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talos Gold Transmutation

10/2/2005 5:07:36
PM
If one accepts geophyicists explaination that gold element is formed
from supernovae
and that all gold on Earth came from gold atoms drifting in universe,
then why is gold only found on Earth, and not other planetoids such as
Moon, Mars, and especially
Venus and Mercury which are more dense than Earth.
The reason is, gold is not created from supernovae. Gold is made from
electrical discharge with sulphur and mercuric sulphide. This mixture
would have been present on Earth eons ago with super charged
lightning strikes around the Earth.
This created the present day gold deposits. Actually, gold can be
manufactured
in laboratory. No need to look for it in natural state.
World economic order will collapse once the truth is known about gold
manufacture.

replies will be listed below this message edit

Replies 1 - 10 (out of 10 total)

Philip Edwards Gee thanks for the info, I will get right on it!
10/3/2005 1:49:10
AM

Legat "World economic order will collapse once the truth is known about gold
10/3/2005 2:35:33 manufacture.
AM "

This is not neccasarily true, as you probably know the human folk have
learned to make artificial diamonds from coal, but it was even more
expensive, because there is a huge pressure and heat needed, to make
this conversion. Russians along with this expensive way, which was
stolen by Americans, also came up with a cheap way, but this
technology is not yet revealed, as it might shatter the current diamond
markets, and people like diamonds because they are rare and
expensive, not common like glass. So even if someone came up with a
cheaper way of aquiring gold than mining, then they are more likely to
hide it, at least for the time being, maybe because the governments
control & protect their natural reciurce markets.

phenomenon If gold can already be made in labs, then who ever funded the start of
10/3/2005 8:43:42 the project, made a good investment because you can make double the
AM goods for minimal cost. Then this theory contradicts with the theory of
the Nephelim who created man and eslaved him to mine for gold. If our
technology is still primitave to galactic standards, wouldnt you think
aliens could make their own gold? hhhhm.

DEATH eVADER The problem is even though Diamond, Gold and Silver is hailed as
10/6/2005 11:18:06 Jewlery. They could and eventually will be required for the next
AM generation for industrial use

UFO23 I don't know if gold has been found on other planets or asteroids, but if
10/6/2005 1:02:03 not then it is strange.The explanation for this would be this:Gold is heavy
PM element and is very deep under the surface because heave and dense
elements tend to concentrate in the middle of the planet or other object.
And I doubt that gold can be ever created artificial like diamonds.I
watched on TV about this and technology is very advanced about
creating diamons.They can create different colors,red,green
diamonds.But they don't know how gold is created.They suppose it is
created when two neutron strars collide.If this is so this is a very seldom
event and gold must be very rare element even in universe.

gfcgame What A HELL are you talking about?

r
10/7/2005 Make gode now!
9:12:09 Make da*m diamonds now!
PM
I don´t give a da*m to this already failed economic killing bilions for petrol!

***************************************************************************
Liks to make diamonds: (sell for cheap as cuturated ones 4$ +)
**************************************************************************

http://www.rangeguide.net/diamonds.htm
http://www.zyra.org.uk/make-dmd.htm

Some fabrics: (not all)

http://www.hypocrites.com/article14801.html
http://www.geniebusters.org/26_Mistry.htm
http://www.sandia.gov/media/diamond.htm
http://www.diamonex.com/abouttech_dlc.htm

*******************************************************************************************
Link to make gold easy, bur risky (joe champion was arrested because that)
*******************************************************************************************
Joe champion recipe:
http://users.rcn.com/zap.dnai/gold.htm
http://www.rexresearch.com/adept/aa1agau.htm
http://www.drjoechampion.com/Transmutation/Isotopic%20phonon%20spacing.ht
m

how make gold using plasma:

http://jnaudin.free.fr/cfr/index.htm
jnaudin now offline, take this pdf link:
 http://www.lenr-canr.org/acrobat/CirilloDtransmutat.pdf

discoveries about gold bacteria:

http://www.abc.net.au/science/k2/trek/4wd/Over44.htm
http://www.prophetau.com/alluvialreport/index.htm

How make gold reaching ilumination or something like this:

http://www.soulinvitation.com/immortality/

********************************************
To melt iron use microwave like this!
********************************************
http://home.c2i.net/metaphor/mvpage.html

You will say: I don´t believe, your dreamin, like triyng to fly without wings...
Yeah.. yeah.. why don´t you try make ovnis using your monitor at all?
http://jnaudin.free.fr/lifters/main.htm

Americans really know this? Noone belive I can, I don´t have a cent to buy
materials to do such.
Money doesnt matter. 2012 something wil happen..... big shift I guess.

UFO23 If it were so easy to make diamonds or gold,then everybody with a

10/9/2005 11:56:09 microwave oven would be a rich man.The reality is that nobody knows
AM how to make gold.Perhaps aliens know.It they can make solar
systems,then why not gold.

gfcgamer
11/4/2005 10:29:40 ARE YOU STUPID ISN`T? DID YOU HEARD?
PM
I SAID IS MORE EASY THAM THAT STUPID particle aceleration!

AT LEAST READ MY LINKS BEFORE SAY ANITHING!

HERE THE LINK FOR THE VIDEO VIDEO VIDEO DAM*M*M*M!

http://jlnlabs.imars.com/cfr/lorio/fusionefredda.wmv
http://jlnlabs.imars.com/cfr/lorio/transmut.wmv

SEE THE METALS GENERATAD IN THIS PICTURE ('AU' is G-O-L-D

ok?)

http://jlnlabs.imars.com/cfr/lorio/index4.htm

FINISHED!
 gfcgamer
11/4/2005 10:40:43 BIG PRESSURE?????
PM http://pubs.acs.org/cen/images/8205/8205cover_GEMESIScxd.JPG

READ FULL REPORT DA*M*M*M

http://pubs.acs.org/cen/coverstory/8205/8205diamonds.html

AND MORE.
http://www.wired.com/wired/archive/11.09/diamond.html

OK now for your big interests in sell yours pressurized diamonds, bann
me if you wish.

gfcgamer OOOOOPS That last report must beLyeing about such pressure!
11/4/2005 11:00:55
PM What About Coating a inch of diamnod???
http://www.geniebusters.org/26_Mistry.htm

1er link:

A Complete Procedure to Produce Diamonds

LOW ENERGY NUCLEAR TRANSMUTATION /
ALCHEMY
 Special thanks to Joe Champion for sharing this technology on the Internet.

Range Guide has featured Ancient Astroglyphs, ancient science and alchemy
from "The Book" thanks to BJ Spurlock, a "Keeper of The Book." Men like these
have contributed to our understanding and make the Internet voyage we take at
the Range Guide website more exciting. But the real fun is getting a better
perspective that makes our lives "lighter". I feel this research needs financial
support even though the information gleened is being given freely in hope that
the spiritual as well as the biological health leaps that can be made from
digesting the rediscovered minerals will be shared abroad, so your comments
and donations are appreciated. Please continue contact with us as we follow this
developement. Special thanks to another researcher, Barry Carter for helping me
understand White Gold/M-State elements better. -Elder

Making diamonds in the microwave / Joe Champion Recipe [Do not do this
experiment without competent adult supervision!]:

STEP 1

Using a pyrex microwave cooking dish with lid, place two charcoal brickets
covered with 4 ounces of peanut butter inside. Microwave on high for 60 minutes
at 10 minute intercals.

STEP 2

When cool enough to handle, take the dish outdoors and place on top of an unlit
barbque grill. Remove the lid form the dish and saturate the charcoal and residue
with charcoal lighter fluid. Light the charcoal (Note: At this time the diamonds
are made, this procedure is reducing the excess carbon to ash.)

STEP 3

At this time you should have a dish full of a gray/black soot. Carefully scrape this
soot into a dark colored dish and gently wash. The ash will wash away leaving
the diamonds you've produced.
If you decide to experiment with recipes other than the one above, do so with
competent adult supervision and in extremely well ventilated areas or outdoors.
Joe Champion has released the recipe above due to its safety and lack of possible
toxicity in your kitchen

Superconductibity and Modern Alchemy

Has the Philosopher's Stone Been found?

In March of 1988, David Hudson filed U.S. and worldwide patents on eleven
orbitally rearranged monatomic elements, Ormes, which he discovered in a form
not previously recognized. This a totally new form of matter, the confirmation of
which will be presented by Mr. Hudson with scientific references and data
compiled by some of the most acclaimed research laboratories in the world.

David Hudson is a fourth generation Arizon farmer who became interested in

extracting gold and silver form the "tailings" of old mining sites near is 675 acre
farm. When he began the recovery process he soon discovered that gold and
silver were being lost because of of the buildup of a powdery substance referred
to as "ghost gold" by miners and metallurgists. Hudson's cruiosity led him to
work with spectroscopists at Cornell University and other labs to discover the
elemental ingredients of this powder. Initial findings of the sam;le yielded iron,
silica and aluminum. Further extraction of these elements left 98% of the powder
intact. The surprise was that this 98% consisted of nothing which could be
identified through normal spectroscopic analysis. Hudson knew that this
"nothing" could be seen, felt, tasted and weighted. It had to be something and he
was determined to find out what it was. In the course of his research he found a
paper from the Soviet Academy of Sciences stating that a proper spectroscopic
analysis required a 300 second burn instead of the 15 second burn used in the
United States. Utilizing the Soviet technizue of fractional vaporization, Hudson
discovered that his sample contained the elements palladium, platinum,
ruthenium, rhodium, iridium and osmium. Even more astoundin was his
discovery that each of the nonmetallic elemental forms was a superconductor, a
substance which allows an electric current to flow without the resistance even in
the absence of a continually applied potential.

Hudson continued his research and found papers by the US Naval Research
Facility showing that cells of living tissues commicate with each other by a
process identical to superconductivity, but the nature of the superconducting
substance was unknown. On a huch, Hudson analyzed the brain tissue of pigs and
cattle and found that brain dry matter weight was 5% rhodium and iridium!
As a result of Hudson's research, he knew that the electrons flowing through a
superconductor pair off and are converted to a light frequency in the process. He
theorized that this might be the same process occurring in human cells. Hudson
discovered papers published by Bristo-Myers-Squibb Laboratories and others
which indicated intense experimentation was being done utilizing precious
elements in the treatment of cancer. These elements were shown to interact with
the cell by a vibrational frequency or by light transfer to correct the mutent DNA.
When Hudson applied his proprietary method of analysis to Essiac Tea(an
alternative treatment for cancer), he discovered high levels of rhodium and
iridium. He also found that acemannan, a derivative of the aloe vera plant
currently being tested on AIDS patients is 90% rhodium.

David Hudson's life took an abrupt turn in 1990 when his uncle brought him a
Time-Life book, Secrets of the Alchemists. The goal of the alchemists was to
make a white powder of gold that would serve as the container of the "light of
life". This search for the white powders has been termed the search for the
philosopher's stone. Encyclopaedia Britannica says: "The stone, also referred to
as the "tincture" or the "powder"....was allied to an elixir of life...Inasmuch as
alchemy was concered not only with the search for a method of upgrading less
valuable metals but also of perfecting the human soul, the philosopher's stone
was thought to cure illnesses, prolong life and bring about spiritual
revitalization."

A new line of thought consumed David Hudson. He read over 500 books on
alchemy and religion including The Bible...finding many references to the white
powder. He talked to Rabbis well versed in the ancient secrets of Judaism who
told him of "white powders" available only to the priest of Solomon's Temple.
This is referred to as "manna"-food of the gods. Hudson's research has led him to
believe that ingesting the manna enabled the preists to approach the Ark of the
Covenant without being killed.

In his lecture, Hudson will give fascinating details about the Ark and a scientific
explanation behind the mann's protection. He will also discuss where the priests
obtained their formula for making the white powders and how this formula was
lost after the Temple was destroyed. He will explain his theories about the
Essenes and why he thinks Mary was given the white powders of gold in
preparation for the conception and birth of Jesus.

Nostradamus predicted that by 1999 "occult gold" would be known to science.

Other prophecies indicate the discovery of this "occult gold" would be made by a
direct descendant of the Davidic blood line. According to the book, Holy Blood,
Holy Grail, the Davidic blood line is continued today in the French du Gulse
family name. Long after his research into the white powders began, David
Hudson discovered he was a direct descendnt of this French family.

Could David Hudson be the one chosen to fulfill these ancient prophecies?
Revelation 2:17 says "...To him that overcometh will I give to eat of the hidden
manna and will give him a white stone and in the stone a new name written,
which no man knoweth saving he that recieveth it."

Products Recommended by Range Guide

The Water
Living Water has been a field of research for me going on 20 years. My first
introduction to the amazing power of water began then with these words
from my great friend, Billy Joe Spurlock, "water will become the most
important thing on Earth". If Billy Joe said so, I knew it was inevitable.
Billy Joe is one of the world's foremost astro-physicists, specializing in
nuclear wave theory, and it was he that told me many things about the
ancient science of Atlantis, Lemuria, and MU. Billy Joe worked directly with
Werner Van Braun and Albert Einstein. Billy Joe, and his associates sought
to harness an understanding of how our universe works and to use the
knowledge for the good of mankind, not like many that took the knowledge
and used it for war and enslavement. Over the years we have worked
together in research, proving many of Billy Joe's scientific methods.

If you have trouble believing in the power of water (important to have salt
also), then I recommend that you read what Dr. Fereydoon Batamanghelidj,
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Click Google video buttons below to see 4 video segments with hyper-physicist and
inventor Dan Nelson at a Winter 2006 seminar (3-day seminar on 3 DVD's available
for a donation of $40).
Click Google video button below to see a short video segment with Dan from early
2006.

While living in Montana, I had the great opportunity to meet Dan Nelson (I
don't believe in coincidence). He had a great interest in water as well. And at
that time he was still collaborating with Lloyd Mear. He had just begun to
share the early versions of his enhanced water. I tried some of this water for
myself, having recently had my own "near death experience", and sought to
give it a try. I have to say that I owe a great deal to Dan Nelson for being
here writing this for you at the beginning of 2006. The result of our meeting
several years ago, the best water in the world (not just my opinion, many
other researchers agree) was officialy labeled and on the market. I
volunteered to do the graphics and design for the label in accordance with
the guidelines I was told would satisfy the FDA.

This was the original labeled water when it first came out in 2 liter:

After 2 months of changes with the government of the State of Utah, I finally
obtained approval for the first label for Dan's water so that it could go on
the market. I called it "The Water". It has gone through several upgrades
since that time, especially with Dan's new invention that he initally called the
"Virtual Photon Laser". The laser, together with specific
mathematical/geometric formulas, encodes the oscillating resonant energies
or "information" in The Water by creating fractal patterns that remain in
motion in The Water. Later on, I interviewed Dan Nelson, and my friend,
Gloria Thiede transcribed the interview so that it could be published. Soon
after the interview was published on my website - Range Guide - the news
went worldwide, and interest began to mount exponentially. I've been
marketing the product wholesale for $35 to my club members ever since,
and many have changed their lives for the better as I did by drinking The
Water. The "concentrate" makes at least 8 gallons for drinking. No specialty
water compares when it comes to maximum hydration of cells quickly.

Dan Nelson and Lloyd Mear collaborated on the formulation of The Water
back in 2001. Dan Nelson’s previous experience with technologically
enhanced water began with his use of Patrick Flanagan’s Crystal Energy
concentrate based on silica micro-clusters with high surface zeta potential.
One parameter of Patrick Flanagan’s water, which has never been
discussed, is the molecular spin-state expressed in bio-angstroms. The bio-
angstrom reading is indicative of the actual water particle configuration.
For example, low spin-state (quantum-state) water is composed of
fundamental water particles, which are quite large by molecular standards
and are actually micron sized particles. Flanagan’s Micro-clusters in water
generated an impressive spin-state of 7,500 bio-angstroms when diluted
according to his recommendations, whereas most drinking water rates
anywhere between 3,000 and 6,000 bio-angstroms. The water inside all living
cells clocks at 8,500 bio-angstroms. Water such as Flanagan’s Crystal
Energy rates a lower interfacial (surface) tension of 59 dynes/cm as opposed
to the nominal 75 dynes/cm of most tap water.

These facts have been greatly misunderstood and misinterpreted. Lower

interfacial tension, while making water a more efficient solvent and wetting
agent, does not make water a more efficient hydrating agent. Water must
enter the cell through active protein channels in the cell membrane wall
called “aquaporin”. Despite the state of the art achievement of Crystal
Energy in lowering interfacial tension, Flanagan’s technology only resulted
in a 15% reduction in micron sized water particles to particles in the
nanometer range. Micron water will not traverse the cell membrane wall by
virtue of its size. The aquaporin only allow for the passage of the nanometer
sized constituents of ingested water through the cell wall.

Dan Nelson’s development of a new class of laser, which he now refers to as

the “Geometric Laser”, makes possible the total engineering of a given
volume of water to achieve a 100% conversion of the fundamental water
particle to sub nanometer size. This water actually supports no water
particle larger than (.4) nanometer. This is achieved by energizing the water
with energy turned back to the water from vacuum space around the
particles. In other words, the Geometric Laser exposes the water to negative
entropy (reverse thermodynamics) and places it in a high quantum state.
One of Lloyd Mear’s associates with a PhD in geophysics referred to this
engineered water as “gyro” water. Dan responded by agreeing with the
terminology as long as it was understood that “gyro” was simply a metaphor
for the permanency of the spin state properties imparted to the water by the
Geometric Laser and not to some nano technology aspect.

Any water exposed to the Geometric Laser assumes a minimum spin state of
1.8 million bio-angstroms. The athletic performance enhancement water
that was produced jointly by Dan Nelson and Lloyd Mears clocks in at 12
million bio-angstroms. This water has a measured interfacial tension of 20
dynes/cm. However, the extraordinary hydrating properties of this water
can be attributable, not to the reduced interfacial tension, but to the
breaking down of the fundamental particle size to the sub nanometer range.
These minimally small water particles now impart new and amazing
properties and capabilities to water which must be experienced to
appreciate.

The science of thermodynamics involves the movement of heat - the

reversible transformation of heat into other forms of energy such as
mechanical energy. The first law of thermodynamics deals with the
conservation of energy. The second law, commonly referred to as the
entropy principle, refers to the degradation of the total energy in a system.
Normally, entropy would be a microscopic variable describing a bulk
property of matter - a quantitative measure of how disorganized a physical
system is. So the second law says, for any "closed" system, the entropy
(magnitude of disorganization) always increases. First of all, the law of
entropy increase is statistical, not absolutely certain. According to the laws
of quantum mechanics, at the quantum level there is said to be time
reversibility, things can happen in any direction. The arrow of time can
point in either direction for entities on the atomic/molecular scale. On the
micro level, nothing seems to have a preference for one movement of time
over the other. Forward or backward time movement is irrelevant to a
molecule until we make the transition from thinking in terms of chemical
thermodynamics to thinking in terms of quantum thermodynamics.

Entropy can decrease in an "open" system. An example would be the

ordered deposition of ions in a crystal lattice. The manifest growth of order
is decreased entropy. Water enjoys the status of being an "open" system in
its liquid phase. Liquid water is in an uncondensed phase. Heat transfer
decreases entropy and water by shifting it into a condensed phase via the
deposition of molecules in the ice lattice or the highly ordered fractal pattern
of a snowflake. All three states of water (liquid, bulk, ice-fractal flakes)
represent what would be considered highly coherent quantum states. Water
is actually a crystal (so are we) in its uncondensed/liquid phase. Instead of
phase shifting water to its condensed phase, we have developed a unique
approach to decreasing the entropy of water while locking it into its
uncondensed phase. This approach brings about a substantially higher
coherent quantum state regarding liquid water. This involves the
restructuring of water's crystalline molecular units into substantially
smaller units. Supporting these smaller molecular units is the proprietary
function of quantum thermodynamics. Water, as an open system, is
exponentially susceptible to the quantum state of the vacuum medium or
what is often referred to a zero point energy.

