IAEA RADIATION TECHNOLOGY SERIES No.

Radiotracer Generators for

Industrial Applications
 IAEA RADIATION TECHNOLOGY SERIES PUBLICATIONS

One of the main objectives of the IAEA Radioisotope Production and Radiation
Technology programme is to enhance the expertise and capability of IAEA Member States
in utilizing the methodologies for radiation processing, compositional analysis and industrial
applications of radioisotope techniques in order to meet national needs as well as to assimilate
new developments for improving industrial process efficiency and safety, development and
characterization of value-added products, and treatment of pollutants/hazardous materials.
Publications in the IAEA Radiation Technology Series provide information in the areas
of: radiation processing and characterization of materials using ionizing radiation, and industrial
applications of radiotracers, sealed sources and non-destructive testing. The publications have
a broad readership and are aimed at meeting the needs of scientists, engineers, researchers,
teachers and students, laboratory professionals, and instructors. International experts assist the
IAEA Secretariat in drafting and reviewing these publications. Some of the publications in this
series may also be endorsed or co-sponsored by international organizations and professional
societies active in the relevant fields.
There are two categories of publications: the IAEA Radiation Technology Series and
the IAEA Radiation Technology Reports.

IAEA RADIATION TECHNOLOGY SERIES

Publications in this category present guidance information or methodologies and analyses

of long term validity, for example protocols, guidelines, codes, standards, quality assurance
manuals, best practices and high level technological and educational material.

IAEA RADIATION TECHNOLOGY REPORTS

In this category, publications complement information published in the IAEA Radiation

Technology Series in the areas of: radiation processing of materials using ionizing radiation,
and industrial applications of radiotracers, sealed sources and NDT. These publications
include reports on current issues and activities such as technical meetings, the results of IAEA
coordinated research projects, interim reports on IAEA projects, and educational material
compiled for IAEA training courses dealing with radioisotope and radiopharmaceutical related
subjects. In some cases, these reports may provide supporting material relating to publications
issued in the IAEA Radiation Technology Series.
All of these publications can be downloaded cost free from the IAEA web site:

http://www.iaea.org/Publications/index.html

Further information is available from:

Marketing and Sales Unit

International Atomic Energy Agency
Vienna International Centre
PO Box 100
1400 Vienna, Austria

Readers are invited to provide feedback to the IAEA on these publications. Information
may be provided through the IAEA web site, by mail at the address given above, or by email to:

[email protected]
RADIOTRACER GENERATORS FOR
INDUSTRIAL APPLICATIONS
 The following States are Members of the International Atomic Energy Agency:

AFGHANISTAN GREECE PAKISTAN

ALBANIA GUATEMALA PALAU
ALGERIA HAITI PANAMA
ANGOLA HOLY SEE PAPUA NEW GUINEA
ARGENTINA HONDURAS PARAGUAY
ARMENIA HUNGARY PERU
AUSTRALIA ICELAND PHILIPPINES
AUSTRIA INDIA POLAND
AZERBAIJAN INDONESIA PORTUGAL
BAHRAIN IRAN, ISLAMIC REPUBLIC OF QATAR
BANGLADESH IRAQ
REPUBLIC OF MOLDOVA
BELARUS IRELAND
ROMANIA
BELGIUM ISRAEL
RUSSIAN FEDERATION
BELIZE ITALY
RWANDA
BENIN JAMAICA
JAPAN SAUDI ARABIA
BOLIVIA
BOSNIA AND HERZEGOVINA JORDAN SENEGAL
BOTSWANA KAZAKHSTAN SERBIA
BRAZIL KENYA SEYCHELLES
BULGARIA KOREA, REPUBLIC OF SIERRA LEONE
BURKINA FASO KUWAIT SINGAPORE
BURUNDI KYRGYZSTAN SLOVAKIA
CAMBODIA LAO PEOPLE’S DEMOCRATIC SLOVENIA
CAMEROON REPUBLIC SOUTH AFRICA
CANADA LATVIA SPAIN
CENTRAL AFRICAN  LEBANON SRI LANKA
REPUBLIC LESOTHO SUDAN
CHAD LIBERIA SWEDEN
CHILE LIBYA SWAZILAND
CHINA LIECHTENSTEIN SWITZERLAND
COLOMBIA LITHUANIA SYRIAN ARAB REPUBLIC
CONGO LUXEMBOURG TAJIKISTAN
COSTA RICA MADAGASCAR THAILAND
CÔTE D’IVOIRE MALAWI THE FORMER YUGOSLAV 
CROATIA MALAYSIA REPUBLIC OF MACEDONIA
CUBA MALI TOGO
CYPRUS MALTA TRINIDAD AND TOBAGO
CZECH REPUBLIC MARSHALL ISLANDS
TUNISIA
DEMOCRATIC REPUBLIC  MAURITANIA
TURKEY
OF THE CONGO MAURITIUS
UGANDA
DENMARK MEXICO
UKRAINE
DOMINICA MONACO
DOMINICAN REPUBLIC MONGOLIA UNITED ARAB EMIRATES
ECUADOR MONTENEGRO UNITED KINGDOM OF 
EGYPT MOROCCO GREAT BRITAIN AND 
EL SALVADOR MOZAMBIQUE NORTHERN IRELAND
ERITREA MYANMAR UNITED REPUBLIC 
ESTONIA NAMIBIA OF TANZANIA
ETHIOPIA NEPAL UNITED STATES OF AMERICA
FIJI NETHERLANDS URUGUAY
FINLAND NEW ZEALAND UZBEKISTAN
FRANCE NICARAGUA VENEZUELA
GABON NIGER VIETNAM
GEORGIA NIGERIA YEMEN
GERMANY NORWAY ZAMBIA
GHANA OMAN ZIMBABWE

The Agency’s Statute was approved on 23 October 1956 by the Conference on the Statute of the
IAEA held at United Nations Headquarters, New York; it entered into force on 29 July 1957. The
Headquarters of the Agency are situated in Vienna. Its principal objective is “to accelerate and enlarge the
contribution of atomic energy to peace, health and prosperity throughout the world’’.
 IAEA RADIATION TECHNOLOGY SERIES No. 5

RADIOTRACER GENERATORS FOR

INDUSTRIAL APPLICATIONS

INTERNATIONAL ATOMIC ENERGY AGENCY

VIENNA, 2013
 COPYRIGHT NOTICE

All IAEA scientific and technical publications are protected by the terms of
the Universal Copyright Convention as adopted in 1952 (Berne) and as revised in
1972 (Paris). The copyright has since been extended by the World Intellectual
Property Organization (Geneva) to include electronic and virtual intellectual
property. Permission to use whole or parts of texts contained in IAEA
publications in printed or electronic form must be obtained and is usually subject
to royalty agreements. Proposals for non-commercial reproductions and
translations are welcomed and considered on a case-by-case basis. Enquiries
should be addressed to the IAEA Publishing Section at:

Marketing and Sales Unit, Publishing Section

International Atomic Energy Agency
Vienna International Centre
PO Box 100
1400 Vienna, Austria
fax: +43 1 2600 29302
tel.: +43 1 2600 22417
email: [email protected]
http://www.iaea.org/books

© IAEA, 2013
Printed by the IAEA in Austria
April 2013
STI/PUB/1579

IAEA Library Cataloguing in Publication Data

Radiotracer generators for industrial applications. — Vienna : International

Atomic Energy Agency, 2013.
p. ; 24 cm. — (IAEA radiation technology series, ISSN 2220–7341 ;
no. 5)
STI/PUB/1579
ISBN 978–92–0–135410–5
Includes bibliographical references.
1. Radioisotopes — Industrial applications. 2. Radioactive tracers.
I. International Atomic Energy Agency. II. Series.

IAEAL 13–00797
 FOREWORD

Radiotracers have been widely used throughout industry to optimize

processes, solve problems, improve product quality, save energy and reduce
pollution. Their technical, economic and environmental benefits have been
recognized by both the industrial and the environmental sectors. The most
important radiotracer techniques have been transferred to many developing
Member States through IAEA Technical Cooperation projects.
However, in spite of their manifest benefits, radiotracer techniques continue
to be underutilized, not only by developing countries but also by more
industrialized nations. There are a number of factors that restrict the usage of the
radioisotope techniques, but chief among them is the timely availability of
suitable radiotracers. Ensuring timely availability of suitable radionuclides is a
main hurdle to the use of radiotracer techniques in industry. For developing
countries that do not possess radioisotope production facilities, the long time
required for import of radionuclides not only completely rules out the use of short
half-life nuclides, but also makes it impossible for the radioisotope applications
teams to respond to problems of an urgent nature. Many possible radiotracer
investigations are not being carried out in developing countries because of this
problem.
Even in industrialized countries, radionuclide supply is often a problem, as
many of the former suppliers of industrial radionuclides have switched their
production facilities to serve the more lucrative radiopharmaceuticals market.
Obtaining continuity of supply of radionuclides with which to carry out extended
studies in difficult-to-access locations, such as offshore oil platforms, is also a
significant challenge.
Making use of tracers from radionuclide generators can alleviate the
difficulties associated with radioisotope supply. Two commercially available
medical radionuclide generators, 99Mo/99mTc and 113Sn/113mIn, have been used for
this purpose, but their use has been restricted because their half-lives are
relatively short and only a limited number of radiotracers derived from them have
been proven under industrial conditions.
Recognizing the potential usefulness of several radionuclide generators,
including 68Ge/68Ga and 137Cs/137mBa and of radiotracers derived from them, the
Agency organized a Coordinated Research Project (CRP) on the Evaluation and
Validation of Radionuclide Generator-based Radiotracers for Industrial
Applications. The objectives of the CRP, which was implemented over the period
2007–2011, was to coordinate the development of industrial radionuclide
generators and to validate generator based radiotracers for use in harsh industrial
conditions. It was anticipated that an important outcome would be the production
of radionuclide generators designed specifically for industrial purposes. Their
cost would be considerably lower than those of medical generators since the high
costs of the facilities required to produce generators suitable for in vivo use can
be avoided.
The IAEA facilitates the transfer of technology, and an important part of
this process is the provision of relevant literature that may be used for reference
purposes or as an aid to teaching. This monograph contains guidelines for the
selection and preparation of radiotracers derived from radionuclide generators, as
well as reports from participants of the CRP. The book has been prepared with
contributions from all CRP participants. The IAEA wishes to express thanks to
all the contributors and especially to T. Bjørnstad and T.S. Charlton for their
contributions to this publication. The IAEA officers responsible for this
publication were Joon-Ha Jin and P. Brisset of the Division of Physical and
Chemical Sciences.
 CONTENTS

1. INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

2. THEORETICAL ASPECTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

2.1. Mother/daughter nuclear relationships

and the Bateman equation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
2.2. Radioactive equilibrium . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
2.2.1. Secular equilibrium . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
2.2.2. Transient equilibrium . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
2.3. Radionuclide generator principle . . . . . . . . . . . . . . . . . . . . . . . . 12
2.3.1. Properties of an ideal IRNG . . . . . . . . . . . . . . . . . . . . . . 13
2.3.2. Additional specific criteria for an IRNG. . . . . . . . . . . . . 14
2.4. Radionuclide generator types . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
2.4.1. Generators based on mother fixed on to
solid support in columns . . . . . . . . . . . . . . . . . . . . . . . . . 18
2.4.2. Column based generator with a heating cap . . . . . . . . . . 21
2.4.3. Radionuclide generators based on separation by
solvent extraction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
2.4.4. Generators based on separation by distillation or
sublimation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
2.4.5. Generators based on cryogenic distillation . . . . . . . . . . . 27
2.4.6. Generators based on chemical precipitation . . . . . . . . . . 30
2.4.7. Generators based on electrochemical separation . . . . . . 32
2.4.8. Generators based on SLM separation . . . . . . . . . . . . . . . 34
2.4.9. Special case: Generator based on electrostatic
radionuclide separation . . . . . . . . . . . . . . . . . . . . . . . . . . 37
2.5. Radiotracer generators based on radionuclide generators . . . . . 39
2.5.1. Design of an IRNG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
2.5.2. Activity requirement . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
2.5.3. Industrial tracing situations . . . . . . . . . . . . . . . . . . . . . . . 43
2.6. Examples of radiotracer generators not based on
a mother/daughter nuclear relationship. . . . . . . . . . . . . . . . . . . . 51
2.6.1. The methyl bromide generator . . . . . . . . . . . . . . . . . . . . 51
2.6.2. Radionuclide generators from on-site activation
with isotropic neutron sources . . . . . . . . . . . . . . . . . . . . 53
2.6.3. Radionuclide (radiotracer) generators based on
on-line use of neutron generators . . . . . . . . . . . . . . . . . . 56
3. SELECTION OF POTENTIALLY USEFUL
RADIONUCLIDE GENERATORS AND PRODUCTION
OF THE MOTHER RADIONUCLIDES. . . . . . . . . . . . . . . . . . . . . . . 58

3.1. Requirements for IRNGs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

3.2. Potentially useful radionuclide generators for industrial
and environmental tracer applications . . . . . . . . . . . . . . . . . . . . 59
3.2.1. General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
3.2.2. Mass attenuation of actual gamma energies . . . . . . . . . . 61
3.2.3. The 44Ti/44Sc radionuclide generator. . . . . . . . . . . . . . . . 62
3.2.4. The 68Ge/68Ga radionuclide generator. . . . . . . . . . . . . . . 70
3.2.5. The 82Sr/82Rb radionuclide generator . . . . . . . . . . . . . . . 83
3.2.6. The 99Mo/99mTc radionuclide generator . . . . . . . . . . . . . 91
3.2.7. The 113Sn/113mIn radionuclide generator . . . . . . . . . . . . . 103
3.2.8. The 137Cs/137mBa radionuclide generator. . . . . . . . . . . . . 109
3.2.9. The 144Ce/144Pr radionuclide generator . . . . . . . . . . . . . . 124
3.2.10. The 172Hf/172Lu radionuclide generator. . . . . . . . . . . . . . 134

4. GUIDELINES FOR USE OF

RADIONUCLIDE GENERATORS FOR
RADIOTRACERS FROM EXPERIMENTS . . . . . . . . . . . . . . . . . . . 139

4.1. Planning a radiotracer experiment . . . . . . . . . . . . . . . . . . . . . . . 139

4.2. Guidelines for transportation of containers of 
radionuclide generators. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 140
4.2.1. The regulatory framework . . . . . . . . . . . . . . . . . . . . . . . 140
4.2.2. Classification of packages. . . . . . . . . . . . . . . . . . . . . . . . 140
4.2.3. Marking and labelling the package
and documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 141
4.3. Guidelines for the evaluation of radionuclide generators . . . . . . 142
4.3.1. Elution of tracer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 142
4.3.2. Elution efficiency and breakthrough test . . . . . . . . . . . . 143
4.3.3. Methods to reduce breakthrough and to increase
the shelf life of radionuclide generators . . . . . . . . . . . . . 144
4.4. Guidelines for preparation of radiotracers from radionuclide
generator based radioisotopes . . . . . . . . . . . . . . . . . . . . . . . . . . . 145
4.5. Guidelines for validation of radionuclide generator based
radiotracers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 147
4.5.1. Thermal stability tests . . . . . . . . . . . . . . . . . . . . . . . . . . . 148
4.5.2. Sorption stability tests. . . . . . . . . . . . . . . . . . . . . . . . . . . 148
4.5.3. Microbial stability tests. . . . . . . . . . . . . . . . . . . . . . . . . . 148
 4.5.4. Partitioning tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 148
4.5.5. Dynamic flooding tests . . . . . . . . . . . . . . . . . . . . . . . . . . 149
4.5.6. Radiochemical purity tests . . . . . . . . . . . . . . . . . . . . . . . 149
4.6. Guidelines for radiological safety in the application of
radionuclide generator based radiotracer . . . . . . . . . . . . . . . . . . 149
4.6.1. Radiation dose considerations for the injection of
radiotracer generators in field tests . . . . . . . . . . . . . . . . . 149
4.6.2. Regulatory framework . . . . . . . . . . . . . . . . . . . . . . . . . . 151

5. PREPARATION OF RADIOTRACERS FROM GENERATOR

PRODUCED RADIONUCLIDES. . . . . . . . . . . . . . . . . . . . . . . . . . . . 153

5.1. Radiotracers from the 68Ge/68Ga generator . . . . . . . . . . . . . . . . 153

5.1.1. Aqueous 68Ga tracers . . . . . . . . . . . . . . . . . . . . . . . . . . . 154
5.1.2. Organic 68Ga tracers . . . . . . . . . . . . . . . . . . . . . . . . . . . . 157
5.1.3. Solid 68Ga tracers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 158
5.2. Radiotracers from the 99Mo/99mTc generator. . . . . . . . . . . . . . . . 159
5.2.1. Aqueous 99mTc tracers . . . . . . . . . . . . . . . . . . . . . . . . . . . 159
5.2.2. Organic 99mTc tracers. . . . . . . . . . . . . . . . . . . . . . . . . . . . 160
5.2.3. Solid 99mTc tracers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 160
5.3. Radiotracers from the 113Sn/113mIn generator . . . . . . . . . . . . . . . 161
5.3.1. Aqueous 113mIn tracers. . . . . . . . . . . . . . . . . . . . . . . . . . . 162
5.3.2. Organic 113mIn tracers . . . . . . . . . . . . . . . . . . . . . . . . . . . 162
5.3.3. Solid 113mIn tracers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 162
5.4. Radiotracers from the 137Cs/137mBa generator. . . . . . . . . . . . . . . 164
5.4.1. Aqueous 137mBa tracers . . . . . . . . . . . . . . . . . . . . . . . . . . 164
5.4.2. Organic 137mBa tracers. . . . . . . . . . . . . . . . . . . . . . . . . . . 165
5.4.3. Solid 137mBa tracers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 165
5.5. Radiotracers from the 44Ti/44Sc generator. . . . . . . . . . . . . . . . . . 165

6. CASE STUDIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 166

6.1. Aqueous phase tracing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 166

6.1.1. Measuring the water intake to a power station
using the 99Mo/99mTc generator . . . . . . . . . . . . . . . . . . . . 167
6.1.2. Studies of the aqueous phase in multiphase flow
in a hydrate loop using a 137Cs/137mBa generator . . . . . . 168
6.1.3. Semi-continuous measurement of effluent flow rate
in open channels using a 137Cs/137mBa generator . . . . . . 169
6.1.4. RTD studies on a hot water sterilizer using
a 99Mo/99mTc generator . . . . . . . . . . . . . . . . . . . . . . . . . . 172
 6.1.5. Industrial emission tomography experiments with
68
Ga and 137mBa . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 174
6.1.6. Investigation of the performance of a sand filter on
a wastewater treatment plant. . . . . . . . . . . . . . . . . . . . . . 177
6.2. Organic phase tracing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 178
6.2.1. Measurement of organic flows using
a 113Sn/113mIn generator . . . . . . . . . . . . . . . . . . . . . . . . . . 178
6.2.2. Tracer studies on a multiphase reactor in
a pilot plant . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 181
6.3. Solid tracing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 182
6.3.1. RTD studies on attritioners in the silica sand
industry using a 99Mo/99mTc generator . . . . . . . . . . . . . . 182
6.3.2. Visualization of water and sludge flows through a
clarifier using a 113Sn/113mIn generator . . . . . . . . . . . . . . 184
6.4. Gas tracing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 186
6.4.1. A radiotracer pig test for leak inspection
in an underground gas pipeline . . . . . . . . . . . . . . . . . . . . 186

REFERENCES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 191
BIBLIOGRAPHY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 201
CONTRIBUTORS TO DRAFTING AND REVIEW . . . . . . . . . . . . . . . . . 203
 1. INTRODUCTION

Radiotracer technology is used in industry to optimize processes, solve

problems, improve product quality, save energy and reduce pollution. Creative
application of radiotracer methodology may contribute to the economic
development and technological advancement of all countries. The evolution of
radiotracer technologies has been influenced by enormous developments in
radiotracer preparation techniques, production of a wide range of radionuclides of
varying half-lives, radiation detection techniques, data processing and
visualization practices. Over the years, the IAEA has contributed to the
development of radiotracer technology and its transfer to developing Member
States. Significant progress has been made, enabling the countries to establish
national radiotracer groups, and the most important industrial radiotracer
techniques have been transferred to many developing Member States through
IAEA Technical Cooperation projects.
The rapid progress in radiotracer investigations realized over the past two
decades has stimulated broad interest in the use of short lived gamma emitting
radionuclides, as many industrial radiotracer applications typically require
tracing the radioactivity for a few minutes to several days. In some cases where
gas transport is involved, transit times down to seconds must be measured.
However, tracers based on long lived radionuclides have often been used in such
applications owing to the difficulty and expense involved in obtaining shorter
lived radiotracers. Consequently, at the completion of the tests, residual
radioactive nuclides are discharged into commercial products or into
environmental waters, or they must be stored safely until the radioactivity dies
away. Although the quantities of discharged radionuclides are small (typically
less than megabecquerel amounts), government regulations must nevertheless be
strictly adhered to. It would be much more satisfactory to use shorter lived
radiotracers whenever possible.
In cases where particularly high radioactivity is required, the use of short
lived radionuclides is a distinct improvement on the use of long lived
radionuclides. Because they decay quickly, they are more acceptable in these
days of concern over radioactive contamination of the environment. Additionally,
by using short lived tracers, it is possible to repeat measurements at intervals
without having to worry about the activity remaining in the system from the
previous test.
Although the potential of short half-life gamma emitting radionuclides for
industrial tracer investigations is high, there are practical problems associated
with their use. Essentially, they can be used only in locations close to their places
of manufacture, since their short half-life limits the transportation time and thus

1
the shipping distances. Timely availability of short lived radiotracers at the
investigation site is one of the main hurdles that prevent the widespread
utilization of short lived radioactive tracers in industry.
Industrial radiotracer generators (IRTGs), based on industrial radionuclide
generators (IRNGs), could be an attractive option for obtaining the desired
radiotracer, at or in close proximity to the industrial investigation site, as
required. Such generators remove the dependence on proximity to radioisotope
production facilities. Another advantage is the ease with which the daughter
product (short lived radionuclides) can be separated on demand and converted
into a radiotracer by some tailor-made labelling procedure on-site. Radionuclide
generators also represent a cost effective strategy to ensure a continuous and
reliable supply of short lived radionuclides for radiotracer investigations. This
facilitates work at remote locations and also makes possible the provision of a
rapid response service for problems of an urgent nature.
Radionuclide generators have been in existence for over 50 years, and are
widely used for the production of radiopharmaceuticals. In spite of their
extensive use in hospitals over the years, commercially available medical
radionuclide generators have limited applications in industrial and environmental
radiotracer studies because of their relatively short shelf lives and the relatively
low energies of the gamma rays from their daughters.
Additionally, concern has also been expressed regarding their use under
harsh industrial and environmental conditions where the effects of the
temperature, pressure, pH and chemical composition of the process streams may
impact adversely on their performance. These potential weaknesses substantially
limit the industrial applicability of the radiotracers produced from the generators
used in nuclear medicine.
Large scale use of short lived radionuclides in radiotracer application
requires that IRNGs should be available. The issues that need to be addressed in
fabricating IRNGs are different from those associated with the manufacture of
medical generators. In the development of IRNGs, it is essential to utilize mother
radionuclides with long physical half-lives of months or years to meet problems
related to the logistics of storage and transportation. The production of the
radionuclide generator, selection/development of sorbent material, construction
of the generator system, devising a chemical method for the separation of the
daughter radionuclide from its mother radionuclide and the post-elution chemical
manipulation of the daughter radionuclide are factors that should be addressed
adequately while developing IRNGs and IRTGs. Furthermore, IRNGs and IRTGs
must meet regulatory and quality control requirements. Though several forms of
radionuclide generator systems for medical applications have been reported in the
literature, the column chromatographic system is most suitable for use in
industrial applications as it can readily be adapted for use in harsh environments.

2
 It is anticipated that IRNGs will be inexpensive in comparison to medical
radionuclide generators, as there is no need to adhere to the stringent
pharmaceutical regulatory requirements. A major deterrent to the use of IRNGs at
the present time is their commercial unavailability. The commercial production of
IRNGs is perceived to be economically unattractive, as the numbers that are
likely to be required are relatively small. As a result, there are very few
companies around the world that currently supply IRNGs, and the number is, if
anything, decreasing. A practical solution to these problems is to use the expertise
and facilities of Member States to develop and validate a few selected IRNGs in
order to encourage their utilization in industrial radiotracer studies.
To address the need of IRNGs for radiotracer investigation, the IAEA
implemented a Coordinated Research Project (CRP) on the Evaluation and
Validation of Radioisotope Generator-based Radiotracers for Industrial
Applications from August 2007 to March 2011. The aim of the CRP was to create
technical capabilities in developing countries for the fabrication and use of
IRNGs for radiotracer application.
The production of the selected IRNGs requires basic infrastructure such as
shielded processing facilities, quality control laboratories and waste handling
facilities, which are generally available at national or regional facilities. To
ensure wide use of the generators in industrial radiotracer applications, the
physical properties of the daughter radionuclide and the chemical and physical
properties of its labelled compounds should be suitable for a large variety of
applications. In many cases, it is necessary to provide specific tracers for specific
applications. Once produced, the radiotracer must be validated at the conditions
under which it is to be used.
The specific objectives of the CRP were:

• Development of radiotracers from IRNG based radionuclides;

• Development of portable systems for production of radiotracers (IRTGs)
using IRNG based radionuclides;
• Provision of guidelines for preparation and validation of IRNG based
radiotracers;
• Development of techniques for enhancing the long term stability of IRNGs.

The CRP succeeded in developing a few useful IRNGs and protocols for the
preparation and validation of a number of IRNG based radiotracers. Since it is
advisable to minimize manual handling in the labelling process, the development
of integrated and automatized labelling procedures to produce IRTGs has been a
topic of interest. This technology can be utilized by Member States.
Although many mother/daughter pairs have the potential to be used as
radionuclide generator systems, only a few were selected for evaluation. The

3
selection was made on the basis of half-lives, radiation type and energy and on
ease of production and labelling. This publication describes the results of
research undertaken in the utilization of 68Ge/68Ga, 137Cs/137mBa, 99Mo/99mTc and
113
Sn/113mIn generators for radiotracers. This includes development of column
materials, development of protocols for the elution of the daughter radionuclide,
evaluation of the generators for extended periods of time, preparation of aqueous,
organic and solid tracers and quality control of the radiotracers in laboratory
experiments conducted under simulated industrial conditions. In addition, some
attention has been given to 44Ti/44Sc, 144Ce/144Pr and 172Hf/172Lu generators.
This publication is the output of the work carried out at participating
institutions in several Member States under the mandate of the CRP. This
publication provides a unique source of information pertaining to the
development and use of IRNGs, preparation of radiotracers, IRTGs, and their use
in troubleshooting and optimizing industrial processes. The report will generate
awareness in the radiotracer community and could be a suitable technology
resource for guidance in research, development and applications.
This publication is organized into six sections. Section 1 provides an
introduction and Section 2 deals with the theoretical aspects of mother/daughter
nuclear relationships, radionuclide generator principles, mother/daughter
separation approaches and radiotracer generators. Section 3 provides the nuclear
characteristics of several IRNGs, their area of usefulness and limitations. It
describes the production and processing of the parent species required for
preparation of radionuclide generator systems of current interest. Section 4
provides information relating to the methodology of preparing tracers from the
generator derived radionuclides, together with quality assurance guidelines.
Section 5 provides general guidelines for chemical preparation of radiotracers
from the generators, validation of the generators and safety aspects of their
transportation and use. These guidelines should be followed as far as possible.
The need for chemical manipulation of the eluted compound is also discussed.
Several procedures are described, some of them being sufficiently mature to be
adopted for industrial applications. Section 5 also discusses experience in the use
of available IRNGs. Section 6 uses case studies to illustrate the validation of
IRNGs in the laboratory and their use in the industrial environment. The case
studies described in this section are concerned with typical problems in industry
and the environment encountered in all countries.
The information contained herein should enable the reader to understand
the routes of production, handling and quality evaluation of IRNGs and IRTGs.
The references included in individual sections will be very useful to tracer groups
for preparing documentation on the production and/or use of generator systems.
Commercial availability of IRNGs and IRTGs will ensure timely accessibility of

4
radiotracers based on short lived radionuclides and help Member States to realize
more fully the economic benefits to be derived from radiotracer technology.

2. THEORETICAL ASPECTS

2.1. MOTHER/DAUGHTER NUCLEAR RELATIONSHIPS

AND THE BATEMAN EQUATION

A nuclear mother/daughter relationship consists of a radionuclide (mother)

that, upon radioactive decay, produces another, but shorter lived, daughter
radionuclide (i.e. T1/2(mother) > T1/2(daughter)). The nuclear chart contains more
than 110 mother/daughter nuclear relationships from the lightest, 28Mg/28Al, to
the heaviest below uranium with some practical use, 234Th/234mPa. Some of them
may be useful for industrial purposes.
The decay process is illustrated in the schematic and simplified decay
scheme in Fig. 1. The mother radionuclide is indexed by 1, the daughter
radionuclide is indexed by 2 and the granddaughter indexed by 3.
In this decay scheme, N(t) is the number of mother radionuclides at time
t = t, N(0) is the initial number of mother radionuclides at time t = 0, D(t) is the

FIG. 1. Simplified decay scheme of a radionuclide generator illustrating the decay of the
mother into the daughter and further into the granddaughter.

5
disintegration rate at time t = t, D(0) is the disintegration rate at time t = 0, T1/2 is
the half-life of the nuclide and λ is the decay constant, λ = ln2/T1/2.
The mathematical relationship between the parameters is described by the
Bateman equation. The Bateman equation is not a single equation; rather, it is a
method of setting up differential equations describing the decay in the chain of
interest.
For the first derivation, it is supposed that N2(0) = 0 and N3(0) = 0 and that
the granddaughter product is stable, which is the case for most useful
radionuclide generators. The stability of the granddaughter is characterized by the
fact that λ3 = 0.
Then, one can set up the following differential equation for the decrease of
the number of parent nuclides as a function of time:

dN 1 (t )
= -1 N 1 (t ) (1)
dt

The solution of Eq. (1) leads to the well-known decay equation of a single
radioactive nuclide, i.e.:
-1t
N 1 (t ) = N 1 (0)e (2)

Since the disintegration rate is defined by:

D1 (t ) = 1 N 1 (t ) (3)

it follows from Eqs (2) and (3) that:

D1 (t ) = D1 (0)e -1t (4)

Similarly, one may set up a differential equation for the number of daughter
nuclides at any time t. Supposing that the only source of the daughter nuclide is
from decay of the mother nuclide, i.e. N2(0) = 0, then:

dN 2 (t )
= 1 N 1 (t ) -  2 N 2 (t ) (5)
dt

6
 Equation (5) describes the rate of change of the daughter nuclides that is
equal to the supply by the decay of the mother and diminished by the rate of loss
through its own decay. The solution of this equation results in the following
expression:

1
N 2 (t ) = N 1 (0)
 2 - 1
(e -1t - e -2t ) (6)

In analogy with Eq. (4):

2
D 2 (t ) = D1 (0)
 2 - 1
(e -1t - e -2t ) (7)

For the sake of completeness, the corresponding equations for the

granddaughter will also be provided. Equation (7) describes the rate of change of
the number of atoms of the granddaughter fed only by the decay of the daughter.
Since the granddaughter is stable, the number of atoms is continuously
accumulating:

dN 3 (t )
=  2 N 2 (t ) (8)
dt

The number of stable granddaughter nuclides at any time t will then be the
initial number of mother nuclides minus the remaining number of mother
nuclides at time t minus the existing number of daughter nuclides at time t,
expressed by:

N 3 (t ) = N 1 (0) - N 1 (t ) - N 2 (t ) (9)

Introducing Eqs (2) and (6) gives:

1
N 3 (t ) = N 1 (0) - N 1 (0)e -1t - N 1 (0)
 2 - 1
(e -1t - e -2t ) (10)

7
 Rearranging Eq. (10) gives:

⎡ ⎤
N 3 (t ) = N 1 (0) ⎢⎢1 −
1
(2
 e −1t
−  e )⎥
− 2t ⎥
(11)
⎣  2 − 1
1
⎦

For more information on these subjects, see Refs [1–3].

2.2. RADIOACTIVE EQUILIBRIUM

Equilibrium is a condition established in a mother/daughter mixture when

both mother and daughter are radioactive and when the daughter’s half-life is
shorter than that of the mother. If the daughter’s half-life exceeds that of the
parent, equilibrium will never be reached. There are two types of equilibrium:
secular and transient.

2.2.1. Secular equilibrium

Strict definitions of secular and transient equilibria hardly exist. However, it

may be regarded that if T1/2,1 >> T1/2,2, a condition of secular equilibrium exists.
This means that the activity of the mother radionuclide does not decrease
measurably during a reasonable period of time, i.e. subsequent elutions of the
daughter with equal spacing in time will yield the same daughter activity
(provided the elution efficiency stays constant). This situation for the general case
is illustrated in Fig. 2.
A practical example is illustrated in Fig. 3, which shows the activities
(disintegration rates) in becquerels for the mother and the daughter nuclides and
their activity ratios for the generator system 137Cs/137mBa, which is an example of
secular equilibrium. Here, T1/2(137Cs) = 30 a and T1/2(137mBa) = 2.55 min, giving a
half-life ratio of T1/2(137Cs)/T1/2(137mBa) = 6.18 × 106.
In the equilibrium mixture, the daughter appears to decay with the half-life
of the parent. When the daughter is isolated from the mixture, it has its own
expected half-life. Perhaps the simplest explanation for their appearing to be
equal is that the daughter cannot decay until it is formed, and so the rate of
formation of the daughter equals the rate of decay of the parent, which is very
slow.
Thus, in secular equilibrium, mixture activity of the mother stays
approximately constant while the daughter activity grows to a constant value.
Correspondingly, their ratio (mother/daughter) decreases in the beginning and

8
 Instantaneous
elution
of daughter
FIG. 2. Illustration of growth of daughter activity with subsequent ‘instantaneous’ elutions
at equal time intervals in a generator system under secular equilibrium.

FIG. 3. Activity of mother (137Cs) and daughter (137mBa) and ratio of their activities (right axis)
for a 137Cs/137mBa generator where the initial number of 137Cs radionuclei has been set to
N1 = 1015.

9
approximates a constant value after a time t > 10T1/2,2. Often, one says that for
secular equilibrium, Eq. (6) may be simplified to:

1
N2 » ⋅ N 0 ⋅ e -1⋅t (12)
 2 - 1 1

since T1/2,1 >> T1/2,2  λ1 << λ2  exp(−λ1t) >> exp(−λ2t) so that the last
exponential can be neglected. This leads again to:

N 1  2 - 1
» (13)
N2 1

and

D1 (t )  2 - 1
» (14)
D 2 (t ) 2

This expression is only strictly valid for t > 10T1/2,2. For t >> 10T1/2,2 and
T1/2,1 >> T1/2,2, λ1 in Eq. (14) can be omitted, and the ratio of the disintegration
rates is ~1.

2.2.2. Transient equilibrium

If T1/2,1  T1/2,2, i.e. the half-life of the mother is not several orders of
magnitude larger than the half-life of the daughter and, in addition, the mother
decays considerably during the period of application, then transient equilibrium is
established. This situation is illustrated generally in Fig. 4.
In order to exemplify transient equilibrium, the mother/daughter
relationship 72Se/72As is chosen.
Figure 5 illustrates the activities in becquerel for the mother (D1) and the
daughter (D2) nuclides and their activity ratios. Here, T1/2(72Se) = 8.5 d and
T1/2(72As) = 26.0 h, giving a half-life ratio of T1/2(72Se)/T1/2(72As) = 7.85.
There is a rule of thumb regarding how long it takes to reach equilibrium:

• Transient equilibrium is reached in ~4T1/2,2;

• Secular equilibrium is reached in ~6T1/2,2.

10
FIG. 4. Illustration of growth of daughter activity with subsequent ‘instantaneous’ elutions
at equal time intervals in a generator system under transient equilibrium.

FIG. 5. Activity of mother ( 72Se) and daughter ( 72As) and the ratio of their activities for
a 72Se/ 72As generator where the initial number of 72Se radionuclei has been set to N1 = 1015.

The activity of the daughter radionuclide obtained per elution cycle (batch)
is the main parameter for the application of a generator system. The activity of the
daughter radionuclide generated at a given time can be calculated using the above

11
equations. However, the useful amount of activity for a radiotracer experiment
also depends on the elution efficiency of the generator as well as the chemical
yield in the labelling process, as will be illustrated later.
It should also be mentioned here that in real applications, interest is focused
mainly on the gamma decay rate of a certain gamma energy than on the total
disintegration rate of the daughter radionuclide. The gamma intensity (or gamma
yield) can be found in decay schemes for the individual radionuclides, for
instance, in the ‘Table of Isotopes’ [4] for the different gamma energies.
Such intensities for single gamma lines of special interest following beta
decay range between 50 and 100%. For + decay, the intensity can reach 200%
for the 511 keV annihilation radiation, here defined by the + branching ratio. It is
now possible to define a gamma activity, A, for a special gamma line. The shape
of the gamma activity line is identical to the shape of the daughter activity in
Figs 2 and 4, and is derived by multiplying these activities by the proper gamma
intensity.

2.3. RADIONUCLIDE GENERATOR PRINCIPLE

A radionuclide generator is a self-contained system housing a

mother/daughter mixture in equilibrium and designed to produce a daughter
radionuclide formed by the decay of a mother radionuclide free from
contamination of the mother [5–7]. The mother/daughter nuclear relationships
offer the possibility to make radionuclide generators to separate the short lived
daughter at suitable time intervals. For practical reasons, most radionuclide
generator systems that can be used for industrial radiotracer applications involve
secular equilibrium, where the parent radionuclide has a half-life significantly
longer than that of the daughter. This scenario permits long shelf life of the
generator.
There must be a method of removing the daughter and leaving the mother
behind to regenerate more daughter activity. The daughter radionuclide is a
different chemical element to the mother, and will therefore exhibit chemical and
physical properties different from those of the mother. With this difference in
characteristics between mother and daughter radionuclides, the latter can usually
be separated by chemical or physical means. It is said that the daughter is eluted
from the generator (a radionuclide generator is also commonly called a ‘cow’ and
the elution process ‘milking of the cow’). Once the activity of the daughter is
recovered, there is a growth of the daughter activity on the generator until it again
reaches equilibrium with the mother. This separation and growth can be
continued as long as there are useful amounts of the parent radionuclide
available, and the breakthrough of the mother stays within acceptable limits.

12
Thus, the useful shelf life of a radionuclide generator depends mainly on the half-
life of the mother and on the radiation resistance of the generator constituents.
Separation may be performed before equilibrium is reached, and the amount of
daughter activity recovered will depend on the time elapsed since the last
separation. In most cases, the generator can be eluted after 1–2 half-lives of the
daughter; 50–75% of the equilibrium activity has then been generated.

2.3.1. Properties of an ideal IRNG

An ideal IRNG should possess the following properties [8, 9]:

• The chemical and/or physical properties of the daughter must be different

from those of the mother to permit efficient separation of daughter from
mother.
• The separation of the daughter radionuclide should be easy and efficient
using appropriate chemical or physical techniques.
• The daughter radionuclide separation should involve no violent chemical
reactions.
• Human intervention in generator operation should be minimal to minimize
radiation dose.
• The daughter radionuclide to be used as a tag on tracers for radiotracer
investigations should be short lived and gamma emitting.
• In any case, a gamma emitter with a high gamma branching ratio is
desirable.
• The elution yield and purity of the daughter radionuclide should be within
the acceptable range.
• The physical half-life of the parent should be long enough for extending the
shelf life of the generator.
• The generator constituents (i.e. eventual column packing material, liquids
involved, tubings and fittings) should be radiation resistant.
• The daughter chemistry should be amenable to the preparation of a wide
variety of compounds for radiotracer applications (such as water tracing, oil
tracing, particle tracing, etc.).
• Shielding, handling and transportation of the generator, even across
national borders, should be straightforward.
• The granddaughter should be stable (or very long lived) to limit concern
about site contamination, environmental persistence and waste disposal
issues.

13
2.3.2. Additional specific criteria for an IRNG

Although many parent/daughter pairs have been evaluated as radionuclide

generator systems in a clinical context, only a few generators are suitable for
routine industrial and research use. While selecting parent/daughter pairs, the
following criteria need to be satisfied [8, 9]:

• Half-life of the mother radionuclide: It is important to select a generator

with an appropriately long half-life of the mother radionuclide. A generator
that remains useful for a period of several months to a year or more may be
appropriate for industrial applications. In some cases, it should be possible
to install the generator ‘permanently’, for instance, to monitor the
operations of a multiphase separator over time.
• Half-life of the daughter radionuclide: The daughter radionuclide should
have a half-life that is compatible with the duration of the radiotracer study.
Half-lives in the range of several minutes to several hours or more are
useful for most fluid and particle industrial tracing operations. For cases
involving tracing of gas transport, transit times of the order of seconds may
be expected, and radiotracers with half-lives of the order of minutes are
most useful. However, the present document has no special focus on gas
monitoring.
• Type and energy of radiation of daughter radionuclide: Gamma ray
emitting radionuclides are preferred for most industrial applications
because of the ability of gamma radiation to penetrate the wall of a vessel or
pipeline. For some investigations, a simple gamma ray spectrum
(containing one single photo peak) is desirable (for instance, in simple
residence time distribution (RTD) experiments, flow rate monitoring, etc.).
In other types of investigation, two or more gamma rays with a certain
energy difference are desirable (when depth information, for instance, from
a chemical reaction vessel, is required).
• Availability and cost of mother radionuclide: An ideal situation would be if
the selected radionuclide generators (see later) were commercially
available. However, in most cases, they are not at the present time, and will
probably not be (in industrially suitable versions) for the foreseeable future
since the global market probably is too small. The minimum requirement is
then that the mother radionuclides should be readily producible in reactors
or cyclotrons at reasonable costs.

In line with the criteria cited in paragraphs 2.3.1 and 2.3.2, some nuclear
genetic relationships have been found to be suitable for production of IRTGs.
Some potential generators are listed and specified in Table 1.

14
 TABLE 1. POTENTIAL RADIONUCLIDE GENERATORS FOR INDUSTRIAL RADIOTRACER APPLICATIONS

Mother nuclides Daughter nuclides

Radionuclide generator Applicationsa
Production Half-life Decay mode Main E (keV) Half-life Decay mode Main E (keV)
44 45
Ti/44Sc Sc(p,2n)44Ti 60 a EC 67 (94.4%), 3.93 h + 511 (188.7%), –
78 (96.0%) 1157 (99.9%)
68 69
Ge/68Ga Ga(p,2n)68Ge 270 d EC No  1.135 h + 511 (178.3%), –, 
1077 (3.2%)
82
Sr/82Rb Mo(p,spall.) 25.6 d EC No  1.273 min + 511 (190.9%), –, 
85
Rb(p4n)82Sr 776 (15.1%)
99
Mo/99mTc Fission product 60 h − 740 6.00 h  141 (89.4%) –, 
113 112
Sn/113mIn Sn(n,)113Sn 115 d EC No  1.65 h  392 (64.1%) –, 
137
Cs/137mBa Fission product 30.0 a − No  2.55 min  661 (90.1%) –, 
144
Ce/144Pr Fission product 285 d − 133 17.3 min  696 (1.34%) –, 
172 173
Hf/172Lu Ta(p,2n)172Hf 1.87 a EC 24, 125 6.7 d  1093 (63.0%) –, 

Note: Intensities taken from Nuclear Data Evaluation Research, Japan Atomic Energy Agency Group, http://www.ndc.jaea.go.jp/NuC/index.html,
modified on 2011/05/09.
a
 Flow rate measurement,  residence time distribution measurement,  leak detection and location,  mixing study,  mass balance,
 positron emission tomography,  single particle tracing,  sediment transport study,  nuclear science education.

