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Anodic stripping voltammetric analysis of trace arsenic(III) enhanced by mild hydrogen-evolution at a bimetallic Au-Pt nanoparticle modified glassy carbon electrode

机译:双金属Au-Pt纳米粒子修饰的玻碳电极上由温和氢逸出增强的痕量砷(III)的阳极溶出伏安法分析

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摘要

A glassy carbon electrode (GCE) modified with electrodeposited bimetallic Au-Pt nanoparticles (Au-PtNPs) was applied to sensitively detect As(III) by linear sweep anodic stripping voltammetry (ISASV). In 0.5 M aqueous H2SO4, atomic hydrogen and molecular hydrogen were easily electrogenerated at the Pt sites on Au-PtNPs/GCE, which can chemically reduce As(III) to As(0) and enhance the cathodic preconcentration of As(0) at both the Pt sites and the neighboring Au sites. Since the As(0)-Au affinity is weaker than the As(0)-Pt affinity, the preconcentrated As(0) can be rapidly oxidized onear the surface Au sites of Au-PtNPs/GCE, yielding sharper and higher LSASV current peaks. Under optimum conditions (700 s preconcentration at -0.1 V, 5 V s(-1)), the LSASV peak current for the As(0)-As(III) oxidation responded linearly to As(III) concentration from 0.005 to 3.0 mu M with a limit of detection (LCD) of 3.7 nM (028 ppb) (S/N = 3), while that for the As(III)-As(V) oxidation was linear with As(III) concentration from 0.01 to 3.0 mu M with a LCD of 6.0 nM (0.45 ppb) (S/N = 3). This method was applied for analysis of As(III) in real water samples. (C) 2015 Elsevier B.V. All rights reserved.
机译:用电沉积双金属Au-Pt纳米粒子(Au-PtNPs)修饰的玻碳电极(GCE)通过线性扫描阳极溶出伏安法(ISASV)灵敏地检测As(III)。在0.5 M的H2SO4水溶液中,Au-PtNPs / GCE上的Pt位置容易产生原子氢和分子氢,可以将As(III)化学还原为As(0)并提高As(0)的阴极预浓Pt站点和附近的Au站点。由于As(0)-Au亲和力弱于As(0)-Pt亲和力,因此预浓缩的As(0)可以在Au-PtNPs / GCE的表面Au位上/附近快速氧化,从而产生更清晰,更高的LSASV当前的峰值。在最佳条件下(-0.1 V,5 V s(-1)时700 s的预浓),As(0)-As(III)氧化的LSASV峰值电流对0.005至3.0 mu的As(III)浓度线性响应M的检出限(LCD)为3.7 nM(028 ppb)(S / N = 3),而As(III)-As(V)的氧化与As(III)浓度在0.01至3.0之间呈线性关系液晶显示屏为6.0 nM(0.45 ppb)的μM(S / N = 3)。该方法用于实际水样中砷(Ⅲ)的分析。 (C)2015 Elsevier B.V.保留所有权利。

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