Korolczuk Mieczyslaw, Moroziewicz Aleksandra, Grabarczyk Malgorzata
Faculty of Chemistry, Maria Curie Sklodowska University, 20-031, Lublin, Poland.
Anal Bioanal Chem. 2005 Aug;382(7):1678-82. doi: 10.1007/s00216-005-3358-2. Epub 2005 Jul 14.
Procedures for trace cobalt determinations by adsorptive stripping voltammetry at in situ and ex situ plated bismuth film electrodes are presented. These exploit the enhancement of the cobalt peak obtained by using the Co(II)-dimethylglyoxime-cetyltrimethylammonium bromide-piperazine-N,N'-bis(2-ethanesulfonic acid) system. The calibration graph for an accumulation time of 120 s was linear from 2 x 10(-10) to 2 x 10(-8) mol L(-1). The relative standard deviation from five determinations of cobalt at a concentration of 5 x 10(-9) mol L(-1) was 5.2%. The detection limit for an accumulation time of 300 s was 1.8 x 10(-11) mol L(-1). The proposed procedure was applied to cobalt determination in certified reference materials and in tap and river water samples.
介绍了在原位和异位镀铋膜电极上采用吸附溶出伏安法测定痕量钴的方法。这些方法利用了通过使用钴(II)-丁二酮肟-十六烷基三甲基溴化铵-哌嗪-N,N'-双(2-乙磺酸)体系获得的钴峰增强效应。累积时间为120 s时的校准曲线在2×10⁻¹⁰至2×10⁻⁸ mol L⁻¹范围内呈线性。在浓度为5×10⁻⁹ mol L⁻¹时对钴进行五次测定的相对标准偏差为5.2%。累积时间为300 s时的检测限为1.8×10⁻¹¹ mol L⁻¹。所提出的方法应用于标准参考物质以及自来水和河水样品中钴的测定。