IP Library Granted Patent US 7,169,268
Granted Patent B2
US 7,169,268 · App. 10/456,655 · Granted Jan 30, 2007

Color stabilization of amines

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Quick Facts
Patent No.
US 7,169,268
App. No.
10/456,655
Granted
Jan 30, 2007
Kind
B2
Abstract

The present invention concerns a process for providing tertiary amine products which are color-stable, and have a greatly reduced tendency to take on color during their storage. According to the invention, an ethyleneamine derivative is added to the distillation pot prior to or during the distillation of the tertiary amine product. Preferably, the ethyleneamine derivative has a higher boiling point than the desired tertiary amine product so as to preclude the ethyleneamine from distilling over with the tertiary amine.

Claims (21)

1. A process for producing a color-stable tertiary amine product comprising the steps of:

a) providing a distillation apparatus having a boiling pot portion, a condenser, and receiver, wherein the distillation apparatus comprises a last tower of a distillation train;

b) feeding a major amount of a desired tertiary amine product in said boiling pot, said tertiary amine having the chemical structure:

in which x may be any integer between 1 and 8, including 1 and 8; wherein R 1 may be hydrogen, hydroxy, or the group:

wherein Y may be: i) hydrogen; ii) any alkyl group, whether straight-chain, branched, or cyclic containing between 1 and 10 carbon atoms, including 1 and 10; or iii) the group—(CH 2 ) x OH in which x may be any integer between 1 and 8, including 1 and 8; and wherein Z may be: i) hydrogen; ii) any alkyl group, whether straight-chain, branched, or cyclic containing between 1 and 10 carbon atoms, including 1 and 10; iii) the group—(CH 2 ) x OH in which x may be any integer between 1 and 8, including 1 and 8; or iv) an aminoalkyl group defined by the formula:

in which m may be any integer between 1 and 6, including 1 and 6; and S and T are each independently selected from the group consisting of: hydrogen, or any C 1 to C 6 alkyl group; and R 2 , and R 3 may each independently be: i) hydrogen; ii) any alkyl group, whether straight-chain, branched, or cyclic containing between 1 and 10 carbon atoms, including 1 and 10; or iii) the group—(CH 2 ) x OH in which x may be any integer between 1 and 8, including 1 and 8;

c) feeding a minor amount of an ethyleneamine derivative which has a boiling point higher than said desired tertiary amine product at standard temperature and pressure, said ethyleneamine derivative being selected from the group consisting of: ethylenediamine; aminoethylethanolamine; diethylenetriamine; triethylenetetramine; tetraethylenepentamine; pentaethylenehexamine; 1,2-propylenediamine; N-(2-hydroxypropyl)ethylenediamine; N-(2-hydroxybutyl)ethylenediamine; N-(2-hydroxyethyl)-1,2-propylenediamine; N-(2-hydroxypropyl)-1,2-propylenediamine; and N-(2-hydroxybutyl)-1,2-propylenediamine in said boiling pot of said last tower;

d) distilling said desired tertiary amine product and said ethyleneamine derivative by providing heat to said boiling pot portion so as to cause vaporization of said desired tertiary amine product and its subsequent condensation in said condenser to produce the color-stable tertiary amine product, wherein said distilling provides final distillation of said desired tertiary amine product; and

e) collecting said color-stable tertiary amine product in said receiver, wherein said ethyleneamine derivative is present in said pot portion in any amount between about 0.001% and about 20% by weight based on the total amount of tertiary amine present in said pot portion.

2. A process according to claim 1 wherein the difference between the boiling point of said desired tertiary amine product and said ethyleneamine derivative is at least five degrees Centigrade.

3. A process according to claim 1 wherein the difference between the boiling point of said desired tertiary amine product and said ethyleneamine derivative is ten degrees Centigrade or more.

4. A process according to claim 1 wherein said tertiary amine is selected from the group consisting of: methyldiethanolamine, N,N-dimethylethanolamine, bis-(2-dimethylaminoethyl) ether, pentamethyldiethylenetriamine, 2-(2-dimethylaminoethoxy) ethanol, triethylamine, and N,N,N′-trimethyl-N′-hydroxyethyl-bisaminoethylether.

