氢解
催化作用
水滑石
煅烧
木质素
化学
环己醇
有机化学
协同催化
氢氧化物
化学工程
工程类
作者
Han-Bing Gao,Le‐Le Qiu,Fa-Peng Wu,Jian Xiao,Yunpeng Zhao,Liang Ji,Yonghui Bai,Fang-Jing Liu,Jing‐Pei Cao
出处
期刊:Fuel
[Elsevier]
日期:2023-04-01
卷期号:337: 127196-127196
被引量:8
标识
DOI:10.1016/j.fuel.2022.127196
摘要
Catalytic hydrogenolysis of CO bonds in lignin provides a promising route to produce high value-added biofuels and chemicals. However, designing highly active and stable catalysts for this process is still a challenge. Herein, a series of Ni/Al2O3 catalysts were synthesized by calcination and reduction of layered double hydroxide precursors, and their activities were evaluated in the catalytic conversion of lignin-derived compounds. Diphenyl ether was completely converted with a 100% monomeric selectivity (cyclohexane and cyclohexanol) over the optimized Ni/Al2O3-500 under the optimal conditions of 200 ℃, 0.5 MPa H2 and 1.5 h, indicating the excellent catalytic activity in the cleavage of CO bonds of the catalyst. The excellent catalytic performances of Ni/Al2O3-500 were originated from its relatively large specific surface area, well-developed porosity, small crystallite size, high Ni0 concentration and strong interaction between the active metal and support. The reusability experiments show that Ni/Al2O3-500 possesses a relatively high stability for six reuses. Moreover, various lignin model compounds can be completely converted to corresponding monomeric products over Ni/Al2O3-500, indicating the applicability of this ingenious catalyst. The application of the hydrotalcite-derived Ni-based catalysts with high activity and stability provides a promising approach for the efficient hydrogenolysis of lignin derivatives.
科研通智能强力驱动
Strongly Powered by AbleSci AI