康彩艳, 蒋治良, 蒋若舟, 莫琪. 光化学氧化甲基紫2.5次微分极谱法间接测定痕量铁[J]. 分析测试技术与仪器, 1996, (4): 20-23.
引用本文: 康彩艳, 蒋治良, 蒋若舟, 莫琪. 光化学氧化甲基紫2.5次微分极谱法间接测定痕量铁[J]. 分析测试技术与仪器, 1996, (4): 20-23.
Kang Caiyan, Jiang Zhiliang, Jiang Ruozhou, Mo Qi. Indirect Differential Polarographic Determination of Trace Iron[J]. Analysis and Testing Technology and Instruments, 1996, (4): 20-23.
Citation: Kang Caiyan, Jiang Zhiliang, Jiang Ruozhou, Mo Qi. Indirect Differential Polarographic Determination of Trace Iron[J]. Analysis and Testing Technology and Instruments, 1996, (4): 20-23.

光化学氧化甲基紫2.5次微分极谱法间接测定痕量铁

Indirect Differential Polarographic Determination of Trace Iron

  • 摘要: 在稀硫酸介质中及活化剂草酸存在条件下,痕量铁(Ⅲ)对甲基紫光化学褪色慢反应有强烈催化作用,甲基紫的光化学产物于-0.70V处产生一个2.5次微分极谱波.以该产物作指示组分,采用2.5次微分极谱检测技术,研究了利用此体系测定铁的影响因素,建立了一个检出限和测定范围分别为3μg/L和6~300μg/L铁的光化学分析新方法,并用于茶叶分析.

     

    Abstract: Fe(Ⅲ) has strong effect on the photocatalytic oxidation of methyl violet in dilute sulfuric acid medium. The irradiation source was an UV lamp, and oxalic acid was used as the activator. The photochemicl oxidation product of methyl violet exhibits a 2.5 order differential palarographic wave at -0.70V vs. SCE. So this ware was chosen as an indicator for the oxidation reaction. On this ground, a novel photochemical-voltammetric method for the indirect determination of 6~300 μg/L Fe in tea samples was established. The detection limit was 3 μ g/L Fe.

     

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