Canadian Patents CA 1228833A1 Gas Electrical Hydrogen Generator PDF Download: CA1228833A1-Gas_Electrical_Hydrogen_Generator.pdf (51) INT. CL. C25B 1/04 Consumer and Consommation Corporate Affairs Canada et Corporations Canada (11) (A) No. 1 228 833 (45) ISSUED 871103 (52) CLASS 204-152 C.R. CL. 322-1as) ca) CANADIAN PATENT «2 (54) Gas Electrical Hydrogen Generator {72) Meyer, Stanley A.,U.S.A. {21) APPLICATION No. (22) FILED (30) PRIORITY DATE DISTRIBUTED BY THE PATENT OFFICE, OTTAWA. CCA-274 {11-82) C-2388 Illustrations ABSTRACT: A hydrogen gas generator system for converting water into hydrogen and oxygen gasses, in combination with a magnetic particle accelerator for voltage/current amplification. The hydrogen gas generator encompasses an array of plates immersed in water in a pressure tight enclosure. Direct current voltage applied to the plates causes the hydrogen/oxygen gasses to disassociate from the water molecule. The upper portion of the container is a hydrogen/oxygen collection chamber for maintaining a predetermined gas pressure. A hydrogen/oxygen gas mixture outlet means connected to the collection chamber of the generator includes a magnetic polarizer for establishing a magnetic field and thereby imparting a magnetic potential to the hydrogen gas and the oxygen gas atoms as they are being pressure released from the collection chamber. Attached to the gas outlet means is a non-magnetic conductive loop of tubing. A coil wound around the tubing will have a voltage induced therein as the pressure velocity polarized magnetized gas particles pass there through. The induced voltage has utilization as an electrical power source. The hydrogen and oxygen gas may be utilized (such as) in a burner system or alternatively returned to the gas storage portion of the hydrogen generator in a closed-loop arrangement for recycling. CROSS REFERENCE AND BACKGROUND: There is disclosed in my co-pending Canadian patent application, filed February 4, 1983, Serial Number 420,908, for, Hydrogen Generator, a hydrogen gas generating system. The apparatus comprises a pressure tight enclosure for a water bath having immersed therein an array of plates. The hydrogen and oxygen atoms are disassociated from the water molecule by the application of a non-regulated, non- filtered, low-power, direct current voltage potential to the plates having water passing therebetween. The plates are non-oxidizing and of similar metal to comprise a sub-atomic action non-electrolysis system. The upper portion of the container is a hydrogen/oxygen storage chamber for maintaining a predetermined level. In my co-pending Canadian patent application, Serial Number 420,890, for, Controlled Hydrogen Gas Flame, filed February 4, 1983, there is disclosed a hydrogen gas burner. The nozzle in that burner is connected to the storage area or gas collection chamber via an appropriate line. The port in the nozzle has an opening of a controlled size and configuration, related to the size of the flame and the temperature and velocity of the burning gas mixture. Also, in my co-pending Canadian patent application, Serial Number 420,909, for Electrical Particle Generator, filed Feb. 4, 1983, there is disclosed an electrical generating system. The non-magnetic pipe is Filled with the discrete gas particles having a magnetic polarized field placed thereon, The magnetic charged gas particles, proceed through the pipe at a high velocity dependent on the pressure in the gas generator storage chamber. As the magnetic particles pass through the core of the winding there is induced a voltage/current therein, that may be utilized in the same manner as any other electrical source. The hydrogen/oxygen gas mixture emitted from the opposite end of the pipe is connected to a gas burner where the hydrogen/ gas mixture may be utilized such as for a flame as shown in my co-pending Canadian application, Serial Number 420,890. When the flame is not in use the gas is directed back by alternate means to the storage chamber in the hydrogen generator in a closed loop arrangement.  SUMMARY OF INVENTION: The present invention utilizes the basic principle of a particle accelerator and the principle of inducing a voltage current in a secondary winding by passing a magnetic element there through in combination with a hydrogen gas generator. The particle accelerator utilizes the principles of my co-pending application, Serial Number, 420,909, and the hydrogen generator is particularly that of my co-pending patent application, 420,908. The structure comprises an electrical inductive winding, having a large number of turns and an output for utilizing the voltage current induced therein. The inductive winding “is positioned around an endless - closed loop, non-magnetic pipe or tubing. The hydrogen gas generator encompasses an array of plates immersed in a pressure tight enclosure. Direct current voltage applied to the plates causes the hydrogen/oxygen gasses to disassociate from the water molecule. The upper portion of the container is a hydrogen/oxygen storage chamber for maintaining a predetermined gas pressure. A hydrogen/oxygen gas mixture outlet means connects the non-magnetic tubing to the storage chamber of the generator. Adjacent the outlet a magnetic polarizer establishes a magnetic field and imparts a magnetic potential to the hydrogen and the oxygen gas being pressure released from the outlet.  The apparatus comprises a non-magnetic pipe in a closed loop having a substantial amount of magnetized particles encapsulated therein. A magnetic accelerator assembly is positioned on the pipe includes an inductive primary winding with a low voltage input. A secondary winding is positioned on the pipe opposite to the primary winding. Upon voltage being applied to the primary winding the magnetized particles accelerate through the increased magnetic accelerator assembly with immense velocity. The velocity accelerated particles induce an electrical voltage/ current potential as they pass through the secondary winding. In a closed-loop system the process is continuous. The increased secondary voltage current is utilized in a direct current or alternate current amplifier arrangement. OBJECTS: It is. a principal object of the present invention to provide a hydrogen gas electrical generator capable of producing a voltage/current much greater in magnitude heretofore possible. Another object of the present invention is to provide such a hydrogen gas electrical generator utilizing magnetized elements and wherein the magnetized elements are charged gas particles from a hydrogen generator. Another object of the present invention is to provide such a hydrogen gas electrical generator in combination with a controlled output hydrogen generator. Another object of the present invention is to provide such an electrical generator that may be utilized with a hydro- gen generator having another utility output for alternative generation. A further object of the present invention is to provide such an electrical generator that utilizes components readily available and adaptable to the simplified embodiment. Other objects and features of the present invention will become apparent from the following detailed description when taken in conjunction with the drawings in which: BRIEF DESCRIPTION OF DRAWINGS Figure 1 is a simplified illustration of the principles of the invention, in cross section showing the particles voltage/ current amplifier together with the hydrogen generator in a preferred embodiment. Figure 2 is a magnetic particle tubing, in an electrical schematic circuit arrangement, illustrating the induced direct and alternating current voltage. DETAILED DESCRIPTION OF DRAWINGS: Referring now to Figure 1 there is illustrated the invention of the preferred embodiment in a simplified schematic arrangement. The generator 10 comprises an airtight pressure enclosure/housing 15. The housing 15 is filled with water 12 to a predetermined level. Immersed in the water 12 is an array of plates 14. In the preferred embodiment of the invention of Figure 1, as disclosed in my co-pending application Serial Number 420,908. The plates 14 are in pairs of similar non-oxidizing metal. A negative voltage current potential and a positive voltage current potential from source 16 is applied to alternate plates of the array 14. The generation of hydrogen/ oxygen is a sub-atomic process, i.e., not electrolysis. That is, the applied potential to the plates causes the hydrogen and oxygen atoms to disassociate themselves from the water molecule. Accordingly, the process is operative with any water irrespective of its purity or amount of contamination.  It is understood, of course, that the hydrogen generator may be that of the electrolysis process---although more costly and less, efficient. In that event the plates 14 would be an anode and cathode and the water would be distilled water with a chemical added. The released hydrogen gas depicted as particles 20a xxx n and oxygen gas particles 22a xxx n are collected and stored in the chamber 23 together with other released gasses such as nitrogen 21a xxx. The chamber 23 further includes switch means 57 to shut off the electrical source 16 to the generator system when the pressure in the chamber 23 sensed by pressure gauge, 55, achieves a predetermined level. In the operation of the hydrogen generator as a burner, as disclosed in the co-pending patent application Serial Number 420,890, the outlet tube 25 is connected directly to the nozzle 40 to obtain the flame 45. upon ignition. The operation of the gas burner is not. altered in the present invention. There is interposed in the line 25, a magnetic polarizer 30 having magnetic poles 32 and 34. The magnetic polarizer 30 may be a permanent magnet or an electrical magnet capable of creating a magnetic field 36 across the non-magnetic tubing 25, The magnetic field 36 in turn imparts a magnetic charge to the gasses released from the storage chamber 33. The hydrogen gas particles become positively magnetically charged and the oxygen particles become negatively magnetically charged - producing a magnetized gas - mixture.  Also connected to the outlet tubing 25 adjacent to the magnetic polarizer 30 is a series of loops of non-magnetic tubing 50. The tubing in its loop configuration can be any one of the arrangements illustrated in my co-pending patent application, Serial Number 420,890. The opposite end 51 of the looped tubing 50 is connected via a ¥Y connection either to the burner assembly 40, via line 35, or a return line 42 to the storage chamber 23. As aforesaid, the storage chamber 23 is maintained at a predetermined pressure; and once the pressure is attained the gas particles will be expelled into outlet line 25 with a substantial velocity. The pressure released particles become charged by the magnetic polarizer 30 and pass through the entire loop arrangement of tubing 50. The loop arrangement of tubing 50 has wound thereon a substantial number of turns 60a xxx n in a winding. The number and size of the turns is related to the tubing configuration and voltage current output. The magnetically charged gas particles traveling with a high pressure velocity pass through the tubing 50. As the magnetically charged gas particles pass through the core of the winding, there is induced a voltage current therein through its inductive field. The output voltage current is utilized via terminals 70-72. Upon demand for the flame, (such as for heat) from demand circuit 65, the valve 37 is opened causing the gas mixture to go to the nozzle 40 and provide the flame 45a upon ignition. Upon satisfaction of the demand, the valve 37 will close and thereby cause the gas mixture to return to the collection chamber 23 via close loop line 42. In this arrangement the pump 45 will turn on and cause a continuous circulation of the gas through the closed loop. One way check valve 49 assures that no gas enters line 42 when the pump 45 is quiescent. If the gas in the collection chamber is of the preset pressure, as sensed at gauge 55, the voltage via terminal 16 will be cut-off discontinuing the generation of gas. With particular reference to Figure 2 there is illustrated, partly in schematic and partly pictorial, the preferred embodiment of the invention. Initially it is noted that the pump 45 of Figure 1 has been replaced by the particle accelerator 46. The accelerator 46 is a non-mechanical/no moving part element and therefore not subject to wear. The hydrogen and oxygen gases have placed thereon a magnetic field potential. Hence, as the magnetized gases approach the accelerator 46 they are attracted and as they pass the center of the accelerator they are propelled there through. Other propulsion means in lieu of the pump 45 of Figure 1 or the accelerator 46 of Figure 2 may be utilized. The volume of the hydrogen/oxygen gas as directed by the storage area 23 and the pressure of the hydrogen/oxygen gas stored therein determines the magnetic field strength. The greater the pressure, the greater the velocity; and, in turn, the greater the voltage/current output. The induced current/voltage can be, at the output 70- 72, either direct current, or alternating current, or both. With reference to Figure 2, the simplified schematic illustrates a direct current voltage in parallel connected windings of coil 74 and an alternating current in series connected windings of coil 75. The number of coils 74a xxx n of coil 74 will determine the ripple frequency of the direct current voltage and its amplitude. Similarly, the number of windings 75a xHxX n will determine the alternating frequency of the alternating current voltage and its amplitude in coil 75. More importantly, the aforesaid ripple frequency of the single polarity voltage of coil 74 and alternating frequency of the alternating voltage of coil 75 can be altered, varied, and controlled. That is, the frequency is a function of the number of discrete windings of the coils times the velocity of the gas per second. The velocity of the gas, in turn, is varied by varying its magnetic field; and the magnetic field is varied by varying the pressure of the gases in the chamber 23. Further, it has been found that the increase in pressure of the gases in chamber 23 increases the velocity of the gas exponentially. Simply, an arithmetical increase in pressure of the gases released results in a geometrical increase in frequency and amplitude of the output voltage from either the direct current winding 74 or the alternating current winding 75. There will be instances where an increase in velocity (pressure) is needed to increase the output voltage of the electrical generator but the generation of more hydrogen gas may be undesirable. That is, for instance when’the flame 45A is a con- trolled gas mixture flame. The addition of more hydrogen will increase the temperature of the combustibility of the mixture and will increase its velocity. The utility of the flame, if not quenched, will be affected proportionately. Accordingly, to increase the gas pressure in chamber 23 other non-combustible gasses 2la xxx n, such as nitrogen are added via pressure inlet means to the mixture. Although certain and specific embodiments are shown and described, alternatives and modifications may be had without departing from the spirit and scope of the invention. THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS: 1. Apparatus comprising: a housing having a water reservoir for retaining water therein and a gas collection chamber; a pair of similar non-oxidizing exciter elements positioned in said water reservoir and adapted to be connected to a voltage potential that creates a negative charge on one of the exciter elements and a positive charge on the other and thereby release gases including hydrogen and oxygen from water in the reservoir; a non-magnetic tubing connected at one end to said collection chamber via an outlet therefrom; a magnetic polarizer positioned for magnetically charging gas flowing through said tubing; and an inductive winding positioned over said tubing downstream from said polarizer whereby flux lines of magnetized gas passing through said tubing and traversing said inductive winding induce a current/voltage in said inductive winding. 