Modelling the mechanical and strain recovery behaviour of partially crystalline PLA
View/ Open
Sweeney_et_al_Polymers (4.510Mb)
Download
Publication date
2019-08-13Rights
© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).Peer-Reviewed
YesOpen Access status
openAccessAccepted for publication
2019-08-09
Metadata
Show full item recordAbstract
This is a study of the modelling and prediction of strain recovery in a polylactide. Strain recovery near the glass transition temperature is the underlying mechanism for the shape memory in an amorphous polymer. The investigation is aimed at modelling such shape memory behaviour. A PLA-based copolymer is subjected to stress–strain, stress relaxation and strain recovery experiments at large strain at 60 C just below its glass transition temperature. The material is 13% crystalline. Using published data on the mechanical properties of the crystals, finite element modelling was used to determine the effect of the crystal phase on the overall mechanical behaviour of the material, which was found to be significant. The finite element models were also used to relate the stress–strain results to the yield stress of the amorphous phase. This yield stress was found to possess strain rate dependence consistent with an Eyring process. Stress relaxation experiments were also interpreted in terms of the Eyring process, and a two-process Eyring-based model was defined that was capable of modelling strain recovery behaviour. This was essentially a model of the amorphous phase. It was shown to be capable of useful predictions of strain recovery.Version
Published versionCitation
Sweeney J, Spencer P, Nair K et al (2019) Modelling the mechanical and strain recovery behaviour of partially crystalline PLA. Polymers. 11(8): 1342.Link to Version of Record
https://doi.org/10.3390/polym11081342Type
Articleae974a485f413a2113503eed53cd6c53
https://doi.org/10.3390/polym11081342