IP Library › Granted Patent US 11,441,027
Granted Patent B2
US 11,441,027 · App. 16/755,945 · Granted Sep 13, 2022

Epoxy resin composition, prepreg, and fiber-reinforced composite material

Inventors: Akihiko Ito (Ehime, JP); Hiroaki Sakata (Ehime, JP)
Assignee: TORAY INDUSTRIES, INC.
C08L63/00C08G59/245C08G59/28C08G59/3227C08G59/4014C08J5/04C08J5/24C08K5/5397C08L81/06C08L2201/02C08L2205/03
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Quick Facts
Patent No.
US 11,441,027
App. No.
16/755,945
Granted
Sep 13, 2022
Kind
B2
Abstract

The purpose of the present invention is to provide an epoxy resin composition which has excellent viscosity stability, and when cured, can provide a resin cured product which has high flame retardancy and excellent mechanical properties, and a prepreg and fiber-reinforced composite material using the epoxy resin composition. An embodiment of the epoxy resin composition according to the present invention which achieves the purpose contains all components [A]-[C]. [A]: A reactive diluent having a specific structure and a viscosity of 2 Pa·s or less at 25° C. [B]: An epoxy resin having three of more functional groups. [C]: An amine-based curing agent having a specific structure.

Claims (48)

1. An epoxy resin composition comprising:

at least one reactive diluent [A] having a viscosity of 2 Pas or less at 25° C. and selected from the group consisting of a reactive diluent having a structure represented by general formula (4), a reactive diluent having a structure represented by general formula (7), and a reactive diluent having a structure represented by general formula (8);

at least one trifunctional or higher functional epoxy resin [B] selected from the group consisting of N,N,O-triglycidyl-m-aminophenol, N,N,O-triglycidyl-p-aminophenol, N,N,O-triglycidyl-4-amino-3-methylphenol, N,N,N′,N′-tetraglycidyl-4,4′-methylenedianiline, N,N,N′,N′-tetraglycidyl-2,2′-diethyl-4,4′-methylenedianiline and N,N,N′,N′-tetraglycidyl-m-xylylenediamine;

at least one amine-based hardener [C] selected from the group consisting of an amine-based hardener having a structure represented by general formula (2) and an amine-based hardener having a structure represented by general formula (3);

optionally, a non-phosphorus-containing aromatic polyamine hardener provided in an amount of up to 90 parts by mass based on 100 parts by mass total of [C] and the aromatic polyamine hardener; and

at least one thermoplastic resin [D] composed of a polyaryl ether skeleton:

wherein in the general formula (4), R 3 and R 4 each independently represent at least one selected from the group consisting of a hydrogen atom, an aliphatic hydrocarbon group with a carbon number of 1 to 4, an alicyclic hydrocarbon group with a carbon number of 3 to 6, an aromatic hydrocarbon group with a carbon number of 6 to 10, a halogen atom, an acyl group, a trifluoromethyl group and a nitro group; and X 3 represents one selected from the group consisting of —O—, —S—, —CO—, —C(═O)O— and —S 2− ;

wherein in the general formula (7), R 7 and R 8 each independently represent at least one selected from the group consisting of a hydrogen atom, an aliphatic hydrocarbon group with a carbon number of 1 to 4, an alicyclic hydrocarbon group with a carbon number of 3 to 6, an aromatic hydrocarbon group with a carbon number of 6 to 10, a halogen atom, an acyl group, a trifluoromethyl group and a nitro group, with the proviso that both of R 7 and R 8 are not hydrogen atoms;

wherein in the general formula (8), R 9 and R 10 each independently represent a direct bond, an alkylene group with a carbon number of 1 to 8, a phenylene group or a cyclohexylene group; and R 11 represents one selected from the group consisting of a hydrogen atom, an aliphatic hydrocarbon group with a carbon number of 1 to 4, an alicyclic hydrocarbon group with a carbon number of 3 to 6, an aromatic hydrocarbon group with a carbon number of 6 to 10, a halogen atom, an acyl group, a trifluoromethyl group and a nitro group;

wherein in the general formula (2), R 1 represents a hydrocarbon group with a carbon number of 2 to 4; and in the general formula (3), R 2 represents a hydrogen atom or an amino group;

wherein [A] is present in an amount of 10 to 50 parts by mass and [B] is present in an amount of 50 to 90 parts by mass, totaling 100 parts by mass; and

wherein [C] is present in amount to provide a phosphorus atom content of 1.0 to 5.0% by mass, based on the overall mass of the epoxy resin composition.

2. The epoxy resin composition according to claim 1 , wherein [A] comprises a reactive diluent having a structure represented by general formula (4) or a reactive diluent having a structure represented by general formula (7).

3. The epoxy resin composition according to claim 1 , wherein R 3 and R 4 of the general formula (4) is a hydrogen atom.

4. The epoxy resin composition according to claim 1 , wherein at least one of R 7 and R 8 of the general formula (7) is a methyl group.

5. The epoxy resin composition according to claim 1 , wherein [A] is selected from the group consisting of N,N-diglycidyl-4-phenoxyaniline, N,N-diglycidyl-o-toluidine, N,N-diglycidyl-m-toluidine, N,N-diglycidyl-p-toluidine, N,N-diglycidyl-2,3-xylidine, N,N-diglycidyl-2,4-xylidine, N,N-diglycidyl-3,4-xylidine, 1,4-cyclohexanedimethanol diglycidyl ether, and 1,4-cyclohexanediethanol diglycidyl ether.

6. The epoxy resin composition according to claim 1 , wherein [A] is present in an amount of 20 to 40 parts by mass and [B] is present in an amount of 60 to 80 parts by mass, totaling 100 parts by mass.

