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Showing posts with label fuel cell. Show all posts
Showing posts with label fuel cell. Show all posts

Sunday, 5 January 2014

Water Fuelled Cars: The Stanley Meyer Fuel Cell

Water Fuelled Cars
The Stanley Meyer Fuel Cell


 


Eye-witness accounts suggest that US inventor Stanley Meyer has developed an electric cell which will split ordinary tap water into hydrogen and oxygen with far less energy than that required by a normal electrolytic cell.

In a demonstration made before Professor Michael Laughton, Dean of Engineering at Mary College, London, Admiral Sir Anthony Griffin, a former controller of  the British Navy, and Dr Keith Hindley, a UK research chemist. Meyer's cell, developed at the inventor's home in Grove City, Ohio, produced far more hydrogen/oxygen mixture than could have been expected by simple electrolysis.

Where normal water electrolysis requires the passage of current measured in amps, Meyer's cell achieves the same effect in milliamps. Furthermore, ordinary tap water requires the addition of an electrolyte such as sulphuric acid to aid current conduction; Meyer's cell functions at greatest efficiency with pure water.

According to the witnesses, the most startling aspect of the Meyer cell was that it remained cold, even after hours of gas production.

Meyer's experiments, which he seems to be able to perform to order, have earned him a series of US patents granted under Section 101. The granting of a patent under this section is dependent on a successful demonstration of the invention to a Patent Review Board.

Meyer's cell seems to have many of the attributes of an electrolytic cell except that it functions at high voltage, low current rather than the other way around. Construction is unremarkable. The electrodes --- referred to as "excitors" by Meyer --- are made from parallel plates of stainless steel formed in either flat or concentric topography. Gas production seems to vary as the inverse of the distance between them; the patents suggest a spacing of 1.5 mm produces satisfactory results.

The real differences occur in the power supply to the cell. Meyer uses an external inductance which appears to resonate with the capacitance of the cell --- pure water apparently possesses a dielectric constant of about 5 --- to produce a parallel resonant circuit. This is excited by a high power pulse generator which, together with the cell capacitance and a rectifier diode, forms a charge pump circuit. High frequency pulses build a rising staircase DC potential across the electrodes of the cell until a point is reached where the water breaks down and a momentary high current flows. A current measuring circuit in the supply detects this breakdown and removes the pulse drive for a few cycles allowing the water to "recover".

Research chemist Keith Hindley offers this description of a Meyer cell demonstration: "After a day of presentations, the Griffin committee witnessed a number of important demonstration of the WFC" (water fuel cell as named by the inventor).

A witness team of independent UK scientifc observers testified that US inventor Stanley Meyer successfully decomposed ordinary tap water into constituent elements through a combination of high, pulsed voltage using an average current measured only in milliamps. Reported gas evolution was enough to sustain a hydrogen /oxygen flame which instantly melted steel.

In contrast with normal high current electrolysis, the witnesses report the lack of any heating within the cell. Meyer declines to release details which would allow scientists to duplicate and evaluate his "water fuel cell". However, he has supplied enough detail to the US Patent Office to persuade them that he can substantiate his 'power-from-water' claims.

One demonstration cell was fitted with two parallel plate "excitors". Using tap water to fill the cell, the plates generated gas at very low current levels --- no greater than a tenth of an amp on the ammeter, and claimed to be milliamps by Meyer --- and this gas production increased steadily as the plates were moved closer together and decreased as they were separated. The DC voltage appeared to be pulsed at tens of thousands of volts.

A second cell carried nine stainless steel double tube cell units and generated much more gas. A sequence of photographs was taken showing gas production at milliamp levels. When the voltage was turned up to its peak value, the gas then poured off at a very impressive level.

"We did notice that the water at the top of the cell slowly became discolored with a pale cream and dark brown precipitate, almost certainly the effects of the chlorine in the heavily chlorinated tap water on the stainless steel tubes used as "excitors".

He was demonstrating hydrogen gas production at milliamp and kilovolt levels.

"The most remarkable observation is that the WFC and all its metal pipework remained quite cold to the touch, even after more than twenty minutes of operation. The splitting mechanism clearly evolves little heat in sharp contrast to electrolysis where the electrolyte warms up quickly."

