Production of liquid fuels from Kraft lignin over bimetallic Ni-Mo supported on ZIF-derived porous carbon catalyst

被引:6
|
作者
Guo, Ge [1 ]
Li, Wenzhi [1 ,2 ]
Ahmed, Tauseef [1 ]
Hu, DuoDuo [3 ]
Cui, Ru [3 ]
Zhang, Baikai [1 ]
Zhang, Xia [1 ]
机构
[1] Univ Sci & Technol China, Lab Basic Res Biomass Convers & Utilizat, Hefei 230026, Peoples R China
[2] Hefei Comprehens Natl Sci Ctr, Inst Energy, Hefei 230031, Peoples R China
[3] Univ Sci & Technol China, Hefei Natl Lab Phys Sci, Microscale & Dept Chem, 96 Jinzhai Rd, Hefei 230026, Peoples R China
关键词
C-O BOND; SELECTIVE HYDRODEOXYGENATION; PLATFORM CHEMICALS; DEPOLYMERIZATION; CLEAVAGE; HYDROTREATMENT; ALKYLPHENOLICS; PHENOLICS; EFFICIENT;
D O I
10.1039/d1ra05354j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Non-noble bimetallic NiMo supported on zeolitic imidazolate framework-derived porous carbon (NiMo@FDC) catalyst for lignin depolymerization has been successfully developed. The synergism between Ni and Mo species in NiMo@FDC catalyst could promote the catalytic cleavage of C-O linkages in Kraft lignin. At a low reaction temperature of 240 degrees C and under 4 MPa H-2, the lignin liquefaction yield was 98.85 wt% and minimum coke yield was 1 wt%, particularly when using 10%NiMo@FDC catalyst. Additionally, at a high reaction temperature of 300 degrees C and under 2 MPa H-2, there was an overall yield of 86 wt% of liquid product and 42 wt% of petroleum ether soluble product. The higher heating value (HHV) increased from 27.65 MJ kg(-1) to 34.11 MJ kg(-1). In the cycling experiment, the bifunctional catalyst also demonstrated reversability and stability. The synergy of Ni hydrogenation sites and Mo coupled adsorption sites identified a possible mechanism path, which could offer considerable potential for lignin depolymerization.
引用
收藏
页码:37932 / 37941
页数:10
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