US2020165734A1PendingUtilityA1
Electrochemical reactor and process
Est. expiryMay 31, 2031(~4.9 yrs left)· nominal 20-yr term from priority
Inventors:Wayne E. Buschmann
C25B 15/02C25B 15/08C25B 1/265C01D 1/04C01B 15/01C25B 1/14C25B 1/34C25B 1/22C25B 9/00C01B 7/01C01B 11/062C25B 1/26C25B 1/00C01B 17/745C25B 1/30C01B 11/06C01B 15/027C25B 1/24C07C 51/02C01B 15/00C25B 9/08C25B 3/02C25B 9/19C25B 3/25C25B 3/23
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Claims
Abstract
The electrochemical reactors disclosed herein provide novel oxidation and reduction chemistries and employ in-creased mass transport rates of materials to and from the surfaces of electrodes
Claims
exact text as granted — not AI-modified1 . An electrochemical reactor for producing chemical species, said electrochemical reactor comprising a first half-cell comprising an anode electrode and an anolyte, a second half-cell comprising a cathode electrode and a catholyte, a gas distributor introduces gas adjacent to at least one of said anode electrode and/or said cathode electrode and an ion permeable separator separating said first half-cell and said second half-cell.
2 . The electrochemical reactor of claim 1 wherein the chemical species produced is determined according to the composition of said anolyte, the composition of said catholyte, the composition of the gas distributed adjacent to at least one of said anode electrode and/or said cathode electrode, and the ion permeability of said ion permeable separator.
3 . The electrochemical reactor of claim 2 wherein the chemical species produced is determined according to the pH of said anolyte, the pH of said catholyte, the voltage applied to said anode electrode, the electric current applied to said anode electrode, the voltage applied to said cathode electrode, and the electric current applied to said cathode electrode.
4 . The electrochemical reactor of claim 1 wherein the gas feed volume flow rate to said cathode electrode and/or anode electrode is from about 100 to about 1400 times greater than the liquid anolyte or liquid catholyte flow rate.
5 . The electrochemical reactor of claim 4 wherein said cathode electrode exhibits electroactivity over greater than 50% of its specific surface area, and
wherein said cathode electrode has a specific surface area greater than about 1 m 2 per 1 m 2 superficial area, preferably a specific surface area greater than about 5 m 2 per 1 m 2 superficial area, more preferably a specific surface area greater than about 10 m 2 per 1 m 2 superficial area, and even more preferably a specific surface area greater than about 100 m 2 per 1 m 2 superficial area.
6 . The electrochemical reactor of claim 4 wherein the composition of the gas is from about 20% oxygen to about 93% oxygen.
7 . The electrochemical reactor of claim 1 wherein said chemical species produced are selected from the group consisting essentially of: hydrogen peroxide, superoxide, alkali, acids, citric acid, sodium hypochlorite, hypochlorites, sulfate acids, chlorine, and chlor-alkali.
8 . A method for using a flow pathway in the electrochemical reactor of claim 5 to produce at least one product chemical species, said flow pathway comprising:
introducing said liquid anolyte into said first half-cell wherein at least one chemical species of said liquid anolyte is oxidized at said anode electrode, and
introducing said liquid catholyte into said second half-cell wherein said gas distributor introduces said gas into said liquid catholyte and creates a multiphase catholyte solution, and
wherein said gas distributor introduces said gas into said cathode electrode, and
wherein at least one chemical species of said multiphase catholyte solution is reduced at said cathode electrode, and
wherein the reduced multiphase catholyte solution and/or the oxidized liquid anolyte contains said at least one product chemical species, and
wherein the reduced multiphase catholyte solution flows out of said second half-cell, and
wherein the oxidized liquid anolyte flows out of said first half-cell.
9 . The method of claim 8 wherein said at least one product chemical species is selected from the woup consisting essentially of: hydrogen peroxide, superoxide, alkali, acids, citric acid, sodium hypochlorite, hypochlorites, sulfate acids, chlorine, and chlor-alkali.
10 . An electrochemical reactor for reducing and/or oxidizing chemical species, said electrochemical reactor comprising a first half-cell comprising an anode electrode and an anolyte, a second half-cell comprising a cathode electrode and a catholyte, a gas distributor introduces gas adjacent to at least one of said anode electrode and/or said cathode electrode and an ion permeable separator separating said first half-cell and said second half-cell.
