Grabarczyk Malgorzata, Adamczyk Marzena
Department of Analytical Chemistry and Instrumental Analysis, Faculty of Chemistry, Maria Curie-Sklodowska University, 20-031 Lublin, Poland.
J Anal Methods Chem. 2017;2017:1486497. doi: 10.1155/2017/1486497. Epub 2017 Aug 28.
A simple, fast, and inexpensive voltammetric method for the simultaneous determination of trace bismuth(III) and lead(II) using (Hg(Ag)FE) as a working electrode was optimized. For adsorptive stripping voltammetric determination of Bi(III) and Pb(II) in a single scan, the cupferron was applied as a complexing agent. Experimental conditions under which these elements can be simultaneously detected include 0.1 mol L acetate buffer (pH = 4.6), 1 × 10 mol L cupferron, accumulation potential -0.05 V, and accumulation time 30 s. The experiments were performed without deaeration of the solutions. The calibration graph was linear from 2 × 10 mol L to 1 × 10 mol L for the simultaneous presence of bismuth and lead. The detection limits for preconcentration time of 30 s were 6.7 × 10 mol L and 8.8 × 10 mol L for bismuth and lead, respectively. The application of this procedure was tested by analyzing certified reference material (SPS-WW1 Wastewater) and Lake Zemborzyce water (eastern areas of Poland).
优化了一种使用(汞(银)膜电极)作为工作电极同时测定痕量铋(III)和铅(II)的简单、快速且廉价的伏安法。对于在单次扫描中吸附溶出伏安法测定铋(III)和铅(II),使用铜铁试剂作为络合剂。能够同时检测这些元素的实验条件包括0.1 mol·L醋酸盐缓冲液(pH = 4.6)、1×10 mol·L铜铁试剂、富集电位-0.05 V以及富集时间30 s。实验在溶液未除气的情况下进行。对于铋和铅同时存在的情况,校准曲线在2×10 mol·L至1×10 mol·L范围内呈线性。预富集时间为30 s时,铋和铅的检测限分别为6.7×10 mol·L和8.8×10 mol·L。通过分析有证标准物质(SPS-WW1废水)和泽姆博尔济采湖湖水(波兰东部地区)对该方法的应用进行了测试。