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US4440914A Expired / Lapsed US ⏱️ 0.0 years remaining

Solid epoxy resin systems

Assignee: BASF Corp
•
Filing: 1982-09-20
•
Granted: 1984-04-03
•
Expires: 2002-09-20
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Abstract

Abstract Solid epoxy resin systems comprising the reaction products of a polyepoxide compound with a functionality greater than two, a diglycidyl ether of a polyhydric phenol and a polyhydric phenol; said systems being applicable for use in a variety of applications and particularly in combination with phenolic novolac hardeners for molding applications.

Inventors

  • 👤 David Helfand
  • 👤 Ralph F. Sellers

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 17:07
CPC Classifications
C; C08; C08G; C08G59/00; C08G59/02; C08G59/04; C08G59/06; C08G59/066; C08G59/18; C08G59/20; C08G59/32; C08G59/38

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 123 words
A solid advanced epoxy resin comprising the reaction product resulting from a catalyzed advancement reaction of (a) a polyepoxide resin having a functionality greater than two, said resin (1) corresponding to the formula ##STR4## wherein R is H or CH 3 and n is about 0.2-6.0, or (2) being the tetraglycidyl ether of tetra[hydroxyphenyl)ethane; (b) a diglycidyl ether of a polyhydric phenol or the alkyl or halogen derivatives thereof; and (c) a polyhydric phenol or the alkyl or halogen derivatives thereof; components (a) and (b) being present in concentration ranges of from 60-90%, by weight, and 10-40%, by weight, respectively, and component (c) being present in a concentration range of 2 to 23%, based on the total weight of components (a) and (b).
Claim 2
Dependent Claim 123 words
A solid advanced epoxy resin comprising the reaction product resulting from a catalyzed advancement reaction of (a) a polyepoxide resin having a functionality greater than two, said resin (1) corresponding to the formula ##STR4## wherein R is H or CH 3 and n is about 0.2-6.0, or (2) being the tetraglycidyl ether of tetra[hydroxyphenyl)ethane; (b) a diglycidyl ether of a polyhydric phenol or the alkyl or halogen derivatives thereof; and (c) a polyhydric phenol or the alkyl or halogen derivatives thereof; components (a) and (b) being present in concentration ranges of from 60-90%, by weight, and 10-40%, by weight, respectively, and component (c) being present in a concentration range of 2 to 23%, based on the total weight of components (a) and (b).
Claim 3
Dependent Claim 16 words
The resin product of claim 1, wherein component (a) is the epoxidation product of cresol novolacs.
Claim 4
Dependent Claim 15 words
The resin product of claim 1, wherein component (a) is the tetraglycidyl ether of tetra[hydroxyphenyl]ethane.
Claim 5
Dependent Claim 36 words
The resin product of claim 1, wherein component (b) is selected from the group consisting of diglycidyl ethers of bisphenols corresponding to the formula ##STR5## wherein m is 0-50 and X is --CH 2 , ##STR6##
Claim 6
Dependent Claim 18 words
The resin product of claims 2 or 3, wherein component (b) in the diglycidyl ether of bisphenol A.
Claim 7
Dependent Claim 15 words
The resin product of claim 1, wherein component (c) is bisphenol F, A or S.
Claim 8
Dependent Claim 12 words
The resin product of claim 5, wherein component (c) is bisphenol A.
Claim 9
Dependent Claim 18 words
The resin product of claim 1, wherein component (a) is present in a concentration of 65-75%, by weight.
Claim 10
Dependent Claim 26 words
The resin product of claim 6, wherein component (c) is present in a concentration of 5-12%, based on the total weight of components (a) and (b).
Claim 11
Dependent Claim 36 words
The resin product of claim 1 comprising the reaction product of 70 parts epoxy cresol novolac, 30 parts of the diglycidylated ether of bisphenol A and 11 parts of bisphenol A, all parts being by weight.
Claim 12
Dependent Claim 36 words
The resin product of claim 1 comprising the reaction product of 70 parts epoxy cresol novolac, 30 parts of the diglycidylated ether of bisphenol A and 9 parts of bisphenol A, all parts being by weight.
Claim 13
Dependent Claim 39 words
The resin product of claim 1 comprising the reaction product of 70 parts of the tetraglycidyl ether of tetra[hydroxyphenyl]ethane, 30 parts of the diglycidylated ether of bisphenol A and 8 parts of bisphenol A, all parts being by weight.
Claim 14
Dependent Claim 22 words
A heat curable composition which comprises the resin product of either of claims 1, 10, 11 or 12 and a hardener therefor.
Claim 15
Dependent Claim 16 words
The cured product obtained from the elevated temperature curing of the curable mixture of claim 13.
Claim 16
Dependent Claim 26 words
A molding composition comprising a resin product of either claims 1, 10, 11 or 12, an inert filler material, a novolac hardener and a curing accelerator.
Claim 17
Dependent Claim 15 words
The molding composition of claim 15, wherein said novolac hardener is a phenol novolac hardener.
Claim 18
Dependent Claim 17 words
The cured molding composition obtained from the elevated temperature curing of the molding composition of claim 15.

References Cited (Backward Citations)

US3367990A Cited
US3100756A Cited
US3452116A Cited
US3488404A Cited
DE2505345A1 Cited
US4169187A Cited
US4288565A Cited
GB2055843A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-04-03 1987-10-03 1988-04-03 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-04-03 1991-10-03 1992-04-03 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-04-03 1995-10-03 1996-04-03 $7700.00 Window Closed / Lapsed

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