IP Library Granted Patent US 8,357,826
Granted Patent B2
US 8,357,826 · App. 12/579,991 · Granted Jan 22, 2013

Methods and apparatus for synthesis of alcohols from syngas

Inventor: Karl Kharas (Louisville, CO)
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Quick Facts
Patent No.
US 8,357,826
App. No.
12/579,991
Granted
Jan 22, 2013
Kind
B2
Abstract

This invention provides a method for producing ethanol and 2-propanol from syngas, the method comprising: (a) converting syngas into methanol using a methanol-synthesis catalyst; (b) converting methanol into ethylene and propylene using a methanol-to-olefins catalyst; and (c) hydrating ethylene into ethanol and propylene into 2-propanol. As taught herein, the combined yield of the ethanol and the 2-propanol from biomass can be at least 100 gallons per dry ton biomass. In certain embodiments, the yield of ethanol is at least 100 gallons per dry ton biomass. In some embodiments, the yield of 2-propanol is at least 50 gallons per dry ton biomass.

Claims (42)

1. A method for producing ethanol and 2-propanol from methanol, said method comprising:

(a) converting methanol, in the presence of a methanol-to-olefins catalyst, into a stream including ethylene and propylene;

(b) feeding said stream from step (a) and water to a first hydration zone under suitable conditions for hydration of propylene to 2-propanol; and

(c) feeding at least a portion of the output of said first hydration zone, and optionally additional water, to a second hydration zone under suitable conditions for hydration of ethylene to ethanol.

2. The method of claim 1 , wherein said methanol is derived from syngas.

3. The method of claim 2 , wherein said syngas is derived from biomass.

4. The method of claim 1 , wherein said methanol-to-olefins catalyst comprises an aluminosilicate zeolite.

5. The method of claim 4 , wherein said aluminosilicate zeolite is selected from the group consisting of ZSM-5, ZSM-11, ZSM-12, ZSM-23, ZSM-35, and ZSM-48.

6. The method of claim 1 , wherein said methanol-to-olefins catalyst comprises a silicoaluminophosphate.

7. The method of claim 6 , wherein said silicoaluminophosphate is selected from the group consisting of SAPO-5, SAPO-8, SAPO-11, SAPO-16, SAPO-17, SAPO-18, SAPO-20, SAPO-31, SAPO-34, SAPO-35, SAPO-36, SAPO-37, SAPO-40, SAPO-41, SAPO-42, SAPO-44, SAPO-47, and SAPO-56.

8. The method of claim 7 , wherein said silicoaluminophosphate is SAPO-34.

9. The method of claim 6 , wherein said silicoaluminophosphate further includes one or more transition metals.

10. The method of claim 9 , wherein said one or more transition metals is selected from the group consisting of Mn, Ni, and Co.

11. The method of claim 10 , wherein said silicoaluminophosphate includes Ni.

12. The method of claim 11 , wherein said methanol-to-olefins catalyst is Ni—SAPO-34.

13. The method of claim 9 , wherein the ratio of silicon to said transition metal is selected from about 1 to about 500.

14. The method of claim 13 , wherein said ratio is selected from about 10 to about 200.

15. The method of claim 1 , wherein in step (a), the molar ratio of ethylene to propylene is greater than about 2.

16. The method of claim 15 , wherein in step (a), said molar ratio of ethylene to propylene is greater than about 10.

17. The method of claim 1 , wherein step (b) is conducted in the presence of one or more olefin-hydration catalysts selected from zeolites, supported acids, acidic resins, and heteropoly acids.

18. The method of claim 1 , wherein step (c) is conducted in the presence of one or more olefin-hydration catalysts selected from zeolites, supported acids, acidic resins, and heteropoly acids.

19. The method of claim 18 , wherein said one or more olefin-hydration catalysts comprises supported phosphoric acid.

20. The method of claim 1 , wherein step (b) and/or step (c) is conducted in the presence of an olefin-hydration catalyst comprising sulfuric acid.

21. The method of claim 1 , wherein said first hydration zone is located in a first reactor and said second hydration zone is located in a second reactor.

22. The method of claim 1 , wherein both of said hydration zones are located in a single reactor.

23. The method of claim 1 , wherein the temperature within said first hydration zone is lower than the temperature within said second hydration zone.

24. The method of claim 23 , wherein said temperature within said first hydration zone is selected from about 125-200° C. and said temperature within said second hydration zone is independently selected from about 200-250° C.

25. The method of claim 1 , wherein at least a portion of water produced from reactions during step (a) is used for said hydrating during step (b), step (c), or both steps (b) and (c).

26. The method of claim 25 , wherein substantially all of the water produced during step (a) is fed to step (b), step (c), or both steps (b) and (c).

27. The method of claim 1 , further comprising generating butenes during step (a).

28. The method of claim 27 , further comprising hydrating said butenes to 2-butanol during step (b).

29. The method of claim 1 , wherein during step (b) and/or step (c), one or more dialkyl ethers are generated, and wherein said method further comprises removing at least a portion of said dialkyl ethers.

30. The method of claim 1 , further comprising the step of separating unhydrated olefins from alcohols by distillation.

31. The method of claim 1 , further comprising the step of separating unhydrated olefins from alcohols by absorption of said alcohols into water.

32. The method of claim 1 , further comprising the step of separating unhydrated olefins from alcohols by absorption of said alcohols into dimethyl ether.

33. The method of claim 1 , further comprising separating said ethanol and/or said 2-propanol from water.

34. The method of claim 1 , further comprising separating said ethanol from said 2-propanol.

35. A method for producing ethanol and 2-propanol from methanol, said method comprising:

(a) converting methanol, in the presence of SAPO-34 or Ni—SAPO-34, into a stream including ethylene and propylene;

(b) feeding said stream from step (a) and water to a first hydration zone under suitable conditions for catalytic hydration of propylene to 2-propanol; and

(c) feeding at least a portion of the output of said first hydration zone and water to a second hydration zone under suitable conditions for catalytic hydration of ethylene to ethanol,

wherein the temperature in said second hydration zone is higher than the temperature in said first hydration zone.

Assignments (5)
SECURITY AGREEMENT Recorded Jan 2, 2014
From: MAVERICK BIOFUELS, INC.
To: OLD BLUFF CAPITAL, INC.
Reel/Frame 031910/0442 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2012
From: RANGE FUELS, INC.
To: MAVERICK BIOFUELS, INC.
Reel/Frame 029432/0879 →
ABANDONMENT AND TERMINATION OF ASSIGNMENT OF ECONOMIC INTERESTS IN INTELLECTUAL PROPERTY Recorded Mar 23, 2012
From: AGSOUTH FARM CREDIT, ACA
To: RANGE FUELS, INC.; RANGE FUELS SOPERTON PLANT, LLC
Reel/Frame 027922/0555 →
SECURITY AGREEMENT Recorded Apr 22, 2010
From: RANGE FUELS, INC.; RANGE FUELS SOPERTON PLANT, LLC
To: AGSOUTH FARM CREDIT, ACA
Reel/Frame 024274/0720 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2009
From: KHARAS, KARL
To: RANGE FUELS, INC.
Reel/Frame 023582/0143 →
Continuity (2)
Provisional Application 61105858 · Oct 16, 2008
Related Publication 20100099926A1 · Apr 22, 2010