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The role of molecular networks and thermally activated processes in the deformation behavior of polymers
Author(s) -
Ward I. M.
Publication year - 1984
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.760241003
Subject(s) - materials science , shrinkage , composite material , deformation (meteorology) , polymer , stress (linguistics) , polyethylene , slip (aerodynamics) , birefringence , optics , thermodynamics , philosophy , linguistics , physics
The deformation behavior of three polymers, polyethylene terephthalate (PET), polymethylmethacrylate (PMMA), and linear polyethylene (LPE) is considered in terms of two key factors, the stretching of a molecular network and the influence of thermally activated processes. In PET the observation of a natural draw ratio leads to studies of shrinkage, shrinkage force, and optical birefringence to define the nature of the network. The network is further exemplified by measurements of the molecular reorientation in deformation bands, spectroscopic studies of molecular orientation in drawing, and the concept of a true stress‐strain curve. Yield and plastic deformation are also to be considered as thermally activated processes, but it appears that a major part of the flow stress is associated with the stretching of the molecular network. In PMMA the concept of a true stress strain curve also appears to be valuable, but the possibility of network breakdown during deformation has to be admitted as an extra complexity. In LPE the concept of a molecular network embracing both crystalline and non‐crystalline material is helpful in understanding the drawing behavior. There is also direct evidence for the existence of a network from measurements of shrinkage and shrinkage force, and the existence of a true‐stress strain curve. However, the dominant contribution to the flow stress now appears to come from thermally activated processes, with a key contribution from a small activation volume process which is tentatively associated with slip in the crystalline regions.