Accelerator systems for low-temperature curing
View Patent ↗Composition comprising as component A) a 1-imidazoly[mothyl-substituted 2-naphthol compound of the general formula (I) where R 1 , R 2 and R 3 each independently of one another are H; C 1-17 alkyl; C 3-12 cycloalkyl, optionally substituted by c1-4 alkyl groups; C4 -20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 -alkyl groups; C 7-15 ,phonylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; or aromatic or aliphatic C 3-12 acyf; R 4 , R 5 , R 6 , R 7 , R 8 , and R 9 each independently of one another are H; C 1-12 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyf groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; C 1-12 alkoxy; or OH; and as component B) a phenol which is liquid at room temperature, the weight ratio of component A) to component B) being from 10:90 to 80:20 as accelerator for curable epoxy resin compositions which are used as a compression moulding compound, sinter powder, encapsulating system, casting resin, or for producing prepregs and laminates having very good interlaminar shear strength values using impregnating methods or injection methods, for producing components, especially components of large surface area.
1. Composition comprising as component A) a 1-imidazolylmethyl-substituted 2-naphthol compound of the general formula (I)
where
R 1 , R 2 , and R 3 each independently of one another are H; C- 1-17 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; or aromatic or aliphatic C 3-12 acyl;
R 4 , R 5 , R 6 , R 7 , R 8 and R 9 each independently of one another are H; C 1-12 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; C 1-12 alkoxy; or OH; and
as component B) a phenol selected from the group consisting of 1,4-n-pentylphenol, n-hexylphenol, n-heptylphenol, n-octyphenol, n-decylphenol, and O,O′ -diallyl-bisphenol A which is liquid at room temperature, with a weight ratio of component A) to component B) being from 30:70 to 70:30 and wherein the composition is a liquid.
2. Composition according to claim 1 , wherein R 1 , R 2 and R 3 each independently of one another are H; C 1-12 alkyl; phenyl; or C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups.
3. Composition according to claim 2 , wherein R 2 and R 3 are each H; and R 1 is C 1-12 alkyl; phenyl; or C 7-15 phenylalkyl, optionally substituted by 1- 3 C 1-4 alkyl groups.
4. Composition according to claim 3 , wherein R 2-9 are a hydrogen atom and R 1 is C 1-4 alkyl, or phenyl, optionally substituted by 1-3 C 1-4 alkyl groups.
5. Composition according to claim 1 , wherein component B) is O,O′-diallyl-bisphenol A.
6. Curable composition comprising;
a) an epoxy resin whose epoxide content is from 0.1 to 11 epoxide equivalents/kg;
b) from 5 to 40 parts by weight, based on the total weight of the curable composition, a liquid composition comprising a 1-imidazolylmethyl-substituted 2-naphthol compound of the general formula (I)
where
R 1 , R 2 , and R 3 each independently of one another are H; C 1-17 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; or aromatic or aliphatic C 3-12 acyl;
R 4 , R 5 , R 6 , R 7 , R 8 and R 9 each independently of one another are H; C 1-12 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; C l-12 alkoxy; or OH; and
a phenol selected from the group consisting of 1,4-n-pentylphenol, n-hexylphenol, n-heptylphenol, n-octyphenol, n-decylphenol, and O,O′-diallyl-bisphenol A which is liquid at room temperature, the weight ratio of the 1-imidazolylmethyl- substituted 2-naphthol compound to phenol being from 30:70:70:30;
c) a curing agent for the epoxy resin having from 0.5 to 1.5 functional groups per epoxide group; and optionally
d) one or more additives.
7. Composition according to claim 6 , wherein the curing agent is an amine or polyamine.
8. Composition according to claim 7 , characterized in that the curing agent is a polyoxypropylenediamine.
9. Composition according to claim 6 , characterized in that the epoxy resin is a glycidyl ether, glycidyl ester, N-glycidyl or N,O-glycidyl derivative of an aromatic or heterocyclic compound, or a cycloaliphatic glycidyl compound.
10. A prepreg comprising a curable composition according to claim 6 .
11. A method for making a curable composition comprising adding to an epoxy resin a curing agent, a liquid composition comprising a 1-imidazolylmethyl-substituted 2-naphthol compound of the general formula (I)
where
R 1 , R 2 , and R 3 each independently of one another are H; C 1-17 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; or aromatic or aliphatic C 3-12 acyl;
R 4 , R 5 , R 6 , R 7 , R 8 and R 9 each independently of one another are H; C 1-12 alkyl; C 3-12 cycloalkyl, optionally substituted by C 1-4 alkyl groups; C 4-20 cycloalkyl-alkyl, optionally substituted by C 1-4 alkyl groups; C 6-10 aryl, optionally substituted by 1-3 C 1-4 alkyl groups; C 7-15 phenylalkyl, optionally substituted by 1-3 C 1-4 alkyl groups; C 3-17 alkenyl; C 3-12 alkynyl; C 1-12 alkoxy; or OH; and
a phenol selected from the group consisting of 1,4-n-pentylphenol, n-hexylphenol, n-heptylphenol, n-octyphenol, n-decylphenol, and O,O′-diallyl-bisphenol A which is liquid at room temperature, the weight ratio of the 1-imidazolylmethyl-substituted 2-naphthol compound to phenol being from 30:70 to 70:30.