2. The apparatus of Claim 1 further comprising: gas utilization means connected to the other end of said tubing for utilizing said generated hydrogen/oxygen gas mixture. 3. The apparatus of Claim 1 further comprising: a nozzle connected to the other end of said tubing, said nozzle having a port of pre-determined size and configuration through which the gases are expelled, and means for igniting said gases. 4. The apparatus of Claim 1 further comprising: control means for maintaining a predetermined gas pressure in said collection chamber. 5. The apparatus of Claim 1 further comprising: a pressure gauge for determining the pressure in said collection chamber, and switch means for controlling the voltage potential source to terminate the generation of hydrogen/oxygen gases upon said collection chamber attaining a predetermined pressure. 6. The apparatus of Claim 1 further comprising: a gas line tubing connected to the other end of said non-magnetic tubing and to said collection chamber in a closed loop arrangement. 7. The apparatus of Claim 1 further comprising: a gas line tubing connecting the other end of said non-magnetic tubing to said collection chamber in a closed loop arrangement, and means in said gas line tubing for maintaining said polarized hydrogen and oxygen atoms circulating through said non-magnetic tubing. 8. The apparatus of Claim 1 further comprising: a gas line tubing connected to the other end of said non-magnetic tubing and to said collection chamber in a closed loop arrangement, and a unidirectional valve connected to the end of said gas line tubing connected to said collection chamber. 9. The apparatus of Claim 1 further comprising: a gas line tubing and gas utilization means, a Y-type connector for alternately connecting said gas line tubing to said gas utilization means and said collection chamber in a closed loop arrangement. 10. The apparatus of Claim 1 further comprising: a gas line tubing and gas utilization means, a Y-type connector for alternately connecting said gas line tubing to said gas utilization means said collection chamber in a closed loop arrangement, two directional valve means, and a demand circuit connected to said valve means for selectively connecting said gas line tubing to said gas utilization means or said collection chamber in response to pre-determined conditions. ll. An apparatus comprising: a gas generator housing having a gas collection chamber for maintaining a preset volume of gas therein under pressure, outlet means from said gas collection chamber, a non-magnetic tubing connected to said outlet means, a magnetic polarizer positioned adjacent said outlet means between said chamber and said tubing for magnetically charging gas expelled from said chamber through said outlet means, and an inductive coil positioned over said non-magnetic tubing whereby the flux lines of magnetized gas passing through said tubing and traversing said inductive coil, induce a current/voltage therein. 12. The apparatus of Claim 11 wherein: said gas is a combustible gas, and utilization means connected to the opposite end of said non-magnetic tubing for utilizing said gases. 13. The apparatus of Claim 11 wherein: said coil comprises a plurality of windings wound in parallel, and wherein said induced voltage/current therein is of a single polarity. 14. The apparatus of Claim 11 wherein: said coil comprises a plurality of windings connected in series polarity. 15. The apparatus of Claim 11 wherein: said coil comprises a plurality of windings and wherein the number of said plurality of windings is determinative of the frequency of the said induced voltage/current therein. 16. The apparatus of Claim 11 further comprising: means for varying the pressure of said gas in said collection chamber to vary the output frequency of said induced voltage in said coils. 17. The apparatus of Claim 11 further comprising: means for varying the generation of said gas to vary the pressure of said gas in said collection chamber to vary the output frequency of said induced voltage in said coils. 18. The apparatus of Claim 11 further comprising: means for adding non-combustible gases to said collection chamber to vary the pressure of said gas in said collection chamber to vary the output frequency of said induced voltage in said coils. 19. The apparatus of Claim 11 wherein: said non-magnetic tubing further comprises means connected thereto for returning said magnetized gas to said collection chamber, and means for recirculating said gas through said chamber, said non-magnetic tubing and said last named means. 20. The apparatus of Claim 11 wherein: said non-magnetic tubing further comprises means connected thereto for returning said magnetized gas to said collection chamber, a particle accelerator for recirculating said gas through said chamber, said tubing, and said last named means. 21. Apparatus comprising: a closed vessel suitable for maintaining a volume of water therein, and permitting the addition of water thereto; a pair of electrically conductive exciter elements formed of a same non-reactive material located in said vessel in a predetermined spatial relationship to one another and adapted to be connected to a source of a voltage potential that creates a potential difference between an arbitrary electrical ground and the source output with one of said exciter elements being connected to said arbitrary electrical ground and the other of said exciter. elements being connected to said source output, whereby there is formed a nominally positive electrical voltage zone in water adjacent said exciter element connected to said output and a nominally negative voltage zone in water adjacent said exciter element connected to said electrical ground as the voltage potential is applied thereto to a degree such that the hydrogen atoms and the oxygen atoms disassociate from water molecules in the vessel and are released in the form of a gas mixture; a gas collection chamber for maintaining a volume of said gas released from water when in the vessel and a potential difference is applied to said exciter elements; a non-magnetic tubing connected at an outlet from said collection chamber; a magnetic polarizer positioned adjacent the end of said tubing as the gas is expelled from said outlet; and an inductive winding positioned over said tubing wherein flux lines of the magnetized gas passing through said tubing, traverse said inductive winding and induce a current in said inductive winding. CA1235669A1 Controlled Hydrogen Gas Flame PDF Download: SMeyer-CA1235669A1-Controlled_Hydrogen_Gas_Flame.pdf Consumer and Consornmation aS Corporate Affairs Canada el Corporations Canada (11) (A) No. 1 235 669 (45) ISSUED 880426 (52) CLASS 204-78 C.R. CL. 204-1664 (51) INT. CL. c25B 1/04us ca GANADIAN PATENT «2 (54) Controlled Hydrogen Gas Flame (72) Meyer, Stanley A.,U.S.A. (21) APPLICATION No. 420,890 (22) FILED 830204 (30) PRIORITY DATE U.S.A. (411,977) 820825 No. OF CLAIMS 9 Canada DISTRIBUTED BY THE PATENT OFFICE, OTTAWA, CCA-274 (11-82) VX   Illustrations ABSTRACT A sustained controllable gas flame. The hydrogen generator utilized provides gasses from water having impurities and other gasses entrapped therein. The hydrogen generator has a chamber for holding a quantity of water and a pair of non-oxidizing electrodes are located in the chamber. A rippling wave form electric potential is applied across the electrodes without any change of polarity and the current flow is limited. The gasses separated from the water comprise combustible gasses such as hydro- gen and oxygen and non-combustible gasses, such as nitrogen. The nitrogen, oxygen and hydrogen are mixed as they are released in the process and collected as a mixture of gasses in a collection chamber of the generator. A nozzle having one or more ports of a given configuration is connected through a line to the uppermost region of the gas collection chamber of the hydrogen generator. The nitrogen reduces the velocity and temperature of the burning flame from that of the hydrogen/oxygen mixture. To further control the temperature and velocity of the burning gas mixture there ‘6 added to the collection chamber other non-burnable gasses. The configuration of the nozzle and its port opening for sustaining a flame is dependent on the mixture of gasses utilized and restricted thereby. An increase in the size of the flame requires additional port openings to prevent blowout. This invention relates to apparatus for generating gases from water and for the controlled burning of such generated gases. The present invention utilizes the hydrogen/oxygen generator disclosed and claimed in my co-pending Canadian Patent Application Serial No. 420,908 filed 4 February, 1983 and entitled " HYDROGEN GENERATOR SYSTEM ". In the process disclosed in said application for separating hydrogen and oxygen atoms from water having impurities, water is passed between two plates of similar non-oxidizing metal. No electrolyte is added to the water. The one plate has placed thereon a positive potential and the other a negative potential from a very low amperage direct— current power source. The action of the direct current voltage on the non-electrolytic water causes the hydrogen and oxygen atoms to be separated and also released are other gases entrapped in the water such as nitrogen. Contaminants in the water that are not released as gases are forced to separate from the water and may be collected or utilized and disposed of in a Known manner. Direct current acts as a static force on the water molecules and a non-regulated rippling direct current acts as a dynamic force. Pulsating the direct current further enhances the release of the hydrogen and oxygen atoms from the water molecules, The electrolysis process for generating hydrogen and oxygen gas from water is well known in the art. It is, of course, further understood with a proper mixture of oxygen gas, the hydrogen gas is combustible and under ideal conditions a flame, may be had. Reference is made to U.S. Patent 4,184,921. However, in that the burning velocity of hydrogen is so great (265-325 cm./sec. versus 37-45 cm./sec. for gasoline) the hydrogen ensuing from a nozzle will not under ordinary circumstances sustain a flame. Therefore, to sustain a flame at a nozzle attached to a hydrogen generator the burning velocity of the hydrogen gas must be reduced. It has been found that all water in its natural state whether it be tap water, well water, sea water, or fresh water is a saturate of ambient air. Further, in that ambient air contains a substantial amount of nitrogen, all natural water will have entrapped therein nitrogen. Again, the percentage of nitrogen entrapped in natural water has been determined to be a fixed percentage and very uniform irrespective of the source of the water or its impurities. A principal object of the present invention is to provide a new and improved hydrogen/oxygen generator that is operable from a water source that provides hydrogen/oxygen output that will have a sustained burn. Another object of the present invention is to provide a hydrogen/oxygen generator that in addition to the hydrogen and oxygen gases releases non-combustible nitrogen gas capable of reducing the burning velocity and temperature of a pure hydrogen/oxygen flame. A further object of the present invention is to provide a hydrogen generator that includes the controlled addition of other non-combustible gases to the gas chamber thereof to thereby further control the burning velocity and temperature of the hydrogen gas. In accordance with the present invention a nozzle is connected to a gas collection chamber via an appropriate line and has a port opening of a controlled size and configuration, related to the size of the flame and the temperature and velocity of the burning gas mixture. To maintain the flame, i.e. prevent blowout, additional nozzles are included when the overall flame size is to be increased. More particularly there is provided in accordance with the present invention an apparatus for generating gases from water and for the controlled burning of the gases generated