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

被引:0
作者
Zhu, Rui [1 ,2 ]
Gao, Fang [1 ,2 ]
Li, Xinglong [3 ]
机构
[1] Jiangnan Univ, Sch Biotechnol, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Key Lab Ind Biotechnol, Minist Educ, Wuxi 214122, Peoples R China
[3] Anhui Univ Sci & Technol, Aust Hefei Inst Adv Res, Sch Carbon Neutral Sci & Engn, Hefei 231131, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxidation; 5-Hydroxymethylfurfural; 2,5-furandicarboxylic acid; Bimetallic cobalt and manganese catalyst; Tert-butyl hydroperoxide; AEROBIC OXIDATION; BIOMASS; BASE; HMF; SUPPORT;
D O I
10.1016/j.mcat.2025.115135
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
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页数:10
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