Manual Detector Fluorescencia
Manual Detector Fluorescencia
Manual Detector Fluorescencia
Before using the instrument, read the safety instructions and precautions carefully. Be sure to observe the safety instructions in this manual and the WARNING/CAUTION labels on the instrument. Keep this manual in a safe place nearby so it can be referred to whenever needed.
Copyright
NOTICE: 1. Information contained in this document is subject to change without notice for improvement. 2. This manual is copyrighted by Hitachi High-Technologies Corporation with all rights reserved. No part of this manual may be reproduced, transmitted or disclosed to a third party in any form or by any means without the express written permission of Hitachi High-Technologies Corporation. 3. This document does not provide any warranty or permission for industrial properties or any rights to grant license lawfully and without infringement.
PREFACE
Thank you very much for purchasing Chromaster 5440 FL Detector. The Chromaster 5440 FL Detector is specifically designed for fluorescence detection of sample components in a liquid chromatograph system. Note that physiologically or biologically active samples are not applicable to the Chromaster 5440 FL Detector because of possible infection with bacteria or viruses. This product is intended for use by persons having a basic knowledge of chemical analysis. Remember that improper use of analytical instruments, chemicals or samples would result not only in wrong analytical data but also in consequences adverse to safety. Note that it is allowed only for persons having a basic knowledge of chemical analysis procedures to use this instrument. Carefully read this instruction manual before attempting operation. For proper use of the software, please acquaint yourself with it. The liquid chromatograph system comprises a pump unit for delivering mobile phases, a sample introduction unit for injecting samples (autosampler, manual injector), a column unit for separating components of each sample, a column oven unit for maintaining the column at a constant temperature, and a detector unit for detecting separated sample components as electric signals. Before using the liquid chromatograph system, read carefully the instruction manual accompanying each of these units so that you can carry out analysis properly.
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IMPORTANT
Warranty on Product
Limited Warranty The Chromaster 5440 FL Detector is warranted to be free from defects in material or workmanship under normal use within the product specifications indicated in this manual and under conditions given below. This warranty is void if the software is not used according to the instruction manual. The manufacturer makes no warranties, either express or implied, except as provided herein, including without limitation thereof, warranties as to marketability, merchantability, for a particular purpose or use, or against infringement of any patent. No oral or written information or advice given by the manufacturer, its dealers, distributors, agents or employees shall create a warranty or in any way increase the scope of this warranty. Scope of Warranty Any parts which prove to be defective in design or workmanship during the warranty period will be repaired, adjusted or replaced without charge. A substitute part may be used for repair, or replacement with an equivalent product may be made instead of repair. Such system components as a personal computer and printer to be updated frequently for improvement may not be available in original versions at the time of replacement. Note that this warranty does not apply to the instrument after it is discarded, or if modified by the user or resold without permission from the manufacturer, consumable parts, and any failure of lifetime-expired parts. The manufacturer assumes no liability for any damage to data or application software due to any possible fault or failure of this instrument. Warranty Period One year from the date of initial installation. (In case a separate warranty document has been issued, the warranty period indicated in it takes precedence over the above period.)
IMPORTANT - 1
Warranty Limitations and Exclusions Disclaimer of Warranty THE MANUFACTURER MAKES NO WARRANTIES, EITHER EXPRESS OR IMPLIED, EXCEPT AS PROVIDED HEREIN, INCLUDING WITHOUT LIMITATION THEREOF, WARRANTIES AS TO MARKETABILITY, MERCHANTABILITY, FOR A PARTICULAR PURPOSE OR USE, OR AGAINST INFRINGEMENT OF ANY PATENT. IN NO EVENT SHALL THE MANUFACTURER BE LIABLE FOR ANY DIRECT, INCIDENTAL OR CONSEQUENTIAL DAMAGES OF ANY NATURE, OR LOSSES OR EXPENSES RESULTING FROM ANY DEFECTIVE PRODUCT OR THE USE OF ANY PRODUCT. NO ORAL OR WRITTEN INFORMATION OR ADVICE GIVEN BY THE MANUFACTURER, ITS DEALERS, DISTRIBUTORS, AGENTS OR EMPLOYEES SHALL CREATE A WARRANTY OR IN ANY WAY INCREASE THE SCOPE OF THIS WARRANTY. Note that the following cases are excluded from the scope of this warranty, i.e., these cases are beyond the coverage of free-of-charge repair even during the warranty period indicated above. (a) Failure due to operation at a place not meeting the installation requirements specified by the manufacturer. (b) Failure due to power supply voltage/frequency other than specified by the manufacturer or due to abnormality in power supply. (c) Corrosion or deterioration of the tubing due to impurities contained in reagent, gas, air or cooling water supplied by the user. (d) Corrosion of the electric circuits or deterioration of the optical elements due to highly corrosive atmospheric gas. (e) Failure due to use of software, hardware or spare parts not supplied by the manufacturer. (f) Failure due to use not described in the manual or improper repair not approved by the manufacturer. (g) Failure due to maintenance or repair by other than service personnel qualified by the manufacturer. (h) Failure due to relocation or transport conducted not under the supervision of the manufacturer after the initial installation of the instrument. (i) Failure due to disassembly, modification or relocation not approved by the manufacturer. (j) Failure due to acts of God, including fire, earthquake, storm, flood, lightning, social disturbance, riot, crime, insurrection, terrorism, war (declared or undeclared), radioactive pollution, contamination with harmful substance, etc.
IMPORTANT - 2
(k) Failure of the hardware, or damage to the system software, application software, data or hard disk due to computer virus infection. (l) After disposal of this instrument, after its resale without prior approval from the manufacturer, consumable parts, and failure of any part that have reached the end of its service life. (m) Failure due to a life-limited part that has exceeded the end of its useful lifetime. Limitations of Liability Hitachi High-Technologies shall not be liable in contract or in tort (including, without limitation, negligence, strict liability or otherwise) for claims by third parties (other then for bodily injury or property damage), for economic losses of any kind or for any special, incidental, indirect, consequential, punitive or exemplary damages, arising in any way out of the performance of, or failure to perform, this instrument, even if Hitachi High-Technologies could foresee or has been advised of the possibility of such damages. Disclaimer of Liability for Industrial Properties of a Third Party Hitachi High-Technologies does not assume any liability for a third partys complaint regarding infringement of any patent rights or industrial properties with respect to products manufactured through use of the equipment supplied by Hitachi High-Technologies or its related companies or application of said instrument.
