Plastic Deformation of Semicrystalline Polyethylene under Extension, Compression, and Shear Using Molecular Dynamics Simulation

Plastic deformation of the stack of alternating crystal and amorphous layers typical of semicrystalline polyethylene is studied by molecular dynamics simulation. A previous investigation of the semicrystalline layered stack undergoing isochoric extension1 is extended here to include several new mode...

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Main Authors: Kim, Jun Mo, Locker, Rebecca, Rutledge, Gregory C.
Drugi avtorji: Massachusetts Institute of Technology. Department of Chemical Engineering
Format: Article
Jezik:en_US
Izdano: American Chemical Society (ACS) 2015
Online dostop:http://hdl.handle.net/1721.1/96081
https://orcid.org/0000-0001-8137-1732
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author Kim, Jun Mo
Locker, Rebecca
Rutledge, Gregory C.
author2 Massachusetts Institute of Technology. Department of Chemical Engineering
author_facet Massachusetts Institute of Technology. Department of Chemical Engineering
Kim, Jun Mo
Locker, Rebecca
Rutledge, Gregory C.
author_sort Kim, Jun Mo
collection MIT
description Plastic deformation of the stack of alternating crystal and amorphous layers typical of semicrystalline polyethylene is studied by molecular dynamics simulation. A previous investigation of the semicrystalline layered stack undergoing isochoric extension1 is extended here to include several new modes of deformation: isostress extension, isostress compression, and isochoric shear, at 350 K and deformation rates of 5 × 107 and 5 × 106 s–1. The observed stress–strain responses are interpreted in terms of the underlying structural evolution of the material for each mode of deformation. Under tensile deformation, crystallographic slip was observed at low strains (0 < e3 < 0.08) regardless of deformation rate. Different yield mechanisms were observed for the different deformation rates. To explain the response at intermediate strains (0.08 < e3 < 0.26), we introduce the concept of “bridging entanglements”, which are temporary, physical bridges between crystal lamellae comprising entanglements involving chain segments belonging to different crystal lamellae. At high strains (e3 > 0.26), melting and recrystallization were observed at the slower deformation rate, while surface melting and cavitation were observed at the faster deformation rate. Under compressive deformation at the slower deformation rate, crystallographic slip was again observed at low strains. For the faster compressive deformation, an initial period of rapid stress growth at low strain was observed. This initial stress growth then transitions to a process of fine crystallographic slip at a strain of e3 = −0.005. At intermediate strains under compressive deformation, the release of bridging entanglements is observed for both strain rates. However, no melting or recrystallization phenomena were observed under compression, even at the highest strains simulated (e3 = −0.33). Under shear deformation, interlamellar slip was observed for both zx and zy shear (strain gradient parallel to stacking direction). Chain segments tend to stretch and align in the shear direction. Interestingly, under shear deformation this semicrystalline polyethylene exhibits transient behavior typical of non-Newtonian fluids.
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spelling mit-1721.1/960812022-09-29T22:21:18Z Plastic Deformation of Semicrystalline Polyethylene under Extension, Compression, and Shear Using Molecular Dynamics Simulation Kim, Jun Mo Locker, Rebecca Rutledge, Gregory C. Massachusetts Institute of Technology. Department of Chemical Engineering Rutledge, Gregory C. Kim, Jun Mo Rutledge, Gregory C. Plastic deformation of the stack of alternating crystal and amorphous layers typical of semicrystalline polyethylene is studied by molecular dynamics simulation. A previous investigation of the semicrystalline layered stack undergoing isochoric extension1 is extended here to include several new modes of deformation: isostress extension, isostress compression, and isochoric shear, at 350 K and deformation rates of 5 × 107 and 5 × 106 s–1. The observed stress–strain responses are interpreted in terms of the underlying structural evolution of the material for each mode of deformation. Under tensile deformation, crystallographic slip was observed at low strains (0 < e3 < 0.08) regardless of deformation rate. Different yield mechanisms were observed for the different deformation rates. To explain the response at intermediate strains (0.08 < e3 < 0.26), we introduce the concept of “bridging entanglements”, which are temporary, physical bridges between crystal lamellae comprising entanglements involving chain segments belonging to different crystal lamellae. At high strains (e3 > 0.26), melting and recrystallization were observed at the slower deformation rate, while surface melting and cavitation were observed at the faster deformation rate. Under compressive deformation at the slower deformation rate, crystallographic slip was again observed at low strains. For the faster compressive deformation, an initial period of rapid stress growth at low strain was observed. This initial stress growth then transitions to a process of fine crystallographic slip at a strain of e3 = −0.005. At intermediate strains under compressive deformation, the release of bridging entanglements is observed for both strain rates. However, no melting or recrystallization phenomena were observed under compression, even at the highest strains simulated (e3 = −0.33). Under shear deformation, interlamellar slip was observed for both zx and zy shear (strain gradient parallel to stacking direction). Chain segments tend to stretch and align in the shear direction. Interestingly, under shear deformation this semicrystalline polyethylene exhibits transient behavior typical of non-Newtonian fluids. Exxon Mobil Corporation 2015-03-19T16:23:55Z 2015-03-19T16:23:55Z 2014-04 2014-03 Article http://purl.org/eprint/type/JournalArticle 0024-9297 1520-5835 http://hdl.handle.net/1721.1/96081 Kim, Jun Mo, Rebecca Locker, and Gregory C. Rutledge. “Plastic Deformation of Semicrystalline Polyethylene Under Extension, Compression, and Shear Using Molecular Dynamics Simulation.” Macromolecules 47, no. 7 (April 8, 2014): 2515–2528. https://orcid.org/0000-0001-8137-1732 en_US http://dx.doi.org/10.1021/ma402297a Macromolecules Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. application/pdf American Chemical Society (ACS) Prof. Rutledge via Erja Kajosalo
spellingShingle Kim, Jun Mo
Locker, Rebecca
Rutledge, Gregory C.
Plastic Deformation of Semicrystalline Polyethylene under Extension, Compression, and Shear Using Molecular Dynamics Simulation
title Plastic Deformation of Semicrystalline Polyethylene under Extension, Compression, and Shear Using Molecular Dynamics Simulation
title_full Plastic Deformation of Semicrystalline Polyethylene under Extension, Compression, and Shear Using Molecular Dynamics Simulation
title_fullStr Plastic Deformation of Semicrystalline Polyethylene under Extension, Compression, and Shear Using Molecular Dynamics Simulation
title_full_unstemmed Plastic Deformation of Semicrystalline Polyethylene under Extension, Compression, and Shear Using Molecular Dynamics Simulation
title_short Plastic Deformation of Semicrystalline Polyethylene under Extension, Compression, and Shear Using Molecular Dynamics Simulation
title_sort plastic deformation of semicrystalline polyethylene under extension compression and shear using molecular dynamics simulation
url http://hdl.handle.net/1721.1/96081
https://orcid.org/0000-0001-8137-1732
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