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采用分散液液微萃取结合高效液相色谱法测定水样中的四种芳香胺。

Determination of four aromatic amines in water samples using dispersive liquid-liquid microextraction combined with HPLC.

作者信息

Wang Xuedong, Fu Lingyan, Wei Guohui, Hu Jia, Zhao Xinna, Liu Xiujuan, Li Yanyan

机构信息

School of Environmental Sciece and Public Health, Wenzhou Medical College, Wenzhou, China.

出版信息

J Sep Sci. 2008 Sep;31(16-17):2932-8. doi: 10.1002/jssc.200800273.

Abstract

A new method for the determination of four aromatic amines in water samples was developed by using dispersive liquid-liquid microextraction (DLLME) technique combined with HPLC-variable wavelength detection (HPLC-VWD). In this extraction method, 0.50 mL methanol (as dispersive solvent) containing 25.0 microL tetrachloroethane (as extraction solvent) was rapidly injected by a syringe into 5.00 mL water sample. Accordingly, a cloudy solution was formed. After centrifugation for 2 min at 4000 rpm, the fine droplets of the tetrachloroethane containing the analytes were sedimented in the bottom of the conical test tube (7+/-0.2 microL). Then, 5.0 microL of the settled phase was determined by HPLC-VWD. Parameters such as the kind and volume of extraction solvent and dispersive solvent, extraction time, and salt concentration were optimized. Under the optimum conditions, the enrichment factors ranged from 41.3 to 94.5. Linearity was observed in the range of 5-5000 ng/mL. The LODs based on S/N of 3 ranged from 0.8 to 1.8 ng/mL. The RSDs (for 400 ng/mL of p-toluidine and o-chloroaniline, 100 ng/mL of p-chloroaniline and p-bromoaniline) varied from 4.1 to 5.3% (n=6). The water samples collected from rivers and lakes were successfully analyzed by the proposed method and the relative recoveries were in the range of 85.4-111.7% and 90.2-101.3%, respectively.

摘要

采用分散液液微萃取(DLLME)技术结合高效液相色谱-可变波长检测(HPLC-VWD),开发了一种测定水样中四种芳香胺的新方法。在该萃取方法中,用注射器将含有25.0微升四氯乙烷(作为萃取溶剂)的0.50毫升甲醇(作为分散溶剂)快速注入5.00毫升水样中。相应地,形成了浑浊溶液。在4000转/分钟下离心2分钟后,含有分析物的四氯乙烷细液滴沉淀在锥形试管底部(7±0.2微升)。然后,用HPLC-VWD测定5.0微升的沉淀相。对萃取溶剂和分散溶剂的种类和体积、萃取时间和盐浓度等参数进行了优化。在最佳条件下,富集因子在41.3至94.5之间。在5-5000纳克/毫升范围内观察到线性关系。基于3倍信噪比的检测限在0.8至1.8纳克/毫升之间。相对标准偏差(对于400纳克/毫升的对甲苯胺和邻氯苯胺、100纳克/毫升的对氯苯胺和对溴苯胺)在4.1%至5.3%之间(n = 6)。所提出的方法成功地分析了从河流和湖泊采集的水样,相对回收率分别在85.4-111.7%和90.2-101.3%范围内。

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