Bringing any pure water to a higher coherent quantum state and

maintaining it there requires the manipulation of quantum
thermodynamics. This is accomplished with a unique Laser that actually
produces a time reversed particle wave. Technically, this is a virtual particle
wave running in the near ultraviolet end of the spectrum. This laser has a
higher degree of phase coherence (by a factor of 100) than a conventional
EM laser no matter where the EM laser is running in the visual spectrum.
The virtual laser imposes coherence (structure) on the vacuum medium
around and through a given volume water and rotates energy out of vacuum
into the fundamental water molecules. As entropy decreases (time reversed
energy always runs thermodynamics in reverse) water physically expresses
this by reorganizing fundamental particles to acquire a higher coherent
quantum state. The molecular units jump from the lower (ground) state in
mathematical predictable quantized stages with different crystalline shapes
of progressively smaller size. This technology has exceeded in reducing
micron size particles to less than one-half nanometer.

In considering our product, remember that what you start with has a lot to
do with what your end product becomes. The Water starts out with a base
water that comes from an ancient aquifer 8,000 feet below the surface. Out
of approximately 5,000 samples from around the world, this water was
selected as the best water in the world to use as the base water for making
The Water. The base water is called "Pure Telluride" (from the Telluride,
Colorado area).

All bottled waters are not created equal. Pure Telluride Natural Spring
Bottled Water comes from a spring deep in the Colorado Rocky Mountains.
This natural spring water is known for its smooth taste and well-balanced
mineral content including a high level of H- (H negative), a youth preserving
anti-oxidant. Bottled at the source in the mountains overlooking Telluride,
this natural spring water is filtered for centuries through volcanic geology.

Pure Telluride water naturally contains extra electrons, also known as H-, a
naturally occurring antioxidant. Free radicals or unstable molecules from
poor diets, bad water, pollution, and stress attach themselves to stable
molecules, stealing their electrons and making them unstable. This causes a
deficiency in our body, which leads to illness as well as premature cellular
degeneration. The antioxidants in Pure Telluride water help replace these
stolen electrons. The antioxidants are necessary for helping the body
maintain health and fight dis-ease. Most tap and bottled water contain free
radicals. Levels of H- present in products - the higher the negative number,
the higher the concentration of energy. Positive levels of H cause free
radicals and indicate a low concentration of energy. The following
substances were tested with an ORP (oxidation reduction potential) meter to
measure the level of H. (The following facts and information found from
Electron Extra in Anchorage, Alaska.)

Pure Telluride water -27

Soda pop +480
Evian water +200
Tap water +140
Bottled juice +350

Information reported by the United States Environmental Protection

Agency reports that in 1999, there were 27 million Americans using tap
systems that violated health standards. The majority of those health-based
violations were for bacteria contamination. Some of the violations were due
to chemical contamination. What are you drinking? Do you know what's in
your water? Modern filtration and purification treatments have rendered
water void of natural elements. Szent-Gyorgyi, in his book Pathology of
Water, made the association that muscle tissue, cartilage, connective tissue,
including skin, aged or became less pliable with time due to lack of good
water provided to cells and tissues. If you are interested in purchasing Pure
Telluride to use with our other products or to drink alone, we have it
available for drop-shipment to your door. Remember, it's already in The
Water (the base).

March of this year [2006], Dan completed construction of his new laser and
another new water enhancement device, and the result is that instead of
using 8 ounces in your drinking water [1 gallon], one only needs 2 ounces.
Now, we are shipping a 16 ounce bottle that do the same job [and then
some!] as the previous 2 liter bottle originally produced for Range Guide
Expiditions. The Water is truly a legendary product, unsurpassed in the
field of specialty water.

Also this year, I am working with Dan in a collaborative effort to produce

another separate upgrade of The Water that includes my product called
"BIONAID". BIONAID is a specialty water that has a very interesting
particle called "Bion". It has been researched in labs for over 15 years, and
the results are unsurpassed regarding products with non-colloidal [under
.004 microns] silver nano-particles. The process that makes BIONAID
results in creating an incredibly small particle consisting of an atom of silver
covalently bonded with an enormous amount of oxygen atoms that results in
producing all the desired health enhancing aspects of silver without all the
worries of colloidal silver. We are continuing research with adding
BIONAID with The Water, and so far we have seen the addition of The
Water reduced the silver ppm's in BIONAID from 2.83 to 1.14 ppms.
BIONAID, like The Water, is so rich in it's constituents and properties that
it can be diluted into drinking water the same as The Water, i.e., 2 ounces
per gallon. Again, we highly recommend mixing The Water and BIONAID
with Pure Telluride, or at least the best drinking water you can find.

While we do not [and will not] use "doom and gloom" to sell products to our
members, we believe that it is very wise to always have plenty of our
specialty water on hand for emergencies. We are continuing to see that pure,
living water, especially enhanced specialty water like The Water, is rapidly
becoming the most precious substance on planet Earth. We only want the
best, and we endeavor to bring the best to you and your family. We realize
that our products are not cheap, but we prefer natural alternatives, for
ourselves, over the soaring costs of questionable drugs and their side effects.
Our personal goal for ourselves is never being in the position of having to
rely on third-party health care - just do what it takes to maintain our health
ourselves and place that responsibility upon our own shoulders. And as time
has proven to us over and over again, we, personally, have faired much
better in the long run for taking this position. Nevertheless, this information
is not intented to replace the advice or services of "health care
professionals". Likewise, the opinions and information here have not been
evaluated by the FDA, and come soley from our personal experience and
research. We make no medical claims and never will. The results of these
products vary from individual to individual as we are all unique and have
our own unique challenges, and some things take longer for some of us.
The Water is $35 per 16oz bottle/$360 per case [12 16oz bottles]. One 16
ounce bottle, adding 2 ounces per gallon of drinking water makes 8 gallons
of mix which normally lasts for a month. My own personal experience with
The Water taught me to respect The Water, so I start out the first few days
with only 1 or 2 8oz glasses of the mix. Please realize that we all have been
accustomed to very dead and/or recycled water, and even water from wells
and springs are greatly lacking in essential properties compared to Pure
Telluride. So do not be suprised if you notice detoxing effects along with the
energetic feeling that has commonly been reported by users.

At the very beginning, a few years ago, I drank it straight and felt so good
the first couple of days, but then all that energy and cleansing power really
began to break out all those toxins out of my body very fast, including toxins
in my head, that NEEDED to be removed, and I had a dull headache for a
few days. It was worth it to me, it saved my life. This proved to me right at
the beginning that I had something very powerful and effective. Now that
the product is even more powerful, it is best to start out a little at a time and
see how you do, then add a little more as you continue to monitor your body
systems. There has never been any need to drink more than 3 8oz ounce
glasses of the mix a day. Again, the water molecules are so small that they
penetrate living tissues very effectively, especially with the high spin energy
too. If the water got any smaller in this product we'd be selling gas instead of
liquid. Water is the universal solvent, so one should expect to have their
bodies cleansed by this water. Dan recently measured the energy field
emmanating from The Water and he got energy readings 470 feet away from
the bottle. Presently it is also measuring to around 76 million bio-angstroms.

Along with what Dan has done, I have also employed "HADO", as
developed by Dr. Emoto and associates, and ancient "Light Language" to
The Water, making this product exclusively unique from the water products
of other people that sale Dan's water under other brand names. Remember,
"The Water" is the original and we are the ones on the cutting edge in water
technology. And as mentioned, BIONAID is also being added. Therefor, The
Water sets the standard in specialty waters world-wide.

The Water is not intended as a dental treatment and has no flouride added
(like most bottled water products). Wish we could tell you all the incredible
testimonies about The Water, but we cannot without putting us in the
position of having The Water classified as a drug by the FDA. I can't even
tell you that "a glass of water cured my dehydration", so please do not ask
us if this "heals" any specific thing, as we make no claims that The Water
does any specific thing for your medical benefit. You smart folks will figure
it out! Thanks for visiting! And remember, you didn't get here by
coincidence. - Elder

Why is water so important to maintain?

Read on:
AMAZING SECRETS FOR HEALTH AND
WELLNESS
Secret # 1: Heartburn is a signal of water shortage in the
upper part of the gastrointestinal tract. It is a major
thirst signal of the human body. The use of antacids or
tablet medications in the treatment of this pain does not
correct dehydration, and the body continues to suffer as
a result of its water shortage.
Tragedy: Not recognizing heartburn as a sign of
dehydration and treating it with antacids and pill
medications will, in time, produce inflammation of the
stomach and duodenum, hiatal hernia, ulceration, and
eventually cancers in the gastrointestinal tract, including
the liver and pancreas.
Secret # 2: Rheumatoid joint pain - arthritis - is a signal
of water shortage in the painful joint. It can affect the
young as well as the old. The use of pain-killers does not
cure the problem, but exposes the person to further
damage from pain medications. Nutritional intake of
quality water and small amounts of salt will allow the
body itself to cure this problem.
Secret # 3: Low back pain and ankylosing arthritis of the
spine are signs of water shortage in the spinal column
and discs - the water cushions that support the weight of
the body.
Tragedy: Not recognizing arthritis and low back pain as
signs of dehydration in the joint cavities and treating
them with pain-killers, manipulation, acupuncture, and
eventually surgery will, in time, produce osteoarthritis
when the cartilage cells in the joints have eventually all
died. It will produce deformity of the spine. It will
produce crippling deformities of the limbs. Pain
medications have their own life-threatening
complications.
Secret # 4: Heart pain - angina - is a sign of water
shortage in the heart/lung axis.
Secret # 5: Migraine headache is a sign of water need by
the brain and the eyes. The type of dehydration that
causes migraine might eventually cause inflammation of
the back of the eye and possibly loss of eye sight.
Secret #6: Colitis pain is a signal of water shortage in the
large gut. It is associated with constipation because the
large intestine constricts to squeeze the last drop of water
from the excrements - thus the lack of water lubrication.
Tragedy: Not recognizing colitis pain as a sign of
dehydration will cause persistent constipation. Later in
life, it will cause fecal impacting: it can cause
diverticulitis, hemorrhoids and polyps, and appreciably
increases the possibility of developing cancer of the colon
and rectum.
Secret # 7: Asthma, which also affects 14 million children
and kills several thousand of them every year, is a
complication of dehydration in the body. It is caused by
body´s drought management. In asthma free passage of
air is obstructed so that water does not leave the body in
the form of vapor - the winter steam. Increased quality
water intake may prevent asthma attacks. Asthmatics
may also need to take more quality salt to break the
mucus plugs in the lungs that obstruct the free flow of air
in and out of the air sacs. Talk to your medical
professional about this.
Tragedy: Not recognizing asthma as the indicator of
dehydration in the body of a growing child not only will
sentence many thousands of children to die every year,
but will permit irreversible genetic damage to establish
in the remaining 14 million asthmatic children.
Secret # 8: Hypertension is a state of adaptation of the
body to a generalized drought, when there is not enough
water to fill all the blood vessels that diffuse water into
vital cells. As part of the mechanism of reverse osmosis,
when water from the blood serum is filtered and injected
into important cells through minute holes in their
membranes, extra pressure is needed for the "injection
process." Just as we inject I.V. "water" in hospitals, so
the body injects water into tens of trillions of cells all at
the same time. Quality water and some salt intake may
bring blood pressure back to normal! Ask your doctor!
Tragedy: Not recognizing hypertension as one of the
major indicators of dehydration in the human body, and
treating it with diuretics that further dehydrate the body
will, in time, cause blockage by cholesterol of the heart
arteries and the arteries that go to the brain. It will cause
heart attacks and small or massive strokes that paralyze.
It will eventually cause kidney disease. It will cause brain
damage and neurological disorders, such as Alzheimer's
disease.
Secret # 9: Adult-onset diabetes is another adaptive state
to severe dehydration of the human body. To have
adequate water in circulation and for the brain's priority
water needs, the release of insulin is inhibited to prevent
insulin from pushing water into all body cells. In
diabetes, only some cells get survival rations of water.
Quality water and some salt may reverse adult-onset
diabetes in its early stages. Consult a physician.
Tragedy: Not recognizing adult-onset diabetes as a
complication of dehydration will, in time, cause massive
damage to the blood vessels all over the body. It will
cause eventual loss of the toes, feet and legs from
gangrene. It will cause eye damage, even blindness.
Secret # 10: High cholesterol levels are an indicator of
early drought management by the body. Cholesterol is a
clay-like material that is poured in the gaps of some cell
membranes to safeguard them against losing their vital
water content to the osmotically more powerful blood
circulating in their vicinity. Cholesterol, apart from
being used to manufacture nerve cell membranes and
hormones, is also used as a "shield" against water
taxation of other vital cells that would normally exchange
water through their cell membranes.
Secret # 11: Depression, loss of libido, chronic fatigue
syndrome, lupus, multiple sclerosis, muscular dystrophy.
These conditions may be caused by prolonged chronic
dehydration. They may clear up once the body becomes
well and regularly hydrated with QUALITY WATER. In
these conditions, exercising one's muscles should be part
of the treatment program. Again, the information above
is not intended to replace competent medical attention by
health care providers. Consult a medical professional for
your medical needs. This information is presented for
research purposes only, and not intended for medical
advice.

Following is an overview of the importance of this

technology in my own words, then some comments
by the inventor. In the past few weeks I've gotten
everything I can get my hands on in an effort to
understand the chemistry of water so that I can
better understand it and then relate to the public
the no-nonsense, no-hype aspects of this discovery.
I wish to present that to you now.

For the record though, John Ellis has exhibited

very poor business ethics. After asking him and his
office for several years to provide me with the
research reports he advertises, he has not sent me
the first page. This is not the proper way to do
business and he deserves any scolding that comes
his way for that. On top of that he has a very poor
attitude on the phone with his customers. As a
matter of fact, he’s downright arrogant. It’s a
shame. I have had good personal results with his
machine, but I have no hard evidence to share, just
my own testimony. I’ll never forget how the water
put 9 pounds of good weight on a child having
eating problems after nearly dying from E-Coli,
how my wind improved and could hold notes much
longer on wind instruments, and that bowl of jello
made with his water that tasted fresh a month later.

Ponder this: While minerals, vitamins, amino

acids, enzymes, etc, are vital in our diets, why must
we have water and air daily to live? We can fair
well during the day without everything else, but we
must have air and water. Why do our bodies
demand these two things? As we have learned from
parents and teachers, we must have oxygen. Every
time we breathe air and drink a glass of water we
get the vital oxygen our bodies demand.

There is something happening to us we should

consider besides the simple understanding that our
bodies use the oxygen in air and water to sustain
us. The more we exercise, the more air and water
we need, and thus oxygen and hydrogen.
The answer, under closer examination, rests in the
understanding of what is in the oxygen and
hydrogen that is in the air and water we consume.
What is in the oxygen and hydrogen? Answer:
Electrons. Yes, there are other things, even smaller
than the electrons in the atoms, but simply put,
electrons surrounding the nucleus of the atom are
the particles that sustain the chemical-biological
exchange at the atomic level that fuels our bodies
and allows chemical exchanges with minerals and
other nutrients in our diets that keeps us healthy.

We have also come to learn that there is a

substantial amount of electricity in our bodies,
particularly in the brain. We are electrical. Within
every square inch of our bodies there is an average
of 10,000 volts of electricity! The normal fat in our
bodies prevents our bodies from going up in flames
because of the incredible amount of electricity
within us.

Therefore, when our bodies begin to lose the

electricity, we begin to lose energy. Without the
electricty being replaced within our bodies, they
die. And then it is obvious why we must constantly
breath the air and regularly drink water. As water
is the medium for carrying the electrical energy
throughout our bodies, deep into every cell,
likewise it is clear to us that the air we breath
immediately hits the blood in our lungs so that the
blood becomes the critical life-force medium that
also carries the electrical energy throughout our
bodies. In this aspect we realize the
chemical/electrical basics of how our bodies
function.

And so the real no-nonsense, no-hype reason why

this invention has the miraculous health aspects
that it has is because it produces water and air that
is loaded with electrons. Thus it is loaded with
energy in the form that our bodies
require...naturally...the way our bodies were
designed to handle. But don't let this simplicity
gloss over your ability to percieve the awesome
dynamics of this concept. It is a matter of life and
death.

Considering that we attempt to determine whether

there is life as we know it on Mars or other planets
by first seeking to establish whether there is water
to be present, we should then be able to understand
the significance of this discovery. Life on Earth
depends on water. The chemical reactions in all
plants and animals that support life take place in a
water medium. Water not only provides the medium
to make these life-sustaining reactions possible, but
water itself is often an important reactant or
product of these reactions. In short, the chemistry
of life is water chemistry.

What is so different about the water produced by

this invention that has gotten so much attention by
those of us that study and apply the healing arts?
Well, lets look at what water is and see if we can
visualize the difference.

Water consists of two hydrogen atoms covalently

bonded to one oxygen atom (H2O). "Normal" tap-
water consists of a water molecule cluster containg
10 - 13 water molecules that have a weak bond,
while the water molecule cluster produced by this
new invention contains many more water
molecules. And not only are there many more
molecules in the water molecule cluster, these
clusters have a stronger bond, and they are bonded
together into an amazing12-faced crystalline
cluster. And we have learned that crystalline
structures have the ability to store and transmit
energy. Considering this, we can begin to see the
unique properties of this cluster. And since it is
larger, it holds many more electrons.

The reason why this has happened is because the

water molecule is stretched in the invention's
distillation process and the shape of the water
molecule is changed. As John states below, labs
have confirmed that there is a 10 degree increase
in the distance between the two hydrogen atoms
bonded to the one oxygen atom. Therefore, we have
a "new puzzle piece that forms a different puzzle."
Its is believed that this is how water once was long
ago. This large crystalline water molecule cluster
appears to be the ultimate water molecule
cluster...the best it can be. I have presented my
artistic representation of this electrically-charged
water molecule cluster below. The addition of an
ozone bulb to the invention now produces a super-
charged water molecule cluster.

Are you beginning to see the bigger picture? Our

bodies have been striving to function in a modern-
day environment which has air and water that has
been depleted of vital electrons. We have suffered
more "dis-ease" and fatigue because of this simple
fact. Our bodies have strived to get the energy they
need to function from those pitiful, tired and
abused water and air molecules. We have done
everything we can imagine to change water back to
its pristine condition...oxygenating it, ozonating it,
ionizing it, you name it...but we have not been
successful. But now, we have the opportunity to
utilize a powerful, electrically charged water
molecule cluster because of John Ellis' invention.
It has the potential to change our environment
significantly for the better. I consider it one of the
most important contributions in modern history.

Consider another aspect of this concept. Most of us

have heard of "free-radicals" and the discovery of
"anti-oxidants", and why these have been
considered the keys to understanding why our
bodies become weak and un-healthy, and what we
can do to help prevent the damage of free-radicals.
In a nutshell, what is happening with free-radicals
that hurts us is that they steal electrons from good
tissues within our bodies, and anti-oxidants are
utilized to block this theft by free-radicals that are
seeking electrons to replace the ones they are
missing. FYI, "reduction" means the addition of
an electron while "oxidation" means the loss of an
electron. So simple, isn't it? Thus you can see how
an electron-rich water molecule acts as the
ultimate anti-oxidant, and why un-healthy, "dis-
ease" causing anaerobic microorganisms (which
cannot live in free oxygen/electron environments)
are destroyed by the electron-rich water produced
by this invention. Furthermore, with this
knowledge you may also see why the phenomenal
claims keep pouring in from all around the
country, such as those mentioned below by the
inventor. - Elder Hale/Certified Iridologist and
Herbologist

Now, some comments from the inventor:

Most Vitamins, "OXYGEN and BODY

ELECTRIC PRODUCTS," water purifiers and
distillers CAN'T WORK without the
ELECTRONS found in CHARGED WATER(tm)
!
Ordinary Distillers should not be used to make
healthy water for a number of reasons:

1. They concentrate the very chemicals you want

to remove.

2. They waste electricity because the raw water is

put directly into the boiler; So, the only way for
pollutants to get out of ordinary distillers is
through their coil. This means you drink them.

Instead, our Living Water Machine(tm) preheats

the water using heat from the condenser. Next, it
drives the preheated water down into a vortex
with a lot of oxygen to strip out the organics
before the water even goes into the boiler. Once it
is in the boiler, as noted earlier, the water is
recycled about 400 times for every gallon of water
that you distill!

Unlike ordinary stills that cost around $1500, our

machines are small, compact units that are great
for home or travel use and they are low cost
considering that they are made of durable
stainless steel.

Ordinary stills produce water that you wouldn't

even want if you understand the distillation
process! They are only a little better than other
water purification products that are readily
available.

