A series of new wholly aromatic polyesters was synthesized by melt polycondensation of 1-phenyl-2,6-naphthalenedicarboxylic acid (PNDA) and &acetates of various aromatic diols. The aromatic diols studied are hydroquinone (HQ), methylhydroquinone (MHQ), phenylhydroquinone (PHQ), (a-phenylisopropy1)hy
Synthesis and characterization of soluble aromatic polyesters derived from substituted terphenyl and quinquephenyl diols
β Scribed by F. Kakali; K. G. Gravalos; J. K. Kallitsis
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 622 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
Rigid aromatic polyesters containing alkoxy or phenyl-substituted oligophenyls were prepared. Soluble polymers were obtained also in cases where phenyl-substituted quinquephenyl diols were combined with asymmetric phenyl-substituted terephthalic acid. The synthesized polyesters were characterized by viscosimetry, gel permeation chromatography, thermal analysis, and dynamic mechanical analysis. The temperature dependence of the intrinsic viscosity was sensitive to the type of side groups. Thermogravimetry has shown that polyesters with aromatic substituents were stable up to 380-400OC. The glass transition temperatures of the polyesters with aromatic side groups were in the 220-260Β°C range as determined by DSC. Polyesters with hexyloxy side chains show crystallinity. Dynamic mechanical analysis showed that in the cases where aromatic substituents were used to increase solubility, the obtained polymers have very useful mechanical properties at high temperatures. The polymer having the quinquephenyl unit in the main chain has an almost constant modulus up to 340Β°C.
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