Process for producing butadiene from ethanol with in situ regeneration of the catalyst of the second reaction step

Patent metadata

Field	Value
Publication number	US-11401219-B2
Application number	US-201917415806-A
Country	US
Kind code	B2
Filing date	Dec 13, 2019
Priority date	Dec 21, 2018
Publication date	Aug 2, 2022
Grant date	Aug 2, 2022

Abstract

The present invention relates to a process for producing butadiene from ethanol, in two reaction steps, comprising a step a) of converting ethanol into acetaldehyde and a step b) of conversion into butadiene, said step b) simultaneously implementing a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being equal to 2 or a multiple thereof, comprising a catalyst, said regeneration step comprising four successive regeneration phases, said step b) also implementing a regeneration loop for the inert gas and at least one regeneration loop for the gas streams comprising oxygen.

First claim

The invention claimed is:

1. A process for producing butadiene from ethanol, comprising at least the following steps:
a) a step of converting ethanol into acetaldehyde, to produce an ethanol/acetaldehyde effluent, wherein the step of converting ethanol into acetaldehyde is carried out in at least one reaction section (A) fed with a stream comprising the ethanol and operated in the presence of a catalyst (Ca);
b) a butadiene producing step carried out in at least one reaction-regenerative section in which are simultaneously performed a reaction step and a regeneration step in (n+n/2) fixed-bed reactors, n being an integer equal to 2 or a multiple thereof, said (n+n/2) fixed-bed reactors each comprising at least one fixed bed of a catalyst (Cb), said (n+n/2) fixed-bed reactors functioning in parallel and in sequence so that said reaction step starts in each of said reactors with a time shift equal to half of the catalytic cycle time of said catalyst (Cb), said reaction-regenerative section comprising a regeneration loop for inert gas and at least one regeneration loop for a gas stream comprising oxygen, and so that, at each instant:
b1) said reaction step is operated in n of said fixed-bed reactors, n being as defined above, fed at least with a fraction of said ethanol/acetaldehyde effluent obtained from step a), at a temperature of between 300 and 400° C., at a pressure of between 0.1 and 1.0 MPa, for a time equal to the catalytic cycle time of said catalyst (b), to produce a reaction effluent comprising butadiene, and
b2) said regeneration step is operated in n/2 of said fixed-bed reactors for a total time equal to half of the catalytic cycle time of said catalyst (Cb), and comprises the following four successive phases:
i) a stripping phase operated at a temperature of between 300 and 400° C., under a stream of inert gas, said phase i) starting on conclusion of the reaction step b1); and then
ii) a first combustion phase operated on conclusion of phase i) under a gas stream comprising said inert gas and oxygen in a content of less than or equal to 1 vol % relative to the total volume of said gas stream, at a temperature of between 300 and 450° C.; and then
iii) a second combustion phase operated on conclusion of the first combustion phase ii) under a gas stream comprising said inert gas and oxygen in a content of greater than or equal to 2 vol % relative to the total volume of said gas stream, at a temperature of between 390 and 550° C.; and then
iv) a final stripping phase operated at a temperature of between 550° C. and 300° C., under a stream of said inert gas.

2. The process as claimed in claim 1 , in which the reaction section of step a) is operated at a temperature of between 200 and 500° C., and at a pressure of between 0.1 and 1.0.

3. The process as claimed in claim 1 , in which said fixed-bed reactors used in said reaction step b1) are also fed with an additional supply of ethanol and/or a supply of acetaldehyde, the feed flow rates being such that the mole ratio between the total molar amount of ethanol relative to the total molar amount of acetaldehyde entering said fixed-bed reactors of said reaction step b1) is between 1 and 5.

4. The process as claimed in claim 1 , in which the integer n is equal to 2 and said reaction-regenerative section of step b) comprises three fixed-bed reactors.

5. The process as claimed in claim 1 , in which said reaction step b1) is operated at a temperature of between 300 and 360° C.

6. The process as claimed in claim 1 , in which said reaction step b1) is operated at a pressure of between 0.2 and 0.4 MPa.

7. The process as claimed in claim 1 , in which the catalytic cycle time of said catalyst (Cb) for the butadiene conversion step b) is greater than or equal to 1 day, and less than or equal to 20 days.

8. The process as claimed in claim 1 , in which the inert gas of the regeneration step b2) is nitrogen, carbon dioxide (CO 2 ) or a mixture thereof.

9. The process as claimed in claim 1 , in which said stripping phase i) is operated at a temperature of between 330 and 370° C.

10. The process as claimed in claim 1 , in which the flow rate of inert gas of said stripping phase i) is between 0.5 and 1.5 Nm 3 /h/kg of catalyst.

11. The process as claimed in claim 1 , in which said first combustion phase ii) is operated under a gas stream comprising an oxygen content of between 0.1 and 1 vol % relative to the total volume of said gas stream.

12. The process as claimed in claim 1 , in which said first combustion phase ii) is operated at a temperature of between 330 and 430° C.

13. The process as claimed in claim 1 , in which said first combustion phase ii) is operated at a flow rate of gas stream of between 3.5 and 5.0 Nm 3 /h/kg of catalyst.

14. The process as claimed in claim 1 , in which said second combustion phase iii) is operated under a gas stream comprising an oxygen content of between 2 and 20 vol % relative to the total volume of said gas stream.

15. The process as claimed in claim 1 , in which said second combustion phase iii) is operated at a constant temperature of between 390 and 430° C. followed by a temperature increase ramp of 10 to 30° C./h and then a phase at a constant temperature of between 460 and 510° C.

16. The process as claimed in claim 1 , in which said second combustion phase iii) is operated at a flow rate of gas stream of between 2.5 and 3.5 Nm 3 /h/kg of catalyst.

17. The process as claimed in claim 1 , in which said final stripping phase iv) is operated on a temperature decrease ramp of 50 to 150° C./h followed by a phase at a constant temperature of between 300 and 400° C.

18. The process as claimed in claim 1 , in which said final stripping phase iv) is operated under a stream of said inert gas, at a flow rate of between 0.5 and 1.5 Nm 3 /h/kg of catalyst.

19. The process as claimed in claim 1 , in which said first combustion phase ii) is operated at a constant temperature of between 330 and 370° C. followed by a temperature increase ramp of 10 to 30° C./h and then a phase at a constant temperature of between 390 and 430° C.

20. The process as claimed in claim 1 , in which the reaction section of step a) is operated at a temperature of between 250 and 300° C., and at a pressure of between 0.1 and 0.3 MPa.

Assignees

• Ifp Energies Now
• Michelin & Cie

Inventors

• Drobyshev Kirill
• Dastillung Rejane
• Gabelle Jean-Christophe
• Rolland Matthieu

Classifications

• C07C2523/20

  Vanadium, niobium or tantalum · CPC title

• B01J23/94

  of catalysts comprising metals, oxides or hydroxides of the iron group metals or copper · CPC title

• B01J23/20 Primary

  Vanadium, niobium or tantalum · CPC title

• C07C1/2072

  by condensation (C07C2/86 takes precedence) · CPC title

• B01J19/245

  placed in series · CPC title