Selective Hydrogenation of 5-Hydroxymethylfurfural via Zeolite Encapsulation to Avoid Further Hydrodehydroxylation

被引：37
作者：
Chen, Qiang [1 ,2 ]
Li, Tianhao [2 ]
Zhou, Yiming [2 ]
Bi, Yunfei [3 ]
Guo, Shuai [4 ]
Liu, Xuan [2 ]
Kang, Haozhe [2 ]
Wang, Mengyue [2 ]
Liu, Lei [4 ]
Xing, Enhui [3 ]
Yang, Dongyuan [5 ,6 ]
机构：
[1] Sun Yat Sen Univ, Sch Chem Engn & Technol, Zhuh Ai 519082, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, Xian 710049, Shaanxi, Peoples R China
[3] Sinopec, Res Inst Petr Proc, Beijing 100083, Peoples R China
[4] Chinese Acad Sci, Inst Proc Engn, Beijing 100190, Peoples R China
[5] Shaanxi Yanchang Petr Grp Corp Ltd, Xian 710065, Shaanxi, Peoples R China
[6] Dalian Inst Chem Phys, Xian Clean Energy Chem Res Inst, Xian 710065, Shaanxi, Peoples R China
来源：
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH | 2020年 / 59卷 / 26期
基金：
中国国家自然科学基金;
关键词：
TOTAL-ENERGY CALCULATIONS; METAL-CLUSTERS; CO OXIDATION; NANOPARTICLES; EFFICIENT; SIZE; NANOCRYSTALS; DISPERSION; CATALYSTS; ATOMS;
D O I：
10.1021/acs.iecr.0c01320
中图分类号：
TQ [化学工业];
学科分类号：
0817 ;
摘要：
Pt nanoparticles encapsulated into zeolite Y (denoted as Pt@Y) exhibited approaching 100% catalytic selectivity to 2,5-bis-(hydroxymethyl)-furan (BHMF) at full conversion of 5-hydroxymethylfurfural (HMF) in the presence of H-2, coupled with good reusability. Zeolite Y constrained HMF to be adsorbed on encapsulated Pt nanoparticle surface via either the end of aldehyde groups or hydroxyl groups in thermodynamically unfavorable end-on mode to enlarge the gap in the activation energies between hydrogenation of aldehyde groups and hydrodehydroxylation of hydroxyl groups to favor selectivity enhancement via avoidance of further hydrodehydroxylation at moderate conditions, which provide a general method to avoid thermodynamics-regulated flat-lying conformation for simultaneous activation on the furan ring, aldehyde, and hydroxyl groups.
引用
收藏
页码：12004 / 12012
页数：9
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