15
 After further evaluation of the existing and potential generators and the
anticipated demands for industrial investigations, it was decided to put most
emphasis on the following three radionuclide generators: 68Ge/68Ga, 113Sn/113mIn
and 137Cs/137mBa. In addition, some attention has been paid to 44Ti/44Sc,
99
Mo/99mTc, 144Ce/144Pr and 172Hf/172Lu.
In recent decades, the majority of developments of radionuclide generators
has been mainly driven by the need for new short lived radiopharmaceuticals,
both for diagnostics and therapy in nuclear medicine. The methods and
techniques developed are, of course, tailor-made for the physical, microbiological
and chemical system of the human body. Thus, the technology developed on
generator design, chemical form of the eluted radionuclides and the tracer
molecules derived from these radionuclides cannot necessarily be applied for
other purposes.
In the paragraphs below, a survey of different radionuclide generator types
are given.

2.4. RADIONUCLIDE GENERATOR TYPES

A radionuclide generator makes available a daughter radionuclide produced

from the decay of a parent radionuclide. The goal is to acquire the daughter
radionuclide from the parent with a sufficiently large decontamination factor
DF = NM/ND, where NM and ND are the number of atoms of the mother and the
daughter, respectively, in the purified daughter radionuclide fraction. In general,
the DF should be in the range 10−5 to 10−7. There are technical and environmental
arguments for these numbers: with regard to the quality of most industrial
investigations, a DF of 10−5 can be readily accepted.
Environmental considerations may require lower limits of mother
breakthrough. The required decontamination factor may depend on the nature of
the mother radionuclide. If the mother is not very long lived and decays
exclusively by electron capture, a decontamination factor in the lower end may be
acceptable.
In principle, a radionuclide generator system designed for use in industrial
radiotracer applications should be simple, give reproducible mother/daughter
separation results and provide a high yield of the daughter radionuclide.
There are various radionuclide generator principles. Some of them are listed
below:

• Mother fixed on solid support in column (ion exchanger/reversed phase),

elution of daughter by simple aqueous solution (salinity, pH).

16
• Mother on solid support in column, elution by aqueous phase with
complexing agent (plus salinity and pH), to ease removal of daughter
radionuclide, possibly extractable into organic solution.
• Mother on solid support in column, elution by organic solution, possibly
with complexing agent to convert daughter directly into a complex
extractable into organic solution.
• Mother on solid support in column, elution by cold, hot or wet air (gas) to
produce the daughter as a gas tracer.
• Mother on solid support in column, elution by hot air (gas) to volatilize the
daughter, which may be converted by chemistry to aqueous, organic or
solid tracer.
• Mother dissolved in liquid (organic), separation of daughter by
liquid–liquid extraction, whereupon the daughter may be converted to
various types of tracers.
• Mother as a gas and the daughter, which may have a much lower vapour
pressure, precipitating on container walls. Mother and daughter are then
separated by cryopumping followed by conversion of daughter to various
tracer types.
• Mother dissolved in aqueous solution. Separation of the daughter is
achieved by selective precipitation with carrier.
• Mother dissolved in aqueous solution. Separation of the daughter is carried
out by electrodeposition.
• Mother dissolved in aqueous solution. Separation of the daughter
performed by electrolysis.
• The supported liquid membrane (SLM) generator where the mother is
dissolved in an aqueous solution and separation of mother and daughter
takes place over a passive extracting membrane between the mother
radionuclide reservoir and an extraction liquid reservoir.
• Generator involving a gaseous component in the decay chain where
separation is achieved by electrostatic attraction on a cathode in the gas
phase.
• Generators not based on a mother/daughter relationship, but on use of a
small isotropic neutron source for production of short lived radionuclides
by neutron irradiation, separation of reaction products by chemical or
physical methods.

Some of these principles are briefly described below.

17
 FIG. 6. Principle of a column based radionuclide generator.

2.4.1. Generators based on mother fixed on to solid support in columns

The most common radionuclide generators are based on sorption of the

mother radionuclide on a column support material with subsequent and selective
elution of the daughter radionuclide from the column with some elution agent
(Fig. 6) while the mother remains on the column support. This category includes
those mentioned above. Both organic and inorganic supports are used. The most
common organic supports are cation and anion exchanger materials based on
styrene–divinylbenzene co-polymer with ionogenic groups such as –SO3H and
–N(CH3)3Cl, respectively.
Here, the H+ and Cl− are exchangeable with other cations and anions,
respectively. Inorganic materials are most often stable (or even refractory) metal
oxides like Al2O3, TiO2, MnO2, ZnO, SnO, SnO2, etc., but other types of material
are used as well.
For high activity generators, which are intended for a long shelf life
(say >100 d), it is important that radiation damage on the support material by
radiolysis is kept at a minimum. In these cases, inorganic material is preferred
whenever possible.
When performing parent/daughter separation, there are many aspects that
must be considered: separation scheme, column type, column dimension,
chemical nature of the mobile phase, species of interest, sample throughput and

18
reagent usage for elution of daughter radionuclide [9]. This technique offers the
following advantages:

• Selectivity: Separation selectivity is ensured by the selection of a suitable

separation scheme.
• Sensitivity: High sensitivities down to the picomol range could be achieved,
which is extremely important in using carrier free mother radionuclide.
• Speed of separation: The time necessary to perform the separation becomes
an increasingly important aspect because of the short half-life of the
daughter radionuclide.
• Operational simplicity: A major advantage of this technique in contrast to
other techniques is its technical simplicity that not only reduces the
radiation exposure to the operating personal, but also precludes the site
contamination in an operational set-up.
• Stability of the separator columns: The stability of separator columns very
much depends on the chemical nature of the packing material being used
and the radiation characteristics of the mother and daughter radionuclides
(alpha and high energy beta decay is more detrimental than EC decay). The
shelf life also depends on the storage conditions (if possible, long time
storage of the generator should be carried out with the column in a dried-out
form in order to reduce degradation due to radiolysis of the liquid with
formation of very reactive radicals).
• Frequent elution repeatability: The system can be operated repeatedly
during the shelf life of the generator, and the operations can readily be made
automatic if required.
• Product reproducibility: Product reproducibility can be excellent, provided
that measures are taken to ensure standardization in the elution procedure
and high radiation stability of the column material.
• Elution performance: This system provides unmatched performance in
terms of yield and ensures high chemical and radiochemical purity of the
daughter radionuclide.

Normally, elution liquids contain no carrier of the daughter radionuclide.

Thus, the daughter radionuclide product will be of high specific activity and is
referred to as ‘carrier free’. In some cases, the elution and the following
chemistry may be eased by addition of a certain amount of stable elemental
carrier. Generators of this type are small in size and simple to build, and the
daughter radionuclide is availed by a simple elution process. A schematic
diagram of a column chromatography generator system appropriate for industrial
radiotracer applications is shown in Fig. 7.

19
FIG. 7. Schematic diagram of a column based radionuclide generator with a small column
system to the left and the column placed in a lead shield to the right [10].

Other column based methods, where the column itself constitutes the
generator or where the column separation plays a major role in separating
mother and daughter, may, in principle, also include extraction chromatography,
partition chromatography, adsorption chromatography and gel permeation
chromatography in various forms.
Novel extraction chromatographic resins exhibiting enhanced parent metal
ion retention capacity, excellent selectivity, improved radiation and chemical
stability offer promise in the development of radionuclide generators [11].
Although extraction chromatography has been shown to provide a means of
performing a number of separations of potential use in radionuclide generator
systems, the application of the technique to generator development has thus far
been limited.
For partition and adsorption chromatography, many of the same arguments
may be applied.
Low capacity, limited radiation stability, long term instability of the column
under harsh industrial conditions and bleeding organic impurities under repeated
elution are among the factors that inhibit its wide scale applicability for the
preparation of IRNGs.

20
FIG. 8. Principle of a column based radionuclide generator with a high temperature heating
cap [8].

Gel permeation chromatography has already, to some extent, been

developed for generator production of radionuclides [12, 13], but is not
considered further in the present publication.

2.4.2. Column based generator with a heating cap

A variation of the generator type described above is the case where the
daughter product is not a gas, but may still be evaporated from the column at
elevated temperatures (up to >1000C). The requirement is that the daughter
element has a considerably higher vapour pressure than the mother element in the
form in which it is bound to the column material. This kind of separation
principle has been developed for laboratory studies but, to our knowledge, has not
yet been implemented in radionuclide generators. One example may be the
generator 128Ba/128Cs where the mother nuclide is fixed in a ceramic column
packing material as BaO, and Cs is removed by evaporation at T > 1000C. The
principle is sketched in Fig. 8.

21
FIG. 9. Illustration of a solvent extraction generator with continuously flowing organic and
aqueous phases [10].

2.4.3. Radionuclide generators based on separation by solvent extraction

Solvent extraction is a technique in which an organic solvent, with or

without an extractant, is used to separate the daughter radionuclide from its
mother [14].
The method is based on the relative solubility of the mother and the
daughter radioelements in two immiscible liquids, usually water and an organic
solvent. After agitation for a sufficient length of time, the layers are allowed to
separate. If the aqueous phase originally contains the mother, the organic liquid,
now containing the daughter radionuclide, is removed, and the aqueous layer
containing the mother radionuclide is kept for subsequent daughter recovery.
It is also possible for the mother radionuclide to be dissolved in the organic
phase. In this case, the daughter would be stripped into the aqueous phase for
further processing. The principle of the process is illustrated in Fig. 9 for a
generator that is based on continuously flowing liquids and on-line phase
separation (either by mixer settlers or by continuously operating centrifuges).
In order to optimize separation, complexing agents may be added to the
aqueous phase and extraction agents to the organic phase, and, most often, pH,
ion strength and temperature are important parameters to consider. The separation

22
of mother and daughter is governed by their respective distribution ratios in the
selected organic–aqueous system. The distribution ratio D for a chemical species
is defined as:

(C M )org (C D )org
DM = and D D = (15)
(C M )aq (C D )aq

where CM and CD are, respectively, the concentrations of the mother and the
daughter radionuclides (expressed by their activities corrected for decay and
gamma branching ratios), in the organic (org) and aqueous (aq) phases.
In the case where the mother radionuclide is dissolved in the aqueous phase,
a good separation is achieved in one separation step if, for instance, DD > 100 and
DM < 0.01. If the mother nuclide reservoir consists of the organic phase, a good
separation is obtained in one separation step if DM > 100 and DD < 0.01.
An example of the first situation is the separation of 144Pr from 144Ce (the
144
Ce/144Pr generator) where 144Ce is dissolved in the aqueous phase. This can
be achieved by extraction of 144Ce4+ with, for instance, diethylhexyl
orthophosphoric acid (HDEHP) dissolved in an organic (kerosene) solvent
from an aqueous and weak acidic (HNO3) solution. The 144Pr3+ will remain in
the aqueous phase.
A variation of the extraction method is illustrated in Fig. 10. In this
example, the mother radionuclide is dissolved in an aqueous solution that is
slightly acidified in order to avoid hydroxide formation of metal cations. After
growing-in of the daughter to an acceptable level, the aqueous solution is
percolated through a column where the column support has been impregnated
with an organic phase containing an appropriate extracting agent for the daughter.
In this process, the daughter nuclides will be sorbed in a narrow band near the top
of the column, together with traces of the mother nuclide. The exit solution from
the column containing the mother is pumped back to the mother nuclide reservoir.
In order to purify the daughter fraction, there are two alternative routes to
follow:

(i) An elution liquid is applied that effectively removes (strips) any remaining
mother activity from the column, leaving pure daughter activity in a
somewhat broadened distribution on the column. The daughter is then
removed from the column and dissolved into an aqueous phase by stripping
with (often) more acidic solution.

23
FIG. 10. Illustration of a generator where the mother nuclide is in an aqueous phase and the
mother/daughter separation is achieved by percolating the aqueous fluid through an extraction
chromatography column [8].

(ii) A specially engineered elution liquid is applied for the chromatographic

separation of the daughter and its mother contaminant as the fluid moves
through the column at moderate speed. Under these conditions, the mother
and daughter have different affinities to the column material. Owing to this
difference, the mother and daughter will move with different speeds down
the column, and exit at the end in different chromatographic bands. This
procedure is illustrated in Fig. 10.

Novel extraction chromatographic resins exhibiting enhanced parent metal

ion retention capacity, excellent selectivity, improved radiation and chemical
stability offer promise in the development of radionuclide generators [15].
Another version of the solvent extraction method is represented by
Ref. [16]. Here, a small static extractor is constructed for extraction of 99mTcO4−
with methyl-ethyl-ketone (MEK) from an aqueous solution of 99MoO42− with an
efficiency of >80% after three extraction cycles.
An example of a generator where the daughter is extracted into the organic
phase while the mother remains in the aqueous phase is the 99Mo/99mTc generator
based on extraction by MEK. An alkaline solution of 99MoO42− is extracted with
highly purified MEK. The daughter nuclide in the form of 99mTcO4− is extracted

24
into the MEK solution, while the molybdate remains in the basic aqueous
solution. The MEK phase will then be isolated, washed and finally evaporated to
dryness. The 99mTc compound is redissolved in an isotonic saline solution for
preparation of radiopharmaceuticals by off-line labelling procedures. This
procedure makes use of low specific activity 99Mo and produces 99mTc at high
purity and high radioactivity concentration [12, 17–19].
Advantages of the solvent extraction process are as follows:

• Offers selective separation due to the use of a specific extracting reagent

mixture designed for the purpose.
• A high separation (or decontamination) factor is achievable.
• Quick separation process.
• High capacity: low specific activity mother can be used, for instance, by
addition of carrier, both for the mother and the daughter to ease the
separation process.
• Low running costs: the costs of the chemicals involved are low.
• Regeneration and recharging are possible.
• The process is scalable (volumes and activity) to a certain degree as per the
need (see below).

Disadvantages of the solvent extraction process are as follows:

• There may be a limit to the activity concentration due to radiolytic reactions

in the solvent chemicals that may, over time, degrade the solvent itself and
change the chemical state of both mother and daughter nuclides and thus
interfere with the separation process.
• Operation of this system requires highly skilled and trained personnel.
• Considerable volumes of organic extractants may be required to achieve
satisfactory performance, dependent on the design of the generator.
• Thus, the operation of the solvent extraction generator may be complicated
and cumbersome.
• There is also a potential for cross-contamination of the aqueous stream with
the organic solution mainly due to formation of (relatively stable) micro-
emulsions.
• The handling of considerable volumes of organic reagents may pose
possible fire or explosion hazards. This can be counteracted by selecting
solvents with low vapour pressure.

The technical difficulties make this procedure less desirable than the
standard chromatographic generator system, and this system is not widely used.

25
Generators based on the solvent extraction technique are generally not the first
choice for the preparation of an IRNG.

2.4.4. Generators based on separation by distillation or sublimation

In this method, the mother/daughter equilibrium mixture is chemically

treated to form a compound in which the daughter radionuclide will have lower
boiling points, whereas the parent is non-volatile.
There are two versions:

(i) The distillation method, which operates with the mother solution in a liquid
solvent under moderate temperatures (<150C);
(ii) The sublimation method, which operates under reduced pressure (vacuum),
either with solid mother nuclide matrices or melts at elevated temperatures
(>150C).

For both versions, on heating the mixture, the vapour will be richer in the
daughter radionuclide that is distilled out of the mother solution. The process is
illustrated in Fig. 11.
In order to facilitate the separation, a chemical compound may be mixed
into the mother solution for version (i) and led over the solid matrix or melt in the
form of a gas for version (ii). These components react with the daughter
radionuclide and make it more volatile. The evaporate then condenses as a
purified compound on a cooled surface, for instance, a cold finger, leaving the
non-volatile parent radionuclide behind. Once heating ceases (and the vacuum is
removed for version (ii), the purified compound may be collected from the
cooling zone, either by removing the cold finger or, as illustrated in Fig. 11, by
directing a dissolving liquid into the apparatus and collecting the solution
containing the daughter nuclide in a separate vessel. The distillation or
sublimation processes are relatively fast, permitting the use of a low specific
activity mother, and generating a daughter radionuclide of high purity. However,
the success of these methods depends upon the possibility of forming a volatile
daughter product compound with sufficient vapour pressure difference with
respect to the mother nuclide. The necessary equipment is relatively bulky, partly
fragile and requires careful operation. Automated versions suitable for operation
under harsh industrial conditions have yet to be developed.
An example of this methodology is one version of the 99mTc generator that
uses the difference in volatilities of the oxides of molybdenum and technetium to
achieve a separation. Reactor produced 99Mo is placed in a tube furnace and
oxygen is passed over the heated, finely powdered metal. Technetium forms the

26
FIG. 11. Radionuclide generator based on sublimation (or distillation) of the volatile daughter
radionuclide or a compound of the radionuclide from a mother radionuclide matrix.

oxide species Tc2O7, which becomes volatile at temperatures of 550°C, while

molybdenum oxides have a much higher sublimation temperature of above
1000°C. The sublimated 99mTc2O7 can be trapped by cooling followed by
dissolution in an aqueous solution [20, 21]. Figure 12 sketches the principle of
such a generator, adapted from Ref. [21].

2.4.5. Generators based on cryogenic distillation

Cryogenic separation of a gaseous daughter radionuclide from the mother

radionuclide represents an effective strategy to providing an efficient separation
with a high purity of the daughter product. It represents the selective removal
either of the daughter radionuclide in the gaseous form from the non-volatile

27
FIG. 12. Concept of the sublimation generator SICCATEC, where 99mTc is separated as
99m
Tc2O7 from the irradiated porous MoO3–V2O5–SiC target material in a flow of air, caught in
the alumina based Tc filter and subsequently redissolved in distilled water or a slightly saline
solution [21].

mother or the removal of the gaseous mother radionuclide from the non-volatile
daughter by connecting a closed chamber of the mother/daughter mixture to a
cold chamber where either the volatile daughter or the volatile mother is
solidified, leaving the other component in the original mixture chamber.
An effective cryogenic separation depends on a low vapour pressure for one
of the components and a high vapour pressure for the other component at room
(or moderately elevated) temperature. Figure 13 illustrates the principle of a
cryogenic distillation.
An example of this type of generator is the 122Xe/122I mother/daughter
relationship where the volatile mother 122Xe is cryopumped away from the
original mixture, leaving the less volatile 122I behind. Cryogenic pumping is a low

28
FIG. 13. Schematic illustration of various steps in operation of a cryogenic distillation
generator, from top to bottom.

29
temperature physical approach to separation, in which the mother or daughter
radionuclide is isolated directly by phase change.
The main advantage of cryogenic separation is that both a large quantity
and a high purity of the daughter radionuclide are achievable. The yield of this
separation is generally >90%.
A major disadvantage of cryogenic separation is the amount of energy
required to provide the refrigeration necessary for the process, particularly for
dilute gas streams. The cooling may be performed with liquid N2, but at remote
locations, electrically cooling equipment may be required. Cryogenic separation
requires the use of significant amounts of process equipment at considerable
capital cost. It is technically difficult to make a lightweight portable version.

2.4.6. Generators based on chemical precipitation

The relative solubility of the mother and daughter metal ion in a chemical
environment can be exploited for the selective separation of the daughter
radionuclide from the mother. When solubility of the mother and the daughter
metal salts are very different, they can be separated by precipitation. The
component that exhibits the lowest solubility will be precipitated first. One
converts the component into an insoluble form or by changing the ionic
composition of the solution or by adjusting pH and temperature, for instance.
Under certain defined conditions, the solubility of every salt is governed by the
solubility product Ksp. For a chemical reaction of the form:

mCn + nAm−  CmAn

the stoichiometric solubility product of the compound CmAn is expressed by:

m n
K sp = [C ] ⋅ [ A] (16)

If the actual ionic concentrations are so large that their product according to
Eq. (16) exceeds Ksp for the particular compound, one has reached the required
conditions for precipitation. In a stringent treatment of this subject area, one should,
in fact, use the thermodynamic solubility product instead, where the concentrations
C and A are exchanged with the expressions aCC and aAA, respectively, where a
is the ionic activity and  is the activity coefficient. Hence, the condition for
precipitation is defined by Eq. (17), where SR is the saturation index:

m n
[ C ] ⋅ [ A]
SR = ³1 (17)
K sp

30
FIG. 14. Schematic illustration of a chemical precipitation system with precipitation of the
daughter nuclide.

The practical implementation of the process involves adding a specific

precipitating reagent containing the counter ion of the ionic compound of interest
to the mother/daughter equilibrium mixture to precipitate either the mother or the
daughter ions or ionic compounds.
In order to achieve a high chemical yield and an acceptable
decontamination factor for the purified daughter product, carrier substances may
be added for both the mother and daughter nuclides. Most often, a large excess of
the added precipitation agent is used. This reduces the need for a high carrier
concentration. Thus, a higher specific activity can be achieved.
Such precipitation methods can be systematically developed by sequencing
of pH, adjusting the added portions of precipitating agents, and selecting the
optimum temperature time period for quantitative precipitation. A schematic
illustration of a chemical precipitation system is depicted in Fig. 14.
Advantages of the precipitation process are as follows:

• Convenient, simple process that provides the only practical method of

separation in some cases;
• Can be highly selective and virtually quantitative (depending on a low Ksp
value);
• High degree of decontamination is possible (depending on the relative
values of Ksp,daughter and Ksp,mother);

31
 • Provides a large range of scale, both with respect to amounts treated and to
the number of chemical elements for which the method is applicable;
• Not energy or resource intensive compared with other techniques
(e.g. solvent extraction).

Disadvantages of the precipitation process are as follows:

• This system is applicable to those cases where there is a significant

difference in solubility product of the actual compound of the mother and
daughter radionuclide.
• It is sensitive to many chemical parameters such as concentration of the
reactants, order of mixing, reaction temperature, etc., and any deviation
from the standard operating procedure may result in failure.
• The multistep separation process to digest, filter or wash the precipitate
may be time consuming and labour intensive.
• The precipitation often has to be complemented by some other separation
method to purify the daughter product.
• It is hardly possible to achieve a carrier free (non-carrier added) product, so
the specific activity (in the case of an isotopic carrier) or the activity
concentration (in the case of a non-isotopic carrier) will not be very high.

One example of a generator where precipitation plays a main part is given

in Ref. [22], where 90Y is separated from its mother 90Sr by precipitation of the
90
Sr followed by subsequent purification of the 90Y by column chromatography.

2.4.7. Generators based on electrochemical separation

The principle of the electrochemical separation of a daughter radionuclide

(or its compound) from its mother radionuclide (or its compound) is based on a
difference in their electrochemical potential. The practical implementation of the
separation process comprises the steps of dissolving the mother/daughter
equilibrium mixture in an electrolyte followed by selective deposition of the
daughter radionuclide on an electrode in accordance with their electrochemical
potential.
This deposition can be achieved either by a spontaneous process or by
applying an external voltage. Both variations are treated briefly below.
Spontaneous deposition, also called autodeposition (and sometimes
incorrectly even electroplating or electrodeposition), is based on a difference in
electronegativity between the mother and the daughter. For preferential
deposition of the daughter, it has to exhibit a higher reduction potential than the
mother.

32
FIG. 15. Schematic illustration of a spontaneous deposition (autodeposition) process illustrated
by the separation of 210Po (T1/2 = 138.4 d) from its grandmother 210Pb ( T1/2 = 22.3 a).

Spontaneous deposition can take place on metallic surfaces with a lower

reduction potential. The process is often demonstrated in primary courses in
chemistry by dipping a rod of metallic zinc into an electrolyte of copper ions
(Cu2+). Metallic copper is spontaneously deposited (reduced to Cu0) on the zinc
rod, while the zinc rod is correspondingly dissolved (oxidized to Zn2+). For the
210
Pb/210Bi/210Po nuclear genetic relationship, the 210Po may be separated by
autodeposition of a metallic nickel surface [23]. It is reported to be a very robust
method. This creates potential for development of a 210Pb/210Po radionuclide
generator for special purpose use. In this case, deposition on to a silver surface
would be required since the nickel surface may also partly deposit the progeny
210
Bi and 210Pb [24]. A schematic outline of the method is given in Fig. 15. The
spontaneous deposition method has not yet been extensively exploited for more
general mother/daughter separation in radionuclide generator technology.
The electrolysis method, also called electroplating (or electrodeposition),
comprises an electrolyte containing the mother/daughter radionuclide mixture,
two electrodes of an inert material like platinum and an external power source
with variable high voltage connected to the electrodes, forming a cathode and an
anode. The negative potential applied to the cathode causes the daughter
radionuclide (as a positively charged ion) to be reduced and deposited on to the
surface of the cathode. Reversing the potential causes the deposited daughter

33
radionuclide to return back to the aqueous phase, thus allowing its recovery
[11, 19, 25, 26].
Advantages of electrochemical separation are:

• Electrolysis requires few steps and product yield is high.

• Capacity is not limited by the amount of adsorbent or extractant.
• Simple to operate.
• Requires low cost equipment.
• Relatively fast process.
• Permits carrier free and clean separation from the parent.

Disadvantages of electrochemical separation are:

• Not a universal method; still in developmental stage with respect to

radionuclide generators.
• Applicable to those systems where there is a significant E0 difference of
parent and daughter.
• A generator version suitable for field application has yet to be developed.
• Production of gaseous components during electrolysis must be taken care of
to reduce any explosion danger (H2 production).

A typical example of this method is the 90Sr/90Y generator developed at

Bhabha Atomic Research Centre (BARC), India [25]. The experimental set-up is
depicted in Fig. 16. In this generator, the separation of 90Y from 90Sr is achieved
due to the difference between the electrochemical potentials of Y3+ and Sr2+. On
applying a suitable electric potential, 90Y is selectively deposited at the cathode
from a mixture of 90Sr and 90Y. The generator involves two electrolysis steps of
purification. The first electrolysis is performed for 90 min in 90Sr(NO3)2 feed
solution at pH2–3 at a potential of –2.5 V with a 100–200 mA current using
platinum electrodes. The second electrolysis is performed for 45 min in
3M HNO3 at a potential of −2.5 V with 100 mA current. In this step, the cathode
from the first electrolysis containing 90Y is used as the anode, whereby the
yttrium again redissolves and is deposited on a fresh circular platinum cathode.
The 90Y deposited on the circular cathode after the second electrolysis is
dissolved in acetate buffer for further production of useful tracer compounds.

2.4.8. Generators based on SLM separation

This separation technique is basically a continuously operated extraction

stripping process. It includes the operation of an extracting liquid membrane

34
 90 90
FIG. 16. Schematic diagram of electrolytic separation of Y from a Sr/ 90Y electrolyte
mixture, adapted from Ref. [22].

where the solute (daughter radionuclide) partitions between three liquid phases:
the feed, the membrane and the receiving phases. This may be described as the
‘supported liquid membrane’ (SLM) technique.
The organic liquid (possibly including an extractant) is immobilized within
the pores of a porous membrane. The porous membrane itself serves only as a
framework or supporting layer for the organic liquid film. Such a membrane can
be easily prepared by impregnating a hydrophobic porous membrane with a
suitable organic solvent possibly modified with an extractant. The membrane can
be defined essentially as a barrier, which separates two aqueous phases and
restricts the transport of the mother radionuclide in a selective manner. The
transport through the membrane is affected by the concentration gradient across
it. The feed aqueous solution initially contains the mother/daughter equilibrium
mixture.

35
 FIG. 17. Two chamber SLM 90Sr/ 90Y generator, adapted from Ref. [22].

Separation of the daughter from the mother by transport of the daughter

through the membrane requires that the distribution ratio DD (Eq. (15)) for the
daughter to the organic phase in the membrane is high and the distribution ratio
DM for the mother correspondingly low. Then, the separation factor will be high.
The aqueous solution present on the opposite side of the membrane, which is
initially free from the daughter radionuclide, is referred to as the strip solution.
For an efficient stripping (or back extraction) of the daughter from the organic
phase in the membrane, the strip solution has to be designed so as to make the
DD value as low as possible on the stripping side of the membrane.
The performance of the process is strongly affected by the properties of the
organic solvent and the selectivity of the possible complexing agent or extraction
agent used in the membrane, the carrier concentration for the daughter or
holdback carrier for the mother, the fluid dynamic of the phases (viscosity) and
the membrane characteristics such as pore size and pore size distribution. In
contrast to ordinary solvent extraction, this overall process is governed by
kinetics and concentration differences rather than equilibrium parameters
[27–29]. The principle of the process is sketched in Fig. 17.
Advantages of the SLM separation technique are:

• It offers selective separation depending on the selectivity of specific

extracting reagents.
• Simple operation, both extraction and stripping are feasible in one stage,
and the process does not include manual interaction.
• It does not use any external force such as pressure or high tension, but is based
on difference of the chemical potential as a driving factor of the process.
• Larger interfacial area permits high efficiency.

36
 Disadvantages of the SLM separation technique are:

• It is not yet a mature technology but still under development. A version

suitable for industrial application has yet to be developed.
• Transport processes of the daughter are slow (slow kinetics), so it cannot be
used for very short lived daughter activity.
• The equipment is still somewhat mechanically unstable, especially due to
short lifetime and instability of the membrane.
• The release of the organic phase from the pores of an SLM into the receiver
chamber represents a problem as it leads to chemical impurity in the
separated product.
• It is essential to recharge the membrane periodically.

A generator system using the above concept has been developed for the
preparation of carrier free 90Y from 90Sr in BARC, India [27] by employing an
SLM using 2-ethylhexyl-2-ethylhexyl phosphonic acid (KSM-17 equivalent to
PC 88A) supported on a poly-tetrafluoro-ethylene (PTFE) membrane (Fig. 17).
After adjusting to pH2 with NaOH, the 90Sr/90Ysolution is used as a feed in a
single stage membrane cell partitioned with a PTFE membrane impregnated with
KSM-17 and having a feed and receiver compartment with 5.0 mL capacity each.
The receiver compartment is filled with a 0.5M HNO3 or 0.5M HCl stripping
solution. Yttrium-90 alone is preferentially transported across the membrane,
leaving behind 90Sr in the feed compartment. This technique can yield 90Y in
millicurie levels in a pure and carrier free form. The feed can be reused repeatedly
after allowing for 90Y buildup.
Out of all the generator principles briefly described above, it was decided
that the chromatographic type generator was to be the method of choice for
further development in the CRP, which is the basis for this publication. The
chromatographic type radionuclide generator has, at this stage, the best overall
potential for being further developed into a suitable radiotracer generator for
industrial application by coupling a selective chemical treatment for the daughter
radionuclide of interest to a suitable radionuclide generator.

2.4.9. Special case: Generator based on electrostatic radionuclide

separation

When one of the decay products in the decay chain from the mother
radionuclide is gaseous, it may emanate from the mother radionuclide compound.
The following decay will produce positively charged daughter products that may
be collected on an electrode at negative charge. One example is generation of
carrier free 212Pb from decay of 228Th through the following decay chain:

37
 FIG. 18. Schematic diagram of the electrostatic 228Th →▪▪▪→ 212Pb generator.

228
Th (1.913 a) ⎯⎯
→ 224 Ra (3.66 d) ⎯⎯
→ 220 Rn (55.6 s)
⎯⎯
→ 216 Po (0.15 s) ⎯⎯
→ 212 Pb (10.68 h)

Here, both the very short lived 216Po, as well as 212Pb itself, will be collected
at the cathode during alpha decay of their progeny. This generator was first
published by Rutherford in 1900 and is often referred to as ‘Rutherford’s thorium
cow’ [30].
Thorium-228 is readily found in compounds of the naturally occurring
mother 232Th. If the thorium compound is ‘old’, i.e. at least 60 years since its
elemental isolation in order to allow for in-growth of its decay product 228Ra
(5.75 a), the 228Th is in nuclear equilibrium with 232Th. Therefore, the emanating
compound normally loaded into the generator is ordinary ThO2. A sketch
illustrating the principle of operation of the generator is given in Fig. 18.
The high tension is normally in the range 100–1000 V, the amount of ThO2
is 10–100 g and the collection time 10–24 h. After the collection period, the

38
platinum foil is removed and the deposited 212Pb rinsed off (dissolved) with dilute
nitric acid. If there is a need for several experiments during 1 d (or one collection
period), several generators may be connected in parallel (battery of generators)
on the same high temperature source. In order to achieve a sufficiently high
emanation rate from the ThO2 powder, it has to be finely grained and
preferentially heated to some 50–60C. A 212Pb activity of 0.5–5 Ci may be
obtained per collection. The operation and typical generator yields are given in
Ref. [31].
Out of all the generator principles briefly described above, it was decided
that the chromatographic type generator was to be the method of choice for
further development in the CRP, which is the basis for this publication. The
chromatographic type radionuclide generator has, at this stage, the best overall
potential for being further developed into a suitable radiotracer generator for
industrial application by coupling a selective chemical treatment for the daughter
radionuclide of interest to a suitable radionuclide generator.

2.5. RADIOTRACER GENERATORS BASED ON 

RADIONUCLIDE GENERATORS

Radionuclides from radionuclide generators are the first step on the way to
producing radiotracers for use in industrial process studies [32]. Radionuclide
generators make radionuclides readily available at locations remote from
irradiation facilities (reactors or particle accelerators). In addition, the short half-
life of the daughter radionuclide ensures that any radioactive waste remaining
after an industrial investigation is minimal and that any contamination of plant,
product streams or environment discharges is negligible.
Although it is sometimes possible to use the daughter radionuclide directly
to trace process streams, more often, it is necessary to chemically modify it so as
to ensure full compatibility with the stream to be traced.

2.5.1. Design of an IRNG

For industrial applications, the most common type of generator is the

column type, described in Section 2.4.1. The designs of the components of a
column based radionuclide generator will vary from one manufacture to another,
but the objective is always to facilitate the separation and elution of the daughter
radionuclide from the parent radionuclide. The components in a typical column
based generator are given below.
Column: The column, usually glass, containing a bed of sorbent as a support
to which the mother radionuclide will bind strongly and not be washed off during

39
the subsequent elution of the daughter radionuclide. Removal of the daughter
radionuclide from the sorbent column is attributed to the lack of affinity of the
daughter radionuclide for the sorbent, whereas the mother radionuclide is
essentially completely bound to the sorbent and cannot be removed by the elution
liquid, regardless of the volume of eluent passing through the column. Removal
of the mother radionuclide requires an eluent of different chemical composition.
Tubing: Tubing is connected to the column to allow it to be washed with an
eluent or rinsing solution. In a traditional generator design, the inlet tube will
generally be accessible usually via a needle on to which a vial of the eluent can be
attached as needed. Other generator designs provide an internal reservoir of
eluent for this purpose. The outlet tube is also accessible and generally terminates
as a needle to which an empty collecting vial can be attached. Most generators
use an evacuated vial for collection so that eluent from the inlet side is drawn
through the column and into the outlet vial. No pumps are needed. The driving
force is the evacuated vial that creates a very significant differential pressure over
the column since the eluent side of the generator is always at atmospheric
pressure.
Filters: Filters serve to maintain the integrity of the sorbent bead within the
column so as to prevent fluid channelling that would reduce the elution
efficiency. The filters are usually glass frits with pore sizes suitable to remove any
small particles of the sorbent from the eluted sample. The filters can also be made
of porous plastic materials (for instance, polyethylene or Teflon).
Catcher column: Some generators come with a catcher column. This
column contains a bed made of the same absorber material as the main column
and is mounted at the outlet side of the main column. The purpose is to catch
(bind chemically) any mother radionuclides that might have been eluted from the
main column. The catcher column should be readily exchangeable without
needing to dismantle the lead shield around the main column (see below).
Shielding: Heavy shielding is required for operator safety, as both the parent
and the daughter radionuclides emit radiation. The glass column acts as a partial
shield, but cannot stop the penetrating gamma radiation. Most generators will
therefore have a lead shield around the column and outlet tubing. Additional
shielding is used during the collection process and, of course, the eluted daughter
radionuclide must be shielded once it is collected from the generator.
Handles: Generators are contained in a housing and have handles to allow
manual or mechanical lifting and positioning. There is a cover to protect the inlet
and outlet needles and appropriate labelling on the generator housing.
One typical generator design is shown in Fig. 7. Another design is given in
Fig. 19.

40
FIG. 19. Left: A column generator in its lead shield. Elution is performed by a vacuum vial,
also in a lead shield. Right: A typical lead-shielded and closed radionuclide generator.

A set-up where the generator is eluted with a vacuum pump from an

external elution liquid reservoir is illustrated in Fig. 20.
Principal features of the generator to be determined before use are the
elution yield of the daughter as a function of the eluant flow rate and the degree of
mother breakthrough. The activity requirements must be considered in order to
optimize the elution flow rate in relation to the total injected volume, the duration
of the examination and the residence time of the system to be studied.
Once the activity of the daughter is eluted, there is a growth of the daughter
on the column until it again reaches a maximum and finally is in close
equilibrium with the mother. This elution and regrowth can be continued as long
as there are useful amounts of the mother radionuclide available. Elution may be
performed before equilibrium is reached, and the amount of daughter activity
eluted will depend on the time elapsed since the last elution.
Radionuclide generators intended for radiotracer applications must meet
regulatory and quality control requirements. The production of the mother
radionuclide in nuclear reactions by irradiation in a reactor or a particle
accelerator, its separation from the target material, and the chemical and technical
construction of the radionuclide generator are factors that must be considered
carefully, so that the end result is a generator that is efficient and easy to operate.
Processes for the production of radionuclide generator systems for radiotracer
applications should follow good manufacturing practice standards.

41
FIG. 20. A generator set-up that is eluted by means of a peristaltic vacuum pump and with a
catcher column outside the main generator housing for easy detection of mother radionuclide
breakthrough.

For some applications, it is possible to incorporate the generator into the

tracer injection system. The system software initiates the elution of the generator
at preset intervals and also controls the duration of the elution and the flow rate of
the eluent. Such a system can be mounted permanently on a process stream for
purposes of routine monitoring.
The choice of a specific daughter radionuclide for any given application
depends on the following factors:

• Energy of photon emitted (in some cases, more than one photon energy);
• Half-life;
• Elution yield;
• Physical and chemical form, which leads into the next point;
• Possibility of converting the radionuclide into a useful radiotracer for
various tracing scenarios.

2.5.2. Activity requirement

Estimating the required activity is an important step in any industrial

experiment with radioactive sources. For radiotracers, the lower limit of the

42
activity is determined by the measurement sensitivity of the detector, desired
accuracy, dilution between injection and detection points, and background
radiation level. The upper limit is set by radiological safety considerations. The
amount of the required activity depends on the following factors:

• Desired accuracy;
• Efficiency of measurement or calibration factor of the detection system;
• Expected level of dilution/dispersion;
• Half-life of the daughter radionuclide;
• Background radiation level and number of repeated measurements;
• Mode of injection and detection (delta function versus continuous or
extended pulse width);
• Expected losses of activity (should not really happen).

2.5.3. Industrial tracing situations

Industrial conditions for radiotracer applications vary considerably from

case to case. Basically, the following conditions may be encountered in a
radiotracer experiment:

• High temperature (up to hundreds or thousands of degrees celsius);

• High pressure (up to hundreds of megapascals);
• Vast volume (up to millions of cubic metres);
• Multiple phases (solids, liquids (aqueous, organic, supercritical), gases);
• Complex processes;
• Quick transit time (down to milliseconds);
• Complex media;
• Unexpected tracer degradation (microbiological attack, sorption, thermal or
chemical degradation);
• Adsorption potential;
• Harsh working environment.

The increasing application of generator produced radiotracers in industry

has stimulated the extensive development of a multitude of new radiotracers and
novel radiolabelling procedures. Radiolabelling with these short lived
radionuclides represents a remarkable challenge. Special attention has to be paid
to synthesis time and specific labelling techniques due to the short physical half-
life of the respective radionuclides. Development of procedures for producing
radiotracers for industrial application must take this into account.

43
2.5.3.1. Aqueous liquid tracing

The radionuclide eluted from a radionuclide generator can be of various

chemical forms. In order for the eluted radionuclide to be used directly as a
passive radiotracer, the chemical form of the radioactive daughter compound
should possess the following properties.
The radioactive material should be soluble in the process stream under the
prevailing conditions of pH, temperature and pressure. It should not degrade in
any way and not behave differently from the traced material itself.
Ideally, the radionuclide eluted from the generator should be in a chemical
form that is physically and chemically compatible with the material to be traced
so that it can be injected into the process stream of interest without delay and
without complicated chemical manipulation. However, in most cases, the
generator eluate does not satisfy all these characteristics. In order to utilize the
eluted radionuclides effectively for radiotracer investigation, further chemical
manipulation is most often necessary.
Chemical conversion makes the production of a wide spectrum of
appropriate radiotracers possible, and opens up the window for utilization of
these compounds in different situations. The eluted radionuclide is generally
treated with an appropriate ligand to form an inert complex having sufficient
thermal stability. For water tracing, the best performing tracers are anionic. In
simple one component water tracing, neutral and positively charged compounds
may be used depending on the process to be traced. In multiphase flow, where
one component is water and the other an oleic phase, a neutral component can
only be used if it does not contain a lipophilic fraction, which makes it soluble in
the oil phase as well as in the water. In addition, for very short lived
radionuclides, the synthesis process must be rapid in order to avoid detrimental
decay during the process.
In order to develop synthesis and/or labelling techniques that can be
adopted for industrial tracing, it is a good starting point to look at the work
conducted for labelling of radiotracers for nuclear medicine purposes. Of course,
this is a much simpler system than encountered in most industrial situations,
especially when considering the temperature, acidity and chemical compositions
of the systems to be investigated.
Radiopharmaceutical scientists have designed, developed and tested many
potentially useful and ‘on the spot’ labelling kit formulations using ‘cold’ kits. A
cold kit contains the ligand to be complexed, an adequate quantity of reducing or
oxidizing agent (if needed), a buffer to adjust the pH to suit the labelling
conditions and other required chemical components or modifiers. Radiolabelling
with kits is fairly easy, can be easily accomplished with high complexation yield
and provides a novel route to make radiotracers. Kit formulations are not only

44
effective in carrying out the tasks, but also save time during field tracer
investigations.
Here, two such examples are illustrated:

(i) The eluted chemical form of 99mTc from the 99Mo/99mTc radionuclide
generator is pertechnetate, 99mTcO4−. This anion is a good water tracer
provided the temperature is below about 90C and the chemical conditions
are not reducing. At reducing conditions, technetium is reduced from
oxidation state +7 to +4 and forms 99mTcO2. This is a non-charged molecule
that will attach to any solid surface and not behave as a water tracer any
more. Hence, 99mTc has to be stabilized preferably as an anion by
complexation with suitable ligands. Such a ligand is EDTA, a readily
obtained chelate. It has been shown to be effective in the process evaluation
of wastewater treatment plants as it precludes absorption of the
radiolabelled molecule on the vessel or pipe walls or on suspended solids
during the course of tracing [33].
(ii) A radiotracer experiments was carried out on a model of a rectangular
settler with a volume of 3 m3. Several different aqueous phase tracers
were injected consecutively. The tracers were (i) non-radioactive
fluorescine (a strongly coloured dye that, in these experiments, is taken
as a reference water tracer), (ii) the eluate from a 68Ge/68Ga generator
eluted with 0.1N HCl solution and no further treatment and (iii) 68Ga
complexes with 1,4,7-triazacyclononane-1,4,7-triacetic acid (NOTA) and
1,4,7,10-tetrazacyclododecane-1,4,7,10-tetraacetic acid (DOTA).

