色谱

• 技术与应用 • 上一篇    

气相色谱法测定水产品中残留的呋喃丹

王淼 1,2,李荣2,邹世平2   

  1. 1.College of Fisheries, Huazhong Agricultural University, Wuhan 430070, China; 2.Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Jingzhou 434000, China
  • 收稿日期:2008-04-16 修回日期:2008-07-16 出版日期:2008-11-30 发布日期:1983-06-25
  • 通讯作者: 邹世平
  • 基金资助:

Determination of carbofuran residue in aquatic products by gas chromatography

WANG Miao1,2, LI Rong2, ZOU Shiping2   

  1. 1.College of Fisheries, Huazhong Agricultural University, Wuhan 430070, China; 2.Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Jingzhou 434000, China
  • Received:2008-04-16 Revised:2008-07-16 Online:2008-11-30 Published:1983-06-25
  • Contact: ZOU Shiping

摘要: 以草鱼(Ctenopharyngodon idellus)、南美白对虾(Penaens vannamei)为实验材料,建立了水产品中呋喃丹残留量的气相色谱测定方法。样品经乙腈提取,正己烷去脂肪,Al2O3柱净化后进样分析。本方法线性范围为0.1~10.0 mg/L,相关系数r ≥0.9995;当呋喃丹的加标水平在0.02~1.0 mg/kg时,其回收率为78%~90%,相对标准偏差为2.49%~9.59%;方法的检出限为0.02 mg/kg。

关键词: 残留量, 呋喃丹, 气相色谱, 水产品

Abstract: A capillary gas chromatographic (GC) method was developed for the determination of carbofuran residue in aquatic products (Ctenopharyngodon idellus and Penaens vannamei). The sample was extracted with acetonitrile, defatted by hexane, re-extracted by acetoacetate and cleaned up with a Al2O3 column, and then determined by GC. The standard curve was linear in the investigated range of 0.1-10.0 mg/L. The correlation coefficients were more than 0.9995, the recoveries were 78%-90% with the relative standard deviations of 2.49%-9.59%at the spiking levels of 0.02-10.0 mg/kg. The detection limit of carbofuran was 0.02 mg/kg.

Key words: aquatic products , carbofuran, residue, gas chromatography (GC)