Bimetallic Co-Mn catalyzed chemselective oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2025-04-18 DOI:10.1016/j.mcat.2025.115135
Rui Zhu , Fang Gao , Xinglong Li
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Abstract

The development of efficient catalysts for the stepwise oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-diformyl furan (DFF), 5-hydroxymethyl-2-furancarboxylic acid (HMFCA), 5-Formyl-2-furancarboxylic acid (FFCA) or 2,5-furandicarboxylic acid (FDCA) is critical for biomass valorization. Herein, we reported a bimetallic Co-Mn catalyst anchored on nitrogen-doped porous carbon, which was used for the oxidation of HMF to FDCA, avoiding the use of high temperature and high-pressure oxygen. High FDCA selectivity (>95 %) was achieved through reaction condition optimization. And HMF→DFF→FFCA→FDCA was considered to be the main reaction pathway during the whole oxidation process. Additionally, the chemical environment of the constituent elements of the used catalyst was analyzed by XPS. TEM revealed that the catalyst retained its porous structure and excellent metal dispersion after the reaction. This structural stability was corroborated by sustained >90 % FDCA selectivity over five consecutive reaction cycles. This work established a dual-metal synergy strategy for multi-step oxidation pathways, offering insights into the design of robust catalysts for biomass-derived platform molecule upgrading.

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双金属Co-Mn催化5-羟甲基糠醛化学选择性氧化制备2,5-呋喃二羧酸
5-羟甲基糠醛(HMF)逐步氧化为2,5-二甲酰呋喃(DFF)、5-羟甲基-2-呋喃羧酸(HMFCA)、5-甲酰基-2-呋喃羧酸(FFCA)或2,5-呋喃二羧酸(FDCA)的高效催化剂的开发对于生物质再生至关重要。本文报道了一种锚定在氮掺杂多孔碳上的双金属Co-Mn催化剂,该催化剂用于将HMF氧化为FDCA,避免了使用高温高压氧气。通过优化反应条件,获得了较高的FDCA选择性(95%)。认为HMF→DFF→FFCA→FDCA是整个氧化过程的主要反应途径。此外,用XPS分析了所用催化剂组成元素的化学环境。TEM结果表明,反应后催化剂保持了多孔结构和良好的金属分散性能。在连续的五个反应周期中,FDCA的选择性持续达到90%,证实了这种结构的稳定性。这项工作为多步氧化途径建立了双金属协同策略,为生物质衍生平台分子升级的稳健催化剂设计提供了见解。
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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