Evaluation of Dispersive Liquid-Liquid Microextraction Coupled with Gas Chromatography-Microelectron Capture Detection (GC-.MU.ECD) for the Determination of Organochlorine Pesticides in Water Samples

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  • ZHAO Zhonghua
    State Key Laboratory for Lake Science and Environment Research, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences Graduate School, Chinese Academy of Sciences
  • ZHANG Lu
    State Key Laboratory for Lake Science and Environment Research, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences
  • WU Jinglu
    State Key Laboratory for Lake Science and Environment Research, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences
  • JIN Miao
    State Key Laboratory for Lake Science and Environment Research, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences
  • FAN Chengxin
    State Key Laboratory for Lake Science and Environment Research, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences

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  • Evaluation of dispersive liquid-liquid microextraction coupled with gas chromatography-microelectron capture detection (GC-μECD) for the determination of organochlorine pesticides in water samples
  • Evaluation of dispersive liquid liquid microextraction coupled with gas chromatography microelectron capture detection GC ミュー ECD for the determination of organochlorine pesticides in water samples

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Abstract

The extraction efficiency of a dispersive liquid–liquid microextraction (DLLME) method coupled with gas chromatography–microelectron capture detection (GC-μECD) for the simultaneous determination of 20 organochlorine pesticides (OCPs) in water samples was evaluated. The optimum conditions of DLLME for OCP measurement in water sample were determined with 10 μL of carbon tetrachloride (CCl4) and 1.5 mL of acetone as the extraction and dispersive solvents, respectively, all measurements were conducted under room temperature without the addition of salt. OCPs were extracted with good recoveries (60.35 – 107.89%) by the proposed method, except for heptachlor and aldrin due to the specific physico-chemical properties of these chemicals. Quantitative analysis showed that the relative standard deviations (RSDs) were below 9% and rather wider linear ranges (LRs) of 0.1 – 50 μg/L were obtained. The limits of detection (LODs) were in the range of 0.21 – 11.65 ng/L and no significant matrix effects were observed. Obtained results demonstrated that DLLME coupled with GC-μECD was rapid, convenient and efficient for OCP analysis in water samples.

Journal

  • Analytical Sciences

    Analytical Sciences 27 (5), 547-, 2011

    The Japan Society for Analytical Chemistry

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