Epoxy Networks Modified by a New Class of Oligomeric Silsesquioxanes Bearing Multiple Intramolecular Rings Formed through SiOC Bonds
✍ Scribed by Ignacio E. dell'Erba; Diana P. Fasce; Roberto J. J. Williams; Rosa Erra-Balsells; Yuko Fukuyama; Hiroshi Nonami
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 153 KB
- Volume
- 289
- Category
- Article
- ISSN
- 1438-7492
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✦ Synopsis
Abstract
Summary: A new class of silsesquioxane (SSO), containing species with two to nine Si atoms bearing multiple intramolecular rings formed through SiOC bonds, was synthesized as a glassy powder. It was characterized by UV‐MALDI‐TOF MS, ^29^Si NMR and FT IR. Solutions containing different amounts of SSO in the diglycidyl ether of bisphenol A (DGEBA), were homopolymerized in the presence of (4‐dimethylamino)pyridine (DMAP) as initiator, leading to SSO‐modified epoxy networks. SSO species were covalently bonded to the epoxy network without any evidence of phase separation. The SSO addition provoked an increase in the elastic modulus in the glassy state explained by an increase in the cohesive energy density. The SSO addition gave also place to an increase in the intensity of tan δ and a decrease in both the glass transition temperature and the elastic modulus in the rubbery state. This was explained by a decrease in crosslink density associated with the flexibility of SSO structures. DMAP was much more effective than other usual initiators (like benzyldimethylamine, BDMA), in increasing the crosslink density of the resulting epoxy network. This led to high values of the glass transition temperature and the elastic modulus in the rubbery state.
Schematic representation of the chemical structure of the most significant species containing three Si atoms, present in the silsesquioxane.
imageSchematic representation of the chemical structure of the most significant species containing three Si atoms, present in the silsesquioxane.