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

IF 5.2 2区 化学 Q1 CHEMISTRY, APPLIED Catalysis Today Pub Date : 2024-09-30 DOI:10.1016/j.cattod.2024.115086
Toyese Oyegoke , Achraf Sadier , Sara Navarro-Jaén , Alessia Ventimiglia , Nikolaos Dimitratos , Franck Dumeignil , Baba El-Yakubu Jibril , Robert Wojcieszak , Carine Michel
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引用次数: 0

摘要

木质纤维素生物质有望生产有价值的化学品。在可能的关键反应中,使用 O2 作为最终氧化剂和支撑金催化剂将 5-hydroxymethylfurfural (HMF) 氧化成 2,5-呋喃二甲酸 (FDCA) 是一条很有前景的路线,但存在碳平衡问题。本研究通过计算建模探索了金(111)模型催化剂上将 HMF 氧化成 FDCA 的机理。我们的研究结果确定了主要中间体(HMFCA)以及 HMF 和 HMFCA 的主要降解途径。由于我们预测 HMF 的降解率较高,因此我们设计了一种分两步进行的实验方法:使用低温完全转化 HMF 并改善碳平衡,然后升温将 HMFCA 中间体转化为 FDCA。这种方法取得了成功,在 8 小时内达到了 FDCA 的高产率(90%),同时碳平衡保持在 97% 以上。
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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 %.
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来源期刊
Catalysis Today
Catalysis Today 化学-工程:化工
CiteScore
11.50
自引率
3.80%
发文量
573
审稿时长
2.9 months
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.
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