US20110048961A1 - System and Method for Refilling an Electrolyzer Tank from a Water Reservoir - Google Patents
System and Method for Refilling an Electrolyzer Tank from a Water Reservoir Download PDFInfo
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- US20110048961A1 US20110048961A1 US12/868,438 US86843810A US2011048961A1 US 20110048961 A1 US20110048961 A1 US 20110048961A1 US 86843810 A US86843810 A US 86843810A US 2011048961 A1 US2011048961 A1 US 2011048961A1
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- Prior art keywords
- water
- make
- electrolyzer
- electrolyte
- pump
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 143
- 238000000034 method Methods 0.000 title claims description 11
- 239000003792 electrolyte Substances 0.000 claims abstract description 58
- 238000005868 electrolysis reaction Methods 0.000 claims abstract description 51
- 239000007789 gas Substances 0.000 claims abstract description 45
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000001257 hydrogen Substances 0.000 claims abstract description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 26
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000001301 oxygen Substances 0.000 claims abstract description 20
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 claims abstract description 9
- 239000012530 fluid Substances 0.000 claims description 5
- 230000032258 transport Effects 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 238000004891 communication Methods 0.000 claims description 3
- 230000003213 activating effect Effects 0.000 claims 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 6
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 5
- 229910001882 dioxygen Inorganic materials 0.000 description 5
- 230000000630 rising effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 235000012206 bottled water Nutrition 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 238000003411 electrode reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Images
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
- C25B15/02—Process control or regulation
-
- 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
- C25B15/08—Supplying or removing reactants or electrolytes; Regeneration of electrolytes
-
- 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
Definitions
- the present invention relates generally to electrolyzer systems, and more specifically to systems for controlling fluid level within an electrolyzer, and most specifically to a system and method for maintaining electrolyte level and concentration within a water electrolyzer tank.
- the purpose of this invention is to create a highly efficient water electrolyzer that, for a give amount of hydrogen produced, also minimizes both the mass and volume of the device.
- a related objective of the invention is to create an electrolyzer that will have no electro-mechanical moving parts and that will be constructed to ensure high reliability even under harsh road conditions.
- Electrolysis of water is the decomposition of water (H 2 O) into oxygen (O 2 ) and hydrogen gas (H 2 ) due to an electric current being passed through the water.
- An electrical power source is connected to two electrodes, or two plates (typically made from some inert metal such as platinum or stainless steel), which are placed in the water.
- Hydrogen will appear at the cathode (the negatively charged electrode, where electrons are transferred to water molecules), and oxygen will appear at the anode (the positively charged electrode where electrons are transferred from water molecules to the electrode).
- the generated amount of hydrogen is twice the amount of oxygen, and both are proportional to the total electrical charge transmitted through the water. Electrons carry the current in the circuit external to the electrolysis cell and in the electrodes, while charged ions carry electric current through the water or electrolyte solution.
- an oxidation reaction occurs, where water is oxidized to generate oxygen gas and giving electrons to the anode.
- Electric current is carried through the electrolyte solution by way of movement of ions such as H + (aq) or OH ⁇ (aq).
- ions such as H + (aq) or OH ⁇ (aq).
- these ions are in very low concentration so an additional electrolyte must be added to allow practical values of current to flow.
- an alkalis such as Sodium Hydroxide (NaOH) or Potassium Hydroxide (KOH) is added in quite high concentrations.
- KOH Potassium Hydroxide
- a typical value for KOH would be about 30 wt %, the concentration at which the electrical conductivity reaches a maximum.
- N the number of moles of gas released by a current 1 in time t
- N I*t /( n*F ) (1)
- rate of hydrogen production is given by
- the minimum voltage required to electrolyze water is 1.23 V but higher voltages must be applied in order to increase the current. Voltage drops occur at the electrodes due to overpotential and across the electrolyte gap between to two electrodes.
- Overpotential ( ⁇ ) refers to the difference between the applied potential necessary to produce a current i and the equilibrium potential E 0 at zero current
- the overpotential is related to the current density by
- i 0 is a constant relating to the particular electrode reaction and the surface on which it occurs, e.g. platinum in KOH
- ⁇ is a constant usually with a value of 0.5
- F is the Faraday constant
- R the gas constant and T temperature in K
- A is the active area of the electrode
- I is the actual measured current.
- the gap between to two electrodes is filled with conducting electrolyte but does incur a potential drop. This potential drop is given by
- V electrolyte I*R (7)
- I is the current and R the resistance of the electrolyte
- A is the effective electrode area and d the electrode separation
- ⁇ is the conductivity of the electrolyte which is a function of the electrolyte composition and concentration and temperature.
- V E 0 + ⁇ anode ⁇ cathode +IR (9)
- V E 0 +B anode 1 n i 0 /i ⁇ B cathode 1 n i 0 /i+IR (10)
- the voltage can be reduced by increasing the effective surface area of the electrodes, reducing the electrode separation, increasing the concentration and temperature of the electrolyte and by catalyzing the electrodes which has the effect of increasing the value of i 0 .
- ⁇ G 0 and ⁇ H 0 are the standard Cibbs Energy Change and standard Enthalpy change for the electrolysis reaction.
- the maximum efficiency is 120%. This is greater than 100% because in principle the reaction can extract heat from the surroundings. In practice, however, the efficiency is below 100% because the driving voltage is always greater than 1.23 V.
