This article reports the glass transition temperatures of poly-( p-phenylenediamine-alt-2,6-diformyl multiphenyl) predicted by both the group contribution method and the molecular dynamics simulations. The related modeling method and the degree of polymerization, density, specific volume, radius of volume, radius of rotation, and non-bonding energy terms with temperature are analyzed in depth. The bulk modulus, shear modulus, compressibility, Young’s modulus, and Poisson’s ratio of poly-( p-phenylenediamine-alt-2,6-diformyl multiphenyl) at room temperature are simulated by molecular dynamics. The results show that the simulated glass transition temperatures of poly-( p-phenylenediamine-alt-2,6-diformyl multiphenyl) are greater than 480 K, which indicates that poly-( p-phenylenediamine-alt-2,6-diformyl multiphenyl) can be expected to be used as a high-temperature-resistant material. As the number of rigid benzene rings on the molecular side chain increases, the glass transition temperature decreases, with an average decrease of 10 K for each additional benzene ring. The free volume theory can explain the glass transitions of poly-( p-phenylenediamine-alt-2,6-diformyl multiphenyl). The modulus and density of poly-( p-phenylenediamine-alt-2,6-diformyl multiphenyl) change accordingly with an increase of rigid benzene rings on the side chain, probably due to the fact that the flexibility of the polymers changes accordingly as the number of benzene rings on the side chain increases.
Using the group contribution method and molecular dynamics to predict the glass transition temperatures and mechanical properties of poly-(p-phenylenediamine-alt-2, 6-diformyl multiphenyl)
