Mesophase pitch is regarded as a profoundly promising candidate for the production of advanced carbon-based multifunctional materials such as carbon fibers, carbon microspheres, and carbon foams owing to its excellent intrinsic properties. Consequently, a deeper understanding of pyrolytic chemistry is indispensable for the efficient and environmentally friendly utilization of mesophase pitch. In this study, details about the structure compositions and microscopic morphologies of petroleum-driven mesophase pitch (pMP) were investigated through ultimate, FTIR, XPS, and C-NMR analyses. Furthermore, a large-scale molecular model of typical pMP with 11,835 atoms was constructed to unveil the comprehensive pyrolysis behaviors and the underlying reactions. Significantly, the evolution of specific chemical bonds and the decomposition of crucial molecular fragments were elucidated within an amalgamation of experimental TG-FTIR/MS and ReaxFF MD simulation. Accordingly, three fundamental reaction stages were artificially divided, including the low-temperature reaction, rapid thermal decomposition, and the molecular condensation reaction. During the rapid thermal decomposition stage, the cleavages of C-C and C-O bonds cooperatively contributed to the formation of CH and HO gaseous products. As the temperature escalated to the molecular condensation stage, the pyrolysis process was governed by the dehydrogenation condensation, accompanied by an augmentation of C-C and H-H bonds and a diminution of C-O and C-H bonds. Additionally, the rare graphitization phenomenon was observed, suggesting a remarkable degree of structural organization in pMP. Overall, the results of ReaxFF MD simulations complement experimental observations, successfully reproducing the microstructure of pMP and atomic-scale pyrolysis behavior, thereby providing invaluable insights for the rational guidance of efficient utilization of pMP and other related carbonaceous precursors.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11547812PMC
http://dx.doi.org/10.3390/ma17215318DOI Listing

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