{"title":"Catalytic Oxidation Process and Thermal Characteristics of Toluene and Butyl Acetate Vapor in an Oven","authors":"Kenichiro Inoue","doi":"10.59796/jcst.v14n1.2024.17","DOIUrl":null,"url":null,"abstract":"Toluene vapor and butyl acetate vapor were oxidized at 523 K in an oven using the Pt/Co3O4-CeO2, Pt/Al2O3, and Co3O4-CeO2 catalysts and a comparison of activity and thermal characteristic among three different catalysts was conducted. The conversion into CO2 was estimated from the change in temperature of a catalyst bed during the oxidation reaction. A relation between heat capacity of the gas and amount of solvent molecule oxidized was clarified. In the oxidation with Pt/Al2O3 catalyst, the butyl acetate could not be completely oxidized, and part remained. Butanol and butanal were formed as by-products of the butyl acetate in the oven, which contained moist air. In the oxidation with Co3O4-CeO2 catalyst, although no butyl acetate remained, some toluene remained and the amount of butanol and butanal increased somewhat after passage over the catalyst bed. By using a catalyst that combined platinum and Co3O4-CeO2 with the original method, both the toluene and butyl acetate were almost completely oxidized at 523 K.","PeriodicalId":36369,"journal":{"name":"Journal of Current Science and Technology","volume":"22 11","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Current Science and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.59796/jcst.v14n1.2024.17","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Multidisciplinary","Score":null,"Total":0}
引用次数: 0
Abstract
Toluene vapor and butyl acetate vapor were oxidized at 523 K in an oven using the Pt/Co3O4-CeO2, Pt/Al2O3, and Co3O4-CeO2 catalysts and a comparison of activity and thermal characteristic among three different catalysts was conducted. The conversion into CO2 was estimated from the change in temperature of a catalyst bed during the oxidation reaction. A relation between heat capacity of the gas and amount of solvent molecule oxidized was clarified. In the oxidation with Pt/Al2O3 catalyst, the butyl acetate could not be completely oxidized, and part remained. Butanol and butanal were formed as by-products of the butyl acetate in the oven, which contained moist air. In the oxidation with Co3O4-CeO2 catalyst, although no butyl acetate remained, some toluene remained and the amount of butanol and butanal increased somewhat after passage over the catalyst bed. By using a catalyst that combined platinum and Co3O4-CeO2 with the original method, both the toluene and butyl acetate were almost completely oxidized at 523 K.