IP Library Granted Patent US 9,840,588
Granted Patent B2
US 9,840,588 · App. 12/642,420 · Granted Dec 12, 2017

Epoxy resin curing compositions and epoxy resin systems including same

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Quick Facts
Patent No.
US 9,840,588
App. No.
12/642,420
Granted
Dec 12, 2017
Kind
B2
Abstract

Disclosed are epoxy resins exhibiting a highly favorable combination of tensile strength and elongation with respect to prior art epoxy systems. The elastomeric epoxy resin systems of the invention are prepared utilizing a curing agent containing at least one monoprimary amine, and are particularly useful in applications such as, for example, castings, potting, composites, crack sealing, coatings, adhesives, roofing materials, flooring or reinforced membranes.

Claims (29)

1. A composition comprising an epoxy resin system, the epoxy resin system comprising a reaction product of:

an epoxy resin component; and

a curing agent comprising:

a monoprimary amine represented by any one of the formulae R′—O—R—NH 2 , R′S—R—NH 2 , R′ 2 N—R—NH 2 , R′ 2 P—R—NH 2 , or R′ 3 Si—RNH 2 wherein each of R or R′ is independently a hydrocarbyl group such that a combination of R plus all R′ groups contains a total of between about 8 and about 50 carbon atoms; and

an adduct of a polyepoxide and a compound having two or more primary amine moieties linked to a common central organic moiety;

wherein when cured, the reaction product of the epoxy resin component and the curing agent exhibits a tensile strength of >1 MPa, and an elongation of >100% as measured by ASTM D-368 at 25° C.

2. The composition of claim 1 wherein the curing agent further comprises an amine terminated polyamide which is the reaction product of a dimerized fatty acid or hydrogenated dimerized fatty acid with an amine containing one primary and one secondary amine group or two secondary amine groups.

3. The composition of claim 2 wherein the amine terminated polyamide is prepared by reacting:

(a) carboxylic acids selected from C 18 -C 60 dicarboxylic acids, C 18 -C 60 dicarboxylic acid derivatives and mixtures thereof, wherein the carboxylic acids optionally contain di- or polycarboxylic acids or acid derivatives having from 4 to 20 carbon atoms in an amount ranging from 0-10% based on all carboxylic acids; and

(b) at least one amine having the formula:

R 1 —NH—R 2 —NH—R 3

wherein R 1 has a total number of carbon atoms from 0 to about 20 and is selected from the group consisting of hydrogen, alkyl, cycloalkyl, alkenyl, arylalkyl, hydroxyalkyl, alkoxyalkyl, cyanoalkyl, alkylthioalkyl, dialkylaminoalkyl, aryl, alkylaryl, cyanoaryl, alkoxyaryl, alkylthioaryl, and dialkylaminoaryl;

R 3 has a total number of carbon atoms from 1 to about 20 and is selected from the group consisting of alkyl, cycloalkyl, alkenyl, arylalkyl, hydroxyalkyl, alkoxyalkyl, cyanoalkyl, alkylthioalkyl, dialkylaminoalkyl, aryl, alkylaryl, cyanoaryl, alkoxyaryl, alkylthioaryl, and dialkylaminoaryl; and

R 2 is (CR 4 R 5 ) n , wherein n is from 2 to about 20, R 4 is independently selected for each (CR 4 R 5 ) from the group consisting of H, alkyl, aryl, hydroxyl, alkoxy, alkylthio, dialkylamino and cyano; and R 5 is independently selected for each (CR 4 R 5 ) from the group consisting of H, alkyl and aryl.

4. The composition of claim 2 wherein the amine terminated polyamide is prepared by reacting:

at least one C 18 -C 50 dicarboxylic acid, dicarboxylic acid ester or dicarboxylic acid chloride with an aminoalkylpiperazine having the formula:

wherein R 1 is hydrogen and R 2 is —R 3 —NH 2 wherein R 3 is a divalent aliphatic linkage with optional —CHR 4 and —CR 4 R 5 units, wherein R 4 and R 5 are independently alkyl groups.

5. The composition of claim 1 wherein the monoprimary amine is represented by the formula R′—O—R—NH 2 wherein each of R or R′ is independently a hydrocarbyl group such that a combination of R plus R′ contains a total of between about 8 and about 50 carbon atoms.

6. The composition of claim 1 wherein the monoprimary amine is represented by the formula R′ 2 N—R—NH 2 wherein each of R or R′ is independently a hydrocarbyl group such that a combination of R plus both R′ groups contains a total of between about 8 and about 50 carbon atoms.

