CA2590421A1 - Multi-cell single voltage electrolysis apparatus and method of using same - Google Patents
Multi-cell single voltage electrolysis apparatus and method of using same Download PDFInfo
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- CA2590421A1 CA2590421A1 CA002590421A CA2590421A CA2590421A1 CA 2590421 A1 CA2590421 A1 CA 2590421A1 CA 002590421 A CA002590421 A CA 002590421A CA 2590421 A CA2590421 A CA 2590421A CA 2590421 A1 CA2590421 A1 CA 2590421A1
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- 238000005868 electrolysis reaction Methods 0.000 title claims abstract description 146
- 238000000034 method Methods 0.000 title claims abstract description 61
- 229910052751 metal Inorganic materials 0.000 claims abstract description 115
- 239000002184 metal Substances 0.000 claims abstract description 115
- 239000012528 membrane Substances 0.000 claims abstract description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 39
- 239000000463 material Substances 0.000 claims description 33
- 239000003792 electrolyte Substances 0.000 claims description 31
- 239000007788 liquid Substances 0.000 claims description 31
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 21
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 20
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 20
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 20
- 239000010439 graphite Substances 0.000 claims description 20
- 229910002804 graphite Inorganic materials 0.000 claims description 20
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 19
- 239000001257 hydrogen Substances 0.000 claims description 19
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- 239000010935 stainless steel Substances 0.000 claims description 11
- 229910001220 stainless steel Inorganic materials 0.000 claims description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 10
- 229910000831 Steel Inorganic materials 0.000 claims description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 10
- 229910017052 cobalt Inorganic materials 0.000 claims description 10
- 239000010941 cobalt Substances 0.000 claims description 10
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 10
- 229910052802 copper Inorganic materials 0.000 claims description 10
- 239000010949 copper Substances 0.000 claims description 10
- 229910052742 iron Inorganic materials 0.000 claims description 10
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 10
- 229910052759 nickel Inorganic materials 0.000 claims description 10
- 229910052763 palladium Inorganic materials 0.000 claims description 10
- 229910052697 platinum Inorganic materials 0.000 claims description 10
- 239000010959 steel Substances 0.000 claims description 10
- 229910052725 zinc Inorganic materials 0.000 claims description 10
- 239000011701 zinc Substances 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 8
- 239000010936 titanium Substances 0.000 claims description 8
- 238000001816 cooling Methods 0.000 claims description 7
- 229910052719 titanium Inorganic materials 0.000 claims description 7
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical class [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims description 5
- XLYOFNOQVPJJNP-DYCDLGHISA-N deuterium hydrogen oxide Chemical compound [2H]O XLYOFNOQVPJJNP-DYCDLGHISA-N 0.000 claims description 5
- XLYOFNOQVPJJNP-NJFSPNSNSA-N ((18)O)water Chemical compound [18OH2] XLYOFNOQVPJJNP-NJFSPNSNSA-N 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- 238000012546 transfer Methods 0.000 claims description 4
- 229910045601 alloy Inorganic materials 0.000 claims description 3
- 239000000956 alloy Substances 0.000 claims description 3
- 230000020169 heat generation Effects 0.000 claims description 2
- 238000012544 monitoring process Methods 0.000 claims 4
- 229910001069 Ti alloy Inorganic materials 0.000 claims 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 238000004891 communication Methods 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 18
- 238000005457 optimization Methods 0.000 description 18
- 239000002803 fossil fuel Substances 0.000 description 11
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 10
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000000926 separation method Methods 0.000 description 5
- 238000009835 boiling Methods 0.000 description 4
- 239000002826 coolant Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-ZSJDYOACSA-N Heavy water Chemical compound [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910001882 dioxygen Chemical group 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000003345 natural gas Substances 0.000 description 3
- 239000002028 Biomass Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 229910001200 Ferrotitanium Inorganic materials 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003034 coal gas Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 239000012811 non-conductive material Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000000243 photosynthetic effect Effects 0.000 description 1
- -1 polypropylene, tetrafluoroethylene Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000000629 steam reforming Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000001149 thermolysis Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/02—Hydrogen or oxygen
- C25B1/04—Hydrogen or oxygen by electrolysis of water
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B15/00—Operating or servicing cells
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Abstract
A method and apparatus for achieving high output efficiency from an electrolysis system (100) using a plurality of electrolysis cells all located within a single electrolysis tank (101) is provided. Each individual electrolysis cell includes a membrane (105-107), a plurality of metal members comprised of at least a first and second metal member (117/118; 125/126) and at least a third and fourth metal member (121/122; 129/130), and a plurality of high voltage electrodes comprised of at least an anode (119; 127) and a cathode (123; 131). Within each cell, the high voltage anode is interposed between the first and second metal members and the high voltage cathode is interposed between the third and fourth metal members. The high voltage applied to the high voltage electrodes is pulsed.
Description
MULTI-CELL SINGLE VOLTAGE ELECTROLYSIS APPARATUS AND
METHOD OF USING SAME
FIELD OF THE INVENTION
The present invention relates generally to electrolysis systems and, more particularly, to a high efficiency electrolysis system and methods of using same.
BACKGROUND OF THE INVENTION
Fossil fuels, in particular oil, coal and natural gas, represent the primary sources of energy in today's world. Unfortunately in a world of rapidly increasing energy needs, dependence on any energy source of finite size and limited regional availability has dire consequences for the world's economy. In particular, as a country's need for energy increases, so does its vulnerability to disruption in the supply of that energy.
Additionally, as fossil fuels are the largest single source of carbon dioxide emissions, a greenhouse gas, continued reliance on such fuels can be expected to lead to continued global warming. Accordingly it is imperative that alternative, clean and renewable energy sources be developed that can replace fossil fuels.
Hydrogen-based fuel is currently one of the leading contenders to replace fossil fuel. There are a number of techniques that can be used to produce hydrogen, although the primary technique is by steam reforming natural gas. In this process thermal energy is used to react natural gas with steam, creating hydrogen and carbon dioxide. This process is well developed, but due to its reliance on fossil fuels and the release of carbon dioxide during production, it does not alleviate the need for fossil fuels nor does it lower the environmental impact of its use over that of traditional fossil fuels. Other, less developed hydrogen producing techniques include (i) biomass fermentation in which methane fermentation of high moisture content biomass creates fuel gas, a small portion of which is hydrogen; (ii) biological water splitting in which certain photosynthetic microbes produce hydrogen from water during their metabolic activities; (iii) photoelectrochemical processes using either soluble metal complexes as a catalyst or semiconducting electrodes in a photochemical cell; (iv) thermochemical water splitting using chemicals such as bromine or iodine, assisted by heat, to split water molecules;
(v) thermolysis in which concentrated solar energy is used to generate temperatures high enough to split methane into hydrogen and carbon; and (vi) electrolysis.
Electrolysis as a means of producing hydrogen has been known and used for over 80 years. In general, electrolysis of water uses two electrodes separated by an ion conducting electrolyte. During the process hydrogen is produced at the cathode and oxygen is produced at the anode, the two reaction areas separated by an ion conducting diaphragm.
Electricity is required to drive the process. An alternative to conventional electrolysis is high temperature electrolysis, also known as steam electrolysis. This process uses heat, for example produced by a solar concentrator, as a portion of the energy required to cause the needed reaction. Although lowering the electrical consumption of the process is desirable, this process has proven difficult to implement due to the tendency of the hydrogen and oxygen to recombine at the technique's high operating temperatures.
A high temperature heat source, for example a geothermal source, can also be used as a replacement for fossil fuel. In such systems the heat source raises the temperature of water sufficiently to produce steam, the steam driving a turbine generator which, in turn, produces electricity. Alternately the heat source can raise the temperature of a liquid that has a lower boiling temperature than water, such as isopentane, which can also be used to drive a turbine generator. Alternately the heat source can be used as a fossil fuel replacement for non-electrical applications, such as heating buildings.
Although a variety of alternatives to fossil fuels in addition to hydrogen and geothenmal sources have been devised, to date none of them have proven acceptable for a variety of reasons ranging from cost to environmental impact to availability.
Accordingly, what is needed is a new energy source, or a more efficient form of a current alternative energy source, that can effectively replace fossil fuels without requiring an overly complex distribution system.
The present invention provides such a system and method of use.
SUMMARY OF THE INVENTION
The present invention provides a method and apparatus for achieving high output efficiency from an electrolysis system using a plurality of electrolysis cells all located within a single electrolysis tank. Each individual electrolysis cell includes a membrane which separates the portion of the electrolysis tank containing that electrolysis cell into two regions.
Additionally, each electrolysis cell includes a plurality of metal members and a plurality of high voltage electrodes. The plurality of metal members includes at least a first and second metal member contained within the first region of the electrolysis cell and at least a third and fourth metal member contained within the second region of the electrolysis cell. The plurality of high voltage electrodes includes at least a first high voltage anode contained within the first region of the electrolysis cell and interposed between the first and second metal members, and a first high voltage cathode contained within the second region of the electrolysis cell and interposed between the third and fourth metal members. The high voltage applied to the high voltage electrodes is pulsed.
Preferably the high voltage pulses occur at a frequency between 50 Hz and 1 MHz, and more preferably at a frequency of between 100 Hz and 10 kHz. The pulse duration is preferably between 0.01 and 75 percent of the time period defined by the frequency, and more preferably between 1 and 50 percent of the time period defined by the frequency. Preferably the high voltage is between 50 volts and 50 kilovolts, more preferably between 100 volts and 5 kilovolts.