The obtained RTD functions indicated that the directly eluted 68Ga (in the
form of solvated Ga3+) did not work as a water tracer in the settler. However, the
complex compounds of gallium were stable in the water phase and were not
adsorbed on the vessel walls. These complexes can be recommended as tracers of
the water phase in similar experiments and under similar experimental
conditions [34].
The preparation procedure is as follows:

• Elute Ga3+ from the generator with about 5 mL of 0.1N HCl solution;
• Add about 1 mL of a 0.01M solution of the macrocyclic compounds DOTA
or NOTA;
• Adjust pH to 3.5;
• Heat the mixture to 90–95°C for 20–30 min.

45
 The above procedure for 68Ga3+ ion complexation with DOTA and NOTA
can be recommended as a useful synthetic route for production of 68Ga labelled
passive water phase tracers of 68Ga eluted on-site from the 68Ge/68Ga generator.
Table 2 summarizes some of the common applications of radiotracers.

TABLE 2. SOME EXAMPLES OF CHEMICAL MODIFICATIONS OF

RADIONUCLIDES ELUTED FROM THREE SELECTED GENERATORS
AND APPLICATIONS OF THESE ‘MODIFIED’ RADIOLABELLED
COMPOUNDS
Generator
Labelled phase
137
Cs/137mBa 99
Mo/99mTc 113
Sn/113mIn

Surface water 137m

Ba–EDTAa 99m
TcO4− (as eluted) 113m
In–DTPA
137m
Ba–DTPAb
113m
Groundwater Too short lived Unstable? In–DTPA

Water WWTPc 137m

Ba–EDTA 99m
Tc–EDTA 113m
In–DTPA
137m
Ba–DTPA
99m
Sludge WWTP Too short lived TcO4− +SnCl2 → 99mTcO2, 113mIn3+ will sorb
sorption on to particles on to particles
99m
Mud in surface water Too short lived TcO4− + SnCl2, 113m
In3+ will sorb
reaction as above on to particles
137m
Organic phase Ba–DC18C6d– 99mTcO4− + TBPf,
tested <120°C HDNNSe i.e. generator eluted
directly with TBP
113m
Catalyst in organic In3+ will sorb
phase tested <120°C on to particles

HTg/HPh water 99m

TcO4− + 8 hydroxy
(<350°C, 40 bar) quinoline
99m
TcO4− + TcMAG3a
a
EDTA: ethylene diamine tetraacetic acid.
b
DTPA: diethylene triamine pentaacetic acid.
c
WWTP: wastewater treatment plant.
d
DC18C6: crown ether: dicyclo-hexano-18-crown-6.
e
HDNNS: dinonylnaphthalenesulphonic acid.
f
TBP: tributyl phosphate.
g
HT: high temperature.
h
HP: high pressure.

46
2.5.3.2. Organic phase tracing

By using optimal reaction conditions, the daughter radionuclide can be

extracted from an aqueous phase into a non-miscible organic liquid. Several
solvent extraction reaction mechanisms are possible, most involving extra
complexing agents (for instance, chelate formers) and some also involving adduct
formers. Some examples are given below.

(a) Technetium-99m tracer in MEK

The 99Mo/99mTc generator based on an MEK solvent extraction system

(Section 2.4.3) can be used to obtain 99mTc in MEK. An alkaline solution of
18.5 GBq (500 mCi) sodium molybdate [99Mo] solution (7.4–14.8 GBq
(200–400 mCi) per g Mo) is transferred into the extraction system. After
extraction, the MEK phase is sampled by extracting an aliquot that can be used
directly for organic phase tracing.

(b) Gallium-68 tracer in isopropyl ether

The solvent extraction method was used to prepare a 68Ga tracer suitable for
use in a single organic phase. Gallium-68 is eluted in 4N HCl (20 mL) from a
68
Ge/68Ga generator based on a TiO2 column. This acid (and chloride)
concentration is sufficient to ensure that the chemical form of gallium is 68GaCl3,
which is non-charged. 10N HCl (20 mL) was added to the eluted 4N HCl
solution in order to make it 6M, which is the optimum molarity to ensure
maximum extraction of 68Ga. Isopropyl ether (20 mL) was used to extract 68Ga
from the aqueous phase (two sequential extractions) without addition of extra
extraction agents. Efficient liquid mixing was achieved by bubbling nitrogen
through the combined fluids for 10 min.

(c) Gallium-68 tracer in MEK

The 68Ga is eluted with 1M HCl. A few mL of the aqueous phase containing
68
Ga is equilibrated with an equal volume of MEK to extract 68Ga.

(d) Gallium-68 labelled acetylacetonate, Ga(acac)3

The 68Ga3+ in the form of GaCl3 is eluted from an ionic 68Ge/68Ga/SnO2

generator with 1M HCl. The solution was evaporated by heating to dryness in a
test tube. The residue was dissolved in an ethanol solution containing 0.002%
acetylacetone. The solution was heated for 20 min in a 65°C water bath to

47
facilitate formation of 68Ga labelled acetylacetonate. The complex is suitable for
oil tracing in single phase flow, but it has not been tested sufficiently in
multiphase processes.

(e) Barium-137m complex with DC18C6 and HDNNS

A radionuclide column generator consisting of 137Cs absorbed on

K2[CoFe(CN)6] coated silica gel is eluted with a mixture of 0.1M HCl and
0.145M NaCl. The eluate is vigorously stirred with a solution of DC18C6 and
HDNNS (1:2) and 1-dodecanol in isooctane. The resulting complex shows a high
distribution ratio, also at elevated temperatures (60C). It has also been tested
with formation waters from oil reservoirs and shows acceptably low back
extraction [35]. This complex (patent pending) may be used for multiphase oil
tracing under typical oil–water separator conditions in the petroleum industry.

2.5.3.3. Solid tracing

Radiotracing using radiolabelled solid particles is an important tool to

obtain invaluable information about movement of solid particulate material in
industrial fluid flow, deposition in mines, geological tracing, surface water and
river transport and movements of shore sediments. A few methods are described
briefly below.
The degree of labelling may be proportional to the volume of the non-
porous part of the solid material or proportional to the surface (internal and/or
external) of the particle.

(a) Electrostatic sorption/ion exchange techniques

The generator eluate can be directly used for labelling solid particles
utilizing electrostatic sorption/ion exchange techniques. This kind of labelling is,
in principle, proportional to the surface of the particle. A larger percentage of the
daughter radionuclide can be adsorbed at low tracer concentrations because a
larger surface area is available compared to the amount of tracer present. Dilution
with carrier decreases the amount of tracer adsorbed because the carrier is
competing for adsorption, and the relative amount of the radioactive label
interacting with the adsorbate is much less. Such a technique depends on the
following factors:

• Chemical state of the radionuclide: Adsorption increases with increasing

charge on the ion.

48
• Nature of the surface material: Surfaces that have a negative charge or that
contain hydroxyl groups can interact with cations through electrostatic
attraction and hydrogen bonding, respectively. For tracing of geological
matter (sands), the charge should typically be positive.
• Surface area: Porous particles have larger surface areas than typical
crystalline particles and have, therefore, a higher capacity for sorption. In
addition, internal surfaces are shielded against wear and erosion of the
radiolabel. If the pore size distribution throughout the particle is
homogeneous and constant, the labelling in this case can also be taken to be
proportional to the volume of the particle.
• pH: Generally, adsorption decreases with a lower pH (higher hydrogen ion
concentration) because the ions interact with negatively charged surfaces,
and the hydronium ions compete with other cations for the available
binding sites.

Examples include:

• Labelling of organic ion exchange material: The daughter radionuclide

eluted from the generator can be equilibrated with a specific amount of ion
exchange material after adjusting the pH of the external solution. In this
way, cation exchangers (with negatively charged sorption sites) can be
labelled with a suite of cationic radionuclides. Likewise, anion exchangers
(with positively charged sorption sites) can be labelled with radionuclides
of anionic form. Organic ion exchangers, for instance, based on
polymerization of styrene with divinylbenzene as a cross linker, represent a
flexible structure that may expand or contract, depending on the ion
strength in the surrounding solution. As such, one can hardly define a
difference between surface and volume labelling; in this case, it is both.
• Labelling of geological and other inorganic material: Natural inorganic
sorbents such as various clays (kaolinite, illite, montmorillonite,
vermiculite, etc.), perlite, glass wool, sands (silicate rich or carbonaceous),
volcanic ash, etc. can also be used for preparing solid radiotracers. The
procedure is similar to the previous one. The process is based on the
adsorption of the radiolabel on to, or into (for porous material), the
available surface of the solid particles.

While choosing a sorbent, the following points must be considered:

• Rate and capacity of absorption/adsorption;

• Retention capacity (i.e. is the absorption thermodynamically irreversible in
the intended tracing process?);

49
 • Physical shielding of the label (i.e. can it be removed by erosion or wear?);
• Ease of application.

(b) Internal labelling

When the starting point is a radionuclide generator, there is only one form
of internal labelling (disregarding the above comment on organic ion
exchangers): the radiolabelled solid particles are produced by chemical
precipitation of the material that contains the radiolabel. It can be direct
precipitation with a carrier concentration with stable isotopes of the same
chemical element or it can be by co-precipitation with other chemical elements.
Further treatment of the precipitate involves crushing and, possibly,
grinding before sieving into special particle size fractions. For precipitation with
a carrier of the same element, one always ensures that all the particles are
homogeneously labelled (i.e. activity in Bq/g is constant), regardless of the
particle size. For the case of co-precipitation, two situations have to be
considered:

(i) Precipitation is performed in a thoroughly stirred solution, in which case,

one achieves a homogeneous precipitation, i.e. the precipitated material is
homogeneously labelled throughout the precipitate volume and the particles
fabricated from the precipitate are also all homogeneously labelled (and the
activity concentration is constant for all particles).
(ii) If vigorous stirring is not carried out, there is the risk that the precipitation
will be non-homogeneous. The first formed core particles have a higher
activity concentration than the precipitated layers that grow on the initial
particles. Thus, there will be a concentration gradient from high activity
in the core towards lower activity at the precipitate surface at the end of
the precipitation process. The various particles produced subsequently
will then not have a homogeneous volumetric label: those from the
surface area will have lower activity and those from the core will have
higher activity.

(c) Preparation of radiocolloids

It is also possible to generate radiocolloids by chemical reactions such as

hydrolysis. A method of forming an aerosol is to produce a liquid spray with a gas
jet. The process can be facilitated by separating the liquid into droplets with
electrostatic repulsions by applying a charge to the liquid. Emulsions are usually
prepared by vigorously shaking the two immiscible phases together, often with
the addition of an emulsifying agent, e.g. a surfactant such as soap, in order to

50
stabilize the product formed. Semi-solid colloids, known as gels, may possibly be
formed from the cooling of lyophilic sols that contain large linear molecules and
have a much greater viscosity than the solvent.

2.6. EXAMPLES OF RADIOTRACER GENERATORS NOT BASED ON

A MOTHER/DAUGHTER NUCLEAR RELATIONSHIP

2.6.1. The methyl bromide generator

Methyl bromide (CH382Br) is a radiolabelled gamma emitting gas used for

gas tracing. Since it is oil soluble, it is also used as a tracer for organic liquids in
single phase tracing, especially for localization of leaks in underground pipelines.
When dealing with strongly radioactive organic liquids, autoradiolysis is always
an issue. Ideally, such tracer molecules should be prepared just before use. Below
is a description of how to generate CH382Br on-site from concentrated solutions
of reactor produced 82Br−.
Neutron irradiation of potassium bromide (KBr) is regularly carried out at
reactors to produce 82Br− (T1/2 = 36 h) for tracing of aqueous systems, and the
availability of this radionuclide is relatively good. The transformation of solid
radioactive potassium bromide to gaseous methyl bromide is carried out in a
mobile chemical reactor, called a methyl bromide generator. It consists of a
lead-shielded chamber containing the irradiated KBr. The KBr is dissolved in
sulphuric acid and dimethylsulphate is added. Upon heating, the gaseous reaction
product CH382Br is formed together with non-radioactive CH379Br and CH381Br
according to the reaction:

2KBr + (CH3)2SO4 → 2CH3Br + K2SO4

The gaseous products are condensed in a second lead shielded and actively
cooled chamber from where it can be injected in aliquots. The generator is
pictured in Fig. 21.
One important feature in the development of such a system is to enable
storage of the CH3Br gas in a ‘cryocanister’ that prevents its release to the
atmosphere. The canister has sufficient capability to store large quantities of
CH382Br for the useful lifetime of the radiolabel (about 1 week).
Depending on the requirements in the various industrial tracing situations,
generator activities up to 379 GBq (10 Ci) can be prepared and transported.
Different versions of mobile generators have been constructed with total
weights ranging from 100 kg up to 400 kg to enable production of the required

51
 FIG. 21. Photograph and schematic diagram of the CH382Br radiotracer generator.

activity for various experiments. The fact that this particular generator design
allows radioactive KBr to be transported separately in well shielded lead
containers, allows for simpler logistics: it is simpler to transport a very small
volume of radiolabelled solid salt than the corresponding activity as a radioactive
gas.
The production process of CH382Br at the work site is as follows:

• Crush the quartz ampoule containing the solid salt K82Br using a special
integrated crusher.

52
 • Add sulphuric acid and methyl sulphate agents to the reactor for the
dissolution of K82Br.
• Clean the crusher and make it ready for the next operation.
• Close the valves connected to the reaction chamber to seal it off to prevent
any accidental leakages.
• Heat the reactor to 70C for about 30 min. The chemical reaction starts.
• Close the top valve on the collection chamber and open carefully the valve
between the chambers.
• The temperature of the cooling chamber is brought to 5°C (liquefaction
temperature of methyl bromide) by submerging the chamber in dry ice. The
CH382Br gas is transported from the reaction chamber to the collection
chamber by cryopumping and condensed there.
• Allow natural heating of the collection chamber by removing the dry ice.
Once the storage tank reaches ambient temperature, release of CH382Br gas
is possible.
• Connect special containers to the exit valve on the collection chamber and
open the valve to transfer CH382Br to the containers.
• CH382Br can be dispensed from the container into special ampoules for
injection in subsequent tracer experiments.
• Clean and prepare the containers to make the system ready for another
synthesis operation.

2.6.2. Radionuclide generators from on-site activation

with isotropic neutron sources

Table 3 shows a number of short lived radionuclides that can be produced

by irradiation with isotopic neutron sources because of very high activation cross-
sections of target nuclides.
The calculated reaction yields are based on the following assumptions:

• Irradiation time: 10T1/2.

• Thermal neutron flux: 109 n·cm–2·s–1.
• Amount of target material: 1 g molecule (mol = 6.023 × 1023 target atoms).

Typical commercial neutron sources are 252Cf (spontaneous fission with

emission of neutrons) and 241Am/Be, in which neutrons are generated by the
following  particle reaction:

9
Be + 4He → 12C + n

53
 TABLE 3. NUCLEAR DATA AND CALCULATED REACTION YIELDS (IN NUMBER OF  EVENTS EXPRESSED AS

54
BECQUERELS OF THE MAIN  RAY ENERGY) FOR SEVERAL SHORT LIVED RADIONUCLIDES THAT MAY BE
PRODUCED BY SMALL ISOTOPIC NEUTRON SOURCES
Radionuclide Half-life Nuclear reaction nth cross-section  energy (intensity) Irradiation time Reaction yield of 
52 51
V 3.75 min V(n, ) 4.9 b 1434 keV (99.75%) 37.5 min 2.9 GBq
56 55
Mn 2.58 h Mn(n, ) 13.3 b 847 keV (100%) 25.8 h 8.0 GBq
60m 59
Co 10.5 min Co(n, ) 20.7 b 59 keV (100%) 105 min 12.4 GBq
80g 79
Br 17.6 min Br(n, ) 8.3 b 616 keV (50.7%) 176 min 2.5 GBq
104 103
Rh 42 s Rh(n, ) 134 b 556 keV (100%) 7 min 80.4 GBq
108g 107
Ag 2.41 min Ag(n, ) 36 b 663 keV (51.8%) 24.1 min 11.2 GBq
110g 109
Ag 24 s Ag(n, ) 87 b 658 keV (48.2%) 4 min 25.2 GBq
116m 115
In 54 min In(n, ) 73 b 1294 keV (95.7%) 540 min 41.9 GBq
FIG. 22. Activation of solid target with thermal neutrons from a small isotopic neutron source
(upper part) followed by dissolution of the target and complexation of the radionuclide of
interest (lower part) to produce a suitable tracer compound.

The process is schematically illustrated in Fig. 22.

Decay of 252Cf by alpha emission (96.91% probability) and spontaneous
fission (3.09% probability) results in an overall half-life of 2.645 a and neutron

55
emission of 2.314 × 106 s−1·µg–1, with a specific activity of 19.832 GBq per µg
(0.536 mCi/µg). Thus, it is an intense neutron emitter that is routinely
encapsulated in compact, cylindrical source capsules. A source the size of a
person’s little finger can emit up to 1011 neutrons/s. However, the use of such a
source requires bulky and heavy shielding. For instance, a 3 mg source requires a
cylindrical transport container of height 121 cm, diameter 112 cm and weight
1723 kg.
The 252Cf sources of several different neutron outputs are, in principle,
available commercially, but are expensive in the sizes needed to produce a slow
neutron flux of 109 n·cm–2·s–1, which is used in the calculation of the reaction
yields in Table 3. However, a lower flux may still be of interest. The yields given
are then simply scaled down linearly with the neutron flux.
The half-life of 241Am is 432 a, and neutron sources based on this
radionuclide have therefore a much longer useful lifetime than the 252Cf sources.
However, the neutron output is lower. In general, for commercially available
sources, the neutron output is 2.2 × 106 n·s–1·Ci–1. Typical commercial source
strengths are in the range 1 Ci (smoke detectors) to >20 Ci (irradiators, oil well
logging tools, etc.). The strongest sources will produce fluxes in the range
105–106 n·cm–2·s–1, which is three to four orders of magnitude lower than the flux
used for the calculations in Table 3. The results are yields of the order of
megabecquerels, which may nevertheless still be useful for some tracing
purposes.
Transportable neutron generators utilizing the T(d,n) or the D(d,n) reaction
can also be used for radionuclide production, as described briefly in Section 2.6.3
below.

2.6.3. Radionuclide (radiotracer) generators based on

on-line use of neutron generators

Tracers to follow a mass flow can be generated in situ if the flowing

material contains an activable component. For illustration purposes, the most
obvious and simple example is activation of water itself with fast (14 MeV)
neutrons from a neutron generator based on the reaction T(d,n)4He. This
activation leads to the nuclear reaction:

16
O + n14 MeV → 16N + p

Nitrogen-16 is radioactive with a half-life of 7.13 s and emits high energy 

rays of 6.1 and 7.1 MeV. This process is possible due to recent development of
small sealed tube and transportable neutron generators.

56
FIG. 23. Schematic diagram of a pulse of a tracer induced in a mass flow by a short (or pulse)
irradiation with a neutron generator, and the subsequent downstream detection of gamma
radiation.

The principle of activation, or ‘tracer injection’, with subsequent radiation

measurement is illustrated in Fig. 23.
Although activation of 16O has been used as an example here, there is a suite
of other radionuclides that may be generated in situ by this method, but whether
or not the above technique is feasible depends to a considerable degree on the
nature and the elemental composition of the flow. If the flow does not have an
appropriate concentration of activable elements that produce useful tracers, it is
possible to inject easily activable material into it.
Examples of useful activation reactions are 12C(n,2n)11C (T1/2 = 20.3 min),
14
N(n,2n)13N (T1/2 = 9.97 min), 19F(n,p)19O (T1/2 = 26.9 s), 20Ne(n,p)20F
(T1/2 = 11.0 s), 24Mg(n,2n)23Mg (T1/2 = 11.32 s), 28Si(n,p)28Al (T1/2 = 2.25 min),
31
P(n,2n)30P (T1/2 = 2.50 min), 37Cl(n,)34P (T1/2 = 12.4 s), 55Mn(n,p)55Cr
(T1/2 = 3.50 min), etc.

57
 3. SELECTION OF
POTENTIALLY USEFUL RADIONUCLIDE GENERATORS
AND PRODUCTION OF THE MOTHER RADIONUCLIDES

3.1. REQUIREMENTS FOR IRNGs

In order to conduct proper radiotracer investigations, various requirements

need to be met before starting the actual test. The most important of all the
requirements is the ‘RADIOTRACER’ itself.
Some medical radionuclide generators like 99Mo/99mTc and 113Sn/113mIn are
being used for a few applications in industry and the environment. The use of
these generators is limited because of low photon energy and short half-life of the
radionuclide and limitations of compatibility and stability of the radiolabelled
tracer molecule (direct generator eluate) under harsh industrial conditions. There
are several potentially useful nuclear genetic relationships that may form the
basis for development of radionuclide generators for industrial applications. For a
radionuclide generator to be suitable for industrial use, the following criteria need
to be satisfied.

(a) Availability: Ideally, the radionuclide generator should be commercially

available at a reasonable cost.
(b) Half-life of the mother radionuclide: For use at remote locations, it is
important to select a generator with an appropriately long half-life. A
generator that remains useful for a period of 1 year may be good for
industrial applications.
(c) Half-life of the daughter radionuclide: The daughter radionuclide, used as a
radioactive tracer or tag on the radioactive tracer for industrial applications
should have a half-life varying typically from several minutes to several
hours.
(d) Type and energy of radiation from the daughter radionuclide: Gamma ray
emitting radionuclides are preferred for most industrial applications
because of the ability of gamma radiation to penetrate the often substantial
thickness of material from which the process plant is constructed. Gamma
rays of energy 140 keV and upwards have been found to be useful, in some
cases, gamma energies >500 keV are required.
(e) Physicochemical properties of the eluted daughter: Ideally, the material
eluted from the generator should be in a form that is physically and
chemically compatible with the material to be traced so that it can be
injected into the process stream of interest without delay and without
complicated chemical treatment. A radionuclide generator that includes a

58
 suitable chemical processing unit enabling the eluted daughter to be
transformed directly into a suitable industrial radiotracer will be preferable.
(f) Easy logistics: Packing, transport and subsequent handling at the industrial
site must be technically easy and readily implemented within the governing
regulations.

3.2. POTENTIALLY USEFUL RADIONUCLIDE GENERATORS FOR

INDUSTRIAL AND ENVIRONMENTAL TRACER APPLICATIONS

3.2.1. General

Based on the requirements that need to be met for radiotracer applications

under harsh industrial and/or field conditions, the radionuclide generators that
have been selected and proposed for use as the basis for generating appropriate
short lived radiotracers in developing and industrialized countries are listed in
Table 4.
Demands from developing and industrialized countries are somewhat
different, mainly due to differing availabilities of the various radionuclide
generators. It was supposed that due to less fluent transport and procurement
conditions in developing countries, parent nuclides with longer half-lives (at least
100 d) and daughter nuclides with longer half-lives (at least of the order of
minutes) should be considered necessary for these countries.
Table 4 lists some important nuclear characteristics such as half-lives and
photon energies and the proposed application environment for the various
radionuclide generators. The table also indicates whether the given radionuclide
generator is commercially available or not.
The following paragraphs give details of the most relevant generator
systems, selected from Table 4. For these generator systems, the following,
relevant parameters are discussed in detail:

• Daughter gamma energy;

• Daughter half-life;
• Parent half-life;
• Production and expected yield;
• Separation technique and chemical form of daughter;
• Availability and current status;
• Possible applications.

59
 TABLE 4. OVERVIEW OF SELECTED GENERATOR SYSTEMS

60
Mother Daughter
Generator
Half-life Decay mode  energy (keV) Production Half-life Main emission Main photon keV (%)
44 45
Ti/44Sc 47.3 a EC 67, 78 Sc(p,2n)44Ti 3.92 h + 511 (188.6%)
1157 (99.9%)
68 69
Ge/68Ga 270 d EC no  Ga(p,2n)68Ge 1.135 h + 511 (178.3%)
1077 (3.2%)
82 85
Sr/82Rb 25.6 d EC no  Rb(p,4n)82Sr 1.273 min + 511 (190.9%)
776 (15.1%)
99 235
Mo/99mTc 60 h − 740 U(n,f) 6.00 h  141 (89.4%)
113 112
Sn/113mIn 115 d EC no  Sn(n,)113Sn 1.65 h  392 (64.1%)
137 235
Cs/137mBa 30.0 a − no  U(n,f) 2.55 min  661 (90.1%)
144 235
Ce/144Pr 285 d − 133 U(n,f) 17.3 min  696.5 (1.34%)
172 175
Hf/172Lu 1.87 a EC 24, 125 Lu(p,4n) 6.7 d  1093 (63.2%)
3.2.2. Mass attenuation of actual gamma energies

The penetrating power of the various actual gamma energies from the
selected radionuclide generators is of interest in order to judge and evaluate the
usefulness of a certain radionuclide for the various industrial monitoring
operations that may be of interest. The selected absorbers, iron (Fe) and water
(H2O), simulate steels and most actual liquid solutions, respectively.
In order to estimate this penetrating power, let us first repeat some
necessary theory. A narrow beam of monoenergetic photons with initial intensity
I0, penetrating a layer of material with mass thickness x, density  and linear
absorption coefficient , exits from the absorber with intensity Ix, given by the
Lambert–Beer law:

⎡ ⎛μ⎞ ⎤
I x = I 0 ⋅ exp ⎢−⎜⎜ ⎟⎟⎟ ⋅ x⎥ (18)
⎢ ⎜⎝ ρ ⎟⎠ ⎥
⎣ ⎦

Let us calculate now the half-value thickness d1/2 for the various relevant
energies for the absorbers iron and water. This d1/2 parameter is defined as the
linear thickness of the absorber that reduces the exit intensity (Ix) to half the value
of the initial intensity (I0). Solving x from Eq. (18) gives:

⎛I ⎞ ⎛ μ ⎞⎟
x = ln ⎜⎜⎜ 0 ⎟⎟⎟ ⎜⎜ ⎟ (19)
⎜⎝ I x ⎟⎠ ⎝⎜ ρ ⎟⎠

Setting Ix = 0.5I0 gives:

⎛μ⎞
x = 0.693 ⎜⎜ ⎟⎟⎟ (20)
⎜⎝ ρ ⎠

and since x = d:

⎧⎛ μ ⎞ ⎪⎫
⎪
d 1/ 2 = 0.693 ⎪
⎨⎜⎜⎜ ⎟⎟⎟ ⋅ ρ ⎪
⎬ (21)
⎪
⎩⎝ ρ ⎠ ⎪
⎪ ⎪
⎭

which is the equation used for calculation of the linear half-value thicknesses.
The primary data on mass absorption coefficients are taken from Ref. [36]
and recalculated for the actual gamma energies. The primary data for the energy
region of interest are plotted in Fig. 24.

61
FIG. 24. Mass attenuation coefficients, /, as a function of gamma energy in the energy range
100–3000 keV for the two absorbers iron (Fe) and water (H2O) [36].

Calculated mass attenuation coefficients and the corresponding half-

thickness values are given in Table 5.
The d1/2 data are plotted in Fig. 25.

3.2.3. The 44Ti/44Sc radionuclide generator

Relevant nuclear data for this radionuclide generator system are given in
Table 4 and the decay scheme of 44Sc is given in Fig. 26.

3.2.3.1. Relevant nuclear properties

(a) Daughter photon emission

The high branching positron emission (94.27%) with maximum/mean

positron energy of 1.5/0.6 MeV is followed by emission of intense 511 keV
annihilation photons. This photon energy is adequate for penetrating metal walls
of vessels and pipes for on-line measurements in industry. The annihilation
character with two 511 keV photons moving in opposite directions allows for
coincidence detection and positron emission tomography (PET). This offers

62
 TABLE 5. MASS ATTENUATION COEFFICIENTS AND THE CORRESPONDING HALF-THICKNESS VALUES
Mass attenuation coefficient Mass attenuation coefficient Half-value thickness Half-value thickness
Radionuclide Gamma energy (keV) (/, cm2/g) (/, cm2/g) (d1/2, cm) (d1/2, cm)

Iron Water Iron Water

99m
Tc 141 0.2280 0.1541 0.39 4.50
172
Lu 181 0.1652 0.1421 0.53 4.88
113m
In 392 0.0953 0.1071 0.93 6.47
44 68 82
Sc, Ga, Rb 511 0.0834 0.0961 1.06 7.21
137m
Ba 661 0.0740 0.0862 1.19 8.04
144
Pr 697 0.0722 0.0843 1.22 8.22
82
Rb 776 0.0682 0.0800 1.29 8.67
172
Lu 912 0.0630 0.0742 1.40 9.34
68
Ga 1077 0.0580 0.0684 1.52 10.13
172
Lu 1093 0.0576 0.0679 1.53 10.20
44
Sc 1157 0.0559 0.0660 1.58 10.50
144
Pr 1489 0.0490 0.0578 1.80 11.99
144
Pr 2186 0.0415 0.0476 2.13 14.55

Note: Mass attenuation (or mass absorption) coefficients for the relevant gamma energies in iron (simulating steel) and water (simulating most
aqueous and many organic solutions) and the half-thicknesses for the actual combinations of gamma energies and absorbers. The numbers are
calculated on the basis of data in Ref. [36].

63
FIG. 25. Half-value thicknesses, d1/2, for water (which simulates with sufficient accuracy most
aqueous solutions and a number of organic liquids) and iron (which simulates steels) as a
function of gamma energy.

potential for determination of the radionuclide distribution with high local

resolution. In addition, the highly abundant 1157 keV photons (99.9%) allow for
on-line measurements of morphological distributions. A gamma spectrum is
shown in Fig. 27.

(b) Daughter half-life

The daughter half-life of 3.92 h is suitable for industrial measurements of

medium duration.

64
FIG. 26. Decay scheme of the ground state of 44Sc to stable 44Ca [37].

FIG. 27. Gamma spectrum of 44Sc accumulated with an HPGe detector.

65
(c) Mother half-life

Mother half-life of 47.3 a offers long term application without replacing the
generator. The lifetime of the generator is then dominated by the stability of the
support (column) material, which again may be affected by the radiation field.

3.2.3.2. Production and expected yield

There are several possible production routes for 44Ti. Examples are the
45
Sc(p,2n)44Ti reaction and proton induced spallation on V or Cr targets. High
production yields of several gigabecquerels per batch are achievable at
accelerators, providing that sufficient proton flux and long term irradiations are
available.

3.2.3.3. Generator designs and elution strategy

The 44Ti is, for instance, fixed on an anion exchanger bed as titanate
An early report [38] states that 44Sc in oxidized form (Sc3+) is eluted with
(TiO32−).
0.1M oxalic acid in 0.2M HCl. The radiochemical yield is 60–70%, the eluent
volume 30–50 mL and a breakthrough of 44Ti ~10−3%.
Other reports on the 44Ti/44Sc generator system are:

• Zirconium oxide column bed, 0.01M HCl eluent, 42–46% radiochemical

yield and parent breakthrough of 5 × 10−4% [39];
• Solvent extraction with organic phase of 1% 1-phenyl-3-methyl-4-capryl-
pyrazolone-5 in methyl-isobutyl-ketone, with 90% recovery in 10 mL
eluent, 44Ti breakthrough is measured at 10−6 [40];
• Polyantimonic acid inorganic ion exchanger and HCl/(NH4)C2O4 eluent
systems give 80% yield and breakthrough of 10−7 [41];
• Other metal oxides/HCl eluent systems are under investigation.

Recent developments with similar chemistry [42] have led to improved

performance and the only currently working generator system. About 185 MBq
(5 mCi) of 44Ti were obtained by the reaction 45Sc(p,2n)44Ti in a cyclotron with a
beam energy of 25 MeV and a current of 200 A. Subsequently, 44Ti was
separated from the 1.5 g massive scandium target using cation exchange
chromatography on a large column (44Ti/NatSc purification, BioRad AG-50Wx8,
200–400 mesh, H+ form). Ion exchange studies have been performed
systematically using AG-1x8 (200–400 mesh Cl− form) and AG-50x8
(200–400 mesh H+ form) resin in H2C2O4/HCl solution in order to evaluate the
potential of ion exchange based generators. The Kd values for both Sc and Ti were

66
determined in batch experiments using different concentrations of HCl/oxalic
acid mixtures. Both 44Ti(44Sc) and 46Sc were used as isotopic tracers for Ti(IV)
and Sc(III) distributions. The best conditions for efficient separation and for the
design of generators are achieved by eluting the AG-1x8 resin with a mixture of
0.2M HCl and 0.1M H2C2O4.
For subsequent 44Sc labelling reactions, post-elution processing of the 44Sc
fraction may be required. The 44Sc may, for example, be absorbed on-line directly
and selectively from the eluate on a cation exchange cartridge. In this case, the
mixture of reduced acid concentrations consisting of 0.06–0.008M HCl and
0.005M H2C2O4 in the elution liquid offer the optimum Kd value for Sc(III)
adsorption.
Further studies with this generator system concerned the effect of ‘direct’
and ‘reverse’ elution procedures. The ‘reverse’ washing procedure after each
‘forward’ elution using the same liquid mixture of 0.2M HCl and 0.1M oxalic
acid promotes a long term stability of the 44Ti/44Sc generator. In addition,
periodical washing with the same mixture allows for focusing the 44Ti
distribution on the ion exchange column. The effect is a smaller breakthrough of
44
Ti. The standard forward elution strategy resulted in an increasing breakthrough
of 44Ti, which amounts to 50% desorption of 44Ti after about 30 elutions and an
almost complete release of 44Ti after 50 elutions. In contrast, the breakthrough of
44
Ti in the case of the reverse elution scheme is negligible for the first ten
elutions, and increases only slightly in the following 40 elutions. The maximum
breakthrough for the reverse elution/washing procedure for 44Ti is about 0.2%.
The elution procedure for the final 185 MBq 44Ti/44Sc generator defines an
elution volume per batch of 20 mL of a mixture of 0.005M H2C2O4 and 0.07M
HCl.

3.2.3.4. From eluted radionuclide to 44Sc labelled tracer

Post-elution processing studies were performed to reduce the volume and

acidity of 44Sc eluate from the 44Ti/44Sc generator and to reduce the amount of
44
Ti in the final product for the syntheses of 44Sc labelled radiotracers.
To reduce the volume of the 44Sc eluate, an additional column filled with the
cationic resin BioRad AG-W50x8 (H+ form) was connected with the primary
generator in such a way that the eluate passed directly through the cation
exchanger. In this process, the 44Sc(III) is adsorbed on the cationic resin, from
which it can be eluted by 3 mL of 0.25M ammonium acetate at pH4.0. This
solution is now ready for labelling and complexation. Subsequently, the cation
exchanger column is reconditioned by washing with 1 mL of 4M HCl and 1 mL
of water in order to prepare the generator system for the next elution sequence.

67
FIG. 28. Schematic diagram of 44Ti/44Sc generator together with post-elution processing of
44
Sc eluates and generator associated syntheses of 44Sc labelled compounds [42].

Finally, around 160 MBq of 44Sc is obtained daily in 3 mL 0.25M ammonium

acetate buffer (pH4.0). The generator system is sketched in Fig. 28.

68
 The operational procedure is as follows:

• The 20 mL generator elution liquid, consisting of a mixture of

0.005M H2C2O4 and 0.07M HCl, is percolated through the 44Ti/44Sc
generator (forward elution) with a flow rate of 1 mL/min by use of a
syringe.
• The eluted 44Sc(III) adsorbs on-line on the small cationic cartridge between
the three-way valves I and II. The 44Sc(III) is retained on the column,
whereas the generator eluate continues to the waste vial (line 2).
• The cation exchange resin is then washed with 2–4 mL of H2O in order to
remove the remaining traces of the initial eluate solution. The wastewater is
directed to the waste vial. Subsequently, 5 mL of air is blown through the
cation exchanger column, and the 44Sc is eluted by pressing slowly 3 mL of
0.25M ammonium acetate buffer (pH4.0) slowly (0.7 mL/min) through the
column with a 2 min break after each 1 mL. The 44Sc is collected in an
11 mL glass reaction vial through flow line 4.
• Again, air is passed through the column to remove traces of the ammonium
acetate buffer solution remaining in the interstitial volume of the column
and in the dead volume of the connecting flow lines.
• Reconditioning of the cation exchange column is achieved by washing with
1 mL of 4M HCl and finally by 1 mL H2O through flow line 4.
• Finally, the generator column is conditioned by sucking 20 mL of a liquid
mixture consisting of 0.2M HCl and 0.1M oxalic acid through the column
from the ‘reverse’ elution mixture reservoir by means of a syringe. Thus,
the column is prepared for the next elution.

Using this post-processed fraction, radiolabelling yields of >96% were

obtained when 30 µL (21.1 nmol) of DOTATOC was added to 3 mL of the 44Sc
eluate (pH4.0) and heated in the oil bath for 25 min at 95ºC [43]. Microwave
assisted labelling speeded up 44Sc complexation with DOTATOC. After 1 min of
microwave heating reaction, the yield was >95% and increased up to 98% during
the next 2 min.

3.2.3.5. Availability and current status

Low production rates require production of 44Ti at dedicated accelerators.

Nevertheless, 44Ti in >370 MBq (10 mCi) batches are commercially available. To
date, no commercial 44Ti/44Sc radionuclide generator systems are available.
Research and development are currently in progress.

69
 68
FIG. 29. Decay scheme of Ga to stable 68Zn [44].

3.2.3.6. Possible applications

The 44Ti/44Sc radionuclide generator provides an optimum choice of long

shelf life, a medium half-life and an optimum decay mode of the daughter.
Modules might be designed for synthesis of 44Sc labelled environmental and
industrial tracers. The 3.92 h half-life of 44Sc and the high positron branching
ratio of 94% may stimulate the application of 44Sc labelled tracers for the study of
flow structures in various types of mass transport by the PET technique. In
addition, the high energy gamma emission of 1157 keV appears to be ideal for
industrial purposes due to the penetrating power of these gamma rays. By
measuring the counting rate ratio of the 511 keV and 1157 keV photons using
detection equipment with spectroscopic properties, some information about the
depth distribution of the traced mass flow components can be achieved.

3.2.4. The 68Ge/68Ga radionuclide generator

Relevant nuclear data for this radionuclide generator system are given in
Table 4 and the decay scheme of 68Ga is given in Fig. 29.

70
3.2.4.1. Relevant nuclear properties

(a) Daughter photon emission

The parent radionuclide 68Ge decays via electron capture to

68
Ga (T½ = 270.95 d). The 68Ga formed subsequently decays (T½ = 67.63 min) to
stable 68Zn (see the decay scheme of 68Ga in Fig. 29). Gallium-68 is a positron
emitter with 89% positron branching accompanied by low intensity photon
emission (1077.4 keV, 3.23%). The 68Ge itself does not emit significant photon
radiation.
The high branching positron emission (89%) with maximum and mean
positron energies of 1.9 and 0.79 MeV, respectively, provides intense 511 keV
annihilation photon emission. This photon energy is adequate for transmission
through thick metal walls and detection outside of industrial vessels or tubings,
and is therefore suitable for on-line measurements in the industry. As for the case
of 44Sc above, the annihilation character with two 511 keV photons moving in
opposite directions allows for coincidence detection and PET. This offers the
potential for determination of the radionuclide distribution with high local
resolution. In addition, the counting rate ratio of the 511 keV photon and the
1077.4 keV gamma ray allows for on-line measurements of depth distributions of
the traced material in an industrial mass flow. A gamma spectrum is shown in
Fig. 30.

(b) The daughter half-life

The daughter half-life of 67.63 min offers industrial measurements of

medium to short duration.

(c) The mother half-life

The mother half-life of 270.95 d offers a shelf life of the generator of about
1.5–2 a.

(d) Main production routes and expected yield of the mother radionuclide

There are several possible production routes for 68Ge. Two of the most
convenient are the 66Zn(,2n) reaction (66Zn abundance: 27.8%) and the
69
Ga(p,2n) reaction (69Ga abundance: 60%). The first reaction has a yield of about
37–74 kBq (1–2 Ci) A/h, while the second reaction has a higher yield [about

71
 FIG. 30. Gamma spectrum of 68Ga accumulated with an HPGe detector.

740 kBq (20 Ci)], and would be the primary choice for routine production for
beam energies around 25 MeV [45]. The useful energy range for production is
35–13 MeV (see the excitation function in Fig. 31). High production yields of
several gigabecquerels per batch are achieved at accelerators providing sufficient
proton flux (>100 A).

3.2.4.2. Generator systems, separation techniques and chemical form of 

the daughter

The chemical details of the individual 68Ge/68Ga generator systems

developed during the last 50 years (as mainly stimulated by radiopharmaceutical
chemistry and nuclear medical applications of 68Ga labelled tracers for biological
systems) are given in Table 6.
Early attempts to adopt liquid–liquid extraction chemistry for routine
generator use were not sustainable and concentrated mainly on column based
generators.

