Germanium(W) can be determined using adsorptive cathodic stripping voltammetry in the presence of 3,4-dihydroxybenzaldehyde (DHB). The sensitivity of the voltammetric technique was improved greatly by the addition of vanadium(W) to the sample. The reduction current of the adsorbed germanium(W)-DHB c
Determination of Se(IV) in On-Line System by Cathodic Stripping Voltammetry
โ Scribed by Mieczyslaw Korolczuk; Malgorzata Grabarczyk
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 155 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1040-0397
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โฆ Synopsis
Abstract
A sensitive and selective onโline 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 1ร10^โ9^โ mol L^โ1^ to 4ร10^โ8^โ mol L^โ1^ for accumulation time of 180โ s. The relative standard deviation was 6.1% (n=5) for a Se(IV) concentration of 1ร10^โ8^โ mol L^โ1^. The detection limit estimated from (3 ฯ) for an accumulation time of 180โ s was about 4ร10^โ10^โ mol L^โ1^. The validation of the procedure proposed was made by a recovery tests for tap and river water samples.
๐ SIMILAR VOLUMES
A cathodic stripping procedure has been developed for the determination of mebendazole. An 8 min accumulation time on a 0.1 M acetic acid/acetate pH=5 buffer solution gives rise to a detection limit of 3 x lo-l1 M. An extraction with ether has been developed for the determination of mebendazole in u
Using a copper microelectrode of ร5-mm diameter, the concentration of Se(IV) was determined by cathodic stripping voltammetry either from HClO 4 (0.1 M) or from NaClO 4 (0.1 M) supporting electrolytes. The preconcentration time of 15 s was chosen as optimal, and calibration graphs were constructed f
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## Abstract A sensitive and selective onโline 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