- V is the cell operating voltage at a given current.
- V is given by equation (10).
- the cell voltage is about 2 V, and this would give an efficiency of about 74%.
- the most energy efficient electrolyzer is one that minimizes the overall cell impedance.
- the impedance of the electrolyzer is minimized by reducing the electrode gap, increasing the electrolyte conductivity and increasing the number of cells in series, usually to six.
- the electrode area is optimized to reduce cell impedance but to remain within the chosen current draw from the alternator.
- the electrolyte is potassium hydroxide the maximum conductivity occurs at about 28% by weight potassium hydroxide.
- An electrolyzer with 6 cells in series with stainless steel electrodes of 200 cm 2 and a spacing of 1 cm immersed in 28% KOH will operate at 12 V and about 30 A and produce about 1.3 L/min of hydrogen.
- This electrolyzer would require a minimum volume of about 1.5 L of electrolyte or about 1 L of water. This amount of water would be consumed in about 16.5 hours. Clearly the electrolyzer would cease to function as designed well before the 1 L of water was consumed.
- both the means of detection of water content and of transporting water between the two reservoirs should contain no moving parts, electrical contacts, switches or require any external control circuitry.
- a water electrolyzer system includes an electrolysis chamber for production of hydrogen and oxygen and a water reservoir from which make-up water is transported to the electrolysis chamber to maintain a constant hydrogen output.
- a system for controlling electrolyte level and concentration within a water electrolyzer includes an electrolysis chamber containing electrolyte for production of hydrogen and oxygen, a water reservoir containing make-up water and separated from the electrolysis chamber through a check valve that opens only when electrolyte level drops to a predetermined level, and a gas lift pump within the water reservoir connected to the electrolysis chamber through the check valve, the gas lift pump having electrodes immersed in the make-up water. Energization of the electrodes creates bubbles that transport the make-up water to the electrolysis chamber to maintain a desired concentration of the electrolyte during the production of hydrogen and oxygen.
- a method according to the invention maintains concentration of an electrolyte in a water electrolyzer during electrolysis of water.
- the method prescribes steps for containing the electrolyte within an electrolysis chamber, providing a water reservoir containing make-up water, connecting the make-up water to the electrolyte through a check valve that opens only when the electrolyte in the electrolysis chamber drops below a predetermined level, immersing a gas lift pump within the water reservoir so that the gas lift pump is in fluid communication with the electrolysis chamber through the check valve, and energizing the gas lift pump to transport the make-up water to the electrolysis chamber.
- FIG. 1 is a schematic diagram of one embodiment of a system according to the invention for maintaining concentration of an electrolyte in a water electrolyzer during electrolysis of water.
- the following disclosure presents an exemplary embodiment of the invention for refilling an electrolyzer tank from a water reservoir.
- the invention provides a highly reliable, robust and passive control system (and related methods) for maintaining electrolyte level and electrolyte concentration within an electrolyzer tank.
- This technology rectifies the limitations of prior fluid level control systems, particularly those employed in water electrolyzers designed for use with internal combustion engines.
- an electrolyzer may be optimized for efficiency and operational life.
- FIG. 1 an exemplary embodiment of the invention is depicted in the form of a schematic for a water electrolyzer.
- a container 2 holds an amount of water 4 , the free surface of which is labeled 3 and container 23 holds an amount of electrolyte 21 , the free surface of which is 19 .
- containers 2 and 23 may be formed within a common outer shell and separated by an inner wall 24 .
- Water may be added to container 2 via the filling port 1 , which may be closed during normal operation.
- the water may be distilled water, de-ionized water, bottled water, tap water or water containing some deliberately added chemical such as KOH.
- the electrolyte may be added to container 23 via the filling port 16 .
- the electrolyte may be added as solid KOH, NaOH, K 2 CO 3 , Na 2 CO 3 or as soluble salts, carbonates, or hydroxides with Group 1A or Group 2A metals from the periodic table.
- the solid alone may be added through port 16 , then water may be added from container 2 via gas lift pump 11 to achieve or maintain a desired electrolyte concentration.
- Electrodes 22 in the electrolysis chamber 23 are immersed in the electrolyte 21 and are connected to a supply of electric current 13 by wires 14 .
- the schematic depicts two unipolar electrodes 22 although three or more are possible in a serial array of electrodes, including one or more bipolar electrodes in the array that occupy intermediate positions between unipolar electrodes at either end of the array.
- an electrochemical reaction will occur that will produce hydrogen at the negative electrode (or cathode) and oxygen at the positively charged electrode (or anode).
- the mixture of these gasses will form bubbles that rise to the surface 19 of the electrolyte 21 .
- the gasses will then escape through vent 15 .
- float ball 20 and port 18 form a check valve that allows make-up water to flow into container 23 , but prevents the leakage of electrolyte 21 past port 18 .
- electrolyte level and composition is maintained constant, within some acceptable level of tolerance.
- Other check valve designs are possible within the scope of the invention.
- the check valve, and any parts thereof, preferably operate as passive components, and should be selected for high reliability.
- the gas lift pump 11 utilizes gas bubbles produced by electrolysis of water 4 by electrodes 7 . Only two electrodes 7 are required for the gas lift pump to operate, although more than two electrodes may be utilized, if desired.
