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Determination of triclocarban by direct and adsorptive stripping voltammetric methods on a glassy carbon electrode

机译:玻碳电极上直接和吸附溶出伏安法测定三氯卡班

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The first report of TCC electrochemical oxidation is presented aiming at its determination in personal care products and drinking water samples at trace levels, using square wave voltammetry (SWV) direct and adsorptive stripping modes. Electrochemical responses of TCC were evaluated using different voltammetric techniques over a wide pH range on a glassy carbon electrode (GCE), demonstrating irreversible and diffusion-controlled processes. The numbers of protons and electrons associated with the oxidation reactions were estimated. The most selective and sensitive response (acetate buffer, pH 5.4) was used for the development of SWV methods, under optimum conditions. A linear response range from (1.8-21) x 10(-9) mol L-1 with a limit of detection (LOD) of 3.2 x 10(-10) mol L-1, 1000 times lower than SWV direct mode, was obtained for SWV adsorptive stripping mode, including the acceptable levels of repeatability (rsd = 4.1%) and reproducibility (rsd = 5.4%) and has been applied to TCC determination in personal care products at levels ranging from 0.21 to 0.49 % m m(-1) (average recovery of 95.3%) and drinking water (average apparent recovery of 95.4%) samples, with excellent analytical performance using simple and low cost instrumentation.
机译:提出了TCC电化学氧化的第一份报告,旨在通过方波伏安法(SWV)直接和吸附剥离模式测定个人护理产品和饮用水中的痕量水平。在宽的pH范围内,在玻璃碳电极(GCE)上使用不同的伏安技术评估了TCC的电化学反应,证明了不可逆和扩散受控的过程。估计了与氧化反应有关的质子和电子的数目。在最佳条件下,SWV方法的开发使用了最具有选择性和敏感性的反应(乙酸缓冲液,pH 5.4)。线性响应范围为(1.8-21)x 10(-9)mol L-1,检测限(LOD)为3.2 x 10(-10)mol L-1,比SWV直接模式低1000倍通过SWV吸附剥离模式获得,包括可接受水平的重复性(rsd = 4.1%)和再现性(rsd = 5.4%),并已应用于个人护理产品中TCC的测定,含量范围为0.21至0.49%mm(-1) )(平均回收率为95.3%)和饮用水(平均表观回收率为95.4%)样品,使用简单且低成本的仪器具有出色的分析性能。

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