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Simultaneous conduction of two- and three-phase hollow-fiber-based liquid-phase microextraction for the determination of aromatic amines in environmental water samples

机译:同时进行两相和三相中空纤维液相微萃取测定环境水样中的芳香胺

摘要

This paper describes a simultaneously performed two-/three-phase hollow-fiber-based liquid-phase microextraction (HF-LPME) method for the determination of aromatic amines with a wide range of pK(a) (-4.25 to 4.6) and log K(ow) (0.9-2.8) values in environmental water samples. Analytes including aniline, 4-nitroaniline, 2,4-dinitroaniline and dicloran were extracted from basic aqueous samples (donor phase, DP) into the microliter volume of organic membrane phase impregnated into the pores of the polypropylene hollow fiber wall, then back extracted into the acidified aqueous solution (acceptor phase, AP) filling in the lumen of the hollow fiber. The mass transfer of the analytes from the donor phase through the organic membrane phase into acceptor phase was driven by both the counter-coupled transport of hydrogen ions and the pH gradient. Afterwards, the hollow fiber was eluted with 50 mu L methanol to capture the analytes from both the organic membrane and the acceptor phase. Factors relevant to the enrichment factors (EFs) were investigated. Under the optimized condition (DP: 100 mL of 0.1 M NaOH with 2 M Na(2)SO(4); organic phase: di-n-hexyl with 8% trioctylphosphine oxide (TOPO); AP: 10 mu L of 8 M HCl; extraction time of 80 min), the obtained EFs were 405-2000, dynamic linear ranges were 5-200 mu g/L (R > 0.9976). and limits of detection were 0.5-1.5 mu g/L. The presence of humic acid (0-25 mg/L dissolved organic carbon) had no significant effect on the extraction efficiency. The proposed procedure worked very well for real environmental water samples with microgram per liter level of analytes, and good spike recoveries (80-103%) were obtained. (C) 2008 Elsevier B.V. All rights reserved.
机译:本文介绍了同时进行的两相/三相中空纤维液相微萃取(HF-LPME)方法,用于测定范围广泛的pK(a)(-4.25至4.6)和log的芳香胺环境水样品中的K(ow)(0.9-2.8)值。从碱性含水样品(供体相,DP)中提取包括苯胺,4-硝基苯胺,2,4-二硝基苯胺和双氯仑在内的分析物,注入微升体积的有机膜相中,该有机膜相浸入聚丙烯中空纤维壁的孔中,然后反萃取至酸化的水溶液(受体相,AP)填充在中空纤维的内腔中。分析物从供体相通过有机膜相到受体相的质量转移是由氢离子的反向耦合传输和pH梯度共同驱动的。然后,将中空纤维用50μL甲醇洗脱,以从有机膜和受体相中捕获分析物。研究了与富集因子(EFs)相关的因子。在优化条件下(DP:100 mL的0.1 M NaOH和2 M Na(2)SO(4);有机相:二正己基和8%的三辛基氧化膦(TOPO); AP:10μL的8 M HCl;提取时间80分钟),得到的EF为405-2000,动态线性范围为5-200μg / L(R> 0.9976)。检出限为0.5-1.5μg/ L。腐殖酸(0-25 mg / L溶解的有机碳)的存在对萃取效率没有显着影响。所提出的方法对于实际环境水样品(每克分析物微克每升水平)非常有效,并获得了良好的加标回收率(80-103%)。 (C)2008 Elsevier B.V.保留所有权利。

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