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Application of headspace liquid-phase microextraction using ionic liquid as extractant combined with gas chromatography-hydrogen flame ionization detector to the determination of BTEXs in water

机译:采用离子液体作为萃取剂与气相色谱 - 氢火焰电离检测器相结合的施用顶空液相微萃取在水中BTEX的测定

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This paper presents a new headspace-liquid-phase microextraction (HS-LPME) strategy for extraction and preconcentration of benzene, toluene, ethyl- benzene, and o-, m- and p-xylenes (BTEXs) from aqueous samples. A typical room temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM]PF_6), was used as extractant, and the extract was subsequently determined by gas chromatography-hydrogen flame ionization detection (GC-FID). Parameters such as ionic liquid volume, sampling temperature, extraction time, stirring rate and salt content, were found to have significant effects on the HS-LPME. The optimized experimental conditions for extraction of target compounds were: 4μL of [BMIM]PF_6, 20 min extraction time, a stirring rate of 800 rpm and 40% sodium nitrate (w/v) in a sample solution at temperature of 70 °C. The proposed method provided good recoveries in the range of 94.7~101.0%, and the related standard deviations (RSDs) (n=10) of 2.5~9.3%. The limits of detection (LODs) varied from 9.8 to 38.9 μg L~(-1) (S/N = 3) using GC-FID. This novel method was applied to the analysis of BTEXs in lake water and river water.
机译:本文介绍了来自含水样品的苯,甲苯,乙烯 - 苯和O-,M-和乙烯基(BTEX)的萃取和预浓缩的新的顶空 - 液相微萃取(HS-LPME)策略。使用典型的室温离子液体,1-丁基-3-甲基咪唑鎓六氟磷酸钡([BMIM] PF_6)作为萃取剂,随后通过气相色谱 - 氢火焰电离检测(GC-FID)测定提取物。发现诸如离子液体体积,取样温度,提取时间,搅拌速率和盐含量的参数对HS-LPME产生显着影响。用于萃取目标化合物的优化实验条件为:4μl[Bmim] pF_6,20分钟提取时间,在70℃的温度下在样品溶液中搅拌800rpm和40%硝酸钠(w / v)。该方法提供了良好的回收率在94.7〜101.0%的范围内,相关标准偏差(RSDS)(N = 10)为2.5〜9.3%。使用GC-FID,检测限度(LOD)的限制在9.8至38.9μg1〜(s / n = 3)中变化。这种新方法应用于湖水和河水中BTEX的分析。

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