Rosemount 2100A Process Total Organic Carbon TOC Analyzer-Rev E Manuals & Guides

Page 1
Rosemount Analytical
M
ODEL
P
ROCESS TOTAL ORGANIC CARBON
A
NALYZER
I
NSTRUCTION MANUAL
2100A
748263-E
Page 2
OTICE
N
The information contained in this document is subject to change without notice.
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®
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Manual Part Number 748263-E March 2001 Printed in U.S.A.
Rosemount Analytical Inc.
4125 East La Palma Avenue
Anaheim, California 92807-1802
Page 3
C
ONTENTS
PREFACE .................................................................... P1
SAFETY SUMMARY ..........................................................................................P1
SPECIFICATIONS - OPERATIONAL.................................................................P4
SPECIFICATIONS - PERFORMANCE...............................................................P4
SPECIFICATIONS - SAMPLE REQUIREMENTS..............................................P4
SPECIFICATIONS - AMBIENT REQUIREMENTS.............................................P5
SPECIFICATIONS - DATA OUTPUT.................................................................P5
SPECIFICATIONS - UTILITY REQUIREMENTS ...............................................P5
SPECIFICATIONS - PHYSICAL.........................................................................P6
SPECIFICATIONS - OPTIONAL TYPE Z PURGE.............................................P6
CUSTOMER SERVICE, TECHNICAL ASSISTANCE AND FIELD SERVICE.............P7
RETURNING PARTS TO THE FACTORY.........................................................P7
TRAINING ......................................................................................................P7
DOCUMENTATION............................................................................................P7
S
ECTION
1.1 SYSTEM DESCRIPTION ............................................................................1
1.2 TYPICAL APPLICATIONS...........................................................................1
1.3 PRINCIPLE OF OPERATION......................................................................2
1. I
NTRODUCTION
.............................................. 1
SECTION 2. INSTALLATION............................................... 4
2.1 GENERAL INFORMATION .........................................................................5
2.2 SAMPLE CONDITIONING...........................................................................5
2.3 LOCATION..................................................................................................5
2.4 UTILITIES AND SUPPLIES .........................................................................6
2.4.1 ELECTRICAL CONNECTIONS .....................................................6
2.4.1.1 Power.............................................................................6
2.4.1.2 Signal.............................................................................6
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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2.4.1.3 Alarm............................................................................. 6
2.4.2 GAS, LIQUID CONNECTIONS ..................................................... 6
2.4.2.1 Sample In...................................................................... 6
2.4.2.2 Sample Drain................................................................. 8
2.4.2.3 Reagent......................................................................... 8
2.4.2.4 Standard......................................................................... 8
2.4.2.5 Carrier Gas..................................................................... 8
2.4.2.6 Vent................................................................................ 9
2.4.2.7 Waste ............................................................................. 9
2.4.2.8 Condensate Trap Drain................................................. 9
2.5 INSTALLATION........................................................................................... 10
2.5.1 Mounting Instrument...................................................................... 10
2.5.2 Electrical ..................................................................................... 10
2.5.2.1 Power............................................................................. 10
2.5.2.2 Signal.............................................................................. 10
2.5.2.3 Alarm.............................................................................. 13
2.5.3 Piping ..................................................................................... 14
2.5.3.2 Drain............................................................................... 14
2.5.3.3 Standard........................................................................ 15
2.5.3.4 Reagent......................................................................... 15
2.6 OPTIONAL TYPE Z PURGE....................................................................... 15
SECTION 3. INITIAL START-UP..........................................16
3.1 START-UP PROCEDURE.......................................................................... 17
SECTION 4. OPERATION AND MAINTENANCE.....................22
4.1 OVERVIEW................................................................................................. 23
4.2 PREPARING REAGENT............................................................................. 24
4.3 REPLACING PUMP TUBES....................................................................... 26
4.4 CALIBRATION CHECK............................................................................... 28
4.5 IR ZERO, SPAN CHECK............................................................................ 30
4.6 TOC ZERO, SPAN CHECK........................................................................ 32
4.7 SEDIMENT REMOVAL............................................................................... 34
4.8 PUMP MOTOR BEARINGS........................................................................ 34
4.9 TOC ALARM............................................................................................... 34
4.10 PREPARATION FOR SHIPMENT............................................................ 35
4.11 CLEANING INFRARED ANALYZER OPTICAL UNIT............................... 38
4.12 CLEANING CONDENSATE TRAP ........................................................... 39
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March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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SECTION 5. PREPARATION OF STANDARDS ...................... 41
5.1 STANDARDS PREPARATION....................................................................41
5.2 BACKGROUND TOC COMPENSATION ....................................................43
SECTION 6. CIRCUIT DESCRIPTIONS ................................. 47
6.1 GENERAL ...................................................................................................47
6.2 INPUT SIGNAL CONDITIONER..................................................................47
6.3 LINEARIZER................................................................................................ 47
6.4 ZERO AND SPAN .......................................................................................47
6.5 RECORDER OUTPUTS..............................................................................47
6.6 ALARM OUTPUT.........................................................................................48
6.7 DISPLAY .....................................................................................................48
6.8 POWER SUPPLY........................................................................................48
SECTION 7. TROUBLESHOOTING....................................... 49
S
ECTION 8. REPLACEMENT PARTS................................... 59
8.1 RECOMMENDED SPARE PARTS..............................................................59
8.2 REPLACEMENT PARTS (NUMERICALLY)................................................60
8.3 REPLACEMENT PARTS (ALPHABETICALLY)...........................................62
GENERAL PRECAUTIONS FOR HANDLING & STORING HIGH PRESSURE CYLINDERS WARRANTY FIELD SERVICE AND REPAIR FACILITIES
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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FIGURES
1-1. Simplified Model 2100A Flow Diagram (TOC Version).............................. 3
1-2. Simplified Model 2100A Flow Diagram (TC Version)................................. 3
2-1. Inner Compartment.................................................................................... 7
2-2. Electrical Connection to PC Board............................................................. 7
2-3. Inner Panel Layout..................................................................................... 11
2-4. Opening Control Panel (loosen two panel fasteners)................................. 12
2-5. Block Wiring Diagram (115VAC)................................................................ 12
2-6. Block Wiring Diagram (230VAC)................................................................ 13
2-7. Purge Option Mounting.............................................................................. 16
3-1. Alarm Readout Button (press and hold while adjusting setpoint)............... 21
4-2. Removing Pump Head............................................................................... 27
4-3. Remove Old Pump Tube ........................................................................... 27
4-4. Connecting New Pump Tube..................................................................... 27
4-5. Fastening Tube Ends................................................................................. 27
4-6. Engaging Pump Shaft................................................................................ 27
4-7. Installing New Pump Tube......................................................................... 27
4-8. Positioning Pump Tube.............................................................................. 29
4-9. Installing Pump Head................................................................................. 29
4-10. Installing Knurled Screws......................................................................... 29
4-11. Straightening Pump Tube ........................................................................ 29
4-12. Set Switch to IR CAL ............................................................................... 31
4-13. Injecting Zero Gas.................................................................................... 31
4-14. Adjusting IR ZERO to 000........................................................................ 31
4-15. Injecting Span Gas................................................................................... 31
4-16. Adjusting IR SPAN Value......................................................................... 31
4-17. Set IR Switch To Normal.......................................................................... 31
4-18. Reagent Pump Switch ............................................................................. 32
4-19. Adjusting TOC ZERO............................................................................... 33
4-20. Sample Selector Valve............................................................................. 33
4-21. Turning Reagent Pump ON...................................................................... 33
4-22. Adjusting TOC SPAN............................................................................... 33
4-23. Infrared Analyzer Optical Unit - Exploded View....................................... 38
4-24. Condensate Trap Assembly..................................................................... 39
T
ABLES
iv
4-1. Application Data......................................................................................... 25
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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DRAWINGS (LOCATED IN REAR OF MANUAL)
655369 Outline and Mounting Dimensions, Model 2100A 655376 Piping Diagram, Model 2100A 660871 Block Wiring Diagram, 230VAC 660872 Block Wiring Diagram, 115VAC 837484 Schematic Diagram, Model 2100A 837519 Type Z Purge Option
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748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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P
REFACE
SAFETY SUMMARY
To avoid explosion, loss of life, personal injury and damage to this equipment and on-site property, all personnel authorized to install, operate and service the Model 340 Trace Moisture Analyzer should be thoroughly familiar with and strictly follow the instructions in this manual. Save these instructions.
DANGER is used to indicate the presence of a hazard which will cause severe personal injury, death, or substantial property damage if the warning is ignored
WARNING is used to indicate the presence of a hazard which can cause severe personal injury, death, or substantial property damage if the warning is ignored.
CAUTION is used to indicate the presence of a hazard which will or can cause minor personal injury or property damage if the warning is ignored.
NOTE is used to indicate installation, operation, or maintenance information which is important but not hazard-related.
WARNING: ELECTRICAL SHOCK HAZARD
Do not operate without doors and covers secure. Servicing requires access to live parts which can cause death or serious injury. Refer servicing to qualified personnel.
For safety and proper performance this instrument must be connected to a properly grounded three-wire source of power.
Alarm switching relay contacts wired to a separate power source must be disconnected before servicing.
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
P1
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REFACE
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WARNING: POSSIBLE EXPLOSION HAZARD
This analyzer is of a type capable of analysis of sample gases which may be flammable. If used for analysis of such gases, the detection section of the analyzer must be either in an explosion proof enclosure suitable for the hazard classification of the gas, or protected by a continuous dilution purge system in accordance with Standard ANSI/NFPA-496-1986 (Chapter 8) or IEC Publication 79-2-1983 (Section Three).
If explosive gases are introduced into this analyzer, the sample containment system must be carefully leak checked upon installation and before initial startup, during routine maintenance and any time the integrity of the sample containment system is broken, to ensure that the system is in leak proof condition. Leak check instructions are provided in Section 4.2.
Internal leaks resulting from failure to observe these precautions could result in an explosion, causing death, personal injury or property damage.
WARNING: HIGH PRESSURE GAS CYLINDERS
Fuel, air and calibration gas cylinders are under pressure. Mishandling of gas cylinders could result in death, injury or property damage. See General Precautions for Handling and Storing High Pressure Cylinders, in the rear of this manual.
CAUTION: PARTS INTEGRITY
Tampering or unauthorized substitution of components may adversely affect safety of this product. Use only factory documented components for repair.
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March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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REFACE
P
WARNING: MERCURY HAZARD
The ultraviolet light generating lamp contains mercury. Lamp breakage could result in mercury exposure. Mercury is highly toxic if absorbed through the skin or ingested, or if the vapors are inhaled.
Handle lamp assembly with extreme care. If lamp if broken, avoid skin contact and inhalation in the area of the lamp or the mercury spill.
]Immediately clean up and dispose of the mercury spill and lamp residue as follows:
Wearing rubber gloves and goggles, collect all droplets of mercury by
means of a suction pump and aspirator bottle with a long capillary tube. (Alternatively, a commercially available mercury spill clean up kit, such as J.T. Baker product No. 4439-01, is recommended.)
Carefully sweep any remaining mercury and lamp debris into a dust
pan.
Carefully transfer all mercury, lamp residue and debris into a plastic
bottle which can be tightly capped.
Label and return to hazardous material reclamation center.
Do not place in trash, incinerate or flush down sewer.
Cover any fine droplets of mercury in non-accessible crevices with
calcium polysulfide and sulfur dust.
748263-E Rosemount Analytical March 2001
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REFACE
P
S
PECIFICATIONS
- O
PERATIONAL
PRINCIPLE
Ultraviolet/persulfate oxidation to CO2
D
ETECTION METHOD
Non-Dispersive Infrared (NDIR)
TOC RANGE - SINGLE RANGE (PPM CARBON)
0 to 2 0 to 5 0 to 10 0 to 20 0 to 50 0 to 100 0 to 200 0 to 500 0 to 1000 0 to 2000 0 to 5000
SPECIFICATIONS - PERFORMANCE
R
EPRODUCIBILITY
1
R
ESPONSE TIME
±2% fullscale
Less than 5 minutes for 90% of fullscale for most ranges
SPECIFICATIONS - SAMPLE REQUIREMENTS
F
LOW RATE SAMPLE INLET
50 to 2000 ml/min. depending on sample availability and response required
F
LOW RATE SIDE STREAM
1.1 to 15 ml/min. depending on reactor range
I
NLET PRESSURE
Constant 2 psig minimum, 15 psig maximum at sample inlet
T
EMPERATURE
35°F to 160°F (2°C to 71°C)
S
USPENDED SOLIDS
Sample must be free of particles larger than 100 micro ns
C
HLORIDES
Up to 1000 ppm (wt)
1
±5% for 0 to 2, 0 to 500, and 0 to 5000 ppm. For better reproducibility, consult factory. Absolute accuracy of analysis
depends upon the accuracy of the calibration standards.