"The results appear to suggest efficient and controllable gas production that responds rapidly to demand and yet is safe in operation. We clearly saw how increasing and decreasing the voltage is used to control gas production. We saw how gas generation ceased and then began again instantly as the voltage driving circuit was switched off and then on again." 


"After hours of discussion between ourselves, we concluded that Stan Meyer did appear to have discovered an entirely new method for splitting water which showed few of the characteristics of classical electrolysis. Confirmation that his devices actually do work come from his collection of granted US patents on various parts of the WFC system. Since they were granted under Section 101 by the US Patent Office, the hardware involved in the patents has been examined experimentally by US Patent Office experts and their seconded experts and all the claims have been established."

"The basic WFC was subjected to three years of testing. This raises the granted patents to the level of independent, critical, scientific and engineering confirmation that the devices actually perform as claimed."

The practical demonstration of the Meyer cell appears substantially more convincing than the para-scientific jargon which has been used to explain it. The inventor himself talks about a distortion and polarization of the water molecule resulting in the H:OH bonding tearing itself apart under the electrostatic potential gradient, of a resonance within the molecule which amplifies the effect.

Apart from the copious hydrogen/oxygen gas evolution and the minimal temperature rise within the cell, witnesses also report that water within the cell disappears rapidly, presumably into its component parts and as an aerosol from the myriad of tiny bubbles breaking the surface of the cell.

Meyer claims to have run a converted VW on hydrogen/oxygen mixture for the last four years using a chain of six cylindrical cells. He also claims that photon stimulation of the reactor space by optical fibre piped laser light increases gas production.

The inventor is a protegee' of the Advanced Energy Institute.

From Electronics World & Wireless World (January 1991)



Water Electrolysis
Canadian Patent # 2,067,735
Water Fuel Injection System
Stanley Meyer

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 water molecules occurs.


Description

This invention relates to a method and apparatus useful in producing thermal combustive energy from the hydrogen component of water…

The invention of this present application represents a generational improvement in methods and apparatus useful in the utilization of water as a fuel source. In brief, the present invention is a microminiaturized 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 eliminated 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 fuel. 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.


Figures 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 3 and Figure 3A respectively show a side cross-section view and frontal view of an alternatively configured in injector.





Figure 4 shows a disk array of injectors.


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 (H2O) 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 # 4,936,961 and co-pending application serial # 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 resonant 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 (O) in 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


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 capacitive 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 are shown as 6A1 and 6A2 and 6B1 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 fro 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 approximately 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 0.10 to 0.15 inch in diameter; the ionized gas orifice is 0.15 to .20 inch diameter; and the non-combustible gas orifice is 0.20 to 0.25 inch 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 or ore volts at a frequency tuned to 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 o the mixture. In a spark-plug sized injector, the voltage zone will typically extend longitudinally about 0.25 to 1.0 inch to permit sufficient dwell time of the water mist and gas mixture between the conductive surfaces 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. In a confined zone such as a piston/cylinder engine, gas detonation under resonant conditions produces explosive physical power.

In the voltage zone, the time share ration 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 # 4,936,961 and application serial # 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 (H2O) 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 to that the 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 1 leading to first distribution disc 1A 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 o the injector. Conductive elements 7A and 7B (7A and 7B depict opposite sides if 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 of micro-nozzles 1A1, 2A1, 3A1, etc., 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 degree 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 1A1. 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 2A1 and 3A1, 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 126 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 if 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 liquefied ambient air gases alone with water can be substituted as a fuel source.

The injector assembly is design variable and is retrofitable 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 (3) nozzle configuration leading to the polarization (voltage) and combustion zones in which one nozzle 31A, 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 capacitive 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, 4, 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 established 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.


via Rex Research @ http://www.rexresearch.com/meyerhy/meyerhy.htm#elworld and http://www.rexresearch.com/meyerhy/2067735.htm

For more about the Stanley Meyer cell from the Rex Research site see http://www.rexresearch.com/meyerhy/meyerhy.htm


For more information about fuel from water see http://nexusilluminati.blogspot.com/search/label/water%20fuel
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Friday, 28 September 2012

Stanley Meyer’s Water Fuel Cell: How He Ran a Car on Water


Stanley Meyer’s Water Fuel Cell
How He Ran a Car on Water




http://api.ning.com/files/MCLsVHbQ4G7aBo7di-9ueRwAy-4O8vDmndnGEs1tC*Nt52qWopBXxpIRWnfa5Bjd3bC3779Wpt*oYB-LwyDGpZLz2fJcR3sr/06stanleymeyersdunebuggy.jpg


Eyewitness accounts suggest that US inventor Stanley Meyer has developed an electric cell which will split ordinary tap water into hydrogen and oxygen with far less energy than that required by a normal electrolytic cell.

