Crystalline polyamides from branched chain diamine and terephthalic acid
AssigneeCiba-Geigy Corporation
InventorsJosef Pfeifer, Heinz Peter
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Abstract
The partially crystalline polyamides according to the invention are obtained by reacting terephthalic acid, or an amide-forming derivative thereof, with a diamine of the formula ##STR1## in which R.sub.1 and R.sub.2 singly or together are organic radicals. The reaction mixture can also contain up to 30% by weight of other amide-forming substances (aminocarboxylic acids or lactams, or mixtures of dicarboxylic acids and diamines), provided the formation of the partial crystallinity of the resulting polyamides is retained. The polyamides are suitable for producing moulded products of the most varied types. They are particularly applicable for producing filaments and fibres.
Claims7
A partially crystalline fiber-forming polyamide of essentially stoichiometric amounts of (1) terephthalic acid, or of an amide-forming derivative thereof, with (2) a diamine of the formula (I) ##STR5## in which R.sub.1 is alkyl having 1-4 C atoms,
- R.sub.2 is alkyl having 1-8 C atoms, or
- R.sub.1 and R.sub.2 together with the linkage C atom to which they are attached are in both cases cycloalkyl having 4-6 C atoms,
- (3) from zero to 5% by weight of an aminocarboxylic acid of the formula (II)
- HOOC--Z.sub.1 --NH.sub.2 (II)
- in which Z.sub.1 is alkylene having 5 to 11 C atoms, or of a corresponding lactam, or (4) zero to 30% by weight of an essentially stoichiometric mixture of a dicarboxylic acid of the formula (III)
- HOOC--Z.sub.2 --COOH (III)
- in which Z.sub.2 is an aliphatic radical having at least 2 C atoms, or a carbocyclic-aromatic radical in which the carbonyl groups are bound to different ring C atoms which are not adjacent, or of an amide-forming derivative thereof, with a diamine of the formula (IV)
- H.sub.2 N--Z.sub.3 --NH.sub.2 (IV)
- in which Z.sub.3 is ##STR6## straight-chain alkylene having 2-12 C atoms, or a cycloaliphatic or araliphatic radical;
- and wherein the defined weight percentages in the case of amide-forming derivatives of terephthalic acid and of the dicarboxylic acid of the formula (III) relate to identical functional groups.
Dependencies are inferred from the claim text.