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Headspace in-tube microextraction coupled with micellar electrokinetic chromatography of neutral aromatic compounds
被引:4
|作者:
Cho, Sung Min
[1
]
Park, Bum Su
[2
]
Jung, Woo Sung
[2
]
Lee, Sang Won
[2
]
Jung, Yunhwan
[2
]
Chung, Doo Soo
[1
]
机构:
[1] Seoul Natl Univ, Dept Chem, Seoul 151747, South Korea
[2] Seoul Sci High Sch, Seoul 110530, South Korea
来源:
关键词:
Headspace extraction;
BTEX;
In-tube microextraction;
Capillary electrophoresis;
SOLID-PHASE MICROEXTRACTION;
SINGLE-DROP MICROEXTRACTION;
SOLVENT-EXTRACTION;
SAMPLE STACKING;
CAPILLARY;
PRECONCENTRATION;
SEPARATION;
INJECTION;
D O I:
10.1016/j.talanta.2015.11.035
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
Headspace (HS) extraction can be carried out easily and aptly via single drop microextraction coupled with capillary electrophoresis (CE). However, one drawback is the difficulty of keeping the single drop stably at the capillary tip. To solve this problem, we have recently demonstrated HS in-tube microextraction (ITME) of acidic compounds such as chlrophenols in an acidic sample using a basic run buffer plug in the separation capillary for CE as an acceptor phase. In this report, an organic acceptor plug in a capillary was used to extract neutral organic volatile pollutants such as BTEX (benzene, toluene, ethylbenzene, and m-xylene). After extraction, the analytes enriched in the organic acceptor plug were analyzed with micellar electrokinetic chromatography (MEKC). The enrichment factors for BTEX in a standard solution were up to 350 under an optimal condition of 25 degrees C for 20 min. As an application, BTEX spiked into bottled water were analyzed with HS-ITME-MEKC, and the enrichment factors for BTEX were up to 320. The limits of detections were 1-4 ppb, which are at least 200 times lower than the US Environmental Protection Agency guidelines for drinking water, except benzene. The entire procedure of HS-ITME-MEKC was carried out automatically using a commercial CE instrument. (C) 2015 Elsevier B.V. All rights reserved.
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页码:729 / 733
页数:5
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