OTM-39 Method for Determination of Oxygen, Carbon Monoxide and Nitrogen Oxides from

Stationary Sources using Portable Gas Analyzers Equipped with Electrochemical Sensors
This method was submitted by Innovative Environmental Solutions, Inc. under contract to the Pipeline
Research Council International (PRCI) on behalf of the PRCI member companies to EPA’s Office of Air
Quality, Planning and Standards, Air Quality Assessment Division, Measurement Technology Group
(MTG) for (1) inclusion into the Other Test Method (OTM) category on EPA’s Air Emission Measurement
Center (EMC) website at: https://www.epa.gov/emc/emc-other-test-methods and (2) consideration as a
broadly applicable alternative test method. OTM-39 has now been approved for use at (1)
Industrial/Commercial/Institutional Steam Generating Units subject to 40 CFR Part 60, Subpart Db 1, (2)
stationary spark ignition internal combustion engines subject to 40 CFR Part 60, Subpart JJJJ 2, and (3)
Reciprocating Internal Combustion Engines subject to 40 CFR Part 63, Subpart ZZZZ 3, see
https://www.epa.gov/sites/production/files/2018-05/documents/alt138.pdf.

Supporting data for this OTM were provided by PRCI can can be found at the links below:
1) Considerations for Developing a New Electrochemical Cell Portable Analyzer Test Method, Innovative
Environmental Solutions, Inc., for the Pipeline Research Council International, Inc., Catalog PR-312-
14206-R01, May 2015

https://www.prci.org/Research/CompressorPumpStation/CPSProjects/CPS-11-6/3235/15171/15170.aspx

2) Portable Analyzer Test Method Update for Common Analyzers Phase 2 Report, Innovative Environmental
Solutions, Inc., for the Pipeline Research Council International, Inc., Catalog PR-312-17204-R01, August
2017

https://www.prci.org/Research/CompressorPumpStation/CPSProjects/CPS-11-6A/3241/141821/125629.aspx

3) Portable Analyzer Test Method Update for Common Analyzers Phase 3 Report, Innovative Environmental
Solutions, Inc., for the Pipeline Research Council International, Inc., Catalog PR-312-17204-R01, October
2017

https://www.prci.org/Research/CompressorPumpStation/CPSProjects/CPS-11-6A/3241/136252/125634.aspx

The posting of a test method on the OTM portion of the EMC website is neither an endorsement by
EPA regarding the validity of the test method nor a regulatory approval of the test method. The
purpose of the OTM portion of the EMC website is to promote discussion of developing emission
measurement methodologies and to provide regulatory agencies, the regulated community, and the
public at large with potentially helpful tools.

Other Test Methods are test methods which have not yet been subject to Federal rulemaking. Each of
these methods, as well as the available technical documentation supporting them, have been reviewed
by the EMC staff and have been found to be potentially useful to the emission measurement
community. The types of technical information reviewed include field and laboratory validation studies;
results of collaborative testing; articles from peer-reviewed journals; peer-review comments; and quality
assurance (QA) and quality control (QC) procedures in the method itself. A table summarizing the

1
Oxygen Measurements
2
Nitrogen Oxides, Carbon Monoxide, and Oxygen Measurements
3
Carbon Monoxide, and Oxygen Measurements
available technical information for each method can be found at the link below. As noted above, the EPA
strongly encourages the submission of additional supporting field and laboratory data as well as
comments in regard to these methods. These methods may be considered for use in federally
enforceable State and local programs (e.g., Title V permits, State Implementation Plans (SIP)) provided
they are subject to an EPA Regional SIP approval process or permit veto opportunity and public notice
with the opportunity for comment. The methods may also be considered to be candidates to be
alternative methods to OTM-40 2 meet Federal requirements under 40 CFR Parts 60, 61, and 63;
however, they must be approved as alternatives through a separate action under §§60.8(b), 61.13(h),
or 63.7(f) before a source may use them for this purpose. Consideration of the applicability of an OTM
for a particular purpose should be based on the stated applicability, the supporting technical
information outlined in the table, or regulatory actions including approval as an alternative test method
or inclusion in a SIP.

These methods are available for application without EPA oversight for other non-EPA program uses
including state permitting programs and scientific and engineering applications. As many of these
methods are submitted by parties outside the Agency, the EPA staff may not necessarily be the technical
experts on these methods. Therefore, technical support from EPA for these methods is limited, but the
table contains contact information for the developers so that you may contact them directly. Also, be
aware that these methods are subject to change based on the review of additional validation studies or
on public comment as a part of adoption as a Federal test method, the Title V permitting process, or
inclusion in a SIP.

Method History

Initial Posting – 08/24/2020

EPA advises all potential users to review the method and all appendices carefully before application of
this method.
OTM 039

OTM-39 Method for Determination of Oxygen, Carbon Monoxide and Nitrogen Oxides from Stationary
Sources using Portable Gas Analyzers Equipped with Electrochemical Sensors

1.0 Scope and Application

This test method is a procedure for measuring nitrogen oxides (NO and NO2), carbon monoxide (CO), and
oxygen (O2) concentrations in controlled and uncontrolled emissions from reciprocating engines,
combustion turbines, boilers, and process heaters firing natural gas using portable gas analyzers with
electrochemical sensors. Quality assurance and quality control requirements are included to assure that you,
the tester, collect data of known and acceptable quality for each testing program. This method does not
completely describe all equipment, supplies, and sampling and analytical procedures you will need, but
instead refers to other test methods for some of the details. Therefore, to obtain reliable results, you should
also have a thorough knowledge of these additional methods which are found in 40 CFR Part 60,
Appendices A-1 and A-3:
(a) Method 1—Sample and Velocity Traverses for Stationary Sources.
(b) Method 4—Determination of Moisture Content in Stack Gases.
(c) Method 7E—Determination of Nitrogen Oxides Emissions from Stationary Sources (Instrumental
Analyzer Procedure).

