IP Library Granted Patent US 10,195,603
Granted Patent B2
US 10,195,603 · App. 15/628,023 · Granted Feb 5, 2019

Production of ethylene with nanowire catalysts

Inventors: Erik C. Scher (San Francisco, CA); Fabio R. Zurcher (Brisbane, CA); Joel M. Cizeron (Redwood City, CA); Wayne P. Schammel (Brisbane, CA); Alex Tkachenko (San Francisco, CA); Joel Gamoras (Vallejo, CA); Dmitry Karshtedt (San Francisco, CA); Greg Nyce (Pleasanton, CA)
Assignee: Siluria Technologies, Inc.
B01J35/06B01J21/066B01J21/10B01J23/10B01J23/22B01J23/34B01J35/0013B01J37/0018B01J37/031B01J37/08B01J37/10B82Y30/00C01F5/02C01F5/14C01F7/02C01F11/02C01F17/0043C01G25/00C01G31/02C01G41/02C01G45/00C01G45/006C01G45/02C07C2/84C07C5/48C10G2/33C10G9/00C01P2002/52C01P2002/72C01P2004/04C01P2004/16C01P2004/54C01P2004/84C01P2006/12C07C2521/10C07C2523/02C07C2523/04C07C2523/10C07C2523/30C07C2523/34C07C2523/75C10G2300/1025C10G2300/70C10G2400/02C10G2400/20C10G2400/22Y02P20/52Y02P30/40
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,195,603
App. No.
15/628,023
Granted
Feb 5, 2019
Kind
B2
Abstract

Nanowires useful as heterogeneous catalysts are provided. The nanowire catalysts are useful in a variety of catalytic reactions, for example, the oxidative coupling of methane to ethylene. Related methods for use and manufacture of the same are also disclosed.

Claims (39)

1. A method for the preparation of ethylene from methane, the method comprising contacting a mixture comprising oxygen and methane at a temperature below 600° C. with a catalytic nanowire, thereby producing C2 hydrocarbons at a selectivity of greater than 30%, wherein the catalytic nanowire comprises one or more elements from any of Groups 1 through 7, lanthanides, actinides or combinations thereof in the form of oxides, hydroxides, oxyhydroxides, sulfates, carbonates, oxide carbonates, oxalates, phosphates, hydrogenphosphates, dihydrogenphosphates, oxyhalides, hydroxihalides, oxysulfates or combinations thereof.

2. The method of claim 1 , wherein the one or more elements are in the form of oxides.

3. The method of claim 1 , wherein the catalytic nanowire comprises Mg, Ca, La, W, Mn, Mo, Nd, Sm, Eu, Pr, Zr or combinations thereof.

4. The method of claim 1 , wherein the catalytic nanowire comprises MgO, CaO, La 2 O 3 , Na 2 WO 4 , Mn 2 O 3 , Mn 3 O 4 , Nd 2 O 3 , Sm 2 O 3 , Eu 2 O 3 , Pr 2 O 3 , Mg 6 MnO 8 , NaMnO 4 , Na/Mn/W/O, MnWO 4 or combinations thereof.

5. The method of claim 1 , wherein the catalytic nanowire further comprises one or more dopants comprising metal elements, semi-metal elements, non-metal elements or combinations thereof.

6. The method of claim 5 , wherein the dopant comprises Li, Na, K, Mg, Ca, Ba, Sr, Eu, Sm, Co or Mn.

7. The method of claim 6 , wherein the catalytic nanowire comprises Li/MgO, Ba/MgO, Sr/La 2 O 3 , Mg/Na/La 2 O 3 , Sr/Nd 2 O 3 , or Mn/Na 2 WO 4 .

8. The method of claim 1 , wherein the catalytic nanowire has a ratio of effective length to actual length of less than one.

9. The method of claim 1 , wherein the catalytic nanowire has a ratio of effective length to actual length of one.

10. The method of claim 1 , wherein the temperature ranges from 550° C. to below 600° C.

11. The method of claim 1 , wherein the temperature ranges from 500° C. to 550° C.

12. A method for preparing a downstream product of ethylene, the method comprising converting ethylene into a downstream product of ethylene, and the method comprising contacting a mixture comprising oxygen and methane at a temperature below 600° C. with a catalytic nanowire, thereby producing C2 hydrocarbons at a selectivity of greater than 30%, wherein the catalytic nanowire comprises one or more elements from any of Groups 1 through 7, lanthanides, actinides or combinations thereof in the form of oxides, hydroxides, oxyhydroxides, sulfates, carbonates, oxide carbonates, oxalates, phosphates, hydrogenphosphates, dihydrogenphosphates, oxyhalides, hydroxihalides, oxysulfates or combinations thereof.

