Polyurethanes cured with amines and their preparation
Polyurethane prepolymers are described which are prepared from 2,4′-diiso-cyanate diphenylmethane (2,4′-MDI), a polyol component and an aliphatic diisocyanate. These prepolymers can be cured with aliphatic, cycloaliphatic and/or aromatic amines to form a cured urethane elastomer. In comparison to cured urethane elastomers based on monomeric 2,4′-MDI, these prepolymers provide elastomers with extended pour life, i.e. they exhibit a slower rate of viscosity buildup after curative and prepolymer are mixed which results in a reduced propensity to crack during the curing process and gives the opportunity to cast larger parts. In comparison to polyurea/urethanes prepared from cured TDI-prepolymers and which optionally include H12-MDI, the prepolymers of the invention have better health and safety aspects.
1. A polyurethane elastomer comprising the reaction product of:
(a) an NCO-terminated prepolymer prepared by reacting:
(1) diphenylmethane diisocyanate having a 2,4′-MDI isomer content of greater than 80% by weight,
with
(2) a high molecular weight polyol selected from the group consisting of polyalkyleneether polyols having a number average molecular weight of 250 to 10,000, polyester polyols having a number average molecular weight of 250 to 10,000 and mixtures thereof,
at a temperature of between 30° C. and 150° C. for a time sufficient to form the NCO-terminated prepolymer, with the OH groups of said polyol being reacted with the NCO groups of said diphenylmethane diisocyanate in an stoichiometric ratio of NCO groups to OH groups in the range of 1.5:1 to 20:1;
(b) an aliphatic diisocyanate selected from the group consisting of the isomers of 1,1′-methylene-bis-(4-isocyanatocyclohexane), 1,4-cyclohexane diisocyanate, isophorone diisocyanate 1,3-xylylene diisocyanate, hexamethylene diisocyanate, the isomers of m-tetramethylxylylene diisocyanate (TMXDI), mixtures thereof and prepolymers thereof;
and
(c) an aliphatic and/or aromatic di- or polyamine;
wherein the reactants - are present in amounts such that the equivalent ratio of NCO groups to the sum of NCO-reactive groups of the resultant elastomer is in the range of from 0.8:1 to 1.2:1.
2. The polyurethane elastomer according to claim 1 , wherein (c) said di- or polyamine is selected from the group consisting of 4,4′-methylene-bis-(2-chloroaniline), 3,5-diamino-4-chlorobenzoic acid isobutyl ester and 4,4′-methylene-bis-(3-chloro-2,6-diethylaniline).
3. A process for the production of polyurethane elastomers comprising:
(A) reacting
(a1) diphenylmethane diisocyanate having a 2,4′-isomer content of greater than 80% by weight
with
(a2) a high molecular weight polyol selected from the group consisting of polyalkyleneether polyols having a number average molecular weight of 250 to 10,000, polyester polyols having a number average molecular weight of 250 to 10,000 and mixtures thereof,
at a temperature of between 30° C. and 150° C. for a time sufficient to form an NCO-terminated prepolymer, with the OH groups of said polyol being reacted with the NCO groups of said diphenylmethane diisocyanate in an equivalent ratio of NCO groups to OH groups in the range of 1.5:1 to 20:1;
(B) adding
(b) an aliphatic diisocyanate selected from the group consisting of the isomers of 1,1′-methylene-bis-(4-isocyanatocyclohexane), 1,4-cyclohexane diisocyanate, isophorone diisocyanate, 1,3-xylylene diisocyanate, hexamethylene diisocyanate, the isomers of 1,1,4,4-tetramethylxylylene diisocyanate, mixtures thereof and prepolymers thereof,
to the NCO-terminated prepolymer formed in step (A);
and
(C) reacting the mixture from step (B) with
(c) an aliphatic and/or aromatic di- or polyamine, in a sufficient amount to effectively cure the polyurethane;
wherein the reactants are present in amounts such that the equivalent ratio of NCO groups to the sum of NCO-reactive groups of the resultant elastomer is in the range of from 0.8:1 to 1.2:1.
4. The polyurethane elastomer of claim 3 , wherein (c) said di- or polyamine is selected from the group consisting of 4,4′-methylene-bis(2-chloroaniline), 3,5-diamino-4-chlorobenzoic acid isobutyl ester and 4,4′-methylene-bis(3-chloro-2,6-diethylaniline).