IP Library Granted Patent US 8,748,540
Granted Patent B2
US 8,748,540 · App. 13/264,962 · Granted Jun 10, 2014

Compositions comprising solvated aromatic amines and methods for the preparation thereof

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,748,540
App. No.
13/264,962
Granted
Jun 10, 2014
Kind
B2
Abstract

The present invention provides a composition comprising a solvated aromatic amine and a liquid carrier, wherein said solvated aromatic amine is the reaction product of an aromatic amine and at least one of any anhydride, an isocyanate or an acid in the liquid carrier. The present invention also provides a method of preparing a composition comprising a solvated aromatic amine and a liquid carrier, said method comprising the steps of providing a reaction mixture comprising: a) an aromatic amine; b) at least one of an anhydride, an isocyanate or an acid; and c) a liquid carrier; and heating the reaction mixture at an elevated temperature to provide the solvated aromatic amine in the liquid carriers. The present invention further provides the use of the compositions for the preparation of the curable compounds and for gasoline resistant coatings.

Claims (62)

1. A curable compound comprising:

a resin; and

a hardener, said hardener comprising a composition comprising a solvated aromatic amine and a liquid carrier, wherein said solvated aromatic amine is the reaction product of an aromatic amine and at least one of an anhydride, or an acid in the liquid carrier, and wherein

said aromatic amine is diphenyl aromatic amine, trimethylene glycol di-p-amino benzoate, methylene his methyl anthranilate, methylene-bis chloroaniline, methylene his chlorodiethylbenzamine or a combination thereof,

said anhydride is methylhexahydrophthalic anhydride, dodecenyl succinic anhydride, nadic methyl anhydride or a combination thereof,

said acid is oleic acid or citric acid, and

said liquid carrier is a non-volatile liquid carrier.

2. The curable compound according to claim 1 , wherein the resin comprises isocyanate.

3. The curable compound according to claim 2 , wherein the isocyanate is methylene diisocyanate, toluene diisocyanate, isophorone diisocyanate, associated prepolymers thereof and combinations thereof.

4. The curable compound according to claim 1 , wherein the composition comprising the solvated aromatic amine and the liquid carrier is prepared in accordance with a method comprising

providing a reaction mixture comprising:

a) said aromatic amine,

b) said anhydride or acid,

and

c) said liquid carrier;

and

heating the reaction mixture at an elevated temperature, wherein the elevated temperature is the temperature at which the aromatic amine is solvated by the liquid carrier.

5. The curable compound according to claim 1 , further comprising at least one low molecular weight polyol.

6. A composition comprising a solvated aromatic amine and a liquid carrier;

wherein said solvated aromatic amine is the reaction product of an aromatic amine and at least one of an anhydride, or an acid in the liquid carrier,

wherein said aromatic amine is diphenyl aromatic amine, trimethylene glycol di-p-amino benzoate, methylene bis methyl anthranilate, methylene-bis chloroaniline, methylene his chlorodiethylbenzamine or a combination thereof;

wherein the anhydride is methylhexahydrophthalic anhydride, dodecenyl succinic anhydride, nadic methyl anhydride or a combination thereof;

wherein said acid is oleic acid or citric acid; and

wherein said liquid carrier is a non-volatile liquid carrier.

7. The composition according to claim 6 , wherein the non-volatile liquid carrier comprises castor oil, castor oil triol, di octyl phthalate, 2-ethylhexyl diphenyl phosphate, dibasic ester, di butyl phthalate, polyether polyol, caprolactone, propylene carbonate or combinations thereof.

8. A composition according to claim 6 , wherein the composition is prepared in accordance with a method comprising:

providing a reaction mixture comprising:

a) said aromatic amine,

b) said anhydride or acid

c) said liquid carrier;

and

heating the reaction mixture at an elevated temperature, wherein the elevated temperature is the temperature at which the aromatic amine is solvated by the liquid carrier.

