Suppr超能文献

用于在线管内固相微萃取的不锈钢管内纳米结构聚苯胺 - 聚吡咯复合涂层的电镀

Electroplating of nanostructured polyaniline-polypyrrole composite coating in a stainless-steel tube for on-line in-tube solid phase microextraction.

作者信息

Asiabi Hamid, Yamini Yadollah, Seidi Shahram, Esrafili Ali, Rezaei Fatemeh

机构信息

Department of Chemistry, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Iran.

Department of Chemistry, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Iran.

出版信息

J Chromatogr A. 2015 Jun 5;1397:19-26. doi: 10.1016/j.chroma.2015.04.015. Epub 2015 Apr 11.

Abstract

In this work, a novel and efficient on-line in-tube solid phase microextraction method followed by high performance liquid chromatography was developed for preconcentration and determination of trace amounts of parabens. A nanostructured polyaniline-polypyrrole composite was electrochemically deposited on the inner surface of a stainless steel tube and used as the extraction phase. Several important factors that influence the extraction efficiency, including type of solid-phase coating, extraction and desorption times, flow rates of the sample solution and eluent, pH, and ionic strength of the sample solution were investigated and optimized. Under the optimal conditions, the limits of detection were in the range of 0.02-0.04 μg L(-1). This method showed good linearity for parabens in the range of 0.07-50 μg L(-1), with coefficients of determination better than 0.998. The intra- and inter-assay precisions (RSD%, n=3) were in the range of 5.9-7.0% and 4.4-5.7% at three concentration levels of 2, 10, and 20 μg L(-1), respectively. The extraction recovery values for the spiked samples were in the acceptable range of 80.3-90.2%. The validated method was successfully applied for analysis of methyl-, ethyl-, and propyl parabens in some water, milk, and juice samples.

摘要

在本研究中,开发了一种新型高效的在线管内固相微萃取方法,随后结合高效液相色谱用于痕量对羟基苯甲酸酯的预富集和测定。一种纳米结构的聚苯胺 - 聚吡咯复合材料通过电化学沉积在不锈钢管的内表面,并用作萃取相。研究并优化了几个影响萃取效率的重要因素,包括固相涂层类型、萃取和解吸时间、样品溶液和洗脱液的流速、pH值以及样品溶液的离子强度。在最佳条件下,检测限在0.02 - 0.04 μg L(-1)范围内。该方法在0.07 - 50 μg L(-1)范围内对对羟基苯甲酸酯具有良好的线性,测定系数优于0.998。在2、10和20 μg L(-1)三个浓度水平下,批内和批间精密度(RSD%,n = 3)分别在5.9 - 7.0%和4.4 - 5.7%范围内。加标样品的萃取回收率在80.3 - 90.2%的可接受范围内。该经过验证的方法成功应用于一些水、牛奶和果汁样品中甲基、乙基和丙基对羟基苯甲酸酯的分析。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验