1,1-Bis[4-(4-carboxyphenoxy)phenyl]cyclohexane (III) and 1,1-bis[4-(4aminophenoxy)phenyl]cyclohexane (V) were prepared in two main steps starting from the aromatic nucleophilic substitution of p-fluorobenzonitrile and p-chloronitrobenzene, respectively, with 1,1-bis(4-hydroxyphenyl)cyclohexane in th
Effect of structure on properties of aromatic polyamides
β Scribed by I. K. Varma; Ramakant Kumar; A. B. Bhattacharyya
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 442 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Polyamides were prepared by reacting 3,5-diamino benzoic acid (DAB) and/or 1,3-bis( 3-amino benzamido) benzene ( ABB ) with terephthaloyl chloride in N,N-dimethylacetamide. Five polymer samples having different contents of pendant carboxyl groups were prepared by changing the molar ratios of DAB : ABB in the initial monomer feed as 1 : 0 ( C ) , 3 : 1 ( C3A), 1 : 1 (CA) , 1 : 3 ( CA3), and 0 : 1 (A). The inherent viscosities of the polymers ranged from 0.198 to 0.478 dL/g. DSC and TG studies indicated loss in weight in the temperature range of 80-200Β°C due to absorbed moisture.
The major loss in weight was observed above 400Β°C. The anaerobic char yield a t 800Β°C depended on the backbone structure and was found to range from 25 to 40%. The resistivities of polyamide film was determined a t 110 and 130Β°C and was found to decrease with an increase in carboxyl content. The dielectric constant of C and C3A polymer films was determined at frequencies ranging from 100 Hz to 1 MHz and at 110 and 130Β°C and was found to decrease with an increase in frequency or decrease in COOH content in the backbone.
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