Abstract

A technique for stripping determination of mercury traces in air employing a glassy carbon electrode is described. The sample is passed at 2 liters min −1 for 2 hr through an absorber containing 0.2 M potassium permanganate and 10% w v sulfuric acid (1:1). After reduction with hydroxylamine hydrochloride, the determination is carried out in 0.12 M potassium thiocyanate at pH 2.0 ± 0.2 in the presence of 0.2 ppm of cupric ions. Calibration curves were found to be linear in the range 20 ppb-1 ppm Hg(II) in the cell. The accuracy of the method was tested over simulated samples and it was found to be better than 95%; the relative standard deviation was 5% or less. The limit of detection of mercury in air was approximately 10 μg m −3.

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