P4
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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S
PECIFICATIONS
TEMPERATURE
35°F to 122°F (2°C to 50°C) Protect from heating effect of direct sunlight
H
UMIDITY
0 to 90% relative humidity
S
PECIFICATIONS
L
OCAL READOUT
Electroluminescent backlighted liquid crystal display (LCD) reading of organics in ppm (carbon)
A
NALOG OUTPUT
– S
Voltage Output: 0 to 1 VDC; 0 to 10 mV DC
A
NALOG OUTPUT
– O
Current Output: 4 to 20 mA DC isolated, 500 ohm load maximum
A
LARM
Single 100% adjustable, high or low, DPDT 10A, 240 VAC (30 VDC) relay contacts
- A
- D
TANDARD
PTIONAL
MBIENT REQUIREMENTS
ATA OUTPUT
SPECIFICATIONS - UTILITY REQUIREMENTS
P
OWER
P
OWER
C
ARRIER GAS
D
RAIN
V
ENT
R
EAGENT
– S
TANDARD
115 VAC ±10%, 50/60 Hz, 1 phase, 3 amps, 350 watts
– O
PTIONAL
230 VAC ±10%, 50/60 Hz, 1 phase, 1.5 amps, 350 watts
200 to 500 scc/min. nitrogen, 1/8-inch tubing (see Table 4-1 for pressure)
Open atmospheric: 1/2-inch minimum inner diameter 2 L/min. maximum, 1/2-inch NPT
Atmospheric operation only. 1 L/min. maximum 1/2-inch NPT gas flow Connection normally not required
19 L/mo. (all ranges except 0-5000 ppm) to 47 L/mo. (0 to 5000 ppm)
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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REFACE
P
S
PECIFICATIONS
- P
HYSICAL
ELECTRICAL CLASSIFICATION – STANDARD
General purpose (non-hazardous locations)
E
LECTRICAL CLASSIFICATION
– O
PTIONAL
Air Purge, Type Z, ANSI/NFPA 496 for Class I, Division 2 hazardous locations
ENCLOSURE
NEMA-3R
D
IMENSIONS
23.7 x 15.0 x 8.3 (600 x 380 x 210) H x W x D
W
EIGHT
(115 VAC) 60 lb. (27.2 kg) (230 VAC) 65 lb. (29.5 kg)
S
HIPPING WEIGHT
(115 VAC) 75 lb. (34 kg) (230 VAC) 80 lb. (36.3 kg)
SPECIFICATIONS - OPTIONAL TYPE Z PURGE
P
URGE GAS
Inert gas, such as nitrogen, supplied through 1/8-inch tubing at 20 psig
O
PERATING PRESSURE
.2 inch H2O
I
NLET PRESSURE
Constant 2 psig minimum, 15 psig maximum at sample inlet
T
EMPERATURE
35°F to 160°F (2°C to 71°C)
S
USPENDED SOLIDS
Sample must be free of particles larger than 100 micro ns
C
HLORIDES
Up to 1000 ppm (wt)
P6
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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C
USTOMER SERVICE
For order administration, replacement Parts, application assistance, on-site or factory repair, service or maintenance contract information, contact:
, T
ECHNICAL ASSIST ANCE AND FIELD SERVICE
Rosemount Analytical Inc.
Process Analytical Division
Customer Service Center
1-800-433-6076
RETURNING PARTS TO THE FACTORY
Before returning parts, contact the Customer Service Center and request a Returned Materials Authorization (RMA) number. Please have the following information when you call: Model Number, Serial Number, and Purchase Order Number or Sales Order
Number.
Prior authorization by the factory must be obtained before returned materials will be accepted. Unauthorized returns will be returned to the sende r, f re ight collect.
When returnin g any pro duct o r compon ent t hat has be en expo sed to a toxic, corrosi ve or other hazardous material or used in such a hazardous environment, the user must attach an appropriate Material Safety Data Sheet (MSDS.) or a written certification that the material has been decontaminated, disinfected and/or detoxified.
Return to:
Rosemount Analytical Inc.
4125 East La Palma Avenue
Anaheim, California 92807-1802
USA
T
RAINING
A comprehensive Factory Training Program of operator and service classes is available. For a copy of the Current Operator and Service Training Schedule contact the Technical Services Depart men t at:
Rosemount Analytical Inc.
Phone: 1-714-986-7600
FAX: 1-714-577-8006
D
OCUMENTATION
The following Model 340 Trace Moisture Analyzer instruction materials are available. Contact Customer Service or the local representative to order.
081854 Instruction Manual (this document)
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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I
NTRODUCTION
1
1.1 SYSTEM DESCRIPTION
The Model 2100A is a continuous, on-line organics analyzer for industrial water analysis applications with fullscale ranges from 0 to 2 ppm to 0 to 5000 ppm total organic carbon. This reliable, low maintenance, industry-proven analyzer offers a real-time, accurate analysis of organic levels in a variety of process water streams.
This model utilizes continuously operating ultraviolet-promoted persulfate oxidation to convert organic carbon to carbon dioxide. This CO2 is then measured by an accurate non-dispersive infrared detector. Output is calibrated to read parts-per-million (ppm) carbon. This cost effective, rugged industrial design provides fast response and simple operation. The Model 2100A has been proven successful in a wide variety of applications.
1.2 TYPICAL APPLICATIONS
EMICONDUCTOR PLANTS
S
Reclaimed water Deionized water plant input
HEMICAL/PETROCHEMICAL PLANTS
C
Cooling water Waste water Organic loading of process streams Product loss monitoring
OOD/BEVERAGE PLANTS
F
Cooling water Waste water Condensate return Ion exchange effluent Rinse water
OWER PLANTS
P
Cooling water Boiler feedwater Condensate return Waste water
ATER/WASTEWA TER PLANTS
W
Raw and finished water quality Potable water Effluent water
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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NTRODUCTION
I
1.3 PRINCIPLE OF OPERATION
Refer to Figures 1-1 (TOC Version) and 1-2 (TC Version). The Model 2100A uses ultraviolet promoted persulfate oxidation with infrared detection to continuously determine concentration of soluble, non-volatile reactive organics. When a sample containing organic compounds is mixed with a persulfate solution and exposed to ultraviolet radiation, it is oxidized to CO2, as shown in the following equation:
Organics + [S2O8] -2 + H2O ½ CO2 + [SO4] -2 + H2SO
UV
4
The concentration Of CO2 is then determined with an infrared analyzer. If dissolved CO and inorganic carbon are removed prior to oxidation, then the CO2 generated after oxidation is indicative of the organics content in the sample.
Sample is introduced continuously into the Model 2100A through a sample bypass either by means of process pressure or an optional sample pump. A sidestream for analysis is continuously pumped at a constant rate and acidified with a sodium or ammonium persulfate/phosphoric acid solution. The phosphoric acid reacts with any inorganic carbon compounds (i.e., carbonates and bicarbonates) which may be present to form CO2. This acidified solution is then sparged with carrier gas (nitrogen) to remove the CO2 and is passed through a liquid/gas separator to vent the CO2. The liquid is introduced to the reaction chamber where it is exposed to high intensity (184.9 nm) ultraviolet light.
The UV radiation catalyzes the persulfate oxidation of the remaining organic carbon to CO2. The CO2-containing carrier gas is passed through a condensate trap to remove moisture,
and then through a non-dispersive infrared analyzer which measures the CO2 concentration.
2
In the TC Version, both organic and inorganic carbon are measured. The sparge system is removed from this configuration, which allows all gases to pass through the infrared detector.
The Model 2100A electronics linearize and scale the infrared detector signal to equate to ppm carbon organics concentration which is read out continuously on the digital display while simultaneously transmitting an analog signal proportional to the ppm carbon reading. This proven concept provides quick, real-time response while maintaining high accuracy.
2
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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NTRODUCTION
I
IGURE
F
1-1. S
IMPLIFIED MODEL
2100A F
LOW DIAGRAM
(TOC V
ERSION
)
IGURE
F
748263-E Rosemount Analytical March 2001
1-2. S
IMPLIFIED MODEL
2100A F
LOW DIAGRAM
Model 2100A Process Total Organic Carbon Analyzer
(TC V
ERSION
)
3
Page 19
NTRODUCTION
I
NOTES
4
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
Page 20
I
NSTALLATION
2
2.1 GENERAL INFORMATION
This section contains instructions on site requirements, utilities, pre-operation checkout, installation and pre tart-up preparations for the Model 2100A Process Total Organic Carbon Analyzer.
2.2 SAMPLE CONDITIONING
Application parameters of the Model 2100A are influenced by the following typical user criteria:
Measurement objective
Physical plant arrangement
Nature of test sample.
Performance of the Model 2100A depends upon the integrity of the sample. Therefore, each Model 2100A system installation may be unique with respect to conditioning of the sample.
The sample flow rate supplied to the Model 2100A by a typical sample system is many times greater than the minimum flow required. This serves to:
Reduce lag time
Minimize change in sample composition
Optimize functioning of basic sample conditioning elements
Optimize compatibility with commercially available pumps and pipe sizes
The analyzer sample inlet system, therefore, is designed to handle an input flow rate of 2 L/min maximum. A sidestream flow of 1. 1 to 15 ml/min is taken for analysis from the flowing inlet sample.
Maximum admissible particle size in the sample supplied to the unit is 100 micron diameter.
2.3 LOCATION
The installation site must be near the sample access point to assure good sample integrity and minimum input lag time. The location must be level, covered and adequately enclosed to provide the unit with good ventilation but without high concentrations of dust or dirt in the air. Ambient operating temperature range is 35°F to 122°F (2°C to 50°C) at 90% maximum relative humidity. The Model 2100A must be isolated from strong vibrations (as may be caused by large motors, pumps, etc.) and protected from the heating effect of direct sunlight.
748263-E Rosemount Analytical March 2001
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Page 21
NSTALLATION
I
Note The standard Model 2100A is designed for installation only in unclassified,
non-hazardous locations. If equipped with an optional air purge system and installed and operated per Type Z of standard ANSI/NFPA 496, the Model 2100A may be located in a Class I, Division 2 classified location as defined in the National Electrical Code (ANSI/NFPA 70).
Actual outside dimensions of the Model 2100A are found in Table 1-1 and drawing 655369.
2.4 UTILITIES AND SUPPLIES
2.4.1 ELECTRICAL CONNECTIONS
2.4.1.1 P
A 115 VAC, 50/60 Hz (optional 230 VAC, 50/60 Hz), 1 phase, 15 A service line with ground is required. Protection by circuit breaker or fuse is necessary. A 14-inch power conduit opening is located on the top right side (frontal view, this and subsequent references) of the Model 2100A cabinet. Power should be wired to the power terminal strip (Figure 2-1).
2.4.1.2 S
Analog output signals of 0 to 1 VDC, 10 mV DC, or optional 4 to 20 mA DC are provided for external stripchart recorders or other signal processing equipment. A separate 1/2-inch conduit opening is located on the top right side of the Model 2100A cabinet for signal wiring. Signal should be wired from terminal board TB1 (Figures 2-1, 2-2). To prevent electrical interference, signal wiring should be run in conduit separate from the power wiring. W here possible, signal cable should be a twisted pair with overall shield and outer insulating jacket. The shield should be grounded at one end only. W hen not used, the signal conduit opening should be plugged with an appropriate watertight plug such as Caplugs part number BP 7/8.
2.4.1.3 A
The Model 2100A has one set of fully adjustable 10 A, 240 VAC (30 VDC), DPDT alarm contacts for either high or low TOC alarming. If used, the alarm wiring should be connected to TB2 (Figure 2-2). Either the power or the analog signal conduit opening may be used, depending upon the voltage level present in the users alarm system.
OWER
IGNAL
LARM
2.4.2 GAS, LIQUID CONNECTIONS
2.4.2.1
The process sample must be supplied at a small positive, constant pressure (2 psig min., 15 psig max.). A 1/4-inch NPT sample inlet connection is provided on the lower left side of the Model 2100A cabinet. Refer to drawing 655369 for recommended installation. For installations where pressure is greater than 2 psig, some means of throttling and flow indication such as a rotameter with throttling valve is desirable. Sample flow may be in the
6
SAMPLE IN
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
Page 22
NSTALLATION
I
range of 50 to 2000 ml/min, with a preferred flow of at least 1000 ml/min to minimize sample transport lag time.
The sample must not contain particles larger than 100 microns in diameter.
IGURE
F
IGURE
F
2-1. I
2-2. E
NNER COMPARTMENT
LECTRICAL CONNECTION TO
PC B
OARD
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
7
Page 23
NSTALLATION
I
2.4.2.2 S
AMPLE DRAIN
A 1/2-inch NPT connection is provided on the left side of the Model 2100A cabinet. This drain should slope directly to an open atmospheric drain, using 1/2-inch minimum O.D. tubing or 1/2-inch minimum diameter pipe with no pockets or obstructions which might introduce back pressure at the analyzer drain connection. See drawing 655369 for recommended installation. A special 1/2-inch elbow with vent hole is supplied separately for making this drain connection.
