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The pH Dependence of the Oxidation Reaction of SO_2 at a Platinum Electrode Studied by Voltammetric and In Situ Infrared Spectroscopic Measurements

机译:伏安法和原位红外光谱法研究铂电极上SO_2氧化反应的pH依赖性

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摘要

The electrooxidation of S(IV)-contained species in the aqueous solution of sodium sulfite at a polycrystalline Pt electrode was studied by cyclic voltammetry and in situ infrared spectroscopy as a function of solution pH (1 ≤ pH ≤ 5). The diffusion-controlled anodic current observed at > 0.7 V vs. Ag ∣ AgCl ∣ KCl sat. decreased in the solution of pH larger than 2, and reached a minimum value at pH 5. On the other hand, the activation effect by pre-polarization of the Pt electrode was observed in all of the pH solutions investigated. In situ infrared spectroscopic measurements undertaken during the oxidation reaction indicated that the main oxidation products were S(VI) species assignable either to HSO_4~-or SO_4~(2-).
机译:通过循环伏安法和原位红外光谱研究了溶液中pH值(1≤pH≤5)下亚硫酸钠水溶液中多晶Pt电极上含S(IV)的物质的电氧化。相对于Ag vsAgCl∣KCl饱和溶液,在> 0.7V下观察到的扩散控制阳极电流。在大于2的pH溶液中pH降低,并在pH 5达到最小值。另一方面,在所有研究的pH溶液中均观察到Pt电极预极化的活化作用。在氧化反应过程中进行的原位红外光谱测量表明,主要氧化产物是可归属于HSO_4〜-或SO_4〜(2-)的S(VI)物种。

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  • 来源
  • 会议地点 Vienna(AT);Vienna(AT);Vienna(AT)
  • 作者单位

    Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Technology, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502 Japan;

    Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Technology, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502 Japan;

    Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Technology, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学电源、电池、燃料电池;
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