Peer-Reviewed Journal Details
Mandatory Fields
Beni, V,Newton, HV,Arrigan, DWM,Hill, M,Lane, WA,Mathewson, A;
2004
January
Analytica Chimica Acta
Voltammetric behaviour at gold electrodes immersed in the BCR sequential extraction scheme media - Application of underpotential deposition-stripping voltammetry to determination of copper in soil extracts
Validated
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Optional Fields
BCR sequential extraction scheme soil extracts voltarnmetric analysis gold electrodes underpotential deposition SCREEN-PRINTED ELECTRODES MERCURY-FREE TRACE DETERMINATION CARBON ELECTRODES FILM ELECTRODES SILVER ELECTRODE LEAD SEDIMENT METALS SINGLE
502
195
206
The development of mercury-free electroanalytical systems for in-field analysis of pollutants requires a foundation on the electrochemical behaviour of the chosen electrode material in the target sample matrices. In this work, the behaviour of gold working electrodes in the media employed in the BCR sequential extraction protocol, for the fractionation of metals in solid environmental matrices, is reported. All three of the BCR sequential extraction media are redox. active, on the basis of acidity and oxygen content as well as the inherent reducing or oxidising nature of some of the reagents employed: 0.11 M acetic acid, 0.1 M hydroxylammonium chloride (adjusted to pH 2) and I M ammonium acetate (adjusted to pH 2) with added trace hydrogen peroxide. The available potential ranges together with the demonstrated detection of target metals in these media are presented. Stripping voltammetry of copper or lead in the BCR extract media solutions reveal a multi-peak behaviour due to the stripping of both bulk metal and underpotential metal deposits. A procedure based on underpotential deposition-stripping voltammetry (UPD-SV) was evaluated for application to determination of copper in 0.11 M acetic acid soil extracts. A preliminary screening step in which different deposition times are applied to the sample enables a deposition time commensurate with UPD-SV to be selected so that no bulk deposition or stripping occurs thus simplifying the shape and features of the resulting voltammograms. Choice of the suitable deposition time is then followed by standards addition calibration. The method was validated by the analysis of a number of BCR 0.11 M acetic acid soil extracts. Good agreement was obtained been the UPD-SV method and atomic spectroscopic results. (C) 2003 Elsevier B.V. All rights reserved.
DOI 10.1016/j.aca.2003.10.006
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