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 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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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. |
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ISSN: | 0037-9875 1884-2259 |
DOI: | 10.2115/fiber.35.T13 |