Long Jiajie, Nagaosa Yukio
Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, University of Fukui, Bunkyo, Fukui, Japan.
Anal Sci. 2007 Nov;23(11):1343-6. doi: 10.2116/analsci.23.1343.
A very sensitive and simple method is presented for the determination of Se(IV) by Osteryang square-wave cathodic stripping voltammery (OSWCSV). The method is based on the reduction of Se(IV) with Bi(III) onto an edge-plane type of pyrolytic graphite substrate, followed by a cathodic potential scan. OSWCSV studies indicate that the reduced selenium produced a distinct catalytic hydrogen wave at -1150 mV vs. Ag/AgCl. The peak height of the catalytic hydrogen wave was directly proportional to the initial Se(IV) concentration in the ranges of 0.1 - 1.0 and 1.0 - 20.0 microg L(-1) (correlation coefficients 0.9800 and 0.9901, respectively) when the optimized parameters were used. A 3sigma detection limit of 0.025 microg L(-1)0 Se(IV) was obtained at 30 s deposition time. The relative standard deviation was 4.0% on replicate runs (n = 12) for the determinations of 0.10 microg L(-1) Se(IV). Analytical results of natural water samples demonstrate that the proposed method is applicable to speciation analysis of Se(IV) and Se(VI).
提出了一种用奥斯特杨方波阴极溶出伏安法(OSWCSV)测定Se(IV)的非常灵敏且简单的方法。该方法基于用Bi(III)将Se(IV)还原到边缘平面型热解石墨基底上,随后进行阴极电位扫描。OSWCSV研究表明,还原后的硒在相对于Ag/AgCl为 -1150 mV时产生明显的催化氢波。当使用优化参数时,催化氢波的峰高在0.1 - 1.0和1.0 - 20.0 μg L⁻¹范围内与初始Se(IV)浓度成正比(相关系数分别为0.9800和0.9901)。在30 s沉积时间下获得了0.025σ检测限为0.025 μg L⁻¹的Se(IV)。对于0.10 μg L⁻¹ Se(IV)的测定,重复运行(n = 12)时相对标准偏差为4.0%。天然水样的分析结果表明,所提出的方法适用于Se(IV)和Se(VI)的形态分析。