ISSN:
1022-1352
Keywords:
Chemistry
;
Polymer and Materials Science
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
,
Physics
Notes:
Differential scanning calorimetry (DSC) and X-ray diffraction analysis were performed to study the multiple melting behavior and crystal forms of neat syndiotactic polystyrene (s-PS) in comparison with its miscible blends with amorphous atactic polystyrene (a-PS) or poly(2,6-dimethyl-p-phenylene oxide) (PPO). For neat s-PS annealed at 242 to 250°C, three melting peaks of changing intensity were observed (labeled I, II, and III from low to high temperature), while if annealed at high temperatures (254°C or higher) only two melting peaks were left. The missing peak was determined to be Peak-III for s-PS annealed at high temperatures. For the s-PS/a-PS or s-PS/PPO blends, two melting peaks were observed, and the missing peak is Peak-II. The missing Peak-II in the blend systems is attributed to the β-modification. Apparently, the condition of s-PS being compatible with a-PS or PPO is unfavorable for generating the β-modification upon melt crystallization. This study also showed that Peak-I is associated with the β-modification. Peak-III may be associated with the less stable β′ form, which can be transformed to the β form upon annealing at high temperatures. For the s-PS/a-PS or s-PS/PPO blends upon annealing at higher temperatures, Peak-III quickly decreases, leaving only a single melting peak (Peak-I) for the blends. The phenomenon of the decrease of Peak-III crystals in the blend is similar to that for neat s-PS annealed at high temperatures.
Additional Material:
7 Ill.
Type of Medium:
Electronic Resource
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