Abstract
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 α-modification. Apparently, the condition of s-PS being compatible with a-PS or PPO is unfavorable for generating the α-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.
Original language | English |
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Pages (from-to) | 2041-2049 |
Number of pages | 9 |
Journal | Macromolecular Chemistry and Physics |
Volume | 199 |
Issue number | 9 |
DOIs | |
Publication status | Published - 1998 Sep |
All Science Journal Classification (ASJC) codes
- Condensed Matter Physics
- Physical and Theoretical Chemistry
- Organic Chemistry
- Polymers and Plastics
- Materials Chemistry