1.1 Analytes.

This method measures the concentrations of nitrogen oxides (NO and NO2), carbon monoxide (CO), and oxygen
(O2) as determined using an electrochemical portable analyzer.

Table 1-1 Analyte list

Analyte CAS No Sensitivity (minimum detectable limit)
Nitric oxide (NO) 10102-43-9 < 2% of calibration gas value
Nitrogen dioxide (NO2) 10102-44-0 < 2% of calibration gas value
Carbon Monoxide (CO) 630-08-0 < 2% of calibration gas value
Oxygen (O2) 7782-44-7 < 2% of calibration gas value

1.2 Applicability.

This method is intended for the measurement of nitrogen oxides (NO and NO2), carbon monoxide (CO), and/or
oxygen (O2) in stationary source emissions for the purposes of conducting performance tests to demonstrate
compliance with an applicable emissions standard. The use of this method for performance tests used to
demonstrate compliance with federal emissions standards or monitoring requirements must be approved by the
EPA Administrator. This method is available for application without Federal oversight for other non-federal
program uses including state permitting programs and engineering applications.

1.3 Data Quality Objectives (DQO).

This method is designed to provide high-quality data for the determinations described above. In these and other
applications, the principal objective is to ensure data accuracy at the emission levels that are at or below the
emissions target. To meet this objective, the use of EPA traceability protocol calibration gases and measurement

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system performance tests are required.

1.4 Data Quality Assessment for Low Emitters.

This test method includes specific considerations for “low” emission testing where measured emissions of NO are
expected to be 20 ppmv or less. Emissions greater than 20 ppmv are considered and noted as “general” emissions
levels in this method. This includes sensor resolution, calibration gas concentration and thermal stability
requirements.

2.0 Summary of Method

A gas sample is continuously extracted from an emission source exhaust duct and conveyed to a portable gas
analyzer for determination of O2, and NO, NO2, and/or CO gas concentrations using electrochemical gas sensors.
Portable gas analyzer design specifications, performance specifications, and test procedures are provided to
ensure reliable performance. Electrochemical gas sensors are designed to detect and quantify the concentration
of a specific gas by measuring the flow of current resulting from the electrochemical reaction of that gas on an
electrode surface. The sensor is comprised of two electrodes, the sensing electrode and the counter electrode, that
are held at a precisely chosen constant relative potential. By selecting the flow rate and sensor design such that
every molecule that reaches the electrode surface is oxidized, the current response curve is predictable. This type
of design is known as “mass transport limited” or “diffusion controlled.” The electrochemical sensor range is
determined by the sensor manufacturer.

Note: This method incorporates technology specific characteristics of electrochemical portable gas analyzers and is not
technology neutral.

Table 2 – 1 Instrument Technology Requirements

Instrumentation Technology Requirement
Portable Gas Analyzer Sensing Technology Electrochemical Sensors
Temperature Monitoring Sensor Temperature Display
Zero-Calibration Automatic
Maintenance Annual by Authorized Service or Manufacturer

3.0 Definitions

3.1 Ambient air rinse means the gas analyzer sample stream is ambient air. This occurs for a set amount of
time between measurements. It is also referred to as purging, breathing, or rinsing. It is required between the
introduction of each analyte calibration gas during system verification and between sample runs for emissions
tests.

Note: Ambient rinses should be at least 5 minutes in length unless otherwise stated in the method. The duration
of the ambient air rinse must be sufficient to refresh the surface of the electrodes inside the sensor. Without an
ambient air rinse, electrochemical sensors will become "saturated”and the output will drift. The amount of time
for the ambient air rinse is generally dependent upon the gas concentration and the time of exposure.
3.2 Calibration error means the percentage difference between the gas concentration measured by the gas
analyzer and the known concentration of the calibration gas.
3.3 Calibration gas means a gas mixture containing an analyte at a known concentration and produced and

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certified in accordance with “EPA Traceability Protocol for Assay and Certification of Gaseous Calibration
Standards,” September 1997, as amended August 25, 1999, EPA-600/R-97/121 or more recent updates. The system
verification tests require the use of calibration gas prepared according to this protocol.
3.3.1 Daily calibration gas means the calibration gas ranges listed in Table 7-1 of this method.
3.3.2 Span calibration gas means the known concentration of a gas in an appropriate diluent gas according to
Table 3-1.
3.3.3 Mid-level calibration gas means a known concentration of a gas in an appropriate diluent gas
according to Table 3-1.
3.3.4 Low-level calibration gas means a NO calibration gas of between the concentration of 5 – 25
ppmv.
3.3.5 Zero calibration gas means a calibration gas which meets requirements under the definition for
“zero air material” in 40 CFR 72.2.

Table 3-1. Linearity Gas Concentrations (As Certified)

Analyte Mid-level calibration gas Span calibration gas concentration
concentration (ppmv) (ppmv)
CO 100 2000
COlow 100 300
NO 100 500
NOlow 100 200
NO2 100 300
O2 15% 20.9%

3.4 Interference check means the procedure for quantifying cross-sensitivities from components in the stack
gas other than the target analyte.
3.5 Linearity check means a periodic check of a gas analyzer to verify the linear response of the
electrochemical sensors in a gas analyzer over a range of gas concentrations. Linearity checks must be performed
at least every calendar quarter for each analyte or whenever an electrochemical sensor is replaced.
3.6 Low emitters means sources (e.g., turbines) in which the concentration of NO does not exceed 20 ppmv.
3.7 Measurement range means the portable gas analyzer manufacturer-determined range of concentration
within which the sensor will operate with the specified accuracy and excess of this range is considered overload.

