Distinguishing Kinetics and Mechanistic Approaches of Ce(IV) Efficient Oxidation of Cadaverine in HClO4 and H2SO4 Media

IF 1.6 4区 化学 Q4 CHEMISTRY, PHYSICAL
Nada Alqarni
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引用次数: 0

Abstract

The kinetics of highly efficient oxidation of cadaverine (CAD) by Ce(IV) in both HClO4 and H2SO4 solutions were examined using UV–Vis absorption spectra at numerous temperatures. The last products of CAD oxidation were recognized as ammonia and 5-aminopentanal, that is, an essential organic compound in both biological and chemical settings. From the obtained data, it's clear that the reactions’ kinetics demonstrated a first-order dependence in [CeIV], where they exhibited lower than unit orders with regard to [CAD] over the studied concentration range. In HClO4 and H2SO4, the oxidation reactions showed positive and negative incomplete unit orders in [H+], correspondingly. Based on the obtained results, the mechanistic reactions’ pathways were suggested. The reliable rate laws were derived, and the reactions’ rate constants were estimated. In addition, the activation and thermodynamic parameters were calculated and discussed. This study illuminated the role of the oxidant, medium, temperature, and other conditions on the oxidation kinetics and mechanisms of these redox systems.

Abstract Image

Ce(IV)在HClO4和H2SO4介质中高效氧化尸胺的区分动力学和机理研究
采用紫外-可见吸收光谱研究了Ce(IV)在HClO4和H2SO4溶液中高效氧化尸胺(CAD)的动力学。CAD氧化的最后产物被认为是氨和5-氨基戊二醛,即生物和化学环境中必需的有机化合物。从获得的数据来看,很明显,反应动力学在[CeIV]中表现出一级依赖性,在研究的浓度范围内,它们表现出低于[CAD]的单位阶数。在HClO4和H2SO4中,[H+]的氧化反应分别呈现正、负不完全单元序。在此基础上,提出了反应机理的途径。导出了可靠的反应速率规律,并对反应速率常数进行了估计。此外,还对活化和热力学参数进行了计算和讨论。本研究阐明了氧化剂、介质、温度和其他条件对这些氧化还原体系的氧化动力学和机理的作用。
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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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