11 . The electrochemical reactor of claim 10 wherein the chemical species reduced and/or oxidized is determined according to the composition of said anolyte, the composition of said catholyte, the composition of the gas distributed adjacent to at least one of said anode electrode and/or said cathode electrode, and the ion permeability of said ion permeable separator.
12 . The electrochemical reactor of claim 11 wherein the chemical species reduced and/or oxidized is determined according to the pH of said anolyte, the pH of said catholyte, the voltage applied to said anode electrode, the electric current applied to said anode electrode, the voltage applied to said cathode electrode, and the electric current applied to said cathode electrode.
13 . The electrochemical reactor of claim 10 wherein the gas feed volume flow rate to said cathode electrode and/or anode electrode is from about 100 to about 1400 times greater than the liquid anolyte or liquid catholyte flow rats.
14 . The electrochemical reactor of claim 13 wherein said cathode electrode exhibits electroactivity over greater than 50% of its specific surface area, and
wherein said cathode electrode has a specific surface area greater than about 1 m 2 per 1 m 2 superficial area, preferably a specific surface area greater than about 5 m 2 per 1 m 2 superficial area, more preferably a specific surface area greater than about 10 m 2 per 1 m 2 superficial area, and even more preferably a specific surface area greater than about 100 m 2 per 1 m 2 superficial area.
15 . The electrochemical reactor of claim 13 wherein the composition of the gas is from about 20% oxygen to about 93% oxygen.
16 . The electrochemical reactor of claim 10 wherein said chemical species reduced and/or oxidized are selected from the group consisting essentially of: molecular oxygen, hydroxyl radicals, hydroxide ions, hydrogen ions, hydrogen peroxide, superoxide, oxygen, water, alkali, acids, citric acid, sodium hypochlorite, hypochlorites, sulfate acids, hypochlorous acid, chlorine, and chlor-alkali
17 . A method for using a flow pathway in the electrochemical reactor of claim 14 to reduce and/or oxidize at least one chemical species, said flow pathway comprising:
introducing said liquid anolyte into said first half-cell wherein at least one chemical specics of said liquid anolytc is oxidized at said anode electrode, and introducing said liquid catholyte into said second half-cell wherein said gas distributor introduces said gas into said liquid catholyte and creates a multiphase catholyte solution, and
wherein said gas distributor introduces said gas into said cathode electrode, and
wherein at least one chemical species of said multiphase catholyte solution is reduced at said cathode electrode, and
wherein the reduced multiphase catholyte solution and/or the oxidized liquid anolyte contains said at least one chemical species that has been reduced and/or oxidized, and
wherein the reduced multiphase catholyte solution flows out of said second half-cell, and
wherein the oxidized liquid anolyte flows out of said first half-cell.
18 . The method of claim 17 wherein said at least one chemical species that has been reduced and/or oxidized are selected from the group consisting essentially of: molecular oxygen, hydroxyl radicals, hydroxide ions, hydrogen ions, hydrogen peroxide, superoxide, oxygen, water, alkali, acids, citric acid, sodium hypochlorite, hypochlorites, sulfate acids, hypochlorous acid, chlorine, and chlor-alkali.
19 . An electrochemical reactor, said electrochemical reactor comprising:
a containment boundary, a gas chamber, a gas distributor, a cathode chamber, a three dimensional cathode, a separator, an anode chamber, a three dimensional anode, and wherein said containment boundary contains said gas chamber, said gas distributor, said cathode chamber, said three dimensional cathode, said separator, said anode chamber, said three dimensional anode, and wherein said gas chamber is defined on a first side by said containment boundary and on a second side by a first side of said gas distributor, and wherein a second side of said gas distributor is in contact with and defines a first side of said cathode chamber, and wherein said cathode chamber is further defined on a second side by a first side of said separator, and wherein said cathode chamber contains said three dimensional cathode, and wherein said anode chamber is in contact with and defined on a first side by a second side of said separator, and wherein said anode chamber is further defined on a second side by said containment boundary, and wherein said anode chamber contains a three dimensional anode.
20 . The electrochemical reactor of claim 19 wherein the superficial area of said second side of said gas distributor is equal to or greater than the superficial area of a side of said three dimensional cathode that faces said second side of said gas distributor, and
wherein said superficial area of said second side of said gas distributor is separate from said three dimensional cathode.
