Efficient oxidative coupling of methane processes and systems

Patent metadata

Field	Value
Publication number	US-9567269-B2
Application number	US-201615076480-A
Country	US
Kind code	B2
Filing date	Mar 21, 2016
Priority date	Mar 17, 2015
Publication date	Feb 14, 2017
Grant date	Feb 14, 2017

Abstract

The present disclosure provides oxidative coupling of methane (OCM) systems for small scale and world scale production of olefins. An OCM system may comprise an OCM subsystem that generates a product stream comprising C 2+ compounds and non-C 2+ impurities from methane and an oxidizing agent. At least one separations subsystem downstream of, and fluidically coupled to, the OCM subsystem can be used to separate the non-C 2+ impurities from the C 2+ compounds. A methanation subsystem downstream and fluidically coupled to the OCM subsystem can be used to react H 2 with CO and/or CO 2 in the non-C 2+ impurities to generate methane, which can be recycled to the OCM subsystem. The OCM system can be integrated in a non-OCM system, such as a natural gas liquids system or an existing ethylene cracker.

First claim

What is claimed is:

1. A method for performing oxidative coupling of methane (OCM), comprising:
(a) directing oxygen (O 2 ) and methane (CH 4 ) to an OCM unit that is upstream of a separations unit, wherein said OCM unit is integrated with and in fluid communication with a cracking unit, wherein in said OCM unit, said O 2 and said CH 4 react in an OCM process to yield a product stream comprising compounds with two or more carbon atoms (C 2+ compounds), including ethylene (C 2 H 4 );
(b) directing at least a portion of said C 2+ compounds to said cracking unit to yield a first stream having a concentration of C 2 H 4 that is increased with respect to said product stream, wherein said at least said portion of said C 2+ compounds is directed to said cracking unit without passage through said separations unit; and
(c) directing said first stream to said separations unit to yield a second stream having a concentration of C 2 H 4 that is increased with respect to said first stream, wherein (a)-(c) are performed at a carbon efficiency of at least about 0.50.

2. The method of claim 1 , further comprising directing one or more alkanes to said cracking unit.

3. The method of claim 2 , wherein said one or more alkanes are directed to said cracking unit along a stream external to said OCM unit.

4. The method of claim 2 , wherein said one or more alkanes comprise ethane (C 2 H 6 ).

5. The method of claim 2 , wherein said one or more alkanes are included in said product stream.

6. The method of claim 1 , wherein said cracking unit is substantially adiabatic.

7. The method of claim 1 , wherein said OCM unit is substantially adiabatic.

8. The method of claim 1 , wherein said at least said portion of said C 2+ compounds is directed to a treatment unit prior to being directed to said cracking unit.

9. The method of claim 1 , wherein an inlet temperature of said OCM unit is at most about 600° C.

10. The method of claim 1 , wherein said OCM unit comprises a plurality of OCM reactors.

11. The method of claim 1 , wherein said cracking unit comprises a plurality of cracking vessels.

12. The method of claim 1 , further comprising, prior to (c), directing said first stream from said cracking unit into a compressor, which compressor increases a pressure of said first stream.

13. The method of claim 1 , said separations unit in (c) yields a third stream comprising hydrogen (H 2 ) and carbon monoxide (CO) or carbon dioxide (CO 2 ) from said first stream or said second stream.

14. The method of claim 13 , further comprising directing said third stream to a methanation unit to react said H 2 with said CO or CO 2 to form CH 4 .

15. The method of claim 14 , wherein said methanation unit has a methanation catalyst that converts CO or CO 2 into CH 4 at a selectivity for the formation of CH 4 that is at least about 10-fold greater than a selectivity of said catalyst for formation of coke from said CO or CO 2 .

16. The method of claim 14 , further comprising directing at least a portion of said CH 4 from said methanation unit to said OCM unit.

17. The method of claim 1 , wherein carbon atoms output as hydrocarbons include at least a portion of said C 2+ compounds and excludes CO and CO 2 .

18. The method of claim 1 , further comprising using a power generation unit in thermal communication with said OCM unit to generate power from at least a portion of heat liberated by said OCM process.

19. The method of claim 1 , wherein at least 90% of energy used to operate said cracking unit and said separations unit is derived from heat liberated by said OCM process.

Assignees

• Siluria Technologies Inc

Inventors

• Radaelli Guido
• Rafique Humera A
• Vuddagiri Srinivas
• Scher Erik C
• Mccormick Jarod
• Cizeron Joel
• Patel Bipinkumar
• Lakhapatri Satish

Classifications

• C07C2/84 Primary

  catalytic · CPC title

• C07C1/0425

  Catalysts; their physical properties · CPC title

• B01J2208/00283

  involving reactant liquids · CPC title

• C07C1/12

  from carbon dioxide with hydrogen · CPC title

• B01J2208/00176

  outside the reactor · CPC title