首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development of a liquid chromatography tandem mass spectrometry method for trace analysis of trisiloxane surfactants in the aqueous environment: An alternative strategy for quantification of ethoxylated surfactants
【24h】

Development of a liquid chromatography tandem mass spectrometry method for trace analysis of trisiloxane surfactants in the aqueous environment: An alternative strategy for quantification of ethoxylated surfactants

机译:液相色谱串联质谱法在水环境中痕量分析三硅氧烷表面活性剂的开发:乙氧基化表面活性剂定量的另一种策略

获取原文
获取原文并翻译 | 示例
       

摘要

Trisiloxane surfactants, often referred to as superspreaders or superwetters, are added to pesticides to enhance the activity and the rainfastness of the active substance by promoting rapid spreading over hydrophobic surfaces. To fill the lack of data on the environmental occurrence of these compounds, we have developed and validated a method for their trace analysis in the aqueous environment. The method is based on liquid-liquid extraction followed by liquid chromatography and tandem mass spectrometry. The oligomeric distribution of trisiloxane surfactant in a reference solution was determined by a theoretical calculation and by experimental measurements. Based on these results, the quantification was performed by comparison with a calibration made with a single homologue instead of a mixture of homologues. This approach avoids a time-consuming synthesis of pure homologues and reduces the risk of wrong estimation of the concentration because of different response factors of the sample and the standard. Such an approach could be applied to the quantification of other ethoxylated surfactants following a similar distribution. The validation was performed from 2 to 250. ng/L (total surfactant concentration) in deionized water, tap water, and river water (Rhine water). Knowing the oligomeric distribution of the polymer in the reference solution, the corresponding calibration ranges were estimated for individual homologues. Limits of quantification were found to be between 0.37. ng/L and 15. ng/L. The total recovery of sample preparation was between 77% and 116%. Matrix effects were lower than 10% with river water and the relative standard deviation evaluated over ten identical samples of spiked river water was below 12%.
机译:将三硅氧烷表面活性剂(通常称为超级分散剂或超级润湿剂)添加到农药中,以促进在疏水性表面上的快速扩散,从而提高活性物质的活性和耐雨性。为了弥补有关这些化合物在环境中发生的数据的不足,我们开发并验证了在水性环境中进行痕量分析的方法。该方法基于液-液萃取,然后进行液相色谱和串联质谱分析。通过理论计算和实验测量确定参考溶液中三硅氧烷表面活性剂的低聚物分布。基于这些结果,通过与使用单个同源物而不是同源物混合物进行的校准进行比较来进行定量。这种方法避免了耗时的纯同系物合成,并降低了由于样品和标准品的响应因子不同而导致浓度估计错误的风险。可以将这种方法应用于遵循相似分布的其他乙氧基化表面活性剂的定量分析。验证是在去离子水,自来水和河水(莱茵水)中以2至250. ng / L(总表面活性剂浓度)进行的。知道参考溶液中聚合物的低聚物分布,就可以估算出各个同系物的相应校准范围。发现定量限在0.37之间。 ng / L和15 ng / L。样品制备的总回收率在77%至116%之间。对于河水,基体效应低于10%,对十个相同的加标河水样品评估的相对标准偏差低于12%。

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