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疏水性离子液体反胶束电膜技术提取环境水中的四环素

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建立了一种基于1-丁基-3-甲基咪唑双三氟甲磺酰亚胺盐([Bmim][NTf2])和1-癸基-3-甲基咪唑双三氟甲磺酰亚胺盐([C10mim][NTf2])的疏水离子液体反胶束电膜提取(IL-RM-EME)样品前处理方法,用于环境水样中四环素(TC)的检测.支撑液膜(SLM)种类、膜孔径、电压、供相和受相溶液pH值和含盐量等对四环素的提取效率均有较大的影响,单因素条件优化结果显示,在不添加盐条件下,使用[Bmim][NTf2]离子液体SLM、PC膜孔径为5μm、电压为30 V、供相pH=2.5以及受相pH=7.5时,IL-RM-EME对TC的提取率最高,达到77.8%,远高于中性(吐温85-异丙醇-正己烷)反胶束电膜体系(41.4%).与传统的样品前处理方法相比,本方法具有操作简单、环境污染小、试剂消耗少和费用低等优势,在环境有机污染物检测中具有良好的应用前景.
Electromembrane Extraction of Tetracycline in Environmental Water Using Hydrophobic Ionic Liquid Reverse Micelle
A hydrophobic ionic liquid reverse micelle electromembrane extraction (IL-RM-EME) method based on 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([Bmim][NTf2]) and 1-decyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C10mim][NTf2]) was developed for pretreatment of tetracycline (TC) in environmental water samples in this work. The experimental results indicated that the type of supported liquid membrane (SLM),membrane pore size,voltage,pH of donor/acceptor phase solution and salt content had great influences on the extraction efficiency of tetracycline. Under the optimal conditions of single factors,including using[Bmim][NTf2]ionic liquid SLM components,PC membrane with pore size of 5μm,30 V of voltage,donor phase at pH 2.5,acceptor phase at pH 7.5,and none salt added,the best extraction efficiency of IL-RM-EME to TC of 77.8% was obtained. This extraction efficiency was much higher than that of neutral (Tween 85-isopropyl alcohol-n-hexane) reverse micelle membrane system (41.4%). Compared with traditional sample pretreatment method,the proposed method had many advantages such as simple operation,less environmental pollution,less reagent consumption and low cost. Moreover,the proposed method showed a good application prospect in detection of environmental organic pollutants.

Ionic liquidReverse micellesElectromembrane extractionTetracycline

费家裕、陈小锋、王孟歌、李明

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扬州大学环境科学与工程学院,扬州225127

离子液体 反胶束 电膜提取 四环素

2024

分析化学
中国化学会 中国科学院长春应用化学研究所

分析化学

CSTPCD北大核心
影响因子:1.423
ISSN:0253-3820
年,卷(期):2024.52(11)