Process for producing 1,3-butadiene from a feedstock comprising ethanol

Patent metadata

Field	Value
Publication number	US-9776933-B2
Application number	US-201415039881-A
Country	US
Kind code	B2
Filing date	Nov 28, 2014
Priority date	Nov 29, 2013
Publication date	Oct 3, 2017
Grant date	Oct 3, 2017

Abstract

Production of 1,3-butadiene ethanol, that is more than 50% of the total weight of feedstock:
A) conversion of feedstock and of ethanol effluent from separation B to a conversion effluent being a majority of 1,3-butadiene, water and ethylene, and to a hydrogen effluent, operating at a pressure between 0.1 and 1.0 MPa, a temperature between 300 and 500° C. in the presence of at least one catalyst; B) separation of conversion effluent originating from A and hydration effluent from C to an ethanol effluent, a butadiene effluent, a water effluent and an ethylene effluent; C) hydration of ethylene fed by ethylene effluent and/or water effluent both from separation B, to produce an ethanol hydration effluent then being recycled to separation B.

First claim

The invention claimed is:

1. A process for the production of 1,3-butadiene from a feedstock rich in ethanol, in which the ethanol represents more than 50% of the total weight of said feedstock, comprising at least:
stage A) conversion of at least said feedstock rich in ethanol and of ethanol effluent originating from separation stage B to a conversion effluent comprising a majority of 1,3-butadiene, water and ethylene, and to a hydrogen effluent, operating at a pressure of 0.1 to 1.0 MPa, at a temperature of 300 to 500° C. in the presence of at least one catalyst;
stage B) separation of at least said conversion effluent originating from A and the hydration effluent originating from C to at least an ethanol effluent, a butadiene effluent, a water effluent and an ethylene effluent;
stage C) hydration of the ethylene fed at least by said ethylene effluent and/or said water effluent both originating from stage B, in order to produce a hydration effluent comprising ethanol, said hydration effluent then being recycled to stage B.

2. The process according to claim 1 , in which said stage A is operated at a pressure of 0.1 to 0.5 MPa.

3. The process according to claim 1 , in which said stage A is operated in one reaction stage and in which said feedstock rich in ethanol is mixed with the ethanol effluent originating from stage B before feeding said stage A.

4. The process according to claim 3 , in which said stage A is operated in the presence of a zinc aluminate catalyst or chromium-doped MgO—SiO 2 catalyst, at a temperature of 380 to 430° C.

5. The process according to claim 1 , in which said stage A is operated in two reaction stages, a first reaction stage converting the ethanol to acetaldehyde in the presence of a catalyst at a mass ratio of ethanol to acetaldehyde in effluent of said first reaction stage being of 2:1 to 4:1, said feedstock rich in ethanol feeding said first reaction stage and said ethanol effluent originating from stage B feeding said second reaction stage, in a mixture with said effluent from said first reaction stage.

6. The process according to claim 5 , in which the second reaction stage of stage A is operated in the presence of a catalyst of silica with an oxide of tantalum, zirconium or niobium, the second reaction stage of stage A being operated at a temperature of 320 to 370° C., the first reaction stage of said stage A being operated at a temperature of 200 to 300° C.

7. The process according to claim, in which stage B is: distillation, cryogenic distillation, washing with solvent, extractive distillation, liquid-liquid extraction, passing through a sieve, membrane separation or combinations thereof.

8. The process according to claim 1 , in which said stage C is an indirect hydration, in which, in a first reaction stage, the ethylene reacts in the presence of concentrated sulphuric acid at a reaction temperature of 50 to 150° C., in a two-phase gas/liquid medium and in a second stage, the products formed in the first stage are hydrolyzed in order to form a majority of ethanol at a temperature of 70 and 100° C.

9. The process according to claim 1 , in which said stage C is a direct hydration operating in gas phase, at a reaction temperature comprised between 200 and 400° C., in the presence of a heterogeneous catalyst based on inorganic acids.

10. The process according to claim 1 , in which said feedstock rich in ethanol comprises acetaldehyde, at a mass ratio of ethanol to acetaldehyde of 2:1 to 4:1.

11. The process according to claim 1 , in which the purity of the ethylene flow feeding hydration stage C is 65 to 99.9% by weight.

12. The process according to claim 1 , in which the purity of the ethylene flow feeding hydration stage C is 65 to 75% by weight.

13. The process according to claim 5 , wherein the catalyst is a mixture of chromium oxide and copper oxide.

14. The process according to claim 9 , wherein the heterogeneous catalyst is phosphoric acid deposited on a silica-based support.

15. The process according to claim 1 , wherein ethylene effluent is fed to stage C without further purification.

Assignees

• Ifp Energies Now
• Michelin & Cie
• Michelin Rech Tech

Inventors

• Dastillung Rejane
• Cadran Nicolas
• Jacquin Marc
• Huyghe Raphael
• Fischer Beatrice

Classifications

• C07C2521/06

  Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof · CPC title

• C07C11/167

  1, 3-Butadiene · CPC title

• C07C1/20 Primary

  starting from organic compounds containing only oxygen atoms as heteroatoms · CPC title

• C07C2523/26

  Chromium · CPC title

• Y02P30/42

  Cross-Sectional Technologies · mapped topic