Toyese Oyegoke , Achraf Sadier , Sara Navarro-Jaén , Alessia Ventimiglia , Nikolaos Dimitratos , Franck Dumeignil , Baba El-Yakubu Jibril , Robert Wojcieszak , Carine Michel
{"title":"用金支撑催化剂促进 5-羟甲基呋喃氧化成 2,5-呋喃二甲酸:通过 DFT 计算优化反应参数并揭示降解机理","authors":"Toyese Oyegoke , Achraf Sadier , Sara Navarro-Jaén , Alessia Ventimiglia , Nikolaos Dimitratos , Franck Dumeignil , Baba El-Yakubu Jibril , Robert Wojcieszak , Carine Michel","doi":"10.1016/j.cattod.2024.115086","DOIUrl":null,"url":null,"abstract":"<div><div>Lignocellulosic biomass holds promise for producing valuable chemicals. Among possible key reactions, the 5-hydroxymethylfurfural (HMF) oxidation to 2,5-furandicarboxylic acid (FDCA) using O<sub>2</sub> as a final oxidant and supported Au catalysts is a promising route but that suffers from carbon balance issues. This study explores the mechanism of HMF oxidation to FDCA on a Au(111) model catalyst using computational modeling. Our results identify the main intermediate (HMFCA) and the major degradation pathways from HMF and HMFCA. Since we predict a higher degradation rate for HMF, we designed an experimental two-step approach, using a low temperature to convert fully HMF and improve the carbon balance and then raising the temperature to convert the HMFCA intermediate into FDCA. This approach was successful, reaching a high yield in FDCA (>90 %) in 8 hours while keeping the carbon balance above 97 %.</div></div>","PeriodicalId":264,"journal":{"name":"Catalysis Today","volume":"445 ","pages":"Article 115086"},"PeriodicalIF":5.2000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhancing 5-hydroxymethylfurfural oxidation to 2,5-furan-dicarboxylic acid with Au-supported catalysts: Optimizing reaction parameters and unraveling degradation mechanism through DFT calculations\",\"authors\":\"Toyese Oyegoke , Achraf Sadier , Sara Navarro-Jaén , Alessia Ventimiglia , Nikolaos Dimitratos , Franck Dumeignil , Baba El-Yakubu Jibril , Robert Wojcieszak , Carine Michel\",\"doi\":\"10.1016/j.cattod.2024.115086\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Lignocellulosic biomass holds promise for producing valuable chemicals. Among possible key reactions, the 5-hydroxymethylfurfural (HMF) oxidation to 2,5-furandicarboxylic acid (FDCA) using O<sub>2</sub> as a final oxidant and supported Au catalysts is a promising route but that suffers from carbon balance issues. This study explores the mechanism of HMF oxidation to FDCA on a Au(111) model catalyst using computational modeling. Our results identify the main intermediate (HMFCA) and the major degradation pathways from HMF and HMFCA. Since we predict a higher degradation rate for HMF, we designed an experimental two-step approach, using a low temperature to convert fully HMF and improve the carbon balance and then raising the temperature to convert the HMFCA intermediate into FDCA. This approach was successful, reaching a high yield in FDCA (>90 %) in 8 hours while keeping the carbon balance above 97 %.</div></div>\",\"PeriodicalId\":264,\"journal\":{\"name\":\"Catalysis Today\",\"volume\":\"445 \",\"pages\":\"Article 115086\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2024-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Today\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0920586124005807\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Today","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0920586124005807","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Enhancing 5-hydroxymethylfurfural oxidation to 2,5-furan-dicarboxylic acid with Au-supported catalysts: Optimizing reaction parameters and unraveling degradation mechanism through DFT calculations
Lignocellulosic biomass holds promise for producing valuable chemicals. Among possible key reactions, the 5-hydroxymethylfurfural (HMF) oxidation to 2,5-furandicarboxylic acid (FDCA) using O2 as a final oxidant and supported Au catalysts is a promising route but that suffers from carbon balance issues. This study explores the mechanism of HMF oxidation to FDCA on a Au(111) model catalyst using computational modeling. Our results identify the main intermediate (HMFCA) and the major degradation pathways from HMF and HMFCA. Since we predict a higher degradation rate for HMF, we designed an experimental two-step approach, using a low temperature to convert fully HMF and improve the carbon balance and then raising the temperature to convert the HMFCA intermediate into FDCA. This approach was successful, reaching a high yield in FDCA (>90 %) in 8 hours while keeping the carbon balance above 97 %.
期刊介绍:
Catalysis Today focuses on the rapid publication of original invited papers devoted to currently important topics in catalysis and related subjects. The journal only publishes special issues (Proposing a Catalysis Today Special Issue), each of which is supervised by Guest Editors who recruit individual papers and oversee the peer review process. Catalysis Today offers researchers in the field of catalysis in-depth overviews of topical issues.
Both fundamental and applied aspects of catalysis are covered. Subjects such as catalysis of immobilized organometallic and biocatalytic systems are welcome. Subjects related to catalysis such as experimental techniques, adsorption, process technology, synthesis, in situ characterization, computational, theoretical modeling, imaging and others are included if there is a clear relationship to catalysis.