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PS/EPDM blends prepared by in situ-polymerization of styrene in the presence of EPDM are immiscible and show two phases. Furthermore, the dynamic mechanical behavior of injected specimens is quite different from that of noninjected blends. This is attributed to the differences in morphology before and after injection molding. The morphology of the noninjected blends consists of PS spherical domains covered by a thin layer of EPDM, whereas the injected blends show elastomeric dispersed phase morphology in a rigid matrix. SEM analysis was important to elucidate the changes in the dynamic mechanical behavior of PS/EPDM blends, but TEM analysis is more precise for morphological characterization and yielded the real average diameter of EPDM particles. Comparing the average diameters for the PS/EPDM blends obtained from SEM and TEM analyses, the diameters obtained from the SEM analysis are wider than those of TEM which is due to the solvent extraction effect on the blend morphology. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009

PS/EPDM blends formed by in situ polymerization of styrene in the presence of EPDM were prepared. EPDM has excellent resistance to factors such as weather, ozone and oxidation and it could be a good alternative for substituting polybutadiene-based rubbers in PS toughening. The PS/EPDM blends present two phases, an EPDM elastomeric phase dispersed into a rigid matrix. The blends show higher thermal stability than polystyrene homopolymer due to the stabilizing effect of EPDM incorporation. The mechanical properties of in situ polymerized PS/EPDM blends with different compositions were evaluated before and after accelerated photoaging and compared with the properties of HIPS submitted to the same aging conditions. The blend containing 17 wt % of EPDM presents an increase in the impact resistance of 210% in comparison with the value of PS. Although the initial mechanical properties of HIPS are superior, a pronounced drop was observed after an exposure time. For example, after the aging period, all PS/EPDM blends showed higher strain at break than HIPS. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008

In this study, the mechanical properties of in situ polymerized PS/EPDM blends with different composition were evaluated before and after accelerated photoaging and compared with the properties of commercial HIPS submitted to similar aging conditions (ASTM G53). The mechanical properties of the PS/EPDM blends as well as their photochemical stability are influenced by the polymerization temperature and blend composition. Although the initial mechanical properties of HIPS are superior in comparison with the in situ polymerized PS/EPDM blends, a pronounced drop of them was observed already for short time exposure. For example, after the aging period, all PS/EPDM blends showed higher strain at break than HIPS. Because PS/EPDM blends present higher resistance to photoaging stability than HIPS, the mechanical properties of the HIPS become worse than the other blends as the aging time increases. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007

Polystyrene/AES blends formed by the in situ polymerization of styrene in the presence of poly(acrylonitrile-g-(ethylene-co-propylene-co-diene)-g-styrene) (AES) were prepared. AES is a commercial elastomer obtained by the radical copolymerization of styrene and acrylonitrile in the presence of an ethylene–propylene–diene terpolymer (EPDM). The polystyrene/AES blends presented two phases: an EPDM elastomeric phase dispersed in a rigid matrix. The phase behavior was strongly affected by the polymerization temperature. The blends showed higher thermal stability than the polystyrene homopolymer because of the stabilizing effect of EPDM incorporation. The mechanical properties were influenced by the polymerization temperature and blend composition. The blend prepared at 60°C with 13.0 wt % AES presented an enhancement of 60% in the impact resistance, whereas the blend prepared at 80°C with 21.8 wt % AES presented an enhancement of 150% in the strain at break. Both blends had these properties improved with a small loss in the Young's modulus. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007