IMPORTANT - 3
(b) A maintenance & service contract is available for servicing the instrument after the warranty period has ended (service available at charge). (c) Maintenance parts and consumables will be supplied during the useful life of this instrument (7 years). And even though parts and/or units (when available) will continue to be supplied after the specified useful life has ended (for up to 10 years), they are not intended to extend the useful life of the instrument. Also, substitutes may be supplied in the event of discontinuance of manufacture of certain parts or units. (d) Some main components of the instrument other than maintenance parts and consumables may not be available in the event of discontinuance of manufacture of the main unit. If repair cannot be provided in the case of instrument malfunction, we recommend that you consider discontinuing use and replacing the instrument.
IMPORTANT - 4
IMPORTANT - 5
If you need to discard this product or discard user serviceable parts: Please contact your local sales representative or distributor who will inform you of the recycle of the product. You might be charged for the costs arising from take-back and recycling. 2. In other Countries outside the EU
If you wish to discard this product, please contact your local authorities and ask for the correct method of disposal.
Other Precautions
Handling of Chemicals and Samples (a) The user is responsible for following relevant laws and regulations in handling, storage and disposal of chemicals and samples used in analytical operation with this instrument. (b) Reagents, standard solutions and accuracy-control samples shall be handled, stored and discarded as instructed by the respective suppliers. (c) Physiologically or biologically active samples are not applicable to this instrument because of possible infection with bacteria or viruses.
IMPORTANT - 6
Disturbance by Electromagnetic Wave This instrument conforms to Class A in the EN standards EN61326 (first edition 2002-02). Avoid installing this instrument near equipment whose data will be affected by electromagnetic noise within the permissible range of this standard. Also, data of this instrument may be affected by electromagnetic noise or the instrument itself may malfunction. In the room where this instrument is installed, the following electric devices must not be brought: Devices which emit radio waves such as mobile phone, transceiver, wireless telephone and similar small-power device. Trademark Acknowledgments EmpowerTM are registered trademarks or trademarks of Waters Corporation USA.
IMPORTANT - 7
SAFETY SUMMARY
Before using the Chromaster 5440 FL Detector, be sure to read the following safety instructions carefully. The hazard warnings which appear on the warning labels on the product or in the manual have and signal word one of the following alert headings consisting of a safety alert symbol WARNING or CAUTION. : The alert symbol shown at left precedes every signal word for hazard warnings, and appears in safety-related descriptions in the manual. To prevent possible hazards or injury, be sure to follow the safety precautions preceded by this symbol. Indicates a potentially hazardous situation which, if not avoided, will or can result in death or serious injury. Indicates a potentially hazardous situation which, if not avoided, will or can result in minor or moderate injury.
WARNING : CAUTION :
The following signal word NOTICE or NOTE is used to indicate precautionary instructions concerning possible property damage. NOTICE Used to indicate a potentially hazardous situation which, if not avoided, will or can result in damage to users property, serious damage to the instrument, damage to data, or environmental pollution, though personal injury may not be incurred. Used to indicate explanatory information for ensuring proper instrument operation and accurate measurement while preventing any possible damage to the instrument.
NOTE
Be sure to observe the precautionary instructions in the manuals accompanying the instrument. Do not perform any operation or action other than described in these manuals. On occurrence of any trouble in the instrument, notify the nearest sales service representative of Hitachi High-Technologies. Keep in mind that the hazard warnings in the manuals or on the product cannot cover every possible case, as it is impossible to predict and evaluate all circumstances beforehand. Always be alert and use your common sense.
SAFETY - 1
SAFETY SUMMARY
General Safety Precautions
Safety Precautions During Use
WARNING
If an abnormal condition such as unusual noise, odor or fumes occurs during operation of the instrument, the power supply should be turned off immediately. Disconnect the power cord plug from the power outlet. Then, after providing proper safety measures as required, contact the nearest service representative of Hitachi High-Technologies. Using the instrument in such an abnormal condition could result in an electric shock or fire.
WARNING
The internal CD-ROM or CD-R/W drive of the PC is provided with a laser beam source. In normal operation of the PC containing the laser beam source, no laser beam harmful to human health will be emitted outside. Note, however, that if a laser beam leaking out of the PC accidentally gets into the eye, eye injury could occur. When using the PC, carefully read the laser-related safety precautions described in the PC manual. Be sure to observe these instructions and the following precautions:
(a) Do not open the panel of the laser device. There are no user-serviceable parts
inside.
(b) On any other laser device, do not attempt to operate or adjust.
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SAFETY SUMMARY
WARNING precautions in the Manual WARNING
Ignition of Flammable Chemicals This instrument is not explosion-proof. In unattended operation, do not use organic solvents having an ignition point below 70 C (Section 3.6, 4.4) Beware of ignition hazard when using flammable chemicals such as organic solvents.
(a) Do not bring a heat or flame source near the instrument. (b) Well-ventilate the laboratory room where the instrument is used. (c) Always check the following conditions. If an abnormality is found, stop operation
immediately. Leakage of solvent or waste solution. Leakage of solvent inside the instrument.
(Section 3.6, 4.4) When using flammable chemicals, be careful about possible ignition due to static electricity. To prevent the build-up of static electricity, use a conductive container for waste solution employ and provide proper grounding connection to it. (Section 3.6, 4.4)
Explosion of Vapor from Flammable Chemicals If a flammable chemical such as organic solvent leaks from the flow path of the instrument and its vapor concentration reaches the explosion limit, it could cause spontaneous combustion with dangerously explosive results. When using a flammable and readily volatile chemical, be sure to check for leakage from the instrument flow path and ventilate the laboratory room adequately. (Section 3.6, 4.4)
SAFETY - 3
SAFETY SUMMARY
WARNING precautions in the Manual(Continued) WARNING
Electric Shock due to Contact with Inside of Instrument When removing the pump cover for part replacement, etc., there is a risk of electric shock. Be sure to turn OFF the power switch and disconnect the power cord from the receptacle in advance. (Section 5.2) Electric Shock due to Improper Grounding This instrument is designed in conformity with the specifications of Class I in Annex H of the IEC 61010-1 (International Electrotechnical Commission Standards) Issue 1. To prevent an electric shock hazard, provide a proper grounding connection.
