Effect of MnO2 Crystal Structure on Aerobic Oxidation of 5-Hydroxymethylfurfural to 2,5-Furandicarboxylic Acid

被引:444
作者
Hayashi, Eri [1 ]
Yamaguchi, Yui [1 ]
Kamata, Keigo [1 ,3 ]
Tsunoda, Naoki [1 ]
Kumagai, Yu [2 ,3 ]
Oba, Fumiyasu [1 ]
Hara, Michikazu [1 ,4 ]
机构
[1] Tokyo Inst Technol, Inst Innovat Res, Lab Mat & Struct, Yokohama, Kanagawa 2268503, Japan
[2] Tokyo Inst Technol, Mat Res Ctr Element Strategy, Yokohama, Kanagawa 2268503, Japan
[3] Japan Sci & Technol Agcy JST, Precursory Res Embryon Sci & Technol PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan
[4] Japan Sci & Technol Agcy JST, Adv Low Carbon Technol Res & Dev Program ALCA, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
OCTAHEDRAL MOLECULAR-SIEVES; OXYGEN REDUCTION REACTION; BASE-FREE CONVERSION; SELECTIVE OXIDATION; WATER OXIDATION; VACANCY FORMATION; MANGANESE OXIDES; CATALYTIC PERFORMANCE; HIGHLY EFFICIENT; PHASE OXIDATION;
D O I
10.1021/jacs.8b09917
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aerobic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA) as a bioplastics monomer is efficiently promoted by a simple system based on a nonprecious-metal catalyst of MnO2 and NaHCO3. Kinetic studies indicate that the oxidation of 5-formyl-2-furancarboxylic acid (FFCA) to FDCA is the slowest step for the aerobic oxidation of HMF to FDCA over activated MnO2. We demonstrate through combined computational and experimental studies that HMF oxidation to FDCA is largely dependent on the MnO2 crystal structure. Density functional theory (DFT) calculations reveal that vacancy formation energies at the planar oxygen sites in alpha- and gamma-MnO2 are higher than those at the bent oxygen sites. beta- and lambda-MnO2 consist of only planar and bent oxygen sites, respectively, with lower vacancy formation energies. Consequently, beta- and lambda-MnO2 are likely to be good candidates as oxidation catalysts. On the other hand, experimental studies reveal that the reaction rates per surface area for the slowest step (FFCA oxidation to FDCA) decrease in the order of beta-MnO2 > lambda-MnO2 > gamma-MnO2 alpha-MnO2 > delta-MnO2 > epsilon-MnO2; the catalytic activity of beta-MnO2 exceeds that of the previously reported activated MnO2 by three times. The order is in good agreement not only with the DFT calculation results, but also with the reduction rates per surface area determined by the H-2-temperature-programmed reduction measurements for MnO2 catalysts. The successful synthesis of high-surface-area beta-MnO2 significantly improves the catalytic activity for the aerobic oxidation of HMF to FDCA.
引用
收藏
页码:890 / 900
页数:11
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