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Radiant Energy Research Manual -version 2.0.1 by Bruce A. Perreault
The actual mechanics and electronics of building and validating a radiant energy
prototype is relatively simple. It is fun and easy.

Those involved in building prototypes must first confront some serious issues
before beginning. I will try to enumerate a few pitfalls and make descriptions as
clear as I can. This will fortunately and blessedly push some of you off the fence,
but for others it will be viewed as a challenge.

What are the most important assets to begin with?
1.
Dedication
2. Motivation
3. Passion
4. DO instead of just theorizing.

The "hands-on-imperative" must be at the very core of your being.
What is the second most important thing?
The lone wolf researcher will need a lot of skills if their project is to succeed.
Among the most valuable skills are those involving electronics technology, plus
some familiarity with machine shop practice and materials. A good sense of
organization and being able to stand back and see the big picture along with a
lot of plain good old common sense is a must have.

What about if I have few tools and skills but have the dedication?
Then you need to have some cash.... the green stuff. You will have to buy the
skills, knowledge and the time of others. You can farm out electronics and
machining chores but it will be expensive. The more that you can do for yourself
the better off you will be.

A fully equipped, skilled, advanced amateur energy experimenter might slip by
for just over $500.00 for everything! If you already have basic tools then a proof
of concept prototype should cost around $400.00 to build. Later you can build a
more powerful prototype to replace the proof of concept design. Your basic
working design will not have to be replaced. You will add more components as
your research progresses. Simple dedication goes a long way watching, paying
attention to details and doing it right the first time. With this borne in mind you
could complete a powerful prototype for around $5.000.00 that could provide
power for the average home. However, it is not my intention at this time to
instruct you on how to build a home power unit. At this time it is my intention 1
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to validate the technology, refinements still have to be made. When my
technology is validated by others then I will move on to designing and building
a home power unit. To reach this height public support must be gained.

Are there any dangers?
Yes, of course there is, there are any number of ways to wind up in an early
grave! Most of the lethal dangers can be avoided with skills. Otherwise, you
must pick up the skills as you go along. Read first and do second. Reference
books and a solid, broad based scientific library is your true asset. Know the
danger zones in the various disciplines you are going to come across.

Electrical:
Alpha fission circuitry uses high voltages from 5KV to 300KV at low amperages, direct current. This current may not electrocute you but caught within its grip
could cause you to hit something and cause serious bodily damage. If you get
knocked into a sharp object or suffer head injury by a shock while working on a
power unit it may not be your first but it could definitely be your last!

Machining:
Crushed and mangled hands to the unwary, metal splinters in eyes or skin.
Welding:
Burns and eye damage hazards.
Vacuum Technology:
Imploding glass bell jars, power valves, can scatter glass splinters at high
velocity into face and body.

Radiation:
This is not much of a problem using alpha fission, neutrons are not emitted.
Radiation in a concentrated state may produce harmful x-rays that can burn you.
My rule is that if does it not burn you then there is no need to worry. With some
degree of respect, like with many other potentially dangerous chemicals, it does
not pose an over whelming degree of safety hazard.

The paranoia about radiation is absolutely senseless! Nuclear bomb-era scientists
were paid large sums of money to create this perpetuating mind set. Their story 2
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was designed to keep other countries from building nuclear weapons and it is
used today to keep people from ripping off radioactive inventories.

Do you have the right stuff?
If you think that you have what it takes and have a burning passion for this
research then you are probably ready to begin. This is not a place for whiney
mentality. If you become frustrated or fail in your experiments have the courage
and good grace to realize that you did it to yourself and make the effort to find
out where you made your mistakes.

More than likely, you are going into this research with what you have learned in
books that have been designed to hide certain facts from you. Do not expect
results over night! Learn all that you need to learn by careful observation,
educate yourself, search out the truth first, let nature be your guide.

Fundamental Principle
My present research involves the development of a standard Alpha Fission Reactor
for commercial applications. This technology in a nut-shell is basically a clean
neutron-free way to speed up and release the energy contained in isotopic
materials. The energy released can be used directly to heat hot water, homes or
businesses. It's polonium by-product can be designed into radiolytically assisted
fuel-cells or capture capacitors to directly produce electricity. This energy source is
no mystery to me. It can be explained simply and does not break any laws of
science. It is a very old source of energy being extracted and harnessed in a very
unconventional way.

Direct Energy Conversion
I have made a number of discoveries over the past years in my line of research. I
designed two new types of capacitors. My thermoelectric capacitor discovery I
believe to be the common factor to several "free energy" devices of yesteryear.
These are electrolytic capacitors that are constructed with thermally differing
plates. When pulsed with energy they are heated like any other capacitor. They
are unique in that they convert this normally wasted heat into usable electrical
energy.

