解聚
催化作用
木质素
氢解
甲醇
化学
有机化学
溶剂
香兰素
双金属片
碳纤维
产量(工程)
材料科学
复合数
冶金
复合材料
作者
Yun Wu,Qi Dang,Tong Wu,Taoning Lei,Kaige Wang,Zhongyang Luo
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-03-15
卷期号:37 (7): 5206-5219
被引量:12
标识
DOI:10.1021/acs.energyfuels.3c00063
摘要
Due to their diverse functional groups and structural composition, carbon-based catalysts exhibit superior performance in various catalytic reaction systems, such as hydrogenolysis, hydrogenation, and oxidation. Herein, we propose an effective strategy of lignin liquid-phase depolymerization by applying the designed lignin-based carbon catalysts to produce aromatic chemicals. A series of Ni–Mo bimetallic carbon-based catalysts were synthesized to explore the effect of different preparation methods on the catalytic activity. The results demonstrate that the embedded Ni–Mo/C-WMO catalyst with multi-active sites of Ni, MoO3, and Mo2C results in a prominent catalytic effect on lignin depolymerization. The Ni–Mo/C-WMO catalyst can achieve a lignin conversion of 87.62% with a 42.25% monophenol yield in the methanol and water system. With the synergistic contribution of multiple active sites of the catalyst and the mixed-solvent system (water, methanol, and 1, 4-dioxane), a remarkably high yield of 62.95% of mono-phenolic compound was achieved at 260 °C and 3 MPa N2 with a reaction time of 4 h. The selectivity of 2-methoxy-4-methylphenol and 2-methoxy-4-ethylphenol in liquid products was 40.85 and 36.42%, respectively. Vanillin, a typical product from lignin depolymerization reported in the literature, was further degraded to monophenol in this system. The outcomes also confirmed that the in situ hydrogen production system of methanol and water coupled with 1,4-dioxane facilitated the lignin depolymerization significantly.
科研通智能强力驱动
Strongly Powered by AbleSci AI