IP Library Granted Patent US 10,577,698
Granted Patent B2
US 10,577,698 · App. 15/334,012 · Granted Mar 3, 2020

Electrochemical reactor and process

Inventor: Wayne E. Buschmann (Boulder, CO)
Assignee: Clean Chemistry, Inc.
C25B1/30C01B7/01C01B11/06C01B11/062C01B15/00C01B15/01C01B15/027C01B17/745C01D1/04C07C51/02C25B1/00C25B1/14C25B1/22C25B1/24C25B1/26C25B1/265C25B1/34C25B3/02C25B9/00C25B9/08C25B15/02C25B15/08
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Quick Facts
Patent No.
US 10,577,698
App. No.
15/334,012
Filed
Oct 25, 2016
Granted
Mar 3, 2020
Kind
B2
Art Unit
1794
USPC
204/265
Abstract

The electrochemical reactors disclosed herein provide novel oxidation and reduction chemistries and employ increased mass transport rates of materials to and from the surfaces of electrodes therein.

Claims (50)

1. A method for producing a chemical product including hydrogen peroxide, the method comprising:

introducing a liquid anolyte into a first half-cell of an electrochemical reactor, wherein at least one chemical species of said liquid anolyte is oxidized at an anode electrode of the first half-cell;

introducing a liquid catholyte into a cathode chamber of a second half-cell of the electrochemical reactor, wherein a porous cathode electrode permeable to gas and liquid is disposed in the cathode chamber;

introducing a feed of a gas into the cathode chamber through an electrically-nonconductive, hydrophobic, gas-permeable gas distributor to mix with said liquid catholyte and create in the cathode chamber a multiphase catholyte solution including a liquid phase and a gas phase with the multiphase catholyte solution in contact with the cathode electrode;

generating hydrogen peroxide in the cathode chamber, comprising reducing at least one chemical species of said multiphase catholyte solution at said cathode electrode;

removing a reduced multiphase catholyte product comprising the hydrogen peroxide from said second half-cell and removing an oxidized liquid anolyte product from said first half-cell; and

after performing the generating hydrogen peroxide for a period of time, discontinuing operation of the electrochemical reactor to stop the generating hydrogen peroxide, after the discontinuing performing a catholyte electrode reactivation process and after performing the catholyte electrode reactivation process re-commencing operation of the electrochemical reactor to re-restart the generating hydrogen peroxide, wherein the catholyte electrode reactivation process comprises:

subjecting the cathode electrode in the cathode chamber to electrochemical reduction; and

flushing the cathode electrode in the cathode chamber with an activation solution comprising peroxyacetic acid;

and wherein:

the electrochemical reactor further comprises:

an ion permeable separator separating the first half-cell and the second half-cell, wherein the ion permeable separator is disposed to one side of the cathode electrode and the gas distributor is disposed to an opposing side of the cathode electrode;

a housing enclosing the first half-cell, the second half-cell and the ion permeable separator; and

a gas chamber disposed within the housing and located on a side of the gas distributor opposite the cathode chamber and the cathode electrode; and

the generating hydrogen peroxide comprises applying electrical power to the electrochemical reactor to provide electrical current through an electrical current conduction path through the electrochemical reactor, the electrical current conduction path including the anode electrode and the cathode electrode and not including the gas distributor.

2. The method of claim 1 , comprising during the generating hydrogen peroxide, also generating superoxide in the cathode chamber, and wherein the multiphase catholyte product comprises hydrogen peroxide and superoxide.

3. The method of claim 1 , wherein the electrochemical reactor has a tubular configuration comprising the anode electrode, the ion permeable separator, the cathode electrode and the gas distributor as nested tubular features within a tubular containment boundary of the housing.

4. The method of claim 3 , wherein the gas chamber comprises an annular space disposed between the tubular containment boundary and the gas distributor.

5. The method of claim 1 , comprising prior to the introducing the gas into the cathode chamber through the gas distributor, flooding the cathode chamber, from the gas distributor through the cathode electrode to the ion separator, with the catholyte solution.

6. The method of claim 1 , wherein during the generating hydrogen peroxide, the introducing the feed of the gas comprises introducing the feed of the gas into the cathode chamber through the gas distributor with a pressure differential across the gas distributor between the gas chamber and the cathode chamber in a range of from 0.5 to 15 psig.

7. The method of claim 1 , wherein during the generating hydrogen peroxide, the introducing the feed of the gas comprises introducing the feed of the gas into the cathode chamber through the gas distributor with a differential pressure across the gas distributor between the gas chamber and the cathode chamber in a range of from 0.5 to 15 psig and at volume flow rate of the gas feed to the cathode chamber of from 100 to 1400 times greater than a liquid flow rate of the catholyte solution to the cathode chamber.

8. The method of claim 7 , wherein volume flow rate of the gas feed is in a range of from 3 to 70 milliliters per minute per square centimeter of a surface area of the gas distributor exposed to the cathode chamber.

