A new aromatic polyamide containing a pendant ethoxycarbonyl group was successfully synthesized from the reaction between 4,4Ј-diamino-2Ј-ethoxycarbonylbenzanilide and terephthaloyl chloride. The new polymer was soluble in organic solvents such as N-methyl-2-pyrrolidone and dimethylacetamide, and a
Preparation and physical properties of poly(4,4′-diamino-3′-carbamoylbenzanilide terephthalamide) and poly(4,4′-diamino-3′-carbamoylbenzanilide isophthalamide) films
✍ Scribed by Seog Joo Kang; Sung Il Hong; Chong Rae Park
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 140 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
To prepare thermally stable and high-performance polymeric films, new solvent-soluble aromatic polyamides with a carbamoyl pendant group, namely poly(4,4Јdiamino-3Ј-carbamoylbenzanilide terephthalamide) (p-PDCBTA) and poly(4,4Ј-diamino-3Ј-carbamoylbenzanilide isophthalamide) (m-PDCBTA), were synthesized. The polymers were cyclized at around 200 to 350 °C to form quinazolone and benzoxazinone units along the polymer backbone. The decomposition onset temperatures of the cyclized m-and p-PDCBTAs were 457 and 524 °C, respectively, lower than that of poly(p-phenylene terephthalamide) (566 °C). For the p-PDCBTA film drawn by 40% and heat-treated, the tensile strength and Young's modulus were 421 MPa and 16.4 GPa, respectively. The film cyclized at 350 °C showed a storage modulus (EЈ) of 1 ϫ 10 11 dyne/cm 2 (10 GPa) over the temperature range of room temperature to 400 °C.
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