5. A process for producing a color-stable tertiary amine product comprising the steps of:

a) providing a distillation apparatus having a boiling pot portion, a condenser, and a receiver, wherein the distillation apparatus comprises a last tower of a distillation train;

b) feeding a major amount of a desired tertiary amine product in said boiling pot, said tertiary amine having the chemical structure:

in which x may be any integer between 1 and 8, including 1 and 8; wherein R 1 may be hydrogen, hydroxy, or the group:

wherein Y may be: i) hydrogen; ii) any alkyl group, whether straight-chain, branched, or cyclic containing between 1 and 10 carbon atoms, including 1 and 10; or iii) the group—(CH 2 ) x OH in which x may be any integer between 1 and 8, including 1 and 8; and wherein Z may be: i) hydrogen; ii) any alkyl group, whether straight-chain, branched, or cyclic containing between 1 and 10 carbon atoms, including 1 and 10; iii) the group—(CH 2 ) x OH in which x may be any integer between 1 and 8, including 1 and 8; or iv) an aminoalkyl group defined by the formula:

in which m may be may be any integer between 1 and 6, including 1 and 6; and S and T are each independently selected from the group consisting of: hydrogen, or any C 1 to C 6 alkyl group; and R 2 , and R 3 may each independently be: i) hydrogen; ii) any alkyl group, whether straight-chain, branched, or cyclic containing between 1 and 10 carbon atoms, including 1 and 10; or iii) the group—(CH 2 ) x OH in which x may be any integer between 1 and 8, including 1 and 8;

c) feeding a minor amount of an ethyleneamine derivative which has a boiling point that is lower than said desired tertiary amine product at standard temperature and pressure, said ethyleneamine derivative being selected from the group consisting of: ethylenediamine; aminoethylethanolamine; diethylenetriamine; triethylenetetramine; tetraethylenepentamine; pentaethylenehexamine; 1,2-propylenediamine; N-(2-hydroxypropyl)ethylenediamine; N-(2-hydroxybutyl)ethylenediamine; N-(2-hydroxytheyl)-1,2-propylenediamine; N-(2-hydroxypropyl)-1,2-propylenediamine; and N-(2-hydroxybutyl)-1,2-propylenediamine in said boiling pot of said last tower;

d) distilling said desired tertiary amine product and said ethyleneamine derivative by providing heat to said boiling pot portion so as to cause vaporization of said desired tertiary amine product and its subsequent condensation in said condenser to produce the color-stable tertiary amine product, wherein said distilling provides final distillation of said desired tertiary amine product; and

e) collecting said color-stable tertiary amine product in said receiver, wherein said ethyleneamine derivative is present in said pot portion in any amount between about 0.001% and about 20% by weight based on the total amount of tertiary amine present in said pot portion, and wherein the distillation apparatus is configured to continuously recycle the ethyleneamine to a feed to the distillation apparatus, while simultaneously distilling the desired tertiary amine product at a different location in the colunm.

Assignments (8)
TERMINATION AND RELEASE OF SECURITY INTEREST IN UNITED STATES TRADEMARKS AND PATENTS Recorded Jun 13, 2018
From: JPMORGAN CHASE BANK, N.A.
To: HUNTSMAN PETROCHEMICAL CORPORATION (N/K/A HUNTSMAN PETROCHEMICAL LLC)
Reel/Frame 046356/0616 →
CORRECTIVE ASSIGNMENT TO CORRECT THE NATURE OF CONVEYANCE FROM AN ASSIGNMENT TO A SECURITY AGREEMENT PREVIOUSLY RECORDED ON REEL 025857 FRAME 0137. 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 026515/0641 →
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 025857/0137 →
RELEASE OF SECURITY INTEREST Recorded Feb 8, 2011
From: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT (F/K/A BANKERS TRUST COMPANY, AS COLLATERAL AGENT)
To: HUNTSMAN INTERNATIONAL LLC; HUNTSMAN ADVANCED MATERIALS LLC; HUNTSMAN ADVANCED MATERIALS AMERICAS LLC; HUNTSMAN ETHYLEMEAMINES LLC; HUNTSMAN PETROCHEMICAL LLC
Reel/Frame 025765/0853 →
SECURITY INTEREST Recorded Nov 17, 2005
From: HUNTSMAN PETROCHEMICAL CORPORATION
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
Reel/Frame 016987/0496 →
SECURITY AGREEMENT Recorded Jan 28, 2005
From: HUNSTMAN PETROCHEMICAL CORPORATION
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS AGENT
Reel/Frame 015661/0547 →
GRANT OF SECURITY INTEREST IN U.S. TRADEMARKS AND PATENTS Recorded Dec 4, 2003
From: HUNTSMAN PETROCHEMICAL CORPORATION
To: DEUTSCHE BANK TRUST COMPANY AMERICAS (FORMERLY KNOWN AS BANKER TRUST COMPANY), AS COLLATERAL AGENT
Reel/Frame 014782/0186 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 6, 2003
From: SU, WEI-YANG; POSEY, MARK L.; WEEME, MAARTEN P. TER
To: HUNTSMAN PETROCHEMICAL CORPORATION
Reel/Frame 014160/0310 →