The worst water is probably bottled water

because of the lack of industry standards and the
fact that viruses, parasites and bacteria are
always a problem!

Also Super viruses, parasites and bacteria have

learned to survive anything but intense heat!
ANY LAB will tell you, these other methods can't
work without the ELECTRONS found in
CHARGED WATER because OXYGEN levels
have dropped to as low as 8%, in today's water
molecules are SMALLER and CAN'T HOLD the
additional donor ELECTRONS (from OXYGEN)
needed to make them work!! As a result,
VIRUSES and BACTERIA are mutating out of
control... CAUSING almost ANY problem you
can name! Our patented method STRETCHES
TODAY'S WATER MOLECULES... so they can
take on more donor electrons!

Just putting OXYGEN into water does

NOTHING (unless you are a fish)... the molecules
must first be stretched to consume oxygen, while
taking on donor electrons! WATCH OUT!! There
is a lot of outright fraud out there! It's EASY TO
PROVE because most products are activated by
the ELECTRONS in WATER, since YOU are
75% water (blood is 94%) it's these
ELECTRONS that make a product work!

MOST VITAMINS CAN'T WORK because there

aren't enough donor electrons to make them
work! It's like a leaf that falls off of a tree, the
nutrients are still there, but it's
ELECTRICALLY DEAD...they must be
reactivated by ELECTRONS! Since OUR
WATER'S MOLECULES are LARGER (as any
lab will confirm), they HOLD MORE
ELECTRONS...like it was when OXYGEN was
at 38% and rainwater was highly charged,
explaining the incredible ages mentioned in the
BIBLE! THAT'S WHAT OUR PRODUCT
DOES, nature's way or God's way if you will!

This is a MOMENTOUS BREAKTHROUGH

because ELECTRONS KILL VIRUSES
(ordinary water doesn't have enough
ELECTRONS), returns wells to purity, stretched
molecules STAY THAT WAY, only a SMALL
amount changes a lot of ordinary water, STORES
INDEFINITELY (you CAN'T do that with
ordinary water... look at the Expiration Dates)
and PURIFIES ITSELF!

NO WATER IN THE WORLD CAN DO ANY

OF THESE THINGS...again, an ordinary water
molecule is TOO SMALL...any lab that studies
the properties of water can PROVE IT TO YOU!
DON'T listen to all the scientific jargon about
products! All you need to know is: IS THE
WATER MOLECULE LARGER (it isn't)? If it
isn't, the product can't work regardless of what
they tell you. This was recently confirmed again
by a Bio-Tech firm that tested TWO of our fine-
tuned machines in their labs.

Most importantly, our water molecule is

LARGER with the same molecular weight as an
ordinary water molecule and since the electrons
kill viruses, they are using the water for
proprietary medical applications. They also
found the angle between the hydrogen atoms is 10
degrees greater, the viscosity is different and it
has a beautiful crystalline structure at ROOM
TEMPERATURE that's dodecahydronal (12
planes). Obviously, God given!! Also, for special
applications we can INCREASE the ENERGY
LEVELS even HIGHER! The implications of
JOHN ELLIS' WATER MOLECULES(tm) are
INCREDIBLE as user reports continue to pour
in! The ONLY water a thinking person would
want!
YOU are ELECTRONS...along with FOOD,
WATER and AIR... NO WONDER people get
such AMAZING results!! With OXYGEN
dropping from 38% to as low as 8%, it's causing
BIG problems!! However, most people don't
realize it until it's TOO LATE!! THE LIVING
WATER MACHINE(tm) is a little 6 pound
machine you can use anywhere! And this is why
its Range Guide Approved...only the best will do.

The World's only No Steam Pressure Water

Distillers!!

"Chlorine does not work on the new super

bacteria" U.S. Water News - Dec. '88!

It's scientifically impossible for ordinary water

distillers to make pure water because of their
high steam pressure (pollutants are carried over
with the steam)!

Our patents show we stop the boiling and recycle

the water every 20 seconds! In this way, there is
no steam pressure and the water gets purer and
purer as it recycles.

Viruses are so tiny they pass through any air

filter, water filter, reverse osmosis machine,
ozone machine or ordinary distiller with bacteria
that also survive the other methods.

Here is how we handle the new untreatable

viruses and bacteria that are everywhere:

We use intense heat (the way they get rid of

infectious waste)!!

Like tea leaves, viruses, parasites and bacteria

are very light.

As the water boils, they are frothed to the

surface. Then, as the water goes out of the boiler
to be recycled, the deadly microorganisms are left
on the two heaters and the sides of the boiler.
Since the heaters are now out of water, the
intense heat destroys them...

...this process repeats 400 times for every gallon

of water you distill to get all of the deadly
microorganisms!

Research chemist Herman Meinke has grown 18

foot corn, gigantic vegetables etc. and one major
university, after turning a well pump off and
pouring this amazing water down a well (pump
off 4 hrs.) was AMAZED to find BACTERIA had
gone from SKY HIGH to ZERO! NO OTHER
WATER CAN DO ALL THESE THINGS!! It's
TRULY "DISTILLED NATURE'S WAY!"
Using the water to make ordinary ice cubes:
Although the ENERGY is still there, it will only
express itself when it's not raining! Osmosis in
trees and plants STOPS when it's raining and
starts again when it's DRY! Water processed
TRULY nature's way (God's way if you will) is
"programmed" to respond this way. This is the
water our Lord wants you to have!
Below is a picture of the inventor. How would you
like to look like that when you're pushing 70
YEARS OLD?! He still holds the reverse-curl
weight lifting record, a record normally
considered to be held by men no older than 45.
John states that he feels stronger now than when
he held the discus throwing record in his youth.

No medical claims are being presented in the

above information or anywhere else on this
website. You are encouraged to discuss this
developement and its significance with your
personal health-care experts. This information is
for educational purposes, and for the promotion
of world-wide awareness of this technology.

Check out John's homepage to order and talk

with the manufacturer. Be sure to tell John that
Elder sent you, and to send me research
information he’s been promising for years!

If you want to see the latest technology I’ve

discovered that does not require buying any
expensive equipment see THE WATER! And be
sure to check out the link below about Miracle II!

The Platinum Cannon Shipwreck

A modern tale of Alchemy
 [email protected]

Links to
related Author's note- What you read here may seem incredible,
topics: impossible or and highly unlikely...but keep an open
mind....every word is true. If I had not had an open mind when
this advernture first begain in 1996, I would have ignorantly
The Platinum
walked away from one of the most interesting and exciting
Cannon Shipwreck
shipwreck stories of the 20th Century.....
Joe Champion

David Hudson The

(semi-technical
lecture) Platinum
David Hudson
Cannon
(made easy)
Shipwreck
20th Century (On the Trail of the
Alchemy Modern Day Alchemist)

The Mango Metal

Report By David Econopouly

Bookstore The question which one should ask after review of his
research is not whether one can produce precious metals
Order The by low energy nuclear transmutation but to what level will
Platinum this technology expand.
Cannon
Shipwreck Exotic Research Report- October/November/December 1996
(written about Joe Champion)
Books.
Click here
"The "treasure" is comprised of two types of materials:
Silver-colored metallic artifacts such as cannons,
cannonballs, dore bars, ingots and other assorted
objects; and a grayish-tan dry chemical, hardened by
almost 200 years of salt-water submersion into the shape
of the wooden barrels that had housed it before rotting
away. The artifacts, at first glance, appeared to be simply
metal and a limestone compound. But oddly enough very
few people could agree on exactly what they were used
for, or for that matter, even what they were made of. That
was one of the first oddities that caught my attention after
my early meeting with Michael. It seemed to me that metal
is metal, often made up of different elements in
combination, but metal none-the-less. So why couldn't our
20th Century science conclusively identify the metals that
were produced almost 200 years ago by more primitive
scientists then ours? According to Dayne Chastain a
retired metallurgist in Oklahoma it was because "The
Spanish could do amazing things with metals but their
technology has been lost", but I was not to talk to Dayne
for yet another month."

"As the hours passed a stream of documents continued to

flow into my hands. One that especially caught my
interest was written on the letterhead of Dayne Chastain
and Associates that took the figures from the German
Institute Assay and multiplied the per ounce value of each
of the elements times the number of ounces in the 2,900
pound carronade. The total value on the precious metals
came to $13,612,954.00. That was a lot of money for a
cannon and I was beginning to see why Michael remained
interested in selling his artifacts despite the fact that he
was unsuccessful for 6 years."

"Another document was on the letterhead of Bremer

Technology Corporation located in Las Veas, Nevada.
This was addressed to "Mr. Fisher". I had heard of Mel
Fisher through a couple of TV specials and news reports
about him, so his involvement in the project caught my
attention.
The first paragraph began "We just completed the
analysis of the three samples submitted by Mr. Dayne
Chastain. As you see the values measured of the sample
#1(Cannon Ball) and sample #2(Cannon) show very high
values of Gold and the Platinum Group Elements. The
values of the Gold and the Platinum Group are probably
not as free metals present and therefore not alloyed with
base metals. To break the bond of those
clusters(molecules) it is necessary to use the Bremer
Technology which will do exactly that." There was
mention of something called an "Electron-beam furnace",
but at that point I had no idea what that was."

""After I got them from the water I set them in my yard. I

asked my Haitian gardener to clean them off and went to
town. When I came back I couldn't believe my eyes…he
had gouged these holes in them. I yelled at him 'What did
you do to my cannons?' He replied, 'I didn't do nothin',
Michael, I just tap dis wit' my machete and pieces fall off.'"
Michael explained to me that the craters seemed to be
filled with some sort of metallic putty to fair out the
cannons so that they were straight, fair and smooth.
This was starting to get extremely interesting to me. The
Platinum Cannons that Michael had may not have been
cannons at all, but large chunks of metal that were made
to look like cannons. Were the cannonballs just chunks of
metal made to look like cannonballs? The hatch? Add to
this 100 barrels of a limestone-like material which Michael
claimed were laced with precious metals and some pretty
interesting theories were developed."

""There is no place in our salvage license that states we

must sell our artifacts by auction.", Patsy began. Minister
Allen didn't appear to have much interest in the subject so
she asked him pointedly "Have you read the license
terms?" The Minister replied very matter of factly, "No."
and for all intents and purposes, that was the end of the
Patsy's meeting with him.
Well, at least we knew that even if we did find a buyer for
the carronade, we would still not be able to sell it. We
were not deterred as we half expected some resistance
from the government and so decided that we would have
to find an alternative plan if the artifacts contained the
precious metal content we believed them to have.
Michael who is as patriotic towards his country and as
honest as a man can be was being pushed to the limits
and I believe his statement to me surprised even himself.
"If we find a buyer, we will sell it to them…even if we have
to smuggle it out." With that settled we would continue
our search to ascertain the value of the artifacts."

"Once the samples were sent off, we eagerly awaited the

results. The first phone call from Walter was a complete
surprise that left me completely baffled and just a bit
worried.
"Congratulations!", Walter began, "You are the owners of
the first Atomic Cannon!". When I asked him what he
meant, he told me that his assay indicated that the
samples that we sent had him contained Uranium. I was
expecting positive results from him, but this was a little
too positive."

""Hudson knew that this "nothing could be seen, felt,

tasted and weighed. It had to be something and he was
determined to find out what it was. In the course of his
research he found a paper from the Soviet Academy of
Sciences stating that a proper spectroscopic analysis
required a 300 second burn instead of the 15 second burn
used in the United States. Utilizing the Soviet technique of
fractional vaporization, Hudson discovered that his
sample contained the elements palladium, platinum,
ruthenium, rhodium, iridium and osmium. Even more
astounding was his discovery that each of the nonmetallic
elemental forms was a superconductor, a substance
which allows an electric current to flow without resistance
even the absence of a continually applied potential.""

"He went on to talk about a man by the name of Dr. Merkle

who was producing an organic crystaline compound that
was being used by people who had debilitating diseases
such as diabetes and heart disease. He mentioned his
brother who was having great success in the battling of
his diabetes using this crystal formula, but emphasized
that he is not able to make any claims. This turned out to
be one more coincidence- I was to find out later that
Dayne and Dr. Merkle had worked together on a project
and had testified before a Senate committee on the
utilization of polymer in the recovery of oil.
At the end of our conversation Dan told me that I needed
to contact a man by the name of Joe Champion. He was
the one that was making gold."

"It was mid-September and the package was sitting on my

desk when I got in from lunch. It was from Dayne and
inside there was a hand-written message on yellow-lined
paper that said "David, I ran across this in cleaning out
my bookshelf. I thought I had put this in the
O.U.(Oklahoma University) package. I'm glad I didn't. It
tells a lot about the Pt. Metals and their complexes. I'm
sure it will interest you." The package was a surprise to
me as I was not aware that he was going to send me
anything. I opened it up and it was a spiral-bound
manuscript, zerox-copied and about 80 pages long. It was
called 20th- Century Alchemy. I began to read the preface-
"Twentieth Century Alchemy is a publication which covers
the debate which has plagued man for milleniums. 'Can
one cause an element to change from itself to another by
a chemical reaction?" Well, my good friend, Dr. John O'M
Bockris from Texas A&M University is now conjuring a
new breed of scientists fluttering throughout their
laboratories adorned in their black robes, wearing conical
hats with their pet horned toads, sprinkling elixir on lead
to convert it to gold.""

"After I answered his questions, he explained his theory

to me. He believed that the "limestone" material, and not
the metal artifacts, was the important discovery and that it
was actually an elixir used by the Spanish to convert base
metals into precious metals. He cautioned me that this
wasn't definite, but that a lot of the facts seemed to point
in that direction. He also suggested that there was a good
chance that the cannons and artifacts merely a thin layer
of platinum covering them. He speculated that this might
have been a chemical reaction which was a result of the
close proximity of the elixir to the artifacts mixing with a
small electrical current naturally produced by salt water.
He theorized that over a period of 200 years the iron may
have been transformed into a thin layer of precious metals
that was identified by the assays performed over the
previous six years."

""Before entering the crux of this memorandum please

allow me the opportunity to state that the story regarding
your discovery is fascinating.
It is my understanding that you are dealing with two types
of unknown material at this time. The first being,
approximately 100 barrels of a gray substance that is
unknown and the second being cannons and other
assorted metallic artifacts of unknown origin.
Continuing, it is my understanding and after physical
communication with Mr. Dayne Chastain and others, you
have found by observation that the material when treated
with esoteric processes appears to contain high levels of
precious metals. Also, it is my understanding that you
have had Mr. Zig Bremmer and his associates in Germany
test the material and report high levels of platinum,
associated platinum group elements and gold.
Completing my thoughts on this subject, it is also my
understanding that you have had numerous other
investigators tell you that the value of the find is
enormous, while others in the "main stream" have stated
its value to be of nothing greater than its artifactual worth.
Having stated this, allow me to enter into a pliable
scenario as to the potential truth of your treasure. For
discussion purposes, let us forget the metallic artifacts
found near the wreckage and concentrate only on the
 barrels.
Being a study and expert in the field of low energy nuclear
reactions, I would have to guess that the barrels contain
material that is now known as a "trigger" for low energy
nuclear events. This modern day term is no more than its
lesser accepted term, elixir. The trigger is something that
allows for the conversion of a base metal to a precious
metal. If you are dealing in the world of sanity, you would
immediately discount such thoughts as reality. However,
in the real world of science, this is now starting to be
recognized as a physical observation. I will explain more
and provide a reference later in this document.""

To Order The Platinum Cannon Shipwreck....click here

Philosopher's Stone/Elixir of Life

Transcript of a David Hudson Lecture
Simplified version of David Hudson's research

Dean Stonier is the director of the Global Sciences group, based out of Denver,
Colorado. Dean introduced David as having worked on this project for over 17
years. David says his research efforts began about 19 years ago. He had been in
agriculture, made a lot of money and began buying gold and silver as an inflation
hedge. From this point, it will be from a first person standpoint.

I came across a lot of refiners in the Phoenix area who were working with
precious metals. They informed me that there were people who we reproducing
precious metals from natural sources. The technique involved using cyanide to
recover gold from old mining sites where they had dumped the tailings from the
mine.
Since I was a successful farmer, I could easily go into mining of this nature
because I had water trucks, road graders, earth movers and backhoes. The idea
was to accumulate gold and silver without having to pay taxes. Later, I became
aware of how to recover gold using the Heap Leach Cyanide System.

In any recovery operation, once you get down to hard pan, it just won't go any
further, that is when you are leaching soluble salts through the soil. The heap
leach system moves gold and silver solutes down to a plastic membrane where
they collect as a slurry. This is pumped up and recovered through your carbon
and refining process. In this recovery process, I was actually recovering gold and
silver from this sludge and fire assay when I found I was recovering something
else which was causing losses in the recovered gold and silver.

No one knew what this problem material was and since I was not a chemist or a
physicist, I had no idea. It had a specific gravity, it would recover in the molten
lead just as if it was gold or silver, it did not float out of the lead, but when I
cupel the lead down, there was nothing.

The people involved in mining and metallurgical work are familiar with this
mystery substance, giving it the name of 'ghost gold', it is a non-issuable, non-
identifiable form of gold. At this point, I became involved with a gentleman who
does emission spectroscopy, we then became aware of work done by under the
auspices of the Soviet Academy of Sciences.

Emission spectroscopy involves taking a carbon electrode and placing your

sample on that carbon electrode. You then run another carbon electrode down
from above it and you strike an arc. As the current burns the carbon electrodes
and the sample in the electric arc, the elements in the sample will ionize and give
off specific light frequencies. This is the basis of spectroscopic Analysis or DC
Arc Emission Spectroscopy.

In this analysis, it is normally run for a period of about 10 to 15 seconds before

the carbon electrode burns away. American spectroscopists will tell you that
anything that is there will be ionized and will be read in this emission
spectroscopy. Our material indicated it was iron, silica and aluminum.

It took me three years to get rid of the iron, silica and aluminum, once that was
done, I still had 98% of the material. This material on the DC arc did not indicate
to be anything. The material was taken back to Cornell University, where I
worked with a gentleman who helped me on analyze this mystery substance.
We used X-ray analysis with 8 different X-ray heads, tunneling microscopy,
diffraction, fluorescent microscopy, all these wonderful technologies, and the
spectroscopist confirmed the presence of iron, silica and aluminum. Once again,
we worked to remove these elements from the sample. When they no longer
showed up on the spectroscopic analysis, the spectroscopist pronounced that
there was now nothing, yet there was still material present.

According to the Soviet Academy of Sciences, proper spectroscopic analysis

requires a 300 second burn instead of the 15 seconds as done in the US. When
you do this, you have to sheath the electrode with an inert gas to remove all
oxygen and prevent the electrode from burning away too fast. The equipment
was setup to use argon as the inert gas so they could achieve a 300 second burn.

Using this process, within the first 15 seconds, we got the standard readings of
iron, silica and aluminum and sometimes traces of calcium.

After that, nothing else was read until 90 seconds into the burn, where palladium
began to read, at 110 seconds, platinum began to read, at 130 seconds, ruthenium
began to read, at 140-150 seconds rhodium began to read, at 190, iridium began
to read, at 220 osmium begins to read. This is called fractional vaporization by
the Russians.

When you understand that the boiling temperature of iron is to these elements as
the boiling temperature of water is to iron. You can't get iron hotter than the
boiling temperature of water until all the water is gone. This is the basis of the
cooling system in your car, as long as there is water in the radiator, that motor
never gets that hot, but once that water is gone, only then can the metal get hot
enough to approach the boiling temperature of the iron.

The same applies to the carbon arc, all of the iron, silica and aluminum are taking
off the heat that the arc is putting into it, and so its not until all of that is gone,
that you can reach the temperatures of the denser elements.

The boiling temperature of these elements is about 5200 to 5300 degrees

centigrade, the maximum temperature of a DC arc is theoretically about 5450 to
5500 degrees centigrade, measured at the center of the arc. The material sits on
the electrode, so it can't get to the maximum temperature of the arc. This material
had to get rid of all its impurities and all the energy of the arc had to literally be
concentrated on the sample, until the elements come off IN THE SEQUENCE of
their boiling temperatures. The lowest is palladium, followed by platinum,
ruthenium, rhodium, etc. They come off all by themselves at a time when nothing
else can be in the sample.
Getting 600,000 to 700,000 counts of iridium versus a 12,000 count of carbon arc
background, we ran this material for 2 and « years, everyday, we prepared
commercial standards. We ran the standards and found they read correctly in the
first 15 seconds. As the electrode continues to burn, at 90 seconds, bang, here
comes the palladium and the following elements.

