Process for making cyclohexanone and/or phenol

Patent metadata

Field	Value
Publication number	US-10294178-B2
Application number	US-201615551839-A
Country	US
Kind code	B2
Filing date	Jan 15, 2016
Priority date	Mar 31, 2015
Publication date	May 21, 2019
Grant date	May 21, 2019

Abstract

In a process for separating a mixture comprising cyclohexanone and phenol, a solid-phase basic material, such as basic ion-exchange resin, is used to remove acid and/or sulfur from the mixture prior to separation. The process results in reduced amount of contamination such as cyclic ethers in the cyclohexanone and/or phenol products.

First claim

The invention claimed is:

1. A process for separating a first mixture comprising cyclohexanone, phenol, cyclohexylbenzene, and a sulfuric acid, comprising the following steps:
(I) contacting the first mixture with a pre-distillation solid-phase basic material to produce a second mixture comprising the sulfuric acid at a concentration lower than in the first mixture;
(II) supplying the second mixture into a distillation column operating at a temperature of at least 120° C. and no higher than the decomposition temperature of the sulfuric acid;
(III) obtaining an upper effluent and a lower effluent from the first distillation column, wherein the upper effluent has a higher concentration in cyclohexanone than the lower effluent, and the lower effluent has a higher cyclohexylbenzene concentration than the upper effluent;
(IV) supplying at least a portion of the upper effluent and an extractive distillation solvent into an extractive distillation column, wherein portion of the upper effluent is obtained by contacting a part of the upper effluent with a pre-extraction solid-phase basic material which is the same as or different from the pre-distillation solid-phase basic material;
(V) obtaining an upper cyclohexanone effluent and a lower extraction effluent from the extractive distillation column wherein the upper cyclohexanone effluent comprises cyclohexanone at a concentration of at least 90 wt %, and the lower extraction effluent comprises phenol and the extractive distillation solvent;
(VI) supplying at least a portion of the lower extraction effluent to a solvent distillation column; and
(VII) obtaining an upper phenol effluent and a lower solvent effluent from the solvent distillation column.

2. The process of claim 1 , wherein at least one of the following conditions is met:
(i) the first mixture comprises sulfur at a total concentration in a range from 80 ppm to 2000 ppm by weight, based on the total weight of the first mixture; and
(ii) the first mixture comprises sulfuric acid at a concentration in a range from 80 ppm to 2000 ppm by weight, based on the total weight of the first mixture.

3. The process of claim 1 , wherein at least one of the following conditions is met:
(i) the second mixture comprises sulfur at a total concentration no greater than 10 ppm by weight, based on the total weight of the second mixture; and
(ii) the second mixture comprises sulfuric acid at a concentration no greater than 10 ppm by weight, based on the total weight of the second mixture.

4. The process of claim 1 , wherein at least one of the following conditions is met:
(i) the upper effluent comprises sulfur at a total concentration no greater than 10 ppm by weight, based on the total weight of the upper effluent; and
(ii) the upper effluent comprises sulfuric acid at a concentration no greater than 10 ppm by weight, based on the total weight of the upper effluent.

5. The process of claim 1 , wherein the first distillation column operates at a temperature of at least 150° C.

6. The process of claim 1 , wherein the first distillation column operates at a temperature higher than the disassociation temperature of at least one of the following: (i) pentane-1,5-diamine sulfuric acid complex; (ii) 1-methyl-hexane-1,5-diamine sulfuric acid complex; (iii) 2-methyl-pentane-1,5-diamine sulfuric acid complex; and (iv) hexane-1,6-diamine sulfuric acid complex.

7. The process of claim 1 , wherein the pre-distillation solid-phase basic material is selected from: (i) oxides of alkali metals alkaline earth metals, and zinc; (ii) hydroxides of alkali metals alkaline earth metals, and zinc; (iii) carbonates of alkali metals alkaline earth metals, and zinc; (iv) bicarbonates of alkali metals alkaline earth metals, and zinc; (v) complexes of two or more of (i), (ii), (iii), and (iv); (vi) solid amines; (vii) ion-exchange resins; and (viii) mixtures and combinations thereof.

