Specimens of high-density low-density polyethylene were uniaxially compressed at nominally constant strain-rates ranging from 0.000066 to 0.66 sec-1 at temperatures from 77° to 350°K and hydrostatic pressures from 0.001(latm) to 4 K bar. It was shown that there were significant effects of temperature, pressure and strain rate on both polyethylenes. At small strains (O.O1), the time-temperature and time-pressure superpositions were used successfully to construct the master curves of stress versus reduced strain-rate. These master curves, which were found to have been taken in the range of linear-viscoelastic behaviour of the polymers, were employed to derive the stress-relaxation moduli and the relaxation spectra. The viscoelastic response to temperature and pressure of high-density polyethylene in the transition zone between the γ and α relaxations, and that of low-density polyethylene in the transition zone between the γ and β relaxations have been found to be controlled by the same molecular motion. This motion, an Arrhenius-type activated process, was identified as involving molecular segments of six to eight carbon atoms with an activation energy of 22 Kcal/mole and an activation volume of 110 cm3/mole.
| Identifer | oai:union.ndltd.org:ADTP/277005 |
| Date | January 1971 |
| Creators | Dao, Kim Chung, 1941- |
| Publisher | ResearchSpace@Auckland |
| Source Sets | Australiasian Digital Theses Program |
| Language | English |
| Detected Language | English |
| Rights | Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated., http://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm, Copyright: The author |
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