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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Simultaneous derivatization and dispersive liquid-liquid microextraction of anilines in different samples followed by gas chromatography-flame ionization detection
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Simultaneous derivatization and dispersive liquid-liquid microextraction of anilines in different samples followed by gas chromatography-flame ionization detection

机译:苯胺同时衍生和分散液-液微萃取不同样品中的苯胺,然后进行气相色谱-火焰电离检测

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摘要

A new method based on simultaneous derivatization and dispersive liquid-liquid microextraction in one step is developed for determination of five anilines in different aqueous samples. In this method, acetonitrile containing microlitre-level of butylchloroformate was rapidly injected into aqueous sample by a syringe. After centrifugation of the cloudy solution, the fine droplets of the butylchloroformate containing the derivatized analytes were sedimented in the bottom of the conical test tube. Then, 0.5 μL of the settled phase was injected into gas chromatography-flame ionization detector. Under optimum conditions the enrichment factors, extraction recoveries and enhancement factors were high and ranged between 197 and 298, 47 and 69%, and 4.7and 6.2, respectively. Linearity was observed in the range of 10-10,000 μg L ~(-1) (except for 4-chloroaniline), and the relative standard deviations (RSD %) were lower than 5.2% (n=6). The limits of detection of the six anilines ranged from 1 to 3 μg L ~(-1). Different aqueous samples including tap, river and well waters as well as wastewaters were successfully analyzed. In this method the extraction solvent and derivatization agent are the same and the derivatization reaction was carried out under mild conditions. This method has several advantages over other reported techniques, being very simple, rapid and less hazardous for the environment.
机译:建立了一种基于同时衍生化和液-液微分散分散的新方法,用于测定不同含水样品中的五种苯胺。在这种方法中,用注射器将含有微升水平的氯甲酸丁酯的乙腈快速注入水性样品中。将浑浊的溶液离心后,含有衍生化的分析物的氯甲酸丁酯的细小液滴沉积在锥形试管的底部。然后,将0.5μL的沉淀相注入气相色谱-火焰电离检测器中。在最佳条件下,富集因子,提取回收率和增强因子较高,分别介于197和298、47%和69%,4.7和6.2之间。在10-10,000μgL〜(-1)范围内观察到线性(4-氯苯胺除外),相对标准偏差(RSD%)小于5.2%(n = 6)。六种苯胺的检出限为1-3μgL〜(-1)。成功分析了不同的水样,包括自来水,河水,井水以及废水。在该方法中,萃取溶剂和衍生剂相同,并且衍生反应在温和的条件下进行。与其他已报道的技术相比,此方法具有多个优点,非常简单,快速且对环境的危害较小。

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