IP Library Granted Patent US 7,919,652
Granted Patent B2
US 7,919,652 · App. 11/365,079 · Granted Apr 5, 2011

Process to produce an enriched composition through the use of a catalyst removal zone and an enrichment zone

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Quick Facts
Patent No.
US 7,919,652
App. No.
11/365,079
Granted
Apr 5, 2011
Kind
B2
Abstract

A process is provided for producing an enriched carboxylic acid compositions produced by contacting composition comprising a carboxylic acid with an enrichment feed in an enrichment zone to form an enriched carboxylic acid composition. This invention also relates to a process and the resulting compositions for removing catalyst from a carboxylic acid composition to produce a post catalyst removal composition.

Claims (26)

1. A process to produce an enriched composition comprising terephthalic acid, said process comprising:

(a) subjecting a cooled carboxylic acid composition comprising terephthalic acid, and a wash feed to a catalyst removal zone in a terephthalic acid process to form a post catalyst removal composition, a wash liquor, and a catalyst rich liquor;

(b) contacting an enrichment feed with said post catalyst removal composition comprising terephthalic acid, to form said enriched composition; wherein said enrichment feed comprises at least one compound selected from the group consisting of isophthalic acid, phthalic acid, benzene-tricarboxylic acid isomers, hydroxybenzoic acid isomers, hydroxymethylbenzoic acid isomers, dicarboxybiphenyl isomers, dicarboxystilbene isomers, tricarboxybiphenyl isomers, tricarboxybenzophenone isomers, dicarboxybenzophenone isomers, dicarboxybenzil isomers, form-acet-hydroxybenzoic acid isomers, acet-hydroxymethylbenzoic acid isomers, and phthaldehyde isomers; wherein said enriched composition is enriched in at least one of said compounds relative to said post catalyst removal composition.

2. The process according to claim 1 wherein said cooled carboxylic acid composition is cooled to a temperature ranging from about 5° C. to about 195° C.

3. The process according to claim 1 wherein said cooled carboxylic acid composition is cooled to a temperature ranging from about 20° C. to about 195° C.

4. The process according to claim 3 wherein said wash feed is at a temperature ranging from about 20° C. to about 90° C.

5. The process according to claim 1 wherein said wash feed is at a temperature ranging from about 5° C. to about 195° C.

6. The process according to claim 1 wherein at least two of said compounds are enriched by at least 1000 ppmw.

7. A process to produce an enriched composition comprising terephthalic acid, said process comprising:

(a) oxidizing paraxylene in a primary oxidation zone to form a crude carboxylic acid composition comprising terephthalic acid;

(b) optionally subjecting said crude carboxylic acid composition to a liquid displacement zone to form a slurry composition;

(c) cooling and optionally enriching said slurry composition or said crude carboxylic acid composition in a cooling zone to form a cooled carboxylic acid composition;

(d) subjecting said cooled carboxylic acid composition, and a wash feed to a catalyst removal zone to form a post catalyst removal composition and a catalyst rich liquor;

(e) contacting said enrichment feed with said post catalyst removal composition comprising terephthalic acid, to form said enriched composition; wherein said enrichment feed comprises at least one compound selected from the group consisting of isophthalic acid, phthalic acid, benzene-tricarboxylic acid isomers, hydroxybenzoic acid isomers, hydroxymethylbenzoic acid isomers, dicarboxybiphenyl isomers, dicarboxystilbene isomers, tricarboxybiphenyl isomers, tricarboxybenzophenone isomers, dicarboxybenzophenone isomers, dicarboxybenzil isomers, form-acet-hydroxybenzoic acid isomers, acet-hydroxymethylbenzoic acid isomers, and phthaldehyde isomers; wherein said enriched composition is enriched in at least one of said compound relative to said post catalyst removal composition.

8. The process according to claim 7 wherein said primary oxidation zone comprises at least one oxidation reactor operated at a temperature from 110° C. to 200° C.

9. The process according to claim 7 wherein said catalyst removal zone has a wash ratio of about 0.2 to about 6.

10. The process according to claim 7 wherein said catalyst removal zone has a wash ratio of about 0.2 to about 2.

11. The process according to claim 7 wherein said catalyst removal zone has a wash ratio of about 0.5 to about 2.0.

12. The process according to claim 7 wherein said catalyst removal zone has a wash ratio of about 0.2 to about 1.0.

13. The process according to claim 7 wherein said cooled carboxylic acid composition is cooled to a temperature ranging from about 20° C. to about 90° C.

14. The process according to claim 7 wherein said cooled carboxylic acid composition is cooled to a temperature ranging from about 5° C. to about 195° C.

15. The process according to claim 13 wherein said cooled carboxylic acid composition is cooled to a temperature ranging from about 5° C. to about 195° C.

16. The process according to claim 7 wherein said wash feed is at a temperature ranging from about 20° C. to about 90° C.

17. The process according to claim 7 wherein said wash feed is at a temperature ranging from about 5° C. to about 195° C.

18. The process according to claim 7 wherein a liquid displacement zone is between the crystallization zone and cooling zone.

19. The process according to claim 1 wherein at least two of said compounds are enriched by at least 1000 ppmw.

Assignments (3)
CHANGE OF NAME Recorded Jan 11, 2022
From: GRUPO PETROTEMEX, S.A. DE C.V.
To: ALPEK POLYESTER, S.A. DE C.V.
Reel/Frame 058691/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2011
From: EASTMAN CHEMICAL COMPANY
To: GRUPO PETROTEMEX, S.A. DE C.V.
Reel/Frame 025728/0217 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2006
From: GIBSON, PHILIP EDWARD; PARKER, KENNY RANDOLPH; O'MEADHRA, RUAIRI SEOSAMH
To: EASTMAN CHEMICAL COMPANY
Reel/Frame 017499/0140 →