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将均相液-液萃取与分散液-液微萃取相结合,用于从水样中萃取和预富集多环芳烃,然后采用带有火焰离子化检测的气相色谱法进行分析。

Coupling of homogeneous liquid-liquid extraction and dispersive liquid-liquid microextraction for the extraction and preconcentration of polycyclic aromatic hydrocarbons from aqueous samples followed by GC with flame ionization detection.

作者信息

Farajzadeh Mir Ali, Khiavi Elahe Behboudi, Khorram Parisa, Mogaddam Mohammad Reza Afshar

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran.

出版信息

J Sep Sci. 2017 Jan;40(2):497-505. doi: 10.1002/jssc.201600894. Epub 2016 Dec 28.

Abstract

In the present study, a simple and rapid method for the extraction and preconcentration of some polycyclic aromatic hydrocarbons in water samples has been developed. In this method, two sample preparation methods were combined to obtain high extraction recoveries and enrichment factors for sensitive analysis of the selected analytes. In the first stage of the method, a homogeneous solution containing an aqueous solution and cyclohexyl amine is broken by the addition of a salt. After centrifugation, the upper collected phase containing the extracted analytes is subjected to the following dispersive liquid-liquid microextraction method. Rapid injection of the mixture of cyclohexyl amine resulted from the first stage and 1,1,2-trichloroethane (as an extraction solvent) into an acetic acid solution is led to form a cloudy solution. After centrifuging, the fine droplets of the extraction solvent are settled down in the bottom of the test tube, and an aliquot of it is analyzed by gas chromatography. Under the optimum extraction conditions, enrichment factors and limits of detection for the studied analytes were obtained in the ranges of 616-752 and 0.08-0.20 μg/L, respectively. The simplicity, high extraction efficiency, short sample preparation time, low cost, and safety demonstrated the efficiency of this method relative to other approaches.

摘要

在本研究中,开发了一种简单快速的方法用于提取和预富集水样中的某些多环芳烃。在该方法中,将两种样品制备方法相结合,以获得高提取回收率和富集因子,用于对选定分析物进行灵敏分析。在该方法的第一阶段,通过加入盐使含有水溶液和环己胺的均匀溶液分层。离心后,将含有萃取分析物的上层收集相进行以下分散液液微萃取方法。将第一阶段得到的环己胺混合物与1,1,2-三氯乙烷(作为萃取溶剂)快速注入乙酸溶液中,形成浑浊溶液。离心后,萃取溶剂的细小液滴沉淀在试管底部,取其一份进行气相色谱分析。在最佳萃取条件下,所研究分析物的富集因子和检测限分别在616 - 752和0.08 - 0.20 μg/L范围内。该方法的简单性、高萃取效率、短样品制备时间、低成本和安全性证明了其相对于其他方法的有效性。

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