Note: A sensor manufacturer may recommend a nominal range of 0 – 4000 ppm with an overload level of 5000 ppm. The
portable gas analyzer manufacturer using this sensor may conservatively recommend a measurement range of 0 – 4000
ppm. Post checks must be performed whenever a gas analyzer reading is above 80% of the measurement range. For the
analyzer described above, a post check would be required when readings are observed in excess of 3,200 ppm (80% of 4000
ppm).
3.8 Measurement system means the total equipment required for the determination of gas concentration. The
measurement system consists of the following major subsystems:

(a) data recorder – a computer or digital recorder for recording measurement data.
(b) electrochemical sensor – that portion of the system that senses the gas to be measured and
generates an output proportional to its concentration, or any sensor that uses diffusion-limited
oxidation and reduction reactions to produce an electron flow or current between a sensing electrode
and a counter electrode. Referred to as “sensor”.
(c) external interference gas scrubber – device filled with scrubbing agent used to remove
interfering compounds upstream of some electrochemical sensors.

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(d) sample interface – that portion of a system used for one or more of the following: sample
acquisition, sample transport, sample conditioning, or protection of the electrochemical sensors from
particulate matter and condensed moisture.
(e) temperature device – temperature measurement device(s) installed 1) immediately next to an
electrochemical sensor to measure and record the temperature within the analyzer (Ts) and 2) mounted
on the external surface of the portable gas analyzer to measure and record the temperature of the ambient
environment (Ta).
3.9 Response time means the amount of time, as measured on the data recorder, required for the
measurement system to display 90 % of the concentration of the calibration gas.
3.10 Sample run means the event of collecting and measuring the emissions from a single location from the
stack or duct. A test normally consists of a specific number of sample runs.
3.11 Test means a series of sample runs required by the applicable regulation.
3.12 Sensor stability time means the elapsed time from the start of the response time to the time when the sensor
stability criteria of less than 1.0% per minute change is achieved.
3.13 Stability check means the procedure for demonstrating that an electrochemical sensor response to the
calibration gas provides a stable output. Defined as less than 1.0% per minute change in measured concentration
during minutes 4 to 5 in the time period immediately following the 2 minutes allotted for the response time.
3.14 Thermal check means calculation of change in temperature with respect to time to demonstrate that the
portable gas analyzer system has sufficiently equilibrated to the test environment. This is a measurement of
thermal stability and defined as a temperature change of less than 1.1°C (2°F) in 15 minutes.
3.15 Thermal stability means calculation of the change in ambient temperature, TA, or sensor temperature,
Ts, during the system performance tests, sample collection test or post-check system verification.
4.0 Interferences
4.1 Analytical Interferences. NO and NO2 can interfere with CO concentration measurements from
electrochemical sensors, and NO2 can interfere with NO concentration measurements from electrochemical
sensors. To mitigate any interference concerns, the use of gas scrubbers immediately prior to an
electrochemical sensor is acceptable and to eliminate any confounding effects calibration criteria must be met
using calibration gases prepared as a single analyte standard balanced in nitrogen or synthetic air.
4.2 Sampling Interface Interferences. Sampling interface interferences prevent the transport of target
analytes to the instrumentation or have the potential to damage the measurement system components (water
condensation and moisture, for example). You must adhere to the manufacturer’s recommended procedures
and specific provisions and performance criteria included in this method to eliminate sampling interface
interferences.

5.0 Safety
This method may require you to work with hazardous materials and in hazardous conditions. We encourage
you to establish safety procedures before using the method. Among other precautions, you should become
familiar with the safety recommendations in the gas analyzer user's manual. Occupational Safety and Health
Administration (OSHA) regulations concerning cylinder and noxious gases may apply. NO and NO2 are toxic
and dangerous gases. Nitric oxide is immediately converted to NO2 upon reaction with air and NO2 is a
highly poisonous and insidious gas. Inflammation of the lungs from exposure may cause only slight pain or
pass unnoticed, but the resulting edema several days later may cause death. A concentration of 100 ppm is
dangerous for even a short exposure, and 200 ppm may be fatal. All calibration gases must be handled with
utmost care and with adequate ventilation.

6.0 Equipment and Supplies

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6.1 This section presents an example of key equipment and supplies designed for this application. Any
electrochemical measurement system that meets the performance and design specifications in this test method
may be used.
6.2 Sample Transport and Conditioning System. The sample transport and conditioning system shall be designed and
operated to preclude water condensation that can affect the accuracy of the readings and to prevent moisture contact
with the electrochemical sensors. The essential components are described below.
6.2.1 Sample Probe. Glass, stainless steel, or other non-reactive material of sufficient length to
traverse the sample points in the source exhaust duct. Probe assembly is to minimize condensation and
scrubbing of NO2 or other water miscible gas species.
6.2.2 Particulate Filters. Filters at the probe, the inlet, or outlet of the moisture removal system, and/or
at the inlet or within the body of the gas analyzer are recommended to prevent accumulation of
particulate material in the measurement system and extend the useful life of the components. Filters
shall be fabricated of materials that are nonreactive with the sample gas.
6.2.3 Sample Line. The sample line from the probe to the conditioning system/sample pump should be
made of Teflon or other material that does not absorb or otherwise alter the sample gas. For NOx testing,
heated or proven design which prevents scrubbing of NO2 or other water miscible gas species is
required.
6.2.4 Moisture Removal System. A device to dry the sample to prevent scrubbing of NO2 or other
water miscible gas species.
6.2.5 Sample Pump. A device to pull the sample gas through the system at a consistent flow rate. The
pump wetted surfaces should be constructed of material that is nonreactive with the sample gas.

