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Adsorption voltammetric techniques for the determination of uranium(VI) with 2,5-dichloro-3,6-dihydroxy-1,4-benzoquinone as complex forming reagent

Identifieur interne : 002B22 ( Main/Exploration ); précédent : 002B21; suivant : 002B23

Adsorption voltammetric techniques for the determination of uranium(VI) with 2,5-dichloro-3,6-dihydroxy-1,4-benzoquinone as complex forming reagent

Auteurs : Sylvia Sander [Allemagne] ; Günter Henze [Allemagne]

Source :

RBID : ISTEX:7F372AB8F9051371A929416A7FD5D9EC1DA2EF28

Abstract

Abstract: Uranium (VI) can be determined by adsorptive voltammetric techniques, as its chloranilic acid complex, over a wide concentration range. Differential pulse polarography is useful for quantification of uranium between 0.1 and 1.5 mg/l; for the range from 10 to 500 μg/l differential pulse voltammetry and for ultra-trace analysis between 0.024 and 40 μg/l adsorptive stripping voltammetry are preferred. The standard deviation for the 3σ-detection limit of 24 ng/l uranium was found to be 8%. In the trace analysis of metals in aquatic environmental systems by adsorptive stripping voltammetry it is normally necessary to decompose polluted water samples by UV irradiation or microwave digestion. The advantage of the developed method is the fact that no sample pretreatment is necessary.

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DOI: 10.1007/BF00323474


Affiliations:


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<div type="abstract" xml:lang="en">Abstract: Uranium (VI) can be determined by adsorptive voltammetric techniques, as its chloranilic acid complex, over a wide concentration range. Differential pulse polarography is useful for quantification of uranium between 0.1 and 1.5 mg/l; for the range from 10 to 500 μg/l differential pulse voltammetry and for ultra-trace analysis between 0.024 and 40 μg/l adsorptive stripping voltammetry are preferred. The standard deviation for the 3σ-detection limit of 24 ng/l uranium was found to be 8%. In the trace analysis of metals in aquatic environmental systems by adsorptive stripping voltammetry it is normally necessary to decompose polluted water samples by UV irradiation or microwave digestion. The advantage of the developed method is the fact that no sample pretreatment is necessary.</div>
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