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The determination of gold by anodic stripping voltammetry

A method is described for the routine determination of gold as its chloride or cyanide complex by anodic stripping voltammetry at a glassy carbon electrode coupled to a microprocessor-controlled voltammeter. The preferred supporting electrolyte is 0.1 M HCl/0.32 M HNO 3, with plating at −200 mV or −...

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Bibliographic Details
Published in:Analytica chimica acta 1988, Vol.209 (1-2), p.193-203
Main Authors: Lintern, Melvyn, Mann, Alan, Longman, Dale
Format: Article
Language:English
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Summary:A method is described for the routine determination of gold as its chloride or cyanide complex by anodic stripping voltammetry at a glassy carbon electrode coupled to a microprocessor-controlled voltammeter. The preferred supporting electrolyte is 0.1 M HCl/0.32 M HNO 3, with plating at −200 mV or −1200 mV (vs. Ag/AgCl). The stripping peak potentials range from 830 to 1150 mV (vs. Ag/AgCl) depending on concentration and plating time. Precision (percent relative standard deviation) is better than 5 % for a range of concentrations between 5 μg l −1 and 1000 μg l −1. The detection limit is about 5 μg l −1 for a 5-min plating period. Interferences from Cu, Hg, Ag and other electroactive species are overcome by preliminary extraction with diethyl ether.
ISSN:0003-2670
1873-4324
DOI:10.1016/S0003-2670(00)84562-6