IP Library Granted Patent US 10,875,997
Granted Patent B2
US 10,875,997 · App. 14/374,824 · Granted Dec 29, 2020

Blends of liquid epoxy and solid phenoxy resins

Inventors: Helga De Velder (Ottignies-Louvain-la-Neuve, BE); Alain Leroy (Ottignies-Louvain-la-Neuve, BE); Jean Riviere (Ottignies-Louvain-la-Neuve, BE); Eckhard Rühle (Esslingen, DE)
Assignee: HEXION INC.
C08L63/00C08J5/24C08G2650/56C08L2201/54Y10T428/24994Y10T428/249921Y10T442/652
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Quick Facts
Patent No.
US 10,875,997
App. No.
14/374,824
Granted
Dec 29, 2020
Kind
B2
Abstract

This invention relates to epoxy resin formulations for preforms to be used in molding processes, especially resin transfer molding processes and to methods for preparing the performs. The epoxy formulation is based on liquid or solid epoxy resins blended, with medium to high molecular weight, phenoxy resins. These formulations are highly compatible with epoxy curable injection resins, and more over are reacted in the polymeric matrix, without reducing the glass transition temperature (Tg) of the cured composite material.

Claims (21)

1. An epoxy resin formulation consisting essentially of a blend of:

a solid phenoxy resin comprising an average molecular weight between 30000 to 65000 daltons, and

a liquid epoxy resin selected from a diglycidyl ether of biphenol, bisphenol, hydrocarbyl-substituted biphenol, hydrocarbyl-substituted bisphenol, phenol- or hydrocarbyl-substituted bisphenol-aldehyde novolac resin, unsaturated hydrocarbon-phenol or hydrocarbyl-substituted phenol resin, with a level of the solid phenoxy resin on the liquid epoxy resin in the range of from 10 to 25 weight %, and with a level of the liquid epoxy resin on the solid phenoxy resin in the range of from 75 to 90 weight %, wherein the solid phenoxy resin comprises a linear resin terminated with phenolic functions and wherein the phenoxy resins are based on advanced bis-phenol A glycidyl ether with bis-phenol A; and

a solvent,

wherein the epoxy resin formulation does not contain a curing agent and/or a curing catalyst, and wherein the solvent is water.

2. The epoxy resin formulation of claim 1 wherein the solid phenoxy resin is present in an amount between 10 and 20 weight %.

3. A film based material comprising the epoxy resin formulation of claim 1 .

4. A fiber based material comprising:

the epoxy resin formulation of claim 1 and

an infusion curable epoxy resin system comprising an epoxy resin and a curing agent and/or a curing catalyst.

5. The fiber based material of claim 4 wherein the fibers are placed in one direction per layer.

6. The fiber based material of claim 4 in contact with a curable infusion system.

7. The fiber based material of claim 6 wherein the infusion system is based on epoxy curable resins.

8. The epoxy resin formulation of claim 1 wherein the epoxy resin is a diglycidyl ether of Bisphenol A having an epoxide equivalent weight of from about 185 to about 250.

9. An epoxy resin formulation consisting of a blend of:

a solid phenoxy resin comprising an average molecular weight between 30000 to 65000 daltons,

a liquid epoxy resin selected from a diglycidyl ether of biphenol, bisphenol, hydrocarbyl-substituted biphenol, hydrocarbyl-substituted bisphenol, phenol- or hydrocarbyl-substituted bisphenol-aldehyde novolac resin, unsaturated hydrocarbon-phenol or hydrocarbyl-substituted phenol resin, with a level of the solid phenoxy resin on the liquid epoxy resin in the range of from 10 to 25 weight %, and with a level of the liquid epoxy resin on the solid phenoxy resin in the range of from 75 to 90 weight %, wherein the solid phenoxy resin comprises a linear resin terminated with phenolic functions and wherein the phenoxy resins are based on advanced bis-phenol A glycidyl ether with bis-phenol A; and

optionally a solvent.

10. The epoxy resin formulation of claim 9 wherein the solid phenoxy resin is present in an amount between 10 and 20 weight %.

11. The epoxy resin formulation of claim 9 wherein the epoxy resin is a diglycidyl ether of Bisphenol A having an epoxide equivalent weight of from about 185 to about 250.

12. The epoxy resin formulation of claim 9 wherein the solvent is water.

Assignments (13)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2022
From: HEXION INC.
To: WESTLAKE EPOXY INC.
Reel/Frame 061611/0876 →
PARTIAL TERMINATION AND RELEASE OF SECURITY INTEREST IN SPECIFIED PATENTS (ABL) Recorded Feb 1, 2022
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 058932/0915 →
PARTIAL TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS (TERM LOAN) Recorded Feb 1, 2022
From: JPMORGAN CHASE BANK, N.A.
To: HEXION INC.
Reel/Frame 058932/0923 →
PATENT SECURITY INTEREST (ABL) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049740/0770 →
PATENT SECURITY INTEREST (TERM LOAN) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049741/0425 →
PATENT SECURITY INTEREST ASSIGNMENT AGREEMENT Recorded Apr 3, 2019
From: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS THE PRIOR COLLATERAL AGENT
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS THE CURRENT COLLATERAL AGENT
Reel/Frame 048788/0617 →
RELEASE OF SECURITY INTEREST Recorded Feb 23, 2017
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: HEXION INC. (FORMERLY KNOWN AS MOMENTIVE SPECIALTY CHEMICALS INC.)
Reel/Frame 041793/0811 →
SECURITY INTEREST Recorded Feb 13, 2017
From: HEXION INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 041693/0888 →
SECURITY INTEREST Recorded Feb 16, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 034967/0872 →
CHANGE OF NAME Recorded Feb 3, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: HEXION INC.
Reel/Frame 034882/0816 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 15, 2014
From: DE VELDER, HELGA; LEROY, ALAIN; RIVIERE, JEAN; RUEHLE, ECKARD
To: MOMENTIVE SPECIALTY CHEMICALS INC.
Reel/Frame 034509/0229 →
SECURITY INTEREST Recorded Oct 22, 2014
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 034003/0145 →
SECURITY INTEREST Recorded Oct 22, 2014
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST COMPANY, AS COLLATERAL AGENT
Reel/Frame 034003/0182 →