- a shroud 8 may completely or partially surround the electrodes 7 . Bubbles of hydrogen and oxygen that form on electrodes 7 rise and are trapped by the shroud 8 to form a larger or aggregate bubble 6 . As the bubble 6 grows in size it will periodically release a rising bubble 12 into gas lift pump tube 11 . As the rising bubbles 12 rise in tube 11 they will push water from within shroud 8 into tube 11 and lift the water to the point 9 where it may flow into container 23 via an open valve 18 .
- valve port 18 In the event that valve port 18 is closed, then the water may exit tube 11 via an overflow opening 10 and fall back into the water container 2 .
- the electrolysis gasses of hydrogen and oxygen will also exit via opening 10 and then pass into container 23 via the gas pressure equalization port 17 .
- a horizontal segment 25 of tube 11 may be level at zero degrees with respect to the container bottom.
- the angle of segment 25 may depart slightly from zero (positively or negatively), or the cross sectional shape of segment 25 may be conical, to promote water flow into port 18 , or to promote the continued travel of bubbles 12 away from the water to prevent obstruction of the flow path.
- opening 10 may be designed to promote the escape of the electrolysis gases. For example, opening 10 may be enlarged beyond the diameter of tube 11 , or it may include one or more sharp edges for dividing or bursting bubbles 12 that rise to the top of the conduit.
- a lower end segment 26 of tube 11 may extend into and below the top of shroud 8 , as shown. In this way, segment 26 may form a primary chamber 27 wherein a bubble 6 may expand until it achieves a size sufficient to allow a portion of the bubble to wrap around the outer wall of segment 26 and break away as a rising bubble 12 . In another embodiment, a segment 26 may be configured to promote the release of an entire bubble 6 into tube 11 .
- the size and frequency of rising bubbles 12 , and the configuration of tube 11 and segment 26 should provide a supply of make-up water to container 23 that compensates for water lost from container 23 through electrolysis, evaporation and droplet formation.
- the gas lift pump 11 should be designed to cause a flow rate of water into container 23 in an amount equal to or greater than the actual rate of water loss from container 23 .
- some amount of make-up water supplied by the gas lift pump will remain within horizontal segment 25 in contact with the float ball, poised to replenish container 23 as soon as the level of electrolyte 21 drops below the predetermined minimum level.
- the size and frequency of rising bubbles 12 may be determined by adjusting the current and the size of segment 6 and inner chamber 27 .
- the gas lift pump may be energized using power supply 13 , or it may be energized from an independent power source. In the case where the power supply provides a constant voltage or current, the operation of the gas lift pump may be controlled by selecting the size and composition of electrodes 7 .
- gas lift pump 11 may produce bubbles by a means other than electrolysis.
- gas lift pump 11 may be a motorized pump that pumps air into the make-up water to produce bubbles, much like a fish tank water pump used to oxygenate an aquarium.
- a water electrolyzer system generally configured as disclosed herein optimizes electrolyzer operation in a number of ways.
- the overall weight of the electrolyzer is minimized by limiting the volume of the heavier electrolyte to the smallest volume (container 23 ) required for producing a desired amount of electrolysis gasses.
- the total volume of make-up water may be selected to achieve a desired operating time between refills. Because water is lighter than the electrolyte, the separation of make-up water from the electrolyte allows the total liquid weight of the electrolyzer (water plus electrolyte) to be minimized.
- electrical efficiency of the electrolyzer is maximized by maintaining a constant volume and concentration of electrolyte between the electrodes 22 .
- the ability to maintain a constant electrolyte concentration allows a designer to minimize heat losses for the duration of the electrolyzer duty cycle by optimizing electrolyzer performance based on power supply and electrode configuration. And with respect to reliability, the absence of moving parts, and the absence of control electronics, reduces the overall probability of system failure.
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- Chemical Kinetics & Catalysis (AREA)
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- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Automation & Control Theory (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Abstract
A system for controlling electrolyte level and concentration within a water electrolyzer includes an electrolysis chamber containing electrolyte for production of hydrogen and oxygen, a water reservoir containing make-up water and separated from the electrolysis chamber through a check valve that opens only when electrolyte level drops to a predetermined level, and a gas lift pump within the water reservoir connected to the electrolysis chamber through the check valve and having electrodes immersed in the make-up water. Energization of the electrodes creates bubbles that transport the make-up water to the electrolysis chamber to maintain a desired concentration of the electrolyte during the production of hydrogen and oxygen.
Description
- This application claims priority to U.S. Provisional Application 61/236,828, which was filed on Aug. 25, 2009 and which is fully incorporated herein by reference.
- 1. Field of the Invention
- The present invention relates generally to electrolyzer systems, and more specifically to systems for controlling fluid level within an electrolyzer, and most specifically to a system and method for maintaining electrolyte level and concentration within a water electrolyzer tank.
- 2. Description of Related Art
- The recovery of hydrogen and oxygen gas by means of electrolysis of water has been practiced for over a century. More recently, water electrolyzers have been used for the purpose of generating and supplying a small stream of hydrogen and oxygen gas as a fuel supplement to internal combustion engines. The hydrogen/oxygen gas stream is usually only a fraction of a percent of the intake combustion air flow but evidence has been presented to show that this small stream can reduce emissions of particulates from diesel engines and in some cases also reduce emissions of NOx and provide small increases in engine fuel efficiency. Typically these water electrolyzers are powered by electrical current from the vehicle battery or alternator and are fitted to the back of the cab compartment of a truck or under the hood of a car.