72
 FIG. 31. Excitation function for the reaction 69Ga(p,2n)68Ge [46].

The early column based generator systems eluted 68Ga with 0.005N EDTA
solutions from 68Ge, absorbed on alumina or zirconium oxides [46]. It provided
non-charged 68Ga–EDTA complexes. Elution efficiencies have been almost
quantitative, and the thermodynamically very stable Ga–EDTA complex appears
to be a suitable water tracer at moderate temperatures (<80–90C).
However, the high complex stability prevented the direct use of this eluate
for further 68Ga labelling reactions. Analogously, 68Ge was retained on antimony
oxide Sb2O5 and 68Ga was eluted with oxalate solutions [51]. Anion exchange
resins using dilute hydrofluoric acid solutions as eluent allowed high purity
separations due to the significant differences of distribution coefficients of the
elements [53]. The breakthrough of 68Ge was <10−4 for up to 600 elutions, and the
68
Ga yield was >90%. In all these cases, further application of the generator
eluate for 68Ga labelling reactions was not possible or difficult due to the strong
gallium fluoride complex.
As Ge(IV) is known to form a very stable complex with phenolic groups, its
adsorption on a 1,2,3-trihydroxybenzene (pyrogallol)–formaldehyde resin was
utilized to elute 68Ga3+ (or a mixture of chloride complexes) in strong (1M)
hydrochloric acid [55]. Average yields of 68Ga of 75% during a period of 250 d
were reported. The Ge breakthrough was <0.5 ppm, with no detectable radiolytic

73
 TABLE 6. THE 68Ge/68Ga GENERATORS FROM PUBLISHED LITERATURE

74
Column material Elution agent Elution yield Reference

Al2O3, ZrO2 Elution agent: 0.005M EDTA Ga recovery 70% [47]

Ga eluted as EDTA complex

Hydrated MnO2 Elution agent: 1M HNO3 Ge ret.>99%, Ga elut.>97% [48]

Probably eluted as Ga3+

Hydrated MnO2 Elution agent: 1M HClO4 Ge ret.>99%, Ga elut.>97% [48]

Probably eluted as Ga3+

Hydrated antimony pentoxide Elution agent: 14M HNO3 Ge ret.>99%, Ga elut.>97% [48]
Probably eluted as Ga3+

Acidic aluminium oxide, Al2O3 Elution agent: 1M HClO4 Ge ret.>99%, Ga elut.>97% [48]
Probably eluted as Ga3+

Tin dioxide, SnO2 Elution agent: 1M HCl Ge ret.>99%, Ga elut.>97% [48]

Probably eluted as Cl complex

Tin dioxide, SnO2 Elution agent: 1M HNO3 Ge ret.>99%, Ga elut.>97% [48]

Probably eluted as Ga3+

Al(OH)3, Fe(OH)3 Elution agent: weak HCl — [49, 50]

Probably eluted as Cl complex

SnO2, ZrO2, TiO2 Elution agent: 1M HCl Ga recovery 70–80% [51]

Probably eluted as Cl complex Ge leakage 10−6–10−5% per bolus
 TABLE 6. THE 68Ge/68Ga GENERATORS FROM PUBLISHED LITERATURE (cont.)
Column material Elution agent Elution yield Reference

No column: solvent extraction process Extraction: 8-hydroxy-quinoline in chloroform at Ga recovery as Ga–oxine complex: [51]
pH5 with Ge4+holdback carrier followed by 70–80% Ge breakthrough <0.003%
evaporation to dryness

Antimony pentoxide Sb2O5 Elution agent: oxalate solution — [52]

Probably eluted as oxalate complex Ga(Ox)x3 − x a

Tin dioxide , SnO2 Elution agent: 1M HCl Ga recovery 75–90% [53]

Probably eluted as Cl complex Ge leakage <0.0002% per elution

Anion exchanger, BioRad AG1-8x, Elution agent: 0.01M HF Ga recovery >90% [54]
probably sorbed as GeF62− Ga eluted as GaFx3 − x a Ge leakage <10–4 for 600 elutions

Anion exchanger, BioRad AG1-8x, Elution agent: 0.5M HCl Ga recovery 75% [55]
probably sorbed as GeF62− Form of Ga in eluate as Cl complex Ge leakage <0.5 ppm

Hydrous zirconium oxide Elution agent: not given Ga recovery 30–40% [56]
Ge leakage <10 ppm

Anion exchanger, Elution agent: weak acid, Recovery and leakage not given [56]
probably sorbed as GeF62− no further details known

Pyrogallol/formaldehyde 1M HCl Ga recovery 60% [55]

condensation product Probably eluted as Cl complex Ge leakage <10–3%

Pyrogallol/formaldehyde Elution agent: 0.3M HCl Ga recovery 60% [57]

condensation product Probably eluted as Cl complex Ge leakage <10–3% per elution

75
 TABLE 6. THE 68Ge/68Ga GENERATORS FROM PUBLISHED LITERATURE (cont.)

76
Column material Elution agent Elution yield Reference

Tin(II) oxide, SnO Elution agent: HCl (conc. not given) Recovery and leakage not given [58]
Probably eluted as Cl complex

Tin(IV) dioxide, SnO2 Elution agent: 1M HCl Recovery and leakage not given [59]
Probably eluted as Cl complex

Tin(IV) oxide, SnO2 Elution agent: 1N HCl Recovery and leakage not given [60, 61]
Ga eluted as Cl complex
Ether extraction from 6N HCl
Probably extracted as GaCl3

Iron(III) oxide, -Fe2O3 Elution agent: HCl (pH2) Ga recovery 50–70% [62]
(alpha-ferric oxide) Probably eluted as Cl complex Ge leakage <2 × 10–4% elution

Cerium(IV) oxide, CeO2 Elution agent: 0.02M HCl Ga recovery 45% [63]
Probably eluted as Cl complex Ge leakage <0.007

Cerium(IV) oxide, CeO2 Elution agent: 0.02M HCl Ga recovery 56% in 0.5 mL [64]
Probably eluted as Cl complex Ge leakage not detected

Tin(IV) oxide, SnO2 Elution agent: 1M HCl Ga recovery 55–75% [65]

Probably eluted as Cl complex Ge leakage ~10−7

Iron(III) oxide, -Fe2O3 Elution agent: 0.05M HCl Ga recovery 90% [66]
(alpha-ferric oxide) Probably eluted as Cl complex Ge leakage <1.8 × 10–4% elution
 TABLE 6. THE 68Ge/68Ga GENERATORS FROM PUBLISHED LITERATURE (cont.)
Column material Elution agent Elution yield Reference

Hydrated SnO2 Elution agent: 0.1M HCl Ga recovery ~88% in 2 mL eluate [67]
Probably eluted as Cl complex Ge leakage not given

Tin(IV) oxide, SnO2 Elution agent: 0.1M HCl Ga recovery 60–70% in 4 mL eluate [68]
Probably eluted as Ga3+ Ge leakage not given

Al2O3 treated with 0.1M NaOH Elution agent: 0.1M HCl Ga recovery 50–70% [69]
Probably eluted as Cl complex Ge leakage 2 × 10–4%

Styrene–divinylbenzene co-polymer Elution agent: citric or phosphoric acid Elution yield not given [70]
with N-methylglucamine groups Ga eluted as a low affinity complex Ge leakage <4 × 10–4%

Hydrous ZrO2 Elution agent: 0.1N HCl Elution yield 30–40% [56]
Probably eluted as Cl complex Ge leakage 10–3% at 0.5 mL/min

Hydrous or crystalline SnO2 Elution agent: 1M HCl Elution yield ~65% [71]
Probably eluted as Cl complex Ge leakage ~6 × 10–4%
a
Where x = 1 or 2.

77
by-products for a 370 MBq (10 mCi) generator. The pyrogallol–formaldehyde
resin was found to be resistant to radiation degradation. An organic macroporous
styrene–divinylbenzene co-polymer containing N-methylglucamine groups was
developed to provide 68Ga with a solution of a low affinity gallium chelating
ligand such as citric or phosphoric acid [69]. The 68Ge breakthrough was
<0.0004% of the 68Ge adsorbed on the resin. These generator strategies are
currently taken up by a commercial system distributed by ITG, Germany.
Ionic 68Ge/68Ga generators were developed, avoiding the formation of a
stable 68Ga–ligand complex in the eluate system. This strategy is achieved for
both 68Ga(OH)4− and 68Ga3+, providing eluates. Indeed, 68Ga has been eluted in
0.1M NaOH solution as gallate anion from alumina columns [72]. A comparison
of performances of alumina/EDTA, alumina/NaOH and tin oxide/HCl generators
[60], however, indicated superior characteristics for the latter system in terms of
68
Ge breakthrough and 68Ga3+ elution efficiency in 1M hydrochloric acid. The
68
Ge/68Ga generators, which provide 68Ga3+ ions (or 68GaClx3−x complexes where
x = 1 or 2) in the eluate, are based on inorganic matrices like Al2O3, Al(OH)3,
Fe2O3, Fe(OH)3, SnO2, ZrO2, TiO2 and CeO2. The SnO2 showed the best
performance in terms of low 68Ge breakthrough (10–6–10–5% per elution) and
high 68Ga elution efficiency (70–80% per elution) with 1M hydrochloric acid.
Figure 32 provides a sketch of the various development attempts towards the
present-day design of 68Ge/68Ga radionuclide generators for routine application in
the medical area, and which, with some adjustment, can also be applied for
industrial purposes.

3.2.4.3. Commercial availability of the 68Ge/68Ga radionuclide generator

For commercial generator productions, a modified TiO2 phase has been

used by Cyclotron Ltd, Obninsk, Russian Federation, since about 2000. These
generators are eluted with 0.1N HCl and show initial 68Ga elution yields of about
80%, with 68Ge breakthrough of about 1 × 10–3%. These data deteriorate over
time (e.g. after about 1 year) or with increasing number of elutions (e.g. 200),
approaching values of about 50% of 68Ga elution and about 10–2% of 68Ge
breakthrough.
A similar generator is available from Eckert & Ziegler known as ‘IGG 100’
(Fig. 33(a)), which provides improved elution characteristics. The elution
efficiency of 68Ga from the fresh generator is ~70%. This value can drop
somewhat if the generator is not eluted for a few days. The 68Ge breakthrough
typically ranges from 3 × 10–5%, when new, to 5.0 × 10–3% after 200 elutions.
Breakthrough can increase up to 1.0 × 10–3% if the generator is not eluted for a
few days. After a break in use, the generator should be pre-eluted with 10 mL of
0.1M HCl 1 d prior to the intended use.

78
FIG. 32. Summary illustration of some published column concepts: liquid–liquid extraction
(left), column based with inorganic column fill material (centre) and column based with
organic (polymer) column filling material (right).

Other systems using a SnO2 based solid phase are produced at Themba
Labs, Republic of South Africa, and delivered by IDB Holland B.V., see
Fig. 33(b). The generator should be eluated with 0.6M HCl. The yield in 5 mL of
eluant is not <80%. The 68Ge breakthrough is <0.002% at the reference date.
Recently, the China Institute of Atomic Energy (CIAE) started delivery of a
few test series of generators also based on SnO2 support. The generators have
been made available to participants in a recent IAEA CRP entitled Evaluation and
Validation of Radionuclide Generator-based Radiotracers for Industrial
Applications, which ended in 2011.
Typical performance data for these generators are displayed in Figs 34 and
35. The generators are produced without the need for sterile conditions because,
for most industrial applications, this is not a requirement. Hence, the production
process can be made somewhat simpler than for generators intended for medical
use, and this should be reflected in a somewhat cheaper price. The elution yield,
which is initially around 60%, seems to deteriorate somewhat, but not
dramatically, in the long term, as displayed in Fig. 35.

79
FIG. 33. (a) The IGG 100 68Ge/68Ga radionuclide generator, Eckert & Ziegler AG, Berlin.
(b) The 68Ge/68Ga generator produced by iThemba Labs and delivered by IDB Holland B.V.

FIG. 34. Typical elution yield of the CIAE 68Ge/68Ga radionuclide generator over the first
12 weeks after the generator was received in the IFE testing laboratory [73].

80
FIG. 35. Example of measured elution yield of the CIAE 68Ge/68Ga radionuclide generator
over the first 3 years after the generator quality check at the production laboratory. A 3 year
period is about the useful lifetime of a 68Ge/68Ga generator. The generator has been eluted
several times within short time periods that are spaced by several months [74].

Variations in 68Ge breakthrough over the first 11 elutions (one per week) of
the CIAE produced generator are given in Fig. 36.
Part of the breakthrough is due to tiny particles from the primary column
bed containing 68Ge. An acceptable breakthrough fraction should be <10–5.
Hence, an improved bed filter support and a secondary (catcher) column should
be implemented for this generator.
An example of an elution curve is given in Fig. 37. Around 80% of the
activity is collected in a volume of 3 mL (fraction 6–8). This is an acceptably
small volume for further complexation reactions.
The 68Ge/68Ga radionuclide generator has been investigated for almost
50 years, since the cyclotron independent availability of positron emitting 68Ga
via the 68Ge/68Ga system had always attracted research in basic nuclear chemistry,
as well as in radiopharmaceutical chemistry. However, it took decades and
generations of research to finally reach a level of 68Ge/68Ga radionuclide
generator designs adequate to the modern requirements of radiometal labelling
chemistry. This landmark can directly be associated to the radiochemical concept
of providing cationic 68Ga3+ rather than 68Ga fluoride, oxalate or EDTA
complexes as eluates. In about 2001, Cyclotron Ltd, Obninsk, Russian

81
FIG. 36. Example of 68Ge breakthrough during elution of the CIAE 68Ge/68Ga radionuclide
generator during the first 11 weeks after the generator was received in the IFE testing
laboratory [73].

FIG. 37. Example of a 68Ga elution curve of the CIAE 68Ge/68Ga radionuclide generator [75].

82
Federation, offered such systems with 68Ge absorbed on modified TiO2 columns
and 68Ga eluted using 0.1N HCl.
The exciting perspective for the 68Ge/68Ga radionuclide generator system,
however, asks for systematic chemical, radiochemical, technological and
radiopharmaceutical efforts, to guarantee reliable, highly efficient and
industrially approved 68Ge/68Ga generator systems. The production of the
radionuclide generator parent, its separation from the target material, and the
chemical and technical concept of the separation of the daughter radionuclide are
factors that result in an efficient and easy application of the generator. The IAEA
has recently initiated a comprehensive review on the production of several
generator mother nuclides which includes discussion of 68Ge [76]. The
radiochemistry of 68Ge was covered comprehensively in 1996 [77], and a more
recent compilation on radionuclide generators systems including 68Ge/68Ga can
be found in Ref. [78]. Recent reviews on the 68Ga radiopharmaceutical and
coordination compounds appeared in 2008 [79, 80].

3.2.4.4. Possible applications

Post-processing systems have been developed for fast generator processing,

including syntheses and purification of 68Ga tracers. In parallel with the
increasing interest for PET imaging related to medicine, there is a potential for
application of the positron annihilation radiation and the PET method also in
various industrial examinations.
Gallium-68 tracers suitable for aqueous, organic and solid phase tracers for
industrial and environmental examinations have partly been developed already,
and this development continues. One main feature of the generator is that it can
be used three to four times per day at close to maximum activity, allowing
repeated studies. Another feature of this radionuclide is the photon energy of
1077 keV, which is coincident with the annihilation radiation, allowing for
additional in-depth information from the study of volume flow with ‘ordinary’
RTD measurement techniques.

3.2.5. The 82Sr/82Rb radionuclide generator

Relevant nuclear data for this radionuclide generator system are given in
Table 6 and the partial decay scheme of 82Sr is given in Fig. 38.

83
FIG. 38. Decay scheme of 82Rb to stable 82Kr [81]. Newer data suggest that the absolute
intensity of the 776.5 keV gamma ray is 15.1%.

3.2.5.1. Relevant nuclear properties

(a) Photon emission of the daughter radionuclide

The 82Rb has a high branching positron emission (96%) with

maximum/mean kinetic energy of 3.38 MeV, providing intense 511 keV
annihilation photon emission in addition to a relatively strong gamma ray at
776.5 keV with an intensity of about 15%. The photon energies are adequate for
transmission through thick metal walls and detection outside of the vessel or
tubing, and therefore suitable for on-line measurements in the industry.
Annihilation character might allow for coincidence detection with potential of
determination with high local resolution of the radionuclide distribution. The
single photon, together with the annihilation radiation, provide for some depth
resolution close to the vessel walls. A gamma spectrum is given in Fig. 39.

84
 68
FIG. 39. Gamma spectrum of Ga accumulated with an HPGe detector.

(b) Half-life of the daughter radionuclide

The daughter half-life of 1.273 min offers industrial measurements of very

short duration and provides for frequent measurement repetitions.

(c) Half-life of the mother radionuclide

The mother half-life of 25.6 d offers the generator a shelf life of about
2 months.

(d) Main production route and expected yield

The most common production route of 82Sr is the 85Rb(p,4n)82Sr reaction,

but it is also produced by the 82Kr(3He,3n)82Sr reaction and the NatMo(p,spall.)
process. The optimal proton energy range for the (p,4n) reaction is 65–40 MeV,
the maximum on the excitation function being at about 50 MeV (Fig. 40). One of

85
 FIG. 40. Excitation function for the 85Rb(p,4n)82Sr reaction [44].

the important contaminants is 85Sr, which is produced simultaneously when

natural rubidium is used as the target material. Recently, Qaim et al. [82]
determined that an incident proton energy of 60 MeV or above is recommended.
The 85Sr impurity then corresponds to <20%.
Some data on target materials and irradiation yields are summarized in
Table 7.
According to Fig. 41, the excitation curve maximum for the 82Kr(3He,3n)
reaction is around 32–33 MeV, and there is useful production down to about
22 MeV. However, the shape of the curve above 34 MeV is not considered. When
natural krypton is used as the target material, the 82Sr production begins at
approximately 18 MeV and increases to a maximum of 80 mb at 62 MeV [83].
The 83,85Sr are contaminants simultaneously produced in relative amounts that
depend on the utilized effective energy range, and there is no energy range that
allows pure 82Sr production alone.
The calculated thick target yield at end of bombardment from 90–20 MeV
was 1290 kBq·μA–1·h–1. At low beam intensities (up to 3 A), the experimental
yields were close to the values calculated from the excitation function. However,
at 15 A, the end of bombardment production yield decreased by 50% to
630 kBq·μA–1·h–1 owing to gas density reduction in the beam strike area. For the
spallation reaction on the Mo target, there is a requirement for 600–800 MeV
protons. Commercial generators with up to 3.7 GBq (100 mCi) are available.

86
TABLE 7. IRRADIATION CONDITIONS AND YIELDS FROM THE
CURRENT SUPPLIERS OF 82Sr [83]
Laboratory Target Irradiation conditions Yields (EOB
MBq·μA–1·h–1)a

Brookhaven National Laboratory RbCl 2 targets (96–74 and 10.5

66–44 MeV)
14 d irradiation

Institute for Nuclear Research, Rb metal 100–40 MeV 18

Moscow

Los Alamos National Laboratory RbCl 2 targets:

97–71 MeV 13.3
65–45 MeV 8.2

iThemba Labs RbCl 61–44 MeV 8.6

a
Batch sizes typically range from approximately 65 to 450 GBq; EOB: end of bombardment.

FIG. 41. Excitation function for the 82Kr(3He,3n)82Sr reaction [46, 84, 85].

87
3.2.5.2. Generator systems, separation techniques and chemical form of
the daughter

The 82Sr/82Rb generator has, by now, had more than 30 years of

development. Table 8 intends to give a flavour of the various generator types that
have been developed and tested during this period.
Synthetic organic resins such as BioRex-70 and Chelex-100 and inorganic
ion exchangers such as ZrO2 and Al2O3 were developed and 82Rb eluted with
2% NaCl solutions. Other systems utilize hydrated SnO2, with 82Rb eluted with
physiological NaCl solution (Fig. 42). Elution yields as high as close to 100% and
breakthrough as low as 10–9/mL have been reported (see Table 8).
Today, the generator is routinely used, especially in clinical practice in
hospitals. As 82Rb is injected intravenously directly from the generator, 82Rb must
be obtained from the generator in a sterile pyrogen free physiological medium.
This requirement is not necessary in general in industrial applications unless,
possibly, when examinations are carried out in the food processing industry.

3.2.5.3. Availability and current status

• Commercial generators with up to 3.7 GBq (100 mCi) are available. Up to

July 2011, the company Bracco Diagnostics Inc. provided a generator with
the trade name CardioGen-82®. It has recently been temporarily withdrawn
from the market. This recall was initiated following discussions with the
US Food and Drug Administration regarding reports of unexpected
radiation exposure in two individuals who underwent cardiac PET scans
with CardioGen-82. This kind of question is, of course, not of importance
for industrial applications, but the withdrawal affects commercial generator
availability.
• The generator is routinely used in clinical practice, but has not yet been
used in industrial studies.
• There is an established radionuclide generator separation chemistry which
is easily modified for use in field applications.

3.2.5.4. Possible applications

This generator is useful for the study of mass flow in systems where the
flow structure changes frequently, for example, during parameter tuning for
process optimization. The short half-life of the daughter radionuclide permits
frequent elutions and repeated examinations of a frequency of, perhaps, one
elution/injection every 5 min.

88
 TABLE 8. SOME REFERENCES SHOWING THE DIVERSITY OF COLUMN MATERIAL AND GENERATOR
PROPERTIES DURING 30 YEARS OF GENERATOR DEVELOPMENT
Column material Elution agent Elution yield Reference

Chelating cation exch.: Chelex-100 0.2M NH4Cl Sep. factor Sr/Rb: >107 [86]
Elution yield 80% in 15 mL

Cation exch.: BioRex 70 2% NaCl Sep. factor Sr/Rb: 107–108 [87]
Chelating cation exch.: Chelex-100 Sep. factor Sr/Rb: 5 × 104

SnO2 (hydrous) Physiological saline = 0.9% Best results:  [55]

82
Ti(OH)4 NaCl Sr breakthrough: <10–9/mL
polyantimonic acid Elution yield: 90% at a flow rate of 30 mL/min

Al2O3 2% NaCl Sep. factor Sr/Rb: 106–107 [88]

Elution yield 70–90% in 25 mL
82
Dual column: 1.8% NaCl, pH9–10 Sr breakthrough: <5 × 10–5/mL [89]
basic Al203 + Chelex-100, Elution yield 66% at elution rate 18 mL/min
82 2+
Sr loading on the Al2O3
at pH9–10

SnO2·xH2O Physiological saline Sep. factor Sr/Rb: 105 [90]

Elution yield 100% in 47 mL at elution rate 25 mL/min

Hydroxyapatite, [91]
general formula M10(PO4)6(OH)2
where M is various metals

89
90
TABLE 8. SOME REFERENCES SHOWING THE DIVERSITY OF COLUMN MATERIAL AND GENERATOR
PROPERTIES DURING 30 YEARS OF GENERATOR DEVELOPMENT (cont.)
Column material Elution agent Elution yield Reference

SnO2 Physiological saline Sep. factor Sr/Rb: 5 × 106 [92]

Elution yield 10–40% in 15 mL

SnO2 Saline, eluted as Rb+ No significant breakthrough after 20 L saline [93]

Sodium non-atitanate: NaCl (0.001–1M), eluted Separation factor Sr/Rb >5.5 × 104 using 0.1M NaCl [94]
Na4Ti9O20·xH2O as Rb+

A special non-regular
column approach
82
Sr2+ + 82Rb+ in nuclear Selective sorption of 82Rb+  Separation factor of 82Sr/82Rb: >104 at 0.5M HNO3 Method possible
secular equilibrium in by inorganic ion exch.: leaving 82Sr2+ in solution. 82Rb+ eluted quantitatively on the basis of
solution cryptomelane with strong (>6M HNO3) Ref. [95]
MnO2 = KMn(IV)6Mn(II)2O16
where K is exchangeable
FIG. 42. Example of a 82Sr/82Rb generator with a catcher column to reduce breakthrough of
82
Sr and a modifier liquid to prepare the 82Rb solution, either for direct infusion or for further
synthesis into an applicable tracer for various fluid phases [89].

3.2.6. The 99Mo/99mTc radionuclide generator

Relevant nuclear data for this radionuclide generator system are given in
Table 4, and the simplified and partial decay scheme of 99mTc is given in Fig. 43.

3.2.6.1. Relevant nuclear properties

(a) Photon energy of the daughter

Decay of the mother radionuclide 99Mo populates several excited states in

the daughter 99Tc, but only the two states at 920.5 keV and 142.6 keV are of

91
FIG. 43. Decay scheme of 99Mo to excited states in 99Tc including the long lived state at
142.6 keV, which may then be regarded as a separate radionuclide 99mTc [83].

importance due to spin/parity difference restrictions for the other states. The long
lived excited state at 142.6 keV in 99Tc constitutes the isomer 99mTc. It decays
primarily by conversion of electron emission to the first excited state in 99Tc at
140.5 keV, which again decays by internal transition (IT) to the ground state
primarily by emission of an intense gamma ray with energy of 140.5 keV. The
ground state is very long lived and decays by negatron emission to stable 99Ru.
The 99Mo/99mTc radionuclide generator has mainly been developed for
nuclear medical purposes. Today, 99mTc, in the form of 99mTcO4− (and many other
compounds) is the main ‘workhorse’ for a variety of examinations in nuclear
medicine. Therefore, detection equipment such as position sensitive gamma
cameras and other instruments for single photon emission computed tomography
(SPECT) (collimators and scintillation crystal thicknesses) have been optimized
for 140.5 keV.
Although the gamma energy of 140.5 keV is not optimal for many
industrial examinations (too low an energy), the choice of this radionuclide in the
present text is due to its wide availability around the world. In several cases, i.e.
in laboratory flow equipment and in smaller industrial systems, the energy is
sufficient for transmission through the flowing medium and through the
enclosing walls of the equipment. The photon energy is appropriate for many
common detector materials such as plastic scintillators and smaller detectors such

92
 99m
FIG. 44. Gamma spectrum of Tc accumulated with a Ge(Li) detector.

as CdTe, but is, of course, also readily detected with other common solid
scintillation detectors such as NaI(Tl), CsI(Tl), BGO and BaF2, by HPGe
semiconductor detectors, and even with liquid scintillation adopted to a flowing
liquid stream. A gamma spectrum is provided in Fig. 44.

(b) Half-life of the daughter

The daughter half-life of 6.02 h covers industrial experiments with a

duration of the order of 1 d, and is the one daughter radionuclide considered in the
present text with the longest half-life. A generator can be eluted at a frequency of
a few hours and still give adequate activity because generators can be provided
with a high initial activity. Thus, several experiments (3–5) can be performed
during 1 d following individual elutions of the generator. Alternatively, and
especially in the start when the generator is ‘fresh’, one single elution will
provide sufficient activity for several experiments/injections.

93
(c) Half-life of the mother

The mother half-life of 66 h (2.7 d) provides for a shelf life of about 2 weeks.
It also allows for transport of the generators to remote locations (for instance,
offshore installations), even with surface transportation. A special point of interest
is that when such a generator has become useless for hospitals, it may still be useful
for technical and industrial tracer examinations. Thus, the generator can be
inherited from hospitals after 2.5 half-lives to a cheaper price and utilized the
following week before returned to the production company for decommissioning.

(d) Main production routes

(i) Production by fission of 235U

Over 80% of diagnostic nuclear medical imaging today uses

radiopharmaceuticals containing 99mTc, entailing over 30 million investigations
per year. Over 95% of the 99Mo required for 99mTc generators is produced by the
fission of 235U targets (99Mo cumulative fission yield 6.1%) in nuclear research
reactors. These reactors are multipurpose installations and not dedicated only to
medical radionuclide production. In addition, the duty cycle (up-time) of the
various reactors differs considerably from about 100 d/year for some to about
300 d/year for others.
During the last two decades a number of research reactors, which
previously were available for radionuclide production, have been shut down, and
the expression ‘neutron drought’ has been invented to describe the current
situation. Hence, there are at present only a few main 99Mo production sites
around the world that utilize the fission production method, see Fig. 41.
In most reactors, the target material is highly enriched 235U (HEU) to ensure
maximum production for the neutron flux available, while others use uranium of
lower 235U content (LEU) with correspondingly lower production rates. This kind
of production is followed by chemical processing of the target to isolate 99Mo in a
close to carrier free condition. This is a very complicated process, and only a few
laboratories around the world are equipped to take on this task. The main
processing facilities are shown in Fig. 45. An example of irradiation yield with
this method is given in Table 9.
After isolation of 99Mo, the radionuclide is shipped to other laboratories for
production of the 99Mo/99mTc generator. Various laboratories use different
methods, but most of the methods are based on a chromatographic or ion
exchange column where 99mTc is extracted by column elution, although the
column support may vary somewhat. The most important laboratories are shown
in Fig. 45.

94
FIG. 45. The most important reactor facilities for irradiation of 235U (HEU or LEU),
processing of the irradiated target for isolation of 99Mo and manufacturing facilities for the
99
Mo/99mTc generator.

TABLE 9. EXAMPLE OF IRRADIATION YIELD OF 99Mo FROM FISSION

OF A 235U TARGET [96]
Parameter Value

Neutron flux 1.5 × 1014 n·cm–2·s–1

235
U/Al target alloy 4.2 g 235U, 45% enriched

Irradiation time 20–200 h

Irradiation yield 7.4–18.5 TBq (200–500 Ci) per batch

The mother nuclide 99Mo is extracted from a fission mixture in alkaline

solution, in the form of molybdate anion, 99MoO42−. This solution is acidified in
order to form oligomers of 99Mo compounds for better adsorption characteristics
on the chromatographic column. The 99Mo is fixed on a pre-acidified alumina
(Al2O3) column. The 99mTc is eluted from the column easily with 0.9% NaCl
solution (physiological solution) in the form of 99mTcO4−. The 99Mo breakthrough
is generally of the order of 10–4.

95
 98
(ii) Production by neutron activation of Mo

Molybdenum-99 may also be produced by thermal neutron capture in the

stable molybdenum isotope 98Mo. The isotopic abundance in natural
molybdenum is 24.13%, but the reaction cross-section is, however, only 0.14 b.
The irradiation yield depends on the following four parameters: (i) isotopic
abundance (which may be increased by a factor of four by using isotopically
enriched material), (ii) amount of target material irradiated, (iii) neutron flux in
the irradiation channel and (iv) irradiation time. An example of an attainable
yield is given in Table 10.
However, since one has to irradiate macro-amounts of target material, the
specific activity in the irradiated target is rather low. This means that the small
size columns, which are sufficient for fission produced 99Mo, will not be
applicable here. One needs column material and column sizes large enough to
absorb higher quantities of Mo. For this purpose, molybdate gel columns, for
instance, have been developed [97].

(iii) Production by charged particle reactions

Much has been written in the literature about the 99Mo/99mTc generator.
Therefore, some useful references on this subject are presented in Table 11 and
some brief descriptions on the preparation of a few column based generators and
a generator based on solvent extraction are given.

99
TABLE 10. EXAMPLE OF IRRADIATION YIELD OF Mo FROM
NEUTRON IRRADIATION OF A Mo TARGET [96]
Parameter Value

Neutron flux 1.6 × 1014 n·cm–2·s–1

MoO3 target material, natural abundance 99–120 g

Irradiation time 1 week

Irradiation yield 1.48 TBq (40 Ci) per batch

96
TABLE 11. SOME USEFUL REFERENCES FOR THE PRODUCTION AND
USE OF A 99Mo/99MTc RADIONUCLIDE GENERATOR
Subject/title Reference

Fission molybdenum for medical use [96]

Alternative technologies for 99mTc generators [96]

Management of waste from 99Mo production [96]

Production technologies for 99Mo and 99mTc [96]

Manual for reactor produced radioisotopes [96]

99m
Tc generators, chemistry and preparation of radiopharmaceuticals [98]
99
Mo production using LEU targets [99]

Radionuclide generator technology [100]

Sol–gel processed ceramics for 99Mo/99mTc generator materials [101]

Conversion of 99Mo production from HEU targets [102]

99m
Tc gel generator usage with the aid of post-elution concentration [103]
of pertechnetate
99m
Tc generators: technology considerations and the IAEA contributions [104]
99m
Tc pharmaceuticals [105]

Polymer embedded nanocrystalline titania sorbent for 99Mo/99mTc generator [106]

Medical isotope production without highly enriched uranium [107]

Recovery of 99mTc from low specific activity (n,γ)99Mo based on [108]
solvent extraction and column chromatography

Separation of 99Mo from nitric acid medium by alumina [109]

A novel electrochemical technique for the production of clinical grade 99mTc [110]
using (n,γ)99Mo

Magnesium molybdate compounds as a matrix for 99Mo/99mTc generators [111]

97
FIG. 46. Production of 99Mo/99mTc generators based on chromatographic quality alumina at
the Centre of Isotopes in Cuba [112].

3.2.6.2. Generator systems, separation techniques and chemical form of 

the daughter

(a) Preparation of 99Mo/99mTc generators with alumina

The adsorption of the molybdate ion on the alumina is strongly affected by

the pH. The sorption capacity of the alumina that is used in the preparation of the
generators (chromatographic quality) at pH4.0 is ~20 mg of Mo per g of alumina,
but it falls quickly to 2 mg/g at somewhat higher pH values. Figure 46 shows a
picture from a typical generator production line.
For the preparation of a 3.7 GBq (100 mCi) generator, the following
procedure is followed:

• A quantity of chromatographic alumina (80–100 mesh) is washed with

distilled water, and the fine particles are eliminated by decantation.

98
 • About 10 g of alumina is transferred to a glass column with appropriate
support (Teflon and polyethylene filters) in the bottom and on the top of the
bed.
• The column is washed with 0.1M sterile and apyrogen HCl or HNO3 until a
pH of 1–2 is reached in the effluent.
• To prepare the loading solution, transfer the 99Mo to a beaker with 4 mL of
distilled water. Add 6M HNO3 until a pH of 3.0 ± 0.5. At smaller pH values,
the molybdenum can precipitate. In such a case, the precipitate may be
redissolved by adding NH4OH. Dilute the solution with distilled water until
25 mL.
• Percolate slowly the 99Mo solution through the column.
• Subsequently, wash the column with 100 mL of 0.1M HCl.
• Wash again the column with 75 mL of isotonic saline solution.
• Capture some drops of the last 10–20 mL of the washing liquid at the exit of
the column and transfer them to a test tube with some milligrams of
potassium ethyl xantate. Add two drops of 2M HCl. A red colour would
indicate that the 99Mo is eluting from the column, which should not happen.
In order to qualify the column and measure any trace of 99Mo breakthrough,
it is necessary to perform  spectrometry on a sample of the eluate and
follow the decay for a few half-lives of the 99mTc.
• Finally, the column should be end capped, placed in the shield and
autoclaved.

For industrial use, the requirements mentioned above (pyrogen free, sterile,
autoclaved) are not necessary for most industrial applications if the generator is
not going to be used in the drug or food industry.
Another method for preparation of a generator based on alumina is making
use of the reaction of the molybdate with phosphoric acid to produce
phosphomolybdate according to:

12MoO42− + H3PO4 + 21HNO3 → PMo12O40

3−
+ 21NO3− + 12H2O

The phosphomolybdate is subsequently loaded on to the column. This

system is not used for the production of medical generators due to traces of
phosphorous in the eluate of 99mTcO4−, but may be a good alternative when
preparing generators for industrial radiotracer applications.

99
(b) Preparation of generators of 99Mo/99mTc on other solid supports

(i) Hydrated zirconium oxide

Another 99mTc generator has been developed by using zirconium oxide as

the column material (e.g. see Ref. [113]). The 99Mo is loaded on to the zirconium
oxide with 0.01M HCl. The 99mTc is eluted with an acidic solution of MEK
solution: 5% v/v in 0.01M HCl. The technetium is complexed as a
H99mTcO4–MEK complex that is dissolvable in organic liquids. As such, the
complex may be directly used as a tracer of the organic phase.
In order to prepare a tracer for the aqueous phase, for instance, as 99mTcO4−,
MEK may be removed by evaporation, and the resulting residue leached with, for
instance, physiological saline solution.

(ii) Manganese dioxide

In the same way, one may adsorb the molybdate on to hydrated manganese
dioxide. The sorption capacity for 99Mo of the MnO2 is rather low. Therefore, this
procedure is impracticable for 99Mo generated by the (n,)99Mo reaction due to
the presence of macro-amounts of natural molybdenum. However, for 99Mo
produced by fission, where the carrier concentration is lower, this column support
is suitable for a 99Mo/99mTc generator. Molybdate retention during application on
the column consisting of 1 g MnO2 material of 99.7% has been reported [114].
The pertechnetate can be eluted with acidified water (pH  5) or 0.9% NaCl. An
elution yield >80% in 5 mL was achieved.

(iii) Hydrated titanium dioxide

Hydrated titanium dioxide has a higher absorption capacity for molybdate

than alumina. The exchange capacity was found to be 58 mg MoO3− per g
hydrated TiO2 and 50 mg MoO3− per g A12O3 at 0.1M HC1 [115]. The properties
of a column containing 2 g anhydrous TiO2 showed an elution efficiency of ~85%
in 10 mL 0.9% NaCl solution, and the breakthrough of 99Mo was reported to be
<10–3%.

(iv) Zirconium molybdophosphate–99Mo gel

Low and medium specific activity of (n,)99Mo produced by neutron

irradiation of MoO3 can be incorporated in an insoluble gel structure, which after
granulation, efficiently releases 99mTc on elution.

100
 Preparation of the ZrMP–99Mo gel was as follows [116]:

• 2 g of neutron irradiated MoO3 was dissolved in 5M NaOH by warming

with addition of a few drops of H2O2 according to the reaction:

MoO3 + 2NaOH  Na2MoO4 + H2O

• The molybdate–99Mo solution formed was converted into

molybdophosphate–99Mo by reacting with a calculated amount of
NaH2PO4·3H2O (160 mg) according to the reaction:

12Na2MoO4 + NaH2PO4 + 25HNO3  H3PMo12O40 + 25NaNO3 + 12H2O

• HNO3 was added to adjust the pH to 4.5. The molybdophosphate–99Mo

solution formed was added slowly to a zirconium oxynitrate (4.19 g)
solution during stirring.

• The temperature was raised to 55–66C. A zirconium molybdophosphate–

99
Mo gel was formed according to the reaction:

H3PMo12O40 + ZrO(NO3)2·xH2O  ZrMP·xH2O (gel)

The properties of the ZrMP column (2 g) were: elution yield varied in the
range 66–90% and the 99Mo breakthrough was <4 × 10–4%.

(v) Silica gel

Other researchers adsorbed the 99Mo on silica gel from a solution of ammonium
molybdate. A yield of 95% was achieved after the elution of the 99mTc with ketone.

(vi) Other generator types

Of the other generator types not treated further here are the ones based on
separation by solvent extraction [108], the generator based on electrochemical
separation [110] and the generator based on separation by sublimation of volatile
Tc2O7 [117].

3.2.6.3. Availability and current status

The 99Mo/99mTc generator is readily available at relatively affordable prices.

Activities in the range 2.5–25 GBq are available with 7 d precalibration. There

101
are presently about five main producers of 99Mo, with two more in the pipeline
(Fig. 41), and all of them base the production on fission of 235U. In addition, there
are four main laboratories that carry out the separation of 99Mo from the target
material. An additional seven laboratories are the main manufacturers of the
generators, most of them based on small size alumina columns. These are
convenient for further refinement in a radiotracer generator system because they
are a small size and require moderate shielding.
In addition to the main producers (90–95% of the total production), there
are a number of other research reactors that produce locally medium to low
specific activity 99Mo by irradiation of a Mo based target. The target separation
and the manufacture of the generator are also carried out locally. However, the
column sizes are more voluminous and the elution volumes considerably larger,
and their use in an IRTG system becomes somewhat more cumbersome.
Long lived 99gTc, which is the decay product of the 99mTc, remains below
exemption level, even for the highest activity of 99Mo/99mTc radionuclide
generators.

3.2.6.4. Possible applications

The 99Mo/99mTc radionuclide generators can be used in several types of

industrial tracer examinations where:

• Wall thickness does not exceed a few millimetres (for steel);

• The enclosing material container is made of glass, plastic or any other
lighter materials;
• A bypass stream is arranged for easier detection;
• Detectors are immersed into the medium to be measured;
• Sampling techniques are used.

The 99Mo/99mTc generator is often regarded as inappropriate for use in

industrial monitoring operations because of the relatively short half-life of the
mother and the low energy of the 99mTc gamma ray. However, the half-thickness
of the 140 keV gamma ray (4 mm of steel), while too low for studies on high
pressure plants, is still sufficient for use in pipes and vessels with wall thicknesses
up to about 10–15 mm. It is also rightly argued that the normal chemical form in
the generator eluate, 99mTcO4−, while a useful water tracer at oxidizing (aerobic)
conditions, is a strong oxidation agent (valence state 7+) and will easily be
reduced to lower valence states under reducing conditions.

102
 For instance, TcO2 is a common reduced form (valence state 4+). Therefore,
labelling techniques are needed to produce useful 99mTc− labelled tracers for
water, organic fluids and solids under varying experimental conditions.
Undisputed positive arguments for industrial use of this generator are that
this is the most widely used generator in nuclear medicine. As such, it is available
worldwide from a number of suppliers, usually at a few days’ notice and at a cost
that is not prohibitive. Additionally, from a public relations point of view,
prospective clients often perceive a radionuclide that is used for medical
applications as more user friendly.
Although the chemistry of technetium is very well known, its multiple
states of oxidation can be an obstacle for labelling certain compounds and
reagents. In addition, most of the labelling chemistry has the development of
methods to produce labelled compounds for in vivo use in the human body as a
primary goal. Thus, thermal and chemical stability at elevated temperatures of
these compounds have, in general, not been thoroughly examined. It is still
largely a remaining task to develop a suite of useful industrially applicable tracers
for harsh experimental conditions.

3.2.7. The 113Sn/113mIn radionuclide generator

Relevant nuclear data for this radionuclide generator system are given in
Table 4 and the simplified and partial decay scheme of 113mIn is given in Fig. 47.

3.2.7.1. Relevant nuclear properties

(a) Photon energy of the daughter

The EC decay of 113Sn feeds mainly (98.2%) the first excited state at
391.69 keV in 113In. The transition from this excited state to the ground state is
M4 (spin difference I = 4 and parity change), which means that the transition is
hindered and therefore also converted to a considerable degree (conversion
coefficient measured to αK = 0.437 ± 0.007 [118]). Therefore, the excited state is
‘long lived’ with a half-life of 99.5 min. Thus, 113In in this excited state may be
regarded as a separate radionuclide, 113mIn.
The energy of the IT of 391 keV is sufficient for transmission through thin
metal or plastic walls and detection outside of the vessel or tubing and therefore
also suitable for on-line measurements in the industry. A gamma spectrum is
provided in Fig. 48.

103
FIG. 47. Decay scheme of 113Sn to excited states in 113In, including the long lived state at
391.69 keV, which may then be regarded as a separate radionuclide 113mIn [83].

(b) Half-life of the daughter

The half-life of the daughter is suitable for at least two examinations per
day in the same experimental system provided they are spaced by 5 h or more, i.e.
the activity from the first injection is largely dead at the time of the second
injection, and the buildup of 113mIn is sufficient for a new elution.

(c) Half-life of the mother

The half-life of 115 d offers about 1 year of application without replacing

the generator.

104
 113m
FIG. 48. Gamma spectrum of In accumulated with a Ge(Li) detector.

(d) Main production routes

(i) Neutron reactions

The main production route is through the 112Sn(nth,)113Sn reaction in a

nuclear reactor. Since the isotopic abundance of 112Sn in natural tin is only 0.97%
and the thermal cross-section only of the order of 1 b (see excitation function in
Fig. 49), the target material should be isotopically enriched with respect to 112Sn.
Enrichments >95% are commercially available (Trace Sciences International).
By using the experimental parameters given, the average activity obtained
(calculated at the end of activation) is about 30 mCi/mg Sn (with 81.7%
enrichment in 112Sn).
It is also possible to produce 113Sn by the reaction 114Sn(n,2n)113Sn using
14 MeV neutrons from the D(T,n)4He reaction in a neutron generator. However,
this is a marginal production method because the flux in the generators is limited
(maximum around 1011 ncm−2s−1), the reaction cross-section is 1270  115 mb
[119] and the isotope fraction for 114Sn only 0.65%. However, isotopically

105
 FIG. 49. Excitation function for the neutron capture reaction 112Sn(n,)113m+gSn [119].

enriched material is commercially available from Trace Sciences International

(60–90+%) and from NIDO/Oak Ridge National Laboratory (>61%).

(ii) Charged particle reactions

Charged particle reactions with moderate energies (15–70 MeV) may also
be used for production of 113Sn. For these reactions, the target material is, for
instance, either indium or cadmium. Some of the most applicable reactions are
listed in Table 12.