thereby comprising: a housing having a chamber for containing natural water therein including entrapped non-combustible gases; a pair of similar non-oxidizing electrodes in said chamber and adapted to be connected to a source of rippling wave form direct current voltage in which the current flow is restricted to provide a force action on water in said chamber, which liberates the hydrogen atoms and oxygen atoms from said water as well as non-combustible gases dissolved in said water and thereby producing a mixture of hydrogen, oxygen and non— combustible gases; a gas collection chamber in said housing for collecting and intermixing said released gases; and a nozzle attached to the gas collection chamber of said housing including an inlet for receiving said mixture of hydrogen, oxygen and non-combustible gases; said nozzle having a port of predetermined size and configuration for expelling said mixed gases at a rate so as to sustain a flame from the gases that are liberated from the water. Description Of Drawings: The invention is illustrated by way of example in the accompanying drawings wherein: Figure 1 is a cross-sectional view of a hydrogen generator illustrating the features of the present invention in. its most preferred embodiment incorporated therein; and Figure 2 is a front face view of a nozzle having increased number of nozzle ports to increase the flame size. Referring to the drawings the hydrogen generator 10 is the subject of my aforementioned co-pending application Serial No. 420,908. The generator 10 comprises a closed watertight housing 12 having a quantity of natural water 13 in the bottom thereof. Submerged in the water 13 is a pair of plates 15 (one not shown) which have a direct current low amperage voltage, applied thereto via connector 11 during operation. As get forth in my co-pending patent application supra, the electrical potential applied to the similar non-oxidizing metal plates is a sub-atomic action. In this way the hydrogen atoms 14 a xxx n and the oxygen atoms 18 a xxx n are released from the water molecule. Unlike the electrolysis process for generating hydrogen from distilled water, the hydrogen generator of my aforementioned patent application, utilizes water 13 that need not be pure --~ simply any water irrespective of contaminants and source. Natural water such as tap, well, sea, or fresh water is an absorber of ambient air and since ambient air contains a substantial amount of nitrogen gas so does the natural water with the ambient air absorbed therein. In operation of the hydrogen generator, the gases released from natural water are thus nitrogen, hydrogen and oxygen. In the preferred embodiment utilizing tap water, the nitrogen gasses 16 a xxx n are intermixed with the hydrogen gases 14 a xxx n and the oxygen gases 18 a xxx n in the chamber 19 of the hydrogen generator 10. Upon release of the gases via line 24 and nozzle 20 and then port 22 the gas mixture is ignited to provide flame 25. The flame 25 is sustained in that the nitrogen gases 16 a xxx n reduces the burning velocity and temperature of the hydrogen gas 14 a Xxx Nn. A realistic and practical manner of further controlling the burning velocity and temperature of the hydrogen gases 14 a xxx n, is by adding non-combustible gases directly to the hydrogen and oxygen gases generated. This is accomplished by inlet 30 to the upper gas chamber 19 of the hydrogen generator. Valve means 35 is adjustable to control the amount of non- combustible gases 37, added to the gas chamber 19. The nozzle 20 connected to the chamber 19 of the generator 10 via line 17, is of a given configuration to permit a predetermined quantity of gases to be expelled from the port 22. The port size is dependent on the gases generated, and collected in the chamber 19, the pressure of the chamber 19 of the generator 10, and the size of the flame desired. To increase the size of the flame 25 would appear to be a simple matter of increasing the rate of gases generated. However, an increase of gases merely causes a blowout at the port or opening 22 of the nozzle 20. This flame blowout will occur since an increase in hydrogen gas generation disrupts the ratio of the initial mixture even though the percentages remain constant. Typically, tap water contains known percentages of hydrogen, oxygen, and nitrogen. The percentages vary somewhat dependent on the other gases that may be trapped in the tap water. The increase in production will not affect the percentages but it must be appreciated that the volume of the gases will be proportionately increased. In turn, the volume being directly related to pressure, the pressure will be similarly increased. To effectively reduce or counteract the velocity due to the increased pressure of the hydrogen gas mixture in the chamber 19 a large port 22 would appear to be capable of handling the increased pressure, but as aforesaid, a larger port with a high velocity hydrogen gas mixture will cause a flame blowout. To sustain a larger flame with increased pressure, additional nozzles having ports 22 a xxx n or, a nozzle 20 with multiple ports 22 a xxx n as shown in Figure 2, can be used. The larger the desired flame the greater will be the number of ports required. It can be understood that a port that will not 5 sustain a flame does present a safety factor relative to hydrogen spark back to the chamber 19. Hence, controlling the size of the port 22 in effect provides a quencher of hydrogen spark back.   Although certain and specific embodiments are shown and described it is within the scope and spirit of the present invention to include alternatives and modifications thereto.  THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS: 1. An apparatus for generating gases from water and for the controlled burning of the gases generated thereby comprising: a housing having a chamber for containing natural water therein including entrapped non-combustible gasses; a pair of similar non-oxidizing electrodes in said chamber and adapted to be connected to a source of rippling wave form direct current voltage in which the current Flow is restricted to provide a force action on water in said chamber, which liberates the hydrogen atoms and oxygen atoms from said water as well as non-combustible gases dissolved in said water and thereby producing a mixture of hydrogen, oxygen and non-combustible gases; a gas collection chamber in said housing for collecting and intermixing said released gases; and a nozzle attached to the gas collection chamber of said housing including an inlet for receiving said mixture of hydrogen, oxygen and non-combustible gases; said nozzle having a port of predetermined size and configuration for expelling said mixed gases at a rate so as to sustain a flame from the gases that are liberated from the water. 2. The apparatus of Claim 1 including means for separately introducing non-combustible gases to said gas collection chamber. 3. The apparatus of Claim 2 including valve means for controlling the amount of non-combustible gases introduced into said chamber. 4. The apparatus of Claim 1 wherein said nozzle has a plurality of separate ports to thereby control the flame. 5. A method of producing a combustible gaseous mixture and sustaining controlled burning thereof comprising: (a) providing a quantity of water in a water holding chamber having a pair of similar non-oxidizing electrodes therein; (b) applying a rippling wave form electric potential across said electrodes without any change of polarity and limiting the current flow so as to liberate hydrogen atoms and oxygen atoms from the water molecules as well as non-combustible gases dissolved in the water and thereby provide combustible and non-combustible gases; (c) collecting and intermixing said gases; and (ad) providing a nozzle having at least one port of predetermined size and configuration such that the gaseous mixture flows therethrough at a rate so as to sustain a flame. 6. The method of Claim 5 including the step of burning said gaseous mixture at said nozzle port. 7. The method of Claims 5 or 6 including the step of adding further non-combustible gases to said intermixed gases to provide a combustible gas mixture with a selected burn rate. 8. The method of Claim 7 including the step of burning said gaseous mixture at said nozzle port. 9. The method of Claims 7 or 8 including the step of adding further non-combustible gases to said intermixed gases to provide a combustible gas mixture with a selected burn rate. CA2067735A1 Water Fuel Injection System PDF Download : SMeyer-CA2067735A1-Water_Fuel_Injection_System.pdf   Consommation et Corporations Canada Bureau des brevets Ottawa, Canada K1A 0C9 Consumer and Corporate Affairs Canada Patent Office (21) (Al) 2,067,735 (22) 1991/05/17 (43) 1992/11/185 (51) INTL.CL. CO1B~-003/04 (19) (cA) APPLICATION FOR CANADIAN PATENT (12) (54) Water Fuel Injection System (72) Meyer, Stanely A. - U.S.A. j; (73) Same as inventor (57) 13 Claims Notice: The specification contained herein as filed 78/e‘Geo’s CCA 3254 (10-89) 41 2067735 ABSTRACT An injector system comprising an -improved method and apparatus useful in the production of a hydrogen containing fuel gas from water in a process in which the dielectric property of water and/or a mixture of water and other components determines a resonant condition that produces a breakdown of the atomic bonding of atoms in the water molecule. The injector delivers a mixture of water mist, ionized gases and non-combustible gas to a zone or locus within which the breakdown process leading to the release of elemental hydrogen from the water molecules occurs.  Illustrations WATER FUEL INJECTION SYSTEM This invention relates to a method and apparatus useful in producing thermal combustive energy from the hydrogen component of water. In my patent no. 4,936,961, “Method for the Production of a Fuel Gas," I describe a water fuel cell which produces a gas energy source by a method that utilizes water as a dielectric component of a resonant electrical circuit. in my patent no. 4,826,581, “Controlled Process for the Production of Thermal Energy From Gases and Apparatus Useful Therefore," I describe a method and apparatus for obtaining the: enhanced release of thermal energy from a gas mixture including hydrogen and oxygen in which the gas ‘is subjected to various electrical, ionizing and electromagnetic fields. In my co-pending application serial no. 07/460,859, "Process and Apparatus for the Production of Fuel Gas and the Enhanced Release of Thermal Energy from Fuel Gas," I describe various means and methods for obtaining the release of thermal/combustive energy from the hydrogen (H) component of a fuel gas obtained from the disassociation of a water (H20) molecule by a process which utilizes the dielectric properties of water in a resonant circuit; and in that application I more thoroughly describe the physical dynamics and chemical aspects of the water-to-fuel conversion process. The invention of this present application represents a generational improvement in methods and apparatus useful in 2067735 the utilization of water as a fuel source, In brief, the present invention is a micro-miniaturized water fuel cell and permits the direct injection of water, and its simultaneous transformation into a hydrogen containing fuel, in a combustion zone, such as a cylinder in an internal combustion engine, a jet engine, or furnace. Alternatively the injection system of the present invention may be utilized in any non-engine application in which a concentrated flame or heat source is desired, for example, welding. The present injection system eliminates the need for an enclosed gas pressure vessel in a hydrogen fuel System and thereby reduces a potential physical hazard heretofore associated with the use of hydrogen-based fuels. The system produces fuel on demand in real-time operation and sets up an integrated environment of optimum parameters so that a water-to-fuel conversion process works at high efficiency. The preferred embodiment of the invention is more fully explained below with reference to the drawings in which: Figure 1 figuratively illustrates the sections and operating zones included in a single injector of the invention. Figure 2A is a side cross sectional view: Figure 2B is a frontal view from the operative end; and Figure 2C is an exploded view -- of an individual injector.  