Preferably the liquid within the tank is comprised of one or more of; water, deuterated water, tritiated water, semiheavy water, heavy oxygen water, and/or any other water containing an isotope of either hydrogen or oxygen. Preferably the liquid within the electrolysis tank includes an electrolyte with a concentration in the range of 0.05 to 10 percent by weight, more preferably in the range of 0.05 to 2.0 percent by weight, and still more preferably in the range of 0.1 to 0.5 percent by weight.
The electrodes and the metal members can be fabricated from a variety of materials, although preferably the material for each is selected from the group consisting of steel, nickel, copper, iron, stainless steel, cobalt, manganese, zinc, titanium, platinum, palladium, carbon, graphite, carbon-graphite and alloys thereof.
In at least one embodiment, the electrolysis system is cooled. Cooling is preferably achieved by thermally coupling at least a portion of the electrolysis system to a portion of a conduit containing a heat transfer medium. The conduit can surround the electrolysis tank, be integrated within the walls of the electrolysis tank, or be contained within the electrolysis tank.
In at least one embodiment, the electrolysis system also contains a system controller. The system controller can be used to perform system optimization, either during an initial optimization period or repeatedly throughout system operation.
METHOD OF USING SAME
FIELD OF THE INVENTION
The present invention relates generally to electrolysis systems and, more particularly, to a high efficiency electrolysis system and methods of using same.
BACKGROUND OF THE INVENTION
Fossil fuels, in particular oil, coal and natural gas, represent the primary sources of energy in today's world. Unfortunately in a world of rapidly increasing energy needs, dependence on any energy source of finite size and limited regional availability has dire consequences for the world's economy. In particular, as a country's need for energy increases, so does its vulnerability to disruption in the supply of that energy.
Additionally, as fossil fuels are the largest single source of carbon dioxide emissions, a greenhouse gas, continued reliance on such fuels can be expected to lead to continued global warming. Accordingly it is imperative that alternative, clean and renewable energy sources be developed that can replace fossil fuels.
Hydrogen-based fuel is currently one of the leading contenders to replace fossil fuel. There are a number of techniques that can be used to produce hydrogen, although the primary technique is by steam reforming natural gas. In this process thermal energy is used to react natural gas with steam, creating hydrogen and carbon dioxide. This process is well developed, but due to its reliance on fossil fuels and the release of carbon dioxide during production, it does not alleviate the need for fossil fuels nor does it lower the environmental impact of its use over that of traditional fossil fuels. Other, less developed hydrogen producing techniques include (i) biomass fermentation in which methane fermentation of high moisture content biomass creates fuel gas, a small portion of which is hydrogen; (ii) biological water splitting in which certain photosynthetic microbes produce hydrogen from water during their metabolic activities; (iii) photoelectrochemical processes using either soluble metal complexes as a catalyst or semiconducting electrodes in a photochemical cell; (iv) thermochemical water splitting using chemicals such as bromine or iodine, assisted by heat, to split water molecules;
(v) thermolysis in which concentrated solar energy is used to generate temperatures high enough to split methane into hydrogen and carbon; and (vi) electrolysis.
Electrolysis as a means of producing hydrogen has been known and used for over 80 years. In general, electrolysis of water uses two electrodes separated by an ion conducting electrolyte. During the process hydrogen is produced at the cathode and oxygen is produced at the anode, the two reaction areas separated by an ion conducting diaphragm.
Electricity is required to drive the process. An alternative to conventional electrolysis is high temperature electrolysis, also known as steam electrolysis. This process uses heat, for example produced by a solar concentrator, as a portion of the energy required to cause the needed reaction. Although lowering the electrical consumption of the process is desirable, this process has proven difficult to implement due to the tendency of the hydrogen and oxygen to recombine at the technique's high operating temperatures.
A high temperature heat source, for example a geothermal source, can also be used as a replacement for fossil fuel. In such systems the heat source raises the temperature of water sufficiently to produce steam, the steam driving a turbine generator which, in turn, produces electricity. Alternately the heat source can raise the temperature of a liquid that has a lower boiling temperature than water, such as isopentane, which can also be used to drive a turbine generator. Alternately the heat source can be used as a fossil fuel replacement for non-electrical applications, such as heating buildings.
Although a variety of alternatives to fossil fuels in addition to hydrogen and geothenmal sources have been devised, to date none of them have proven acceptable for a variety of reasons ranging from cost to environmental impact to availability.
Accordingly, what is needed is a new energy source, or a more efficient form of a current alternative energy source, that can effectively replace fossil fuels without requiring an overly complex distribution system.
The present invention provides such a system and method of use.
SUMMARY OF THE INVENTION
The present invention provides a method and apparatus for achieving high output efficiency from an electrolysis system using a plurality of electrolysis cells all located within a single electrolysis tank. Each individual electrolysis cell includes a membrane which separates the portion of the electrolysis tank containing that electrolysis cell into two regions.
Additionally, each electrolysis cell includes a plurality of metal members and a plurality of high voltage electrodes. The plurality of metal members includes at least a first and second metal member contained within the first region of the electrolysis cell and at least a third and fourth metal member contained within the second region of the electrolysis cell. The plurality of high voltage electrodes includes at least a first high voltage anode contained within the first region of the electrolysis cell and interposed between the first and second metal members, and a first high voltage cathode contained within the second region of the electrolysis cell and interposed between the third and fourth metal members. The high voltage applied to the high voltage electrodes is pulsed.
Preferably the high voltage pulses occur at a frequency between 50 Hz and 1 MHz, and more preferably at a frequency of between 100 Hz and 10 kHz. The pulse duration is preferably between 0.01 and 75 percent of the time period defined by the frequency, and more preferably between 1 and 50 percent of the time period defined by the frequency. Preferably the high voltage is between 50 volts and 50 kilovolts, more preferably between 100 volts and 5 kilovolts.
Preferably the liquid within the tank is comprised of one or more of; water, deuterated water, tritiated water, semiheavy water, heavy oxygen water, and/or any other water containing an isotope of either hydrogen or oxygen. Preferably the liquid within the electrolysis tank includes an electrolyte with a concentration in the range of 0.05 to 10 percent by weight, more preferably in the range of 0.05 to 2.0 percent by weight, and still more preferably in the range of 0.1 to 0.5 percent by weight.
The electrodes and the metal members can be fabricated from a variety of materials, although preferably the material for each is selected from the group consisting of steel, nickel, copper, iron, stainless steel, cobalt, manganese, zinc, titanium, platinum, palladium, carbon, graphite, carbon-graphite and alloys thereof.
In at least one embodiment, the electrolysis system is cooled. Cooling is preferably achieved by thermally coupling at least a portion of the electrolysis system to a portion of a conduit containing a heat transfer medium. The conduit can surround the electrolysis tank, be integrated within the walls of the electrolysis tank, or be contained within the electrolysis tank.
In at least one embodiment, the electrolysis system also contains a system controller. The system controller can be used to perform system optimization, either during an initial optimization period or repeatedly throughout system operation.
A further understanding of the nature and advantages of the present invention may be realized by reference to the remaining portions of the specification and the drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is an illustration of an exemplary embodiment of the invention utilizing a three cell configuration;
Fig. 2 is an illustration of an alternate embodiment based on the configuration shown in Fig. 1 utilizing multiple sets of metal members for each cell;
Fig. 3 is an illustration of an alternate embodiment based on the configuration shown in Fig. 1 utilizing multiple sets of high voltage electrodes for each cell;
Fig. 4 is an illustration of an alternate embodiment based on the configuration shown in Fig. I utilizing multiple sets of metal members and multiple sets of high voltage electrodes for each cell;
Fig. 5 is an illustration of an alternate embodiment utilizing a cylindrically-shapedtank;
Fig. 6 is an illustration of an alternate embodiment based on the configuration shown in Fig. 1 utilizing a switching power supply;
Fig. 7 is an illustration of an alternate embodiment based on the configuration shown in Fig. 1 utilizing a switching power supply with an internal pulse generator;
Fig. 8 is an illustration of one mode of operation;
Fig. 9 is an illustration of an alternate mode of operation that includes initial process optimization steps;
Fig. 10 is an illustration of an alternate, and preferred, mode of operation in which the process undergoes continuous optimization;
Fig. 11 is an illustration of an alternate embodiment of Fig. I utilizing multiple high voltage supplies; and Fig. 12 is an illustration of an alternate embodiment of Fig. 1 that includes a system controller.
DESCRIPTION OF THE SPECIFIC EMBODIMENTS
Fig. 1 is an illustration of an exemplary, and preferred, embodiment of the invention which can be used, for example, as a heat generator. Electrolysis system 100 includes a tank 101 comprised of a non-conductive material, the size of the tank depending primarily upon the desired output level for the system, for example the desired heat production. Although tank 101 is shown as having a rectangular shape, it will be appreciated that the invention is not so limited and that tank 101 can utilize other shapes, for example cylindrical, square, irregularly-shaped, etc. Tank 101 is substantially filled with liquid 103. In at least one preferred embodiment, liquid 103 is comprised of water with an electrolyte, the electrolyte being either an acid electrolyte or a base electrolyte. Exemplary electrolytes include potassium hydroxide and sodium hydroxide. The term "water" as used herein refers to water (H20), deuterated water (deuterium oxide or D20), tritiated water (tritium oxide or T20), semiheavy water (HDO), heavy oxygen water (H2180 or H2170) or any other water containing an isotope of either hydrogen or oxygen, either singly or in any combination thereof (for example, a combination of H20 and D20).
