Teledyne 6650 User Manual

UV-Photo-X
OPERATING INSTRUCTIONS FOR
MODEL 6650B
UV-Photo-X Fluorescence Analyzer
P/N M6650
02/15/2006
ECO # xx-xxxx
DANGER
time even after the power is turned off and disconnected. Only authorized personnel should conduct maintenance and/or servicing. Before
conducting any maintenance or servicing, consult with authorized supervisor/manager.
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Model 6650
Copyright © 2006 Teledyne Analytical Instruments
All Rights Reserved. No part of this manual may be reproduced, transmitted, transcribed, stored in a retrieval system, or translated into any other language or computer language in whole or in part, in any form or by any means, whether it be electronic, mechanical, magnetic, optical, manual, or otherwise, without the prior written consent of Teledyne Analytical Instruments, 16830 Chestnut Street, City of Industry, CA 91749-1580.
Warranty
This equipment is sold subject to the mutual agreement that it is warranted by us free from defects of material and of construction, and that our liability shall be limited to replacing or repairing at our factory (without charge, except for transportation), or at customer plant at our option, any material or construction in which defects become apparent within one year from the date of shipment, except in cases where quotations or acknowledgements provide for a shorter period. Components manufactured by others bear the warranty of their manufacturer. This warranty does not cover defects caused by wear, accident, misuse, neglect or repairs other than those performed by Teledyne or an authorized service center. We assume no liability for direct or indirect damages of any kind and the purchaser by the acceptance of the equipment will assume all liability for any damage which may result from its use or misuse.
We reserve the right to employ any suitable material in the manufacture of our apparatus, and to make any alterations in the dimensions, shape or weight of any parts, in so far as such alterations do not adversely affect our warranty.
Important Notice
This instrument provides measurement readings to its use r, an d serves as a tool b y whic h valuable data can be gathered. The information provided by the instrument may assist the user in eliminating potential hazards caused by his process; however, it is essential that all personnel involved in the use of the instrument or its interface, with the process being measured, be properly trained in the process itself, as well as all instrumentation related to it.
The safety of personnel is ultimately the responsibility of those who control process conditions. While this instrument may be able to provide early warning of imminent danger, it has no control over process conditions, and it can be misused. In particular, any alarm or control systems installed must be tested and understood, both as to how they operate and as to how they can be defeated. Any safeguards required such as locks, labels, or redundancy, must be provided by the user or specifically requested of Teledyne at the time the order is placed.
Therefore, the purchaser must be aware of the hazardous process conditions. The purchaser is responsible for the training of personnel, for providing hazard warning methods and instrumentation per the appropriate standards, and for ensuring that hazard warning devices and instrumentation are maintained and operated properly.
Teledyne Analytical Instruments, the manufacturer of this instrument, cannot accept responsibility for conditions beyond its knowledge and control. No statement expressed or implied by this document or any information disseminated by the manufacturer or its agents, is to be construed as a warranty of adequate safety control under the user’s process conditions.
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UV-Photo-X
Safety Messages
Your safety and the safety of others is very important. We have provided many important safety messages in this manual. Please read these messages carefully.
A safety message alerts you to potential hazards that could hurt you or others. Each safety message is associated with a safety alert symbol. These symbols are found in the manual and inside the instrument. The definition of these symbols is described below:
GENERAL WARNING/CAUTION: Refer to the instructions for details on the specific danger. These cautions warn of specific procedures which if not followed could cause bodily Injury and/or damage the instrument.
CAUTION: HOT SURFACE WARNING: This warning is specific to heated components within the instrument. Failure to heed the warning could result in serious burns to skin and underlying tissue.
WARNING: ELECTRICAL SHOCK HAZARD: Dangerous voltages appear within this instrument. This warning is specific to an electrical hazard existing at or nearby the component or procedure under discussion. Failure to heed this warning could result in injury and/or death from electrocution.
Technician Symbol: All operations marked with this symbol are to be performed by qualified maintenance personnel only.
NOTE: Additional information and comments regarding a specific component or procedure are highlighted in the form of a note.
