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Determination of selenium (Ⅳ) by stripping voltammetry on a copper-doped mercury film electrode

机译:汽提伏安法测定铜掺杂汞膜电极中的硒(Ⅵ)

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The need to measure the concentration of Se in food, environmental objects etc is well-known. The stripping voltammetry is one of the commonly used methods for that. In some processes Se is accumulated in the form of a hardly soluble compounds in the presence of a suitable metal ions, normally copper. Cu~(2+) + 2e +Hg → Cu~0(Hg) (1) SeO_3~(2-) + xCu(Hg) + 6H~+ + 4e → Cu_xSe(Hg) + 3H_2O (2) The electrochemical reduction of the precipitate thus obtained results in the formation of the charachteristic peak on the voltammogram, its height being proportional to the concentration of Se in the solution: Cu_xSe(Hg) + 2H~+ + 2e → H_2Se + xCu(Hg). (3) Good sensitivity and reproducibility were found for the case of the mercury drop electrode only so far. The use of the mercury film electrode results in the considerably worse metrological characteristics of the analysis (Lange and Scholz 1997). The present work aims at the development of the method of Se (Ⅳ) determination by stripping voltammetry on the the mercury drop electrode, pre-doped with Cu, which was not done so far.
机译:需要测量食物中SE的浓度,环境对象等是众所周知的。剥离伏安法是其中常用的方法之一。在一些方法中,Se在合适的金属离子存在下以难以溶于化合物的形式累积,通常是铜的。 Cu〜(2+)+ 2E + Hg→Cu〜0(Hg)(1)SEO_3〜(2-)+ XCU(HG)+ 6H〜+ + 4E→CU_XSE(HG)+ 3H_2O(2)电化学减少由此获得的沉淀物导致形成伏安图上的Characteristic峰值,其高度与溶液中Se的浓度成比例:Cu_xSE(Hg)+ 2H〜+ 2E→H_2SE + XCU(Hg)。 (3)仅对汞滴电极的情况下发现了良好的敏感性和再现性。使用汞薄膜电极的使用导致分析的显着比计度特征(Lange和Scholz 1997)。本作者旨在通过剥离汞滴电极上的伏安法测定Se(Ⅵ)测定的方法,预先掺杂Cu,这是迄今为止未进行的。

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