Core-shell composite particles were prepared by a heterocoagulation and annealing process, in which control of the number of chemical linkages in the interfacial zone without changing other properties was possible using Γve kinds of small size shell particles (SP) with di β erent carboxyl charge dens
Viscoelastic behaviour of epoxy resins modified with poly(methyl methacrylate)
β Scribed by Mondragon, I.; Remiro, P. M.; Martin, M. D.; Valea, A.; Franco, M.; Bellenguer, V.
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 252 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
The viscoelastic behaviour of a stoichiometric diglycidyl ether of bisphenol-A, (DGEBA), 4,4@-diaminodiphenylmethanes (DDM)s epoxy matrix modiΓed with several amounts of poly(methyl methacrylate) (PMMA) has been studied by dynamic-mechanical analysis. Mixtures pre-cured at 80Β‘C ranged from transparency to opacity as thermoplastic content changed from 5 to 15 wt%. These changes have been attributed to variations in the ratio between polymerization rate and phase separation rate when PMMA content increased in the mixtures. When PMMA segregated from the epoxy matrix during curing, it had no inΓuence on the crosslinking density of the epoxy phase. The clear decrease of temperature and activation energy of the b relaxation with respect to those values for the neat matrix, observed for the 5 wt% PMMA-containing mixture but not for the 15 wt% PMMA-containing one, are proposed to be a consequence of physical interactions between the PMMA chains and some epoxy oligomers. The dissimilar variation of the height of the u relaxation with frequency when compared to that for the other relaxations studied, outlines the signiΓcance of physical factors inΓuencing this relaxation.
Society of ( 1998 Chemical Industry
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Poly(methyl methacrylate) (PMMA, M n = 232 000) was used to modify a stoichiometric epoxy (diglycidyl ether of bisphenol A; DGEBA)Β±anhydride (methyl tetrahydrophthalic anhydride; MTHPA) thermoset. PMMA concentrations in the range 3Β±7 wt% led to morphologies consisting of a continuous PMMA-rich regio
Poly(urethane acrylate)/poly(glycidyl methacrylate-co-acrylonitrile) coreshell composite particles were prepared using two-stage emulsion polymerization. Composite particle sizes were varied from 48 to 200 nm by introducing polyoxyethylene groups into the urethane acrylate molecules. The morphology