{"title":"阳离子表面活性剂对Ru(III)催化高铁酸盐氧化L-谷氨酸的影响","authors":"Abhishek Srivastava, Madhav Krishna Goswami, Rajeev Kumar Dohare, Neetu Srivastava, Krishna Srivastava","doi":"10.1002/kin.21646","DOIUrl":null,"url":null,"abstract":"<p>In CTAB micellar medium, the kinetic investigation of Ru(III) promoted oxidation of L-glutamic acid (Glu) by [Fe(CN)<sub>6</sub>]<sup>3−</sup> was carried out by recording the decline in absorbance at 420 nm, which corresponds to [Fe(CN)<sub>6</sub>]<sup>3−</sup>. By adjusting one variable at a time, the progression of the reaction has been inspected as a function of [OH<sup>−</sup>], ionic strength, [CTAB], [Ru<sup>3+</sup>], [Glu], [Fe(CN)<sub>6</sub><sup>3−</sup>], and temperature using the pseudo-first-order condition. The findings demonstrate that [OH<sup>−</sup>], [CTAB], and [Glu] are the key parameters that have a discernible impact on reaction rate. In the studied concentration range of Ru(III), [Fe(CN)<sub>6</sub>]<sup>3−</sup>, and at lower [Glu] and [OH<sup>−</sup>], the reaction displays first-order kinetics. The incremental trend in reaction rate with electrolyte concentration demonstrates a positive salt effect. CTAB substantially catalyzes the process, and after reaching a maximum, the rate remains nearly constant at increased [CTAB]. The observed decline in the CMC of CTAB may be caused by the reduced repulsion between the positively charged heads of the surfactant molecules caused by the negatively charged OH<sup>−</sup>, and [Fe(CN)<sub>6</sub>]<sup>3−</sup>. The activation parameters also support the outer-sphere electron transfer mechanism as recommended by us.</p>","PeriodicalId":13894,"journal":{"name":"International Journal of Chemical Kinetics","volume":null,"pages":null},"PeriodicalIF":1.5000,"publicationDate":"2023-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Effect of cationic surfactant on Ru(III) catalyzed L-glutamic acid oxidation by hexacyanoferrate(III)\",\"authors\":\"Abhishek Srivastava, Madhav Krishna Goswami, Rajeev Kumar Dohare, Neetu Srivastava, Krishna Srivastava\",\"doi\":\"10.1002/kin.21646\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In CTAB micellar medium, the kinetic investigation of Ru(III) promoted oxidation of L-glutamic acid (Glu) by [Fe(CN)<sub>6</sub>]<sup>3−</sup> was carried out by recording the decline in absorbance at 420 nm, which corresponds to [Fe(CN)<sub>6</sub>]<sup>3−</sup>. By adjusting one variable at a time, the progression of the reaction has been inspected as a function of [OH<sup>−</sup>], ionic strength, [CTAB], [Ru<sup>3+</sup>], [Glu], [Fe(CN)<sub>6</sub><sup>3−</sup>], and temperature using the pseudo-first-order condition. The findings demonstrate that [OH<sup>−</sup>], [CTAB], and [Glu] are the key parameters that have a discernible impact on reaction rate. In the studied concentration range of Ru(III), [Fe(CN)<sub>6</sub>]<sup>3−</sup>, and at lower [Glu] and [OH<sup>−</sup>], the reaction displays first-order kinetics. The incremental trend in reaction rate with electrolyte concentration demonstrates a positive salt effect. CTAB substantially catalyzes the process, and after reaching a maximum, the rate remains nearly constant at increased [CTAB]. The observed decline in the CMC of CTAB may be caused by the reduced repulsion between the positively charged heads of the surfactant molecules caused by the negatively charged OH<sup>−</sup>, and [Fe(CN)<sub>6</sub>]<sup>3−</sup>. The activation parameters also support the outer-sphere electron transfer mechanism as recommended by us.</p>\",\"PeriodicalId\":13894,\"journal\":{\"name\":\"International Journal of Chemical Kinetics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2023-04-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Chemical Kinetics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/kin.21646\",\"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.21646","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Effect of cationic surfactant on Ru(III) catalyzed L-glutamic acid oxidation by hexacyanoferrate(III)
In CTAB micellar medium, the kinetic investigation of Ru(III) promoted oxidation of L-glutamic acid (Glu) by [Fe(CN)6]3− was carried out by recording the decline in absorbance at 420 nm, which corresponds to [Fe(CN)6]3−. By adjusting one variable at a time, the progression of the reaction has been inspected as a function of [OH−], ionic strength, [CTAB], [Ru3+], [Glu], [Fe(CN)63−], and temperature using the pseudo-first-order condition. The findings demonstrate that [OH−], [CTAB], and [Glu] are the key parameters that have a discernible impact on reaction rate. In the studied concentration range of Ru(III), [Fe(CN)6]3−, and at lower [Glu] and [OH−], the reaction displays first-order kinetics. The incremental trend in reaction rate with electrolyte concentration demonstrates a positive salt effect. CTAB substantially catalyzes the process, and after reaching a maximum, the rate remains nearly constant at increased [CTAB]. The observed decline in the CMC of CTAB may be caused by the reduced repulsion between the positively charged heads of the surfactant molecules caused by the negatively charged OH−, and [Fe(CN)6]3−. The activation parameters also support the outer-sphere electron transfer mechanism as recommended by us.
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.