Methods and devices for removing impurities from electrolytes

Patent metadata

Field	Value
Publication number	US-12074353-B2
Application number	US-201917270623-A
Country	US
Kind code	B2
Filing date	Oct 23, 2019
Priority date	Oct 23, 2018
Publication date	Aug 27, 2024
Grant date	Aug 27, 2024

Abstract

The present disclosure provides methods and devices for preparing electrolyte solutions containing unwanted impurities at the pg/L levels. The methods generally comprise electrochemically reducing the impurity to a precipitated, plated, or volatilized form, and removing that reduced form from electrolyte solution. This disclosure describes the methods and devices for effecting such methods, and the electrochemical solutions derived or derivable from such methods.

First claim

What is claimed is:

1. A method for preparing an electrolyte solution having reduced impurity levels, the method comprising:
a. electrochemically reducing an impurity in an initial electrolyte solution, the initial electrolyte solution further comprising a redox active electrolyte at a concentration of at least 0.5 M, under conditions sufficient to generate an electrochemically treated electrolyte solution containing a reduced form of the redox active electrolyte and a reduced form of the impurity, wherein the redox active electrolyte comprises a metal ligand coordination compound comprising Al, Ca, Co, Cr, Sr, Cu, Fe, Mg, Mn, Mo, Ni, Pd, Pt, Ru, Sn, Ti, V, Zn, or Zr;
b. heating the electrochemically treated electrolyte solution at a temperature in a range of from 20° C. to about 105° C.;
c. purging the electrochemically treated electrolyte solution; and
d. separating the reduced form of the impurity from the electrochemically treated solution,
so as to provide a final electrolyte solution having a final concentration of the impurity that is less than about 10 mg/L or less than about 10 mg impurity per mol of the redox active electrolyte in the redox active electrolyte solution (“mg/mol”).

2. The method of claim 1 , wherein the final concentration of the impurity in the final electrolyte solution is:
(i) less than 5 mg/L, less than 2.5 mg/L, less than 1 mg/L, less than 500 μg/L, less than 250 μg/L, less than 100 μg/L, less than 50 μg/L, less than about 40 μg/L, less than about 30 μg/L, less than about 20 μg/L, less than about 10 μg/L, less than about 5 μg/L, or less than about 1 μg/L of one or more of a given impurity; or
(ii) less than 5 mg/mol, less than 2.5 mg/mol, less than 1 mg/mol, less than 500 μg/mol, less than 250 μg/mol, less than 100 μg/mol, less than 50 μg/mol, less than about 40 μg/mol, less than about 30 μg/mol, less than about 20 μg/mol, less than about 10 μg/mol, less than about 5 μg/mol, or less than about 1 μg/mol of one or more of a given impurity.

3. The method of claim 1 , wherein the impurity comprises a form of antimony, arsenic, germanium, tin, or a combination thereof.

4. The method of claim 1 , wherein the electrochemical treatment is performed in an electrochemical cell.

5. The method of claim 4 , wherein the reduced form of the impurity is separated by plating within the cathode of the electrochemical cell.

6. The method of claim 1 , wherein the reduced form of the impurity precipitates from the electrochemically treated electrolyte solution.

7. The method of claim 6 , wherein the precipitated reduced form of the impurity is removed by filtration.

8. The method of claim 1 , wherein the reduced form of the impurity is a volatile hydride.

9. The method of claim 8 , wherein the volatile hydride is arsine (AsH 3 ), germane (GeH 4 ), stannane (SnH 4 ), stibine (SbH 3 ), or a combination thereof.

10. The method of claim 1 , wherein the electrochemical treatment is an electrochemical reduction is performed at an oxidation reduction potential that is more negative than the reduction potential of the impurity.

11. The method of claim 1 , wherein the temperature of the heating step (a) is in a range of about 35° C. to about 95° C.

12. The method of claim 1 , wherein the inert gas is nitrogen or argon.

13. The method of claim 1 , wherein steps a and b are performed simultaneously.

14. The method of claim 1 , wherein steps a and b are performed sequentially.

15. The method of claim 1 , further comprising oxidizing the reduced form of the redox active electrolyte in the final electrolyte solution.

16. The method of claim 15 , wherein the oxidizing is performed by purging the final electrolyte solution with an oxidant.

17. The method of claim 15 , wherein the oxidizing is done using hydrogen peroxide.

18. The method of claim 15 , wherein the oxidizing is performed while heating the final electrolyte solution.

19. The method of claim 15 , wherein the oxidizing is performed at a temperature of about 65° C. or greater, preferably at a temperature of about 85° C. or greater, more preferably at a temperature of about 105° C. or greater.

20. The method of claim 18 , wherein the oxidizing is performed using a hydrogen evolution catalyst.

21. The method of claim 20 , wherein the hydrogen evolution catalyst is activated carbon, carbon cloth, carbon felt, carbon paper, Ti mesh, Ti felt, expanded Ti mesh, Pt-plated Ti mesh, or a combination thereof.

22. The method of claim 1 , wherein the redox active electrolyte comprises a metal ligand coordination compound comprising Co, Cr, Cu, Fe, Mn, Mo, Ru, Sn, Ti, V, or Zr.

23. An electrolyte solution prepared according to the method of claim 1 .

24. The method of claim 15 , wherein the redox active electrolyte further comprises an organic active material.

25. The method of claim 24 , wherein the organic active material is carbon or an aromatic hydrocarbon.

26. The method of claim 25 , wherein the aromatic hydrocarbon is a quinone, hydroquinone, viologen, pyridinium, pyridine, acridinium, or catechol.

27. The method of claim 1 , wherein the temperature of the heating is in a range of about 45° C. to about 85° C.

28. The method of claim 16 , wherein the oxidant is oxygen.

Assignees

• Lockheed Martin Energy Llc

Inventors

• Norman Zachariah M
• Papandrew Alexander B
• Reece Steven Y
• Klet Rachel Christine
• Millard Matthew

Classifications

• Y02E60/50

  Fuel cells · CPC title

• H01M2300/0002

  Aqueous electrolytes · CPC title

• H01M8/188

  by recharging of redox couples containing fluids; Redox flow type batteries · CPC title

• H01M8/08

  Fuel cells with aqueous electrolytes · CPC title

• H01M4/9041

  Metals or alloys (H01M4/92 takes precedence) · CPC title