About 85% of the reading occurs way out there towards the end of the burn. In
other words the people buying these precious metal standards are only reading
about 15% to 20% of the sample and assuming it is everything.

Short burn times are in error when used to determine standards, the Soviet
Academy of Sciences has the most advanced method currently known. Basically,
(David must still be referring to an analysis of off-the-shelf standards here) we
find 6-8 oz per ton of palladium, 12-13 oz per ton of platinum, 150 oz per ton of
osmium, 200 oz per ton of ruthenium, 600 oz. per ton of iridium, 1200 oz per ton
of rhodium.(this was done using spectroscopic analysis)

The best deposit in the world is in South Africa, they are mining 1/3 of one ounce
per ton. That's all the platinum group elements. They go a «mile down in the
ground and follow an 18 inch seam to get this material. I say there are about 2400
oz per ton of these precious elements instead of the 1/3 of one ounce that is
currently being recovered. No one else knows it is there and no one else can
analyze for it.

The gentleman spectroscopist who helped me with this analysis winded up

getting starry-eyed and went off to Germany. There he studied at the Institute for
Spectroscopy, where he claimed he had found precious elements in natural
materials, all of which I paid for. I have since learned to protect my knowledge
and willingness to share so openly with contracts.

We ran these experiments for 2+ years and have now created commercially pure
standards which were helping us to perfect this analytical technique. I later went
to a chemist who I was told was one of the best analytical chemists that the state
of Arizona had to offer. This was all explained to the chemist and he became so
interested that he volunteered his own time to help research this phenomenon.

This chemist worked with me for over 3 and a half years at no charge. Basically,
we were running the procedures that the Soviet Academy recommended. When
we were finished, we had separated, through analytical chemistry, 6-8 oz. per ton
of palladium, 12-13 oz. per ton of platinum, 150 oz. per ton of osmium, 200 oz.
per ton of ruthenium, 600 oz. per ton of iridium, 1200 oz. per ton of rhodium, the
same values as found in spectroscopic analysis.
From the analytical chemical tests, all the solution colors were correct, all the
oxidation reduction potentials were basically correct, all the physical this, heated
it in a tube furnace under oxygen at 850 degrees centigrade for an hour to
dehydrate it until we had this red brown oxide.

We took 1/3 of the sample out and put it in a beaker and sealed it. We then
placed the other 2/3 back into the tube furnace, hydrogen reduced it until we got
a gray powder, just like rhodium is supposed to look.

We take that out, take half the sample, place in another vial and seal it, returning
the other half of this gray powder to the furnace where it is cooked at 1000
degrees under argon, and it turns SNOW WHITE. We take that out, put it in
another vial, seal it and send all the three sealed samples out for spectroscopic
analysis.

The analysis was done by a commercial firm called SpectraChem in Los

Angeles, they do most of the work for the aerospace industry, the man who runs
the instrument is the president of the Spectroscopic Association. The red brown
dioxide analyzed to be iron, the reduced hydrogen material was aluminum and
calcium, and the white material, annealed under argon was calcium and silicon

The point being that there was no consistency in the analysis of the three
materials even though they were all three the same element, that material is
99.9% pure rhodium.

The commercial standards that you buy are not technically correct. The chloride
salt, the sulfate salt that you buy from Johnson/Massey and Englehart are not
technically correct. The material like tri-chloride that is sold as RHCL3 (rhodium
trichloride), is in fact a salt that is closer to RH12CL36, it still has metal/metal
bonds. When you add a reductant to the solution, the chlorine drops away, but
you still have metallics, because they have never NOT been metallics...

These colloidal particles begin to nucleate and come out of solution as metal, but
they've never NOT been metal. Even in solution and filtered through a millipore
filter, they have the metal/metal bonds and they never lose those. In the world of
an atom, we found that if you disaggregate the rhodium to the monoatomic state,
the last particle you come up with is HRHCL4, which is the acid trichloride,
when you take away the chlorine, you have hydrogen rhodide, a rhodide actually
is a minus one, not a plus one and the physical properties of the rhodide are more
like an iodide than that of a metal.
Monoatomic gold as a chloride has a forest green color, commercial gold
chloride is gold or a light green depending on how much you dilute it. No one
offers monoatomic gold commercially.

Edgar Cayce says you should use gold chloride solution in his Wet Cell
Appliance. When you put the green gold chloride solution in the wet cell it works
about 20 times better. This is the true elemental chemistry of the precious
elements and it applies to all of these elements, osmium, ruthenium, rhodium,
iridium, palladium, platinum and gold.

When you dissolve metallic gold into aqua regia, you convert to chloride to get
rid of all the nitric. All you really have is a cluster of metallic gold. I don't care
how long you boil this, it never will dissolve to the monoatom. The diatonic
bonds of gold are so profoundly strong, and if you really think about it, gold has
an electronic structure of 5d106s1 and that in itself tells you it will never go to
the monoatom.

All of the other S1 elements are lithium, sodium, potassium, rubidium, cesium,
these are explosively reactive substances that we call the alkaline metals. If you
throw them in water, they burn. Gold has the same structure as these alkaline
metals. Gold gets a hold of itself and it will not let go. You can get it down to the
diatom, but it will never go farther than that, so the best that you can ever hope
for, is AU2CL6. You never lose the diatonic bond, and that's why when you
refine gold, you always get 99.9% recovery, because its real easy to recover, it
never loses its metallic character.

But if you know how to take those metallic bonds apart and get monoatomic
gold, which is what mother nature did by literally dissolving it to a single atom
when it comes up out of the earth, about 98% of the gold comes up as
monoatomic gold, about 2% comes up as metal. A diamond and carbon are the
same element, a diamond is a high energy crystalline form of carbon.

We have developed our analytical method over the centuries to recover the
yellow gold. When it is dissolved to the monoatomic, it never comes back as
yellow gold, it is not metallic and it has no metallic character. In fact, one of the
things we did is we submitted the material to thermo-gravimetric analysis, out in
Palo Alto.

When you produce monoatomic gold, it is kind of gray-black as hydrogen oride,

under an inert gas, you can heat it and the proton lets go, in the same way that
amorphous silicon is produced as selane to amorphous silicon. It is SIH where
this is HAU. When that proton is annealed away, it goes to a snow-white powder,
it loses 4/9ths of its weight.

How can it lose 4/9ths of its weight and yet if you take it back to metal, it GAINS
BACK the 4/9ths of the weight? In fact, in the heating of this, the heating coil is
actually around this quartz tube to control the atmosphere so nothing is
interfering. The heating coil is BIFILAR WOUND to cancel all magnetic fields.

Yet, this material as we kept annealing it over and over, this white material
would literally levitate, weighing less than the pan it was sitting in, if it wasn't in
there, the pan would weigh more than when the powder was in it.

In cooling, sometimes it would go to 200% or 300% the weight, heat it and it

goes to less than nothing and cool it and it weighs 300% more than what you
started with. This only happens in this white powder form using this thermo-
gravimetric analyzer. They actually give you magnetic standards that you put in
the machine and heat it and it lets go its oxide as chloride, you can weigh it as
you do this and everything works fine.

You take 100% of gold and make the hydrogen oride pellet and it weighs 103%,
but you anneal it and it goes to 5/9ths or about 62-63% of the beginning weight,
and yet, the mass has never left, its still there.

The manufacturer says if you were cooling the sample, you must have
superconductor, but because you are heating the sample, this stuff makes no
sense at all. This led us to investigate the properties of superconductivity.
Basically, the powder should allow the flow of current with no resistance if it is
truly superconducting. This was attempted with a voltmeter and nothing
happened, we learned that a superconductor is a material that has a single
wavelength within the sample, much like a laser, it has a single frequency within
it. When you hook up the electrodes to the superconducting material, by
definition a superconductor does not allow any voltage potential to exist in the
sample. It will sustain a perfect amperage with NO voltage.

To get the electron off the wire and INTO the SAMPLE, it takes voltage, to get
the electron out of the sample and INTO the WIRE it again takes voltage. But the
sample doesn't allow voltage if it is truly superconducting. The only way to get
energy into a perfect superconductor is to 'tune' the vibrational frequency OF
THE ELECTRONS on the wire to match the frequency of the powder and then
energy flows on WITH NO PUSH. It does not have to come off, it just flows on
and on without coming off. The only way to get it off, is you have to tune the
vibrational frequency of the wire that it's coming into to the frequency of the
superconductor, and then apply a voltage potential and then it comes out, the
amazing thing is it does not HAVE to come out.

When you learn that the electrons are going into the superconductor by
PAIRING, it is a TIME FORWARD electron, pairing with a TIME REVERSED
electron and they call this a Cooper Pair.

When the electrons pair, THEY CONVERT TO LIGHT, it is no longer a particle

but becomes pure light. Any amount of light can exist in any space time, if it has
no particle aspect, so the light flows onto it and it gets more and more light, but it
does not reside in any space time. The only way you can prove it is a
superconductor, is as the energy flows within it, it produces around it a Meissner
field. This field will not allow any voltage potential into the sample. It has no
north/south pole, the only material we know to have this property. It will not
allow any voltage potential or any electromagnetic energy to enter the sample.

So what color does it have to be if it REFLECTS ALL LIGHT, if it absorbs all

light, it is BLACK, if it reflects all light, it must be WHITE. Superconductor will
respond to magnetic fields of 2 X 10 to the minus 15 ergs. There are 10 to the
18th power ergs in a gauss and the Earth's magnetic field, as detectable by a
compass, is about .78 gauss. So if there are 10 to the 18th ergs in a gauss, this erg
must really be a tiny measure of magnetic energy. Do you know how they see
your thoughts in your brain? With a superconductor measuring tiny magnetic
changes in the brain. This material is so sensitive to magnetic fields that when it
goes to the white powder form and loses 4/9ths of its weight, what it is doing is
flowing light within it, in response to the earth's magnetic field There is so much
current flowing in it that it levitates 4/9ths of its weight ON THE EARTH'S
MAGNETIC FIELD. Your hand has sufficient amperage that if passed under this
tube, The material floats, it is that sensitive to magnetic fields. All of these
elements do this, ruthenium, osmium, iridium, rhodium, palladium, platinum,
gold, silver, copper, cobalt and nickel. In 1988, we filed US and worldwide
patents on this form of matter. At that time, I was working with General Electric
on fuel cells. I was told if I was the first to understand it, the first to make it, then
I could be the first to patent it.

The work I was doing with GE was with fuel cells, providing my 'alleged'
rhodium to be used in the fuel cells. When it was received by GE, they analyzed
no rhodium, yet they put it on carbon, mounted it in the fuel cells and it works. It
does what only rhodium will do. After operating the fuel cell for two to three
weeks, they take it out and now there is rhodium in the electrode. They were
puzzled as to where the rhodium was coming from, since it had been analyzed
before being inserted and no rhodium was found.
In 1988, I filed these patents for Orbitally Re-arranged Monoatomic Elements,
ORMES....Orme Gold, Orme Platinum, Orme Palladium....(you could just as
easily says 'ghost gold', 'ghost platinum', etc.... Jerry)

About 1990, my uncle showed me a Time-Life book on Secrets of the

Alchemists. I put it off because I thought there was nothing in alchemy that could
be of use to me. He kept after me and showed me a section where it talks about a
white powder made from gold. The goal of the alchemists was to make a white
powder of gold, that would serve as the container of the light of life. If you stand
in its presence, you don't age, if you partake of it, you live forever.

So I begrudgingly read the book and have now read 500 to 600 books on
alchemy and it's history. All of it goes back to a man the Hebrews called Enoch,
the Egyptians called Thoth, in Greece, they call him Hermes Trimesgritus, all the
same man.

It is claimed he ascended by partaking of the white drops, the man who never
died, he ascended because he was so perfect.

We have found, and this in the standard Bristol/Myers Squibb literature, that over
the last four or five years, there is tremendous research going on with precious
elements and cancer treatment. The precious elements have been found to inter-
react with the cell by a vibrational frequency or by alight transfer to correct the
DNA. Any incorrect part of the DNA is corrected by the precious element.

It perfects the cells of our body. The element going into our body is not a metal,
the element is not a heavy metal, the element is AN ELEMENT, and so there is
no heavy metal POISONING. You can eat any amount of this white flour you
want to and it won't hurt you, it goes through your digestive system.

In fact, we took some brain tissue from a pig and a cow and we analyzed it, first
we destroyed the organic matter and did a metals analysis. Over 5%of the brain
tissue by dry matter weight is RHODIUM and IRIDIUM and no one knows it,
because it can't be directly measured. The elements are flowing the light of life in
your body, the elements are in fact, what the light is.....(remember, this is
ORME-RHODIUM and ORME-IRIDIUM, detected by the 300 second
spectroscopic analysis.... Jerry)

I can show you four papers by the US Naval Research Facility where they have
PROVEN that the cells communicate with each other by a process identical to
superconductivity, but they can't figure out WHAT is superconducting. It is these
'stealth' atoms at work. The atoms that are in your body, the atoms that flow
perpetually the light of life, but no one knows they are there, because they don't
identify by (normal) instrumental analysis.

And the reason they don't identify is also in the literature, since 1986, some of the
top physicists in the world, at the Niels Bohr Institute, at Argonne National Labs
and at Berkeley Brookhaven have found that there is a group

of elements at the center of the periodic table that goes to this strange state of
existence. Most of these publications occurred from 1988 on, but my patent was
filed first.

What they found, was that the nucleus of these elements deforms, goes to a high
spin state, called a high spin nuclei, and theoretically the high spin nuclei should
be superconductors, because high spin nuclei pass energy from one atom to the
next with NO NET LOSS OF ENERGY. This is what is in your body, this is
what flows as the light of life.

When you understand that a superconductor flows with only a single frequency
of light. In fact, that light is a NULL light. In other words, it consists of two
waves, that are mirror images of each other. Because of this mirror symmetry,
there is NO WAVE, it APPEARS to cancel. But this null wave that is not
measurable directly is what produces the aura around your body. THE AURA IS
THE MEISSNER FIELD from the superconductivity.

There are still many mystery areas within living tissues. In our body we have
what is called 'junk DNA'. There are over 30 aspects of DNA which No one can
figure out what they are there for. We only use 15% of our brain, what is the
other 85% there for? Did we evolve a brain we don't use? It's as if we existed at
one time in a higher state of enlightenment and we have fallen to the state we
exist in right now.

There is some material from ancient Egypt that provides some insight into this
white powder, it is called the Egyptian Book of the Dead and the Papyrus of Ani,
by Budge. This is the oldest book of the Dead, found about 3500 BC in the tomb
of Pepi the 2nd. It says, I am purified of all imperfections, what is it? I sin like
the golden hawk of Horus, what is it? I pass by the immortals without dying,
what is it? I come before my father in heaven, what is it?

It goes on and on, always asking what is it?

Do you know that the Hebrews worked in Egypt for many generations, they were
the artisans and metallurgists. When they left Egypt, Bezalial the goldsmith
prepared the bread of the presence of god. Bezalial prepared this bread that the
high priest partook of, the mellets(sp?) of that priest.

The word in Hebrew that literally means What is it? is Manna. The word manna
literally translates verbatim to a question, What is it? Look in the travels of
Josephus and you will see that this is so. The very same words that were used in
Old Kingdom Egypt in 3500 BC.

Basically, these elements are naturally in your body, primarily rhodium and
iridium, but gold (OR?), means gold or the highest light. The Bible says that
Moses told the Hebrew people that they had not kept the Covenant, so the Manna
was to be taken from them, but it will come back in the end times when we
would be a nation of high priests, not an elect high priesthood. This is the food,
this is the light, that you take in your body.

In fact, if you ask a Rabbi if he ever heard of the white powder of gold, he says,
yes, we know of the white powder of gold, but to our knowledge No one knows
how to make it since the destruction of the first Temple, the Temple of Solomon.

This knowledge was not completely lost, the high priests who left the temple
when it was destroyed went out on the desert and organized the community
known as Qumrun, they were the Essenes. If you get copies of the Dead Sea
Scrolls Uncovered, which Eiseman and Wise just translated, this in ancient Egypt
was known as the GOLDEN TEAR from the EYE OF HORUS.

It was the white powder of gold mixed in water. It was called that which issues
from the mouth of the creator. The spittle. Not the word of God, but the spittle, or
the semen of the father in Heaven. If you mix the white powder in water, it
doesn't really dissolve, it forms a gelatinous suspension, and it looks just like a
vial of semen. I know this because, being a farmer, I know what semen looks like
that we use on our farm.

You have to understand the symbolism, the understanding of; prepare yourself
like a bride in the bridal chamber, purify and cleanse yourself, prepare yourself
for the coming of the father in Heaven. To be inseminated by this father in
Heaven in the bridal chamber, to totally be regenerated, to be purified, to be
cleansed.

Every cell in your body will be taken back to the state it is supposed to be, when
you were a teenager or a child. It perfects the DNA, and closes the light within
the body until you literally reach a point where the light body exceeds the
physical body.
In ancient Egypt, they said you have a physical body you must feed so it can
grow and become what is meant to be. If you don't feed that child, he never
grows, he never becomes the person he is supposed to be. But you also have to
feed the spirit body, you have to feed the KA, so it can grow and become what its
meant to be. And most of you are not feeding your KA. It is sitting there like a
little runt inside your body. The texts say you must feed the KA with the semen
of the father in heaven.

And the KA grows and grows, becoming ever more enlightened, until you reach
a point where the light body exceeds the material body, you literally light up the
room when you walk in.

The gifts that go with this are perfect telepathy, you can know good and evil
when it is in the room with you, you can project your thoughts into someone
else's mind, you can levitate, you can walk on water, because It is flowing so
much light in you, you literally don't attract to gravity. When you understand that
your body can now exclude all magnetic and other fields, including gravity, you
are no longer of this space time, you become a fifth dimensional being. You
literally can think where you'd like to be and you can go there and disappear from
here.

These ancient texts specify the appearance of other attributes such as healing
with the laying on of hands, they claim you can resurrect the dead within two or
three days after they die. Instead of using electrical paddles, you have so much
energy in you, you can literally embrace these people and bring energy and life
back into them. Sounds pretty far out. Most groups don't receive this very well.

It works. We haven't achieved everything yet, but it has done miraculous things.
We started with very incremental amounts, 2 milligrams. There are 32,000
milligrams in an ounce, we start with 2 milligrams. We have gone up to 50
milligrams, over a period of 60 to 90 days and have had amazing results, it is the
light that corrects the cells. Christ said to his disciples, don't touch me, I don't
have on my earthly garments. They said, when will we see you again. Christ
replied, when you have prepared the proper food and when you have on your
proper garments. What is the proper food? It is the food of the angels, the food of
the gods, the manna, the what is it? The proper garment, is your garment of
glory, your rainbow garment, your Meissner field is what science calls it, and
literally its about 1000 times what you have now. The amazing thing about
superconductors is they don't have to touch for energy to flow from one
superconductor to the other. Electricity has to touch for electricity to flow.
Superconductors can sit at a distance from each other, and as long as they are
resonant to each other, they are AS ONE. They function as one.
When you have your perfect superconducting body, you are no longer of this
space time. You are a light being, your mind is one with other people's minds.
You literally know their thoughts and they know your thoughts. You're one mind
and you are one heart and this is science.

For those of you who don't believe it, it does not make any difference, because
this is science, it is here. The Bible says that the man who will plant the golden
tree of life, which in Hebrew is the ORME tree, the name of my patent, and I had
no idea of this when I filed my patent.

My cousin joined the Mormon church and they told her to do our genealogy. My
thrice great grandmother is Hanna Deguies, daughter of Christopher Deguies,
brother of Claude Deguies, who if you read the book, Holy Blood, Holy Grail,
you know who the Deguies' are.

Nostradamus worked with the Deguies family and Nostradamus prophesied that
by 1999, the occult gold will be known to science. The old enemy of religion and
philosophy is science. But in fact, science will serve up the confirmation and
science will be the one to bring this to the world.

