Delineating nature of stress responses during ductile uniaxial extension of polycarbonate glass. (20th April 2016)
- Record Type:
- Journal Article
- Title:
- Delineating nature of stress responses during ductile uniaxial extension of polycarbonate glass. (20th April 2016)
- Main Title:
- Delineating nature of stress responses during ductile uniaxial extension of polycarbonate glass
- Authors:
- Lin, Panpan
Liu, Jianning
Wang, Shi-Qing - Abstract:
- Abstract: We carry out simultaneous mechanical and IR-thermal-imaging-based temperature measurements of tensile extension on untreated, milled (mechanically "rejuvenated") and melt-stretched bisphenol A-polycarbonate (PC). The extension is found to cause significant buildup of both excess internal energy u2 and plastic dissipation. The magnitude of u2 is one to two orders of magnitude higher than the energy involved in rubbery elastic deformation. While the ratio of u2 to the mechanical work w decreases with increasing rate of extension for untreated PC, milled PC is found to be more dissipative at lower rates. Homogeneous extension of melt-stretched PC in the post-yield regime including strain hardening behavior reveals largely non-dissipative responses, emphasizing the plastic deformation of glassy polymer may not be fully dissipative. The experimental results clearly indicate that a significant component of stress can be intrasegmental leading to the observed buildup of internal energy by distortions of covalent bonds. The glassy polymer physics at the chain level complements the more familiar idea of inter-segmental dissipation as the dominant event during plastic deformation. Graphical abstract: Highlights: Simultaneous mechanical and thermal measurements of a glassy polymer reveal significant internal (potential) energy storage during large ductile extension. The internal energy buildup is both intrasegmental and intersegmental in origin. Strain hardening involvesAbstract: We carry out simultaneous mechanical and IR-thermal-imaging-based temperature measurements of tensile extension on untreated, milled (mechanically "rejuvenated") and melt-stretched bisphenol A-polycarbonate (PC). The extension is found to cause significant buildup of both excess internal energy u2 and plastic dissipation. The magnitude of u2 is one to two orders of magnitude higher than the energy involved in rubbery elastic deformation. While the ratio of u2 to the mechanical work w decreases with increasing rate of extension for untreated PC, milled PC is found to be more dissipative at lower rates. Homogeneous extension of melt-stretched PC in the post-yield regime including strain hardening behavior reveals largely non-dissipative responses, emphasizing the plastic deformation of glassy polymer may not be fully dissipative. The experimental results clearly indicate that a significant component of stress can be intrasegmental leading to the observed buildup of internal energy by distortions of covalent bonds. The glassy polymer physics at the chain level complements the more familiar idea of inter-segmental dissipation as the dominant event during plastic deformation. Graphical abstract: Highlights: Simultaneous mechanical and thermal measurements of a glassy polymer reveal significant internal (potential) energy storage during large ductile extension. The internal energy buildup is both intrasegmental and intersegmental in origin. Strain hardening involves considerable elastic deformation, leading to much higher energy than that associated with rubbery elasticity. The high intrasegmental stress is plausibly due to emergence of chain tension in load-bearing strands of the chain network. … (more)
- Is Part Of:
- Polymer. Volume 89(2016)
- Journal:
- Polymer
- Issue:
- Volume 89(2016)
- Issue Display:
- Volume 89, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 89
- Issue:
- 2016
- Issue Sort Value:
- 2016-0089-2016-0000
- Page Start:
- 143
- Page End:
- 153
- Publication Date:
- 2016-04-20
- Subjects:
- Glassy polymers -- Internal energy -- Plastic dissipation -- Strain hardening
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00323861 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.polymer.2016.02.051 ↗
- Languages:
- English
- ISSNs:
- 0032-3861
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2782.xml