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January 2, 1991
MEYER.ASC

PLEASE PASS THIS AROUND TO EVERYONE WHO WOULD HAVE EVEN THE SLIGHTEST INTEREST IN THIS SUBJECT. ANYONE WHO DOES AUTO REPAIR, AUTO UPGRADES, ENGINEERING, GARAGE TINKERING WILL FIND THIS AND OTHER INFO TO COME VERY INTERESTING!

"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."

What does this mean to you ??? How will it affect YOUR life ???

Let me tell you why this is EXTREMELY IMPORTANT TO YOU !

This is just about the MOST IMPORTANT THING YOU HAVE EVER READ !

Think of the BILLIONS of U.S. dollars being spent on "stuff" that is pumped out of the ground. We send that money to ANOTHER COUNTRY ! (and they fight and kill each other and want more).

If this invention can be installed in YOUR EXISTING CAR you would not have to spend another DIME on GAS !

This would mean that those BILLIONS of dollars would stay here in the good old USA and be used for medical research, new technologies, space exploration and lots of other things.

IT WOULD MAKE YOUR LIFE SO MUCH BETTER !

Besides getting rid of lots of pollution. You could run the two most power hungry devices in your house (your Air Conditioner and Refrigerator) on a system using this device... The applications are endless !!!!

THIS IS SO IMPORTANT ! I CAN'T SAY THIS ENOUGH !

STOP WHATEVER YOU ARE DOING AND GET THIS INFORMATION AND OTHER DATA THAT IS TO COME TO SOMEONE WHO KNOWS WHAT TO DO WITH IT ! TAKE A DAY OFF WORK, TURN OFF THE TV FOR A FEW DAYS !

PASS IT OUT, PRINT IT OUT AND SEND IT TO RADIO STATIONS, FAX IT, UPLOAD IT TO EVERY BBS YOU CAN THINK OF !

You know the OIL companies (greedy !) will fight like DOGS to keep us from using this technology ! DON'T LET THIS HAPPEN ! MAKE THIS INFORMATION PUBLIC KNOWLEDGE !!! GET IT OUT THERE ! DON'T EXPECT SOMEONE ELSE TO DO IT FOR YOU !

You can see the following article in full and a color picture of the device by visiting your local library and picking up this magazine.

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Reprinted in part from an article in "ELECTRONICS WORLD + WIRELESS WORLD" January 1991:

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 Queen 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 1.5mm 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 miliamps. 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 "waterfuel cell". However, he has supplied enough detail to the US Patents 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 Steve 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.

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Meyer Patents: (up to Sep, 1991)

4936961 - Method for the production of a fuel gas (get this)
4826581 - Controlled.. production of thermal energy from gases
4798661 - Gas generator voltage control circuit (get this)
4613304 - Gas electrical hydrogen generator (get this)

There are others of his, which do not typically apply to his "generator":

4613779 - Power isolation device
4465455 - Startup and shutdown for a hydrogen burner
4421474 - Hydrogen gas burner
4389981 - Hydrogen gas injector
4275950 - Light Lens
4265224 - Solar storage system
3970070 - Solar heating system

There are several ways to obtain these patents, but the easiest one gets them sent directly to your door.

The Patent office will send you each patent for $1.50 each, post paid! If you get the above 4 patents, thats $6!

It's very simple, you just put your check in an envelope, put a piece of notebook paper in it with your name and address and the numbers of the patents you want to:

Commissioner of Patents & Trademarks
Washington, DC 20231

That's all there is to it! You really need all four because bits and peices of details are spread over all four patents! Please don't let this get buried ! PASS THIS INFO OUT !!!

Copies of the Patents will be scanned and made into GIF files when they are available. Further information is comming so keep your eyes peeled but don't let that stop you from passing out this info !!!

January 2, 1991
MEYER2.ASC

METHOD FOR THE PRODUCTION OF A FUEL GAS (US Pat # 4,936,961)

Related Application:

This is a continuation-in -part of my co-pending application Ser. No. 081,859, filed 8/5/87, now U.S. Pat. No. 4,826, 581.

Field of Invention:

This invention relates to a method of and apparatus for obtaining the release of a fuel gas mixture including hydrogen and oxygen from water.

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BACKGROUND OF THE PRIOR ART

Numerous processes have been proposed for separating a water molecule into its elemental hydrogen and oxygen components. Electrolysis is one such process. Other processes are described in the United States patents such as 4,344,831; 4,184,931; 4,023,545; 3,980, 053; and Patent Corporation Treaty application No. PCT/US80/1362, Published 30 April, 1981.