Note: An aged or weak sample pump will result in a low flow rate. An inadequate flow rate will result in low bias
and false negative readings. Pumps must be included in annual gas analyzer maintenance. Flow rate must be
visibly monitored either by an intrinsic flow rate meter or by placing a flow rate control valve upstream of the gas
analyzer during system verification and at the exhaust (to measure flow) of the gas analyzer during source testing.
6.2.6 System Verification Assembly. A tee-fitting to attach to the probe tip for introducing calibration
gases at ambient pressure during the system verification. The vented end of the tee should have a flow
indicator to ensure sufficient calibration gas flow. A schematic of an acceptable calibration assembly is
shown in Figure 17-1. Any other similar method, such as a demand flow regulator, that introduces
calibration gases at the probe at atmospheric pressure may be used.
6.2.7 Gas Flow Rate Control. A gas flow rate control valve and rotameter, or equivalent, to maintain a
constant sampling rate during system performance tests and to measure and record the flow rate during
source testing. The flow during the system verification and source testing must be within 10 % of each
other. The rate control components shall be fabricated of materials that are non-reactive with the sample
gas.
6.2.8 Interference Gas Scrubber. A device used to remove interfering compounds upstream of a CO
electrochemical sensor. The measurement system must provide the operator with a means of determining
when the scrubbing agent is exhausted (that is, visible color change indication, or electronic ppm hour
counter, or equivalent).
6.2.9 Sensor Temperature Indicator. A thermocouple, thermistor, or other device must be used to
monitor and display the sensor temperature. The temperature may be monitored at the surface or within
the sensor. Sensor temperature must be monitored, recorded, and visibly displayed.
6.2.10 Ambient Temperature Indicator. A thermocouple, thermistor, or other device must be used to
monitor the ambient temperature of the portable gas analyzer. The temperature should be monitored at the
surface of the gas analyzer. Instrument ambient temperature must be monitored, recorded, and visibly
displayed.
6.3 Portable Gas Analyzer. An instrument containing electrochemical sensors to determine the NO, NO2,

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CO, and O2 concentrations in the sample gas stream. These analyzers must be operated per manufacturer
instructions in addition to the following requirements:

(a) The gas analyzer shall contain electrochemical sensors with a minimum resolution of 1.0 ppm for
“general” range emission testing or 0.1 ppm for “low” emitter testing (i.e., < 20 ppm).
(b) The gas analyzer must be adequately charged prior to operation. Analyzers which have not been
operated within the last 30 calendar days, or have no battery charge remaining, must be fully
charged per the manufacturer’s specifications to ensure 100% bias on the NO sensor.

Note: NO sensors operate with an electrical bias, if no charge or not enough charge remains then the bias on
the NO sensor will be inadequate. Only when the analyzer is fully charged will the NO sensor electrical bias
will be restored. If this sensor operates with an inadequate bias, it could be biased low and may not stabilize
at the concentration of the calibration gas.
(c) The manufacturer’s maintenance procedures should be followed, and any required or suggested
calibration and annual maintenance must be performed. This can be completed by the manufacturer,
the operator, or a third party, although a record of this maintenance shall be maintained an provided
to the applicable authority upon request.
6.4 Data Recorder. A computer, or digital recorder, for recording measurement data. The data recorder
resolution (that is, readability) must be at least 1 ppmv for CO, NO, and NO2 for general testing; at least 0.1
ppmv for CO, NO, and NO2 for low emitter testing (i.e., < 20 ppm); at least 0.1% O2 for oxygen
measurements; and 0.1° C (0.2⁰F) for temperature. Alternatively, a digital or analog meter that complies with
these resolution specifications may be used to obtain the gas analyzer responses and the readings may be
recorded manually. The data recorder must be capable of reading at a minimum of 10 second intervals.

7.0 Reagents and Standards

7.1 Measurement Range. The measurement range for each analyte is determined by the electrochemical sensor
design and specified by the portable gas analyzer manufacturer.
7.2 Calibration Gases. The calibration gases for the gas analyzer shall be CO in nitrogen or CO in synthetic
air, NO in nitrogen, NO2 in synthetic air or nitrogen, and O2 in nitrogen. Each calibration gas must be certified
(or recertified) within an uncertainty of 2.0 percent in accordance with “EPA Traceability Protocol for Assay and
Certification of Gaseous Calibration Standards” September 1997, as amended August 25, 1999, EPA-600/R-
97/12. Zero gas must meet the requirements under the definition for “zero air material” in 40 CFR 72.2. The
calibration gas must be used before it’s expiration date and the cylinder gas pressure must be greater than the
minimum pressure of use. It is acceptable to prepare calibration gas mixtures from EPA Traceability Protocol
gases in accordance with Method 205 in appendix M to 40 CFR Part 51, however blended gases which contain
multiple analytes are not permitted.
7.3 Calibration Gas Concentrations. Use the appropriate calibration gas for the calibration check of each
sensor. Select the appropriate low-level or high-level calibration gas listed in Table 7-1 for each analyte to be
measured. The calibration gas concentration may not exceed the measurement range of the analyzer and/or
electrochemical sensor. If the expected gas concentration is greater than the high-level calibration gas
concentrations, the high-level concentration must be selected.

