Revealing the deformation mechanism of amorphous polyethylene subjected to cycle loading via molecular dynamics simulations

QH Fang and YY Tian and H Wu and J Li, RSC ADVANCES, 8, 32377-32386 (2018).

DOI: 10.1039/c8ra05868g

Despite tremendous efforts being devoted to the study of the deformation behavior of polyethylene, the deformation mechanism of an amorphous polyethylene polymer under cycle shear-loading remains largely unknown. Here, we report the cycle shear deformation mechanism of an amorphous polyethylene polymer using molecular dynamics (MD) simulations. The stress-strain behaviors, including the elastic, yield, strain hardening, and strain softening regions, are qualitatively in agreement with the previous results. The values of the yield stress, Young's modulus and ultimate strength obtained from MD simulations are consistent with the previous data. The effects of the shear strain rate, temperature, and cycle shear-loading number on the stress-strain behaviors are investigated. Higher strain rate and a lower temperature result in a higher strength in the amorphous polyethylene polymer, attributed to the agglomeration of high local strains. With the increase of the cycle shear-loading number, the high strain region gradually expands from the upper and lower surface to the interior of the polyethylene polymer matrix, which provides the origin of crack initiation. The energy contributions are used in elucidating the inherent deformation mechanisms within the elastic, yielding, strain hardening, and strain softening regions, and the variation trend of energy is consistent with the stress-strain response.

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