13. The method of claim 12 , wherein the one or more elements are in the form of oxides.

14. The method of claim 12 , wherein the catalytic nanowire comprises Mg, Ca, La, W, Mn, Mo, Nd, Sm, Eu, Pr, Zr or combinations thereof.

15. The method of claim 12 , wherein the catalytic nanowire comprises MgO, CaO, La 2 O 3 , Na 2 WO 4 , Mn 2 O 3 , Mn 3 O 4 , Nd 2 O 3 , Sm 2 O 3 , Eu 2 O 3 , Pr 2 O 3 , Mg 6 MnO 8 , NaMnO 4 , Na/Mn/W/O, MnWO 4 or combinations thereof.

16. The method of claim 12 , wherein the catalytic nanowire further comprises one or more dopants comprising metal elements, semi-metal elements, non-metal elements or combinations thereof.

17. The method of claim 16 , wherein the dopant comprises Li, Na, K, Mg, Ca, Ba, Sr, Eu, Sm, Co or Mn.

18. The method of claim 17 , wherein the catalytic nanowire comprises Li/MgO, Ba/MgO, Sr/La 2 O 3 , Mg/Na/La 2 O 3 , Sr/Nd 2 O 3 , or Mn/Na 2 WO 4 .

19. The method of claim 12 , wherein the catalytic nanowire has a ratio of effective length to actual length of less than one.

20. The method of claim 12 , wherein the catalytic nanowire has a ratio of effective length to actual length of one.

21. The method of claim 12 , wherein the downstream product of ethylene is natural gasoline.

22. The method of claim 12 , wherein the downstream product of ethylene comprises 1-hexene, 1-octene or combinations thereof.

23. The method of claim 12 , wherein the temperature ranges from 550° C. to below 600° C.

24. The method of claim 12 , wherein the temperature ranges from 500° C. to 550 ° C.

25. A method for the preparation of a downstream product of ethylene, the method comprising:

converting methane into ethylene by contacting a mixture comprising oxygen and methane at a temperature below 600° C. with a catalytic nanowire, thereby producing C2hydrocarbons at a selectivity of greater than 30%; and

oligomerizing the ethylene to prepare a downstream product of ethylene, wherein the catalytic nanowire comprises one or more elements from any of Groups 1 through 7, lanthanides, actinides or combinations thereof in the form of oxides, hydroxides, oxyhydroxides, sulfates, carbonates, oxide carbonates, oxalates, phosphates, hydrogenphosphates, dihydrogenphosphates, oxyhalides, hydroxihalides, oxysulfates or combinations thereof.

26. The method of claim 25 , wherein the one or more elements are in the form of oxides.

27. The method of claim 25 , wherein the catalytic nanowire comprises Mg, Ca, La, W, Mn, Mo, Nd, Sm, Eu, Pr, Zr or combinations thereof.

28. The method of claim 25 , wherein the catalytic nanowire comprises MgO, CaO, La 2 O 3 , Na 2 WO 4 , Mn 2 O 3 , Mn 3 O 4 , Nd 2 O 3 , Sm 2 O 3 , Eu 2 O 3 , Pr 2 O 3 , Mg 6 MnO 8 , NaMnO 4 , Na/Mn/W/O, MnWO 4 or combinations thereof.

29. The method of claim 25 , wherein the catalytic nanowire further comprises one or more dopants comprising metal elements, semi-metal elements, non-metal elements or combinations thereof.

30. The method of claim 29 , wherein the dopant comprises Li, Na, K, Mg, Ca, Ba, Sr, Eu, Sm, Co or Mn.

31. The method of claim 30 , wherein the catalytic nanowire comprises Li/MgO, Ba/MgO, Sr/La 2 O 3 , Mg/Na/La 2 O 3 , Sr/Nd 2 O 3 , or Mn/Na 2 WO 4 .

32. The method of claim 25 , wherein the catalytic nanowire has a ratio of effective length to actual length of less than one.

33. The method of claim 25 , wherein the catalytic nanowire has a ratio of effective length to actual length of one.

34. The method of claim 25 , wherein the downstream product of ethylene is natural gasoline.

35. The method of claim 25 , wherein the downstream product of ethylene comprises 1-hexene, 1-octene or combinations thereof.

36. The method of claim 25 , wherein the temperature ranges from 550° C. to below 600° C.

37. The method of claim 25 , wherein the temperature ranges from 500° C. to 550° C.

Continuity (4)
Continuation 13115082 · May 24, 2011
Provisional Application 61425631 · Dec 21, 2010
Provisional Application 61347774 · May 24, 2010
Related Publication 20180117579A1 · May 3, 2018
Cited By (4)
US 12,227,466 US 12,447,465 US 12,612,344 US 12,655,075