{"title":"用非线性Poisson−Boltzmann方程和静电自由能模型模拟胶束催化的双分子离子反应","authors":"Arnab Karmakar, Sumit Kumar Jana","doi":"10.1002/kin.21647","DOIUrl":null,"url":null,"abstract":"<p>The hydrolysis reactions of crystal violet (CV) and <i>p</i>-nitrophenyl acetate (PNPA) by sodium hydroxide in cetyltrimethylammonium bromide (CTAB) micellar solution were studied in this work. Combined with the Boltzmann probability of ionic species in an electrostatic potential field, a model with a numerical scheme was developed based on the nonlinear Poisson−Boltzmann equation in the micelle-cell consisting of the reactants and the surfactant. The numerical solution gives the ionic species distribution in the micelle phase and the radius of the micelle-phase. The dielectric constant of the micelle-phase varies in the range of 39.8−54.4. The second-order reaction rate constants in the micelle-phase were determined using the electrostatic and dipolar free energy models. For the basic hydrolysis of CV and PNPA, the overall second-order rate constants are three to five times and 1.4 times greater than the corresponding values in water, respectively. The rate enhancement occurs due to the distribution of the reactive ionic species in the cell region and the enhancement of the Coulombic and dipolar interactions among the ionic and polar reactants.</p>","PeriodicalId":13894,"journal":{"name":"International Journal of Chemical Kinetics","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2023-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Modeling of micellar-catalyzed bimolecular ionic reactions by a nonlinear Poisson−Boltzmann equation and an electrostatic free energy model\",\"authors\":\"Arnab Karmakar, Sumit Kumar Jana\",\"doi\":\"10.1002/kin.21647\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The hydrolysis reactions of crystal violet (CV) and <i>p</i>-nitrophenyl acetate (PNPA) by sodium hydroxide in cetyltrimethylammonium bromide (CTAB) micellar solution were studied in this work. Combined with the Boltzmann probability of ionic species in an electrostatic potential field, a model with a numerical scheme was developed based on the nonlinear Poisson−Boltzmann equation in the micelle-cell consisting of the reactants and the surfactant. The numerical solution gives the ionic species distribution in the micelle phase and the radius of the micelle-phase. The dielectric constant of the micelle-phase varies in the range of 39.8−54.4. The second-order reaction rate constants in the micelle-phase were determined using the electrostatic and dipolar free energy models. For the basic hydrolysis of CV and PNPA, the overall second-order rate constants are three to five times and 1.4 times greater than the corresponding values in water, respectively. The rate enhancement occurs due to the distribution of the reactive ionic species in the cell region and the enhancement of the Coulombic and dipolar interactions among the ionic and polar reactants.</p>\",\"PeriodicalId\":13894,\"journal\":{\"name\":\"International Journal of Chemical Kinetics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2023-04-13\",\"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.21647\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Chemical Kinetics","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/kin.21647","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Modeling of micellar-catalyzed bimolecular ionic reactions by a nonlinear Poisson−Boltzmann equation and an electrostatic free energy model
The hydrolysis reactions of crystal violet (CV) and p-nitrophenyl acetate (PNPA) by sodium hydroxide in cetyltrimethylammonium bromide (CTAB) micellar solution were studied in this work. Combined with the Boltzmann probability of ionic species in an electrostatic potential field, a model with a numerical scheme was developed based on the nonlinear Poisson−Boltzmann equation in the micelle-cell consisting of the reactants and the surfactant. The numerical solution gives the ionic species distribution in the micelle phase and the radius of the micelle-phase. The dielectric constant of the micelle-phase varies in the range of 39.8−54.4. The second-order reaction rate constants in the micelle-phase were determined using the electrostatic and dipolar free energy models. For the basic hydrolysis of CV and PNPA, the overall second-order rate constants are three to five times and 1.4 times greater than the corresponding values in water, respectively. The rate enhancement occurs due to the distribution of the reactive ionic species in the cell region and the enhancement of the Coulombic and dipolar interactions among the ionic and polar reactants.
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.