正丁醇萃取-原子荧光光谱法间接测定茶叶中的钼  

Indirect Determination of Molybdenum in Tea with N-butyl Alcohol Extraction by Atomic Fluorescence Spectrometry

作　　者：廖朝东[1] 耿国兴[2] 陆建平[2] 唐艳葵[2] 

机构地区：[1]广西卫生职业技术学院,南宁530004 [2]广西大学化学化工学院,南宁530021

出　　处：《分析化学》2012年第6期964-967,共4页Chinese Journal of Analytical Chemistry

基　　金：国家自然科学基金项目(No.51168001)资助

摘　　要：建立了正丁醇萃取原子荧光光谱法间接测定茶叶中钼的方法。基于As?和钼酸铵在0.3 mol/LH2SO4介质中能形成砷钼杂多酸,且形成的杂多酸可以被有效地萃取到有机溶剂中,原子荧光光谱法直接测定有机相中的砷,间接得到钼的含量。在优化的实验条件下,钼含量在0.09～15.0-g/L范围内呈良好的线性关系,方法的检出限是0.09-g/L,相对标准偏差为2.3%,据此对不同茶叶样品进行分析,加标回收率为95.2%～96.9%。本方法对茶叶中Mo的检测结果与电感耦合等离子体原子发射光谱法相符合。An analytical method for indirect determination of molybdenum in tea sample is established using atomic fluorescence spectrometry（AFS）.Based upon the heteropoly arsenomolybdic acid,formed between As and ammonium molybdate in 0.3 mol/L of sulfuric acid and extractable perfectly by n-butyl alcohol,measuring the arsenic in organic phase,in term of the stoichiometric relationship between arsenic and molybdenum,the concentration of molybdenum can be measured.Under the optimized condition,the results show that the linearity between the concentration of molybdenum and its fluorescence intensity is 0.09-15.0 μg/L,the limit of detection is 0.09 μg/L,and the relative standard deviation is 2.3%.The method has been applied to the determination of molybdenum in tea samples with the recoveries of 95.2%-96.9%.The method was validated by inductively coupled plasma atomic emission spectrometry（ICP-AES）,and the analytical results were in good.

关 键 词：钼 砷 茶叶 原子荧光光谱 正丁醇 

分 类 号：O657.31[理学—分析化学]