A new high-speed hollow fiber based liquid phase microextraction method using volatile organic solvent for determination of aromatic amines in environmental water samples prior to high-performance liquid chromatography

被引:40
作者
Sarafraz-Yazdi, A. [1 ]
Mofazzeli, F. [2 ]
Es'haghi, Z. [3 ]
机构
[1] Ferdowsi Univ Mashhad, Fac Sci, Dept Chem, Mashhad, Iran
[2] Islamic Azad Univ, Quchan Branch, Dept Chem, Quchan, Iran
[3] Payame Noor Univ, Fac Sci, Dept Chem, Tehran, Iran
关键词
Hollow fiber based liquid phase microextraction (HF-LPME); Aromatic amines; High-performance liquid chromatography (HPLC); Water analysis; GAS-CHROMATOGRAPHY; MASS-SPECTROMETRY; AZO DYES; EXTRACTION; OPTIMIZATION; POLLUTANTS; DRUGS;
D O I
10.1016/j.talanta.2009.04.015
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new and fast hollow fiber based liquid phase microextraction (HF-LPME) method using volatile organic solvents coupled with high-performance liquid chromatography (HPLC) was developed for determination of aromatic amines in the environmental water samples. Analytes including 3-nitroaniline, 3-chloroaniline and 4-bromoaniline were extracted from 6 mL basic aqueous sample solution (donor phase, NaOH 1 mol L-1) into the thin film of organic solvent that surrounded and impregnated the pores of the polypropylene hollow fiber wall (toluene, 20 mu L). then back-extracted into the 6 mu L acidified aqueous solution (acceptor phase, HCl 0.5mol L-1) in the lumen of the two-end sealed hollow fiber. After the extraction, 5 mu L of the acceptor phase was withdrawn into the syringe and injected directly into the HPLC system for the analysis. The parameters influencing the extraction efficiency including the kind of organic solvent and its volume, composition of donor and acceptor phases and the volume ratio between them, extraction time, stirring rate, salt addition and the effect of the analyte complexation with 18-crown-6 ether were investigated and optimized. Under the optimal conditions (donor phase: 6 mL of 1 mol L-1 NaOH with 10% NaCl: organic phase: 20 mu L of toluene; acceptor phase: 6 mu L of 0.5 mol L-1 HCl and 600 m mol L-1 18-crown-6 ether; pre-extraction and back-extraction times: 75 s and 10 min, respectively; stirring rate: 800 rpm), the obtained EFs were between 259 and 674, dynamic linear ranges were 0.1-1000 mu g L-1 (R > 0.9991), and also the limits of detection were in the range of 0.01-0.1 mu g L-1. The proposed procedure worked very well for real environmental water samples with microgram per liter level of the analytes, and good relative recoveries (91-102%) were obtained for the spiked sample solutions. (C) 2009 Elsevier B.V. All rights reserved.
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页码:472 / 478
页数:7
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