Combined Use of Liquid-Liquid Microextraction and Carbon Nanotube Reinforced Hollow Fiber Microporous Membrane Solid-Phase Microextraction for the Determination of Triazine Herbicides in Water and Milk Samples by High-Performance Liquid Chromatography

被引:34
作者
Wu, Chunxia [1 ]
Liu, Yuan [2 ]
Wu, Qiuhua [1 ]
Wang, Chun [1 ]
Wang, Zhi [1 ]
机构
[1] Agr Univ Hebei, Coll Sci, Key Lab Bioinorgan Chem, Baoding 071001, Hebei, Peoples R China
[2] Agr Univ Hebei, Coll Agr, Baoding 071001, Hebei, Peoples R China
关键词
Hollow fiber microporous membrane solid-phase microextraction; Multi-walled carbon nanotube; Triazine herbicides; High-performance liquid chromatography; Water samples; Milk samples; MICROWAVE-ASSISTED EXTRACTION; GAS-CHROMATOGRAPHY; MASS-SPECTROMETRY; CAPILLARY-ELECTROPHORESIS; AQUEOUS SAMPLES; PRECONCENTRATION; ADSORBENTS; PESTICIDES; ATRAZINE; METABOLITES;
D O I
10.1007/s12161-011-9280-7
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A simple, efficient and environmentally friendly method for the extraction and determination of five triazine herbicides in water and milk samples was developed by simultaneous liquid-liquid microextraction and carbon nanotube reinforced hollow fiber microporous membrane solid-phase microextraction coupled with high-performance liquid chromatography-diode array detection. The parameters that affect the extraction efficiencies, including the type and concentration of multi-walled carbon nanotube, type of membrane solvent and desorption solvent, the type and volume of the extraction solvent in sample solution, extraction time and temperature, the pH of sample solution, stirring rate, and ionic strength were investigated and optimized. Under the optimum conditions, the method shows a good linearity within a range of 0.5-200 ng mL(-1) for water samples and 1-200 ng mL(-1) for milk samples, with the correlation coefficients (r) varying from 0.9991 to 0.9998 and from 0.9989 to 0.9994, respectively. The limits of detection were in the range between 0.08 and 0.15 ng mL(-1) for water samples and 0.3 and 0.5 ng mL(-1) for milk samples, while the relative standard deviations varied from 4.6% to 6.9% and from 5.3% to 7.7%, respectively. The recoveries of the target analytes at spiking levels of 5.0 and 50.0 ng mL(-1) were in the range from 86.6% to 106.8% for water samples and from 81.3% to 97.4% for milk samples. The results demonstrated that the developed method was an efficient pretreatment and enrichment procedure for the determination of triazine pesticides in real water and milk samples.
引用
收藏
页码:540 / 550
页数:11
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