蒋励, 殷忠. 电感耦合等离子体质谱法测定水中砷的方法改进[J]. 环境卫生学杂志, 2013, 3(4): 369-372.
    引用本文: 蒋励, 殷忠. 电感耦合等离子体质谱法测定水中砷的方法改进[J]. 环境卫生学杂志, 2013, 3(4): 369-372.
    Jiang Li, Yin Zhong. Improvement of Method on Arsenic Monitoring in Water conducted by Inductively Coupled Plasma Mass Spectrometry[J]. Journal of Environmental Hygiene, 2013, 3(4): 369-372.
    Citation: Jiang Li, Yin Zhong. Improvement of Method on Arsenic Monitoring in Water conducted by Inductively Coupled Plasma Mass Spectrometry[J]. Journal of Environmental Hygiene, 2013, 3(4): 369-372.

    电感耦合等离子体质谱法测定水中砷的方法改进

    Improvement of Method on Arsenic Monitoring in Water conducted by Inductively Coupled Plasma Mass Spectrometry

    • 摘要:
      目的 对电感耦合等离子体质谱法测定水中砷存在的影响因素进行改进, 为水中砷的准确定量提供新方法。
      方法 样品直接用碰撞反应池电感耦合等离子体质谱仪(ICP-MS)进行测定分析。用钇(89Y)内标校正基体干扰和漂移, 用高性能Xs接口降低非质谱干扰, 用碰撞反应池技术(CRCT模式)消除质谱干扰。
      结果 方法的标准曲线最佳线性范围:0~20 μg/L, 相关系数为0.9999。方法检出限0.064 μg/L, 最低检出浓度为0.19 μg/L, 相对标准偏差1.4%~4.0%, 回收率为95.7%~104.0%。分析2个标准参考物质, 结果在标准范围内。
      结论 此方法检出限低、简便、快速、准确, 能用于水中砷的准确测定。

       

      Abstract:
      Objectives To improve the influencing factors of inductively coupled plasma mass spectrometry method for the determination of arsenic in water and to provide a new method for accurate quantitative analysis of arsenic in water.
      Methods Samples were directly determined by inductively coupled plasma mass spectrometry based on collided reaction cell technology.Internal standard element of Yttrium (89Y) was used to correct matrix interference and signal drifting; high-performance Xs interface was used to reduce non-mass spectrum interferences, and collided reaction cell technology (CCT mode) was used to eliminate mass spectrum interferences.
      Results The optimal linear range of the standard curve for this method was 0~20 μg/L with a correlation coefficient of 0.9999.The detection limit of the method was 0.064 μg/L; the lowest quantitative limit was 0.19 μg/L; the relative standard deviation was 1.4%~4.0% and the recovery rate was 95.7%~104.0%. The detection results of two standard reference materials were satisfactory.
      Conclusions The detection limit of the method was low; and the method was simple, fast, accurate, and suitable for accurate quantitative analysis of arsenic in water.

       

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