A series of new aromatic poly(amide-imide)s were synthesized by the triphenyl phosphite-activated polycondensation of the diimide-diacid, 2,5-bis(trimellitimido)chlorobenzene (I) with various aromatic diamines in a medium consisting of N-methyl-2-pyrrolidone (NMP), pyridine, and calcium chloride. Th
Synthesis and characterization of new poly(amide-imide)s based on 1,4-bis(trimellitimido)-2,5-dichlorobenzene
β Scribed by Chin-Ping Yang; Guey-Sheng Liou; Shyh-Yau Chang; Shin-Haur Chen
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 141 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
A series of new aromatic poly(amide-imide)s were synthesized by the triphenyl phosphite-activated polycondensation of the diimide-diacid, 1,4-bis(trimellitimido)-2,5-dichlorobenzene (I), with various aromatic diamines in a medium consisting of N-methyl-2-pyrrolidone (NMP), pyridine, and calcium chloride. The poly(amideimide)s had inherent viscosities of 0.88 -1.27 dL g Οͺ1 . The diimide-diacid monomer (I) was prepared from 2,5-dichloro-p-phenylenediamine with trimellitic anhydride. All the resulting polymers were amorphous and were readily soluble in a variety of organic solvents, including NMP and N,N-dimethylacetamide. Transparent, flexible, and tough films of these polymers could be cast from N,N-dimethylacetamide or NMP solutions. Cast films had tensile strengths ranging from 92 to 127 MPa, elongations at break from 4 to 24%, and initial moduli from 2.59 to 3.65 GPa. The glass transition temperatures of these polymers were in the range of 256Β°-317Β°C, and the 10% weight loss temperatures were above 430Β°C in nitrogen.
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