Homogeneous Liquid-Liquid Microextraction for Determination of Organophosphorus Pesticides in Environmental Water Samples Prior to Gas Chromatography-Flame Photometric Detection

被引:32
作者
Berijani, Sana [1 ]
Sadigh, Mirhanif [2 ]
Pournamdari, Elham [3 ]
机构
[1] Islamic Azad Univ, South Tehran Branch, Dept Appl Chem, Fac Sci, Tehran, Iran
[2] Univ Sci & Culture, Dept Civil Engn, Tehran, Iran
[3] Islamic Azad Univ, Islamshahr Branch, Dept Chem, Coll Sci, Islamshahr, Iran
关键词
SOLID-PHASE MICROEXTRACTION; CLOUD-POINT EXTRACTION; SINGLE-DROP MICROEXTRACTION; CONVENTIONAL MICROSYRINGE; CAPILLARY-ELECTROPHORESIS; MASS-SPECTROMETRY; ORGANIC-COMPOUNDS; AQUEOUS SAMPLES; HUMAN BLOOD; GC-MS;
D O I
10.1093/chromsci/bmw020
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, homogeneous liquid-liquid microextraction (HLLME) was developed for preconcentration and extraction of 15 organophosphorus pesticides (OPPs) from water samples coupling with gas chromatography followed by a flame photometric detector (HLLME-GC-FPD). In this method, OPPs were extracted by the homogeneous phase in a ternary solvent system (water/acetic acid/chloroform). The homogeneous solution was excluded by the addition of sodium hydroxide as a phase separator reagent and a cloudy solution was formed. After centrifugation (3 min at 5,000 rpm), the fine particles of extraction solvent (chloroform) were sedimented at the bottom of the conical test tube (10.0 +/- 0.5 mu L). Furthermore, 0.5 mu L of the sedimented phase was injected into the GC for separation and determination of OPPs. Optimal results were obtained under the following conditions: volume of the extracting solvent (chloroform), 53 mu L; volume of the consolute solvent (acetic acid), 0.76 mL and concentration of sodium hydroxide, 40% (w/v). Under the optimumconditions, the enrichment factors of (260-665), the extraction percent of 75.8-104%, the dynamic linear range of 0.03-300 mu g L-1 and the limits of detection of 0.004-0.03 mu g L-1 were obtained for the OPPs. This method was successfully applied for the extraction and determination of the OPPs in environmental water samples.
引用
收藏
页码:1061 / 1067
页数:7
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