IP Library Granted Patent US 8,969,613
Granted Patent B2
US 8,969,613 · App. 13/664,549 · Granted Mar 3, 2015

Removal of aldehydes in acetic acid production

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Quick Facts
Patent No.
US 8,969,613
App. No.
13/664,549
Granted
Mar 3, 2015
Kind
B2
Abstract

A system and method for removing acetaldehyde from an acetic acid system, including providing a solution from the acetic acid system, the stream having methyl iodide and acetaldehyde, and contacting the solution with an ion-exchange resin and/or liquid catalyst.

Claims (37)

1. A method for removing acetaldehyde from an acetic acid system, comprising:

providing a solution comprising methyl iodide and acetaldehyde from the acetic acid system; and

contacting the solution with an ion-exchange resin, wherein contacting the solution with the ion-exchange resin converts at least a portion of the acetaldehyde to yield an oligomer

wherein the oligomer comprises crotonaldehyde.

2. The method of claim 1 , comprising removing the oligomer from the solution.

3. The method of claim 2 , wherein removing comprises distilling the solution and discharging the oligomer in a bottom stream of the distilling.

4. The method of claim 2 , wherein removing comprises adsorbing at least a portion of the oligomer onto the ion-exchange resin, and further comprising regenerating the ion-exchange resin.

5. The method of claim 4 , wherein regenerating comprises:

heating the ion-exchange resin to a temperature above about 21° C.; and

separating the oligomer from the ion-exchange resin.

6. The method of claim 4 , wherein regenerating comprises heating the ion-exchange resin having the adsorbed oligomer to a temperature of about 80° C. or greater.

7. The method of claim 1 , comprising recovering methyl iodide from the solution, and recycling the recovered methyl iodide to within the acetic acid system.

8. The method of claim 1 , wherein the solution comprises less than 1 wt % water, and wherein the ion-exchange resin comprises a strongly acidic ion-exchange resin.

9. The method of claim 1 , wherein contacting the solution with the ion-exchange resin occurs at room temperature for at least about 30 minutes, and wherein the mass ratio of aldehyde to ion-exchange resin is in a range of about 0.1 to about 2.0.

10. The method of claim 1 , wherein the acetic acid system comprises a decanter, the process further comprising removing a heavy phase stream comprising the solution from the decanter, and passing the heavy phase stream to a resin vessel comprising the ion-exchange resin, and wherein contacting the solution is performed in the resin vessel.

11. A method of operating an acetic acid production system, comprising:

(i) flashing a reaction mixture discharged from an acetic acid production reactor into a vapor stream and a liquid stream, the vapor stream comprising acetic acid, water, methanol, methyl acetate, methyl iodide, and acetaldehyde;

(ii) distilling the vapor stream into: (1) a product side stream comprising acetic acid and water; (2) a bottoms stream; and (3) an overhead stream comprising methyl iodide, water, methyl acetate, acetic acid, and acetaldehyde;

(iii) condensing the overhead stream into: (1) a light, aqueous phase comprising water, acetic acid, and methyl acetate; and (2) a heavy, organic phase comprising methyl iodide, acetic acid, water, and the acetaldehyde;

(iv) converting the acetaldehyde in at least a portion of the heavy, organic phase to an oligomer, wherein the converting step comprises contacting the at least a portion of the heavy, organic phase with an ion-exchange resin to convert the acetaldehyde to the oligomer; and

(v) distilling the at least a portion of the heavy, organic phase after contact with the ion-exchange resin into a vapor stream comprising methyl iodide and a bottoms stream comprising the oligomer, wherein the oligomer is crotonaldehyde.

12. The method of claim 11 , comprising:

adsorbing the oligomer onto the ion-exchange resin, wherein the oligomer comprises crotonaldehyde; and

regenerating the ion-exchange resin to separate the crotonaldehyde from the ion-exchange resin.

13. The method of claim 11 , wherein converting comprising contacting the at least a portion of the heavy, organic phase with methanesulfonic acid (MSA) as a catalyst to convert the acetaldehyde to the oligomer.

14. A method of producing acetic acid, comprising:

reacting methanol and carbon monoxide in the presence of a carbonylation catalyst to produce a crude stream comprising acetic acid;

purifying the crude stream to produce a product stream comprising the acetic acid, wherein the purifying generates a methyl iodide stream comprising methyl iodide acetaldehyde; and

contacting the methyl iodide stream with an ion-exchange resin to convert the acetaldehyde to crotonaldehyde to reduce an amount of acetaldehyde in an acetic acid system producing the acetic acid.

15. An acetic acid production system comprising:

a reactor to react methanol and carbon monoxide in the presence of a carbonylation catalyst to form acetic acid;

a flash vessel that receives a reaction mixture comprising the acetic acid from the reactor;

a distillation column that receives a vapor stream from the flash vessel;

a decanter that receives a condensed overhead stream from the distillation column; and

a resin vessel that receives a heavy, organic phase comprising methyl iodide and acetaldehyde from the decanter, the resin vessel having an ion-exchange resin to convert the acetaldehyde to an oligomer

wherein a majority by weight of the heavy, organic phase is methyl iodide, and

wherein the oligomer comprises crotonaldehyde.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2014
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: LYONDELLBASELL ACETYLS, LLC
Reel/Frame 033182/0019 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2012
From: HALLINAN, NOEL C.; SALISBURY, BRIAN A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 029218/0144 →