A typical electrolysis system used to decompose water into hydrogen and oxygen gases utilizes relatively high concentrations of electrolyte. The present invention, however, has been found to work best with relatively low electrolyte concentrations, thereby maintaining a relatively high initial water resistivity. Preferably the water resistivity prior to the addition of an electrolyte is on the order of 1 to 28 megohms. Preferably the concentration of electrolyte is in the range of 0.05 percent to 10 percent by weight, more preferably the concentration of electrolyte is in the range of 0.05 percent to 2.0 percent by weight, and still more preferably the concentration of electrolyte is in the range of 0.1 percent to 0.5 percent by weight.
The electrolysis system of the invention includes multiple electrolysis cells, an electrolysis cell defined herein as having at least two metal members and a high voltage cathode interposed between the two metal members within a first region of the cell, and at least two metal members and a high voltage anode interposed between the two metal members within a second region of the cell, the two cell regions separated by a membrane. In the embodiment illustrated in Fig. 1, electrolysis tank 101 includes three electrolysis cells, the three cells including membranes 105-107, respectively. It should be understood that the invention is not limited to an electrolysis system with a specific number of cells, rather the number of cells depends primarily on the desired output level (e.g., heat production) and the size of the electrolysis tank.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is an illustration of an exemplary embodiment of the invention utilizing a three cell configuration;
Fig. 2 is an illustration of an alternate embodiment based on the configuration shown in Fig. 1 utilizing multiple sets of metal members for each cell;
Fig. 3 is an illustration of an alternate embodiment based on the configuration shown in Fig. 1 utilizing multiple sets of high voltage electrodes for each cell;
Fig. 4 is an illustration of an alternate embodiment based on the configuration shown in Fig. I utilizing multiple sets of metal members and multiple sets of high voltage electrodes for each cell;
Fig. 5 is an illustration of an alternate embodiment utilizing a cylindrically-shapedtank;
Fig. 6 is an illustration of an alternate embodiment based on the configuration shown in Fig. 1 utilizing a switching power supply;
Fig. 7 is an illustration of an alternate embodiment based on the configuration shown in Fig. 1 utilizing a switching power supply with an internal pulse generator;
Fig. 8 is an illustration of one mode of operation;
Fig. 9 is an illustration of an alternate mode of operation that includes initial process optimization steps;
Fig. 10 is an illustration of an alternate, and preferred, mode of operation in which the process undergoes continuous optimization;
Fig. 11 is an illustration of an alternate embodiment of Fig. I utilizing multiple high voltage supplies; and Fig. 12 is an illustration of an alternate embodiment of Fig. 1 that includes a system controller.
DESCRIPTION OF THE SPECIFIC EMBODIMENTS
Fig. 1 is an illustration of an exemplary, and preferred, embodiment of the invention which can be used, for example, as a heat generator. Electrolysis system 100 includes a tank 101 comprised of a non-conductive material, the size of the tank depending primarily upon the desired output level for the system, for example the desired heat production. Although tank 101 is shown as having a rectangular shape, it will be appreciated that the invention is not so limited and that tank 101 can utilize other shapes, for example cylindrical, square, irregularly-shaped, etc. Tank 101 is substantially filled with liquid 103. In at least one preferred embodiment, liquid 103 is comprised of water with an electrolyte, the electrolyte being either an acid electrolyte or a base electrolyte. Exemplary electrolytes include potassium hydroxide and sodium hydroxide. The term "water" as used herein refers to water (H20), deuterated water (deuterium oxide or D20), tritiated water (tritium oxide or T20), semiheavy water (HDO), heavy oxygen water (H2180 or H2170) or any other water containing an isotope of either hydrogen or oxygen, either singly or in any combination thereof (for example, a combination of H20 and D20).
A typical electrolysis system used to decompose water into hydrogen and oxygen gases utilizes relatively high concentrations of electrolyte. The present invention, however, has been found to work best with relatively low electrolyte concentrations, thereby maintaining a relatively high initial water resistivity. Preferably the water resistivity prior to the addition of an electrolyte is on the order of 1 to 28 megohms. Preferably the concentration of electrolyte is in the range of 0.05 percent to 10 percent by weight, more preferably the concentration of electrolyte is in the range of 0.05 percent to 2.0 percent by weight, and still more preferably the concentration of electrolyte is in the range of 0.1 percent to 0.5 percent by weight.
The electrolysis system of the invention includes multiple electrolysis cells, an electrolysis cell defined herein as having at least two metal members and a high voltage cathode interposed between the two metal members within a first region of the cell, and at least two metal members and a high voltage anode interposed between the two metal members within a second region of the cell, the two cell regions separated by a membrane. In the embodiment illustrated in Fig. 1, electrolysis tank 101 includes three electrolysis cells, the three cells including membranes 105-107, respectively. It should be understood that the invention is not limited to an electrolysis system with a specific number of cells, rather the number of cells depends primarily on the desired output level (e.g., heat production) and the size of the electrolysis tank.
Membranes 105-107 permit ion/electron exchange between the two regions of each cell while keeping separate the oxygen and hydrogen bubbles produced during electrolysis.
Maintaining separate hydrogen and oxygen gas regions is important as a means of minimizing the risk of explosions due to the inadvertent recombination of the two gases.
Additionally, separating the regions allows the collection of pure hydrogen gas and pure oxygen gas.
Accordingly similar polarity electrodes are grouped together with the membranes keeping groups separate. Exemplary membrane materials include, but are not limited to, polypropylene, tetrafluoroethylene, asbestos, etc.
As noted herein, the present system is capable of generating considerable heat.
Accordingly, system components such as the electrolysis tank (e.g., tank 101) and the membranes (e.g., membranes 105-107) that are expected to be subjected to the heat generated by the system must be fabricated from suitable materials and designed to indefinitely accommodate the intended operating temperatures as well as the internal tank pressure. For example, in at least one preferred embodiment the system is designed to operate at a temperature of approximately 90 C at standard pressure. In an alternate exemplary embodiment, the system is designed to operate at elevated temperatures (e.g., 100 C to 150 C) and at sufficient pressure to prevent boiling of liquid 103. In yet another alternate exemplary embodiment, the system is designed to operate at even higher temperatures (e.g., 200 C to 350 C) and higher pressures (e.g., sufficient to prevent boiling). Accordingly, it will be understood that the choice of materials (e.g., for tank 101 and membranes 105-107) and the design of the system (e.g., tank wall thicknesses, fittings, etc.) will vary, depending upon the intended system operational parameters, primarily temperature and pressure.
Other standard features of the electrolysis tank are gas outlets for any hydrogen and oxygen gases generated within the tank. In the exemplary embodiment shown in Fig. 1, the oxygen gas produced at the anodes will exit tank 101 at gas outlets 108-109 while hydrogen gas produced at the cathodes will exit the tank at gas outlets 110-111.
Replenishment of liquid 103 is preferably through a separate conduit, for example conduit 113. In at least one embodiment of the invention, another conduit 115 is used to remove liquid 103 from the system. Alternately, each cell can include one or more conduits for liquid 103 replenishment. If desired, a single conduit can be used for both liquid removal and replenishment. It will be appreciated that the system can either be periodically refilled or liquid 103 can be continuously added at a very slow rate during system operation.
In the embodiment illustrated in Fig. 1, each cell includes four metal members, two members per cell region, and two high voltage electrodes (i.e., one cathode and one anode).
In the illustrated embodiment, the first cell includes membrane 105, metal members 117/118 and interposed high voltage anode 119, and metal members 121/122 and interposed high voltage cathode 123. Noting that adjacent cells preferably co-use sets of electrodes/members as shown, the second cell includes membrane 106, metal members 121/122 and interposed high voltage cathode 123, and metal members 125/126 and interposed high voltage anode 127.
The third cell includes membrane 107, metal members 125/126 and interposed high voltage anode 127, and metal members 129/130 and interposed high voltage cathode 131.
Preferably and as shown, the faces of the individual electrodes and the individual metal members are parallel to one another. It should be understood, however, that the faces of the individual electrodes and the individual metal members do not have to be parallel to one another.
In a preferred embodiment, all of the electrodes and metal members are comprised of titanium. In another preferred embodiment, all of the electrodes and metal members are comprised of stainless steel. It should be appreciated, however, that other materials can be used and that the same material does not have to be used for both the metal members and the high voltage electrodes, nor does the same material have to be used for all of the metal members, nor does the same material have to be used for both the high voltage anodes and the high voltage cathodes. In addition to titanium and stainless steel, other exemplary materials that can be used for the metal members and the high voltage electrodes include, but are not limited to, copper, iron, cobalt, steel, manganese, zinc, nickel, platinum, palladium, carbon, graphite, carbon-graphite, and alloys of these materials. Preferably the surface area of each of the faces of the metal members (i.e., members 117, 118, 121, 122, 125, 126, 129 and 130 in Fig. 1) is a large percentage of the cross-sectional area of tank 101, typically on the order of at least 40 percent of the cross-sectional area of tank 101, and often between approximately 70 percent and 90 percent of the cross-sectional area of tank 101. The high voltage electrodes may be larger, smaller or the same size as the metal members. Although the separation distance between electrodes is dependent upon a variety of factors (e.g., tank size, voltage/current, etc.), in at least one preferred embodiment the separation between the closest metal members positioned on either side of a membrane (e.g., in Fig. I members 118/121, members 122/125 and members 126/129) is between 2 millimeters and 15 centimeters.
