IP Library Granted Patent US 7,217,771
Granted Patent B2
US 7,217,771 · App. 10/485,440 · Granted May 15, 2007

Epoxy resin

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Quick Facts
Patent No.
US 7,217,771
App. No.
10/485,440
Granted
May 15, 2007
Kind
B2
Abstract

Compositions containing: (a) a liquid epoxy resin; (b) an aliphatic or cycloaliphatic primary monoamine and/or an aliphatic or cycloaliphatic disecondary diamine; (c) a latent curing agent for the epoxy resin (a) which does not react until temperatures above 70° C. (measured by means of DSC at a heating rate of 10° C./min); (d) a photopolymerizable compound; and (e) a photoinitiator; the ratio of the number of equivalents of epoxy groups to that of photopolymerizable groups being 1:0.01 to 1:0.7, are suitable as impregnating resins.

Claims (15)

1. Composition containing

(a) a liquid epoxy resin,

(b) an aliphatic or cycloaliphatic primary monoamine and/or an aliphatic or cycloaliphatic disecondary diamine,

(c) a latent curing agent for the epoxy resin (a) which does not react until temperatures above 70° C. (measured by means of DSC at a heating rate of 10° C./min),

(d) a photopolymerizable compound and

(e) a photoinitiator,

the ratio of the number of equivalents of epoxy groups to that of photopolymerizable groups being 1:0.01 to 1:0.07 and wherein the composition contains 0.25–0.75 aminehydrogen equivalent of the component (b) per epoxide equivalent of the epoxy resin (a).

2. Composition according to claim 1 , containing a bisphenol diglycidyl ether or an epoxy novolak as component (a).

3. Composition according to claim 1 , containing bisphenol A diglycidyl ether or an epoxycresol novolak as component (a).

4. Composition according to claim 1 , containing a primary monoamine as component (b).

5. Composition according to claim 1 , containing benzylamine, n-octylamine, 2-phenylethylamine, 3-(2-ethylhexyloxy)propylamine or 2-(2-aminoethoxy)ethanol as component (b).

6. Composition according to claim 1 , containing diaminodiphenylsulphone, dicyandiamide, phenylimidazole and 2,4,6-tris(dimethylaminomethyl)phenol as component (c).

7. Composition according to claim 1 , containing an acrylic acid ester or a methacrylic acid ester as component (d).

8. Composition according to claim 1 , containing ethylene glycol dimethacrylate, 1,4-butanediol dimethacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2-ethoxyethyl methacrylate, 1,1,1-trimethylolpropane trimethacrylate, pentaerythritol tetraacrylate or dipentaerythritol pentacrylate as component (d).

9. Composition according to claim 1 , containing isopropylthioxanthone or 2-methyl-1-[4-(methylthio) phenyl]-2-morpholinopropan-1-one as component (e).

Assignments (5)
TERMINATION AND RELEASE OF SECURITY INTEREST IN UNITED STATES TRADEMARKS AND PATENTS Recorded Jun 13, 2018
From: JPMORGAN CHASE BANK, N.A.
To: HUNTSMAN ADVANCED MATERIALS AMERICAS INC. (N/K/A HUNTSMAN ADVANCED MATERIALS AMERICAS LLC)
Reel/Frame 046352/0893 →
CORRECTIVE ASSIGNMENT TO CORRECT THE NATURE OF CONVEYANCE FROM ASSIGNMENT TO SECURITY AGREEMENT PREVIOUSLY RECORDED ON REEL 025855 FRAME 0192. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 28, 2011
From: DEUTSCHE BANK TRUST AG NEW YORK BRANCH, AS RESIGNING ADMINISTRATIVE AGENT AND COLLATERAL AGENT
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 026515/0735 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 28, 2011
From: DEUTSCHE BANK TRUST AG NEW YORK BRANCH, AS RESIGNING ADMINISTRATIVE AGENT AND COLLATERAL AGENT
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 025855/0192 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 22, 2006
From: SETIABUDI, FRANS
To: HUNTSMAN ADVANCED MATERIALS AMERICAS INC
Reel/Frame 017832/0921 →
SECURITY INTEREST Recorded Jan 20, 2006
From: HUNTSMAN ADVANCED MATERIALS AMERICAS, INC.
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS AGENT
Reel/Frame 017164/0639 →