Liquid-liquid-liquid microextraction of nitrophenols with a hollow fiber membrane prior to capillary liquid chromatography

被引:127
作者
Zhu, LY [1 ]
Zhu, L [1 ]
Lee, HK [1 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
关键词
liquid-liquid-liquid microextraction; extraction methods; hollow-fiber membranes; water analysis; environmental analysis; nitrophenols;
D O I
10.1016/S0021-9673(01)00906-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple liquid-liquid-liquid microextraction device utilizing a 2 cmX0.6 mm I.D. hollow fiber membrane was used to preconcentrate nitrophenols from water sample prior to capillary liquid chromatography (cLC) analysis. The extraction procedure was induced by the pH difference inside and outside the hollow fiber. The donor phase outside the hollow fiber was adjusted to pH similar to1 with HCl; the acceptor phase was NaOH solution used at various concentrations. Organic solvent was immobilized into the pores of the hollow fiber. With stirring, the neutral nitrophenols outside the fiber were extracted into the organic solvent, then back extracted into 2 ld of basic acceptor solution inside the fiber. The acceptor phase was then withdrawn into a microsyringe and injected into the cLC system directly. This technique used a low-cost disposable extraction "device" and is very convenient to operate. Up to 380-fold enrichment of analytes could be achieved. This procedure could also serve as a sample clean-up step because large molecules and basic compounds were not extracted into the acceptor phase. The RSD (n=6) was less than 6.2%, while the linear calibration range was from I to 200 mug/ml with r >0.998. The procedure was applied to the analysis of seawater. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:407 / 414
页数:8
相关论文
共 26 条
[1]   Large volume injection of acidic pesticides by reversed-phase micro high-performance liquid chromatography [J].
Cappiello, A ;
Famiglini, G ;
Berloni, A .
JOURNAL OF CHROMATOGRAPHY A, 1997, 768 (02) :215-222
[2]   Membrane solid-phase extraction with closed vessel microwave elution for the determination of phenolic compounds in aqueous matrices [J].
Chee, KK ;
Wong, MK ;
Lee, HK .
MIKROCHIMICA ACTA, 1997, 126 (1-2) :97-104
[3]  
FINGLER S, 1987, MIKROCHIM ACTA, V11, P163
[4]   DETERMINATION OF PHENOLS IN SEA-WATER BY LIQUID-CHROMATOGRAPHY WITH ELECTROCHEMICAL DETECTION AFTER ENRICHMENT BY USING SOLID-PHASE EXTRACTION CARTRIDGES AND DISKS [J].
GALCERAN, MT ;
JAUREGUI, O .
ANALYTICA CHIMICA ACTA, 1995, 304 (01) :75-84
[5]   Detection of more than 50 substituted phenols as their t-butyldimethylsilyl derivatives using gas chromatography mass spectrometry [J].
Heberer, T ;
Stan, HJ .
ANALYTICA CHIMICA ACTA, 1997, 341 (01) :21-34
[6]   Determination of alkyl, chloro and mononitrophenols in water by sample-acetylation and automatic on-line solid phase extraction gas chromatography mass spectrometry [J].
Jahr, D .
CHROMATOGRAPHIA, 1998, 47 (1-2) :49-56
[7]  
LEE HB, 1993, J CHROMATOGR, V636, P263
[8]   Solid-phase microextraction and gas chromatography mass spectrometry for determining chlorophenols from landfill leaches and soil [J].
Lee, MR ;
Yeh, YC ;
Hsiang, WS ;
Hwang, BH .
JOURNAL OF CHROMATOGRAPHY A, 1998, 806 (02) :317-324
[9]   Quantitative analysis of pesticides by capillary column high performance liquid chromatography combined with solid-phase extraction [J].
Liu, WP ;
Lee, HK .
TALANTA, 1998, 45 (04) :631-639
[10]  
Llompart M, 2000, J MICROCOLUMN SEP, V12, P25, DOI 10.1002/(SICI)1520-667X(2000)12:1<25::AID-MCS4>3.0.CO