Molecular simulations of crazes in glassy polymers under cyclic loading

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Main Authors: Laschuetza, Tobias, Ge, Ting, Seelig, Thomas, Rottler, Joerg
Format: Preprint
Published: 2024
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author Laschuetza, Tobias
Ge, Ting
Seelig, Thomas
Rottler, Joerg
author_facet Laschuetza, Tobias
Ge, Ting
Seelig, Thomas
Rottler, Joerg
contents We study with molecular dynamics simulations of a generic bead-spring model the cyclic crazing behaviour of glassy polymers. The aim is to elucidate the mechanical response of sole fibrillated craze matter as well as its interaction with bulk material. The macroscopic stress response exhibits a hysteresis, which is quasi stationary after the first cycle and largely independent of deformation rate and temperature. It results from a complex interplay between constraints imposed by the entanglement network, pore space and pore space closure. Once the craze fibrils are oriented, stretching of the covalent backbone bonds leads to a rapid stress increase. In the initial stages of unloading, a loss in entanglement contact yields a quick stress relaxation in the backbone. During unloading, the craze fibrils undergo a rigid body (i.e.\ stress-free) folding motion due to the surrounding pore space, so that the structural behaviour of craze fibrils during unloading is most accurately described as string-like. The reloading response depends significantly on the degree of pore space closure and the enforced intermolecular interaction during unloading. It ranges from a linear stress increase to a re-cavitation with a re-drawing response. Compared to the bulk stiffness, the craze stiffness is two orders of magnitude lower and as a result, the macro response of coexisting craze and bulk matter is governed by the sole fibrillated craze matter.
format Preprint
id arxiv_https___arxiv_org_abs_2406_14383
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Molecular simulations of crazes in glassy polymers under cyclic loading
Laschuetza, Tobias
Ge, Ting
Seelig, Thomas
Rottler, Joerg
Soft Condensed Matter
We study with molecular dynamics simulations of a generic bead-spring model the cyclic crazing behaviour of glassy polymers. The aim is to elucidate the mechanical response of sole fibrillated craze matter as well as its interaction with bulk material. The macroscopic stress response exhibits a hysteresis, which is quasi stationary after the first cycle and largely independent of deformation rate and temperature. It results from a complex interplay between constraints imposed by the entanglement network, pore space and pore space closure. Once the craze fibrils are oriented, stretching of the covalent backbone bonds leads to a rapid stress increase. In the initial stages of unloading, a loss in entanglement contact yields a quick stress relaxation in the backbone. During unloading, the craze fibrils undergo a rigid body (i.e.\ stress-free) folding motion due to the surrounding pore space, so that the structural behaviour of craze fibrils during unloading is most accurately described as string-like. The reloading response depends significantly on the degree of pore space closure and the enforced intermolecular interaction during unloading. It ranges from a linear stress increase to a re-cavitation with a re-drawing response. Compared to the bulk stiffness, the craze stiffness is two orders of magnitude lower and as a result, the macro response of coexisting craze and bulk matter is governed by the sole fibrillated craze matter.
title Molecular simulations of crazes in glassy polymers under cyclic loading
topic Soft Condensed Matter
url https://arxiv.org/abs/2406.14383