N-phenylmaleimide-styrene-p-hydroxystyrene terpolymers (PMSH), containing pendant p-hydroxyphenyl groups as functionalities, were prepared and used to improve the toughness of bisphenol-A diglycidyl ether epoxy resin cured with p,p'-diaminodiphenyl sulphone. The terpolymers were effective as modifie
Modification of bismaleimide resin with N-phenylmaleimide-styrene-p-hydroxystyrene and N-phenylmaleimide-styrene-p-allyloxystyrene terpolymers
β Scribed by Takao Iijima; Kohji Ohnishi; Wakichi Fukuda; Masao Tomoi
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 574 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
N-Phenylmaleimide-styrene-p-hydroxystyrene terpolymers (PMSH) and N-phenylmaleimide-styrene-p-allyloxystyrene terpolymers (PMSA), containing pendant functionalities, were prepared and used to improve the toughness of the bismaleimide resin composed of bis(4-maleimidediphenyl)methane and o,o-diallyl bisphenol A. PMSH (0.5 mol % p-hydroxystyrene [HSt] unit) was more effective as a modifier than PMSA (0.5 mol % p-allyloxystyrene unit). When using 5 wt % of PMSH with 0.5 mol % HSt unit, the fracture toughness (K IC ) for the modified resin increased 60% with only a modest loss of flexural strength and with retention in flexural modulus and the glass transition temperature. Morphologies of the modified resins changed from particulate to cocontinuous and to inverted phase structures, depending on the modifier structure and content. The most effective improvement of properties for the modified resins could be attained because of the cocontinuous structure. The toughening mechanism was discussed in terms of the morphological characteristics of the modified bismaleimide resin systems.
π SIMILAR VOLUMES
Emulsion copolymerization of N-phenylmaleimide (PMI) with styrene (St) was conducted via semibatch and batch methods. The effect of monomer mixture composition and method of copolymerization on copolymer structure-property relationships was investigated. The semibatch copolymers have a homogeneous m
The copolymerization and addition reaction of styrene (S) with N-phenylmaleimide (PMI), either neat or in xylene, have been found to proceed at 125Β°C in the presence of 2,2,6,6-tetramethylpiperidin-1-yloxy (TEMPO) radicals. TEMPO-terminated alternating S-PMI copolymers and comonomer adducts were obt