3.2.7.2. Generator systems, separation techniques and chemical form of

the daughter

Presently available 113Sn/113mIn generators use high specific activity 113Sn,

which cannot be produced in low and medium flux research reactors, even with
enriched 112Sn.
However, relatively low specific activity of 113Sn, 75–115 GBq (2–3 Ci)
per g, may still be produced in sufficient amounts in low and medium flux
research reactors by irradiation of enriched metallic 112Sn. After dissolving the
irradiated target in HCl, the resulting 113SnCl4 is firmly adsorbed on hydrous
zirconium oxide from 3–4M NaCl solutions of pH1.3–1.5 and the elution of
113m
In is effected by dilute HCl. The yield of such a generator is typically 70% of

106
TABLE 12. EXAMPLES OF CHARGED PARTICLE REACTIONS FOR
PRODUCTION OF 113Sn
Energy Emax at
Nuclear reaction Cross-section max at Emax
cross-section maximum
113
In(p,n)113Sn
115
In(p,3n)113Sn 30 MeV 1850 mb (113m+gSn)a
Nat
In(p,xn)113Sn, x = 1, 3 28 MeV 780 mbb
113
In(d,2n)113Sn 11–19 MeV ~1000 mbb
Nat
In(3He,xn)113Sb → 113Sn, x = 3, 5
Nat
In(3He,pxn)113Sn, x = 2, 4 55 MeV 700 mbc
Nat
In(,pxn)113Sn, x = 3, 5 85 MeV 850 mbc
Nat
Cd(3He,xn)113Sn, x = 2–4 38 MeV 400 mbc
Nat
Cd(,xn)113Sn, x = 1–5 55 MeV 270 mbc
a
Numerical value from Ref. [120].
b
Numerical values from Ref. [121].
c
Numerical values from Ref. [122].

the theoretically available ll3mIn activity [123]. Breakthrough of 113Sn has been
consistently <0.01% of the 113mIn activity.
Hydrous zirconium oxides may be produced with varying degrees of
hydration, and the different forms may show somewhat different performance
characteristics with respect to tin loading, 113mIn elution and 113Sn breakthrough.
Generators containing up to 25 GBq (700 mCi) of 113Sn have been prepared,
yielding pure 113mIn suitable for medical use [124].
Other column types reported include the following:

• Glass beads [125] that have been eluted with 0.16M NaCl and gave 73%
yield with 0.042% breakthrough.
• Activated carbon [126] with an exchange capacity of Sn(IV) ~7.6 meq/g,
elution efficiency of 113mIn 80% by using 10 mL of 0.2M HCl–80% acetone
with flow rate 1 mL/min. A secondary catcher column of the anion
exchanger Dowex 1x8 is used to capture any breakthrough of 113Sn.

107
 • Experiments with various tungstocerate(IV) gel matrices [127, 128], for
instance, 12-tungstocerate(IV) column with the formula
113
H4[CeO4·W12O36]·18H2O, for sorption of Sn(IV) from 0.1M HCl
solution and elution of 113mIn(III) using the same solution.
• Tests on the 12-molybdenocerate(IV) column matrix [129] with focus on
the chemical conditions to optimize the loading capacity and efficiency and
on the elution efficiency as a function of time.
• Hydrated antimony pentoxide column (2 g/column, 50–100 mesh) [130],
elution at 0.5M HCl, elution yield >60% in 18 mL, but decreases with
number of elutions.
• Silica gel based on absorption of 113Sn in the presence of bromine water and
0.4M HCl. The absorption capacity was 6 mg Sn per g silica gel, the
absorption efficiency >99% and the Sn/In separation factor >104 for the
elution liquid pH > 1.2. In general, the silica gel system had superior
operating characteristics when compared to the hydrous zinc oxide system:
higher recovery of 113mIn over a greater pH range was observed [131].
• Organic Chelex-100 (iminodiacetic functional group) or BioRex-63
(a phosphonic resin) ion exchangers for chromatographic separation [132].
0.1N hydrochloric acid is used as eluent with a separation yield of 60–70%
and a separation factor of 105.

The chemical form of 113mIn in the eluate from the various generators
mentioned here is mainly as the cations In3+ at low chloride concentration. At
higher Cl− concentrations, chloride complexes like InCl2+, and even InCl2+, will
occur. At strong Cl– concentrations, the chemical form may be converted to the
anionic form InCl4−.

3.2.7.3. Availability and current status

Since this generator has lost some interest in nuclear medicine, the number
of commercial producers seems to have been reduced to only a handful on the
global scale. Two companies that still deliver the generator are Polatom in Poland
and SSC RF-IPPE in the Russian Federation. Alternatively, 113Sn may be
purchased, for instance, from Polatom, and the generator produced in the
purchaser’s own laboratories according to the procedure outlined in Fig. 50.

108
FIG. 50. Example of irradiation–target dissolution–column material preparation–column
loading sequence [133].

3.2.7.4. Potential and existing applications

• Potential for application in a variety of industrial situations (chemical,

petroleum, metallurgical industries, etc.), with tailor-made 113mIn tracers as
probes for aqueous, organic or solid material;
• Applications for logging in oil wells [134];
• Used in studies of wastewater treatment plants;
• Used for surface labelling of coal and accompanying minerals;
• Can be used for monitoring movements of fines in surface water flows in
environmental situations;
• Syntheses and purification of 113mIn tracers for industry is possible due to
the experiences from analogous syntheses of 111In labelled tracers used in
nuclear medicine and SPECT imaging.

3.2.8. The 137Cs/137mBa radionuclide generator

Relevant nuclear data for this radionuclide generator system are given in
Table 4 and the simplified and partial decay scheme of 137mBa is given in Fig. 51.

109
FIG. 51. Decay scheme of 137Cs to a ‘long lived’ excited state in 137Ba at 661.6 keV, which may
then be regarded as a separate radionuclide, 137mBa [83].

3.2.8.1. Relevant nuclear properties

(a) Photon energy of the daughter

The gamma energy (IT) of the daughter of 661 keV, with high intensity
(89.9%), is sufficient for transmission through medium thick (<20 mm) metal
walls and detection outside of the vessel or tubing. Therefore, it is suitable for
on-line measurements in the industry using common sized NaI(Tl) scintillation
detectors (for instance, d × l = 25 mm × 38 mm for narrow detector positions and
50 mm × 50 mm for general applications). A gamma spectrum is given in Fig. 52.

(b) Half-life of the daughter

The daughter half-life of 2.55 min restricts the use to a maximum 10 min
per injected batch, but offers possibilities of cyclic industrial measurements of
short duration: after about 20 min, the system has no memory of the preceding
tracer injection. This is valuable for systems with fast mass transport and which
require frequent measurements, especially in situations and periods where
running parameters are adjusted in order to optimize the process.

110
 137m
FIG. 52. Gamma spectrum of Ba accumulated with a Ge(Li) detector.

(c) Half-life of the mother

The physical half-life of 137Cs is 30 a. However, the useful life of the

generator is significantly less. The shelf life is dependent upon the detailed
construction and physicochemical properties of the system. Radiolytic reactions
due to beta and gamma interactions in the generator matrix may slowly lead to
breakdown of the matrix and thereby ruin the elution properties of the generator.
Still, if column material is selected for the best radiation resistance (mainly
inorganic materials), and the generator is properly stored in periods where it is not
in use (it should be stored under dry conditions), the shelf life of the generator can
be many years, possibly as much as >10 a. This long life of the generator makes
it suitable for the provision of tracers at remote locations over an extended period
of time, and also for possible use in permanent installations at inaccessible places,
such as in subsea oil installation equipment. It is possible to incorporate the
generator into installed equipment to automatically provide an ongoing supply of
tracer for semi-continuous flow rate measurement.

111
(d) Main production routes

Neutron reactions: the only viable production route of the mother nuclide
137
Cs for large scale industrial use is by fission of uranium through the reaction
235
U(n,f)137Cs and recovery of the 137Cs from the mixture of fission products. The
accumulated fission yield is 6.236%. Very high activities can be achieved by this
method, and the inventory of 137Cs on a global basis is large. The main use of this
radionuclide is as a solid source in gamma sterilization plants, mass measurement
equipment for the industry (gamma transmission tomography) and in industrial
radiography for checks of quality of weldings, for instance.
It is, in principle, also possible to produce carrier free 137Cs in reactors by
thermal neutron irradiation of 136Xe to produce short lived (3.83 min) 137Xe
followed by beta decay. The total reaction is 136Xe(n,)137Xe → 137Cs. However,
this production route is not practical due to the long half-life of 137Cs, an isotopic
abundance of 136Xe of 8.9% and a low production cross-section of 0.26 b.
Charged particle reactions: it is, of course, also possible to produce 137Cs by
charged particle induced fission, for instance, of 232Th or NatU in medium to high
energy particle accelerators.
Another production method for carrier free 137Cs is by irradiation of 136Xe
by deuterons using a small particle accelerator capable of producing 12–15 MeV
deuterons. The reaction is 136Xe(d,n)137Cs, but it is not a practical production
route due to the same arguments as for the (n,) reaction above.

3.2.8.2. Generator systems, separation techniques and chemical form of

the daughter

Most of the generator systems developed and studied are based on columns
with sorption media of different types: zirconium phosphate, zirconium vanadate,
ammonium phosphomolybdate, titanium hexacyanoferrate or cupric cobalt
ferrocyanide and several other inorganic adsorbents using EDTA and other eluent
solutions. Ion exchange columns eluted with 0.9% NaCl provided highest yield
and breakthrough of <10–3. A selection of various column systems is summarized
in Table 13.
A typical microscopy picture of the granular column support material silica
gel coated with the active ion exchange material potassium–copper–
hexacyanoferrate is given in Fig. 53. The particle sizes are in the range
0.25–0.85 mm.

112
 TABLE 13. SELECTION OF PUBLISHED DATA ON 137Cs/137MBa GENERATORS AND COLUMN SUPPORT MATERIAL
USED FOR SELECTIVE SEPARATION OF 137Cs FROM COMPLEX REACTION MIXTURES, BUT WHICH HAVE NOT
YET BEEN UTILIZED IN GENERATORS
Column material Column loading fluid and elution agent Yield and breakthrough Reference

Cobaltferrocyanides of the form Loading with 0.1M HCl Yield (IS): 83 ± 7% in 10 mL [135]
M[CoFe(CN)6], where M may be Ni, Zn, Elution with isotonic saline (IS) Yield (HCl): 85 ± 10% in 10 mL [136]
Fe(II) or Cu(II) or 0.1M HCl Breakthrough: <10–4%
The latter is preferred

Zirconium phosphate Elution with HNO3 Elution yield: 30% [137]

Breakthrough: <10–3%

(Anionic resin + MoO3−)+  Loading capacity: 0.48 meq/g dry Elution yield: not given [138]
(H2NH3PO4 + 7.5M HNO3) R-AMP Breakthrough: ‘completely free
 R-AMP = (NH4)3PO4·12MoO3 Elution with 0.1M or 0.3M HNO3 from the parent’

Support bed (various org. polymers) loaded Various elution agents, Elution yield: 65–79% in 10 mL up [139]
with the extractant dicarbollide H+ in optimum conditions for to 50 elutions
nitrobenzene, the formula is 10–4M HNO3 + 2.5 × 10–3M Ba(NO3)2 Contamination of 137Cs <0.1%
((-(3)-1,2-B9C2H11)2 CoIII)–

1. Copper–cobaltferrocyanide, Cu[CoFe(CN)6] CCS loading: wide pH range Yield CCS: high [140]
2. Zirconium phosphate (ZrP) CCS elution: IS or 0.1M HCl Breakthrough CCS: <10–4% [141]
ZrP loading: pH2 Yield ZrP: 58% in 3 mL
ZrP elution: 0.5M HNO3 Breakthrough ZrP: 2%

Zirconium vanadate (ZrV)–formula Exch. capacity: 4.02 meq/g Elution yield: high [142]
Zr(HVO4)2·nH2O Elution with 0.1M NH4Cl Breakthrough: 137Cs not detected

113
 TABLE 13. SELECTION OF PUBLISHED DATA ON 137Cs/137MBa GENERATORS AND COLUMN SUPPORT MATERIAL

114
USED FOR SELECTIVE SEPARATION OF 137Cs FROM COMPLEX REACTION MIXTURES, BUT WHICH HAVE NOT
YET BEEN UTILIZED IN GENERATORS (cont.)
Column material Column loading fluid and elution agent Yield and breakthrough Reference

6-Tungstocerate(IV) gel matrix Elution with Elution yield: high and reproducible [143]
0.9% NaCl + 0.1M HCl over ~1 year
Radionuclide purity: >99.99%

Polyoxometalate of the form Exch. capacity for Cs+: 2.29 mmol/g Elution yield: none with 0.01M HCl High [144]
Na2(H2O)4(H3O)[Al(OH)6Mo6O18] Loading with 0.01M HCl but no numbers given with ascorbic acid
Elution with 0.5% ascorbic acid Breakthrough: no 137Cs detected in eluate

Potassium–cobalt–hexacyanoferrate on silica Exch. capacity for Cs+: 0.311 mmol/g Elution yield: 65–75% in 10 mL [145]
gel: K2[CoFe(CN)6]–SiO2 Loading and elution with Breakthrough fraction: ~4 × 10–6
0.1M HCl + 0.9% NaCl

Potassium–copper–hexacyanoferrate on silica Exch. capacity for Cs+: 0.060 mmol/g Elution yield: >80% in 10 mL [112]
gel: K2[CuFe(CN)6]–SiO2 Elution with 0.9% NaCl Breakthrough: <10–4%

Ammonium molybdophosphate (AMP) Elution with Elution yield: >80% breakthrough: [146]
impregnated alumina microspheres 0.1M NH4NO3 + 0.5M HNO3 solution ‘Acceptable radionuclidic purity suitable
(AMP–Al2O3) for industrial radiotracer investigations’

Interesting column supports not yet further described or utilized in generators

Titanium phosphates (TiP) and combined Not described Not described [147]
titanium phosphate–ammonium
molybdophosphate (TiP–AMP)
 TABLE 13. SELECTION OF PUBLISHED DATA ON 137Cs/137MBa GENERATORS AND COLUMN SUPPORT MATERIAL
USED FOR SELECTIVE SEPARATION OF 137Cs FROM COMPLEX REACTION MIXTURES, BUT WHICH HAVE NOT
YET BEEN UTILIZED IN GENERATORS (cont.)
Column material Column loading fluid and elution agent Yield and breakthrough Reference

Selective sorption of radioactive caesium and High sorption efficiency of both Not described [148]
strontium on stannic molybdophosphate ion Cs+ and Sr2+ (Ba2+ has not been tested)
exchanger

Ammonium molybdophosphate–alumina Studied kinetics Not described [149]

(AMP–Al2O3) Other properties not described

SiO2–potassium–cobalt–hexacyanoferrate, Exch. capacity 0.38 meq Cs/g Not described [150]

SiO2–K2CoFe(CN)6 Distribution coeff. for Cs: for
HCl 0.001–3M = 7.5 × 104 and 5.8 × 104

Organic ion exchanger SuperLig644 with Not described Not described [151]
proprietary structure

Potassium–copper–nickel–hexacyanoferrate(II) Exch. capacity: 2.25 mmol/g of Cs Not described [152]

with composition Loading efficiency: >99% [153]
K2.3Cu0.65Ni1.7[Fe(CN)6]2·13H2O [154]
also called K–Cu–Ni–CNF

Ni–CNF, K–Ni–CNF and K–Cu–Ni–CNF Not described Not described [155]

absorbed into a porous matrix of
polyacrylonitrile, PAN

Ammonium–phosphor–molybdate Not described Not described [156]

(NH4)3PO4(MoO3)12·4H2O on activated carbon

115
FIG. 53. Micrograph of the granular column support material silica gel (SiO2·xH2O) coated
with the active ion exchange material K2[CuFe(CN)6] [112].

Generators recently developed and studied by the contributors to the

present document are in particular based on the following column support
materials:

• Potassium–copper–hexacyanoferrate on silica gel, K2[CuFe(CN)6]–SiO2, in

short denoted KCuFC–SiO2, developed at INSTEC in Cuba [112];
• Potassium–cobalt–hexacyanoferrate on silica gel, K2[CoFe(CN)6]–SiO2 , in
short denoted KCoFC–SiO2, developed at CIAE in China [145];
• Ammonium molybdophosphate impregnated alumina microspheres,
possibly of the form {(NH4)3PO4(MoO3)12–Al2O3}·xH2O, in short, denoted
AMP–Al2O3, developed at BARC in India [146].

A sketch of the crystal structure of the active ion exchanging part in the
column support material is, for illustration purposes only, given in Fig. 54 for the
case of the CIAE generator. By changing the cobalt atoms for copper atoms, the
figure also illustrates the INSTEC generator. Here, it is the blue spheres
(potassium ions) that are exchangeable with 137Cs+.

116
FIG. 54. Crystal structure unit cell of the active ion exchange material K2[CoFe(CN)6] [145].
Each connecting line between red and green spheres represents a CN ligand.

117
FIG. 55. Ion exchange capacity (in mmol/g) and distribution ratio Kd (defined by Eq. (18)) of
137
Cs+on the column support material K2[CoFe(CN)6]–SiO2 as a function of pH [145].

FIG. 56. Elution efficiency of 137mBa2+ and corresponding breakthrough of 137Cs in 10 mL of the
elution mixture 0.1M HCl + 0.9% NaCl for the column support material K2[CoFe(CN)6]–SiO2
as a function of time [145].

The properties of all these three generators seem to be acceptable for

sufficiently stable operations over at least a few years. Examples of ion exchange
capacities, elution efficiencies and breakthrough properties are given in Figs 55
and 56.

118
 Here, Ai is the initial activity concentration (Bq/mL), Aeq is the activity
concentration (Bq/mL) in the liquid at distribution equilibrium, V is the liquid
volume used (mL) and m is the mass of the ion exchanger material or column
support material (g):

( Ai - Aeq ) ⋅ V
Kd = mL/g (22)
Aeq ⋅ m

Figure 57 shows the elution efficiency of a test production of an industrial

version of the CIAE generator of the same activity, ~1.7 GBq. The generator was
eluted for the first time 330 d after quality check and calibration in the CIAE
laboratory, and the measured efficiency amounts to ~60% as compared with the
65% claimed by the manufacturer. The general trend was a reduction to ~40% at
the end of the nearly 2 years of application, as compared with ~50% for a
corresponding period measured in the manufacturer’s laboratory. The abrupt drop

FIG. 57. Elution yield of 137mBa from K2[CoFe(CN)6]–SiO2 (an industrial version of the CIAE
generator) as a function of time after it has been used for various industrial tracing operations.
The colour code relates to different and narrow spaced elutions for the same colour with
different storage periods in between [74].

119
FIG. 58. Elution efficiency of 137mBa2+ and corresponding breakthrough of 137Cs in 5 mL of the
elution mixture 0.1M NH4NO3 + 0.5M HNO3 for the column support material
–
[(NH4 )3PO4(MoO3 )12 Al2O3]·xH2O as a function of time [146].

in the beginning of the ‘red’ elution period is explained by improper storage: the
generator probably went dry without the operator noticing, hence there is a
recovery of the efficiency after a few elution cycles [74].
Figure 58 shows that the ion exchange capacity of the K2[CoFe(CN)6]–SiO2
column decreases somewhat, but not dramatically, with increasing pH, while the
distribution ratio stays fairly constant over the pH range shown at
Kd = 2.2 × 104 mL/g, which is somewhat less than that reported by Mardan et al.
[150]. In order to secure optimum capacity and minimum breakthrough of
caesium, the column is both loaded and eluted with a mixture of 0.1M HCL and
0.9% NaCl.
Figure 58 also shows that the initial elution efficiency of 137mBa from the
same column is around 65%, but decreases to about 50% in the course of the 600 d
testing period. The corresponding breakthrough of 137Cs is around 4 × 10–5% per
mL in the beginning, but there is an increasing tendency towards the end of the
testing period. The activity of 137Cs on this test generator was ~1.7 GBq (~45 mCi).

120
 The elution efficiency of 137mBa for the APM/Al2O3 generator
manufactured at BARC (5 mL of the elution mixture 0.1M NH4NO3
+ 0.5M HNO3) is shown in Fig. 58. It is, on average, ~80% and stays stable over
the testing period of 180 d. This is significantly higher than for the previously
described KCoFeC/SiO2 based generator. The corresponding breakthrough of
137
Cs is also fairly stable over the testing period and amounts to some
0.005–0.01% per 5 mL (10–3–2 × 10–3% per mL), which is acceptable but not as
good as for the previously described KCoFeC/SiO2 based generator [146].
The real shelf lives of the generators are yet to be determined. The main
problem is probably the disintegration of the column support material into fines
that are not retained by the ordinary filters but transported by the elution liquid.
These particles will then also contain the mother nuclide 137Cs. Breakthrough
might arise to an unacceptable level. The material breakdown may be due to a
combination of radiolysis, chemical interactions from the elution liquid and the
physical erosion effect of the eluting liquid.
Measures to increase the shelf life would probably be:

• To mount extra exchangeable filters for 137Cs carrying fines of the column
material;
• To install an extra exchangeable catcher column for ionic 137Cs+;
• To store the generator between application periods under controlled wet
conditions and in a tempered area.

The set-up of column based 137mBa generators may be somewhat different

from laboratory to laboratory. One such set-up developed and used at BARC in
India [146] is sketched in Fig. 59. It shows the elution operation process where a
vial filled with the elution liquid is mounted at the generator top on a needle that
penetrates a septum in the lid of the elution flask, thus connecting this liquid to
the column support material. Another needle, also penetrating this septum, is
leading air into the bottle during the elution process. A second bottle, also with a
septum in the lid and originally evacuated, is sucking the elution liquid through
the column and is receiving the eluate containing the 137mBa activity. The
generator system is a small size and transportable. During transport, a combined
lead shield and lid seals off the generator top. The external dimensions of the
BARC generator are Ø = 90 mm and h = 163 mm.
Another 137mBa generator recently developed at CIAE in China [145] uses a
peristaltic pump to create suction during the generator elution process. The
external dimensions are larger, the shielding thicker and the weight
correspondingly heavier. The 44 kg still makes it readily transportable.

121
FIG. 59. Schematic diagram of the 137Cs/137mBa generator set-up developed and used at BARC,
India [146].

Extensive reviews of column materials (ion exchangers) and partly also

liquid extraction agents for selective separation of 137Cs from aqueous systems
are given in Refs [157–159], but elution properties of 137mBa have not necessarily
been considered. However, the experiences described here may be important for
further development of radiotracer generators.
An example of an alternative generator is provided by the equilibrium
mixture of 137Cs+ and 137mBa2+ which is loaded on to a column of Amberlite
IRC-50 modified by incorporating an amide group. Barium is fixed, while
caesium runs unhindered through. Subsequently, 137mBa is recovered from the
column by eluting with 0.01M EDTA at a pH of 10 [160]. There are, however,
three drawbacks with this method: firstly, the need for handling radioactive
solutions of the long lived 137Cs for each separation operation; secondly, these
operations steal valuable time which results in a lower separated activity of

122
137m
Ba; thirdly, production of a strong Ba–EDTA complex makes it more difficult
and time consuming to use the activity in other labelling operations.

3.2.8.3. Availability and current status

Caesium-137 is primarily used in sealed sources for mass measurements

(density), industrial radiography and in large irradiation facilities for treatment of
sludges and for sterilization purposes. Therefore, the radionuclide itself is readily
available worldwide at a reasonable price because it is separated in large amounts
from fission waste.
Commercial generators with a relatively low activity of 0.37 MBq (10 µCi)
are available (e.g. from TEL-Atomic Inc.), but they are primarily intended for use
as educational instruments.
A 0.74 GBq (20 mCi) 137Cs/137Ba generator has been produced by Atom
Hightech Co. Ltd in China, but it is, for the moment, unclear whether this
generator is still available. However, both the generator from CIAE in China and
the one from BARC in India described in the text above show promise. These
organizations are large and have the necessary competence and facilities to be
future manufacturers for the world market of industrial versions of the
137
Cs/137mBa generators.

3.2.8.4. Potential and existing applications

• The generator can be used many times per day at maximum activity,
allowing repeated studies.
• Post-processing methods to synthesize a variety of industrial 137mBa tracers
for aqueous/environmental, organic, solids and multiphase purposes are
under development. Promising results have been obtained recently to
synthesize a 137mBa labelled tracer for oil in multiphase flow experiments,
see Ref. [161]. The kinetics of the labelling process is fast and may easily
be automatized.
• Simpler labelling, for instance, to generate a stable water tracer, can be done
directly in the elution process by application of a suitable complexing agent
in the elution liquid.

There are several advantages with this generator:

• For injection into product streams: The short half-life ensures that by the
time the material leaves the plant, the radioactivity is at a negligible level.
• For investigations on systems with recirculation: The short half-life ensures
that buildup of activity in the stream does not become a problem.

123
FIG. 60. Schematic diagram of a possible set-up for a 137mBa generator integrated with a
chemistry unit for complexation of the Ba2+ ion if needed, and also integrated with a tracer
injection system. A number of electronic or pneumatic valves are not shown. The equipment
may be operated automatically by a PC with auxiliary electronic equipment.

• Where repeat measurements are required: The system regenerates rapidly

so that the tracer is available over an extended period.
• For solids tracing: The main application of 137mBa labelled compounds will
be in fluid tracing. However, the primary chemical form eluted for most
column support media described above is Ba2+. This can be used directly to
label solids that are cation exchangers, such as various clays.

Owing to the short half-life of 137mBa (2.55 min), it will be desirable to

engineer the generator into a system that is automatically operated and which is
directly associated with a proper injection system. A possible arrangement is
sketched in Fig. 60.

3.2.9. The 144Ce/144Pr radionuclide generator

Relevant nuclear data for this radionuclide generator system are given in
Table 4 and the simplified and partial decay scheme of 137mBa is given in Fig. 61.

124
FIG. 61. Partial decay scheme of 144Pr to excited states in 144Nd whose ground state is a very
long lived nuclide with  decay to stable 140Ce. In practice, this ground state may be regarded
as ‘stable’ [83].

3.2.9.1. Relevant nuclear properties

(a) Photon energy of the daughter

A total of 97.8% of the beta decay of 144Pr goes directly to the ground state
of ‘stable’ 144Nd, with no associated gamma rays. The most abundant gamma rays
at 699.5 keV have an absolute intensity of 1.34%. However, the 144Ce/144Pr
nuclear genetic relationship is of interest as an industrial nuclide generator for
several other reasons:

• The combination of the mother half-life (relatively long) and the daughter
half-life (medium short) covers a time combination not offered by any of
the other generators considered in the present document.

125
 144
FIG. 62. Gamma spectrum of Pr accumulated with a Ge(Li) detector.

• The daughter energy of 699 keV is sufficient for transmission through

medium thick (some mm) metal walls and detection outside of the vessel or
tubing and offers therefore the possibility for on-line measurements in the
industry.
• The two main gamma energies from decay of 144Ce of 133.5 keV (11.1%)
and 80.1 keV (1.36%) are easy to shield, so the source strength (activity of
144
Ce) can be rather high (several GBq, several hundred mCi) in order to
compensate for the low gamma intensity of 144Pr.
• If the source strength is sufficiently high, all three gamma energies may be
utilized in industrial measurements. The high energies penetrate several cm
of steel, and the combination of the three makes it possible to obtain depth
information in tanks or large pipelines. A gamma spectrum is given in
Fig. 62.

126
(b) Half-life of the daughter

A daughter half-life of 17.3 min offers industrial measurements of short-to-

medium duration.

(c) Half-life of the mother

A half-life of 285 d offers some 2–3 a of application without replacing the

generator.

(d) Main production routes

Fission (for instance, thermal neutron induced fission of 235U or 239Pu or

high energy particle induced fission of 238U or 232Th) is the only viable and
effective production method for 144Ce. The cumulative chain yield of mass
number A = 144 for thermal neutron fission of 235U is 5.459%, which is relatively
high. The 144Ce is then isolated from the fission mixture. Cerium belongs to the
lanthanide series. The oxidation state with highest stability of most lanthanides is
3+. This implies that the chemistry of all lanthanides is very similar and their
individual separations are correspondingly challenging. However, cerium is also
stable in the 4+ state, and this simplifies the separation, both from other fission
products, and from other lanthanides: a lanthanide group separation from other
fission products is performed first. This is followed by a specific isolation
(mainly by solvent extraction) of four valent cerium from the lanthanide group.
A key element in the production of a 144Ce/144Pr radionuclide generator is,
of course, the high efficiency separation of 144Ce from the mixture of fission
products. Three methods will briefly be mentioned: the first one is based on
continuous production comprising electromagnetic separation, the second one on
continuous production comprising chemical separations and the third one on
batch wise irradiation followed by chemical separations. The first two have not
yet developed to their full potential for production of sources of sufficient
strength.

Method 1, continuous on-line production:

• Nuclear reaction: High energy particle induced fission of uranium;

144
• Separation: Element selective surface ionization of the precursor Cs
(T1/2 = 1.0 s) followed by electromagnetic separation and collection of the
mass separated A = 144 beam, which rapidly accumulates in long lived
144
Ce.

127
 144
FIG. 63. Method 1 for production of Ce.

This process has been implemented, for instance, at the ISOLDE laboratory
at CERN. Figure 63 gives somewhat more detailed information of the method. At
ISOLDE/CERN, 144Cs is selectively produced at a target temperature of 2000C
and an ionization temperature of 1000C with an ionization efficiency of 90%.
In Fig. 63, the left picture gives a rough principle sketch of particle induced
nuclear reactions in a high temperature target, surface ionization of diffusing
nuclear reaction products followed by extraction and acceleration in an electric
field of the generated ions before mass analysis in a magnetic field and collection
of the mass separated particle beam. In the same figure, the right picture shows
experimental production yields at ISOLDE for Cs isotopes normalized to a 1 A
600 MeV proton and/or a 1 particle A 910 MeV 3He irradiated target consisting
of 16.4 g/cm2 of uranium impregnated carbon cloth [162].
So far, this method has not been used for large scale production of strong
sources of 144Ce. For that to happen, the actual production yield has to increase
considerably relative to the numbers in Fig. 63. This can be achieved by:

• Applying a thicker target, say a factor of ten higher than the one mentioned
in Fig. 63;
• Applying a higher particle (proton) flux, say 100 A;
• Using a tungsten surface ionization source and increasing the ionization
temperature to 2000C or higher, resulting in partial ionization also of 144La
and 144Ce;
• Keeping the target temperature at >2000C to maintain a high diffusion rate
of relatively volatile fission products out of the target matrix.

128
FIG. 64. Schematic diagram of a continuous on-line production and separation set-up for Ce
isotopes based on fission of 235U in a thermal reactor.

Assuming the same overall efficiency for production of 144Cs with these
parameters might result in a production time of ~1000 s in order to obtain a 144Ce
source of 10 MBq.

Method 2, continuous on-line production:

235
• Nuclear reaction: Thermal fission of U in a thin target where fission
fragments recoil out of the thin target into a recoil chamber volume;
• Separation: The recoiling fission fragments are trapped in a sweeping gas
(most often containing salt clusters of NaCl or KCl) and transported with a
gas jet through a thin capillary to a continuously running chemical
separation apparatus based on solvent extraction.

This process has been used to isolate and study short lived isotopes of light
lanthanide elements in the SISAK equipment. Figure 64 sketches the principles
of the process.
The gas jet transport of fission products is guided to the SISAK
radiochemical separation system, which is based on solvent extraction and final
catchment of 144Ce on a column with a solid support composed of HDEHP
impregnated PVC powder. A delay line inserted in the aqueous phase between
mixer/centrifuge units 1 and 2 ensures sufficient decay to 144Ce of the precursor
144
La (T1/2 = 40 s).

129
FIG. 65. Schematic diagram off-line and batch wise radiochemical separation procedure for
isolation of 144Ce from PUREX HLW.

An alternative route is to apply a system for separation of lanthanum

(144La), sorption of the 144La on an ion exchanger and let 144Ce grow in.
This system has not yet been used for production of strong sources of 144Ce,
and no attempt has been made here to calculate production yields.

Method 3, batch wise production:

235
• Nuclear reaction: Thermal neutron induced fission of U or high energy
particle induced fission of uranium or thorium performed in high flux
reactors or at high flux accelerators;
• Separation: Chemical dissolution of the irradiated target followed by a
multistep chemical separation scheme, mainly manually operated, in a hot
cell.

This procedure and the reprocessing of high level waste (HLW) mainly
from the nuclear energy industry, are those primarily used at present for
production of radiochemically pure sources and solutions of 144Ce. Some of the
relevant methods for off-line batch separation of 144Ce from a fission mixture
include chromatographic methods, solvent extraction where electro-oxidation is a
key element and more ordinary solvent extraction methods. The separation of
144
Ce from HLW is illustrated in Fig. 65.

130
 The acronym KSM-17 (Fig. 65) represents the organic complexant
2-ethylhexyl hydrogen 2-ethylhexyl phosphonate. The overall chemical yield is
~70%, and the decontamination factor >105. Figure 65 is based on a procedure
described in Ref. [144].

3.2.9.2. Generator systems, separation techniques and chemical form of

the daughter

Since neither 144Ce nor 144Pr are considered radiopharmaceutical species of

interest, the literature on their separation in the form of a radionuclide generator
is rather poor. A few publications exist, however, and some of these are
summarized in Table 14, although the most recent relevant publication dates from
1987. The various relevant types of information given in the respective references
are not comprehensive, and important data on elution yields and mother
breakthrough are indicated only in a few cases. Hence, the lifetime of the various
generators reported cannot be reliably estimated. A recent thorough search of the
available literature has not revealed any more recent attempts to develop and
study the 144Ce/144Pr generator. There seems, therefore, to be a need to develop
and study new/improved generators based on the 144Ce/144Pr nuclear genetic
relationship.

3.2.9.3. Availability and current status

The 144Ce/144Pr radionuclide generator is not commercially available at

present. However, radiochemical solutions of pure 144Ce (+ equilibrium activity
of 144Pr) can probably be purchased from a few radiochemical companies. Thus,
generators can be produced on an individual basis in the various radiochemistry
laboratories where published information can be taken as a starting point for
further studies and improvements.
The availability of 144Ce depends on reactors producing fission products.

3.2.9.4. Possible applications

Owing to the short half-life of 144Pr (17.3 min), the generator can be used
many times per day at maximum activity, allowing repeated studies. Of special
interest is the fact that this radionuclide emits three well-spaced gamma photons
of 696 keV, 1489 keV and 2185 keV. This enables information of the depth
distribution of the 144Pr labelled tracer in extended volumes, and will complement
those radiotracers with fewer useful gamma photons.

131
 TABLE 14. THE 144Ce/144Pr GENERATORS AND COLUMN SUPPORT MATERIAL USED FOR SELECTIVE

132
SEPARATION OF 144Pr FROM AN INVENTORY OF RADIOCHEMICALLY PURE 144Ce
Generator material Chemistry involved Yields

Filter material of ‘insoluble’ and freshly formed To an equilibrium mixture of 144Ce/144Pr The solution is percolated through the freshly formed
Ce(IO3)4 in 5M HNO3 is added 1M NaBrO3 to Ce(IO3)4 and 144Ce(IV) is fixed by the mechanism of
oxidize Ce(III) to Ce(IV) isotopic exchange. The 144Pr runs unhindered
through. The 144Ce labelled Ce(IO3)4 may be
redissolved by adding H2O2 and the precipitation
process repeated after in-growth
144
Column support material is Dowex-1 To an equilibrium mixture of 144Ce/144Pr Pr is quantitatively eluted by 10 mL 9M HNO3.
(100–200 mesh) on nitrate form prepared is added NaBrO3 in 9M HNO3 to oxidize Contamination of 144Ce is <0.2%
by treating with 6M HNO3 and 0.5M NaBrO3 Ce(III) to Ce(IV)
144
1–3 mL liquid mixture of 144Ce/144Pr in Addition of solid NaBiO3 to oxidize Pr is left in the aqueous phase in a ‘pure’ form
3M HNO3 Ce(III) to Ce(IV)
Add methyl-isobutyl-ketone (hexone)
to extract Ce(IV) into organic phase
144
Filter paper impregnated with MnOx with A 144Ce/144Pr equilibrium mixture is Pr is separated from 144Ce by the ring oven
Mn having an average oxidation number of +3 administered on to the centre of the technique: with 0.06–0.07M trichloroacetic acid as
filter paper wash solution, 144Pr can be concentrated in the ring
zone with 80–90% yield and decontamination factors
>103

Column support material of MnO2 — —

 TABLE 14. THE 144Ce/144Pr GENERATORS AND COLUMN SUPPORT MATERIAL USED FOR SELECTIVE
SEPARATION OF 144Pr FROM AN INVENTORY OF RADIOCHEMICALLY PURE 144Ce (cont.)
Generator material Chemistry involved Yields
144
Column support material of MnO2 prepared by Carrier free 144Ce (probably as Ce(IV)?) Pr is eluted with 6 mL of 0.1M HNO3
mixing MnSO4 and KMnO4, followed by is loaded on to the column in 0.1M HNO3
filtering, washing, drying, grinding and sieving.
Fraction of 72–120 mesh is dispersed in 0.1M
HNO3 and filled into a column
144
Column support material of Al2O3 coated Ce(III) oxidized to Ce(IV) and absorbed Pr elution with 1% KIO3 in 1M HNO3 with an
with MnO2 on the column as Ce(IO3)4 elution yield >60% and a radionuclide purity >99.9%
144
Column support material of zirconium Ce(III) oxidized to Ce(IV) by NaBrO3  Pr eluted with water at pH7 or slightly higher
phosphate (possibly of the form in H2SO4 medium and 144Ce(IV) fixed
Zr(HPO4)2·nH2O) on column
144
Column support material of crystalline Ce fixed on column material Elution of 144Pr with a ‘suitable’ elution agent
zirconium arsenate (possibly Zr3(AsO4)4(H2O)2)
144
Column of Dowex 1x8, washed with 2M HCl The 144Ce solution in 6M HNO3 and Pr was eluted with 3 mL of a mixture of 
and preconditioned with 6M HNO3 and 0.2M KBrO3 was applied to the column 1M HNO3, 6M NaNO3 and 0.2M KBrO3
0.3M KBrO3 and washed with a mixture of 1M HNO3, The elution yield was ~75% and the contamination
6M NaNO3 and 0.2M KBrO3 of 144Ce <0.02%

133
FIG. 66. Partial decay scheme of 172Lu to excited states in 172Yb whose ground state is stable
[81].

Post-processing systems to synthesize a variety of industrial 144Pr tracers as

aqueous, environmental, organic and solid tracers are possible. However,
systematic studies on suitable tracers for aqueous and organic fluids, and
mapping of their thermal, chemical and microbial stability have not yet been
carried out to a sufficient degree.

3.2.10. The 172Hf/172Lu radionuclide generator

Relevant nuclear data for this radionuclide generator system are given in
Table 4, and the simplified and partial decay scheme of 172Lu is given in Fig. 66.

134
FIG. 67. Gamma spectrum of 172Lu accumulated with a Ge(Li) detector. The most interesting
energies are marked in red.

3.2.10.1. Relevant nuclear properties

(a) Gamma energies of the daughter

The decay scheme in Fig. 66 is only a partial decay scheme. The complete
scheme is rather complex: there are relatively abundant gamma energies from
79 keV to 1093 keV. A gamma spectrum of 172Lu is given in Fig. 67. It is very
complicated with all its gamma peaks, and it would therefore be preferable to use
this radionuclide in combination with a detector with high energy resolution.
The high abundance 1093 keV (63%) and 900 keV (30%) photons are
optimal for transmission through thick metal walls and detection outside of the
vessel or tubing. The low energy gamma rays at 79 keV and 181 keV are sensitive
to smaller mass thicknesses. Hence, this radionuclide is suitable for a suite of
on-line measurements in the industry.

135
(b) Half-life of the daughter

The daughter half-life of 6.7 d is adequate for relatively long duration

(weeks) investigations, and is the longest lived considered in the present
document.

(c) Half-life of the mother

The half-life of the mother radionuclide of 1.87 a offers, in principle, very

long time (several years) application without replacing the generator, provided
that the generator column keeps up its performance with acceptable quality with
respect to elution yield and mother breakthrough.

(d) Main production routes

At moderate beam energies, the mother radionuclide is produced by

Nat
Yb(p,xn)172Hf (typically 30–40 MeV), 175Lu(p,4n)172Hf (typically 40–50 MeV)
or, for instance, 169Tm(7Li,4n)172Hf (beam energy 35 MeV) reactions. The yields
are relatively small at beam intensities of a few particle A. The highest yields
have been achieved in proton induced spallation processes on Ta, W or other high
Z targets. Sophisticated separation chemistry to isolate 172Hf from tantalum or
spallation targets has been developed. Eventually, cooling periods are required to
minimize the amount of other co-produced and more short lived hafnium
radionuclides.
An example of the complex chemistry involved in working up the hafnium
from an irradiated tantalum target is given in Fig. 68. This is essentially a
procedure developed at Los Alamos National Laboratory. For a period of
approximately 2 months, a tantalum metal target was irradiated at the Isotope
Production Facility (A-6) at LAMPF. The target was irradiated with ~750 MeV
protons with an intensity of ~350 A. The irradiation area received ~1022 protons
(6 × 105 A/h) during this 2 month period. The tantalum target consisted of three
slabs of the metal. Each slab weighed ~250 g for a total target weight of 770 g.
The slabs measured 8 cm2 and 0.32 cm thick.
Chemistry was started approximately 2 months after the irradiation. At that
time, the radiation level of the target was >500 R/h at 1.5 m.
The overall chemical yield for 172Hf was estimated at >90%, for Lu ~90%
and for gadolinium and europium 60–70%. The amount of 172Hf at the end of
irradiation was estimated to be ~0.25 TBq (~6.7 Ci).

136
FIG. 68. Schematic diagram of the chemical procedure developed at LAMPF for working up
the hafnium (including 172Hf) and heavier lanthanides from the mixture of spallation products
after 750 MeV proton irradiation of a tantalum metal target.

3.2.10.2. Generator systems, separation techniques and chemical form of

the daughter

While the literature is rich on papers dealing with chemical complexation of

Lu isotopes due to the radiopharmaceutical use of 177Lu, it is correspondingly
poor on development of 172Hf/172Lu generators. One useful example is the
following: a 172Hf/172Lu radionuclide generator based on extraction
chromatography with HDEHP as the extractant and Chromosorb-102 as the inert
support has been developed in India [163]. A column (0.5 cm × 4.0 cm) was filled
with 1.5 g of the inert support Chromosorb-102 (100–200 mesh). Each gram of
Chromosorb-102 was impregnated with 100 mg of HDEHP.
The mother 172Hf, dissolved in 5M HNO3, was loaded on to the column.
The Lu generated could be eluted quantitatively by using 5M HNO3. The 172Lu
172

obtained by this method was free from detectable 172Hf activity (<4 × 10–5 of
172
Hf).

137
 The characteristics of the column material remained unchanged during
2 years of operation. This has demonstrated the suitability of the technique for
availing 172Lu for radiotracer investigation.

3.2.10.3. Availability and current status

At present, there is no commercial availability of this generator. During

production, there is a limited batch yield of about 10 mCi, which is, however,
sufficient to prepare generator systems.