Figure 3A and Figure 3B respectively show. a side cross-section view and frontal view of an alternatively configured injector. Figure 4 shows a disk array of injectors (No 3B in Patent - Assumed 3 is 3B) Figure 5 shows the resonance electrical circuit including the injector. Figure 6 depicts the inter-relationship of the electrical and fuel distribution components of an injector system. Although I refer to an “injector” herein, the invention relates not only to the physical configuration of an injector apparatus but also to the overall process and system parameters determined in the apparatus to achieve the release of thermal energy. In a basic outline, an injector regulates the introduction “into a combustion zone of process constituents and sets up a fuel mixture condition permitting combustion. That combustion condition is triggered simultaneously with injector operation in real time correspondence with control parameters for the process constituents. In the fuel mixture condition that is created by the injector, water (H20) is atomized into a fine spray and mixed with (1) ionized ambient air gases and (2) other non-combustible gases such as nitrogen, argon and other rare gases, and water vapor. (Exhaust gas produced by the combustion of hydrogen with oxygen is a non-combustible water vapor. This water vapor and other inert gases resulting from combustion may be recycled from an exhaust outlet in the injector system back into the input mixture of non-combustible gases.) The fuel mix is introduced at a consistent flow rate maintained under a predetermined pressure. In the triggering of the condition created by the injector, the conversion process described in my patent no. 4,936,961 and co-pending application serial no. 07/460,859 is set off spontaneously on a “micro” level in a predetermined reaction zone. The injector creates a mixture, under pressure in a defined zone (or locus), of water, ionized gases and non-combustible gases, Pressure is an important factor in the maintenance of the reaction condition and causes the water mist/gas mixture to become intimately mixed, compressed, and destabilized to produce combustion when activated under resonance conditions of ignition. In accordance with the aforementioned conversion process of my patent and application, when water is subjected to a resonance condition water molecules expand and distend; electrons are ejected from the water molecule and absorbed by ionized gases; and the water molecule, thus destabilized, breaks down into its elemental components of hydrogen (2H) and oxygen (0) in the combustion zone. The hydrogen atoms released from the molecule provide the fuel source in the mixture for combustion with oxygen. The present invention is an application of that process and is outlined in Table I: TABLE I Image Text: Injector Mixture + Pr ndition = Thermal Energy (1) Water Mist (1) Release Under (1) Heat pressure into and Combustion Zone or and (2) Internal . : Combustion (2) Ionized Gas (2) Resonance utilizing Engine the dielectric (Explosive property of water force) as a capacitor and or and . (3) Jet Engine (3) Non-Combustible (3) Unipolar pulsing . Gas at high voltage or (4) Other application The process occurs as water mist and gases are injected under pressure into, and intimately mixed in the combustion zone and an electrically polarized zone. In the electrically polarized zone, the water mixture is subjected to a unipolar pulsed direct current voltage that is tuned to achieve resonance in accordance with the electrical, mass and other characteristics of the mixture as a dielectric in the environment of the combustion zone. The resonant frequency will vary according to injector configuration and depends upon the physical characteristics, such as mass and volume of water and gases in the zone. As my prior patents and application point out, the resonant condition in the capacitative circuit is determined by the dielectric properties of water: (1) as the dielectric in a capacitor formed by adjacent conductive surfaces and (2) as the water molecule itself is a polar dielectric material. At resonance, current Flow in the resonant electrical circuit will be minimized and voltage will peak. The injector system provides a pressurized fuel mixture for subjection to the resonant environment of the voltage ‘ combustion zone as the mixture is introduced to the zone. In a preferred embodiment, the injector includes concentrically nested serial orifices, one for each of three constituent elements of the fuel mixture. (It may be feasible to combine and process non-combustible and ionized gases in advance of the injector. In this event only two orifices are required, one for the water and the other for the combined gases.) The orifices disperse the water mist and gases under pressure into a conically shaped activation and combustion zone (or locus). Figure 1A shows a transverse cross-section of an injector in which supply lines for water 1 ionized gas 2 and non-combustible gas 3 feed into a distribution disk assembly 4 having concentrically nested orifices. The fuel mixture passes. through a mixing zone 5 and voltage zone 6 created by electrodes or conductive surfaces 7a and 7b (positive) and 8 (negative or ground). Electrical field lines as shown as 6al and 6a2 and 6bl and 6b2. Combustion (i.e., the oxidation of: hydrogen) occurs in the zone 9. Ignition of the hydrogen can be primed by a spark or may occur spontaneously as a result of the exceptionally high volatility of hydrogen. and its presence in a high voltage field. Although a differentiation of the mixing zone, the voltage zone and the combustion zone is made in explaining the invention, that differentiation relates to events or conditions in a process continuum, and ‘as is evident from Figure 1, the zones are not physically discrete. In the zone(s), there is produced an "excited" Mixture of vaporized water mist, ionized gases and other non-combustible gases all of which have been instantaneously released from under high pressure. Simultaneously, the released mixture is exposed to a pulsed voltage in the zone/ locus at a frequency corresponding to electrical resonance. Under these conditions, outer shell electrons of atoms in the water molecule are destabilized and molecular time share is interrupted. Thus, the gas mixture in the injector zone is subjected to physical, electrical and chemical interactive forces which cause a breakdown of the atomic bonding forces of the water molecule. Process parameters are determined based on the size of a particular injector. In an injector sized appropriately for use to provide a fuel mixture to a conventional cylinder in a passenger vehicle automobile engine, the injector may resemble a conventional spark plug. In such an injector, the water orifice is .10 to .15 inch in diameter; the ionized gas orifice is -15 to -20 inch in diameter; and the non-combustible gas orifice is .20 to .25 inch in diameter. In such a configuration, the serial orifices increase in size from the innermost orifice, as appropriate to a concentric configuration. As noted above, the introduction of the fuel components is desirably maintained at a constant rate; maintenance of a back pressure of about 125 pounds per square inch for each of the three fuel gas constituents appears satisfactorily useful for a “spark-plug* injector. In the Pressurized environment of the injector, spring loaded one-way check valves in each supply line,’ such as 14 and 15, maintain pressure during pulse off times. The voltage zone 6 surrounds the pressurized fuel mixture and. provides an electrically charged environment of pulsed direct current in the range from about 500 to 20,000 and more volts at a frequency tuned into the resonant characteristic of the mixture. This frequency will typically lie within the range of from about 20 KHz to about 50 KHz, dependent, as noted above, on the mass flow of the mixture from the injector and the dielectric property of the mixture. In a, spark-plug sized injector, the voltage zone will typically extend longitudinally about -25 to 1.0 inch to permit sufficient dwell time of the water mist and gas mixture between the conductive sufaces 7 and 8 that form a Capacitor so that resonance occurs at a high voltage pulsed frequency and combustion is triggered. In the zone, an energy wave is formed related to the resonant pulse frequency. The wave continues to pulse through the flame in the combustion zone. The thermal energy produced is released as heat energy. Ina confined zone such as a piston/cylinder engine, gas detonation under resonant conditions produces explosive physical power. In the voltage zone, the time share ratio of the hydrogen and oxygen atoms comprising the individual water molecules in the water mist is upset in accordance with the process explained in my aforementioned patent no. 4,936,961 and application serial no. 07/460,859. To wit, the water molecule which is itself a polar structure, is distended or distorted in shape by being subjected to the polar electric field in the voltage zone. The resonant condition induced in the molecule by the unipolar pulses upsets the molecular bonding of shell electrons such that the water molecule, at resonance, breaks apart into its constituent atoms. In the voltage zone, the water (H20) molecules are excited into an ionized state; and the pre-ionized gas component of the fuel mixture captures the electrons released from the “water molecule. In this manner at the resonant condition, the water molecule is destabilized and the constituent atomic elements of the molecule, 2H and O, are released; and the released hydrogen atoms are available for combustion. The non-combustible gases in the fuel mixture reduce the burn rate of hydrogen to that of a hydrocarbon fuel such as gasoline -or kerosene from its normal burn rate (which is approximately 2.5 times that of gasoline). Hence the presence of non-combustible gases in the fuel mixture moderates energy release and modulate the rate at which the free hydrogen and oxygen molecules combine in the combustion process. The conversion process does not spontaneously occur and the condition in the zone must be carefully fine tuned to achieve an optimum input flow rate for water and the gases corresponding to the maintenance of a resonant condition. The input water mist and gases may likewise be injected into the zone in a physically pulsed [on/off] manner corresponding to the resonance achieved. In an internal combustion engine, the resonance of the electrical circuit and the physical pulsing of the input mixture may be required to be related to the combustion cycle of the reciprocating engine. In this regard, one or two conventional spark plugs may require a spark cycle tuned in correspondence to the ‘conversion cycle resonance so that combustion of the mixture will occur. Thus, the input flow, conversion rate and combustion rate are interrelated and optimally should each be tuned in accordance with the circuit resonance at which conversion occurs. The injection system of the present invention is suited to retrofit applications in conventionally fueled gasoline and diesel internal combustion engines and conventionally fueled jet aircraft engines. EXAMPLE 1 Figures 2A, 2B and 2C illustrate a type of injector useful, inter alia as a fuel source for a conventional internal combustion engine. In the cross-section of Figure 2A, reference numerals corresponding to identifying numerals used in Figure 1 show a supply line for water l leading to first distribution disc la and supply line for ionized gas 2, leading to second distribution disc 2a. In the cross section, the supply line for non-combustible gas 3 leading to distribution disc 3a is not illustrated, however, its location as a third line should be self-evident. The three discs comprise distribution disc assembly 4. The supply lines are formed in an electrically insulating body 10 surrounded by electrically conductive sheath/housing 11 having a threaded end segment 12.   A central electrode 8 extends the length of the injector. Conductive elements 7a and 7b (7a and 7b depict oppositive sides of the diameter in the cross-section of a circular body) adjacent threaded section 12 form, with electrode 8, the electrical polarization zone 6 proximate to combustion zone 9. An electrical connector 13 may be provided at the other end of the injector. (As used herein “electrode” refers to the conductive surface of an element forming one Side of a capacitor.) In the frontal view of Figure 2B it is seen that each disc comprising the distribution disc assembly 9, includes a plurality o£ micro-nozzles lal, 2al, 3al, etec,, for the outlet of the water and gases into the polarization/voltage and combustion zones. The exploded view of Figure 2C shows another view of the injector and additionally depicts two supply line inlets 16 and 17, the third not being shown (because of the inability to represent the uniform 120° separation of three lines in a two-dimensional drawing). In the injector, water mist (forming droplets in the range, for example, of from 10 to 250 microns and above, with size being related to voltage intensity) is injected into fuel-mixing and polarizing zone by way of water spray nozzles lal. The tendency of water to form a “bead" or droplet is a parameter related to droplet mist size and voltage intensity. Ionized air gases and non-combustible gases, introduced through nozzles 2al and 3al1, are intermixed with the expelling water mist to form a fuel-mixture which enters into voltage zone 6 where the mixture is exposed to a pulsating, unipolar high intensity voltage field (typically 20,000 volts at 50 Khz or above at the resonant condition in which - current flow in the circuit (amps) is reduced to a minimum) created between electrodes 7 and 8. Laser energy prevents discharge of the ionized gases and provides additional energy input into the molecular destabilization process that occurs at resonance. It is preferable that the ionized gases be subjected to laser (photonic energy) activation in advance of the introduction of the gases into ‘the zone(s); although, for example, a fiber optic conduit may be useful to direct photonic energy directly into the zone. Heat generated in the zone, however, may affect the operability of such an alternative configuration. The electrical polarization of the water molecule and a resonant condition occurs to destabilize the molecular bonding of the hydrogen and oxygen atoms. By Spark ignition, combustion energy is released. To ensure proper flame projection and subsequent flame stability, pumps for the ambient air, non-combustible gas and water introduce these components to the injector under static-pressure up to and beyond 125 psi.  Flame temperature is regulated by controlling the volume flow-rate of each fluid-media in direct relationship to applied voltage intensity. To elevate flame temperature, fluid displacement is increased while the volume flow rate of non-combustible gases is maintained or reduced and the applied voltage amplitude is increased. To lower flame temperature, the fluid flow rate of non-combustible gases is increased and pulse voltage amplitude is lowered. To _ establish a predetermined flame temperature, the fluid media and applied voltage are adjusted independently. The flame-pattern is further maintained as the ignited, compressed, and moving gases are projected from the nozzle-ports in distribution disc assembly 4 under pressure and the gas expands in the zone and is ignited.  