Farahani Hadi, Norouzi Parviz, Dinarvand Rassoul, Ganjali Mohammad Reza
Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, P.O. Box 14155-6455, Tehran, Iran.
J Chromatogr A. 2007 Nov 23;1172(2):105-12. doi: 10.1016/j.chroma.2007.10.001. Epub 2007 Oct 10.
A simple, rapid and efficient method, the dispersive liquid-liquid microextraction (DLLME) in conjunction with gas chromatography-mass spectrometry (GC-MS), has been developed for the extraction and determination of phthalate esters (dimethyl phthalate, diallyl phthalate, di-n-butyl phthalate, benzyl butyl phthalate, dicyclohexyl phthalate and di-2-ethylhexyl phthalate) in water samples. Factors relevant to the microextraction efficiency, such as the kind of extraction, the disperser solvent and their volume, the salt effect and the extraction time were investigated and optimized. Under the optimized extraction conditions (extraction solvent: chlorobenzene, volume, 9.5microL; disperser solvent: acetone, volume, 0.50mL, without salt addition and extraction time below 5s), the figures of merit of the proposed method were evaluated. The values of the detection limit of the method were in the range of 0.002-0.008microgL(-1), while the RSD% value for the analysis of 1microgL(-1) of the analytes was below 6.8% (n=4). A good linearity (0.9962>/=r(2)>/=0.9901) and a broad linear range (0.02-100microgL(-1)) were obtained. The method exhibited enrichment factors and recoveries, ranging from 681 to 889 and 68.1 to 88.9%, respectively, at room temperature (25+/-1 degrees C). Finally, the proposed method was successfully utilized for the preconcentration and determination of the phthalate esters in different real water samples and satisfactory results were obtained.
已开发出一种简单、快速且高效的方法——分散液液微萃取(DLLME)结合气相色谱 - 质谱联用(GC - MS),用于萃取和测定水样中的邻苯二甲酸酯(邻苯二甲酸二甲酯、邻苯二甲酸二烯丙酯、邻苯二甲酸二正丁酯、邻苯二甲酸苄基丁酯、邻苯二甲酸二环己酯和邻苯二甲酸二(2 - 乙基己基)酯)。研究并优化了与微萃取效率相关的因素,如萃取剂种类、分散剂溶剂及其体积、盐效应和萃取时间。在优化的萃取条件下(萃取溶剂:氯苯,体积9.5微升;分散剂溶剂:丙酮,体积0.50毫升,不添加盐且萃取时间低于5秒),对所提方法的性能指标进行了评估。该方法的检测限在0.002 - 0.008微克/升范围内,而对1微克/升分析物进行分析时的相对标准偏差(RSD%)值低于6.8%(n = 4)。获得了良好的线性关系(0.9962≥r²≥0.9901)和较宽的线性范围(0.02 - 100微克/升)。在室温(25±1℃)下,该方法的富集因子和回收率分别为681至889以及68.1%至88.9%。最后,所提方法成功用于不同实际水样中邻苯二甲酸酯的预浓缩和测定,并获得了满意的结果。