3.2.10.4. Possible applications

The 172Hf/172Lu generator is an excellent source for availing 172Lu for

industrial radiotracer applications. As displayed in Fig. 66, 172Lu emits a
multiplicity of gamma rays in its decay, with energies from 79 keV to 1622 keV,
including a 63% abundant 1094 keV gamma transition. The high energy
radiations of 172Lu allow its use as a radiotracer in most types of industrial
application, in particular, for investigation of processes inside thick walled pipes
and vessels.
The 172Lu exhibits general rare earth chemistry, including complexation
with a wide variety of chelating agents and thus permits the preparation of a wide
variety of industrial radiotracers. Moreover, Lu exists only in the +3 oxidation
state. Any redox complications of its solution chemistry are thus eliminated.
Since 177Lu is a popular radiopharmaceutical agent, one has a good starting point
for production of industrial radiotracers. However, much work remains to be done
to prepare aqueous, organic and solid tracers based on 172Lu. Stress studies on
thermal, chemical and microbial stability for various temperatures and chemical
compositions are especially important for industrial radiotracers.
The 6.7 d half-life of 172Lu is a valuable asset for real time radiotracer
experiments. Moreover, the 6.7 d half-life of 172Lu is convenient for generator
post-elution chemical manipulations, tracer shipment to remote sites and
experimental utilization.
The long half-life of the parent radionuclide 172Hf (T1/2 = 1.87 a) ensures
convenient cost effective availability of 172Lu for long periods of time, provided
there is sufficient stability of the column support against chemical and
radiolytical degradation.

138
 4. GUIDELINES FOR USE OF
RADIONUCLIDE GENERATORS FOR
RADIOTRACERS FROM EXPERIMENTS

Most tracer studies on industrial process plants are carried out over
relatively short time periods, ranging from several seconds to a few hours at
maximum. For such studies, radionuclide generators provide a useful means of
providing short lived radionuclides on-site. For the effective and safe utilization
of radionuclide generators in industry, it is important to ensure that:

— The radionuclide generator is of robust construction, suitable for use in the

industrial environment.
— The radionuclide generator is transported safely to and from the worksite.
— Appropriate, written operating instructions and safety procedures for the
generator are in place and are adhered to.
— An appropriate procedure is followed to produce the radiotracer from the
radionuclide generator eluate.
— The radiotracer is appropriate for the system to be traced.

4.1. PLANNING A RADIOTRACER EXPERIMENT

Prior to carrying out any work on an industrial site with a radionuclide

generator, detailed planning is required. The three basic principles of radiation
protection as set out by the ICRP, namely, justification, optimization and dose
limitation, must be given due consideration.
The proposed work must be discussed with, and approved by, a radiation
protection adviser. It is important that a job specific work procedure should be
compiled and that this should address the doses that might be received by those
carrying out the fieldwork. This should include a description of the controlled and
supervised areas that need to be set up. It should also contain a contingency plan
describing the actions to be taken in the event of an accident.
Before work can commence, a permit to work must be obtained from the
plant supervisor. In carrying out work with radioactive material, it is possible that
the radiation from the scanning source may interfere temporarily with the
operation of any nuclear level gauge in the near vicinity. The plant operators must
be made aware of this possibility and, if necessary, these instruments should be
put on manual control for the duration of the measurements.
Prior to the elution taking place, a controlled area will need to be
established at the worksite. This is generally done by ‘roping-off’ an area around

139
the injection point. For a controlled area, the dose rate outside the rope barrier
should not exceed 2.5 µSv/h. The controlled area should be divided into ‘clean’
and ‘dirty’ areas. Facilities to enable any required decontamination of the field
engineer must be available and a gamma radiation dose rate meter and a
contamination monitor must be to hand.

4.2. GUIDELINES FOR TRANSPORTATION OF CONTAINERS OF

RADIONUCLIDE GENERATORS

The packing and transportation of radioactive material is governed by

stringent rules and regulations. The first set of rules and regulations for the safe
transport of radioactive material was published by the IAEA in 1961 and based
on ICRP recommendations, which forms the basis for all national and
international regulations. These regulations are constantly reviewed, revised and
updated from time to time by the ICRP and the IAEA. Recently, the IAEA has
published revised regulations for the safe handling and transport of radioactive
material [164].

4.2.1. The regulatory framework

The transport of radionuclide generators is controlled by the same

regulations that apply to the transport of all radioactive material. General
guidelines for transport operations are provided in the IAEA safety standard,
Regulations for the Safe Transport of Radioactive Material 2009 Edition [164].
The normal modes of transportation are road, air and sea. Transport is rarely
carried out by rail.
Road transport is controlled by national regulations. Sea transport is
controlled by the International Maritime Dangerous Goods Code. Air transport is
controlled by the International Air Transport Association Dangerous Goods
Regulations. These regulations are revised annually or every two years, and,
therefore, care should be taken to ensure that the current edition is used.

4.2.2. Classification of packages

Packages containing radioactive material are categorized for transport on

the basis of their surface dose rate and on their transport index. The transport
index is the number obtained by measuring the highest dose rate obtained at a
distance of 1 m from any surface of the package in microsieverts per hour divided
by 10. This number should be rounded up to one decimal place.

140
 The packaging of radioactive material is tightly controlled. If the quantity
of the parent radionuclide in an isotope generator is below 10–4 of the A2 value,
then it may be possible to transport the radioisotope generator as an excepted
package. In the vast majority of cases, the radioisotope generators used for field
studies are in excess of these quantities and must, therefore, be transported as
Type A packages. This involves the use of approved, certified Type A transport
containers. To be certified as a Type A transport container, the design type must
have undergone rigorous tests, including drop tests, penetration tests and
temperature cycling.
Depending upon the transport index and the surface dose rate, the package
will be designated as I-White, II-Yellow, III-Yellow, as indicated in Table 15.
Where the transport index satisfies the condition for one category but the
surface radiation level satisfies the condition for a different category, the package
must be assigned to the higher category of the two.

4.2.3. Marking and labelling the package and documentation

The shipper of the radioisotope generator is responsible for ensuring that

the correct marks and labels are on the package before it is transported. Any
irrelevant markings or labels already on the package should be removed. The
package should then be marked with each of the following:

• Proper shipping name: In the case of a radionuclide generator, this will be

radioactive material, Type A package.
• United Nations number preceded by the letters ‘UN’. In this case, it will be
UN 2915.
• The full name and address of the shipper.
• The full name and address of the consignee.

TABLE 15. TRANSPORT INDEX

Transport index Maximum radiation level at any point on Category
the external surface

0 Not more than 0.005 mSv/h I-White

More than 0 but not more than 1 More than 0.005 mSv/h but not more than II-Yellow
0.5 mSv/h

More than 1 but not more than 10 More than 0.5 mSv/h but not more than III-Yellow
2 mSv/h

141
 • Type A package identification is in the format: TYPE A/International
Vehicle Registration Code/name of the manufacturer or other identification
specified by the competent authority of the country of origin or design.
• The package must bear the correct labels and again this is the responsibility
of the shipper. There are two types of label: hazard labels, set at an angle of
45°, and handling labels. The hazard labels are either I-White, II-Yellow or
III-Yellow.

After the generator has been correctly packaged and labelled the shipment
should be documented by completing the appropriate shippers declaration
document for either road, sea or air transportation. It is essential that the
information given in this document is exactly the same as that on the package.

4.3. GUIDELINES FOR THE EVALUATION OF RADIONUCLIDE

GENERATORS

Before using the generator, it is recommended that a measurement of the

surface dose rate on the generator containment be carried out and that a swipe test
be performed close to the eluate exit to check for any loose contamination.

4.3.1. Elution of tracer

The isotope generator should be taken into the controlled ‘dirty’ area in
readiness for elution. While the parent nuclide has a certain amount of shielding
so that it may be transported safely, the eluate vessel has none. Some suitable
form of shielding is, therefore, required. This can be in the form of a small lead
brick wall or lead lined pot.
It is recommended that the daughter radionuclide should be eluted by
applying suction only. No pressure should be built up inside the ion exchange
column, as it is likely to disrupt the integrity of the column packing material. This
may also cause bleeding of any parent radionuclide that is not strongly bound to
the adsorbent.
The elution should be carried out in accordance with the elution procedure
provided by the producer of the generator. An example is given in Fig. 69.
On completion of work, the field engineer should monitor thoroughly
before leaving the controlled area.

142
 FIG. 69. Procedure for eluting the generators.

4.3.2. Elution efficiency and breakthrough test

When a daughter radionuclide from the generator is eluted, it is possible to

elute the mother nuclide from the column material along with the product. This is
likely to interfere with the tracer studies and may cause environmental pollution.
This must be measured and kept within permissible limits. The presence of
excessive metal ions of column material in the eluate indicates lack of stability of
the generator column.
Before field application, the following laboratory tests are to be conducted
with the eluate of the generator to evaluate its performance:

• Assess physical appearance — whether clear or whether any turbidity is

present.
• Measure the activity of the daughter radionuclide by an absolute counting
technique to determine the elution efficiency.
• Measure the elution efficiency as a function of time and number of elutions
and total eluate volume.
• Check the  ray spectrum of the decayed eluate to measure the breakthrough
of the mother radionuclide.

143
 FIG. 70. The catcher columns installed to the Cs/Ba generator and Ge/Ga generator.

4.3.3. Methods to reduce breakthrough and to increase the shelf life of

radionuclide generators

For the radionuclide generators such as 137Cs/137mBa, 68Ge/68Ga and

44
Ti/44Sc, and the long half-lives of their parent radionuclides, it is particularly
important to avoid breakthrough. However, since the possibility of breakthrough
cannot be completely eliminated, the following techniques are used to prevent
contamination of the eluate by the long lived mother radionuclide.

4.3.3.1. Catcher columns

Elution and breakthrough tests to study the effect of catcher columns were
carried out in the Republic of Korea with the 68Ge/68Ga and 137Cs/137mBa
generators produced in China by the CIAE. The catcher column packing
materials are the same as those used in the generators (SnO2 for the 68Ge/68Ga
generator and KCoFC–SiO2 for the 137Cs/137mBa generator).
By adding the catcher column (Fig. 70) to the 137Cs/137mBa generator and to
the Ge/68Ga generator, the breakthroughs decreased dramatically.
68

4.3.3.2. Recycling elution

The group at Mainz in Germany has developed efficient and fast on-line
protocols for post-processing of the generator eluate. The generator daughter is
trapped using cation exchange purification while the rest of the eluate is directed
into a waste vial. This results in several advantages:

• The post-processing takes 4 min, with overall recovery yields of 97 ± 2%

for 68Ga and 90 ± 2% for 44Sc.
• It results in volume reduction along with chemical and radiochemical
purification.

144
 • This procedure leads to almost complete removal of metallic impurities,
including the mother breakthrough, down to only becquerel levels.
• Since the content of the mother nuclide in the daughter is negligible, the
generators can be used with a significantly extended shelf life.
• The breakthrough is easily collected in waste vials. From these collected
waste volumes, the mother nuclide may be chemically processed for
recycling.

4.4. GUIDELINES FOR PREPARATION OF RADIOTRACERS FROM

RADIONUCLIDE GENERATOR BASED RADIOISOTOPES

It is a requirement of any tracer that it should mimic the behaviour of the

material into which it is introduced and that it should faithfully follow that
material through the system of interest. Thus, in selecting a tracer for a particular
application, care must be taken to ensure its physical and chemical stabilities
under the prevailing process conditions.
The generator systems selected in Table 16 provide daughter radionuclides
of different half-lives, different gamma energies and different chemical
properties. Except for 68Ge/68Ga and 99Mo/99mTc generators, which can be used
with organic eluants, all the other daughters are available in aqueous solutions of
acidic or neutral pH in the form of anions (TcO4–) or cations (Ba2+, Ga3+, Sc3+,
In3+, Pr3+, Lu3+).
Tracers may be required to study aqueous, organic or solid systems. To
synthesize chemical species compatible with these systems using the above
radioactive cations, several strategies, such as complex formation, sorption,
reduction and solvent extraction, are employed.
Aqueous eluates may be used as aqueous radiotracers, provided they are
applied to simple aqueous systems. However, as the metal cations tend to be
adsorbed on to solid surfaces, it is necessary to make anionic metal complexes
using chelating agents (La), such as EDTA, DOTA and NOTA. The complexes
move with aqueous media without significant absorption on to surrounding solid
materials.
Complexes of the cations with ligands (Lb) with a backbone substituted
lipophilic group are used as organic radiotracers with low solubility in aqueous
solutions and high solubility in organic solutions. Complexes of the cations with
bifunctional ligands (Lc) linked via one of their functional groups covalently to a
transport vector, such as solid particles, and via the other functional group to
metal radionuclides providing strong complex formation are used as solid tracers.
This may also be true of nanoparticles.

145
 TABLE 16. CHEMICAL FORM OF DAUGHTER RADIONUCLIDES FROM SELECTED GENERATOR SYSTEMS AND

146
POSSIBILE TRACER SYNTHESIS
Tracer synthesis strategies
Generator Eluant Chemical form
Aqueous Organic Solid

68
Aqueous (HCl) [Ga(H2O)6]3+ Ga–La Ga–Lb Ga–Lc, sorption
Ge/68Ga
Acetylacetone Ga(acac) Ga(acac)
44
Ti/44Sc Aqueous (HCl) [Sc(H2O)6]3+ Sc–La Sc–Lb Sc–Lc, sorption
172
Hf/172Lu Aqueous (HCl) [Lu(H2O)n]3+ Lu–La Lu–Lb Lu–Lc, sorption
144
Ce/144Pr Aqueous (HCl) [Pr(H2O)6]3+ Pr–La Pr–Lb Pr–Lc, sorption
137
Cs/137mBa Aqueous(NaCl) [Ba(H2O)n]2+ Ba–La, BaCl2 Ba–Lb Ba–c, sorption
113
Sn/113mIn Aqueous (HCl) [In(H2O)6]3+ In–La In–Lb In–Lc, sorption, reduction

99
Aqueous(NaCl) [TcO4]– [TcO4]– Solvent extraction Reduction to TcO2
Mo/99mTc
Tri-n-butylphosphate Tc(TBP) Tc(TBP)
a
Chelating agents.
b
Ligands.
c
Bifunctional ligands.
4.5. GUIDELINES FOR VALIDATION OF RADIONUCLIDE GENERATOR
BASED RADIOTRACERS

After having produced a radiotracer candidate, this should be subjected to a

sequence of laboratory tests to validate its applicability to the industrial
investigation in hand. Tracer candidates which do not pass the tests are unlikely
to be appropriate and should not be considered further.
Most industrial radiotracer applications involve the use of physical tracers
to study the physical dynamics of phases. In these cases, passive tracers are
normally used. For radionuclide generator based passive radiotracers, the
following items should be considered for validation:

• Flow behaviour similarity (no size exclusion or ion exclusion owing to

electric charges);
• Physical stability (no evaporation, segregation or mechanical rupture);
• Chemical stability (no chemical degradation, sorption, partitioning or
precipitation);
• Biological stability (not affected by microbial activity in the traced system);
• Thermal survivability (no significant thermal degradation in the system
under study);
• Pressure survivability (not affected by increasing or decreasing pressure);
• Labelling efficiency (readily possible to label the intended physical phase);
• Radioactivity (suitable half-life and radiation characteristics);
• Specific radioactivity (may, in some cases, need a high specific
radioactivity);
• Radiochemical purity (concentration of other compounds labelled with the
same radionuclide within acceptable limits);
• Radionuclide impurity (concentration of other radionuclides present not
detrimental for the intended tracing operation);
• Density control (in cases where identical density is required, i.e. for particle
tracing);
• Packaging and handling (appropriate procedures have to be implemented in
each case);
• Chemical toxicity (has to be as low as possible and data sheets have to be
provided).

Detailed guidelines should be developed for validation of specific

radionuclide generator based radiotracers for specific applications.

147
4.5.1. Thermal stability tests

Thermal stability tests are carried out in closed (sealed) vials of

polypropylene (<100C), borosilicate glass or quartz glass containing the
pertinent liquid medium. If testing at high pressures is needed, one may have to
use steel, hastalloy or titanium vials. Parameters tested may be temperature,
pressure, pH, ion composition, concentration of multivalent ions, etc.
The degradation products of a radiotracer normally behave differently from
the radiotracer. Removal of the degradation products can normally be done by ion
exchange or solvent extraction. In many cases, the degradation products adsorb
on to the walls of the vials and are, therefore, removed from the solution. The
quotient Rx,t/Rx,0 should be recorded as a function of the parameters tested, where
Rx,t is counting rate of the radiotracer still in solution after a time t for the
parameter value x and Rx,0 is the corresponding counting rate at time zero. For a
good tracer, this value should be constant, with a value of 1.

4.5.2. Sorption stability tests

For radiotracers that are supposed to come into contact with solid material,
sorption tests should be conducted. In nature, they are similar to the thermal
stability tests, the only difference being that the vials contain the solid material as
a finely divided substrate. Sometimes, it is appropriate to carry out the thermal
and sorption tests together in the same vial. The results will then show the
composite effect, which may be sufficient for the purpose.

4.5.3. Microbial stability tests

For tracers which have a chance to be biodegraded, corresponding stability

tests have to be conducted under aerobic and anaerobic conditions. The
experiments are similar to those described above.

4.5.4. Partitioning tests

Tracer molecules, which are non-charged and which contain at least one
substituent (ligand) with a lipophilic character, can partition between aqueous and
organic phases. For a passive water tracer, for instance, this is undesirable.
Therefore, the partition coefficient (distribution ratio), KD = [Tr]0/[Tr]w, of these
molecules should be measured for actual liquid systems (water type and
composition and organic phase type and composition) as a function of actual
parameters (temperature, salinity, pH, etc.).

148
 Here, [Tr]0 is the concentration of tracer in the organic phase at distribution
equilibrium and [Tr]w is the corresponding concentration in the aqueous phase.
The experiments are carried out in simple equipment such as a separation funnel
at ambient conditions, and more advanced equipment as temperature and/or
pressure increases.

4.5.5. Dynamic flooding tests

Tracer candidates that have passed the preceding tests continue to the final
laboratory test, which is a dynamic experiment where the tracer candidate is
injected as a sharp low volume pulse, together with a standard reference tracer
(mainly HTO for water) into a liquid stream. The stream enters the test system,
which should simulate the industrial conditions as closely as possible (except for
volume). In-line detectors can be applied on the exit fluid stream or samples can
be taken at regular intervals so that the tracer production curves can be recorded.
There will be one curve for the standard reference tracer and one for each tracer
candidate. The latter production curves should resemble those of the standard
reference as closely as possible. From these tests, it is possible to extract
quantitative information on, for instance, sorption on to solid substrates or
partitioning between fluids. This test is the last test in the laboratory before the
systems developed are tested in the field.

4.5.6. Radiochemical purity tests

The radiochemical purity of radiotracer is very important for the accuracy

of tracer experiments. For example, any uncomplexed form of 113mIn in the
113m
In-EDTA tracer will be adsorbed in the system during the process
investigation. The radiochemical purity of the generator eluate or radiotracer can
be determined by a paper chromatographic technique using standard protocol.

4.6. GUIDELINES FOR RADIOLOGICAL SAFETY IN THE APPLICATION

OF RADIONUCLIDE GENERATOR BASED RADIOTRACER

4.6.1. Radiation dose considerations for the injection of radiotracer

generators in field tests

Prior to carrying out work with a radionuclide generator based radiotracer,

it is necessary to make an estimate of the radiation dose that may potentially be
received by the persons carrying out the project, by the workforce on the

149
industrial site and by members of the general public. The method of making this
assessment will clearly vary from case to case.
As an example, the radiation dose received by the radiotracer practitioner
under the following conditions should be considered:

• Activity of the radionuclide: 3.7 GBq (100 mCi) considered as a point

source.
• Distance of the operator to the source: 1 m.
• Duration of the injection operation: 1 min without shielding
(elution + transfer to injection system).
• Shielding of the injection system: 3 cm thick lead shielding.

The results of the dose calculations are presented in Table 17. The
conclusion is that under normal conditions, the gamma radiation dose to the
operator is very low. It is also worth pointing out that in many cases, the activities
required for field tests are significantly lower than those used in the above
calculations. However, if, for any potential application, the calculation should
indicate the potential for a significant radiation dose to be received, then
measures must be taken to reduce that dose to a level as low as reasonably
achievable (ALARA). Such measures might include the provision of additional
shielding, or the use of remote handling equipment.
It can almost always be shown that the potential dose to workers on the
industrial site where the project is being carried out will be negligible, because of
the dilution of the tracer in the process stream, the shielding provided by the thick
metal walls of process vessels, the short half-life of the radionuclide, etc.
However, should the potential for a significant dose to workers, or to members of

TABLE 17. DOSE FROM 3.7 GBq RADIOTRACER INJECTION FOR FOUR
RADIONUCLIDES
Dose rate at 1 m
Dose rate at 1 m from Dose for 1 min
Nuclide activity from the external walls
the unshielded source operation
(3.7 GBq) of the injection system
(µSv/h) (µSv)
(µSv/h)
99m
Tc 70 1.2 4  10–20
113m
In 150 2.5 9  10–2
68
Ga 470 7.8 8.6
137m
Ba 300 5.0 15

150
the general public exist and should it prove impossible to reduce the dose to an
acceptable level by altering the test procedure, then the project must not be
undertaken.
Despite the fact that the radiation doses received by the operator and
workers on-site are negligible, there is still an obligation on the part of the
radioisotope practitioner to keep the worker on-site fully informed about the
nature of the work that is being carried out, explaining clearly the potential risk
due to radiation dose and the precautions that will be taken to ensure that the
work can be carried out safely.

4.6.2. Regulatory framework

The regulatory requirements for the conduct of radiotracer experiments are

determined at a national level. These vary from country to country, but are
commonly determined with reference to safety standards and guidelines issued by
the IAEA and the ICRP. At the highest level, the IAEA’s Fundamental Safety
Principles [165] are relevant to environmental radiotracer applications in
requiring that:

• The benefits of an activity must outweigh the radiation risk (Principle 4).
• Activities should be optimized to ensure exposures are ALARA
(Principle 5).
• Radiation exposure to ecosystems should be limited to ensure protection of
populations of a species (as distinct from individual organisms)
(Principle 7).

These principles are binding on the IAEA for its own operations, and they
are also recommended for use by Member States in relation to their own
activities.
The IAEA International Basic Safety Standards for Protection against
Ionizing Radiation and for the Safety of Radiation Sources [166] lists the
requirements for the use of radiation and radioactive material. An environmental
radiotracer application can be considered to be a planned exposure, as defined in
this publication, which covers applications of radiation and radioactive material
in industry, agriculture and research.
National regulations covering the use of radiotracers in the environment
vary from jurisdiction to jurisdiction and it is not appropriate to address these
comprehensively here. Generally, the regulation of radiotracer activities is carried
out in three ways:

151
 (i) Licensing of an organization to possess and use radioisotopes;
(ii) Licensing of individuals to handle radioisotopes;
(iii) Approval for the release of a radioisotope tracer into the environment.

The injection of a radiotracer into the environment for the purposes of

studying environmental processes is, in effect, a radioactive discharge and is
considered by many national jurisdictions to be a form of radioactive waste
disposal. In some jurisdictions, the limits applied to environmental radiotracer
studies are derived from those applied to waste discharges.
In most cases, there is a requirement for pre-approval of each radiotracer
experiment either by the national regulator (e.g. France, Indonesia, Sweden,
Uruguay) or, in some cases, by a radiation safety body within the applicant’s
organization (e.g. Australia, Brazil, Republic of Korea) where general licensing
for radiotracer studies has already been obtained. The application for approval
requires a radiation safety assessment of the release to be carried out, addressing
the following aspects:

• Purpose of the experiment and justification for the use of radiotracers;

• Location of the experiment and predicted radioactivity levels in the
environment during and following the release;
• Radiological dose calculations for planned radiation exposure of workers
and the public and potential unintended exposures;
• Safety measures and monitoring to be employed to minimize radiological
dose and risk of injury to workers and to the public during and following the
experiment.

In the majority of jurisdictions, a radiological risk assessment is only

required for humans potentially exposed to the radiotracer. An underlying
assumption is that the environmental impact of radiotracer releases is negligible
owing to the rapid dispersion of the radiotracer in the receiving environment.
However, in some jurisdictions, particularly Australia, it is also a requirement to
address the environmental impact of the radiotracer study in conducting the risk
assessment.
General guidelines for the safe handling of radioisotopes have been issued
by the ICRP and the IAEA from time to time [165, 167, 168].
Generally, safety regulations include justification of the use of radiotracer,
optimization of radiation exposures and the annual dose limits in order to prevent
unnecessary exposure. Justification implies that the competent authority should
not allow the use of radiation unless a net positive benefit arises from its use.
The design of a radiotracer experiment has to ensure optimization of
radiation exposures. All the exposures have to be ALARA. The optimization of

152
radiation exposures depends initially on selecting the most appropriate
radioisotope for the project and ensuring that the activity used is kept to a
minimum, consistent with achieving the aims of the project. Additionally,
distance, time and shielding are used to minimize the dose received:

• The dose rate at a point varies in inversely proportion to the square of the
distance between the source and the point. Therefore, radiation workers
have to maintain the maximum possible distance between themselves and a
radiation source.
• The dose received is directly proportional to the time spent in handling the
source. Thus, the time spent handling the source should be minimized.
• The radiation intensity at a point reduces exponentially with the thickness
of shielding material. Thus, an optimum thickness of the shielding material
has to be used between the source and a radiation worker.

The relevant annual dose limits have to be taken into account and no
individual must be exposed to more than the prescribed limit. These dose limits
recommended by the ICRP are 1 mSv/a for a member of the public and 20 mSv/a
for a radiation worker [169].

5. PREPARATION OF RADIOTRACERS FROM

GENERATOR PRODUCED RADIONUCLIDES

5.1. RADIOTRACERS FROM THE 68Ge/68Ga GENERATOR

The high energy photon (1077 keV, abundance: 3.2%) emitted by 68Ga can
be detected through thick metal walls and so is suitable for on-line measurements
on industrial process plants. Gallium-68 is a positron emitter and so the
coincidence detection of annihilation radiation (511 keV, abundance: 178.3%)
presents the possibility of determining local radionuclide distributions with high
resolution.
There is an increasing demand for 68Ga for PET imaging in medicine, but,
in addition, there is good potential for a variety of 68Ga compounds as aqueous,
organic and solid phase tracers for industrial applications. The fact that the
generator can be used three to four times per day at maximum activity, allowing
repeated radiotracer studies, is a particular advantage in this respect. Commercial
68
Ge/68Ga generators are produced using modified TiO2 columns, modified SnO2

153
columns, modified (nano-particular) ZrO2 matrices, as well as organic resins.
Common to all systems, hydrochloric acid with concentrations ranging from
0.01N to 1.0N is used for the elution of 68Ga.
In order to avoid any radioactive contamination of the systems under
investigation and the environment around them, it is very important to make sure
that the concentration of the mother nuclide in the eluate is as low as that
specified by the supplier of the generator. Therefore, the eluate needs to be
carefully monitored throughout the life of the generator to check for the
breakthrough of the mother radionuclide and also to ensure that the elution
efficiency continues to be satisfactory.
For preparation of 68Ge/68Ga generators, several radiochemical criteria are
relevant, such as effective separation strategies providing high 68Ga elution yields
and low 68Ge breakthrough, long term stability and the type of eluate useful for
subsequent labelling reactions (low volume, low pH, high purity, etc.). The eluate
is obtained as a complex of 68Ga tetrachloride in hydrochloric acid solutions. The
68
Ga complex starts to hydrolyze and begins to form hydroxides at pH4. These
tend to form colloids or pseudocolloids with unknown physicochemical
characteristics and migration behaviour. In consequence, 68Ga should be
transformed into species that are chemically stable under environmental
conditions. In neutral pH, the 68Ga cation is easily adsorbed on to the surface of
solids, creating a stable bonding. Therefore, for the tracing of liquid systems,
68
Ga should be transformed into species that are stable in aqueous or organic
media.
Thus, the eluate from the 68Ge/68Ga generator can be used either for the
labelling of solid particles (by surface adsorption) as solid tracers or for the
synthesis of 68Ga–ligand complexes of very high thermodynamic and kinetic
stabilities, capable of ‘surviving’ any harsh physical and chemical conditions in
the industrial system to be studied.

5.1.1. Aqueous 68Ga tracers

5.1.1.1. The eluate of a 68Ge/68Ga generator

The eluate of a 68Ge/68Ga generator was tested as a radiotracer on a large

scale laboratory installation at the INCT in Warsaw, Poland (a model of a
rectangular settler on a wastewater plant). A fluorescent dye was used as a
reference tracer for the water. RTD analysis demonstrated that the mean residence
time of the 68Ga was significantly longer than that of the fluorescent dye. The
authors attributed this to the sorption of the Ga3+ species on to solids in the
system. This indicates that the unmodified eluate from the generator is not a
reliable water tracer.

154
 The hydrated Ga(III) ion is only stable under acidic conditions and the
insoluble species Ga(OH)3 is formed as the pH increases. Between pH3 and 9.5,
insoluble Ga(OH)3 is the predominant species, whereas above pH9.6, the soluble
tetrahydroxigallate anion, Ga(OH)4–, is formed.

Ga(H2O)3+ 2+
6 + H2O  Ga(OH)(H2 O)5 + H3O
+

Ga(H2O)3+ 3–
6 + 6HCl  GaCl6 + 6H3O
+

> 4M

5.1.1.2. Gallium-68-ligand complexes

As 68Ga exists in trivalent cationic form, its compatibility with aqueous

media without significant absorption on to surrounding materials can be
achieved by producing a complex compound with the chelating agents such as
DOTA (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid), NOTA
(1,4,7-triazacyclononane-1,4,7-triacetic acid) and EDTA (ethylene-diamine-
tetraacetic acid).
The group at the Korea Atomic Energy Research Institute (KAERI) used
DOTA in order to stabilize the Ga3+ ion in the aqueous phase. The method of
preparing Ga–DOTA is given below:

— Elution of Ga3+ ion from the 68Ge/68Ga generator;

— Addition of the DOTA solution (2 mg of DOTA in 0.2 mL of 50mM sodium
acetate buffer, pH5.5);
— Regulation of pH by using sodium hydroxide and sodium acetate solution
(~pH3);
— Heating the solution to ~90°C for 15 min;
— Cooling the solution by ice or cold water.

After the synthesis, thin layer chromatography (TLC) was performed on

0.8 cm × 7.5 cm TLC plates (Kieselgel 60 F-254, Merck) with 75% methanol.
The activity distribution on the plates was measured by a TLC radioisotope
scanner (TRACER-MASTER20, Berhold). Figure 71 shows the thin layer
chromatograms of Ga3+ ion and the Ga–DOTA complex, respectively.
Figure 71(a) shows that the Ga ion remained the spotting point of the plate
(Rf = 0). On the other hand, Fig. 71(b) shows that there is no peak at the origin
and that the activity has moved to the centre of the plate (Rf = 0.45). This means
that all the Ga ions were changed to the Ga–DOTA complex.
The group at Mainz University in Germany developed an efficient and fast
on-line protocol based on a cation exchange purification method for on-line

155
 Distance (cm) Distance (cm)

Spotting Solvent Spotting Solvent

point front point front

(a) 68Ga3+ ion (Rf = 0) (b) 68Ga-DOTA (Rf = 0.45)

68
FIG. 71. Thin layer chromatograms of Ga ion and 68Ga-DOTA.

radiopharmaceutical syntheses. The key step in this procedure consists of the

direct transfer of the initial 0.1N HCl 68Ga eluate to a cation exchanger. Owing to
high distribution coefficients, 68Ga is quantitatively adsorbed on to only about
50 mg of the resin directly from the generator eluate.
Low volumes of a mixture of 1.0 mL of 80% acetone/0.15N HCl are
applied to purify 68Ga from Ge(IV), Ti(IV), Zn(II) and Fe(III). Admixture of
0.4 mL of a 98% acetone/0.05N HCl is sufficient to completely desorb 68Ga from
the resin and to transfer this purified fraction on-line to a labelling vial.
The processing takes 4 min, with overall 68Ga recovery yields of 97 ± 2%.
This efficient and simplified system for processing 68Ga eluates results in volume
reduction along with chemical and radiochemical purification. This procedure
leads to almost complete removal of metallic impurities, including 68Ge
breakthrough, thus providing the purified 68Ga in a form useful for direct
labelling with acceptable pH, volume and purity.
For subsequent syntheses, the 400 µL fraction of the 80%
acetone/0.15N HCl mixture containing the processed 68Ga is transferred to 5 mL
of water, containing appropriate amounts of, for example, DOTA–TOC (such as
20 µg). The resulting mixture is pH2.3. Owing to the high purity of the
68
Ga fraction and the fact that buffer systems (which may introduce a load of
metallic impurities) are not needed, high labelling yields of >95% are achieved
with about 5 min of heating to just below 100°C.

156
 The group at the INCT in Poland compared the behaviour of the
radiotracers 68Ga–NOTA (Fig. 71) and 68Ga–DOPA (obtained from
radiopharmaceutical elution of the generator), with that of fluorescein (classical
water tracer) in investigating the settler of a wastewater treatment plant. The RTD
curves of these tracers showed very good similarity within the limits of
experimental error. Thus, it was concluded that 68Ga–NOTA and 68Ga–DOPA are
appropriate tracers of water and water-like systems. The major disadvantage of
these two ligands is that they are more expensive than EDTA and DTPA, so their
use to trace industrial water systems may not be justified, especially since
68
Ga–EDTA is a proven tracer for aqueous systems.

5.1.2. Organic 68Ga tracers

The group in India has developed industrial nano-zirconia based 68Ge/68Ga

generators, which can be used to obtain 68Ga eluted in an acetylacetone medium.
The 68Ge/68Ga solution containing 68Ge at pH2 was percolated into the column at
a flow rate of 0.25 mL/min. The generator column was thoroughly dried by
continuous passage of hot dry air (~60C) through it for 4 h to ensure the sorbent
was free from moisture. After drying the column, it is mandatory to cool it for 30
min. followed by washing with 50 mL of acetylacetone. The generator is eluted
with 4 mL of acetylacetone. The eluate can be used directly as an organic
radiotracer in the oil and petrochemical industries.
The group at Mainz University in Germany uses purified 68Ga adsorbed on
a small cation exchange resin as a means of transferring 68Ga into a labelling
intermediate applicable for use with anhydrous or organic media. The initial
aqueous generator eluate is transferred on-line on to a cation exchange resin.
From this resin, 68Ga is eluted with different acetone based, non-aqueous solvent
systems.
More than 95% of the generator eluted 68Ga is obtained from the cation
exchange resin using a mixture of 600 µL of 98% acetone/2% acetylacetone
providing 68Ga(acac)3 as the labelling agent. Water-insoluble macrocyclic
polypyrrole derivatives were chosen as model compounds for a proof-of-
principle labelling of lipophilic compounds with 68Ga. Labelling of two different
porphyrin derivatives was performed in chloroform in a focused microwave
synthesis system in yields of up to 97% within 1 min. On the basis of these
results, this novel procedure of providing 68Ga(acac)3 offers a wide scope of
application for this labelling agent.
Figure 72 illustrates the prototype of such a ligand, which is difficult to
dissolve in an aqueous solution. However, even DOTA or NOTA based

157
 CH3
HO

CH3

OH
H 3C

Cl
N N CH3

Ga

N N

H 3C CH3

C
O C
OH OH
O

FIG. 72. Gallium-68-hematoporphyrin.

macrocyclic ligands may be applied where those ethyl structures have been
conjugated to lipohilic moieties such as aliphatic or aromatic carbohydrates.

5.1.3. Solid 68Ga tracers

The efficient operation of the fluidized catalytic cracking unit (FCCU) is

critical to the profitability of a refinery, and radioactive tracers are widely used
for troubleshooting operational problems and for process optimization. The
68
Ge/68Ga generator can be used to label the FCCU catalyst. If appropriate
radioisotope handling facilities are available at the work site, catalyst powder can
be soaked in the eluate from the generator and, after drying, injected into the
FCCU. Where this is not possible, the eluate from the generator can be injected
directly into the FCCU riser as a pulse, to provide in situ labelling. Both of the
above approaches have been used successfully to study the behaviour of the
catalyst in FCCU risers, primarily to measure its velocity and to study its
distribution over the riser cross-section.
An investigation into the sorption of Ga ions eluted from the 68Ge/68Ga
generator on to bentonite has been carried out. After about 20 min, the firm and
complete sorption of the 68Ga was observed. Rinsing the bentonite showed that
approximately 98% of the activity was associated with the solid phase. It is,
therefore, feasible that labelled bentonite particles could be used as a tracer of the
solid phase.

158
5.2. RADIOTRACERS FROM THE 99Mo/99mTc GENERATOR

The 99Mo/99mTc generator is used extensively in nuclear medicine and is

widely available worldwide. For this reason, the somewhat short half-life of
99
Mo is not too severe a disadvantage. The 6 h half-life of the daughter 99mTc is
appropriate for a wide range of studies in industry and the environment.
Radiotracers from the 99Mo/99mTc generator have the potential for application in a
variety of industrial situations, with tailor-made 99mTc tracers suitable for
aqueous, organic or solid media.
The gamma ray (140 keV) emitted by 99mTc has a half-thickness of 5 mm of
steel and, thus, allows process investigation inside a vessel of wall thickness up to
about 20 mm. It is not appropriate for use on high pressure plants owing to the
greater wall thickness of the process vessels.

5.2.1. Aqueous 99mTc tracers

5.2.1.1. Eluate from a 99Mo/99mTc generator

The eluate of the 99Mo/99mTc generator is sodium pertechnetate

99m
(Na TcO4), which is the chemical form preferably used by radiotracer teams to
label aqueous systems in which the redox potential of the system is not enough
for the chemical reduction of the species TcO4−. In such circumstances,
experience has shown that Na99mTcO4 is a good tracer of the water phase, and can
be used for:

• Water tracing in wastewater treatment plants for RTD measurement;

• Water tracing in surface bodies (rivers, sea) for the study of the dispersion
of effluents and for dispersion coefficient measurements;
• Water tracing for water infiltration coefficient measurements in soil;
• Determination of water channelling in petroleum industry boreholes.

Because of the low gamma energy of 99mTc gamma ray, detectors

submerged in large scale water systems sense only radiotracer in the immediate
vicinity, so that localized flow patterns can be observed.
Some authors have reported adsorption of technetium during studies on
units of wastewater treatment plants or in very reducing environments. This may
be because, in such environments, the TcO4– ion can be metabolized by
microorganisms or can be reduced to TcO2, TcO(OH)2 or Tc2+. In those forms, it
can produce radiocolloids and be adsorbed. In such a case, the use of the
complexes 99mTc–EDTA or 99mTc–DTPA is recommended.

159
5.2.1.2. Aquacomplex ion [99mTc(CO)3(H2O)3]+

Although the RTD of this ion is similar to that obtained with K82Br when
tracing wastewater in a settler, the use of this compound is not recommended
because its chemical stability is only about 3 h and its preparation is rather
complicated.

5.2.2. Organic 99mTc tracers

5.2.2.1. Non-aqueous 99Mo/99mTc generator

The industrial 99Mo/99mTc generator developed by India with the aid of

chromatographic alumina can be used to obtain 99mTc in a non-aqueous medium
(TBP). This generator system is based on the selective extraction of 99mTc, with
appreciable yield and with high radiochemical and radionuclidic purities.
It has also been reported that nearly 85% of the 99mTc retained in the column
is eluted in a volume of 5 mL. The performance of the generator remains
consistent over a period of two weeks, which is the normal shelf life of a
99
Mo/99mTc generator. This approach provides 99mTc at industrial sites in a
medium soluble in hydrocarbon solvents, for radiotracer applications. The
physical properties of TBP (melting point: –76°C; boiling point: 289°C; flash
point: 146°C; water solubility: 6 g/L) and its miscibility with most hydrocarbons
make it an attractive tracer.
It has also been reported that MEK is used as an eluant in the 99Mo/99mTc
generator, which is produced by the Indian Radiation and Isotopic Technology
Association. Yields greater than 95% have been achieved by extracting the
99m
TcO4– with MEK. However, under conditions of high temperature or salinity,
such as those usually found in multiphase systems in the petroleum industry, the
thermal and chemical stabilities of this radiotracer have still to be proven.

5.2.2.2. Solvent extraction method

The extraction of pertechnetate (99mTcO4–) with organic solvents is

employed for the preparation of organic 99mTc tracers. TBP and tri-n-octylamine
are two of the most used extractants, either on their own or mixed with other
solvents.

5.2.3. Solid 99mTc tracers

For solid phase labelling (particle tracers), the generator eluate (99mTcO4–)
can be reduced to TcO2 using an aqueous solution of SnCl2. The reduced form can

160
be used to label solid particles, which can be used for radiotracer investigations,
such as:

• Sludge tracing in wastewater treatment plants for RTD measurements;

• Mud tracing in surface water (rivers, sea) for particle dispersion in effluent
studies and dispersion coefficient measurements;
• Mud tracing in the sea for dredging and dumping studies (dumping
efficiency, advection, dilution, dispersion coefficients, etc.).

The eluate (99mTcO4–) and the particles (always in an aqueous medium) are
mixed with a reducing solution of SnCl2 (concentration 20 g/L) so as to achieve a
concentration (i.e. the ratio of the mass or particles to the mass of SnCl2) of
approximately 3.
After 10–15 min stirring, the particles are labelled with better than 90%
efficiency. The stability of the labelled particles must be tested under the
conditions of the system to be investigated, especially for high temperature
applications. An example of this procedure applied to sand labelling is as follows:

• First dry the sand and take a 200 g sample.

• Take ~20–30 g of SnCl2 and dissolve it in 20 mL of water.
• Add 1 mCi of 99mTc together with 20 mL of water to the sand and stir until
they are mixed homogeneously.
• Then, mix in the SnCl2 solution.
• Wash the sand three times.
• Add sufficient water to make it easy to inject into the system inlet.

5.3. RADIOTRACERS FROM THE 113Sn/113mIn GENERATOR

The radionuclide 113mIn has the potential for application in a variety of

industrial situations using tailor-made 113mIn tracers as probes for aqueous,
organic or solid material. A wide variety of 113mIn labelled tracers can be
synthesized using information obtained from the radiopharmaceutical literature.
Dual phase systems with solid/liquid are often encountered in various
industrial process units that are designed to separate or purify the components.
Understanding the dynamic behaviour of each phase is very important in order to
investigate the performance of the system. Indium-113m compounds can be used
for the selective labelling of both phases.
The gamma energy (391 keV) is sufficiently high for 113mIn tracers to be
used for on-line measurements in most industrial plant. Indium is extracted from

161
the 113Sn/113mIn generator using 0.1N HCl solution to obtain the 113m
In3+ ion in
chloride solution.

5.3.1. Aqueous 113mIn tracers

The 113mIn3+ ion can be complexed with multidentate ligands such as EDTA
and DTPA for aqueous tracing in dual phase systems. For many years, the
radiotracer pulse velocity technique using the 113mIn–EDTA complex has been
applied routinely to the measurement of process flow rates on industrial plants.
Comparison of the results obtained with the 113mIn–EDTA complex with those
obtained using K82Br solution (which is known to be a good tracer for water), has
shown that the results are identical, within the limits of accuracy of the
measurements (±2%).

5.3.2. Organic 113mIn tracers

The eluate of the 113Sn/113mIn generator was mixed with methanol to be used
as an organic tracer for the measurement of velocity and volume flow rate of
petrol flowing through a 10 cm diameter pipe at ambient temperature using the
pulse velocity technique. The Reynolds number for this flow was 1.7 × 105,
indicating that it is fully turbulent. The measured results were in excellent
agreement with the results obtained using the well-known organic radiotracer,
82
Br labelled paradibromobenzene dissolved in toluene.
Similar studies were carried out on fuel oil flow in a 20 cm diameter
pipeline and, again, there was good agreement between the results obtained with
the generator eluate and those obtained with the paradibromobenzene tracer.
It is, perhaps, going too far to suggest that on the basis of these two
measurements, the eluate from the generator is a good tracer for any fully
turbulent flow organic, but these results are encouraging. Further to this, since the
chemistry of gallium is very similar to that of indium, it is reasonable to suppose
that the eluate from the 68Ge/68Ga would also be a satisfactory tracer for pulse
velocity measurements of turbulent flow in organic liquids.

