IP Library Granted Patent US 10,087,538
Granted Patent B2
US 10,087,538 · App. 15/279,926 · Granted Oct 2, 2018

Process for recovering alkali metals and sulfur from alkali metal sulfides and polysulfides

Inventor: John Howard Gordon (Salt Lake City, UT)
Assignee: FIELD UPGRADING LIMITED
C25C1/02C01B17/22C01B17/34C10G32/02C25B1/00C25C3/02C10G2300/202
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Quick Facts
Patent No.
US 10,087,538
App. No.
15/279,926
Granted
Oct 2, 2018
Kind
B2
Abstract

Alkali metals and sulfur may be recovered from alkali monosulfide and polysulfides in an electrolytic process that utilizes an electrolytic cell having an alkali ion conductive membrane. An anolyte includes an alkali monosulfide, an alkali polysulfide, or a mixture thereof and a solvent that dissolves elemental sulfur. A catholyte includes molten alkali metal. Applying an electric current oxidizes sulfide and polysulfide in the anolyte compartment, causes alkali metal ions to pass through the alkali ion conductive membrane to the catholyte compartment, and reduces the alkali metal ions in the catholyte compartment. Liquid sulfur separates from the anolyte and may be recovered. The electrolytic cell is operated at a temperature where the formed alkali metal and sulfur are molten.

Claims (41)

1. A process for oxidizing an alkali metal monosulfide or alkali metal polysulfide comprising:

obtaining an electrolytic cell comprising an alkali ion conductive membrane configured to selectively transport alkali ions, the membrane separating an anolyte compartment configured with an anode and a catholyte compartment configured with a cathode;

introducing into the anolyte compartment an anolyte comprising an alkali metal monosulfide, an alkali metal polysulfide, or a mixture thereof and an anolyte solvent that partially dissolves elemental sulfur;

introducing into the catholyte compartment a catholyte wherein the catholyte comprises at least one of a molten alkali metal and a solvent;

applying an electric current to the electrolytic cell at an operating temperature thereby:

i. oxidizing the alkali metal monosulfide or polysulfide in the anolyte compartment to form liquid elemental sulfur and alkali metal ions;

ii. causing the alkali metal ions to pass through the alkali ion conductive membrane from the anolyte compartment to the catholyte compartment; and

iii. reducing the alkali metal ions in the catholyte compartment to form liquid elemental alkali metal;

allowing liquid elemental sulfur to become saturated in the anolyte; and

separating the liquid elemental sulfur from the anolyte to form a second liquid phase.

2. The process according to claim 1 where the liquid elemental sulfur separates from the anolyte in a settling zone that is within the electrolytic cell.

3. The process according to claim 1 where the liquid elemental sulfur separates from the anolyte in a settling zone that is external to the cell.

4. The process according to claim 1 where the separation of liquid elemental sulfur from the anolyte includes one or more of the separation techniques selected from gravimetric, filtration, and centrifugation.

5. The process according to claim 1 , wherein the alkali ion conductive membrane is substantially impermeable to anions, the catholyte solvent, the anolyte solvent, and dissolved sulfur.

6. The process according to claim 1 , wherein the alkali ion conductive membrane comprises in part an alkali metal conductive ceramic or glass ceramic.

7. The process according to claim 1 , wherein the alkali ion conductive membrane comprises a solid MSICON (Metal Super Ion CONducting) material, where M is Na or Li.

8. The process according to claim 1 , wherein the anolyte solvent comprises one or more solvents selected from N,N-dimethylaniline, quinoline, tetrahydrofuran, 2-methyl tetrahydrofuran, benzene, cyclohexane, fluorobenzene, thrifluorobenzene, toluene, xylene, tetraethylene glycol dimethyl ether (tetraglyme), diglyme, isopropanol, ethyl propional, dimethyl carbonate, dimethoxy ether, dimethylpropyleneurea, formamide, methyl formamide, dimethyl formamide, acetamide, methyl acetamide, dimethyl acetamide, triethylamine, diethyl acetamide, ethanol and ethyl acetate, propylene carbonate, ethylene carbonate, and diethyl carbonate.

9. The process according to claim 1 , wherein the anolyte solvent comprises from about 60-100 vol. % polar solvent and 0-40 vol. % apolar solvent.

