Abstract
The kinetics of the delayed elasticity in inorganic glasses is explained by a molecular rearrangement mechanism with a distribution of activation energies. An experimental method is described by means of which the spectrum of activation energies for the recovery creep process can be determined. Two such spectra, for a soda-lime-silica glass, and for fused silica are presented. The distributions are strongly skewed toward the high-energy side with peaks at 61 and 42.5 kcal/mole for these two glasses, respectively. In soda-lime-silica the rearranging regions are of ionic size, while in fused silica they contain a large number of ions.
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Dates
Type | When |
---|---|
Created | 21 years, 6 months ago (Feb. 9, 2004, 11:55 a.m.) |
Deposited | 1 year, 7 months ago (Feb. 1, 2024, 7:46 p.m.) |
Indexed | 3 months, 1 week ago (May 26, 2025, 3:05 a.m.) |
Issued | 57 years, 1 month ago (Aug. 1, 1968) |
Published | 57 years, 1 month ago (Aug. 1, 1968) |
Published Print | 57 years, 1 month ago (Aug. 1, 1968) |
@article{Argon_1968, title={Delayed Elasticity in Inorganic Glasses}, volume={39}, ISSN={1089-7550}, url={http://dx.doi.org/10.1063/1.1656927}, DOI={10.1063/1.1656927}, number={9}, journal={Journal of Applied Physics}, publisher={AIP Publishing}, author={Argon, A. S.}, year={1968}, month=aug, pages={4080–4086} }