IP Library Granted Patent US 7,001,977
Granted Patent B2
US 7,001,977 · App. 10/472,100 · Granted Feb 21, 2006

Adducts of polyalkylene glycol monoglycidyl ethers and amine compounds

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Quick Facts
Patent No.
US 7,001,977
App. No.
10/472,100
Granted
Feb 21, 2006
Kind
B2
Abstract

The present invention relates to adducts obtainable by reaction of: A) an amine compound containing 2 or more than 2 amino groups: with B) a polyalkylene glycol monoglycidyl ether of general formula (I), in which R independently of one another (for n>1), is an —H or —CH, radical, and n=1 to 50, characterized in that the reaction ratio of components A) and B) is selected in such a way that the resultant adduct contains 2 or more than 2 amine hydrogen groups: to curable compositions based on these adducts with epoxy resins, and to the use of these curable compositions as casting resin, adhesive, matrix resin, tooling resin or as coating composition, in particular for self-flowing coatings.

Claims (24)

1. An adduct obtainable by reaction of:

A) an amine compound containing two or more than two amino groups, with

B) a polyalkylene glycol monoglycidyl ether of the general formula (I)

 in which R, independently of one another (for n>1), is an —H or —CH 3 radical, and n is 1 to 50;

 wherein the reaction ratio of components A) and B) is selected in such a way that the resultant adduct contains two or more than two amine hydrogen groups.

2. An adduct according to claim 1 , wherein n is 3 to 35 for the polyalkylene monoglycidyl ether of the general formula (I).

3. An adduct according to claim 1 , wherein the polyalkylene glycol monoglycidyl ether is prepared by the addition of epichlorohydrin onto polyalkylene glycol, and wherein said polyalkylene glycol has a mean molecular weight of from 200 to 2000.

4. The adduct of claim 3 , wherein said polyalkylene glycol is polypropylene glycol or polyethylene glycol.

5. An adduct according to claim 1 , wherein component A) is a cycloaliphatic, heterocyclic, aromatic polyamine, or imidazoline-containing polyaminoamide.

6. An adduct according to claim 1 , wherein the component A) is selected from the group consisting of isophoronediamine, xylylenediamine, bis(aminomethylcyclohexyl)methane and 2,2,4(2,4,4)-trimethylhexamethylene-1,6-diamine, triethylenetetramine, N-aminoethylpiperazine, 1,2-diaminocyclohexane and norbornanediamine.

7. An adduct according to claim 1 , wherein an excess of the amine compound is reacted with the polyalkylene glycol monoglycidyl ether.

8. The adduct of claim 7 , wherein from 1.5 to 10 times the molar amount of amine is introduced, and the polyalkylene glycol monoglycidyl ether is added thereto.

9. The adduct of claim 8 , wherein from 4 to 6 times the molar amount of amine is introduced.

10. A curable composition comprising

a) an epoxide compound containing on average more than one epoxide group per molecule; and

b) an adduct according to claim 1 .

11. A curable composition according to claim 10 , wherein n is 3 to 35 for the polyalkylene monoglycidyl ether of the formula (I).

12. A curable composition according to claim 10 , wherein the adduct b) is present in an amount such that from 0.5 to 1.25 functional groups of b) are present in the composition per epoxide group of component a).

13. A curable composition according to claim 12 , wherein the adduct b) is present in an amount such that from 0.75 to 1.25 functional groups of adduct b) are present in the composition per epoxide group of component a).

14. A curable composition according to claim 10 , wherein component a) is derived from a polyhydric or polycyclic phenol.

15. A curable composition according to claim 14 , where the phenol is bisphenol A, bisphenol F or a novolak.

16. The curable composition of claim 15 further comprising a reactive diluent.

17. A curable composition according to claim 10 , further comprising a diluent.

18. A product obtained by curing a composition according to claim 10 .

Assignments (6)
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 →
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 →
CHANGE OF NAME Recorded Mar 24, 2005
From: VANTICO INC.
To: HUNTSMAN ADVANCED MATERIALS AMERICAS INC.
Reel/Frame 015959/0722 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2003
From: SCHERZER, WOLFGANG; VOLLE, JORG; FITZEK, DORIS
To: VANTICO INC.
Reel/Frame 014858/0207 →