Catalytic hydrogenolysis of lignin and model compounds over highly dispersed Ni-Ru/Al2O3 without additional H2

Selective hydrogenolysis of lignin is an attractive strategy for valorizing lignin to fuels/value-added chemicals and developing novel and highly active heterogeneous catalysts is crucial. Herein, a highly dispersed Ni-Ru/Al2O3 catalyst prepared by a coprecipitation method using layered double hydroxide as precursor was reported. Various lignin model compounds were used to evaluate the catalyst activity. The results show that all the model compounds can be completely transformed into arenes and phenol below 150 ? using isopropanol as hydrogen source, and the latter was easily reduced to cyclohexanol. Kinetics study reveals that apparent activation energies increase in the order: benzyl phenyl ether (90.6 kJ/mol) < phenethoxybenzene (126.7 kJ/mol) < diphenyl ether (172.2 kJ/mol). 2D HSQC NMR analysis exhibits that most of C-O linkages in lignin were cleaved during hydrogenolysis over Ni-Ru/Al2O3 . The results indicate that the bimetallic Ni-Ru catalyst has a high activity for catalyzing hydrogenolysis of lignin and model compounds. The catalyst was characterized with multiple tools. The results suggest that Ni and Ru nanoparticles in the catalyst are highly dispersed and a strong interaction exists between Ni and Ru, which should be responsible for promoting the hydrogenolysis of lignin and model compounds.

Automated summary

Selective hydrogenolysis of lignin can be achieved using a highly dispersed Ni-Ru/Al2O3 catalyst. The catalyst exhibits high activity for the hydrogenolysis of lignin and model compounds, with the apparent activation energy depending on the structure of the substrates.