Process for the production of polyamide-polyureas and dispersions thereof in water

Claim 2

A process for the production of linear, segmented, polyamide ureas having carboxyl groups which are situated directly on the main chain and which are non-statistically arranged comprising reacting polyisocyanates with primary and/or secondary polyamines in the presence of tetracarboxylic acid dianhydrides at a temperature of from 10° to 100° C., the reactants being selected in such a way that from 0.05 to 0.6 acid anhydride groups and from 0.4 to 4 NCO-groups are used per amino group.

Claim 3

The process of claim 1, wherein said polyisocyanates are isocyanate-terminated prepolymers and said polyamines are diamines.

Claim 4

The process of claim 2, wherein said dianhydride is selected from the group consisting of (a) Pyromellitic acid dianhydride (1,2,4,5-benzene tetracarboxylic acid dianhydride); (b) Bicyclo-(2,2,2)-oct-(7)-ene-2,3,5,6-tetracarboxylic acid-2,3:5,6-dianhydride; (c) Perylene-3,4,9,10-tetracarboxylic acid dianhydride; (d) Naphthalene tetracarboxylic acid dianhydride; (e) Tetracarboxylic acid anhydrides of the following formulae ##STR6## in which R represents a C 1 -C 12 -alkylene, --CO--, --O--, --S--, --SO 2 -bridge, the alkylene bridge optionally also containing hetero atoms.

Claim 5

The process of claim 2, wherein said dianhydride is selected from the group consisting of pyromellitic acid anhydride, benzophenone tetracarboxylic acid dianhydride, and esters of trimellitic acid anhydride.

Claim 6

The process of claim 1 wherein the reaction is carried out at a temperature of from 20° to 60° C.

Claim 7

The process of claim 1 wherein the reactants are selected in such a way that from 0.1 to 0.5 acid anhydride groups and from 0.8 to 2.5 NCO-groups are used per amino group during the reaction.

Claim 8

The process of claim 1 wherein acetone is used as a solvent during the reaction.

Claim 9

A process for the production of aqueous dispersions of linear, segmented, polyamide ureas having carboxyl groups which are situated directly on the main chain and which are non-statistically arranged, said polyamide ureas produced by reacting polyisocyanates with primary and/or secondary polyamines in the presence of tetracarboxylic acid dianhydrides at a temperature of from 10° to 100° C., the reactants being selected in such a way that from 0.05 to 0.6 acid anhydride groups and from 0.4 to 4 NCO-groups are used per amino group, said process comprising converting the carboxyl groups of the polyadduct into carboxylate groups by at least partial neutralization, and dispersing the resulting polyadduct, containing ionic groups, in water.

Claim 10

A process for the production of aqueous dispersions of linear, segmented, polyamide ureas having carboxyl groups which are situated directly on the main chain and which are non-statistically arranged, said polyamide ureas produced by reacting polyisocyanates with primary and/or secondary polyamines in the presence of tetracarboxylic acid dianhydrides at a temperature of from 10° to 100° C., the reactants being selected in such a way that from 0.05 to 0.6 acid anhydride groups and from 0.4 to 4 NCO-groups are used per amino group, said process comprising converting the carboxyl groups of the polyadduct into carboxylate groups by at least partial neutralization, and dispersing the resulting polyadduct, containing ionic groups, in water.

Claim 11

The process of claim 8, wherein said polyisocyanates are isocyanate-terminated prepolymers and said polyamines are diamines.

Claim 12

The process of claim 9, wherein said dianhydride is selected from the group consisting of (a) Pyromellitic acid dianhydride (1,2,4,5-benzene tetracarboxylic acid dianhydride); (b) Bicyclo-(2,2,2)-oct-(7)-ene-2,3,5,6-tetracarboxylic acid-2,3:5,6-dianhydride; (c) Perylene-3,4,9,10-tetracarboxylic acid dianhydride; (d) Naphthalene tetracarboxylic acid dianhydride; (e) Tetracarboxylic acid anhydrides of the following formulae ##STR7## in which R represents a C 1 -C 12 -alkylene, --CO--, --O--, --S--, --SO 2 -bridge, the alkylene bridge optionally also containing hetero atoms.

Claim 13

The process of claim 9, wherein said dianhydride is selected from the group consisting of pyromellitic acid anhydride, benzophenone tetracarboxylic acid dianhydride, and esters of trimellitic acid anhydride.