IP Library Granted Patent US 10,287,454
Granted Patent B2
US 10,287,454 · App. 14/906,365 · Granted May 14, 2019

Coating compositions

Inventors: Thomas Klotzbach (Essen, DE); Michael Fiedel (Essen, DE); Michael Ferenz (Essen, DE)
Assignee: Evonik Degussa GmbH
C09D183/06C09D183/04C08G77/18C08G77/80
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Quick Facts
Patent No.
US 10,287,454
App. No.
14/906,365
Granted
May 14, 2019
Kind
B2
Abstract

The present invention relates to coating compositions comprising A) alkoxy-functional arylpolysiloxanes and/or alkoxy-functional aryl-alkylpolysiloxanes, B) at least one crosslinking catalyst and optionally C) at least one alkoxysilane and D) optionally further auxiliaries and additives, where the fraction of the alkoxy groups is at least 10 wt %, based on the sum of components A) and C).

Claims (73)

1. A coating composition comprising a mixture of

A) an alkoxy-functional arylpolysiloxane and/or alkoxy-functional aryl-alkylpolysiloxane comprising alkoxy groups;

B) a crosslinking catalyst selected from the group of the guanidines or amidines;

C) an alkoxysilane comprising alkoxy groups; and

D) optionally further auxiliaries and additives,

wherein the alkoxy groups is at least 10 wt %, based on the sum of components A) and C);

wherein the coating composition comprises from 10 to 70 wt % based on the mixture components A) and C) of alkoxy-functional arylpolysiloxanes and/or alkoxy-functional aryl-alkylpolysiloxanes; and

from 0.001 to 15 wt % based on the mixture components A) and C) of the crosslinking catalyst; and C) from 10 to 80 wt % based on the mixture components A) and C); and

wherein the alkoxy-functional arylpolysiloxanes and/or alkoxy-functional aryl-alkylpolysiloxanes are of the general formula (I):

R a Si(OR′) b O (4−a−b)/2   (I)

in which 0<a<2, 1<b<4 and a+b<4 and

R is selected from an aromatic moiety having 6 to 20 carbon atoms or from a mixture of an aromatic moiety having 6 to 20 carbon atoms and an alkyl group consisting of 1 to 8 carbon atoms, and

R′ is an alkyl group consisting of 1 to 8 carbon atoms,

wherein the coating composition has full mechanical and chemical stability resulting from a combination of physical volume drying of less than 6.5 hours under a pressure of 101325 Pa, with a temperature of 23° C., and with an ambient relative atmospheric humidity of approximately 40% and, at the same time, chemical crosslinking by hydrolysis-condensation with sufficient moisture introduced into the oven.

2. The coating composition according to claim 1 , wherein component A) comprises alkoxy-functional phenylpolysiloxanes.

3. The coating composition according to claim 2 , wherein alkoxysilanes C) used are those of the formula (II)

R c Si(OR′) d   (II)

0≤c≤2, 1≤d≤4, c+d=4

in which R is an alkyl group of 1 to 8 carbon atoms, a cycloalkyl group of 3 to 8 carbon atoms or an aromatic moiety having 6 to 20 carbon atoms and R′ is an alkyl group having 1 to 8 carbon atoms.

4. The coating composition according to claim 1 , wherein component A) comprises alkoxy-functional phenylmethylpolysiloxanes.

5. The coating composition according to claim 4 , wherein the phenyl:methyl ratio is in the range from 1:0.1 to 0.1:1.

6. The coating composition according to claim 4 , wherein alkoxysilanes C) used are those of the formula (II)

R c Si(OR′) d   (II)

0≤c≤2, 1≤d≤4, c+d=4

in which R is an alkyl group of 1 to 8 carbon atoms, a cycloalkyl group of 3 to 8 carbon atoms or an aromatic moiety having 6 to 20 carbon atoms and R′ is an alkyl group having 1 to 8 carbon atoms.

7. The coating composition according to claim 1 , wherein the alkoxy-functional arylpolysiloxanes and/or alkoxy-functional aryl-alkylpolysiloxanes A) are present as solvent-free 100% resin or in the form of a resin solution.

8. The coating composition according to claim 7 , wherein alkoxysilanes C) used are those of the formula (II)

R c Si(OR′) d   (II)

0≤c≤2, 1≤d≤4, c+d=4

in which R is an alkyl group of 1 to 8 carbon atoms, a cycloalkyl group of 3 to 8 carbon atoms or an aromatic moiety having 6 to 20 carbon atoms and R′ is an alkyl group having 1 to 8 carbon atoms.

9. The coating composition according to claim 1 , wherein alkoxysilanes C) used are those of the formula (II)

R c Si(OR′) d   (II)

0≤c≤2, 1≤d≤2, c+d=4

in which R is an alkyl group of 1 to 8 carbon atoms, a cycloalkyl group of 3 to 8 carbon atoms or an aromatic moiety having 6 to 20 carbon atoms and R′ is an alkyl group having 1 to 8 carbon atoms.

10. The coating composition according to claim 9 , wherein component A) comprises alkoxy-functional phenylmethylpolysiloxanes.