Table 7-1. Calibration gas concentrations (as certified)

Analyte Low-level calibration gas High-level calibration gas
concentration range (ppmv) concentration range (ppmv)
CO 95 - 105 1900 - 2100
NO 95 - 105 475 - 525
NO2 95 - 105 95 - 105

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O2 Dry ambient air (20.9% O2) Dry ambient air (20.9% O2)
Example 1: If the expected gas concentration is 200 ppm CO, the selection of low-level or high-level calibration gas will be
based upon the measurement range of the sensor. In most cases, the installed sensor will be a low CO sensor with an upper
limit of around 500 ppm measurement range, and therefore, low-level calibration gas will be selected to not overrange the
sensor.

Example 2: If the expected gas concentration is 2500 ppm CO, this is in excess of the high-level calibration gas of 1900 -
2100 ppm and therefore, the high-level calibrations gas must be selected.
7.4 Linearity Check. Instrument preventative maintenance must be carried out and documented on an annual
basis. It is required that analyzer manufacturer’s maintenance procedures be followed, and an annual calibration
and maintenance be performed. This can be completed by the manufacturer, the operator, or a third party. The
linearity check must challenge the instrument through the entire measurement range with at least a span calibration
gas, mid-level calibration gas, and zero gas as listed in Table 3-1. The absolute value of the difference between
the gas value and the analyzer response shall not be greater than 2.5% of the span gas value. If you choose to
challenge at additional ranges, the difference between the gas value and the analyzer response shall not be greater
than 2.5% of the span calibration gas value for each range.
8.0 Sample Collection, Preservation and Storage

Emission Test Procedure: Since you are allowed to choose different options to comply with some of the
performance criteria, it is your responsibility to identify the specific options you have chosen and to document
that the performance criteria for that option have been met.
8.1 Sampling Location. Select a sampling site following EPA Method 1 or 1A (40 CFR Part 60,
Appendix A).
8.2 Stratification Tests. Perform stratification testing according to procedures found in Section 8.1.2 of EPA
Method 7E (40 CFR Part 60, Appendix A), unless otherwise specified by the applicable subpart or rule.
8.3 Initial Measurement System Performance Tests. Before measuring emissions, you must perform the
procedures:
(a) Calibration Gas Verification
(b) Linearity Verification
(c) Equipment Verification
(d) System Warm-up
(e) Leak Check
(f) Zero Calibration Error
(g) System Verification
(h) Low-emitter Verification (if applicable)
8.4 Calibration Gas Verification. Obtain a certificate from the gas manufacturer documenting the quality of
the gas. Confirm that the manufacturer certification is complete and current. Ensure that your calibration gas
certifications have not expired. This documentation should be available on-site (i.e., test location) for inspection.
8.5 Linearity Verification. At least once per calendar quarter in which the gas analyzer is in use or whenever
a sensor is replaced, perform the linearity check on the system after the system verification process by
challenging each sensor with a span calibration gas, a mid-level calibration gas, and a zero calibration gas per the
requirement in Section 7.4. The absolute value of the difference between the gas value and the analyzer response
shall not be greater than 2.5% of the span gas value. This documentation should be available on-site for
inspection and must be reported.
8.6 Equipment Verification. Assemble the sampling system by following the manufacturer’s recommended
procedures; verify through visual, electronic, or other suitable method that the gas scrubbing agent is not
depleted; inspect the particulate filter(s) through visual, electronic, or other suitable method; and record all
observations on an appropriate form.
8.7 System Warm-up and Thermal Check. Power the gas analyzer, and with the pump running, record the time,
and the ambient and sensor temperatures (TA,Ts). Allow the gas analyzer and sample interface to warm-up

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according to manufacturer’s recommendations. After the recommended warm-up and the gas analyzer is stable,
record the time, and ambient and sensor temperatures (TA,Ts) again and calculate the thermal response
(TCA,TCs) according to Equation OTM-39-1 or OTM-39-2 . When the system warm-up is complete, zero the
analyzer according to the manufacturers recommendation prior to the leak check, zero calibration error, and
system verification.

Note: The gas analyzer is stable when either TA or Ts changes less than 1.1°C (2°F) in 15 minutes.
8.8 Leak Check. With the pump running, perform a leak check by plugging the sample line and
observing that the gas flow rate is less than 0.03 l/min, or alternatively, by injecting an oxygen free gas
through the sampling probe tip and verifying that the O2 reading is less than or equal to 0.2%; record the
result of the check.
8.9 Zero Calibration Error. Introduce the zero calibration gas at the probe tip using the calibration assembly.
During the zero calibration error, make no adjustments to the system except those necessary to achieve the
correct calibration gas flow rate through the gas analyzer. Allow the electrochemical sensors’ responses to
stabilize for at least 30 seconds before recording the results and calculate the zero calibration error according to
Equation OTM-39-3. The requirement for the zero calibration error is that the CO, NO, and NO2 response must
be ≤3.0% of the value of the calibration gas used, while the O2 response must be ≤ 0.3% O2. If the method
specifications are not met, take corrective actions and repeat the zero calibration error.
8.10 System Verification: Pretest Response Time, Stability, and Calibration Error. The following procedure is
prescriptive and designed to evaluate the health and accuracy of the electrochemical sensors used in the portable
gas analyzers. Figure 17-2 (CO and NO) and Figure 17-3 (NO2) present an example of the portable gas analyzer
response during the system verification cycle. Conduct the system verification at the facility being tested
immediately prior to the start of a sample collections test. Keep the gas analyzer in the same location until the
post-test calibration error is conducted. The system verification must be completed for each test or series of tests
located at the same location.
8.10.1 Response Time.
8.10.1.1 Turn the pump on and introduce the CO calibration gas to the sample line through the
probe, or tubing as appropriate, per Figure 17-1 and ensure that the calibration gas flows through all
parts of the sample interface. Check the calibration gas flow rate on the instrument monitor or an
excess flow rotameter (if applicable), record the flow rate (e.g., lpm, cfm), and then perform an
ambient rinse.
8.10.1.2 Stop the ambient rinse and reconnect the sample line, as needed, and observe the
display for a reading of CO. The first detection of CO is time zero (Time 0) for the response
time. Recheck and record the flow rate. Record the time in seconds (i.e., response time) it
takes to achieve 90% of the full calibration gas value. If the response time is greater than 2
minutes, this indicates a thermal stability or sensor integrity issue and requires corrective action
prior to testing. Stop the system verification, troubleshoot, and repeat the response time.

