کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1182788 | 1491646 | 2013 | 6 صفحه PDF | دانلود رایگان |

A novel analytical method was developed for the extraction and determination of five chloroacetanilide herbicides (alachlor, acetochlor, metolachlor, butachlor and pretilachlor) in water and green tea samples by graphene-based magnetic solid phase extraction and dispersive liquid-liquid microextraction followed by gas chromatography-flame ionization detection (GC-FID). Some important experimental parameters that could influence the extraction efficiency were investigated. Under the optimum conditions, as high as 3399 to 4002 fold enrichment factors for the herbicides were achieved. A good linearity was obtained in the range of 0.1–50.0 μg L−1 for all the five herbicides with the correlation coefficients (r) varying from 0.9973 to 0.9993. The limits of detection ranged from 0.01 to 0.03μg L−1. The method was applied to the analysis of the chloroacetanilide herbicides in environmental water and green tea samples with a satisfactory result. The recoveries of the method for the analytes were in the range from 80.2% to 105.3%, and the relative standard deviations were between 3.8% and 5.8%.
A graphene-based magnetic solid phase extraction coupled with dispersive liquid-liquid microextraction was developed to extract five chloroacetanilide herbicides from water and green tea samples followed by gas chromatography-flame ionization detection. The method has the advantages such as simplicity and high sensitivity.Figure optionsDownload as PowerPoint slide
Journal: Chinese Journal of Analytical Chemistry - Volume 41, Issue 8, August 2013, Pages 1177–1182