Cyclohexanone-containing products and processes for making the same

Patent metadata

Field	Value
Publication number	US-10745336-B2
Application number	US-201816621123-A
Country	US
Kind code	B2
Filing date	Apr 24, 2018
Priority date	Jun 28, 2017
Publication date	Aug 18, 2020
Grant date	Aug 18, 2020

Abstract

Disclosed are processes for making cyclohexanone from a feed mixture comprising cyclohexylbenzene, cyclohexanone, phenol, 3-cylclohexenone and optionally 2-cyclohexenone, comprising feeding the feed mixture to a first distillation column and hydrogenating a fraction from the first distillation column in a hydrogenation reactor separate from the first distillation in the presence of a hydrogenation catalyst under hydrogenation conditions. A cyclohexanone-rich upper effluent comprising 3-cyclohexenone and 2-cyclohexenone at low concentrations can be obtained from the first distillation column.

First claim

The invention claimed is:

1. A process for producing cyclohexanone from a first feed mixture comprising cyclohexylbenzene, cyclohexanone, phenol, and 3-cyclohexenone, the process comprising:
feeding the first feed mixture into a first distillation column at a first feeding location on the first distillation column;
obtaining a lower cyclohexylbenzene-rich effluent from the first distillation column;
obtaining a first upper effluent from a first upper effluent location on the first distillation column above the first feeding location, the first upper effluent comprising cyclohexanone, cyclohexanol, and is substantially free of phenol and 3-cyclohexenone;
obtaining a middle effluent from a middle effluent location on the first distillation column above the first feeding location and below the first upper effluent location, the middle effluent comprising cyclohexanone, phenol, and 3-cyclohexenone;
feeding at least a portion of the middle effluent to a hydrogenation reactor, where the middle effluent contacts with hydrogen in the presence of a hydrogenation catalyst under hydrogenation conditions to produce a hydrogenation reactor effluent substantially free of 3-cylcohexenone;
feeding at least a portion of the hydrogenation reactor effluent to the first distillation column at a recycle location between the middle effluent location and the first upper effluent location, wherein:
the recycle location is 6 to 30 stages above the middle effluent location; and
the conversion of phenol in the hydrogenation reactor is no higher than 99%.

2. The process of claim 1 , wherein:
the concentration of 3-cyclohexenone in the first feed mixture is in the range from 30 ppm by weight to 1 wt %, based on the total weight of the first feed mixture;
the first feed mixture optionally comprises 2-cyclohexenone at a concentration in the range from 30 ppm by weight to 1 wt %, based on the total weight of the first feed mixture; and the hydrogenation reactor effluent is substantially free of 2-cyclohexenone.

3. The process of claim 1 , wherein in the hydrogenation reactor, the conversion of 3-cyclopexenone is at least 95%, and the conversion of the optional 2-cyclohexenone, if present, is at least 95%.

4. The process of claim 1 , wherein the recycle location is 10 to 20 stages above the middle effluent location.

5. The process of claim 1 , wherein in the hydrogenation reactor, the conversion of phenol is in the range from 30 to 99%.

6. The process of claim 5 , wherein in the hydrogenation reactor, the conversion of phenol is in the range from 40 to 80%.

7. The process of claim 1 , wherein:
the hydrogenation catalyst comprises at least one of the following elements: Fe, Co, Ni, Ru, Rh, Pd, Re, Os, Ir, and Pt; and
the hydrogenation conditions comprise a temperature in the range from 25° C. to 300° C. and a hydrogen partial pressure in the range from 50 to 2000 kPa (absolute pressure).

8. The process of claim 1 , further comprising feeding at least a portion of the hydrogenation reactor effluent to the hydrogenation reactor.

9. The process of claim 1 , wherein the first feed mixture further comprises water and light acids, the first middle effluent comprises water and light acids, and the first middle effluent is stripped of water and/or light acids before being fed into the hydrogenation reactor.

