首页> 外文期刊>Analytical chemistry >Injection port derivatization following ion-pair hollow fiber-protected liquid-phase microextraction for determining acidic herbicides by gas chromatography/mass spectrometry
【24h】

Injection port derivatization following ion-pair hollow fiber-protected liquid-phase microextraction for determining acidic herbicides by gas chromatography/mass spectrometry

机译:离子对中空纤维保护液相微萃取后的进样口衍生化,用于气相色谱/质谱法测定酸性除草剂

获取原文
获取原文并翻译 | 示例
       

摘要

Injection port derivatization following ion-pair hollow fiber-protected liquid-phase microextraction (LPME) for the trace determination of acidic herbicides (2,4-dichlorobenzoic acid, 2,4-dichlorophenoxyacetic acid, 2-(2,4-dichlorophenoxy) propionic acid, 3,5-dichlorobenzoic acid, 2-(2,4,5-trichlorophenoxy) propionic acid) in aqueous samples by gas chromatography/mass spectrometry (GC/MS) was developed. Prior to GC injection port derivatization, acidic herbicides were converted into their ion-pair complexes with tetrabutylammonium chloride in aqueous samples and then extracted by 1-octanol impregnated in the hollow fiber. Upon injection, ion pairs of acidic herbicides were quantitatively derivatized to their butyl esters in the GC injection port. Thus, several parameters related to the derivatization process (i.e., injection temperature, purge-off time) were evaluated, and main parameters affecting the hollow fiber-protected LPME procedure such as extraction organic solvent, ion-pair reagent type, pH of aqueous medium, concentration of ion-pair reagent, sodium chloride concentration added to the aqueous medium, stirring speed, and extraction time profile, optimized. At the selected extraction and derivatization conditions, no matrix effects were observed. This method proved good repeatability (RSDs < 12.3%, n = 6) and good linearity (r(2) >= 0.9939) for spiked deionized water samples for five analytes. The limits of detection were in the range of 0.51-13.7 ng.L-1 (S/N = 3) under GC/MS selected ion monitoring mode. The results demonstrated that injection port derivatization following ion-pair hollow fiber-protected LPME was a simple, rapid, and accurate method for the determination of trace acidic herbicides from aqueous samples. In addition, this method proved to be environmentally friendly since it completely avoided open derivatization with potentially hazardous reagents.
机译:离子对中空纤维保护液相微萃取(LPME)后进样口衍生化,用于痕量测定酸性除草剂(2,4-二氯苯甲酸,2,4-二氯苯氧基乙酸,2-(2,4-二氯苯氧基)丙酸通过气相色谱/质谱(GC / MS)开发了水性样品中的乙酸,3,5-二氯苯甲酸,2-(2,4,5-三氯苯氧基)丙酸)。在GC进样口衍生化之前,将酸性除草剂与四丁基氯化铵在水溶液样品中转化为离子对络合物,然后通过浸渍在中空纤维中的1-辛醇萃取。进样后,酸性除草剂的离子对在GC进样口中被定量衍生为它们的丁酯。因此,评估了与衍生化过程相关的几个参数(例如,注入温度,吹扫时间),并且影响了中空纤维保护的LPME程序的主要参数,例如萃取有机溶剂,离子对试剂类型,水性介质的pH ,离子对试剂的浓度,添加到水性介质中的氯化钠浓度,搅拌速度和萃取时间曲线均已优化。在选定的提取和衍生条件下,未观察到基质效应。对于加标的去离子水样品中的五种分析物,此方法证明了良好的重复性(RSDs <12.3%,n = 6)和良好的线性度(r(2)> = 0.9939)。在GC / MS选择的离子监测模式下,检出限为0.51-13.7 ng.L-1(S / N = 3)。结果表明,离子对中空纤维保护的LPME之后的进样口衍生化方法是一种从含水样品中测定痕量酸性除草剂的简单,快速,准确的方法。此外,由于完全避免了潜在危险试剂的开放衍生,因此该方法被证明对环境无害。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号