“…Noticeably, both RGE and C9PR have only one dominating pyrolysis stage, between 500 and 800 K, accompanied by the cracking of branching chains and the ring-opening reaction of cyclic compounds, and the reaction-order model is found to be the most probable reaction mechanism for pyrolysis of various resins. Results from TG–FTIR/MS analyses show that it is more difficult to crack the bio-based resin into phenyl than the petroleum-based resin, clearly revealing that the tricyclic phenanthrene structures in the bio-based resins are highly thermally stable and require higher pyrolysis temperatures than the cycloaliphatic and aromatic rings in the petro-based resins, and similar results have been reported. , Before starting pyrolysis, a small amount of compounds is released due to the evaporation of moisture and the cracking of weak chemical bonds, which may reduce the fitting quality of the kinetic model. , Among them, the cracking of weak chemical bonds of RGE and HRGE consists of the decarboxylation reaction and the cracking of methyl and isopropyl, with concomitant formation of CO, CO 2 , CH 3 OH, ethane, propane, CH 4 , and isopropanol, which is well supported by the results of TG–FTIR/MS analyses. Similarly, the branching chains of C9PR and HC9PR are cracked first to form straight-chain alkanes and olefins, such as ethane, propane, ethene and propylene.…”