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首页> 外文期刊>Analytical Sciences >Determination of Selenium(IV) by Catalytic Stripping Voltammetry with an in situ Plated Bismuth-film Electrode
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Determination of Selenium(IV) by Catalytic Stripping Voltammetry with an in situ Plated Bismuth-film Electrode

机译:原位镀铋膜电极催化溶出伏安法测定硒(IV)

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摘要

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 µg L-1 (correlation coefficients 0.9800 and 0.9901, respectively) when the optimized parameters were used. A 3σ detection limit of 0.025 µg L-10 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 µg 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).
机译:提出了一种非常灵敏和简单的方法,用于通过Osteryang方波阴极溶出伏安法(OSWCSV)测定Se(IV)。该方法基于用Bi(III)将Se(IV)还原到边缘平面类型的热解石墨衬底上,然后进行阴极电势扫描。 OSWCSV研究表明,相对于Ag / AgCl,还原的硒在-1150 mV处产生了明显的催化氢波。当使用优化参数时,催化氢波的峰高与初始Se(IV)浓度成正比,范围为0.1-1.0和1.0-20.0 µg L-1(分别为0.9800和0.9901)。在30 s的沉积时间下,获得的3σ检出限为0.025 µg L-10 Se(IV)。测定0.10 µg L-1 Se(IV)的重复运行(n = 12)的相对标准偏差为4.0%。天然水样的分析结果表明,该方法适用于Se(IV)和Se(VI)的形态分析。

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