In the voltage zone several functions occur Simultaneously to initiate and trigger thermal energy-yield. Water mist droplets are exposed to high intensity pulsating voltage fields in accordance with an electrical polarization process that separates the atoms of the water molecule and causes the atoms to experience electron ejection. The polar nature of the water molecule which facilitates the formation of minute droplets in the mist appears to cause a relationship between the droplet size and the voltage required to effect the process, i.e. the greater the droplet size, the higher the voltage required. The liberated atoms of the water molecule interact with laser primed ionized ambient air gases to cause a highly energized and destabilized mass of combustible gas atoms to thermally ignite. Incoming ambient air gases are laser primed and ionized when passing through a gas processor; and an electron extraction circuit (Figure 5) captures and consumes in sink 55 ejected electrons and prevents electron flow into the resonant circuit. In terms of performance, reliability and safety, ionized air gases and water fuel liquid do not become volatile until the fuel mixture reaches the voltage . and combustion zones. Injected non-combustible gases retard and control the combustion rate of hydrogen during gas ignition. In alternate applications, laser primed ionized liquid oxygen and laser primed liquid hydrogen stored in separate fuel-tanks can be used in place of the fuel mixture, or liquified ambient air gases alone with water can be substituted as a fuel-source. The injector assembly is design variable and is retrofit-able to fossil fuel injector ports conventionally used in jet/rocket engines, grain dryers, blast furnaces, heating systems, internal combustion engines and the like. EXAMPLE II A flange mounted injector is shown in cross-Section in Figure 3 which shows the fuel mixture inlets and illustrates an alternative three (3) nozzle configuration leading to the polarization (voltage) and combustion zones in which one nozzle 3la, 32a and 33a for each of the three gas mixtures is provided, connected to supply lines 31 and 32 (33 not . shown). Electrical polarization zone 36 is formed between electrode 38 and surrounding conductive shell 37. The capacitative element of the resonant circuit is formed when the fuel mixture, as a dielectric, is introduced between the conductive surfaces of 37 and 38. Figure 3A is a frontal view of the operative end of the injector. EXAMPLE III Multiple injectors may be arranged in a gang as shown in Figure 4 in which injectors 40, 41, 42, 43, 44, 45, 46, 47, 48 and 49 are arranged concentrically in an assembly 50. Such a ganged array is useful in applications having intensive energy requirements such as jet aircraft engines, and blast furnaces. EXAMPLE IV The basic electrical system utilized in the invention is depicted in Figure 5 showing the electrical polarization zone 6 which receives and processes the water and gas mixture as a capacitive circuit element in a resonant charging circuit formed by inductors 51 and 52 connected in series with diode 53, pulsed voltage source 54, electron sink 55 and the zone/locus 6 formed from conductive elements 7 and 8. In this manner, electrodes. 7 and 8 in the injector form a capacitor which has electrical characteristics dependent on the dielectric media (e.g., the water mist, ionized gases, and non-combustible gases) introduced between the conductive elements. Within the macro-dielectric media, however, the water molecules themselves, because of their polar nature, can be considered micro-capacitors. EXAMPLE V Fuel distribution and management systems useful with the injector of this application are described in my co-pending applications for patent, PCT/US90/6513 and PCT/US90/6407  A distribution block for the assembly is shown in Figure 6. In Figure 6 the distribution block pulses and synchronizes the input of the fuel components in sequence with the electrical pulsing circuit. The fuel components are injected into the injector ports in synchronization with the resonant frequency to enhance the energy wave pulse extending from the voltage zone through the flame. In the configuration of Figure 6, the electrical system is interrelated to distribution block 60, gate valve 61 and separate passageways 62, 63, and 64 for fuel components. The distributor produces a trigger pulse which activates a pulse shaping circuit that forms a pulse having a width and amplitude determined by resonance of the mixture and establishes a dwell time for the mixture in the zone to produce combustion. As in my referenced application regarding control and management and distribution systems for a hydrogen containing fuel gas produced from water, the production of hydrogen gas is related to pulse frequency on/off time. In the system shown in Figure 6, the distributor block pulses the fluid media introduced to the injector in relationship to the resonant pulse frequency of the circuit and to the operational on/off gate pulse frequency. In this Manner the rate of water conversion (i.e., the rate of fuel production by the injector) can be regulated and the pattern of resonance in the flame controlled. What is claimed is: 1. The improved method of converting water into a hydrogen containing fuel comprising: providing a mist of water in a defined zone determined by conductive members, the surfaces: of which define the opposite plates of a capacitive element in a resonant circuit, and subjecting the water mist in the zone to a unipolar pulsing electrical signal, such that resonance of the circuit is achieved, whereby hydrogen is disassociated from water molecules in the zone as a gas. 2. The method of claim 1 in which the resonant circuit is an electrical circuit including an inductive member 3. The method of Claim 2 in which the inductive member is in series relationship with the capacitive element. 4. The method of Claim 1 in which non-combustible gases are injected with water into the zone. 5. The method of Claim 1 in which ionized gases are injected with water into the zone.  6. The method of Claim 5 in which the ionized gases are subjected to excitation by photons. 7. The method of Claim 1 or Claim 2 or Claim 3 or Claim 4 or Claim 5 or Claim 6 including the oxidation of the hydrogen gas released to produce thermal energy. 8. The method of Claim 1 or Claim 2 or Claim 3 or Claim 4 or Claim 5 or Claim 6 including the oxidation of the hydrogen gas released to produce an explosive force of combustion. 9. The method of Claim 1 or Claim 2 or Claim 3 or Claim 4 or Claim 5 or Claim 6 in which the media in the zone is subjected in the zone to physical pulsing corresponding to the resonance of the circuit. 10. Apparatus useful in a method for the conversion of water into a hydrogen fuel including: electrically conductive surfaces that form the opposite surfaces of an electrically capacitive element in a circuit; means for injecting water as.a fine mist into the zone defined by the electrically conductive surfaces; and  means for achieving resonance in the circuit at a frequency determined substantially by the dielectric properties of the water in the zone, whereby hydrogen is disassociated from water molecules in the zone as a gas. 11. Apparatus in accordance with Claim 10 including means for the injection of gases with water into the zone to produce a mixture and in which the resonant frequency is related to the dielectric properties of the mixture. 12. Apparatus in accordance with Claim 10 or Claim ll including means for causing ignition of the hydrogen gas. 13. Apparatus in accordance with Claim 10 or Claim 11 including further means for subjecting the media in the zone to physical pulsing. CA1234774A1 Hydrogen Generator System PDF Download: SMeyer-CA1234774A1-Hydrogen_Generator_System.pdf Y e Consumer and Consommation ~ Corporate Affairs Canada et Corporations Canada (11) (a) wo. 1-234 774 (45) ISSUED 880405 (52) CLASS 204-78 C.R. CL. 204-1644 (51) INT. CL. C25B 1/04aa) cs) CANADIAN PATENT a2 (54) Hydrogen Generator System (72) Meyer, Stanley A., | U.S.A. . : (21). APPLICATION No. 420,908 (22) FILED 830204 mo ! r No. OF CLAIMS 15 | Canad DISTRISUTED BY THE PATENT OFFICE, OTTAWA. CCA-274 (11-82) ABSTRACT Process and apparatus for dissociating hydrogen atoms from a water molecule by electrical force. Particularly, the separation of the hydrogen and oxygen atoms from the water molecule by the application of a non-regulated, non- filtered, low-power, direct current voltage electrical potential applied to two non-oxidizing similar metal plates having water passing therebetween. The direct current voltage may be continuous, but the action can be enhanced by pulsing the non-regulated and non-filtered direct current voltage. The apparatus comprises various. constructional configurations and alternative embodiments for segregating the generated hydrogen gas from the oxygen gas. The water need not be pure and may contain contaminants. The release of the hydrogen and oxygen atoms causes the contaminants to fall away, thereby enabling the system to be utilized in a liquid slurry removal system. Alternatively, the recombining of the hydrogen and oxygen would give pure water.  Background 1234774 The potential availability of hydrogen as a Supplement to and eventually complete replacement of the present day available fuels is most appreciated. The efficiency of hydrogen as a fuel and its pollution free qualities further enhances its attractiveness. The prior art systems have been Successful in splitting the Sos. . hydrogen atoms from the oxygen. However, cost per Btu is most prohibitive and completely restricts the known process from commercialization. The most commonly understood method of separating the hydrogen and oxygen atoms from water is electrolysis. This comprises placing a direct current voltage to.a solution of water and potassium hydroxide. When current flows, an exchange of ions and electrons occurs between the electrodes. Hydrogen atoms collect at the negative electrode (cathode) and oxygen atoms at the positive electrode (anode). A Separation between electrodes separates the gases. Significantly, this process requires a chemical solution; that is, it does not Operate when using pure water. Furthermore, the cast per million Btu is in the order of three times the cost of gasoline. Other electrolysis processes have been devised and disclosed but are more sophisticated, complicated, complex and costly with attendant unreliability. Another Process under Study. comprises nuclear energy to supply heat in a thermal of the hydrogen dissociation. The problems with the process include the lack of container materials that can withstand temperatures involved (900°C) and a practical method of attaining such temperatures. The addition of inorganic compounds to the water permits lower temperatures but again, adds to the complexity of the process & commercial method known as the Bosch process, consists in passing steam over highly heated carbon in the presence of a Suitable catalyst. Carbon monoxide, CO, and hydrogen are first formed as shown in the following equation: The resulting carbon monoxide then reacts with more steam, forming carbon dioxide and hydrogen: The carbon dioxide is Separated from the hydrogen by passing the mixture through water under pressure; the carbon dioxide dissolves in the water and leaves the hydrogen pure or nearly so. Another process consists in the action of steam on methane, CH4. The equations for the reactions that take place are: The resulting carbon dioxide and hydrogen are separated as in Bosch process. In a similar way, hydrogen may be obtainéd ‘from other hydrocarbons.  Hydrogen is also obtained as a by-product from processes designed to prepare other substances, for example in the preparation of chlorine by electrolysis of sodium chloride solution: and other important processes. The symbol (aq) tells us that the substances are present in water (aqueous) solutions.  Finally, there is the natural way of attaining hydrogen by photosynthesis. At best the process is still in the laboratory small-scale stage and those in the art acknowledge the process can produce hydrogen with an efficiency of only 373%. It is generally acknowledged by scientists that every form of hydrogen production must be explored ~~ even 1£ it is too costly, inefficient, or impractical. But, more significantly, hydrogen will be the fuel of the future. The only question remains how and when it will be produced. Reference is made to the publication Cheaper Hydrogen. Popular Science, September 1981, pages 10 through 14, that reviews and updates the above-noted processes. Summary of Invention The process of the present invention, unlike those of the prior art, is a simple, efficient, and low cost process for separating the hydrogen and oxygen atoms from water. No chemicals are added to the water and the electrical power utilized is only negligible. In its most fundamental concept the water (which may be uncontaminated or pure water, salt water, or contaminated water) is passed between two plates of similar non-oxidizing metal. The one plate has placed thereon a positive potential and the other a negative potential from a very low direct current voltage power source. The hydrogen atoms are separated and collected for utilization. The contaminants in the water are dissociated and the dissociated parts may be collected and disposed of or utilized. This in turn leads to recombining the hydrogen’ and oxygen to form pure water. The direct current voltage is non-regulated and non-filtered. Experimentation demonstrated that the direct current voltage acts as a static force on the water molecules; whereas the rippling direct current voltage acts as a dynamic force . Pulsating the direct current further results in a dynamic force and enhances considerably the splitting of the atoms from the water molecules, The apparatus for carrying out the process is extremely simple and can be manufactured most inexpensively. Certain plate arrangements and configurations are disclosed with graphical illustration of relative efficiency. Alternative structure for separating and collecting the hydrogen from the oxygen is disclosed. Objects It is accordingly a principal object of the present invention to provide method and means that is operable for producing hydrogen and oxygen from any natural water irrespective of its purity. Another object of the present invention is to provide a hydrogen/oxygen generator that is operable from very low electrical power, extremely efficient, and wherein the cost o£ Operation is minimal. Another object