10. A process for oxidizing an alkali metal monosulfide or alkali metal polysulfide comprising:

obtaining a first electrolytic cell comprising a first alkali ion conductive membrane configured to selectively transport alkali ions, the membrane separating a first anolyte compartment configured with a first anode and a first catholyte compartment configured with a first cathode;

introducing into the first anolyte compartment a first anolyte comprising an alkali metal monosulfide, an alkali metal polysulfide, or a mixture thereof and an anolyte solvent that partially dissolves elemental sulfur;

introducing into the first catholyte compartment a first catholyte, wherein the catholyte comprises at least one of a molten alkali metal and a solvent;

applying an electric current to the first electrolytic cell thereby:

i. oxidizing the alkali metal sulfide or polysulfide in the first anolyte compartment to form a higher level polysulfide and alkali ions;

ii. causing the alkali metal ions to pass through the first alkali ion conductive membrane from the first anolyte compartment to the first catholyte compartment; and

iii. reducing the alkali metal ions in the first catholyte compartment to form elemental alkali metal;

transporting anolyte from the first electrolytic cell to a second electrolytic cell comprising a second alkali ion conductive membrane configured to selectively transport alkali ions, the membrane separating a second anolyte compartment configured with a second anode and a second catholyte compartment configured with a cathode and a second catholyte;

applying an electric current to the second electrolytic cell thereby:

i. oxidizing polysulfide in the second anolyte compartment to form liquid elemental sulfur and alkali metal ions;

ii. causing the alkali metal ions to pass through the alkali ion conductive membrane from the second anolyte compartment to the second catholyte compartment; and

iii. reducing the alkali metal ions in the second catholyte compartment to form liquid elemental alkali metal;

allowing liquid elemental sulfur to become saturated in the anolyte in the second electrolytic cell; and

separating the liquid elemental sulfur from the anolyte to form a second liquid phase.

11. The process according to claim 10 where the liquid elemental sulfur separates from the anolyte in a settling zone that is within the second electrolytic cell.

12. The process according to claim 10 where the liquid elemental sulfur separates from the anolyte in a settling zone that is external to the second electrolytic cell.

13. The process according to claim 10 where the separation of liquid elemental sulfur from the anolyte includes one or more of the separation techniques selected from gravimetric, filtration, and centrifugation.

14. The process according to claim 10 , wherein the first alkali ion conductive membrane and the second alkali ion conductive membrane is substantially impermeable to anions, the catholyte solvent, the anolyte solvent, and dissolved sulfur.

15. The process according to claim 10 , wherein the first alkali ion conductive membrane and the second alkali ion conductive membrane comprises in part an alkali metal conductive ceramic or glass ceramic.

16. The process according to claim 10 , wherein the first alkali ion conductive membrane and the second alkali ion conductive membrane comprises a solid MSICON (Metal Super Ion CONducting) material, where M is Na or Li.

17. The process according to claim 10 , wherein the anolyte solvent comprises one or more solvents selected from N,N-dimethylaniline, quinoline, tetrahydrofuran, 2-methyl tetrahydrofuran, benzene, cyclohexane, fluorobenzene, thrifluorobenzene, toluene, xylene, tetraethylene glycol dimethyl ether (tetraglyme), diglyme, isopropanol, ethyl propional, dimethyl carbonate, dimethoxy ether, dimethylpropyleneurea, formamide, methyl formamide, dimethyl formamide, acetamide, methyl acetamide, dimethyl acetamide, triethylamine, diethyl acetamide, ethanol and ethyl acetate, propylene carbonate, ethylene carbonate, and diethyl carbonate.

18. The process according to claim 10 , wherein the anolyte solvent comprises from about 60-100 vol. % polar solvent and 0-40 vol. % apolar solvent.

Assignments (4)
MERGER AND CHANGE OF NAME Recorded Sep 21, 2018
From: FIELD UPGRADING LIMITED; ENLIGHTEN INNOVATIONS INC.
To: ENLIGHTEN INNOVATIONS INC.
Reel/Frame 047586/0443 →
CONFIRMATORY LICENSE Recorded Jul 11, 2018
From: CERAMATEC, INC.
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 046320/0069 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 8, 2017
From: CERAMATEC, INC.
To: FIELD UPGRADING LIMITED
Reel/Frame 043788/0907 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2017
From: GORDON, JOHN H
To: CERAMATEC, INC.
Reel/Frame 041986/0849 →
Continuity (6)
Division 14210891 · Mar 14, 2014
Continuation In Part 12576977 · Oct 9, 2009
Provisional Application 61781557 · Mar 14, 2013
Provisional Application 61103973 · Oct 9, 2008
Related Publication 20170016128A1 · Jan 19, 2017
Related Publication 20170275771A9 · Sep 28, 2017