4.6 Article

Ultrasound-assisted surfactant-enhanced emulsification microextraction for the determination of carbamate pesticides in water samples by high performance liquid chromatography

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1217, Issue 11, Pages 1773-1778

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2010.01.060

Keywords

Ultrasound-assisted surfactant-enhanced emulsification microextraction; Carbamate pesticides; High performance liquid chromatography; Water samples

Funding

  1. Natural Science Foundations of Hebei [B2008000210]
  2. Scientific Research Foundation of Education Department of Hebei Province [2009132]

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A novel ultrasound-assisted surfactant-enhanced emulsification microextraction (UASEME) coupled with high performance liquid chromatography-diode array detection has been developed for the extraction and determination of six carbamate pesticides (metolcarb, carbofuran, carbaryl, pirimicarb, isoprocarb and diethofencarb) in water samples in the UASEME technique,Tween 20 was used as emulsifier, and chlorobenzene and chloroform were used as dual extraction solvent Without using any organic dispersive solvent that is normally required in the previously described common dispersive liquid-liquid microextraction method. Parameters that affect the extraction efficiency, Such as the kind and volume of the extraction solvent, the type and concentration of the surfactant, Ultrasound emulsification time and salt addition. were investigated and optimized for the method. Under the optimum conditions, the enrichment factors were in the range between 170 and 246 The limits of detection of the method were 0 1-0 3 ng mL(-1) and the limits of quantification were between 0.3 and 0.9 ng mL(-1). depending on the compounds. The linearity of the method was obtained in the range of 0 3-200 ng mL(-1) for metolcarb, carbaryl, pirimicarb. and diethofencarb. 0 6-200 ng mnL(-1) for carbofuran, and 0 9-200 ng mL(-1) for isoprocarb, with the con elation coefficients (r) ranging from 0 9982 to 0 9998 The relative standard deviations varied from 3 2 to 4.8% (n = 5). The recoveries of the method for the six carbamates from water samples at spiking levels of 1.0, 10 0, 50.0 and 100 0 ng mL(-1) were ranged from 81 0 to 97 5% The proposed UASEME technique has demonstrated to be simple, practical and environmentally friendly for the determination of carbamates residues in river, reservoir and well water samples (C) 2010 Elsevier B V All rights reserved

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