Isotactic, atactic, and syndiotactic poly(methyl methacrylates) (PMMAs) (designated as iPMMA, aPMMA, and sPMMA) were mixed with poly(styrene-co-phydroxystyrene) (abbreviated as PHS) containing 15 mol % of hydroxystyrene separately in 2-butanone to make three polymer blend systems. Differential scann
Miscibility of polymer blends of poly(styrene-co-4-hydroxystyrene) with bisphenol-A polycarbonate
β Scribed by Guangxian Li; J. M. G. Cowie; V. Arrighi
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 181 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
The miscibility of blends of bisphenol-A polycarbonate (BAPC) and tetramethyl bisphenol-A polycarbonate (TMPC) with copolymers of poly(styrene-co-4-hydroxystyrene) (PSHS) was studied in this work. It has been demonstrated that BAPC is miscible with PSHS over a region of approximately 45-75 mol % hydroxyl groups in the copolymer. TMPC has a wider miscible window than BAPC when blended with PSHS. The blend miscibility was considered to be driven by the intermolecular attractive interactions between the hydroxyl groups of the PSHS and the electrons of the aromatic rings of both polycarbonates (PCs). As the FTIR measurements showed, after blending of BAPC with PSHS, there is no visible shift of the carbonyl band of BAPC at 1774 cm Οͺ1 , whereas the stretching frequency of the free hydroxyl groups of the copolymers at 3523 cm Οͺ1 disappeared. The large positive values of the segment interaction energy density parameter B st-HS calculated from the group contribution approach indicated that the intramolecular repulsive interaction may also have played a role in the promotion of the blend miscibility.
π SIMILAR VOLUMES
Analog calorimetry is used as a tool to study the interaction of polystyrene, PS, with bisphenol-A polycarbonate, PC, and with tetramethyl bisphenol-A polycarbonate, TMPC. Electrostatic charge calculations were used as a guide to divide polymer repeat units and analogs into groups. A mean-field bina
The miscibility of poly(4-hydroxystyrene-co-methoxystyrene) (HSMS) and poly(e-caprolactone) (PCL) was investigated by differential scanning calorimetry and Fourier transform infrared spectroscopy (FTIR). HSMS/PCL blends were found to be miscible in the whole composition range by detecting only a gla
In the presence of polycarbonate (PC), the polymerization of diglycidyl ether of bisphenol A (DGEBA) and bisphenol A in the melt was initiated to prepare blends of poly(hydroxyether of bisphenol A) (phenoxy) and PC. The polymerization reaction started from the initially homogeneous ternary mixture c