- To further improve the effectiveness of these devices it is necessary to minimize their volume and mass and maximize their energy efficiency for a given intended hydrogen or oxygen output. Furthermore it is important to operate an electrolyzer that can function reliably for thousands of hours in extremes of temperature, and in the presence of continuous shock and vibration and road grime and grit.
- The purpose of this invention is to create a highly efficient water electrolyzer that, for a give amount of hydrogen produced, also minimizes both the mass and volume of the device. A related objective of the invention is to create an electrolyzer that will have no electro-mechanical moving parts and that will be constructed to ensure high reliability even under harsh road conditions.
- Principles of Electrolyzers and of Electrolysis
- The science and engineering principles behind the design and operation of water electrolyzers are well known and understood. Some general principles follow.
- Electrolysis of water is the decomposition of water (H2O) into oxygen (O2) and hydrogen gas (H2) due to an electric current being passed through the water. An electrical power source is connected to two electrodes, or two plates (typically made from some inert metal such as platinum or stainless steel), which are placed in the water. Hydrogen will appear at the cathode (the negatively charged electrode, where electrons are transferred to water molecules), and oxygen will appear at the anode (the positively charged electrode where electrons are transferred from water molecules to the electrode). The generated amount of hydrogen is twice the amount of oxygen, and both are proportional to the total electrical charge transmitted through the water. Electrons carry the current in the circuit external to the electrolysis cell and in the electrodes, while charged ions carry electric current through the water or electrolyte solution.
- In the water at the negatively charged cathode, a reduction reaction takes place, with electrons (e−) from the cathode being given to water molecules to form hydrogen gas:
- Cathode (reduction): 2H2O(1)+2e−→H2(g)+2OH−(aq)
- At the positively charged anode, an oxidation reaction occurs, where water is oxidized to generate oxygen gas and giving electrons to the anode.
- Anode (oxidation): H2O(1)→1/2O2(g)+2H+(aq)+2e−
- Combining these two reactions with
- H2O(1)→2H+(aq)+2OH−(aq)
- yields the overall decomposition of water into oxygen and hydrogen:
- Overall reaction: 2H2O(1)→2H2(g)+O2(g)
- For every two electrons the number of hydrogen molecules produced is twice the number of oxygen molecules. Assuming equal temperature and pressure for both gases, the produced hydrogen gas has therefore twice the volume of the produced oxygen gas. In acid solution the reactions and standard electrode potentials are
-
2H +(aq)+2e − →H 2(g)E 0=0.00V -
1/2O 2(g)+2H +(aq)+2e − →H 2 O(1) E0=1.23V - giving a Standard EMF of 1.23V.
- In base solution the reactions and standard electrode potentials are
-
2H 2 O(1)+2e − →H 2(g)+2OH −(aq)E0=−0.83V -
1/2O 2(g)+2H 2 O(1)+2e −→2OH −(aq)E0=0.40V - giving a Standard EMF of 1.23V.
- Electric current is carried through the electrolyte solution by way of movement of ions such as H+(aq) or OH−(aq). However in pure water these ions are in very low concentration so an additional electrolyte must be added to allow practical values of current to flow. Typically an alkalis such as Sodium Hydroxide (NaOH) or Potassium Hydroxide (KOH) is added in quite high concentrations. A typical value for KOH would be about 30 wt %, the concentration at which the electrical conductivity reaches a maximum.
- Faraday's Law provides the relationship between the current and the rate of electrolysis,
- where N the number of moles of gas released by a current 1 in time t is given by
-
N=I*t/(n*F) (1) - N is the number of electrons required to deliver one mole of gas, for hydrogen n=2 for oxygen n=4. Thus the rate of hydrogen production is given by
-
ΔI/Δt=I/(2*F) (2) - The minimum voltage required to electrolyze water is 1.23 V but higher voltages must be applied in order to increase the current. Voltage drops occur at the electrodes due to overpotential and across the electrolyte gap between to two electrodes.
- Overpotential (η) refers to the difference between the applied potential necessary to produce a current i and the equilibrium potential E0 at zero current,
-
η=E−E 0 (3) - For the anode where oxygen is produced the overpotential is related to the current density by
-
i=i 0exp(−bη) (4) -
where -
b=αnF/RT and i=I/A (5) - and where i0 is a constant relating to the particular electrode reaction and the surface on which it occurs, e.g. platinum in KOH, α is a constant usually with a value of 0.5, F is the Faraday constant, R the gas constant and T temperature in K, A is the active area of the electrode and I is the actual measured current. A similar equation exists for the cathode but with different values of i0 and α. These equations can also be expressed in terms of the overvoltage as
-
η=B1n i 0 −B1ni=B1n i 0 /I (6) - where B=1/b.
- The gap between to two electrodes is filled with conducting electrolyte but does incur a potential drop. This potential drop is given by
-
V electrolyte =I*R (7) - where I is the current and R the resistance of the electrolyte, and where
-
R=A/d*κ (8) - where A is the effective electrode area and d the electrode separation, κ is the conductivity of the electrolyte which is a function of the electrolyte composition and concentration and temperature.
