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首页> 外文期刊>Journal of Chromatographic Science >Trace determination of dichlorvos in environmental samples by room temperature ionic liquid-based dispersive liquid-phase microextraction combined with HPLC
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Trace determination of dichlorvos in environmental samples by room temperature ionic liquid-based dispersive liquid-phase microextraction combined with HPLC

机译:室温离子液体基分散液相微萃取-HPLC法测定环境样品中的敌敌畏

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Using 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM] [PF6]) room temperature ionic liquid (RTIL) as extraction solvent, tetrahydrofuran (THF) as disperser solvent, the organophosphorus pesticide dichlorvos in water was determined by dispersive liquid- liquid microextraction (DLLME) combined with high-performance liquid chromatography. Factors affecting RTIL-DLLME (type of disperser solvent, amount of RTIL, volume of disperser solvent, percentage of NaCl and volume and pH of water sample) were optimized by the single-factor method, obtaining the most favorable results when using 65 μL of [BMIM][PF6] and 260 μL of THF to extract the compound from an 8-mL water sample at pH 5.0 containing 25% (w/v) of NaCl. Under these optimum conditions, an enrichment factor of 215-fold was obtained. The calibration curves were linear in the concentration range of 2-1,000 μg/L. The limit of detection calculated at a signal-to-noise ratio of 3 was 0.2 μg/L. The relative standard deviations (RSD) for six replicate experiments at 20, 100 and 200 μg/L concentration levels were 1.8%, 1.3% and 1.3 %, respectively. Then the proposed method was applied to the analysis of three different water sample sources (tap, farm and rain water) and the relative recoveries and RSD of spiked water samples were 95.6-102.4% and 0.6-3.1%, respectively, at three different concentration levels of 20, 100 and 200 μg/L.
机译:使用六氟磷酸1-丁基-3-甲基咪唑鎓盐([BMIM] [PF6])室温离子液体(RTIL)作为萃取溶剂,四氢呋喃(THF)作为分散剂,通过分散液-液微萃取法测定水中的有机磷农药敌敌畏(DLLME)与高效液相色谱结合。通过单因素方法优化了影响RTIL-DLLME的因素(分散剂溶剂的类型,RTIL的量,分散剂溶剂的量,NaCl的百分比以及水样品的体积和pH值),当使用65μLHPLC时,可获得最佳结果[BMIM] [PF6]和260μLTHF从pH值为5.0的8毫升水样品中提取化合物,其中含有25%(w / v)的NaCl。在这些最佳条件下,获得了215倍的富集因子。校准曲线在2-1,000μg/ L的浓度范围内呈线性。以3的信噪比计算的检测极限为0.2μg/ L。六个重复实验在20、100和200μg/ L浓度水平下的相对标准偏差(RSD)分别为1.8%,1.3%和1.3%。然后将该方法用于三种不同水样源(自来水,农田水和雨水)的分析,加标水样在三种不同浓度下的相对回收率和RSD分别为95.6-102.4%和0.6-3.1%。浓度为20、100和200μg/ L。

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