Large-scale carbon-mineralization through oxalatization
View Patent ↗The present invention is broadly concerned with mineralization methods that assist in permanent carbon storage. The methods provide a storage mechanism for oxalic acid generated by existing or future-developed carbon capture and conversion methods that convert CO2 to oxalic acid. That oxalic acid can be injected into a subsurface rock formation containing non-carbonate rock to form oxalates or oxalate hydrates. Alternatively, oxalic acid can be mixed with mine tailings, well drilling dirt, crushed rocks, etc., that contain desired non-carbonate rock minerals, to promote mineralization.
1. A mineralization method comprising contacting oxalic acid with a component chosen from non-carbonate rocks, non-carbonate minerals, or mixtures thereof under conditions to cause formation of one or both of a metal oxalate or metal oxalate hydrate, wherein:
said non-carbonate rocks comprise less than about 40% by weight of metal carbonates and are chosen from basalt, peridotite, or mixtures thereof;
said non-carbonate minerals comprise less than about 40% by weight of metal carbonates and are chosen from plagioclase, olivine, pyroxenes, amphiboles, glauconite, dunite, or mixtures thereof.
2. The method of claim 1 , wherein said contacting comprises injecting said oxalic acid into a rock formation comprising said component.
3. The method of claim 2 , wherein said rock formation comprises a subsurface formation.
4. The method of claim 2 , wherein said contacting comprises co-injecting oxalic acid and liquified CO 2 .
5. The method of claim 1 , wherein said contacting comprises mixing said oxalic acid with said component.
6. The method of claim 5 , wherein said component is present in mine tailings, well drilling dirt, or a mixture thereof.
7. The method of claim 1 , wherein said oxalic acid is present in an aqueous solution.
8. The method of claim 1 , wherein said component comprises a metal oxide, a metal oxide in a silicate, or mixtures thereof.
9. The method of claim 8 , wherein:
said non-carbonate rock comprises at least about 20% by weight metal oxide; and
said non-carbonate mineral comprises at least about 30% by weight metal oxide.
10. The method of claim 8 , wherein said metal oxide comprises an oxide of a metal chosen from alkaline earth metals, transition metals, or mixtures thereof.
11. The method of claim 8 , wherein said metal oxide comprises an oxide of a metal chosen from magnesium, iron, calcium, or mixtures thereof.
12. The method of claim 1 , wherein said metal oxalate hydrate comprises magnesium oxalate dihydrate, ferrous oxalate dihydrate, calcium oxalate monohydrate, or mixtures thereof.
13. The method of claim 1 , wherein said component comprises at least about 20% by weight magnesium oxide, at least about 8% by weight iron oxide, or both, based on the total weight of the component taken as 100% by weight.
14. The method of claim 1 , wherein said component has an initial quantity of total metal oxides and at least about 75% by weight of said initial quantity is converted to one or both of said metal oxalate or metal oxalate hydrate.
15. The method of claim 14 , wherein at least about 75% by weight of said initial quantity is converted to one or both of said metal oxalate or metal oxalate hydrate within about 30 days of said contacting.
16. The method of claim 1 , wherein said component has a quantity of magnesium oxide and at least about 50% by weight of said quantity of magnesium oxide is converted to one or both of magnesium oxalate or magnesium oxalate hydrate.
17. The method of claim 16 , wherein at least about 50% by weight of said quantity of magnesium oxide is converted to one or both of said magnesium oxalate or magnesium oxalate hydrate within about 7 days of said contacting.
18. The method of claim 1 , wherein the molar ratio of oxalic acid to total metal oxide in the component is about 1:20 to about 1:1.
19. The method of claim 1 , wherein said oxalic acid is produced from:
CO 2 captured from air;
CO 2 captured from point sources;
low-concentration CO 2 from point sources directly;
biomass whose growth removed CO 2 from air; or
mixtures thereof.
20. The method of claim 1 , wherein said contacting results in double the number of carbon atoms being consumed per metal atom when compared to the number of carbon atoms consumed per metal atom to form a metal carbonate.
21. A system for carrying out the method of claim 1 .
22. The reaction product formed by the method of claim 1 .