My capture capacitors are essentially unique fuel cells that are supplied with
hydrogen and oxygen as fuel that is generated from a radiolytic reaction.
Normally a radiolytic reaction only has an efficiency of around 5% because the
hydrogen and oxygen recombines and generates heat. However, by using
thermally differing plates additional energy gains may be achieved. My system
takes advantage of two processes, radiolysis and the thermoelectric effect. 3
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An Unsuspected Source of Energy
There is a source of energy that could provide us with all of our energy needs for
countless of generations. With this energy we can reach for the stars, or at the very least
explore our own solar system. The fuel that I speak of is called Polonium. It releases
more energy than any single element ever to be discovered by man or woman.
Polonium was the first element discovered by Madame Curie in 1898 while seeking the
cause of radioactivity of pitchblende. Her electroscope showed it separating with
bismuth. Polonium is also called Radium F. Polonium is a very rare natural element.
Uranium ores contain only about 100 micrograms of this element per ton. It is found in
Radium and its abundance is only about two tenths of one percent. In 1934, it was
found that when natural bismuth (Bi 209 ) was bombarded by neutrons, Bi 210 , the parent
of polonium, was created. Milligram amounts of polonium are now prepared this way,
by using the high neutron fluxes of nuclear reactors. Polonium-210 is a low-melting,
fairly volatile metal, 50% of which is vaporized in air in 45 hours at 131° F. It is an alpha
emitter with a half-life of 138.39 days. A milligram emits as many alpha particles as five
grams of radium. This represents a whopping five curies per 1/ 1000 th of a gram,
making Polonium 5,000 times more powerful than radium. The energy released by its
decay is so large (140W/ g) that a capsule containing about half a gram reaches a
temperature above 932° F. A few curies of polonium exhibits a blue glow, caused by
excitation of the surrounding gas. Almost all its alpha radiation is stopped within the
container that it is stored, where it gives up its energy. For these reasons polonium is an
attractive lightweight source of energy. Twenty five isotopes of polonium are known,
with atomic masses ranging from 194 to 218. Polonium-210 has been the most readily
available. Isotopes of mass 209 (half-life 103 years) and mass 208 (half-life 2.9 years) can
be prepared by alpha, proton, or deuteron bombardment of lead or bismuth in a
cyclotron, but this method has proved to be quite expensive.

However, there is another way to produce Polonium fuel, the Moray method. This
involves speeding up the decay process of uranium ores. This method electronically
excites alpha particles into fissioning. With this type of reaction it is possible to speed up
the half-life of uranium from 4.4 Billion years to a half-life of around 25 years. The by-product
of which is Polonium. With a reactor using this process no fission fragments
result as is the case of today's commercial neutron reactors. The neutron reactor
produces several magnitudes of deadly toxic radio isotopes. The alpha fission process
speeds radioactive decay the same way that occurs naturally except at a much more
speeded pace. Conventional nuclear reactors speed up decay by brute force and crack
atoms into many jagged fragments. While the alpha reactor gently creates the right
conditions for an isotope to follow its natural path of decay. Furthermore, once
Polonium decays it leaves behind only stable lead elements in its wake. This lead can
then be used safely for other purposes.

WARNING
Polonium is very dangerous to handle in even milligram or microgram amounts. Damage arises from the complete absorption of the energy
of the alpha particle into tissue. The maximum permissible body burden for ingested polonium is only 0.03 micro-curies, which represents
a particle weighing only 6.8 x 10 -12 12g. Weight for weight it is about 2.5 x 10 11 times as toxic as hydrocyanic acid. The maximum
allowable concentration for soluble polonium compounds in air is about 2 x 10 -11 microcuries/ cm 3 . If it is respected, like anything else it
poses little risk. So, you don't want to take apart a capture capacitor. Getting this material into your blood stream via an open wound on
your body could be fatal. If the capture capacitor remains sealed then there is nothing to worry about. 4
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High-voltage Power Inverter for Alpha Fission
I use a special flyback transformer that has a low resistance over-wind that has
wire windings added to its ferrite core. The high-voltage, high-frequency is the
result of the transformer being driven into resonance at about 143Khz. The
flyback transformer T1 outputs around 10KV, 15KV peak to peak at the above
mentioned frequency and is inputted to a solid-state multiplier section. The
multiplier steps up and rectifies the voltage to about -300KV optimally. This
extreme voltage is utilized to power the Alpha Fission Reactor. The heat that
results can be used directly for homes, businesses, or factories. Polonium can also
be obtained by this method to supply the alpha particles required in the assembly
of radiolytic capture capacitors.