(a) Be sure to use the grounded 3P power cable, which is supplied as a standard
accessory for the instrument. The use of a different type of power cable may result in an electric shock hazard. Connect the 3P power cable to a grounded 3P power outlet.
(b) If a grounded 3P power outlet is not available, use a grounded 3P table tap or a
3P-2P adapter. In this case, be sure to provide proper grounding connection. For grounding connection, use a screw having a diameter of M4 or higher and a turn count of 3 or more in threading, and a wire having a thickness of 1.25 mm. (APPENDIX 1) Inflammation or Injury due to Toxic, Corrosive or Stimulative Solvent When using a toxic, corrosive or stimulative solvent, be careful not to incur a physical inflammation or injury. For details of the properties of each solvent and how to handle it, refer to the relevant Material Safety Data Sheets (MSDS). Be sure to handle each solvent properly.
(a) Wear proper protective clothes (e.g., safety goggles) so that a solvent will not
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SAFETY SUMMARY
WARNING precautions in the Manual(Continued) WARNING
Injury due to Xenon Lamp Explosion [In use] When the cumulative turn-on time of the xenon lamp exceeds the guaranteed useful lifetime, the electrodes evaporate and the scattered matter sticks to the bulb wall, so its blackening progresses and heat dissipation is hindered. As a result, the internal bulb temperature (pressure) will rise abnormally to cause a danger of burst, etc. Replace the xenon lamp with a new one before its cumulative turn-on time exceeds the guaranteed useful lifetime.
P/N J851152 J851153 Part Name 150 W xenon lamp Long-life xenon lamp Useful Lifetime 500 hours 1,000 hours
(Section 3.5) [At replacement] Before removing the xenon lamp for replacement, turn off the xenon lamp (turn off power to the instrument) and then wait for at least one hour until the xenon lamp becomes sufficiently cool to reduce its internal pressure the normal safety level. (Section 5.2) If a strong shock or impact is applied to the xenon lamp or if the surface of its quartz glass part is scratched, it may explode and scatter glass pieces, resulting in personal injury. Be sure to wear proper protective gear such as safety goggles, safety mask, thick long sleeves, and gloves when handling the xenon lamp. (Section 5.2) [At mounting] When loosening or tightening the retaining nut for the xenon lamp, be careful not to apply excessive force to its glass bulb part. Never hold and turn the glass bulb part for loosening/tightening. (Section 5.2)
SAFETY - 5
SAFETY SUMMARY
WARNING precautions in the Manual(Continued) WARNING
Injury due to Xenon Lamp Explosion [At mounting] (Continued) Do not touch the quartz glass part of the xenon lamp with bare hands. If the quartz glass part of the xenon lamp is contaminated with dust or fingerprints, wipe it using a gauze sheet or absorbent cotton cloth slightly moistened with high-quality alcohol. If the xenon lamp is turned on with dust or fingerprints left on the surface of the quartz glass part, it may cause contamination burn-in to decrease the mechanical strength of the glass part, resulting in explosion of the xenon lamp. (Section 5.2) Be sure to mount the xenon lamp in the specified direction. If the mounting direction (polarity) is wrong, the cathode will be consumed significantly to disable turn-on of the lamp. Mount the lamp so that the '+' (anode) mark on it will be positioned at the support metal of the lamp holder. If the lamp with its cathode consumed excessively is used continuously, pressure inside the lamp bulb may become too high, causing possible explosion. To prevent this, replace the lamp with a new one immediately if its cathode has been consumed substantially. (Section 5.2) If the nut on the lamp base and wiring part is loose, the contact resistance between them will increase due to poor contacting. This could generate a large amount of heat to make the lamp extremely hot, resulting in possible explosion. To prevent this, be sure to tighten the nut securely. (Section 5.2) [At disposal] The xenon lamp is filled with high-pressure gas (approx. 1 MPa at room temperature, approx. 4 MPa under operating condition), and this high-pressure gas still remains in the xenon lamp after it is demounted for replacement.For disposal of the used xenon lamp, wrap it with a thick cloth (e.g., triple-folded cotton cloth) completely and crush its glass part with a hammer or the like. Then, discard the xenon lamp as a dangerous waste item properly. If the xenon lamp is discarded without being crushed, it could explode due to possible impact at the time of disposal, scattering glass pieces to cause personal injury. (Section 6.2)
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SAFETY SUMMARY
CAUTION Precautions in the Manual CAUTION
Touching Hot Part Could Result in Burns The light source lamp and its cover become hot during operation and remain hot for a while even after power-off. They can severely burn you if touched. Before replacement of the lamp, turn power off and wait for about 30 minutes until it cools down sufficiently. (Section 5.2) Direct Gazing at Illuminating Xenon Lamp Could Cause Eye Damage The xenon lamp radiates intense ultraviolet light when it is on. If you look at the illuminating xenon lamp during coarse adjustment of its position, your eyes could be damaged. Do not look at the xenon lamp directly when it is lit. Be sure to wear tinted safety glasses to prevent possible eye damage. (Section 5.2) Heavy Instrument This instrument weight as much as 23 kg. When carrying this instrument, exercise care not to incur injury by dropping it accidentally. Be sure to hold the right and left parts of the instrument securely when moving it. (Section 2.1) Prevention of Instrument Tipover Personal injury could be incurred if the instrument tips over. When installing the instrument, provide a proper means for preventing the instrument from tipping over accidentally. (APPENDIX 1) Fatigue due to Long-Hour Operation If you keep working with the display monitor and keyboard for long hours, your eyes and body will be fatigued to jeopardize your health. When working with the display monitor for a long time, take a break for 10 to 15 minutes per hour for health of your eyes and body. (Chapter 3)
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SAFETY SUMMARY
WARNING and CAUTION Labels on Instrument
The warning labels shown below are attached on the Chromaster 5440 FL Detector. Read the warning labels carefully, and check the instructions on them to attain a clear understanding with reference to actual parts. Periodically check the appearances of these warning labels to see if they are clean to allow easy reading over a safe distance. If any one of the warning labels becomes illegible due to deterioration, contact your local Hitachi High-Technologies Corporation sales representative or service office of Hitachi High-Technologies Corporation sales representative for replacement with a new one.
