Process for the preparation of polyisocyanates containing biuret and/or higher polyuret groups and use thereof as synthesis component in the preparation of polyurethane plastics

Claim 2

A process for the preparation of polyisocyanates containing biuret and/or higher polyuret groups comprising reacting secondary diamines corresponding to the formula: R.sub.1 --NH--R.sub.2 --NH--R.sub.3 with excess quantities of organic diisocyanates corresponding to the formula: R.sub.4 (NCO).sub.2 wherein R 1 and R 3 , which may be the same or different, each represents an aliphatic hydrocarbon radical containing from 1 to 20 carbon atoms which may also be attached to one another with incorporation of the basic diamine skeleton to form a 5- or 6-membered ring, or a cycloaliphatic hydrocarbon radical containing from 4 to 15 carbon atoms; and R 2 and R 4 , which may be the same or different, each represents an aliphatic hydrocarbon radical having a total of from 2 to 20 carbon atoms optionally containing ester groups or a cycloaliphatic hydrocarbon radical containing from 4 to 15 carbon atoms, at least 2 carbon atoms being arranged between the two nitrogen atoms; characterized in that (a) the reaction is carried out in the presence of catalytic quantities of strong acids which form mixed carbamic acid anhydrides with isocyanates, and (b) the reaction product is clear and contains virtually no difficultly soluble polyurea.

Claim 3

A process for the preparation of clear polyisocyanates containing biuret and/or higher polyuret groups, but containing virtually no difficultly soluble polyureas comprising reacting secondary diamines corresponding to the formula: R.sub.1 --NH--R.sub.2 --NH--R.sub.3 with excess quantities of organic diisocyanates corresponding to the formula: R.sub.4 (NCO).sub.2 wherein R 1 and R 3 , which may be the same or different, each represents an aliphatic hydrocarbon radical containing from 1 to 20 carbon atoms which may also be attached to one another with incorporation of the basic diamine skeleton to form a 5- or 6-membered ring, or a cycloaliphatic hydrocarbon radical containing from 4 to 15 carbon atoms; and R 2 and R 4 , which may be the same or different, each represents an aliphatic hydrocarbon radical having a total of from 2 to 20 carbon atoms optionally containing ester groups or a cycloaliphatic hydrocarbon radical containing from 4 to 15 carbon atoms, at least 2 carbon atoms being arranged between the two nitrogen atoms; characterized in that the reaction is carried out in the absence of catalysts to form urea diisocyanate corresponding to the formula: ##STR3## and subsequently reacting said urea diisocyanates thus formed in the presence of catalytic quantities of strong acids which form mixed carbamic acid anhydrides with isocyanates, with more diisocyanate corresponding to the formula: R.sub.4 (NCO).sub.2 or with another diisocyanate corresponding to the formula: R.sub.5 (NCO).sub.2 wherein R 5 corresponds to the definition of R 4 but is not the same as R 4 .

Claim 4

A process for the preparation of clear polyisocyanates containing biuret and/or higher polyuret groups, but containing virtually no difficultly soluble polyureas comprising reacting secondary diamines corresponding to the formula: R.sub.1 --NH--R.sub.2 --NH--R.sub.3 with excess quantities of organic diisocyanates corresponding to the formula: R.sub.4 (NCO).sub.2 wherein R 1 and R 3 , which may be the same or different, each represents an aliphatic hydrocarbon radical containing from 1 to 20 carbon atoms which may also be attached to one another with incorporation of the basic diamine skeleton to form a 5- or 6-membered ring, or a cycloaliphatic hydrocarbon radical containing from 4 to 15 carbon atoms; and R 2 and R 4 , which may be the same or different, each represents an aliphatic hydrocarbon radical having a total of from 2 to 20 carbon atoms optionally containing ester groups or a cycloaliphatic hydrocarbon radical containing from 4 to 15 carbon atoms, at least 2 carbon atoms being arranged between the two nitrogen atoms; characterized in that the reaction is carried out in the absence of catalysts to form urea diisocyanate corresponding to the formula: ##STR3## and subsequently reacting said urea diisocyanates thus formed in the presence of catalytic quantities of strong acids which form mixed carbamic acid anhydrides with isocyanates, with more diisocyanate corresponding to the formula: R.sub.4 (NCO).sub.2 or with another diisocyanate corresponding to the formula: R.sub.5 (NCO).sub.2 wherein R 5 corresponds to the definition of R 4 but is not the same as R 4 .

Claim 5

A process for producing polyurethane by reacting a polyisocyanate with active hydrogen containing material, wherein said polyisocyanate is the polyisocyanate as produced by the process of claims 1 or 2, optionally blocked with blocking agents for isocyanate groups.