- The Current Voltage Characteristic for a single cell is therefore given by
-
V=E 0+ηanode−ηcathode +IR (9) -
V=E 0 +B anode1n i 0 /i−B cathode1n i 0 /i+IR (10) - It can be seen that for a given current the voltage can be reduced by increasing the effective surface area of the electrodes, reducing the electrode separation, increasing the concentration and temperature of the electrolyte and by catalyzing the electrodes which has the effect of increasing the value of i0.
- The maximum efficiency of an Electrolyzer c, is given by,
-
ε=ΔH 0 /ΔG 0 - where ΔG0 and ΔH0 are the standard Cibbs Energy Change and standard Enthalpy change for the electrolysis reaction. For water electrolysis the maximum efficiency is 120%. This is greater than 100% because in principle the reaction can extract heat from the surroundings. In practice, however, the efficiency is below 100% because the driving voltage is always greater than 1.23 V.
- The actual efficiency is given by
-
ε=ΔH 0/(nFV) - where V is the cell operating voltage at a given current. V is given by equation (10).
- At a practical current density of about 2 A cm−2, the cell voltage is about 2 V, and this would give an efficiency of about 74%.
- Electrolyzer Design
- From the above descriptions and equations it can be shown that the most energy efficient electrolyzer is one that minimizes the overall cell impedance. For an electrolyzer supplied with current from a vehicle alternator operating at a constant voltage of approximately 13 V and with a current draw limited to 20 to 30 A, the impedance of the electrolyzer is minimized by reducing the electrode gap, increasing the electrolyte conductivity and increasing the number of cells in series, usually to six. Under these circumstances the electrode area is optimized to reduce cell impedance but to remain within the chosen current draw from the alternator.
- If the electrolyte is potassium hydroxide the maximum conductivity occurs at about 28% by weight potassium hydroxide. An electrolyzer with 6 cells in series with stainless steel electrodes of 200 cm2 and a spacing of 1 cm immersed in 28% KOH will operate at 12 V and about 30 A and produce about 1.3 L/min of hydrogen. This electrolyzer would require a minimum volume of about 1.5 L of electrolyte or about 1 L of water. This amount of water would be consumed in about 16.5 hours. Clearly the electrolyzer would cease to function as designed well before the 1 L of water was consumed.
- To facilitate long periods of operation between additions of water and to maintain electrolyzer energy efficiency it is necessary to add water as required to the electrolyzer, for example, from a water reservoir. In conventional practice, this requires a means for detecting the loss of water from the electrolyte and a means of transporting water from the reservoir to the electrolyte and a means of detecting when sufficient water has been added to replenish the water content. An electrolyzer is inherently a very robust device. Provided that the electrodes are not corroded by the applied potentials or reaction with the electrolyte or produced gasses then operational reliability is very high. However, the introduction of electro-mechanical level detectors, valves and pumps can severely reduce reliability, especially when exposed to the harsh environment experienced by devices operating large diesel engines such as long haul trucks, bull dozers, cranes, etc. Ideally both the means of detection of water content and of transporting water between the two reservoirs should contain no moving parts, electrical contacts, switches or require any external control circuitry.
- The present invention discloses exemplary systems and methods for refilling an electrolyzer tank from a water reservoir. In one embodiment, a water electrolyzer system according to the invention includes an electrolysis chamber for production of hydrogen and oxygen and a water reservoir from which make-up water is transported to the electrolysis chamber to maintain a constant hydrogen output.
- In another embodiment, a system for controlling electrolyte level and concentration within a water electrolyzer includes an electrolysis chamber containing electrolyte for production of hydrogen and oxygen, a water reservoir containing make-up water and separated from the electrolysis chamber through a check valve that opens only when electrolyte level drops to a predetermined level, and a gas lift pump within the water reservoir connected to the electrolysis chamber through the check valve, the gas lift pump having electrodes immersed in the make-up water. Energization of the electrodes creates bubbles that transport the make-up water to the electrolysis chamber to maintain a desired concentration of the electrolyte during the production of hydrogen and oxygen.
- A method according to the invention maintains concentration of an electrolyte in a water electrolyzer during electrolysis of water. The method prescribes steps for containing the electrolyte within an electrolysis chamber, providing a water reservoir containing make-up water, connecting the make-up water to the electrolyte through a check valve that opens only when the electrolyte in the electrolysis chamber drops below a predetermined level, immersing a gas lift pump within the water reservoir so that the gas lift pump is in fluid communication with the electrolysis chamber through the check valve, and energizing the gas lift pump to transport the make-up water to the electrolysis chamber.
- Other systems, methods, features and advantages of the invention will be or will become apparent to one with skill in the art upon examination of the following figures and detailed description. It is intended that all such additional systems, methods, features and advantages be included within this description, be within the scope of the invention, and be protected by the accompanying claims. Component parts shown in the drawings are not necessarily to scale, and may be exaggerated to better illustrate the important features of the invention. In the drawings, like reference numerals designate like parts throughout the different views, wherein:
-
FIG. 1 is a schematic diagram of one embodiment of a system according to the invention for maintaining concentration of an electrolyte in a water electrolyzer during electrolysis of water. - The following disclosure presents an exemplary embodiment of the invention for refilling an electrolyzer tank from a water reservoir. The invention provides a highly reliable, robust and passive control system (and related methods) for maintaining electrolyte level and electrolyte concentration within an electrolyzer tank. This technology rectifies the limitations of prior fluid level control systems, particularly those employed in water electrolyzers designed for use with internal combustion engines. Using the technology of the present invention, an electrolyzer may be optimized for efficiency and operational life.
