Strong Inhibition of the Fe3+ + H2O2 Reaction by Ethanol: Evidence against the Free Radical Theory

IF 2.1 4区 化学 Q3 CHEMISTRY, PHYSICAL
M. L. Kremer
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引用次数: 8

Abstract

The effect of ethanol on the catalytic decomposition of H2O2 by Fe3+ was investigated. While expecting a simple competitive oxidation of C2H5OH, far more complex kinetics were encountered experimentally: already minute amounts of C2H5OH (1% of H2O2) had a powerful retardation effect on the disappearance of H2O2. This fact indicated the operation of an intricate mechanism. It excluded the possibility of OH• radicals being the active agents in the oxidation: OH• radicals generated by radiolysis react with C2H5OH with a very high rate constant. The interpretation of the experimental results was based on a mechanism involving iron in a +5 oxidation state (FeO3+) as the active intermediate and its binding in complex structures in which activity is reduced. The question of free radical versus non-radical mechanisms is discussed. The conclusions differ from generally accepted concepts in relation to the Fenton and related reactions.
乙醇对Fe3+ + H2O2反应的强抑制:反对自由基理论的证据
研究了乙醇对Fe3+催化分解H2O2的影响。虽然期望C2H5OH的简单竞争性氧化,但实验中遇到了更复杂的动力学:已经有微量的C2H5OH(1%的H2O2)对H2O2的消失有强大的延缓作用。这一事实表明一种复杂的机制在起作用。它排除了OH•自由基作为氧化活性剂的可能性:OH•自由基与C2H5OH以非常高的速率常数发生反应。实验结果的解释是基于一种机制,涉及铁在+5氧化态(FeO3+)作为活性中间体及其结合在复杂结构中活性降低。讨论了自由基与非自由基机理的问题。结论不同于一般接受的关于芬顿反应和相关反应的概念。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
5
审稿时长
2.3 months
期刊介绍: The journal covers the fields of kinetics and mechanisms of chemical processes in the gas phase and solution of both simple and complex systems.
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