Religion has tried to do it for 2000 years and has failed miserably. The world is
no durned good, people are no durned good, they are greedy and selfish. The
capitalist system has worn out, because it is based on the selfishness and greed of
man. But science can take this to the world in 4 to 5 years. Once it is accepted
and understood by scientists, the breakthroughs will be astronomical. Basically
what I have done is create a basic analytical breakthrough. What it means, is you
can fill yourself with this light. As you read in the Dead Sea Scrolls Uncovered,
not only did the Qumrun community have a metallurgical foundry in the center
of the city, you also find out that the Teacher of Righteousness, this thing that
they were totally preoccupied with, wasn't Moses or Christ. It says the high priest
SWALLOWED the Teacher of Righteousness which was the Holy Spirit, it is the
light, the zero point light that is not measurable. But it is in fact, the light or god
force within us. It is the teacher that shows us how to know all things, we don't
have to read or study, we just know.

Supposedly, when your light body exceeds your material body, you don't have to
eat food. You can if you want, but you don't have to. You have perfect telepathy,
how much more could you ever be judged, than for everyone to know your heart
and your mind.

Everything about you is known, no more hidden agendas, no more lies, no more
deceit. Everything is known, this is called the opening of the book of life. In
Revelations, it says blessed be the man who will overcome, for he shall be given
the hidden manna, the white stone of purest kind upon which will be written a
new name, you will not be the same person.

It's encoded in your DNA, waiting to be activated. It says, at 1160 degrees, the
white powder of gold fuses to gold glass, its a transparent glass, just like window
glass. In Revelations, written by John the Revelator, one of the three inner
disciples, it says the streets of the New Jerusalem will be paved with gold so pure
as like unto transparent glass and the foundations of New Jerusalem will be made
of gold like unto transparent glass. This is the gold glass, the very basis of the
New Jerusalem, the very basis of raising ourselves and our consciousness to this
higher state.

This OR, the highest light, that will literally activate all our DNA, will cause us
to use all of our brain AGAIN and we will return back to the original state we
were created to be in before we fell to this animalistic existence we know now.

These elements are in all of the herbs that EFFECT regeneration, in the herbal
teas and in many of the vegetables you vegetarians are eating. You get them in
small amounts. Through work, dedication, years of study, meditation, you can
achieve similar results, but it really is tough to be a Tibetan monk.

This is called the Keys to the Kingdom, you insert it, turn it and the door is open.
It is your decision to step through the door. We are in the process of building a
refinery, producing 65 million milligrams per day, it will be available in 8 or 9
months and I have to give it away, I can't sell it.

I of course will solicit donations, I have to GIVE it to people, if they find it of

benefit, they can make a contribution. There is a book being written on it, it will
be out in 8 to 9 months also. It will be called ORMUS, it will be in all
bookstores, we are not sure it will be published by one of the big houses, most
likely, we will publish it ourselves. It will be a biography, it will be the story of
my quest for the Holy Grail with all the details. The material will be available to
all who seek it for the correct reasons at no charge.

A nre website has been developed for research in Aetheric Energy -

AethericEnergy.org.. This with give you the latest developments in this research
and mention some new products. For a vast and comprehensive study of this
issue go to the White Gold Website and also Barry Carters Website that is loaded
with historical documentation, case studies and instructions. I'd like to publicly
thank Barry for his assistance in helping me understand this mysterious discovery
better. You will want to listen to David Hudson's Lectures.
--

2DO LINK

How to make DIAMOND

Diamond is carbon, so, how about turning
ordinary carbon graphite into valuable diamond?
How to make diamond:
1. melt down some iron
2. dissolve some ordinary carbon in it
3. drop the molten iron with carbon in water
4. dissolve the iron in acid

It's true, this really does make diamonds, but

they are very small and not of very high quality.
Safety point: Melting down iron is not practical in the average household
kitchen, and the writers of this page take no liability for any
consequences of anyone being silly enough to try this! Plus, there are
easier ways of making money, so please don't try this without some
seriously industrial equipment.

--

4TO LINK
A bulk process for making diamonds

"Lucky Lab Accident Yields New Recipe For Diamond Coating"

by Malcolm W. Browne, The New York Times, 3/12/96, pages B5 and B10

"By unintentionally substituting the wrong gas for one they intended to use for
hardening tools, workers at a small metallurgical company have accidentally hit
upon a potentially valuable method for coating objects with a hard diamond film.

"Specialists trying to learn why and how the method works warn that it has yet to
prove its worth in industrial processing. But if the new diamond-coating
technique proves to be as cheap, fast and effective as its inventors say, it may
revolutionize the manufacture of machine tools, automobile engines, ships,
beverage cans and much more, materials experts say.

"Although the discovery was made two years ago, it has not been reported in
scientific journals, and information about it has spread mainly by word of mouth.

"The discoverer of the new method is Pravin Mistry, a 43-year-old British

metallurgist who founded a small, privately owned engineering company, QQC
Inc, in Dearborn, Michigan... Mr. Mistry's company specializes in applying
coatings to industrial objects so as to impart desirable properties.

" 'This is an interesting instance of technology leading science,' said Dr. Rustum
Roy, who heads the Diamond and Related Materials Center at Pennsylvania State
University. 'There is no question that this fellow is coating all kinds of things
with diamond, and doing it astonishingly rapidly and well, under conditions that
no scientists imagined would work.'

"Part of Mr. Mistry's method involves four powerful and finely tuned laser
beams, which interact as they scan the surface of an object as it is coated. As Mr.
Mistry explains it, the scanning takes place in a gaseous environment, and the
intense heat at the spot where the lasers converge breaks up some of the gas into
an electrically charged plasma. The lasers also vaporize a very thin layer of the
object being coated. ... By continuing to deposit atoms from the hot gas on the
coated object, the thickness of the coating can be rapidly increased to up to a half
inch, Mr. Mistry said.
"In 1994, Mr. Mistry's group made its discovery while using this interacting laser
technique to apply a coating of hard titanium diboride to the surface of an
aluminum object. An error in their procedure set the stage for a surprise that may
prove to be immensely profitable for all concerned: someone accidentally
substituted carbon dioxide for the nitrogen gas used in the process. A dense
coating formed rapidly, but it did not consist of the intended titanium diboride. It
turned out to be diamond.

"News of the discovery spread rapidly among materials experts, who were
amazed that Mr. Mistry's technique for coating objects with diamond films was
reportedly 1000 times faster than existing diamond-coating techniques.
Moreover, the Mistry process promised to form particularly strong bonds
between the coating and the metal objects to which it was applied, a vital
requirement for hardened machine tools.

"The United States Navy, Army and Air Force, and the Defense Department's
Advanced Research Projects Agency, as well as automotive companies, are
following developments with interest.

" 'I have seen objects coated using Mr. Mistry's process, and I can verify that the
coating is diamond,' said Dr. Robert Pohanka, director of materials research at
the Office of Naval Research in Arlington, Virginia. 'I have visited the plant and
seen the equipment.'

"Mr. Mistry said in interviews that the technique was in its infancy, but that all
indications suggested that the coating was cheap and could be applied in closely
controlled shapes and thicknesses, with excellent adhesion to objects.

"If the Mistry process lives up to expectations, Dr. Pohanka said, it could be used
to apply hard coatings to gears and bearings, to cover pumps and other machinery
with corrosion-resistant coatings... and to harden engine components to reduce
wear.

"Dr. Roy, whose research group has undertaken an investigation of the scientific
basis of the Mistry process, believes it could be used almost like a paint brush to
apply coatings of diamond or other special materials. 'Mr. Mistry's equipment is
operated by robots under computer control,' he said, 'and since the method is so
flexible, it might some day be possible to coat an entire ship's hull with a film
made of diamond or some other protective material.' "
Apparently Pravin Mistry and his colleagues are stuck on the idea of applying a
coating of diamond to an existing object. It has not occurred to them that the
substrate is just a substrate -- the diamond itself is the main thing. This technique
could be used to make all kinds of things out of diamond.

Lasers don't have to be macroscopic (see, for example, Stephen R. Forrest,

"Lasing from a molecular sieve," Nature, 28 January 1999, page 294, and
Michael Brooks, "Heart of Chaos," New Scientist, 9 January 1999, page 28).
Given microscopic lasers, the Mistry process could be used to make very fine-
grained diamond structures.

However, the Mistry process is not molecular nanotechnology. The carbon

atoms are not singled out and put in place individually, they are deposited from
a gas (or plasma) onto a surface. This will still be true even if the lasers are
miniaturized. The Mistry process is inherently a bulk process.

--

5TO LINK

Super-hard material thickly coats metals, plastics; also

stands alone

Wear-resistant diamond coating created by

Sandia scientists
ALBUQUERQUE, N.M. -- Eliminate stress, the saying goes, and you live
longer. Apparently the same is true of certain diamond coatings.

A team of Sandia National Laboratories scientists has developed a simple,

inexpensive way to relieve the normal internal stresses of amorphous
(noncrystalline) diamond films -- a significant advance in producing wear-
resistant coatings.

This should mean improved protection and extended lifetimes for metal tools,
auto parts, and even plastics, such as those used in biomedical devices. The film,
for which Sandia, a U.S. Department of Energy (DOE) laboratory, has applied
for a patent, may be one important step in making diamond coatings
commonplace.
Diamond has been used as a hard, wear-resistant material at least as far back as
Pliny the Elder in ancient Rome, who used diamond shards as tools. The science
novelist Arthur C. Clarke, who wrote the book 2001, predicts in his
novel 2061: Odyssey Three, that in less than a century, it will be customary to
protect buildings from weather damage through use of diamond coatings.

The researchers published papers on their work in Applied Physics

Letters (December 29, 1997) and the Journal of Electronic Materials (September
1997). They presented talks at the Materials Research Society meeting in Boston
in December 1997.

How is the Sandia coating different?

Ordinarily, amorphous diamond films contain very high levels of compressive
stress, equivalent to a pressure of 70,000 atmospheres within the plane of the
film. These high levels of stress cause the film to peel off its substrate, which
limits the film's thickness, and also makes it impossible to create large-area free-
standing membranes -- coatings without substrates -- that could serve as
transparent windows for X-ray or electron optics.

The new material enables the creation of thick, stress-free, amorphous diamond
coatings, never before successfully achieved. The stress-free coatings are harder
than any known coating, except for crystalline diamond.

Because they are stress-free, the coatings have also been used to create very thin,
large-area, free-standing membranes.

"The stress-free coatings represent a major advance over other types of diamond
coatings," says Sandia researcher Tom Friedmann, who with Sandia colleague
John Sullivan, originated the stress-relief technique.

Unlike crystalline diamond coatings, which require high temperatures to deposit

and have very rough surfaces, the stress-free coatings are deposited at room
temperature and are extremely smooth. "Furthermore, these stress-free coatings
are almost identically as hard as the crystalline films," says Friedmann. These
coatings are also much more stable than amorphous diamond films that contain
hydrogen -- industry's most common hard carbon coating. As Friedmann points
out, "Diamond coatings that contain hydrogen tend to degrade at temperatures as
low as 200 degrees Celsius. The stress-free coatings show negligible degradation
up to 800 degrees Celsius."

Ultrahard, chemically inert

To date, the team has made stress-free films more than seven microns thick, has
applied the thick coatings to plastic substrates, and has made free-standing
membranes more than one inch in diameter and less than 600 angstroms thick.
One angstrom is about equal to the diameter of a carbon atom. Because the films
are stress free, deposition to almost any thickness is conceivable, and the
researchers believe they could easily create even larger, thinner membranes.

Measurements show that the amorphous diamond coating is 90 percent as hard

and stiff as crystalline diamond, the hardest known material. The films have other
desirable properties as well -- they are wear resistant, have a low coefficient of
friction, and are inert to almost all chemicals, which makes them suitable for use
in harsh environments.

An additional feature, says Sullivan, is that "we not only can eliminate stress but
we can control it. We can make a tensile film -- a film that wants to contract and
pull taut like a drumhead. This is important for making membranes."

How is it made?
The process uses a pulsed laser on a graphite target to deposit, at room
temperature, an amorphous carbon film with a high percentage of diamond-like
bonds but with high initial stress.

"Then," says Friedmann, "we discovered that when the deposited material is
heated, these films lose their stress, yet retain their diamond-like properties. In
contrast, amorphous diamond films that contain hydrogen convert to graphite
upon heating."

"The stress relaxation that occurs in the stress-free coatings is uniquely different
from other types of stress relaxation we have seen in the past," says Sullivan. The
process seems to involve short-range bond rearrangement as opposed to long
range atomic migration which occurs in many other materials. "The surprising
thing is that the hardness seems to be unaffected by the subtle rearrangements,"
says Friedmann.

The work is funded by Sandia's Laboratory-Directed Research and Development

program for leading-edge, proof-of-principle research. DOE funds are used to
continue development.

Companies interested in joint development of the material should contact

Sandia's Technology Partnership Center at the number listed below for industrial
contacts. Sandia is a multiprogram DOE laboratory, operated by a subsidiary of
Lockheed Martin Corp. With main facilities in Albuquerque, N.M., and
Livermore, Calif., Sandia has major research and development responsibilities in
national security, energy, and environmental technologies.

--

7MO LINK

TRANSMUTATION RECIPES FOR MAKING GOLD

The National Security Agency is EXTREMELY hostile to

the distribution of the below

COMMENTS ON TRANSMUTATION ARE BELOW THE RECIPES; also links which

provide the images and an htm file that will help with visualization of the
atom as it truly is.

You will want to examine this new source of highly detailed information

at the bottom is a letter from someone who followed instructions with a bit of
creative ingenuity and had solid success.

Last modified March 03, 2006

RECIPE # 1
************
It was Joe Champion who was, I believe, imprisoned for this process.
************

Joe Champion
4833 Woodmere Fairway E-1
Scottsdale, Arizona 85251

(602)481-6249 (home)
Personal Profile:

SUMMARY OF DIRECTION

Research into the Field of Low Energy 1989 - Present

Nuclear Transmutation

In 1989 I was fortunate to witness a phenomena which for all intents and
purposes has been ruled by the established scientific community as an
impossible event. In my observation of an experiment being performed by a
non-scientific person, I observed what appeared to be the instant conversion
of one element to another. This "conversion" occurred under conditions
wherein the applied energies were lower than those normally considered
possible.

Replication of this event under controlled conditions caused me to consider

the fact that nuclear events could occur under two sets of conditions; the
accepted norm of "high energy physics" and under a low energy nuclear
exchange.

Since the initial introduction to this event, I have dedicated full time to the
cause and potential effects of this discovery. In an attempt to fully
comprehend my findings I have collaborated with institutions throughout
the world to solidify my position and priority.
Work Experience;

Discovery Publishing 1992 - Present

Westboro, Wisconsin
Phoenix, Arizona

Performed functional testing of low energy nuclear transmutation reactions.

Position includes interaction with academic, government and private
research laboratories. Both domestic and international, to assimilate
foundation data that low energy nuclear events do in fact occur in nature
and are reproducible under controlled laboratory conditions. Information
gathered was published in professional and public journals

Instituto TE.S.R.E.

Roberto A. Monti

LOW ENERGY TRANSMUTATIONS

(cold fusions and cold fissions)
Introduction.
At the end of October 1988 I made a summary of the ideas about
the structure of the atom which I developed since I was a student (1).
At the beginning of February 1989 a new model of the atom was
completed, and in light of this new model, I reconstructed the Periodic
Table of the Elements (2).
I have never had the possibility to make any experiment, but the
experimental foundations of this model could be found, in my opinion, in
the papers of Thomson, Parson, Lewis, Allen, Harkins, Kervran and
Borghi (3).
Finally, at the beginning of 1991, I made a summary of my ideas
about aether and matter in two papers (4), (5).
Since that time I was waiting for the occasion to make some
experiments.
This occasion came to me in April 1992, through Prof. Bockris.
The results of these experiments are the following:

***********

The final product of the ignition showed in crease of B (beta)

radiation greater than twice the measured background.
The mixture before ignition contained less than 20 p.p.m. of gold.
After the ignition, the mixture contained more than 400 p.p.m. of
gold.

Experiment 2.

Experiment 2 consisted in the ignition of the following mixture of

chemicals:

Gold ore 100 g (Action Mining, 0.047 Oz./ton Au,

0.14 Oz./ton Ag).

PbO 20 g (Johnson Matthey, 99.99%)

C 150 g (Johnson Matthey, 300 mesh, 99.5 %)

KNOs 450 g (Baker, 99.2 %)

S 30 g (Spectrum)

Hg2Cl2 20 g (Fisher, 99.8 %)

Fire assay Flux No ("o" is superscript) 486, Action Mining

Services Inc.
The final product of the ignition showed the following results:

1) The total B (beta) radiation count was 2.2 -10^4 CPM and five
different energy peaks were observed.

2) The mixture before ignition contained certainly less than 20

p.p.m.
of gold
 After the ignition, the mixture contained 1700 p.p., of gold.
'em

Consiglio Nationale Delle Richerce

Instituto TE.S.R.E.
( Studio e Technologie delle Radiazioni Extraterrestri)
Via De Castagnoli I 40129 Bologna
Tel 051-28 7011 Fax 229702 - telex 511250 CNR BO I

Roberto A. Monti

COLD FUSION AND COLD FISSION : EXPERIMENTAL EVIDENCE

FOR THE ALPHA-EXTENDED MODEL OF THE ATOM.

Summary.

Part I ; A new model of the atom.

On the basis of Thomson's, Parson's, Lewis, Allen's and Harkins' hypotheses

a new model of the atom is advanced, characterized by the following
features: 1) substantial asymmetry of the Coulomb electric and magnetic
fields of electrons and protons: 2) existence of positions of stable
electromagnetic equilibrium of electrons in the vicinity of nuclei; 3) the
neutron is a particular "bond state" of the hydrogen atom; 4) the nuclei,
whose dimensions are greater than supposed by Rutherford, are composite
structures of hydrogen atoms, of period 4 (Alpha-extended model); 5)
Physical and chemical properties of each atom depend on the various,
possible, isomeric configurations.

In the light of this new model, the Periodic Table of the Elements has been
reconstructed.

Part II : Experimental evidence for the Alpha-extended model.

The genesis of the elements and the Slpha-extended model of the atom are
shown by means of: 1) neutron synthesis, starting from a cold plasma of
protons and electrons; 2) the synthesis of deuterium, Tritium, Helium-3 and
Helium-4, starting from the hydrogen, ultra cold neutrons and thermal
neutrons; 3) the production an decay of Helium-B; 4) the production and
decay of the nuclei from 11 a (alpha?) to 18 a (alpha?) ; 5) "cold fusion" of
Iron-56 ; 6) cold fission; 7) carbon isomeric configurations (allotropic
forms); 8) cold fusion in metal lattices; 9) biological cold fusions and cold
fissions (weak energy transmutations); 10) the distribution of the scattered
radiation.
 Reference.

(1) R.A. Monti. A brief history of the atom, cold fusion and cold fission.
Proceedings of the international Conference: "What Physics for the next
century?" Ischia, Italy, 29 Ray-I June 1991
RECIPE # 3

In response to many questions about this:

The Quartz Geode is what should be used instead of the ceramic

mortar when using the procedure followed in Recipe #1, avoiding
the absorption of the Arsenic and the diminishment of results.

The electrodes inserted into the mixture are copper coated or copper.

No sources for parts and equipment are available, you will have to check
locally.

There IS a device that will plug into house current and give the
specified
electrical input in DC. That device costs $250.00.

The process can take up to five hours. Be meticulous and precise in

measurements. Keep exact records. Do not try this to get rich. You may
get into deep trouble.

Small things can frustrate immediate success. Be cautious and patient.

This can result in explosions. The vapors are also dangerous.

......... zeropoint

items needed

1. 1/4 oz. silver shavings 99% pure

2. 3 oz. sulfur powder (pharmaceutical grade)
3. 10 oz. Cinnabar with no TRACES of gold (also known as
a mineral, Mercuric Sulfide, Hgs)- powder it
4. 1 quartz geode
5. 4 12 volt car batteries
6. 2 lead (Pb - the element) copper electrodes

place all shavings and powder into Quartz Geode, connect

car batteries to equal 48 volts at 3 amp per minute, place
leads into powder in Quartz Geode. Wait 25 minutes

produces 1.75 ounces of gold

don't get greedy, do exactly as stated

larger amounts at one time will produce radioactive gold,

you can repeat the procedure to make more gold. Wear
mask!!!!!!!! and gloves!!!!

