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Simultaneous determination of trace lead and cadmium in water samples by adsorptive stripping voltammetry using gallic acid as a selective chelating agent

机译:没食子酸作为选择性螯合剂的吸附溶出伏安法同时测定水中的痕量铅和镉

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摘要

This work describes a procedure for the simultaneous determination of cadmium and lead in some food and water samples using an adsorptive stripping voltammetric method. The method is based on the adsorptive accumulation of 2,3,4-trihydroxybenzoic acid (gallic acid (GA)) complexes of these elements onto a hanging mercury drop electrode, followed by the reduction of the adsorbed species. Optimal analytical conditions were found to be 0.10 M borate buffer (pH 6.2), 2.5 x 10(-5) M GA, an accumulation potential of -0.1 V (Versus SCE), an accumulation time of 80 s and a scan rate of 60 mV/s. The peak current is proportional to the concentration of lead and cadmium over the range of 0.50-70.00 ng mL(-1) and 0.20-35.00 ng mL(-1), respectively, and the detection limit is 0.014 ng mL(-1) and 0.011 ng mL(-1) for lead and cadmium, respectively, for a 80 s adsorption time. The propose method was applied to the determination of lead and cadmium in water and food samples with satisfactory results.
机译:这项工作描述了一种使用吸附溶出伏安法同时测定某些食品和水样品中镉和铅的程序。该方法基于这些元素的2,3,4-三羟基苯甲酸(没食子酸(GA))络合物在堆积的汞滴电极上的吸附性积累,然后减少了所吸附的物质。发现最佳分析条件是0.10 M硼酸盐缓冲液(pH 6.2),2.5 x 10(-5)M GA,-0.1 V的累积电势(相对于SCE),80 s的累积时间和60的扫描速率毫伏/秒峰值电流分别与0.50-70.00 ng mL(-1)和0.20-35.00 ng mL(-1)范围内的铅和镉浓度成正比,检出限为0.014 ng mL(-1)铅和镉的吸附时间分别为0.011 ng mL(-1)和80 s。该方法用于水和食品中铅和镉的测定,结果令人满意。

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