In a demonstration made before Professor Michael Laughton, Dean of Engineering at Mary College, London, Admiral Sir Anthony Griffin, a former controller of  the British Navy, and Dr Keith Hindley, a UK research chemist. Meyer's cell, developed at the inventor's home in Grove City, Ohio, produced far more hydrogen/oxygen mixture than could have been expected by simple electrolysis.

Where normal water electrolysis requires the passage of current measured in amps, Meyer's cell achieves the same effect in milliamps. Furthermore, ordinary tap water requires the addition of an electrolyte such as sulphuric acid to aid current conduction; Meyer's cell functions at greatest efficiency with pure water.

According to the witnesses, the most startling aspect of the Meyer cell was that it remained cold, even after hours of gas production.

Meyer's experiments, which he seems to be able to perform to order, have earned him a series of US patents granted under Section 101. The granting of a patent under this section is dependent on a successful demonstration of the invention to a Patent Review Board.

Meyer's cell seems to have many of the attributes of an electrolytic cell except that it functions at high voltage, low current rather than the other way around. Construction is unremarkable. The electrodes --- referred to as "excitors" by Meyer --- are made from parallel plates of stainless steel formed in either flat or concentric topography. Gas production seems to vary as the inverse of the distance between them; the patents suggest a spacing of 1.5 mm produces satisfactory results.

The real differences occur in the power supply to the cell. Meyer uses an external inductance which appears to resonate with the capacitance of the cell --- pure water apparently possesses a dielectric constant of about 5 --- to produce a parallel resonant circuit. This is excited by a high power pulse generator which, together with the cell capacitance and a rectifier diode, forms a charge pump circuit. High frequency pulses build a rising staircase DC potential across the electrodes of the cell until a point is reached where the water breaks down and a momentary high current flows. A current measuring circuit in the supply detects this breakdown and removes the pulse drive for a few cycles allowing the water to "recover".

Research chemist Keith Hindley offers this description of a Meyer cell demonstration: "After a day of presentations, the Griffin committee witnessed a number of important demonstration of the WFC" (water fuel cell as named by the inventor).

A witness team of independent UK scientifc observers testified that US inventor Stanley Meyer successfully decomposed ordinary tap water into constituent elements through a combination of high, pulsed voltage using an average current measured only in milliamps. Reported gas evolution was enough to sustain a hydrogen /oxygen flame which instantly melted steel.

In contrast with normal high current electrolysis, the witnesses report the lack of any heating within the cell. Meyer declines to release details which would allow scientists to duplicate and evaluate his "water fuel cell". However, he has supplied enough detail to the US Patent Office to persuade them that he can substantiate his 'power-from-water' claims.

One demonstration cell was fitted with two parallel plate "excitors". Using tap water to fill the cell, the plates generated gas at very low current levels --- no greater than a tenth of an amp on the ammeter, and claimed to be milliamps by Meyer --- and this gas production increased steadily as the plates were moved closer together and decreased as they were separated. The DC voltage appeared to be pulsed at tens of thousands of volts.

A second cell carried nine stainless steel double tube cell units and generated much more gas. A sequence of photographs was taken showing gas production at milliamp levels. When the voltage was turned up to its peak value, the gas then poured off at a very impressive level.

"We did notice that the water at the top of the cell slowly became discolored with a pale cream and dark brown precipitate, almost certainly the effects of the chlorine in the heavily chlorinated tap water on the stainless steel tubes used as "excitors".

He was demonstrating hydrogen gas production at milliamp and kilovolt levels.

