On-line coupling of supercritical CO2 extraction with reversed-phase liquid chromatography for the quantitative analysis of analytes in aqueous matrices

被引:21
|
作者
Wang, ZY [1 ]
Ashraf-Khorassani, M [1 ]
Taylor, LT [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24061 USA
关键词
water analysis; supercritical fluid extraction; environmental analysis; interfaces; SFE-LC; progesterone; phenanthrene; pyrene; caffeine;
D O I
10.1016/j.chroma.2004.01.041
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The first report of on-line coupled supercritical fluid extraction (SFE) with reversed-phase liquid chromatography for the quantitative analysis of analytes in aqueous matrices is described. Two commercial systems (e.g. SFE and HPLC) were connected via a single six-port injection valve. By using water to eliminate residual decompressed CO2 gas in the solid-phase extraction trap, quantitative extraction and transfer were achieved for the target analytes (progesterone, phenanthrene, and pyrene) spiked in water, as well as in real samples (urine and environmental water). During each extraction, no restrictor plugging was realized. Extraction temperature and pressure were optimized. Different amounts of salt were added to the aqueous matrix to enhance ionic strength and thus extraction efficiency. Methanol and 2-propanol were used as CO2 modifiers. Compared with dynamically mixing modifier with the CO2 extraction fluid, pre-spiking the same amount of modifier in the extraction vessel enhanced the recovery similar to30% for progesterone, phenanthrene, and pyrene due to a "co-extraction effect". (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:221 / 227
页数:7
相关论文
共 50 条