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OBJECTS OF THE INVENTION

It is an object of the invention to provide a fuel cell and a process in which molecules of water are broken down into hydrogen and oxygen gases, and other formerly dissolved within the water is produced. As used herein the term "fuel cell" refers to a single unit of the invention comprising a water capacitor cell, as hereinafter explained, that produces the fuel gas in accordance with the method of the invention.

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Brief Description of the Drawings

FIG. 1 illustrates a circuit useful in the process.
FIG. 2 shows a perspective of a "water capacitor" element used in the fuel cell circuit.
FIGS. 3A through 3F are illustrations depicting the theoretical bases for the phenomena encountered during operation of the invention herein.

Description of the Preferred Embodiment:

In brief, the invention is a method of obtaining the release of a gas mixture including hydrogen on oxygen and other dissolved gases formerly entrapped in water, from water consisting of:

(A) providing a capacitor, in which the water is included as a dielectric liquid between capacitor plates, in a resonate charging choke circuit that includes an inductance in series with the capacitor;

(B) subjecting the capacitor to a pulsating, unipolar electric voltage field in which the polarity does no pass beyond an arbitrary ground, whereby the water molecules within the capacitor are subjected to a charge of the same polarity and the water molecules are distended by their subjection to electrical polar forces;

(C) Further subjecting in said capacitor to said pulsating electric field to achieve a pulse frequency such that the Pulsating electric field induces a resonance within the water molecule;

(D) continuing the application of the pulsating frequency to the capacitor cell after resonance occurs so that the energy level within the molecule is increased in cascading incremental steps in proportion to the number of pulses;

(E) maintaining the charge of said capacitor during the application of the pulsing field, whereby the co-valent electrical bonding of the hydrogen and oxygen atoms within said molecules is destabilized such that the force of the electrical field applied, as the force is effective within the molecule, exceeds the bonding force of the molecule, and hydrogen and oxygen atoms are liberated from the molecule as elemental gases; and

(F) collecting said hydrogen and oxygen gases, and any other gases that were formerly dissolved within the water, and discharging the collected gases as a fuel gas mixture.

The process follows the sequence of steps shown in the following Table 1 in which water molecules are subjected to increasing electrical forces. In an ambient state, randomly oriented water molecules are aligned with respect to a molecule polar orientation.

They are next, themselves polarized and "elongated" by the application of an electrical potential to the extent that covalent bonding of the water molecule is so weakened that the atoms dissociate and the molecule breaks down into hydrogen and oxygen elemental components.

Engineering design parameters based on known theoretical principles of electrical circuits determine the incremental levels of electrical and wave energy input required to produce resonance in the system whereby the fuel gas comprised of a mixture of hydrogen, oxygen, and other gases such as air test were formerly dissolved within the water, is produced.

TABLE 1

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Process Steps:

The sequence of the relative state of the water molecule and/or hydrogen/oxygen/other atoms:

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A. (ambient state) random
B. Alignment of polar fields
C. Polarization of molecule
D. Molecular elongation
E. Atom liberation by breakdown of covalent bond
F. Release of gases

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In the process, the point of optimum gas release is reached at a circuit resonance. Water in the fuel cell is subjected to a pulsating, polar electric field produced by the electrical circuit whereby the water molecules are distended by reason of their subjection to electrical polar forces of the capacitor plates.

The polar pulsating frequency applied is such that the pulsating electric field induces a resonance in the molecule. A cascade effect occurs and the overall energy level of specific water molecules is increased in cascading, incremental steps.

The hydrogen and oxygen atomic gases, and other gas components formerly entrapped as dissolved gases in water, are released when the resonant energy exceeds the co-valent bonding force of the water molecule. A preferred construction material for the capacitor plates is stainless steel T-304 which is non-chemical reactive with water, hydrogen, or oxygen.

An electrically conductive material which is inert in the fluid environment is a desirable material of construction for the electrical field plates of "water capacitor" employed in the circuit.

Once triggered, the gas output is controllable by the attenuation of operational parameters. Thus, once the frequency of resonance is identified, by varying the applied pulse voltage to the water fuel cell assembly, gas output is varied.

By varying the pulse shape and/or amplitude or pulse train sequence of the initial pulsing wave source, final gas output is varied. Attenuation of the voltage field frequency in the form of OFF and ON pulses likewise affects output.