- Referring to
FIG. 1 , an exemplary embodiment of the invention is depicted in the form of a schematic for a water electrolyzer. In normal operation, acontainer 2 holds an amount of water 4, the free surface of which is labeled 3 andcontainer 23 holds an amount ofelectrolyte 21, the free surface of which is 19. In one embodiment, 2 and 23 may be formed within a common outer shell and separated by ancontainers inner wall 24. Water may be added tocontainer 2 via the fillingport 1, which may be closed during normal operation. The water may be distilled water, de-ionized water, bottled water, tap water or water containing some deliberately added chemical such as KOH. The electrolyte may be added tocontainer 23 via the fillingport 16. The electrolyte may be added as solid KOH, NaOH, K2CO3, Na2CO3 or as soluble salts, carbonates, or hydroxides with Group 1A or Group 2A metals from the periodic table. Alternatively the solid alone may be added throughport 16, then water may be added fromcontainer 2 viagas lift pump 11 to achieve or maintain a desired electrolyte concentration. -
Electrodes 22 in theelectrolysis chamber 23 are immersed in theelectrolyte 21 and are connected to a supply of electric current 13 bywires 14. The schematic depicts twounipolar electrodes 22 although three or more are possible in a serial array of electrodes, including one or more bipolar electrodes in the array that occupy intermediate positions between unipolar electrodes at either end of the array. When electric current flows from thepower supply 13 to theelectrodes 22 an electrochemical reaction will occur that will produce hydrogen at the negative electrode (or cathode) and oxygen at the positively charged electrode (or anode). The mixture of these gasses will form bubbles that rise to thesurface 19 of theelectrolyte 21. The gasses will then escape throughvent 15. As the electrolysis proceeds, water in the electrolyte is converted into hydrogen and oxygen and the volume of the electrolyte incontainer 23 diminishes. The height of theelectrolyte surface 19 will drop to below a predetermined minimum level, causing afloat ball 20 to drop and open avalve port 18. This allows make-up water fromcontainer 2 to flow intocontainer 23 via thegas lift pump 11. As water flows intocontainer 23, the level of the electrolyte will rise, causingball 20 to rise and seat against thevalve port 18, thereby shutting off the flow of water fromgas lift pump 11. In this respect,float ball 20 andport 18 form a check valve that allows make-up water to flow intocontainer 23, but prevents the leakage ofelectrolyte 21past port 18. By this means the electrolyte level and composition is maintained constant, within some acceptable level of tolerance. Other check valve designs are possible within the scope of the invention. The check valve, and any parts thereof, preferably operate as passive components, and should be selected for high reliability. - The
gas lift pump 11 utilizes gas bubbles produced by electrolysis of water 4 byelectrodes 7. Only twoelectrodes 7 are required for the gas lift pump to operate, although more than two electrodes may be utilized, if desired. Ashroud 8 may completely or partially surround theelectrodes 7. Bubbles of hydrogen and oxygen that form onelectrodes 7 rise and are trapped by theshroud 8 to form a larger oraggregate bubble 6. As thebubble 6 grows in size it will periodically release a risingbubble 12 into gaslift pump tube 11. As the rising bubbles 12 rise intube 11 they will push water from withinshroud 8 intotube 11 and lift the water to thepoint 9 where it may flow intocontainer 23 via anopen valve 18. In the event thatvalve port 18 is closed, then the water may exittube 11 via anoverflow opening 10 and fall back into thewater container 2. The electrolysis gasses of hydrogen and oxygen will also exit via opening 10 and then pass intocontainer 23 via the gaspressure equalization port 17. - In one embodiment, a
horizontal segment 25 oftube 11 may be level at zero degrees with respect to the container bottom. In another embodiment, the angle ofsegment 25 may depart slightly from zero (positively or negatively), or the cross sectional shape ofsegment 25 may be conical, to promote water flow intoport 18, or to promote the continued travel ofbubbles 12 away from the water to prevent obstruction of the flow path. In another embodiment, opening 10 may be designed to promote the escape of the electrolysis gases. For example, opening 10 may be enlarged beyond the diameter oftube 11, or it may include one or more sharp edges for dividing or burstingbubbles 12 that rise to the top of the conduit. - In another embodiment, a
lower end segment 26 oftube 11 may extend into and below the top ofshroud 8, as shown. In this way,segment 26 may form aprimary chamber 27 wherein abubble 6 may expand until it achieves a size sufficient to allow a portion of the bubble to wrap around the outer wall ofsegment 26 and break away as a risingbubble 12. In another embodiment, asegment 26 may be configured to promote the release of anentire bubble 6 intotube 11. - For proper operation, the size and frequency of rising
bubbles 12, and the configuration oftube 11 andsegment 26 should provide a supply of make-up water tocontainer 23 that compensates for water lost fromcontainer 23 through electrolysis, evaporation and droplet formation. In other words, thegas lift pump 11 should be designed to cause a flow rate of water intocontainer 23 in an amount equal to or greater than the actual rate of water loss fromcontainer 23. In one mode of operation, when the float ball closes the check valve, some amount of make-up water supplied by the gas lift pump will remain withinhorizontal segment 25 in contact with the float ball, poised to replenishcontainer 23 as soon as the level ofelectrolyte 21 drops below the predetermined minimum level. Replenishment of the make-up water through the check valve will raise the float ball, causing re-closure of the check valve. In this manner, transfer of make-up water intocontainer 23 according to the invention guarantees a passive, self-governing control of electrolyte volume at or near the predetermined minimum level. - Given a steady-state operation of the gas lift pump, the size and frequency of rising
