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首页> 外文期刊>Chromatographia >Fast analysis of synthetic pyrethroid metabolites in water samples using in-syringe derivatization coupled hollow fiber mediated liquid phase microextraction with GC-ECD
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Fast analysis of synthetic pyrethroid metabolites in water samples using in-syringe derivatization coupled hollow fiber mediated liquid phase microextraction with GC-ECD

机译:注射器中衍生化中空纤维介导的液相微萃取-GC-ECD快速分析水样中的拟除虫菊酯代谢物

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摘要

A fast and efficient method has been demonstrated for the trace determination of six important metabolites of synthetic pyrethroids including cis- and trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylic acid (cis- and trans-Cl_2CA), cis-3-(2,2-dibromovinyl)-2,2- dimethylcyclopropane-1-carboxylic acid (cis-Br_2CA), 4-fluoro-3-phenoxybenzoic acid (4-F-3-PBA), 3-phenoxybenzoic acid (3-PBA), and 2-phenoxybenzoic acid (2-PBA) in environmental water samples using hollow fiber (HF)-mediated liquid-phase microextraction (LPME) coupled with in-syringe derivatization (ISD) followed by gas chromatography (GC) with electron capture detector (ECD) analysis. This method utilizes a HF membrane segment impregnated with extraction solvent as the LPME sampling probe, which was connected to a microsyringe pre-filled with derivatizing agents, and it was immersed into sample solution for extraction. After extraction, the extracting solution was subjected to derivatization reaction that was performed inside the syringe barrel followed by GC-ECD analysis. Under optimal conditions, the best extraction efficiency was obtained using sampling probe (2.0 cm hollow fiber) impregnated with 1-octanol immersed into water sample (5.0 mL, adjusted pH below 1.0) and stirring (1,250 rpm) for 10 min at 70 C and diisopropylcarbodiimide (2 μL) and 1,1,1,3,3,3-hexafluoro-2-propanol (1 μL) were the derivatizing agents used. The detection limits of 3 ng mL~(-1) for cis- and trans-Cl_2CA, 2 ng mL~(-1) for cis-Br_2CA, 6 ng mL~(-1) for 4-F-3-PBA, and 0.6 ng mL~(-1) for 3-PBA and 2-PBA. The method showed good linearity (R ~2 = 0.973-0.998), repeatability from 4.0 to 13 % (n = 5), recovery from 79.2 to 95.7 %, and enrichment factors ranged between 109 and 159 for target analytes spiked in water samples. The proposed method and conventional methods were compared. Results suggested that the proposed HF-LPME-ISD/GC-ECD method was a rapid, simple, inexpensive, and eco-friendly technique for the analysis of metabolites of pyrethroids.
机译:已经证明了一种快速有效的方法来痕量测定合成拟除虫菊酯的六种重要代谢物,包括顺式和反式-3-(2,2-二氯乙烯基)-2,2-二甲基环丙烷-1-羧酸(顺式和反式) -Cl_2CA),顺式-3-(2,2-二溴乙烯基)-2,2-二甲基环丙烷-1-甲酸(cis-Br_2CA),4-氟-3-苯氧基苯甲酸(4-F-3-PBA),使用空心纤维(HF)介导的液相微萃取(LPME)与注射器内衍生化(ISD)结合进行环境水样品中的3-苯氧基苯甲酸(3-PBA)和2-苯氧基苯甲酸(2-PBA)气相色谱(GC)和电子捕获检测器(ECD)分析。该方法利用浸有萃取溶剂的HF膜片段作为LPME采样探针,将其连接到预先填充有衍生剂的微注射器上,然后浸入样品溶液中进行萃取。提取后,对提取液进行在注射器筒内进行的衍生化反应,然后进行GC-ECD分析。在最佳条件下,使用浸有1-辛醇的采样探针(2.0厘米中空纤维)浸渍在水样品(5.0毫升,pH值调节至1.0以下)中并在70℃下搅拌(1,250 rpm)10分钟,可获得最佳萃取效率。二异丙基碳二亚胺(2μL)和1,1,1,3,3,3-六氟-2-丙醇(1μL)是使用的衍生剂。顺式和反式Cl_2CA的检出限为3 ng mL〜(-1),顺式Br_2CA的检出限为2 ng mL〜(-1),4-F-3-PBA的检出限为6 ng mL〜(-1), 3-PBA和2-PBA的浓度为0.6 ng mL〜(-1)。该方法显示出良好的线性(R〜2 = 0.973-0.998),可重复性从4.0%增至13%(n = 5),回收率从79.2%增至95.7%,对于水样中加标的目标分析物,富集系数在109至159之间。比较了所提出的方法和常规方法。结果表明,所提出的HF-LPME-ISD / GC-ECD方法是一种快速,简便,廉价且环保的技术,可用于分析拟除虫菊酯的代谢物。

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