"got this off the net"

====> source is traced to:
http://www.geocities.com/Area51/9357/ <<== at this site,
go to the link for "tribute" .... You will find that the cinnabar
which Is WILDLY variable in price, from less than $200 to $900/oz,
can be substituted with one ounze of mercury. ***If you go into the
"tribute" section you will find another link to where the original
handwritten copy is found. *** Do not hesitate to call the webmaster
by phone to consult on this or to give information such as sources for
cheap materials. Also, the quartz geode with LARGE crystals may be
superior.
A frequently asked question is about the electrodes. These should
be LEAD on the outside with copper feeds to the battery or the rheostat.
Don't talk too much about what you are doing. USA is expected to go
down the toilet beginning summer 1999, then, there will be too much
chaos for much policing, and you can be more public, if money is worth
anything.

A FOURTH PROCESS/RECIPE from France!

This site will eventually and soon include the explanations for how these
effects are possible. It is very simple but depends on the visualization of the
ACTUAL shape of the atoms involved and how they interact. This
information is dispersed throughout the page and will be pathed to this first
link dealing with transmutation.

It was an ancient Arabic text which caused the infamous quest to make gold
from base metals. The text described the testing of a preparation of
medicine, "if when flame is applied to the powder, the powder turns to gold,
the medicine is ready and should be taken." This science depends on the
facts articulated in the new science of ORMES. The formation of ORMES as
described in the link to David Hudson's site. The means of determining the
nature of the shape of the atom and of its substructure is esoteric in nature,
Kundalini.

The results of many overunity inventors end up in being piles of dust... the
metal device turns to powder on the lab bench, as is described in
japanese.htm. It is this powder that is the key. It is possible to make ORMES
that when ingested do heal. Subsequent eating of certain of these
preparations render the person a spirit who may spend millions of years in
the state of the ethereal and require special fixation to be able to materialize.
It is suggested that various diabolical practises are merely rituals intended
to give purchase to the material world to persons who very long ago ate such
preparations but cannot orient to our state without contrivances by fools
who engage is certain practises. The ability to manipulate matter and
circumstances in this manner, scalar physics and, with respect to
transmutation itself, frank CORRECT chemistry/physics, is that "magic"
which the Holy Bible says will disappear, e.g., be forgotten. The keeping of
this science from the public is designed to allow maximum shock value when
it is implemented.

Paranormal Observations Of ORMES Atomic structure This link is defunct

in its original location and is provided with images that show the atomic
structure and substructure as visualized by the unusual means described in
this large htm file. The images will be hooked up to the htm by April 2, 1998.
And otherwise placed in this paragraph. The viewing of the images and the
understanding of what they show will explain the simplicity of
transmutation. bar.gif, dumbell.gif, dumbval.gif, subhelix.gif, rebal.gif. ftp/
pictures/ subdirectory. Gold atom in rest state, dumbval shows gold in high-
pin state. Flanges at ends are valence attachment points which, in high spin
state allow for Cooper Pairing of the atom with itself or another atom.
subhelix.gif shows substructure of the atom itself. bar.gif shows another one
of the several types of atomic configuration for another element.

 BACK TO MAIN PAGE,

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at: Electrifying Times Magazine

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Contact information

Fourth Millennium
[email protected]
(510) 285-7681

From: "Fourth Millennium"

Subject: PERSONAL SUCCESS WITH GOLD MANUFACTURE

You are welcome, Very welcome. Do be discrete about this. USA itself is
using this process to help to fund SDI (star wars). Their colleagues don't like
for the cat to be out of the bag. later. zeropoint From: xxxx Subject:
Feedback from Web site/gold

Hi to all at ZAP

I am writing to say THANK YOU THANK YOU THANK YOU THANK

YOU THANK YOU THANK YOU THANK YOU THANK YOU THANK
YOU..

I have just completed the successful transmutation of gold as given by the

recipe on your site. This is the one involving the use of silver, mercury &
sulpher.

I was very skeptical that this could possibly work, but since I had on hand
some .999% pure silver in coins,( Liberty Silver 1 oz ) I was able to proceed
with only the minor expense of purchasing the sulfur and Cinnabar
(mercury). I was also concerned with the possible fumes from the reaction
and so arranged an extractor fan to suck out fumes via a 6in chimney flue
using a discarded computor cooling fan. this worked well and no problems
were experienced with dangerous fumes. Another concern was the
regulating of the current to 3 amps a min, this is a non scientific term as
current flow is not measured in time but in instantaneous amperage, well in
any event we set up a Rheostat to limit current to 3amps as the flow rate.
using a dashboard lamp dimmer from a wrecked truck and a multimeter to
show the current.

The whole thing sure looked weird in the shed, but WOW the results say it
all... I am astonished that this kind of information is available, and even
more amazed that it WORKS.

I have several more coins to file down to powder, that's the hard part, I
didn't want to use a grindstone for fear of contamination of the formula with
stone particles, maybe I will give it a go as it seems a lot of the mixture is
dross in any event, and I am sure a few micrograms of stone will be
absorbed as part of it, after it cools and hardens.

Once again THANK YOU, I am now sure I will be able to produce about 50
oz gold with the remaining silver I have on hand and then we will see what
to do next.

You may be interested to know that here in xxxxxxxxxx a person who finds
gold as in prospecting, does not have to pay tax on it, it is redeemable for
cash at the xxxxxxxxxxxx, some 120 miles from where I live, when I have
finished the 50 oz

I will pour it all into one bar and take it up there, the estimated value is
$12500:00 xx, so you can see why I am so happy. thanks again...

Contact Information
 Fourth Millennium
[email protected]

(510) 717-9737
toes show picture is
fake

http://users.rcn.com/zap.dnai/gold.htm

Alchemist's Formula for making Gold

This formula came from Cynthia Schneider Drayer Philip Schneider's ex-
wife. I Mark Allen Pitt make no claims as to this formula actually working
or not since I have not made any Gold using this formula. Please make all
inquires to Cynthia as to the formula's validity.
Her email address is as follows Click here to email Cynthia Schneider
Drayer [email protected]

Wear rubber gloves and Gas Mask when working with this Formula to
protect yourself from Mercury Poisoning.

1/4 OZ Silver Shavings 99.9% pure.

3 OZ Sulfur Powder Pharmaceutical grade.

10 OZ Cinnabar (also known as a mineral, Mercuric Sulfide, Hgs) - powder

it, or 1 OZ Mercury with no traces of Gold .

1 Quartz Geode.

4 12 Volt Car Batteries.

2 Lead Copper Electrodes.

Place all shavings and powder into Quartz Geode.

Connect Car Batteries to equal 48 Volts at 3 Amps per minute.

Place Leads into powder in Quartz Geode wait 25 minutes.

Produces 1.75 OZ of Gold.

Don't get greedy, do this exactly as stated above, larger amounts at one time
will produce Radioactive Gold. You can repeat the procedure to make more
Gold.

Paranormal Observations of ORMEs Atomic Structure

by Gary

Between August 1895 and October 1933, Charles W. Leadbeater and Annie
Besant of the Theosophical Society conducted clairvoyant studies of the atomic
structure of the elements. Both of these individuals had previously awakened
kundalini; Leadbeater has described his having done so by pranayama, which is
the same method I used. After kundalini has been awakened, and after the ajna
chakra (brow chakra) is fully functioning, it is possible to extend one's
consciousness, specifically the faculty of vision, through great ranges in
magnification capability, and either up or down in objective size. In yogic
writings, this is part of what is allegorically referred to as the ability to make
oneself very small or very large at will. These are the first and second of the eight
major siddhis, the Sanskrit Anima and Mahima. The actual nature and extent of
many of the siddhis, or paranormal powers, are often (intentionally) described
allegorically, and so are widely misunderstood. Anima and Mahima actually each
refer to several different things.

One of these, or what actually happens, and is being referred to in the case of
these observations, is that a projection from the ajna chakra is formed by the
yogi; the functional aperture and gain of this protuberant projection or filament
can be controlled by the yogi, according to the scale of the object under
observation. This extended faculty is symbolically depicted in ancient Egyptian
iconography by the small serpent on the pharaoh's forehead, which is dismissed
by most Egyptologists as being just a part of the headdress. By its means, one is
capable of seeing objects far smaller and far more distant than is possible by
means of any man-made instruments yet devised. Leadbeater, for example,
describes an entire spectrum of particle sizes below the subatomic particles
which make up physical atoms.

The results of Leadbeater's and Besant's investigations were published serially as

articles in the magazine, The Theosophist. The material was later arranged and
published in 1909 in a book titled "Occult Chemistry", which was revised in a
second edition in 1919. In 1951, a much enlarged and revised third edition (396
pages) was published in Adyar, Madras, India. I am fortunate to have copies of
these two later editions. Over twenty years ago, in the 1970's, I corresponded at
length with the Theosophical Society's Olcott Library, and they graciously
provided me with a good deal of further information. Since that time, and during
my own studies, I have awaited in hopes that the Theosophical Society would
reprint all the original material. This has not yet occurred, though I continue to
hope for it. Editions of Occult Chemistry are now very rare and difficult to find.
[R. A. Kessinger has done a reprint of this book. It is available from them at:
P.O. Box 160, Kila, MT 59920, phone (406) 756-0167, fax (406) 257-5051, e-
mail : [email protected]]

However, a British physicist named Stephen Phillips became aware of this

material, and in 1980 published a book titled "Extra-Sensory Perception of
Quarks", describing the two Theosophist's work and interpreting it in the light of
modern atomic theory. Though the atomic structures observed by the yogic
faculty, as described by Leadbeater and Besant, did not make much sense to their
contemporaries, present day theories of atomic structure and particle physics
make their descriptions much more recognizable, validated, and startlingly
accurate, as Dr. Phillips was amazed to discover.

Phillip's book was published before the high spin state was recognized, and so he
does not discuss it from this aspect. However, he does notice how the
observations match the Higgs superconducting vacuum model, recognizes non-
Abelian monopoles with Nielsen-Olesen vortices as carrying quantized flux, and
identifies the mechanisms at work underlaying quark stability, among many other
things. All in all, he did a fine job of it. [Extra-Sensory Perception of Quarks, by
Stephen M. Phillips, PhD, 1980, Theosophical Publishing House, Wheaton IL,
ISBN 0-8356-0227-3, US $15.00]
David's ORME patent literature specifically names cobalt, nickel, silver, gold,
palladium, platinum, ruthenium, rhodium, iridium, and osmium as exhibiting the
orbitally rearranged state, with the attendant room temperature superconductivity.
Later, he announced in his lectures, that he finds that mercury also exhibits the
same behavior. As far as I am aware, he has not yet publicly suggested any other
elements (excepting only mercury) are capable of stable ORME states and high
temperature superconductivity, beyond those listed in his patent literature.

Now, as Leadbeater and Besant's work has already been published, presenting a
great deal on this subject (even if it is not widely known), and it has been
available for some time now, and monatomics are also now becoming more
widely recognized, and a certain requisite amount of discussion has taken place
regarding it, (thanks to Dr. Phillips), it is at last permissible to comment on the
information that has been released occultly, with greater openness, and from the
perspective of monatomic research.

Based on these published materials, and on certain studies I have done, I may
now relate some further information regarding monatomic forms of the physical
elements, their shapes as monatomics, some additional light on
superdeformation, superdeformation's relation to the high spin state, and what
these several factors have to do with the manifestation and development of
superconductivity.

As monatomics (single, isolated atoms), the elements are yogically observed to

display shapes, which turn out to resemble certain of the platonic solids and other
unanticipated shapes, more than the Bohr atom most people think of. However,
valence structures, subatomic structures, and numerous other complex
phenomena can be identified, given patient study, so that the physical basis for
our theories are nearly all seen to be revealed, even if they are not implemented
quite as we had supposed. The valences take the form of rod-, bar-, and funnel-
like shapes, with the large end of the funnel cone pointed outwards. The valence
shapes, nuclei shapes, and other observed macro features are of course not solid
forms, but are swept volume envelopes, made by the rapidly moving particles
which compose the atoms. I will be referring to the "valence structures" etc.;
these are equivalent to "orbitals" as used in the ORME acronym.

Dr. Phillips has observed that incongruencies exists between the valences
observed yogically, and those predicted by theory, that the number and nature of
the valence structures actually observed (in the monatomic state) are not as
would be expected, according to present scientific theories of atomic structure.
And he has made an effort to reconcile the two, theory and observation. Valency,
as observed, can be seen in some cases to be comprised of sets of half valences,
so that there are two valence structures for each of the valences allotted in our
present theory, and other variations in other cases. Dr. Phillips puzzles over this
at length in his book. Unfortunately, he never quite makes the connection (though
he comes to within a hair of it), or it fails to occur to him, as to how these sets of
"half" valences (for instance) relate to, and are responsible for, the forming of
Cooper pairs. But he seems so pleased to at last be seeing how atoms really work,
that he doesn't greatly mind this "problem".

Phillips concludes that the majority of the atoms observed by the investigators,
and presumed to be monatomic, are actually diatomic, and points out that this
assumption clears up most of the apparent difficulties. In this article I will refer
to the observed forms as monatomic, for continuity with the original
investigators, as much as for any other reasons. (1) Dr. Phillips' book, sadly, has
not received much attention. Scientists do not enjoy giving up their theories, but
few would argue that the theories as they stand today shall forever remain
unchanged. I recommend that those interested read his book, for a hint at what
the theories will be... changing to.

The physical structural arrangement of elemental atoms, and particularly how the
valence structures are arranged in the atom, are observed to develop as several
recurring periodic patterns of form. Leadbeater and Besant soon found that the
structural patterns do not fit well into the Mendelyeev table (which has been
found so useful for predicting chemical properties), but the observed structural
periodicity is nicely predicted by the periodic system proposed by Sir William
Crookes, which was later refined by Jinarajadasa into a quadruple leminscate.
Crookes-type tables, which can be represented by a multi-level 3-dimensional
figure 8 pattern, fit the data far better from a structural characteristics standpoint,
**for the purely singular and monatomic forms of the elements**. This is an
important point to remember, as the elements have dramatically different shapes
when they are observed in chemical combinations.

The elements in Table 1 (below) are yogically or paranormally observed to have

shapes which appear as moderately high aspect symmetrical dipoles, when
examined as single atoms; ie, apart from chemical-, cluster-, lattice-, or
crystalline- influences. They all show symmetry of rotation about their major
axis, as well as mirror symmetry about a plane bisecting their major axis. They
were aptly termed "dumbbell shaped" by Leadbeater and Besant; the valence
funnels are dipolarly disposed on either end of the atom, giving them a distinctive
dumbbell shape.
 Dumb-Bell Shaped Atom

In the case of the dumbbell shaped atoms, which might be considered as one of
the most puzzling shapes to someone seeing it for the first time, it is arranged as
follows. The main or central body envelope is a swept volume which is
approximately represented by imagining an elliptical solid, or ellipsoid of
revolution, formed by spinning an ellipse on its major axis. The aspect ratio of
the major/minor axes (speaking only of the central structure) is greater for
smaller atoms in this family, like sodium, where it is approximately 4:1, and
becoming relatively "fatter" in the heavier atoms. Monatomic gold has a central
body of about 2:1 aspect.
 Gold Atom

Each element in the dumbbell shaped group has a total of 24 valence funnels;
there are 12 at each end of the atom, representing 6 sets of half valences. The 12
funnels are arranged a bit like blades of a ceiling fan, which rotate on the major
elliptical axis of the central body, hence the dumbbell look. The ends of the
valence funnels are slightly staggered, alternating up and down slightly as you go
around the atom.

Within the central ellipsoid form and the valence structures are found smaller
forms (and similarly so for the other element family shapes), which Phillips has
managed to relate to protons, neutrons, quarks, and their components. Of course
quarks, let alone baryons, leptons, omegons, etc. were unheard of when this
information was first published. The smallest particles which make up the
physical atom are referred to by Leadbeater and Besant as "ultimate physical
atoms", since they seem to be the constituent particle from which all the
subatomic particles are built up. They have called these "Anu", after the Sanskrit
name for the ultimate particles of matter (it is the same root term used in Anima,
"the size of an atom"). There are two types of these, termed + and -. The Anu
"particles" are composed of whirls of energy which spin in opposite senses
between the + and - varieties. These whirls of energy, when magnified under
increasing power by yogic vision, are themselves composed of smaller spirals,
and those of smaller spirals, and so on, down through 7 layers of nesting.
 Nested Spirals

The Anu are many orders of magnitude smaller than the subatomic particles, and
the subatomic particles are in turn many orders of magnitude smaller than the
elemental physical atoms of the periodic chart. The Anu, and more complex
particles, all move at enormous velocities, sweeping out the shapes that I am
referring to, and the atom is an extremely active thing to see. It is ceaslessly
throbbing, pulsating, spinning, gyrating and precessing with amazing rapidity and
vigor when so viewed. Not at all like the billiard ball protons and neutrons with
the spherical electron shells many would expect to see. But our dashed
expectations are our own fault, rather than Nature's. Still, we are better prepared
now than at any time before to understand the remaining secrets of atomic
structure; we must only recognize that things are far more complex than we have
ever previously supposed. (2)

Table 1 elements are all structurally similar, despite the fact that under our
present periodic arrangement samarium (for example) inserts columnarly in VIII
between ruthenium and osmium, and sodium falls in group IA with the alkalis.
Most of the nonmetallic halides are found, by this faculty, to similarly be
dumbbell shaped in their monatomic states. Of the elements in this family, David
has already observed ORME state superconductivity which develops in gold,
silver, and copper.
  Table 1

"Dumbbell" group monatomics, predicted to exhibit the ORME superconducting

state.

 Sodium
 Chlorine
 Copper +
 Bromine
 Silver +
 Iodine
 Samarium
 Erbium
 Gold +
 Astatine
 Berkelium
 Lawrencium

+ Already specifically named in David Hudson's patent literature.

The inclusion of an alkali metal like sodium, most of the halides, and so on, flies
in the face of existing interpretations as to the underlying causes of the ORME
phenomena (which is presently postulated to be a consequence of partly filled
orbitals). Many of the elements I suggest in this article to possess
superconducting ORME states are, of course, nowhere near the center of the
Mendelyeev periodic table, where elements with partly filled orbitals are placed.

It would be good to recall at this point that the periodic table was originally
developed only as a means of helping us understand the laws governing the
elements' chemical properties, and we should not fall into the trap of
extrapolating its fine success in this regard to imply that it also applies to, or
continues to hold true for, monatomic shapes. To assume that chemical properties
are a reflection of an element's monatomic-form structure is not supported by
yogic observations. There is little hope in discovering an element's atomic
propensity for having an ORME state by peering at the Mendelyeev periodic
table. This phenomena has little to do with orbital filling as shown there.
However, the phenomena and the reasons behind it become clear and plain when
viewed yogically.
The actual reasons that certain elements exhibit stable ORME states, form
Cooper pairs, and display Type 2 superconductivity (as David has correctly
described them as doing), lies in their structural characteristics, and these
particular structural characteristics only occur in the monatomic forms of
elements, and then only among certain monatomic-form structural families. The
valence forming structures (ie, 'orbitals') of the elements named in David's patent
literature (as well as mercury, and others), are seen to "rearrange" precisely as
David has indicated, and this rearrangement is indeed what leads to their
extraordinary properties. Other elements, discussed in this article, not yet
acknowledged as ORMEs by David, shall eventually be found to exhibit this
same behavior, under appropriate conditions.

The elements which can potentially exhibit room temperature (and higher)
superconductivity do not necessarily immediately or spontaneously rearrange
themselves into a superconducting ORME state upon disaggregation. They first
require an impetus to set them rapidly spinning. High spin is a necessary
condition for this rearrangement to occur; it is the first step in how the ORME
state is reached. (It should be apparent that to have a rapidly spinning single atom
means that it is monatomic.) However, the relatively low energy of thermal
collision forces is sufficient to get them spinning fast enough. Simple glancing
thermal collisions knock the monatomic atom into a rapid spin, and that is how
the high spin state leading to ORME transition is most commonly achieved. That
is the reason behind why David had to heat the monatomic material in order to
transform it into a superconducting ORME state. It is indeed a strange
consequence that thermal energy transfer, in the form of a spin-imparting
collision, may act to lower the atomic energy temperature, but it is an
observationally evident effect.

