Total Organic Carbon (TOC) Analyzer

Off-line Monitoring System TA-1.0

The product uses the electrical conductivity difference detection technology, with high accuracy and short response time. The instrument completely conforms to the requirements of the national pharmacopoeia, and it can meet the offline testing requirements for the deionized water such as pharmaceutical water (injection water and purified water) and ultrapure wate

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导言
Working Principle

This instrument adopts the principle of ultraviolet catalytic oxidation, to oxidize the organic matter in the sample into carbon dioxide, where the test of carbon dioxide test uses the direct conductivity method, to determine the total organic carbon content through the test of the difference between the total carbon content in the sample after oxidation reaction and the total inorganic carbon content in the sample without oxidation, i.e., the total organic carbon (TOC) = total carbon (TC) – total inorganic carbon (TIC)

1. The rotating quartz glass tube coated with titanium dioxide; 2. UV lamp; 3. Conductivity sensor; 4. Delay coil; 5. Peristaltic pump

Features

There is no need of nitrogen, oxygen, acid reagent and oxidant, so the operation is simple and the cost is low
The intelligent level is high, as it is equipped with automatic sampler, and the system suitability validation can be done automatically
It is in conformity with the test scheme as specified in the new edition of state pharmacopoeia
It can be used in off-line laboratory, to meet the test and cleaning validation for organic carbon injection water and purified water
It has the limit alarm design, and when the test sample exceeds the prescribed limit, the instrument makes automatic alarm

Parameters

Power Supply100 – 240 VAC, 50HZ, 120W
Conductivity Detection Range0.055us/cm-8.000us/cm
Measure Range0.001mg/L~1.0 mg/L (1~1000ppb)
Accuracy±3%
Resolution0.001mg/L
Analyzing TimeContinues Analyzing
Response Time5mins
Measuring Limit0.001 mg/L
Sample Temperature1-99°C
Applied RangeOffline in the Laboratory/Cleaning Validation
Authority ManagementUser name and password login/ to meet FDA 21CFR PART 11 requirements
Audit trailCustom-made
Print FunctionExternal Printer
Historical Records>=3years
Data CopyUSB disk to export the data
Display ScreenColor Touch Screen
Weight8.5KG
Dimension (mm)400*240*270
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