Faculty of Chemistry, Maria Curie-Sklodowska University, M.C. Sklodowska Sq. 3, 20-031 Lublin, Poland.
Talanta. 2011 Apr 15;84(2):393-9. doi: 10.1016/j.talanta.2011.01.057. Epub 2011 Jan 26.
A differential pulse adsorptive stripping voltammetric method has been developed for molybdenum trace determination in environmental water samples containing organic compounds. It was proved that interferences from the organic matrix such as surface active substances and humic substances could be removed by the addition of resin to the analysed sample prior to voltammetric measurement. The parameters for Mo(VI) determination in the presence of resin, using a hanging mercury drop as the working electrode, were examined systematically for two complexing agents: cupferron and chloranilic acid. The detection limits estimated from 3 times the standard deviation for a low Mo(VI) concentrations were equal to 5 × 10(-11) and 3 × 10(-10) mol L(-1) for cupferron and chloranilic acid, respectively. At the optimized conditions the quantitative Mo(VI) determination in the presence of even 50 mg L(-1) of surface active compounds can be performed. The proposed procedures were validated in the course of Mo(VI) determination in certified reference material NASS-5 and in the course of studying recovery of Mo(VI) from spiked river water samples.
一种差分脉冲吸附溶出伏安法已被开发用于测定环境水样中的钼痕量,其中水样含有机化合物。研究证明,通过在进行伏安测量之前向分析样品中添加树脂,可以去除来自有机基质(如表面活性剂和腐殖质)的干扰。在存在树脂的情况下,使用悬汞滴作为工作电极,系统地检查了两种络合剂:铜铁试剂和氯邻苯二甲酸用于测定 Mo(VI)的参数。从低 Mo(VI)浓度的 3 倍标准偏差估算的检测限分别为 5×10(-11)和 3×10(-10) mol L(-1),适用于铜铁试剂和氯邻苯二甲酸。在优化条件下,即使存在 50 mg L(-1)的表面活性剂,也可以进行定量 Mo(VI)测定。在 NASS-5 认证参考物质中 Mo(VI)的测定过程中和从加标河水样品中回收 Mo(VI)的研究过程中验证了所提出的程序。