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Determination of trace levels of Pb(II) in tap water by anodic stripping voltammetry with boron-doped diamond electrode

机译:掺硼金刚石电极阳极溶出伏安法测定自来水中痕量铅(II)

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摘要

A simple and rapid method to determine traces of lead in the Hatyai city tap water by square wave anodic stripping voltammetry with boron-doped diamond (BDD) electrode has been studied. The parameters in the preconcentration steps studied included electrolyte influences, pH, concentrations, and volumes. Effective preconcentration of trace lead was achieved at pH 1.26. The appropriate electrolyte was found to be 0.2 M potassium nitrate (KNO _3) in 0.05 M nitric acid (HNO_3) to make all lead ionic. By scanning potential in the negative direction, the stripping peak was obtained at - 0.460 V. Instrumental parameters including deposition potential, deposition time, scan rate, modulation amplitude, and equilibration time were optimized. The detection limit was found to be 0.3 μg/l. The accuracy was verified by analysing the standard reference material. Several interfering ions were studied and it was found that the method was not significantly affected by these coexisting ions and can be applied satisfactorily to lead determination in water samples. The results from determination of Pb~(2+) using the studied method and ICP-OES were compared and found to be in good agreement. The concentrations of lead in various water samples from eleven regions in Hatyai city were found to be in the range of 0.0-0.8 μg/l, lower than the drinking water contamination standard (< 10.0 μg/l) issued by the World Health Organization.
机译:研究了用掺硼金刚石(BDD)电极通过方波阳极溶出伏安法测定合艾市自来水中痕量铅的简便方法。研究的预浓缩步骤中的参数包括电解质的影响,pH,浓度和体积。在pH 1.26时有效地富集了痕量铅。发现合适的电解质是在0.05 M硝酸(HNO_3)中的0.2 M硝酸钾(KNO _3),使所有铅离子化。通过在负方向上扫描电势,可在-0.460 V处获得剥离峰。对包括沉积电势,沉积时间,扫描速率,调制幅度和平衡时间在内的仪器参数进行了优化。检出限为0.3μg/ l。通过分析标准参考物质验证了准确性。对几种干扰离子进行了研究,发现该方法不受这些共存离子的影响很大,可以令人满意地应用于水样中铅的测定。比较了所研究方法与ICP-OES测定Pb〜(2+)的结果,发现结果吻合良好。研究发现,合艾市11个地区的各种水样中铅的含量在0.0-0.8μg/ l的范围内,低于世界卫生组织发布的饮用水污染标准(<10.0μg/ l)。

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