IP Library Granted Patent US 7,790,920
Granted Patent B2
US 7,790,920 · App. 12/283,329 · Granted Sep 7, 2010

Preparation of acetic acid

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 7,790,920
App. No.
12/283,329
Granted
Sep 7, 2010
Kind
B2
Abstract

A process for producing acetic acid is disclosed. The process comprises carbonylating methanol to form a reaction mixture comprising a catalyst, catalyst stabilizer, acetic acid, methanol, methyl iodide, methyl acetate, water, and carbon monoxide and introducing at least a portion of the reaction mixture to a distillation column to separate into a bottom steam comprising the catalyst and catalyst stabilizer, a sidedraw stream comprising acetic acid and water, and an overhead stream comprising methanol, methyl acetate, methyl iodide, and water. The process of the invention eliminates the use of flash tank.

Claims (16)

1. A process for producing acetic acid, said process comprising:

(a) carbonylating methanol in the presence of a catalyst selected from the group consisting of rhodium catalysts and iridium catalysts, catalyst stabilizer, water and methyl iodide to form a reaction mixture comprising the catalyst, catalyst stabilizer, acetic acid, methanol, methyl iodide, methyl acetate, and water; and

(b) withdrawing the reaction mixture and feeding it to a distillation column to separate into a bottom stream comprising the catalyst and catalyst stabilizer, a sidedraw stream comprising acetic acid and water, and an overhead stream comprising methanol, methyl acetate, methyl iodide, and water; wherein no flash tank is used between steps (a) and (b).

2. The process of claim 1 , wherein the bottom stream of step (b) is recycled to the carbonylation of step (a).

3. The process of claim 1 , wherein the overhead stream of step (b) is recycled to the carbonylation of step (a).

4. The process of claim 1 , wherein the overhead stream is phase-separated to a light, aqueous phase comprising water, acetic acid, and methyl acetate and a heavy, organic phase comprising methyl iodide and methyl acetate.

5. The process of claim 4 , wherein the heavy, organic phase is recycled to the carbonylation of step (a).

6. The process of claim 4 , wherein the light, aqueous phase is recycled to the distillation of step (b) or to the carbonylation of step (a).

7. The process of claim 1 , further comprising distilling the sidedraw stream to remove water.

8. The process of claim 1 , wherein the catalyst is a rhodium catalyst.

9. The process of claim 8 , wherein the catalyst stabilizer is selected from the group consisting of pentavalent Group VA oxides, metal iodide salts, and mixtures thereof.

10. The process of claim 8 , wherein the catalyst stabilizer is a phosphine oxide.

11. The process of claim 8 , wherein the catalyst stabilizer is triphenylphosphine oxide.

12. The process of claim 8 , wherein the catalyst stabilizer is a metal iodide salt.

13. The process of claim 8 , wherein the catalyst stabilizer is lithium iodide.

14. The process of claim 1 , wherein the concentration of water in step (a) is up to 10 wt % of the reaction mixture.

Assignments (15)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2014
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: LYONDELLBASELL ACETYLS, LLC
Reel/Frame 033182/0019 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032137/0156 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032123/0799 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: BANK OF AMERICA, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032138/0134 →
APPOINTMENT OF SUCCESSOR ADMINISTRATIVE AGENT Recorded Jan 23, 2014
From: UBS AG, STAMFORD BRANCH
To: BANK OF AMERICA, N.A.
Reel/Frame 032137/0639 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: CITIBANK, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032125/0296 →
SECURITY AGREEMENT Recorded May 19, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 024402/0681 →
SECURITY AGREEMENT Recorded May 18, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024397/0818 →
SECURITY AGREEMENT Recorded May 7, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 024342/0801 →
SECURITY AGREEMENT Recorded May 6, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024342/0421 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, LP
Reel/Frame 024337/0285 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, LP
Reel/Frame 024337/0020 →
SECURITY AGREEMENT Recorded Oct 30, 2009
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 023449/0138 →
SECURITY AGREEMENT Recorded Apr 9, 2009
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
Reel/Frame 022708/0830 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2008
From: BRTKO, WAYNE J.; FITZPATRICK, MICHAEL E.; SALISBURY, BRIAN A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 021576/0092 →