CAUTION: THE ANALYZER SHOULD ONLY BE USED FOR THE
PURPOSE AND IN THE MANNER DESCRIBED IN THIS MANUAL.
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IF YOU USE THE ANALYZER IN A MANNER OTHER THAN THAT FOR WHICH IT WAS INTENDED, UNPREDICTABLE BEHAVIOR COULD RESULT POSSIBLY ACCOMPANIED WITH HAZARDOUS CONSEQUENCES.
This manual provides information designed to guide you through the installation, calibration and operation of your new analyzer. Please read this manual and keep it available.
Occasionally, some instruments are customized for a particular application or features and/or options added per customer requests. Please check the front of this manual for any additional information in the form of an Addendum which discusses specific information, procedures, cautions and warnings that may be peculiar to your instrument.
Manuals do get lost. Additional manuals can be obtained from Teledyne at the address given in the Appendix. Some of our manuals are available in electronic form via the internet. Please visit our website at: www.teledyne-ai.com.
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UV-Photo-X
Table of Contents
Safety Messages ..........................................................................iii
Table of Contents..........................................................................v
List of Figures vii
Introduction ...................................................................................1
1.1 Theory of Operation 1
1.2 Filter Based Flurometer Description 2
Definition of Terms........................................................................4
2.1 Excitation Filter 4
2.2 Emission Filter 4
2.3 Measure Detector 4
2.4 Span Filter 4
2.5 Background Fluorescence 5
2.6 Sensitivity 5
2.7 Specificity 5
2.8 Signal-to-Noise Ratio 5
2.9 Signal-to-Background Ratio 6
2.10 Dynamic Range 6
2.11 Linearity 6
2.12 Process Background 6
2.13 Mode 1 Initialization 6
2.14 Mode 2 Initialization 7
Diagnostics & Controls.................................................................8
3.1 Front Panel Controls 8
Hardware Installation....................................................................9
4.1 Physical 9
4.2 Optical 9
4.3 Electrical 10
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Model 6650
Setup & Operation....................................................................... 12
5.1 First Power-Up Following Installation 13
5.2 Application Engineering 14
5.3 Initialization for Process Monitoring: Mode 2 Operation 15
5.3.1 Case 1: Process monitoring following hardware setup without application engineer 15
5.3.2 Case 2: Process monitoring without application engineering 15
5.3.3 Case 3: Process monitoring following application engineering 16
5.4 Initialization for Process Monitoring: Mode 1 Operation 18
5.5 Adjusting the Display 19
5.6 Adjusting the 20 mA Level 20
5.7 Adjusting the 20 mA Level 21
5.8 Diagnostics 22
5.8.1 Front Panel Lamp Diagnostics 22
5.8.2 Rectifying the Problem: Flashing Yellow Indicators 23
5.8.3 Rectifying the Problem: Red Indicators 24
Specifications.............................................................................. 26
6.1 General Measurement Specifications 26
6.2 Transmitter Specifications 27
6.3 Mechanical Specifications of Analysis Cell/Probe. 28
Appendix...................................................................................... 30
A-1 Application Engineering Assistance 30
A-1.1 Series 1 - Initializing the Unit and Determination of the Probe/Analyzer Signal Level 30
A-1.2 Determination of the Probe/Transmitter Fluorescence in a Non-Fluorescing Liquid: 32
A-1.3 Determination of the Process Fluorescence: 33 A-2 Notes 36 A-3 Recommended 2-Year Spare Parts List 37
Index............................................................................................. 38
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UV-Photo-X
List of Figures
Figure 1-1: Molecular Fluorescence Example.............................1
Figure 3-1: Photo-X Front Panel Controls...................................8
Figure 4-1: Top view of Flurometer............................................11
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DANGER
COMBUSTIBLE GAS USAGE
This is a general purpose instrument designed for usage in a nonhazardous area. It is the customer's responsibility to ensure safety especially when combustible gases are being analyzed since the potential of gas leaks always exist.
The customer should ensure that the principles of operating of this equipment are well understood by the user. Misuse of this product in any manner, tampering with its components, or unauthorized substitution of any component may adversely affect the safety of this instrument.
