Ni5Fe5/Al2O3 catalytic hydrogenolysis of lignin: mechanism investigation and selectivity regulation

被引:0
作者
Shen, Zhensheng [1 ,2 ]
Wang, Wei [1 ,2 ]
Pan, Lun [1 ,2 ,3 ]
Huang, Zhenfeng [1 ,2 ]
Zhang, Xiangwen [1 ,2 ,3 ]
Shi, Chengxiang [1 ,2 ]
Zou, Ji-Jun [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Minist Educ, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
[3] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
关键词
LIGNOCELLULOSE FRACTIONATION; PHENOLIC MONOMERS; DEPOLYMERIZATION; CONVERSION; BIOMASS; RU; CHEMICALS; CLEAVAGE; FRAGMENTATION; NI;
D O I
10.1039/d3gc01988h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of novel catalysts to regulate product selectivity and insight into the mechanism of lignin hydrogenolysis are important for the comprehensive utilization of lignocellulose. Herein, we present a non-precious bimetallic catalyst Ni5Fe5/Al2O3 with improved catalytic performance relative to commercial Pd/C and Ni-10/Al2O3 for hydrogenolysis of woody sawdust. In particular, the selectivity of propylguaiacol and propylsyringol is 79.1%. We developed kinetic experimental studies on beta-O-4 model compounds and directly monitored the coniferyl alcohol or sinapyl alcohol intermediates in the reaction system for the first time. This directly demonstrates the lignin hydrolysis reaction pathway with simultaneous breakage of C-alpha-OH and C-beta-O. In the catalytic system, the reason for the difference in selectivity between Ni5Fe5/Al2O3 and other catalysts is their different hydrogenation pathways for intermediates coniferyl alcohol or sinapyl alcohol. Our work provides both an efficient catalyst and insight into understanding and regulating the mechanism of lignin hydrogenolysis.
引用
收藏
页码:7782 / 7793
页数:12
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