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Effects of maleated syndiotactic polystyrene on the morphology, mechanical properties, and crystallization behavior of syndiotactic polystyrene/polyamide 6 blends
Author(s) -
Quan Zhang Xue,
Son Younggon
Publication year - 2003
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.12213
Subject(s) - compatibilization , polystyrene , maleic anhydride , materials science , crystallization , tacticity , polyamide , polymer chemistry , polymer blend , fourier transform infrared spectroscopy , chemical engineering , composite material , polymer , polymerization , copolymer , engineering
The compatibilization of syndiotactic polystyrene (sPS)/polyamide 6 (PA‐6) blends with maleic anhydride grafted syndiotactic polystyrene (sPS‐ g ‐MA) as a reactive compatibilizer was investigated. The sPS/PA‐6 blends were in situ compatibilized by a reaction between the maleic anhydride (MA) of sPS‐ g ‐MA and the amine end group of PA‐6. The occurrence of the chemical reaction was substantiated by the disappearance of a characteristic MA peak from the Fourier transform infrared spectrum. Morphology observations showed that the size of the dispersed PA‐6 domains was significantly reduced and that the interfacial adhesion was much improved by the addition of sPS‐ g ‐MA. As a result of reactive compatibilization, the impact strengths of the sPS/PA‐6 blends increased with an increase in the sPS‐ g ‐MA content. The crystallization behaviors of the blends were affected by the compatibilization effect of sPS‐ g ‐MA. A single melting peak of sPS in the noncompatibilized blend was gradually split into two peaks as the amount of the compatibilizer increased. A single crystallization peak of PA‐6 in the noncompatibilized blend became two peaks with the addition of 3 wt % sPS‐ g ‐MA. The new peak was a result of the fractionation crystallization. As the amount of sPS‐ g ‐MA increased, the intensity of the new peak increased, and the original peak nearly disappeared. Finally, the crystallization peak of PA‐6 disappeared with 20 wt % sPS‐ g ‐MA in the blend. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2502–2506, 2003