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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Optimization of derivatization procedure and gas chromatography-mass spectrometry method for determination of bensulfuron-methyl herbicide residues in water
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Optimization of derivatization procedure and gas chromatography-mass spectrometry method for determination of bensulfuron-methyl herbicide residues in water

机译:衍生化方法的优化和气相色谱-质谱法测定水中苯磺隆-甲基除草剂的残留量

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摘要

A simple and efficient technique based on liquid phase extraction with CH2Cl2 solvent followed by derivatization with (C2H5)(2)O center dot BF3 solution and confirmation analysis with GC-MS analytical method was developed for detecting the bensulfuron-methyl (BSM) residues in water. Box-Behnken response surface methodology was employed for optimization of the derivatization efficiency. According to the optimization model, the derivatization time of 45 min, derivatization temperature at 55 degrees C and 0.2 mL (C2H5)(2)O center dot BF3 solvent were selected as the optimal derivatization condition for obtaining the maximum desirability of response. Method validation was performed at 6 working standard levels (0.05, 0.1, 0.2, 0.5, 1.0, 5.0 mu g/mL) and the linearity of the calibration curve was linear well over the 6 fortification levels with the squared correlation coefficient of determination r(2) = 0.998 and the LOD was found to be 0.1 mu g/L for BSM herbicide. The mean value of BSM was detected from 0.0414 to 4.7542 mu g/mL at levels from 0.05 to 5 mu g/mL with the recoveries remained at the acceptable level (42.8-95.0%) with the RSD values from 3.5% to 6.2%, which is more accptable and desirable than the results obtained by LC methods. Moreover, the method allowed the determination of BSM residue in real paddy field water samples at concentrations between 0.0902 and 3.4605 mu g/L. Average recovery rates of the BSM spiked at levels 0.1, 0.2, 0.5, 1.0 mu g/mL into thirty water samples ranged from 74.1% and 94.1% with the relative standard derivation (RSD) values from 1.9% to 6.7%. (C) 2015 Elsevier B.V. All rights reserved.
机译:开发了一种简单高效的技术,该方法基于用CH2Cl2溶剂进行液相萃取,然后用(C2H5)(2)O中心点BF3溶液进行衍生化,并使用GC-MS分析方法进行确认分析,以检测苯并磺隆中的甲基(BSM)残留物。水。采用Box-Behnken响应面方法优化衍生化效率。根据优化模型,选择45分钟的衍生时间,55摄氏度的衍生温度和0.2 mL(C2H5)(2)O中心点BF3溶剂作为最佳衍生条件,以获得最大的响应期望。方法验证是在6个工作标准水平(0.05、0.1、0.2、0.5、1.0、5.0μg / mL)下进行的,并且校准曲线的线性在6个设防水平上均呈线性关系,相关系数为r( 2)= 0.998,发现BSM除草剂的LOD为0.1μg / L。在0.05至5μg / mL的水平下检测到BSM的平均值为0.0414至4.7542μg / mL,回收率保持在可接受的水平(42.8-95.0%),RSD值从3.5%至6.2%,这比LC方法获得的结果更易于接受和期望。此外,该方法还可以测定实际稻田水样中BSM残留量,浓度在0.0902至3.4605μg / L之间。在30个水样中,BSM的平均回收率分别为0.1、0.2、0.5、1.0μg / mL,分别为74.1%和94.1%,相对标准偏差(RSD)值为1.9%至6.7%。 (C)2015 Elsevier B.V.保留所有权利。

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