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Adsorptive stripping voltammetric determination of vanadium as chloranilic acid complex

Identifieur interne : 000613 ( Istex/Corpus ); précédent : 000612; suivant : 000614

Adsorptive stripping voltammetric determination of vanadium as chloranilic acid complex

Auteurs : Sylvia Sander ; Günter Henze

Source :

RBID : ISTEX:A3959C2344F7EFA18736C0BEC8834A30CBBF7223

Abstract

Abstract: Traces of vanadium(V) can be determined up to 21 ng/l by adsorptive stripping voltammetry using 2,5-dichloro-1,4-dihydroxy-3,6-benzoquinone (chloranilic acid) as complex forming reagent. The complex is stable in a 0.1 mol/l acetate buffer (pH 4.6) solution and adsorbed at the electrode surface in a potential range between −150 mV and −400 mV. The adsorption process is solved by alternating current (ac) voltammetric measurements. The method is applied to different real samples.

Url:
DOI: 10.1007/s0021663560259

Links to Exploration step

ISTEX:A3959C2344F7EFA18736C0BEC8834A30CBBF7223

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<Para>Traces of vanadium(V) can be determined up to 21 ng/l by adsorptive stripping voltammetry using 2,5-dichloro-1,4-dihydroxy-3,6-benzoquinone (chloranilic acid) as complex forming reagent. The complex is stable in a 0.1 mol/l acetate buffer (pH 4.6) solution and adsorbed at the electrode surface in a potential range between −150 mV and −400 mV. The adsorption process is solved by alternating current (ac) voltammetric measurements. The method is applied to different real samples.</Para>
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<abstract lang="en">Abstract: Traces of vanadium(V) can be determined up to 21 ng/l by adsorptive stripping voltammetry using 2,5-dichloro-1,4-dihydroxy-3,6-benzoquinone (chloranilic acid) as complex forming reagent. The complex is stable in a 0.1 mol/l acetate buffer (pH 4.6) solution and adsorbed at the electrode surface in a potential range between −150 mV and −400 mV. The adsorption process is solved by alternating current (ac) voltammetric measurements. The method is applied to different real samples.</abstract>
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