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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:SO_2氧化反应在通过伏安和原位红外光谱测量研究的铂电极处的氧化反应

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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在多晶PT电极的亚硫酸钠水溶液中的S(IV)阳性物种的电氧化作为溶液pH(1≤ph≤5)的函数。观察到的扩散控制的阳极电流> 0.7V与Ag | AGCL | kcl坐了。在pH大于2的溶液中降低,并在pH 5处达到最小值5.另一方面,在研究所有pH溶液中观察到通过PT电极的预极化的激活效果。在氧化反应期间进行的原位红外光谱测量结果表明,主要氧化产物是S(VI)物种,可分配给HSO_4〜 - 或SO_4〜(2-)。

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