"The most remarkable observation is that the WFC and all its metal pipework remained quite cold to the touch, even after more than twenty minutes of operation. The splitting mechanism clearly evolves little heat in sharp contrast to electrolysis where the electrolyte warms up quickly."

"The results appear to suggest efficient and controllable gas production that responds rapidly to demand and yet is safe in operation. We clearly saw how increasing and decreasing the voltage is used to control gas production. We saw how gas generation ceased and then began again instantly as the voltage driving circuit was switched off and then on again."

"After hours of discussion between ourselves, we concluded that Stan Meyer did appear to have discovered an entirely new method for splitting water which showed few of the characteristics of classical electrolysis. Confirmation that his devices actually do work come from his collection of granted US patents on various parts of the WFC system. Since they were granted under Section 101 by the US Patent Office, the hardware involved in the patents has been examined experimentally by US Patent Office experts and their seconded experts and all the claims have been established."

"The basic WFC was subjected to three years of testing. This raises the granted patents to the level of independent, critical, scientific and engineering confirmation that the devices actually perform as claimed."

The practical demonstration of the Meyer cell appears substantially more convincing than the para-scientific jargon which has been used to explain it. The inventor himself talks about a distortion and polarization of the water molecule resulting in the H:OH bonding tearing itself apart under the electrostatic potential gradient, of a resonance within the molecule which amplifies the effect.

Apart from the copious hydrogen/oxygen gas evolution and the minimal temperature rise within the cell, witnesses also report that water within the cell disappears rapidly, presumably into its component parts and as an aerosol from the myriad of tiny bubbles breaking the surface of the cell.

Meyer claims to have run a converted VW on hydrogen/oxygen mixture for the last four years using a chain of six cylindrical cells. He also claims that photon stimulation of the reactor space by optical fibre piped laser light increases gas production.

The inventor is a protégé of the Advanced Energy Institute.

-         KeelyNet File MEYER1.ASC
Excerpts from:
-          
-         Electronics World & Wireless World
-         (January 1991)

http://www.waterpoweredcar.com/images/waterdunebuggy.jpg

Molecular Dissociation of Water:
A Project for the Experimenter

by Dan Danforth

In the original setup that Stan Meyer showed us, he used 36 volts as the basic potential applied to the reaction chamber. He also commented that stainless steel ( 410 not 403 ) was the only metal that could be used as oxides formed with all others. His original chamber used 18 inch long by 0.375 inch diameter (o.d.) rod surrounded by 1 inch diameter (i.d.) 16 inch long pipe. The reason for the difference in length is for mechanical ease of construction. My prototype used 14 inch long rod and 12 inch long pipe of similar diameters as the drawing indicates.

Having a severe lack of parts diversity here in Sri-Lanka, I was only able to obtain a 24 volt. 8 amp transformer and built my circuitry around that. The final output is 20 volts with Ml reading 10 amps to the pulsing circuit which generates a symmetrical square wave ( 50% duty cycle ) to the flyback inductor connected in series with the chamber as the schematic shows. The flyback high voltage spike is directed across the chamber via c* end d*. The use of a high voltage spike alone, without the current being delivered through the liquid, will not cause the disassociation to take place. This I verified using an ignition coil in place of the inductor and applied the secondary with halfwave rectification and blocking capacitor to prevent burn out to the chamber with no results. Apparently the current in the water aligns the molecules appropriately to allow the high voltage spike to do its work which in my opinion is the stimulation of molecular resonance. Once Stan's unit was made to begin breakdown (which takes 6 to 8 seconds) he was able to reduce both current and voltage to miniscule proportions. I attribute this to sympathetic oscillation of the aligned molecules, requiring very little in the way of additional excitation. A phenomenon akin to Tesla's super resonance... resulting in Stan discovering that he only had to supply three pulses in ten to satisfy the requirement of the chamber. I have not yet had the opportunity to duplicate this portion of the experiment but, in time I will.

Duplication of the device described in these pages, however, will produce the phenomena and hopefully launch other enterprising end inventive souls on to designing their own refined models. It would be nice to have feedback so that we can all collectively work to bring about the transition to non-pollution energy.

P.S.- Though electrical circuit is by no means optimised, but represents instead the result of parts availability here. Any good technician could improve on it quite readily.