7. The composition of claim 1 wherein the compound having two or more primary amine moieties linked to a common central organic moiety may comprise an amine compound selected from the group consisting of aliphatic polyamines, cycloaliphatic polyamines, polyglycoldiamines, polyoxypropylene diamines, polyoxypropylenetriamines, araliphatic polyamines, heterocyclic amines, aromatic polyamines, and combinations thereof, having two or more primary amine moieties linked to a common central organic moiety.

8. The composition of claim 1 wherein the epoxy resin system further comprises a monofunctional or polyfunctional epoxy diluent.

9. The composition of claim 1 wherein the epoxy resin system further comprises a polyacrylate or polymethacrylate ester of a polyol.

10. The composition of claim 1 wherein the epoxy resin system further comprises an accelerator.

11. The composition of claim 10 wherein the accelerator comprises a compound selected from the group of alkylbenzenesulfonates, phosphonates, sulfates, tetrafluoroborates, carboxylates and nitrates of Groups IA, IIA and transition metals of the Periodic Table, inorganic acids, carboxylic acids, phenolic compounds, imidazoles, cyanamide compounds, sulfonamides, imides, and combinations thereof.

12. The composition of claim 1 wherein the composition is free of asphalt.

13. The composition of claim 1 wherein the monoprimary amine comprises one or more amines selected from the group consisting of octyl 3-aminopropyl ether, 2-ethylhexyl 3-aminopropyl ether, lauryl 3-aminopropyl ether, myristyl 3-aminopropyl ether, stearyl 3-aminopropyl ether, oleyl 3-aminopropyl ether, behenyl 3-aminopropyl ether and tridecyl 3-aminopropyl ether (linear or branched) and combinations thereof.

14. The composition of claim 1 wherein the curing agent has a Brookfield viscosity of 3000 cP or less at 25° C.

15. The composition of claim 1 wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a Tg below 30° C. as measured by Differential Scanning calorimetry.

16. The composition of claim 2 , wherein, when cured, the reaction product of the epoxy resin component and the curing agent exhibits a T g below 30° C. as measured by Differential Scanning calorimetry.

Assignments (17)
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 (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 (ABL) Recorded Jul 12, 2019
From: HEXION INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 049740/0770 →
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (030146/0970) Recorded Jul 9, 2019
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
To: HEXION INC. (FORMERLY KNOWN AS MOMENTIVE SPECIALTY CHEMICALS INC.)
Reel/Frame 049706/0264 →
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 (SUCCESSOR BY MERGER TO WILMINGTON TRUST FSB), AS COLLATERAL AGENT
To: HEXION INC. (FORMERLY KNOWN AS HEXION SPECIALTY CHEMICALS INC.); BORDEN CHEMICAL FOUNDRY, LLC; HEXION INVESTMENTS INC. (FORMERLY KNOWN AS BORDEN CHEMICAL INVESTMENTS, INC.); HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; HEXION INTERNATIONAL INC. (FORMERLY KNOWN AS BORDEN CHEMICAL INTERNATIONAL INC.); OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
Reel/Frame 041793/0001 →
SECURITY INTEREST Recorded Feb 13, 2017
From: HEXION INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 041693/0888 →
CHANGE OF NAME Recorded Feb 3, 2015
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: HEXION INC.
Reel/Frame 034882/0816 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 030146/0970 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 030146/0946 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Mar 28, 2013
From: JPMORGAN CHASE BANK, N.A.
To: MOMENTIVE SPECIALTY CHEMICALS INC. (F/K/A HEXION SPECIALTY CHEMICALS, INC.)
Reel/Frame 030111/0021 →
CHANGE OF NAME Recorded Oct 20, 2011
From: HEXION SPECIALTY CHEMICALS, INC.
To: MOMENTIVE SPECIALTY CHEMICALS INC.
Reel/Frame 027096/0480 →
SECURITY AGREEMENT Recorded Feb 5, 2010
From: HEXION LLC; HEXION SPECIALTY CHEMICALS, INC.; BORDEN CHEMICAL FOUNDRY, LLC; BORDEN CHEMICAL INVESTMENTS, INC.; HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; BORDEN CHEMICAL INTERNATIONAL, INC.; OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 023905/0451 →
SECURITY INTEREST Recorded Jan 29, 2010
From: HEXION SPECIALTY CHEMICALS, INC.; BORDEN CHEMICAL FOUNDRY, LLC; BORDEN CHEMICAL INVESTMENTS, INC.; HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; BORDEN CHEMICAL INTERNATIONAL, INC.; OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
To: WILMINGTON TRUST FSB, AS COLLATERAL AGENT
Reel/Frame 023963/0038 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2009
From: CORLEY, LARRY STEVEN; ASH, CARLTON E.
To: HEXION SPECIALTY CHEMICALS, INC.
Reel/Frame 023677/0973 →