In Fig. 1, high voltage power source 133 supplies power to all of the high voltage electrodes. Preferably the high voltage generated by source 133 is within the range of 50 volts to 50 kilovolts, and more preferably within the range of 100 volts to 5 kilovolts. Rather than continually apply voltage to the electrodes, source 133 is pulsed, preferably at a frequency between 50 Hz and 1 MHz, and more preferably at a frequency of between 100 Hz and 10 kHz.
The pulse width (i.e., pulse duration) is preferably between 0.01 and 75 percent of the time period defined by the frequency, and more preferably between 1 and 50 percent of the time period defined by the frequency. Thus, for example, for a frequency of 150 Hz, the pulse duration is preferably in the range of 0.67 microseconds to 5 milliseconds, and more preferably in the range of 66.7 microseconds to 3.3 milliseconds. Alternately, for example, for a frequency of 1 kHz, the pulse duration is preferably in the range of 0.1 microseconds to 0.75 milliseconds, and more preferably in the range of 10 microseconds to 0.5 milliseconds.
Although voltage source 133 can include internal means for pulsing the source output, preferably an external pulse generator 135 controls a high voltage switch 137 which, in turn, controls the output of voltage source 133 as shown, and as described above. Other means for pulsing the voltage sources are clearly envisioned, for example using a switching power supply coupled to an external pulse generator or using a switching power supply with an internal pulse generator.
If multiple pulse generators are used, for example for use with multiple high voltage sources, preferably means such as a system controller are used to insure that the pulses generated by the individual pulse generators are simultaneous.
As previously noted, the electrolysis process of the invention generates considerable heat. To withdraw that heat so that it can be used, and to prevent the liquid within the tank from becoming too hot and boiling at a given temperature, and to prevent possible damage to those system components that may be susceptible to damage, in the preferred embodiments of the invention the system includes means to actively cool the system to within an acceptable temperature range. For example, in at least one preferred embodiment the cooling system does not allow the temperature to exceed 90 C. Although it will be appreciated that the invention is not limited to a specific type of cooling system or a specific implementation of the cooling system, in at least one embodiment the electrolysis tank is surrounded by a coolant conduit 139, portions of which are shown in Figs. 1-7, 11 and 12. Within coolant conduit 139 is a heat transfer medium, for example water. Coolant conduit 139 can either surround a portion of the electrolysis tank as shown, or be contained within the electrolysis tank, or be integrated within the walls of the electrolysis tank. The coolant pump and heat withdrawal system is not shown in the figures as cooling systems are well known by those of skill in the art.
As will be appreciated by those of skill in the art, there are numerous minor variations of the system described herein and shown in Fig. 1 that will function in substantially the same manner as the disclosed system. As previously noted, alternate configurations can utilize fewer or greater numbers of cells, differently sized/shaped tanks, different electrolytic solutions, and a variety of different electrode/metal member configurations and materials.
Additionally the system can utilize a range of input powers, frequencies and pulse widths (i.e., pulse duration). In general, the exact configuration depends upon the desired output level as well as available space and power. Figs. 2-5 illustrate a few alternate configurations, including the use of multiple sets of metal members for each cell (e.g., Fig. 2), multiple sets of high voltage electrodes for each cell (e.g., Fig. 3), multiple sets of metal members and high voltage electrodes for each cell (e.g., Fig. 4), and a horizontal cylindrical tank (e.g., Fig. 5).
Fig. 2 illustrates an alternate embodiment of the system shown in Fig. 1, the alternate configuration replacing metal member 117 with three metal members 201-203, replacing metal member 118 with three metal members 205-207, replacing metal member 121 with three metal members 209-211, replacing metal member 122 with three metal members 213-215, replacing metal member 125 with three metal members 217-219, replacing metal member 126 with three metal members 221-223, replacing metal member 129 with three metal members 225-227, and replacing metal member 130 with three metal members 229-23 1.
Fig. 3 illustrates an alternate embodiment of the system shown in Fig. 1, the alternate configuration replacing high voltage electrode 119 with two high voltage electrodes 301-302, replacing high voltage electrode 123 with two high voltage electrodes 303-304, replacing high voltage electrode 127 with two high voltage electrodes 305-306, and replacing high voltage electrode 131 with two high voltage electrodes 307-308.
Maintaining separate hydrogen and oxygen gas regions is important as a means of minimizing the risk of explosions due to the inadvertent recombination of the two gases.
Additionally, separating the regions allows the collection of pure hydrogen gas and pure oxygen gas.
Accordingly similar polarity electrodes are grouped together with the membranes keeping groups separate. Exemplary membrane materials include, but are not limited to, polypropylene, tetrafluoroethylene, asbestos, etc.
As noted herein, the present system is capable of generating considerable heat.
Accordingly, system components such as the electrolysis tank (e.g., tank 101) and the membranes (e.g., membranes 105-107) that are expected to be subjected to the heat generated by the system must be fabricated from suitable materials and designed to indefinitely accommodate the intended operating temperatures as well as the internal tank pressure. For example, in at least one preferred embodiment the system is designed to operate at a temperature of approximately 90 C at standard pressure. In an alternate exemplary embodiment, the system is designed to operate at elevated temperatures (e.g., 100 C to 150 C) and at sufficient pressure to prevent boiling of liquid 103. In yet another alternate exemplary embodiment, the system is designed to operate at even higher temperatures (e.g., 200 C to 350 C) and higher pressures (e.g., sufficient to prevent boiling). Accordingly, it will be understood that the choice of materials (e.g., for tank 101 and membranes 105-107) and the design of the system (e.g., tank wall thicknesses, fittings, etc.) will vary, depending upon the intended system operational parameters, primarily temperature and pressure.
Other standard features of the electrolysis tank are gas outlets for any hydrogen and oxygen gases generated within the tank. In the exemplary embodiment shown in Fig. 1, the oxygen gas produced at the anodes will exit tank 101 at gas outlets 108-109 while hydrogen gas produced at the cathodes will exit the tank at gas outlets 110-111.
Replenishment of liquid 103 is preferably through a separate conduit, for example conduit 113. In at least one embodiment of the invention, another conduit 115 is used to remove liquid 103 from the system. Alternately, each cell can include one or more conduits for liquid 103 replenishment. If desired, a single conduit can be used for both liquid removal and replenishment. It will be appreciated that the system can either be periodically refilled or liquid 103 can be continuously added at a very slow rate during system operation.
In the embodiment illustrated in Fig. 1, each cell includes four metal members, two members per cell region, and two high voltage electrodes (i.e., one cathode and one anode).
In the illustrated embodiment, the first cell includes membrane 105, metal members 117/118 and interposed high voltage anode 119, and metal members 121/122 and interposed high voltage cathode 123. Noting that adjacent cells preferably co-use sets of electrodes/members as shown, the second cell includes membrane 106, metal members 121/122 and interposed high voltage cathode 123, and metal members 125/126 and interposed high voltage anode 127.
The third cell includes membrane 107, metal members 125/126 and interposed high voltage anode 127, and metal members 129/130 and interposed high voltage cathode 131.
Preferably and as shown, the faces of the individual electrodes and the individual metal members are parallel to one another. It should be understood, however, that the faces of the individual electrodes and the individual metal members do not have to be parallel to one another.
In a preferred embodiment, all of the electrodes and metal members are comprised of titanium. In another preferred embodiment, all of the electrodes and metal members are comprised of stainless steel. It should be appreciated, however, that other materials can be used and that the same material does not have to be used for both the metal members and the high voltage electrodes, nor does the same material have to be used for all of the metal members, nor does the same material have to be used for both the high voltage anodes and the high voltage cathodes. In addition to titanium and stainless steel, other exemplary materials that can be used for the metal members and the high voltage electrodes include, but are not limited to, copper, iron, cobalt, steel, manganese, zinc, nickel, platinum, palladium, carbon, graphite, carbon-graphite, and alloys of these materials. Preferably the surface area of each of the faces of the metal members (i.e., members 117, 118, 121, 122, 125, 126, 129 and 130 in Fig. 1) is a large percentage of the cross-sectional area of tank 101, typically on the order of at least 40 percent of the cross-sectional area of tank 101, and often between approximately 70 percent and 90 percent of the cross-sectional area of tank 101. The high voltage electrodes may be larger, smaller or the same size as the metal members. Although the separation distance between electrodes is dependent upon a variety of factors (e.g., tank size, voltage/current, etc.), in at least one preferred embodiment the separation between the closest metal members positioned on either side of a membrane (e.g., in Fig. I members 118/121, members 122/125 and members 126/129) is between 2 millimeters and 15 centimeters.
In Fig. 1, high voltage power source 133 supplies power to all of the high voltage electrodes. Preferably the high voltage generated by source 133 is within the range of 50 volts to 50 kilovolts, and more preferably within the range of 100 volts to 5 kilovolts. Rather than continually apply voltage to the electrodes, source 133 is pulsed, preferably at a frequency between 50 Hz and 1 MHz, and more preferably at a frequency of between 100 Hz and 10 kHz.