of the present invention is to provide a. hydrogen/oxygen generator using water containing contaminants, and thereafter recombining the hydrogen/oxygen to form pure water. Still another object of the present invention is to provide a hydrogen/oxygen generator that utilizes apparatus of simple and low cost materials, and which structure can be made in varying sizes, and duplicated without loss of efficiency. Other objects and features of the present invention will become apparent from a reading of the detailed description of the preferred embodiment and its alternative structures when taken in conjunction with the drawings in which:  BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is an illustration in cross~section of the operable constructed preferred embodiment of the present invention; Figure 2 illustrates a coaxial cluster or array of plates utilized in the embodiment of Figure 1; Figure 3 is a first alternative plate arrangement, a concentric coaxial array; Figure 4 is another alternative plate arrangement, a flat plate array; Figure 5 diagrammatically illustrates applying a voltage potential to several plates; Figure 6 illustrates the principles of the present invention in its most simplified embodiment; ‘Figure 7 is the preferred embodiment shown in Figure 1 except in this illustration, the view is perspective; Figure 8 is a graphical illustration of amperage versus gas generated, and effect as to condition of water; Figure 9 is a graphical illustration of D.c. voltage versus gas generated, and increases in water temperatures; . . generation Figure 10 is a graphical illustration of. gas generator versus tube length in a tubular plate arrangement; ‘Figure 11 is a graphical illustration of applied power versus gas generated for pure water;  Figure 12 is a graphical illustration of gas generation for three different geometrical configurations of plate structure; Figure 13 is a graphical illustration of gas generated with the plates having increasing separation; Figure 14 is a graphical illustration of electrical costs versus gas generated, and increases in Exciter Plate 5; Figure 15 is a graphical illustration of different applied power versus gas generated, for various types of water conditions; and Figure 16 is a graphical illustration of gas generated versus pulse direct current repetition rate.  Detailed Description of Invention as Depicted in Drawings With particular reference now to Figure 6, there is illustrated schematically in cross-section the invention in its most simplified embodiment. A structure 110 contains water supply 15 comprising molecules 62a xxx 62n, of hydrogen 38a xxx 38n, oxygen, 39a xxx 39n, and foreign substances 64a xxx 64n. A pair of plates 9a and 9b consisting of non-oxidizing metal ~- and both of the same metal, are submerged in the water 15. Attached to terminal 32 on the first of the plates 9a is a wire having its other end connected to the negative terminal power source 30 and another wire is connected to terminal 31 on Plate 9b the other end of such wire being connected to the positive terminal of the aforesaid direct current voltage electrical source 30, The direct current voltage applied to the water passing between plates 9a and 9b is sufficient to dissociate the hydrogen atoms 38a xxx 38n and oxygen atoms 39a xxx 39n (appearing as bubbles) from the water molecules 62a xxx 62n. The forceful action of the applied potential attacks the Molecule structure of the water and not its atomic structure. The foreign substance or contaminants 64a xxx 64n are broken” away from the water molecule 62a xxx 62n, and spill over the outside area of the plates 9a and 9b to a collector at the bottom of the tank 10. The hydrogen gas 63a xxx 63n and oxygen gas 65a xxx 65n rises above the liguid. The gases are separated, collected and thereafter utilized all as set forth below. The process shown with the apparatus of Figure 6 is operable, as depicted schematically, in its most crude form. To increase and enhance the action, the process and the apparatus are improved upon as shown in the constructed and preferred embodiment of Figure 1 (a cross~sectional view) and Figure 7 (a perspective view). The voltage source 30 (shown schematically in Figure 5) supplies a direct current voltage that is rectified but not filtered and not regulated. That is, the direct current voltage is rippled and unregulated. The varying amplitude $S3K5, ripples, in terms of applied force act as a constant static physical force. The amount of electrical power required by the hydrogen/oxygen generator of the preferred embodiment, as illustrated, is surprisingly minimal. For the embodiment shown in Figures 1, 2 and 7, the power source 30 supplies 12 volts at J ampere. It can be appreciated, that increasing the voltage would enhance the forceful action upon the water molecule. The correlation of gas generated vs, electrical energy is graphically illustrated in Figure 11. The gas generated is a linear function of the magnitude of voltage applied. However, there is a serious limitation to increasing the voltage. As the voltage/current is increased the temperature of the water increases and eventually reaches a condition where steam is generated -- as illustrated graphically in Figure 9. Further, as shown graphically in Figure 8, the current versus gas , generated is also a function of the type of water utilized. Therefore, in lieu of increasing the electrical power to enhance the action on the water molecules, other conditions must be considered. The first is to alter the plate source direct current voltage waveform, With particular reference to Figure 5 there is illustrated an electronic switch for switching on and off the rippled D.C. output of supply 30. The- ripple is not removed. The plates 32a XXX. 32n are connected to a common ground 34. The positive terminals 33a xxx 33n are connected respectively to contacts 31a Xxx 31n of switch 35 rotatively making and breaking contact with the direct-current voltage source 30. In function the pulsed rippled output voltage functions to forcefully apply to the water molecules a dynamic force, the pulse repetition rate determining the amount of gas generated. Other structured factors affecting the hydrogen gas generation comprise altering (1) plate size, (2) plate spacing, (3) number of plates, and (4) the plate configuration. All of these factors have been taken into consideration in the development of a plate configuration to provide optimum results for a preferred embodiment. With reference to Figure 2, there is shown an array or cluster of tubular plates utilized in the preferred embodiment of Figures 1 and 7. The term "plate" hereinafter, is intended to convey a large area electrical surface; and whether the surface is flat, curved, tubular or otherwise, is of no consequence except as hereinafter defined. Particularly, each tubular plate comprises an outside tube 32a XXX 32n, and an inside tube 33a xxx 33n. Connecting each of the inner tubes 33a xxx 33n is a terminal wire 34; and connecting each of the outside tubes through a common ground is a terminal wire 36. The two terminal wires 34 and 36 are connected to the positive and negative side respectively of the direct current voltage source 30. Intermediate the outside and inside tubes are a series of spacers 35a Xxx 35n.. The coaxial tubes in an array are shown pictorially in the perspective view of Figure.7. With particular reference to Figure 3 there is illustrated, as an alternative to that utilized in the preferred.embodiment, another plate arrangement and configuration... This concentric ring array comprises a series of co-axial radially spaced tubes with equal spacing between adjacent tubes. The center tube 38a and the alternate tubes 38b.and 38c serve as the positive plates connected to positive wire terminal 34. Each of the tubular plates 38a, 38b, and 38c is interconnected via connectors 8a and 8b to wire terminal 34. The three spacers 39a, 39b, and 39c maintain a uniform spacing between the respective tubular plates. With particular reference to Figure 4 there is shown still another plate arrangement and configuration. In this embodiment, shown in cross-section, the positive plates 9a xxx 9n are interconnected by electrode 12a whereas the negative plates lla xxx lin are interconnected by the electrode 12b. With particular reference to Figure 12 there is illustrated graphically the efficiency of the tubular plate array of Figure 2, the cluster tubular array of Figure 3, and the flat plate array of Figure 4. Specifically there is shown the gas generation versus the plate configuration. It can be appreciated from this graph why the embodiment of Figure 1 includes the cluster tubular array of Figure 2. As stated above another factor affecting the gas generation output is the plate separation. With particular reference to Figure 13 there is illustrated graphically plate Spacing versus gas generation. As can be seen, the greater the spacing the less gas generation. The efficiency versus spacing of the plates is a linear decrease with spacing. As stated above, the applied direct current voltage across the positive current voltage plates having water therebetween is a force applied -- in the nature of a physical force -- to the water molecules. The applied force is sufficient to cause the hydrogen and oxygen atoms to dissociate themselves from the Water molecule and anything else that may be included therewith. In the aforementioned prior art system of hydrogen gas generation such as the electrolysis process, it is essential that the water be distilled or otherwise made pure.  To determine the relative differences of the amount of gas generated versus the purity of the water, analysis was made of distilled water, rain water, city tap water, river water, well water untreated, well. water treated, and sea water. The results of gas generation versus electrical power are illustrated in Figures 8 and 15 graphically for each of the waters tested. It appears that water containing contaminants aids gas generation; however, the nature of the water contaminants appears to have no significance. The hydrogen atoms and oxygen atoms dissociate themselves from the water molecule. Anything else that may be included in the water is also bombarded loose and overflows the tank 37 and falls to the bottom 43. Having now examined the applied electrical force phenomena the physical configuration of the electrical plates, the power applied, and the condition of the water, reference is made specifically to-the construction, function and operation of the hydrogen gas generator of the present invention which is shown in cross-section in Figure 1 and in perspective in Figure 7. The container 10 is a square elongated box configuration completely enclosing and sealing the components as hereinafter described. Water, from which the hydrogen gas is to be taken, enters via inlet 42 to the chamber 36. The water is pumped or enters under normal pressure from a source via line 56. As mentioned above, the water need not be pure and hence may originate from any source. The water from source 42 enters chamber 36 which is a free area to an open top enclosure 37. The water entering chamber 36 is caused to rise upwardly through the plates of the cluster 60 previously described in more detail relative to Figure 2.  Applied to the inner tubular structures is a positive direct current voltage, and to the outer tubular structures of the cluster array 60 is applied a negative direct current voltage. The direct current voltage is applied via terminals 4 connected to a suitable direct current voltage power source 30. The hydrogen gas is depicted in Figure 1 as a solid circle 38 whereas the oxygen gas is depicted as the open circles 39. OSes The separated hydrogen and oxygen“gas rise into the accumulator chamber 47, Not all of the water molecules are broken up into their various atomic components. Thus, the unspent water 41 spills over the top of chamber 37 and drops down through outer chamber 54 and back to reservoir 43. As aforesaid, it is not necessary to utilize pure (uncontaminated) water, the intake water will include several forms of contaminants. As best understood, when the water molecule is bombarded with the dynamic and static electrical force, the contaminants adhering to the water molecules are shaken loose and released therefrom. The contaminants, too, rise to the top of chamber 37 and fill a part of the spillway 41. in that the contaminants do not contain hydrogen or oxygen, there will be no atomic breakup. The combination of water with contaminants drops down into extraction chamber 43. In the extraction chamber 43 most of the sediment or sludge will drop to the bottom of. the chamber 32. The water with most of the sediment removed passes through the ports 33a xxx 33n, through charcoal filter 31, and into return water chamber 44, The uppermost portion of the water in chamber 44 drops into Standpipe. 35. The water cleansed of substantially all contaminants, exits via pipe 45 and then through line 55 and back to inlet pipe 42. The combined water from inlets 55 and 56 is again processed as aforesaid. THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS : 1. A system for the release of hydrogen and oxygen gas from natural water having no electrolyte added thereto, comprising: a housing of non-corrosive, non-reactive, and non-oxidizing material, simi laa a pair of’electrical voltage conductive plates sSimitarly of . NON Gorrodeble : : : : a non-reactive, 1 and non-oxidizing material positioned in said housing with a spatial relationship to one another, means for passing said natural water between said plates; and means connecting one of said plates to a negative output terminal and the other of said plates to a positive output terminal of a variable D.c. voltage source which includes circuit means for restricting the current thereof to a negligible value relative to the magnitude of the voltage, Said voltage forming a positive electrical voltage zone adjacent said plate having said positive terminal connected thereto and a negative voltage zone adjacent said plate having said negative output terminal connected thereto, voltage when applied to said plates having a sufficient magnitude to cause the hydrogen atoms of the water molecule to be attracted to said negative zone, and the oxygen atoms to be attracted to said positive zone, and thereby force the hydrogen atoms and the oxygen atoms to disassociate themselves from the water molecule at a rate in dependence on the magnitude of the voltage applied to said plates. 