Limiting acetic acid production in ethane ODH process

Patent metadata

Field	Value
Publication number	US-12325684-B2
Application number	US-202118008312-A
Country	US
Kind code	B2
Filing date	May 25, 2021
Priority date	Jun 9, 2020
Publication date	Jun 10, 2025
Grant date	Jun 10, 2025

Abstract

The present disclosure relates to limiting the production of acetic acid in an oxidative dehydrogenation process to convert ethane to ethylene. The process of oxidative dehydrogenation includes feeding acetic acid, along with ethane and oxygen into an oxidative dehydrogenation reactor where contact with a catalyst leads to conversion of the ethane into ethylene and acetic acid. By including acetic acid in the feed, the amount of acetic acid produced may be limited and the ratio of ethylene produced to ethane consumed may increase.

First claim

The invention claimed is:

1. A process for the oxidative dehydrogenation of ethane comprising contacting a feed stream comprising ethane, oxygen, and acetic acid with an oxidative dehydrogenation catalyst under oxidative dehydrogenation conditions in an oxidative dehydrogenation reactor to produce a product stream comprising ethylene, unreacted ethane, water, and acetic acid, wherein the concentration of acetic acid in the feed stream is from 0.5 to 10 vol % of the feed stream.

2. The process according to claim 1 , wherein the concentration of acetic acid in the feed stream is from 2 to 5 vol % of the feed stream.

3. The process according to claim 1 , wherein the concentration of acetic acid in the feed stream is greater than 2 vol % of the feed stream.

4. The process according to claim 1 , further comprising a downstream separation process wherein the product stream is separated into a liquid stream comprising water and acetic acid, and a gaseous components stream comprising ethylene and unreacted ethane, and recycling to the reactor as part of the feed stream at least a portion of the liquid stream.

5. The process according to claim 4 , wherein the liquid stream is diluted with water to achieve the desired amount of acetic acid in the feed stream.

6. The process according to claim 4 , wherein a split fraction of the liquid stream is adjusted to achieve the desired amount of acetic acid in the feed stream.

7. The process according to claim 1 , wherein the feed stream to the reactor comprises:
i) from 0.5 to 10 vol % acetic acid;
ii) an oxygen to ethane molar ratio from 0.5 to 0.7; and
iii) H 2 O and CO 2 in a molar ratio such that the feed composition is outside the flammability limits.

8. The process according to claim 1 , wherein the reactor operates at a temperature from 300° C. to 425° C.

9. The process according to claim 1 , wherein the reactor operates at a temperature from 315° C. to 400° C.

10. The process according to claim 1 , wherein the reactor operates at a pressure from 0.5 psig to 100 psig.

11. The process according to claim 1 , wherein the reactor operates at a pressure from 15 psig to 504 psig.

12. The process according to claim 1 , wherein the gas hourly space velocity of the product stream is from 500 h −1 to 30000 h −1 .

13. The process according to claim 1 , wherein the gas hourly space velocity of the product stream is from 1000 h −1 to 15000 h −1 .

14. The process according to claim 1 , wherein the gas hourly space velocity of the product stream is from 500 h −1 to 4000 h −1 .

15. The process according to claim 1 , wherein the catalyst comprises one or more catalyst selected from the group consisting of:
i) catalysts of the formula:
Mo a V b Te c Nb d Pd e O f

wherein: a, b, c, d, e and f are the relative atomic amounts of the elements Mo, V, Te, Nb, Pd and O, respectively; and when a=1, b=0.01 to 1.0, c=0.01 to 1.0, d=0.01 to 1.0, 0.00≤e≤ 0.10 and f is a number to satisfy the valence state of the catalyst;
ii) catalysts of the formula:
Mo a E k G l O f

wherein: E is selected from the group consisting of Ba, Ca, Cr, Mn, Nb, Ta, Ti, Te, V, W and mixtures thereof; G is selected from the group consisting of Bi, Ce, Co, Cu, Fe, K, Mg, V, Ni, P, Pb, Sb, Si, Sn, Ti, U, and mixtures thereof; a=1; k is 0 to 2; 1=0 to 2, with the proviso that the total value of 1 for Co, Ni, Fe and mixtures thereof is less than 0.5; and fis a number to satisfy the valence state of the catalyst;
iii) catalysts of the formula:
V m Mo n Nb o Te p Me q O f

wherein: Me is a metal selected from the group consisting of Ta, Ti, W, Hf, Zr, Sb and mixtures thereof; m is from 0.1 to 3; n is from 0.5 to 1.5; o is from 0.001 to 3; p is from 0.001 to 5; q is from 0 to 2; and f is a number to satisfy the valence state of the catalyst; and
iv) catalysts of the formula:
Mo a V r X s Y t Z u M v O f

wherein: X is at least one of Nb and Ta; Y is at least one of Sb and Ni; Z is at least one of Te, Ga, Pd, W, Bi and Al; M is at least one of Fe, Co, Cu, Cr, Ti, Ce, Zr, Mn, Pb, Mg, Sn, Pt, Si, La, K, Ag and In; a=1.0 (normalized); r=0.05 to 1.0; s=0.001 to 1.0; t=0.001 to 1.0; u=0.001 to 0.5; v=0.001 to 0.3; and f is a number to satisfy the valence state of the catalyst.

16. The process according to claim 4 , wherein the liquid stream comprises less than 10 vol % of acetic acid.

17. The process according to claim 1 , wherein the selectivity to ethylene is from 75% to 99%.

18. The process according to claim 1 , wherein the selectivity to CO 2 is equal to or less than 10%.

19. The process according to claim 1 , wherein the selectivity to CO is equal to or less than 11%.

20. The process according to claim 1 , wherein the feed stream to the reactor comprises from 2 to 3 vol % of acetic acid, 29 to 57 vol % of H 2 O, 16 to 26 vol % of C 2 H 6 , 8 to 14 vol % of O 2 , and 17 to 28 vol % of CO 2 .

21. The process according to claim 4 , wherein a makeup stream and the gaseous components stream are contacted with a second oxidative dehydrogenation catalyst under oxidative dehydrogenation conditions in a second oxidative dehydrogenation reactor to produce a second product stream comprising ethylene, unreacted ethane, water, and acetic acid, wherein an overall concentration of acetic acid of the makeup stream and the gaseous components stream entering the second oxidative dehydrogenation reactor is from 0.5 to 10 vol %.

22. The process according to claim 21 , further comprising a second downstream separation process wherein the second product stream is separated into a second liquid stream comprising water and acetic acid, and a second gaseous components stream comprising ethylene and unreacted ethane, and recycling at least a portion of the second liquid stream to the oxidative dehydrogenation reactor as part of the feed stream or to the second oxidative dehydrogenation reactor as part of the makeup stream.

Assignees

• Nova Chemicals International Sa

Inventors

• Olayiwola Bolaji
• Goodarznia Shahin
• Simanzhenkov Vasily
• Aiffa Mohamed
• Serhal Kamal
• Ladd Robert
• Gent David

Classifications

• C07C53/08

  Acetic acid (pyroligneous acid C10C; preparation of vinegar C12J) · CPC title

• C07C51/15 Primary

  by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis · CPC title

• C07C2527/057

  Selenium or tellurium; Compounds thereof · CPC title

• C07C2523/28

  Molybdenum · CPC title

• C07C2523/20

  Vanadium, niobium or tantalum · CPC title