Rear panel
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SAFETY SUMMARY
WARNING and CAUTION Labels on Instrument
(3) Explosion of Vapor from Flammable Chemicals
(4) Electric Shock due to Contact with Light
Front View
(4) Ignition of Flammable Chemicals
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SAFETY SUMMARY
WARNING and CAUTION Labels on Instrument
(7) Before Turning on Xenon Lamp
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SAFETY SUMMARY
NOTICE
Precautions on Use of Solvents Fluororesin, PEEK, quartz and SUS316 materials are used for the wetted parts of the instrument. Never use solvents that would corrode these materials. This instrument has internal parts made of materials that could be corroded by strongly acidic solutions, strongly alkaline solutions or organic solvents. Take care not to spill these corrosive solutions or solvents into the inside of the instrument. If a corrosive solution or solvent spills inside, wipe it off immediately. For use of the liquid leak sensor, follow the instructions given below.
(a) Turn on the leak sensor function when feeding a solvent. (b) The leak sensor function may remain inactive in cases where the amount of leakage
precautions
is too small. Furthermore, leakage of a highly volatile solvent may not be detected. Be sure to check for liquid leakage regularly to prevent a possible serious accident regardless of whether the leak sensor is activated or not.
(a) In routine inspection of the instrument, visually check for liquid leakage before
attempting measurements.
(b) In periodic inspection of the instrument, check that the leak sensor works normally.
(Section 2.5) Referring to the instruction manual accompanying each module unit of the liquid chromatograph system, set up the automatic liquid feed stop function (such as the pressure limiter function of the pump unit) to prevent a possible trouble. (Section 4.3)
Disposal of Waste Solution Be sure to collect waste solution and treat it for proper disposal in accordance with the relevant laws and regulations regarding water pollution control and sewage treatment. Improper treatment of waste solution may result in environmental pollution and could also lead to a penalty.
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SAFETY SUMMARY
NOTICE precaution (Continued)
Accuracy and Precision of Measured Values Carry out periodic inspection and check whether the system is operating normally. If necessary, conduct measurement on a control sample. Possible Carryover When examining the results of measurements, take account of the possibility of occurrence of a carryover. Otherwise, a correct judgment may not be formed. Since fluororesin and quartz materials are used for the wetted parts of piping, particular attention should be paid when analyzing samples that are likely to be adsorbed by these materials.
Before Turning on Xenon Lamp Again After the xenon lamp is turned off, it remains very hot for a while. Under this condition, it is not allowed to turn on the xenon lamp again for measurement. Before turning on the xenon lamp again, wait for at least five minutes.
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CONTENTS
PREFACE ...............................................................................................................1 ABOUT THIS MANUAL ..........................................................................................2 IMPORTANT .....................................................................................IMPORTANT-1 Warranty on Product ................................................................IMPORTANT-1 Installation, Relocation and After-sale Technical Service ....IMPORTANT-3 Technical Seminars and Training Courses for Users ...........IMPORTANT-4 Estimated Life time of the Instrument.....................................IMPORTANT-4 Caution on Disposal of Instrument .........................................IMPORTANT-5 Disposal of This Instrument and Its Parts ..............................IMPORTANT-5 Precautions on CE Conformity Marking .................................IMPORTANT-5 Other Precautions.....................................................................IMPORTANT-6 SAFETY SUMMARY ........................................................................ SAFETY-1 General Safety Precautions ........................................................... SAFETY-2 WARNING Precautions in the Manual ........................................... SAFETY-3 CAUTION Precautions in the Manual ............................................ SAFETY-7 WARNING and CAUTION Labels on Instrument........................... SAFETY-8 NOTICE Precautions....................................................................... SAFETY-11
1. OUTLINE ................................................................................................................ 1-1 1.1 Isocratic System .......................................................................................... 1-1 1.2 Low-Pressure Gradient System .................................................................. 1-2 FUNCTIONS ........................................................................................................... 2-1 2.1 Name and Function of Each Part on FL detector ...................................... 2-1 2.2 Name and Function of Each Part on UI Pad (Option)................................ 2-3 2.3 Description of Fluorometry ......................................................................... 2-6 2.3.1 Principle of fluorometry .................................................................... 2-6 2.3.2 Advantages of fluorometry ............................................................... 2-8 2.3.3 Notes on fluorescence analysis........................................................ 2-11 2.3.4 Principle of operation ....................................................................... 2-16 2.3.5 Features of light source ................................................................... 2-17 2.4 Specifications .............................................................................................. 2-17 OPERATION .......................................................................................................... 3-1 3.1 Basic Operation ........................................................................................... 3-1 3.1.1 Power supply ................................................................................... 3-1 3.1.2 Parameter setting............................................................................. 3-4 3.1.3 Auto Zero adjustment....................................................................... 3-6
2.
3.
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3.2
3.3
3.4
3.5
3.6
3.7
3.1.4 Wavelength setting .......................................................................... 3-6 3.1.5 Shutdown procedure ........................................................................ 3-7 3.1.6 Flushing the flow cell after use......................................................... 3-7 UTLTY Setting .............................................................................................. 3-8 3.2.1 Offset setting ................................................................................... 3-8 3.2.2 Time constant setting....................................................................... 3-9 3.2.3 Use time progrum setting ................................................................. 3-10 3.2.4 PMT voltage setting ......................................................................... 3-11 3.2.5 Other settings .................................................................................. 3-12 GLP Functions ............................................................................................. 3-17 3.3.1 Xe lamp logbook data display .......................................................... 3-17 3.3.2 Xe lamp logbook data resetting........................................................ 3-18 3.3.3 Hg lamp logbook data display .......................................................... 3-20 3.3.4 Hg lamp logbook data resetting ....................................................... 3-21 3.3.5 Key lock setting................................................................................ 3-23 3.3.6 Wavelength accuracy check by using Hg lamp ................................ 3-24 3.3.7 Xe lamp energy check ..................................................................... 3-25 Operating Instructions ................................................................................ 3-27 3.4.1 Time program setting ....................................................................... 3-27 3.4.2 Time program starting...................................................................... 3-33 3.4.3 Time program stopping .................................................................... 3-33 3.4.4 Time program operation examples................................................... 3-33 3.4.5 Spectrum measurement................................................................... 3-37 3.4.6 Recorder and spectrum output factors setting.................................. 3-41 3.4.7 Marker operation.............................................................................. 3-45 Set Up Setting .............................................................................................. 3-46 3.5.1 Communication channel (CH) setting............................................... 3-46 3.5.2 Thermo cell setting........................................................................... 3-47 3.5.3 Liquid crystal display contrast setting ............................................... 3-49 3.5.4 Standard xenon lamp lifetime setting ............................................... 3-50 Before Performing Analysis ........................................................................ 3-52 3.6.1 Selection of mobile phase and cautions on handling........................ 3-53 3.6.2 Characteristics of organic solvents................................................... 3-56 3.6.3 Cautions on static electricity............................................................. 3-60 Preparation................................................................................................... 3-61 3.7.1 Degassing and removing dust from mobile phase............................ 3-61 3.7.2 Degassing mobile phase.................................................................. 3-61 3.7.3 Removing dust from mobile phase................................................... 3-64 3.7.4 Sample pretreatment ....................................................................... 3-65
4.
