Polymorphic crystal forms and morphology of syndiotactic polystyrene in miscible states
β Scribed by E. M. Woo; Fu Sun Wu
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 366 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-6266
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β¦ Synopsis
X-ray diffraction and optical microscopy characterization were performed to evaluate the phenomenon of alteration of polymorphism of syndiotactic polystyrene (s-PS) in the presence of other blending miscible polymers: poly(2,6-dimethyl-pphenylene oxide) (PPO) or atactic polystyrene (a-PS). Both β£ and β€ crystal forms were observed in the neat s-PS sample, but only β€-form crystal was found in miscible blends of s-PS with a-PS or PPO. The order and neighboring chain segments of neat s-PS are different from those of s-PS/PPO or s-PS/a-PS blends; thus, it is plausible that the greater randomness in the melt state of s-PS/a-PS or s-PS/PPO blends might be unfavorable for formation of β£-form crystals from melts. The final spherulitic morphology the s-PS/a-PS or s-PS/PPO blends suggests that the amorphous-state miscibility of does not change much the spherulitic structure of s-PS. The radial growth rate is, in general, depressed with the presence of blending miscible polymers in s-PS of equal T g or PPO of higher T g .
π SIMILAR VOLUMES
Dynamic viscoelasticity and dynamic birefringence measurements were performed on a quenched amorphous sample of a syndiotactic polystyrene, sPS. The measurements were carried out at temperatures where crystallization did not occur above the glass transition temperature. The data were analyzed with a
Fourier transform infrared (FTIR) spectra of syndiotactic polystyrene (s-PS) semicrystalline samples have been examined by using the spectral subtraction approach. For the crystalline forms including trans-planar chains (trigonal a and orthorhombic b) a number of conformational and structural order