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微波消解-基体改进剂GFAAS法测定食品中铬
引用本文:冯银凤,周日东,黄诚,吴惠刚,欧阳珮珮,陈秀惠.微波消解-基体改进剂GFAAS法测定食品中铬[J].中国热带医学,2008,8(12):2243-2244.
作者姓名:冯银凤  周日东  黄诚  吴惠刚  欧阳珮珮  陈秀惠
作者单位:中山市疾病预防控制中心,广东,中山,528403
摘    要:目的建立微波消解一石墨炉原子吸收法测定食品中铬的分析方法。方法样品经微波消解,以磷酸铵溶液、硝酸+抗坏血酸作混合基体改进剂。样品经稀释后利用仪器全自动进样系统,采用石墨炉原子吸收法测定食品中铬的含量。结果选定了最佳测量条件,该方法的灵敏度、精密度均能满足检测工作的需求。本法铬的含量0-15.0μg/L范围内呈线性关系,线性相关系数大于0.998,本法检出限为0.16μg/L。相对标准偏差为1.9%-2.6%,加标回收率为92.8%~103.8%。结论本法简便、快速、灵敏度和精密度高。适用于食品中铬含量的测定。

关 键 词:微波消解  石墨炉原子吸收法  混合基体改进剂  食品中铬

Determination of Chromiun in food by microwave dissolution and GFAAS
Affiliation:FENG Yin-feng, ZHOU Ri-dong, HUANG Cheng,et al. (Zhongshan Munipical Center for Disease Control and Prevention, Zhongshan 528403, Guangdong, P. R. China)
Abstract:Objective To determine the chromium in food by microwave dissolution and graphite furnace atomic absorption spectroscopy. Methods The samples were digested by close-vessel microwave dissolution system. (NHg)3PO4, HNO3,L-Ascorbic acid were used as the matrix modifier to reduce the interference, Results The range of calibration curve was 0-15.0 Ixg/L and the correlation coefficient was over 0.998. The detection limit was 0.16}xg/L, the relative standard deviation 1.9%~2.6% and recovery 92.8%- 103.8%. Conclusions This method is simple, rapid and the analytical results meet the demands of accuracy and precision.
Keywords:GFAAS  Matrix modifier  Chromium in food
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