bubbles 12 may be determined by adjusting the current and the size ofsegment 6 andinner chamber 27. The gas lift pump may be energized usingpower supply 13, or it may be energized from an independent power source. In the case where the power supply provides a constant voltage or current, the operation of the gas lift pump may be controlled by selecting the size and composition ofelectrodes 7. - In another embodiment of the invention,
gas lift pump 11 may produce bubbles by a means other than electrolysis. For example,gas lift pump 11 may be a motorized pump that pumps air into the make-up water to produce bubbles, much like a fish tank water pump used to oxygenate an aquarium. - A water electrolyzer system generally configured as disclosed herein optimizes electrolyzer operation in a number of ways. With respect to weight, the overall weight of the electrolyzer is minimized by limiting the volume of the heavier electrolyte to the smallest volume (container 23) required for producing a desired amount of electrolysis gasses. In
container 2 the total volume of make-up water may be selected to achieve a desired operating time between refills. Because water is lighter than the electrolyte, the separation of make-up water from the electrolyte allows the total liquid weight of the electrolyzer (water plus electrolyte) to be minimized. With respect to power, electrical efficiency of the electrolyzer is maximized by maintaining a constant volume and concentration of electrolyte between theelectrodes 22. The ability to maintain a constant electrolyte concentration allows a designer to minimize heat losses for the duration of the electrolyzer duty cycle by optimizing electrolyzer performance based on power supply and electrode configuration. And with respect to reliability, the absence of moving parts, and the absence of control electronics, reduces the overall probability of system failure. - Exemplary embodiments of the invention have been disclosed in an illustrative style. Accordingly, the terminology employed throughout should be read in a non-limiting manner. Although minor modifications to the teachings herein will occur to those well versed in the art, it shall be understood that what is intended to be circumscribed within the scope of the patent warranted hereon are all such embodiments that reasonably fall within the scope of the advancement to the art hereby contributed, and that that scope shall not be restricted, except in light of the appended claims and their equivalents.
Claims (20)
1. A water electrolyzer comprising:
an electrolysis chamber for production of hydrogen and oxygen; and
a water reservoir from which make-up water is transported to the electrolysis chamber to maintain a constant hydrogen output.
2. The water electrolyzer of claim 1 further comprising a gas lift pump transporting the make-up water from the water reservoir to the electrolysis chamber.
3. The water electrolyzer of claim 2 wherein activating gas in the gas lift pump is supplied via electrolysis of the make-up water.
4. The water electrolyzer of claim 3 further comprising a primary chamber in the gas lift pump and a pump lift tube adjacent to the primary chamber, the primary chamber configured to accumulate bubbles from the electrolysis of the make-up water and to promote formation of an aggregate bubble and release of the aggregate bubble into the pump lift tube to force make-up water to a higher level.
5. The water electrolyzer of claim 2 further comprising the gas lift pump fitted with a check valve that allows flow of the make-up water into the electrolysis chamber only when electrolyte level within the electrolysis chamber drops below a predetermined minimum level.
6. The water electrolyzer of claim 4 further comprising the gas lift pump having an overflow opening allowing gas to escape from the pump lift tube and allowing excess make-up water to spill back into the water reservoir when the check valve is closed.
7. A water electrolyzer comprising:
an electrolysis chamber containing electrolyte for production of hydrogen and oxygen;
a water reservoir containing make-up water;
a check valve separating the electrolysis chamber from the water reservoir; and
a gas lift pump within the water reservoir, the gas lift pump in fluid communication with the electrolysis chamber through the check valve and having electrodes immersed in the make-up water;
whereby energization of the electrodes transports the make-up water to the electrolysis chamber to maintain a desired concentration of the electrolyte during the production of hydrogen and oxygen.
8. The water electrolyzer of claim 7 wherein the check valve comprises a float ball at least partially immersed in the electrolyte.
9. The water electrolyzer of claim 7 wherein the electrodes and the electrolysis chamber are energized by a common power supply.
10. The water electrolyzer of claim 7 wherein the electrodes are energized by an independent power supply.
11. The water electrolyzer of claim 7 wherein the inner wall includes a gas pressure equalization port between the electrolysis chamber and the water reservoir.
12. The water electrolyzer of claim 7 further comprising a primary chamber in the gas lift pump and a pump lift tube adjacent to the primary chamber, the primary chamber configured to accumulate bubbles from electrolysis of the make-up water and to promote formation of an aggregate bubble and release of the larger bubble into the pump lift tube to force make-up water toward the check valve.
13. The water electrolyzer of claim 7 further comprising the gas lift pump having an overflow opening allowing gas to escape from the pump lift tube and allowing excess make-up water to spill back into the water reservoir.
14. The water electrolyzer of claim 13 wherein the overflow opening has a diameter greater than a diameter of the pump lift tube to promote escape of the aggregate bubble.
15. The water electrolyzer of claim 13 wherein the overflow opening comprises an edge for dividing the aggregate bubble to promote escape of gasses from the pump lift tube.
