Catalytic spectrophotometric determination of trace selenium in microemulsion after separation and e

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A new catalytic spectrophotometric method was developed for the determination of trace amount of Se(IV) in microemulsion medium. The method is based on the catalytic effect of traces of Se(IV) on the oxidation of 2’,4’-dichlorophenylfluorone (p-CPF) by potassium bromate with HNO3 as an activator in the presence of nonionic microemulsion medium. Under optimum conditions, the calibration graph is linear in the range of 0.4-15 μg?L?1 of Se(IV) at 480 nm. The detection limit achieved is 9.86 × 10?10 μg?L?1. Samples were dissolved and the obtained trace Se(IV) was separated and enriched by sulphydryl dextrane gel (SDG). The method has been applied for determination of trace selenium with satisfactory results. A new catalytic spectrophotometric method was developed for the determination of trace amount of Se (IV) in microemulsion medium. The method is based on the catalytic effect of traces of Se (IV) on the oxidation of 2 ’, 4’-dichlorophenylfluorone (p -CPF) by potassium bromate with HNO3 as an activator in the presence of nonionic microemulsion medium. Under optimum conditions, the calibration graph is linear in the range of 0.4-15 μg · L -1 of Se (IV) at 480 nm. The detection limit achieved was 9.86 x 10? 10 μg? L? 1. Samples were dissolved and the obtained trace Se (IV) was separated and enriched by sulphydryl dextrane gel (SDG). The method has been applied for determination of trace selenium with satisfactory results.
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