Catalytic hydropyrolysis of lignin: Insights into the effect of Ni catalyst and hydrogen using ReaxFF molecular dynamics simulation

Abstract

Catalytic hydropyrolysis (CHP) of lignin as an emerging technology provides an efficient way of utilizing waste resources and promoting the production of alternative fuels and valuable bio-based products. The reinforcement of selective catalysts and hydrogen facilitates the overall conversion process but the mechanism remains difficult to clarify due to the complex nature of the system. This work employs a ReaxFF reactive molecular dynamics simulation method to explore the CHP of lignin dimer DMPD and the reaction mechanism at the molecular level. The results suggest that the hydropyrolysis (HP) system achieves a deoxygenation degree of 12.0 % for liquid products and the incorporation of hydrogen into pyrolysis suppresses the production of CO while promoting H2O and CH4 generation. The introduction of the Ni catalyst in the CHP system results in a liquid product yield of 68.9 wt % at 2000 K with a higher deoxygenation degree of 14.6 % due to the participation of a large amount of •H radicals species dissociated on the catalyst surface. The CHP reactions remarkably promote the production of phenols such as guaiacol and catechol and catechol is more likely to generate from the dynamic evolution of reaction intermediates. The integrated system also improves the production of H2O and light hydrocarbons like CH4 and C2H6. The first-order kinetic model reveals that the average activation energies of C-C, C-H, C-O bonds, and DMPD in the CHP system are significantly reduced to 113.12, 55.79, 59.99, and 132.17 kJ/mol in contrast to HP. The results indicate that the CHP system is more favorable for producing desirable liquid products with lower energy barriers.