The flyback T1 has one added primary coil. A feed-back coil is also added that is
180 degrees out of phase with the primary coil. These two coils are hand-wound
onto the flyback T1 ferrite core. The circuit is driven by one Mosfet Q1. Full core
saturation occurs with this design and a minimal amount of energy is consumed.
The frequency is variable with control pot R4. This allows fine tuning of the
frequency, driving T1 out of resonance where it can reduce over-all output
voltage from the flyback for various adjustments. Capacitor C3 and the primary
windings form a tank circuit to effect flyback oscillation. Resistor R2 limits
current to the gate of Q2. R1 provides the circuit imbalance to start oscillation.

PARTS LIST
Resistors
R1 & R2 – 100 ohms 1 watt
R3 – 470 ohms ˝ watt
R4 – 10,000 ohms potentiometer

Capacitors C1 --470µF 25 volt electrolytic
C2 --. 01µF 25 volt ceramic
C3 --. 27µF 100 volt ceramic or foil
C4 --2200µF 25 volt electrolytic

Semiconductors Q1 – Motorola TIP 100 Darlington
NPN Power transistor.
Q2 --IRF540 MOSFET
D1 – 8 volt Zener diode ˝ watt

Miscellaneous--electrical T1 --Modified flyback transformer -*
see text.
Miscellaneous --hardware 2-inch square perforated construction
board.
Mosfet needs a good heat sink.

Inverter Power Circuitry
Assembled & Tested --$130.00
* Batteries and case not included....

We offer a 30-day, no questions asked,
unconditional money-back guarantee!

This guarantee is null and void if a
product is returned damaged due to
misuse! It must be returned in resalable
condition...

Please add 10% for shipping... 5
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This circuit draws about ˝ watt when properly constructed. I use a small 12-volt
direct current (dc) computer processing unit (CPU) fan, that is normally used in
personal computers, to cool the Mosfet heat sink.

Assembly
1. Spread out and identify electronic components and hardware. Confirm
resistor values by using resistor color codes.

2. Insert and solder all electronic and electrical components onto a 2-inch
square piece of perforated construction board.

3. Using 16-gauge magnet wire, wind two coils consisting of 10 turns each onto
the flyback core. These coils are wound side by side. Then wrap these coils
tight with electrical tape.

4. Mount Q1 & Q2 onto transistor heat sinks.
5. Recheck all wiring according to the schematic.
Test Circuit
6. Turn R4 fully counter-clock-wise, switch S1 to off, insert 10 amp fuse into it's
holder.
7. Connect the negative probe of an amp-meter to supply ground. The positive
probe is connected to the negative terminal on a twelve-volt power supply.
8. Now connect the positive terminal on your power supply to the positive
input of the high-voltage, high-frequency inverter circuit.
9. Next, turn on power switch S1, notice a reading of Ľ amp on your meter.
Slowly adjust R4 clock-wise and there should be a rise in your reading to
about ˝ amp. You should also see some ion glow around the output
terminal. This is the lowest operational output that this circuit put out and
can be used continuously in this mode without overheating. Continue to turn
R7 and you should then notice a sharp rise in your reading. This is the
maximum operational mode and you should be reading around 1 amp. Do
not continue to operate in this mode as the Mosfet can become quickly
damaged without being cooled.
10. You can enclose the flyback in a 6-inch PVC tube. Seal around all wire feeds
using silicon sealant. Use PVC plumber's cement to seal tube pieces. Make
sure that your circuit is functioning properly before making final seals.
11. I use a small 12-volt dc personal computer processing unit (CPU) fan to cool
the heat sink to avoid damage to the Mosfet.
12. The output of the flyback is terminated to a suitable hardware bolt. 6
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Electronically induced Alpha Fission
United States Patent No. 4,961,880 Electrostatic Voltage Excitation Process and Apparatus is very similar to the setup that I am using here to create
alpha fission. The difference is that I am using solid-state components instead of a Van De Graaf machine. I was delighted to find this

patent in March as it validates what I have been trying to tell folks all along. All the numbers and figures are outlined in this patent... I will continue to develop this invention.

