US2024410032A1PendingUtilityA1
Carbon dioxide based mining for carbon negative mineral recovery
Assignee: BATTELLE MEMORIAL INSTITUTEPriority: Jun 12, 2023Filed: Jun 12, 2024Published: Dec 12, 2024
Est. expiryJun 12, 2043(~16.9 yrs left)· nominal 20-yr term from priority
E21B 43/28C22B 3/42C22B 3/165C22B 23/0461C22B 15/0065C22B 23/0407C22B 3/04C22B 23/0453C22B 3/205
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Claims
Abstract
A mineral recovery solution may include a liquid or supercritical carbon dioxide component. The mineral recovery solution may include a water component. The mineral recovery solution may include a chelator component.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A mineral recovery solution comprising:
a liquid or supercritical carbon dioxide component; a water component; and a chelator component.
2 . The mineral recovery solution of claim 1 , wherein the chelator component is present in a range of from about 0.01 mol % to about 7 mol % of the mineral recovery solution.
3 . The mineral recovery solution of claim 2 , wherein the chelator component is present in a range of from about 0.01 mol % to about 0.2 mol % of the mineral recovery solution.
4 . The mineral recovery solution of claim 1 , wherein the chelator component comprises a chelator capable of chelation with nickel, iron, cobalt, copper, or mixtures thereof.
5 . The mineral recovery solution of claim 1 , wherein the chelator component comprises a single chelator or a mixture of at least two different chelators.
6 . The mineral recovery solution of claim 5 , wherein the single chelator or mixture of at least two different chelators comprises EDTA (ethylenediaminetetraacetic acid), or EDDS (Ethylenediamine-N,N′-disuccinic acid), CDTA (cyclohexane diamine tetra acetic acid), PDTA (Propylenediamine-N,N,N′,N′-tetraacetic acid), and PDTA (1,3-propanediaminetetraacetic acid) ortho-Phenylenediamine-N,N,N′,N′-tetraacetic acid.
7 . The mineral recovery solution of claim 5 , wherein the single chelator comprises ethylenediaminetetraacetic acid.
8 . The mineral recovery solution of claim 1 , wherein the liquid or supercritical carbon dioxide component is in range of from about 2 mol % to about 95 mol % of the mineral recovery solution.
9 . The mineral recovery solution of claim 8 , wherein the liquid or supercritical carbon dioxide component is in range of from about 50 mol % to about 95 mol % of the mineral recovery solution.
10 . The mineral recovery solution of claim 1 , wherein the liquid or supercritical carbon dioxide component is a supercritical carbon dioxide.
11 . A method of recovering a mineral, the method comprising:
delivering a mineral recovery solution to a subterranean location, the mineral recovery solution comprising:
a liquid or supercritical carbon dioxide component;
a water component; and
a chelator component;
chelating a mineral with the chelator component to form a chelated mineral; mineralizing the liquid or supercritical carbon dioxide component; and recovering the chelated mineral.
12 . The method of claim 11 , wherein
the liquid or supercritical carbon dioxide component is in range of from about 0.01 mol % to about 7 mol % of the mineral recovery solution; the chelator component is present in a range of from about 0.5 mol % to about 7 mol % of the mineral recovery solution; and the chelator component comprises a single chelator or a mixture of at least two different chelators, the single chelator or mixture of at least two different chelators comprises EDTA (ethylenediaminetetraacetic acid), or EDDS (Ethylenediamine-N,N′-disuccinic acid), CDTA (cyclohexane diamine tetra acetic acid), PDTA (Propylenediamine-N,N,N′,N′-tetraacetic acid), and PDTA (1,3-propanediaminetetraacetic acid) ortho-Phenylenediamine-N,N,N′,N′-tetraacetic acid.
13 . The method of claim 11 , wherein the mineral comprises nickel, iron, cobalt, copper, or mixtures thereof.
14 . The method of claim 11 , wherein at least 90 mol % of the mineral is chelated.
15 . The method of claim 11 , wherein the method is a carbon net negative method.
16 . A method of forming a mineral recovery solution, the method comprising:
contacting a liquid or supercritical carbon dioxide component and a chelator component.
17 . The method of claim 16 , further comprising contacting water with the liquid or supercritical carbon dioxide component and a chelator component.
18 . The method of claim 16 , wherein the liquid or supercritical carbon dioxide component and the chelator component are located in separate storage tanks prior to contact with each other and are contacted at a subterranean location.
19 . The method of claim 18 , wherein an amount of the liquid or supercritical carbon dioxide component and the chelator component is controlled by a manifold in fluid communication with the liquid or supercritical carbon dioxide component and the chelator component.
20 . The method of claim 18 , further comprising further separate storage tank comprising a second chelator component.Join the waitlist — get patent alerts
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