Method for recycling pyrolysis tail gas through conversion into formic acid

Patent metadata

Field	Value
Publication number	US-10760004-B2
Application number	US-201815935654-A
Country	US
Kind code	B2
Filing date	Mar 26, 2018
Priority date	Mar 24, 2017
Publication date	Sep 1, 2020
Grant date	Sep 1, 2020

Abstract

This disclosure describes systems and methods for using pyrolysis tail gas as the source for additional hydrogen to be used in the pyrolysis reaction. Tail gas is separated from the pyrolysis products and a portion of the tail gas is converted into formic acid (HCOOH). The formic acid is then injected into the pyrolysis reactor where it becomes the donor of two monohydrogen atoms and is ultimately converted into CO2 under reaction conditions. In this fashion, a closed loop pyrolysis hydrogen donor system may be created utilizing a generally non-toxic intermediary derived from the pyrolysis reaction products. This disclosure also describes using a ruthenium catalyst supported on particles of activated carbon to improve the yield of pyrolysis reactions.

First claim

What is claimed is:

1. A method comprising:
providing a first stream containing at least some methane and supercritical carbon dioxide;
converting at least some of the methane and the supercritical carbon dioxide in the first stream into formic acid; and
injecting at least some of the formic acid into a pyrolysis reaction.

2. The method of claim 1 wherein the first stream is derived from pyrolysis reaction products.

3. The method of claim 2 further comprising:
pyrolyzing a feedstock to generate the pyrolysis reaction products.

4. The method of claim 1 wherein the first stream includes at least some tail gas from a pyrolyzed feedstock.

5. The method of claim 1 further comprising:
maintaining the carbon dioxide in the supercritical state during the converting operation.

6. The method of claim 3 further comprising:
mixing the formic acid with the feedstock to obtain a feedstock and formic acid mixture; and
pyrolyzing the feedstock and formic acid mixture to generate pyrolysis reaction products including at least some tail gas.

7. The method of claim 6 , wherein the mixing further comprises:
mixing the formic acid and the feedstock at a temperature less than 100 ° C. and a pressure less than 1 MPa.

8. The method of claim 3 wherein the pyrolyzing is performed using supercritical carbon dioxide at a first temperature from 150-600 ° C. and a first pressure from 7-12 MPa and the feedstock is selected from bituminous coal, sub-bituminous coal, lignite, and anthracite.

9. The method of claim 3 further comprising:
mixing the feedstock with a ruthenium catalyst supported on particles of activated carbon to obtain a feedstock and ruthenium catalyst mixture; and
pyrolyzing the feedstock and ruthenium catalyst mixture to generate pyrolysis reaction products including at least some tail gas.

10. The method of claim 2 further comprising:
mixing a feedstock with formic acid and a ruthenium catalyst supported on particles of activated carbon to obtain a feedstock/formic acid/ruthenium catalyst mixture; and
pyrolyzing the feedstock/formic acid/ruthenium catalyst mixture to generate pyrolysis reaction products including at least some tail gas.

11. The method of claim 9 , wherein the particles of activated carbon have a mean particle diameter of less than 25.4 mm measured by passing through a 1 inch US Mesh.

12. A method comprising:
pyrolyzing a feedstock to generate an output stream containing carbon dioxide and pyrolysis reaction products, the pyrolysis reaction products including at least some tail gas;
converting at least some of the tail gas and carbon dioxide from the output stream to formic acid;
injecting at least some of the formic acid into the step of pyrolyzing the feedstock.

13. The method of claim 12 further comprising:
separating a portion of the at least some tail gas and carbon dioxide from the output stream containing carbon dioxide and pyrolysis reaction products.

14. The method of claim 12 further comprising:
separating a stream of methane and carbon dioxide from the output stream containing carbon dioxide and pyrolysis reaction products; and
converting at least some of the separated methane and carbon dioxide to formic acid.

15. The method of claim 12 wherein the pyrolyzing is performed using supercritical carbon dioxide at a first temperature from 150-600 ° C. and a first pressure from 7-12 MPa.

16. The method of claim 13 wherein the feedstock is selected from bituminous coal, sub-bituminous coal, lignite, and anthracite.

17. A method of pyrolyzing coal comprising:
pyrolyzing a first feedstock comprising coal in a carbon dioxide atmosphere in a reactor at a temperature and pressure at which the carbon dioxide is in a supercritical state to generate reaction products including at least some methane;
removing at least some of the supercritical carbon dioxide and reaction products from the reactor;
separating at least some methane and carbon dioxide from the removed supercritical carbon dioxide and reaction products to generate a first stream including at least methane and carbon dioxide;
dry reforming at least a portion of the first stream to generate a second stream including at least hydrogen and carbon monoxide;
converting at least a portion of the second stream into a third stream including hydrogen and carbon dioxide using the water-gas shift reaction;
converting at least a portion of the third stream into formic acid via a formic acid generation reaction; and
combining at least some of the generated formic acid with the first feedstock prior to or during pyrolysis of the first feedstock, or combining at least some of the generated formic acid with a second feedstock of a separate, different pyrolysis reactor.

Assignees

• Terrapower Llc
• Univ Washington State

Inventors

• Garcia-Perez Manuel
• Walter Joshua C

Classifications

• C07C51/00 Primary

  Preparation of carboxylic acids or their salts, halides or anhydrides (of acids by hydrolysis of oils, fats or waxes C11C) · CPC title

• C10K3/00

  Modifying the chemical composition of combustible gases containing carbon monoxide to produce an improved fuel, e.g. one of different calorific value, which may be free from carbon monoxide · CPC title

• C10K3/04

  reducing the carbon monoxide content {, e.g. water-gas shift [WGS]} · CPC title

• C07C51/15

  by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis · CPC title

• C10G1/02

  by distillation · CPC title