MAINTENANCE AND TROUBLESHOOTING ........................................................ 4-1 4.1 Operational Check ....................................................................................... 4-1 4.2 Performance Checks ................................................................................... 4-1 4.2.1 Xe lamp energy check ..................................................................... 4-1 4.2.2 Wavelength accuracy check by using Hg lamp ................................ 4-2
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4.3
4.4
4.5 4.6 5.
4.2.3 Sensitivity check .............................................................................. 4-2 4.2.4 Wavelength accuracy check and calibration .................................... 4-15 4.2.5 Leak sensor check ........................................................................... 4-18 4.2.6 Drain tray check ............................................................................... 4-20 Periodic Checks ........................................................................................... 4-21 4.3.1 Xe lamp energy check ..................................................................... 4-21 4.3.2 Wavelength accuracy check using Hg lamp..................................... 4-21 4.3.3 Lamp logbook check ........................................................................ 4-22 Flow Cell Unit Checks ................................................................................. 4-23 4.4.1 Check and washing of flow cell ........................................................ 4-24 4.4.2 Disassembly and cleaning of flow cell .............................................. 4-26 4.4.3 Leakage from the flow cell ............................................................... 4-29 4.4.4 Cautions on storage of the flow cell ................................................. 4-30 Troubleshooting .......................................................................................... 4-31 Error Messages ............................................................................................ 4-33
SPARE PARTS ...................................................................................................... 5-1 5.1 Replacement Parts and Consumables ....................................................... 5-1 5.2 Lamp Replacement ...................................................................................... 5-3 5.2.1 Xe lamp replacement ....................................................................... 5-3 5.2.2 Hg lamp replacement ....................................................................... 5-17 5.3 Fuse Replacement ....................................................................................... 5-20 INDEX .................................................................................................................... 6-1
6.
APPENDIX APPENDIX 1. INSTALLATION ........................................................... APPENDIX1-1 1. Unpacking.............................................................................. APPENDIX1-1 2. Installation Conditions............................................................ APPENDIX1-2 3. Installation Place.................................................................... APPENDIX1-5 4. Installation Environment......................................................... APPENDIX1-5 5. Checking the Contents .......................................................... APPENDIX1-6 6. Assembling ............................................................................ APPENDIX1-7 6.1 Removal of Transport Screws....................................... APPENDIX1-7 APPENDIX 2. DESCRIPTION ON CONTACT SIGNAL COMMUNICATION....................................................... APPENDIX2-1 1. Outline ................................................................................... APPENDIX2-1 2. Contact Signals Entering the e-line connector ....................... APPENDIX2-1 3. Individual Contacts of Each Unit ............................................ APPENDIX2-4 APPENDIX 3. GLOSSARY ................................................................. APPENDIX3-1 FLOWPATH FIGURES................................................................. APPENDIX3-4 1. Isocratic System .................................................................... APPENDIX3-4 2. Low Pressure Gradient System ............................................. APPENDIX3-4
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1.
OUTLINE
The liquid chromatograph system consists of a pump for feeding a mobile phase, a sample introducing section (autosampler, manual injector) for injecting a sample, a column for chromatographic separation of the injected sample, a column oven for maintaining the column at a constant temperature, and a detector section for detecting a signal of a separated component of the sample. In addition, a degassing unit for deaerating an eluent, a gradient device for varying a mixing ratio of eluents with time, and other optional devices are incorporated in the system.
1.1
Isocratic System
The isocratic system has a simple configuration in which singlesolvent analysis is performed.
Chromaster 5440 Fluorescence detector Detector cell
Injection valve Chromaster 5210 Autosampler Wash pump Degassing unit Syringe valve Drain
Fig. 1-1 Isocratic System (1) (2) (3) An eluent is fed by the pump through the degassing unit. A sample is injected from the autosampler. The injected sample is separated through the column which is maintained at a constant temperature by the column oven.
1-1
(4)
Each component separated from the sample is then detected as a signal by the detector.
1.2
Chromaster 5310 Column oven Mixer Organizer Column Injection valve Chromaster 5210 Autosampler Wash pump 4-way joint Degassing unit Proportioning valve Syringe valve Drain
Fig. 1-2 Low Gradient System (1) Each of plural eluents is fed from the degassing unit to the low-pressure unit. In the low-pressure unit, the eluents are mixed at a prespecified ratio. Through the mixer, the mixture eluent is delivered. A sample is injected by the autosampler. The injected sample is separated through the column which is maintained at a constant temperature by the column oven. Each component separated from the sample is detected as a signal by the detector.
(2)
(6)
1-2
2.
2.1
FUNCTIONS
Power switch
Left door
UI pad
Right door
LED
Fig. 2-1 Front Panel Power switch UI pad (option) LEDs : Turns power ON/OFF. : A keypad required for unit operation. : Four LED indicators are provided for indicating the following states.
Doors (upper and lower right/left) : Three doors are provided. Drain tray : A tray for liquid leakage
Designation (Color) CH1 (blue, orange) CH2 (blue, orange) Xe LAMP (blue) PROG. RUN (blue) Blue : Orange : Blue : Orange : Blue Blue : : LED Indication CH1 operation mode. An error has occurred in CH1 operation mode. CH2 operation mode. An error has occurred in CH2 operation mode. Xe lamp is lit. Time program is in execution.
