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原子荧光光谱法测定刺五加不同部位中砷、锑、汞和硒的含量

[Determination of arsenic, antimony, mercury and selenium in different parts of Acanthopanax senticosus harms by atomic fluorescence spectrometry].

作者信息

Liu Chun-Tao, Hou Hai-Ge, Fan Nai-Ying, Li Han-Hui

机构信息

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

出版信息

Guang Pu Xue Yu Guang Pu Fen Xi. 2010 Apr;30(4):1123-5.

Abstract

A method for the determination of arsenic, antimony, mercury and selenium in different parts (root, stem, leaf and fruit) of acanthopanax senticosus harms using hydride generation atomic fluorescence spectrometry with microwave digestion was developed. Under the optimized experimental conditions, the concentration of arsenic, antimony, mercury and selenium showed a linear relationship with the fluorescence intensity. The detection limit of arsenic was 0.068 ng x mL(-1), and the RSD was 1.05%. The detection limit of antimony was 0.155 ng x mL(-1), and the RSD was 1.32%. The detection limit of mercury was 0.014 ng x mL(-1), and the RSD was 2.03%. The detection limit of selenium was 0.052 ng x mL(-1), and the RSD was 2.34%. The method was checked in terms of accuracy and precision using the standard reference substance of hair (GBW07601), and proved to be sensitive and rapid with satisfactory results. The content of arsenic, mercury and selenium is high in the leaf, and that of antimony is higher in the root than in other parts.

摘要

建立了一种采用微波消解-氢化物发生原子荧光光谱法测定刺五加不同部位(根、茎、叶和果实)中砷、锑、汞和硒的方法。在优化的实验条件下,砷、锑、汞和硒的浓度与荧光强度呈线性关系。砷的检出限为0.068 ng·mL⁻¹,相对标准偏差为1.05%。锑的检出限为0.155 ng·mL⁻¹,相对标准偏差为1.32%。汞的检出限为0.014 ng·mL⁻¹,相对标准偏差为2.03%。硒的检出限为0.052 ng·mL⁻¹,相对标准偏差为2.34%。采用头发标准物质(GBW07601)对该方法的准确性和精密度进行了检验,结果表明该方法灵敏、快速,结果令人满意。叶中砷、汞和硒的含量较高,根中锑的含量高于其他部位。

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