2.4.2.3 R
EAGENT
A 1/8-inch tubing connection is located at the left side of the Model 2100A cabinet for connection to the persulfate reagent reservoir supplied with the instrument. A continuous 10-foot length of 3/16-inch O.D.
Teflon tubing runs through this fitting for connection to the reagent reservoir. To connect the reservoir, drill a 1/4-inch hole in the center of the reservoir cap and insert the Teflon tube into the hole until the tube reaches the bottom of the reservoir. Stainless steel tube ferrules attached to the tube end act as a weight to prevent the tube from floating. See drawing 655369 for proper installation. Refer to Section 4.2 and Table 4-1 for special instructions about reagent preparation.
CAUTION: CORROSION HAZARD
Do not use metal tubing or fittings for reagent connection.
2.4.2.4 S
TANDARD
This 1/8-inch tubing connection, located on the lower left side of the Model 2100A cabinet, is for introducing a prepared calibration standard for calibration of the analyzer, or for introducing a "grab sample" for analysis. For the recommended calibration standard, see Table 4-1 and refer to Section 5. A continuous 4 to 5-foot length of Teflon tubing runs through this connection directly to the sample select valve. The free end of this tube should be inserted into a sample container at atmospheric pressure. A stainless steel nut and ferrules attached to the free end of this tube act as a weight to prevent the tube from float­ing. The sample is pumped out of the container by the sample pump internal to the analyzer when the pump is running and the sample selector valve is rotated to the "Standard" position. See Section 3, INITIAL START-UP, and Section 4, OPERATION and MAINTENANCE, for operational details. See drawing 655369 for recommended installation.
2.4.2.5 C
ARRIER GAS
A 1/8-inch tubing connection is located on the lower left side of the Model 2100A for a suitable carrier gas. A 1/8-inch tube is recommended but 1/4-inch tubing with a 1/8-inch adapter may be necessary to avoid pressure drop if the distance from gas supply to instrument exceeds 5 to 10 feet.
8
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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Carrier gas may be clean, dry CO2-free nitrogen. It should be supplied at 75 to 100 psig at instrument inlet. Set the internal carrie r gas regulator according to requirements un ique to each individual instrument, as outlined on the Data Sheet at the back of the manual. Carrier gas consumption is between 200 and 500 cc/min depending upon the TOC fullscale range. See drawing 655369 for recommended installation.
2.4.2.6 V
ENT
A 1/2-inch tubing vent connection is located on the lower left side of the Model 2100A. This vent carries the combined flow of drying gas and CO2-containing carrier and sparge gas. Normally no tubing is required for this vent. In fact, the preferred installation requires no external tubing or piping connected to the vent connection. If it is necessary to route this vent outside, 1/2-inch O.D. minimum tubing or 1/2-inch tubing minimum pipe should be used. The tubing should be as short as possible and must slope downward throughout, with no pockets where condensation might collect and cause varying back pressure. See drawing 655369.
CAUTION: BACK PRESSURE HAZARD
The "Sample Drain" and "Waste Drain" must not be connected together. Both drains should be run separately into a common open atmospheric drain. These lines must slope all the way to the open drain, with no pockets or obstructions which might introduce back pressure at the analyzer drain connection. Only the special vented male elbow supplied with the analyzer should be used for making the first connection to the analyzer "Waste Drain."
2.4.2.7 W
ASTE
A 1/2-inch NPT waste drain connection is located on the lower left side of the Model 2100A. This drain must be connected to a 1/2-inch minimum plastic or 316SS tubing or pipe, and must continuously slope downward unobstructed to an open atmospheric drain. To assure proper venting of this drain, a special 1/2-inch plastic male elbow with a drilled vent hole is provided with the analyzer. Use only this connector for the first waste fitting out of the analyzer.
Note Use only plastic or 316SS material in the "Waste Drain" line. This line contains a
persulfate salt, which will corrode most metals. Do not use copper or brass.
2.4.2.8 C
ONDENSATE TRAP DRAIN
The self-draining condensate trap requires a 3/8" I.D. hose attached to its drain stem. See drawing 655369. The hose should be directed to an open drain or container. Allow water to
748263-E Rosemount Analytical March 2001
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NSTALLATION
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drain freely. Keep the drain hose above the water level of the drain or container. Do not obstruct the drain stem.
2.5 INSTALLATION
2.5.1 M
OUNTING INSTRUMENT
1. Find a suitable location to mount the Model 2100A as discussed in Section 2.3.
2. The dimensional drawing for the unit is drawing 655369. Use either the dimensional drawing or the module itself to locate and drill analyzer mounting holes. Mounting brackets are provided with the analyzer.
2.5.2 E
LECTRICAL
Refer to Figure 2-4. Turn OFF (lower portion of switch pushed in) the "MAIN POWER," "LAMP," and both "PUMP" switches located on the control panel inside the analyzer. Open this panel (Figure 2-5) and make all electrical connections to the analyzer as follows.
WARNING: ELECTRICAL SHOCK HAZARD
Installation and servicing requires access to shock hazard level voltages which can cause death or serious injury. Refer servicing to qualified personnel.
For proper performance and safety, this instrument must be connected to a properly grounded three-wire source of electrical power.
2.5.2.1 P
OWER
Refer to Figures 2-1 and 2-6 (115 VAC) or 2-7 (230 VAC). Connect power to the terminal strip mounted in the upper right corner of the back panel. For
115 VAC instruments, connect "Hot" line to "HOT" terminal and "Neutral" line to "NEU" terminal. For 230 VAC instruments, which are typically not polarized, connect the "Ground" line to "GND" terminal and the other two lines to the "Ll" and “L2" terminals.
2.5.2.2 S
IGNAL
Refer to Figures 2-1 and 2-2. Connect Analog Signal wiring to the appropriate output signal terminals of the electronics
board, which is located under the top panel of the Model 2100A. Since the board is rotated 1800 upon mounting, these terminals, from left to right, read "420 mA +", "4-20 mA –“, "GND", "0-10 mV", and "0-1 V". The terminals marked "0-1 V" and "0-10 mV" are positive, and "GND" is negative. The "4-20 mA " ter min al s are electr i cal l y isolated.
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Note "0-1 V" and "0-10 mV" outputs are present on all instruments. A 4 to 20 mA signal is
present only if the optional 4 to 20 mA output has been purchased. This output is obtained from a plug-in module which may be added at a later time if desired.
A shielded, twisted-pair cable is recommended for all signal wiring. The shield should be grounded at one end only, normally at the recorder or other receiver end.
IGURE
F
748263-E Rosemount Analytical March 2001
2-3. I
NNER PANEL LAYOUT
Model 2100A Process Total Organic Carbon Analyzer
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IGURE
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2-4. O
PENING CONTROL PANEL (LOOSEN TWO PANEL FASTENERS
)
IGURE
F
12
2-5. B
LOCK WIRING DIAGRAM
(115VAC)
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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2.5.2.3 A
LARM
Refer to Figures 2-1 and 2-2.
WARNING: ELECTRICAL SHOCK HAZARD
Alarm switching relay contacts wired to a separate power source must be disconnected before servicing.
Connect alarm wires to the appropriate terminals (TB2) located on the electronics board. These are DPDT contacts capable of switching up to 10 A at 240 VAC. They may be used for driving alarm annunciators, lights, horns or other devices. Power must be supplied by your alarm actuating circuit, if needed.
IGURE
F
748263-E Rosemount Analytical March 2001
2-6. B
LOCK WIRING DIAGRAM
(230VAC)
Model 2100A Process Total Organic Carbon Analyzer
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2.5.3 P
IPING
Refer to drawing 655369. To maintain sample integrity, the quality of the input samp le line is very imp ortant . The input
line should be clean and made from an inert material. New Teflon or stainless steel tubing is strongly recommended.
Connect a 1/4-inch line from sample point to the sample inlet of the manifold. It is recommended that a flowmeter with a throttling valve be installed in this line for flow control. Desired flowrate is 1 L/min, but may be 50 to 2000 ml/min, depending upon desired response time and sample availability.
CAUTION
Do not turn on sample until installation is complete.
2.5.3.2 D
RAIN
Refer to drawing 655369. The Model 2100A has two drains located on the lower left side of the analyzer and a drain
from the condensate trap. The two-drain system was designed to eliminate sample con­tamination in those cases when it is desired to return the sample to the water system.
The drain designated "waste" contains oxidation products and persulfate not found in the sample stream and MUST NOT be returned to the water system. The drain designated "Sample Drain!' contains only process sample and may be returned to the water system.
If the sample drain is to be used in a sample return configuration, the drain line must meet the same criteria as the sample line. If the sample overflow is directed to a drain, then the material used to pipe the excess sample to the drain is not critical.
1. Connect a 1/2-inch. O.D., 10-ft. maximum length line from the "Sample Drain" to an open drain.
2. Connect a 1/2-inch line to the "Waste" drain located on the lower left side of the cabinet. The other end of the line should be routed to an appropriate open drain. This is a waste line containing oxidized compounds and the persulfate oxidation medium.
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CAUTION: BACK PRESSURE HAZARD
The drain lines must not be connected together before entering the open drain. Connecting the drain lines or using a sealed drain can cause back pressure, leading to excessive signal noise or actual flooding and damage to the instrument.
Also, the Sample Drain line should drain freely to an open drain if possible. Do not bend line more than 45 degrees from the vertical position because it may cause excessive pressure.
Any other condition which would cause back pressure in the drain lines must be avoided.
3. Connect a 1/2-inch line to the condensate trap drain. The other end of the line should be routed to an appropriate open drain. This is a waste line that may contain small amounts of oxidized compounds and the persulfate oxidation medium.
2.5.3.3 S
TANDARD
The "Standard" inlet located on the lower left side of the cabinet is used to introduce a calibration solution or to introduce a "grab" sample for analysis. Turn the selector valve on the inner panel to "Standard" for oper a ti on o f the "Stan dar d" inl et.
The Teflon tube may be inserted into a glass bottle or other calibration standard container.
2.5.3.4 R
EAGENT
Insert the 1/16-inch Teflon tube through the reagent reservoir cap into the container until the tube end rests on the reservoir bottom. Do not use metal tubing or fittings for this line. The reagent will react with most metals except 316SS. Refer to Section 4.2 for reagent preparation procedures.
2.6 OPTIONAL TYPE Z PURGE
Refer to Figure 2-8, and drawings 655369 and 837519 in Appendix A. The Model 2100A can be fitted with an optional Type Z purge (PN 837519). This option, which is installed on the instrument's right side, allows the unit to be placed in a Class I, Division 2 hazardous location per Standard ANSI/NFPA 496.
The Type Z purge supplies an inert gas, such as nitrogen, to the interior of the instrument casing. Administer purge gas to flowmeter at 20 psig. Adjust flowmeter for operation at .2 inch H2O.
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WARNING: POSSIBLE EXPLOSION HAZARD
For instruments equipped with the optional Type Z air purge installed in a Class 1, Division 2 (or equivalent) Hazardous Location, enclosure shall not be opened unless the area is known to be non-hazardous or unless all devices within have been de-energized. Power shall not be restored after enclosure has been opened until enclosure has been purged for 10 minutes.
IGURE
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16
2-7. P
URGE OPTION MOUNTING
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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S
TARTUP PROCEDURE
3
3.1 START-UP PROCEDURE
The purpose for this section is to provide step-by-step instructions, as follows, for first-time start-up of the unit.
1. A selector valve, located on the inner panel, is labeled "Standard" and "Process Sample". Turn this valve to the "Standard" position. Flow process sample through the sample inlet at a rate greater than 50 ml/min but not greater than 2000 ml/min. Check for leaks both inside and outside and correct any found. Allow the system to flush for at least one hour while proceeding with start-up.
2. Turn on drying gas, then carrier gas, and check for leaks using SNOOP PN 837801) or other leak detection solution.
3. Loosen 2 panel fasteners (Figure 2-5). Open inner panel and set carrier pressure according to the Data Sheet at the back of the manual.
Note This setting will change as the analyzer warms up and should be reset after about 2 hours.
4. Ensure that all switches on the inner panel are off (lower portion of switch pushed in).
5. Turn on external power to the instrument.
6. Turn on power switch ("on" position to the left) on the left side of the electronics board behind inner panel at the top of the unit.
7. Turn on main power switch (upper portion of switch pushed in) on upper right corner of panel.
At this point, heater, heater fan and front panel digital display on the front of the outer door should be operating.