The overall apparatus thus includes an electrical circuit in which a water capacitor having a known dielectric property is an element. The fuel gases are obtained from the water by the disassociation of the water molecule. The water molecules are split into component atomic elements (hydrogen and oxygen gases) by a voltage stimulation process called the electrical polarization process which also releases dissolved gases entrapped in the water.

From the outline of physical phenomena associated with the process described in Table 1, the theoretical basis of the invention considers the respective states of molecules and gases and ions derived from liquid water. Before voltage stimulation, water molecules are randomly dispersed throughout water in a container.

When a unipolar voltage pulse train such as shown in FIGS. 3B through 3F is applied to positive and negative capacitor plates, an increasing voltage potential is induced in the molecules in a linear, step like charging effect.

The electrical field of the particles within a volume of water including the electrical field plates increases from a low energy state to a high energy state successively is a step manner following each pulse-train as illustrated figuratively in the depictions of FIG. 3A through 3F.

The increasing voltage potential is always positive in direct relationship to negative ground potential during each pulse. The voltage polarity on the plates which create the voltage fields remains constant although the voltage charge increases. Positive and negative voltage "zones" are thus formed simultaneously in the electrical field of the capacitor plates.

In the first stage of the process described in Table 1, because the water molecule naturally exhibits opposite electrical fields in a relatively polar configuration (the two hydrogen atoms are positively electrically charged relative to the negative electrically charged oxygen atom), the voltage pulse causes initially randomly oriented water molecules in the liquid state to spin and orient themselves with reference to positive and negative poles of the voltage fields applied.

The positive electrically charged hydrogen atoms of said water molecule are attracted to a negative voltage field; while, at the same time, the negative electrically charged oxygen atoms of the same water molecule are attracted to a positive voltage field.

Even a slight potential difference applied to inert, conductive plates of a containment chamber which forms a capacitor will initiate polar atomic orientation within the water molecule based on polarity differences.

When the potential difference applied causes the orientated water molecules to align themselves between the conductive plates, pulsing causes the voltage field intensity to be increased in accordance with FIG. 3B. As further molecule alignment occurs, molecular movement is hindered.

Because the positively charged hydrogen atoms of said aligned molecules are attracted in a direction opposite to the negatively charged oxygen atoms, a polar charge alignment or distribution occurs within the molecules between said voltage zones, as shown in FIG. 3B. And as the energy level of the atoms subjected to resonant pulsing increases, the stationary water molecules become elongated as shown in FIGS. 3C and 3D. Electrically charged nuclei and electrons are attracted toward opposite electrically charged equilibrium of the water molecule.

As the water molecule is further exposed to an increasing potential difference resulting from the step charging of the capacitor, the electrical force of attraction of the atoms within the molecule to the capacitor plates of the chamber also increase in strength. As a result, the co-valent bonding between which form the molecule is weakened - and ultimately terminated. The negatively charged electron is attracted toward the positively charged hydrogen atoms, while at the same time, the negatively charged oxygen atoms repel electrons.

In a more specific explanation of the "sub-atomic" action the occurs in the water fuel cell, it is known that natural water is a liquid which has a dielectric constant of 78.54 at 20 degrees C. and 1 atm pressure. [Handbook of Chemistry and Physics, 68th ed., CRC Press(Boca Raton, Florida (1987-88)), Section E-50. H20(water)].

When a volume of water is isolated and electrically conductive plates, that are chemically inert in water and are separated by a distance, are immersed in water, a capacitor is formed, having a capacitance determined by the surface area of the plates, the distance of their separation and the dielectric constant of water.

When water molecules are exposed to voltage at a restricted current, water takes on an electrical charge. By the laws of electrical attraction, molecules align according to positive and negative polarity fields of the molecule and the alignment field . The plates of the capacitor constitute such as alignment field when a voltage is applied.

When a charge is applied to a capacitor, the electrical charge of the capacitor equals the applied voltage charge; in a water capacitor, the dielectric property of water resists the flow of amps in the circuit, and the water molecule itself, because it has polarity fields formed by the relationship of hydrogen and oxygen in the co-valent bond, and intrinsic dielectric property, becomes part of the electrical circuit, analogues to a "mircocapacitor" within the capacitor defined by the plates.

In the Example of a fuel cell circuit of FIG. 1, a water capacitor is included. The step-up coil is formed on a conventional torroidal core formed of a compressed ferromagnetic powered material that will not itself become permanently magnetized, such as the trademarked "Ferramic 06# "Permag" powder as described in Siemens Ferrites Catalog, CG-2000-002-121, (Cleveland, Ohio) No. F626-1205". The core is 1.50 inch in diameter and 0.25 inch in thickness. A primary coil of 200 turns of 24 gauge coppe r wire is provided and coil of 600 turns of 36 gauge wire comprises the secondary winding.

