STRUCTURE AND PROPERTIES OF WHOLLY AROMATIC NYLON COPOLYMERS

Wholly aromatic nylon copolymers were prepared by low-temperature solution polycondensation in N-methyl-2-pyrrolidone solvent from diamine of p-phenylene(P) or m-phenylene(M) and diacid chloride of terephthaloyl(T) or isophthaloyl(I). Copolymer compositions measured by IR method for P/M-I copolymers...

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Veröffentlicht in:Sen'i Gakkaishi 1979/01/10, Vol.35(1), pp.T13-T18
Hauptverfasser: Kiyotsukuri, Tsuyoshi, Tsujimoto, Keizo
Format: Artikel
Sprache:eng
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Zusammenfassung:Wholly aromatic nylon copolymers were prepared by low-temperature solution polycondensation in N-methyl-2-pyrrolidone solvent from diamine of p-phenylene(P) or m-phenylene(M) and diacid chloride of terephthaloyl(T) or isophthaloyl(I). Copolymer compositions measured by IR method for P/M-I copolymers are nearly equal to comonomer compositions. Melting point measured by DTA method and crystallinity measured by X-ray method decrease and solubility increases, by the copolymerization. Films were prepared by casting from as-polymerized solutions of P/M-I copolymers. Tensile strength, Young's modulus, elongation and dynamic modulus near room temperature increase with increasing comonomer content. Retention of dynamic modulus at higher temperature increases with increasing P content of copolymers. Some discussion was made on these results.
ISSN:0037-9875
1884-2259
DOI:10.2115/fiber.35.T13