Tor Ali
Selcuk University, Department of Environmental Engineering, 42031 Campus-Konya, Turkey.
J Chromatogr A. 2006 Aug 25;1125(1):129-32. doi: 10.1016/j.chroma.2006.06.081. Epub 2006 Jul 21.
A drop-based liquid phase microextraction and gas chromatographic-electron capture detection (GC-ECD) method was described for the determination of chlorobenzenes including chlorobenzene, 1,2-dichlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene and 1,2,3-trichlorobenzene in 5 ml of water. The method used 2 microl of n-hexane as extraction solvent, 5 min extraction time, a stirring rate of 600 rpm and sample ionic strength of 3 M maintained with sodium chloride at 25 degrees C (ambient temperature). The limits of detection (LODs) ranged from 0.004 microg l(-1) (for 1,3-dichlorobenzene) to 0.008 microg l(-1) (for monochlorobenzene). The dynamic linear range for all investigated chlorobenzenes was 1-50 microg l(-1). Recoveries of chlorobenzenes from fortified distilled water are over 90% for three different fortification levels (5, 15 and 45 microg l(-1)) and relative standard deviations of the recoveries are below 6%. Analysis of fortified (5 microg l(-1)) real water samples revealed that matrices had no adverse effect on extraction efficiency of proposed method. The recovery of fortified real water samples was from 90 to 94% with relative standard deviations below 6%.
描述了一种基于液滴的液相微萃取和气相色谱-电子捕获检测(GC-ECD)方法,用于测定5毫升水中的氯苯,包括氯苯、1,2-二氯苯、1,3-二氯苯、1,4-二氯苯和1,2,3-三氯苯。该方法使用2微升正己烷作为萃取溶剂,萃取时间为5分钟,搅拌速率为600转/分钟,在25℃(环境温度)下用氯化钠将样品离子强度保持在3M。检测限(LOD)范围为0.004微克/升(对于1,3-二氯苯)至0.008微克/升(对于一氯苯)。所有研究的氯苯的动态线性范围为1-50微克/升。对于三种不同的加标水平(5、15和45微克/升),从加标蒸馏水回收氯苯的回收率超过90%,回收率的相对标准偏差低于6%。对加标(5微克/升)实际水样的分析表明,基质对所提出方法的萃取效率没有不利影响。加标实际水样的回收率为90%至94%,相对标准偏差低于6%。