Abstract

This paper describes an electrochemical stripping procedure for ultratrace measurements of zirconium, in which preconcentration is achieved by the adsorption of a zirconium—Solochrome Violet RS complex onto a hanging mercury drop electrode. Cyclic voltammetry was used to characterize the interfacial and redox behaviour. For a 10-min preconcentration time, the detection limit found was 2.3 × 10 −10 M. Optimal experimental conditions were found to be use of a stirred acetate buffer (pH 4.6) solution with Solochrome Violet RS concentration 1.5 × 10 −6 M, a preconcentration potential of −0.3 V and linear scan mode. A 60-fold enhancement of the response is obtained following 5-min preconcentration. With preconcentration for 60 sec, calibration plots for zirconium are linear for the 1.1 × 10 −8−1.1 × 10 −7 M range. The relative standard deviation at 5.5 × 10 −8 M is 1.7%. Possible interferences by surface-active organic materials and other trace metals have been investigated. Zirconium added to a sea-water sample at the 10 ng/ml level was readily determined.

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