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  • Glove Integrity Tester
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  • Sample Pre-treatment
  • Microbial Limit Test
  • Endoscope Microbial Test
  • TOC Analyzer
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  • Glove Integrity Tester
  • Sterility Test
  • Sample Pre-treatment
  • Microbial Limit Test
  • Endoscope Microbial Test
  • TOC Analyzer
  • Filter Integrity Tester
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    TOC Analyzer WOT100
    TOC Analyzer WOT100
    TOC Analyzer WOT100
    TOC Analyzer WOT100
    TOC Analyzer WOT100

    Clean equipment is vital to the pharmaceutical industry due to potential cross contamination between product runs of various drugs.

    Total Organic Carbon (TOC) analysis is a widely accepted way to analyze for residual pharmaceutical components.

    WOT-100 TOC analyzer adopts the UV light-activated persulfate oxidation method. 

    TOC content is determined by first removing inorganic carbon (IC) from the sample through the addition of

    phosphoric acid. The organic carbon is oxidized to carbon dioxide (CO2) using UV oxidation with

    sodium persulfate. The CO2 produced is then swept to the non-dispersive infrared detector (NDIR) and

    measured. 

    Based on above steps, we can get the TC and TIC, thus the TC - TIC= TOC.

    Features

    UV light-activated persulfate oxidation method. 

    Equipped with eight-way rotary valve for automatic acid intaking, oxidant intaking, sample intaking ,purge and waste discharge.

    Poweful software compliance with  the requirements of 21CFR Part 11, audit trail, CSV(Computerized System Validation).

    Remove halide and bicarbonate interference;

    Low cost, main consumables are Phosphoric acid solution and Sodium persulfate solution;

    Wide detemination range.

    Easy to calibration, support the one point and multi-point calibration.

    Built-in aeration tank, when testing NPOC, a series of processes such as aeration, acid addition and sample injection are completed by the instrument automatically.


    Technical Parameters

    Power supply:          (220±10%)VAC 50/60Hz

    Power consumption: 300W
    Indication error: ±5%
    Repeatability: RSD≤3%
    Determination Range:(0-100.000)mg/L
    Analysis time: 4 min.
    Required sample temperature:(1-95)℃
    Ambient temperature:(10-40)℃

    Noise:≤55dB(A)

    Dimensions: 55cm×50cm×53cm

    Net Weight: 35Kgs

    Applications

    Cleaning validation in pharmaceutical industry

     

     

    Technical specifications are subject to change without notice. Copyright reserved by Tailin.