H2O2与Fe2+和Fe3+离子反应的初始步骤:自由基理论的不一致性

Reactions Pub Date : 2023-02-20 DOI:10.3390/reactions4010010
M. L. Kremer
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引用次数: 1

摘要

考虑到自由能的变化,自由基理论中假设的H2O2与Fe2+和Fe3+反应的初始步骤是不一致的。自由基理论不能解释由Fe3+引起的H2O2分解或氧化。在高[H2O2]条件下与Fe2+离子的反应中,O2的演化达到一个极限,这个极限是自由基模型所不能预见的。在较低的[H2O2]中,由于所使用的方程中不允许进行替换,因此解释无效。因此,由H2O2产生的自由基似乎不能为这些反应的模型构建提供合适的基础。非自由基模型在解释实验结果方面更为成功。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Initial Steps in the Reaction of H2O2 with Fe2+ and Fe3+ Ions: Inconsistency in the Free Radical Theory
Consideration of the changes in free energy shows that the assumed initial steps in reactions of H2O2 with Fe2+ and Fe3+ in the free radical theory are not consistent. The free radical theory is unable to account for the Fe3+-initiated decomposition of H2O2 or for oxidations by it. In reactions with Fe2+ ions at high [H2O2], where O2 evolution reaches a limit, such limit is not foreseen by the free radical model. At lower [H2O2], because of a disallowed substitution in the equation used, the interpretation is not valid. It appears, therefore, that free radicals derived from H2O2 do not provide a suitable basis for constructing models for these reactions. Non-radical models are more successful in interpreting experimental results.
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