In-line coupling headspace liquid-phase microextraction with capillary electrophoresis

被引:24
|
作者
Xie, Hai-Yang [1 ]
He, You-Zhao [1 ]
Gan, Wu-Er [1 ]
Yu, Chang-Zhu [1 ]
Han, Fang [1 ]
Ling, Da-Si [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China
基金
美国国家科学基金会;
关键词
Headspace liquid-phase microextraction; Capillary electrophoresis; In-line coupling; Sample pretreatment; Preconcentration; SINGLE-DROP MICROEXTRACTION; IONIC LIQUID; GAS-CHROMATOGRAPHY; PRECONCENTRATION METHOD; SOLVENT-EXTRACTION; SAMPLE PREPARATION; WATER; PERFORMANCE; PHENOLS;
D O I
10.1016/j.chroma.2009.12.028
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An analytical technique of in-line coupling headspace liquid-phase microextraction (HS-LPME) with capillary electrophoresis (CE) was proposed to determine volatile analytes A special covet unit of the sample vial was adopted in the coupling method To evaluate the proposed method, phenols were used as model analyzes The parameters affecting the extraction efficiency were investigated. Including the configuration of acceptor phase, kind and concentration of acceptor solution, extiaction temperature and rime. salt-our effect, sample volume. etc The optimal enrichment factors of HS-LPME were obtained with the sample volume of about half of sample vials, which were confirmed by both the theoretical prediction and experimental results The enrichment factors were obtained from 520 to 1270 The limits of detection (LODs. S/N=3) were in the range from 0 5 to t ng/mL each phenol The recoveries were from 87 2% to 92 7% and the relative standard deviations (RSDs) were lower than 5 7% (n=6) The proposed method was successfully applied to the quantitative analysis of the phenols in tap water, and proved to be a simple, convenient and reliable sample preconcentration and determination method for volatile analyzes In water samples (C) 2009 Elsevier 13 V All rights reserved
引用
收藏
页码:1203 / 1207
页数:5
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