21 . A method for using a flow pathway in the electrochemical reactor of claim 20 to produce at least one chemical species, said flow pathway comprising:
introducing an anolyte flow into said anode chamber wherein at least one chemical species of said anolyte flow is oxidized at said three dimensional anode, and
introducing a catholyte flow into said cathode chamber wherein said gas distributor introduces a gas into said catholyte flow and creates a multiphase catholyte solution, and
wherein said gas distributor introduces said gas into said three dimensional cathode, and
wherein at least one chemical species of said multiphase catholyte solution is reduced at said three dimensional cathode, and
wherein the reduced multiphase catholyte solution flows out of said cathode chamber, and
wherein the oxidized anolyte flow flows out of said anode chamber, and
wherein the reduced multiphase catholyte solution and/or the oxidized anode flow contains said at least one chemical species produced.
22 . The method of claim 21 wherein said at least one chemical species produced is selected from the group consisting essentially of: hydrogen peroxide, superoxide, alkali, acids, citric acid, sodium hypochlorite, hypochlorites, sulfate acids, chlorine, and chlor-alkali.
23 . A tubular electrochemical reactor, said tubular electrochemical reactor comprising:
a tubular gas chamber, a tubular gas dispersion tube, a cathode flow channel, a tubular cathode, a tubular separator, a tubular anode, a tubular anolyte chamber, a tubular anolyte chamber housing, and wherein said tubular gas chamber resides within and i s defined by the interior surface of said tubular gas dispersion tube, and wherein the exterior surface of said tubular gas dispersion tube forms the interior side of said cathode flow channel, and wherein the interior surface of said tubular separator forms the exterior side of said cathode flow channel, and wherein said tubular cathode resides within said cathode flow channel, and wherein the exterior surface of said tubular separator forms the interior side of said tubular anolyte chamber, and wherein the exterior side of said tubular anolyte chamber is formed by the interior surface of said tubular anolyte chamber housing, and wherein said tubular anode resides within said tubular anolyte chamber.
24 . The tubular electrochemical reactor of claim 23 further comprising a first toroidal seat plate, a second toroidal seat plate, a first end plate, a second end plate, a first toroidal cathode current distributor and compression ferrule, a second toroidal cathode current distributor and compression ferrule, and
wherein a second side of said first toroidal seat plate forms a first end of said tubular anolyte chamber by bridging a first end of said interior surface of said tubular anolyte chamber housing at an exterior portion of said first toroidal seat plate and a first end of said exterior surface of said tubular separator at an interior portion of said first toroidal seat plate, and
wherein a first side of said second toroidal seat plate forms a second end of said tubular anolyte chamber by bridging a second end of said interior surface of said tubular anolyte chamber housing at an exterior portion of said second toroidal seat plate and a second end of said exterior surface of said tubular separator at an interior portion of said second toroidal seat plate, and
wherein a second side of said first toroidal cathode current distributor and compression ferrule contacts a first end of said tubular cathode, and
wherein said second side of said first toroidal cathode current distributor and compression ferrule bridges a first end of said tubular separator and a interior surface of said first toroidal seat plate, and
wherein a first side of said second toroidal cathode current distributor and compression ferrule contacts a second end of said tubular cathode, and
wherein said first side of said second toroidal cathode current distributor and compression ferrule bridges a second end of said tubular separator and a interior surface of said second toroidal seat plate, and
wherein a second side of said first cnd plate forms a first end of said tubular gas chamber, and
wherein said second side of said first end plate forms a first end of said tubular gas dispersion tube, and
wherein said second side of said first end plate compresses said first toroidal cathode current distributor and compression ferrule between said second side of said first end plate and said first side of said first toroidal seat plate, and
wherein a first side of said second end plate forms a second end of said tubular gas chamber, and
wherein said first side of said second end plate forms a second end of said tubular gas dispersion tube, and
wherein said first side of said second end plate compresses said second toroidal cathode current distributor and compression ferrule between said first side of said second end plate and a second side of said second toroidal seat plate.
25 . The tubular electrochemical reactor of claim 24 further comprising at least one cathode electrical feed through post in said first and said second end plate, at least one catholyte intlet/outlet port in said first and said second end plate, at least one gas inlet/outlet port in said first and said second end plate, at least one anolyte inlet/outlet port in said tubular anolyte chamber housing, at least one anode electrical feed through post that passes through said tubular anolyte chamber housing and makes contact with said tubular anode at at least one anode current collector tab.