There are two primary frequencies that produce the best results. They are: 14,372 Hz and 43,430 Hz. The former is about 50% more efficient, but it seems that just about any frequency between 9 KHz and 143,762 KHz works quite well. (1) This is because the nature of the wave form ( a spike ) is rich in harmonics and one of them is bound to be close to one of the two primary frequencies.

Use of permanent magnets may also increase efficiency. I'll give you the outcome of that attempt in my next letter along with the plans for what I hope to be a much improved version.

Note: Sub-harmonics of the two primary frequencies at which dissociation will occur:

43430 Hz                         143762 HZ
SUBHARMONIC           SUBHARMONIC
1st  21715  HZ                 1st  71881  HZ
2nd  14476.67 HZ             2nd  47920.67 HZ
3rd  15517.5  HZ              3rd  35840.1  HZ
4th  8686                           4th  28752.4  HZ


*1500 VOLTS IS THE MINIMUM REQUIRED FOR MOLECULAR RINGING TO BEGIN.

Source publication: Unknown... Scanned from very bad photocopy.










Excerpts from Water Fuel Cell News Release # 4 (Winter/Spring 87/88) :

"The Birth of New Technology: The Hydrogen Fracturing Process & Related Water Fuel Cell Technology"

by Marcia Thompson

The purpose of establishing the Hydrogen Fracturing technology which ahs been developed is to use energy from the atom to produce a system which would lend itself to mass production. Meyer is now in the process of integrating the Electrical Polarization Generator (EPG) into the Hydrogen Fracturing Process. The Electrical Polarization Generator is in essence a gas battery which produces electric energy directly from the fuel cell gases without chemical interaction.

The significance of the voltage is that it is a potential energy source, not consumed energy. The most significant point is that the influence of voltage has a phenomenal effect on the splitting of the water molecule and does it in a controlled state. Voltage from the Electrical Polarization Generator separates the water molecule economically by not consuming power. It's a new technology --- bringing the water molecule from a liquid to gas ionization state, which in turn sets up the Hydrogen Fracturing Process of destabilization of the gas atoms to release their atomic energy. The process consumes very little power to accomplish this task.

The Voltage Intensifier Circuit (VIC) patent development had to be fully developed to bring on the voltage phenomenon where very low energy is being consumed.

In conjunction with this development, a new Electron Grid Extractor Circuit (EGEC) has been fully developed to extend the operability of the Hydrogen Gas Gun technology, which sets up the hydrogen fracturing process. The Voltage Intensifier Circuit patent development and Electron Grid Extraction Circuit had to be fully developed to bring on the voltage phenomenon where very low energy is being consumed.
What is this Hydrogen Fracturing Process? Since the Water Fuel Cell (WFC) dissociates the water molecule by the stimulation of voltage, this voltage technology has now been applied to the Fuel Cell gas atoms to release their atomic energy. Meyer discovered that not only can the water molecule be split into its component parts, but it is also possible to separate the atoms of gases into their component parts by the same voltage stimulation, releasing a tremendous amount of thermal explosive energy from the atom under a controlled state. Under this process, preliminary tests show that energy yields from one gallon of water are predicted to equal that of 44,000 to 108,000 barrels of oil. The Hydrogen Fracturing Process is environmentally safe since the gas atoms are split into their component parts, releasing explosive thermal energy from the gas atom. The nucleus remains intact.


In conjunction to the Hydrogen Fracturing Process of the Water Fuel Cell technology, Meyer is now working out systems mechanics of retrofitting the EPG system to the entire Water Fuel Cell system. The entire systems mechanics are now being integrated together into a package system which, when miniaturized, will lend itself to production. All of these previous steps have been necessary to ensure the system lends itself to the economics of mass production with costs held down.

Beyond the Electrical Particle Generator (EPG) system, which utilizes a magnetized gas to produce electrical energy, work is continuing on the Electrical Polarization Generator to optimize its operational performance, which is also required for mass production. The EPG system is now being prepared for design interfacing with the existing WFC technology.

To reach the maximum operational effect of the EPG system, several types of magnetized gases are being developed and tested. Meyer is also developing the technology to enhance the electromagnetic deflection of the gas to optimize the EPG system still further. This development phase is now being considered for systems economics with regard to manufacturing techniques.