5.3.3. Solid 113mIn tracers

Because 113mIn is eluted in cationic form, the solid phase can be labelled by
mixing the 113mIn cation with solid particles, such as sand. In doing this, the pH of
the generator eluate should be adjusted to a value where optimum sorption of In3+
will occur. For example, 113mInCl3 is a good tracer of sediments. Experience has
shown that 113mInCl3 eluted from an indium generator can be used for:

162
 • Sludge tracing in wastewater treatment plants for RTD measurements;
• Mud tracing for dumping site studies;
• Catalyst tracing for RTD measurements.

Indium is easily fixed on fine solid particles by simple adsorption of the

hydrolyzed ion without any pretreatment. Although the extraction efficiency
decreases from 80% with 0.1N HCl to 70% with 0.08N HCl, it can be the
preferred method to prevent mud flocculation, which is low, under 0.1M HCl per
kilogram of mud or sludge. The fixation efficiency is always between 95 and
98%.
The natural adsorption capacity of sand particles can vary depending upon
the sand origin and grain size distribution, but it is always quite low, typically less
than 12%. Thus, it may be necessary to carry out a pretreatment of the sand
particles to increase the adsorption efficiency. The pretreatment can be performed
as follows:

• Step 1: Treatment with nitric acid to clean the sand of organic matter and
impurities, and to create microholes at the surface of the grains.
• Step 2: Treatment with NaOH for the formation of a superficial silica gel is
helpful for the adsorption, retention and resistance of the radionuclide
deposit.
• Step 3: Tin chloride for its reducing properties.
• Step 4: Silver coating to exchange silver with tracer.

Reactions that are supposed to occur are reduction of silver nitrate.

Sn2+ + 2Ag+ → Sn4+ + 2Ag0

The silver coated sand is stored under distilled water to avoid any oxidation
which would transform Ag0 in AgO. The In3+ in the chloride solution is added to
the silver coated sand and the following reduction and exchange reactions occur:

• Reduction of In3+ by remaining tin: Sn2+ + 2In3+→ 3Sn4+ + 2In0

• Reduction of In3+ by silver: 3Ag0 + In3+ → In0 + 3Ag+

The natural sand labelling method has two main disadvantages: surface
labelling and risk of erosion during the transport of the grains. However,
following the above process, the fixation efficiency is more than 80% and the
resistance to mechanical erosion is quite sufficient.
The 113Sn/113mIn generator can be used to label the FCCU catalyst. If
appropriate radioisotope handling facilities are available at the work site, the

163
catalyst powder can be soaked in the eluate from the generator and, after drying,
injected into the FCCU. Where this is not possible, the eluate from the generator
can be injected directly into the FCCU riser as a pulse, to provide in situ labelling.
Both of the above approaches have been used successfully to study the behaviour
of the catalyst in FCCU risers, primarily to measure its velocity and to study its
distribution over the riser cross-section.

5.4. RADIOTRACERS FROM THE 137Cs/137mBa GENERATOR

Commercially available 137Cs/137mBa generators are of very low activity

(typically 370 kBq). They are used in educational establishments for
demonstration purposes only. However, the parent radioisotope, 137Cs, may be
procured from commercial suppliers and can be used for the construction of
generators to meet the needs of individual users.
The main drawback of the 137mBa as radiotracer is its short half-life
(T½ = 2.5 min). Even so, it is suitable for many industrial tracer applications. The
short half-life of the 137mBa ensures that there is no possibility of buildup of
radioactivity in the system being studied. The half-life of the parent isotope (30 a)
facilitates long term storage and the gamma ray energy of the daughter (660 keV)
is high enough for most industrial applications.
The long lived parent nuclide (137Cs) provides a renewable source of
radiotracer over a period of years. This opens up the possibility of using a
137
Cs/137mBa generator as the source of tracer in permanently installed plant
instrumentation. As described in Section 6.1.3, a flowmeter based on this
generator operated successfully on the effluent outfall of a major chemical
complex to provide semi-continuous monitoring of the effluent flow rate.

5.4.1. Aqueous 137mBa tracers

There may, sometimes, be a need for chemical treatment/complexation, but

in most cases, especially in water and water-like media, the eluted tracer
(137mBaCl2) is used directly after milking from the generator. Some typical
applications of this generator are:

• Flow rate measurement for flowmeter calibration.

• Mixing studies of reactors which operate with Newtonian low viscosity
fluids under turbulent regimes. The homogenization time in the vessel
should be comparable with the half-life of 137mBa.

164
 The 137mBaCl2 eluted from the generator was used to characterize the
mixing efficiency of a pilot crystallizer. The results confirmed the suitability of
the tracer. A further study confirmed that the 137mBaCl2 tracer was appropriate for
use in RTD measurements in a ceramic membrane module.
Water–oil distribution experiments have been carried out using barium
complexes as tracers undert ambient conditions. Aqueous phase Ba complexes of
EDTA, DTPA and 18C6 (ethylene oxide cyclic hexamer). The results showed that
no oil phase partitioning was observed with Ba–EDTA, Ba–DTPA or Ba–18C6.
The degree of sorption to reservoir rock material was acceptably low. Therefore,
these complexes may prove applicable to the study of water transport in general,
as well as in commingled multiphase fluid handling systems such as separators
and scrubbers in the petroleum industry.

5.4.2. Organic 137mBa tracers

Barium complexes with DC18C6 and HDNNS show promise as tracers for
organic phases. They are generally applicable to single phase flow of organic
liquids. It is also probable that they could be applied to commingled multiphase
flow in oil installations, but further work is needed to confirm this.

5.4.3. Solid 137mBa tracers

There is no obvious reason why the 137Cs/137mBa generator should not be

used for the in situ labelling of an FCCU catalyst by injecting the eluate from the
generator directly into the FCCU riser.
The half-life of the 137mBa (2.55 min) is certainly sufficiently long for riser
studies, since the typical residence time of catalyst in the riser is generally no
more than 10 s. The 660 keV gamma rays are sufficiently energetic to penetrate
the thick walls and refractory lining of the vessel.

5.5. RADIOTRACERS FROM THE 44Ti/44Sc GENERATOR

The 44Ti/44Sc radionuclide generators may be of interest for medical

imaging as well as for industrial applications. The 3.92 h half-life of 44Sc and the
high positron branching of 94% may stimulate the application of 44Sc labelled
PET radiopharmaceuticals.
In addition, the high energy photon emission of 1.157 MeV appears to be
ideal for industrial purposes. However, both 44Ti production and 44Ti/44Sc
generator design present challenges for basic radiochemistry.

165
 The 44Ti/44Sc radionuclide generators have been investigated in a few cases
only over recent decades. The general concept has been to elute 44Sc from ion
exchange based generators. The 44Sc is finally obtained as complex of weak
ligands such as halogenides (e.g. chloride) and/or oxalate.
For liquid systems, however, 44Sc should be transformed into species stable
in the aqueous or non-aqueous media (i.e. not undergoing hydrolysis in neutral
pH or formation of colloids or unspecific surface absorption). Scandium-44 starts
to hydrolyze at about pH5 and is already forming hydroxides. These tend to form
colloids or pseudo-colloids with unknown physicochemical properties.
Therefore, it is essential to transform 44Sc into species that are chemically stable
under harsh environmental conditions. In the industrial context, 44Sc could
possibly be used for the synthesis of particles for solids tracing or, as ligand
complexes, with very high thermodynamic and kinetic stabilities for liquid
tracing in harsh industrial environments.

6. CASE STUDIES

Case studies of industrial applications carried out using tracers from

radionuclide generators are presented. They have been selected to illustrate
important features and advantages of radionuclide generators as used in the
industrial context.

6.1. AQUEOUS PHASE TRACING

In most cases, the liquids used for the elution of radionuclide generators are
aqueous in nature. For this reason, it is often possible to use the eluants directly,
or with minimal modification, as tracers for aqueous systems. In other cases, it
has been found necessary to incorporate the radionuclide into a chemical complex
to render it appropriate for use as a tracer. The case histories described below are
illustrative of both of the above scenarios.

166
6.1.1. Measuring the water intake to a power station
using the 99Mo/99mTc generator

This case study describes how a commercially available 99Mo/99mTc

generator was used to measure extremely large flows of water through closed
conduits.
A coal fired power station received its water supply from a nearby lake.
Water was pumped from the lake to the power station via six rising mains, with a
total water intake of approximately 120 m3/s. It was very important that the six
water pumps (one on each riser) were properly balanced so that the whole system
was operating at optimum efficiency. Thus, to achieve optimal operation, it was
necessary to measure accurately the water flow up each riser. This had proved
difficult using conventional measurement methods: each main was 2.7 m in
diameter, and there were concerns about the accuracy of the installed flow
instrumentation.
It was therefore decided to use a radiotracer pulse velocity technique to
measure the flow rate up each riser for comparison with the power consumption
of the corresponding water pump.
As the power station was located at a significant distance from the nearest
nuclear reactor and because a series of flow rate measurements were required
over a period of time, it was decided to use a radioisotope generator to provide the
tracer. A 99Mo/99mTc generator of activity 40 GBq was selected, and this was
eluted appropriately to provide the 2.6 GBq tracer pulses required for each
measurement.
Measurements were carried out using the standard pulse velocity
methodology. The tracer was injected as a sharp pulse into the pump suction, as
shown in Fig. 73.
A pair of radiation detectors mounted at a measured separation on the riser
measured the passage of the tracer pulse so that the flow velocity could be
measured. Since the internal cross-sectional area of the main was known, the
volume flow rate could be calculated. The accuracy of each measurement was
±1% at 95% confidence limits.
Significant differences in pump efficiency were found, with delivery flow
rates varying between 16 and 21 m3/s.
The measurements are perhaps noteworthy as being among the largest
liquid flows that have ever been measured using a pulse velocity technique in a
closed conduit.
Owing to the large diameter of the mains, and because detectors mounted
externally would only sense radiation that originated within approximately

167
 FIG. 73. Water intake flow rate measurement.

150 mm of the pipe wall, there were concerns initially that the flow
measurements might be unrepresentative of the true velocity profile across the
main.
This problem was resolved by performing a separate test in which, at each
detector station, blanked-off tubes were inserted through flanges as far as the
centre of the riser.
Velocity measurements were made with detectors positioned at the
centreline, at the half-radius position and at the surface of the riser. No significant
differences in velocity were observed, thus confirming that the measurements
obtained with the detectors mounted external to the risers were reliable.
Since cooling water leaving the power station was returned to the lake, and
this was an environmentally sensitive location, it was important to avoid any
buildup of the radioactive tracer. Neglecting the very large dilution of tracer in the
volume of lake water, which in itself was sufficient to ensure that the tracer
concentration was at a negligible level, the 6.02 h half-life of the 99mTc provided
an additional measure of reassurance and facilitated official approval for the
measurement.

6.1.2. Studies of the aqueous phase in multiphase flow in a hydrate loop

using a 137Cs/137mBa generator

A 740 MBq 137Cs/137mBa generator supplied by Atom Hightech Co. Ltd

(China) has been used to study the velocity of the aqueous phase inside a hydrate
flow loop using the pulse velocity technique described in Section 6.1.1.

168
 FIG. 74. Aqueous phase velocity measurements in a hydrate flow loop.

Understanding hydrate dynamics in oil production systems is essential for flow

assurance in deepwater production fields. In this project, which is part of a much
larger study, the velocity in the loop was measured using the eluate from the
generator as tracer. Eight detectors were deployed, and from their responses, the
velocities in different parts of the loop and under different sets of flow conditions
were determined. The detector responses obtained from a single injection of
approximately 7 MBq of 137mBa are shown in Fig. 74.
The study required many successive injections of the tracer, and it was
found that the 137mBa eluate was ideal for this purpose. Its rapid decay (half-life
2.5 min) ensured that background activity did not buildup in the loop, and repeat
measurements every 10 min were thereby facilitated. Checks carried out on water
drained from the loop confirmed that residual contamination was negligible.

6.1.3. Semi-continuous measurement of effluent flow rate in open channels

using a 137Cs/137mBa generator

This case study describes how a 137Cs/137mBa generator was used to provide
the tracer required by an instrument permanently installed on the effluent outfall
of a major chemical complex to provide semi-continuous monitoring of the
effluent flow rate. It is perhaps the only example of the use of the radioactive
tracer technique automatically, in on-line measurement and control.

169
 FIG. 75. Principles of the constant rate dilution method of flow rate measurement.

As the requirement for improved environmental management becomes ever

more important, there is an increasing need to carefully control all effluent
discharges from industrial premises. Before the discharges can be controlled, they
must first be monitored. Measurement of liquid effluent flow rate can be
particularly difficult as the flows are very often in open conduits of irregular
cross-section, such as drainage ditches. The traditional approach to flow
measurement is to make use of flumes or weirs and to relate the water head to the
flow rate. Such systems are notoriously inaccurate, as they are severely affected
by silt buildup, and frequent calibration is needed.
One approach is to use a constant rate radioisotope dilution method to
provide measurement of the volume flow rate in the effluent channel for
comparison with the readings of the installed meter. The principles of this method
are shown in Fig. 75.
This is arguably the most commonly used method of effluent flow rate
measurement. It is relatively simple to apply, and provides a direct measurement
of the volume flow rate of the effluent, independent of any assumptions about the
shape of the conduit, depth or velocity of the liquid.
It is also possible to apply a dilution measurement using pulse injection
rather than constant rate injection. This ‘total count’ method is discussed
extensively in the literature. Essentially, it can be shown that the flow, Q, in the
stream is related to the total activity, A, injected and the total count, N, recorded
by a downstream detector by:

Q = AF/N (23)

170
 FIG. 76. Installed effluent flow rate meter based on a 137Cs/137mBa generator.

where F is a constant depending on the efficiency of the detector and the counting
geometry. F can be determined by calibration.
This approach has advantages over the constant rate injection technique in
that it requires a smaller activity of radiotracer. In addition, once the constant F
has been determined, repeat measurements can be carried out simply and reliably.
The demand for spot checks of effluent flow rates in the main outfall from a
major chemical complex increased to a point where a continuous — or at least,
semi-continuous — measurement was needed. To satisfy this requirement, an
installed flowmeter, based upon the radioisotope ‘total count’ method was
developed. This instrument is shown schematically in Fig. 76.
A water pump and a solenoid valve, operated by relays in the control unit,
are used to control the injection of radioactive material from the generator. The
water pump feeds clean water to the radioisotope generator, and the eluted 137mBa

171
is then pumped into the coil at the base of the counting chamber where its
radioactivity is measured.
The activity is then pumped into the effluent stream. A sample pump, well
downstream of the tracer injection point extracts a sample of effluent over a time
interval sufficient to span the transit of the injected tracer pulse, and this sample
is also subjected to radioassay in the counting chamber.
The radioactivity counts for the injected water and sampled effluent are fed
to a microprocessor that computes the flow rate in the effluent stream using the
‘total count’ algorithm. The efficiency factor, F, of the system is derived from on-
line calibration data.
Devices of this type operated successfully for several years on industrial
complexes in the UK. Periodic spot checks carried out using a constant rate
dilution method indicated that the accuracy of the measurement was ±2.5% at a
flow rate of approximately 5000 m3/h. The ability to install this device without
the need for expensive civil engineering — as would be required for the
installation of a weir — is clearly a very distinct advantage.
The137Cs/137mBa generator is crucial, both to the operation of the device and
to obtaining necessary safety approvals from the relevant legislative authorities.
The long lived 137Cs parent provides a renewable source of radiotracer over a
period of years, while the 2.5 min half-life of the daughter ensures that there is no
possibility of buildup of radioactivity in natural water systems.

6.1.4. RTD studies on a hot water sterilizer using a 99Mo/99mTc generator

A manufacturer of domestic water heaters was developing a new type of

heater for hospitals and surgeries, the purpose of which was to give a supply of
sterilized water, on demand. Calculations had shown that if ordinary tap water
were contacted with superheated water for 2 min, all known pathogens would be
destroyed. It was necessary to conduct tests on the prototype heater to ensure that
it complied with this specification. The most direct way of doing this was to
measure the mean residence time and RTD of the water flowing through the
heater.
The factory producing the heater was in the middle of an urban industrial
site, with a drainage system shared with surrounding public housing. Clearly,
disposal of water contaminated with radioactive tracer was a matter to which
consideration had to be given in planning the measurements. Two different
radioisotope generators were available: 99Mo/99mTc and 137Cs/137mBa.
The 137Cs/137mBa generator was considered first, on the grounds that the
short half-life of the 137mBa (2.55 min) would ensure that the small amount of
radioactive material entering the drain would have decayed to a negligible level
before it passed out of the site boundary. However, the prototype heater was of

172
FIG. 77. Residence time distribution studies to prove the design of a hot water sterilizer using
a 99Mo/99mTc generator.

small volume (approximately 0.5 m3), and the associated pipe work was
correspondingly small. It was found that the heavy shielding needed to collimate
the radiation detectors and to screen out extraneous radiation from the tracer
flowing round the system was too cumbersome. It was therefore decided to use
the 99Mo/99mTc generator. The low energy 140 keV gamma rays could be easily
shielded and collimated using thin lead sheet, which made positioning of the
radiation detectors on the compact pipe work relatively easy. The contaminated
water from the system was simply collected in a container and stored securely for
3 d, after which time, the activity was reduced to a negligible level by radioactive
decay. It was then disposed of to drain.
The measurement set-up is shown in Fig. 77. The results showed that
though there was some back mixing of the water, the flow through the heater was
essentially plug flow in character. The shortest residence time of any element of
the fluid was 2.4 min, which was deemed to be acceptable by the heater
designers.

173
 FIG. 78. The In-SPECT system.

6.1.5. Industrial emission tomography experiments with 68Ga and 137mBa

The eluates from two radioisotope generators, 137Cs/137mBa and 68Ge/68Ga,

were used as tracers in industrial emission tomographic measurement
experiments to visualize the spatial distribution of radioisotope as a function of
time and hence to investigate the flow dynamics of a laboratory scale process
vessel.
The industrial single photon emission computed tomography (In–SPECT)
system consists of 30 50 mm × 50 mm NaI(Tl) detectors connected to 30 single
channel analysers.
Initially, the equipment was tested under static conditions (Fig. 78). Two
cylindrical pipes with different diameter were installed inside a water filled vessel
of diameter 60 cm. The pipes were separated by 17 cm from each other and filled
with various combinations of the radioisotopes eluted from the generators, as
shown in Table 18, which also lists the data accumulation mode of the detectors.

TABLE 18. EXPERIMENTAL DATA FOR TESTS UNDER STATIC

CONDITIONS
Specific activity of the
No. Nuclide (keV) Counting mode radioisotope (mCi/L)

Pipe 1 Pipe 2
68
1 Ga (511) Gross 2.2 —
68
2 Ga (511) Gross 1.1 3.0
137m
3 Cs (662) Gross 6.2 10.4
137m
4 Cs (662) Photopeak 4.0 11.0

174
 FIG. 79. Reconstructed images from the measurements in the static condition.

‘Gross’ means that the detector counts all radiation energies above a threshold set
at a low energy level. In this mode, not only the primary gamma rays, but also
Compton scattered radiation is detected. ‘Photopeak’ means that only energies in
a narrow band about the photopeak are detected, thus discriminating against the
Compton scattered radiation.
The expectation maximization algorithm was applied to the image
reconstruction. Figure 79 shows the reconstructed images from the four cases:

(a) Pipe 1 is filled with 68Ga;

(b) Both pipes are filled with 68Ga;
(c) Both pipes are filled with 137mCs;
(d) Both pipes are filled with 137mCs and only the photopeak was recorded.

Image (a) provides only a rough indication of the location of the pipe. The
low quality of the image is certainly due to the small number of detectors. In
images (b) and (c), the images corresponding to the two pipes are not resolved
because of interference from scattered radiation. In (d), the two pipes are clearly
resolved, and it is also possible to observe the difference in the specific activities
of the radioisotopes they contain. The above measurements clearly show that the
performance of the In–SPECT system is significantly impaired by the scattered
photons. However, counting on the photopeak implies that far fewer gamma ray
photons will be detected than when gross counting is employed, and this clearly
impacts on the counting statistics. For this reason, it is preferable to use a
radioisotope with high gamma ray energy to minimize signal loss from
attenuation in the walls of the vessel.
The experimental arrangement for the measurements under dynamic
conditions is shown in Fig. 80. During the experiment, the flow rate of water was
kept constant at 8.7 L/min, and 2.2 mCi of 68Ga and 9.7 mCi of 137mBa were
injected into the vessel inlet.
Figures 81 and 82 show the pattern of tracer movement for 68Ga and 137mBa,
respectively. The patterns observed with the two tracers are of similar form, but

175
 FIG. 80. Experimental set-up for the measurements under dynamic flow conditions.

FIG. 81. The spatial distribution of 68Ga as a function of time.

137m
FIG. 82. The spatial distribution of Ba as a function of time.

176
those obtained with 137mBa are clearer because of its higher gamma energy and
the resulting improvement in counting statistics.

6.1.6. Investigation of the performance of a sand filter on a wastewater

treatment plant

The 113mIn eluate from a 113Sn/113mIn generator was used to investigate the
performance of a sand filter on a wastewater treatment plant. The filter contained
beds of sand and gravel. The objective of the study was to determine the
wastewater flow model through the system and hence measure the volume
occupied by the sand and gravel.
The 113mIn in the eluate from the generator is of the form of positively
charged ions that tend to be absorbed on to particles. For this reason, the untreated
eluate is a good tracer for flocks and suspended particles. However, by chelating
with EDTA, 113mIn forms a complex compound (113mIn–EDTA), which is very
stable and can be used as a water tracer. This was used as the water tracer to
investigate the flow of wastewater through the sand filter system.
As shown in Fig. 83, the tracer was injected just before the pump upstream
of the filter. Two radiation detectors (D-1 and D-6) were placed between the
pump and the sand filter at a measured separation, so that the flow rate of the
wastewater could be measured using the pulse velocity technique. The RTD of
the wastewater in the filter was measured by detector D-2, placed on the outlet
line of the sand filter. This is shown in Fig. 84. A two-stirred-tanks-in-series
model provided a good fit to the experimental data. The experimental mean
residence time was found to be 747 s.

FIG. 83. Experimental arrangement for sand filter measurements.

177
 FIG. 84. RTD of wastewater through the sand filter.

From the measured wastewater flow rate and the known overall volume of
the sand filter, the theoretical mean residence time was calculated to be 1065 s.
Comparing this figure with the measured mean residence time of 747 s, it was
concluded that 70% of the volume of the filter was occupied by water. The result
showed that the filter was operating satisfactorily. There was no evidence of any
liquid channelling through the system.

6.2. ORGANIC PHASE TRACING

6.2.1. Measurement of organic flows using a 113Sn/113mIn generator

The velocity and volume flow rate of petrol flowing through a 10 cm

diameter pipe at ambient temperature were measured using the integrated pulse
velocity technique. The measurement procedure is identical to that of the normal
pulse velocity technique: a pulse injection of radiotracer, with two downstream
radiation detectors to measure the transit time of the tracer. However, in this
variant of the technique, the detector response curves are integrated. The detector
outputs are then similar to those shown in Fig. 85. From these, the transit time of
the tracer is easily and accurately determined as the time separation between the
two half-heights of the integrated response curves.

178
 FIG. 85. Detector outputs in the integrated pulse velocity technique.

Two tracers were used:

(i) Paradibromobenzene, labelled with 82Br, dissolved in toluene. This is

known to be a reliable tracer for the measurement of the flow rate of organic
liquids.
(ii) The 113mIn eluate from a 113Sn/113mIn generator, supplied by Polatom. The
eluate was mixed with methanol prior to injection.

The results of the tracer injections with paradibromobenzene are shown in

Table 19, while the results obtained with the eluate injections are shown in
Table 20. The detector separation was 7.19 m. The calculations of the mean
transit time and mean flow velocity for radiotracer 82Br give:

• Mean transit time = 5.12 ± 0.09 s;

• Mean flow velocity = 1.40 ± 0.03 m/s.

179
TABLE 19. RESULTS OF INTEGRATED PULSE VELOCITY
MEASUREMENTS USING THE PARADIBROMOBENZENE TRACER
Run number Transit time (s)

1 5.13

2 5.26

3 5.16

4 5.11

5 5.01

6 5.07

TABLE 20. RESULTS OF INTEGRATED PULSE VELOCITY

MEASUREMENTS USING THE 113mIn ELUATE AS A TRACER
Run number Transit time (s)

1 5.10

2 5.01

3 5.44

4 5.01

5 4.87

6 5.10

7 5.25

8 5.10

9 5.27

10 4.92

The calculations of mean transit time and mean flow velocity for
radiotracer 113mIn give:

• Mean transit time = 5.11 ± 0.11 s;

• Mean flow velocity = 1.41 ± 0.03 m/s.

180
 Note that the uncertainty in the mean velocities includes the uncertainty
associated with the measurement of the detector separation (±5 cm).
It is clear that the two sets of results are in excellent agreement with one
another, from which it is concluded that the aqueous eluate from the 113Sn/113mIn
generator is an appropriate tracer for this measurement. The Reynolds number for
this flow is 1.7 × 105, indicating that it is fully turbulent.
Similar studies were carried out on a fuel oil flow in a 20 cm pipeline and
again, there was good agreement between the results obtained with the generator
eluate and with the paradibromobenzene tracer. It is, perhaps, going too far to
suggest that on the basis of these two measurements, the eluate from the generator
is a good tracer for any fully turbulent flow, aqueous or organic, but these results
are encouraging.
Further to this, since the chemistry of gallium is very similar to that of
indium, it is reasonable to suppose that the eluate from the 68Ge/68Ga would also
be a satisfactory tracer for pulse velocity measurements of turbulent flows of
organic liquids.

6.2.2. Tracer studies on a multiphase reactor in a pilot plant

The objective of these experiments was to study the flow patterns of gas,
liquid and solid phases in the reactor. The experiment involved breakthrough
studies of all three phases together with flow pattern visualization using the
SPECT technique. However, concern here is confined to the liquid phase and, to
a lesser extent, the solid phase, RTD measurements.
The RTD of the liquid phase (heptane) was studied using two tracers: 82Br
as a solution of paradibromobenzene in heptane (well known as a reliable tracer
for organic liquids) and an 113mIn–EDTA complex. The 113mIn was eluted from a
113
Sn/113mIn generator and mixed with EDTA to create a stable complex. The
purpose of using two tracers for the liquid phase was to compare their
performance. If 113mIn–EDTA could be validated as a suitable tracer for this
application, it would be possible to use the generator in subsequent tests, thereby
simplifying the logistics of tracer supply.
Tracer was injected as a pulse into the inlet line to the reactor. A collimated
NaI(Tl) detector, 38 mm in height and 50 mm in diameter was placed on the
outlet line. Its response curves for the 82Br and 113mIn tracers are shown in Fig. 86.
The response curves were similar, and it was therefore concluded that
113m
In–EDTA is suitable for tracing organic liquid flows on pilot plants. However,
it must be remembered that the reactor was operating at ambient temperature.
Further validation work is required before its use under high temperature
conditions can be considered to be validated.

181
FIG. 86. Comparison of the detector response curves (area normalized) obtained from the 82 Br
and 113mIn–EDTA liquid phase tracers.

The flow of the solid phase (catalyst) through the vessel was studied using
the catalyst labelled with 113mIn. The tracer was prepared by stirring 5 g of
catalyst powder with 10 cm3 of the eluate from the 113Sn/113mIn generator for
approximately 1 min, after which 99.9% of the indium was adsorbed on to the
catalyst. The labelled catalyst was injected into the inlet line to the reactor using
nitrogen backing pressure. Examples of the response curve of the detector on the
outlet line are presented in Fig. 87.

6.3. SOLID TRACING

6.3.1. RTD studies on attritioners in the silica sand industry using 

a 99Mo/99mTc generator

Attritioners are used in silica sand processing plants to remove impurities

from the silica particles. The silica particles are suspended in water, which is
agitated by a propeller in the attritioner so that the particles impact upon one
another at high velocity and suffer abrasion. Impurities are scrubbed from the

182
FIG. 87. Examples of detector response curves obtained using the In labelled catalyst as the
tracer.

surface of the particles in this process, and are removed by water washing
immediately downstream of the attritioner.
The objective of these studies was to study the RTDs of sand and water
through the attritioner with a view to improving the efficiency of the attrition
process.
The tracer selected to trace the liquid was the pertechnetate eluate from a
99
Mo/99mTc generator. This was known to be a reliable tracer for the water and
was used without any chemical modification.
The solid phase was also labelled with 99mTc. This was done by stirring
samples of sand with the eluate from the 99Mo/99mTc generator, together with
stannous chloride solution, which acted as a reducing agent. This causes the 99mTc
to become fixed to the solid particles in the form of TcO2.
Examples of RTD curves obtained for the liquid and solid phases are given
in Figs 88 and 89, respectively.
The sand passes through the attritioner significantly more quickly than the
liquid. This is not apparent from visual observation, which suggests that the two
phases flow together through the system.
The long tails on the RTD curves are indicative of the presence of dead
zones in the attritioner. This is due to the fact that there are significant gaps
between the attritioner’s propeller and the walls and bottom of the vessel. As a

183
 FIG. 88. Liquid RTD in the attritioner.

FIG. 89. Solid RTD in the attritioner.

result, a significant amount of sand is not subjected to the attrition process.

Design improvements are necessary to reduce the dead zones. This is especially
relevant as the higher quality sand reserves are becoming depleted, making it
necessary to process material with higher levels of impurities. This, in turn,
means that the efficiency of the attrition process must be improved.

6.3.2. Visualization of water and sludge flows through a clarifier using 

a 113Sn/113mIn generator

Indium-113m from a 113Sn/113mIn generator was used to monitor the flow

behaviour of both the water and the sludge in a laboratory scale clarifier.

184
 FIG. 90. Experimental arrangement for the clarifier studies.

There were several reasons for the choice of tracer:

• Firstly, the 0.392 keV gamma rays of 113mIn was very suitable for this study:
this energy was sufficiently high to be detected effectively through the
walls of the clarifier, yet it was still easy to provide shielding using
relatively small thicknesses of lead.
• Secondly, the short half-life of 99.5 min ensured that contamination of the
equipment with radioactivity and disposal of the contaminated water and
sludge would not present problems.
• Thirdly, 113mIn can be used to trace both the water and the sludge. Because
indium exists as a cation of InCl3 in 0.05M HCl solution, it was possible to
label the sludge in situ, simply by adding the eluate from the generator to
the water containing the sludge to be monitored. In order to trace water
flow, however, the indium cation was first reacted with EDTA to produce a
complex compound that is very stable in the water and traces the water flow
faithfully.

The clarifier is shown in Fig. 90.

NaI(Tl) scintillation detectors were installed at the inlet and at the outlet of
the clarifier to monitor the inflow and outflow. The tracer inside the clarifier was
monitored by four collimated 12.5 mm  12.5 mm NaI(Tl) scintillation detectors,
installed in a vertical line. This four detector arrangement was designed to move
sequentially to five preselected measurement positions. The detector response
signals were transmitted to a multichannel data acquisition system and recorded
on a notebook computer. Approximately 5 mCi of radiotracer was used for each
experimental run. This was injected as a pulse into the system just before the
rotary pump upstream of the clarifier.

185
 The results of the water tracing study are presented in Fig. 91 as a series of
five tracer concentration contour maps, while the results of the sludge tracing are
presented in Fig. 92. In contrast to the water, which was observed to move
progressively through the clarifier before being discharged from its outlet, the
sludge remained concentrated on the bottom of the vessel near the inlet.
It is interesting to compare these contour maps with a photograph of the
clarifier taken during the study (Fig. 93). The dark region on the bottom of the
clarifier is the settled sludge.

6.4. GAS TRACING

6.4.1. A radiotracer pig test for leak inspection

in an underground gas pipeline

Bromine-82, labelled CH3Br, produced by the portable methyl bromide

generator was used in conjunction with a pipeline pig to check for the presence of

FIG. 91. Time variation of the water tracer concentration along the clarifier.

186
 FIG. 92. Time variation of the sludge tracer concentration along the clarifier.

FIG. 93. Photograph of the clarifier.

leaks in an underground gas pipeline. The pipeline, of diameter 400 mm and

length 40 km, was buried 2–3 m under the soil surface.
The pig, which was of a rugged, shockproof design, contained a
76 mm × 76 mm NaI scintillation detector, together with a data recorder. It was
capable of 100 h continuous operation, the power for the detector and recording

187
FIG. 94. The pipeline pig showing the pig internals, the assembled pig and the pig being
launched into the pipe.

FIG. 95. Injection of the radiolabelled methyl bromide gas from the generator to the pipeline
using a manual air pump.

units being supplied from batteries. Figure 94 shows the pig in its housing, ready
for launching into the pipeline.
Ten curies of 82Br methyl bromide gas provided by the generator was used
as the radiotracer. The radiotracer gas was injected directly into the operational
pipeline, as illustrated in Fig. 95.

188
 FIG. 96. Data downloaded from the pig.

A manual air pump was connected through a flexible metallic tube to the
gaseous methyl bromide generator on one side and to the injection valve installed
at the pipeline launcher on the other. By operating the air pump, the radiotracer
was injected instantaneously, from the generator into the pipeline. After 2 h, the
radiotracer pig was inserted into the pipeline through the cleaning chamber, as
shown in Fig. 94.
The pig moved downstream under the influence of the flowing gas, taking
approximately 6 h to transit the pipeline. After retrieving the pig at the other end
of the pipeline, the data stored by it were downloaded to a PC. A section of the
data covering a 1 h time interval is shown in Fig. 96.
The red traces shown in Fig. 96 comprise the background counts recorded
by the detector, while the two sharp black peaks correspond to radiation received
by the detector in transiting two small 60Co sources that had been placed near the
pipeline to act as distance markers. Had the radioactive tracer leaked from the
pipeline into the soil, additional peaks would have been observed in the detector
response at locations corresponding to the leak positions. No such peaks were
present, from which it was concluded that the pipeline was not leaking.

189
.
 REFERENCES
[1] FRIEDLANDER, G., KENNEDY, J.W., MACIAS, E.S., MILLER, J.M., Nuclear and
Radiochemistry, John Wiley & Sons, New York (1981).
[2] KNAPP, F.F. (Ed.), Radionuclide Generators: New Systems for Nuclear Medicine
Applications, ACS Symposium Series 241, American Chemical Society, Washington,
DC (1984).
[3] VÉRTES, A., NAGY, S., KLENCSÁR, Z., LOVAS, R.G., RÖSCH, F. (Eds), Handbook
of Nuclear Chemistry, Vol. 1: Basics of Nuclear Science, Springer Verlag, New York
(2010).
[4] FIRESTONE, R.B., SHIRLEY, V.S. (Eds), Table of Isotopes, 8th edn, Lawrence
Berkeley Laboratory, John Wiley & Sons, New York (1999).
[5] LEBOWITZ, E., RICHARDS, P., Radionuclide generator systems, Semin. Nucl. Med. 4
3 (1974) 257–268.
[6] FINN, R., MOLINSKI, V., HUPF, H., KRAMER, H., Radionuclide Generators for
Biomedicals Applications, Oak Ridge Technical Information Ctr (1983).
[7] SAHA, G.B., Physics and Radiobiology of Nuclear Medicine, 3rd edn, Springer (1993).
[8] BJØRNSTAD, T., “Industrial radionuclide generators — status and perspectives”, paper
presented at Conf. on Tracer and Tracing Methods, Ciechocinek, Poland, 2004.
[9] INTERNATIONAL ATOMIC ENERGY AGENCY, Report of Consultants Meeting on
Radionuclide Generators for Industrial Radiotracer Technology, 5–8 December 2005,
IAEA, Vienna (2005).
[10] BJØRNSTAD, T., HOLTEBEKK, T., RUUD, A., The Production of 81mKr Generators at
the Oslo Cyclotron, Technical Research Report 84-02, Institute of Physics Report
Series, University of Oslo (1984).
[11] CHAKRAVARTY, R., DASH, A., KOTHARI, K., PILLAI, M.R.A.,VENKATESH, M.,
A novel 188W/188Re electrochemical generator with potential for medical applications,
Radiochim. Acta 97 6 (2009) 309–317.
[12] BOYD, R.E., The gel generator: A viable alternative source of 99mTc for nuclear
medicine, Appl. Radiat. Isot. 48 8 (1997) 1027–1033.
[13] SARASWATHY, P., et al., “Tc-99m generators for clinical use based on zirconium
molybdate gel and (n,) produced Mo-99: Indian experience in the development and
deployment of indigenous technology and processing facilities”, paper presented at
International RERTR Meeting, Prague, 2007.
[14] RÖSCH, F., KNAPP, F., Jr., “Radionuclide generators”, Handbook of Nuclear
Chemistry (VÉRTES, A., NAGY, S., KLENCSÁR, Z., RÖSCH, F., Eds), Vol. 4, Klüwer
Academic Publishers, Dordrecht (2004) 81–118.
[15] DIETZ, M.L., HORWITZ, E.P., Applications of extraction chromatography in the
development of radionuclide generator systems for nuclear medicine, Ind. Eng. Chem.
Res. 39 9 (2000) 3181–3188.
[16] SKURIDIN, V.S., CHIBISOV, E.V., Development of a small-size extractor for
separation of the 99Mo/99mTc couple, Radiochem. 52 1 (2010) 90–94.
[17] BOYD, R.E., Technetium-99m generators — the available options, Int. J. Appl. Radiat.
Isot. 33 10 (1982) 801–809.

191
[18] NORONHA, O.P.D., Solvent extraction technology of 99Mo-99mTc generator system 1:
An Indian experience — process design considerations, Isot. Environ. Health Stud. 22 2
(1986) 53–57.
[19] CHAKRAVARTY, R., DASH, A., VENKATESH, M., A novel electrochemical
technique for the production of clinical grade 99mTc using (n, γ)99Mo, Nucl. Med. Biol.
37 1 (2010) 21–28.
[20] MOLINSKI, V.J., A review of 99mTc generator technology, Int. J. Appl. Radiat. Isot. 33
10 (1982) 811–819.
[21] MILLER, J., “Procedure for production of 99mTc sublimation generators based on
eutectic SiC–MoO3–V2O5”, Alternative Technologies for 99mTc Generators,
IAEA-TECDOC-852, IAEA, Vienna (1995) 44–46.
[22] JIN XIAO-HAI, et al., “Development of 90Sr/90Y generator technology”, Therapeutic
Radionuclide Generators: 90Sr/90Y and 188W/188Re Generators, Technical Reports Series
No. 470, IAEA, Vienna (2009).
[23] FIGGINS, F.E., The Radiochemistry of Polonium, Rep. NAS-NS 3037, National
Academy of Sciences, US Atomic Energy Commission, Washington, DC (1961).
[24] MATTHEWS, K.M., KIM, C.-K., MARTIN, P., Determination of 210Po in
environmental materials: A review of analytical methodology, Appl. Radiat. Isot. 65
(2007) 267–279.
[25] CHAKRAVARTY, R., et al., Development of an electrochemical 90Sr–90Y generator for
separation of 90Y suitable for targeted therapy, Nucl. Med. Biol. 35 2 (2008) 245–253.
[26] CHAKRAVARTY, R., VENKATESH, M., DASH, A., A novel electrochemical
99
Mo/99mTc generator, J. Radioanal. Nucl. Chem. 290 1 (2011) 45–51.
[27] RAMANUJAM, A., et al., Separation of carrier-free 90Y from high level waste by
supported liquid membrane using KSM-17, J. Radioanal. Nucl. Chem. 247 1 (2001)
185–191.
[28] NAIK, P.W., et al., Separation of carrier-free 90Y from 90Sr by SLM technique using
D2EHPA in n-dodecane as carrier, Sep. Sci. Technol. 45 4 (2010) 554–561.
[29] HAPPEL, S., STRENG, R., VATER, P., ENSINGER, W., Sr/Y separation by supported
liquid membranes based on nuclear track micro filters, Radiat. Meas. 36 (2003)
761–766.
[30] EISWIRTH, M., SCHWANKNER, R., WEIGEL, F., WISHNEVSKY, V., Electrostatic
radionuclide separation — a new version of Rutherford’s “thorium cow”, J. Chem.
Educ. 59 (1982) 608–611.
[31] MELICHER, F., SVOBODA, K., PROKOP, J., BUDSKY, F., “Experience in utilisation
of WR-S reactor with medium neutron flux intensity for 99mTc production in
Czechoslovakia”, paper presented at IAEA Sem. on Radionuclide Generator
Technology, Vienna, 1986.
[32] JENNEWEIN, M., SCHMIDT, A., NOVGORODOV, A.F., QAIM, S.M., RÖSCH, F.,
A no-carrier-added 72Se/72As radionuclide generator based on distillation, Radiochim.
Acta 92 (2004) 245–249.
[33] BORROTO, J.I., DOMINGUEZ, J., GRIFFITH, J., FICK, M., LECLERC, J.P.,
Technetium-99m as a tracer for liquid RTD measurement in opaque anaerobic digester:
Application in a sugar wastewater treatment plant, Chem. Eng. Process 42 11 (2003)
857–865.

