Electro-catalytic oxidation of HMF to FDCA over RuO2/MnO2/CNT catalysts in base-free solution

被引:21
|
作者
Wang, Tianci [1 ]
Song, Yu [1 ]
Zhao, Wanna [1 ]
Zhou, Chunmei [1 ]
Jin, Yuguang [1 ]
Wan, Xiaoyue [1 ]
Dai, Yihu [1 ]
Yang, Yanhui [1 ,2 ]
机构
[1] Nanjing Tech Univ, Jiangsu Natl Synerget Innovat Ctr Adv Mat, Sch Chem & Mol Engn, Inst Adv Synth, Nanjing 211816, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
2,5-FURANDICARBOXYLIC ACID; AEROBIC OXIDATION; HYDROGEN-PRODUCTION; RUTHENIUM DIOXIDE; WATER; CONVERSION; MECHANISM; PLATINUM; AU; PD;
D O I
10.1039/d1nj03292e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) is one of the most attractive reactions to establish a sustainable chemical process based on biomass resources. In this work, a CNT-supported ruthenium-manganese oxide nano-catalyst (RuO2/MnO2/CNT) was employed for the electro-catalytic oxidation of HMF in base-free aqueous solution. The activity test showed that alpha-MnO2 can effectively promote the activity of RuO2 in the oxidation of HMF. In comparison with RuO2/CNT, RuO2/MnO2/CNT possessed a lower activation energy and more than twice the FDCA formation rate. Under the optimized reaction conditions, the RuO2/MnO2/CNT catalyst afforded a FDCA yield of 72.1% in a 0.1 M K2SO4 aqueous solution at a 0.9 V (vs. Ag/AgCl) applied potential. To our knowledge, this is the first demonstration of FDCA formation as the primary product with high yield in an initially neutral electrolyte. The product FDCA can be easily separated after cooling the reaction solution to room temperature.
引用
收藏
页码:21285 / 21292
页数:8
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