7. The epoxy resin composition according to claim 1 , wherein [C] comprises an amine-based hardener having a structure represented by general formula (3).

8. The epoxy resin composition according to claim 7 , wherein R 2 in the general formula (3) is an amino group.

9. The epoxy resin composition according to claim 1 , wherein [D] comprises polyethersulfone.

10. The epoxy resin composition according to claim 9 , wherein [D] is present in amount of 24 to 27 parts by mass based on the total 100 parts by mass of [A] and [B].

11. The epoxy resin composition according to claim 1 , wherein the optional aromatic polyamine hardener is not present, and the epoxy resin composition has a viscosity increase ratio after 2 hours at 80° C. of 7% to 30%, and a cured product of the epoxy resin composition has a flexural modulus of 4.1 to 4.5 GPa and a char production ratio at 650° C. of 25% to 30%.

12. The epoxy resin composition according to claim 1 , wherein the optional aromatic polyamine hardener is present and is 3,3′-diaminodiphenyl sulfone.

13. The epoxy resin composition according to claim 12 , wherein the epoxy resin composition has a viscosity increase ratio after 2 hours at 80° C. of 12% to 47%, and a cured product of the epoxy resin composition has a flexural modulus of 3.8 to 4.8 GPa and a char production ratio at 650° C. of 9% to 17%.

14. A prepreg obtained by impregnating a reinforced fiber with the epoxy resin composition described in claim 1 .

15. A fiber-reinforced composite material obtained by curing the prepreg described in claim 14 .

16. A fiber-reinforced composite material comprising a cured resin obtained by curing the epoxy resin composition described in claim 1 , and a reinforced fiber.

17. An epoxy resin composition comprising

a difunctional glycidyl amine epoxy resin [A′] represented by general formula (4);

at least one trifunctional or higher functional epoxy resin [B] selected from the group consisting of N,N,O-triglycidyl-m-aminophenol, N,N,O-triglycidyl-p-aminophenol, N,N,O-triglycidyl-4-amino-3-methylphenol, N,N,N′,N′-tetraglycidyl-4,4′-methylenedianiline, N,N,N′,N′-tetraglycidyl-2,2′-diethyl-4,4′-methylenedianiline and N,N,N′,N′-tetraglycidyl-m-xylylenediamine;

at least one amine-based hardener [C] selected from the group consisting of an amine-based hardener having a structure represented by general formula (5) and an amine-based hardener having a structure represented by general formula (6);

optionally, a non-phosphorus-containing aromatic polyamine hardener provided in an amount of up to 90 parts by mass based on 100 parts by mass total of [C′] and the aromatic polyamine hardener; and

at least one thermoplastic resin [D] composed of a polyaryl ether skeleton:

wherein in the general formula (4), R 3 and R 4 each independently represent at least one selected from the group consisting of a hydrogen atom, an aliphatic hydrocarbon group with a carbon number of 1 to 4, an alicyclic hydrocarbon group with a carbon number of 3 to 6, an aromatic hydrocarbon group with a carbon number of 6 to 10, a halogen atom, an acyl group, a trifluoromethyl group and a nitro group; and X 3 represents one selected from the group consisting of —O—, —S—, —CO—, —C(═O)O— and —SO 2− ;

wherein in the general formula (5), R 5 represents a hydrocarbon group with a carbon number of 1 to 4; and in general formula (6), R 6 represents a hydrogen atom or an amino group;

wherein [A] is present in an amount of 10 to 50 parts by mass and [B] is present in an amount of 50 to 90 parts by mass, totaling 100 parts by mass; and

wherein [C] is present in amount to provide a phosphorus atom content of 1.0 to 5.0% by mass, based on the overall mass of the epoxy resin composition.

18. The epoxy resin composition according to claim 17 , wherein R 3 and R 4 of the general formula (4) is a hydrogen atom.

19. The epoxy resin composition according to claim 17 , wherein [C′] comprises an amine-based hardener having a structure represented by general formula (6).

20. The epoxy resin composition according to claim 19 , wherein R 6 in the general formula (6) is an amino group.

21. The epoxy resin composition according to claim 17 , wherein [D] comprises polyethersulfone.

22. The epoxy resin composition according to claim 21 , wherein [D] is present in amount of 24 to 27 parts by mass based on the total 100 parts by mass of [A] and [B].

23. The epoxy resin composition according to claim 17 , wherein the optional aromatic polyamine hardener is not present, the epoxy resin composition has a viscosity increase ratio after 2 hours at 80° C. of 7% to 30%, and a cured product of the epoxy resin composition has a flexural modulus of 4.1 to 4.5 GPa and a char production ratio at 650° C. of 25% to 30%.

24. The epoxy resin composition according to claim 17 , wherein the optional aromatic polyamine hardener is present and is 3,3′-diaminodiphenyl sulfone.

25. The epoxy resin composition according to claim 24 , wherein the epoxy resin composition has a viscosity increase ratio after 2 hours at 80° C. of 13% to 47%, and a cured product of the epoxy resin composition has a flexural modulus of 4.3 to 4.6 GPa and a char production ratio at 650° C. of 11% to 17%.

26. A prepreg obtained by impregnating a reinforced fiber with the epoxy resin composition described in claim 17 .

27. A fiber-reinforced composite material obtained by curing the prepreg described in claim 26 .

28. A fiber-reinforced composite material comprising a cured resin obtained by curing the epoxy resin composition described in claim 17 , and a reinforced fiber.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 31, 2020
From: ITO, AKIHIKO; SAKATA, HIROAKI
To: TORAY INDUSTRIES, INC.
Reel/Frame 053639/0945 →
Priority Claims (1)
JP JP2017-205030 · Oct 24, 2017 · national
Continuity (1)
Related Publication 20200247986A1 · Aug 6, 2020