11. The coating composition according to claim 9 , wherein the alkoxy-functional arylpolysiloxanes and/or alkoxy-functional aryl-alkylpolysiloxanes A) are present as solvent-free 100% resin or in the form of a resin solution.

12. The coating composition according to claim 1 , wherein the crosslinking catalyst B) contains no silicon atoms.

13. The coating composition according to claim 1 , wherein the fraction of component B) in the coating composition is 0.1 to 15.0 wt %, based on component A).

14. The coating composition according to claim 1 , wherein the coating composition comprises further auxiliaries and additives as component D).

15. The coating composition according to claim 1 , wherein the coating composition comprises a fraction of component A) of 30 to 50 wt % based on the mixture components A) to C),

of component B) of 0.1 to 3.0 wt % based on the mixture components A) to C), and

of component C) of 20 to 50 wt % based on the mixture components A) to C).

16. A coating system comprising coating compositions according to claim 1 .

17. The coating systems according to claim 16 , wherein the coating system is a paint, an ink or a varnish.

18. The coating composition according to claim 1 , wherein the crosslinking catalyst B) is selected from the group of 1,1,3,3-tetramethylguanidine or 1,8diazabicyclo[5.4.0]-7-undecene.

19. The coating composition according to claim 1 , wherein alkoxysilanes C) used are those of the formula (II)

R c Si(OR′) d   (II)

0≤c≤2, 1≤d≤4, c+d=4

in which R is an alkyl group of 1 to 8 carbon atoms, a cycloalkyl group of 3 to 8 carbon atoms or an aromatic moiety having 6 to 20 carbon atoms and R′ is an alkyl group having 1 to 8 carbon atoms.

20. A coating composition consisting of a mixture of

A) an alkoxy-functional arylpolysiloxane and/or alkoxy-functional aryl-alkylpolysiloxane comprising alkoxy groups;

B) a crosslinking catalyst selected from the group of the guanidines or amidines;

C) an alkoxysilane comprising alkoxy groups; and

D) auxiliaries and additives,

wherein the alkoxy groups is at least 10 wt %, based on the sum of components A) and C);

wherein the coating composition comprises from 10 to 70 wt % based on the mixture components A) and C) of alkoxy-functional arylpolysiloxanes and/or alkoxy-functional aryl-alkylpolysiloxanes; and

from 0.001 to 15 wt % based on the mixture components A) and C) of the crosslinking catalyst; and C) from 10 to 80 wt % based on the mixture components A) and C); and

wherein the alkoxy-functional arylpolysiloxanes and/or alkoxy-functional aryl-alkylpolysiloxanes are of the general formula (I):

R a Si(OR′) b O (4−a−b)/2   (I)

in which 0<a<2, 1<b<4 and a+b<4 and

R is selected from an aromatic moiety having 6 to 20 carbon atoms or from a mixture of an aromatic moiety having 6 to 20 carbon atoms and an alkyl group consisting of 1 to 8 carbon atoms, and

R′ is an alkyl group consisting of 1 to 8 carbon atoms,

wherein the coating composition has full mechanical and chemical stability resulting from a combination of physical volume drying of less than 6.5 hours under a pressure of 101325 Pa, with a temperature of 23° C., and with an ambient relative atmospheric humidity of approximately 40%, and, at the same time, chemical crosslinking by hydrolysis-condensation with sufficient moisture introduced into the oven.

21. The coating composition according to claim 20 , wherein component A) is an alkoxy-functional phenylpolysiloxane.

22. The coating composition according to claim 20 , wherein component A) is an alkoxy-functional phenylmethylpolysiloxane.

23. The coating composition according to claim 22 , wherein the phenyl:methyl ratio is in the range from 1:0.1 to 0.1:1.

24. The coating composition according to claim 20 , wherein the alkoxy-functional arylpolysiloxane or alkoxy-functional aryl-alkylpolysiloxane A) are present as solvent-free 100% resin or in the form of a resin solution.

25. The coating composition according to claim 20 , wherein alkoxysilanes C) used are those of the formula (II)

R c Si(OR′) d   (II)

0≤c≤2, 1≤d≤2, c+d=4

in which R is an alkyl group of 1 to 8 carbon atoms, a cycloalkyl group of 3 to 8 carbon atoms or an aromatic moiety having 6 to 20 carbon atoms and R′ is an alkyl group having 1 to 8 carbon atoms.

26. The coating composition according to claim 20 , wherein the crosslinking catalyst B) contains no silicon atoms.

27. The coating composition according to claim 20 , wherein the fraction of component B) in the coating composition is 0.1 to 15.0 wt %, based on component A).

Assignments (2)
CHANGE OF NAME Recorded Dec 27, 2019
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051428/0710 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2016
From: KLOTZBACH, THOMAS; FIEDEL, MICHAEL; FERENZ, MICHAEL
To: EVONIK DEGUSSA GMBH
Reel/Frame 037788/0481 →
Priority Claims (1)
DE 10 2013 216 781 · Aug 23, 2013 · national
Continuity (1)
Related Publication 20160160081A1 · Jun 9, 2016
Cited By (1)
US 12,404,407