Radioactive emanations expelled from radium, thorium or radioactive ores can be concentrated on a negatively charged conductor. Radioactive matter decays and expels
emanations that will travel to a negative electrode. The collecting distance will depend on the potential of the charged

wire. This emanation, widely known as radon gas, will decay to polonium in a few days.
As an illustration of the enormous activity deposit of polonium, Marckwald stated that a precipitate of 1/ 100 milligram on a copper plate, 4 square centimeters in area, illuminated a zinc
sulfide screen so brightly that it could be seen by an audience of several hundred people.
In a nutshell, polonium is deposited on the wall of an alpha fission reactor by the application of a
negative charge. This deposit accumulates and an intense alpha flux results. The flux is contained
and focuses a tight stream of alpha particles into the isotopic seed material, alpha fission results.

This discovery has enormous implications in the way we obtain energy. It is safe, clean and abundant. I am a
catalyst to getting this technology implemented. Let's all work together and bring positive changes to our world. We are indeed running out of time. Will you make a

difference? The future of our world depends on what you do today...

300KV Voltage Multiplier
Three sections of voltage multiplication are shown here. Beyond six stages will
require good insulating material. Mineral oil is a good choice. A 300KV multiplier
will require forty 15kv capacitors and forty 20kv diodes.

.001/ 15KV ceramic capacitors $2.50@ 20KV diodes $3.00@
15KV Stage $30.00@ Assembled & Tested 300KV multiplier $450.00
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Capture Capacitor Construction Details
The capture capacitor is essentially a fuel cell powered by radiolytic reactions. One of the
most promising designs of the past was the 1961 Allis-Chalmers fuel cell that used silver
and platinum for its metal electrodes. Paper towel may be used as a chemically inert,
porous separator in a proof of concept prototype and is sandwiched between the two
electrodes. The plates may be enclosed in a vacuum cylinder made of glass or a suitable
container. The porous separator must be moistened with a 35% sodium hydroxide (lye)
solution so that ions can pass between the two electrode plates. The plates do not react to
the electrolyte. The electrolyte only serves as an electrically conductive medium.

In a capture capacitor alpha emissions occur through radiolytic decay processes, energy
is absorbed and converted to electrical current. By confining this cell within a suitable
container the energy released is greatly enhanced by natural processes. An all voltage, low
amperage biasing potential keeps this process going. Energy in these cells are "captured"
and then released in the form of electrical energy. A capture capacitor is both an energy
generator and storage cell all in one.

Silver element (anode -) plate forming process
To make the silver electrode, first mix 100 grams of silver oxide with 20 grams of
ammonium chloride, then add distilled water --a drop at a time --until a stiff paste
results. The mixture will give off ammonia gas and will turn to a white color. Working
quickly, smear the paste well into a 1˝ x 6-inch piece of close-mesh iron or copper wire
screening.

It will take about a day for the paste to thoroughly set and harden on the screen, or you
can hasten it by placing it in an oven set at no more than 130° F. When dry, lay screen in a
solution of ammonium chloride (200 grams to 6 oz. of water), for about 1˝ hours to
harden it further. This completes the anode element.

Platinum element (cathode + ) plate forming process
To make the form the platinum electrode, first mix 100 grains of platinum oxide with 20
grams of ammonium chloride, then add distilled water, a drop at a time, until a stiff paste
results. The mixture will give off ammonia gas. Form the positive element directly on the
surface of a 1˝ x 6-inch. piece of .015 inch or thicker nickel screen, which has been
cleaned thoroughly with emery cloth. Working quickly, smear this paste well into a 1˝ x
6-inch piece of close-mesh nickel wire screening.

It will take about a day for this paste to thoroughly set and harden on the screen, or you
can hasten it by placing it in an oven set at no more than 130° F. When dry, lay screen in a
solution of ammonium chloride (200 grams to 6 oz. of water), for about 1˝ hours to
harden it further. 8
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Fill a wide mouthed jar or a 1000 ml. Beaker with 32 oz. of distilled water. Dissolve 150
grams of sodium hydroxide (lye) in this water and add 20 grams of common table salt.
Sodium hydroxide is hard on the hands and clothes in its concentrated form, so don't
handle the crystals with your fingers and always add the crystals to the water slowly.

Mark the platinum oxide/ nickel plate and copper strips minus and plus now to avoid
mistakes. Connect a battery charger or car storage battery to the strips, negative to
platinum/ nickel strip and positive to the two other strips, also a D. C. ammeter or multi-tester
and a l0-ohm 25-watt resister is added in series with the charging current. Turn on
the charging current and adjust the variable resister so that only 1 ampere of charging
current flows. It is important that you observe polarity right at the first charge. Connecting
the positive lead of the charging source to the two iron or copper strips and the negative
lead to the platinum oxide/ nickel strip. This charge must be (2 or 3 hours), because the
oxide negative element must be converted to metallic platinum. It doesn't matter if the
elements gas in this forming charge.