2-1
e-Line
Ground terminal
Fig. 2-2
Rear Panel
Analog signal output unit (Option) :Provides PROCESSOR, RECORDER, MAKER IN terminal. Ground terminal :The terminals for grounding connection (three terminals). Power source connector :Connects the power supply cable. Table 2-2
No. 1 Indication e-line Function 1. Used to transmit the acquired signal (or the acquired spectral data) to other units on the e-line. Also, used to send/receive the instrument parameter data via the e-line. 2. Used for input/output of each contact signal. START IN ERROR IN ERROR OUT BUSY OUT 2 3 LAMP OFF IN AUTO ZERO IN The lamp is turned off by means of a contact signal input. The auto zero function is activated by means of contact signal input.
Input/Output terminal
Remarks 1. The florescence intensity data is output.
2. The program is initiated. An error condition in another instrument is checked. An error condition on this instrument is indicated. The operational status of the instrument is indicated.
2-2
The marker function is activated by means of contact signal input. Analog output for recorder 1. The florescence intensity value at each point of time 2. Stored spectral data Analog output for data processor (integrator) 1. The florescence intensity value at each point of time 2. Stored spectral data
The marker function is started when the short-circuit signal of more than one second is input. The florescence intensity value data is output.
PROCESSOR (option)
2.2
12 13
14
NOTE: Press the ESC key to return to the initial state when you made incorrect operation..
2-3
Table 2-3
No. 1 Indication
A/Z
Key Functions
Function Remarks
Sets display and output to zero at each measuring wavelength. (Auto zero)
WL
SET UP
UTILTY
(1) Sets offset value, time constant, etc (UTILTY). (2) Sets digital communication channel via the e-Line, LCD contrast, and constant temperature flow cell (SET UP) (2) Keep pressing with key simultaneously to change to th setup screen. (2) Press the ESC key to release the key lock.
GLP
(GLP) 5
Selects GLP information. (1) Checks for lamp energy and wavelength accuracy. Displays and resets lamp logbook. (2) Sets the key lock. Selects and sets the time program.
PROG
(Set program) 6
(Arrow)
(1) The monitor screen key: Accesses the previous screen. key: Accesses the next screen. (2) Editing program key: Displays the previous screen. Indicates the last line if it is the first line. key: Displays the next screen. Indicates the first line if it is the last line. (1) Starts the time program. (2) Starts analog output of the stored spectrum. (2) Valid only when connect to the analog signal output unit.
START 7 (Start)
STOP 8 (Stop)
(1) Stops the time program. (2) Stops analog output of the stored spectrum.
2-4
No. 9
Function Used to specify the recorder full-scale range, recorder output speed, and output data.
Remarks
10
SPECT 5 (Spectrum)
Obtains spectrum over a specified wavelength range and stores the spectrum in memory.
11
MARKER 1 (Marker)
12
(1) Used to return from data input mode to the monitor screen. (2) Used to interrupt the recording of the spectrum. (3) Used to release the key lock when keys are locked.
13
DEL (Delete)
Deletes the step which the cursor is pointed while editing a time program. Deletes the step which the cursor is pointed in the input part of TIME. Deletes the item when the cursor points a part other than the input part of TIME. When the ESC key is pressed while - is displayed on the screen, the screen returns to the monitor screen, and cancels the DEL key processing. - is displayed after pressing the DEL key, and the processing will be determined by pressing the ENT key. Accepts entered information.
14
ENT (Enter)
15
CL (Clear)
(1) Used to remove the present data input on the display before the ENT key is pressed (e.g. to erase incorrect data). (2) Also used to reset system when an error condition is indicated.
2-5
2.3
Description of Fluorometry
Excitation
Fluorescence or Phosphorescence Stable condition (Ground state) Radiationless transition 3 2 1 Excited state V = 0 Excited triplet state Light Light Unstable condition (Excited state) Radiationless transition
Excitation light
Fig. 2-4
Figure 3-4 shows the energy level transitions of an organic molecule for the various processes involved in absorption, fluorescence and phosphorescence.
2-6
When light strikes an organic molecule in the ground state, it absorbs radiation of specific wavelengths and several excited states are populated. A part of the excitation (absorbed) energy is lost in vibrational relaxation, i.e. radiationless transition to the lowest vibrational level in the excited state. The molecule can return to the ground state by; (1) (2) Emitting radiation (Fluorescence) Undergoing a radiationless transition to populate the triplet state. The triplet state can emit radiation (Phosphorescence). Generally phosphorescence persists for 10-4 seconds or longer due to the selection rule imposed on the triplet-to-singlet transition. In contrast, fluorescence takes place over a period of 10-8 to 10-9 seconds. Going through a radiationless transition to return directly to the ground state.
(3)
Since a part of the radiation absorbed by the substance is lost as vibrational energy; the energy emitted by the excited state is less than that absorbed by the compound (i.e. the fluorescence wavelength is longer than the excitation wavelength, *Stokes Law). The ratio of the number of photons emitted during fluorescence to the number of photons absorbed is called the quantum efficiency of fluorescence (Fluorescence Yield). If two compounds absorb the same number of photons, the fluorescence intensity of the compound with the larger fluorescence quantum yield will be greater than that from a compound with a lower fluorescence quantum yield. Also, the intensity of the fluorescence emitted by a compound is proportional to the number of photons absorbed by it. Therefore, when a dilute sample is used, the intensity of fluorescence is expressed by: F = KIocl F K Io c l : : : : : : : Fluorescence intensity Instrumental constant Intensity of exciting radiation Concentration of the compound of interest Optical path length of cell Absorptivity of substance Quantum efficiency of substance
2-7
2.3.2 Advantages of fluorometry For verifying the advantage of fluorometry, the limitation of absorbance measurement in its application to low-concentration samples is explained first. In this discussion, we will consider the detection of a sample that has a transmittance of 99% (relative to the blank). If we assume that the inaccuracy of the % transmittance measurement is 0.1%, the reliability of the observed data is as follows: Percent transmittance of blank Percent transmittance of sample Difference (proportional to concentration of sample) 100.0 0.1% 99.0 0.1% 1.0 0.2%
In this example, the uncertainty in the concentration measurement is 20%. In contrast, in fluorometry, a difference in the signal is directly proportional to the concentration of sample. An analysis of the error in the measurement is as follows: Output signal level at measurement of sample Value corresponding to blank Difference (proportional to concentration of sample) 100 0.1 0 0.1 100 0.2
As is evident from this example, the error percentage by fluorometry is not dependent on sample concentration theoretically, so this method is very advantageous for low sample concentrations. In actuality, some error factors will increase relatively as sample concentration falls extremely, but it can generally be said that fluorometry is capable of detecting concentrations at least 3 digits lower than by absorptiometry.
