Zhang W, Zha H, Yao B, Zhang C, Zhou X, Zhong S
Department of Chemistry, Wuhan University, Wuhan 430072, People's Republic of China.
Talanta. 1998 Aug;46(4):711-6. doi: 10.1016/s0039-9140(97)00324-x.
The electrochemical redox mechanism of I(-) ion under different concentrations on gold electrodes was studied in detail using the EQCM technique (a combination of the QCM technique and cyclic voltammetry). The redox behavior of the I(-) ion on a gold microelectrode when no supporting electrolyte was added was compared with a conventional gold microelectrode. Due to the small current and the very low solution iR drop of the microelectrode, the actual oxidation potential of I(-) on the microelectrode was much more negative than that of the conventional electrode and its anodic peak was better defined. Therefore the gold microelectode was employed for the determination of I(-). A linear range of 1.0x10(-5)-0.1 mol l(-1) with a detection limit of 1.0x10(-6) mol l(-1) was obtained on the microelectrode in pure KI aqueous solution. Two samples were measured using this method and the results were in good agreement with those indicated or calculated..
采用电化学石英晶体微天平技术(QCM技术与循环伏安法相结合)详细研究了不同浓度I(-)离子在金电极上的电化学氧化还原机理。将未添加支持电解质时I(-)离子在金微电极上的氧化还原行为与传统金微电极进行了比较。由于微电极电流小且溶液iR降极低,I(-)在微电极上的实际氧化电位比传统电极的氧化电位负得多,其阳极峰更清晰。因此,采用金微电极测定I(-)。在纯KI水溶液中的微电极上获得了1.0×10(-5)-0.1 mol l(-1)的线性范围,检测限为1.0×10(-6) mol l(-1)。使用该方法对两个样品进行了测量,结果与所示或计算结果吻合良好。