Hollow fiber supported liquid-phase microextraction using ionic liquid as extractant for preconcentration of benzene, toluene, ethylbenzene and xylenes from water sample with gas chromatography-hydrogen flame ionization detection

► Ionic liquid-based HF-LPME used for preconcentration of BTEXs from water. ► Separation and detection is performed by GC-FID. ► LODs are better than or comparable with those of other methods. ► No carry-over interference or extraction solvent interference with the analytes. ► Simple, cheap and envi...

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Veröffentlicht in:Journal of hazardous materials 2011-10, Vol.194, p.24-29
Hauptverfasser: Ma, Xiaoguo, Huang, Minghua, Li, Zhihua, Wu, Jianmei
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Sprache:eng
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Zusammenfassung:► Ionic liquid-based HF-LPME used for preconcentration of BTEXs from water. ► Separation and detection is performed by GC-FID. ► LODs are better than or comparable with those of other methods. ► No carry-over interference or extraction solvent interference with the analytes. ► Simple, cheap and environmentally benign. A novel method has been developed for the analysis of benzene, toluene, ethyl-benzene, and o-, m- and p-xylenes (BTEXs) in water using hollow fiber supported liquid-phase microextraction (HF-LPME) followed by gas chromatography-hydrogen flame ionization detection. Ionic liquid 1-butyl-3-methy-limidazolium hexafluorophosphate ([BMIM][PF 6]) was acted as the extractant for extraction and preconcentration of BTEXs from aqueous samples, and a porous-walled polypropylene hollow fiber was utilized to stabilize and protect [BMIM][PF 6] during the extraction process. Various parameters that affect extraction efficiency were investigated in detail, and the optimized experimental conditions were as follows: 8 μL of [BMIM][PF 6] as extraction solvent for the target analytes in 20 mL of sample solution, 30 min of extraction time, a stirring rate of 1400 rpm and 15% NaCl (w/v) in aqueous sample at 25 °C (ambient temperature). The recovery was found to be 90.0–111.5% with RSD ( n = 5) of 1.3–5.4%, and the detection limits (S/N = 3) were in the range of 2.7–4.0 μg/L. The proposed method was simple, cheap, rapid, sensitive and environmentally benign, and could act as an alternative to techniques for BTEXs analysis with expensive instrumentations.
ISSN:0304-3894
1873-3336
DOI:10.1016/j.jhazmat.2011.07.066