Abstract
A nafion-coated antimony film electrode (NSbFE) was prepared ex situ and applied to the model metal ions Pb(II) and Cd(II) by adsorptive stripping voltammetry in the presence of pyrogallol red (PGR). To enhance the electroanalytical performance of the NSbFE, we optimized several operational parameters, including antimony concentration, deposition potential and time used in the preparation of the electrode, and effect of pH, ligand concentration (CPGR), adsorptive potential, and time (Eads, tads). The NSbFE exhibited well developed signals for the reduction of the adsorbed complexes at −0.63 and −0.92V for Pb-PGR and Cd-PGR, respectively, with higher current compared to unmodified electrodes. The optimum parameters for NSbFE preparation consisting of 100mgL−1 Sb(III), 0.5molL−1 HCl at −1.5V (150s) and for the determination of Pb(II) and Cd(II) were pH=4.5 (acetate buffer); CPGR=2.8μmolL−1; Eads=−0.40V and tads=100s. The electrode presents good linear behavior in the examined concentration range from 0.9 to 12.0μgL−1 for both metal ions, with a limit of detection (3σ) of 0.4 and 0.9μgL−1 for Pb(II) and 0.5 and 1.0μgL−1 for Cd(II) using 2-mm and 3-mm diameter glassy carbon electrodes, respectively. The relative standard deviation for a Pb(II) a Cd(II) solution (9.8μgL−1) was 2.0% for six successive assays. The method was validated using certified reference water for trace elements (TMDA-61) with satisfactory results. Finally, the method was applied to the determination of Pb(II) and Cd(II) in tap and mineral water.
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