26 . The tubular electrochemical reactor of claim 25 wherein a second end of said at least one cathode electrical feed through post contacts a first toroidal cathode current distributor and compression ferrule, and
wherein a first end of said at least one cathode electrical feed through post protrudes from a first side of said first end plate, and
wherein a first end of said at least one cathode electrical feed through post contacts a second toroidal cathode current distributor and compression ferrule, and
wherein a second end of said at least one cathode electrical feed through post protrudes from a second side of said second end plate.
27 . The tubular electrochemical reactor of claim 26 wherein at least one catholyte intlet/outlet port in said first and said second end plate forms a channel with said cathode flow channel, and
wherein at least one gas inlet/outlet port in said first and said second end plate forms a channel with said tubular gas chamber, and
wherein at least one anolyte inlet/outlet port in said tubular anolyte chamber housing forms a channel with said tubular anolyte chamber.
28 . A method for using a flow pathway in the tubular electrochemical reactor of claim 27 to produce at least one chemical species, said flow pathway comprising:
introducing an anolyte flow into said tubular anolyte chamber wherein at least one chemical species of said anolyte flow is oxidized at said tubular anode, and
introducing a catholyte flow into said cathode chamber wherein said tubular gas distributor introduces a gas into said catholyte flow and creates a multiphase catholyte solution, and
wherein said tubular gas distributor introduces said gas into said tubular cathode, and
wherein at least one chemical species of said multiphase catholyte solution is reduced at said tubular cathode, and
wherein the reduced multiphase catholyte solution and/or the oxidized anode flow contains said at least one chemical species produced, and
wherein the reduced multiphase catholyte solution flows out of said cathode chamber, and
wherein the oxidized anolyte flow flows out of said tubular anolyte chamber.
29 . The method of claim 28 wherein said at least one chemical species produced is selected from the group consisting essentially of: hydrogen peroxide, superoxide, alkali, acids, citric acid, sodium hypochlorite, hypochlorites, sulfate acids, chlorine, and chlor-alkali.
30 . The tubular electrochemical reactor of claim 27 wherein said tubular separator is selectively permeable to cations.
31 . The tubular electrochemical reactor of claim 27 wherein said tubular separator is selectively permeable to anions.
32 . The tubular electrochemical reactor of claim 27 wherein said tubular cathode has a thickness that is between about 0.1 and 10 millimeters, and preferably between about 0.5 and 5 millimeters and more preferably between about 1 and 3 millimeters.
33 . The tubular electrochemical reactor of claim 27 wherein said tubular cathode exhibits electroactivity over greater than 50% of its specific surface area, and
wherein said tubular cathode has a specific surface area greater than about 1 m 2 per 1 m 2 superficial area, preferably a specific surface area greater than about 5 m 2 per 1 m 2 superficial area, more preferably a specific surface area greater than about 10 m 2 per 1 m 2 superficial area, and even more preferably a specific surface area greater than about 100 m 2 per 1 m 2 superficial area.
34 . A method of making hydrogen peroxide by providing the electrochemical reactor of claim 27 with a catholyte feed, an anolyte feed, a gas feed, a voltage to said tubular cathode, and a voltage to said tubular anode.
35 . A method of making superoxide by providing the electrochemical reactor of claim 27 with a catholyte feed, an anolyte feed, a gas feed, a voltage to said tubular cathode, and a voltage to said tubular anode.
36 . A method of making a mixture of hydrogen peroxide and superoxide in said cathode flow channel of the electrochemical reactor of claim 27 by providing a catholyte feed, an anolyte feed, a gas feed, a voltage to said tubular cathode, and a voltage to said tubular anode of said electrochemical reactor.
37 . A method of making alkaline hydrogen peroxide and citric acid by providing the electrochemical reactor of claim 27 with a catholyte feed, an anolyte feed, a gas feed, a voltage to said tubular cathode, and a voltage to said tubular anode.
38 . A method of making alkaline hydrogen peroxide and sulfate acids by providing the electrochemical reactor of claim 27 with a catholyte feed, an anolyte feed, a gas feed, a voltage to said tubular cathode, and a voltage to said tubular anode.
39 . A method of making alkaline hydrogen peroxide and sodium hypochlorite by providing the electrochemical reactor of claim 27 with a catholyte feed, an anolyte feed, a gas feed, a voltage to said tubular cathode, and a voltage to said tubular anode.Join the waitlist — get patent alerts
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