氯水钌(III)催化酸溴酸盐氧化酒石酸的动力学与机理

Ajaya K. Singh, Ashok K. Singh, Vineeta Singh, S. Singh, B. Singh
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引用次数: 6

摘要

在高氯酸水溶液中,在恒定离子强度下,研究了溴酸钾催化Ru (III)氧化酒石酸的动力学。低浓度溴酸盐反应表现为一级动力学,高浓度溴酸盐反应趋于零级动力学。在酒石酸的氧化过程中观察到与(酒石酸)有关的零级动力学和(Ru (III))的一级动力学。连续加入(H +)和(Cl -)对反应速率有积极的影响。乙酸汞浓度、(Hg(OAc)2)和介质离子强度的变化对反应速率没有显著影响。一阶速率常数随介质介电常数的减小而增大。利用在四种不同温度下观察到的速率常数值来计算活化参数。甲酸和二氧化碳是该反应的主要氧化产物。从动力学研究、化学计量学和产物分析等方面提出了一种合理的反应机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinetics and Mechanism of Aquachlororuthenium (III) Catalyzed Oxidation of Tartaric Acid by Acid Bromate
The kinetics of the oxidation of Ru (III) catalyzed oxidation of tartaric acid by potassium bromate in aqueous perchloric acid medium at constant ionic strength was investigated in the temperature range 303- 318 K. The reactions exhibit first order kinetics at low concentration of bromate, tending to zero order at high concentration. Zero order kinetics with respect to (tartaric acid) and first order kinetics in (Ru (III)) were observed in the oxidation of tartaric acid. A positive effect on the rate of reaction has been found on the successive addition of (H + ) and (Cl - ). Variation in mercuric acetate concentration, (Hg(OAc)2) and ionic strength of the medium did not bring any significant change on the rate of reaction. The first order rate constant increases with decrease in the dielectric constant of the medium. The values of rate constants observed at four different temperatures were utilized to calculate the activation parameters. Formic acid and carbon dioxide have been identified as main oxidation products of the reaction. A plausible mechanism from the results of kinetic studies, reaction stoichiometry and product analysis has been proposed.
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