史晓梅,陈士恒,章 晴,高丁,杨永坛.固相萃取-气相色谱法测定玉米中有机氯和 拟除虫菊酯农药残留量[J].食品安全质量检测学报,2015,6(4):1122-1127
固相萃取-气相色谱法测定玉米中有机氯和 拟除虫菊酯农药残留量
Simultaneous determination of organic chlorine and pyrethroid pesticides residues in corn by solid phase extraction-gas chromatography
投稿时间:2015-03-20  修订日期:2015-04-22
DOI:
中文关键词:  有机氯农药  拟除虫菊酯农药  固相萃取  气相色谱法  玉米
英文关键词:organic chlorine pesticides  pyrethroid pesticides  solid phase extraction  gas chromatography  corn
基金项目:
作者单位
史晓梅 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
陈士恒 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
章 晴 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
高丁 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
杨永坛 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
AuthorInstitution
SHI Xiao-Mei Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
CHEN Shi-Heng Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
ZHANG Qing Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
GAO Ding Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
YANG Yong-Tan Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
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中文摘要:
      目的 建立气相色谱-电子捕获检测器法(GC-ECD)测定玉米中16种有机氯和拟除虫菊酯农药残留量的方法。方法 玉米样品经乙腈超声提取后, 使用Florisil进行固相萃取净化, 样品经氮吹浓缩后, 使用气相色谱电子捕获检测器测定。结果 16种有机氯和拟除虫菊酯农药在0.01~0.5 mg/L浓度范围内呈现良好线性关系, R2大于0.99; 在0.02、0.05、0.2 mg/kg三个添加浓度上回收率范围为71.0%~103%, 相对标准偏差1.28%~8.74%, 检出限在0.1~16 μg/kg之间。结论 该方法前处理操作快速简单, 能够有效净化样品, 满足玉米中有机氯和拟除虫菊酯农药的日常检测和监管工作, 适用于大批次样品的定性定量分析。
英文摘要:
      Objective To develop a method for the simultaneous determination of organic chlorine and pyrethroid pesticides residues in corn by gas chromatography with ECD detector. Methods Corn samples were extracted with acetonitrile by ultra-sonic, and the extracts were purified by solid phase extraction using Florisil, then samples were detected by GC-ECD after concentrated by nitrogen flushing. Results The method showed a good linearity in the range of 0.01~0.5 mg/L for organic chlorine and pyrethroid pesticides with R2>0.99. The recoveries were in the range of 71.0%~103% at 3 spiked levels of 0.02, 0.05, and 0.2 mg/kg for organic chlorine and pyrethroid pesticides, and the relative standard deviations (RSDs) were 1.28%~8.74%. The limit of detection was in the range of 0.1~16 μg/kg. Conclusion The method is suitable for quantitative and qualitative determination of organic chlorine and pyrethroid pesticides residues in a large number of corn samples with a sample and fast pretreatment procedure. Meanwhile, samples can be effectively cleaned up, and it could meet the requirements of daily inspection and supervision work.
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