Makombe Martin, van der Horst Charlton, Silwana Bongiwe, Iwuoha Emmanuel, Somerset Vernon
a Sensorlab, Department of Chemistry, University of the Western Cape , Bellville , South Africa.
b Natural Resources and the Environment (NRE), Council for Scientific and Industrial Research (CSIR) , Stellenbosch , South Africa.
J Environ Sci Health A Tox Hazard Subst Environ Eng. 2016 Jul 2;51(8):597-606. doi: 10.1080/10934529.2016.1159857. Epub 2016 Apr 11.
A sensor for the adsorptive stripping voltammetric determination of rare earth elements has been developed. The electrochemical procedure is based on the oxidation of the rare earth elements complexed with alizarin complexone at a glassy carbon electrode that was in situ modified with an antimony film, during an anodic scan from -0.2 V to 1.1 V (vs. Ag/AgCl) and deposition potential of -0.1 V (vs. Ag/AgCl). The factors influencing the adsorptive stripping capability were optimised, including the complexing agent concentration, plating concentration of antimony and deposition time. The detection of rare earth elements (La, Ce and Pr) were realised in 0.08 M sodium acetate (pH = 5.8) solution as supporting electrolyte, with 2 × 10(-6) M alizarin complexone and 1.0 mg L(-1) antimony solution. Under the optimised conditions, a deposition time of 360 s was obtained and a linear response was observed between 1 and 25 µg L(-1). The reproducibility of the voltammetric measurements was found to be within 5.0% RSD for 12 replicate measurements of cerium(III) concentration of 5 µg L(-1) using the same electrode surface. The detection limits obtained using stripping analysis was 0.06, 0.42 and 0.71 μg L(-1) for Ce(III), La(III) and Pr(III), respectively. The developed sensor has been successfully applied for the determination of cerium, lanthanum and praseodymium in municipal tap water samples.
已开发出一种用于吸附溶出伏安法测定稀土元素的传感器。该电化学方法基于在玻碳电极上,稀土元素与茜素氨羧络合剂形成的络合物在阳极扫描(从 -0.2 V 至 1.1 V(相对于 Ag/AgCl))期间被氧化,玻碳电极已用锑膜原位修饰,沉积电位为 -0.1 V(相对于 Ag/AgCl)。优化了影响吸附溶出能力的因素,包括络合剂浓度、锑的镀覆浓度和沉积时间。在 0.08 M 醋酸钠(pH = 5.8)溶液作为支持电解质、2×10⁻⁶ M 茜素氨羧络合剂和 1.0 mg L⁻¹ 锑溶液的条件下实现了稀土元素(La、Ce 和 Pr)的检测。在优化条件下,获得了 360 s 的沉积时间,在 1 至 25 μg L⁻¹ 之间观察到线性响应。对于使用相同电极表面对 5 μg L⁻¹ 的铈(III)浓度进行 12 次重复测量,伏安测量的重现性在 5.0% RSD 以内。使用溶出分析获得的检测限分别为 Ce(III) 0.06 μg L⁻¹、La(III) 0.42 μg L⁻¹ 和 Pr(III) 0.71 μg L⁻¹。所开发的传感器已成功应用于市政自来水样品中铈、镧和镨的测定。