What does the Hydrogen Fracturing Process (HFP) really do for the system? It destabilizes the mass and electrical equilibrium of the gas atoms, bringing them into a critical state for energy utilization.

The electronics control system determines systems operation and efficiency and is part of the HFP. It complies with both US and foreign patent requirements. It establishes electric circuit interfacing for the operability and efficiency of the HFP. In mass production, it will be reduced to a small, simple circuit component. The control system triggers the HFP and maintains control of it.

The Hydrogen Gas Injector Fuel Cell (HGIFC) is composed of resonant cavities (lower section) in a vertical array which splits water molecules into component parts by stimulation of a high pulse voltage frequency, setting up the resonant action. The liberated hydrogen and oxygen atoms and ambient air gases are stimulated from a liquid to gas ionization state prior to entering the Hydrogen Gas Gun (HGG), located on top of the resonant cavities. Gases are then allowed to go into the Hydrogen Fracturing Process. The thrust nozzle, located at the very top of the system, is an optical thermal lens affixed to the unit which triggers and sustains the Hydrogen Fracturing Process as to the flow rate of fuel cell gases. In mass production, the whole unit forms the Gas Injector Fuel Cell (GIFC). The complete unit will be reduced to a small, extremely light-weight unit. The Hydrogen Fracturing Process is completely environmentally safe. There are no radioactive materials used in the process, and it applies to all EPA standards, plus safety, housing and highway codes…

Hydrogen Gas Gun


Hydrogen Gas Gun


Water Fuel Cell






Excerpts from Raum & Zeit 1(6):63-68 (1990) :


Hydrogen Gas Gun

The Electron Extraction Circuit removes, captures, and consumes the "dislodged" eelctrons (from the gas atoms) to cause the gas atoms to go into and reach "Critical State", forming highly energized combustiblegas atoms having missing electrons. Resistive values (R4, R6, R7) and dielectric constant of gas (Rg) and isolated ground (W) prevents "electron-flow" or "electron deflection" from occurring within the circuit during pulsing operations (at resonant frequency) and, therefore, keeps the gas atoms in critical state by not allowing electron replacement to occur or take place between the moving gas atoms. The "dislodged" negative charged electrons are "destroyed" or "consumed" in the form of heat when Amp Consuming Device (S) such as a light bulb) is positively electrically energized during alternate pulsing operations. Laser activated or laser primed gas ions repel the dislodged electrons being consumed. The Electron Extraction Process is hereinafter called the "Hydrogen Gas Gun" and is placed on top of a Resonant Cavity Assembly.


Thermal Explosive Energy

Exposing the expelling "laser-primed" and electrically charged combustible gas ions (exiting from the Gas Resonant Cavity) to a thermal spark or heat zone causes thermal gas ignition, releasing Thermal Explosive Energy (gtnt) beyond the Gas-Flame Stage...

Thermal Atomic interaction (gtnt) is caused when the combustible gas ions (from water) fail to unite or form a Covalent Linkup or Bond between the water molecule atoms. The oxygen atom having less than four covalent electrons (Electron Extraction Process) is unable to reach "Stable State" ( 6 to 8 covalent electrons required) when the two hydrogen atoms seek to form the water molecule during thermal gas ignition. The absorbed laser energy (Va, Vb, and Vc) weakens the electrical bond between the orbital electrons and the nucleus of the atom. And, electrical attraction force being stronger than normal due to the lack of covalent electrons, "locks onto" and "keeps" the hydrogen electrons... This Atomic Thermal Interaction between combustible gas opns is from now on called the "Hydrogen Fracturing Process".

By simply attenuating or varying the voltage amplitude in direct relationship to voltage pulse rate determines Atmomic Power Yield under control state...

