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微波消解-原子荧光光谱法测定不同种类中药材中的痕量汞

[Determination of trace mercury in different sorts of Chinese herbs by atomic fluorescence spectrometry with microwave digestion].

作者信息

Liu Chun-Tao, Hou Hai-Ge, Yang Jing-Lin, Li Li, Li Han-Hui

机构信息

School of Chemistry, Chemical Engineering and Materials Science, Heilongjiang University, Harbin 150080, China.

出版信息

Guang Pu Xue Yu Guang Pu Fen Xi. 2009 Nov;29(11):3144-6.

Abstract

A method for the determination of trace mercury in different sorts of Chinese herbs using hydride generation atomic fluorescence spectrometry under different microwave digestion conditions was developed. Under the optimized experimental conditions, the linear equation was I(F) = 809.1 x -3.327 5, the correlation coefficient was 0.999 998,and the linear range for mercury was 0-80 ng x mL(-1). The detection limit of mercury was 0.014 ng x mL(-1) (n = 11) and the relative standard deviation was 2.03%. The recoveries for these samples were 96.8%-102.80% (n = 6) while the detection limit of the method was 1.17 ng x g(-1). The method's accuracy and precision for different sorts of Chinese herbs using the standard reference standard substance of rice (GBW08508), poplar leaf (GBW07601), and mytilus edulis (GBW08571) was checked, and the results were found to be basically consistent with the reference values. This method has been proved to be sensitive, simple and rapid with satisfactory results.

摘要

建立了一种在不同微波消解条件下,采用氢化物发生原子荧光光谱法测定不同种类中草药中痕量汞的方法。在优化的实验条件下,线性方程为I(F)=809.1x - 3.3275,相关系数为0.999998,汞的线性范围为0 - 80 ng·mL⁻¹。汞的检出限为0.014 ng·mL⁻¹(n = 11),相对标准偏差为2.03%。这些样品的回收率为96.8% - 102.80%(n = 6),该方法的检出限为1.17 ng·g⁻¹。采用大米(GBW08508)、杨树叶(GBW07601)和贻贝(GBW08571)标准参考物质对该方法测定不同种类中草药的准确性和精密度进行了检验,结果发现与参考值基本一致。该方法具有灵敏度高、操作简单快速、结果令人满意等优点。

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