Catalyst Design for Selective Hydrodeoxygenation of Glycerol to 1,3-Propanediol

被引:48
|
作者
Miao, Gai [1 ,2 ]
Shi, Lei [1 ]
Zhou, Zhimin [1 ,2 ]
Zhu, Lijun [1 ,2 ]
Zhang, Yanfei [1 ,2 ]
Zhao, Xinpeng [1 ,2 ]
Luo, Hu [1 ]
Li, Shenggang [1 ,2 ,3 ]
Kong, Lingzhao [1 ,2 ]
Sun, Yuhan [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Adv Res Inst, CAS Key Lab Low Carbon Convers Sci & Engn, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
基金
中国国家自然科学基金;
关键词
glycerol; heterogeneous catalysis; hydrodeoxygenation; density functional theory calculations; interfaces; TUNGSTEN-OXIDE; NOBLE-METALS; HYDROGENOLYSIS; CONVERSION; WOX; ZEOLITE; MORDENITE; STABILITY; CHEMICALS; ZIRCONIA;
D O I
10.1021/acscatal.0c04167
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
Biomass-derived glycerol is an ideal feedstock for replacing fossil resources in manufacturing propanediols (PDOs) via selective hydrodeoxygenation (HDO) because of the high atomic economy. However, it remains a great challenge to design a competitive HDO catalyst for selectively converting glycerol into 1,3-PDO owing to the higher thermodynamic stability of 1,2-PDO. In this work, theoretical analysis and first principles calculations were adopted for the design and development of an efficient HDO catalyst. The designed Pt/W/beta catalyst has low Pt and W loadings, and exhibits high performance in the HDO reaction with glycerol conversion (84.2%), 1,3-PDO selectivity (46.1%), and total C-3 alcohol selectivity (>90%) under mild reaction conditions. Furthermore, experimental structure-performance relationship of the HDO catalyst was found to be consistent with our first principles prediction, confirming the important role of the interfacial structure in the HDO reaction.
引用
收藏
页码:15217 / 15226
页数:10
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