Elçi L, Sahin U, Oztaş S
Erciyes University, Art and Sciences Faculty, Chemistry Department, Kayseri, Turkey.
Talanta. 1997 Jun;44(6):1017-23. doi: 10.1016/s0039-9140(96)02186-8.
A method for determination of trace amounts of Cu, Fe, Pb, Mn, Zn, Cd, Ni, Bi and Cr in aqueous solutions by flame atomic absorption spectrometry after coprecipitation by using a combination of sodium diethyldithiocarbamate as a chelating agent and cobalt as a carrier element was introduced. Different factors including amounts of reagents, pH of sample solution, standing time, sample volume for the precipitation and matrix effects were examined. Under selected conditions, the relative standard deviation of the combined method of sample treatment, coprecipitation and determination with flame AAS (n = 9) is generally about 3.5-6.9%; the limits of detection (3 s, n = 20) for the analytes were found to be between 4 and 64 microg 1(-1). The procedure was applied to the analysis of sea water and dialysis concentrate samples with quantitative recovery, > or =95%.
介绍了一种通过火焰原子吸收光谱法测定水溶液中痕量铜、铁、铅、锰、锌、镉、镍、铋和铬的方法,该方法采用二乙基二硫代氨基甲酸钠作为螯合剂和钴作为载体元素进行共沉淀。研究了试剂用量、样品溶液pH值、静置时间、沉淀样品体积和基体效应等不同因素。在选定条件下,样品处理、共沉淀和火焰原子吸收光谱法测定相结合的方法(n = 9)的相对标准偏差一般约为3.5-6.9%;分析物的检测限(3s,n = 20)在4至64μg L-1之间。该方法应用于海水和透析浓缩液样品的分析,回收率定量,≥95%。