In the circuit of FIG 1, the diode is a 1N1198 diode which acts as a blocking diode and an electric switch that allows voltage flow in one direction only. Thus, the capacitor is never subjected to a pulse of reverse polarity.

The primary coil of the torroid is subject to a 50% duty cycle pulse. The torroidal pulsing coil provides a voltage step-up from the pulse generator in excess of five times, although the relative amount of step-up is determined by pre-selected criteria for a particular application. As the stepped-up pulse enters first inductor (formed from 100 turns of 24 gauge wire 1 inch in diameter), an electromagnetic field is formed around the inductor, voltage is switched off when the pulse ends, and the field collapses and produces another pulse of the same polarity; i.e., another positive pulse is formed where the 50% duty cycle was terminated. Thus, a double pulse frequency is produced; however, in pulse train of unipolar pulses, there is a brief time when pulses are not present.

By being so subjected to electrical pulses in the circuit of FIG. 1, water confined in the volume that includes the capacitor plates takes on an electrical charge that is increased by a step charging phenomenon occurring in the water capacitor. Voltage continually increases (to about 1000 volts and more) and the water molecules starts to elongate.

The pulse train is then switched off; the voltage across the water capacitor drops to the amount of the charge that the water molecules have taken on i.e. voltage is maintained across the charged capacitor. The pulse train is the reapplied.

Because a voltage potential applied to a capacitor can perform work, the higher the voltage the higher the voltage potential, the more work us performed by a given capacitor. In an optimum capacitor that is wholly non-conductive, zero (0) current flow will occur across the capacitor.

Thus, in view of an idealized capacitor circuit, the object of the water capacitor circuit is to prevent electron flow through the circuit, i.e. such as occurs by electron flow or leakage through a resistive element that produces heat.

Electrical leakage in the water will occur, however, because of some residual conductivity and impurities or ions that may be otherwise present in the water. Thus, the water capacitor is preferably chemically inert. An electrolyte is not added to the water.

In the isolated water bath, the water molecule takes on charge, and the charge increases. The object of the process is to switch off the co-valent bonding of the water molecule and interrupt the sub-atomic force, i.e. the electrical force or electromagnetic force, that binds the hydrogen and oxygen atoms to form a molecule so that the hydrogen and oxygen separate.

Because an electron will only occupy a certain electron shell (shells are well known) the voltage applied to the capacitor affects the electrical forces inherent in the co-valent bond. As a result of the charge applied by the plates, the applied force becomes greater than the force of the co-valent bonds between the atom of the water molecule; and the water molecule becomes elongated. When this happens, the time share ratio of the electron shells is modified.

In the process, electrons are extracted from the water bath; electrons are not consumed nor are electrons introduced into the water bath by the circuit as electrons are conventionally introduced in as electrolysis process. There may nevertheless occur a leakage current through the water.

Those hydrogen atoms missing electrons become neutralized; atoms are liberated from the water. The charged atoms and electrons are attracted to the opposite polarity voltage zones created between the capacitor plates. The electrons formerly shared by atoms in the water co-valent bond are reallocated such that neutral elemental gases are liberated.

In the process, the electrical resonance may be reached at all levels of voltage potential. The overall circuit is characterized as a "resonant charging choke" circuit which is an inductor in series with a capacitor that produces a resonant circuit. [SAMS Modern Dictionary of Electronics, Rudolf Garff, copy right 1984, Howard W. Sams & Co. (Indianapolis, Ind.), page 859.]

Such a resonant charging choke is on each side of the capacitor. In the circuit, the diode acts as a switch that allows the magnetic field produced in the inductor to collapse, thereby doubling the pulse frequency and preventing the capacitor from discharging. In this manner a continuous voltage is produced across the capacitor plates in the water bath; and the capacitor does not discharge. The water molecules are thus subjected to a continuously charged field until the breakdown of the co-valent bond occurs.

As noted initially, the capacitance depends on the dielectric properties of the water and the size and separation of the conductive elements forming the water capacitor.

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EXAMPLE 1

In an example of the circuit of FIG. 1 (in which other circuit element specifications are provided above), two concentric cylinders 4 inches long formed the water capacitor of the fuel cell in the volume of water. The outside cylinder was .75 inch in outside diameter; the inner cylinder was 0.5 inch in outside diameter.

