Review and Outlook on Regulation of Catalyst Activity, Selectivity, and Stability for Biomass Hydrodeoxygenation Reaction in an Aqueous Environment

被引:3
作者
Cheng, Yifan [1 ]
Shan, Hai [1 ]
Guo, Peng [1 ]
Li, Hao [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Natl Local Joint Engn Lab Energy Conservat Chem Pr, Tianjin Key Lab Chem Proc Safety, Tianjin 300130, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
METAL-SUPPORT INTERACTION; PYROLYSIS BIO-OIL; LEVULINIC ACID; GAMMA-VALEROLACTONE; HETEROGENEOUS CATALYSIS; WATER; HYDROGENATION; CARBON; CONVERSION; LIGNIN;
D O I
10.1021/acs.energyfuels.4c00002
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
One extremely promising approach for turning biomass into useful chemicals and fuels is hydrodeoxygenation (HDO). In the hydrodeoxygenation reaction of biomass and its platform chemicals, water can be used as a reactant or cocatalyst on one hand, thus significantly enhancing the catalytic reaction speed and product selectivity. On the other hand, it is green, nontoxic, and inexpensive. Notably, water is also often reported as a destructive factor. Therefore, the optimal functioning of the catalysts can be efficiently sustained by rationally utilizing the physicochemical interaction between the catalysts and water. This study reviews the regulation of activity, selectivity, and stability of biomass hydrodeoxygenation reactions using various catalysts (noble metal catalysts, transition metal catalysts, etc.) in the aqueous environment. The catalyst structure is optimized by adding metal particles, heteroatom doping modification, and other methods, which combine the complementary effect of water and catalyst to accomplish the regulation effect. The stability of the catalysts is further discussed, and methods to improve the resistance to deactivation are summarized. At last, the perspectives are put forth for the purpose of advancing and enhancing future development.
引用
收藏
页码:6644 / 6658
页数:15
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