Stanley Meyer: Water Fuel Cell


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**Stanley MEYER**
**Water Fuel Cell**


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***[Electronics World & Wireless
World](#elworld)*** ( January 1991)   
**[Dan Danforth: Molecular Dissociation of
Water](#danforth)**   
***[Water Fuel Cell News Release](#wfcnews)***
(Winter/Spring 87/88)   
***[Raum & Zeit](#raum)*** 1(6) 63-68
(1990)   
**[Patents Granted](#patents)** (@ 1990)   
**[Water Fuel Cell R&D Format](#rd)**   
***[Infinite Energy](#obit)*** 19: 50-51
(1998) Obituary   
**[Water-Powered Car Video](http://www.lonelantern.org/collection.html)** ( Link to
http://www.lonelantern.org/collection.html target="\_blank" )   
**[USP # 4,936,961](4936961.htm) ~
Method for the Production of a Fuel Gas**   
**[USP # 4,826,581](4826581.htm) ~
Controlled Process for the Production of Thermal Energy from
Gases...**   
**[USP # 4,798,661](4798661.htm) ~
Gas Generator Voltage Control Circuit**   
**[USP # 4,613,304](4613304.htm) ~
Gas Electrical Hydrogen Generator**   
**[USP # 4,465,455](4465455.htm)**
~ **Start-up/Shut-down for a Hydrogen Gas Burner**   
**[USP # 4,421,474](4421474.htm) ~
Hydrogen Gas Burner**   
**[USP # 4,389,981](4389981.htm) ~
Hydrogen Gas Injector System for Internal Combustion Engine**
  
**[Canadian Patent #
2,067,735](2067735.htm) ~ Water Fuel Injection System**   
**[WO 92/07861](wo92.htm) ~ Control
& Driver Circuits for a Hydrogen Gas Fuel Producing Cell**
  
**[USP Appln. 2005/0246059](uspa05.htm) ~ Hydroxyl
Filling Station (Stephen Meyer)**

---

**KeelyNet File MEYER1.ASC**   
Excerpts from:

***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 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.

---



**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
symetricel squarewave ( 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 approprately to allow the high
voltege spike to do its workr 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 phenomena 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 vill.

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 optinised, 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**

![](1hggun2.jpg)

**Hydrogen Gas Gun**   
![](1hggun.jpg)

**Water Fuel Cell**

![](1wfcell.jpg)

---

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 chareged
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 attentuating or varying the voltage amplitude in
direct relationship to voltage pulse rate determines Atmomic
Power Yield under control state...

**Photon Energy Aids Resonant Action**   
![](1photres.jpg)

**Laser-Injected Resonant Cavity**   
![](1lsrinjx.jpg)

**Power Load Distributor**   
![](1pwrload.jpg)

**Destabilizing Combustible Gas Ion**   
![](1destab.jpg)

**LED Laser Array**   
![](1led.jpg)

**Electrical Voltage Zone (Laser-Injected Resonant Cavity)**
  
![](1elvzone.jpg)

**Destabilizing Combustible Gas Ion**   
![](1polrzn.jpg)

**Controlled Energy Yield from Water Atoms**   
![](1yield.jpg)

---

**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.

---