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作 者:叶江雷[1] 弓振斌[1] 林芳[2] 金贵娥[2] 温裕云[2]
机构地区:[1]近海海洋环境科学国家重点实验室(厦门大学) [2]厦门大学海洋与环境学院,福建厦门361005
出 处:《厦门大学学报(自然科学版)》2007年第3期441-444,共4页Journal of Xiamen University:Natural Science
基 金:福建省自然科学基金重点项目(B2200001)资助
摘 要:建立了茶叶中4种有机磷农药——水胺硫磷、亚胺硫磷、甲基对硫磷和伏杀硫磷残留的高效液相色谱测定方法.在45℃加温条件下用乙酸乙酯-正己烷(1:1,by vol.)混合溶剂提取待测目标物、活性炭层析柱净化,用10.0mL乙酸乙酯-正己烷(6:1,by vol.)淋洗待测组分,以Eclipse XDB-Cs色谱柱、乙腈-水混合液梯度洗脱分离、二极管阵列检测器测定.结果表明,上述4种农药在6.5min内能很好地分离;样品中添加的待测组分能定量回收,回收率89.0%~108.0%,相对标准偏差为1.89%~5.96%(1.0μg/mL,n=5),检出限分别为:水胺硫磷9.82μg/kg、亚胺硫磷7.88pg/kg、甲基对硫磷2.19pg/kg、伏杀硫磷0.72pg/kg(dm).A method has been developed for quantitative determination of isocarbophos, phosemet,methyl-parathion,and phosalone residues in tea samples. The pesticide residues were extracted from tea samples with mixture of ethyl acetate and n-hexane (1 : 1, by vol. ) at 45℃. The extracts were then treated with a cartridge packed with active carbon and 10 mL eluant of ethyl acetate and n-hex- ane (6 : 1). The 4 organophosphorus pesticides were separated with Eclipse XDB-C8 column and detected with diode array detector at programmed wavelength. The recoveries for added standard were 89.0%- 108.0 %. The relative standard deviations were 1.89 % - 5.96% (1.0 μg/mL, n=5). The limits of quantitative determination (3a) in dry tea samples were 9.82,7.88,2. 19 and 0.72 pg/kg for isocarbophos, phosemet, methyl-parathion and phosalone, respectively.
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