Example 1 – 100 ppmv calibration gas, must read ≥0.9*100 = 90 ppm within 2 minutes.
Example 2 – 2,000 ppmv calibration gas, must read ≥0.9*2000 = 1800 ppm within 2 minutes.

8.10.2 Stability Check. After the response time has been determined, continue to flow the CO
calibration gas for 240 seconds (4 minutes) from the start of the response test and record the CO, NO,
and NO2 concentrations. Record data every 10 seconds. Allow for the calibration gas to continue to flow
for an additional minute and record the CO concentration at 300 seconds (5 minutes) from the start of the
response time. The difference in the recorded CO concentrations at 300 and 240 seconds must be less
than one percent of the CO calibration gas concentration.

│ppm(300 sec) – ppm (240 sec)│ ≤ 0.01* calibration gas concentration

Example 1 – 100 ppmv calibration gas, | (ppm5min – ppm 4min) | ≤ 0.01 * 100 ≤ 1 ppm

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Example 2 – 2,000 ppmv calibration gas, | (ppm5min – ppm 4min) | ≤ 0.01 * 2000 ≤ 20 ppm

8.10.3 Calibration Error. Average the measured values of the CO response observed (every 10
seconds) during the stability check. This value must be within 5.0% of the calibration gas value.

Example 1 – 100 ppmv calibration gas, 95 ≤ (average of readings minute 4 to 5) ≤ 105

Example 2 – 2,000 ppmv calibration gas, 1900 ≤ (average of readings minute 4 to 5) ≤ 2,100
8.10.4 If the gas analyzer CO measurement passes the specifications in Sections 8.10.1, 8.10.2 and
8.10.3, record the NO and NO2 concentrations measured and calculate the percent interference according
to Equation OTM 39-5. This value must be 5.0% or less. If the gas analyzer CO measurement does not
pass the response time, stability check, calibration error, and/or interference checks, corrective actions
are required. Stop the system verification, troubleshoot, and repeat the system verification starting from
the response time test.
8.10.5 Disconnect the sample line from the gas analyzer, as needed, and perform an ambient air rinse
for 5 minutes; record time and TA and Ts and then turn off the sample pump.
8.10.6 Repeat Sections 8.10.1 through 8.10.5 for NO. If the analyzer NO measurement passes these
specifications, record the NO2 concentration measured during the calibration error check to calculate
interference (according to Equation OTM 39-6).
8.10.7 NO2 System Verification. Introduce the NO2 calibration gas to the sample line through the probe,
or tubing as appropriate, per Figure 17-1, and ensure that the calibration gas flows through all parts of
the sample interface. Check the flow rate on the instrument monitor or excess flow rotameter (if
applicable). Connect the sample line to the gas analyzer, as needed, turn on the pump, and run the NO2
calibration gas for 10 minutes to pre-condition the system. Disconnect the sample line from the gas
analyzer, as needed, and perform an ambient air rinse for 5 minutes.
8.10.8 Repeat Sections 8.10.1 through 8.10.5 for NO2, there are no interferences to record for NO2.
8.10.9 Repeat sections 8.10.1 through 8.10.5 for O2.
8.10.10 Low-emitter Verification Calibration. If the NO measurements are expected to be < 20 ppm, you
must challenge the instrument with a low-level calibration gas and the NO response must be within 5.0%
of the calibration gas value. If the analyzer NO measurement does not pass this specification, you may
not use this analyzer for low emitters.
8.11 Sample Collection Method.
8.11.1 Position the sampling probe at the first or only measurement traverse point and begin sampling
at the same flow rate used during the system verification. You must maintain the sampling flow rate
within 10% of the gas analyzer flow rate value used during the system verification during the entire
sample run.
8.11.2 Allow the sample gas to flow through the sampling system for at least 5 minutes before
recording any data. Sample for an equal period of time at each traverse point for the required run time.
Record concentration values every 15 seconds and TS and TA at least once every 10 minutes. If an
electrochemical sensor is exposed to gas concentrations greater than 80 % of the measurement range
during any sample run, you must perform the post test system verification check.
At least once every 3 hours of clock time, perform an instrument zero calibration check where ambient
air is introduced and the CO, NO and NO2 are allowed to stabilize. Additionally, you must recalibrate
the analyzer with air at the zero level on each occasion when the sampling location changes.