2-8
A graphical description of why fluorescence can provide better sensitivity than absorbance is presented in Fig. 3-5. In this figure, the signal IS is used to represent the difference between the intensity of the incident beam Io and the intensity of the transmitted beam It in absorptiometry. The detection limit is the point where the difference between It and Io is equivalent to the noise level. In contrast, when fluorometry is used, the observed signal IF is directly proportional to the concentration and the background has a fluorescence of zero. When a small signal is observed it is compared to a very small signal (since the blank does not fluoresce) and is readily amplified for detection. In addition, since the fluorescence emission wavelength is different from the excitation wavelength (incident beam wavelength), scattering due to the excitation radiation is negligible.
High concentration Low concentration Is Is High concentration Low concentration IF
Io
Io IF
Amplification
It
It
In addition to providing high sensitivity, fluorescence detection can provide a fluorescence spectrum and an excitation spectrum (which is very similar to the absorbance spectrum). If the sample contains two compounds, selection of the appropriate excitation and emission wavelengths may be used to provide qualitative and quantitative information about the components in the mixture. This point is described in Fig. 3-6. An attempt to quantitate compound B in a mixture of A and B using absorbance will not be successful because the absorbance spectra of the two compounds overlap at all wavelengths (Fig. 3-6 (a)).
2-9
In contrast, if the fluorescence spectra do not overlap (Fig. 3-6 (b)), quantitative analysis of each compound can be made by selecting the appropriate fluorescence emission wavelength (even if the absorption wavelengths of two components are the same).
Absorption spectra Component A Excitation spectra Component A Fluorescence spectra Component B
Component B
(a)
Absorptiometry
(b)
Fluorometry
Table 3-1 compares the analytical information obtained via absorptiometry and fluorometry.
Table 2-4
2 - 10
2.3.3 Notes on fluorescence analysis (1) Raman Scattering When fluorescence is measured, two additional peaks may appear in the spectrum. The Rayleigh peak appears at the excitation wavelength and is due to scattered light, while the Raman peak appears at longer wavelength than the excitation. The position of the Raman band is dependent on the excitation wavelength, while the position of the fluorescence is independent of the excitation wavelength though its peak height changes. Both Rayleigh and Raman scatterings occur due to a solvent. Take care not to mistake them for fluorescence peaks. Table 3-2 presents the position of the Raman peak for a variety of excitation wavelengths. In liquid chromatography, the Raman scattering appears as a background rise. This means that baseline noise increases to disturb high-sensitivity measurement.
Table 2-5
2 - 11
80
40
Raman scattering
20
Fig. 2-7
(2)
Notes on Handling Samples that Contain a High Concentration of the Compound of Interest When the concentration of the compound of interest is relatively high, various error factors will arise. The greatest factor is that the excitation beam is substantially absorbed near the entrance slit of a cell and it cannot reach the cell center adequately. An extreme situation is shown in Fig. 3-8. Fluorescence is emitted near the entrance slit of a cell, but it will not be taken into the emission monochromator.
Excitation beam
2 - 12
If emission occurs only in the entrance area for excitation beam, such a sample needs to be diluted with an appropriate factor before measurement. The second factor is called concentration quenching where activity is disturbed by interaction of molecules. Another potential error that may occur when fluorescence detection is used is the re-absorption of fluorescence (selfabsorption of fluorescence). An example of this phenomenon is shown in Fig. 3-9. Re-absorption of fluorescence occurs when the tail of the shorter-wavelength side of fluorescence spectrum overlaps the tail of the longwavelength side of the excitation spectrum. When this phenomenon occurs, the fluorescence spectrum appears to be somewhat shifted toward the longer-wavelength. This phenomenon will very rarely cause a substantial error in quantitation when fluorescence detection is used, and should not be a cause for concern.
Excitation spectrum Relative intensity
Fluorescence spectrum
Anyway if a high concentration may have caused a measurement error, dilution with an appropriate factor is necessary.
2 - 13
(3)
Second-order and Third-order Radiation The Raman peak is described as a cautionary item when the excitation and emission wavelengths are comparatively close to each other. Conversely, when these wavelengths are comparatively distant from each other, the analyst should be aware of the second and third-order radiation phenomenon. The second-order radiation occurs at a double wavelength of the excitation beam and the third-order radiation arises at a triple wavelength. For instance, if the excitation wavelength is 240 nm, the second-order and third-order excitation occur at 480 and 720 nm, respectively. To eliminate second and third order radiation, it is simply necessary to place a short-wavelength cutoff filter in the path of fluorescing radiation. When the second and/or third-order radiation poses a particular problem, it is recommended to use the optional filter set accessory. In measurement with a chromatograph, the second and third-order radiation appears as a background rise. Therefore, baseline noise will increase to disturb highsensitivity measurement.
(4)
1) Relative intensity 4) 2) 3) 5)
EX 1) 2) 3) 4) 5)
EX 2 Scattering of excitation beam Raman scattering due to mobile phase Fluorescence of impurity Fluorescence of compound of interest Second-order scattering of excitation beam
Wavelength
Fig. 2-10
2 - 14
In measurement of a fluorescence spectrum, many peaks appear besides that of sample fluorescence. It is necessary to find the correct sample peak according to the explanation given above. (5) Temperature Dependency of Fluorescence Intensity In most cases, the fluorescence intensity decreases by 1 to 2% as the temperature of sample increases by 1 C. It should be noted, however, that in some biochemical samples, the fluorescence intensity decreases by approx. 10% as the temperature of sample increases by 1 C.
