Catalytic depolymerization of the dealkaline lignin over Co-Mo-S catalysts in supercritical ethanol

被引:20
作者
Hao, Guojun [1 ]
Liu, Hongying [1 ]
Chang, Zhibing [1 ]
Song, Kechen [1 ]
Yang, Xin [1 ]
Ma, Han [1 ]
Wang, Wenjing [1 ]
机构
[1] China Univ Min & Technol Beijing, Sch Chem & Environm Engn, Lab Utilizat Low Rank Coal, Beijing 100083, Peoples R China
关键词
Lignin depolymerization; Alcoholysis; CoMo sulfide catalyst; Supercritical ethanol; Aromatic compounds; MICROWAVE-ASSISTED DEPOLYMERIZATION; KRAFT LIGNIN; CONVERSION; CHEMICALS; ACID; HYDRODEOXYGENATION; PYROLYSIS;
D O I
10.1016/j.biombioe.2021.106330
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
In this work, lignin depolymerization was examined over CoMo sulfide catalysts supported on different carriers in supercritical ethanol system. The temperature, time, MoS2 and carrier effects on the lignin depolymerization were investigated. 95.76% liquefaction yield with negligible char was achieved over Co-Mo-S/ZrO2 at 340 degrees C for 150 min. The liquid product was mainly composed of C-4-C-8 alcohols, C-4-C-10 esters and C-7-C-10 aromatic compounds. The synergistic effect of active sites and acid-base sites on support played an important role in lignin depolymerization. Furthermore, the Co-Mo-S/ZrO2 catalyst is reusable with 8% loss in liquefaction yield after 5 cyclic runs. We believe that acid/base carriers or additives that can promote the medium to generate abundant free radicals or ions to replace external hydrogen pressure are one of the prospects for the design of depolymerization lignin catalysts.
引用
收藏
页数:11
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