A sensitive and selective adsorptive stripping voltammetric method was employed to determine traces of tin in water samples. The spontaneously formed tin complex with 2,5-dichloro-1,4-dihydroxy-3,6-benzoquinone (chloranilic acid) is adsorbed at the surface of a mercury drop electrode. The analyte ca
Determination of Labile Chromium in Water Samples by Catalytic Adsorptive Stripping Voltammetry in On-Line System
β Scribed by Malgorzata Grabarczyk; Mieczyslaw Korolczuk
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 73 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1040-0397
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β¦ Synopsis
Abstract
A sensitive and selective onβline voltammetric procedure for determination of traces of labile chromium is presented. The pulsed potential accumulation was proposed for the minimization of interferences of surface active substances and foreign ions. The calibration plot was linear from 7Γ10^β10^β molβL^β1^ to 3Γ10^β8^β molβL^β1^ for an accumulation time of 60β s. The relative standard deviation was 4.7% (n=5) for a chromium concentration of 1.5Γ10^β8^β molβL^β1^. The detection limit estimated from (3β Ο) for an accumulation time of 60β s was about 2Γ10^β10^β molβL^β1^. The method was applied for the determination of labile chromium in tap and river water samples.
π SIMILAR VOLUMES
A procedure for the determination of chromium by differential pulse catalytic-adsorptive stripping voltammetry (DPAdSV), using N-(2hydroxyethyl) ethylenediamine-N, N 0 , N 0 -triacetic acid (HEDTA) as complexing agent, has been optimized. The selection of the experimental conditions was made using e
## Abstract A sensitive and selective onβline voltammetric procedure for determination of traces of Se(IV) is presented. The pulsed potential accumulation was proposed for minimization of interferences of surface active substances and foreign ions. The calibration plot was linear from 1Γ10^β9^β mol