Comparison of the phase behaviour of the liquid-crystalline polymer/poly(methyl methacrylate) and poly(vinyl acetate)/poly(methyl methacrylate) blends
β Scribed by Nesterov, Anatoly E; Lipatov, Yuri S.; Horichko, Vitaly V.
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 687 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0959-8103
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β¦ Synopsis
The phase behaviour of blends of a liquid-crystalline polymer (LCP) and poly(methyl methacrylate) (PMMA), as well as the phase state of blends of PMMA and poly(vinyl acetate) (PVA) has been investigated using light scattering and phase-contrast optical microscopy. The blends of LCP and PMMA have been obtained by coagulation from ternary solutions. The cloud point curves were determined. It was established that both pairs demix upon heating, ie have an LCST. In the region of intermediate composition, the phase separation proceeds according to a spinodal mechanism ; however for LCP/PMMA blends, the decomposition proceeds according to a non-linear regime from the very onset. In the region of small amounts of LCP, the phase separation follows a mechanism of nucleation and growth. For PMMA/PVA blends, the spinodal decomposition proceeds according to a linear regime, in spite of the molecular mobility that PVA chains develop at lower temperatures. Only after prolonged heat treatment does the process transit to a non-linear regime. The data show a similarity between the phase behaviour of blends of liquid-crystalline and of Γ½exible amorphous polymers. The distinction consists of the absence of a linear regime of decomposition for LCP-PMMA blends.
π SIMILAR VOLUMES
A poly(viny1 chloride) (PVC)/poly(methyl methacrylate) (PMMA) (80/20 w/w) polymer blend was studied by mechanical spectroscopy. Two relaxations can be distinguished in the glassy state, a very large secondary relaxation in the range of 100 K to 325 K which results from the combination of secondary r
Polymer blends composed of poly ( methyl methacrylate ) ( PMMA ) and poly ( vinyl acetate ) ( PVAc ) were prepared via radical-initiated polymerization of methyl methacrylate ( MMA ) in the presence of PVAc. Differential scanning calorimetry and dynamic mechanical analysis were employed to investiga