Manova A, Strelec M, Cacho F, Lehotay J, Beinrohr E
Slovak University of Technology, Institute of Analytical Chemistry, Radlinskeho 9, 812 37 Bratislava, Slovakia.
Anal Chim Acta. 2007 Apr 4;588(1):16-9. doi: 10.1016/j.aca.2007.01.074. Epub 2007 Feb 6.
Sulphides in water samples were determined by stripping chronopotentiometry in a computer controlled flow system with a flow-through electrochemical cell. The working electrode was a porous glassy carbon electrode coated with Nafion and mercury. The sample was diluted with 0.1 mol L(-1) NaOH and analysed. Sulphides in the sample were collected in the porous electrode as mercury sulphide and then stripped by a current of -500 microA. The limit of detection was found to be 1.6 microg L(-1) and 0.5 microg L(-1) for 1 mL and 5 mL of preconcentrated sample, respectively. The linear range for 1mL sample was found to be 5-400 microg L(-1). The repeatability and reproducibility was found to be 2.6% and 4.8%, respectively. The method was applied to analyses of waste water samples from a tannery.
采用流动注射计时电位法,在计算机控制的流动体系中,使用流通式电化学池测定水样中的硫化物。工作电极是涂有Nafion和汞的多孔玻碳电极。将样品用0.1 mol L(-1) NaOH稀释后进行分析。样品中的硫化物在多孔电极中以硫化汞的形式收集,然后用-500 μA的电流进行溶出。对于1 mL和5 mL预浓缩样品,检测限分别为1.6 μg L(-1)和0.5 μg L(-1)。1 mL样品的线性范围为5-400 μg L(-1)。重复性和再现性分别为2.6%和4.8%。该方法应用于制革厂废水样品的分析。