{"title":"Distinguishing Kinetics and Mechanistic Approaches of Ce(IV) Efficient Oxidation of Cadaverine in HClO4 and H2SO4 Media","authors":"Nada Alqarni","doi":"10.1002/kin.70010","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>The kinetics of highly efficient oxidation of cadaverine (CAD) by Ce(IV) in both HClO<sub>4</sub> and H<sub>2</sub>SO<sub>4</sub> 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 [Ce<sup>IV</sup>], where they exhibited lower than unit orders with regard to [CAD] over the studied concentration range. In HClO<sub>4</sub> and H<sub>2</sub>SO<sub>4</sub>, the oxidation reactions showed positive and negative incomplete unit orders in [H<sup>+</sup>], 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.</p>\n </div>","PeriodicalId":13894,"journal":{"name":"International Journal of Chemical Kinetics","volume":"57 11","pages":"674-683"},"PeriodicalIF":1.6000,"publicationDate":"2025-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Chemical Kinetics","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/kin.70010","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
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.
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.