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   <subfield code="a">Some aspects of the determination of water by the karl fisher method</subfield>
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   <subfield code="a">Conditions for eliminating systematic errors and minimizing random errors in the determination of water in methanol and α-alumina using Karl Fisher reagent with visual end-point detection are studied. The concentration dependence of the relative standard deviation of the determination of water by the Karl Fisher method is found to be linear in RSD-1/c coordinates. To exclude the effect of moisture contained in the titration flask, it is suggested to bind water with a titrant in the presence of a small amount of methanol. The methanol effect (that is, the dependence of the titration results on the water: methanol ratio and the total amount of the titrated water-methanol mixture) is shown to be eliminated in the presence of the products of water interaction with Karl Fisher reagent that form on the water binding stage. It is found that the use of a background dye, methylene blue, eliminates significant systematic errors in the determination of water by the Karl Fisher method, particularly, at low concentrations. It is noted that the visual detection of the titration end-point has some advantages over the automated electrometric versions of the method; in particular, it is characterized by a better reproducibility of the determination of low concentrations of water.</subfield>
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