The pulse width (i.e., pulse duration) is preferably between 0.01 and 75 percent of the time period defined by the frequency, and more preferably between 1 and 50 percent of the time period defined by the frequency. Thus, for example, for a frequency of 150 Hz, the pulse duration is preferably in the range of 0.67 microseconds to 5 milliseconds, and more preferably in the range of 66.7 microseconds to 3.3 milliseconds. Alternately, for example, for a frequency of 1 kHz, the pulse duration is preferably in the range of 0.1 microseconds to 0.75 milliseconds, and more preferably in the range of 10 microseconds to 0.5 milliseconds.
Although voltage source 133 can include internal means for pulsing the source output, preferably an external pulse generator 135 controls a high voltage switch 137 which, in turn, controls the output of voltage source 133 as shown, and as described above. Other means for pulsing the voltage sources are clearly envisioned, for example using a switching power supply coupled to an external pulse generator or using a switching power supply with an internal pulse generator.
If multiple pulse generators are used, for example for use with multiple high voltage sources, preferably means such as a system controller are used to insure that the pulses generated by the individual pulse generators are simultaneous.
As previously noted, the electrolysis process of the invention generates considerable heat. To withdraw that heat so that it can be used, and to prevent the liquid within the tank from becoming too hot and boiling at a given temperature, and to prevent possible damage to those system components that may be susceptible to damage, in the preferred embodiments of the invention the system includes means to actively cool the system to within an acceptable temperature range. For example, in at least one preferred embodiment the cooling system does not allow the temperature to exceed 90 C. Although it will be appreciated that the invention is not limited to a specific type of cooling system or a specific implementation of the cooling system, in at least one embodiment the electrolysis tank is surrounded by a coolant conduit 139, portions of which are shown in Figs. 1-7, 11 and 12. Within coolant conduit 139 is a heat transfer medium, for example water. Coolant conduit 139 can either surround a portion of the electrolysis tank as shown, or be contained within the electrolysis tank, or be integrated within the walls of the electrolysis tank. The coolant pump and heat withdrawal system is not shown in the figures as cooling systems are well known by those of skill in the art.
As will be appreciated by those of skill in the art, there are numerous minor variations of the system described herein and shown in Fig. 1 that will function in substantially the same manner as the disclosed system. As previously noted, alternate configurations can utilize fewer or greater numbers of cells, differently sized/shaped tanks, different electrolytic solutions, and a variety of different electrode/metal member configurations and materials.
Additionally the system can utilize a range of input powers, frequencies and pulse widths (i.e., pulse duration). In general, the exact configuration depends upon the desired output level as well as available space and power. Figs. 2-5 illustrate a few alternate configurations, including the use of multiple sets of metal members for each cell (e.g., Fig. 2), multiple sets of high voltage electrodes for each cell (e.g., Fig. 3), multiple sets of metal members and high voltage electrodes for each cell (e.g., Fig. 4), and a horizontal cylindrical tank (e.g., Fig. 5).
Fig. 2 illustrates an alternate embodiment of the system shown in Fig. 1, the alternate configuration replacing metal member 117 with three metal members 201-203, replacing metal member 118 with three metal members 205-207, replacing metal member 121 with three metal members 209-211, replacing metal member 122 with three metal members 213-215, replacing metal member 125 with three metal members 217-219, replacing metal member 126 with three metal members 221-223, replacing metal member 129 with three metal members 225-227, and replacing metal member 130 with three metal members 229-23 1.
Fig. 3 illustrates an alternate embodiment of the system shown in Fig. 1, the alternate configuration replacing high voltage electrode 119 with two high voltage electrodes 301-302, replacing high voltage electrode 123 with two high voltage electrodes 303-304, replacing high voltage electrode 127 with two high voltage electrodes 305-306, and replacing high voltage electrode 131 with two high voltage electrodes 307-308.
Fig. 4 illustrates an alternate embodiment of the system shown in Fig. 1, the alternate embodiment utilizing the metal member configuration shown in Fig. 2 and the high voltage electrode configuration shown in Fig. 3.
Fig. 5 illustrates an alternate embodiment of the system shown in Fig. 1, the alternate configuration replacing tank 101 with a horizontally configured cylindrical tank 501, replacing membrane 105 with an appropriately shaped membrane 503, replacing membrane 106 with an appropriately shaped membrane 504, replacing membrane 107 with an appropriately shaped membrane 505, replacing metal member 117 with disc-shaped metal member 507, replacing metal member 118 with disc-shaped metal member 508, replacing high voltage electrode 119 with disc-shaped high voltage electrode 509, replacing metal member 121 with disc-shaped metal member 511, replacing metal member 122 with disc-shaped metal member 512, replacing high voltage electrode 123 with disc-shaped high voltage electrode 513, replacing metal member 125 with disc-shaped metal member 515, replacing metal member 126 with disc-shaped metal member 516, replacing high voltage electrode 127 with disc-shaped high voltage electrode 517, replacing metal member 129 with disc-shaped metal member 519, replacing metal member 130 with disc-shaped metal member 520, and replacing high voltage electrode 131 with disc-shaped high voltage electrode 521.
It will be appreciated that the supply electronics (i.e., high voltage power supply, high voltage switch, pulse generator) shown in Figs. 1-5 represent only one exemplary configuration and that other configurations can be used to supply the requisite pulsed and timed power to the high voltage electrodes within the,cells of the electrolysis system of the invention.
Figs. 6 and 7 illustrate two additional alternate, and exemplary, configurations. Specifically, Fig. 6 illustrates a system similar to that shown in Fig. 1, except that high voltage supply 133 and high voltage switch 137 are combined into a single high voltage switching power supply 601. The embodiment illustrated in Fig. 7 combines the pulse generation within the power supply, i.e., high voltage supply 701.
It should be understood that the electrolysis system of the present invention can be operated in a number of modes, the primary differences between modes being the degree of process optimization used during operation. For example, Fig. 8 illustrates one method of operation requiring minimal optimization. As illustrated, initially the electrolysis tank, e.g., tank 101, is filled with water (step 801). Preferably the level of water in the tank at least covers the top of the electrodes. The electrolyte can either be mixed into the water prior to filling the tank or after the tank is filled. The frequency of the pulse generator is then set (step 803) as well as the pulse duration (step 805). The initial voltage setting for the high voltage power supply is also set (step 807). It will be appreciated that the order of set-up is clearly not critical to the electrolysis process. Typically, prior to the initiation of electrolysis, the temperature of the water is at room temperature.
Once set-up is complete, electrolysis is initiated (step 809). During the electrolysis process (step 811), and as previously noted, the water is heated by the process itself.
Eventually, when operation is no longer desirable, the electrolysis process is suspended (step 813). If desired, prior to further operation the tank can be drained (step 815) and refilled (step 817). Prior to refilling the tank, a series of optional steps can be performed. For example, the tank can be washed out (optional step 819) and the electrodes and/or metal members can be cleaned, for example to remove oxides, by washing with diluted acids (optional step 821).
Spent, or used up, electrodes and/or metal members can also be replaced prior to refilling (optional step 823). After cleaning the system and/or replacing electrodes/members as deemed necessary, and refilling the system, the system is ready to reinitiate the electrolysis process.
The above sequence of processing steps works best once the operational parameters have been optimized for a specific system configuration since the system configuration will impact the heat generation efficiency of the process.
Exemplary system configuration parameters that affect the optimal electrolysis settings include tank size, quantity of water, type and/or quality of water, electrolyte composition, electrolyte concentration, electrode size, electrode composition, electrode shape, electrode configuration, electrode separation, metal member size, metal member composition, metal member shape, metal member configuration, metal member separation, cell number, cell separation, initial water temperature, high voltage setting, pulse frequency and pulse duration.
Fig. 9 illustrates an alternate procedure, one in which the process undergoes optimization. Initially the tank is filled (step 901) and initial settings for pulse frequency (step 903), pulse duration (step 905) and high voltage supply output (step 907) are made. Typically the initial settings are based on previous settings that have been optimized for a similarly configured system. For example, assuming that the new configuration was the same as a previous configuration except for the composition of the electrodes, a reasonable initial set-up would be the optimized set-up from the previous configuration.
After the initial set-up is completed, electrolysis is initiated (step 909) and system output is monitored (step 911), for example absolute temperature or the rate of temperature increase. Although system optimization can begin immediately, preferably the system is allowed to run for an initial period of time (step 913) prior to optimization.
The initial period of operation can be based on achieving a predetermined output, for example a specific level of temperature increase, or achieving a steady state output (e.g., steady state temperature).
Alternately the initial period of time can simply be a predetermined time period, for example 6 hours.
After the initial time period is exceeded, the system output (e.g., temperature rate increase, steady state temperature, etc.) is monitored (step 915) while optimizing one or more of the operational parameters. Although the order of parameter optimization is not critical, in at least one preferred embodiment the first parameter to be optimized is pulse duration (step 917).
Then the pulse frequency is optimized (step 918), followed by optimization of the high voltage (step 919). In this embodiment after optimization is complete the electrolysis process is allowed to continue (step 921) without further optimization until the process is halted, step 923. In another, and preferred, alternative approach illustrated in Fig. 10, one or more of optimization steps 917-919 are performed continuously throughout the electrolysis process until electrolysis is suspended.
