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Methods of the determination of inorganic arsenic species by stripping voltammetry in weakly alkaline media

机译:弱碱性介质中溶出伏安法测定无机砷的方法

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摘要

Two methods are considered for the direct determination of trace amounts of As(III) and As(V) in solutions by stripping voltammetry (SVA) using an ensemble of gold microelectrodes (Au-MEA) previously developed by the authors of this paper. In both methods, analyzing a mixture of As(III) and As(V), analysts first record an SVA signal of As(III) in a supporting Na2SO3 electrolyte. To record an analytical SVA signal of As(V), in the first method one should use the reduction of As(V) to As(III) on the surface of an Au-MEA catalyzed by the system Mn(II)/Mn(0) and followed by the formation of As(0) and its anode dissolution. In the second method, the photoreduction of As(V) to As(III) in a Na2SO3 solution is conducted under UV irradiation followed by the reduction of As(III) to As(0) and its electrooxidation on Au-MEA. The two methods are compared taking into account their performance characteristics and interfering ions. To improve the reliability of the results of analysis at an insignificant increase in its cost, we propose the consecutive use of both methods. The procedures are simple and rapid, do not require the removal of dissolved oxygen or toxic reactants, and can be used for the analysis of aqueous solutions at the place of sampling. The results of analyses of real objects, snow, river water, and process solutions are presented.
机译:考虑了两种方法,该方法使用以前由本文作者开发的金微电极(Au-MEA)集合通过溶出伏安法(SVA)直接测定溶液中的痕量As(III)和As(V)。在这两种方法中,分析As(III)和As(V)的混合物时,分析人员首先在支持的Na2SO3电解质中记录As(III)的SVA信号。为了记录As(V)的分析SVA信号,在第一种方法中,应使用由Mn(II)/ Mn(系统)催化的Au-MEA表面上的As(V)还原为As(III) 0),然后形成As(0)及其阳极溶解。在第二种方法中,在紫外线照射下,在Na2SO3溶液中将As(V)光还原为As(III),然后将As(III)还原为As(0),并在Au-MEA上进行电氧化。比较两种方法时要考虑它们的性能特征和干扰离子。为了在不增加成本的情况下提高分析结果的可靠性,我们建议连续使用两种方法。该过程简单,快速,不需要去除溶解的氧气或有毒的反应物,并且可以在取样位置用于水溶液的分析。给出了实物,雪,河水和过程解决方案的分析结果。

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