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Kinetics and Mechanism of the Organic Degradation in Aqueous Solution Irradiated with Gaseous Plasma

机译:气态等离子体辐照水溶液中有机物降解的动力学和机理

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The degradation of organic compounds in an aqueous solution induced by a gaseous plasma, which was sustained locally on the surface of solution by means of contact glow discharge electrolysis, was mechanistically studied. The oxidation of phenol was extensively examined and it was revealed that the rate of disappearance followed the first-order rate law when the initial concentration of phenol was lower than 100 mM. As the initial concentration increased, the rate equation gradually deviated from the first-order and eventually shifted to zero-order above 250 mM. Such a kinetical behavior could be rationalized by assuming the reaction scheme where hydroxyl radical would act as the most responsible key-species for the organic degradation in competition with the coupling to hydrogen peroxide. In addition, the catalytic effects of Fe ions in the solution on the rate of organic degradation were closely investigated and could be consistently explained on the above concept.
机译:从机械上研究了由气态等离子体诱导的水溶液中有机化合物的降解,该降解通过接触辉光放电电解而局部维持在溶液表面上。广泛研究了苯酚的氧化,发现当苯酚的初始浓度低于100 mM时,消失速率遵循一阶速率定律。随着初始浓度的增加,速率方程逐渐偏离一阶,最终在250 mM以上移至零阶。可以通过假设反应方案使这种动力学行为合理化,在该方案中,羟基自由基将是有机降解过程中最负责任的关键物种,与过氧化氢的偶联竞争。另外,溶液中Fe离子对有机降解速率的催化作用已得到密切研究,并可以在上述概念上得到一致解释。

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