Note that the optimization processes described relative to Figs. 9 and 10 assume that (i) the cells physical geometry is fixed and (ii) there is no control over the high voltage applied to individual cell electrodes. If the system does include means for adjusting the physical geometry of the individual cells during electrolysis, for example the spacing between the electrodes within the cells or the cell-to-cell spacing, these parameters can also be altered to further optimize the electrolysis process during system operation. The system can also be configured to provide additional control over the high voltage applied to the cells. For example, the system shown in Fig. 11 uses a pair of high voltage power supplies 1101/1102 and associated high voltage switches 1103/1104. Systems such as these, although more complex, provide further control and therefore potentially greater optimization.
The optimization process described relative to Figs. 9 and 10 can be performed manually. In the preferred embodiment, however, the system or portions of the system are controlled via a system controller such as controller 1201 shown in an alternate embodiment of the configuration illustrated in Fig. 1(i.e., Fig. 12). Assuming that controller 1201 is used to control and optimize the pulse frequency, pulse duration and high voltage, system controller 1201 is coupled to the pulse generator and the voltage supply as shown. If the system controller is only used to control and optimize a subset of these parameters, the system controller is coupled accordingly (i.e., coupled to the pulse generator to control pulse frequency and duration;
coupled to the high voltage source to control the high voltage). In order to allow optimization automation, system controller 1201 is also coupled to a system monitor, for example one or more temperature monitors (e.g., monitor 1203). In at least one preferred embodiment system controller 1201 is also coupled to a monitor 1205, monitor 1205 providing either the pH or the resistivity of liquid 103 within electrolysis tank 101, thereby providing means for determining when additional electrolyte needs to be added. In at least one preferred embodiment system controller 1201 is also coupled to a liquid level monitor 1207, thereby providing means for determining when additional water needs to be added to the electrolysis tank.
Preferably system controller 1201 is also coupled to one or more flow valves 1209 which allow water, electrolyte, or a combination of water and electrolyte to be automatically added to the electrolysis system in response to pHlresistivity data provided by monitor 1205 (i.e., when the monitored pH/resistivity falls outside of a preset range) and/or liquid level data provided by monitor 1207 (i.e., when the monitored liquid level falls below a preset value).
As will be understood by those familiar with the art, the present invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. Accordingly, the disclosures and descriptions herein are intended to be illustrative, but not limiting, of the scope of the invention which is set forth in the following claims.
Fig. 5 illustrates an alternate embodiment of the system shown in Fig. 1, the alternate configuration replacing tank 101 with a horizontally configured cylindrical tank 501, replacing membrane 105 with an appropriately shaped membrane 503, replacing membrane 106 with an appropriately shaped membrane 504, replacing membrane 107 with an appropriately shaped membrane 505, replacing metal member 117 with disc-shaped metal member 507, replacing metal member 118 with disc-shaped metal member 508, replacing high voltage electrode 119 with disc-shaped high voltage electrode 509, replacing metal member 121 with disc-shaped metal member 511, replacing metal member 122 with disc-shaped metal member 512, replacing high voltage electrode 123 with disc-shaped high voltage electrode 513, replacing metal member 125 with disc-shaped metal member 515, replacing metal member 126 with disc-shaped metal member 516, replacing high voltage electrode 127 with disc-shaped high voltage electrode 517, replacing metal member 129 with disc-shaped metal member 519, replacing metal member 130 with disc-shaped metal member 520, and replacing high voltage electrode 131 with disc-shaped high voltage electrode 521.
It will be appreciated that the supply electronics (i.e., high voltage power supply, high voltage switch, pulse generator) shown in Figs. 1-5 represent only one exemplary configuration and that other configurations can be used to supply the requisite pulsed and timed power to the high voltage electrodes within the,cells of the electrolysis system of the invention.
Figs. 6 and 7 illustrate two additional alternate, and exemplary, configurations. Specifically, Fig. 6 illustrates a system similar to that shown in Fig. 1, except that high voltage supply 133 and high voltage switch 137 are combined into a single high voltage switching power supply 601. The embodiment illustrated in Fig. 7 combines the pulse generation within the power supply, i.e., high voltage supply 701.
It should be understood that the electrolysis system of the present invention can be operated in a number of modes, the primary differences between modes being the degree of process optimization used during operation. For example, Fig. 8 illustrates one method of operation requiring minimal optimization. As illustrated, initially the electrolysis tank, e.g., tank 101, is filled with water (step 801). Preferably the level of water in the tank at least covers the top of the electrodes. The electrolyte can either be mixed into the water prior to filling the tank or after the tank is filled. The frequency of the pulse generator is then set (step 803) as well as the pulse duration (step 805). The initial voltage setting for the high voltage power supply is also set (step 807). It will be appreciated that the order of set-up is clearly not critical to the electrolysis process. Typically, prior to the initiation of electrolysis, the temperature of the water is at room temperature.
Once set-up is complete, electrolysis is initiated (step 809). During the electrolysis process (step 811), and as previously noted, the water is heated by the process itself.
Eventually, when operation is no longer desirable, the electrolysis process is suspended (step 813). If desired, prior to further operation the tank can be drained (step 815) and refilled (step 817). Prior to refilling the tank, a series of optional steps can be performed. For example, the tank can be washed out (optional step 819) and the electrodes and/or metal members can be cleaned, for example to remove oxides, by washing with diluted acids (optional step 821).
Spent, or used up, electrodes and/or metal members can also be replaced prior to refilling (optional step 823). After cleaning the system and/or replacing electrodes/members as deemed necessary, and refilling the system, the system is ready to reinitiate the electrolysis process.
The above sequence of processing steps works best once the operational parameters have been optimized for a specific system configuration since the system configuration will impact the heat generation efficiency of the process.
Exemplary system configuration parameters that affect the optimal electrolysis settings include tank size, quantity of water, type and/or quality of water, electrolyte composition, electrolyte concentration, electrode size, electrode composition, electrode shape, electrode configuration, electrode separation, metal member size, metal member composition, metal member shape, metal member configuration, metal member separation, cell number, cell separation, initial water temperature, high voltage setting, pulse frequency and pulse duration.
Fig. 9 illustrates an alternate procedure, one in which the process undergoes optimization. Initially the tank is filled (step 901) and initial settings for pulse frequency (step 903), pulse duration (step 905) and high voltage supply output (step 907) are made. Typically the initial settings are based on previous settings that have been optimized for a similarly configured system. For example, assuming that the new configuration was the same as a previous configuration except for the composition of the electrodes, a reasonable initial set-up would be the optimized set-up from the previous configuration.
After the initial set-up is completed, electrolysis is initiated (step 909) and system output is monitored (step 911), for example absolute temperature or the rate of temperature increase. Although system optimization can begin immediately, preferably the system is allowed to run for an initial period of time (step 913) prior to optimization.
The initial period of operation can be based on achieving a predetermined output, for example a specific level of temperature increase, or achieving a steady state output (e.g., steady state temperature).
Alternately the initial period of time can simply be a predetermined time period, for example 6 hours.
After the initial time period is exceeded, the system output (e.g., temperature rate increase, steady state temperature, etc.) is monitored (step 915) while optimizing one or more of the operational parameters. Although the order of parameter optimization is not critical, in at least one preferred embodiment the first parameter to be optimized is pulse duration (step 917).
Then the pulse frequency is optimized (step 918), followed by optimization of the high voltage (step 919). In this embodiment after optimization is complete the electrolysis process is allowed to continue (step 921) without further optimization until the process is halted, step 923. In another, and preferred, alternative approach illustrated in Fig. 10, one or more of optimization steps 917-919 are performed continuously throughout the electrolysis process until electrolysis is suspended.
Note that the optimization processes described relative to Figs. 9 and 10 assume that (i) the cells physical geometry is fixed and (ii) there is no control over the high voltage applied to individual cell electrodes. If the system does include means for adjusting the physical geometry of the individual cells during electrolysis, for example the spacing between the electrodes within the cells or the cell-to-cell spacing, these parameters can also be altered to further optimize the electrolysis process during system operation. The system can also be configured to provide additional control over the high voltage applied to the cells. For example, the system shown in Fig. 11 uses a pair of high voltage power supplies 1101/1102 and associated high voltage switches 1103/1104. Systems such as these, although more complex, provide further control and therefore potentially greater optimization.
The optimization process described relative to Figs. 9 and 10 can be performed manually. In the preferred embodiment, however, the system or portions of the system are controlled via a system controller such as controller 1201 shown in an alternate embodiment of the configuration illustrated in Fig. 1(i.e., Fig. 12). Assuming that controller 1201 is used to control and optimize the pulse frequency, pulse duration and high voltage, system controller 1201 is coupled to the pulse generator and the voltage supply as shown. If the system controller is only used to control and optimize a subset of these parameters, the system controller is coupled accordingly (i.e., coupled to the pulse generator to control pulse frequency and duration;
coupled to the high voltage source to control the high voltage). In order to allow optimization automation, system controller 1201 is also coupled to a system monitor, for example one or more temperature monitors (e.g., monitor 1203). In at least one preferred embodiment system controller 1201 is also coupled to a monitor 1205, monitor 1205 providing either the pH or the resistivity of liquid 103 within electrolysis tank 101, thereby providing means for determining when additional electrolyte needs to be added. In at least one preferred embodiment system controller 1201 is also coupled to a liquid level monitor 1207, thereby providing means for determining when additional water needs to be added to the electrolysis tank.