8. The process of claim 7 , wherein the pre-distillation solid-phase basic material comprises an ion-exchange resin.

9. The process of claim 8 , wherein the extractive distillation solvent comprises a glycol, and at least one of the upper cyclohexanone effluent and the upper phenol effluent has a total concentration of cyclic ethers produced from condensation reaction(s) of the glycol of no more than 10 ppm by weight, based on the total weight of the respective upper cyclohexanone effluent or the upper phenol effluent.

10. The process of claim 9 , wherein the extractive distillation solvent comprises diethylene glycol, and at least one of the upper cyclohexanone effluent and the upper phenol effluent has a concentration of 1,4-dioxane of no more than 10 ppm by weight, based on the total weight of the respective upper cyclohexanone effluent or the upper phenol effluent.

11. The process of claim 8 , wherein in the liquid medium inside the extractive distillation column, at least one of the following conditions is met:
(i) the total concentration of sulfuric acid is at most 10 ppm by weight, based on the total weight of the liquid medium; and
(ii) the total concentration of sulfur is at most 10 ppm by weight, based on the total weight of the liquid medium.

12. A process for making phenol and/or cyclohexanone from an extraction distillation feed comprising phenol and cyclohexanone, comprising the following steps:
(i) controlling the concentration of an acid in the extraction distillation feed at a level no greater than 10 ppm by weight, based on the total weight of the extraction distillation feed, by contacting at least a portion of the extraction distillation feed with a pre-extraction solid-phase basic material;
(ii) supplying at least a portion of the extraction distillation feed and an extractive distillation solvent into an extractive distillation column;
(iii) obtaining an upper cyclohexanone effluent and a lower extraction effluent from the extractive distillation column, wherein the upper cyclohexanone effluent comprises cyclohexanone at a concentration of at least 90 wt %, and the lower extraction effluent comprises phenol and the extractive distillation solvent;
(iv) supplying at least a portion of the lower extraction effluent to a solvent distillation column; and
(v) obtaining an upper phenol effluent and a lower solvent effluent from the solvent distillation column.

13. The process of claim 12 , wherein the extractive distillation solvent comprises a glycol, and at least one of the upper cyclohexanone effluent and the upper phenol effluent has a total concentration of cyclic ethers produced from condensation reaction(s) of the glycol of no more than 10 ppm by weight, based on the total weight of the respective upper cyclohexanone effluent or the upper phenol effluent.

14. The process of claim 13 , wherein the extractive distillation solvent comprises diethylene glycol, and at least one of the upper cyclohexanone effluent and the upper phenol effluent has a concentration of 1,4-dioxane of no more than 10 ppm by weight, based on the total weight of the respective upper cyclohexanone effluent or the upper phenol effluent.

15. The process of claim 12 , wherein in the liquid medium inside the extractive distillation column, at least one of the following conditions is met:
(i) the total concentration of sulfuric acid is at most 10 ppm by weight, based on the total weight of the liquid medium; and
(ii) the total concentration of sulfur is at most 10 ppm by weight, based on the total weight of the liquid medium.

16. The process of claim 12 , wherein the pre-extraction solid-phase basic material is selected from: (i) oxides of alkali metals

Assignees

• Exxonmobil Chemical Patents Inc

Inventors

• Kuechler Keith H
• Weber Jörg F W
• Poucher Ashley J
• Davis Jason D

Classifications

• C07C37/80

  by extractive distillation · CPC title

• C07C7/12

  by adsorption, i.e. purification or separation of hydrocarbons with the aid of solids, e.g. with ion-exchangers · CPC title

• C07C2601/14

  The ring being saturated · CPC title

• C07C45/79

  by solid-liquid treatment; by chemisorption · CPC title

• C07C37/82

  by solid-liquid treatment; by chemisorption · CPC title