WARNING
Since the use of this instrument is beyond the control of Teledyne, no responsibility by Teledyne, its affiliates, and agents for damage or injury from misuse or neglect of this equipment is implied or assumed.
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UV-Photo-X Introduction
Introduction
1.1 Theory of Operation
The ability to monitor the concentration of an analyte in a process stream is critical for accurate and reliable process control. There are many techniques used to determine the analyte concentration of interest. One of the most sensitive sensing techniques is molecular fluorescence. Fluorescence occurs when a molecule absorbs light energy, either ultraviolet or visible, and rapidly emits light, at some longer wavelength. Fluorescence of this type is referred to as Stokes fluorescence. Fluorimetry characterizes the excitation and emission properties of the molecular species. Figure 1-1 shows an example of the excitation and emission spectrum from a hypothetical fluorophore.
Fluorimetry is concerned with two types of information: 1) The (spectral) wavelength distribution, which is characteristic of the electronic properties of the molecule, and 2) The intensity of the fluorescence, which is typically correlated to the concentration of the fluorescent molecule in the solution.
Figure 1-1: Molecular Fluorescence Example
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Introduction Model 6650
1.2 Filter Based Flurometer Description
The Fluorometer is a filter-based analyzer. The Fluorometer measures the ability of the analyte of interest to absorb light in a narrow spectral region and emit light at a longer wavelength. A filter-based Fluorometer is a good choice when quantitative measurements are desired for a specific analyte in process. Additionally, the Fluorometer provides a relative measurement and can be calibrated with a known concentration standard(s) or correlated to measurements using standard laboratory methods resulting in a quantitative fluorescence.
A filter-based Fluorometer uses optical filters to provide specific excitation or emission wavelengths wavelengths for molecular fluorescence. In the Fluorometer the filters are located internal to the transmitter and are specific to the application. Therefore, the Fluorometer is a dedicated instrument for monitoring only one specific analyte of interest. The filter sets used to configure the instrument are specific to the analyte of interest. In order to monitor a new analyte of interest, the user must return the Fluorometer to TIA for factory reconfiguration. The Fluorometer can be used for both quantitative measurements (determination of analyte concentration) and control measurements (switching of valves once a fluorescence level is attained, for example)
In brief, the Fluorometer works as follows: The light source launches excitation light into a fiber optic cable. The fiber optic cable transfers the excitation light to the Fluorescence probe mounted in the process. The fluorescence probe launches light into the process sample, and collects the molecular fluorescence (emission) from the sample. The emission light is then transferred from the probe through fiber optic cable to the analyzer. The emission light passes through an emission filter in order to remove any residual excitation energy collected by the fluorescence probe. The emission light then impinges a detector and the fluorescence intensity is displayed on the analyzer.
Unlike many fluorescence units on the market, the Fluorometer utilizes a xenon flash lamp to provide excitation energy. This lamp allows the Fluorometer to be easily configured to meet any excitation wavelength requirement with the appropriate filter selection across the entire spectrum. The xenon flash lamp also has an extended lifetime compared to other common UV sources (deuterium, mercury vapor, etc.), which reduces the cost of ownership of the analyzer.
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UV-Photo-X Introduction
The remainder of this manual provides the user with the necessary tools to operate the Fluorometer. In addition to standard operation methods and procedures, a section detailing some application development objectives (Appendix 1) has been provided to aid the user in defining the parameters required to realize optimal process monitoring.
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Definition of Terms Model 6650
Definition of Terms
2.1 Excitation Filter
The excitation filter is used to select the range of wavelengths, the pass band, used to cause or excite the molecular fluorescence. Wavelengths not in the pass band are rejected and ideally never reach the sample. Removal of wavelengths outside the pass band minimizes the possibly of false fluorescence readings due to detection of light from the lamp which mimics the fluorescence signal.
