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首页> 外文期刊>Electrochemistry communications >Dual-signal anodic stripping voltammetric determination of trace arsenic(III) at a glassy carbon electrode modified with internal-electrolysis deposited gold nanoparticles
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Dual-signal anodic stripping voltammetric determination of trace arsenic(III) at a glassy carbon electrode modified with internal-electrolysis deposited gold nanoparticles

机译:内电解沉积金纳米粒子修饰的玻碳电极上双信号阳极溶出伏安法测定痕量砷

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摘要

A glassy carbon electrode (GCE) modified with internal-electrolysis deposited gold nanoparticles (AuNPs_(ied)) was applied to sensitively and selectively detect As(III) by anodic stripping linear sweep voltammetry (ASLSV). The AuNPs_(ied)/GCE was prepared based on the redox replacement reaction between a supporting-electrolyte-free aqueous HAuCl_4 and a copper sheet in saturated KCl separated by a salt bridge. Under optimum conditions (0.5 M aqueous H_2SO_4, 300-s preconcentration at -0.4 V), the ASLSV peak current for the As(0)-As(III) oxidation responded linearly to As(III) concentration from 0.02 to 3 μM with a limit of detection (LOD) of 0.9 nM (0.07 μg L~(-1)) (S/N = 3), while that for the As(III)-As(V) oxidation was linear with As(III) concentration from 0.02 to 1 μM with a LOD of 4 nM (0.3 μg L~(-1)) (S/N = 3). An appropriate high-scan-rate for ASLSV can enhance both the sensitivity and signal-to-noise ratio. This method was applied for analyses of As(III) in real water samples.
机译:应用内部电解沉积的金纳米颗粒(AuNPs_(ied))修饰的玻碳电极(GCE),通过阳极溶出线性扫描伏安法(ASLSV)灵敏且选择性地检测As(III)。 AuNPs(ied)/ GCE是基于无载体电解质的HAuCl_4水溶液和饱和KCl中的铜片(通过盐桥分离)之间的氧化还原置换反应而制备的。在最佳条件下(0.5 M的H_2SO_4水溶液,在-0.4 V时预浓缩300-s),As(0)-As(III)氧化的ASLSV峰值电流对As(III)的浓度从0.02到3μM线性响应,检出限(LOD)为0.9 nM(0.07μgL〜(-1))(S / N = 3),而对于As(III)-As(V)而言,氧化与As(III)浓度呈线性关系0.02至1μM,LOD为4 nM(0.3μgL〜(-1))(S / N = 3)。适当的ASLSV高扫描速率可以提高灵敏度和信噪比。该方法用于分析实际水样中的As(III)。

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