Abstract
The investigation of biomass pyrolysis mechanism is crucial for the advancement of pyrolysis-based technology and it is still quite challenging due to the complex nature of lignocellulosic biomass. The application of reactive molecular dynamics simulation offers a powerful strategy to probe more essential information along the reaction process beyond advanced experimental techniques. In this work, the fast pyrolysis process of a lignin dimer, DMPD with representative β-O-4 linkage, is investigated using the ReaxFF method to explore the reaction characteristics, mechanism, and kinetics. The results elucidate that higher temperatures are favorable for the formation of CO, the transformation of guaiacol to catechol, and the breaking of bonds when varying the temperature from 1400 to 2400 K. Guaiacol achieves the highest yield of 13.37% at 2000 K while catechol and CO obtain the highest yield of 6.67% and 8.22% at 2400 K, respectively. Higher heating rates promote the generation of C5-12 products (increased from 70.59% to 78.23%) and the breaking of C-O bond regarding the investigated range of 15.5–170 K/ps. Based upon the time evolution of the reactant and final product distribution under various operating conditions, a first-order kinetic model is derived to calculate the activation energies of C-C, C-H, C-⎔O bonds, and DMPD to be 122.41, 35.18, 52.58, and 52.18 kJ/mol, respectively. A reaction pathway is proposed from the product distribution along the DMPD pyrolysis at 2000 K. The detailed characteristics from ReaxFF simulations enable a better understanding of the complicated pyrolysis mechanism of biomass from a molecular level.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.