The spin of the atom centrifugally causes the valence structures to deflect from
the normal positions they have as single (monatomic) atoms. Rearrangement of
the valence structures into the ORME configuration then occurs, which, once
formed, is extremely stable for some elements. [For some other elements capable
of forming ORMEs, much greater excitation levels are required, and stability is
also lower.]

Here is how the transition into an ORME works from an observational

standpoint. Assume an atom of one of the appropriate families has just become
disaggregated (let us say, by some means that does not impart substantial kinetic
energy to it) from a lattice, or crystal, or chemical combination, so that it is free
to assume its normal monatomic (family) shape, and is just floating around
without much velocity or spin. In its initial condition, upon disaggregating, its
valence structures will be arranged in their "normal" symmetrically disposed
manner as a monatomic chemical atom. In this shape and condition, it is stable,
though it is, of course, able to chemically combine in normal ways, since its
valences are as yet unaltered.

How long the atom has to wait for a suitable collision depends on the temperature
and population density of its environment. This may be very brief, as some atoms
can make this transition at only moderate temperatures. Even if its environment
is relatively cool, an energetic collision may still occur, it is just less likely.
Eventually (assume), a collision occurs causing it to tumble or spin about its
center of mass.

There is a statistical probability that the collision will impart rotation to the atom,
in (or reasonably near to) one of the possible spin planes which will deform the
valences into one of the possible ORME configurations for the particular atom.

When an atom is set properly spinning and on its way to forming an ORME
configuration, the outreaching valence structures are flung centrifugally from
their normal orientations, and this always happens in the manner that most
increases the atom's moment of inertia in the closest ORME spin plane. For
example, in the case of the dumbbell shaped atoms of Table 1, this would be a
tumbling of the major axis itself (ie, the major axis is rotating around a line
passing through the atom's center of mass and orthogonally bisecting the major
axis), and all the valence structures at either end of the dumbbell swing outwards,
away from the center of mass of the atom, to align or cluster towards parallelism
with the atom's tumbling major axis.

The atom thus deforms as centrifugal forces overcome the forces which hold the
valence structures in their "normal" positions. It just happens fortuitously that the
Coulomb forces which want to keep the valence structures separated, and the
centrifugal forces the valences actually experience under high spin conditions are
similar in magnitude. The atoms and their substructures are extremely stretchy
and springy; this should not come as a big surprise, since after all, they are
basically bundles of forces and masses. As rearrangement of the valence
structures takes place, it acts to reduce the spin of the atom, similar to how
spinning ice skaters can slow down by extending their arms outwards.

However, if enough angular velocity has been achieved, the valence structures
("orbitals") rearrange into two groups, like two bouquets of funnel-like flowers,
with one group swung centrifugally outwards on each end of the tumbling, now
highly elongated atom. In this superdeformed condition, their outermost ends
(where the chemical bonds form) approach each other. When (and if) the
coupling ends of the valence structures come into close enough proximity, they
link together in pairs in a specific manner. In other words, in this superdeformed
condition, the atom becomes able to bond to itself, much the same way it would
bond to another atom, only more tightly. When this happens, it looks a bit like
the atom is "hugging" itself with its multiple valence "arms", all joined together
in pairs. It is like when you stick your hands into the opposite sleeve of your coat
on a cold day. To yogic vision, this is what actually happens physically and
structurally, corresponding to what is termed in modern scientific theory as the
formation of Cooper pairs. It is the forming of a micro-cosmic orbit, so to speak,
at an extremely tiny atomic scale. In a sense, it seems ORMEs are metaphysical,
even from a structural standpoint; they are like the atomic equivalent of the
ancient adage: "Turn inwards, and know thyself."

When the valences are all paired together, the atom will look nothing like it used
to, from a chemical properties or analytical standpoint. No free bonds are left to
form compounds. Externally it appears inert, all closed up, not a valence to be
seen. Its spectral emissions will be entirely different. David's statements here are
right on the mark. This closed-up-armadillo-like structure is why they are
insoluble in the strongest acids, capable of withstanding great temperatures, and
so forth. The internally closed circulating flow, through the self-joined valences,
is the source of their individual Meissner fields.

It is important to note that it is also possible to have partial ORMEs, in which

some of the valences are "normal", and free to form chemical bonds, while the
others, on the same atom, are coupled as Cooper pairs. These "partial" ORMEs
may result from either a marginal collision, resulting in an incomplete ORME
formation; from an odd collision event that knocks two valence structures
together just right to cause them to join; from a fully paired ORME that
experiences a partial uncoupling of its paired valences; and from other less
probable events. Varying degrees of "partiality" are possible, in steps of one
valence structure pair at a time, from all to none. (3) This is a bit like the
Cheshire cat, who gradually disappears, a little at a time, till all you have left is
the smile. Partial ORMEs are less stable; when the still exposed valence portion
of a partial ORME enters into a bond with another element, etc., this can
introduce other internal changes in the partial ORME which disrupt the
remaining Cooper pairs, causing them to decouple. Partial ORMEs having
chemical bonds to other atoms may eventually relax their Cooper pairing and
drop back into a normal metallic or chemical atom state.

There is no question but that many of the naturally occurring and manufactured
ORMEs David has been working with are, in fact, partial ORMEs. The natural
ORME materials found in the tailings and volcanic deposits Dave is using
contain or comprise a mixture of both completely and partially formed ORMEs.
The partially formed ORMEs components exist in varying levels of completeness
in their Cooper pairing. Of this raw material mix, the natural, partially formed
ORME atoms which still remained semi-uncoupled were able to bind with his
cyanide solution. That is why they were able to be caught by the chemical
leaching process of his tailings recovery operation, leading Dave to his path of
discovery. This was only possible, and only happened this way because partially
formed ORMEs still retain some of their metallic attributes. The fully formed
ORMEs do not act like metals at all, and do not in the least interact chemically
with the leaching process cyanide. If all the ORMEs in the tailings had been
100% Cooper paired, they would all still be sitting in those tailings piles, and
Dave would still be growing cotton; the cyanide would have never caught them.

It was only the incompletely or partially formed ORMEs, still weakly metallic,
which were picked up by the recovery solution. Fortunately however, the
partially formed ORMEs still form linkages with fully formed ORMEs through
their Meissner fields, even though the fields of partial ORMEs are weaker. And
so both varieties were carried along together by the recovery process. The partial
ORMEs reacted with the cyanide (using what free metal bonds they had left) and
were washed out with it. These captured partial ORMEs in turn dragged the fully
formed ORMEs along for the ride, pulling them by their Meissner fields like a
big dog on a leash, towing its owner. The 100% ORMEs are easy for these partial
ORMEs to pull around, since the full ORMEs offer no resistance at all. No other
chemical attachment forces can act on them (chemically speaking they are as
slippery as a greased pig), and so they obligingly follow their more chemically
attached partial ORME partners, being pulled along as if they were riding on ball
bearings.

Later, when the solution mix of partial and complete ORMEs is subjected to
further chemical separation methods, the Meissner leash connection between
them eventually gets severed. This is usually through the full ORME's stronger
attraction to the Meissner fields of other full ORMEs, thus breaking up the
partnership. The partials are eventually removed through their still semi-
functional metallic reactivity, as an "impurity" along with the precious metals.
This leaves behind the fully formed ORMEs, clogging up Dave's process
solution, and causing David and his associates so much bafflement when they
were found to resist all known forms of analysis.

Fully formed ORMEs will not react with hydrogen cyanide any more than they
do with aqua regia or anything else. Their main interaction with external world is
through their Meissner fields. In Nature, only other ORMEs, partial or complete,
speak their language. They all ride along together in a world of their own on the
waves of magnetic and electric fields that pass through the earth.
David's patent literature says the following:

"Further, the applications to which the ORMEs are directed will establish their
relationship to a specific T-metal by virtue of the manner in which the ORME
performs in that application as compared to the performance of commercially
available derivatives of the T-metal. An example is the performance of
commercial rhodium as a hydrogen-oxidation catalyst compared with the
performance of the rhodium ORME as used in a hydrogen-oxidation catalyst."

Partial ORMEs will still work, to some extent, depending on the degree of
partiality, in fuel cell catalysis, for the same reason they react with cyanide; a
consequence of the weakened metallic properties they retain. Dave has indicated
in his lectures that some elements in his patent are susceptible to nitric oxide
destabilization as ORMEs (specifically excluding gold, which of course does not
react with nitric oxide, even in its metallic form). This then, strongly suggests
that these are not 100% coupled ORMEs, in which he has observed this effect.
100% coupled ORMEs, regardless of element, will not react with nitric oxide.
They will not do anything in a fuel cell. Nor will they form bonds with cyanide,
acids, etc. By definition, a 100% ORME is one which has nothing -no bonds-
remaining but Cooper pairs, so it *cannot* react chemically; it has become
incapable of doing so. Only partial ORMEs may react with nitric oxide, or other
chemicals. To repeat myself, in 100% ORMEs, all the valence structures are
coupled and closed off.

Dumbbell group atoms of Table 1, with their 24 valence structures capable of

forming up to 12 pairs, thus have from 0 to 12 levels or stages of partiality (ie,
orbital rearrangement), with zero being a normal chemical atom.(4) Bars group
atoms, listed in Table 2 (and discussed later in the article), with 14 valence bars,
may form from 0 to 7 distinct levels of partiality.

Presently, I do not believe Dave or his associates are aware of the distinction
which exists between full and partial ORMEs.(5) It is obvious that
determinations as to whether 100% Cooper paired ORMEs are best suited to, and
should be supplied for, medical and philosophical uses are not possible as long as
there is no such awareness. Depending on the element, only a partial complement
of Cooper pairing may be needed to prevent heavy metal toxicity in the body. For
example, partial pairing, from a toxicity standpoint, is not even an issue for a
nontoxic element, such as gold. But fully paired ORMEs are more effective and
efficient in the intended applications, due to their stronger Meissner fields, which
is the number one active ingredient.
But I shall also suggest that a complement of partial ORMEs helps the body to
utilize ORMEs better. Perhaps, I shall suggest, the body may wish to have a
certain amount of certain partial ORMEs to act as tethers, to keep the 100%
ORMEs on a leash, at the place where they are needed. Perhaps the partial
ORMEs are a natural "handle", provided by Nature to help hold onto their more
slippery cousins. The fact that partial ORMEs that have first been reacted with
HCl are reported to be most effective, eg when administered by injection,
strongly suggests this is so to some degree. [These were partials or the HCl could
not have reacted with them.] Or perhaps partial ORMEs are a hidden danger,
waiting for those who ignore them to learn a tragic lesson from. Perhaps all these
things. The subject of partially formed ORMEs needs to be closely examined, in
the context of its implication for each of these elements.

The subject of partial ORMEs is the main reason I have decided to submit the
information in this article. There is a present lack of understanding here, and
hopefully these explanations will be plain and obvious enough to help remedy
this. I would rather that someone else had pointed out, but this hasn't happened.

Reasonably high yields of fully coupled ORMEs are obtainable by simply

processing monatomics in a finely divided form for a sufficient length of time at
optimum temperature and pressure in an inert gas atmosphere. The inert gas
atoms provide an effective spin-inducing collision mechanism. The lack of
external valencing of the inert gases results in more effective spin-inducing
collisions than for any other medium. Batch yield, or a determination of partial
ORME content can be gauged by screening a sample with aqua regia, fluorine,
hydrocyanic acid, or other powerful reactants, depending on the ORME elements
involved. If it doesn't react with those, it is certifiably highly Cooper paired, and
obviously safe for the body. There are no doubt other partially paired gaussian
distributions for each of the various elements, which may be certifed as safe
under less stringent criteria, but these determinations need to made in an
informed, intelligent, and demonstrative way. There will always be some partials
produced by any practical process. David's methodology, as gleaned from his
lectures, presently seems to include no provision or means to analyze, monitor,
regulate, or optimize the product ratios of these partial forms, let alone assay or
separate partials out according to the discrete levels or stages of their Cooper
pairing.

The stability (or actually, lack of stability) of the ORME states of some of the
other elements I speculate about in this article may render them unsuitable for
consumption. However, any ORME elements which are observed in any quantity
in Nature are arguably stable enough, or they would have long since disappeared
as such forms. I suggest that less stable ORMEs shall nevertheless be found to be
of great interest in other exciting ways.

Loading the ORME atoms with more energy than they can handle will also break
up the Cooper pairs. One way this can happen is as when Dave exposed the
material to direct sunlight. When overloaded, the links between the ends of the
valence funnels or bars burst apart like the joint of a water pipe when forced to
carry too much pressure. This is the structural observation of what happens in a
superconductor collapse, such as occurs with experimental and commercial
superconducting-ring energy storage devices, when too much energy is pumped
into the Meissner field. Most of these devices develop Type 2 superconductivity
using cryogenic temperatures, but the formation of Cooper pairs in the metal
lattices of low temperature superconductors follow valence behavior principles
related to those occurring in ORMEs.(6) The self-bonding of ORMEs has the
decided advantage of not having to contend with local lattice thermal jitter, and
thus functions at high external temperatures.

It appears that overloading is what is occurring in the electro-winning method

Dave uses in his patent literature to reconstitute the group VIII ORMEs into
metals. On this the patent states:

"ORMEs are transformed into their original T-metal by means of a chemical

bonding with an electron-donating element, such as carbon, which is capable of d
orbital electron overlap and "spin flip". When the G-ORME is chemically bonded
to carbon in an aqueous solution of ethyl alcohol under a specific potential,
carbon monoxide is formed and the ORME forms Au+(Au+, a black precipitate,
which under continued application of potential and dehydration reduces to Au+1
(Au-1, a metallic bonded diatom of gold. **This invention establishes that a high
potential applied to the solution forces an electron into the d orbital, thus
eliminating the electron pair.** The first potential, which for G-ORME is
approximately -2.2 V and for other ORMEs is between -1.8 and -2.2 V, re-
establishes the d orbital overlap. The final potential of -2.5 V overcomes the
water potential to deposit gold onto the cathode."

( **'s added.)

And again, later:

"An ORME can be reaggregated to the T-metal form using conventional wet
chemistry techniques, by subjecting the ORME to a two-stage electrical potential
to "oxidize" the element to the metallic form."
It seems that what is happening here, in the description of converting gold
ORMEs (or G-ORMEs, as they are termed) to metal, is that the partial ORMEs
are reacting mildly with the cyanide solution (the carbon referred to), dragging
fully formed ORMEs along in the process, just as I have described earlier as
happening for Dave's heap leaching process. The chemistry that is referred to as
going on is all associated with the weakly metallic aspects of the partial ORMEs
only. The 100% ORMEs don't participate in it. The part I have highlighted
(between **'s), is where the energy loading that breaks the Cooper pairing
occurs, coming from the electric potential in the cell, and Dave is specifically
recognizing that and pointing it out in a subtle way. The mistake is in failing to
understand that partially formed ORMEs are involved, and what their role is in
the process. This is not intended as criticism; the best present theories of atomic
structure which he is applying to the phenomena are simply not yet able to
provide many clues as to the true explanation of what is going on.

In Dave's lectures and in the 5/26/96 interview with binga, he indicates he uses a
chemical analysis on test materials, to determine their ORMEs content, which
appears to take several days of running to complete. This is a proprietary method
he has not given any details on, but has released on disclosure to certain parties
such as MIU. Without knowing the details on this, it is likely for the reasons I
have discussed, that Dave's analysis method (being chemical) acts on partial
ORMEs, though the process may well also accumulate full ORMEs, by Meissner
linkages, similar to the way his tailings recovery process did. I tend to suspect
that this is the case, even though it seems to not yet be apparent to Dave that a
distinction exists in ORMEs, between full and partial varieties.

In determining whether a particular element in the periodic table may exhibit

structural bistability, having both a stable chemical atom state and an ORME
state, there are several factors to consider. Everything about these ORME's
behavior is structural in nature. In order to form a true, complete ORME state, all
the valences must be paired up as Cooper pairs. Ideally (though not in practice)
only elements having a number of valence structures divisible by 4 can exhibit
ORME behavior: the valence structures divide into 2 opposite groups under high
spin. There must also be an even number of valence structures in each spin-
divided group in order to form Cooper pairs, so all the valences "disappear".
Hence the factor of 4. Element families which have a number of valence
structures that is a multiple of 4 meet this ideal, and form symmetrical ORMEs.
There are three atomic structural families among the physical elements that
satisfy this "ideal" criteria. These are called the dumbbell, octahedron, and
tetrahedron families by Leadbeater and Besant (viewed as monatomics), and
have 24, 8, and 4 valence structures, respectively. Gold, silver, and copper from
David's patents are from the dumbbell family. Mercury is from the tetrahedral
family.

All the other elements in David's patent are from another family shape, which
doesn't meet the criteria of having a valence structure count divisible by 4, but
manages to get around this (and very successfully) by utilizing an unbalanced
spin in forming ORMEs. This is the "bars" family, each element having 14
valence structures. These are called bars, as the valence structures resemble bar
shapes, radially projecting from the center of the atom. The valence bars are
(monatomically) disposed towards the 6 face centers and 8 corners of an
imaginary cube (the cube shape is not visible in the atom, but that is how the bars
arrange themselves). When bars elements form monatomics, they form (when
spinning) an unbalanced dipole, with 6 bars (3 Cooper pairing sets) grouped on
one end, and 8 bars (4 Cooper pairing sets) on the other end.

Bar Group Atoms

Besides the dumbbell and bars families, there are also atomic families with
shapes resembling octahedrons, cubes, tetrahedrons, spikes (shaped similar to
carpet tacks), and 6 pointed stars. There is a separate group for hydrogen. I will
not discuss these groups except for briefly mentioning a few elements from some
of them, that appear to have potential for ORMEs formation.

 Table 2

"Bars" group monatomics, predicted to exhibit superconducting ORME states.

This group has the highest thermal-collision statistical probability to form an
ORME state, based on number of possible spin planes, resulting in their having
lower average temperature transition points.
Iron

 Cobalt *
 Nickel *
 Ruthenium *
 Rhodium *
 Palladium *
 Osmium *
 Iridium *
 Platinum *
 Plutonium
 Americium
 Curium
* Already specifically named in David Hudson's patent literature.

The "bars" family, followed by the "dumbbell" family have more possible spin
planes than the "octahedral" and "tetrahedral" families, which can all (potentially,
-even the cubics) form complete sets of Cooper pairs. This gives bars and
dumbbell group elements a statistical advantage, by reducing the number of
thermal collisions necessary for a successful valence rearrangement transition.
This seems to explain why such a high percentage of these elements (bars group
in particular) occur in Nature as ORMEs, and hence why the majority of the
ORMEs David has discovered to date are in this category. The bars group have
long extended valences which bend together to couple relatively easily, and the
large number of them means the required angular deflection (the angle between
the valence bars) is comparatively small compared to the octahedrons, cubics,
and tetrahedrons. All these factors tend to make the bars family ORME states
highly stable and easily formed.

On the other hand, the unbalanced high spin state of bars group elements make
them distinctly more susceptible to the formation of partial ORMEs. This
conclusion also appears substantiated in the higher relative ratio of partial to
complete bars family ORMEs, as found in Nature. Since these elements are the
largest constituent for ORMEs in Dave's volcanic mineral deposits, it is
unavoidable that the production process will generate large amounts of partial
ORMEs, with or without awareness of the fact.

The dumbbell family has an infinite number of spin planes, but they are not
uniformly distributed, being all planes which make up the set that include the line
of the major axis. In other words, if you imagine a spin plane which includes the
line of the major axis, then rotate the spin plane using the major axis line as a
pivot, every angular position the plane can have, as it rotates in this manner,
represents a possible spin plane; there are an infinite number of such spin planes
in 2PI radians. The bars family, on the other hand, while actually having no
"ideal" spin plane possibilities (its valence structures are not multiples of 4) is
nevertheless statistically more likely to benefit from a particular collision. Its
'6+8 arrangement' unbalanced spin plane combinations are evenly distributed,
and valence positional variance, plus the tolerance window for collision angles,
eliminates nearly all non-ORME-forming collision "blind spots". As a result the
bars family enjoys a much greater total number of potentially transitionable
thermal collision vectors.