Attach the anode and cathode electrodes to a strip of wood to test the two electrodes. Fill
another 13-oz. glass tumbler with about 9 oz. of distilled water and slowly dissolve 3 oz.
of sodium hydroxide in this to form the electrolyte of the silver-platinum/ nickel cell.
Suspend the electrodes in this liquid.

To activate and obtain electrical power from a capture capacitor polonium must be pre-induced
into the platinum/ nickel plate. A 300 kilo-volt supply will provide the required
polonium fuel in the form of a by-product of the alpha fission process. The
platinum/ nickel plate must be exposed to a radon rich atmosphere and negatively charged
for several weeks using the 300 kilo-volt source. Final assembly of the capture capacitor
takes place after treatment with the method just described.

* note:
Less expensive anode and cathode materials may be used to perform experiments. I have demonstrated that there only
has to be a thermal difference between two metallic plates to get the desired effect. I have used aluminum and copper
with good success. Aluminum and stainless steel works even better as this combination offers a greater thermal
potential. When using aluminum it is important that the electrolyte used as the thermoelectric junction between the
plates is not too strong or the aluminum will be consumed. A 50% ethylene glycol solution will work or you can use
window cleaner (Windex™) as a suitable substitute. 9
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The Radiolytic Effect Explained compiled by Bruce A. Perreault, August 20 th , 1997
Updated February 9 th , 1998
Of all the radiation-chemical reactions that have been studied in aqueous solution, the most
important is the decomposition of pure water itself. It has been shown by Pierre Curie and
Debierne that a vacuum can not be maintained with a solution of radium salts, that from the
solution a continuous evolution of hydrogen and oxygen takes place.

It must be mentioned that the decomposition of water in any form by alpha particles renders the
practice of sealing radioactive salts in small tubes for long periods of time a dangerous one unless
certain precautions are observed. Accidents involving serious loss of radium have occurred through
the explosion of tubes by accumulated pressure of hydrogen and oxygen. It appears to be
dangerous to heat an old tube or to exert any mechanical stress upon it. It is possible that
weakening of the glass container by the continued radiant energy bombardment enhances the
danger through devitrification of the glass. A far reaching disintegration of quartz containers by
radium rays has been reported.

The wide variety of chemical actions brought about, particularly by alpha particles, is surprising,
and one must be struck by the universality of the phenomenon of chemical change by radiation. We
find that alpha and beta particles, in their passage through molecules, are almost universally
capable of changing them chemically; their action does not depend upon any wave-length relation
with the atom or molecule affected. This is in marked contrast with photo chemical action, where
the specific nature of the reaction and of the system being acted on depends entirely upon the wave-length
of the light, and the capability of being absorbed by a given element or molecule. Owning to
the tremendous kinetic energy of alpha particles they always ionize and frequently produce
chemical changes in substances through which they pass.

Water when exposed to radiation undergoes a breakdown sequence into hydrogen peroxide,
hydrogen radicals and assorted oxygen compounds such as ozone which when converted back into
oxygen releases great amounts of energy. Some of these are explosive. This decomposition is
produced mainly by the alpha particles, that can be entirely absorbed by very thin layers of water.
This fact was not recognized by early experiments.

It has been observed by Runge, Bodländer, Ramsay, Kernbaum, Duane, and Scheuer that a
mixture of hydrogen and oxygen obtained by the decomposition of water by radium radiation
contains an excess of hydrogen. The excess is greater in the early stages of the reaction and has
been found to amount to an excess of 36% in one case. Kernbaum showed that hydrogen peroxide
is formed in water in an amount equivalent to the deficiency of oxygen in the gaseous mixture. As
the quantity of hydrogen peroxide accumulates in the solution a point is reached where its rate of
decomposition just balances the new formation, under which condition of dynamic equilibrium the
gases evolved would have normal composition. This explains the gradual diminution in the
observed excess of hydrogen.

Radiant energy as a catalyst holds the key to obtaining an endless supply of electrical power. Just a
few sprinkles of radium introduced into a weak solution of sodium hydroxide by catalytic action
will produce hydrogen and oxygen for a fuel cell. There is nothing to wear down. The radium
endlessly, day or night, generates hydrogen and oxygen to provide the fuel for a capture capacitor.
The only thing required is to draw off the electrical current so that the gasses will not build up. By
drawing off electrical energy the hydrogen and oxygen will recombine and revert back to water!
The cycle then starts all over again with nothing to replenish!!! 10
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Neutron Oxidation – Reduction Theory Promises non-polluting, portable electronic nuclear direct conversion devices.
The first law of thermodynamics – the principle of the conservation of energy states that "energy is
not created or destroyed; it merely changes its form." It is matter that can not be created nor
destroyed. In fact, energy is a result of matter being transformed from one condition to another.