9. The method of claim 7 , wherein the gas introduced into the cathode chamber through the gas distributor comprises at least 20% oxygen.

10. The method of claim 7 , wherein the cathode electrode has a superficial area disposed toward the gas distributor, and the cathode electrode has a surface area of greater than 10 m 2 per m 2 of the superficial area of the cathode electrode.

11. The method of claim 10 , wherein the cathode electrode comprises continuous carbon fibers.

12. The method of claim 1 , wherein the cathode electrode has a thickness between the gas distributor and the ion permeable membrane in a range of from 0.1 to 10 millimeters.

13. The method of claim 12 , wherein the gas distributor has a thickness between the gas chamber and the cathode chamber in a range of from 1 to 10 millimeters.

14. The method of claim 13 , wherein the gas distributor has a pore diameter rating of less than 10 microns.

15. The method of claim 1 , wherein

the gas distributor comprises a non-conductive, hydrophobic material selected from the group consisting of polyethylene, polypropylene, polytetrafluoroethylene and polyvinylidene difluoride.

16. The method of claim 1 , comprising;

subjecting the multiphase catholyte product to gas-liquid separation to separate the multiphase catholyte product into a separated gas and a separated liquid; and

recycling at least a portion of the separated gas to prepare the feed of the gas to the gas distributor and not recycling any of the separated liquid to the cathode chamber.

17. The method of claim 1 , wherein during the generating hydrogen peroxide, the entire cathode electrode is flooded with the multi-phase catholyte fluid.

18. The method of claim 1 , wherein the reduced multiphase catholyte product has a pH of greater than pH 12.

19. A method for producing a chemical product including hydrogen peroxide, the method comprising:

introducing a liquid anolyte into a first half-cell of an electrochemical reactor, wherein at least one chemical species of said liquid anolyte is oxidized at an anode electrode of the first half-cell;

introducing a liquid catholyte into a cathode chamber of a second half-cell of the electrochemical reactor, wherein a porous cathode electrode permeable to gas and liquid is disposed in the cathode chamber;

introducing a feed of a gas into the cathode chamber through a gas-permeable gas distributor to mix with said liquid catholyte and create in the cathode chamber a multiphase catholyte solution including a liquid phase and a gas phase with the multiphase catholyte solution in contact with the cathode electrode, wherein the gas distributor is an electrically non-conductive, hydrophobic material;

generating hydrogen peroxide in the cathode chamber, comprising reducing at least one chemical species of said multiphase catholyte solution at said cathode electrode; and

removing a reduced multiphase catholyte product comprising the hydrogen peroxide from said second half-cell and removing an oxidized liquid anolyte product from said first half-cell;

wherein:

the electrochemical reactor comprises an ion permeable separator separating the first half-cell and the second half-cell;

the ion permeable separator is disposed to one side of the cathode electrode and the gas distributor is disposed to an opposing side of the cathode electrode;

the electrochemical reactor comprises a housing enclosing the first half-cell, the second half-cell and the ion permeable separator; and

the electrochemical reactor comprises a gas chamber disposed within the housing and located on a side of the gas distributor opposite the cathode chamber and the cathode electrode; and

the method further comprises after performing the generating hydrogen peroxide for a period of time, discontinuing operation of the electrochemical reactor to stop the generating hydrogen peroxide, after the discontinuing performing a catholyte electrode reactivation process and after performing the catholyte electrode reactivation process re-commencing operation of the electrochemical reactor to re-restart the generating hydrogen peroxide, wherein the catholyte electrode reactivation process comprises:

subjecting the cathode electrode in the cathode chamber to electrochemical reduction; and

flushing the cathode electrode in the cathode chamber with an activation solution comprising peroxyacetic acid.

20. The method of claim 19 , wherein the cathode electrode has a superficial area disposed toward the gas distributor, and the cathode electrode has a surface area of greater than 10 m 2 per m 2 of the superficial area of the cathode electrode.

Assignments (4)
SECURITY INTEREST Recorded Sep 16, 2022
From: CLEAN CHEMISTRY, INC.
To: PACIFIC WESTERN BANK D/B/A PACIFIC WESTERN BUSINESS FINANCE
Reel/Frame 061127/0178 →
SECURITY INTEREST Recorded Sep 16, 2020
From: CLEAN CHEMISTRY, INC.
To: SILICON VALLEY BANK
Reel/Frame 053784/0872 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE STATE OF INCORPORATION INSIDE THE ASSIGNMENT DOCUMENT PREVIOUSLY RECORDED AT REEL: 040989 FRAME: 0579. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 15, 2018
From: BUSCHMANN, WAYNE E.
To: CLEAN CHEMISTRY, INC.
Reel/Frame 046385/0913 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2017
From: BUSCHMANN, WAYNE E.
To: CLEAN CHEMISTRY INC.
Reel/Frame 040989/0579 →
Continuity (3)
Continuation 14122185
Provisional Application 61491800 · May 31, 2011
Related Publication 20170114468A1 · Apr 27, 2017
Cited By (2)
US 12,215,460 US 12,685,320