Preferably system controller 1201 is also coupled to one or more flow valves 1209 which allow water, electrolyte, or a combination of water and electrolyte to be automatically added to the electrolysis system in response to pHlresistivity data provided by monitor 1205 (i.e., when the monitored pH/resistivity falls outside of a preset range) and/or liquid level data provided by monitor 1207 (i.e., when the monitored liquid level falls below a preset value).
As will be understood by those familiar with the art, the present invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. Accordingly, the disclosures and descriptions herein are intended to be illustrative, but not limiting, of the scope of the invention which is set forth in the following claims.
Claims (58)
1. An electrolysis system comprising:
an electrolysis tank;
a plurality of electrolysis cells within said electrolysis tank, each of said plurality of electrolysis cells comprising:
a membrane dividing said electrolysis cell into a first region and a second region, wherein said membrane permits ion and electron exchange between said first and second regions;
a plurality of metal members, said plurality of metal members comprised of at least a first metal member and at least a second metal member contained within said first region, and said plurality of metal members comprised of at least a third metal member and at least a fourth metal member contained within said second region;
and a plurality of high voltage electrodes, said plurality of high voltage electrodes comprised of at least a first high voltage anode contained within said first region and interposed between said first metal member and said second metal member, and said plurality of high voltage electrodes comprised of at least a first high voltage cathode contained within said second region and interposed between said third metal member and said fourth metal member;
a high voltage source electrically connected to said plurality of high voltage electrodes of each electrolysis cell; and means for pulsing said high voltage source at a specific frequency and a specific pulse duration.
an electrolysis tank;
a plurality of electrolysis cells within said electrolysis tank, each of said plurality of electrolysis cells comprising:
a membrane dividing said electrolysis cell into a first region and a second region, wherein said membrane permits ion and electron exchange between said first and second regions;
a plurality of metal members, said plurality of metal members comprised of at least a first metal member and at least a second metal member contained within said first region, and said plurality of metal members comprised of at least a third metal member and at least a fourth metal member contained within said second region;
and a plurality of high voltage electrodes, said plurality of high voltage electrodes comprised of at least a first high voltage anode contained within said first region and interposed between said first metal member and said second metal member, and said plurality of high voltage electrodes comprised of at least a first high voltage cathode contained within said second region and interposed between said third metal member and said fourth metal member;
a high voltage source electrically connected to said plurality of high voltage electrodes of each electrolysis cell; and means for pulsing said high voltage source at a specific frequency and a specific pulse duration.
2. The electrolysis system of claim 1, further comprising a system controller coupled to said electrolysis system.
3. The electrolysis system of claim 2, wherein said system controller is coupled to at least one of said high voltage source and said pulsing means.
4. The electrolysis system of claim 2, wherein said system controller is coupled to a temperature monitor.
5. The electrolysis system of claim 4, wherein said temperature monitor is contained within said electrolysis tank.
6. The electrolysis system of claim 2, wherein said system controller is coupled to a flow valve within an inlet line coupled to said electrolysis tank.
7. The electrolysis system of claim 2, wherein said system controller is coupled to a water level monitor within said electrolysis tank.
8. The electrolysis system of claim 2, wherein said system controller is coupled to a pH monitor within said electrolysis tank.
9. The electrolysis system of claim 2, wherein said system controller is coupled to a resistivity monitor within said electrolysis tank.
10. The electrolysis system of claim 1, wherein said pulsing means comprises a pulse generator coupled to said high voltage source.
11. The electrolysis system of claim 10, wherein said pulse generator is integrated within said high voltage source.
12. The electrolysis system of claim 1, wherein said pulsing means comprises a pulse generator coupled to a high voltage switch, wherein said high voltage switch is coupled to said high voltage source.
13. The electrolysis system of claim 1, further comprising means for cooling said electrolysis system.
14. The electrolysis system of claim 13, wherein said cooling means is comprised of a conduit containing a heat transfer medium, wherein a portion of said conduit is in thermal communication with at least a portion of said electrolysis tank.
15. The electrolysis system of claim 14, wherein said portion of said conduit surrounds at least a portion of said electrolysis tank.
16. The electrolysis system of claim 14, wherein said portion of said conduit is contained within said electrolysis tank.
17. The electrolysis system of claim 14, wherein said portion of said conduit is integrated within a portion of a wall comprising said electrolysis tank.
18. The electrolysis system of claim 14, wherein said heat transfer medium is comprised of water.
19. The electrolysis system of claim 1, further comprising a liquid within said electrolysis tank.
20. The electrolysis system of claim 19, wherein said liquid includes at least one of water, deuterated water, tritiated water, semiheavy water, heavy oxygen water, water containing an isotope of hydrogen, or water containing an isotope of oxygen.
21. The electrolysis system of claim 19, further comprising an electrolyte within said liquid, said electrolyte having a concentration of between 0.05 and 10.0 percent by weight.
22. The electrolysis system of claim 19, further comprising an electrolyte within said liquid, said electrolyte having a concentration of between 0.05 and 2.0 percent by weight.
23. The electrolysis system of claim 19, further comprising an electrolyte within said liquid, said electrolyte having a concentration of between 0.1 and 0.5 percent by weight.
24. The electrolysis system of claim 1, wherein an output voltage corresponding to said high voltage source is between 50 volts and 50 kilovolts.
25. The electrolysis system of claim 1, wherein an output voltage corresponding to said high voltage source is between 100 volts and 5 kilovolts.
26. The electrolysis system of claim 1, wherein said first metal member is comprised of a first material, wherein said second metal member is comprised of a second material, wherein said third metal member is comprised of a third material, wherein said fourth metal member is comprised of a fourth material, wherein said first high voltage anode is comprised of a fifth material, wherein said first high voltage cathode is comprised of a sixth material, and wherein said first, second, third, fourth, fifth and sixth materials are selected from the group consisting of titanium, stainless steel, copper, iron, steel, cobalt, manganese, zinc, nickel, platinum, palladium, carbon, graphite, carbon-graphite and alloys of titanium, stainless steel, copper, iron, steel, cobalt, manganese, zinc, nickel, platinum, palladium, carbon, graphite, and carbon-graphite.
27. The electrolysis system of claim 1, wherein said plurality of metal members are comprised of a first material, wherein said plurality of high voltage electrodes are comprised of a second material, and wherein said first and second materials are selected from the group consisting of titanium, stainless steel, copper, iron, steel, cobalt, manganese, zinc, nickel, platinum, palladium, carbon, graphite, carbon-graphite and alloys of titanium, stainless steel, copper, iron, steel, cobalt, manganese, zinc, nickel, platinum, palladium, carbon, graphite, and carbon-graphite.
28. The electrolysis system of claim 1, wherein said metal members within each electrolysis cell are coplanar.
29. The electrolysis system of claim 1, wherein said specific frequency is between 50 Hz and 1 MHz.
30. The electrolysis system of claim 1, wherein said specific frequency is between 100 Hz and 10 kHz.
31. The electrolysis system of claim 1, wherein said specific pulse duration is between 0.01 and 75 percent of a time period defined by said specific frequency.
32. The electrolysis system of claim 1, wherein said specific pulse duration is between 1 and 50 percent of a time period defined by said specific frequency.
33. A method of operating a multi-cell electrolysis system comprising the steps of applying a high voltage to at least a first high voltage anode and a first high voltage cathode contained within each of a plurality of electrolysis cells contained within an electrolysis tank of said electrolysis system, said high voltage applying step further comprising the step of pulsing said high voltage at a first frequency and with a first pulse duration, and wherein said first high voltage anode is interposed between a first metal member and a second metal member within a first region of each of said plurality of electrolysis cells, and wherein said first high voltage cathode is interposed between a third metal member and a fourth metal member within a second region of each of said plurality of electrolysis cells.
34. A method of operating an electrolysis system comprising the steps of:
positioning a plurality of electrolysis cells within an electrolysis tank, wherein each of said electrolysis cells is comprised of a membrane dividing each of said electrolysis cells into a first region and a second region;
filling said electrolysis tank with a liquid;
positioning a plurality of metal members within each of said plurality of electrolysis cells, wherein said plurality of metal members is comprised of at least a first metal member, a second metal member, a third metal member and a fourth metal member, wherein said positioning step further comprises the steps of positioning said first and second metal members within said first region of each of said electrolysis cells and positioning said third and fourth metal members within said second region of each of said electrolysis cells;
positioning a plurality of high voltage electrodes within each of said plurality of electrolysis cells, wherein said plurality of high voltage electrodes is comprised of at least a first high voltage anode and a first high voltage cathode, wherein said positioning step further comprises the steps of positioning said first high voltage anode between said first and second metal members within said first region of each of said electrolysis cells and positioning said first high voltage cathode between said third and fourth metal members within said second region of each of said electrolysis cells; and applying a high voltage to said plurality of high voltage electrodes, said high voltage applying step further comprising the step of pulsing said high voltage at a first frequency and with a first pulse duration.
positioning a plurality of electrolysis cells within an electrolysis tank, wherein each of said electrolysis cells is comprised of a membrane dividing each of said electrolysis cells into a first region and a second region;
filling said electrolysis tank with a liquid;
positioning a plurality of metal members within each of said plurality of electrolysis cells, wherein said plurality of metal members is comprised of at least a first metal member, a second metal member, a third metal member and a fourth metal member, wherein said positioning step further comprises the steps of positioning said first and second metal members within said first region of each of said electrolysis cells and positioning said third and fourth metal members within said second region of each of said electrolysis cells;
positioning a plurality of high voltage electrodes within each of said plurality of electrolysis cells, wherein said plurality of high voltage electrodes is comprised of at least a first high voltage anode and a first high voltage cathode, wherein said positioning step further comprises the steps of positioning said first high voltage anode between said first and second metal members within said first region of each of said electrolysis cells and positioning said first high voltage cathode between said third and fourth metal members within said second region of each of said electrolysis cells; and applying a high voltage to said plurality of high voltage electrodes, said high voltage applying step further comprising the step of pulsing said high voltage at a first frequency and with a first pulse duration.