The elements were created at the beginning of the universe and they can not be destroyed or altered.
The lithium atom for example has a mass that is slightly larger than the hydrogen atom, it is the
center of it's universe and has a resonate frequency representative of it's mass. Having a larger
mass than hydrogen it will vibrate at a lower rate. Logically lithium is heavier than hydrogen
because it is caught by earth's gravitational pull more readily. This analogy may be applied to the
rest of the elements on the chart. It is quite clear that isotopic differences in atomic weights are due
solely to their neutron counts.

I dare to speculate further that the neutrons do not occupy the space where atoms reside, that they
are not part of a "nucleus." The most simplistic expression of the Perreault atom makes the bold
statement that the neutrons reside in balance with electrons in the atomic shells. This concept
implied to exist throughout periodic chart of elements.

Using hydrogen as an example, it represents a positively charged mass that is seen at the center of
its universe, it is an atom that has a specific resonate frequency according to this mass. Three
hydrogen elements are known to exist that are chemically similar but weigh differently. The reason
why they weigh differently is that they individually have a differing combination of electron or
neutrons. They are all hydrogen atoms, however, it is the neutron count in the atomic shells that
determines what isotope of hydrogen it is.

By using this atomic model it can be clearly shown how triple weight hydrogen (tritium) decays to
helium-3. In this particular transformation a charged normal weight hydrogen element (protium)
that carries an excess electron in it's shell can react with a tritium element and emit an electron as a
by-product of this reaction. When this occurs an electron is emitted at an accelerated rate and is
seen as beta energy. This model will not alter the way we view chemistry, however, it will change
how we view nuclear changes. In light of my theory I postulate that isotopic differences in atomic
weights are due solely to the neutron counts in the atomic shells.

Mysteries of nature such as gravitation may be better understood by applying my bold theory.
Lithium for sake of comparison is an atom that has a mass that is slightly larger than the hydrogen 11
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atom, it is the center of it's universe and has a resonate frequency representative of it's mass.
Having a greater mass it will vibrate at a lower rate than that of hydrogen, therefore we may say
that it is caught by earth's gravitational pull more readily and therefore has more weight. This can
also be applied to the rest of the elements on the chart explain their attractions to the earth.

Furthermore it is my contention that the atoms were created at the beginning of the universe and
they can not be destroyed or altered. The good news is that the elements, cosmic soups of atoms
with orbital neutrons and electrons can be altered to serve humankind.

Swedish Stones

Around the year 1911 T. H. Moray was able to power a 16-candlepower carbon-arc lamp at about
half its light output with a simple electrostatic charge obtained from an antenna and ground
connection. So, "radiant energy" power generation was born. In 1912 while Henry Moray was on
mission with the Mormon Church in Upsalla, Sweden, he had a passion for crystal radio reception.
Every spare moment he searched for a mineral that could possibly work as a radio detector. Moray
had found two specimens that worked well as radio detectors. One was the sensitive galena that he
found in a hillside and the other was a white, powdery, stone-like material that he found in a
railway car, located in Abisko, Sweden. From military records we know for certain that the white
material was "fused silica." Back in the early days quartz (silicon dioxide) was crushed and used
for the mining roads. Moray had taken the powdery quartz material, along with its impurities and
fused it with a welding torch knowing that fused silica in those days made a good detector for
crystal radio. He also knew that the galena taken from the hillside would make a good radio
detector material. One day he put the two specimens back to back with a silver catswisker and to
his surprise got wonderful results. In fact, he found that he could drive a small horn speaker with
the combination.