8. Close inner panel and allow instrument to warm while proceeding with start-up.
9. Fill reagent reservoir, a 20 L container. (See Section 4.2, PREPARING REAGENT).
10. Install the reactor cap/lamp assembly to the top of the reactor. Ensure the rubber septum in the glass tube faces towards the front of the instrument. Install retaining springs to the cap and plug in lamp cord to lamp power outlet (Figure 2-4). Connect rubber tubing at lower end of condenser tubing over the rear glass tube on the reactor cap.
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CAUTION: INSTRUMENT DAMAGE
Do not run pumps without carrier gas flow. Damage to the instrument can occur if this requirement is not observed.
11. Fill reagent reservoir, a 20 L container. (See Section 4.2, PREPARING REAGENT).
12. Install the reactor cap/lamp assembly to the top of the reactor. Ensure the rubber septum in the glass tube faces towards the front of the instrument. Install retaining springs to the cap and plug in lamp cord to lamp power outlet (Figure 2-4). Connect rubber tubing at lower end of condenser tubing over the
CAUTION: GLASSWARE HAZARD
This instrument utilizes numerous vessels and other components made of glass. These components are fragile and should be handled carefully to avoid breakage. During installation or maintenance, wear face shield or eye goggles, gloves, and lab coat or long-sleeved clothing. In the event of breakage, immediately pick up and properly dispose of any large pieces. Use a suitable wet/dry shop-type vacuum machine to remove fine pieces. If the UV lamp is broken, refer to Mercury Hazard Warning below.
WARNING: MERCURY HAZARD
The ultraviolet light generating lamp contains mercury. Lamp breakage could result in mercury exposure. Mercury is highly toxic if absorbed through the skin or ingested, or if the vapors are inhaled.
Handle lamp assembly with extreme care. If lamp is broken, avoid skin contact and inhalation in the area of the lamp or the mercury spill.
Immediately clean up and dispose of the mercury spill and lamp residue as follows:
Wearing rubber gloves and goggles, collect all droplets of mercury by means of a suction pump and aspirator bottle with a long capillary tube. (Alternatively, a commercially available mercury spill clean up kit, such as J.T. Baker product No. 4439-01, is recommended.) Carefully sweep any remaining mercury and lamp debris into a dust pan. Carefully transfer all mercury, lamp residue and debris into a plastic bottle which can be tightly capped. Label and return to hazardous material reclamation center. Do not place in trash, incinerate or flush down the sewer. Cover any fine droplets of mercury in non-accessible crevices with calcium polysulfide and sulfur dust.
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WARNING: INTERNAL ULTRAVIOLET LIGHT HAZARD
Ultraviolet light from the reactor lamp can cause permanent eye damage. Do not look directly at the ultraviolet source in the reactor for prolonged periods. Use of ultraviolet filtering glasses is recommended. Never operate the lamp outside the reactor.
Additionally, the lamp may break if fluid flow is interrupted (allowing the lamp to heat up) and then reintroduced to the hot lamp.
WARNING: HAZARDOUS AND CORROSIVE CHEMICAL
This instrument utilizes a user provided chemical reagent which is an aqueous solution (14 to 40%) of either sodium persulfate, Na2S2O8, or ammonium persul­fate, (NH4)2S2O8, acidified with concentrated phosphoric acid, H3P04.
The reagent solution and its constituent chemicals are strong oxidizing agents and are highly corrosive. They can cause severe skin burns and eye damage upon contact. Ingestion could be fatal. Vapors can be very irritating to the skin, mucous membranes, eyes and respiratory tract.
Reagent leakage can cause severe corrosion damage to the instrument's enclosure and/or components and could create an electrical shock hazard. The instrument should be thoroughly checked for leaks during installation and start-up, routinely thereafter, and any time the integrity of the reagent contain­ment system is disrupted (e.g., for tube or fitting replacement).
Chemical salt encrustation at joints or fittings is an early symptom of reagent leakage. If evidence of leakage is discovered, the instrument should be imme­diately shut down and the leak repaired. Salt encrustation is normal at the reactor top interface. Salt buildup must be removed periodically to avoid collection on the case bottom, where the salt will damage the instrument en­closure due to reaction with moisture.
Refer reagent preparation, installation and service to qualified chemical technicians and observe all precautions noted in the safety messages located in appropriate sections throughout this manual.
11. Remove silicone rubber septum from reactor cap and fill reactor with distilled or deionized water. Observe carrier gas bubbling up through reactor.
12. Replace septum.
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13. Insert the reagent tubing into the 20 L reagent container (see step 9 above), and turn on reagent pump.
Note It will take several minutes for the first drops of reagent to reach the sparger. The
reagent flowrate is only approximately 1/2 ml/min. Do not run reagent pump without the sample pump for long periods as reagent may froth and travel upstream in the condenser tube.
14. Observe whether reagent/gas mixture is being blown into sample inlet sparger on the side of the reactor. If not, pull on both pump tube ends while the pump is rotating. Wait until reagent pump is primed and reagent/gas mixture is noted before proceeding.
15. Inse rt the standard line into a container of distilled or deionized water and set Sample Selector Valve to "Standard" positi o n.
16. Turn on standard pump and ensure that flow has increased into sparger (signifying that pump is drawing water from sample container).
17. After approximately an hour, switch IR Calibrate switch to "Calibrate." Open inner panel, check carrier gas pressure, and reset if necessary. Close inner panel. Wait 10 to 15 minutes before proceeding.
18. Calibrate the IR analyzer zero and span. (Section 4.5, IR ZERO, SPAN CHECK).
19. Switch IR Calibrate switch to "Nor mal" and turn on UV lamp. At this point, the digital reading can be expected to increase, perhaps off scale, until all organics in the reactor are oxidized.
20. When TOC reading stabilizes (about 1/2 hr.), the standard sample tubing has been adequately flushed.
21. Set TOC zero and span (See Section 4.6, TOC ZERO, SPAN CHECK).
22. Connect an accurate digital multimeter (DMM) or a recorder to the analog output terminals. Adjust R12 for correct 0 to 1 VDC output or R44 for correct 0 to 10 mV DC output (Figure 2-2). If you have the optional 4 to 20 mA output, set R44 to its lowest setting and short the 0 to 10 mV output to ground. Adjust the 4 to 20 mA zero adjust for 4 mA output.
Note A digital multimeter must be in series with other devices connected to this
output, and total output loop resistance must not exceed 500 ohms.
23. Remove short from 0 to 10 mV terminals, and adjust R44 for 0 to 10 mV reading which corresponds to the digital reading. Then adjust the 4 to 20 mA "span" adjust for correct output.
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24. Remove digital multimeter and reconnect any output wires.
25. Press and hold alarm readout button (Figure 3-1) while adjusting R6 (Figure 2-2) for correct alarm setting on digital display.
Note PC board is mounted upside down at the top of the instrument, inside inner-
panel.
26. Close inner panel.
27. Turn sample select valve to "Process Sample" and close front door.
28. From this point on, inner panel should remain closed. Allowing the temperature-controlled compartment to cool for any period of time may cause water condensation in the dryer.
The analyzer is now ready for analysis of the process stream. IR and TOC zero and span checks should be repeated after the first 24 hours of operation.
IGURE
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748263-E Rosemount Analytical March 2001
3-1. A
LARM READOUT BUTTON (PRESS
AND HOLD WHILE ADJUSTING SETPOINT
)
Model 2100A Process Total Organic Carbon Analyzer
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NOTES
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O
PERATION AND MAINTENANCE
4
4.1 OVERVIEW
The Model 2100A is designed for reliable, low-maintenance operation, requiring the following routine maintenance.
Normal maintenance consists of:
DAILY internal visual check for leaks and loose tubing,
Replenishing reagent, (as required)
Replacing two pump tubes, (every 6 months)
Checking calibration, (as required)
Removing reactor sediment, (as required)
Cleaning IR analyzer, (as required)
These procedures are outlined in this section. They should be followed to ensure analyzer life and performance.
WARNING: HAZARDOUS CHEMICALS
Sodium persulfate (Na2S2O8) and ammonium persulfate [(NH4)2S2O8)] are strong oxidizing agents that may cause fire if placed in contact with other materials. These chemicals and phosphoric acid (H3PO4) are corrosive and may cause se­vere burns if their dust or fumes are exposed to skin, eyes, or mucous membranes, or if they are inhaled.
Use in vent hood or in a well ventilated location. Wear eye goggles, rubber gloves and lab coat when handling all hazardous chemicals.
In the event of contact, flush eyes with water for at least 15 minutes. Flush skin areas with plenty of water. Obtain medical aid immediately.
Refer to the Material Safety Data Sheet, supplied by the chemical manufacturer, for specific information about each chemical.
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4.2 PREPARING REAGENT
The reagent reservoir (5 gal.) supplied with the instrument will hold enough reagent (customer supplied) for up to four weeks of operation, depending on the analyzer's range. Reagent flow is 26 ml/hr. to 65 ml/hr. depending on analyzer range.
To prepare the reagent, refer to Table 4-1 for correct reagent composition, and proceed as follows.
1. Measure out one liter of deionized water.
2. Add sodium or ammonium persulfate [Na2S2O8 or (NH4)2S2O8] and stir until all crystals are dissolved (use 140.0 grams for 14% or 400 grams for 40%).
CAUTION: DISSOLVE COMPLETE USE SPECIFIED CHEMICALS ONLY
Be sure all crystals are completely dissolved. Any un-dissolved crystals will cause excessive wear and premature failure of the reagent pump tube. They may also plug instrument tubing.
Do not use potassium persulfate as a substitute for sodium or ammonium persulfate. Potassium persulfate is less soluble. Therefore, it may leave undissolved crystals or cause crystals to drop out of solution if ambient temperature decreases. These crystals will cause the above-noted problems.
3. Add 5 ml of concentrated phosphoric acid (H3PO4) and stir.
4. Repeat this procedure until at least 10 liters of solution are prepared.
Alternatively, the reagent may be prepared in one batch, but a great deal of agitation will be required to dissolve all of the persulfate. A mechanical stirrer (plastic or stainless steel) will aid this procedure.
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Recommended
TOC
Range
(fullscale)
IR Range
(fullscale)
Sample Pump Head (Model No.)
Persulfate
Reagent
Conc. Type
2
Carrier Gas
Pressure
(psig)
3
Restrictor
(color)
Calibration
Standard
(ppm)
KHP Sucrose
2 0.2 % 7016 14% Sodium 10 Red 1.8 1.8 5 0.2 % 7016 14 % Sodium 15 Red 4.5 4.6 10 0.2 % 7016 14 % Sodium 24 Red 9.0 9.0 20 0.2 % 7014 14 % Sodium 14 Blue 1810 18.0 50 1 % 7014 14 % Sodium 12 Red 45.0 45.0 100 1 % 7014 14 % Sodium 20 Red 90.0 90.0 200 1 % 7014 14 % Sodium 22 Blue 180 180 500 1 % 7013 14 % Sodium 16 Blue Note 1000 10% 7013 14 % Sodium 10 Red Note 2000 10% 7013 40 % Ammonium 10 Red Note 5000 10% 7013 40 % Ammonium 12 Red Note
4
450
4
900
4
1800
4
4500
NOTE: Settings are approximations only. Isopropyl alcohol not recommended for calibration.
ABLE
T
4-1. A
PPLICATION DATA
2
Sodium persulfate is Na2S208 and ammonium persulfate is (NH4)2S208.
3
±20 %.
4
KHP not recommended for calibration at higher ranges but preferred over sucrose at lower ranges.
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4.3 REPLACING PUMP TUBES
CAUTION: REPLACE PUMP TUBES REGULARLY
A pump tube can fail in one of two ways: it may collapse or rupture. A collapsed tube will decrease flow rate or stop flow completely. A ruptured tube will also stop flow. More importantly, it will leak corrosive reagent into pump internals, resulting in pump failure and increased pump tube wear. Therefore, it is important to adhere strictly to a six-month pump tube replacement schedule. Instrument warranty does not cover pump internals damaged by corrosion.
The pump tubes can be expected to last for about twelve months of normal operation. To prevent unexpected analyzer shut- down or possible pump damage, the tubes should be replaced every six months.
Figures 4-1 through 4-11 illustrate the procedure for replacing pump tubes. To replace them, do the following procedure.
1. Turn 3-way valve in instrument to standard position. Pull standard and reagent lines from respective bottles. Allow pumps to run for 15 minutes to flush liquid from lines. Turn off PUMP POWER switches, and shut off carrier gas supply.
This step will prevent unwanted backflow and possible reagent con­tamination during this procedure.
2. Loosen both knurled screws holding the pump head together (Figure 4-1).
3. Pull off the front half of the pu mp head (Figure 4-2).
4. Pull out the old pump tube (Figure 4-3).
5. Replace one end of tubing at a time (to prevent improper re-connection) and secure the new tubing on analyzer tubing with two Ty-Raps on each end to stop leakage (Figures 4-4 and 4-5).
