首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Anodic stripping voltammetric determination of total arsenic using a gold nanoparticle-modified boron-doped diamond electrode on a paper-based device
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Anodic stripping voltammetric determination of total arsenic using a gold nanoparticle-modified boron-doped diamond electrode on a paper-based device

机译:阳极剥离伏安法使用金纳米颗粒改性的硼掺杂金刚石电极在纸张的装置上使用金纳米粒子改性的硼掺杂金刚石测定

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摘要

A multistep paper-based analytical device (mPAD) was designed and applied to the voltammetric determination of total inorganic arsenic. The electrodeposition of gold nanoparticles on a boron-doped diamond (AuNP/BDD) electrode and the determination of total inorganic arsenic is accomplished with a single device. Total inorganic arsenic can be determined by first reducing As(V) to As(III) using thiosulfate in 1.0 mol L-1 HCl. As(III) is then deposited on the electrode surface, and total inorganic arsenic is quantified as As(III) by square-wave anodic stripping voltammetry the potential range between -0.25 V and 0.35 V (vs. Ag/AgCl), best at around 0.05 V. Under optimal conditions, the voltammetric response for As(III) detection is linear in the range from 0.1 to 1.5 mu g mL(-1) and the limit of detection (3SD/slope) is 20 ng mL(-1). The relative standard deviation at 0.3, 0.7 and 1.0 mu g mL(-1) of As(III) are 3.6, 4.3 and 3.3, respectively (10 different electrodes). The results show that the assay has high precision, a rather low working potential, and excellent sensor-to-sensor reproducibility. The method was employed to the determination of total inorganic arsenic in rice samples. Results agreed well with those obtained by inductively coupled plasma-optical emission spectroscopy (ICP-OES).
机译:设计并应用了基于多步纸的分析装置(MPAD)并施加到总无机砷的伏安测定。用单个装置完成金纳米颗粒上的金纳米颗粒对硼掺杂金刚石(AUNP / BDD)电极的测定。通过在1.0mol L-1 HCl中首先使用硫代硫酸盐首先将As(v)降低至(v)至As(III)来确定总无机砷。然后将(III)沉积在电极表面上,并且通过方波阳极溶出伏安法量化总无机砷,其电位范围为-0.25V和0.35V(Vs.AG / AGCL),最佳在最佳条件下约0.05 V.伏安响应(III)检测为0.1至1.5μg(-1)的线性,检测极限(3SD /斜率)为20ng mL(-1 )。为0.3,0.7和1.0μg(-1)的相对标准偏差为(III)分别为3.6,4.3和3.3(10个不同的电极)。结果表明,该测定具有高精度,更低的工作电位,以及出色的传感器到传感器的再现性。该方法用于测定水稻样品中的总无机砷。结果与电感耦合等离子体 - 光发射光谱(ICP-OES)相同吻合。

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