Sometime in late spring of 1925 Moray designed devices that could put out higher wattage's. Often
times people would demand that he draw too much power and the white, stone-like material would
overheat and burn up. When he ran out of this material he was forced to find a substitute. I have
identified Moray's material taken from the hillside as being a type of argenti-zinciferrous-galena,
this he was able to synthetically duplicate, this formula is found in his Electrotherapeutic U. S.
Patent No. 2,460,707. However, he was unable to figure out what the impurities were in his fused
silica
material. This forced him into exhaustive research with semi-conductive materials. Silicon
and ultra-pure germanium were what held the most promise. To increase the sensitivity of these
materials he induced artificial radiation into them. As a result of his experiments he was able to
formulate a satisfactory mixture. It was a triboluminescent zinc comprising pure zinc sulfide that
was doped with a bismuth activator. This material was then exposed to radiation emitted by a
unique high-voltage powered vacuum-tube that contained radium chloride. This created "active
bismuth," today known as polonium-210. It would glow a bluish-green after treatment. This is
what Moray called "artificial radiation." When doped into ultra-pure germanium it made an
excellent transistor type material. Moray called this new synthetic "fission material." This
transistor material is said to have been superior to the Bell Laboratory transistor materials. Moray
was never able to duplicate his fused silica material that produced power. However, he was able
to build cylinders that housed a central corona wire. These cylinders when charged with
electrostatic energy added current to the ions. Excess power could be obtained with certain circuits. 12
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Energy Release by Alpha Disintegration
When positively charged helium atoms (alpha particles) collide with the electron cloud that envelopes
another atom its' positive charge is eventually canceled by these collisions. This is called "absorption." Atoms ring like a bell when impinged upon by
alpha particles. This ringing state generates x-rays. The wavelength of this generated
x-ray depends on the charge of the alpha particle and what type of atom it hits. If the
x-ray generated has an energy level that exceeds 10 MeV it is absorbed by atoms, in which case the neutrons are raised to an excited state and they may be broken loose from the shells of an element or a

neutron may be added to a shell. Isotopes may be created by gaining or losing neutrons in this process. We can efficiently do this by exposing atoms to
alpha particles. From this model it is clear that ENERGY can be created or destroyed by one state to another.

The formation of a chemical compound is in general accompanied by the release of a definite amount of heat per unit mass of compound formed. The burning of a fuel is a chemical reaction in which oxygen
unites with it. The quantity of heat released when a unit of fuel is burned with oxygen is called the heat of combustion. For the average coal this value is from 7,000 to 8,000 calories per gram or 12,000 to 14,000
BTUs per pound.
In contrast, isotopic transformation is accompanied by the release of enormous energy when compared to
conventional oxygen – electron oxidation. However, this does not justify the theory advanced that neutrons occupy the center of atoms. It is my hypothesis that neutrons reside in the orbital shells of

elements and not within the nucleus. To envision this atomic structure one only has to look at our own solar system to see this on a grand scale. Isotopic oxidation – neutron oxidation simply involves the
neutrons. However, the energy involved is much greater because the neutrons represent neutral charge and therefore the binding energy to the elemental shells are of a greater magnitude.

When the unstable isotope of an element reverts back to it's stable state energy is released in the transformation. Now, if incident impinging electrons are impinged upon a naturally occurring element
like U-235 and the wavelength is correct according to the resonate frequency of this element then excess energy can be released. This may be done with any isotope, however, U-235 is "self-fissioning" and under
the right conditions will not require any other source of energy other than what it releases. It will fission by capturing neutrons. Excess energy is released only after the amount of captured neutrons equals the
amount used for the transformation. This is called the "break even" point, beyond this excess energy is released.

We are not limited to the U-235 isotope to use as a fuel source. This element is used in commercial nuclear reactors because it is self-fissioning and requires no external energy to get it to "burn." U-235 is burned by
capturing neutrons. This reaction is deadly to biological materials. What is not generally known is that the U-238 in a commercial reactor does not undergo fission. The only reason for it being there is too capture
neutrons to transform it into weapons grade Plutonium (Pu-239).
U-238 will fission by alpha fission and will not fission by neutron fission. However, there is a hitch to the alpha fission process, the U-238 fuel requires an initial external energy to get it to burn faster than its
normal decay rate. This is not a problem. All that is needed is the right type of spark to speed up the decay rate. This involves a simple and economical alpha fission process, furthermore, ZERO neutrons are
emitted by this process.
Fully deleted U-238, uranium that does not contain U-235, is the answer to our energy needs because it's entire decay chain emits only alpha particles. Alpha particles are stopped by a thin piece of paper and
therefore can be contained safely. No deadly neutrons result, this is my definition of a clean nuclear fuel. The end product is stable lead and can be used for other applications.

