Liquid hardeners for hardening epoxide resins (I)
The present invention relates to novel latent curing agents for curing curable polymer resins, in particular epoxy resins, and to epoxy resin compositions and the use thereof in the production of fiber composites.
1. A liquid curing agent for curing polymer resins comprising:
a) cyanamide;
b) at least one urea derivative of Formula (I)
wherein
R 1 and R 2 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 1 and R 2 together are C3- to C10-alkylene, thereby forming a ring together with the nitrogen atom to which they are attached;
R 3 is selected from the group consisting of hydrogen, C1- to C15-alkyl, C3- to C15-cycloalkyl, aryl, arylalkyl, C1- to C15-alkyl substituted by —NHC(O)NR 1 R 2 , C3- to C15-cycloalkyl substituted by —NHC(O)NR 1 R 2 , aryl substituted by —NHC(O)NR 1 R 2 and arylalkyl substituted by —NHC(O)NR 1 R 2 ;
provided that at least one of R 1 , R 2 , and R 3 is not hydrogen; and,
c) at least one viscosity modifier selected from the group consisting of monools, diols, polyols, ethers, ether alcohols, polyethers, polyether polyols, ketones, aldehydes, nitriles, carboxylic acid esters and mixtures thereof.
2. The liquid curing agent of claim 1 , wherein the cyanamide and the at least one urea derivative of formula (I) are provided in a molar ratio of 1:1 to 4:1.
3. The liquid curing agent of claim 1 , wherein
R 3 is selected from the group consisting of aryl, arylalkyl, aryl substituted by —NHC(O)NR 1 R 2 and arylalkyl substituted by —NHC(O)NR 1 R 2 , or wherein R 3 is represented by the general formula (III)
R 1 and R 2 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 1 and R 2 together are C3- to C10-alkylene, thereby forming a ring together with the nitrogen atom to which they are attached;
R 4 , R 5 , R 6 , R 7 and R 8 are each independently selected from the group consisting of hydrogen, halogen, C1- to C15-alkyl, C3- to C15-cycloalkyl, aryl, arylalkyl, —CF 3 , —NHC(O)NR 1 R 2 , C1- to C15-alkyl substituted with —NHC(O)NR 1 R 2 , aryl substituted by —NHC(O)NR 1 R 2 and arylalkyl substituted by —NHC(O)NR 1 R 2 ;
R 9 and R 10 are each independently selected from the group consisting of hydrogen and C1- to C15-alkyl; and,
n is a number between 0 and 10.
4. The liquid curing agent of claim 1 , wherein
R 1 and R 2 are each independently selected from the group consisting of hydrogen and C1- to C15-alkyl;
R 3 is selected from the group consisting of hydrogen, C1- to C15-alkyl, C3- to C15-cycloalkyl, C1- to C15-alkyl substituted by —NHC(O)NR 1 R 2 , and C3- to C15-cycloalkyl substituted by —NHC(O)NR 1 R 2 .
5. The liquid curing agent of claim 1 , wherein the at least one urea derivative according to formula (I) is selected from the group consisting of 1-methylurea, 1,1-dimethylurea, 1,3-dimethylurea, 3-(3-chloro-4-methylphenyl)-1,1-dimethylurea, 3-(p-chlorophenyl)-1,1-dimethylurea, 3-phenyl-1,1-dimethylurea, 3-(3,4-dichlorophenyl)-1,1-dimethylurea, 1,1′-(methylenedi-p-phenylene)-bis-(3,3-dimethylurea), 3-(3-trifluoromethylphenyl)-1,1-dimethylurea, 1,1′-(2-methyl-m-phenylene)-bis-(3,3-dimethylurea), 1,1′-(4-methyl-m-phenylene)-bis-(3,3-dimethylurea) and mixtures thereof.
