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茶叶中多菌灵和甲萘威农药残留量的测定

Determination the Residue of Carbendazim and Carbaryl in Tea

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【作者】 张雪波上官良敏

【Author】 ZHANG Xue-bo1,2,SHANGGUAN Liang-min1(1.National Tea Quality Supervision and inspection Center(Fujian),Anxi 362400,Fujian,China)(2.Key Laboratory of Tea Biochemistry & Biotechnology,Anhui Agricultural University,Hefei 230036,Anhui,China)

【机构】 国家茶叶质量监督检验中心(福建)安徽农业大学农业部教育部茶叶生物化学与生物技术重点实验室

【摘要】 采用高效液相色谱法测定茶叶中多菌灵和甲萘威农药残留。通过乙腈提取凝胶渗透色谱净化(GPC)和在线浓缩方式预处理;样品检测条件:色谱柱为WatersC18柱(3.0×250mm,5μm),采用乙腈和水为流动相进行梯度洗脱,柱温30℃,流速0.5mL/min,PDA检测器,检测波长为285.2nm和220.3nm,进样量5μL。回收率为84.5%~103.2%;RSD为3.2%~4.5%;多菌灵的农药检测限为0.1μg/mL、甲萘威的农药检测限为0.03μg/mL。

【Abstract】 To determine the residues of carbofuran and carbaryl in tea by GPC-HPLC.The sample was extracted by acetonit ester,purified by gel permeation chromatography(GPC),separated with Waters C18 column(3.0 mm×250 mm×5 μm),water and acetonit rile as mobile phase with gradient elution at column temperature of 30,and a flow rate of 0.5 mL/min,detected with PDA detector,and the wavelength was 285.2 nm and 220.3 nm,and the inpouring was 5μL.The recoveries were 84.5 %~103.2 %,corresponding RSDs were 3.2 %~4.5 % and the detection limit of carbofuran was 0.1μg/mL、the detection limit of carbaryl was 0.03μg/mL

【关键词】 多菌灵甲萘威茶叶凝胶渗透色谱高效液相色谱
【Key words】 CarbendazimCarbarylTeaGPCHPLC
  • 【文献出处】 质量技术监督研究 ,Quality and Technical Supervision Research , 编辑部邮箱 ,2009年02期
  • 【分类号】S481.8
  • 【被引频次】6
  • 【下载频次】199
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