{"title":"酸性水溶液中咖啡因与高锰酸盐离子氧化还原反应动力学的分光光度法研究","authors":"F. Jones, I. Anweting, I. E. Okon, K. Andem","doi":"10.9734/ajocs/2023/v13i3239","DOIUrl":null,"url":null,"abstract":"The kinetics of redox reaction between caffeine (hereafter referred to as CAF) and permanganate ion [MnO4-] has been studied spectrophotometrically in aqueous sulfuric acid medium. One mole of CAF was oxidized by one mole of [MnO4-].The reaction showed first-order kinetics with respect to both [CAF] and [MnO4-]. The investigation was carried out under pseudo-first order condition atI= 0.5 mol dm–3, (Na2SO4), T = 24± 0.1℃ and [H+] = 1.0 × 10–1mol dm-3. The reaction obeys the rate law: -d[MnO4-]/dt = (a+b [H+]) [CAF ] [MnO4-]. The reaction was retarded by increased in ionic strength of the reaction medium. The rate of the reaction showed dependence on acid (in the range used).Added anions and cations were observed to catalyze the reaction rate. Spectroscopic investigation and kinetic study did not suggest intermediate complex formation. An outer–sphere mechanism is proposed for the reaction.","PeriodicalId":8505,"journal":{"name":"Asian Journal of Chemical Sciences","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Spectrophotometric Study of Kinetics of Redox Reaction between Caffeine and Permanganate Ion in Aqueous Acidic Medium\",\"authors\":\"F. Jones, I. Anweting, I. E. Okon, K. Andem\",\"doi\":\"10.9734/ajocs/2023/v13i3239\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The kinetics of redox reaction between caffeine (hereafter referred to as CAF) and permanganate ion [MnO4-] has been studied spectrophotometrically in aqueous sulfuric acid medium. One mole of CAF was oxidized by one mole of [MnO4-].The reaction showed first-order kinetics with respect to both [CAF] and [MnO4-]. The investigation was carried out under pseudo-first order condition atI= 0.5 mol dm–3, (Na2SO4), T = 24± 0.1℃ and [H+] = 1.0 × 10–1mol dm-3. The reaction obeys the rate law: -d[MnO4-]/dt = (a+b [H+]) [CAF ] [MnO4-]. The reaction was retarded by increased in ionic strength of the reaction medium. The rate of the reaction showed dependence on acid (in the range used).Added anions and cations were observed to catalyze the reaction rate. Spectroscopic investigation and kinetic study did not suggest intermediate complex formation. An outer–sphere mechanism is proposed for the reaction.\",\"PeriodicalId\":8505,\"journal\":{\"name\":\"Asian Journal of Chemical Sciences\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-06-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Chemical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.9734/ajocs/2023/v13i3239\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Chemical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/ajocs/2023/v13i3239","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Spectrophotometric Study of Kinetics of Redox Reaction between Caffeine and Permanganate Ion in Aqueous Acidic Medium
The kinetics of redox reaction between caffeine (hereafter referred to as CAF) and permanganate ion [MnO4-] has been studied spectrophotometrically in aqueous sulfuric acid medium. One mole of CAF was oxidized by one mole of [MnO4-].The reaction showed first-order kinetics with respect to both [CAF] and [MnO4-]. The investigation was carried out under pseudo-first order condition atI= 0.5 mol dm–3, (Na2SO4), T = 24± 0.1℃ and [H+] = 1.0 × 10–1mol dm-3. The reaction obeys the rate law: -d[MnO4-]/dt = (a+b [H+]) [CAF ] [MnO4-]. The reaction was retarded by increased in ionic strength of the reaction medium. The rate of the reaction showed dependence on acid (in the range used).Added anions and cations were observed to catalyze the reaction rate. Spectroscopic investigation and kinetic study did not suggest intermediate complex formation. An outer–sphere mechanism is proposed for the reaction.