Nuclear decay by electronic stimulation
My 1996 radiant energy findings show that the decay rate of radioactive matter can be accelerated by confinement and electronic means. Isotopes can be stimulated into storing or giving up excess energy. This
technology indeed holds great rewards. 13
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A non-polluting, neutron free, portable electronically stimulated nuclear reaction process named "Method of Generating Nuclear Decay by Electronic Stimulation," was publicly disclosed by me on the internet on
November 28 th , 1997. My method of nuclear decay by electronic stimulation was first disclosed by me to the United States Patent disclosure office on July 27th, 1996. I do not claim to be the first to use this process
to accelerate nuclear decay by electronic stimulation. T. H. Moray to the best of my knowledge was the first to accomplish this. At the end of March of this year I discovered that about ten years ago another inventor
had also rediscovered the Moray process and received a patent for his work. This inventor has validated that the technology is safe and is clean, no neutrons result. In fact, as documented in the patent, nuclear
waste can be used as a fuel source and the "waste" becomes non-radioactive. This technology could eliminate the need to store fuel and batteries aboard vehicles.

My approach to directly convert radioactive energy into electrical energy is a very old approach with a new twist. This, together with
alpha fission could be the answer to our energy needs. That is if I am permitted to bring it to the world.

However, there is one hitch, radiolysis at best is only 5% efficient. Weather you use an electrolyte or a solid-state semiconductor most of the ions created by the radioactive decay products recombine and heat
is the result. This represents waste in the conversion of radioactive decay to electrical current. For the most
part I have found a way around this recombination by capturing the ions before they get the chance to recombine. This is done by using a fuel-cell process developed by Allis-Chalmers in the early 1960s. The

only requirement is that power is continually drawn from this capture capacitor. If power is not drawn off
then there is no place to store the ions and recombination will occur. Heat will result and may destroy this component.

This discovery, among others, have been the result of my research in the alternative energy field that presently spans about fifteen years. Nuclear decay by electronic stimulation could provide additional
energy to radiant energy conversion processes.

"Ere many generations pass, our machinery will be driven by power obtainable at any point in the universe... it is a mere question of time when men will succeed in attaching their machinery to the very
wheelwork of nature." -Nikola Tesla
My research reveals an artificial process to control and intensify nuclear energy: by confinement and
electronic stimulation to produce oscillations in radiant matter resulting in artificial radiation, to achieve this objective.

Basically, my Radiant Energy Research explores three functions: a) Ions generated by isotopic transformations b) oscillations of ions, c) means to convert isotopic energy release to electrical current, d)
means to accelerate nuclear decay by an electronic method to induce resonance between alpha particles and other elements.

Radiant energy devices under development
For almost fifteen years now I have performed many experiments. The fruits of this research is now taking shape. Many fruits are within grasp but they are not yet quite ripe for the picking. My intent of revealing
my progress to the world is to insure that my work is not done in vain. Through my writings I have attempted to explain the many facets of "radiant energy" and how it is possible to draw power from it. If
radiant energy can be given to the world then humankind will have the potential to reach heights not yet dreamed or conceived of yet. Today I freely give to you the results of my life's work. It is my hope that in
the months to come that with your support that this mode of power generation will become a commercial reality.

Acknowledgments
I would like to thank Calvin Bahlmann for volunteering his expertise in the manufacture of Radiant Energy Products. He is
a fine mechanical engineer and you will be hearing more about him as our projects progress.

I would also like to give thanks to Michael Schuckel who has spent many hours in refining the electronic circuits. His
prime goal is to get this technology out into the marketplace. 14
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WARNING!!!
The information herein is deemed as research material. We can not guarantee results. We
do not take responsibility for accidents due to negligence or ignorance!!! Electricity is
EXTREMELY DANGEROUS and caution should always be used when working around
it. Please take the time to educate yourself sufficiently. If you don't understand something,
investigate further before attempting. Take liberal advantage of encyclopedias, science
books, and other reference materials. This manual was compiled for information purposes
only. We do not control the materials used in construction, the methods of construction,
nor the applications of the construction, therefore; WE ARE NOT RESPONSIBLE FOR
DANGEROUS OR UNDESIRABLE RESULTS. Always use protective gear.

ALL SAFETY PROCEDURES MUST BE CAREFULLY OBSERVED.
MEASURING THE HIGH VOLTAGE IS NOT RECOMMENDED

Copyright Information
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graphics, and graphic elements) are copyrighted ©, 1998 by Nu Energy Horizons, Inc.

All materials may not be reproduced, stored in any retrieval system, or used in any way for
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Send correspondence to: Nu Energy Horizons, P. O. Box 22, Rumney, N. H. 03266

Disclaimer: The author assumes no liability for any incidental, consequential or other
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arising from the use or misuse of the information contained herein are entirely the
responsibility of the user. Although careful precaution has been taken in the preparation
of this material, we assume no responsibility for omissions or errors.


Last Modified: July 2 nd , 1998
www. cyberportal. net/ nuenergy
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