6. The liquid curing agent of claim 1 , wherein the at least one viscosity modifier is selected from the group consisting of monools, diols, polyols, ethers, ether alcohols, polyethers, polyether polyols and mixtures thereof according to the general formula (v):
wherein
R 11 and R 22 are each independently selected from the group consisting of hydrogen, —OH and C1- to C15-alkyl;
R 12 , R 14 , R 16 , R 18 and R 20 are each independently selected from the group consisting of hydrogen, —OH and C1- to C5-alkyl;
R 13 , R 15 , R 17 , R 19 and R 21 are each independently selected from the group consisting of hydrogen, —OH, —NH 2 and C1- to C5-alkyl;
u is a number from 1 to 10;
s and t are each independently a number from 0 to 10, provided that at least one of s and t is a number from 1 to 10;
m is a number from 0 to 10, provided that m is a number from 1 to 10 when s is a number from 1 to 10;
p is a number from 0 to 10, provided that p is a number from 1 to 10 when t is a number from 1 to 10; and,
n, o and q are each independently a number from 0 to 10.
7. The liquid curing agent of claim 1 , wherein the curing agent further comprises d) at least one curing accelerator selected from the group consisting of imidazolines according to formula (VI) and imidazoles according to formula (VII),
wherein:
R 30 is selected from the group consisting of hydrogen, C1- to C20-alkyl, C3- to C20-cycloalkyl, aryl and arylalkyl;
R 32 and R 34 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 32 and R 34 together are C3- to C15-alkylene, thereby forming a ring together with the carbon atom to which they are attached;
R 33 and R 35 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 33 and R 35 together are C3- to C15-alkylene, thereby forming a ring together with the carbon atom to which they are attached.
8. The liquid curing agent of claim 1 , wherein the curing agent further comprises e) a stabiliser selected from the group consisting of inorganic acids and organic acids.
9. The liquid curing agent of claim 1 , wherein the curing agent further comprises e) a stabiliser selected from the group consisting of salicylic acid, phthalic acid, toluenesulfonic acid, sulfuric acid, phosphoric acid, anhydrides thereof and mixtures thereof.
10. The liquid curing agent of claim 1 , wherein the curing agent comprises:
from 1 to 50 parts by weight of the cyanamide,
from 1 to 50 parts by weight of the at least one urea derivative of formula (I), and
from 0.01 to 50 parts by weight of the at least one viscosity modifier.
11. The liquid curing agent of claim 10 , further comprising from 0 to 10 parts by weight of at least one curing accelerator selected from the group consisting of imidazolines of formula (VI) and imidazoles of formula (VII),
wherein:
R 30 is selected from the group consisting of hydrogen, C1- to C20-alkyl, C3- to C20-cycloalkyl, aryl and arylalkyl;
R 32 and R 34 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 32 and R 34 together are C3- to C15-alkylene, thereby forming a ring together with the carbon atom to which they are attached;
R 33 and R 35 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 33 and R 35 together are C3- to C15-alkylene, thereby forming a ring together with the carbon atom to which they are attached.
12. The liquid curing agent of claim 10 , further comprising from 0 to 10 parts by weight of at least one stabilizer.
13. An epoxy resin composition comprising:
a) at least one curable epoxy resin; and,
b) the liquid curing agent of claim 1 .
14. A polyurethane resin composition comprising:
a) at least one curable polyurethane resin; and,
b) the liquid curing agent of claim 1 .
15. A composite material comprising:
a) a carrier material;
b) at least one of a curable epoxy resin and a curable polyurethane resin; and,
c) the liquid curing agent of claim 1 .
16. The composite material of claim 15 , wherein the carrier material is a fiber material.
17. A method of making a composite material comprising:
impregnating a carrier material with a curable composition; and,
curing the impregnated carrier material,
wherein the carrier material is selected from the group consisting of fiber materials, woven fabrics, knitted fabrics and braided fabrics, and
wherein the curable composition comprises a curable polymer resin and the liquid curing agent of claim 1 .
18. The method of claim 17 , wherein the curable polymer resin is at least one of a curable epoxy resin and a curable polyurethane resin.
