Beinrohr E, Cakrt M, Dzurov J, Kottas P, Kozáková E
Department of Analytical Chemistry, Slovak Technical University, 812 37, Bratislava, Slovakia.
Anal Bioanal Chem. 1996 Sep;356(3-4):253-8. doi: 10.1007/s0021663560253.
Trace concentrations of Hg were determined in a flow-system by constant current stripping chronopotentiometry in coulometric mode. Mercury was electrodeposited from the flowing sample solution in an electrochemical flow-through cell on a large surface porous electrode plated with a thin layer of gold. The deposited mercury was then stripped with constant current and the potential change of the working electrode was recorded and evaluated. Since complete electrochemical yields were achieved at both the deposition and dissolution steps, the mercury concentration in the sample solution could be calculated from Faraday's law. The detection limit and reproducibility of the method were about 0.1 ng/ml for 10 ml sample solution and 4%, respectively. The time for a complete analysis was 2 to 5 min. The utility of the method was demonstrated with the analysis of reference materials, water samples, waste materials, plants and charcoal catalysts.
采用恒电流溶出计时电位法的库仑模式,在流动体系中测定痕量汞浓度。汞在电化学流通池中从流动的样品溶液中电沉积到镀有薄层金的大表面积多孔电极上。然后用恒电流溶出沉积的汞,并记录和评估工作电极的电位变化。由于在沉积和溶解步骤中均实现了完全的电化学产率,因此可根据法拉第定律计算样品溶液中的汞浓度。对于10 ml样品溶液,该方法的检测限和重现性分别约为0.1 ng/ml和4%。完整分析所需时间为2至5分钟。通过对标准物质、水样、废料、植物和炭催化剂的分析证明了该方法的实用性。