10. The process of claim 1 , wherein the first feed mixture comprises water and light acids, and the process further comprises obtaining a second upper effluent from the first distillation column at a second upper effluent location above the first upper effluent location, wherein the second upper effluent comprises water and light acids, and is substantially free of phenol.

11. The process of claim 10 , wherein the second upper effluent further comprises cyclohexanone, and the process further comprises:
separating at least a portion of the cyclohexanone from the second upper effluent to obtain a recycle cyclohexanone stream; and
recycling at least a portion of the recycle cyclohexanone stream to the first distillation column at a location below the second upper effluent location.

12. The process of claim 1 , further comprising:
feeding at least a portion of the first upper effluent into a second distillation column;
obtaining an light-components-rich upper effluent from the second distillation column;
obtaining a light-components-depleted lower effluent from the second distillation column;
feeding at least a portion of the light-components-depleted effluent into a third distillation column; and
obtaining a cyclohexanone-rich upper effluent and a lower effluent from the third distillation column.

13. The process of claim 12 , wherein the lower effluent from the third distillation column is a KA oil effluent comprising cyclohexanol at a concentration in the range from 10 to 40 wt %, based on the total weight of the KA oil effluent.

14. The process of claim 12 , wherein the lower effluent from the third distillation column comprises cyclohexanol and cyclohexanone, and the lower effluent is further subject to dehydrogenation to convert at least a portion of the cyclohexanol to cyclohexanone.

15. The process of claim 12 , wherein the cyclohexanone-rich upper effluent from the third distillation column comprises 3-cyclohexenone at a concentration no greater than 20 ppm by weight, based on the total weight of the cyclohexanone-rich upper effluent, and the lower effluent from the third distillation column comprises 3-cyclohexenone at a concentration no greater than 20 ppm by weight, based on the total weight of the lower effluent from the third distillation column.

16. The process of claim 12 , wherein the cyclohexanone-rich upper effluent from the third distillation column comprises 2-cyclohexenone at a concentration no greater than 20 ppm by weight, based on the total weight of the cyclohexanone-rich upper effluent, and the lower effluent from the third distillation column comprises 2-cyclohexenone at a concentration no greater than 20 ppm by weight, based on the total weight of the lower effluent from the third distillation column.

17. The process of claim 12 , wherein the cyclohexanone-rich upper effluent from the third distillation column comprises 2-cyclohexenone ad 3-cyclohexenone in total at a concentration no greater than 20 ppm by weight, based on the total weight of the cyclohexanone-rich upper effluent, and the lower effluent from the third distillation column comprises 2-cyclohexenone and 3-cyclohexenone in total at a concentration no greater than 20 ppm by weight, based on the total weight of the lower effluent from the third distillation column.

18. The process of claim 12 , wherein the cyclohexanone-rich upper effluent from the third distillation column comprises 2-cyclohexenone and 3-cyclohexenone in total at a concentration no greater than 10 ppm by weight, based on the total weight of the cyclohexanone-rich upper effluent, and the lower effluent from the third distillation column comprises 2-cyclohexenone and 3-cyclohexenone in total at a concentration no greater than 10 ppm by weight, based on the total weight of the lower effluent from the third distillation column.

19. The process of claim 1 , wherein the first feed mixture comprises cyclohexylbenzene at a concentration in the range from 20 to 70 wt %, cyclohexanone at a concentration in the range from 10 to 40 wt %, phenol at a concentration in the range from 10 to 40 wt %, 3-cyclohexenone at a concentration in the range from 30 ppm by weight to 1 wt %, and 2-cyclohexenone at a concentration in

Assignees

• Exxonmobil Chemical Patents Inc

Inventors

• Galvan Kendele S
• Becker Christopher L
• Weber Jörg F W
• Malik Ashley J

Classifications

• C07C45/82

  by distillation · CPC title

• C07C45/006

  by hydrogenation of aromatic hydroxy compounds · CPC title

• C07C2601/16

  the ring being unsaturated · CPC title

• C07C45/62 Primary

  by hydrogenation of carbon-to-carbon double or triple bonds · CPC title

• C07C2601/14

  The ring being saturated · CPC title