A new concept of hollow fiber liquid-liquid-liquid microextraction compatible with gas chromatography based on two immiscible organic solvents

被引:63
作者
Ghambarian, Mahnaz [1 ]
Yamini, Yadollah [1 ]
Esrafili, Ali [1 ]
Yazdanfar, Najmeh [2 ]
Moradi, Morteza [1 ]
机构
[1] Tarbiat Modares Univ, Dept Chem, Fac Sci, Tehran, Iran
[2] ACECR, Iranian Res & Dev Ctr Chem Ind, Tehran, Iran
关键词
Liquid-liquid-liquid microextraction; Immiscible organic solvents; Chlorophenols; Gas chromatography-electron capture detection; ELECTRON-CAPTURE DETECTION; PHASE MICROEXTRACTION; WATER SAMPLES; SINGLE DROP; CHLOROPHENOLS; EXTRACTION; SPECTROMETRY;
D O I
10.1016/j.chroma.2010.07.013
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
A new concept of liquid-liquid-liquid microextraction (LLLME) was introduced based on applying two immiscible organic solvents in lumen and wall pores of hollow fiber (HF). With this methodology, analytes of interest can be extracted from aqueous sample, into a thin layer of organic solvent (dodecane) sustained in the pores of a porous hollow fiber, and further into a mu L volume of organic acceptor (acetonitrile or methanol) located inside the lumen of the hollow fiber. Some chlorophenols (CPs) were selected as model compounds for developing and evaluating of the method performance. The analysis was performed by gas chromatography-electron capture detection (GC-ECD) without derivatization. The factors affecting the HF-LLLME of target compounds were investigated and the optimal extraction conditions were established. Under the optimum conditions, preconcentration factors in a range of 208-895 were obtained. The performance of the proposed method was studied in terms of linear dynamic ranges (LDRs from 0.02 to 100 ng mL(-1)), linearity (R-2 >= 0.995), precision (RSD%<= 8.1) and limits of detection (LODs in the range of 0.006-0.2 ng mL(-1)). In addition to preconcentration, HF-LLLME also served as a technique for sample clean-up. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:5652 / 5658
页数:7
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