19. A liquid curing agent for curing polymer resins comprising:
a) cyanamide;
b) at least one urea derivative of Formula (I)
wherein
R 1 and R 2 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 1 and R 2 together are C3- to C10-alkylene, thereby forming a ring together with the nitrogen atom to which they are attached;
R 3 is selected from the group consisting of hydrogen, C1- to C15-alkyl, C3- to C15-cycloalkyl, aryl, arylalkyl, C1- to C15-alkyl substituted by —NHC(O)NR 1 R 2 , C3- to C15-cycloalkyl substituted by —NHC(O)NR 1 R 2 , aryl substituted by —NHC(O)NR 1 R 2 and arylalkyl substituted by —NHC(O)NR 1 R 2 ;
provided that at least one of R 1 , R 2 , and R 3 is not hydrogen; and,
c) at least one viscosity modifier selected from the group consisting of monools, diols, polyols, ethers, ether alcohols, polyethers, polyether polyols, ketones, aldehydes, nitriles, carboxylic acid esters and mixtures thereof, wherein the at least one viscosity modifier has a boiling point of at least 100° C.
20. The liquid curing agent of claim 19 , wherein the cyanamide and the at least one urea derivative of formula (I) are provided in a molar ratio of 1:1 to 4:1.
21. The liquid curing agent of claim 19 , wherein
R 3 is selected from the group consisting of aryl, arylalkyl, aryl substituted by —NHC(O)NR 1 R 2 and arylalkyl substituted by —NHC(O)NR 1 R 2 , or wherein R 3 is represented by the general formula (III)
R 1 and R 2 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 1 and R 2 together are C3- to C10-alkylene, thereby forming a ring together with the nitrogen atom to which they are attached;
R 4 , R 5 , R 6 , R 7 and R 8 are each independently selected from the group consisting of hydrogen, halogen, C1- to C15-alkyl, C3- to C15-cycloalkyl, aryl, arylalkyl, —CF 3 , —NHC(O)NR 1 R 2 , C1- to C15-alkyl substituted with —NHC(O)NR 1 R 2 , aryl substituted by —NHC(O)NR 1 R 2 and arylalkyl substituted by —NHC(O)NR 1 R 2 ;
R 9 and R 10 are each independently selected from the group consisting of hydrogen and C1- to C15-alkyl; and,
n is a number between 0 and 10.
22. The liquid curing agent of claim 19 , wherein
R 1 and R 2 are each independently selected from the group consisting of hydrogen and C1- to C15-alkyl;
R 3 is selected from the group consisting of hydrogen, C1- to C15-alkyl, C3- to C15-cycloalkyl, C1- to C15-alkyl substituted by —NHC(O)NR 1 R 2 , and C3- to C15-cycloalkyl substituted by —NHC(O)NR 1 R 2 .
23. The liquid curing agent of claim 19 , wherein the at least one urea derivative according to formula (I) is selected from the group consisting of 1-methylurea, 1,1-dimethylurea, 1,3-dimethylurea, 3-(3-chloro-4-methylphenyl)-1,1-dimethylurea, 3-(p-chlorophenyl)-1,1-dimethylurea, 3-phenyl-1,1-dimethylurea, 3-(3,4-dichlorophenyl)-1,1-dimethylurea, 1,1′-(methylenedi-p-phenylene)-bis-(3,3-dimethylurea), 3-(3-trifluoromethylphenyl)-1,1-dimethylurea, 1,1′-(2-methyl-m-phenylene)-bis-(3,3-dimethylurea), 1,1′-(4-methyl-m-phenylene)-bis-(3,3-dimethylurea) and mixtures thereof.