9. A method of preparing a composition comprising a solvated aromatic amine and a liquid carrier, said method comprising the steps of:

providing a reaction mixture comprising:

a) an aromatic amine, wherein the aromatic amine is diphenyl aromatic amine, trimethylene glycol di-p-amino benzoate, methylene bis methyl anthranilate, methylene-bis chloroaniline, methylene bis chlorodiethylbenzamine or a combination thereof;

b) at least one of an anhydride, or an acid,

wherein the anhydride is methylhexahydrophthalic anhydride, dodecenyl succinic anhydride, nadic methyl anhydride or a combination thereof,

and

wherein the acid is oleic acid or citric acid; and

c) a liquid carrier;

and

heating the reaction mixture at an elevated temperature, wherein the elevated temperature is the temperature at which the aromatic amine is solvated by the liquid carrier.

10. The method according to claim 9 , wherein the liquid carrier is a non-volatile liquid carrier.

11. The method according to claim 10 , wherein the non-volatile liquid carrier comprises castor oil, castor oil triol, di octyl phthalate, 2-ethylhexyl diphenyl phosphate, dibasic ester, di butyl phthalate, polyether polyol, caprolactone, propylene carbonate or combinations thereof.

12. The method according to claim 9 , wherein the amount of the aromatic amine in the reaction mixture is about 30% to about 60% w/w.

13. The method according to claim 9 , wherein the amount of the anhydride, or the acid in the reaction mixture is about 0.1% to about 10% w/w.

14. The method according to claim 9 , wherein the amount of the liquid carrier in the reaction mixture is about 30% to about 60% w/w.

15. The method according to claim 9 , wherein the elevated temperature is between about 100° C. to about 135° C.

16. The method according to claim 15 , wherein the elevated temperature is about 110° C.

17. The method according to claim 16 , wherein a nitrogen blanket is provided over the reaction mixture.

18. A method of decreasing gasoline permeability of a container, comprising the steps:

coating an inside surface of the container with a curable compound comprising a resin and a hardener, said hardener comprising a composition comprising a solvated aromatic amine and a liquid carrier, wherein said solvated aromatic amine is the reaction product of an aromatic amine and at least one of an anhydride, or an acid in the liquid carrier, and wherein said aromatic amine is diphenyl aromatic amine, trimethylene glycol di-p-amino benzoate, methylene bis methyl anthranilate, methylene-bis chloroaniline, methylene bis chlorodiethylbenzamine or a combination thereof; said anhydride is methylhexahydrophthalic anhydride, dodecenyl succinic anhydride, nadic methyl anhydride or a combination thereof; said acid is oleic acid or citric acid; and said liquid carrier is a non-volatile liquid carrier;

and

curing the curable compound to provide a gasoline resistant coating.

19. The method according to claim 18 , wherein the composition comprising the solvated aromatic amine and the liquid carrier is prepared in accordance with a method comprising

providing a reaction mixture comprising:

a) said aromatic amine

b) said anhydride acid,

c) said liquid carrier;

and

heating the reaction mixture at an elevated temperature, wherein the elevated temperature is the temperature at which the aromatic amine is solvated by the liquid carrier.

20. The method of claim 19 , wherein the gasoline resistant coating decreases gasoline permeability of the container to below about 1.5 g/m 2 /day.

Assignments (2)
SECURITY INTEREST Recorded Aug 21, 2014
From: REVOLUTION LIGHTING TECHNOLOGIES, INC.; LUMIFICIENT CORPORATION; LIGHTING INTEGRATION TECHNOLOGIES, LLC; SEESMART TECHNOLOGIES, LLC; RELUME TECHNOLOGIES, INC.; TRI-STATE LED DE, LLC; VALUE LIGHTING, LLC; SEESMART, INC.; ENVIROLIGHT LED, LLC; SENTINEL SYSTEM, LLC; VALUE LIGHTING OF HOUSTON, LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 033579/0700 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2011
From: ULCAR, JOHN; TOFFEY, ACKAH
To: CROSSLINK TECHNOLOGY, INC.
Reel/Frame 027107/0426 →