Department of Chemistry, Shahid Bahonar University of Kerman, 22 Bahman Boulevard, Kerman 76169, Iran. m
J Hazard Mater. 2011 Feb 28;186(2-3):1739-43. doi: 10.1016/j.jhazmat.2010.12.080. Epub 2010 Dec 22.
In the present work, an efficient microextraction method was applied to separation and preconcentration of Ni(II), Co(II), Pb(II) and Cr(III). This method is dispersive liquid-liquid microextraction based on solidification of floating organic drop, which overcomes the most important problems of each aforementioned technique. The influences of analytical parameters, including pH, extraction solvent volume, disperser solvent type and its volume, concentration of chelating agent, salt effect and extraction time on the quantitative recoveries of nickel, cobalt, lead and chromium ions were investigated. Under the optimized conditions, the limits of detection were 0.2 ng L(-1) for Cr and 1.3 ng L(-1) for Co, Ni and Pb, with a preconcentration factor of 800 times. The relative standard deviations of 6.2% at 6.0 ng L(-1) of Cr and 7.2% at 10 ng L(-1) of Co, Ni and Pb were obtained (n=7). The proposed method was successfully applied for the analysis of ultra trace metals in water and wastewater samples.
在本工作中,应用了一种高效的微萃取方法来分离和预富集 Ni(II)、Co(II)、Pb(II) 和 Cr(III)。该方法是基于悬浮液滴固化的分散液-液微萃取,克服了上述每种技术的最重要问题。考察了分析参数,包括 pH 值、萃取溶剂体积、分散剂溶剂类型及其体积、螯合剂浓度、盐效应和萃取时间对镍、钴、铅和铬离子定量回收的影响。在优化条件下,Cr 的检测限为 0.2 ng L(-1),Co、Ni 和 Pb 的检测限为 1.3 ng L(-1),浓缩倍数为 800 倍。在 6.0 ng L(-1)Cr 和 10 ng L(-1)Co、Ni 和 Pb 时,相对标准偏差分别为 6.2%和 7.2%(n=7)。该方法成功应用于水样和废水样中超痕量金属的分析。