期刊
ANALYTICA CHIMICA ACTA
卷 626, 期 2, 页码 166-173出版社
ELSEVIER
DOI: 10.1016/j.aca.2008.08.001
关键词
liquid-phase microextraction; organochlorine pesticides; gas chromatography-electron; capture detector; solidified microdrop
资金
- Iran National Science Foundation, INSF [86023/06]
A simple and efficient liquid-phase microextraction (LPME) in conjunction with gas chromatography-electron capture detector (GC-ECD) has been developed for extraction and determination of 11 organochlorine pesticides (OCPs) from water samples. in this technique a microdrop of 1-dodecanol containing pentachloronitrobenzene (internal standard) is delivered to the surface of an aqueous sample while being agitated by a stirring bar in the bulk of solution. Following completion of extraction, the sample vial was cooled by putting it into an ice bath for 5 min. Finally 2 mu L of the drop was injected into the GC for analysis. Factors relevant to the extraction efficiency were studied and optimized. Under the optimized extraction conditions (extraction solvent: 1-dodecanol; extraction temperature: 65 degrees C; sodium chloride concentration: 0.25 M; microdrop and sample volumes: 8 mu L and 20 mL respectively; the stirring rate: 750 rpm and the extraction time: 30 min), figures of merit of the proposed method were evaluated. The detection limits of the method were in the range of 7-19 ng L-1 and the RSD% for analysis of 2 mu g L-1 of OCPs was below 7.2% (n = 5). A good linearity (r(2) >= 0.993) and a relatively broad dynamic linear range (25-2000 ng L-1) were obtained. After 30 min of extraction, preconcentration factors were in the range of 708-1337 for different organochlorine pesticides and the relative errors ranged from -10.1 to 10.9%. Finally the proposed method was successfully utilized for preconcentration and determination of OCPs in different real samples. (c) 2008 Elsevier B.V All rights reserved.
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