IP Library Granted Patent US 7,947,239
Granted Patent B2
US 7,947,239 · App. 11/579,713 · Granted May 24, 2011

Carbon dioxide capture and mitigation of carbon dioxide emissions

Assignee: The Trustees of Columbia University in the City of New York
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Quick Facts
Patent No.
US 7,947,239
App. No.
11/579,713
Granted
May 24, 2011
Kind
B2
Abstract

The present invention describes methods and systems for extracting, capturing, reducing, storing, sequestering, or disposing of carbon dioxide (CO 2 ), particularly from the air. The CO 2 extraction methods and systems involve the use of chemical processes, mineral sequestration, and solid and liquid sorbents. Methods are also described for extracting and/or capturing CO 2 via condensation on solid surfaces at low temperature.

Claims (28)

1. A method of extracting or sequestering carbon dioxide, comprising:

(a) dissolving a magnesium bearing silicate in an aqueous acid to form an acidic solution;

(b) increasing the pH of the solution of step (a) to precipitate one or more magnesium components;

(c) carbonating the precipitated magnesium components from step (b) to bind carbon dioxide; and

(d) recovering ammonia gas and acid by thermal decomposition or by electrodialysis.

2. The method according to claim 1 , wherein the acid of step (a) is present in an amount at least 10% in excess of a stoichiometric amount for neutralizing magnesium in the magnesium bearing silicate.

3. The method according to claim 1 , wherein the magnesium bearing silicate of step (a) comprises peridotite rock.

4. The method according to claim 1 , wherein the magnesium bearing silicate of step (a) is selected from serpentine or olivine.

5. The method according to claim 1 , wherein the aqueous acid of step (a) is selected from citric acid, acetic acid, chromic acid, sulfuric acid, orthophosphoric acid, oxalic acid, ammonium bisulfate, or a combination of two or more thereof.

6. The method according to claim 1 , wherein the pH of the acidic solution is less than or equal to about pH 4.5.

7. The method according to claim 1 , further comprising the step of neutralizing the acidic solution of step (a) with a neutralizing agent to precipitate iron and silicate prior to the precipitation of the one or more magnesium components.

8. The method according to claim 7 , wherein the neutralizing step comprises a neutralizing agent selected from ammonia or magnesium hydroxide.

9. The method according to claim 7 , wherein the pH of the neutralized solution is less than or equal to about pH 8.

10. The method according to claim 1 , wherein increasing the pH in step (b) comprises an ammonia-containing reagent.

11. The method according to claim 1 , wherein increasing the pH in step (b) comprises a reagent selected from NaOH, KOH, NH 3 , NH 4 OH, NH 4 HCO 3 , (NH 4 ) 2 CO 3 , Na 2 CO 3 , or a combination thereof.

12. The method according to claim 1 , further comprising following step (c):

(i) washing the precipitated magnesium component to remove residual salt; and

(ii) exposing the precipitated and washed magnesium component to carbon dioxide at elevated temperature and pressure.

13. The method according to claim 12 , wherein the elevated temperature comprises about 300° C. to 500° C. or above.

14. The method according to claim 12 , wherein the elevated pressure comprises about 1 to about 50 atmospheres.

15. The method according to claim 12 , wherein the precipitated magnesium component is magnesium hydroxide or magnesium oxide.

16. The method according to claim 1 , wherein the one or more magnesium components of step (b) is Mg(OH) 2 .

17. The method according to claim 1 , wherein carbon dioxide is extracted or sequestered from air.

18. The method according to claim 1 , wherein the one or more precipitated magnesium components is carbonated in step (c) in a gas solid reaction between magnesium components and carbon dioxide at elevated temperature.

19. The method according to claim 18 , wherein the temperature is about 300° C. to less than about 900° C.

20. The method according to claim 18 , wherein the temperature elevation is performed in an autoclave under pressure.

21. The method according to claim 20 , wherein the pressure is about 1 to about 50 atmospheres or greater.

22. The method according to claim 1 , comprising recovering ammonia gas and acid following step (c) by electrodialysis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2012
From: GRIMES, MAUREEN A., TRUSTEE; PATRICK G. GRIMES TRUST
To: GRDC, LLC
Reel/Frame 028161/0730 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 16, 2010
From: LACKNER, KLAUS S.; KREVOR, SAMUEL C.; ZEMAN, FRANK S.
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 025366/0838 →
Continuity (2)
Provisional Application 60568091 · May 4, 2004
Related Publication 20080031801A1 · Feb 7, 2008