E. Ventura, Rodolpho L. R. Alves, Silmar A. do Monte
{"title":"三个耦合不可逆基本反应的动力学:两个平行混合二阶反应,然后是一个一阶反应","authors":"E. Ventura, Rodolpho L. R. Alves, Silmar A. do Monte","doi":"10.1007/s10910-024-01580-1","DOIUrl":null,"url":null,"abstract":"<div><p>A semi-analytical solution for the time dependence of the concentration of the intermediate is derived, in the case of two parallel mixed second order reactions followed by a first order reaction. The solution is restricted to equal initial concentrations for the reactants, and it is connected to the exponential integral. From the solution and through a proper choice of the dimensionless time (u) and concentration of the intermediate (y) one obtains a very simple relation between the maximum concentration of the intermediate (y<sub>max</sub>) and the time associated with this concentration (u<sub>max</sub>). This relation is governed by a parameter (β) which depends on the three rate constants and on the initial concentration. The smaller is β the larger are u<sub>max</sub> and y<sub>max</sub>, and the slower is the decay of y. An approximate expression connecting u<sub>max</sub> and β, has also been obtained, and it yields maximum errors of ~ 8% and ~ 15% for u<sub>max</sub> and y<sub>max</sub>, respectively. The obtained expression can be very useful from the experimental point of view, as it allows an a priori selection of the most suitable experimental technique to detect the intermediate, simply comparing its time resolution with t<sub>max</sub> (that is, u<sub>max</sub> transformed to a time unit). An illustrative calculation is also discussed.</p></div>","PeriodicalId":648,"journal":{"name":"Journal of Mathematical Chemistry","volume":"62 4","pages":"922 - 935"},"PeriodicalIF":1.7000,"publicationDate":"2024-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The kinetics of three coupled irreversible elementary reactions: two parallel mixed second order reactions followed by a first order reaction\",\"authors\":\"E. Ventura, Rodolpho L. R. Alves, Silmar A. do Monte\",\"doi\":\"10.1007/s10910-024-01580-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A semi-analytical solution for the time dependence of the concentration of the intermediate is derived, in the case of two parallel mixed second order reactions followed by a first order reaction. The solution is restricted to equal initial concentrations for the reactants, and it is connected to the exponential integral. From the solution and through a proper choice of the dimensionless time (u) and concentration of the intermediate (y) one obtains a very simple relation between the maximum concentration of the intermediate (y<sub>max</sub>) and the time associated with this concentration (u<sub>max</sub>). This relation is governed by a parameter (β) which depends on the three rate constants and on the initial concentration. The smaller is β the larger are u<sub>max</sub> and y<sub>max</sub>, and the slower is the decay of y. An approximate expression connecting u<sub>max</sub> and β, has also been obtained, and it yields maximum errors of ~ 8% and ~ 15% for u<sub>max</sub> and y<sub>max</sub>, respectively. The obtained expression can be very useful from the experimental point of view, as it allows an a priori selection of the most suitable experimental technique to detect the intermediate, simply comparing its time resolution with t<sub>max</sub> (that is, u<sub>max</sub> transformed to a time unit). An illustrative calculation is also discussed.</p></div>\",\"PeriodicalId\":648,\"journal\":{\"name\":\"Journal of Mathematical Chemistry\",\"volume\":\"62 4\",\"pages\":\"922 - 935\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-02-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Mathematical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10910-024-01580-1\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Mathematical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10910-024-01580-1","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
The kinetics of three coupled irreversible elementary reactions: two parallel mixed second order reactions followed by a first order reaction
A semi-analytical solution for the time dependence of the concentration of the intermediate is derived, in the case of two parallel mixed second order reactions followed by a first order reaction. The solution is restricted to equal initial concentrations for the reactants, and it is connected to the exponential integral. From the solution and through a proper choice of the dimensionless time (u) and concentration of the intermediate (y) one obtains a very simple relation between the maximum concentration of the intermediate (ymax) and the time associated with this concentration (umax). This relation is governed by a parameter (β) which depends on the three rate constants and on the initial concentration. The smaller is β the larger are umax and ymax, and the slower is the decay of y. An approximate expression connecting umax and β, has also been obtained, and it yields maximum errors of ~ 8% and ~ 15% for umax and ymax, respectively. The obtained expression can be very useful from the experimental point of view, as it allows an a priori selection of the most suitable experimental technique to detect the intermediate, simply comparing its time resolution with tmax (that is, umax transformed to a time unit). An illustrative calculation is also discussed.
期刊介绍:
The Journal of Mathematical Chemistry (JOMC) publishes original, chemically important mathematical results which use non-routine mathematical methodologies often unfamiliar to the usual audience of mainstream experimental and theoretical chemistry journals. Furthermore JOMC publishes papers on novel applications of more familiar mathematical techniques and analyses of chemical problems which indicate the need for new mathematical approaches.
Mathematical chemistry is a truly interdisciplinary subject, a field of rapidly growing importance. As chemistry becomes more and more amenable to mathematically rigorous study, it is likely that chemistry will also become an alert and demanding consumer of new mathematical results. The level of complexity of chemical problems is often very high, and modeling molecular behaviour and chemical reactions does require new mathematical approaches. Chemistry is witnessing an important shift in emphasis: simplistic models are no longer satisfactory, and more detailed mathematical understanding of complex chemical properties and phenomena are required. From theoretical chemistry and quantum chemistry to applied fields such as molecular modeling, drug design, molecular engineering, and the development of supramolecular structures, mathematical chemistry is an important discipline providing both explanations and predictions. JOMC has an important role in advancing chemistry to an era of detailed understanding of molecules and reactions.