IP Library Granted Patent US 10,647,641
Granted Patent B2
US 10,647,641 · App. 16/516,656 · Granted May 12, 2020

Process for the separation of ethylbenzene from other C

Inventors: Alisa Kammafoo (Rayong, TH); Attapong Thirasak (Rayong, TH); Zhongyi Ding (Katy, TX)
Assignees: SCG Chemicals Co., Ltd.; Sulzer GTC Technology US Inc.
C07C7/08B01D3/143B01D3/40C07C15/073B01D2256/24B01D2257/40
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Quick Facts
Patent No.
US 10,647,641
App. No.
16/516,656
Granted
May 12, 2020
Kind
B2
Abstract

Extractive agent compounds are disclosed, with exemplary compounds having Formula (I): wherein R a and R b are independently selected from the group consisting of an oxygen radical, a hydrogen radical, and a hydrocarbyl radical having from about 1 to about 20 carbon atoms, and wherein R 2 -R 6 are independently selected from the group consisting of halo, a hydrogen radical, and a hydrocarbyl radical having from about 1 to about 20 carbon atoms, and further wherein at least two of R 2 -R 6 are halo. Also disclosed are extractive distillation processes, comprising distilling a liquid mixture comprising ethylbenzene, a further C 8 aromatic compound, and an extractive agent compound as described herein. The extractive agent contributes to improved separability of ethylbenzene from the further C 8 aromatic compound. The separability may be quantified in terms of increasing relative volatility of ethylbenzene to the further C 8 aromatic compound or may alternatively be quantified in terms of a competitive factor, D, as described herein.

Claims (30)

1. An extractive distillation process, the process comprising (a) distilling a liquid mixture comprising ethylbenzene, at least one further C 8 aromatic compound, and an extractive agent compound,

wherein the extractive agent compound includes a carbocyclic or heterocyclic ring structure, said ring structure being substituted with at least one NR a R b -group radical and at least two halo radicals, and

wherein R a and R b are independently selected from the group consisting of an oxygen radical, a hydrogen radical, and a hydrocarbyl radical having from about 1 to about 20 carbon atoms.

2. The process of claim 1 , wherein the extractive agent compound includes a carbocyclic ring structure that is an aromatic ring structure.

3. The process of claim 2 , wherein the extractive agent compound is an aromatic compound of Formula (I):

wherein R a and R b are as defined in claim 1 , and

wherein R 2 -R 6 are independently selected from the group consisting of halo, a hydrogen radical, and a hydrocarbyl radical having from about 1 to about 20 carbon atoms, and further wherein at least two of R 2 -R 6 are halo.

4. The process of claim 3 , wherein, in Formula (I), said at least two of R 2 -R 6 are chloro.

5. The process of claim 3 , wherein, in Formula (I), at least R 3 and R 4 are halo.

6. The process of claim 5 , wherein, in Formula (I), R 2 , R 5 , and R 6 are independently selected from the group consisting of a hydrogen radical and a hydrocarbyl radical having from about 1 to about 20 carbon atoms.

7. The process of claim 3 , wherein, in Formula (I), R 2 and R 3 are halo.

8. The process of claim 7 , wherein, in Formula (I), R 4 , R 5 , and R 6 are independently selected from the group consisting of a hydrogen radical and a hydrocarbyl radical having from about 1 to about 20 carbon atoms.

9. The process of claim 1 , wherein, in Formula (I), R a and R b are both oxygen radicals, whereby the NR a R b -group radical is nitro.

10. The process of claim 1 , wherein the extractive agent compound is an isomer of dichloronitrobenzene.

11. The process of claim 1 , wherein the extractive agent compound is 1,2-dichloro-3-nitrobenzene or 1,2-dichloro-4-nitrobenzene.

12. The process of claim 1 , wherein the liquid mixture comprises both 1,2-dichloro-3-nitrobenzene and 1,2-dichloro-4-nitrobenzene.

13. The process of claim 1 , wherein, in Formula (I), R a and R b are both hydrogen radicals, whereby the NR a R b -group radical is amino.

14. The process claim 1 , wherein the extractive agent compound is an isomer of dichloroaniline.

15. The process of claim 1 , wherein the extractive agent compound is 3,4-dichloroaniline.

16. The process of claim 1 , wherein the liquid mixture comprises both an isomer of dichloronitrobenzene and an isomer of dichloroaniline.

17. The process of claim 1 , wherein the liquid mixture comprises (i) 3,4-dichloroaniline and (ii) 1,2-dichloro-4-nitrobenzene or 1,2-dichloro-3-nitrobenzene.

18. A liquid mixture comprising ethylbenzene, at least one further C 8 aromatic compound, and an extractive agent compound, wherein the extractive agent compound is present in the liquid mixture in an amount such that the relative volatility (a) between the ethylbenzene and the at least one further C 8 aromatic compound is at least about 1.14 at 200 millibar (mbar),

wherein the extractive agent compound includes a carbocyclic or heterocyclic ring structure, said ring structure being substituted with at least one NR a R b -group radical and at least two halo radicals, and wherein R a and R b are independently selected from the group consisting of an oxygen radical, a hydrogen radical, and a hydrocarbyl radical having from about 1 to about 20 carbon atoms.

19. An extractive distillation process comprising:

(a) distilling a liquid mixture of a purified feed stream and an extractive agent compound to provide (i) an overhead fraction enriched in ethylbenzene, relative to the liquid mixture, and (ii) a bottoms fraction that, relative to the liquid mixture, is enriched in both the at least one further C 8 aromatic compound and the extractive agent compound, and is depleted in ethylbenzene;

(b) distilling the bottoms fraction to provide (i) a second bottoms fraction enriched in the extractive agent compound, relative to the bottoms fraction, and (ii) a second overhead fraction enriched in the at least one further C 8 aromatic compound, relative to the bottoms fraction; and

(c) recycling at least a portion of the second bottoms fraction to provide at least a portion of the extractive agent compound in the liquid mixture in step (a),

wherein the extractive agent compound includes a carbocyclic or heterocyclic ring structure, said ring structure being substituted with at least one NR a R b -group radical and at least two halo radicals, and wherein R a and R b are independently selected from the group consisting of an oxygen radical, a hydrogen radical, and a hydrocarbyl radical having from about 1 to about 20 carbon atoms.

20. The process of claim 19 , further comprising, prior to step (a),

recovering, as a bottoms fraction from an upstream distillation of an impure feed stream, the purified feed steam comprising ethylbenzene and at least one further C 8 aromatic compound, wherein the purified feed stream is depleted in non-aromatic hydrocarbons, relative to the impure feed stream.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S ADDRESS PREVIOUSLY RECORDED AT REEL: 055043 FRAME: 0345. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Oct 26, 2021
From: SULZER GTC TECHNOLOGY US INC.
To: SULZER MANAGEMENT AG
Reel/Frame 058556/0475 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2021
From: SULZER GTC TECHNOLOGY US INC.
To: SULZER MANAGEMENT AG
Reel/Frame 055043/0345 →
CHANGE OF NAME Recorded Aug 22, 2019
From: GTC TECHNOLOGY US, LLC
To: SULZER GTC TECHNOLOGY US INC.
Reel/Frame 050128/0041 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2019
From: KAMMAFOO, ALISA; THIRASAK, ATTAPONG
To: SCG CHEMICALS CO., LTD.
Reel/Frame 049836/0173 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2019
From: DING, ZHONGYI
To: GTC TECHNOLOGY US, LLC
Reel/Frame 049836/0211 →
Continuity (2)
Provisional Application 62701059 · Jul 20, 2018
Related Publication 20200024217A1 · Jan 23, 2020