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中国精品科技期刊2020
李杨梅, 杨敏, 谭伟, 杨宏兴, 高斯祺, 李桂镇, 王红斌. 多壁碳纳米管固相萃取-气相色谱法检测蔬菜中毒死蜱、丙溴磷和三唑磷农药残留[J]. 食品工业科技, 2014, (19): 316-320. DOI: 10.13386/j.issn1002-0306.2014.19.060
引用本文: 李杨梅, 杨敏, 谭伟, 杨宏兴, 高斯祺, 李桂镇, 王红斌. 多壁碳纳米管固相萃取-气相色谱法检测蔬菜中毒死蜱、丙溴磷和三唑磷农药残留[J]. 食品工业科技, 2014, (19): 316-320. DOI: 10.13386/j.issn1002-0306.2014.19.060
LI Yang-mei, YANG Min, TAN Wei, YANG Hong-xing, GAO Si-qi, LI Gui-zhen, WANG Hong-bin. Determination of chlorpyrifos, triazophos and profenofos in vegetables by gas chromatography with solid phase extraction using multiwalled carbon nanotubes as adsorbent[J]. Science and Technology of Food Industry, 2014, (19): 316-320. DOI: 10.13386/j.issn1002-0306.2014.19.060
Citation: LI Yang-mei, YANG Min, TAN Wei, YANG Hong-xing, GAO Si-qi, LI Gui-zhen, WANG Hong-bin. Determination of chlorpyrifos, triazophos and profenofos in vegetables by gas chromatography with solid phase extraction using multiwalled carbon nanotubes as adsorbent[J]. Science and Technology of Food Industry, 2014, (19): 316-320. DOI: 10.13386/j.issn1002-0306.2014.19.060

多壁碳纳米管固相萃取-气相色谱法检测蔬菜中毒死蜱、丙溴磷和三唑磷农药残留

Determination of chlorpyrifos, triazophos and profenofos in vegetables by gas chromatography with solid phase extraction using multiwalled carbon nanotubes as adsorbent

  • 摘要: 本文以多壁碳纳米管为固相萃取材料,建立了蔬菜中毒死蜱、丙溴磷和三唑磷农药残留的GC-FPD分析方法。样品经乙酸乙酯匀浆提取后,用多壁碳纳米管SPE柱净化,以丙酮∶正己烷(1∶1,v/v)为洗脱剂,浓缩后用丙酮定容,再用GC-FPD进行检测。三种有机磷农药在0.00252.0mg/L范围内呈良好的线性关系,相关系数在0.99980.9999之间,回收率在83.3%96.7%之间,方法的检出限在8.21×10-41.37×10-3mg/kg之间。将该方法推广到莴苣、番茄、豇豆、梨、香菇等9种蔬菜、水果和食用菌中毒死蜱、丙溴磷、三唑磷农药残留的测定,效果较好。 

     

    Abstract: A method based on multiwalled carbon nanotubes as the solid phase extraction material had been developed for the determination of chlorpyrifos, triazophos and profenofos in vegetables by gas chromatographyflame photometric detector ( GC /FPD) .The samples were extracted with ethyl acetate and purified by multiwalled carbon nanotubes column.The eluent was a mixture of acetone∶hexane ( 1∶1, v /v) .Then concentrated and dissolved by acetone before determined by GC /FPD.The results showed that these pesticides had a good linearity in the range of 0.0025~2.0mg /L and the correlations were between 0.9998 and 0.9999.The recoveries rate and limits of detection were 83.3% ~ 96.7% and 8.21 × 10- 4~ 1.37 × 10- 3mg /kg. Application of the method to the analysis of chlorpyrifos, triazophos and profenofos in several samples, we had a satisfactory result.

     

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