6. Rotate and push the pump roller assembly toward the inner back panel to ensure that the assembly shaft is
IGURE
F
4-1. P
UMP HEAD SCREWS
fully engaged (Figure 4-6).
7. Place the new tube over the rollers while keeping tension on the tube toward the right side and remembering that pump outlet is at top, inlet at bottom (Figure 4-7).
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PERATION AND MAINTENANCE
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IGURE
F
IGURE
F
4-2. R
4-3. R
EMOVING PUMP HEAD
EMOVE OLD PUMP TUBE
IGURE
F
IGURE
F
4-5. F
4-6. E
ASTENING TUBE ENDS
NGAGING PUMP SHAFT
IGURE
F
748263-E Rosemount Analytical March 2001
4-4. C
ONNECTING NEW PUMP TUBE
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F
Model 2100A Process Total Organic Carbon Analyzer
4-7. I
NST ALLING NEW PUMP TUBE
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PERATI ON AND MAINTENANCE
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8. With left thumb, press the new pump tube completely under each roller, being careful not to twist or kink the tube, or disengage the roller shaft (Figure 4-8).
9. Holding the tubes in the inlet and outlet grooves in the pump head, reinstall the pump head half, making sure that the pump tube is not pinched between the two pump head halves (Figure 4-9).
10. Install the knurled screws (Figure 4-10).
11. Firmly pull on each set of pump tube ends to remove any kinks or twists from the tube (Figure 4-11).
12. After both pump tubes are re placed, turn on carrier gas supply and verify gas flow through the reactor vessel. Turn on PUMP POWER switches. While the pumps are running, again pull on each pump tube end to remove kinks or twists (Figure 4-11).
WARNING: POSSIBLE INSTRUMENT DAMAGE
Operation of reagent and sample pumps without carrier gas flow can cause damage to the instrument.
13. If pump moves and makes a clicking sound, disassemble the front half of pump head, and seat pump tubing.
Note After a pump tube change, wait 2 hours for warm-up and recalibrate the
analyzer.
4.4 CALIBRATION CHECK
A complete calibration check should be performed periodically at startup and on a daily basis until confidence in longer periods of time has been established.
A calibration check is done in two phases: (1) IR zero and span check and (2) TOC zero and span check.
Note Some analyzer internal components are temperature 8ensitive. For this reason,
the analyzer's inner compartment is heated to a controlled temperature If the inner panel has been opened for maintenance, the panel should be closed for at least two hours to allow for temperature stabilization before proceeding with a calibration check. At initial start-up time, a slightly longer period temperature stabilization may be required before final calibration.
of
130
°°°°
F.
of
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IGURE
F
IGURE
F
4-8. P
4-9. I
OSITIONING PUMP TUBE
NSTALLING PUMP HEAD
IGURE
F
IGURE
F
4-10. I
4-1 1. S
NST ALLING KNURLED SCREWS
TRAIGHTENING PUMP TUBE
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4.5 IR ZERO, SPAN CHECK
The infrared analyzer is subject to very little drift as long as a constant enclosure temperature is maintained. A TOC zero and span check will identify the IR drift that may occur since last calibration. For this reason, an IR zero and span check is required periodically. Figures 4-12 through 4-17 illustrate the procedure for calibrating the IR analyzer.
To Check IR Zero and Span, proceed as follows.
1. Locate zero and span gas canisters (customer supplied; available from Rosemount Analytical, Inc.). Injection needles are taped inside canister caps.
2. Open the analyzer front door and locate the following controls on the control panel (Figure 2-4 for location).
a. IR Ca libra te Switch - W hen t h is switch is in the " Norma l" po sitio n, re acto r gas f lo ws
through the IR detector and the digital display reads TOC concentration. When this switch is in the "IR Calibrate" position, reactor gas bypasses the IR detector and the digital display reads CO2 concentration directly.
b. CAL Gas Fitting - Calibration gas is injected through this fitting and enters the IR
detector directly.
c. IR "Span" and "Zero" - These screwdriver adjusted pots are accessible from the
front of the inner panel. The are used to adjust the M zero and span, respectively.
3. Set IR calibrate switch to "Calibrate" (Figure 4-12).
4. Attach injection needle to zero gas canister and insert into CAL gas fitting (Figure 4-13).
CAUTION: SHARP NEEDLE
Handle the injection needle with care.
5. Inject short bursts of zero gas and observe front panel display. Do not inject continuously because 1) canister may be emptied or 2) the IR cell may be over­pressurized. When reading has stabilized, inject another burst of gas. Repeat until reading remains stable.
6. Adjust IR ZERO until front panel display reads 000. Disregard the decimal point if present (Figure
4-14).
30
Note The zero adjust is very slow in responding. Make a slight adjustment and wait
for the reading to stabilize before making another adjustment. Continue until display reads 000. The display will not register negative numbers in IR calibrate mode.
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PERATION AND MAINTENANCE
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IGURE
F
IGURE
F
4-12. S
4-13. I
ET SWITCH TO
NJECTING ZERO GAS
IR C
AL
IGURE
F
IGURE
F
4-15. I
4-16. A
NJECTING SPAN GAS
DJUSTING
PAN VALUE
IR S
IGURE
IGURE
F
7. Inject another burst of gas to ensure reading has not changed.
748263-E Rosemount Analytical March 2001
4-14. A
DJUSTING
IR ZERO
TO
000
F
Model 2100A Process Total Organic Carbon Analyzer
4-17. S
ET
IR S
WITCH TO
NORMAL
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PERATI ON AND MAINTENANCE
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8. Using the span gas canister, repeat paragraphs 4 and 5 to calibrate span gas (Figure 4-15).
9. After reading has stabilized , adju st "IR Span " (Figure 4 -16) until digita l displa y registers the same CO2 concentration shown on the gas canister (four digits for under 2000 PPM CO2, and three digits for concentrations over 2000 ppm). Ignore any decimal point which may be present on the display. This decimal is only relevant for TOC readout.
10. Set "IR Calibrate" switch back to "Normal" (Figure 4-17).
4.6 TOC ZERO, SPAN CHECK
TOC zero is affected by CO2 in the carrier gas, trace contaminants in the persulfate reagent and IR drift. Normally, concentration of carrier gas CO2 is constant, reagent contaminants are negligible and relatively constant, and IR drift is small. Therefore, unless the above factors are known problems, TOC zero should drift very little and require only occasional checks.
TOC span is affected by sample pump flow rate, carrier gas flow rate and IR span drift. Normally, these factors are also stable. Therefore, TOC span need only be checked every 1 to 2 months.
Inject another burst of gas to ensure reading has not changed. To check TOC zero and span, proceed as follows.
Note Use the following procedure only. Do not use IR zero and span controls for TOC
zero and span.
1. Prepare TOC standard (See Section
5.1, STANDARDS PREPARATION).
2. Connect calibration standard to "Standard" inlet. For maximum accuracy, container should be positioned so that liquid surface is approximately at the same level as the Sample Drain fitting on the side of the Model 2100A. This will assure that the liquid head at the pump inlet is the same for both stream sample and standard.
3. Turn off reagent pump (Figure 4-18). This action turns off both the reagent
IGURE
F
4-18. R
EAGENT PUMP SWITCH
and sample pumps.
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4. After analyzer reading is stable, adjust "TOC Zero" (Figure 4-19) until digital display reads "000".
5. Rotate sample selector valve to "Standard" (Figure 4-20).
6. Turn on reagent pump (sample pump will also start) and wait for stable TOC reading (Figure 4-21).
7. When analyzer reading is stable, adjust "TOC Span" (Figure 4-22) until digital display reads the same TOC as the calibration standard. Analyzer is now calibrated.
8. Rotate sample selector valve to "Process Sample" (Figure 4-20). Analyzer is in normal operation.
IGURE
F
IGURE
F
4-19. A
4-20. S
DJUSTING
AMPLE SELECTOR VALVE
TOC ZERO
IGURE
F
F
4-21. T
IGURE
URNING REAGENT PUMP
4-22. A
DJUSTING
ON
TOC SPAN
748263-E Rosemount Analytical March 2001
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4.7 SEDIMENT REMOVAL
Sediment from the sample may collect in the bottom of the reactor over a period of time. To remove this sediment while analyzer is operating, proceed as follows.
1. Turn off the UV lamp.
2. Remove rubber plug from reactor cap, and insert 1/8-inch O.D. Teflon tube to the bottom of the reactor.
3. Use a syringe or siphon to draw the sediment from the bottom of the reactor (remove as little reactor solution as possible). Refer to Section 4.10, paragraph 6.
4. Remove tube, and replace rubber plug.
5. When norm al reactor liquid level is re-estab lished, turn on the UV lamp and allow the instrument to stabilize. The analyzer will be back to normal operation.
6. Close analyzer door.
7. Discard sediment in an approved chemical disposal container.
4.8 PUMP MOTOR BEARINGS
Pump motor bearings are sealed and do not require lubrication.
4.9 TOC ALARM
The TOC alarm may be adjusted at any point from 0 to 100% and above fullscale. (For location, see Figure 3-1.)
To set this alarm point, proceed as follow s.
1. Press and ho ld ALARM SET SWITCH (S3). Alarm setpoint will now be displayed on the front panel digital readout.
2. W hile still pressing S3, adjust ALARM SET potentiometer (R6) until desired setpoin t is displayed on digital readout. Alarm is now adjusted.
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4.10 PREPARATION FOR SHIPMENT
If the Model 2100A requires shipment or relocation, precautions must be taken to protect the analyzer from the corrosive persulfate reagent. Employ the following procedure to drain and flush the reactor vessel and tubing and prepare the instrument for movement:
Note Please contact factory prior to shipment
CAUTION: GLASSWARE HAZARD
instrument to the factory.
of
This instrument utilizes numerous vessels and other components made of glass. These components are fragile and should be handled carefully to avoid breakage. During installation or maintenance, wear face shield or eye goggles, gloves, and lab coat or long sleeved clothing. In the event of breakage, immediately pick up and properly dispose of any large pieces. Use a suitable wet/dry shop-type vacuum machine to remove fine pieces. See Mercury Warning.
WARNING: MERCURY HAZARD
The ultraviolet light generating lamp contains mercury. Lamp breakage could result in mercury exposure. Mercury is highly toxic if absorbed through the skin or ingested, or if the vapors are inhaled.
Handle lamp assembly with extreme care. If lamp is broken, avoid skin con. tact and inhalation in the area of the lamp or
the mercury spill. Immediately clean up and dispose of the mercury spill and lamp residue as
follows: Wearing rubber gloves and goggles, collect all droplets of mercury by means of
a suction pump and aspirator bottle with a long capillary tube. (Alternatively, a commercially available mercury spill clean up kit, such as J.T. Baker product No. 4439-01, is recommended.) Care. fully sweep any remaining mercury and lamp debris into a dust pan. Carefully transfer all mercury, lamp residue and debris into a plastic bottle which can be tightly capped. Label and return to hazardous material reclamation center. Do not place in trash, incinerate or flush down the sewer. Cover any fine droplets of mercury in non-accessible crevices with calcium polysulfide and sulfur dust.
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1. Open the outer door of the analyzer and turn off the ultraviolet lamp. Reagent and sample pumps remain running, and carrier and drying gases remain flowing.
2. Fill a clean container with clean, deionized or distilled water. Place reagent and standard tubing into this container.
3. Switch the 3-way valve on the inner door from process sample position to standard position.
4. Allow system to flush standard and reagent lines with clean water for 1/2 hour.
5. After this flushing period, remove the standard and reagent lines from the clean water container. Allow liquid to drain for 15 minutes.
6. When standa rd and re agent lines run d ry, rem ove the rubber plug fro m the reac tor ca p and drain the reactor. This can be done by either of the following procedures, with 1/8-inch O.D. Teflon tube and/or syringe.
Insert the tube through the reactor cap to the bottom of the reactor. Use the syringe to extract the liquid.
Altern atively, immerse the tube into a container of clean water, filling the tube with water. Plug one end of the tube with your finger, trapping the water inside, and insert the opposite end through the reactor cap to the bottom of the reactor. Position the opposing end of the tube lower than the reactor bottom, and allow the siphoning process to remove all reactor liquids.
7. Using similar techniques as those in Step 6, fill the reactor with clean water. Ensure that the filling container is positioned higher than the reactor when using the alternative technique above. Continue filling the re actor until a cup of water flows from the waste drain.
8. Repeat Step 6 to drain the reactor. Replace the rubber plug in the reactor cap.
9. Turn off the reagent and sample pumps.
10. Turn off the main power switch.
11. Discontinue the flow of carrier and drying gases. Disconnect the carrier and drying gas lines at the bottom left side of the analyzer.
