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基于溶胶-凝胶的氨基功能化固相微萃取纤维与高效液相色谱联用,结合柱后光化学诱导荧光衍生化法对水样中的拟除虫菊酯类杀虫剂进行荧光检测。

Immersed sol-gel based amino-functionalized SPME fiber and HPLC combined with post-column photochemically induced fluorimetry derivatization and fluorescence detection of pyrethroid insecticides from water samples.

作者信息

Bagheri Habib, Ghanbarnejad Hadi, Khalilian Faezeh

机构信息

Environmental and Bio-Analytical Laboratories, Department of Chemistry, Sharif University of Technology, Tehran, Iran.

出版信息

J Sep Sci. 2009 Sep;32(17):2912-8. doi: 10.1002/jssc.200900044.

Abstract

A method based on direct immersion solid-phase microextraction (DI-SPME) coupled with high performance liquid chromatography combined with post-column photochemically induced fluorimetry derivatization and fluorescence detection (HPLC-PIF-FD) was developed to extract three pyrethroid insecticides, i.e. cyfluthrin, cypermethrin, and flumethrin from water samples. A sol-gel based coating fiber using 3-(trimethoxysilyl propyl) amine as precursor was prepared and used for the extraction of the pyrethroids from groundwater samples. A post-column photochemical reactor was designed and constructed for the derivatization of these environmentally important pollutants to increase their fluorescence sensitivity and determination in HPLC. The parameters affecting extraction process (extraction time and temperature, pH, salt addition, and co-solvent) and desorption step (solvent, desorption time, and temperature) of the analytes from the sol-gel-based fiber, along with photochemical reaction conditions were investigated. The developed method proved to be relatively rapid, simple, and easy and offers high sensitivity and reproducibility. Linear dynamic ranges (LDR) for these insecticides were ranged between 0.25 to 50 microg/L. The regression coefficients were satisfactory (R(2) > 0.984) for these pyrethroids. The limits of detection and limits of quantification varied between 0.09 and 0.35 microg/L and 0.25 and 1.00 microg/L, respectively. Relative standard deviation RSDs values varied between 4.41% and 6.20%. Relative recoveries obtained from analysis of Jajroud river water sample ranged between 94% and 104%.

摘要

建立了一种基于直接浸入式固相微萃取(DI-SPME)结合高效液相色谱,并采用柱后光化学诱导荧光衍生化和荧光检测(HPLC-PIF-FD)的方法,用于从水样中萃取三种拟除虫菊酯类杀虫剂,即氟氯氰菊酯、氯氰菊酯和氟甲菊酯。制备了一种以3-(三甲氧基甲硅烷基丙基)胺为前驱体的溶胶-凝胶涂层纤维,并用于从地下水样中萃取拟除虫菊酯。设计并构建了柱后光化学反应器,用于这些对环境有重要影响的污染物的衍生化,以提高其在高效液相色谱中的荧光灵敏度和测定能力。研究了影响分析物从溶胶-凝胶纤维中萃取过程(萃取时间和温度、pH值、加盐量和共溶剂)和解吸步骤(溶剂、解吸时间和温度)的参数,以及光化学反应条件。所建立的方法证明相对快速、简单且易于操作,具有高灵敏度和重现性。这些杀虫剂的线性动态范围(LDR)在0.25至50μg/L之间。这些拟除虫菊酯的回归系数令人满意(R²>0.984)。检测限和定量限分别在0.09至0.35μg/L和0.25至1.00μg/L之间变化。相对标准偏差(RSD)值在4.41%至6.20%之间变化。对贾鲁德河水样分析获得的相对回收率在94%至104%之间。

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