Poly(ether sulfone) copolymers I-V were synthesized by the nucleophilic substitution reaction of 4,4-dichlorodiphenyl sulfone with varying mole proportions of 4,4-isopropylidene diphenol (bisphenol A) and 4,4-dihydroxydiphenyl sulfone (bisphenol S) using sulfolane as the solvent in the presence of a
Synthesis and characterization of poly(ether naphthalimide)s
β Scribed by Hai Bin Zheng; Zhi Yuan Wang
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 110 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
A series of new poly(ether imide)s containing the naphthalimide moiety were prepared from bis(4-fluorobenzoyl)naphthalimides and several bisphenols by aromatic nucleophilic displacement polymerization. These polyimides had inherent viscosities in the range of 0.31-1.04 dL/g in chloroform and glass transition temperatures of 283.0 -341.6Β°C by differential scanning calorimetry. The onset temperature for 5% weight loss for all the polymers was over 448Β°C, as assessed by thermogravimetry at a heating rate 10Β°C/min in nitrogen. In addition, these novel polyimides exhibited good solubility in organic solvents including N-methyl-2-pyrrolidone, N,N-dimethylformamide, N,N-dimethylacetamide, 1,1,2,2-tetrachloroethane and chloroform.
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