Abstract

The associate formed by triiodide ion and hexadecylpyridinium chloride (cetylpyridinium chloride (CPC)) micelles was used to enhance the kinetic spectrophotometric determination of W VI by its catalytic action on the oxidation of iodide with hydrogen peroxide in an acidic medium. The reaction was monitored spectrophotometrically by measuring the increase in absorbance of I 3 −–CPC associate at 525 nm by the fixed-time method of 3 min from initiation of the reaction. The micellar medium allowed the determination of W VI at concentrations between 4 and 90 ng ml −1 with a detection limit of 2.4 ng ml −1 (i.e. about 12–13 times lower than those of methods implemented in aqueous media). The relative standard deviation for nine replicate analyses was 0.03% for 76.6 ng ml −1 of W VI. The proposed method was applied to the determination of W VI in aqueous extracts of soil sample with no prior separation.

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