Thermal and morphology characterization of blends of poly(ethylene oxide) with poly(vinyl acetate)
β Scribed by N.K. Kalfoglou; D.D. Sotiropoulou; A.G. Margaritis
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 974 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
Thermal and morphology studies were carried out to characterize the mutual miscibility of poly(ethylene oxide)/poly(vinyl acetate) (PEO/PVAC) blends. The techniques used were DSC and polarized microscopy and the study covered the complete composition range. Morphology revealed qualitative differences between melt-pressed and solvent-cast films. Determination of melting point depression (T~) of annealed melt-pressed films allowed determination of the Z12 interaction parameter of the two polymers in the melt, using available theory. To obtain equilibrium T,~ data, the Hoffman-Weeks procedure was applied to take into account the influence of crystal morphology. The results indicate that the blends are miscible at higher PVAC contents (wt fraction 30.4) and Xt2 has a negative value (-0.30) comparable to interaction parameter values of analogous miscible semicrystalline-amorphous blends,
π SIMILAR VOLUMES
To obtain a correlation among structure-morphology-mobility-compatibility properties of poly(ethylene-co-vinyl acetate) (EVA)/poly(vinyl acetate) (PVAc) blends, we have used scanning electron microscopy and solid-state nuclear magnetic resonance in our investigations. The results are discussed in te
## Abstract Poly(vinyl acetate) (PVAc) was added to the crystalline blends of poly(ethylene oxide) (PEO) and poly(Lβlactide) (PLLA) (40/60) of higher molecular weights, whereas diblock and triblock poly(ethylene glycol)βpoly(Lβlactide) copolymers were added to the same blend of moderate molecular w
EVA was blended with phenoxy over the whole range of composition using a twin-screw Brabender. Two-phase separation caused by EVA crystallization was observed in the EVA-rich blends and the dispersed domain of EVA was not clearly shown in the phenoxy-rich blends. Differential scanning calorimetry (D