35. The method of claim 34, further comprising the step of selecting said liquid from the group consisting of water, deuterated water, tritiated water, semiheavy water, heavy oxygen water, water containing an isotope of hydrogen, or water containing an isotope of oxygen.
36. The method of claim 34, further comprising the steps of:
monitoring a liquid level within said electrolysis tank; and adding more of said liquid to said electrolysis tank when said monitored liquid level falls below a preset value.
monitoring a liquid level within said electrolysis tank; and adding more of said liquid to said electrolysis tank when said monitored liquid level falls below a preset value.
37. The method of claim 34, further comprising the step of adding an electrolyte to said liquid.
38. The method of claim 37, further comprising the step of selecting a concentration of said electrolyte to be within a range of 0.05 to 10.0 percent by weight.
39. The method of claim 37, further comprising the step of selecting a concentration of said electrolyte to be within a range of 0.05 to 2.0 percent by weight.
40. The method of claim 37, further comprising the step of selecting a concentration of said electrolyte to be within a range of 0.1 to 0.5 percent by weight.
41. The method of claim 34, further comprising the steps of:
monitoring pH of said liquid within said electrolysis tank; and adding electrolyte to said liquid when said monitored pH falls outside of a preset range.
monitoring pH of said liquid within said electrolysis tank; and adding electrolyte to said liquid when said monitored pH falls outside of a preset range.
42. The method of claim 34, further comprising the steps of:
monitoring resistivity of said liquid within said electrolysis tank; and adding electrolyte to said liquid when said monitored resistivity falls outside of a preset range.
monitoring resistivity of said liquid within said electrolysis tank; and adding electrolyte to said liquid when said monitored resistivity falls outside of a preset range.
43. The method of claim 34, further comprising the steps of:
fabricating said plurality of metal members from a first material;
fabricating said plurality of high voltage electrodes from a second material;
and selecting said first material and said second material from the group consisting of steel, nickel, copper, iron, stainless steel, cobalt, manganese, zinc, titanium, platinum, palladium, carbon, graphite, carbon-graphite and alloys of steel, nickel, copper, iron, stainless steel, cobalt, manganese, zinc, titanium, platinum, palladium, carbon, graphite, and carbon-graphite.
fabricating said plurality of metal members from a first material;
fabricating said plurality of high voltage electrodes from a second material;
and selecting said first material and said second material from the group consisting of steel, nickel, copper, iron, stainless steel, cobalt, manganese, zinc, titanium, platinum, palladium, carbon, graphite, carbon-graphite and alloys of steel, nickel, copper, iron, stainless steel, cobalt, manganese, zinc, titanium, platinum, palladium, carbon, graphite, and carbon-graphite.
44. The method of claim 34, further comprising the steps of:
fabricating said first metal member from a first material;
fabricating said second metal member from a second material;
fabricating said third metal member from a third material;
fabricating said fourth metal member from a fourth material;
fabricating said first high voltage anode from a fifth material;
fabricating said first high voltage cathode from a sixth material; and selecting said first, second, third, fourth, fifth and sixth materials from the group consisting of titanium, stainless steel, copper, iron, steel, cobalt, manganese, zinc, nickel, platinum, palladium, carbon, graphite, carbon-graphite and alloys of titanium, stainless steel, copper, iron, steel, cobalt, manganese, zinc, nickel, platinum, palladium, carbon, graphite, and carbon-graphite.
fabricating said first metal member from a first material;
fabricating said second metal member from a second material;
fabricating said third metal member from a third material;
fabricating said fourth metal member from a fourth material;
fabricating said first high voltage anode from a fifth material;
fabricating said first high voltage cathode from a sixth material; and selecting said first, second, third, fourth, fifth and sixth materials from the group consisting of titanium, stainless steel, copper, iron, steel, cobalt, manganese, zinc, nickel, platinum, palladium, carbon, graphite, carbon-graphite and alloys of titanium, stainless steel, copper, iron, steel, cobalt, manganese, zinc, nickel, platinum, palladium, carbon, graphite, and carbon-graphite.
45. The method of claim 34, further comprising the step of selecting said high voltage within the range of 50 volts to 50 kilovolts.
46. The method of claim 34, further comprising the step of selecting said high voltage within the range of 100 volts to 5 kilovolts.
47. The method of claim 34, further comprising the step of selecting said first frequency to be within the range of 50 Hz to 1 MHz.
48. The method of claim 34, further comprising the step of selecting said first frequency to be within the range of 100 Hz to 10 kHz.
49. The method of claim 34, further comprising the step of selecting said first pulse duration to be between 0.01 and 75 percent of a time period defined by said first frequency.
50. The method of claim 34, further comprising the step of selecting said first pulse duration to be between 1 and 50 percent of a time period defined by said first frequency.
51. The method of claim 34, further comprising the steps of:
monitoring an electrolysis system output; and optimizing an operating parameter of said electrolysis system in response to said monitored electrolysis system output.
monitoring an electrolysis system output; and optimizing an operating parameter of said electrolysis system in response to said monitored electrolysis system output.
52. The method of claim 51, wherein said optimizing step is performed after completing at least 6 hours of continuous electrolysis.
53. The method of claim 51, further comprising the step of selecting said high voltage as said operating parameter.
54. The method of claim 51, further comprising the step of selecting said first frequency as said operating parameter.
55. The method of claim 51, further comprising the step of selecting said first pulse duration as said operating parameter.
56. The method of claim 51, further comprising the step of selecting a rate of heat generation as said monitored electrolysis system output.
57. The method of claim 51, wherein said optimizing step is performed repeatedly.
58. The method of claim 51, wherein said optimizing step is automated.
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US12/151,502 US20080296169A1 (en) | 2007-05-30 | 2008-05-07 | Multi-cell single voltage electrolysis apparatus and method of using same |
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CA2590487A1 (en) * | 2007-05-30 | 2008-11-30 | Kuzo Holding Inc. | Multi-cell dual voltage electrolysis apparatus and method of using same |
CA2590490A1 (en) * | 2007-05-30 | 2008-11-30 | Kuzo Holding Inc. | Pulsed electrolysis apparatus and method of using same |
US10892525B2 (en) * | 2016-06-29 | 2021-01-12 | University Of Kentucky Research Foundation | Rechargeable batteries including high-voltage cathode and redox shuttle conferring overcharge protection |
US10854911B2 (en) * | 2016-07-19 | 2020-12-01 | University Of Kentucky Research Foundation | 1,9,10-substituted phenothiazine derivatives with strained radical cations and use thereof |
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US3954592A (en) * | 1974-07-03 | 1976-05-04 | Beeston Company Limited | Electrolysis apparatus |
GB1552311A (en) * | 1977-03-10 | 1979-09-12 | Inoue Japax Res | Electrolytic gernaration of hydrogen and oxygen |
US4219394A (en) * | 1978-03-22 | 1980-08-26 | Diamond Shamrock Corporation | Membrane assembly for electrolytic cells |
CA1155085A (en) * | 1978-04-14 | 1983-10-11 | Sameer M. Jasem | Electrochemical gas separation including catalytic regeneration |
JPH0217005Y2 (en) * | 1987-03-08 | 1990-05-11 | ||
US6638413B1 (en) * | 1989-10-10 | 2003-10-28 | Lectro Press, Inc. | Methods and apparatus for electrolysis of water |
JP3120521B2 (en) * | 1991-12-24 | 2000-12-25 | カシオ計算機株式会社 | Anodizing method for metal film |
US5587057A (en) * | 1992-03-19 | 1996-12-24 | David M. A. Metzler | Highly conductive liquid media electrocoagulation |
US5989407A (en) * | 1997-03-31 | 1999-11-23 | Lynntech, Inc. | Generation and delivery device for ozone gas and ozone dissolved in water |
US6576096B1 (en) * | 1998-01-05 | 2003-06-10 | Lynntech International, Ltd. | Generation and delivery device for ozone gas and ozone dissolved in water |
US6080288A (en) * | 1998-05-29 | 2000-06-27 | Schwartz; Vladimir | System for forming nickel stampers utilized in optical disc production |
US6126794A (en) * | 1998-06-26 | 2000-10-03 | Xogen Power Inc. | Apparatus for producing orthohydrogen and/or parahydrogen |
US6969457B2 (en) * | 2002-10-21 | 2005-11-29 | General Electric Company | Method for partially stripping a coating from the surface of a substrate, and related articles and compositions |
CA2590487A1 (en) * | 2007-05-30 | 2008-11-30 | Kuzo Holding Inc. | Multi-cell dual voltage electrolysis apparatus and method of using same |
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