Photon Energy Aids Resonant Action


 

Laser-Injected Resonant Cavity

 

Power Load Distributor

Destabilizing Combustible Gas Ion

 

LED Laser Array

Electrical Voltage Zone (Laser-Injected Resonant Cavity)

Destabilizing Combustible Gas Ion

Controlled Energy Yield from Water Atoms

 




Patents Granted

USP # 4,936,961 - Method for the Production of a Fuel Gas
USP # 4,826,581 - Controlled Production of Thermal Energy from Gases
USP # 4,798,661 - Gas generator voltage control circuit
USP # 4,613,779 ~ Electrical Pulse Generator
USP # 4,613,304 ~ Gas Electrical H Generator
USP # 4,465,455 ~ Start-up/Shut-down for H Gas Burner
USP # 4,421,474 ~ H Gas Burner
USP # 4,389,981 ~ H Gas Injector System for IC Engine
USP # 4,275,950 ~ Light-Guide Lense
USP # 3,970,070 ~ Solar Heating System
USP # 4,265,224 ~ Multi-Stage Solar Storage System
USP # 3,970,070 - Solar heating system


Canada Patent # 1,231,872 ~ H Injector System
CP # 1,233,379 ~ H Gas Injector System for IC Engine
CP # 1,235,669 ~ Controlled H Gas Flame
CP # 1,228,833 ~ Gas Electrical H Generator
CP # 1,227,094 ~ H/Air & Non-Combustible Gas Mixing Combustion System
CP # 1,234,774 ~ H Generator System
CP # 1,234,773 ~ Resonant Cavity H Generator...
CP # 1,213,671 ~ Electrical Particle Generator








Water Fuel Cell R&D Format
 
Fuel Cell Technology:

Electrical Polarization Process ~ Producing H gas economically from water by voltage stimulation
Voltage Intensifier Circuit ~ Controls H gas production on demand
Cluster Array ~ Light manufacturing
Resonant Cavity ~Home/transportation
Laser-Injected Resonant Cavity ~ Medium industry
Atom-Injected Resonant Cavity ~ Heavy industry
H Fracturing Process ~ Controlled energy yield from water atoms (Aircraft/rockets)


Processed H Gas:

Rendering H Gas Safe ~ Adjust H gas burn rate to co-equal natural gasQuenching Circuit ~ Anti-Spark back
Quenching Tube ~ Distribute H gas without spark ignition
H Ignition ~ Sustain & maintain H flame regardless of gas rate
Startup/Shutdown Electronic Circuit ~ Automatically reignites H gas after flame-out
H Pipeline Storage ~ Transporting H gas through existing pipelines safely
H Gas Reclaim ~ Recycling water for H re-use & producing pure drinking water


Electrical Power Generation:

Electrical Particle Generator (EPG) ~ Using a magnetized gas or slurry to produce electrical energy without any air-gap
EPG Mechanical Drive System ~ To propel said magnetized gas/slurry by mechanical displacement
EPG Electromagnetic Drive System ~ To propel said magnetized gas/slurry by EM deflection
EPG Laser Drive System ~ To propel said magnetized gas/slurry by photon or particle injection
Magnetic Spin Generator ~ Reorient dyne-axis of said magnetized gas/slurry by variable pulse voltage
Spiral Transformer Configuration ~ Pass electrical energy at high pulse voltage frequencies
Electrical Pulsing Generator ~ EM amplifier that produces a variable voltage frequency


Electrical Feedback Network:

Gas Activated Electrical Generator ~ Using a thermal pump to move said magnetized gas/slurry to produce electricity
Internal Combustion Electrical Generator ~ Using IC engine power by processed H gas to move magnetized gas/slurry to produce electricity
Fluid Drive Electrical Generator ~ Using H gas pressure to move magnetized gas/slurry to produce electricity
Electrical Polarization Generator ~ Using electrically charged gas to produce electrical energy


Others:

Steam Resonator ~ Producing superheated steam by polar-voltage stimulation
Light-Guide Lens Assembly ~ Collects, redirects, transfers & focuses solar energy without any moving parts





Infinite Energy 19: 50-51 (1998):

Stanley Meyer, Water-Fuel Cell Inventor & Promoter, Dies Suddenly

by Eugene Mallove

Stanley A. Meyer, the controversial Ohio inventor who had claimed his technology could produce a hydrogen-oxygen mixture with a minimal energy input (compared with conventional electrolysis) died on March 21, 1998. He had gained a world-wide following of adherents and people who had invested in his activities --- Water Fuel Cell (Grove City, OH). He was famous for his claimed "water fueled car" which was exhibited symbolically in the BBC/CBC 1994 documentary on cold fusion, "Too Close to the Sun".

