Suppr超能文献

采用分散液液微萃取-浮动有机液滴固化高效液相色谱法测定环境水样中的有机磷农药。

Determination of organophosphorus pesticides in environmental water samples by dispersive liquid-liquid microextraction with solidification of floating organic droplet followed by high-performance liquid chromatography.

机构信息

Key Laboratory of Bioinorganic Chemistry, College of Sciences, Agricultural University of Hebei, Baoding 071001, China.

出版信息

Anal Bioanal Chem. 2010 Jul;397(6):2543-9. doi: 10.1007/s00216-010-3790-9. Epub 2010 May 28.

Abstract

A simple dispersive liquid-liquid microextraction based on solidification of floating organic droplet coupled with high-performance liquid chromatography-diode array detection was developed for the determination of five organophosphorus pesticides (OPs) in water samples. In this method, the extraction solvent used is of low density, low toxicity, and proper melting point near room temperature. The extractant droplet could be collected easily by solidifying it in the lower temperature. Some important experimental parameters that affect the extraction efficiencies were optimized. Under the optimum conditions, the calibration curve was linear in the concentration range from 1 to 200 ng mL(-1) for the five OPs (triazophos, parathion, diazinon, phoxim, and parathion-methyl), with the correlation coefficients (r) varying from 0.9991 to 0.9998. High enrichment factors were achieved ranging from 215 to 557. The limits of detection were in the range between 0.1 and 0.3 ng mL(-1). The recoveries of the target analytes from water samples at spiking levels of 5.0 and 50.0 ng mL(-1) were 82.2-98.8% and 83.6-104.0%, respectively. The relative standard deviations fell in the range of 4.4% to 6.3%. The method was suitable for the determination of the OPs in real water samples.

摘要

建立了一种基于悬浮液滴固化分散液相微萃取结合高效液相色谱-二极管阵列检测法用于水样中 5 种有机磷农药(OPs)的测定方法。该方法使用的萃取溶剂密度低、毒性低、熔点接近室温。通过将萃取剂固化在低温下,可以很容易地收集萃取剂液滴。优化了一些影响萃取效率的重要实验参数。在最佳条件下,5 种 OPs(三唑磷、对硫磷、二嗪农、辛硫磷和甲基对硫磷)的浓度范围为 1-200ngmL(-1)时,校准曲线呈线性,相关系数(r)在 0.9991-0.9998 之间。获得了 215-557 的高富集因子。检测限在 0.1-0.3ngmL(-1)之间。目标分析物在 5.0 和 50.0ngmL(-1)加标水平下从水样中的回收率为 82.2-98.8%和 83.6-104.0%,相对标准偏差在 4.4%-6.3%之间。该方法适用于实际水样中 OPs 的测定。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验