The empirical form for the dependence, Tg(n) = Tg(co) (1 + a / n ) , of the glass transition temperature Tg on the average number n of repeat units between crosslinks, is generalized for randomly crosslinked high polymers. The new form, TJn) is based on a correlation study of data for 77 samples of
A generalized theory for the glass transition temperature of crosslinked and uncrosslinked polymers
β Scribed by H. Stutz; K.-H. Illers; J. Mertes
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 729 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0887-6266
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β¦ Synopsis
Abstract
A generalized theory for the glass transition temperature of crosslinked and uncrosslinked polymers has been developed, which takes into account the influences of end groups, branching, and crosslinking, and their functionality distribution. DiBenedetto's theory was found to correctly characterize the influence of crosslinks on the glass temperature. Normalized to constant crosslink functionality, the crosslink constant is a universal parameter suggesting that the entropic theory of glasses is applicable to crosslinked systems. Data on linear polymers and networks from the crosslinking of polymer chains, vinyl/divinylβcopolymers and stepβgrowth polymers, such as polyurethanes, amineβcured epoxies, or inorganic glasses, are presented.
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## Abstract Dynamic mechanical properties and glass transition temperatures were measured for crosslinked polymers derived from diallyl succinate monomers. The mobility of the diester having an elevenβmembered ring and of homologous structures which are introduced in the crosslinked polymer system,