Note External standard and reagent lines must not be cut or disconnected from
bottom left side fittings.
12. Coil and tie the standard and reagent lines, ensuring that no crimping or pinching occurs.
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13. Discontinue flow through sample in connection. Disconnect sample in, sample drain, and waste lines and vent fitting at the bottom left side of the analyzer. Partially insert absorbent material (such as paper towels) into fittings.
14. Turn off power to analyzer at the circuit breaker and remove either the wiring to power terminal strip on the inside rear (upper right) of enclosure or power cord from receptacle.
15. Unplug the ultraviolet lamp from lamp power socket. Press latches on either side of socket to release plug.
16. Remove lower end of the condenser tube from the reactor and fasten to the inner door handle.
17. Remove the two springs that secure the reactor cap to the vessel.
18. Gently remove the reactor cap and ultraviolet lamp from the vessel. Application of a little water to the seam between the two may loosen the fit.
19. Pack the reactor cap/lamp assembly in a suitable (preferably the original) shipping container. Protection from shock and vibration is critical.
20. Insert absorbent material (such as paper towels) into the interior of the reactor vessel. Leave all absorbent materials in place for shipment.
21. Wipe dry the interior of the analyzer. Secure the inner door. Attach shock absorbent material (a sufficient amount to be squeezed between inner and outer doors) to the left side of the inner door handle with tape. Secure the outer door.
22. Carefully remove the analyzer from its mountings, ensuring the standard and reagent lines are not crimped.
23. Tilt instrument side-to-side and back-to-front to drain any remaining liquids from the enclosure.
24. Pack the analyzer on its back in a suitable (preferably the original) shipping container with sufficient packing material on all sides, top and bottom. Seal container properly.
25. Ship the ultraviolet lamp in its own container with, but not inside or attached to, the Model
2100A
enclosure.
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4.11 CLEANING INFRARED ANALYZER OPTICAL UNIT
Introduction of dust or water into the infrared analyzer may cause drift. When adjustment of the zero level with the zero control becomes impossible, check the IR analyzer for contamination.
For maintenance of the IR analyzer, refer to Figure 4-23 and do the following:
1. Shut off reagent pump.
2. Stop the sample gas flow. Purge the interior of the IR analyzer with zero gas, if necessary.
3. Turn main power off.
4. Disconnect the IR analyzer tubes from the optical unit.
5. Remove the two screws that attach the IR analyzer optical unit to the chassis, and remove the unit.
6. Remove the two screws from the IR Detector unit, and remove the measuring cell and source unit as an assembly.
7. If necessary, remove the two screws from the source unit, and disassemble the cell by cutting the rubber sealant.
IGURE
F
4-23. I
NFRARED ANALYZER OPTICAL
U
NIT
XPLODED VIEW
– E
8. Clean both sides of the measuring cell glass and the measuring cell interior with an ethanol-saturated cotton swab.
CAUTION: GAS LEAK HAZARD
During disassembly and e-assembly of the IR measuring cell, avoid excess pressure on the detector and infrared light source unit pipes. Deformation of these pipes may cause a gas leak and malfunction of the analyzer. Proper use of sealant is necessary to operate purge effectively and keep out unwanted CO2.
9. Reassemble by reversing instructions in paragraphs 1 through 7 above. Make sure to replace the o-ring between the cell and detector, to clean off all rubber sealant and to re-apply new sealant where removed.
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PERATION AND MAINTENANCE
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4.12 CLEANING CONDENSATE TRAP
See Figure 4-24.
WARNING: HAZARDOUS AND CORROSIVE CHEMICALS
This instrument utilizes a user provided chemical reagent which is an aqueous solution (14 to 40 %) o f either sodium persulfate, N a2S2O8, or ammonium persulfate, (NH4)2S2O
The reagent solut ion and its co nstituent chemical s are stro ng oxidizing agent s and are highly corrosive. They can cause severe skin burns and eye damage upon contact. Ingestion could be fatal. Vapors can be very irritating to the skin, mucous membranes, eyes and respiratory tract.
Reagent leakage can cause seve re corrosion damage to the instrument's enc losure and/or components and could create an electrical shock hazard. The instrument should be thoroughly checked for leaks during installation and start-up, routinely thereafter, and any time the integrity of the reagent containment system is disrupted (e.g., for tube or fitting replacement).
, acidified with con centrat ed phosph oric acid , H3PO4-
8
Chemical salt encrustation at joints or fittings is an early symptom of reagent leakage. If evidence of leakage is discov­ered, the instrument should be immediately shut down and the leak repaired.
Refer reagent preparation, in­stallation and service to qualified chemical technicians and observe all precautions noted in the safety messages located in appropriate sections thro ughout this manu al.
Condensate Trap
1. Remove the drain hose, loosen and remove the nuts on the tee fitting, and detach the trap from the instrument.
2. Unscrew the body of the Condensate Trap. Clean all parts with deionized water.
3. Reassemble and replace the trap. Replace drain hose.
748263-E Rosemount Analytical March 2001
IGURE
F
4-24. C
Model 2100A Process Total Organic Carbon Analyzer
ONDENSATE TRAP ASSEMBLY
39
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NOTES
40
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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P
REPARATION OF STANDARDS
5
5.1 STANDARDS PREPARATION
CAUTION: SAFETY PRECAUTIONS
Read this entire section before beginning to prepare standard solutions. Observe standard laboratory safety precautions when performing the following
procedures.
To calibrate the readout and analog output of the Model 2100A, a standard sample of known carbon content is required. Calibration should be checked every month or two. The standard sample used for calibration should be somewhat representative of the carbon material expected to be monitored. Carbon concentration should be close to, but slightly less than the analyzer fullscale reading.
Fresh standards are required. Use reagent grade materials only. All equipment and containers used for the carbon standard must be clean and free from
organic contaminants. Clean deionized or distilled water with carbon content less than five percent of the intended concentration is required for the standard.
To prepare a standard sample from a pure solid material, use the following equations to calculate the carbon concentration. Actual sample TOC will be the sum of this calculated value plus background TOC (See Section 5.2, BACKGROUND TOC COMPENSATION).
(1) 1 ppm C = 1 mg C/liter solution
= 1,000 ppb
(2) TOC = mg/L C = (Wt)(n)(12)(1000)
(mw)(V)
(3) Wt/Liter of standard = (desired concentration in ppm C)(mw)
(12)(n)(1000)
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REPARATION OF STANDARDS
P
As an alternative method to prepare a standard sample from a pure liquid material, use the following equations.
(4) Vs = (desired concentration in ppm C)(mw) or
(12)(n)(1000)(d)
(5) mg/L C = (Vs)(d)(n)(12)(11000)
(mw)(V)
Where:
Wt = wei ght of compound in grams mw = molecular weight of compound n = number of carbon atoms per molecule 12 = atomic weight of carbon V = volume of standard in liters Vs = volume of pure liquid compound in ml d = density of pure liquid compound in g/ml at room temperature
At the low concentrations sometimes encountered when using the Model 2100A, it may be more convenient to prepare a concentrated standard, and then use a small measured portion of this solution to prepare diluted standard solutions as required. The higher concentration solution may be stored for some time if refrigerated in a dark brown bottle. Adding 1 or 2 drops of phosphoric acid will also aid in preserving the standard.
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REPARATION OF STANDARDS
P
5.2 BACKGROUND TOC COMPENSATION
All of the above calculations assume that the water used for preparing the standards is pure, with no background TOC. This, of course, is never true. Therefore, in order to determine the true carbon content of the calibration sample, it is necessary to determine background carbon content. The background TOC may be determined by the following procedure.
1. Calibrate the analyzer to the calculated calibration standard value, or if the analyzer has been previously calibrated, simply run the analyzer on the calibration standard and record the analyzer digital reading.
2. Introduce a sample of the "zero water" used for preparing the standard.
3. Record the digital reading.
4. Use the following equations to calculate the background. TOC of the "zero water" used for preparing the standard and the true TOC of the
standard: (6) TOC2 = (R2)(TOCC)
(RS – RZ) (7) TOC = TOCC + TOC Where:
TOC = True TOC
Z
TOC
= TOC of “zero water” = background TOC
TOCC= Calculated TOC from equation (1)
S
R R
= Digital reading of standard
Z
= Digital reading of “zero” water
Z
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REPARATION OF STANDARDS
P
Examples: A. T o prepare a 1 liter 100 ppm standard of sucrose (cane sugar) in water (commonly
used for calibration in sugar plant or waste treatment plant applications), the following calculations apply.
Sucrose (C12H22O11) has a molecular weight of 342.31 and has 12 carbon atoms per molecule.
Therefore:
mw = 342.31 n = 12 Solving Equation (3):
Wt/L = (100)(342.31) = .23772 g
(12)(12)(1000)
0.23772 g of sucrose (easily weighed on a laboratory balance) dissolved in pure water to a final volume of 1 liter will result in a standard of 100 ppm plus background TOC.
B. To prepare a I liter 2 ppm standard of isopropanol (commonly used for
semiconductor industry applications), the following calculations apply. Isopropanol (C3H7OH) has a molecular weight of 60.09, a density of .789 g/ml, and
3 carbon atoms per molecule. Therefore:
mw = 60.09 d = .789 n = 3 Solving Equation (4):
Vs = (2)(60.09) = 0.004231 ml
(12)(3)(1000)(.789)
0.004231 ml is too small to measure with equipment normally found in laboratories. If a 1000 ppm standard is prepared, 2.1154 ml of isopropanol would be required. This is still not a convenient quantity to measure. However, 2 ml is easily measured with a standard pipette. Solving Equation 5 for 2 ml in one liter:
44
mg/L C = (Vs)(d)(n)(12)(1000) = (2)(.789)(3)(12)(1000) = 945.4
(mw)(V) (60.09)(1)
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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REPARATION OF STANDARDS
P
Therefore, 2 ml of isopropanol dissolved in water to a final volume of 1 liter will result in a standard of 945 ppm plus background TOC. When 2 ml of this solution is diluted with water to make one liter of final calibration standard, the concentration will be 1.89 ppm plus background TOC. 1.89 ppm is 94.5% of fullscale for a 0 to 2 ppm (0 to 2000 ppb) fullscale range, an ideal figure with which to work. Similarly, 5 ml of the 945 ppm solution in 1 L will be 4. 725 ppm or 94.5% of fullscale for a 0 to 5 ppm range.
C. To prepare a 1 liter 500 ppm standard of potassium hydrogen phathalate (KBP),
which is a commonly used standard for wastewater applications, the following
calculations apply. KHP(C6H5O4K) has a molecular weight of 204.2 and 8 carbon atoms per molecule. Therefore:
mw = 204.2 n = 8 Solving Equation (3):
wt/L = (500)(204.2) = 1.06354 g
(12)(8)(1000)
1.06354 g of KHP dissolved in pure water to a final volume of 1 liter will result in a standard of 500 ppm plus background TOC. A 1000 ppm sample may be prepared by doubling this amount of KHP.
D. To determine background TOC and true TOC of a sample, the following
calculations apply. A 1000 ppb standard sample is prepared using one of the above methods. The
analyzer is calibrated to read 1000 ppb with this standard. When "zero water" is introduced, the analyzer reads 58. To calculate the background TOC of the sample:
S
R
= 1000 RZ = 58 TOCC = 1000
Using equation (6): TOCZ = (RZ)(TOCC) = (58)(1000) = 61
(RS – RZ) (1000 – 58) The true TOC of the sample is 1061 ppm. Calibrate analyzer to read 1061 with this
standard.
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REPARATION OF STANDARDS
P
NOTES
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C
IRCUIT DESCRIPTIONS
6
6.1 GENERAL
This section describes how the IR detector signal is electronically processed. Refer to the instrument schematic (See Appendix A) and to Figure 2-2 for component location.
6.2 INPUT SIGNAL CONDITIONER
The input signal from the NDIR detector is 10 to 110 mV DC. The two segments of amplifier U1 provide necessary suppression and gain to produce an output signal of 0 to 10 V at test point TP-6. Potentiometer R21 controls the suppression, and potentiometer R16 controls the gain. R21 and R16 are factory set controls and normally require no further adjustment.
6.3 LINEARIZER
The output signal from the NDIR (and therefore, also from the signal conditioner) is non-linear with respect to CO2 concentration. This non-linearity is corrected by generating a non-linear gain of opposite magnitude. The correction signal is generated in three individual straight segments and added together. At any given point, the product of the non-linear input signal and non-linear gain produce a very close approximation to a linear output signal at the output of the linearizer (pin 14, U2). Potentiometers R28, R30, R34, R38, R40 are fac­tory preset and should not be altered under any circumstances.
6.4 ZERO AND SPAN
A piggyback board is mounted on the main printed circuit board. This board contains a dual amplifier and two user controls. A zero control (R8) allows null of the offset due to the presence Of CO2 in the carrier gas. A span control (R7) allows the user to calibrate the instrument against known standards. The output of the zero and span board at TP-1 is 0 to 10 V linear with CO2 concentration.