Spacing from the outside of the inner cylinder to the inner surface of the outside cylinder was 0.0625 inch. Resonance in the circuit was achieved at a 26 volt applied pulse to the primary coil of the torroid at 0KHz, and the water molecules disassociated into elemental hydrogen and oxygen and the gas released from the fuel cell comprised a mixture of hydrogen, oxygen from the water molecule, and gases formerly dissolved in the water such as the atmospheric gases or oxygen, nitrogen, and argon.

In achieving resonance in any circuit, as the pulse frequency is adjusted, the flow of amps is minimized and the voltage is maximized to a peak. Calculation of the resonance frequency of an overall circuit is determined by known means; different cavities have a different frequency of resonance dependant on parameters of the water dielectric, plate size, configuration and distance, circuit inductors, and the like. Control of the production of fuel gas is determined by variation of the period of time between a train of pulses, pulse amplitude and capacitor plate size and configuration, with corresponding value adjustments to other circuit components.

The wiper arm on the second conductor tunes the circuit and accommodates to contaminants in water so that the charge is always applied to the capacitor. The voltage applied determines the rate of breakdown of the molecule into its atomic components. As water in the cell is consumed, it is replaced by any appropriate means or control system.

Variations of the process and apparatus may be evident to those skilled in the art.

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What is claimed is:

1. A method of obtaining the release of a gas mixture including hydrogen and oxygen and other dissolved gases formerly entrapped in water, from water, consisting of:

(A) providing a capacitor in which water is included as a dielectric between capacitor plates, in a resonant charging choke circuit that includes an inductance in series with the capacitor;

(B) subjecting the capacitor to a pulsating, uinpolar electric charging voltage in which the polarity does not pass beyond an arbitrary ground, whereby the water molecules within the capacitor plates;

(C) further subjecting the water in said capacitor to a pulsating electric field resulting from the subjection of the capacitor to the charging voltage such that the pulsating electric field induces a resonance within the water molecules;

(D) continuing the application of the pulsating charging voltage to the capacitor after the resonance occurs so that the energy level within the molecules is increased in cascading incremental steps in proportion to the number of pulses;

(E) maintaining the charge of said capacitor during the application of the pulsating charge voltage, whereby the co-valent electrical bonding of the hydrogen and oxygen atoms within said molecules is destabilized, such that the force of the electrical field applied to the molecules exceeds the bonding force within the molecules, and the hydrogen and oxygen atoms are liberated from the molecules as elemental gases.

2. The method of claim 1 including the further steps of collecting said liberated gases and any other gases that were formerly dissolved within the water and discharging said collected gases as a fuel gas mixture.

*** END OF PATENT TEXT ***

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Note:

1N1198 Diode is also a NTE 5995 or a ECG 5994. It is a 40A 600 PIV Diode (the 40A is over kill and may not be needed).

Stainless Steel "T304" is a type of weldable Stainless, but other types should work the same. "T304" is just the more common type of Stainless tubing available.

The outer tube figures out to be 3/4" 16 gauge (.060 "wall") tube (a common size) cut to 4 inch length.

The inner tube figure out to be 1/2" 18 gauge (.049 "wall", this is a common size for this tube, but the actual gauge cannot be figured from this patent documentation, but this size should work) cut to 4 inch length.

You should also attach the two leads to the Stainless, using Stainless solid rod (1/6 dia would do) and USE LEAD FREE SOLDER ! (you may want the purified water that is returned to drink some day).

You also need to figure out a way to keep the two tubes separated from each other. This could be done with small pieces of plastic. They cannot block the flow of water into/out of the tubes.

It was not indicated if the inner tube is full of water or not. The guess here is that it is full of water, and this doesn't effect the device at all.

The Patent doesn't say but I would think that insulating the leads with some type of tubing up to the tubes would be electrically correct (and probably wouldn't hurt).

The pulse frequency was not printed, it is estimated from the size of the coils and transformer that the frequency doesn't exceed 50 Mhz. Don't depend on this being fact, it's just a educated guess.

The circuit to do this is not shown, just empty boxes. It's time to get out your SCOPE and try things !

Don't forget to share your results with others ! GREED is why this type of thing never gets out into the world to do some GOOD.

If you want to make some money, make something PRACTICAL that WORKS and that PEOPLE can use in their every day lives, then sell it!

Holding onto information like this only hurts ALL OF US !!

Return to Stanley Meyer Main Link Page


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