首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Sample preparation procedure using extraction and derivatization of carboxylic acids from aqueous samples by means of deep eutectic solvents for gas chromatographic-mass spectrometric analysis
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Sample preparation procedure using extraction and derivatization of carboxylic acids from aqueous samples by means of deep eutectic solvents for gas chromatographic-mass spectrometric analysis

机译:通过深对立溶剂的气相色谱 - 质谱分析,使用来自含水样品的羧酸萃取和衍生羧酸的样品制备方法

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The paper presents a new procedure for the determination of organic acids in a complex aqueous matrix using ultrasound-assisted dispersive liquid-liquid microextraction followed by injection port derivatization and GC-MS analysis. A deep eutectic solvent (choline chloride: 4-methylphenol in a 1:2 mol ratio) was used both as an extracting solvent and as a derivatizing agent to yield ion pairs which were next converted to methyl esters of organic acids in a hot GC injection port. The procedure was optimized in terms of selection of a deep eutectic solvent, disperser solvent, and the ratio of their volumes, pH, salting out effect, extraction time, injection port temperature and time of opening the split valve. The developed procedure is characterized by low LOD (1.7-8.3 mu g/L) and LOQ(5.1-25 mu g/L) values, good repeatability (RSD ranging from 4.0 to 6.7%), good recoveries for most of the studied analyte (81.5-106%) and a wide linear range. The procedure was used for the determination of carboxylic acids in real effluents from the production of petroleum bitumens. A total of ten analytes at concentrations ranging from 0.33 to 43.3 mu g/mL were identified and determined in the effluents before and after chemical treatment. The study revealed that in effluents treated by hydrodynamic cavitation an increase in concentration of benzoic acid and related compounds was observed. (C) 2018 Elsevier B.V. All rights reserved.
机译:本文介绍用于有机酸在一个复杂的水性基质使用超声辅助分散液 - 液微确定一个新的程序,然后注射端口衍生化和GC-MS分析。深共晶溶剂(氯化胆碱:4-甲基苯酚以1:2摩尔比)既用作萃取溶剂和作为衍生剂以收率离子对,其被下转换为有机酸的甲基酯在热GC注射港口。该程序是在选择了深刻的共晶的溶剂,分散溶剂,和它们的体积的比例,pH值的条件进行了优化,盐析效应,提取时间,进样口温度和打开所述分割阀的时间。所开发的程序的特征在于低LOD(1.7-8.3亩克/升)和LOQ(5.1-25微米克/ L)的值,重复性好(RSD范围从4.0至6.7%),良好的回收率对于大多数所研究的分析物的(81.5-106%)和线性范围宽。步骤,用于在从生产石油沥青的真实流出物羧酸的确定。在浓度总共十个分析物范围从0.33至43.3微米克/毫升进行鉴定和化学处理之前和之后在流出物来确定。该研究显示,在水力空化处理的废水中观察到的增加苯甲酸和相关化合物的浓度。 (c)2018年elestvier b.v.保留所有权利。

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