6.5 RECORDER OUTPUTS
The voltage at test point TP-1 is 0 to 10 V for a range of zero to fullscale TOC. Voltage outputs are available at TB-3 of 0 to 1 V and 0 to 10 mV for this same range. In addition, a socket is provided for the installation of an optional plug-in module for an isolated 4 to 20 mA signal. The outputs are individually adjustable to provide the 0 to 1 V and 0 to 10 mV signals with digital readings as low as 0 to 500. R12 controls the 0 to 1 V output. R44
748263-E Rosemount Analytical March 2001
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IRCUIT DESCRIPTIONS
C
controls the 0 to 10 mV and the 4 to 20 mA outputs simultaneously. Refer to Section 3.1, paragraphs 22 through 24, for modul e adj ustments.
6.6 ALARM OUTPUT
A DPDT 10 A alarm control is provided as standard. The setpoint is continuously variable over the range of 0 to 2500. The voltage developed at R6 "Alarm Setpoint" is buffered by part of U3 and compared to the signal voltage by another part of U3. If the signal voltage is higher than the set voltage, transistor Q1 and pilot relay K1 are energized. K1 in turn energizes relay K2. Momentarily depressing pushbutton S3 displays the setpoint of the alarm in ppm on the LCD display. Some hysteresis is built into the alarm circuit to prevent relay chattering on the small amount of signal noise normally present. Thus the alarm dropout point is somewhat lower than the alarm energize point.
6.7 DISPLAY
The display module is a 31/2-digit backlighted assembly. The range of the display is 0 to
1999. Provision has been made for adding a decimal point to the display (i.e. 199.9 etc.) by soldering a jumper. This is accomplished by soldering a jumper to the appropriate pair of holes in the D.P. column of the main PC board.
A jumper is provided on the piggyback board to allow 10 volts from the linearizer circuit to read either 1999 for a 0 to .2% IR detector or 1000 for a 0 to 1% or 0 to 10% detector.
6.8 POWER SUPPLY
A power supply provides regulated ±15 VDC for the circuit board (Figures 2-6 and 2-7). Factory-wired jumpers (A,B,C,D) select either 115 V or 230 V, 50/60 Hz operation.
A switch (SW 1) and 1 A fuse (Fl) are provided (See DRAWING 837484 in Appendix A). The switch does not protect the contacts of relay K2. The rectified DC is regulated by separate ±15 V regulators so that the operation is independent of line voltage changes of 20%.
CAUTION: VOLTAGE CONVERSION
Changing jumpers alone is not enough to convert the instrument from 115 VAC to 230 VAC or vice versa. Consult the factory for further information.
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T
ROUBLESHOOTING
7
Should a malfunction occur in the Model 2100A TOC, the chart beginning on page 7-3 will aid in determining and correcting the cause.
WARNING: ELECTRICAL SHOCK HAZARD
Servicing this instrument requires access to shock hazard level voltages which can cause death or serious injury. Refer servicing to qualified personnel. Relay contacts wired to separate power sources must be disconnected before servicing.
WARNING: ULTRAVIOLET LIGHT HAZARD
Ultraviolet light from the reactor lamp can cause permanent eye damage. Do not look directly at the ultraviolet source in the reactor for prolonged periods. Never operate the lamp outside the reactor. Additionally, the lamp may break if fluid flow is interrupted and then reintroduced to the hot lamp.
CAUTION: GLASSWARE HAZARD
This instrument utilizes numerous vessels and other components made of glass. These components are fragile and should be handled carefully to avoid breakage. During installation or maintenance, wear face shield or eye goggles, gloves, and lab coat or long-sleeved clothing. In the event of breakage, im­mediately pick up and properly dispose of any large pieces. Use a suitable wet/dry shop-type vacuum machine to remove fine pieces. Refer to Mercury Warning on next page.
748263-E Rosemount Analytical March 2001
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ROUBLESHOOTING
T
WARNING: HAZARDOUS AND CORROSIVE CHEMICALS
This instrument utilizes a user provided chemical reagent which is an aqueous solution (14 to 40%) of either sodium persulfate, Na2S208, or ammonium per­sulfate, (NH4)2S208, acidified with concentrated phosphoric acid, H3P04-
The reagent solution and its constituent chemicals are strong oxidizing agents and are highly corrosive. They can cause severe skin burns and eye damage upon contact. Ingestion could be fatal. Vapors can be very irritating to the skin, mucous membranes, eyes and respiratory tract.
Reagent leakage can cause severe corrosion damage to the instrument's enclosure and/or components and could create an electrical shock hazard. The instrument should be thoroughly checked for leaks during installation and start-up, routinely thereafter, and any time the integrity of the reagent contain­ment system is disrupted (e.g., for tube or fitting replacement).
Chemical salt encrustation at joints or fittings is an early symptom of reagent leakage. If evidence of leakage is discovered, the instrument should be immediately shut down and the leak repaired. Salt encrustation is normal at the reactor top interface. Salt buildup must be removed periodically to avoid collection on the case bottom, where the salt will damage the instrument enclosure due to reaction with moisture.
Refer reagent preparation, installation and service to qualified chemical technicians and observe all precautions noted in the safety messages located in appropriate sections throughout this manual.
CAUTION: INSTRUMENT DAMAGE
Do not run pumps without carrier gas flow. Damage to the instrument can occur if this requirement is not observed.
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ROUBLESHOOTING
T
WARNING: MERCURY HAZARD
The ultraviolet light generating lamp contains mercury. Lamp breakage could result in mercury exposure. Mercury is highly toxic if absorbed through the skin or ingested, or if the vapors are inhaled.
Handle lamp assembly with extreme care. If lamp if broken, avoid skin contact and inhalation in the area of the lamp or the mercury spill.
]Immediately clean up and dispose of the mercury spill and lamp residue as follows:
Wearing rubber gloves and goggles, collect all droplets of mercury by
means of a suction pump and aspirator bottle with a long capillary tube. (Alternatively, a commercially available mercury spill clean up kit, such as J.T. Baker product No. 4439-01, is recommended.)
Carefully sweep any remaining mercury and lamp debris into a dust
pan.
Carefully transfer all mercury, lamp residue and debris into a plastic
bottle which can be tightly capped.
Label and return to hazardous material reclamation center.
Do not place in trash, incinerate or flush down sewer.
Cover any fine droplets of mercury in non-accessible crevices with
calcium polysulfide and sulfur dust.
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
51
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ROUBLESHOOTING
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SYMPTOM POSSIBLE CAUSE CORRECTION
Digital display dark. No power.
Analog output zero. No power.
UV lamp out. No power.
High sample TOC.
Low carrier flow.
High TOC reading.
Plugged gas restrictor.
Check to see that power is turned on.
Check PC Board power switch (left position).
Check fuse; replace if necessary.
Confirm analyzer calibr ati on with calibration standard. Analyzer grab sample with lab TOC analyzer. Recalibrate if necessary.
Check gas supply pressure and carrier gas pressure setting. Adjust setting and recalibrate analyzer if necessary. Also, see "Low or no gas through reactor" below.
Replace restrictor (located on the carrier regulator).
Low TOC reading.
No sparger air.
Inadequate amount of phosphoric acid in reagent
Low sample TOC.
Carrier gas flow too high.
Check all gas flows. Replace sparger gas restrictor located on the carrier regulator if corroded or plugged. WARNING: DO
NOT OPERATE PUMPS WITH GAS OFF.
Confirm that acid was added (See Section 4). Increase amount if too low.
Check analyzer with calibration standard. Take grab sample for lab analysis.
Check carrier gas pressure setting. Adjust and recalibrate if necessary.
52
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
Page 68
SYMPTOM POSSIBLE CAUSE CORRECTION
Check analyzer with
Analyzer out of calibration.
calibration standard. Recalibrate if necessary.
ROUBLESHOOTING
T
Zero or near zero TOC reading on calibration standard.
Out of reagent.
Check reagent container and refill if necessary.
Check reagent mixing
Reagent improperly mixed.
procedure to be sure reagent has been mixed to proper concentrations.
Weak UV lamp (not likely). Replace lamp.
Check that transformer is
Lamp not burning.
plugged in, lamp is plugged
in and lamp switch is ON. Lamp burned out. Replace lamp. Sample pump turned off. Turn on pump. Reagent pump turned off. Turn on pump. Sample pump not pumping. Repl ace pu mp tub e. Reagent pump not pumping. Replace pump tub e.
Flush out lines to remove
plug, and be sure proper
reagent is being used. DO Reagent pump or reagent tubing plugged.
NOT SUBSTITUTE
POTASSIUM
PERSULFATE FOR
SODIUM PERSULFATE.
Replace pump tube.
Leak in reagent pump inlet causing loss of prime.
Defective reagent pump motor or sample pump motor.
748263-E Rosemount Analytical March 2001
Place two nylon Ty-Raps
around each end of the
pump tubing to assure tight
seal.
Replace motor.
Model 2100A Process Total Organic Carbon Analyzer
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ROUBLESHOOTING
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SYMPTOM POSSIBLE CAUSE CORRECTION
Check infrared analyzer with Infrared analyzer defective or out of calibration.
calibration gases. Replace
or service infrared analyzer
if necessary.
Replace reagent if dirty. Mix
reagent thoroughly until all
crystals are dissolved.
ENSURE POTASSIUM
PERSULFATE HAS NOT
BEEN SUBSTITUTED FOR
SODIUM PERSULFATE,
Short reagent pump tube life.
Dirt or crystals in reagent solution.
OR POTASSIUM OR
SODIUM SULFATE FOR
AMMONIUM
PERSULFATE.
Corroded pump rollers. Replace roller assembly.
Negative TOC reading. Analyzer out of calibration. Analyzer reading does not
change when sample is changed or sample pump is
“IR Calibrate” switch is in “Calibrate” position.
turned on or off.
Excessive back pressure in system is blowing gas out reactor overflow.
After period of normal operation, analyzer reading does not change when sample is changed or sample pump is turned on or
Water in lines to or from IR detector.
off.
Recalibrate (See Section
4.4).
Switch to “Normal”.
Check sample flow lines for
blocked components (valve,
solenoid valve, and
condensate trap).
Remove water and correct
cause. Check IR cell for
water and clean cell if water
is found.
Check to confirm that
analyzer is correctly vented
(See Section 2.4.2.6) and
correct if necessary.
54
Gas leaks.
Check all fittings and tighten
where necessary
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
Page 70
SYMPTOM POSSIBLE CAUSE CORRECTION
ROUBLESHOOTING
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Water in vent lines, either internal or external.
Sparger gas/liquid separator flooded.
Excessive noise on display and analog output only wi th "IR Calibrate" switch in "Normal" position only.
Excessive noise on digital display and on analog output only with "IR Calibrate" switch in either position.
Improper drain and/or vent installation.
Improper drain and/or vent installation.
Correct installation (VERY IMPORTANT). See Section
2.4.2. Correct installation (VERY
IMPORTANT). See Section
2.4.2.
Remove source of back Water or other source of back pressure in vent line.
pressure. Check that all
external vent lines slope
downward (Section 2.4.2.6) Condensate trap blocked.
Clean condensate trap per
Section 4.12. Water or dirt in IR cell. Clean or replace cell. Defective IR analyzer. Replace IR analyzer.
Loose connection.
Check wiring and tighten
connections if necessary. Defective electronics board. Replace electronics board.
Digital display has reading but analog signal incorrect or not present.
No output from 4 to 20 mA terminals (test meter must be in series with 4 to 20 mA loop).
4 to 20 mA output always reads 4 mA with positive readout on the digital display (test meter must be in series with 4 to 20 mA loop).
R12 or R44 not adjusted. Adjust pot.
4 to 20 mA plug-in option not installed or not plugged
Install 4 to 20 mA option. in.
Defective 4 to 20 mA module.
4 to 20 mA plug-in misadjusted.
R44 not adju sted or span pot on 4 to 20 mA plug-in option not adjusted.
Defective 4 to 20 mA module.
Replace plug-in module.
Calibrate 4 to 20 mA
module. (See Section 3.1,
steps 22 to 24.)
Check and adjust R44 first if
necessary. If output still
reads 4 mA, then adjust pot
on plug-in module.
Replace plug-in module.
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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ROUBLESHOOTING
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SYMPTOM POSSIBLE CAUSE CORRECTION
Check carrier gas source
Low carrier gas pressure.
pressure and correct if necessary.
Low or no gas flow through reactor.
Saw-tooth recorder pattern.
Incorrect carrier gas pressure setting.
Adjust to correct setting and recalibrate analyzer .
Replace restrictor. Plugged carrier gas restrictor.
