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

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 lign...

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Detalles Bibliográficos
Autores principales: Guo, Ge, Li, Wenzhi, Ahmed, Tauseef, Hu, DuoDuo, Cui, Ru, Zhang, Baikai, Zhang, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044013/
https://www.ncbi.nlm.nih.gov/pubmed/35498074
http://dx.doi.org/10.1039/d1ra05354j
Descripción
Sumario: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 °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 °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.