4234774 2. The system as set forth in claim 1 including means selectively to vary the voltage and maintain it at a constant level. 3. The system as set forth in claim 1 wherein said variable voltage source further comprises pulsing circuit means and wherein the rate of release of said hydrogen and oxygen gas is directly related to the repetition rate of the voltage output pulses of said pulsing circuit. 4. The system as set forth in claim 3 wherein the magnitude of the output voltage of said variable voltage source is interrelated to the pulse repetition rate of the output pulse of sand pulsing circuit, and wherein the rate of the hydrogen and oxygen atoms disassociating from the water molecule is related to the magnitude of said voltage and the pulse repetition rate of said pulses. 5. The system as set forth in claim 1 wherein said variable voltage source includes means for varying the magnitude of said voltage from 0 volts to in excess of 110 volts and for restricting the current thereof to less than 1 ampere. 6. The system as set forth in claim 1, characterized in that said non-oxidizing plates are coaxial or alternatively have concentric surfaces. 7. The system as set forth in claim 1, characterized in that said non-oxidizing plates are a plurality of plates in an array. 8. The system as set forth in claim 1, characterized in that said non-oxidizing plates are a cluster of coaxial plates in an array. 9. The system as set forth in claim 1, characterized in that said non-oxidizing housing further comprises a gas collection chamber for maintaining a preset volume of gas under pressure. 10, The system as set forth in claim 7, characterized by switching means interconnected to each of said plates in said array and to said voltage source for switching in and out selected ones of said array of plates from said voltage source. 11. The system as set forth in the spacing between the plates, surface area of the plates, the configuration of the plates and plates is adapted to be changed claim 1 wherein at least one of the length of the plates, the the the voltage applied to the so as to alter the production number of plates, rate of hydrogen and oxygen gas. 12. The system as set forth in claim 1 further comprising means to separate the produced hydrogen and oxygen gases. 13. The process of releasing hydrogen and oxygen gas from natural water having no electrolyte added thereto, comprising: passing said natural water through a contained area having nen-daorrodable AGR-EOEEOSLVG, non-reactive electrically conductive plates therein, a pair of similar non-oxidizing, ’ applying a variable D.C. positive voltage across one of said plates and applying a variable D.C. negative voltage across the other of said plates, restricting the current of said variable voltages applied rash to said plates to a negligible value 4p GOS. to said voltage, said positive voltage forming a positive voltage zone adjacent said plate having a positive voltage applied thereto and said negative voltage forming a negative voltage zone adjacent the plate having a negative voltage applied thereto, Said variable voltages applied to said plates being of sufficent magnitude to cause the positive atoms of the water molecule to be attracted to the negative voltage zone and said plate and the negative atoms of the water molecule to be attracted to the positive voltage zone on said other plate, thereby forcing the hydrogen atoms and the oxygen atoms to disassociate themselves from the water molecules at a rate dependent on the magnitude of said variable voltage, and varying the magnitude of the variable voltage applied to said plates to vary the rate at which the hydrogen atoms and the oxygen atoms disassociate themselves from the water molecule. 14, The process of claim 13 further comprises pulsing the variable voltage applied to said plates at a variable repetition rate and varying the physical parameters of said plates in an interrelationship with said variable voltages. 15. The system as set forth in claim 7 further comprising switching means interconnected to each of said plates in said array and to said voltage source for switching in and out selected ones of said array of plates from said voltage source and wherein the number of said plates having said voltage source switched therein is directly related to the rate of hydrogen atoms and oxygen atoms disassociating from said water molecule CA1234773A1 Resonant Cavity Hydrogen Generator That Operates with a Pulsed Voltage Electrical Potential PDF Download: SMeyer-CA1234773A1-Resonant_Cavity_Hydrogen_Generator_That_Operates_with_a_Pulsed_Voltage_Electrical_Potential.pdf Consumer and Consommation Corporate Affairs Canada al Corporations Canada (11) (A) No. 1 234 773 (45) ISSUED 880405 (52) CLASS 204-78 C.R. CL. 158-14 (51) INT. CL. ¢C25B 1/04) (54) Resonant Cavity Hydrogen Generator That Operates With a Pulsed Voltage Electrical Potential (72) Meyer, Stanley A., U.S.A. (21) APPLICATION No. 420 ,902 (22) FILED 830204 (30) PRIORITY DATE U.S.A. (P65,797) 820924 No. OF CLAIMS 22 DISTRIBUTED BY THE PATENT OFFICE, OTTAWA. CCA-274 (11-82)  ABSTRACT A process is disclosed for producing hydrogen and oxygen gasses from water which includes having water in a cavity which has a selected resonant frequency and applying of voltage potential to exciter elements in contact with the in the cavity so that one element maintains a positive charge and the other a negative charge. The voltage potential is pulsed at a frequency matching the resonant frequency of the cavity. The apparatus includes preferably a spherical shell which is a first exciter element formed of an electrically conductive non-reactive material and defines the boundary of a cavity. The cavity has a pre-determined resonant frequency and a second exciter element of the same material as the the first element is located within the cavity in selected spaced relationship therewith. Water can flow into the cavity gasses produced outflow from the top of the cavity, such gasses being obtained from the water in the cavity when an electrical pulsating potential is applied to the exciter elements RESONANT CAVITY FOR A HYDROGEN GENERATOR CROSS REFERENCE: In the non-electrolysis process disclosed and Claimed in my co-pending Canadain patent application, Serial Number 420,908, filed 4 February 1983, for HYDROGEN GENERATOR SYSTEM, for separating hydrogen and oxygen atoms from water, water is passed between two plates of similar non-oxidizing metal. The one plate has placed thereon a positive potential and the other a negative potential from a very low-direct— current power source. The action of the direct current voltage causes the hydrogen and oxygen atoms to be separated. The contaminants in the water also separated out and may be collected or utilized and disposed of. This in turn lends the process to recombining the hydrogen and oxygen into pure water. The direct current voltage applied to the plates is non-regulated and non-filtered. The direct current acts as a static force on the water molecules whereas the rippling direct current voltage acts as a dynamic force. Pulsating the direct current further acts as a dynamic force and enhances considerably the splitting of the atoms from the water molecules. An increase in voltage potential further increases the hydrogen output. Certain plate arrangements and configurations with graphical illustrations of relative efficiency are disclosed. In my co-pending patent application, supra, it was shown that the hydrogen gas generator is variably increased by varying the construction of the exciters; more particularly, by (1) increasing the area of the plates, (2) reducing the Space between the plates, and (3) altering the physical configuration of the plate. SUMMARY OF THE INVENTION: The basic structure of and principles of operation disclosed in the aforesaid co-pending patent application are utilized. The non-oxidizing exciters are of a construction, spherical in a preferred embodiment, with a given spacing between the positive and negative elements to form a resonant cavity at a given frequency. The direct current voltage is pulsed at a repetition rate (frequency) to match the resonant wavelength. At the matched frequency the action cof the 5 pulsed direct current voltage is enhanced considerably. The forceful action on the water molecule causes the molecules to break into their atomic structure at a much more rapid rate; thereafter, the gas atoms are set into motion within the resonant cavity, thereby increasing velocity to a jet-like action as they are released from a port. The single resonant cavity has a controlled size port for the utilization of the high velocity gasses. The resonant cavity plate structure in a preferred arrangement is an array of elements. The gasses emitted from the array are combined and expelled as high velocity gasses from a common nozzle and utilized. A principal object of the present invention is to provide an improved method and apparatus for the separation of hydrogen/oxygen gasses from water. In accordance with one aspect of the present invention there is provided a process for producing a gaseous medium which includes hydrogen and oxygen from water, comprising: providing at least one pair of spaced apart electrically conductive , non-oxidizing exciter elements in association with a cavity having a selected resonant frequency and in which there is water, said exciter elements being in 4 contact with the water in the cavity, applying a voltage potential to said exciter elements such that one element maintains a positive charge and the other a negative charge, 30. and pulsing the voltage patential at a frequency matching the resonant. frequency of the cavity. In accordance with a further aspect of the present invention there is provided apparatus for producing a gaseous, medium which includes hydrogen and oxygen from water 35 comprising a first exciter element formed of an electrically conductive non-reactive material having a surface which defines the boundaries of a cavity, said cavity having a predetermined resonant frequency with a quantity of water therein, a second exciter element of the said same material within said cavity in selected spaced relationship from said first exciter element, means permitting the inflow of water into said cavity and means permitting the outflow of gasses from said cavity, said gasses being obtained from water in the cavity when an electrical pulsating potential is applied to said exciter elements. BRIEF DESCRIPTION OF DRAWINGS: Figure 1 is a schematic illustration of the structure of the present invention in its most simplified arrangement. Figures 2, 2A, and 2B, are a series of waveforms illustrating the pulse rate of the direct current to’ match the resonant frequency of the structure of Figure 1. Figure 3 is a schematic illustration of the utilization of the structure of Figure 1. Figure 4 is a first alternative structure to that shown in Figure 1. Figure 5 is another alternative structure to that shown in Figure 1. Figure 6 is another alternative structure to that shown in Figure 1. Figure 7 and 7A are an array of exciters, such as shown in Figure 1, in a preferred embodiment. Figure 8 is an array of exciters, such as shown in Figure 3, in a preferred embodiment. DETAILED DESCRIPTION OF INVENTION: Reference is now made to the several figures depicting the preferred embodiment of the present invention. Referring to Fig. 1. there is illustrated a device 10 which includes a vessel 5 having therein an outer shell 9 and an inner element 15. The shell 9 has a gas expulsion opening 8 in its uppermost region, and a gas guide 13 flared out from the opening 8. Shell 9 and element 15 are spherical the latter being centrally positioned within the sphere 9 and of much smaller diameter. The outer shell 39 is the grounded negative side and adopted to and connected to a suitable DC voltage source via terminal 16 and wire 17. The inner element 15, is adapted for connection to the positive side of the potential via terminal 18, wire 14 and a support 11 for the element 15 which enters shell 9 through a water intake opening 12 in the lower end thereof. The vessel 5 contains water 4, replenished from a source through faucet 6, at a level above the shell 9 and element 15. The water 4 flows into the cavity of shell 9 through the lower opening 12, As described in my aforesaid patent application the direct current electrical potential is in the nature of a physical force on the water molecule which causes the water molecule to break up into its atomic structure liberating hydrogen and oxygen in gaseous form from the water. Also other gasses, such as nitrogen, that may be entrapped therein will be released. In that the aforesaid process is not an electrolysis process, water of any origin may be used, irrespective of the contaminant content. In the process, as the gasses are released the contaminants will be separated and fall to the bottom of the container. Again, since the process does not in fact generate hydrogen but simply releases the hydrogen, the process is most efficient and not power intensive. The direct current voltage/potential is of extremely low voltage and only of an insignificant current. There is described in the process of my co-pending patent application apparatus and methods for increasing the output of hydrogen for a given voltage/potential input. For instance plate spacing and plate area are discussed; pulsing the direct current and applying an unfiltered direct current all in one manner or another enhances the release of hydrogen, Increasing the voltage/potential will increase the gas output proportionally. In each of the apparatus or methods for increasing the output, the physical force applied to the water molecule is the