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基于液滴的液-液微萃取辅助固相微萃取气相色谱法分析水中挥发性芳烃。

Solid phase microextraction assisted by droplets-based liquid-liquid microextraction for analysis of volatile aromatic hydrocarbons in water by gas chromatography.

机构信息

Department of Chemistry, West University of Timisoara, Timisoara, Romania.

出版信息

J Sep Sci. 2012 Jul;35(13):1651-8. doi: 10.1002/jssc.201101105.

Abstract

A new technique for the analysis of volatile aromatic hydrocarbons by combining liquid-liquid microextraction with solid phase microextraction has been developed. The analytes were extracted from aqueous samples by an immobilized polydimethylsiloxane fiber assisted by the droplets of an appropriate organic solvent. Benzene, toluene, ethylbenzene, and o-xylene were used as target analytes. The main factors potentially affecting the microextraction such as the nature and the volume of organic solvent, polydimethylsiloxane (PDMS) swelling, extraction time, agitation, temperature, and salts were optimized. The method requires a very low consumption of organic solvent. The relative enrichment factor is in the range of 7.1-32.4 for extraction in the presence of dichloromethane at an optimum volume of 18 μL mL(-1) of aqueous sample. This enhancement over regular polydimethylsiloxane fiber is primarily the result of the fiber swelling and of a stable thin layer of organic solvent attached to the surface of the PDMS fiber. The limit of detection ranges from 0.02 to 0.65 ng mL(-1) for the target compounds using a 7-μm bonded polydimethylsiloxane coating and a flame ionization detector. The validity of this method is demonstrated by the analysis of a real waste water sample.

摘要

一种新的分析挥发性芳香烃的技术,将液-液微萃取与固相微萃取相结合。分析物通过固定在聚二甲基硅氧烷纤维上的有机溶剂液滴从水样中提取。苯、甲苯、乙苯和邻二甲苯被用作目标分析物。主要影响微萃取的因素,如有机溶剂的性质和体积、聚二甲基硅氧烷(PDMS)溶胀、萃取时间、搅拌、温度和盐,都得到了优化。该方法需要极低的有机溶剂消耗。在最佳条件下,当二氯甲烷的体积为 18 μL·mL(-1)时,相对富集因子在 7.1-32.4 范围内。与普通聚二甲基硅氧烷纤维相比,这种增强主要是由于纤维溶胀和稳定的薄层有机溶剂附着在 PDMS 纤维表面。使用 7-μm 键合聚二甲基硅氧烷涂层和火焰离子化检测器,目标化合物的检测限范围为 0.02-0.65ng·mL(-1)。通过对实际废水样品的分析验证了该方法的有效性。

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