High purity isoamylene production from tertiary amyl methyl ether decomposition

Patent metadata

Field	Value
Publication number	US-11465949-B2
Application number	US-202117453241-A
Country	US
Kind code	B2
Filing date	Nov 2, 2021
Priority date	Nov 2, 2020
Publication date	Oct 11, 2022
Grant date	Oct 11, 2022

Abstract

Systems and methods for the production of a high purity isoamylene product. The isoamylene in a mixed hydrocarbon stream may initially be converted to TAME via etherification, and a subsequent decomposition of the TAME may result in a high purity isoamylene stream with very low impurities that is suitable for a variety of petrochemical applications, such as for use in the production of fragrances, pesticides, peroxides, polymer antioxidants, UV stabilizers and hydrocarbon resins.

First claim

What is claimed as new and desired to be protected by Letters Patent is:

1. A process for producing a high purity isoamylene stream, the process comprising:
purifying a crude tertiary amyl ether stream, comprising tertiary amyl ether, tertiary amyl alcohol, diisoamylene, C5 hydrocarbons including linear pentenes and pentanes, alcohol, and water, to recover a lights stream comprising the C5 hydrocarbons and tertiary amyl alcohol, a heavies stream comprising diisoamylene, and a tertiary amyl ether containing stream;
feeding the tertiary amyl ether containing stream as a vapor to a decomposition reactor containing a decomposition catalyst;
contacting the tertiary amyl ether with the decomposition catalyst to convert the tertiary amyl ether to isoamylene and alcohol and to recover an isoamylene containing rector effluent;
feeding the isoamylene containing reactor effluent to a separation zone and separating the isoamylene containing reactor effluent into an alcohol stream, a vent stream, an isoamylene product stream, and a heavy oxygenate stream comprising unreacted ethers and tertiary amyl alcohol.

2. The process of claim 1 , wherein the contacting occurs at a reaction temperature in a range from about 130° C. to about 260° C. and at a pressure in a range from about 2 barg to about 12 barg.

3. The process of claim 1 , further comprising:
feeding a C1-C2 alcohol and a mixed C5 stream to a fixed bed reactor containing an etherification catalyst, contacting the C1-C2 alcohol and isoamylene with the etherification catalyst to convert a portion of the isoamylene and C1-C2 alcohol to tertiary amyl ether, and recovering a fixed bed reactor effluent;
feeding the fixed bed reactor effluent to a catalytic distillation reactor for concurrently (i) reacting isoamylene with the C1-C2 alcohol to produce additional tertiary amyl ether and (ii) recovering a bottoms stream comprising the tertiary amyl ether and an overhead stream comprising unreacted C5s and unreacted C1-C2 alcohol; and
feeding the bottoms stream as the crude tertiary amyl ether stream to the purifying step.

4. The process of claim 1 , wherein the purifying a crude tertiary amyl ether stream comprises feeding the crude tertiary amyl ether stream to a divided wall distillation column, and recovering the tertiary amyl ether containing stream as a side draw from the divided wall distillation column.

5. The process of claim 1 , wherein the isoamylene product stream comprises at least 99.8 wt % isoamylene.

6. The process of claim 1 , wherein the alcohol comprises methanol, the tertiary amyl ether comprises tertiary amyl methyl ether, and wherein the alcohol stream comprises at least 99.8 wt % methanol.

7. The process of claim 1 , wherein the alcohol comprises ethanol, and the tertiary amyl ether comprises tertiary amyl ethyl ether.

8. The process of claim 1 , further comprising feeding the heavy oxygenate stream to the purifying step.

Assignees

• Lummus Technology Inc

Inventors

• Barias Rosette
• Chen Liang
• Scott Michael Jon

Classifications

• C07C7/04

  by distillation · CPC title

• C07C1/20 Primary

  starting from organic compounds containing only oxygen atoms as heteroatoms · CPC title

• Y02P20/10

  Process efficiency · CPC title

• C07C7/10

  by extraction, i.e. purification or separation of liquid hydrocarbons with the aid of liquids · CPC title

• C07C29/10

  of ethers, including cyclic ethers, e.g. oxiranes · CPC title