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Commonly Used Sample Preservation Techniques for Laboratory Water – Table 2 (Residual Chlorine, Oils, Carbon, etc.)

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    Common Water Sample Preservation Techniques


    The table lists the requirements for water sample preservation techniques. The preservation time, container material selection, and application of preservation measures all depend on the components and properties of the sample. However, real-world water samples vary greatly, so the requirements listed in the table cannot be absolute guidelines. Therefore, each analyst should verify the applicability of these requirements in their specific work, and the sample collection and preservation methods should be clearly specified when developing analytical method standards. Furthermore, if there are incompatibilities between the analytical method to be used and the protective agent and container material, it is often necessary to take several samples from the same water body and analyze them using different preservation methods to determine the most suitable protection method and container.


    Common Sample Preservation Techniques – Table 2


    (This table only contains general requirements for sample preservation. Due to the complex properties of natural water and wastewater, the stability of each type of sample treated according to the following methods needs to be verified before analysis.)


    1

    Project to be tested

    2

    Container Category

    3

    Save method

    4

    Analysis location

    5

    Storage time

    6

    suggestion

    A

    thing

    reason

    ,

    change

    study

    and

    born

    change

    point

    Analysis

    Residual chlorine

    P or G


    on site


    It is best to analyze on-site, such as

    If that's not possible, use it on-site.

    Excess NaOH fixation. (Preservation)

    Storage should not exceed 6 hours

    carbon dioxide

    P or G


    See pH level



    Dissolved oxygen

    (dissolved oxygen bottle)

    On-site fixed oxygen

    Store in the dark

    On-site, laboratory

    a few hours

    Add 1 mL of 1 mol/L iodometric titration

    Potassium permanganate and 2 mL 1 mol/

    Alkaline potassium iodide

    Fats, oils, carbon

    Hydrogen compounds, stone

    Oils and derivatives

    Rinse the container with the solvent used in the analysis.

    On-site extraction

    Freeze to -20°C

    Laboratory Laboratory

    24 hours a day

    It is recommended to do this immediately after sampling.

    Add to the analysis method

    The extractant used, or the input

    On-site extraction

    Ionic Tablet

    surfactant

    G

    Refrigerate at 2.5℃

    Sulfuric acid acidification pH < 2

    laboratory

    laboratory

    as soon as possible (48 hours)


    Non-ionic type

    surfactant

    G

    Add 40% (v/v) formaldehyde to make the sample contain 1% (v/v) formaldehyde.

    The aldehyde solution should be refrigerated at 2–5°C, and the container should be filled with water sample.

    laboratory

    January


    arsenic


    Add H2SO4 to make pH < 2

    Adjust pH to 12 by adding alkali

    Laboratory Laboratory

    Several months

    Nitric acid acidification cannot be used.

    Domestic sewage and industrial waste

    Water should be used in this way

    sulfides


    Add 2 mL per 100 mL

    Add 2 mol/L zinc acetate to 2 mL of 2 mol/L NaOH and refrigerate.

    laboratory

    24h

    Must be fixed on site

    Total cyanide

    P

    Adjust the pH to >12 using NaOH.

    laboratory

    24h



    Note: ①P – Polyethylene; C – Borosilicate glass. ②A "-" indicates that no preservation measures are taken.

    References
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