A series of new soluble polyamides having isopropylidene and methylsubstituted arylene ether moieties in the polymer chain were prepared by the direct polycondensation of 3,3Ј,5,5Ј-tetramethyl-2,2-bis[4-(4-carboxyphenoxy)phenyl]propane and various diamines in N-methyl-2-pyrrolidinone (NMP) containin
Synthesis and characterization of new soluble polyamides based on 3,3′,5,5′-tetramethyl-2,2- bis[4-(4-aminophenoxy)phenyl]propane and various aromatic dicarboxylic acids
✍ Scribed by Der-Jang Liaw; Been-Yang Liaw
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 140 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
A series of new soluble polyamides having isopropylidene-and methylsubstituted arylene ether moieties in the polymer chain were prepared by the direct polycondensation of 3,3 ,5,5-tetramethyl-2,2-bis[4-(4-aminophenoxy)phenyl]propane (TBAPP ) and various aromatic dicarboxylic acids in N-methyl-2-pyrrolidinone (NMP) using triphenyl phosphite and pyridine as condensing agents. Polymers were produced with high yield and moderate to high inherent viscosities of 0.87-1.56 dL g 01 . All the polymers could be readily dissolved in polar aprotic solvents such as NMP, N,Ndimethylacetamide and N,N-dimethylformamide, as well as less polar solvents such as m-cresol and pyridine. Some of them were even soluble in tetrahydrofuran. These polymers were solution-cast into transparent, flexible, tough films which were further characterized by x-ray and mechanical analysis. All of the polymers were amorphous and the polyamide films had a tensile strength range of 51-100 MPa, an elongation at break range of 4-11%, and a tensile modulus range of 1.90-2.53 GPa. These polyamides had glass transition temperatures between 188-255ЊC and 10% mass loss temperatures in the range of 439-468 and 454-483ЊC in nitrogen and air atmosphere, respectively.
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