2.2 Emission Filter
The emission filter is used to select the range of wavelengths, the pass band, to be passed to the measure detector. Wavelengths not in the pass band are rejected and ideally never reach the sample. It is critical that the excitation wavelengths never reach the detector, since it will respond to excitation light. Excitation light impinging the measure detector results in increased residual background levels, which reduces the dynamic range, the signal-to-noise ratio and the signal-to-blank ratio.
2.3 Measure Detector
The light detector is most often a photomultiplier tube, though photodiodes are increasingly being used. The light passing through the emission filter is detected by the photomultiplier or photodiode. The light intensity, which is proportional to the analyte concentration, is registered as a digital readout.
2.4 Span Filter
The span filter is used to check instrument operation. When a fluorescence filter is employed the span filter fluorescence value is dependent on the initialization method utilized and the standards used during calibration. The span filter is used to verify instrument operation and should not be used to calibrate the instrument.
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UV-Photo-Florescenceefinition of Terms
2.5 Background Fluorescence
The fluorescence signal due to the probe/analyzer optical configuration, stray light, and fluorescence from the background material.
2.6 Sensitivity
The ability of the analyzer to detect a given level of analyte based on the molecular fluorescence from the analyte. The actual limits of detection depend on the properties of the analyte measured and the process conditions. Parameters such as pH, temperature, oxygen content, and background solvent, to name but a few may dramatically alter the fluorescence intensity measured. Typically, detection of parts-per­million (PPM) and parts-per-billion (PPB) analyte levels can be detected. In general, fluorescent measurements are 1,000 to 500,000 times more sensitive than absorbance based photometric measurements. Practically, sensitivity means the minimum analyte concentration that can be measured above background fluorescence in the process.
2.7 Specificity
The ability of the analyzer to monitor one specific analyte in a mixture of background materials without interference from the background materials. In absorbance based photometric measurements, interference problems are common since many materials absorb light, making it difficult to isolate the targeted analyte in a complex mixture. However, Fluorometers are highly specific and less susceptible to interferences because fewer materials exhibit molecular fluorescence. Furthermore, if background materials do absorb and emit light, it is rare that they will emit the same wavelength of light as the analyte of interest.
2.8 Signal-to-Noise Ratio
Signal refers to the emission collected by the fluorescence probe and monitored by the analyzer using the internal span filter. Noise refers to the output from the instrument’s electronics, which is present whether or not sample is being read and any collection of errant wavelengths not removed by the optical filters. Noise is measured by placing the fluorescence probe in air and in complete darkness (no stray light). For process monitoring, the signal-to-noise ratio is not as important as the signal-to background ratio.
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Definition of Terms Model 6650
2.9 Signal-to-Background Ratio
Signal refers to the emission collected from a sample with known analyte concentration by the fluorescence probe and monitored by the analyzer. Background refers to the process liquid containing no analyte of interest and any stray light present in the system. The signal-to­background ratio should be calculated during the application engineering phase of the project. Knowing this ratio will help determine when the stray light level changes and/or the background material fluorescence properties change. Refer to Appendix 1 for additional details.
2.10 Dynamic Range
Dynamic range refers to the range of concentrations an instrument can read, from the minimum to the maximum detectable. The minimum detectable concentration is determined by signal-to-noise and signal-to-background ratios. The maximum detectable concentration is determined by the compound’s chemistry and by factors such as instrument sensitivity ranges, fluorescence (quantum) efficiency, specificity of optical filters, etc.
2.11 Linearity
Fluorescence intensity is typically directly proportional (linear) to concentration. There are, however, factors that affect this linear relationship. For example, variations in temperature, pH, dissolved oxygen content, stray light, turbidity, variation in the chemical composition of the background, etc. can dramatically affect the linearity of the fluorescence response. Practically, the linearity of the measurement is determined during the application engineering phase of the project. Refer to Appendix 1 for details.
2.12 Process Background
The liquid solution used to transport or sustain the analyte of interest in the process. This solution has all the chemical constituents found in the process except the analyte of interest.
2.13 Mode 1 Initialization
Mode 1 initialization is a method for setting up the Fluorometer for process monitoring. Mode 1 initialization is used to setup the
Fluorometer when the fluorescence intensity versus analyte
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