Ragnhild C. Pille, Chang-yu Yu , Gilbert F. Froment
{"title":"Kinetic study of the hydrogen sulfide effect in the conversion of thiophene on supported CoMo catalysts","authors":"Ragnhild C. Pille, Chang-yu Yu , Gilbert F. Froment","doi":"10.1016/0304-5102(94)00152-9","DOIUrl":null,"url":null,"abstract":"<div><p>The hydrodesulfurization of thiophene on a commercial CoMo/alumina catalyst was studied in a Berty type CSTR reactor at 350°C, with partial pressures of hydrogen sulfide in the range of 0.2 to 5.5 bar. A kinetic model with interconversion of active sites is superior to models based on a fixed number of active sites. The proposed mechanism for the interconversion of active sites predicts that the hydrogenation and hydrogenolysis activities of a HDS catalyst can be substantially varied by hydrogen sulfide. The model also explains the controversial hydrogen sulfide effects observed in various types of reactions on CoMo catalysts.</p></div>","PeriodicalId":16567,"journal":{"name":"分子催化","volume":"94 3","pages":"Pages 369-387"},"PeriodicalIF":0.0000,"publicationDate":"1994-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0304-5102(94)00152-9","citationCount":"24","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"分子催化","FirstCategoryId":"1089","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0304510294001529","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Chemical Engineering","Score":null,"Total":0}
引用次数: 24
Abstract
The hydrodesulfurization of thiophene on a commercial CoMo/alumina catalyst was studied in a Berty type CSTR reactor at 350°C, with partial pressures of hydrogen sulfide in the range of 0.2 to 5.5 bar. A kinetic model with interconversion of active sites is superior to models based on a fixed number of active sites. The proposed mechanism for the interconversion of active sites predicts that the hydrogenation and hydrogenolysis activities of a HDS catalyst can be substantially varied by hydrogen sulfide. The model also explains the controversial hydrogen sulfide effects observed in various types of reactions on CoMo catalysts.