POLY(BETA-HYDROXYNONANOATE) AND POLYSTYRENE OR POLY(METHYL METHACRYLATE) GRAFT-COPOLYMERS - MICROSTRUCTURE CHARACTERISTICS AND MECHANICAL AND THERMAL-BEHAVIOR

Authors
Citation
B. Hazer, POLY(BETA-HYDROXYNONANOATE) AND POLYSTYRENE OR POLY(METHYL METHACRYLATE) GRAFT-COPOLYMERS - MICROSTRUCTURE CHARACTERISTICS AND MECHANICAL AND THERMAL-BEHAVIOR, Macromolecular chemistry and physics, 197(2), 1996, pp. 431-441
Citations number
24
Categorie Soggetti
Polymer Sciences
ISSN journal
10221352
Volume
197
Issue
2
Year of publication
1996
Pages
431 - 441
Database
ISI
SICI code
1022-1352(1996)197:2<431:PAPOPM>2.0.ZU;2-T
Abstract
Active polymers containing peroxide groups were synthesized via polyme rization of styrene or methyl methacrylate with oligo(adipoyl 2,5-dime thylhexane-2,5-diyl peroxide) (OAHP) or oligo(2,5-dimethylhexane-2,5-d iyl 4,4'-azobis(4-cyanoperoxyvalerate)) (LUAB). Poly(beta-hydroxynonan oate) (PHN) and the active polymer were mixed, and free radical grafti ng reactions were carried out to optimize mechanical and viscoelastic properties of PHN. The ''active'' vinyl polymers polystyrene (PS) and poly(methyl methacrylate) (PMMA) were grafted onto PHN chains or cleav ed them, depending on the PHN/active polymer mass ratio and the peroxy gen content of the active polymer. The increase in tensile strength (f ) and strain (epsilon) was observed to be maximum in graft copolymers having vinyl polymer contents less than 20 wt.-%. SEM micrographs show ed surface topography. Phase-separated graft copolymers reveal dispers ed phase particles, micrometer and submicrometer sized particles, and holes in the micrographs. The SEM observations are also wholly consist ent with the glass transition temperature behavior obtained from diffe rential scanning calorimetric (DSC) measurements.