Abstract
AbstractNylon 610/65F and nylon 610/65 copolymers were prepared by melt polycondensation from the diethylester of sebacic acid (10) and hexafluoroglutaric acid (5F) or glutaric acid (5) with hexamethylene diamine (6). Reduced specific viscosities of nylon 610/65F were lower than those of nylon 610/65. The crystallinity measured by WAXS and the melting point measured by DTA were depressed by the copolymerization. The melting point depression of nylon 610/65F was much larger than that of nylon 610/65. The thermal decomposition temperature measured by TG was also depressed significantly for nylon 610/65F. The residue at 600°C was increased by the fluorine substitution. The copolymers with higher fluorine content became flame retardant. The solubility was appreciably affected by the fluorine substitution. The contact angle for nylon 610/65F varied in a complicated manner with increasing 65F content and tended to be higher than the corresponding nylon 610/65.
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More From: Journal of Polymer Science Part A: Polymer Chemistry
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