16. The water electrolyzer of claim 12 wherein the gas lift pump comprises a shroud surrounding the electrodes.
17. The water electrolyzer of claim 16 wherein a portion of the gas lift tube extends into the shroud to form the primary chamber.
18. A method for maintaining concentration of an electrolyte in a water electrolyzer during electrolysis of water, comprising:
containing the electrolyte within an electrolysis chamber;
providing a water reservoir containing make-up water;
connecting the make-up water to the electrolyte through a check valve that opens only when the electrolyte in the electrolysis chamber drops below a predetermined level;
immersing a gas lift pump within the water reservoir, the gas lift pump in fluid communication with the electrolysis chamber through the check valve; and
energizing the gas lift pump to transport the make-up water to the electrolysis chamber.
19. The method of claim 18 wherein the energizing step comprises applying electrical energy to electrodes within the gas lift pump to produce bubbles that force the make-up water toward the check valve.
20. The method of claim 19 further comprising energizing the electrodes and the electrolysis chamber from a common power supply.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/868,438 US20110048961A1 (en) | 2009-08-25 | 2010-08-25 | System and Method for Refilling an Electrolyzer Tank from a Water Reservoir |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23682809P | 2009-08-25 | 2009-08-25 | |
| US12/868,438 US20110048961A1 (en) | 2009-08-25 | 2010-08-25 | System and Method for Refilling an Electrolyzer Tank from a Water Reservoir |
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| US20110048961A1 true US20110048961A1 (en) | 2011-03-03 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US12/868,438 Abandoned US20110048961A1 (en) | 2009-08-25 | 2010-08-25 | System and Method for Refilling an Electrolyzer Tank from a Water Reservoir |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US20120073523A1 (en) * | 2010-03-15 | 2012-03-29 | Donald Owens | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US8757107B2 (en) | 2010-05-28 | 2014-06-24 | Hno Greenfuels, Inc. | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US8784619B2 (en) | 2010-05-28 | 2014-07-22 | HNO Green Fuels, Inc. | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US20150056523A1 (en) * | 2012-04-04 | 2015-02-26 | Phinergy Ltd. | Electrolyte system and method of preparation thereof |
| US9399946B2 (en) | 2010-05-28 | 2016-07-26 | Donald W. Owens | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US9453457B2 (en) | 2010-03-15 | 2016-09-27 | HNO Green Fuels, Inc. | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US9476357B2 (en) | 2010-03-15 | 2016-10-25 | HNO Green Fuels, Inc. | Method and apparatus for increasing combustion efficiency and reducing particulate matter emissions in jet engines |
| US9574492B2 (en) | 2010-03-15 | 2017-02-21 | HNO Green Fuels, Inc. | Portable hydrogen supplemental system and method for lowering particulate matter and other emissions in diesel engines at idle |
| EP4116463A3 (en) * | 2021-06-11 | 2023-01-25 | Airbus Defence and Space GmbH | Electrolyzer system and matrix cell therefor |
| CN116222112A (en) * | 2021-12-03 | 2023-06-06 | 青岛海尔电冰箱有限公司 | Electrolytic deoxygenation device and refrigerator with same |
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| US1660147A (en) * | 1920-10-01 | 1928-02-21 | Farley G Clark | Electrolytic gas-generating system |
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Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9453457B2 (en) | 2010-03-15 | 2016-09-27 | HNO Green Fuels, Inc. | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US8449735B2 (en) * | 2010-03-15 | 2013-05-28 | Hno Greenfuels, Inc. | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US9574492B2 (en) | 2010-03-15 | 2017-02-21 | HNO Green Fuels, Inc. | Portable hydrogen supplemental system and method for lowering particulate matter and other emissions in diesel engines at idle |
| US20120073523A1 (en) * | 2010-03-15 | 2012-03-29 | Donald Owens | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US9476357B2 (en) | 2010-03-15 | 2016-10-25 | HNO Green Fuels, Inc. | Method and apparatus for increasing combustion efficiency and reducing particulate matter emissions in jet engines |
| US9267468B2 (en) | 2010-03-15 | 2016-02-23 | Hno Greenfuels, Inc. | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US8784619B2 (en) | 2010-05-28 | 2014-07-22 | HNO Green Fuels, Inc. | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US9399946B2 (en) | 2010-05-28 | 2016-07-26 | Donald W. Owens | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US8757107B2 (en) | 2010-05-28 | 2014-06-24 | Hno Greenfuels, Inc. | Hydrogen supplemental system for on-demand hydrogen generation for internal combustion engines |
| US20150056523A1 (en) * | 2012-04-04 | 2015-02-26 | Phinergy Ltd. | Electrolyte system and method of preparation thereof |
| US11515574B2 (en) | 2012-04-04 | 2022-11-29 | Phinergy Ltd. | Method for producing an electrolyte for a metal air battery |
| EP4116463A3 (en) * | 2021-06-11 | 2023-01-25 | Airbus Defence and Space GmbH | Electrolyzer system and matrix cell therefor |
| US12351925B2 (en) | 2021-06-11 | 2025-07-08 | Airbus Defence and Space GmbH | Electrolyzer system and matrix cell therefor |
| CN116222112A (en) * | 2021-12-03 | 2023-06-06 | 青岛海尔电冰箱有限公司 | Electrolytic deoxygenation device and refrigerator with same |
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