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多壁碳纳米管固相萃取/气相色谱-质谱测定蔬菜中的苯醚甲环唑农药残留
引用本文:张彦军,洪霞,周鑫魁,柴宗龙,王杰斌,袁彩霞,贾亚莉,钱滢文.多壁碳纳米管固相萃取/气相色谱-质谱测定蔬菜中的苯醚甲环唑农药残留[J].食品工业科技,2018,39(8):210-214.
作者姓名:张彦军  洪霞  周鑫魁  柴宗龙  王杰斌  袁彩霞  贾亚莉  钱滢文
作者单位:1. 甘肃省商业科技研究所有限公司, 甘肃兰州 730010;2. 甘肃中商食品质量检验检测有限公司, 甘肃兰州 730010
基金项目:丝绸之路经济带食品质量安全检验检测技术创新合作研究与平台建设(17ZD2WA003)甘肃省公共安全检验检测服务平台(食品行业方向)中国-马来西亚科技交流合作(1604WKCA001)甘肃省动物源性制品安全分析与检测技术重点实验室(1309RTSA025)甘肃-青海食品研究开发与检测联合实验室建设(1606RTSA337)兰白试验区食品安全检验检测技术服务平台。中国马来西亚清真食品及相关产业国际创新合作(1504WKCA094)清真食品检验检测科技服务平台能力建设(1605JTCA011)
摘    要:以多壁碳纳米管(MWCNTs)为固相萃取材料,建立了蔬菜中苯醚甲环唑农药残留的气相色谱-质谱联用(GC-MS)分析方法。样品经乙酸乙酯匀浆提取后,以MWCNTs固相萃取柱净化,用GC-MS进行检测。研究了不同提取溶剂和MWCNTs的量对提取净化效率的影响。结果表明:在最优实验条件下,苯醚甲环唑在0.005~2.0 μg/mL范围内呈良好的线性关系,相关系数为0.9997,检出限为0.001 mg/kg,空白蔬菜样品在0.01、0.10、1.00 μg/mL 3个加标水平下的回收率在84.2%~111.3%之间,相对标准偏差(n=5)为5.3%~11.9%。该方法灵敏度高,选择性好,抗干扰能力强,适合蔬菜中苯醚甲环唑残留量的定性确证分析和定量分析。

关 键 词:多壁碳纳米管    固相萃取    气相色谱-质谱    苯醚甲环唑    蔬菜
收稿时间:2017-09-14

Determination of difenoconazole in vegetables samples by gas chromatography-mass spectrometry using multi-walled carbon nanotubes as solid-phase extraction sorbent
ZHANG Yan-jun,HONG Xia,ZHOU Xin-kui,CHAI Zong-long,WANG Jie-bin,YUAN Cai-xia,JIA Ya-li,QIAN Ying-wen.Determination of difenoconazole in vegetables samples by gas chromatography-mass spectrometry using multi-walled carbon nanotubes as solid-phase extraction sorbent[J].Science and Technology of Food Industry,2018,39(8):210-214.
Authors:ZHANG Yan-jun  HONG Xia  ZHOU Xin-kui  CHAI Zong-long  WANG Jie-bin  YUAN Cai-xia  JIA Ya-li  QIAN Ying-wen
Affiliation:1. Gansu Institute of Business and Technology Co., Ltd., Lanzhou 730010, China;2. Gansu Zhongshang Food Quality Test and Detection Co., Ltd., Lanzhou 730010, China
Abstract:A method based on multiwalled carbon nanotubes(MWCNTs)as the solid phase extraction material had been developed for the determination of difenoconazole in vegetables by gas chromatography-mass spectrometry(GC-MS).The samples were extracted with ethyl acetate,purified by MWCNTs solid phase extraction;and determined by GC-MS. Effects of different extraction solvents and amount of MWCNTs on the determination of difenoconazole were investigated. The results showed that difenoconazole had a good linearity in the range of 0.005~2.0 μg/mL and the correlation was 0.9997 under the optimal conditions. The limit of detection for difenoconazole was 0.001 mg/kg. Tests of recoveries were made by the addition to blank vegetable sample at three spiked levels of 0.01,0.10 and 1.00 μg/mL,and the recoveries were in the range of 84.2%~111.3% with relative standard deviations(RSD,n=5)of 5.3%~11.9%. Therefore,the developed method is suitable for determination of difenoconazole in vegetables qualitatively and quantitatively with satisfactory sensitivity,selectivity,accuracy and precision.
Keywords:
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