IP Library Granted Patent US 10,844,001
Granted Patent B2
US 10,844,001 · App. 16/074,485 · Granted Nov 24, 2020

Process to prepare higher ethylene amines and ethylene amine derivatives

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Quick Facts
Patent No.
US 10,844,001
App. No.
16/074,485
Granted
Nov 24, 2020
Kind
B2
Abstract

The present invention relates to a process to prepare ethylene amines of the formula NH 2 —(C 2 H 4 —NH—) p H wherein p is at least 3 or derivatives thereof wherein one or more units —NH—C 2 H 4 —NH— may be present as a cyclic ethylene urea unit or between two units —NH—C 2 H 4 —NH— a carbonyl moiety is present, by reacting an ethanolamine-functional compound, an amine-functional compound in the presence of a carbon oxide delivering agent, wherein the molar ratio of carbon oxide delivering agent to amine-functional compound is at least 0.6 to 1.

Claims (21)

1. A process of preparing (i) ethylene amines of the formula: NH 2 —(C 2 H 4 —NH—) p H wherein p is at least 3, (ii) derivatives thereof wherein one or more —NH—C 2 H 4 —NH— units are present as a cyclic ethylene urea unit

and/or (iii) derivatives thereof wherein a carbonyl moiety is present between two —NH—C 2 H 4 —NH— units,

said process comprising the following steps:

(a) reacting an ethanolamine-functional compound and an amine-functional compound in the presence of a carbon oxide delivering agent to obtain a mixture of products, at least some of which products are said derivatives thereof wherein one or more units —NH—C 2 H 4 —NH— are present as a cyclic ethylene urea unit, wherein for said reacting the molar ratio of carbon oxide delivering agent to amine-functional compound is at least 0.8:1; and

(b) converting at least some of said derivatives thereof wherein one or more units —NH—C 2 H 4 —NH— are present as a cyclic ethylene urea unit to the corresponding ethylene amines;

wherein:

the ethanolamine functional compound contains a hydroxyl group linked via an ethylene group to an amine group, or its carbamate equivalent, or the ethanolamine functional compound is UAEEA (the urea of aminoethylethanolamine);

the amine functional compound contains no alcohol groups, and contains at least two primary amine groups and optionally more primary, secondary and/or tertiary amine groups, wherein the amine groups are linked to one another via ethylene groups, and optionally by a carbonyl moiety; and

the carbon oxide delivering agent is carbon dioxide or an organic compound selected from urea, linear and cyclic alkylene ureas, mono- or di-substituted alkylene ureas, alkyl and dialkyl ureas, linear and cyclic carbamates and organic carbonates, and derivatives or precursors thereof selected from carbonate salts, bicarbonate salts and carbamic acids and their salts.

2. The process of claim 1 wherein the molar ratio of carbon oxide delivering agent to amine functional compound is between 0.8:1 and 20:1.

3. The process of claim 1 wherein in at least part of the ethanol-amine functional compound one or more —O—C 2 H 4 —NH— units are present as cyclic ethylene carbamate units or, if present, one or more —N—C 2 H 4 —N— units are present in the form of cyclic ethylene urea units.

4. The process of claim 1 wherein in at least part of the amine-functional compound one or more —N—C 2 H 4 —N— units are present in the form of cyclic ethylene urea units.

5. The process of claim 1 wherein the ethanolamine-functional compound is of the formula HO—(C 2 H 4 —NH—) q H wherein q is at least 1 and the amine-functional compound is of the formula NH 2 —(C 2 H 4 —NH—) r H wherein r is at least 1, wherein the sum of q+r is at least 3 and wherein optionally one or more —O—C 2 H 4 —NH— or —N—C 2 H 4 —N— units may be present as a cyclic ethylene urea or cyclic ethylene carbamate units.

6. The process of claim 1 wherein the ethanolamine-functional compound is AEEA (aminoethylethanolamine), CAEEA (the carbamate of aminoethylethanolamine), UAEEA (the urea of aminoethylethanolamine) or a mixture thereof and the amine-functional compound is EDA (ethylenediamine), EU (ethyleneurea) or a mixture thereof.

7. The process of claim 6 wherein the ratio of AEEA, UAEEA+CAEEA to EDA+EU is equal to or higher than 1.

8. The process of claim 1 wherein the ethanolamine-functional compound is MEA (monoethanolamine), CMEA (the carbamate of monoethanolamine) or a mixture thereof and the amine-functional compound is DETA (diethylenetriamine), UDETA (the urea of diethylenetriamine) or a mixture thereof.

9. The process of claim 8 wherein the ratio of MEA+CMEA to DETA+UDETA is higher than 1.

10. The process of claim 1 wherein the ethanolamine-functional compound is MEA (monoethanolamine), CMEA (the carbamate of monoethanolamine) or a mixture thereof and the amine-functional compound is EDA (ethylenediamine), EU (ethyleneurea) or a mixture thereof.

11. The process of claim 10 wherein the ratio of MEA+CMEA to EDA+EU is higher than 2.

12. The process of claim 9 wherein the ratio of MEA+CMEA to DETA+UDETA is higher than 2.

13. The process of claim 11 wherein the ratio of MEA+CMEA to EDA+EU is higher than 3.

Assignments (5)
CHANGE OF NAME Recorded Sep 18, 2019
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 050426/0671 →
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2018
From: EDVINSSON, ROLF KRISTER; KANTZER, EIKE NICOLAS; LARSSON, PER FREDRIK OLMO; TEN KATE, ANTOON JACOB BEREND
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 046533/0529 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2018
From: LAKE, KARL FREDRIK
To: RISE RESEARCH INSTITUTES OF SWEDEN AB; SURFACE, PROCESS AND FORMULATION
Reel/Frame 046533/0556 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2018
From: RISE RESEARCH INSTITUTES OF SWEDEN AB; SURFACE, PROCESS AND FORMULATION
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 046533/0576 →