Abstract
Selenium was determined by cathodic stripping voltammetry in a 1 mol l–1 HCl acid solution containing added CuII. In this medium, selenium was preconcentrated on the hanging mercury drop electrode and stripped cathodically in differential-pulse mode. After a deposition period of 1 min, 0.2 ng ml–1 of selenium could be detected. The method was applied to the analysis of food supplements. Total selenium was determined after digestion of the sample with HNO3—HClO4 and reduction to the electroactive SeIV by heating with HCl. Inorganic selenium (i.e., selenite and selenate) was similarly determined after extraction with dilute sodium hydroxide solution and clean-up on activated carbon. Representative over-the-counter preparations have been analysed.

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