IP Library Granted Patent US 9,296,672
Granted Patent B2
US 9,296,672 · App. 14/111,205 · Granted Mar 29, 2016

Process and plant for the production of methanol from synthesis gas rich in inerts

Inventors: Philipp Marius Hackel (Frankfurt am Main, DE); Rainer Morgenroth (Hattstedt, DE); Andreas Bormann (Frankfurt, DE); Veronika Gronemann (Frankfurt, DE)
Assignee: AIR LIQUIDE GLOBAL E&C SOLUTIONS GERMANY GMBH
C07C29/152Y02E50/18Y10T29/49716
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Quick Facts
Patent No.
US 9,296,672
App. No.
14/111,205
Granted
Mar 29, 2016
Kind
B2
Abstract

A method for producing methanol from inert-rich syngas includes installing a catalytic pre-reactor is upstream of the single or mufti-stage synthesis loop, a first part of the syngas being converted to methanol in the catalytic pre-reactor. Furthermore, an inert gas separation stage, for example a pressure swing adsorption system or a membrane system, is connected downstream of the synthesis loop, whereby a hydrogen-enriched syngas stream can be returned to the synthesis loop. In the processing of methane-rich syngas, the inert gas separation stage may also comprise an autothermal reformer in which methane is converted to carbon oxides and hydrogen, which are also returned into the synthesis loop.

Claims (40)

1. A method for the production of methanol from a synthesis gas comprising hydrogen, a carbon oxide, and an inert component, the process comprising:

(a) passing a first synthesis gas stream as feed stream through at least one methanol pre-reactor, in which a part of the carbon oxide is catalytically converted with hydrogen to obtain methanol;

(b) separating off the methanol produced in (a) to obtain a second synthesis gas stream;

(c) passing the second synthesis gas stream through at least one methanol main reactor, in which a further part of the carbon oxide is catalytically converted with hydrogen to obtain methanol;

(d) separating off the methanol produced in (c) to obtain a third synthesis gas stream;

(e) dividing the third synthesis gas stream into a fourth synthesis gas stream and a fifth synthesis gas stream;

(f) recirculating the fourth synthesis gas stream to the methanol main reactor to form an inner synthesis cycle;

(g) supplying the fifth synthesis gas stream to at least one inert gas separation stage, to obtain a sixth stream depleted of inert components and a purge stream enriched in inert components; and

(h) recirculating the sixth stream to the methanol main reactor to form an outer synthesis cycle,

wherein a space velocity of the methanol main reactor is greater than a space velocity of the methanol pre-reactor.

2. The method of claim 1 , wherein the inert gas separation stage comprises a pressure swing adsorption system.

3. The method of claim 1 , wherein the inert gas separation stage comprises an autothermal reformer.

4. The method of claim 1 , wherein the first synthesis gas stream is obtained by gasification of natural gas with a gas comprising oxygen.

5. The method of claim 1 , wherein the first synthesis gas stream is obtained by gasification of coal with a gas comprising oxygen.

6. The method of claim 1 , further comprising:

(i) supplying the methanol obtained to further product processing.

7. The method of claim 1 , wherein the methanol main reactor is operated in a water-cooled manner.

8. The method of claim 1 , wherein the at least one methanol main reactor comprises:

a first methanol main reactor; and

a second methanol main reactor,

wherein the first methanol main reactor in flow direction is operated in a water-cooled manner, and

wherein the second methanol main reactor in flow direction is operated in a gas-cooled manner.

9. The method of claim 1 , wherein the inert gas separation stage comprises a membrane system.

10. The method of claim 1 , Wherein the inert gas separation stage comprises an autothermal reformer, jointly with a pressure swing adsorption system.

11. The method of claim 1 , wherein the first synthesis gas stream is obtained by gasification of biomass with a gas comprising oxygen.

12. The method of claim 1 , wherein the methanol main reactor is operated in gas-cooled manner.

13. The method of claim 1 , wherein the methanol main reactor is operated in an adiabatic manner.

14. The method of claim 1 , wherein the at least one methanol main reactor consists essentially of:

a first methanol main reactor; and

a second methanol main reactor,

wherein the first methanol main reactor in flow direction is operated in a water-cooled manner, and

wherein the second methanol main reactor in flow direction is operated in a gas-cooled manner.

15. The method of claim 1 , wherein a space velocity of the methanol main reactor is twice space velocity of the methanol pre-reactor.

16. The method of claim 1 , Wherein an inlet temperature of the methanol main reactor is greater than an inlet temperature of the methanol pre-reactor.

17. The method of claim 1 , wherein the synthesis gas comprises 60 vol. % methane.

18. The method of claim 1 , further comprising:

converting methane comprised in the purge stream to further synthesis gas.

19. The method of claim 1 , further comprising:

converting methane comprised in the purge stream to further synthesis gas; and

recycling the further synthesis gas to the methanol main reactor.

Assignments (2)
CHANGE OF NAME Recorded Jul 24, 2014
From: LURGI GMBH
To: AIR LIQUIDE GLOBAL E&C SOLUTIONS GERMANY GMBH
Reel/Frame 033397/0172 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 18, 2013
From: HACKEL, PHILIPP MARIUS; MORGENROTH, RAINER; BORMANN, ANDREAS; GRONEMANN, VERONIKA
To: LURGI GMBH
Reel/Frame 031429/0947 →
Priority Claims (1)
DE 10 2011 017 300 · Apr 15, 2011 · national
Continuity (1)
Related Publication 20140031438A1 · Jan 30, 2014