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于兆水, 张勤, 刘玲. 氢化物发生-原子荧光光谱法测定土壤中水溶态砷(Ⅲ)和砷(Ⅴ)[J]. 岩矿测试, 2012, 31(5): 838-841.
引用本文: 于兆水, 张勤, 刘玲. 氢化物发生-原子荧光光谱法测定土壤中水溶态砷(Ⅲ)和砷(Ⅴ)[J]. 岩矿测试, 2012, 31(5): 838-841.
YU Zhao-shui, ZHANG Qin, LIU Ling. Determination of Water Soluble As(Ⅲ) and As(Ⅴ) in Soil by Hydride Generation-Atomic Fluorescence Spectrometry[J]. Rock and Mineral Analysis, 2012, 31(5): 838-841.
Citation: YU Zhao-shui, ZHANG Qin, LIU Ling. Determination of Water Soluble As(Ⅲ) and As(Ⅴ) in Soil by Hydride Generation-Atomic Fluorescence Spectrometry[J]. Rock and Mineral Analysis, 2012, 31(5): 838-841.

氢化物发生-原子荧光光谱法测定土壤中水溶态砷(Ⅲ)和砷(Ⅴ)

Determination of Water Soluble As(Ⅲ) and As(Ⅴ) in Soil by Hydride Generation-Atomic Fluorescence Spectrometry

  • 摘要: 以氢气发生器为氩-氢火焰提供纯净、稳定的氢气,原子荧光光谱法测定土壤中水溶态和可交换态Sb(Ⅲ)和Sb(Ⅴ)已有应用,本研究进一步将此方法用于测定土壤样品中的As(Ⅲ)和As(Ⅴ)。在0.3 mol/L NaH2PO4-Na2HPO4缓冲液中,采用氢化物发生-原子荧光光谱法测定土壤中水溶态As(Ⅲ)和总砷的含量,通过差减法计算As(Ⅴ)的含量。实验考察了0.02~0.4 mol/L NaH2PO4-Na2HPO4对As(Ⅲ)和As(Ⅴ)测定的影响,结果表明0.3 mol/L NaH2PO4-Na2HPO4可以有效掩蔽As(Ⅴ)。As(Ⅲ)的检出限为2.92 ng/g,总砷的检出限为2.35 ng/g;As(Ⅲ)和As(Ⅴ)的加标回收率分别为96%~104%和101%~103%。本方法不再依靠化学反应产生氢气来点燃并维持氩氢火焰,可在发生氢化反应的任何介质中测定砷,且不需要考虑酸度问题。方法操作简便,准确度高,能满足大批量样品分析要求。

     

    Abstract: Based on the determination method of Sb(Ⅲ) and Sb(Ⅴ) in soil, a method for the determination of water soluble As(Ⅲ) and total arsenic in soil has been established by using Hydride Generation-Atomic Fluorescence Spectrometry (HG-AFS) in the media of 0.3 mol/L NaH2PO4-Na2HPO4. An amount of As(Ⅴ) was obtained by subtracting As(Ⅲ) from total arsenic. The hydrogen was provided from a hydrogen generator instead of chemical reaction to ignite a H2-Ar flame. Therefore, arsenic in any media was measurable since the arsenic was reduced into AsH3. Effects on the determination of As(Ⅲ) and As(Ⅴ) were investigated for concentrations of NaH2PO4-Na2HPO4 from 0.02 mol/L to 0.4 mol/L. The results show As(Ⅴ) can be screened by 0.3 mol/L NaH2PO4-Na2HPO4. The detection limits were 2.92 ng/g for As(Ⅲ) and 2.35 ng/g for total As. The recoveries of As(Ⅲ) and As(Ⅴ) are 96%-104% and 101%-103%, respectively. The method was simple and highly accurate, meeting the requirements for multiple sample analysis.

     

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