24. The liquid curing agent of claim 19 , wherein the at least one viscosity modifier is selected from the group consisting of monools, diols, polyols, ethers, ether alcohols, polyethers, polyether polyols and mixtures thereof according to the general formula (V):
wherein
R 11 and R 22 are each independently selected from the group consisting of hydrogen, —OH and C1- to C15-alkyl;
R 12 , R 14 , R 16 , R 18 and R 20 are each independently selected from the group consisting of hydrogen, —OH and C1- to C5-alkyl;
R 13 , R 15 , R 17 , R 19 and R 21 are each independently selected from the group consisting of hydrogen, —OH, —NH 2 and C1- to C5-alkyl;
u is a number from 1 to 10;
s and t are each independently a number from 0 to 10, provided that at least one of s and t is a number from 1 to 10;
m is a number from 0 to 10, provided that m is a number from 1 to 10 when s is a number from 1 to 10;
p is a number from 0 to 10, provided that p is a number from 1 to 10 when t is a number from 1 to 10; and, n, o and q are each independently a number from 0 to 10.
25. The liquid curing agent of claim 19 , wherein the curing agent further comprises d) at least one curing accelerator selected from the group consisting of imidazolines according to formula (VI) and imidazoles according to formula (VII),
wherein:
R 30 is selected from the group consisting of hydrogen, C1- to C20-alkyl, C3- to C20-cycloalkyl, aryl and arylalkyl;
R 32 and R 34 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 32 and R 34 together are C3- to C15-alkylene, thereby forming a ring together with the carbon atom to which they are attached;
R 33 and R 35 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 33 and R 35 together are C3- to C15-alkylene, thereby forming a ring together with the carbon atom to which they are attached.
26. The liquid curing agent of claim 19 , wherein the curing agent further comprises e) a stabiliser selected from the group consisting of inorganic acids and organic acids.
27. The liquid curing agent of claim 19 , wherein the curing agent further comprises e) a stabiliser selected from the group consisting of salicylic acid, phthalic acid, toluenesulfonic acid, sulfuric acid, phosphoric acid, anhydrides thereof and mixtures thereof.
28. The liquid curing agent of claim 19 , wherein the curing agent comprises:
from 1 to 50 parts by weight of the cyanamide,
from 1 to 50 parts by weight of the at least one urea derivative of formula (I), and
from 0.01 to 50 parts by weight of the at least one viscosity modifier.
29. An epoxy resin composition comprising:
a) at least one curable epoxy resin; and,
b) the liquid curing agent of claim 19 .
30. A polyurethane resin composition comprising:
a) at least one curable polyurethane resin; and,
b) the liquid curing agent of claim 19 .
31. A composite material comprising:
a) a carrier material;
b) at least one of a curable epoxy resin and a curable polyurethane resin; and,
c) the liquid curing agent of claim 19 .
32. A method of making a composite material comprising:
impregnating a carrier material with a curable composition; and,
curing the impregnated carrier material,
wherein the carrier material is selected from the group consisting of fiber materials, woven fabrics, knitted fabrics and braided fabrics, and
wherein the curable composition comprises a curable polymer resin and the liquid curing agent of claim 19 .
33. The method of claim 32 , wherein the curable polymer resin is an epoxy resin.
34. A liquid curing agent for curing epoxy resins comprising
a) cyanamide;
b) at least one urea derivative of Formula (I)
wherein
R 1 and R 2 are each independently selected from the group consisting of hydrogen, C1- to C15-alkyl and C3- to C15-cycloalkyl, or R 1 and R 2 together are C3- to C10-alkylene, thereby forming a ring together with the nitrogen atom to which they are attached;
R 3 is selected from the group consisting of hydrogen, C1- to C15-alkyl, C3- to C15-cycloalkyl, aryl, arylalkyl, C1- to C15-alkyl substituted by —NHC(O)NR 1 R 2 , C3- to C15-cycloalkyl substituted by —NHC(O)NR 1 R 2 , aryl substituted by —NHC(O)NR 1 R 2 and arylalkyl substituted by —NHC(O)NR 1 R 2 ;
provided that at least one of R 1 , R 2 , and R 3 is not hydrogen; and,
c) at least one viscosity modifier selected from the group consisting of monools, diols, polyols, ethers, ether alcohols, polyethers, polyether polyols, ketones, aldehydes, nitriles, carboxylic acid esters and mixtures thereof.