首页 | 本学科首页   官方微博 | 高级检索  
     

气相色谱法同时检测丙炔氟草胺和精异丙甲草胺在绿豆中的残留
引用本文:晏姣,袁桂平,欧晓明,曾利红,梁贵平,胡军和,金晨钟.气相色谱法同时检测丙炔氟草胺和精异丙甲草胺在绿豆中的残留[J].农药,2021(4):282-284,305.
作者姓名:晏姣  袁桂平  欧晓明  曾利红  梁贵平  胡军和  金晨钟
作者单位:湖南化工研究院国家农药创制工程技术研究中心;湖南加法检测有限公司;中化现代农业(湖北)有限公司;湖南人文科技学院农药无害化应用重点实验室/湖南省农田杂草防控技术与应用协同创新中心
摘    要:目的]为了监测丙炔氟草胺和精异丙甲草胺在绿豆等农产品中的残留及环境安全性评价,采用气相色谱仪建立了同时检测绿豆中丙炔氟草胺和精异丙甲草胺残留量的方法。方法]样品中丙炔氟草胺和精异丙甲草胺残留先用二氯甲烷提取,再用二氯甲烷进行液-液分配,浓缩定容后用PSA和C-GCB净化,采用GC-ECD进行检测,色谱柱为DB-608。结果]在0.05~5.0 mg/L的质量浓度范围内,丙炔氟草胺和精异丙甲草胺的峰面积与质量浓度之间呈现出良好的线性关系;在添加质量分数为0.05~2.0 mg/kg时,丙炔氟草胺和精异丙甲草胺在绿豆中的添加回收率分别为90%~105%和80%~94%,相对标准偏差分别为1.1%~3.1%和0.6%~2.6%。该方法的最小检出量(LOD)均为0.05 ng,丙炔氟草胺和精异丙甲草胺在绿豆中的最低检测浓度(LOQ)均为0.05 mg/kg。结论]该方法具有灵敏度、精密度和准确度良好,杂质干扰少等特点,符合农药残留检测分析的基本要求。

关 键 词:丙炔氟草胺  精异丙甲草胺  残留  气相色谱  绿豆

Simultaneous Determination of Flumioxazin and S-Metolachlor Residues in Mung Beans by Gas Chromatography with ECD
YAN Jiao,YUAN Gui-ping,OU Xiao-ming,ZENG Li-hong,LIANG Gui-ping,HU Jun-he,JIN Chen-zhong.Simultaneous Determination of Flumioxazin and S-Metolachlor Residues in Mung Beans by Gas Chromatography with ECD[J].Pesticides,2021(4):282-284,305.
Authors:YAN Jiao  YUAN Gui-ping  OU Xiao-ming  ZENG Li-hong  LIANG Gui-ping  HU Jun-he  JIN Chen-zhong
Affiliation:(National Engineering Center for Agrochemicals,Hunan Research Institute of Chemical Industry,Changsha 410014,China;Hunan J&F Test Co.,Ltd.,Changsha 410014,China;Sinochem Modem Agricultural(Hubei)Co.,Ltd.,Wuhan 430000,China;Key Laboratory of Pesticide Harmless Application/Hunan Provincial Collaborative Innovation Center for Field Weeds Control,Hunan University of Humanities,Science and Technology,Loudi 417000,Hunan,China)
Abstract:Aims]This study aims to establish an analytical method for simultaneous determination of flumioxazin and S-metolachlor residue in mung beans by using gas chromatography with electronic capture detector(GC-ECD)to monitor the residues of flumioxazin and S-metolachlor in mung beans and other agricultural products and the environmental safety assessment.Methods]The flumioxazin and S-metolachlor residues in mung bean samples were extracted with dichloromethane,and cleaned-up through liquid-liquid partition.The concentrated solutions were purified by PSA and C-GCB before analysis.The analysis was performed on a DB-608 steel column.Results]The results showed that there were in good linearity between the concentrations of flumioxazin and S-metolachlor and their corresponding response values within the concentration of 0.05-5.0 mg/L.When the spiked level ranged from 0.05 to 2.0 mg/kg,the average spiked recoveries of flumioxazin and S-metolachlor in mung beans were 90-105 and 80-94%,respectively,with their corresponding relative standard deviation(RSD)of 1.1-3.1 and 0.6-2.6%,respectively.The limit of detection(LOD)of the method were 0.05 ng,and the limit of quantification(LOQ)of flumioxazin and S-metolachlor in mung beans samples were 0.05 mg/kg.Conclusions]The method was proved to meet the basic requirements of pesticide residue analysis on sensitivity,accuracy and precision,and to be suitable for analysis of flumioxazin and S-metolachlor residues in the environmental matrix such as mung beans.
Keywords:flumioxazin  S-metolachlor  residue  GC-ECD  mung beans
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号