Suppr超能文献

使用在线固相萃取熔融核柱色谱法测定水样中氨基甲酸酯类和拟除虫菊酯类杀虫剂的新方法。

New method for the determination of carbamate and pyrethroid insecticides in water samples using on-line SPE fused core column chromatography.

作者信息

Fernández-Ramos C, Satínský D, Solich P

机构信息

Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, Heyrovského1203, 500 05 Hradec Králové, Czech Republic.

Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, Heyrovského1203, 500 05 Hradec Králové, Czech Republic.

出版信息

Talanta. 2014 Nov;129:579-85. doi: 10.1016/j.talanta.2014.06.037. Epub 2014 Jun 26.

Abstract

A new HPLC column-switching method using large volume sample injection and fused-core columns for on-line solid phase extraction have been developed for the determination of the following carbamates and pyrethroids: aldicarb, carbaryl, pirimicarb, carbofuran, kadethrin, flumethrin, fenpropathrin, fenoxycarb, tau-fluvalinate and fenvalerate, in surface water samples. Sudan I was used as internal standard. The proposed method was performed using 100 µl sample injection followed by an on-line solid phase extraction procedure and finally the compounds were identified and quantified by liquid chromatography with ultraviolet detection. The separation was carried out on C-18 reversed phase column based on fused-core particle technology. The influence of the injected sample volume, the variables affecting to SPE process and the conditions for the separation on an analytical column, were studied and optimized. The limits of detection ranged from 5.5 to 8.9 µg L(-1), and limits of quantification from 18.4 to 29.7 µg L(-1), while inter- and intra-day variability was under 15%. This new analytical procedure was satisfactorily applied for the determination of these organic pollutants in surface water samples located in Czech Republic. Concentration levels were found for some of these pollutants up to 26.11 µg L(-1) in the river Elbe and up to 34.53 µg L(-1) in the closed lakes samples.

摘要

已开发出一种新的高效液相色谱柱切换方法,该方法使用大体积进样和熔核柱进行在线固相萃取,用于测定地表水样中的以下氨基甲酸酯类和拟除虫菊酯类化合物:涕灭威、西维因、抗蚜威、克百威、甲氰菊酯、氟氯氰菊酯、甲氰菊酯、苯氧威、氟胺氰菊酯和氰戊菊酯。苏丹红I用作内标。该方法采用100 μl进样,随后进行在线固相萃取程序,最后通过带紫外检测的液相色谱对化合物进行鉴定和定量。分离在基于熔核颗粒技术的C-18反相柱上进行。研究并优化了进样体积、影响固相萃取过程的变量以及分析柱上的分离条件。检测限范围为5.5至8.9 μg L⁻¹,定量限范围为18.4至29.7 μg L⁻¹,日间和日内变异系数均低于15%。这种新的分析方法成功应用于捷克共和国地表水样中这些有机污染物的测定。在易北河中发现这些污染物中的一些浓度水平高达26.11 μg L⁻¹,在封闭湖泊水样中高达34.53 μg L⁻¹。

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