IP Library Granted Patent US 9,238,706
Granted Patent B2
US 9,238,706 · App. 13/498,435 · Granted Jan 19, 2016

Use of guanidine derivatives as curing accelerators for epoxy resins

Inventors: Martin Hitzler (Gottmadingen, DE); Hans-Peter Krimmer (Kirchweidach, DE); Sylvia Strobel (Garching, DE); Monika Brandl (Tacherting, DE)
Assignee: AlzChem AG
C08G59/50C08G59/4021C08G59/686
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Quick Facts
Patent No.
US 9,238,706
App. No.
13/498,435
Granted
Jan 19, 2016
Kind
B2
Abstract

The present invention describes guanidine derivatives of the general formula (I) having the stated meanings for the residues R 1 , R 2 and R 3 as accelerators for cold-curing epoxy resin compositions. The curing of cold-curing epoxy resin systems may advantageously be accelerated with the assistance of these compounds.

Claims (57)

1. A method of accelerating curing of a cold-curing epoxy resin composition comprising adding to the cold-curing epoxy resin a guanidine derivative of Formula (I)

wherein:

R 1 is —CN, —NO 2 or —(C═O)—R 4 ;

R 2 is —H, alkyl, benzyl, phenyl, aryl or —(C═O)—R 4 ;

R 3 is —H or alkyl;

R 4 is —H, alkyl, or —O-alkyl;

wherein, when R 1 is —CN or —(C═O)—R 4 , R 2 is not —H if R 3 is —H;

wherein the cold-curing epoxy resin composition further comprises at least one amine curing agent for the epoxy resin which is activatable at a temperature of <60° C.

2. The method of claim 1 , wherein the guanidine derivative is selected from the group consisting of 1,1-dimethyl-3-cyanoguanidine, 1-acetyl-3-cyanoguanidine, 1-(p-chlorophenyl)-3-cyanoguanidine, nitroguanidine and, 1-methyl-3-nitroguanidine, 1-ethyl-3-nitroguanidine, 1-butyl-3-nitroguanidine, 1-benzyl-3-nitroguanidine.

3. The method of claim 1 , wherein the amine curing agent comprises at least two free amine groups and is selected from the group consisting of an alkyldiamine, an aryldiamine, an alkylpolyamine, an arylpolyamine, and a polyetheramine.

4. The method of claim 1 , wherein the amine curing agent is selected from the group of an ethylenediamine, a diethylenetriamine, a triethylenetetramine, a meta-xylylenediamine, a methylenedianiline, a para-minocyclohexylmethane, an isophoronediamine and a polyetheramine.

5. The method of claim 1 , wherein the guanidine derivative is present in a quantity of 0.1 to 15 wt. % relative to the epoxy resin composition.

6. The method of claim 1 , wherein the guanidine derivative is present in a ratio of 0.1 to 15 parts relative to 100 parts of epoxy resin.

7. The method of claim 1 , wherein the amine curing agent comprises at least two free amine groups and is selected from the group consisting of an alkyldiamine, an aryldiamine, an alkylpolyamine and an arylpolyamine, and wherein the cold-curing epoxy resin composition does not contain a polyetheramine.

8. The method of claim 1 , wherein the amine curing agent is selected from the group of an ethylenediamine, a diethylenetriamine, a triethylenetetramine, a meta-xylylenediamine, a methylenedianiline, a para-aminocyclohexylmethane and an isophoronediamine, and wherein the cold-curing epoxy resin composition does not contain a polyetheramine.

9. A cold-curing epoxy resin composition comprising:

a guanidine derivative of Formula (I)

wherein:

R 1 is —CN, —NO 2 or —(C═O)—R 4 ;

R 2 is —H, alkyl, benzyl, phenyl, aryl or —(C═O)—R 4 ;

R 3 is —H or alkyl;

R 4 is —H, alkyl, or —O-alkyl;

wherein, when R 1 is —CN, or —(C═O)—R 4 , R 2 is not —H if R 3 is —H;

a cold-curing epoxy resin, and an amine curing agent for the epoxy resin which is activatable at a temperature of <60° C.

10. A cold-curing epoxy resin composition according to claim 9 , wherein the curing accelerator is selected from the group consisting of 1,1-dimethyl-3-cyanoguanidine, 1-acetyl-3-cyanoguanidine, 1-(p-chlorophenyl)-3-cyanoguanidine, nitroguanidine, 1-methyl-3-nitroguanidine, 1-ethyl-3-nitroguanidine, 1-butyl-3-nitroguanidine, and 1-benzyl-3-nitroguanidine.

