The anodic stripping voltammetric determination of gold was accomplished on a chemically modified glassy carbon electrode in a solution containing chloride ions. A modifying polymer, polyvinylferrocene, was coated by immersing the glassy carbon surface in its solution in methylene chloride followed by solvent evaporation. Tetrahalo complexes of gold, tetrachloroaurate(III) and tetrabromoaurate(III) ions, were found to be reduced to metallic gold by chemical reduction during immersion of the polymer coated electrode into the solution containing aurate(III) ions. This reaction was utilized as means of preconcentration without the need for cathodic electrolysis prior to the anodic stripping of metallic gold. The effects of the preconcentration period, film thickness and the presence of Cu(II) ions as possible interferants were investigated.

The anodic stripping voltammetric determination of gold was accomplished on a chemically modified glassy carbon electrode in a solution containing chloride ions. A modifying polymer, polyvinylferrocene, was coated by immersing the glassy carbon surface in its solution in methylene chloride followed by solvent evaporation. Tetrahalo complexes of gold, tetrachloroaurate(III) and tetrabromoaurate(III) ions, were found to be reduced to metallic gold by chemical reduction during immersion of the polymer coated electrode into the solution containing aurate(III) ions. This reaction was utilized as means of preconcentration without the need for cathodic electrolysis prior to the anodic stripping of metallic gold. The effects of the preconcentration period, film thickness and the presence of Cu(II) ions as possible interferants were investigated.