192
[34] PALIGE, J., MAJKOWSKA, A., HERDZIK, I., PTASZEK, S., 68Ge/68Ga radioisotope
generator as a source of radiotracers for water flow investigations, Nukleonika 56 1
(2011) 77−80.
[35] STAVSETRA, L., FURE, K., HAUGAN, A., BJØRNSTAD, T., “137mBa oil tracer — for
applications in multiphase separators and scrubbers”, paper presented at Tracer 6, Oslo,
2011.
[36] HUBBELL, J.H., SELTZER, S.M., Tables of X-Ray Mass Attenuation Coefficients and
Mass Energy-Absorption Coefficients from 1 keV to 20 MeV for Elements Z = 1 to 92
and 48 Additional Substances of Dosimetric Interest, NISTIR 5632, The National
Institute of Standards and Technology (NIST), on-line 1996, last update 2004,
http://www.nist.gov/pml/data/xraycoef/index.cfm
[37] BÉ, M.M., et al., Table of Radionuclides (Vol. 1-A = 1 to 150), Monograph BIPM-5,
Bureau International des Poids et Mesures, Sèvres, France (2004) 311.
[38] GREENE, M.W., HILLMAN, M., A scandium generator, Int. J. Appl. Radiat. Isot. 18
(1967) 540–541.
[39] SEIDL, E., LIESER, K.H., Die Radionuklidgeneratoren 113Sn/113mIn, 68Ge/68Ga und
44
Ti/44Sc, Radiochim. Acta 19 (1973) 196–198.
[40] MIRZA, M.Y., AZIZ, A., A scandium generator, Radiochim. Acta 11 (1969) 43–44.
[41] CUI, A., O’BRIEN, H.A., Jr., STEINKRUGER, F.J., TAYLOR, W.A., “A new
inorganic-based 44Ti/44Sc radioisotope generator”, Am. Chem. Soc. Nat. Meeting,
13–18 April 1986, American Chemical Society, Paper Nucl. 91 53 (1990) 26–27.
[42] LOKTIONOVA, N., Development and Evaluation of a 44Ti/44Sc Radionuclide
Generator and Labeling of Biomolecules with 44Sc and 68Ga for PET Imaging, PhD
Thesis, Johannes Gutenberg-Universität (2010).
[43] PRUSZYNSKI, M., LOKTIONOVA, N., MAJKOWSKA, A., ROESCH, F.,
Radiolabeling of DOTATOC with 44T/44Sc generator-derived 44Sc, J. Nucl. Med. 51
Suppl. 2 (2010) 1534.
[44] ENSDF Decay Data in the MIRD (Medical Internal Radiation Dose) Format for 68Ga
(1999),
http://www.orau.org/ptp/PTP%20Library/library/DOE/bnl/nuclidedata/MIRGa68.htm
[45] PAO, P.J., SILVESTER, D.J., WATERS, S.L., A new method for the preparation of
68
Ga-generators following proton bombardment of gallium oxide targets, J. Radioanal.
Chem. 64 1–2 (1981) 267–272.
[46] INTERNATIONAL ATOMIC ENERGY AGENCY, Cyclotron Produced
Radionuclides: Physical Characteristics and Production Methods, Technical Reports
Series No. 468, IAEA, Vienna (2009).
[47] GREENE, M.W., TUCKER, W.D., An improved gallium-68 cow, Int. J. Appl. Radiat.
Isot. 12 (1961) 62–63.
[48] GIRARDI, F., PIETRA, R., SABBIONI, E., Radiochemical separations by retention on
ionic precipitate adsorption tests on 11 materials, J. Radioanal. Chem. 5 (1970)
141–171.
[49] KOPECKY, P., MUDROVA, B., SVOBODA, K., The study of conditions for the
preparation and utilization of a 68Ge–68Ga generator, Int. J. Appl. Radiat. Isot. 24 (1973)
73–80.
[50] KOPECKY, P., MUDROVA, B., 68Ge-68Ga generator for the production of 68Ga in an
ionic form, Int. J. Appl. Radiat. Isot. 25 (1974) 263–268.

193
[51] MALYSHEV, K.V., SMIRNOV, V.V., Gallium-68 yield from hydrated zirconium oxide
based generators, Sov. Radiochim. 17 (1975) 137–140.
[52] EHRHARDT, G.J., WELCH, M.J., A new germanium-68/gallium-68 generator, J. Nucl.
Med. 19 8 (1978) 925–929.
[53] ARINO, H., SKRABA, W.J., KRAMER, H.H., A new 68Ge/68Ga radioisotope generator
system, Int. J. Appl. Radiat. Nuclides 29 (1978) 117–120.
[54] LOC’H, C., MAZIERE, B., COMAR, D., A new generator for ionic gallium-68, J.
Nucl. Med. 21 2 (1980) 171–173.
[55] NEIRINCKX, R.D., DAVIS, M.A., Potential column chromatography for ionic Ga-68.
II: Organic ion exchangers as chromatographic supports, J. Nucl. Med. 21 (1980)
81–83.
[56] SCHUMACHER, J., MAIER-BORST, W., A new 68Ge/68Ga radioisotope generator
system for production of 68Ga in dilute HCl, Int. J. Appl. Radiat. Isot. 32 (1981) 31–36.
[57] DAVIS, M.A., NEIRINCKX, R.D., Generator for Ionic Gallium-68 Based on Column
Chromatography, US Pat. Doc. 4,288,424/A/, United States Patent and Trademark
Office, Alexandria, VA (1981).
[58] NEIRINCKX, R.D., LAYNE, W.W., DAVIS, M.A., SAWAN, S.P., Development of an
ionic 68Ge-68Ga generator III. Chelate resins as chromatographic substrates for
germanium, Int. J. Appl. Radiat. Isot. 33 4 (1982) 259–266.
[59] WELCH, M.J., Preparation of Gallium-68 Radiopharmaceuticals for Positron
Tomography, Progress Report, 1 November 1980–31 December 1983,
Rep. DOE/EV/04318-5, National Technical Information Service, Alexandria, VA
(1983).
[60] McELVANY, K.D., HOPKINS, K.T., WELCH, M.J., Comparison of 68Ge/68Ga
generator systems for radiopharmaceutical production, Int. J. Appl. Radiat. Isot. 35 6
(1984) 521–524.
[61] YANO, Y, et al., Platelet labelling and positron emission tomography in the detection of
sites of vascular injury, J. Nucl. Med. 26 5 (1985) 21, Abstract No. 78.
[62] AMBE, S., 68Ge/68Ga generator with alpha-ferric oxide support, Appl. Radiat. Isot. 39
(1988) 49–51.
[63] SONG, M., BAO, B., A new (68)Ge-(68)Ga generator based on CeO2, Nucl. Technol.
18 7 (1995) 435–439.
[64] BAO, B., SONG, M., A new 68Ge/68Ga generator based on CeO2, J. Radioanal. Nucl.
Chem. 213 4 (1996) 233–238.
[65] TANG, Q., ZHAO, G., LUO, W., LI, D., Preparation and study of a 68Ge-68Ga generator,
J. Nucl. Radiochem. 19 2 (1997) 29–33.
[66] CAO, B., LI, Z., WANG, Y., 68Ge-68Ga generator with alpha-ferric oxide support in
trigonal structure, J. Radioanal. Nucl. Chem. 238 1–2 (1998) 175–178.
[67] LIU, Z., JIA., C., The effect of SnO2xH2O on adsorption characteristics for 68Ge-68Ga
generator, J. Isotopes 12 1 (1999) 27–32.
[68] CHENG, W.-L., YAO, J., LEE, C.-S., LO, A.R., Preparation of 68Ge/68Ga generator with
a binary Ga/Ag electrodepositions as solid target, J. Radioanal. Nucl. Chem. 245 1
(2000) 25–30.
[69] EGAMEDIEV, S.K.H., KHUJAEV, S., MAMATKAZINA, A.K.H., Influence of
preliminary treatment of aluminum oxide on the separation of 68Ge-68Ga radionuclide
chain, J. Radioanal. Nucl. Chem. 246 3 (2000) 593–596.

194
[70] NAKAYAMA, M., et al., A new 68Ge/68Ga generator system using an organic polymer
containing N-methylglucamine groups as adsorbent for 68Ge, Appl. Radiat. Isot. 58 1
(2003) 9–14.
[71] AARDANEH, K., VAN DER WALT, T.N., Ga2O for target, solvent extraction for
radiochemical separation and SnO2 for the preparation of a 68Ge/68Ga generator, J.
Radioanal. Nucl. Chem. 268 1 (2006) 25–32.
[72] LEWIS, R.E., CAMIN, L.L., Germanium-68/gallium-68 generator for the one step
elution of ionic gallium-68, J. Labelled Compd. Radiopharm. 18 (1981) 164.
[73] BJØRNSTAD, T., FURE, K., STAVSETRA, L., HAUGAN, A., “Observations on the
performance of the 68Ge-68Ga test generator produced at CIAE, China: Status per
August 2007”, paper presented at IAEA Mtg on Evaluation and Validation of
Radionuclide Generator-based Radiotracers for Industrial Applications, Vienna, 2011.
[74] CHARLTON, J.S., FIRBY, B., JENKINS, D., “AUSTRALIA/UK: Evaluation of the
68
Ge-68Ga and 137Cs-137mBa generators from CIAE, China – final report”, ibid.
[75] JUNG, S.-H., “Evaluation and improvement of the applicability of IRGs for industrial
process diagnosis tests”, ibid.
[76] RÖSCH, F., KNAPP, F.F., “Radionuclide generators”, Handbook of Nuclear Chemistry
(VÉRTES, A., NAGY, S., KLENCSAR, Z., LOVAS, R.G., RÖSCH, F., Eds), Vol. 4,
Springer, New York (2011) 1935–1976.
[77] MIRZADEH, S., Generator-produced alpha-emitters, Appl. Radiat. Isot. 49 (1998)
345–349.
[78] RÖSCH, F., FILOSOFOV, D.V., Production, radiochemical processing and quality
evaluation of Ge-68, IAEA Radioisotopes and Radiopharmaceuticals Series No. 2,
IAEA, Vienna (2010) 11–28.
[79] FANI, M., ANDRÉ, J.P., MAECKE, H., 68Ga-PET: A powerful generator-based
alternative to cyclotron-based PET radiopharmaceuticals, Contr. Media Mol. Imaging 3
(2008) 67–77.
[80] ROESCH, F., RISS, P.J., The renaissance of the 68Ge/68Ga radionuclide generator
initiates new developments in 68Ga radiopharmaceutical chemistry, Curr. Top. Med.
Chem. 10 16 (2010) 1633–1668.
[81] LEDERER, C.M., SHIRLEY, V.S., Table of Isotopes, 7th edn, Wiley, New York (1978).
[82] QAIM, S.M., et al., Yield and purity of 82Sr produced via the natRb(p,xn)82Sr process,
Appl. Radiat. Isot. 65 2 (2007) 247–252.
[83] JOHN, K.D., MAUSNER, L., RUTH, T.J., Production and processing of 83Sr, IAEA
Radioisotopes and Radiopharmaceuticals Series No. 2, IAEA, Vienna (2010) 31–48.
[84] TARKANYI, F., QAIM, S.M., STOECKLIN, G., Excitation-functions of He-3-particle
and alpha-particle induced nuclear-reactions on natural krypton: Production of Sr-82 at
a compact cyclotron, Appl. Radiat. Isot. 39 (1988) 135–143.
[85] TARKANYI, F., QAIM, S.M., STOECKLIN, G., Excitation-functions of He-3-particle
and alpha-particle induced nuclear-reactions on natural krypton with special reference
to the production of Sr-82, Appl. Radiat. Isot. A 41 (1990) 91.
[86] GRANT, P.M., ERDAL, B.R., O’BRIEN, H.A., Jr., A 82Sr-82Rb isotope generator for
use in nuclear medicine, J. Nucl. Med. 16 4 (1975) 300.
[87] YANO, Y., et al., Rubidium-82 generators for imaging studies, J. Nucl. Med. 18 1
(1977) 46–50.

195
 [88] YANO, Y., CAHOON, J.L., BUDINGER, T.F., A precision flow-controlled Rb-82
generator for bolus or constant-infusion studies of the heart and brain, J. Nucl. Med. 22
11 (1981) 1006–1010.
[89] HORLOCK, P.L., et al., The preparation of a rubidium-82 radionuclide generator, J.
Radioanal. Chem. 64 1–2 (1981) 257–265.
[90] GENNARO, G.P., et al., “A radionuclide generator and infusion system for
pharmaceutical quality Rb-82”, Radionuclide Generators: New Systems for Nuclear
Medicine Applications (KNAPP, F.F., Ed.), American Chemical Society, Washington,
DC (1984) 135–150.
[91] GENNARO, G.P., HANEY, P.S., Strontium-82/Rubidium-82 Generator, US Patent
4,597,951, United States Patent and Trademark Office, Alexandria, VA (1986).
[92] BRIHAYE, C., et al., Preparation and evaluation of a hydrous tin(IV) oxide 82Sr/82Rb
medical generator system for continuous elution, Int. J. Rad. Appl. Instrum. A 38 3
(1987) 213–217.
[93] DEKEMP, R., ALVAREZ-DIEZ, T.M., BEANLANDS, R., VINCENT, J., Manufacture
of strontium-82/rubidium-82 generators and quality control of rubidium-82 chloride for
myocardial perfusion imaging in patients using positron emission tomography, Appl.
Radiat. Isot. 50 6 (1999) 1015–1023.
[94] SYLVESTER, P., MÖLLER, T., ADAMS, T.W., CISAR, A., New ion exchange
materials for use in a 82Sr/82Rb generator, Appl. Radiat. Isot. 61 (2004) 1139–1145.
[95] BILEWICZ, A., BARTOŚ, B., MISIAK, R., PETELENZ, B., Separation of 82Sr from
rubidium target for preparation of 82Sr/82Rb generator, J. Radioanal. Nucl. Chem. 268 3
(2006) 485–487.
[96] INTERNATIONAL ATOMIC ENERGY AGENCY, Manual for Reactor Produced
Radioisotopes, IAEA-TECDOC-1340, IAEA, Vienna (2003).
[97] BOYD, R.E., “The gel generator option”, Production Technologies for Molybdenum-99
and Technetium-99m, IAEA-TECDOC 1065, IAEA, Vienna (1999) 148–156.
[98] ECKELMAN, W.C., COURSEY, B.M. (Eds), Special issue on “99mTc generators,
chemistry and preparation of radiopharmaceuticals”, Int. J. Appl. Radiat. Isot. 33 10
(1982).
[99] ARGONNE, L.N., Mo-99 Production Using LEU Targets, Link to related papers
presented in the RERTR Mtg in Brazil (1998), http://www.rertr.anl.gov/MO99.html
[100] ADLOFF, J.P., LIESER, K.H., Special issue on “Radionuclide generator technology”,
Radiochim. Acta 41 2/3 (1987) 74.
[101] LEE, J.S., et al., “Sol-gel processed ceramics for 99Mo/99mTc generator materials”, 5ICI
(Proc. 5th Int. Conf. Isotopes 2005, Brussels), Medimond, Bologna (2005) 21–26.
[102] BAKEL, A.J., et al., “Progress in technology development for conversion of 99Mo
production from HEU targets — development of new separation schemes, and new
processing equipment”, paper presented at 2006 RERTR Mtg, Cape Town, 2006.
[103] RAMAMOORTHY, N., GOLDMAN, I., ADELFANG, P., Enhanced prospects of 99mTc
gel generator usage with the aid of post-elution concentration of pertechnetate in
ISRS-2007, J. Labelled Compd. Radiopharm. 50 Suppl. 1 (2007) 896.
[104] RAMAMOORTHY, N., “Production and availability of 99mTc generators and of 99Mo:
Technology considerations and the IAEA contributions”, paper presented at
NUCAR-2007 Symp., Mumbai, 2007.

196
[105] ZOLLE, I. (Ed.), Technetium-99 Pharmaceuticals: Preparation and Quality Control in
Nuclear Medicine, Springer (2007).
[106] CHAKRAVARTY, R., et al., Polymer embedded nanocrystalline titania sorbent for
99
Mo-99mTc generator, J. Nanosci. Nanotechnol. 8 (2008) 4447–4452.
[107] NATIONAL RESEARCH COUNCIL OF THE NATIONAL ACADEMIES,
Committee on Medical Isotope Production Without Highly Enriched Uranium: Medical
Isotope Production Without Highly Enriched Uranium (Nuclear and Radiation Studies
Board), The National Academies Press, Washington, DC (2009) 202.
[108] CHATTOPADHYAY, S., DAS, S.S., BARUA, L., A simple and rapid technique for
recovery of 99mTc from low specific activity (n,γ)99Mo based on solvent extraction and
column chromatography, Appl. Radiat. Isot. 68 (2010) 1–4.
[109] YAMAURA, M., et al., “Studies on the separation of 99Mo from nitric acid medium by
alumina”, RERTR 2010 32nd International Meeting on Reduced Enrichment for
Research and Test Reactors,10–14 October 2010, Lisbon, Portugal (2010).
[110] CHAKRAVARTY, R., DASH, A., VENKATESH, M., A novel electrochemical
technique for the production of clinical grade 99mTc using (n,γ)99Mo, Nucl. Med. Biol.
37 (2010) 21–28.
[111] MONROY-GUZMAN, F., JIMENEZ MARTINEZ, T.S., ARRIOLA, H., LONGORIA
GANDARA, L.C., Magnesium-molybdate compounds as matrix for 99Mo/99mTc
generators, Pharmaceuticals 4 (2011) 215–232.
[112] BORROTO, J., et al., “Development of a 137Cs/137mBa radioisotope generator for
educational and industrial radiotracer applications”, paper presented at IAEA Mtg on
Evaluation and Validation of Radionuclide Generator-based Radiotracers for Industrial
Applications, Vienna, 2011.
[113] CHAKRAVARTY, R., et al., Practicality of tetragonal nano-zirconia as a prospective
sorbent in the preparation of 99Mo/99mTc generator for biomedical applications,
Chromatographia 72 9 (2010) 875–884.
[114] SERRANO GÓMEZ, J., GRANADOS CORREA, F., 99mTc generator with hydrated
MnO2 as adsorbent of 99Mo, J. Radioanal. Nucl. Chem. 254 3 (2002) 625–628.
[115] MUSHTAQ, A., MANSOOR, M.S., KARIM, H.M.A., KHAN, M.A., Hydrated
titanium dioxide as an adsorbent for 99Mo-99mTc generator, J. Radioanal. Nucl. Chem.
147 2 (1991) 257–261.
[116] EL-KOLALY, M.T., A 99Mo-99mTc generator based on the use of zirconium
molybdophosphate-99Mo gel, J. Radioanal. Nucl. Chem. 170 2 (1993) 293–298.
[117] MILLER, J., “Procedure for production of 99Tcm sublimation generators based on
eutectic SiC-MoO3-V2O5”, Alternative Technologies for 99Tcm Generators,
IAEA-TECDOC-852, IAEA, Vienna (1995) 44–46.
[118] HANSEN, H.H., DE ROOST, E., MOUCHEL, D., VANINBROUKX, R., Internal
conversion coefficients of the 392 keV γ-ray and half-life of the isomeric state in 113In,
Int. J. Appl. Radiat. Isot. 22 1 (1971) 1–8.
[119] BĔTÁK, E., MIKOŁAJCZAK, R., STANISZEWSKA, J., MIKOŁAJEWSKI, S.,
RURARZ, E., Activation cross sections for reactions induced by 14 MeV neutrons on
natural tin and enriched 112Sn targets with reference to 111In production via radioisotope
generator 112Sn(n,2n)111Sn → 111In, Radiochim. Acta 93 (2005) 311–326.
[120] KOPECKY, J. (Ed.), Atlas of Neutron Capture Cross Sections, INDC(NDS)-362,
IAEA, Vienna (1997) 389.

197
[121] BRODOVITCH, J.C., Excitation Functions and Isomeric Yield Ratios of (p,xn)
Reactions Induced in 75As and 115In by 20–85 MeV Protons, PhD Thesis, McGill Univ.
(1973).
[122] NEVES, M., KLING, A., OLIVEIRA, A., Radionuclides used for therapy and
suggestion for new candidates, J. Radioanal. Nucl. Chem. 266 3 (2005) 377–384.
[123] GANDARIAS-CRUZ, D., OKAMOTO, K., Status of the Compilation of Nuclear Data
for Medical Radioisotopes Produced by Accelerators, Technical Report INDC(NDS)-
209/GZ, IAEA, Vienna (1988) 121.
[124] RAMAMOORTHY, N., NARASIMHAN, D.V.S., MANI, R.S., Studies on the
preparation of 113Sn-113mIn generators, Isot. Environ. Health Stud. 11 7 (1975) 246–249.
[125] TERANISHI, K., YAMAASHI, Y., MARUYAMA, Y., 113Sn-113mIn generator with a
glass beads column, J. Radioanal. Nucl. Chem. 254 2 (2002) 369–371.
[126] ALLAN, K.F., ALI, M.M.S., HANAFI, H.A., EL-AZONY, K.M., Separation of 113mIn
from 113Sn based on activated carbon used as column matrix, J. Radioanal. Nucl. Chem.
284 (2010) 297–301.
[127] EL-SAID, H., MSc Dissertation, Alexandria Univ. (1998).
[128] ABDEL-RAHMAN, H.E.R., Comparative Studies on Tin-113/Indium-113m
Radioisotope Generators based on Tungstocerate (IV) Column Matrices, PhD Thesis,
Helwan Univ. (2002).
[129] ABDEL-HALIM, A.A., Study on 113Sn-113mIn Generator of the Chromatographic
Column Elution Mode, PhD Thesis, Cairo Univ. (2002).
[130] MUSHTAQ, A., MANSUR, M.S., MUHAMMAD, A., Separation of radioindium
(N.C.A.) from neutron irradiated tin and cadmium on hydrated antimony pentoxide, J.
Radioanal. Nucl. Chem. 212 2 (1996) 107–115.
[131] ARINO, H., SKRABA, W.J., KRAMER, H.H., A new 137Cs/137Ba radioisotope
generator system, Int. J. Appl. Radiat. Isot. 24 4 (1973) 197–200.
[132] ONICIU, L., VEGLIA, A., Étude des générateurs d’indium-113m, J. Radioanal. Chem.
24 (1975) 99–114.
[133] INTERNATIONAL ATOMIC ENERGY AGENCY, Manual for Reactor Produced
Radioisotopes, IAEA-TECDOC-1340, IAEA, Vienna (2003).
[134] SUN, W.H., SONG, D.H., HUANG, Y., “Application of 113mIn radiotracer to well
logging”, Isotope Production and Applications in the 21st Century
(STEVENSON, N.R., Ed.) (Proc. 3rd Int. Conf. Vancouver, 1999), World Scientific
Publishing (1999) 226–228.
[135] ARINO, H., REARDON, V.D., Radioactive Barium-137m, CA Patent Document
907287, US Patent 3663177, United States Patent and Trademark Office, Alexandria,
VA (1972) 11.
[136] ARINO, H., KRAMER, H.H., 113Sn/113Inm radioisotope generator systems, Int. J. Appl.
Radiat. Isot. 25 11–12 (1974) 493–496.
[137] RAMAMOORTHY, N., KRISHNAMOORTHY, M., MANI, R.S., Studies on the
preparation of a 137Cs-137mBa generator, Radiochem. Radioanal. Lett. 31 4–5 (1977)
251–264.
[138] MATSUDA, H.T., ABRÃO, A., New Technique for Synthesizing AMP: Precipitation
Inside an Ion-Exchange Resin and its Application to Separation of Cesium from
Fission-products and to a 137mBa Generator, Rep. IPEN-Pub-13, IPEN, São Paulo
(1980).

198
[139] KOPRDA, V., SCASNAR, V., Extraction — chromatographic separation of 137mBa from
137
Cs, J. Radioanal. Nucl. Chem. 121 2 (1988) 415–428.
[140] WANG, Y., LEE, C., CHENG, W., “Study on the preparation of a Cs-137/Ba-137m
radionuclide generator”, Proc. International Topical Conf. on Methods and Applications
of Radioanalytical Chemistry II (MARC-2), Kona, HI (1991).
[141] WANG, Y.M., LEE, C.S., CHENG, W.L., Study on the preparation of a
Cs-137/Ba-137m radionuclide generator, J. Radioanal. Nucl. Chem. 160 2 (1992)
517–527.
[142] ROY, K., PAL, D.K., BASU, S., NAYAK, D., LAHIRI, S., Synthesis of a new ion
exchanger, zirconium vanadate, and its application to the separation of barium and
cesium radionuclides at tracer levels, Appl. Radiat. Isot. 57 (2002) 471–474.
[143] EL-ABSY, M.A., et al., Cs-137/Ba-137m radioisotope generator based on
6-tungstocerate(IV) column matrix, J. Radioanal. Nucl. Chem. 267 1 (2005) 161–167.
[144] DHARA, S., DEY, S., BASU, S., DREW, M.G.B., CHATTOPADHYAY, P., Separation
of 137mBa from 137Cs using new ion exchanger Na2(H2O)4(H3O)[Al(OH)6Mo6O18],
Radiochim. Acta 95 (2007) 297–301.
[145] LI, J., YANG, G., WANG, G., “Development and evaluation of 68Ge-68Ga and
137
Cs-137mBa radionuclide generators for industrial tracer application”, paper presented
at IAEA Mtg on Evaluation and Validation of Radionuclide Generator-based
Radiotracers for Industrial Applications, Vienna, 2011.
[146] CHAKRAVARTY, R., et al., Ammonium molybdophosphate impregnated alumina
microspheres as a new generation sorbent for chromatographic 137Cs/137mBa generator,
J. Chromatogr. A 1220 (2012) 82–91.
[147] BORTUN, A.I., et al., Modified titanium phosphates as cesium selective ion
exchangers, Solv. Extr. Ion Exch. 15 5 (1997) 895–907.
[148] MARAGEH, M.G., HUSAINA, S.W., KHANCHIB, A.R., Selective sorption of
radioactive cesium and strontium on stannic molybdophosphate ion exchanger, Appl.
Radiat. Isot. 50 (1999) 459–465.
[149] SATYANARAYANA, J., MURTHY, G.S., SASIDHAR, P., Adsorption studies of
cesium on a new inorganic exchanger ammonium molybdophosphate-alumina
(AMP-Al2O3), J. Radioanal. Nucl. Chem. 242 1 (1999) 11–16.
[150] MARDAN, A., AJAZ, R., MEHMOOD, A., RAZA, S.M., GHAFFAR, A., Preparation
of silica potassium cobalt hexacyanoferrate composite ion exchanger and its uptake
behavior for cesium, Sep. Purif. Technol. 16 2 (1999) 147–158.
[151] HASSAN, N.M., KING, W.D., McCABE, D.J., HAMM, L.L., JOHNSON, M.E.,
SuperLig644 equilibrium sorption data for cesium from Hanford tank waste
supernates, J. Radioanal. Nucl. Chem. 253 3 (2002) 361–367.
[152] ISHFAQ, M.M., KARIM, H.M.A., KHAN, M.A., Preparation and characterization of
potassium copper nickel hexacyanoferrate(II) as ion exchanger for cesium, J. Radioanal.
Nucl. Chem. 159 2 (1992) 335–342.
[153] NILCHI, A., MALEK, B., MARAGHEH, M.G., KHANCHI, A., Exchange properties
of cyanide complexes — Part I. Ion exchange of cesium on ferrocyanides, J. Radioanal.
Nucl. Chem. 258 3 (2003) 457–462.
[154] NILCHI, A., MALEK, B., MARAGHEH, M.G., KHANCHI, A., Investigation of the
resistance of the potassium copper nickel hexacyanoferrate(II) ion exchanger against
gamma radiation, Radiat. Phys. Chem. 68 5 (2003) 837–842.

199
[155] NILCHI, A., ATASHI, H., JAVID, A.H., SABERI, R., Preparation of PAN-based
adsorbers for separation of cesium and cobalt from radioactive waste, Appl. Radiat. Isot.
65 (2007) 482–487.
[156] FENG, M., et al., Synthesis and characterization of a new activated carbon supported
ammonium molybdophosphate composite and its cesium-selective adsorption
properties, Radiochim. Acta 98 1 (2010) 39–44.
[157] ORTH, R.J., BROOKS, K.P., KURATH, D.E., Review and Assessment of Technologies
for the Separation of Cesium from Acidic Media, Rep. PNL-9874/UC-721, Batelle
Pacific Northwest Laboratory, Richland, WA (1994).
[158] GAUR, S., Determination of Cs-137 in environmental water by ion-exchange
chromatography, J. Chromatogr. A 733 (1996) 57–71.
[159] MUSHTAQ, A., Inorganic ion-exchangers: Their role in chromatographic radionuclide
generators for the decade 1993–2002, J. Radioanal. Nucl. Chem. 262 3 (2004) 797–810.
[160] MAJI, S., BASU, S., Separation of 137mBa from its parent 137Cs from an equilibrium
mixture using amide incorporated Amberlite IRC-50, Radiochim. Acta 95 (2007)
183–188.
[161] BJØRNSTAD, T., HOLTEBEKK, T., RUUD, A., The Production of 81mKr Generators at
the Oslo Cyclotron, Technical Research Rep. 84-02, Institute of Physics Report Series,
University of Oslo (1984).
[162] STAVSETRA, L., FURE, K., HAUGAN, A., BJØRNSTAD, T., “Development of an oil
tracer labelled with 137mBa”, paper presented at 6th International Conf. Tracers and
Tracing Methods (Tracer 6), Oslo (2011).
[163] CHAKRAVARTY, R., et al., Nanoceria-PAN composite-based advanced sorbent
material: A major step forward in the field of clinical-grade 68Ge/68Ga generator, ACS
Appl. Mater. Interfaces 2 7 (2010) 2069–2075.
[164] INTERNATIONAL ATOMIC ENERGY AGENCY, Regulations for the Safe Transport
of Radioactive Material 2009 Edition, IAEA Safety Standards Series No. TS-R-1,
IAEA, Vienna (2009).
[165] INTERNATIONAL ATOMIC ENERGY AGENCY, Fundamental Safety Principles,
IAEA Safety Standards Series No. SF-1, IAEA, Vienna (2006).
[166] INTERNATIONAL ATOMIC ENERGY AGENCY, International Basic Safety
Standards for Protection against Ionizing Radiation and for the Safety of Radiation
Sources, IAEA, Vienna (in preparation).
[167] INTERNATIONAL COMMISSION ON RADIOLOGICAL PROTECTION, Dose
Coefficients for Intakes of Radionuclides by Workers, Publication 68, Pergamon Press,
Oxford and New York (1994).
[168] INTERNATIONAL COMMISSION ON RADIOLOGICAL PROTECTION, General
Principles for the Radiation Protection of Workers, Publication 75, Pergamon Press,
Oxford and New York (1997).
[169] INTERNATIONAL COMMISSION ON RADIOLOGICAL PROTECTION, 1990
Recommendations of the International Commission on Radiological Protection,
Publication 60, Pergamon Press, Oxford and New York (1990).

200
 BIBLIOGRAPHY
BJØRNSTAD, T., Selection of Tracers for Oil and Gas Reservoir Evaluation, Tech. Res.
Rep. IFE/KR/E-91/009, Institute for Energy Technology, Kjeller, Norway (1991).

BJØRNSTAD, T., “Recent and current oil field tracer development for interwell application”,
Proc. 2nd Tracer Workshop, University of Texas at Austin, 14–15 November 1994
(BJØRNSTAD, T., POPE, G. (Eds)), Res. Rep. IFE/KR/E-95/002, Institute for Energy
Technology, Kjeller, Norway (1995).

BJØRNSTAD, T., New Development in Tracer Technology for Reservoir Description, Res.
Rep. IFE/KR/E-98/006, Institute for Energy Technology, Kjeller, Norway (1998).

BJØRNSTAD, T., HAUGEN, O.B., HUNDERE, I.A., Dynamic behavior of radio-labelled

water tracer candidates for chalk reservoirs, J. Petrol. Sci. Eng. 10 (1994) 223.

BJØRNSTAD, T., DUGSTAD, O., GALDIGA, C., SAGEN, J., “Interwell tracer technology in
oil reservoirs: State-of-the-art”, paper presented at Proc. 2nd International Congress on Tracers
and Tracing Methods (TRACER 2), Nancy, France, 2001.

BLET, V., BERNE, Ph., TOLA, F., VITART, X., CHAUSSY, C., Recent developments in
radioactive tracers methodology, Appl. Rad. Isot. 51 (1999) 615–624.

BLET, V., BERNE, Ph., LEGOUPIL, S., VITART, X., Radioactive tracing as aid for diagnosing
chemical reactors, Oil Gas Sci. Technol. 55 (2000) 171.

CHARLTON, J.S., Radioisotope Techniques for Problem-solving in Industrial Process Plants,

Leonard Hill, Glasgow and London, 1986.

CHARLTON, J.S., HURST, J.A., Radioisotope techniques for problem solving in the offshore
oil and gas, J. Pet. Technol. (1992).

CHMIELEWSKI, A.G., et al., “Application of radioisotope techniques”, paper presented at

4th Conf. on Radioisotope Application and Radiation Processing in Industry, Leipzig, 1989.

DUDUKOVIC, M.P., Opaque multiphase flows: Experiments and modeling, Exp. Thermal
Fluid Sci. 26 (2002) 747–761.

FRIES, B.A., “Training the engineer for radiotracer applications in industry”, Radiation
Engineering in the Academic Curriculum (Proc. Study Group Mtg Haifa, 1973), IAEA, Vienna
(1975).

GARDNER, R.P., ELY, J.R., Radioisotope Measurement Applications in Engineering,

Reinhold Publishing Corporation, New York (1967).

201
INTERNATIONAL ATOMIC ENERGY AGENCY, Guidebook on Radioisotope Tracers in
Industry, Technical Reports Series No. 316, IAEA, Vienna (1990).

INTERNATIONAL ATOMIC ENERGY AGENCY, Radiotracer Technology as Applied to

Industry, IAEA-TECDOC-1262, IAEA, Vienna (2001).

INTERNATIONAL ATOMIC ENERGY AGENCY, Tracer Applications in Oil Field

Investigations, IAEA, Vienna (2003).

INTERNATIONAL ATOMIC ENERGY AGENCY, Radiotracer Applications in Industry —

A Guidebook, Technical Reports Series No. 423, IAEA, Vienna (2004).

INTERNATIONAL ATOMIC ENERGY AGENCY, Industrial Process Gamma Tomography,

IAEA-TECDOC-1589, IAEA, Vienna (2008).

INTERNATIONAL ATOMIC ENERGY AGENCY, Leak Detection in Heat Exchangers and

Underground Pipelines Using Radiotracers, IAEA Training Course Series No. 38, IAEA,
Vienna (2009).

JIN, J.-H., et al., Radiotracers and Labelling Compounds for Applications in Industry and
Environment, Report of the CM, Warsaw (2004).

JOHANSEN, G.A., Nuclear tomography methods in industry, Nucl. Phys. A 752 (2005)
696c–705c.

KRAS, J., et al., “New tracer and adsorbents for checking the tightness of technological units in
petroleum industry”, paper presented at 4th Conf. on Radioisotope Application and Radiation
Processing in Industry, Leipzig, 1989.

PLASARI, E., THERESKA, J., LECLERC, J.P., VILLERMAUX, J., Tracer experiments and
residence-time distributions in the analysis of industrial units: Case studies, Nukleonika 44
(1999) 39–58.

THYN, J., et al., Analysis and Diagnostics of Industrial Processes by Radiotracers and
Radioisotope Sealed Sources, Czech Technical University, Prague (2000).

TRACERCO, DiagnosticsTM FCC Study, Brochure, Tracerco, Billingham, United Kingdom

(1998).

TRACERCO, Using Radioisotope Technology to Maximise Efficiency, Petromin (1999)

62–69.

ZEMEL, B., Tracers in the Oil Field, Elsevier Science, Amsterdam (1995).

202
 CONTRIBUTORS TO DRAFTING AND REVIEW
Bjørnstad, T. Institute for Energy Technology, Norway

Borroto Portela, J.I. Agencia de Energía Nuclear y Tecnologías de

Avanzada, Cuba

Brisset, P. International Atomic Energy Agency

Chankow, N. Chulalongkorn University, Thailand

Charlton, J.S. Oatley, Australia

Conejo Solis, M.A. Instituto Tecnológico de Costa Rica, Costa Rica

Dagadu, C.P.K. Ghana Atomic Energy Commission, Ghana

Dash, A. Bhabha Atomic Research Centre, India

Diaz Vargas, F. Comisión Chilena de Energía Nuclear, Chile

Ghiyas-Ud-Din Pakistan Institute of Nuclear Science and Technology,

Pakistan

Jin, J.-H. International Atomic Energy Agency

Li Jinfu China Institute of Atomic Energy, China

Muñoz Anrique, L. Comisión Chilena de Energía Nuclear, Chile

Pinto Ferreira, A. Comissão Nacional de Energia Nuclear, Brazil

Palige, J.M. Institute of Nuclear Chemistry and Technology, Poland

Roesch, F. Institute of Nuclear Chemistry, Germany

Sung-Hee Jung Korea Atomic Energy Research Institute,

Republic of Korea

Vargas, C. Instituto Tecnológico de Costa Rica, Costa Rica

203
.
@





 
 
 

 
  
    
  
 !"

 
#
 $
%&'(
)*+!,*-.-/
+ 01%.-2/.3444456701%.-2/.344''

0$
8
 5(
0 099
 

! " #
:;$)
/3/<=..23< 
+ 01-//>-'&-3'56701-//>-'3'&.

0 8
5(
0 099== 

$%
<
 &>3.6< $ 
/33;*#/343%=&-&% 
+ 0.='33='%>=-&>45670.='33='%>=-&>3

0 85(
0 099
)

?!; .=>-%2! )" " 
@.:2:-
+ 01%.-4&>/%%>56701%.-4&>4%%3

0 85(
0 099

$& 



!
0!
 ? !
+ 
 
"<7/.3-<

?

$'$&(! $
!A )"@ $-&4.'3/.2
+ 01&/3/%%3->-%&56701&/3/'&'/.%&%

08B5(
0 099B

)  %
 
@
"<"C./'D@ .E6=33.3., 


+ 01->'2./.&.56701->'2./.&&>3

0
8 
5(
0 099 


)$
6=
>:"<7/>6=4>2/.
!7.2
+ 01--.&/3.&2&256701--.&/3.2323

0
8
5(
0 099

;$

  .&>$
?2&/-%!!7
+ 01--.&4&3%43/5671--.&4&3%43/

0 $
8 $

5(
0 099 $



"#*
"=F ?F 
=F ?G,,? .3#=>-..-<
+ 01&2//'2&23/356701&2//'2&23/31&2//'2&23///

0  ?8=$ ?5(
0 099=$ ?

&"*
;
 ; < "<7./%,=.%>%< 
+ 01-%./>4444456701-%./>44&4/5
08
 

% 


G. 6 #,.>:,
*?<   *
&3333.
+ 012.////%.42/%9/4567012.////%.42/'

0
 8$ 5(
0 099


< /94/

! # 
..3332
+ 012.../-/%'4'%12.../-/>4/%&567012.../-/'.-.>

0 8$  

 *
;

 

H# ;

<

I"JF
!
%=/3.&%*

+ 01-23/&'2>&>>/&'2>&>%/56701-23/&'2>&>&'

0
8


5(
0



JAPAN
Maruzen Company Ltd, 1-9-18, Kaigan, Minato-ku, Tokyo, 105-0022
Telephone: +81 3 6367 6079 • Fax: +81 3 6367 6207
Email: [email protected] • Web site: http://www.maruzen.co.jp

REPUBLIC OF KOREA
KINS Inc., Information Business Dept. Samho Bldg. 2nd Floor, 275-1 Yang Jae-dong SeoCho-G, Seoul 137-130
Telephone: +02 589 1740 • Fax: +02 589 1746 • Web site: http://www.kins.re.kr

NETHERLANDS
De Lindeboom Internationale Publicaties B.V., M.A. de Ruyterstraat 20A, NL-7482 BZ Haaksbergen
Telephone: +31 (0) 53 5740004 • Fax: +31 (0) 53 5729296
Email: [email protected] • Web site: http://www.delindeboom.com
Martinus Nijhoff International, Koraalrood 50, P.O. Box 1853, 2700 CZ Zoetermeer
Telephone: +31 793 684 400 • Fax: +31 793 615 698
Email: [email protected] • Web site: http://www.nijhoff.nl
Swets and Zeitlinger b.v., P.O. Box 830, 2160 SZ Lisse
Telephone: +31 252 435 111 • Fax: +31 252 415 888
Email: [email protected] • Web site: http://www.swets.nl

NEW ZEALAND
DA Information Services, 648 Whitehorse Road, MITCHAM 3132, Australia
Telephone: +61 3 9210 7777 • Fax: +61 3 9210 7788
Email: [email protected] • Web site: http://www.dadirect.com.au

SLOVENIA
Cankarjeva Zalozba d.d., Kopitarjeva 2, SI-1512 Ljubljana
Telephone: +386 1 432 31 44 • Fax: +386 1 230 14 35
Email: [email protected] • Web site: http://www.cankarjeva-z.si/uvoz

SPAIN
Díaz de Santos, S.A., c/ Juan Bravo, 3A, E-28006 Madrid
Telephone: +34 91 781 94 80 • Fax: +34 91 575 55 63
Email: [email protected], [email protected], [email protected], [email protected]
Web site: http://www.diazdesantos.es

UNITED KINGDOM
The Stationery Office Ltd, International Sales Agency, PO Box 29, Norwich, NR3 1 GN
Telephone (orders): +44 870 600 5552 • (enquiries): +44 207 873 8372 • Fax: +44 207 873 8203
Email (orders): [email protected] • (enquiries): [email protected] • Web site: http://www.tso.co.uk
On-line orders
DELTA Int. Book Wholesalers Ltd., 39 Alexandra Road, Addlestone, Surrey, KT15 2PQ
Email: [email protected] • Web site: http://www.profbooks.com
Books on the Environment
Earthprint Ltd., P.O. Box 119, Stevenage SG1 4TP
Telephone: +44 1438748111 • Fax: +44 1438748844
Email: [email protected] • Web site: http://www.earthprint.com

UNITED NATIONS
Dept. I004, Room DC2-0853, First Avenue at 46th Street, New York, N.Y. 10017, USA
(UN) Telephone: +800 253-9646 or +212 963-8302 • Fax: +212 963-3489
Email: [email protected] • Web site: http://www.un.org

UNITED STATES OF AMERICA

Bernan Associates, 4501 Forbes Blvd., Suite 200, Lanham, MD 20706-4346
Telephone: 1-800-865-3457 • Fax: 1-800-865-3450
Email: [email protected] · Web site: http://www.bernan.com
Renouf Publishing Company Ltd., 812 Proctor Ave., Ogdensburg, NY, 13669
Telephone: +888 551 7470 (toll-free) • Fax: +888 568 8546 (toll-free)
Email: [email protected] • Web site: http://www.renoufbooks.com

Orders and requests for information may also be addressed directly to:
Marketing and Sales Unit, International Atomic Energy Agency
Vienna International Centre, PO Box 100, 1400 Vienna, Austria
Telephone: +43 1 2600 22529 (or 22530) • Fax: +43 1 2600 29302
Email: [email protected] • Web site: http://www.iaea.org/books
12-46311
 R EL AT ED PUBL ICAT IONS

RADIOTRACER APPLICATIONS IN INDUSTRY – A GUIDEBOOK

Technical Reports Series No. 423
STI/DOC/010/423 (281 pp.; 2004)
ISBN 92–0–114503–9 Price: €45.00
CYCLOTRON PRODUCED RADIONUCLIDES: PHYSICAL
CHARACTERISTICS AND PRODUCTION METHODS
Technical Reports Series No. 468
STI/DOC/010/468 (266 pp.; 2009)
ISBN 978–92–0–106908–5 Price: €52.00
RADIOTRACER RESIDENCE TIME DISTRIBUTION METHOD FOR
INDUSTRIAL AND ENVIRONMENTAL APPLICATIONS
Training Course Series No. 31
(2008)
Price: €0.0

www.iaea.org/books
Radionuclide generators represent a cost effective strategy to ensure a continuous
and reliable supply of short lived radionuclides for radiotracer investigations.
Making use of radiotracers from radionuclide generators can alleviate the
difficulties associated with radioisotope supply. Another advantage is the ease
with which the daughter product can be separated on demand and converted into
a radiotracer by some tailor-made labelling procedure at the site. This publication
contains guidelines for the selection and preparation of radiotracers derived from
radionuclide generators. It describes the results of research undertaken in the
characterization of 68Ge/68Ga, 137Cs/137mBa, 99Mo/99mTc and 113Sn/113mIn radiotracer
generators and their validation in industrial process investigations. Radiotracers
have been widely used throughout industry to optimize processes, solve problems,
improve product quality, save energy and reduce pollution. Recent trends in
the industrialization process of developing countries suggest that radiotracer
techniques will continue to play an important role in industry for many years to
come.

INTERNATIONAL ATOMIC ENERGY AGENCY

VIENNA
ISBN 978–92–0–135410–5
ISSN 2220–7341