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非离子表面活性剂作为一种发展方法在两相溶剂浮选微萃取中的应用,用于同时测定水样中三种邻苯二甲酸酯。

Application of non-ionic surfactant as a developed method for the enhancement of two-phase solvent bar microextraction for the simultaneous determination of three phthalate esters from water samples.

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, University of Mazandaran, NirooHavayii Boulevard, 47416-95447, Babolsar, Iran.

Department of Analytical Chemistry, Faculty of Chemistry, University of Mazandaran, NirooHavayii Boulevard, 47416-95447, Babolsar, Iran.

出版信息

J Chromatogr A. 2018 Aug 3;1561:39-47. doi: 10.1016/j.chroma.2018.05.039. Epub 2018 May 20.

Abstract

The extraction of phthalate esters (PEs) from aqueous matrices using two-phase solvent bar microextraction by organic micellar phase was investigated. A short hollow fiber immobilized with reverse micelles of Brij 35 surfactant in 1-octanol was served as the solvent bar for microextraction. Experimental results show that the extraction efficiency were much higher using two-phase solvent bar microextraction based on non-ionic surfactant than conventional two-phase solvent bar microextraction because of a positive effect of surfactant-containing extraction phase in promoting the partition process by non-ionic intermolecular forces such as polar and hydrophobicity interactions. The nature of the extraction solvent, type and concentration of non-ionic surfactant, extraction time, sample pH, temperature, stirring rate and ionic strength were the effecting parameters which optimized to obtain the highest extraction recovery. Analysis of recovered analytes was carried out with high performance liquid chromatography coupled with ultraviolet detection (HPLC-UV). Under the optimum conditions, linearity was observed in the range of 1-800 ng mL for dimethylphthalate (DMP) and 0.5-800 ng mL for diethylphthalate (DEP) and di-n-butyl phthalate (DBP) with correlation determination values above 0.99 for them. The limits of detection and quantification were ranged from 0.012 to 0.03 ng mL and 0.04-0.1 ng mL, respectively. The ranges of intra-day and inter-day RSD (n = 3) at 20 ng mL of PEs were 1.8-2.1% and 2.1-2.6%, respectively. Results showed that developed method can be a very powerful, innovative and promising sample preparation technique in PEs analysis from environmental and drinking water samples.

摘要

采用有机胶束相的双相比溶剂微萃取法从水基质中萃取邻苯二甲酸酯(PEs)。短的中空纤维固定在 1-辛醇中的 Brij 35 表面活性剂的反胶束中作为溶剂微萃取的溶剂棒。实验结果表明,由于含有表面活性剂的萃取相通过非离子分子间力(如极性和疏水性相互作用)促进分配过程,基于非离子表面活性剂的双相比溶剂微萃取的萃取效率比传统的双相比溶剂微萃取高得多。萃取溶剂的性质、非离子表面活性剂的类型和浓度、萃取时间、样品 pH 值、温度、搅拌速度和离子强度是获得最高萃取回收率的影响参数。用高效液相色谱法与紫外检测(HPLC-UV)对回收的分析物进行分析。在最佳条件下,二甲基邻苯二甲酸酯(DMP)的线性范围为 1-800ngmL,二乙基邻苯二甲酸酯(DEP)和邻苯二甲酸二丁酯(DBP)的线性范围为 0.5-800ngmL,相关系数均大于 0.99。检测限和定量限范围分别为 0.012-0.03ngmL 和 0.04-0.1ngmL。在 20ngmL PEs 时,日内和日间 RSD(n=3)的范围分别为 1.8-2.1%和 2.1-2.6%。结果表明,该方法可作为一种非常强大、创新和有前途的环境和饮用水样品中 PEs 分析的样品制备技术。

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