陈啟荣,杨 明,梁 颖,朱琳娜,邵 鹏,范筱京.多壁碳纳米管固相萃取净化-气相色谱质谱联用 同时测定茶叶中26种农药[J].食品安全质量检测学报,2016,7(4):1686-1693
多壁碳纳米管固相萃取净化-气相色谱质谱联用 同时测定茶叶中26种农药
Determination of 26 pesticides in tea by gas chromatography-mass spectro-metry with multi-walled carbon nanotubes as solid-phase
投稿时间:2016-01-14  修订日期:2016-02-25
DOI:
中文关键词:  多壁碳纳米管  茶叶  农药残留  气相色谱质谱联用法
英文关键词:multi-walled carbon nanotubes  tea  pesticides  gas-chromatography-mass spectrometry
基金项目:北京市财政科技创新工程项目(PXM 2013_178305_000004)
作者单位
陈啟荣 北京市理化分析测试中心, 北京市食品安全分析测试工程技术研究中心 
杨 明 北京市理化分析测试中心, 北京市食品安全分析测试工程技术研究中心 
梁 颖 北京市理化分析测试中心, 北京市食品安全分析测试工程技术研究中心 
朱琳娜 北京市理化分析测试中心, 北京市食品安全分析测试工程技术研究中心 
邵 鹏 北京市理化分析测试中心, 北京市食品安全分析测试工程技术研究中心 
范筱京 北京市理化分析测试中心, 北京市食品安全分析测试工程技术研究中心 
AuthorInstitution
CHEN Qi-Rong Beijing Center for Physical and Chemical Analysis, Beijing Engineering Research Center of Food Safety Analysis 
YANG Ming Beijing Center for Physical and Chemical Analysis, Beijing Engineering Research Center of Food Safety Analysis 
LIANG Ying Beijing Center for Physical and Chemical Analysis, Beijing Engineering Research Center of Food Safety Analysis 
ZHU Ling-Na Beijing Center for Physical and Chemical Analysis, Beijing Engineering Research Center of Food Safety Analysis 
SHAO Peng Beijing Center for Physical and Chemical Analysis, Beijing Engineering Research Center of Food Safety Analysis 
FAN Xiao-Jing Beijing Center for Physical and Chemical Analysis, Beijing Engineering Research Center of Food Safety Analysis 
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中文摘要:
      目的 建立一种多壁碳纳米管固相萃取净化-气相色谱质谱联用同时测定茶叶中26种农药的检测方法。方法 样品经乙腈提取, 过滤型多壁碳纳米管柱净化后, 使用气相色谱质谱仪检测。结果 碳纳米管净化能够有效去除茶叶中干扰物质, 简化实验步骤, 降低前处理过程中农药的分解。26种农药在0.04~1.6 μg/mL范围内具有较好的线性。方法的检出限为0.005~0.05 mg/kg, 定量下限为0.015~0.15 mg/kg。采用该方法对茶叶样品进行加标回收率实验, 加标回收率在66.6%~125.5%, 相对标准偏差为0.3%~6.4%(n=5)。结论 该方法快速、准确、灵敏, 适合茶叶中多种农药的同时测定。
英文摘要:
      Objective To determine 26 pesticides in tea by solid-phase extraction with multi-walled carbon nanotubes and gas chromatography-mass spectrometry (GC-MS). Methods The sample was extracted with acetonitrile. After purified by multi-walled carbon nanotubes, the sample solution was detected by GC-MS. Results The established method was simple, and could reduce the pesticides decomposition in pretreatment. The calibration curves of 26 pesticides were linear in the range of 0.04~1.6 μg/mL. The limits of detection for 26 pesticides in tea were in the range of 0.005~0.05 mg/kg, and their limits of quantitation were 0.015~0.15 mg/kg. The spiked recoveries of 26 pesticides in tea sample were between 66.6% and 125.5% with relative standard deviations of 0.3%~6.4% (n=5). Conclusion The proposed method is rapid, accurate and sensitive, which is suitable for simultaneous detection of multiple pesticides.
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