controlling factor. It can be appreciated that limitations may be reached in the control of these dynamic and static forces. in the present invention, the preferred embodiment utilizes in one manner or another, all of the aforementioned output control factors and is directed primarily to pulsing the direct current potential. It has been found that the distance between plates of the exciters will have, or can be adjusted to have, a ‘wavelength or partial wavelength, or a multiple wavelength , related to the motion of the water molecule in travelling from the one plate to the other . Therefore, the structure is constructed to be a resonant cavity at some given frequency of the molecular motion. With specific reference again to Figure 1, the distance from the outer surface of the central element 15 to the inner surface 9a of the outer spherical element 9 will be at some wavelength correlated to the molecular motion of travel. When the wavelength is matched with a physical force equal in frequency to that wavelength the inner area becomes a resonant cavity. As understood in resonant cavities of an electron nature, the molecules are set into motion and will be bombarded back and forth from the one surface to the next continuously so long as the initial force is applied. In the sphere of Figure 1, the directions that the water molecules may travel from the inner sphere 15 to the surface 9a of the other sphere 9 is of an infinite number. Considering a single molecule, the water molecule's motion will under normal conditions be impeded by the water. If the distance between the inner and outer sphere is co-related to a wavelength related to the frequency of the pulsating direct current applied to the water, the water molecule will be set in motion and thereafter enhanced in motion in the resonant cavity 3 and overcome the impediment of water. Further, the molecule upon striking the inside surface of the outer sphere, will be reflected and directed to an angular surface where it again will be reflected. This action continues indefinitely and will continue until the applied energy is terminated. Thus, a resonant cavity causes the water molecule to travel back and forth continuously and at a velocity that increases geometrically. The above-noted single molecule's motion of travel will be further increased in velocity when it is considered that the number of water molecules is infinite and the striking force is not only from surface-to-surface but also from molecule-to-molecule . The enhanced physical action on the water molecule in the resonant cavity 3 will directly affect the breaking up of the molecule into its gaseous atomic structure. As this occurs, the hydrogen, oxygen and other gasses that may be released from the water will be similarly set into motion. The gas atoms will be reflected from the surface 9a and bombard each other in geometric proportion to the energy applied. The water impediment now is relatively insignificant. With reference to the graph of Figure 2, the direct current input voltage a is pulsed at a repetition rate, as shown by waveform 6, (per second) equal to the resonance frequency of the cavity 3 . To enhance the forceful action of the applied pulsed direct current voltage/potential on the water molecule and the sub-atomic action for the release of gasses, the pulsing of the direct current is periodically interrupted as shown in the graph of Figure 2A. That is, the pulse frequency and pulsed direct current C, C1, and C2 is interrupted in uniform intervals d1, d2, and d3. Again, the pulsed direct current may be periodically interrupted , That is, the interruption between pulses C, C1, C2, and C3... is for different time periods: e, e1, e2, and e3. Returning to Figure 1, an opening @ is provided in the uppermost portion of the outer sphere 9 of the resonant cavity 3 structure. The travel of the gas atoms 7 bombarding back and forth in the resonant cavity 3 will eventually pass through the opening 8. However, the movement of the gas atoms 7 has been accelerated as aforesaid and when they pass through the opening 8 they are at an extremely high velocity. That is, the motion of the gas atoms 7 will pass out of opening 8 as though they are jet propelled. The structure of Figure 1 is that of a sphere 9 with another sphere 15 positioned therein. The spacing between the outer surface of the inner sphere 15 to the inner wall 9a of sphere 9 provides a resonant cavity to a given frequency of the physical force of the direct current voltage. Other resonant cavities may be utilized in other arrangements. In Figure 3 the resonant cavity structure 20 is utilized in a first completed self contained embodiment. Water 4 enters via nozzle 19 directly into the chamber of the closed sphere 9. The structure of Figure 3 is substantially identical in operation to that of Figure 1. However, in this embodiment, the opening 8 has a nozzle 2 therein with ports of selected size. The velocity of the gasses being expelled determines the sizes of the ports of the nozzle 2. ‘That is, the ports in the nozzle 2 must be sufficiently large to permit an adequate amount of gas to be expelled to maintain a flame, but not so small that the velocity of the gasses expelled would be so great that combustion cannot be sustained. The direction of the high velocity gasses is controlled by guide 13. The gasses 7. may be ignited by igniter 25 or utilized directly in another manner. The resonant cavities of Figures 1, 3, and 7 are related to the spacing between an outside and an inside spherical structure comprising a resonant cavity to the excited atoms .in the atomic process. Other configurations particularly those shown in the aforesaid co-pending patent application, may be constructed or modified to be resonant cavities. The resonant cavities will enhance the release of the gasses, irrespective of their configuration. However, the structure that is found most productive may be related to its utilization in an operable embodiment. More particularly, the resonant cavity of Figure 4 is an elongated exciter 31. The Spacing between the elements 33 and 36 provide the resonant cavity. The gasses 35 in this embodiment will be jettisoned broadside along the slot 32. I n Figure 5 there is illustrated the coaxial exciter arrangement of the preferred embodiment of the aforementioned co-pending patent application. In this embodiment the spacing 34 between the inner plate 39 and the inner wall of the outer element 37 is adjusted to be resonant at a given frequency. The input direct current is pulsed accordingly. The gasses are propelled along the longitudinal axis of the elements 37 and 39 and expelled from the end 38 of the exciter. Corrugations The exciter 40 of Figure 6 is an improvement over an earlier development in that increased surface area is provided by corrugations in the walls that create the resonant cavity. The corrugations provide an enhancement of the sub-atomic action on the water entering at 44. The spacing 46 between the plate 41 and plate 42 is such that the cavity is resonant at a particular frequency, as aforementioned. However, instead of a forward direct line back-and-forth path of the atom flow, the corrugations of the convex 47 and concave 49 surfaces cause the atoms to move in a forward and backward of back~and-forth path. The increased movement, in turn, increases the sub-atomic action and the velocity of the flow of gasses 45 emitted from the end 43 of exciter 40. Referring now to Figures 7 and 7A, the structure of Figure 1 is in an array of resonant cavities 50a to 50n. Specifically, the housing 51 having water 52 therein includes the array of exciters, having a positive potential applied to its central element 53a to 53n, via terminal 64 and a negative potential to the outer element 55a to 55n. The direct current potential is pulsed in a repetitive frequency, as noted above, to match the frequency of the resonant cavity. The gasses 54a to 54n being released from respective ones of exciters 50a to 50n are directed by the guide walls 56 to the upper chamber 58 wherein the high velocity gasses 54 are accumulated. As the gasses 54 are accumulated the pressure in the upper chamber 58 increases proportionally. With reference to Figure 3, the port 2 is correlated in size of opening relative to the velocity of the gasses. If the port 2 is oversize the velocity of the gasses will be so great that a flame could not be sustained and backfire may occur, hence the port size is limited. In Figure 7, the ports 57a to 57n may be greater in size that the individual port 2 of Figure 3. The individual outputs are not utilized to support a flame hence the significance of limiting the port size and the danger of flashback is not critical. The outputs from each of the exciters are accumulated as gasses 54 in a master chamber 58. With particular reference now to Figure 8 there is illustrated an array of the gas exciters illustrated in Figure 3. The operation of the individual gas exciters is identical to that of Figure 3 except that in the array the several gas flames from the individual exciters are accumulated in chamber 75.  Throughout the above specification the term "plate" is used to denote an element as described. It is specifically understood that the term plate is not to be limited to a flat or planar construction, but may be a structure of any configuration. Although certain embodiments are shown, modification may be had without departing from the spirit and scope of the invention. In the foregoing there is described with reference to the drawings, apparatus for obtaining a gaseous medium which includes hydrogen and oxygen from water. The following is a brief explanation as to what is believed takes place in practicing the invention. A water molecule is exposed to a potential difference physically between one positively charged and one negatively charged electrical voltage zone. The unlike hydrogen and oxygen atoms, already having a positive negative charge in the bound molecule, assume opposing electrical characteristics that are equal. in magnitude and potential. In the zone of potential difference the electrical polarity of the water molecule is stabilized. Although the molecule is stabilized in electrical polarity by the application of the potential difference, the bond between the atoms becomes weakened. The electrical polarization of the water molecule according to the invention is basically a four step process: First, the water molecule is subjected to a potential difference physically in oppositely charged electrical voltage zones. Second, the water molecule becomes electrically polarized. Third, the electrical polarization of the molecule as it affects the electrical charges of the component hydrogen and oxygen atoms greatly weakens  the stability of the overall molecule. And fourth, because the voltage zones are present and have opposite electrical attractions, the electron bonding of the hydrogen and oxygen atoms molecule is broken and the molecule splits into its component atoms. The hydrogen is attracted to the negative electrical voltage zone, while, simultaneously, the oxygen is attracted to the positive electrical voltage zone. Because the bond between the hydrogen and oxygen is already weakened by the first electrical polarization of the water molecule, little energy in the form of applied voltage is needed to actually separate the hydrogen and oxygen atoms. Voltage, a potential energy and not energy consumption (amps), provides the threshold impetus for the atoms to break away from one another in ‘the molecule ina strictly physical process. Hydrogen gas and oxygen gas are released in great amounts with little energy consumed, and without chemical interactions. Once the molecule splits, the liberated hydrogen and oxygen atoms will not recombine. In an explanation of the theory of operation of the invention a water molecule (H20) in a normal state has a molecular bond in a neutral molecule that includes the sharing of electrons between two nominally positive hydrogen atoms and a nominally negative oxygen atom. The molecule itself is in a neutral, uncharged, stable state. In the invention, electrical voltage zones are created. The atoms of the normally neutral water molecule take on an electrical charge; the oxygen atom takes on a negative electrical charge; the hydrogen atoms take on a positive charge. The covalent electron bonding of the molecule is disrupted by the introduced electrical charge and is weakened. Separation of the atoms, and the production of gas, occurs between the plates. The process is preferably done in a non-chemical environment; thus, any form of "natural" water may be utilized without additives or chemicals. Voltage zones are provided by electrically conductive non-oxidizing, non-corrosive, non-reactive excitor plates (formed from a material such as stainless steel) placed in a non-chemical, non-reactive housing. A voltage is applied to the excitor plates to provide a potential energy. Although current leakage will occur because of the residual conductivity of the water in the invention the flow of amperes is limited deliberately in any well known manner so as to be insignificant. Contaminants present in water do not affect the process. Gas production is achieved by pulsing the potential difference that creates the electrical voltage zones in a variable, repetitive manner. In general, the production of gas increases with either or both of the voltage applied and/or the frequency of: the voltage pulse. Because of the ability to control the gas production rate the method and apparatus of the invention provides a fuel cell that is a constant energy source. In practical application, there is no need for secondary storage medium for the gas produced. Natural water is the safest medium in which to store hydrogen atoms until they are needed for consumption. If the fuel cell is ruptured, the only material to spill out would be harmless water. THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS: 1. A process for producing a gaseous medium which includes hydrogen and oxygen from water, comprising: providing at least one pair of spaced apart electrically conductive, non-ox