纺织学报 ›› 2014, Vol. 35 ›› Issue (9): 100-0.

• 染整与化学品 • 上一篇    下一篇

棉花中7种烟碱类农药残留的液相色谱-串联质谱法测定

  

  1. 浙江出入境检验检疫局检验检疫技术中心
  • 收稿日期:2013-09-02 修回日期:2014-04-18 出版日期:2014-09-15 发布日期:2014-09-16
  • 通讯作者: 谢文 E-mail:xw@ziq.gov.cn
  • 基金资助:

    棉花中不同种类农药残留检测技术研究;进出口棉花中农残检测及国际贸易技术壁垒应对体系研究

Determination of Seven Neonicotinoid Pesticides Residues in Cotton samples by Using High Performance Liquid Chromatography Tandem Mass Spectrometry

  • Received:2013-09-02 Revised:2014-04-18 Online:2014-09-15 Published:2014-09-16

摘要: 介绍了应用液相色谱-电喷雾电离三级四极杆质谱(LC-ESI-MS/MS)方法测定棉花中烯啶虫胺、呋虫胺、噻虫嗪、噻虫胺、吡虫啉、啶虫咪和噻虫啉烟碱类农药残留。前处理方法包括添加同位素内标吡虫啉-D4,乙腈提取。该方法采用正离子方式,多反应监测,每种烟碱类杀虫剂各两对离子进行定性、定量分析。方法在0~12.5 ug/L范围内具有良好的线性关系。在10、20和40 ug/kg三个添加水平,平均回收率范围为75.9-98.4%;相对标准偏差小于15.8%;方法检测低限(LOQ)均为10 ug/kg。本方法简便、快速、准确,各项技术指标满足国内外法规的要求,可用于棉花样品中烟碱类农药残留的确证检测。

Abstract: A method for the determination of nitenpyram, dinotefuran, thiamethoxam, clothiandin, imidacloprid, acetamiprid and thiacloprid in cotton samples has been introducted. The isotope internal standard (imidcacloprid-D4) was added into the sample solutions. The sample was extracted with acetonitrile. The ionisation mode used was positive mode with multiple reaction monitoring. The one precursor/two product ion transitions for each neonicotinoids were used. The results show that the working curves were linear in the range of 0~12.5 ug/L. The recoveries were between 75.9-98.4% and the relative standard deviations were less 15.8% at the spiked levels of 10, 20 and 40 ug/kg. The limits of quantitation were 10 ug/kg. The method is simple, rapid, and accurate, and its performance can meet the requirements of the domestic and international legislation. The method adapts to confirm residues of neonicotinoid pesticides in cotton samples.

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