化学
钒
过氧化氢
水溶液
反应速率常数
无机化学
丙酮
化学计量学
动力学
反应机理
反应速率
催化作用
物理化学
有机化学
量子力学
物理
作者
Guodong Du,James H. Espenson
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2005-06-28
卷期号:44 (15): 5514-5522
被引量:21
摘要
The reaction between vanadium(III) and hydrogen peroxide in aqueous acidic solutions was investigated. The rate law shows first-order dependences on both vanadium(III) and hydrogen peroxide concentrations, with a rate constant, defined in terms of -d[H(2)O(2)]/dt, of 2.06 +/- 0.03 L mol(-)(1) s(-)(1) at 25 degrees C; the rate is independent of hydrogen ion concentration. The varying reaction stoichiometry, the appreciable evolution of dioxygen, the oxidation of 2-PrOH to acetone, and the inhibition of acetone formation by the hydroxyl radical scavengers, dimethyl sulfoxide and sodium benzoate, point to a Fenton mechanism as the predominant pathway in the reaction. Methyltrioxorhenium(VII) does not appear to catalyze this reaction. A second-order rate constant for the oxidation of V(3+) by OV(O(2))(+) was determined to be 11.3 +/- 0.3 L mol(-)(1) s(-)(1) at 25 degrees C. An overall reaction scheme consisting of over 20 reactions, in agreement with the experimental results and literature reports, was established by kinetic simulation studies.
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