WARNING: DO NOT
OPERATE PUMPS WITH
GAS OFF.
Leaking fitting. Tighten all fittings. Plugged sparging frit in
reactor.
Clean reactor with acid.
Replace check valve. Plugged carrier gas check valve.
WARNING: DO NOT
OPERATE PUMPS WITH
GAS OFF.
Varying carrier pressure. Instrument carrier gas
supply pressure too low. Defective carrier pressure
regulator.
Install pressure regulator in
supply line to instrument.
Raise carrier supply
pressure.
Replace regulator.
Dryer turning brown or purple.
Infrared analyzer does not respond to calibration gases.
56
Liquid trapped in drain or vent line.
Remove liquid and correct
installation. Normal condition. No corrective action req’d. Empty canisters. Replace canisters.
Loose tube or fitting in IR analyzer.
Tighten or replace fitting or
tubing.
Carefully clean cell windows Dirty IR cell windows.
with soft cotton swab and
ethanol. (See Section 4.11.) Defective IR analyzer.
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
Repair or replace IR
analyzer.
Page 72
SYMPTOM POSSIBLE CAUSE CORRECTION
ROUBLESHOOTING
T
IR reading too low when span gas introduced, and IR span pot at maximum setting.
IR cell windows require frequent cleaning, cell is corroding, smell of chlorine observed at instrument vent.
Analog output normal, but no digital readout or digital readout always reads zero.
UV lamps and pumps operate, but no analog output present and digital display is dark.
"IR Calibrate" switch in “Normal” position.
Switch to "Calibrate" during IR calibration.
Any of above. See above.
High salt concentration in sample.
Contact factory for solutions.
Defective display module. Repair or replace module. Defective ribbon cable. Replace cable.
Defective electronics board.
Blown or defective fuse on electronics board.
Power switch on, electronics board turned off.
Repair or replace electronics board.
Replace fuse on electronics board located at top of analyzer.
Turn on switch (left position).
Analyzer reading seems to drift with ambient temperature changes.
Zero drifts with sample pump off and air carrier flowing.
Sample TOC may be changing with ambient temperature.
Instrument temperature controller set too low.
Defective instrument enclosure temperature control system
Air compressor inlet located too close to source of CO2 or inside building occupied by people.
Instrument air dryer removing varying amounts of CO2.
Confirm analyz er zero and calibration.
Install thermometer and adjust temperature control for 130°F.
Locate and replace defective component.
Move compressor inlet or switch to nitrogen carrier gas. Recalibrate analyzer.
Switch to more stable carrier gas.
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
57
Page 73
ROUBLESHOOTING
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SYMPTOM POSSIBLE CAUSE CORRECTION
Corrosion of IR detector and Tygon tubing.
Air being used as carrier gas. UV lamp oxidizes oxygen to ozone, a corrosive agent.
Use CO2-free nitrogen as
carrier gas. DO NOT USE
AIR OR OXYGEN AS
CARRIER GAS.
58
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
Page 74
R
EPLACEMENT PARTS
8
WARNING: PARTS INTEGRITY
Tampering with or unauthorized ubstitution of components may adversely affect safety of this product. Use only factory-approved components for repair.
8.1 RECOMMENDED SPARE PARTS
Qty
2 010963 2 010964 2 010965 2 010966 2 030504 2 030505 1 070627 Gasket Sleeve, Reactor, Teflon 1 090092 Restrictor, 400 cc, Green 1 090093 Restrictor, 20 cc, Union 1 090094 Restrictor, 50 cc, White 1 090095 Restrictor, Male Connector, 100 cc, Blue 1 090096 1 090868 1 512092 Lamp, Ultraviolet 1 512096 Reactor Cap 1 512097 Reactor Body 1 517798 Septa, Pierced (pkg. of 10) 1 517803 Septa (pkg. of 10) 1 523341 Tubing, 1/8-inch Teflon, 5 feet 2 837353 2 837354 2 837356 1 902515 Check Valve
Part
Number
Description
5
Gas, Zero
5
Gas, Span, 2 to 50 ppm ranges (1,770 ppm CO2 in N2)
5
Gas, Span, 100 to 1,000 ppm ranges (9,020 ppm CO2 in N2)
5
Gas, Span, 2,000 to 5,000 ppm ranges
5
Persulfate, Sodium, 500 g
5
Persulfate, Ammonium, 500 g
5
Restrictor, Male Connector, 200 cc, Blue
5
Filter, Infrared Analyzer, In-line
5
Pump Tube, Norprene 7013, ranges 500 to 5,000 ppm
5
Pump Tube, Norprene 7014, ranges 20 to 200 ppm
5
Pump Tube, Norprene 7016, ranges 2 to 10 ppm
5
Specify analyzer range when ordering.
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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EPLACEMENT PARTS
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8.2 REPLACEMENT PARTS (NUMERICALLY)
Part Number Description
010115 Switch, Rocker 010116 Switch, Rocker (Infrared Analyzer) 010443 010963 010964 010965 010966 030504 030505 070627 Gasket Sleeve, Reactor, Teflon 080014 Container, Reagent, 20 L 080046 Key, Enclosure 080874 Valve, 3-Way, Stainless Steel 080950 Cross, Teflon 090092 Restrictor, 400 cc, Green 090093 Restrictor, 20 cc, Union 090094 Restrictor, 50 cc, White 090095 Restrictor, Male Connector, 100 cc, Blue 090096 Restrictor, Male Connector, 200 cc, Blue 090828 Filter, Collins 090864 090865 090866 090868 Filter, Infrared Analyzer, In-line 152106 Tubing, 1/8-inch O.D. 512092 Lamp, Ultraviolet 512096 Reactor Cap 512097 Reactor Body 517322 Septa, Gas Injector (pkg. of 10) 517798 Septa, Pierced (pkg. of 10) 517803 Septa (pkg. of 10) 523341 Tubing, 1/8-inch Teflon, 5 feet 523893 Fuse, 5 amp (pkg. of 5) 644790 Trap Assembly, TOCA Condensate 655374 Tee, Modified 1/4 T x 1/4 MPT Cres. 748263 Manual, Instruction 837120 Display, Back-lighted (LCD) 837326 Cable, Ribbon (14 Lead) 837353
6 5 5 5 5 5 5
5 5 5
5
Transformer, Step-Down Gas, Zero Gas, Span, 2 to 50 ppm ranges (1,770 ppm CO2 in N2) Gas, Span, 100 to 1,000 ppm ranges (9,020 ppm CO2 in N2) Gas, Span, 2,000 to 5,000 ppm ranges Persulfate, Sodium, 500 g Persulfate, Ammonium, 500 g
Pump Head, 7013 Pump Head, 7014 Pump Head, 7016
Pump Tube, Norprene 7013, ranges 500 to 5,000 ppm
6
Applicable to instruments with serial numbers less than 1000083.
60
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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EPLACEMENT PARTS
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837354 837356
5 5
Pump Tube, Norprene 7014, ranges 20 to 200 ppm
Pump Tube, Norprene 7016, ranges 2 to 10 ppm 837404 Temperature Controller 230 V 837405 Thermistor Assembly 837406 Transformer Assembly, Ultraviolet, 230 V 837407 Printed Circuit Board Assembly, Model 2100A, 115 V 837409 Heater Assembly, 230 V 837411 Cable, 115 V Harness 837414 Transformer Assembly, Ultraviolet, 115 V 837415 Temperature Controller 115 V 837417 Heater Assembly, 115 V 837418 Fan Assembly, 115 V 837419 Fan Assembly, 230 V 837435 Cable, 230 V Harness 837436 Cable, Signal Assembly 837443 Regulator Assembly 837444 Solenoid Assembly, 115 V DC 837445 230V Board Assembly, Model 2100A 837465 Elbow, Waste 837467 Connector, Male 1/8" Modified 837519 Z Purge Kit, Class 1, Division 2, Groups C and D 837555 Current Output, 4 to 20 mA 837564 Motor, 18 rpm, 120 V, 50/60 Hz, Sample Pump 837565 Motor, 7 rpm, 115 V, 50/60 Hz, Sample Pump 837566 Motor, 15 rpm, 230 V, 50/60 Hz, Sample Pump 837567 Motor, 6 rpm, 230 V, 50/60 Hz, Reagent Pump 884873 Filter, Air 25 cfm, 1/8 NPT 899322 Indicator Light, LED, Red 899486 Shipping Kit 901842 Latch, Flush - Lift & Turn 901844 Fastener, Stud, 1/4-Turn, Quick-Release 901845 Fastener, Receptacle, 1/4-Turn, Quick-Release 901961
7
Transformer, Step-Down 902515 Valve, Check
7
Applicable to instruments with serial numbers greater than 1000082.
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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EPLACEMENT PARTS
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8.3 REPLACEMENT PARTS (ALPHABETICALLY)
Part Number Description
837411 Cable, 115 V Harness 837435 Cable, 230 V Harness 837326 Cable, Ribbon (14 Lead) 837436 Cable, Signal Assembly 837467 Connector, Male 1/8" Modified 080014 Container, Reagent, 20 L 080950 Cross, Teflon 837555 Current Output, 4 to 20 mA 837120 Display, Back-lighted (LCD) 837465 Elbow, Waste 837418 Fan Assembly, 115 V 837419 Fan Assembly, 230 V 901845 Fastener, Receptacle, 1/4-Turn, Quick-Release 901844 Fastener, Stud, 1/4-Turn, Quick-Release 884873 Filter, Air 25 cfm, 1/8 NPT 090828 Filter, Collins 090868 Filter, Infrared Analyzer, In-line 523893 Fuse, 5 amp (pkg. of 5) 010965 010964 010966 010963 070627 Gasket Sleeve, Reactor, Teflon 837417 Heater Assembly, 115 V 837409 Heater Assembly, 230 V 899322 Indicator Light, LED, Red 080046 Key, Enclosure 512092 Lamp, Ultraviolet 901842 Latch, Flush - Lift & Turn 748263 Manual, Instruction 837566 Motor, 15 rpm, 230 V, 50/60 Hz, Sample Pump 837564 Motor, 18 rpm, 120 V, 50/60 Hz, Sample Pump 837567 Motor, 6 rpm, 230 V, 50/60 Hz, Reagent Pump 837565 Motor, 7 rpm, 115 V, 50/60 Hz, Sample Pump 030505 030504 837407 Printed Circuit Board Assembly, Model 2100A, 115 V 837445 Printed Circuit Board Assembly, Model 2100A, 230 V 090864 090865
5 5 5 5
5 5
5 5
Gas, Span, 100 to 1,000 ppm ranges (9,020 ppm CO2 in N2) Gas, Span, 2 to 50 ppm ranges (1,770 ppm CO2 in N2) Gas, Span, 2,000 to 5,000 ppm ranges Gas, Zero
Persulfate, Ammonium, 500 g Persulfate, Sodium, 500 g
Pump Head, 7013 Pump Head, 7014
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March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
Page 78
EPLACEMENT PARTS
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Part Number Description
090866 837353 837354 837356
5 5 5 5
Pump Head, 7016
Pump Tube, Norprene 7013, ranges 500 to 5,000 ppm
Pump Tube, Norprene 7014, ranges 20 to 200 ppm
Pump Tube, Norprene 7016, ranges 2 to 10 ppm 512097 Reactor Body 512096 Reactor Cap 837443 Regulator Assembly 090093 Restrictor, 20 cc, Union 090092 Restrictor, 400 cc, Green 090094 Restrictor, 50 cc, White 090095 Restrictor, Male Connector, 100 cc, Blue 090096 Restrictor, Male Connector, 200 cc, Blue 517803 Septa (pkg. of 10) 517322 Septa, Gas Injector (pkg. of 10) 517798 Septa, Pierced (pkg. of 10) 899486 Shipping Kit 837444 Solenoid Assembly, 115 V DC 010115 Switch, Rocker 010116 Switch, Rocker (Infrared Analyzer) 655374 Tee, Modified 1/4 T x 1/4 MPT Cres. 837415 Temperature Controller 115 V 837404 Temperature Controller 230 V 837405 Thermistor Assembly 837414 Transformer Assembly, Ultraviolet, 115 V 837406 Transformer Assembly, Ultraviolet, 230 V 010443 901961
6 7
Transformer, Step-Down
Transformer, Step-Down 644790 Trap Assembly, TOCA Condensate 152106 Tubing, 1/8-inch O.D. 523341 Tubing, 1/8-inch Teflon, 5 feet 080874 Valve, 3-Way, Stainless Steel 902515 Valve, Check 837519 Z Purge Kit, Class 1, Division 2, Groups C and D
748263-E Rosemount Analytical March 2001
Model 2100A Process Total Organic Carbon Analyzer
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EPLACEMENT PARTS
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NOTES
64
March 2001 Rosemount Analytical 748263-EModel 2100A Process Total Organic Carbon Analyzer
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