期刊
JOURNAL OF CHROMATOGRAPHY A
卷 1217, 期 38, 页码 5883-5889出版社
ELSEVIER
DOI: 10.1016/j.chroma.2010.07.033
关键词
Temperature-controlled headspace liquid-phase microextraction; (TC-HS-LPME); Headspace liquid-phase extraction; Thermoelectric cooler (TEC); Chlorobenzenes; Large volume injection
资金
- National Natural Science Foundation of China [20627006]
- Ministry of Science & Technology of China [2007AA06Z419]
- Chinese Academy of Sciences [KJCX2-YW-H18]
A novel temperature-controlled headspace liquid-phase microextraction (TC-HS-LPME) device was established in which volatile solvents could be used as extractant. In this device, a PTFE vial cap with a cylindrical cavity was used as the holder of the extraction solvent. Up to 40 mu l of extraction solvent could be suspended in the cavity over the headspace of aqueous sample in the vial. A cooling system based on thermoelectric cooler (TEC) was used to lower the temperature of extractant in PTFE vial cap to reduce the loss of volatile solvent during extraction process and increase the extraction efficiency. The selection of solvents for HS-LPME was then extended to volatile solvents, such as dichloromethane, ethyl acetate and acetone. The use of volatile extraction solvents instead of semi-volatile solvent reduced the interference of the large solvent peak to the analytes peaks, and enhanced the compatibility of HS-LPME with gas chromatograph (GC). Moreover, the use of larger volume of extractant solvent increases the extraction capacity and the injection volume of GC after extraction, thus improving detection limits. Several critical parameters of this technique were investigated by using chlorobenzenes (CBs) as the model analytes. High enrichment factors (498-915), low limits of detection (0.004-0.008 mu g/L) and precision (3.93-5.27%) were obtained by using TC-HS-LPME/GC-FID. Relative recoveries for real samples were more than 83%. (C) 2010 Elsevier BM. All rights reserved.
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