2 - 15
Plane mirror
Measuring detector
Photomultiplier high voltage circuit Monitor detector amplifier Operational circuit Recorder or integrator Electrical connection Optical path
The beam from the xenon lamp strikes the excitation monochromator that disperses the radiation. Only radiation of the specified wavelength is allowed to pass through the exit slit. After the exit slit, the excitation radiation strikes the sample. The fluorescence (emitted radiation) enters the emission monochromator, where it is dispersed by the monochromator. The selected radiation strikes the measuring detector. On the other hand, the excitation beam which passed through the sample enters the monitor detector via the diffusion plate.
2 - 16
2.3.5 Features of light source The light source thermally dissociates ozone via the heat generated by the xenon lamp itself. This allows the use of a quartz-bulb xenon lamp that produces intense radiation even in the short wavelength region. As a safety measure against failure or stoppage of the cooling fan, a thermal sensor works to extinguish the xenon lamp in about 15 minutes if the fan stops during analysis at a room temperature of 27 C, or in about 20 minutes if the fan was stopped from the beginning, in order to prevent failure or damage of the instrument.
2.4
Specifications
(1) Optical system: Ratio photometry; intensity of transmitted beam is monitored. Light source: Xe lamp (150 W) Hg lamp (for checking wavelength) Excitation wavelength range: 200 to 850 nm/Zero order
(2)
(3) (4)
Emission wavelength range: 250 to 900 nm/Zero order Photomultiplier must be changed at emission wavelength greater than 731 nm. Spectral bandwidth on excitation side: 15 nm
(5) (6)
Spectral bandwidth on emission side: 15 nm, 30 nm (variable) With this instrument, spectrum bandwidth is defined by halfvalue width. Therefore, in order to separate a spectrum completely, a wavelength interval of 30 nm or more is required. Wavelength setting: By communication (e-line) or keyboard
2 - 17
(10) Recorder output (Option): 10 mV Full scale. Full scale 1 to 1000 FLU (settable in steps of 1). (11) Processor output (Option): 1 V Full scale, digital by e-Line. -40 (-40 mV) to 1000(1000 mV) (12) Response: Changeable in 7 steps corresponding to time constants of 0.01 / 0.02 / 0.05 / 0.1 / 0.5 / 1.0 / 2.0 seconds. (13) Sensitivity: (a) With emission-side spectral bandwidth set at 15 nm S/N ratio for Raman peak of water ........ 700 or more (Baseline method) S/N ratio for Raman peak of water ........ 525 or more (Tangent method) (b) With emission-side spectral bandwidth set at 30 nm S/N ratio for Raman peak of water ........ 900 or more (Baseline method) Wavelength: 350 nm, Time constant: 2.0 s (14) Auto Zero range: (15) Offset range: 0 to 1000 FLU
(16) Spectrum memory: Memorized contents.......................Excitation and fluorescence spectra Number of spectra memorized.......4 Measuring wavelength range .........Changeable in measurement condition setting (17) Marker (Option): Place a marker (0.6 mV) on the recording.
(18) Instrumental conditions setup: Following conditions are set and saved in the memory. Full scale range Spectrum measurement range Photo multiplier applied voltage Offset value
2 - 18
(19) Time program Number of programs............... 9 Settable time........................... Up to 600 minutes in increments of 0.1 minute Number of steps storable........ 100 steps for a total of 9 files Programmable parameters ..... Measurement wavelength (Ex and Em) Baseline processing PMT gain (20) GLP support function: Lamp energy check Wavelength accuracy check Lamp lighting time and replacement record (21) Communication facility: e-Line communication (22) External output terminal (Option): Processor: 1 V Full scale Recorder: 10 mV Full scale (23) External I/O contact terminals: Time Program Start Error Input/Output Busy Output (Above contacts are incorporated in e-Line connector, and effective with analog connection.) Auto Zero Input Lamp Off Input (24) Flow cell: Standard, Constant temperature flow cell (Option) Standard 12 L (irradiated capacity) 1.0 MPa 4 to 35 C (non-condensing)
(26) Flow cell withstand pressure: (27) Operating temperature range: (28) Operating humidity range:
25 to 85% RH
2 - 19
(31) Dimensions:
(32) Weight: Approx. 25 kg NOTE: Please contact your local Hitachi HighTechnologies Corporation sales representative about a purchas of the Thermo cell.
2 - 20
3.
OPERATION
The method of FL detector operation using the optional UI pad is described here.
CAUTION
Fatigue due to Long-Hour Operation If you keep working with the display monitor and keyboard for long hours, your eyes and body will be fatigued to jeopardize your health. When working with the display monitor for a long time, take a break for 10 to 15 minutes per hour for health of your eyes and body.
3.1
Basic Operation
First, turn on the power supply to display the 1st LCD monitor screen. Spend one hour or more for warming up time to stabilize the xenon lamp. The numerical value indicated before input is default values or currently set values.
3.1.1 Power supply The power activation operation of autosampler is described here.
Liquid Crystal Display (LCD) UI pad
Power switch
LED
3-1
NOTE:
If the monitor display screen does not appear on the LCD within 3 minutes after turning on the power, or if an error message appears on the LCD, refer to 5.6 Troubleshooting or 5.7 Error Messages.
1) 2)
Turn on the power switch of the detector. Liquid Crystal Display (LCD) presents the initial screen, which changes to the initializing screen after a few seconds. At the same time, a test for self-diagnosis (initialization) is carried out. * The current channel setting LED and the Xe LAMP LED will light in blue.
<Initial screen>
FL Detector 8928148-00 Hitachi High-Technologies Corp.2010
<Initializing screen>
WL DRIVE & LAMP INITIALIZING
The sequence of wavelength drive (check of reference point for drive), lighting of the lamp and auto zeroing is performed. 3) The first monitor screen will be indicated after initializeprocessing is completed normally. Press monitor screen. Press screen. * key to indicate the second and the third ESC key to return to the first monitor
An error message will be presented if an abnormality occurs during initializing. Check Section 4.6.
3-2
The 1st monitor screen (FL indication) TIME 0.0 Ex 250 Em 350 FL 0.0 PROG 1 LAMP Xe [I]
Emission wavelength
Status Program indicator number Lamp indicator Fluorescence intensity key, key or ESC key