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Adsorptive stripping voltammetry of uranium: elimination of interferences from surface active substances and application to the determination in natural water samples

机译:铀的吸附溶出伏安法:消除表面活性物质的干扰并将其应用于天然水样品的测定中

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We report a simple and sensitive stripping voltammetric procedure for determination of trace quantity of U(VI) in environmental water samples containing high concentrations of surfactants. The procedure is based on the adsorptive accumulation of the U(VI)–cupferron complex onto a hanging mercury drop electrode, followed by a reduction of the adsorbed species by a voltammetric scan using differential pulse modulation. The interference from surfactants was eliminated by adsorption of interferents onto an Amberlite XAD-7 or XAD-16 resin. Optimum conditions for removing the surfactants by mixing the analysed sample with resin and for voltammetric measurements of uranium quantification were evaluated. Under optimal conditions the linear calibration plot for U(VI) was achieved in the simultaneous presence of 5.0 mg L?1 anionic, 2.0 mg L?1 cationic and 5.0 mg L?1nonionic surfactants for an accumulation time of 30 s in the range 5.0 × 10?10 to 2.0 × 10?8 mol L?1, and the detection limit for the accumulation time of 30 s was about 1.4 × 10?10 mol L?1. The proposed method was successfully validated using certified reference materials, seawater NASS-5 and rainwater TMRAIN-95...
机译:我们报告了一种简单而灵敏的溶出伏安法,用于测定含有高浓度表面活性剂的环境水样品中的痕量U(VI)。该程序基于U(VI)-铜铁离子络合物在堆积的汞滴电极上的吸附积累,然后通过使用差分脉冲调制的伏安扫描减少吸附的物质。通过将干扰物吸附到Amberlite XAD-7或XAD-16树脂上,消除了表面活性剂的干扰。评估了通过将分析样品与树脂混合以去除表面活性剂的最佳条件,以及对铀定量进行伏安测量的最佳条件。在最佳条件下,同时存在5.0 mg L?1阴离子表面活性剂,2.0 mg L?1阳离子表面活性剂和5.0 mg L?1非离子表面活性剂,并在5.0范围内累积30 s,即可获得U(VI)的线性校准图。 ×10×10 10至2.0×10 -8 mol L·1,并且30s的累积时间的检测极限约为1.4×10×10 mol L·1。使用认证的参考材料,海水NASS-5和雨水TMRAIN-95成功验证了该方法。

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