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Cloud point extraction coupled with microwave or ultrasonic assisted back extraction as a preconcentration step prior to gas chromatography

机译:浊点萃取与微波或超声辅助反萃取相结合,作为气相色谱之前的预浓缩步骤

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Cloud point extraction of nonionic and anionic surfactants was applied as a preconcentration step prior to gas chromatography. No cleanup step preceded chromatographic analysis. The obtained surfactant-rich phase was treated with water-immiscible solvents, and the target analytes were back extracted by short-term microwave application or ultrasonication. A mixture of six PAHs (naphthalene, acenaphthene, fluorene, anthracene, fluoranthene, pyrene) was used as test compounds. The obtained detection limits were in the microgram per liter area. Recoveries of spiked water and soil samples ranged between 92 and 105% while analysis of certified reference materials gave results in good agreement with the certified values. Under the optimum experimental conditions, there was no interference or blocking of the column. According to our results, this approach presents a convenient solution to the up-to-date problem of combining gas chromatography with micellar cloud point extraction.
机译:在气相色谱分析之前,将非离子和阴离子表面活性剂的浊点萃取用作预浓缩步骤。色谱分析之前没有任何清洁步骤。用与水不混溶的溶剂处理所得的富含表面活性剂的相,并通过短期微波应用或超声处理反萃取目标分析物。六个PAH(萘,,芴,蒽,荧蒽,pyr)的混合物用作测试化合物。所获得的检测极限为微克每升面积。加标的水和土壤样品的回收率在92%到105%之间,而经认证的参考物质的分析结果与经认证的值高度一致。在最佳实验条件下,色谱柱没有干扰或阻塞。根据我们的结果,这种方法为结合气相色谱与胶束浊点萃取的最新问题提供了一种方便的解决方案。

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