Atomistic simulation of energetic and entropic elasticity in short-chain polyethylenes

The thermodynamical aspects of polymeric liquids subjected to uniaxial elongational flow are examined using atomistically detailed nonequilibrium Monte Carlo simulations. In particular, attention is paid to the energetic effects, in addition to the entropic ones, which occur under conditions of extreme deformation. Atomistic nonequilibrium Monte Carlo simulations of linear polyethylene systems, ranging in molecular length from C 24 to C 78 and for temperatures from 300 to 450 K , demonstrate clear contributions of energetic effects to the elasticity of the system. These are manifested in a conformationally dependent heat capacity, which is significant under large deformations. Violations of the hypothesis of purely entropic elasticity are evident in these simulations, in that the free energy of the system is demonstrated to be composed of significant energetic effects under high degrees of orientation. These arise mainly from favorable intermolecular side-to-side interactions developing in the process of elongation due to chain uncoiling and alignment in the direction of extension.