Safavi A, Shams E
Department of Chemistry, College of Sciences, Shiraz University, Shiraz 71454, Iran.
Talanta. 2000 May 5;51(6):1117-23. doi: 10.1016/s0039-9140(00)00278-2.
A very sensitive and selective catalytic adsorptive cathodic stripping procedure for trace measurements of cobalt is presented. The method is based on adsorptive accumulation of the cobalt-MTB (methyl thymol blue) complex onto a hanging mercury drop electrode, followed by reduction of the adsorbed species by voltammetric scan using differential pulse modulation. The reduction current is enhanced catalytically by nitrite. The optimum conditions for the analysis of cobalt include pH 9.0 (ammonia buffer), 2.0 muM methyl thymol blue, 0.8 M sodium nitrite and an accumulation potential of -0.5 V (versus Ag/AgCl). The peak current is proportional to the concentration of cobalt over the entire concentration range tested (0.02-500 ng ml(-1)) with a detection limit of 0.005 ng ml(-1) for an accumulation time of 60 s. The method was applied to determination of cobalt in a mineral water sample and some analytical grade salts with satisfactory results.
本文提出了一种用于痕量钴测定的非常灵敏且具有选择性的催化吸附阴极溶出分析方法。该方法基于钴 - 甲基百里酚蓝(MTB)络合物吸附富集到悬汞滴电极上,随后采用差分脉冲调制通过伏安扫描对吸附物种进行还原。亚硝酸盐可催化增强还原电流。分析钴的最佳条件包括pH 9.0(氨缓冲液)、2.0 μM甲基百里酚蓝、0.8 M亚硝酸钠以及 - 0.5 V(相对于Ag/AgCl)的富集电位。在整个测试浓度范围(0.02 - 500 ng ml⁻¹)内,峰电流与钴浓度成正比,对于60 s的富集时间,检测限为0.005 ng ml⁻¹。该方法应用于矿泉水样品和一些分析纯盐中钴的测定,结果令人满意。