Structural consequences arising from the application of stress to polyolefines
Structural consequences arising from the application of stress to polyolefines
Structural consequences involved during the application of stress to high density polyethylene have been studied by infra-red spectroscopy. Two cases were considered: the plastic deformation of polyethylene in the solid state and the smearing-extrusion of polyethylene in the molten state along a moving tube. In the first case, the concentration of carbonyl and vinyl group formed has been correlated to the number of bonds broken during the plastic deformation under different conditions. It was concluded that in a sample exposed to various temperatures, elongations, times, and of various thicknesses, the number of bonds which broke was not consistent with the Peterlin theory of plastic deformation, wherein a set of solid state rearrangements are envisaged producing a fibrous material from a spherulitic lamellar precursor. The research described in the thesis leads to the suggestion that the mechanical work must be concentrated into very small volumes in the neck region leading to localised melting and subsequent recrystallization. In the second case, a high degree of orientation of the molecules has been achieved along the flow direction concentrated mainly at the polymer-tube interface (inside surface). The evidence shows that the structure varies between a spherulitic, or row nucleated structure produced by a `low stress' induced crystallnization on the die-polymer interface (outside surface), and a `high stress' nucleated crystalline structure where chain folded crystals grow epitaxially on very small amounts of highly oriented chains on the inside surface and aligned along the flow direction. (D82525)
University of Southampton
1987
Lator, Bruno Gratien
(1987)
Structural consequences arising from the application of stress to polyolefines.
University of Southampton, Doctoral Thesis.
Record type:
Thesis
(Doctoral)
Abstract
Structural consequences involved during the application of stress to high density polyethylene have been studied by infra-red spectroscopy. Two cases were considered: the plastic deformation of polyethylene in the solid state and the smearing-extrusion of polyethylene in the molten state along a moving tube. In the first case, the concentration of carbonyl and vinyl group formed has been correlated to the number of bonds broken during the plastic deformation under different conditions. It was concluded that in a sample exposed to various temperatures, elongations, times, and of various thicknesses, the number of bonds which broke was not consistent with the Peterlin theory of plastic deformation, wherein a set of solid state rearrangements are envisaged producing a fibrous material from a spherulitic lamellar precursor. The research described in the thesis leads to the suggestion that the mechanical work must be concentrated into very small volumes in the neck region leading to localised melting and subsequent recrystallization. In the second case, a high degree of orientation of the molecules has been achieved along the flow direction concentrated mainly at the polymer-tube interface (inside surface). The evidence shows that the structure varies between a spherulitic, or row nucleated structure produced by a `low stress' induced crystallnization on the die-polymer interface (outside surface), and a `high stress' nucleated crystalline structure where chain folded crystals grow epitaxially on very small amounts of highly oriented chains on the inside surface and aligned along the flow direction. (D82525)
This record has no associated files available for download.
More information
Published date: 1987
Identifiers
Local EPrints ID: 461865
URI: http://eprints.soton.ac.uk/id/eprint/461865
PURE UUID: 1e4a8044-5c5a-4eab-88ef-4537d55a04c8
Catalogue record
Date deposited: 04 Jul 2022 18:57
Last modified: 04 Jul 2022 18:57
Export record
Contributors
Author:
Bruno Gratien Lator
Download statistics
Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.
View more statistics