There were also those who were initially curious about Meyer's work, such as the editor of this magazine, the late Christopher Tinsley of the UK, and the late Admiral of the British Navy, Sir Anthony Griffin, but who became frustrated by being unable --- or, more to the point, not allowed --- to confirm (or reject finally) Meyer's claims.

I have absolutely NO DOUBT today that Stanley Meyer was his own worst enemy. IF --- and a very big IF --- he had discovered the technological process that he had said he had, there is no way that a reasonable, straightforward marketing strategy would have failed to make his technology quickly spread worldwide. He could have become very influential and very rich.

There remains a very strong suspicion that he had no such process, even though he conducted a demonstration (before this writer and another engineer at the Meyer lab in 1993) of the production of copious hydrogen/oxygen gas from what visually seemed like a small input power. But Meyer was exceedingly paranoid and he flatly refused reasonable requests by us and others to test the performance --- the input/out power ratio, even with the proviso that we did not have to "look into his black box" of electronics feeding his rather simply constructed stainless steel electrode, alternating current and voltage cell. The last such refusal --- this one in public and recorded on video tape --- was at the ANE meeting in Denver CO in 1997. Then Meyer loudly and falsely protested to me that he would "lose his patent rights" if he were to release anything but complete, integrated systems --- such as a water-fueled vehicle. Excuses, excuses, excuses...

In 1996, Meyer lost a long-lasting Ohio civil court battle accusing him of "egregious fraud" against a former associate. As was Meyer's custom, he ascribed this and other alleged assaults on him to various conspiracies. To television cameras he suggested that he had been offered huge sums of money to "suppress this technology", but that he had refused those sums. One had the impression that he really believed that there were conspiracies against him. That is a tragedy, a very compounded tragedy if he had actually come up with something novel and useful that he was hiding.

This is a very complex human and scientific story that we shall want to cover in greater detail in a future issue of Infinite Energy. There are other processes and inventions that suggest that splitting water molecules with much greater efficiency than with conventional electrolysis may be possible. Certainly there are other novelties within water --- "cold fusion" to be sure --- that really do produce prodigious quantities of energy, but not in the mode Meyer claimed. For now, here are some of the facts surrounding Meyer's death:

He was apparently eating dinner at a Grove City OH restaurant, when it is reported that he jumped up from the table, yelled that he'd been poisoned", and rushed out into the parking lot, where he collapsed and died. It has been reported by Meyer's associates that Meyer had just secured funding for a $50 million research center near Grove City, but there is no way to confirm or reject this at the moment.


Electronics World & Wireless World ( January 1991)
Dan Danforth: Molecular Dissociation of Water
Water Fuel Cell News Release (Winter/Spring 87/88)
Raum & Zeit 1(6) 63-68 (1990)
Patents Granted (@ 1990)
Water Fuel Cell R&D Format
Infinite Energy 19: 50-51 (1998) Obituary
Water-Powered Car Video ( Link to http://www.lonelantern.org/collection.html )
USP # 4,936,961 ~ Method for the Production of a Fuel Gas
USP # 4,826,581 ~ Controlled Process for the Production of Thermal Energy from Gases...
USP # 4,798,661 ~ Gas Generator Voltage Control Circuit
USP # 4,613,304 ~ Gas Electrical Hydrogen Generator
USP # 4,465,455 ~ Start-up/Shut-down for a Hydrogen Gas Burner
USP # 4,421,474 ~ Hydrogen Gas Burner
USP # 4,389,981 ~ Hydrogen Gas Injector System for Internal Combustion Engine
Canadian Patent # 2,067,735 ~ Water Fuel Injection System
WO 92/07861 ~ Control & Driver Circuits for a Hydrogen Gas Fuel Producing Cell
USP Appln. 2005/0246059 ~ Hydroxyl Filling Station (Stephen Meyer)


From Keelynet via Rex Research @ http://www.rexresearch.com/meyerhy/meyerhy.htm

For more information about water used as fuel see http://nexusilluminati.blogspot.com/search/label/water%20fuel  or http://nexusilluminati.blogspot.com/search/label/h2o2


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