Abstract

A method is proposed for the determination of copper in white-metal bearing alloys by direct controlled-potential electrolysis with a tantalum cathode at −0.32 V vs. SCE in a sulphate/bisulphate buffered electrolyte (pH 2) with fluoroboric acid and sodium tartrate as masking agents. Only Bi(III) interferes. Any co-deposited Bi can be corrected for by its spectrophotometric determination with Semi-Xylenol Orange after preconcentration with La(III) as carrier, from an ammoniacal solution containing the redissolved deposit. Any residual Cu(II) in the electrolyte is determined by spectrophotometry with 2,9-dimethyl-1, 10-phenanthroline. The standard deviation of this method has been found to be 0.03 mg ( n = 12) and its relative standard deviation from 0.03 to 0.17%. It has been successfully used for referee analysis and certification of standard reference materials.

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