Intractable high-T-g thermoplastics processed with epoxy resin: Interfacial adhesion and mechanical properties of the cured blends

Citation
A. Bonnet et al., Intractable high-T-g thermoplastics processed with epoxy resin: Interfacial adhesion and mechanical properties of the cured blends, J POL SC PP, 39(3), 2001, pp. 363-373
Citations number
38
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS
ISSN journal
08876266 → ACNP
Volume
39
Issue
3
Year of publication
2001
Pages
363 - 373
Database
ISI
SICI code
0887-6266(20010201)39:3<363:IHTPWE>2.0.ZU;2-W
Abstract
The intractable, high-temperature-resistant thermoplastics (TPs) polyphenyl enether (PPE) and polyetherimide (PEI) were processed by dissolution into e poxyamine precursors and a subsequent reaction of the precursors. Because t he TP concentration was higher than the critical concentration, the phase s eparation produced a dispersion of crosslinked thermoset (TS) particles int o a TP matrix. The morphology of the blends was examined with transmission electron microscopy and dynamic mechanical thermal spectroscopy, which show ed completion of the phase separation. The interfacial adhesion at the TP-m atrix/TS-particle interface was estimated on TP/TS bilayers to be 10 J/m(2) in PEI blends, whereas it was 70 J/m(2) in PPE blends, where there is stro ng evidence for in situ grafting between PPE phenolic chain ends and glycid yl functions of the reactive TS. Yielding in the compressive mode occurred at an intermediate yield stress between the components' values, and the ane lastic deformation was separated from the plastic deformation. Fractures in the tensile mode occurred through debonding at the matrix/particle interfa ces and coalescence of these defects, which led to microcrack formation and brittle failure. Mode I fracture toughness was, therefore, higher for PPE blends than for PEI blends, a result of the higher interfacial adhesion. Ho wever, a decrease from pure TP was observed. (C) 2000 John Wiley & Sons, In c.