首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Combination of dispersive solid phase extraction and dispersive liquid-liquid microextraction for extraction of some aryloxy pesticides prior to their determination by gas chromatography
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Combination of dispersive solid phase extraction and dispersive liquid-liquid microextraction for extraction of some aryloxy pesticides prior to their determination by gas chromatography

机译:分散固相萃取和分散液 - 液体微萃取在气相色谱法测定之前提取一些芳氧基农药的组合

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In this study a new version of solid phase extraction performed in a narrow-bore tube using large volume of sample followed by dispersive liquid-liquid microextraction has been proposed to achieve a high sensitive analytical method. It has been Used for the extraction and preconcentration of trace concentrations of some pesticides (metalaxyl, haloxyfop-r-methyl, clodinafop-propargyl, diclofop-methyl, and bromopropylate) in different vegetables (potato, tomato, onion, garlic, celery, radish, beet, and carrot) followed by gas chromatography-flame ionization detection. In the proposed method mg-level of a sorbent (C-8) is mixed with a dispersive solvent (iso-propanol) and then dispersed into an aqueous solution placed into a narrow-bore tube. By this action, the sorbent passes through the solution in a short time instead of passing the solution from the cartridge in conventional solid phase extraction in a long time. To achieve high enrichment factors, an appropriate organic solvent (acetonitrile) is used to elute the compounds of interest from the sorbent for the following dispersive liquid-liquid microextraction procedure. Some important parameters which affect the extraction efficiency were studied. Under the optimum extraction conditions, the method showed wide linear ranges (0.08-10,000 mu g L-1). Enrichment factors and extraction recoveries were in the ranges of 1702-4147 and 31-75%, respectively. Detection limits were in the range of 0.02-0.25 mu g L-1 in solution (0.01-0.89 mu g kg(-1) in samples). LOQs were obtained in the range of 0.08-0.83 mu g L-1 in solution (0.04-2.9 mu g kg(-1) in samples). Relative standard deviations of 4-7% (n = 6) and 2-4% (n = 7) were obtained for 10 and 50 mu g L-1 of each analyte, respectively. The relative recoveries obtained in three different concentrations were 80-101%. (C) 2016 Elsevier B.V. All rights reserved.
机译:在该研究中,已经提出了在使用大量样品中的窄孔管中进行的新版本的固相萃取,然后提出了分散液 - 液体微萃取,以实现高敏感的分析方法。它已被用于不同蔬菜(马铃薯,番茄,洋葱,大蒜,芹菜,萝卜)中痕量浓度的痕量浓度的痕量浓度(金属吡酰基,卤昔酯-r-甲基,克里丹替酯 - 丙基,二氯丙杂化物)的萃取和前浓度,甜菜和胡萝卜)随后是气相色谱 - 火焰电离检测。在所提出的方法中,吸附剂(C-8)的Mg水平与分散溶剂(异丙醇)混合,然后分散到置于狭窄孔管中的水溶液中。通过这种动作,吸附剂在短时间内通过解决方案,而不是在长时间内将盒从盒中传递盒。为了达到高富集因子,使用适当的有机溶剂(乙腈)从吸附剂中吸入以下分散液 - 液微萃取方法的感兴趣的化合物。研究了影响提取效率的一些重要参数。在最佳提取条件下,该方法显示宽线性范围(0.08-10,000μgl-1)。富集因子和提取回收率分别为1702-4147和31-75%的范围。检测限为0.02-0.25μgl-1的溶液(样品中0.01-0.89μg(-1))的范围内。在溶液(样品中0.04-2.9μg(-1)的溶液中的0.08-0.83μg1-1的范围内获得LOQ)。每个分析物的10和50μg1-1获得4-7%(n = 6)和2-4%(n = 7)的相对标准偏差。三种不同浓度中获得的相对回收率为80-101%。 (c)2016年Elsevier B.v.保留所有权利。

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