Adsorptive stripping voltammetric determination of vanadium as chloranilic acid complex
Identifieur interne : 002D36 ( Main/Merge ); précédent : 002D35; suivant : 002D37Adsorptive stripping voltammetric determination of vanadium as chloranilic acid complex
Auteurs : S. Sander [Allemagne] ; G. Henze [Allemagne]Source :
- Fresenius' journal of analytical chemistry [ 0937-0633 ] ; 1996.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Vanadium, Eau, Combustible.
English descriptors
- KwdEn :
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 - 400mV. The adsorption process is solved by alternating current (ac) voltammetric measurements. The method is applied to different real samples.
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Pascal:96-0461363Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Benzoquinone derivatives</term>
<term>Chemical analysis</term>
<term>Fuels</term>
<term>Reoxidation</term>
<term>Trace analysis</term>
<term>Vanadium</term>
<term>Vanadium complex</term>
<term>Voltammetry</term>
<term>Water</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Analyse chimique</term>
<term>Analyse trace</term>
<term>Voltammétrie</term>
<term>Réoxydation</term>
<term>Vanadium</term>
<term>Vanadium complexe</term>
<term>Benzoquinone dérivé</term>
<term>Eau</term>
<term>Combustible</term>
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<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Vanadium</term>
<term>Eau</term>
<term>Combustible</term>
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<front><div type="abstract" xml:lang="en">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 - 400mV. The adsorption process is solved by alternating current (ac) voltammetric measurements. The method is applied to different real samples.</div>
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