Catalytic biomass pyrolysis process

Patent metadata

Field	Value
Publication number	US-9944857-B2
Application number	US-201314382822-A
Country	US
Kind code	B2
Filing date	Mar 6, 2013
Priority date	Mar 7, 2012
Publication date	Apr 17, 2018
Grant date	Apr 17, 2018

Abstract

Described herein are processes for converting a biomass starting material (such as lignocellulosic materials) into a low oxygen containing, stable liquid intermediate that can be refined to make liquid hydrocarbon fuels. More specifically, the process can be a catalytic biomass pyrolysis process wherein an oxygen removing catalyst is employed in the reactor while the biomass is subjected to pyrolysis conditions. The stream exiting the pyrolysis reactor comprises bio-oil having a low oxygen content, and such stream may be subjected to further steps, such as separation and/or condensation to isolate the bio-oil.

First claim

The invention claimed is:

1. A catalytic biomass pyrolysis process comprising:
feeding a biomass starting material into a reactor wherein the biomass starting material is subjected to pyrolysis conditions in the presence of a solid catalyst in a reduced state to remove oxygen from the biomass starting material, form a pyrolysis product stream comprising a pyrolysis product, and convert at least a portion of the catalyst to an oxidized state;
transferring the pyrolysis product stream to a separator;
separating a vapor and gas fraction and a solids fraction comprising non-catalyst solids and the solid catalyst;
regenerating the solid catalyst by removing the non-catalyst solids from the solid catalyst;
subjecting the solid catalyst to conditions wherein the solid catalyst is converted back to the reduced state; and
recycling at least a portion of the regenerated and reduced catalyst into the reactor;
wherein the process exhibits a carbon conversion efficiency of about 20% or greater by weight.

2. The process of claim 1 , wherein the biomass starting material comprises a lignocellulosic material.

3. The process of claim 1 , wherein the biomass starting material is particularized with an average particle size of about 25 mm or less.

4. The process of claim 1 , wherein the catalyst is
insensitive to ash present in the biomass or formed in said pyrolysis process.

5. The process of claim 1 , wherein the catalyst comprises an iron oxide.

6. The process of claim 1 , wherein the catalyst comprises a mixed metal oxide.

7. The process of claim 6 , wherein the catalyst comprises a mixture of iron oxide and tin oxide or a mixture of iron oxide and a metallic oxide promoter.

8. The process of claim 7 , wherein the promoter is selected from the group consisting of chromium oxide, nickel oxide, manganese oxide, cobalt oxide, molybdenum oxide, and combinations thereof.

9. The process of claim 1 , wherein the catalyst is a bifunctional catalyst that optionally includes a component that utilizes water-bound hydrogen as a deoxygenation reagent.

10. The process of claim 1 , wherein the catalyst comprises a supported metal.

11. The process of claim 1 , wherein the biomass starting material is fed into the reactor without premixing with the catalyst, or wherein the biomass starting material is fed into the reactor without premixing with a heat transfer medium.

12. The process of claim 1 , wherein the reactor is a transport reactor, and the biomass starting material is transported through the transport reactor at a rate such that the residence time is about 5 seconds or less.

13. The process of claim 1 , wherein the pyrolysis conditions include a temperature of about 200° C. to about 700° C. or a temperature of about 550° C. or less.

14. The process of claim 1 , wherein the catalyst and the biomass starting material are provided in a ratio of about 1:1 to about 100:1 based on mass.

15. The process of claim 1 , wherein the pyrolysis conditions include a pressure of up to about 25 bar (2.5 MPa).

16. The process of claim 1 , wherein removal of oxygen from the biomass starting material is via one or both of direct catalytic deoxygenation and indirect deoxygenation through catalytic hydrogen production and in situ hydrodeoxygenation.

17. The process of claim 1 , further comprising regenerating the catalyst by removing non-catalyst solids therefrom prior to subjecting the catalyst to conditions wherein the catalyst is converted back to the reduced state.

18. The process of claim 1 , wherein the vapor and gas fraction is transferred to a condenser wherein a liquid product is separated from a gaseous fraction.

19. The process of claim 18 , wherein the liquid product is separated into an aqueous phase and a bio-oil.

20. The process of claim 19 , wherein the bio-oil has an oxygen content of about 1% to about 25% by weight on a dry basis based on the overall weight of the bio-oil.

21. The process of claim 1 , wherein the process exhibits a carbon conversion efficiency of about 20% to about 65% by weight.

22. The process of claim 1 , further comprising isolating a bio-oil fraction from the pyrolysis product.

Assignees

• Res Triangle Inst

Inventors

• Dayton David C
• Gupta Raghubir P
• Turk Brian S
• Kataria Atish
• Shen Jian-Ping

Classifications

• C10G2300/1011

  Biomass · CPC title

• B01J23/94

  of catalysts comprising metals, oxides or hydroxides of the iron group metals or copper · CPC title

• B01J23/8892

  Manganese · CPC title

• Y02P20/145

  the feedstock being materials of biological origin · CPC title

• B01J23/85

  Chromium, molybdenum or tungsten · CPC title