Polyaspartimides
View Patent ↗The present invention relates to novel polyaspartimides, their method of production and the use of these polyaspartimides as reactive components for polyisocyanates in two-component polyurethane coating compositions. The polyaspartimides are prepared by reacting a polyether amine with a maleimide.
1. A polyaspartimide of the formula:
where
X represents an n-valent polyether radical obtained by the removal of n amino groups from a polyether amine corresponding to the formula, X—(NH 2 ) n , wherein said polyether amine has a number average molecular weight of from about 200 to about 6000, and may contain further functional groups that either are reactive with isocyanate groups or are inert to isocyanate groups at temperatures of up to 100°C.,
R 2 and R 3 may be the same or different and represent moieties selected from the group consisting of i) hydrogen, ii) straight or branched C 1 to C 8 alkyl groups, which may be substituted with up to three aryl groups containing from 6 to 10 carbon atoms, iii) C 6 to C 10 aryl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms, and iv) together form a five or six-membered cycloalkyl group, with said cycloalkyl group being substituted with from 0 to 3 alkyl groups having from 1 to 3 carbon atoms, R 1 represents a moiety selected from the group consisting of i) hydrogen, ii) straight or branched C 1 to C 8 alkyl groups, which may be substituted with up to three aryl groups containing from 6 to 10 carbon atoms, and iii) C 6 to C 10 aryl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms, and
n represents an integer of from 2 to 4.
2. A process for preparing a polyaspartimide of the formula:
where
X represents an n-valent polyether radical obtained by the removal of a amino groups from a polyether amine corresponding to the formula, X-(NH 2 ) n , wherein said polyether amine has a number average molecular weight of from about 200 to about 6000, and may contain further functional groups that either are reactive with isocyanate groups or are inert to isocyanate groups at temperatures of up to 100°C.,
R 2 and R 3 may be the same or different and represent moieties selected from the group consisting of i) hydrogen, ii) straight or branched C 1 to C 8 alkyl groups, which may be substituted with up to three aryl groups containing from 6 to 10 carbon atoms, iii) C 6 to C 10 aryl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms, and iv) together form a five or six-membered cycloalkyl group, with said cycloalkyl group being substituted with from 0 to 3 alkyl groups having from 1 to 3 carbon atoms,
R 1 represents a moiety selected from the group consisting of i) hydrogen, ii) straight or branched C 1 to C 8 alkyl groups, which .may be substituted with up to three aryl groups containing from 6 to 10 carbon atoms, and iii) C 6 to C 10 aryl groups, which may be substituted with up to three alkyl groups having from 1 to 3 carbon atoms, and
n represents an integer of from 2 to 4, comprising reacting at a temperature of from about room temperature to about 100°C., in solution or in the absence of a solvent, an amine of the formula
X[-N H 2 ] n
with a maleimide at a maleimide to amine group equivalent ratio is from about 0.95:1 to about 1.05:1, and wherein X and n are as defined above.
3. The process of claim 2 , wherein said maleimide is of the formula:
where R 1 , R 2 and R 3 are as defined above.
4. The process of claim 2 , wherein the maleimide to amine group equivalent ratio is 1:1.
5. A two-component coating composition which comprises, as binder,
a) a polyisocyanate component and
b) an isocyanate-reactive component containing
b1) the polyaspartimide of claim 1 ,
b2) optionally other isocyanate-reactive compounds,
wherein the equivalent ratio of isocyanate groups to isocyanate-reactive groups is from about 0.8:1 to about 2.0:1.