Hydrogenolysis of guaiacol and lignin to phenols over Ni/ Nb2O5-HZSM-5 catalyst

被引:0
作者
Ren, Xiaohong [1 ]
Rong, Zeming [1 ]
Yu, Xiaoqiang [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116012, Peoples R China
来源
MOLECULAR CATALYSIS | 2024年 / 569卷
关键词
Water; Hydrogenolysis; Lignin; Guaiacol; REDOX-NEUTRAL DEPOLYMERIZATION; SELECTIVE HYDRODEOXYGENATION; PHASE HYDRODEOXYGENATION; PORE STRUCTURE; ACTIVE-SITES; EFFICIENT; TRANSFORMATION; NANOPARTICLES; PERFORMANCE; STABILITY;
D O I
10.1016/j.mcat.2024.114559
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
Selective hydrogenolysis of CAr-O bonds in lignin to produce aromatic compounds typically necessitates severe conditions. We developed a Ni/Nb2O5-HZSM-5 catalyst that facilitates direct cleavage of guaiacol's aryl ether bonds at reduced temperatures (200 degrees C) and pressure (0.1 MPa H2), achieving a conversion of 89.5 % with the selectivity of phenol at 81.7 %, while retaining its activity after five cycles. The Ni/Nb2O5-HZSM-5 exhibits a higher yield of phenol (49.1 mmolphenol & sdot;gNi1 & sdot;h1), currently achieving the highest phenol yield among Ni-based catalysts. The addition of Nb2O5 enhances the dispersion of Ni and augments the effective surface area. In addition, the strong interaction of Nb with the HZSM-5 changed the electronic state of Nb and enhanced the resistance of the catalyst to high temperature and mechanical stress. Employing this catalyst for lignin depoly-merization in an aqueous medium led to a 17.0 wt% yield of alkyl phenolic compounds. This approach represents an advancement in biomass resource conversion, circumventing the dependency on high-pressure and precious- metal catalysts, and signaling a new trajectory for sustainable biomass utilization in scientific research
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页数:13
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