Note: The actual procedure for performing the instrument zero calibration check will be per the instrument
manufacturer’s instructions. For many portable analyzers, this is automatic upon “power up” of the analyzer.
8.11.3 At the conclusion of each sample run perform the ambient air rinse for a minimum of 5 minutes
and the CO, NO and NO2 responses are ≤3.0% of the concentration measured during the previous run. A

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conservative estimate for the period of time required is shown in Table 8-1
Table 8-1. Ambient Air Rinse
Gas Concentration (ppm) Rinse time (min)
NO < 200 5
200-1000 10
1001 – 2000 20
3000+ 30
NOLOW < 50 5
51- 200 10
201 – 300 20
NO2 <50 5
51- 200 10
201 – 300 20
CO <100 5
101 – 1000 10
1001-2000 15
2001-4000 30
4001-8000 45
8000-10000 60
COLOW < 20 5
21 – 100 10
101 – 200 15
201-500 20

8.12 Post Test requirements

8.12.1 After each test or series of tests, conduct the post-test system verification per the requirements in
Section 8.10. Make no changes to the measurement system or gas analyzer calibration until all of the
calibration error tests have been completed and results have been recorded.
8.12.2 If the response time, stability check, calibration error, or low-emitter verification exceeds the
performance specifications in Section 8.10, all measurements since the previous acceptable checks are
invalid. You may also choose to perform zero or calibration error tests after each test run

9.0 Quality Assurance and Quality Control

Table 9-1 summarizes the QA/QC performance criteria.

Table 9-1. Quality Assurance/Quality Control Criteria

Section QA/QC test or Acceptance Criteria Frequency Corrective

specification action if not met
6.2 Sample Transport See requirements in Section Each test Do not test unless
and Conditioning 6.2.1 – 6.2.11 these criteria are
System met.
6.3 Portable Gas See requirements in Section 6.3. Annually Do not test unless
Analyzer Maintenance must be carried these criteria are
(performance and out and documented by an met.
maintenance) authorized service organization
or appropriately trained
operator.

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6.3 Portable Gas If the gas analyzer has not At least every 30 days or when Do not test unless
Analyzer been operated within the no battery charge remaining this criterion is
(battery charge). last 30 calendar days or met.
when no battery charge
remaining, then it must be
fully charged per the
manufacturer’s
specifications. System
performance checks may
not be performed until
charged.

7.2 Calibration Gas Certified using EPA Each test Do not test unless
Traceability Protocol this criterion is
met.
7.3 Calibration Gas Meet the Low-Range and Each test Do not test unless
Concentration High-Range (as these criteria are
Range(s) appropriate) in Table 7-1 met.
7.4 Linearity Check 2.5% of the span gas in Each Calendar Quarter when in Repeat Linearity
Table 3-1 operation Check.
8.1 Sampling According to EPA Each test Use an alternative
Location Method 1 or 1A sampling location
that meets the
acceptance
criteria.
8.2 Stratification ±5.0% of mean for 1-point Each test Sample at 12
Test sampling; ±10% of mean traverse points or
for 3-point sampling; Space the three
alternatively, all points points at 16.7,
within: ±0.5 ppm of mean 50.0, and 83.3
for 1-point sampling; ±1.0 percent of the
ppm of mean for 3-point measurement
sampling line.
8.6 Gas Scrubber Verify Equipment start-up Replace gas
Sufficient scrubber.
8.7 Thermal Check TA or TS changes less than Equipment start-up Do not test unless
1.1°C (2°F) in 15 minutes. this criterion is
met.
8.8 Leak Check With plugged sample line, Equipment start-up Do not test unless
flow rate is less than 0.3 l/min, this criterion is
or alternatively, inject oxygen met.
free gas and verify oxygen ≤
0.2%
8.9 Zero Calibration CO, NO, NO2 response must Prior to each test Do not test unless
Error be ≤ 3.0% of calibration gas these criteria are
for each analyte, oxygen must met.
be ≤ 0.3% O2
8.10.1 System < 2 minutes (for each analyte) Each test Troubleshoot,
Verification – and repeat
Response Time response time.
8.10.2 System % difference in the recorded Each test Repeat System
Verification – concentrations at 5 and 4 Verification.
Stability Check minutes must be less than
1.0% of the calibration gas
value, for each analyte when
applicable
8.10.3 System < 5.0% of the calibration gas Each test Repeat System
Verification – value Verification.
Calibration

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OTM 039

8.10.4 System Interference may not Calculate interference responses .

Verification - exceed 5.0% for NO (INO) and CO (ICO) using Repeat System
Interference the equations in Section 12 and Verification.
the system performance check
calibration results and average
emission concentrations for the
test
8.10.10 System < 5.0% of the calibration Each test when values are Repeat System
Verification – gas value using a expected to be below 20 ppmv Verification.
Low Emitter calibration gas between 5
Verification and 25 ppmv
8.11.1 Sample Flow rates during system Each run
Collection – verification and source Invalidate the test
Flow Rate testing must be within 10 and repeat.
% of each other
8.11.3 Sample CO, NO, NO2 response At least every 3 hours and after
Do not test unless
Collection – Zero must be ≤ 3.0% of a sampling location changes
this criterion is
Calibration calibration gas for each
met.
Check analyte
8.11.4 Sample CO, NO and NO2 responses After each test run Do not test unless
Collection – are ≤3.0% of the calibration these criteria is
Ambient Air gas used met.
Rinse
8.12.1 Post-test < 2 minutes (for each analyte) Each test Invalidate data
System since previous
Verification – System
Response Verification.
Time
8.12.1 Post-test % difference in the recorded Each test. Invalidate data
System concentrations at 5 and 4 since previous
Verification – minutes must be less than System
Stability 1.0% of the calibration gas Verification.
Check concentration, for each analyte
when applicable
8.12.1 Post-test < 5.0% of the calibration value Each Test Invalidate data
System since previous
Verification – System
Calibration Verification.