11. A cold-curing epoxy resin composition according to claim 9 , wherein the amine curing agent comprises at least one member selected from the group consisting of an alkyldiamine, aryldiamine, alkylpolyamine, arylpolyamine and polyetheramine, wherein the amine curing agent in each case comprises at least two free amine groups.

12. A cold-curing epoxy resin composition according to claim 9 , wherein the amine curing agent is selected from the group of ethylenediamine, diethylenetriamine, triethylenetetramine, meta-xylylenediamine, methylenedianiline, para-aminocyclohexylmethane, isophoronediamine and a polyetheramine.

13. A cold-curing epoxy resin composition according to claim 9 , wherein the composition further comprises at least one member selected from the group consisting of auxiliary substance and an additive.

14. A cold-curing epoxy resin composition according to claim 13 , wherein the auxiliary substance or additive is selected from the group consisting of a reactive diluent, a filler, a rheological additive, a thixotroping agent, a dispersion additive, an anticaking agent, a dye, a pigment, an impact modifier and a flameproofing additive.

15. A method for producing a cold-curing epoxy resin composition according to claim 9 comprising the steps of:

a. providing the cold-curing epoxy resin, wherein the cold-curing epoxy resin has on average more than one epoxy group per molecule,

b. adding the amine curing agent for the cold-curing epoxy resin which is activatable at a temperature of <60° C. ,

c. adding the curing accelerator;

with the proviso that method steps b) and c) proceed in succession or simultaneously.

16. A method according to claim 15 , wherein the amine curing agent is added first and thereafter the curing accelerator is added.

17. A method according to claim 15 , further comprising, adding, before steps b) or c), an auxiliary substance or an additive.

18. A method according to claim 17 , wherein the auxiliary substance or additive is selected from the group consisting of a reactive diluent, a filler, a rheological additive, a thixotroping agent, a dispersion additive, an anticaking agent, a dye, a pigment, an impact modifier and a flameproofing additive.

19. A method according to claim 15 that is conducted without input of heat.

20. A cold-curing epoxy resin composition according to claim 9 , wherein the amine curing agent comprises at least one member selected from the group consisting of an alkyldiamine, aryldiamine, alkylpolyamine and arylpolyamine, wherein the amine curing agent in each case comprises at least two free amine groups, and wherein the cold-curing epoxy resin composition does not contain a polyetheramine.

21. A cold-curing epoxy resin composition according to claim 9 , wherein the amine curing agent is selected from the group of ethylenediamine, diethylenetriamine, triethylenetetramine, meta-xylylenediamine, methylenedianiline, para-aminocyclohexylmethane and isophoronediamine, and wherein the cold-curing epoxy resin composition does not contain a polyetheramine.

22. A method of accelerating curing of a cold-curing epoxy resin composition comprising adding to the cold-curing epoxy resin a guanidine derivative of Formula (I)

wherein:

R 1 is —CN, —NO 2 or —(C═O)—R 4 ;

R 2 is —H, alkyl, benzyl, phenyl, aryl or —(C═O)—R 4 ;

R 3 is —H or alkyl;

R 4 is —H, alkyl, or —O-alkyl;

wherein, when R 1 is —CN or —(C═O)—R 4 , R 2 is not —H if R 3 is —H;

wherein the cold-curing epoxy resin composition further comprises at least one amine curing agent for the epoxy resin which is activatable at a temperature of <60° C., and wherein the cold-curing epoxy resin composition does not contain a polyetheramine.

23. A cold-curing epoxy resin composition comprising:

a curing accelerator comprising guanidine derivative of Formula (I)

wherein:

R 1 is —CN, —NO 2 or —(C═O)—R 4 ;

R 2 is —H, alkyl, benzyl, phenyl, aryl or —(C═O)—R 4 ;

R 3 is —H or alkyl;

R 4 is —H, alkyl, or —O-alkyl;

wherein, when R 1 is —CN or —(C═O)—R 4 , R 2 is not —H if R 3 is —H;

a cold-curing epoxy resin, and an amine curing agent for the epoxy resin which is activatable at a temperature of <60° C. , and wherein the cold-curing epoxy resin composition does not contain a polyetheramine.

Assignments (2)
CHANGE OF NAME Recorded Jul 31, 2018
From: ALZCHEM AG
To: ALZCHEM TROSTBERG GMBH
Reel/Frame 046670/0167 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2012
From: HITZLER, MARTIN; KRIMMER, HANS-PETER; STROBEL, SYLVIA; BRANDL, MONIKA
To: ALZCHEM AG
Reel/Frame 027951/0318 →
Priority Claims (1)
DE 10 2009 052 061 · Nov 5, 2009 · national
Continuity (1)
Related Publication 20120208925A1 · Aug 16, 2012