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固相萃取-气相色谱法测定植物性食品中恶草酮残留量方法研究 被引量:3

Determination of oxadiazon residues in plant food by solid-phase extraction-gas chromatography
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摘要 目的:建立固相萃取一气相色谱法测定植物性食品中恶草酮的方法。方法:采用硅镁吸附剂预处理小柱进行净化,气相色谱电子捕获检测器进行食品中恶草酮残留量测定分析,对前处理和仪器条件进行试验研究。结果:方法的检出限为0.005mg/kg,添加回收率为88.0%-95.0%,相对标准偏差为4.25%-8.21%。结论:该方法的建立具有操作简便、准确、灵敏度高的特点,适合于植物性食品中恶草酮残留量的测定。 Objective:A analysis method was developed for the determination of oxadiazon residues in plant food by solid phase extraction - gas chromatography. Methods: Cleane - up by florisil SPE cartridge and determination of oxacliazon residues in plant food by electron capture detection. Results:The detection limit of the method was 0. 005 mg/kg. The recovery of the method ranged from 88.0% to 95.0%. The relative standard deviation was between 4. 25% and 8.21%. Conclusion:This method is simple,accurate and sensitive and reliable to determine oxadiazon residues in plant food.
出处 《中国卫生检验杂志》 CAS 2007年第9期1626-1626,1633,共2页 Chinese Journal of Health Laboratory Technology
关键词 固相萃取 气相色谱法 植物性食品 恶草酮 残留量 Solid - phase extraction Gas chromatography Plant food Oxadiazon Residues
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参考文献4

  • 1农业部农药检定所.新编农药手册[M].北京:农业出版社,1998,569-572.
  • 2GB2763-2005.食品中农药最大残留量[S].
  • 3Guy R Lambert, William T Padgett, Michal H Veouge Quantitative analysis of alachlor protein adducts by gas chromatography-mass spectrometry [J]. Analy Biochem,1999,268(2):289-296.
  • 4《食品分析大全》编写组.食品分析大全[M].北京:高等教育出版社,1997,685-687.

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