8.12.1 Post-test < 5.0% of the calibration gas Each test when values are Invalidate data
System value using a calibration gas below 20 ppmv since previous
Verification – between 5 and 25 ppmv System
Low Emitter Verification.
Verification

10.0 Calibration and Standardization

10.1 You must operate the instrument per the manufacturer’s recommendations and as described in Section
8. The system verification described in Section 8.10 is required and must meet the specifications in Section 13
before you start the test. Then, after the test commences, you must perform the ambient air rinse after each run
and recalibrate as specified in Section 8.11. Finally, you must perform the post-test System Verification in
Section 8.12 as defined.
10.2 You must include a copy of the manufacturer's certification of the calibration gases used in the testing as
part of the test report. This certification must include the 13 documentation requirements in the EPA Traceability
Protocol for Assay and Certification of Gaseous Calibration Standards, September 1997, as amended August 25,
1999. When Method 205 is used to produce diluted calibration gases, you must document that the specifications

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for the gas dilution system are met for the test. You must also include the date of the most recent dilution system
calibration against flow standards and the name of the person or manufacturer who carried out the calibration in
the test report.

11.0 Analytical Procedures

Because sample collection and analysis are performed together (see Section 8), additional discussion of the
analytical procedure is not necessary.
12.0 Calculations and Data Analysis
12.1 Nomenclature.

Where as:

C = concentration measured, ppm or %

CS = concentration of calibration gas, ppm or %
CE = calibration error, %
CNOG = concentration of NO span gas, ppm NO,
CNOS = concentration of NO in stack gas, ppm NO,
CCOS = concentration of CO in stack gas, ppm CO,
CCOG = concentration of CO span gas, ppm NO2,
CNO2S = concentration of NO2 in stack gas, ppm NO2, and
CNO2G = concentration of NO2 span gas, ppm NO2, and
CNOxS = concentration of NOx in stack gas, ppm NOx.
ICO = CO interference response, %,
INO = NO interference response, %,
RCO-NO = CO response to NO span gas, ppm CO,
RCO-NO2 = CO response to NO2 span gas, ppm CO,
RNO-NO2 = NO response to NO2 span gas, ppm NO,
TCA = Thermal check ambient temperature
TCS = Thermal check sensor temperature
TAF = Ambient temperature (final)
TAI = Ambient temperature (initial)
TSF = Sensor Temperature (final)
TSI = Sensor Temperature(initial)
ZCE = Zero calibration error
12.2 Thermal Check.
Equation OTM 39-1 TCs = TSF - TSI
Equation OTM 39-2 TCA = TAF - TAI

12.3 Calibration Error.

Cs - C
Equation OTM 39-3 CE = 𝑥𝑥 100
Cs
C
Equation OTM 39-4 ZCE = x 100
Cs

12.4 Interference Response.

RCO-NO CNOS RCO-NO2 CNO2S
Equation OTM 38-5 ICO = ��
CNOG
𝑥𝑥
𝐶𝐶COS
�+�C
NO2G
𝑥𝑥
CCOS
�� x100
RNO-NO2 CNO2S
Equation OTM 38-6 INO = �
CNO2G
𝑥𝑥
𝐶𝐶NOxS
� x100
13.0 Method Performance
13.1 Zero Calibration Error. The requirement for the zero-calibration error is that the CO, NO, and NO2

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OTM 039

response must be ≤3.0% of the calibration gas. The O2 response must be ≤ 0.3% O2.
13.2 Linearity Verification. For the zero, mid-level, and span gases; the absolute value of the difference
between the gas value and the analyzer response shall not be greater than 2.5% of the span gas.
13.3 System Verification.
13.3.1 Response Time. The time in seconds it takes to achieve 90% of the full calibration gas
value shall be no greater than 2 minutes.
13.3.2 Stability Check. The difference in the recorded pollutant or diluent concentrations at
300 and 240 seconds must be less than one percent of the calibration gas concentration.
13.3.3 Calibration. The measured values of the pollutant response observed (every 10
seconds) during the stability check. This value must be within 5.0% of the calibration gas
value.
13.3.4 Low-emitter Verification. If the NO measurements are expected to be < 20 ppm, the
NO response must be within 5.0% of the low-level calibration gas value.
14.0 Pollution Prevention
(reserved)
15.0 Waste Management
(reserved)
16.0 References
16.1 Pipeline Research Council International (PRCI) PR-312-14206-R01, “Technical Considerations for
Developing a New Electrochemical Cell Portable Analyzer Test Method,”
16.2 Table 10.1 Testo 350 Combustion & Emission Analyzer Instruction manual, p. 104, 105 0970 3519 en
02 V01.00 en_US
16.3 EPA Methods from 40 CFR Part 60, Appendix A
Method 3A – Determination of Oxygen and Carbon Dioxide Concentrations in Emissions from
Stationary Sources (Instrumental Analyzer Procedure)
Method 7E – Determination of Nitrogen Oxides Emissions from Stationary Sources (Instrumental
Analyzer Procedure)
Method 10 – Determination of Carbon Monoxide Emissions from Stationary Source
Method 20 – Determination of Nitrogen Oxides, Sulfur Dioxide, and Diluent Emissions from
Stationary Gas Turbines
16.4 EPA Methods from 40 CFR Part 63, Appendix A:
Method 301 – Field Validation of Pollutant Measurement Methods from Various Waste Media
16.5 EPA Methods from 40 CFR Part 75, Appendix H:
Revised Traceability Protocol No. 1: Protocol G1 and G2 Procedures

17.0 Tables Diagrams Flowcharts and Validation Data

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OTM 039

Figure 17-1 System Verification Assembly.

Figure 17-2. Example system performance -test checks cycle CO, NO.

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OTM 039

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OTM 039

Figure 17-3. Sequence for Electrochemical Sensor and Gas Analyzer System Performance Check for
NO2

Figure 17-4 Example Data Sheet – Equipment Verification

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OTM 039

Figure 17-5 Example Data Sheet - System warm-up, leak check, and filter/scrubber checks

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OTM 039

Figure 17-6 Example Data Sheet - System Verification

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