Among the octahedrals, titanium, and zirconium appear to have potential for
ORME formation, based on their structural proportions. Titanium and zirconium
are oddities within this family, each having 4 long narrow valence arms which
bifurcate at the very ends. They have a strong affinity for carbon, as their valence
terminations are identical in structure to that of carbon's valences. Most of the
other octahedral elements (and more so with cubics and tetrahedrals) have short
broad valence funnels, which would have a hard time of it, trying to reach around
to each other to form a Cooper pair coupling. Of the other octahedrals, lead looks
like it would be the next most likely possibility; its valence structures are a little
longer, proportionately.

Once the valence structures of an atom have been self-coupled into Cooper pairs,
the atom may (or may not!) remain this way. Upon fully coupling, the valences
have a strong mutual affinity to staying paired; after all, it is coupling to itself,
and so the compatibility factor is pretty high. Many elements highly prefer being
in the ORME state.

Some of Nature's elements form extremely stable and tightly clenched ORMEs.
Other elements simply cannot, or else barely can, bridge the distance to make the
connection, even when spinning enormously fast. These latter cases are much
less stable as ORMEs, though they may still form under appropriate conditions.
Elements having stubby valence structures must be spinning much faster to
deform the valence positions, than elements with longer more gangly valences.
Greater "at rest" separations between valences means that more deformation must
take place before Cooper pairing can occur. Elements with platonically shaped
monatomics having fewer faces are more disadvantaged in this way. Elements
which are less structurally disposed to forming an ORME state will require
proportionately higher collision temperatures, to get to the coupled
superconducting condition, once they have been disaggregated into monatomics.
Consequently, even though the elements of certain structural families may
potentially form ORMEs, some of them, such as many of the octahedrons,
cubics, and especially the tetrahedrons, can only do so under extraordinary
conditions. Even then, once formed they may not have sufficient stability to
remain rearranged when their spin drops below a certain rate. The restoring
forces trying to pull the valences apart will become stronger than the self-
coupling forces, if the atom's spin rate drops too low.

Of the cubics, some of the heavier elements, most notably tantalum and lutetium,
have relatively long valence funnels and may be able to successfully form
Cooper pairs under suitable conditions. Like the bars family, these cubics would
have to enter an unbalanced spin in order to form ORMEs. That is, the cubic
elements must spin so that there are two valence funnels (1 Cooper pairing set)
on one end, with the other four valence funnels (2 Cooper pairing sets) on the
opposite end of the spinning atom, in order for complete pairing to be possible.

Mercury is a special case, coming as it does from the tetrahedral structural

family, with only 4 possible spin planes (2+, 2-) which might form an ORME
superconducting state. How is it that mercury has managed to have this capability
and be discovered already? One might think that the tetrahedrals would be among
the least likely families from which would appear a stable ORME. To yogic
vision, mercury (like Ti and Zr) is seen to be a bit of an oddity, compared to
other elements in its family. It has some major subatomic structures in common
with gold, and while showing the expected structural family features, it is oddly
proportioned quite differently than it might be expected to be as a tetrahedral
family element. These nonconformities enable it to deform more than other
tetrahedrals with the same amount of spin, allowing it to rearrange and achieve a
superconducting state more easily. When it superdeforms, it winds up looking
more like a gold atom that has two big valence structures on each end, rather than
like the other tetrahedrals.

Vaporizing mercury in an inert gas atmosphere of sufficient temperature and

pressure will form Hg-ORMEs. This is an effective means of forming ORMEs
for any element. Seeding this process with some already formed ORMEs will
help catalyze the transition. Occasionally this even occurs in a minor way in
mercury vapor turbines, but has not been recognized. With only four valence
structures, there are only three free state possibilities in the case of mercury:
metallic (chemical) atoms, 50% partial ORMEs (1 set of valence structures
paired), and complete ORMEs (all 4 valence structures paired, into 2 sets).

In David's patent literature, he uses this process in the case of gold:

G-ORME was prepared from metallic gold as follows: ... (19) The monoatomic
gold is placed in a porcelain ignition boat and annealed at 300 C under an inert
gas to remove hydrogen and to form a very chemically and thermally stable
white gold monomer....

This step appears to say that the 300 C temperature and inert gas are mainly there
in order to facilitate removing the hydrogen. The description might leave one
with the impression that if the hydrogen could only be removed in some other
lower temperature manner, perhaps the process would still succeed, and that the
ORMEs form spontaneously. Well, they do, in a manner of speaking, but it is
because of the high temperature, and the presence of the inert gas that the
"spontaneity" happens. As soon as they become monatomic, their exposure to
these conditions gives them an excellent opportunity to experience thermal
collisions, knocking them immediately into the high spin state that leads to their
forming into Cooper paired ORMEs. The environmental conditions are the most
important parts of the equation. Though he has mentioned using welding grade
argon, David says nothing in his patent about the pressure he is doing the
annealing at, and has not mentioned in his lectures whether he has experimented
with gas pressure as a variable. The gas pressure is not a critical factor to success,
but it does impact the process rates.

For each particular element, there shall be found to exist a range, or window, of
conditions of pressure and temperature, depending on which inert gas is used as
the atmosphere, which will result in ORMEs (and partial ORMEs) formation.
Besides the associative ORMEs formation process, there is also a dissociative
process operating simultaneously. As in all other thermally driven reactions of
this nature, the rates of both processes increase with temperature. Optimum
ORMEs formation will occur under specific conditions, and may be arrived at
computationally, but these may also be determined empirically (simple trial and
error) for specific cases. Once the process has remained at some fixed conditions
long enough for the rates to stabilize and reach equilibrium, no significant further
change in product quantity will occur. In ALL cases, the process result will be a
combination of complete and partial ORMEs, to some degree. The object is to set
up the process to maximize or peak the full/partial ORMEs ratio for each
element.

Remember the 300 second spectroscopic burn David refers to in his lectures? I
suggest the following be considered as an explanation of what was happening
there, in illustration of how these two process rates I've just discussed operate. As
a premise, I believe the samples Dave was using in these spectroscopic
experiments were most likely 100% paired ORMEs to start with. The sample
material (I am supposing) had inadvertently been selectively concentrated that
way (as 100% ORMEs), by his tailings recovery process, as explained earlier. I
think he may have had quite a bunch of this material around, that nearly all the
partials had been removed or excluded from, as a side effect of his refinement
operation, and that this was where the materials he was using at the time came
from. But any other 100% source he may have had would produce the same
results. The spectroscopic arc is inert gas shielded, and very hot. Just like what
I've described as an efficient ORMEs formation process, and just like what is in
Dave's patent for making ORMEs.

What do you suppose would happen to 100% ORMEs, under those conditions?
They obviously cannot follow the association process function, since they
already are all 100% paired. The only thing they can do is begin to dissociate,
once the temperature drives the function high enough. Dissociation will continue
until the partial population count (within a particular minute volume in the arc)
becomes high enough that the two rates, associative and dissociative, come to
equilibrium. Dissociation will be the strongly dominant process. ORMEs
vaporized off the sample will be turning into partial ORMEs, as a dissociative
process, as collisions with inert gas atom break their Cooper pairings.

Dissociation for the first element (palladium) seems to commence at 70 seconds

into the burn. At that time, the ORMEs start vaporizing. As soon as the ORMEs
leave the sample's surface, partials begin to form, and spectral lines begin to
show up. Only when ORMEs vaporization and dissociation starts, do platinum
group spectral lines appear, those metal lines being emitted by the unpaired
portions of the newly-dissociated partial ORMEs. The dissociation, is occurring
in an ordinary manner, by means of thermal collisions between the ORMEs and
the hot inert gas atoms occasionally breaking some Cooper pairings in the
ORMEs.

When Dave stopped the burn at 68 seconds, thinking (in those early days) that he
should then have only metals left, he had only succeeded in further purging his
100% paired sample of extraneous impurities of lower boiling point. No
transmutations were occurring, or are needed to explain the results. Only
ordinary associative/dissociative reactions, acting on some very unordinary
orbital arrangements.

Later, when the sample was analyzed, no evidence of metals could be found in it.
Why? Because the sample was still 100% ORMEs, as it had started out. The
dissociation was occurring among the ORME atoms in the arc, just where you
would expect it to be occurring, not in the relatively cooler sample body. These
vaporized and Cooper-dissociated partials, after emitting their spectral lines, get
carried off in the draft of the inert gas. So no metals (or partially metallic
ORMEs) would be expected to remain in the sample. Had the arc vapors been
trapped and condensed, a small quantity of weakly metallic ORMEs would have
been found there. What if the original sample had not been 100% ORMEs, as in
my premise? That seems improbable to me, as the unpaired metallic portions of
the partial ORME atoms would then have shown up in the quantitative chemical
analysis of the sample, both before and after the burn.

In his lectures, Dave often speaks of how the atoms are undetectable, don't match
any known spectral lines, defy analysis, and can't be dissolved in aqua regia.
Then in almost the same breath, he tells of seeing platinum group spectral lines
though no metals can be found, that the material works in fuel cells, can be
analyzed in things like Acemannan, carrot juice, and cow brains using chemical
means, and recovers in his cyanide to the point of clogging things up. Now it's
chemically reactive... now it isn't. These are incongruous statements, and I sense
he is uncomfortable with them. I believe many others sense a problem here, too,
though they haven't been able to put their finger on it. I have tried to explain here,
that the seemingly dual personalities of this stuff are not at all as contradictory as
they seem on the surface. There is an explanation. It just requires a deeper
understanding of what the materials are doing, way down there in the tiny world
of Anima. When you look very, very closely, and see that Cheshire cat smiling at
you, it all makes sense. I hope some of Dave's friends will take this to him. This
is what he needs to know.

At some future time, it may be possible to comment further on these interesting

topics.(7) I invite forum subscribers to pursue this area of study as a potentially
fruitful direction for new discovery. Science has indeed come a long way. But do
not rest just yet.

About the author:

back

Gary describes himself as a kundalini awakened American engineer. Gary is a

single white male in his mid 40s who works as an engineer with a very big US
company. Gary has "a background in physics, electronics, and knows a few
things about chemistry and the elements."
 FOOTNOTES

(1) SO CALLED MONATOMIC ATOMS ARE

DIATOMIC
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To state this plainly, the "monatomic" ORMEs in Hudson's patents are, in fact,
diatomic. It is also clear to me that most of these elements do not exist stably in
an isolated, monatomic state, but quickly disintegrate when forced by the Will to
assume that condition, although they are perfectly stable as such when in
chemical combinations.

(I chose to refer to the elements in my original article as monatomic, prefaced by

an explanation of why I was doing so (quoted above), so that anyone sufficiently
interested in studying the article material carefully would note this and take it
into account in understanding the rest of what I wrote in the article. I knew full
well that this brief note would be lost on most who would read it, but I also knew
that those few who would read it very carefully, which should include any
scientists, would pick it up.

This was done in the hope of making the content of my discussion at least appear
to stand on familiar ground, and so be more acceptable to David Hudson, et al,
through a commonality of sorts in terminology.

My taking this approach also considerably reduced the amount of explanation I

would have had to include, to make the subject intelligible to everyone, who have
been (in the absence of anything else being available) only familiar with ORMEs
theory as propounded by David Hudson. Even so it was a large, rather lengthy
article.)

For diatoms, the number of valences will obviously always be even, ie divisible
by 2, and so Cooper pairing is freed from the objection that atoms with uneven
numbers of electrons could not be completely Cooper paired. The valence
funnels "rotate" (as a consequence of the motion of the particles forming them) in
alternating senses, as viewed in a sequence going around the atom (e.g. a gold
dumbbell - See below). It should be clear that two adjacent funnels, one rotating
clockwise, and one counter-clockwise, will coincide in rotation if the funnels are
distorted into a loop so that the mouths join. They then form a continuous
rotating tubular vortex. This is the physical action corresponding to two electron
spins joining and canceling to form a Cooper pair. A similar effect occurs in
metal lattices at cryogenic temperatures, except that funnels join between
neighboring atoms, rather than on the same atom for an ORME.

Describing ORMEs as monatomic is still justifiable in a sense (albeit technically

inaccurate) since the ORMEs state is still the smallest atomic level division that
most of those elements remain stable and intact at when isolated.

I will also suggest that, (if you will expand on what I have written in my original
article) it should then be obvious that, in addition to the electromagnetic flux
carried by the closed loop funnels of ORMEs, other energies may (and do) also
flow through these circuit paths, and may (and do) do so in parallel with
electromagnetic energy. Since this flux, in moving around this atomic-level
closed circuit, passes through the very heart of the atom, it should not be at all
surprising, and should indeed readily suggest itself to anyone reading my article
and thinking about it that the nuclear strong and weak forces may also participate
in this flow (they do). This ORMEs circuit is one of the few cases in Nature in
which these internal forces may thus develop macroatomic fields, extending
beyond the outer envelope or perimeter of the atoms, and each of these forces
(and others still more esoteric) generates a field, which, like the electromagnetic
Meissner field, has unique properties, according to the laws governing each of
the underlying forces generating those distinct yet co-spatial fields. Like the
electromagnetic Meissner field (which Hudson and others have erred in rushing
to suppose to be the same as the aura) each of these may vary in the amount of
energy they contain, as a function (by specific type) of their flow in the circuit.

Speaking now, in stricter use of the concepts 'monatom' and 'diatom', I offer
some further comments which may be of interest. This is in regards to Brown's
gas.

Diatomic hydrogen is observed to be an ovoid, containing two triangular

"monatoms", each composed of 3 quarks (having 3 anu each). The triangular H
atoms are not identical in the types of their constituent quarks; each hydrogen in
the diatom has the same mass, but differs from the other as a consequence of
their quark components. When dissociated into monatoms, the two separated
hydrogen atoms are stable (ie do not spontaneously dissociate further) but I
would suggest that they would prefer to be paired.

As monatoms, they loosely associate with free particles, forming something like
the atomic equivalent of the double-layer of continuous-phase charge which
forms around colloidal particles to neutralize their remaining charge; it is a less
defined layering for a gaseous continuos phase than for a liquid as far as colloids
are concerned, and this (gas case) is a close analog of what happens in the atomic
state, where the atomic-level vacuum is the continuous phase, and the myriad of
loose and undifferentiated subatomic particles are the matter that the layers are
(dynamically) formed from around the monatoms, as a loose aggregate.

Diatomic oxygen is also an ovoid, containing two spiral shapes, looking very
much like helices of 5 turns each, with each being "wound" in the opposite
direction. Like the hydrogen, each monatom of the O2 diatom is dissimilar, being
more positive or negative, respectively, from its mate. Oxygen is also stable as a
monatom, but also prefers to be paired. It too can use loose matter to neutralize
its monatomic charge, but is entirely much less happy about the situation.

Three such oxygen monatoms may unite to form ozone. These will either be +-+,
or -+-. The helices arrange with their axes parallel, and triangularly spaced as an
isosceles, when viewed end on. Leadbeater noted that the positive variety of
ozone (+-+) tends to rise, though no tendency to move either up or down is noted
for the negative variety. This is further confirmed in that for observations
performed at high altitudes, nearly all the ozone found in the atmosphere is of the
positive type. In any practical ozone generation system, equal amounts of each
type will be formed. While I have not tried it, it appears that it should be possible
to separate these according to species, once formed, by placing ozone gas in a
potential gradient (- on the upper electrode surface) that draws the two types
apart. Ozone that is thus separated by species is substantially more stable and far
less explosive in nature than ordinary heterogeneous ozone.

Oxygen is a very energetic and active element, and is capable of mediating

several type of energies, some of which are not as yet recognized by Science.

(2) OTHER FORCES ARE AT WORK

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There are several forces, flowing between and linking individual anu into
associations of the different subatomic particles, and these forces are seen to
originate from, and return to, higher dimensions. They well-up and later
disappear, in a source/sink fashion, associated with anu forming the ends of their
flow paths in our 3 dimensions. Several types of distinct forces transit along the
different coils or whorls of the anu themselves. Still other types of forces act
through larger particles and atoms, and linking monatoms (for instance) together
into diatomic arrangements. Describing all the forces which can be observed at
work is a real challenge. It will take a great deal of work to separate and quantify
these forces, to reduce them to physics.
As far as I can tell, none of the high energy experiments we can perform actually
"create" (or destroy) matter. But this statement must be qualified. Under
appropriate conditions, particles already existing in the atomic-level background-
vacuum, but still too small (or for other reasons) to be detectable by us, may be
caused to thereby associate, and this association forms a larger particle, which
*is* detectable. This may make it appear that an energetic photon (for example)
was transformed into matter, whereas the photon actually did no more than
provide the energy of association for number of (unseen) particles that were
already present.

Likewise, the mass-to-energy losses that are observed, to balance the equations in
nuclear disintegrations, etc., are also related to the binding energy of particle
associations. The flux between anu is a stream of tiny "particles" (though these
are not hard "particles" any more than the anu are). These tiny particles each have
a minute mass. The mass of this binding energy stream is a function of the length
of the stream; larger particles typically have longer binding streams, since they
are composed of more anu. It is the mass represented by the inter-anu energy
streams, which represents the mass change in (at least many of) our nuclear
equations, apparent as energy. The anu do not change mass, and both types are
the same. The larger particles of matter we observe thus have masses which are
integer multiples of the anu mass, plus however much mass is represented in their
linking, or binding energy stream. There are a number of different ways (lengths
of stream paths) any particular number of anu may be linked. This general
statement on atomic and subatomic particle mass quanta does not, of course,
apply to particles smaller than one anu, such as electrons, photons, etc.

If one takes an anu, and uses the Will to take it apart and completely dissociate it,
this can be done, but as soon as the Will is released, the anu reforms again. It is
like taking a piece of slinky spring, and unwinding it by stretching it out and
pressing it flat on the floor with your hands. But as soon as you let go, it pops
back. The individual anu are each (one discovers) direct force-aspect
manifestations of a higher Will, which generates and sustains all the matter in the
Universe. It is... in very fact, the "Force", which is with us. This Force originates
from a dimension far higher than we (certainly, I) can reach while still clinging to
corporeal form. When we try to conceive of the stupendous number of anu,
throughout all matter of the visible galaxies, which are being held in existence in
such manner, the extent and scope of that Will is truly mind numbing.

If you are interested in gaining insight into the forces at work in ORMEs
systems, you might wish to read a book, first published in 1758, by a Slavic
Jesuit monk named Roger Joseph Boscovich. Its title is "A Theory of Natural
Philosophy - Reducing to a Single Law All the Forces Which Exist in Nature"
[Theoria Philosophiae Naturalis - Redacta ad Unicam Legem Virium in Natura
Existentium]. I believe it is still available from MIT Press, where I got a copy
about twenty years ago.

(3) MONATOMS SLOW IN DISCRETE STEPS

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According to a reference in Scientific American [October 1991, Spin Cycle - The

Spectra of Super Deformed Nuclei, by Philip Yam] from David Hudson's Dallas
presentation:

"A spinning superdeformed nucleus slows down in discrete steps, each time
emitting gamma rays, or highly energetic photons. The emissions produce a
characteristic band of energy spikes all spaced equally apart. The surprise: the
spectra of some different superdeformed nuclei were almost identical."

I suggest that these discrete stepped emissions are the result of rupturing the
valence circuits, one pair at a time, releasing their circuit energy (as an emission).
Since the emission energy is a function of the energy stored in the valence circuit
(and so not constant), when they are observed, as reported, to be the nearly the
same for different elements, then this is only because the atoms were all charged
in their circuits to nearly the same energy level; this is most probably a
consequence of conditions imposed by the instrumentation environment that the
atoms were placed in, and were observed under.

Some of the elements, though capable of forming ORMEs states, are unstable as
such unless kept spinning quite rapidly, and would drop out of the ORMEs
condition as their spin decreased. The changing effect on atomic moment of
inertia is a result of the valence funnels deforming by swinging out into the super
elongated shapes, and the same is true in reverse as they release while spinning
down. This tends to keep angular velocity (spin rate) from changing as it would
normally be expected to, as angular momentum is added or subtracted. If an
observer using conventional methods is unaware that this is happening, it can
lead to incorrect conclusions about their moments of inertia.

(4) ELECTRON ORBITAL MODELS DON'T APPLY

HERE
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Although all elements with the dumbbell structure have 12 pairing levels because
each dumbbell has 24 funnels, and these combine by two's to form 12 pairs, this
has little to do with the number of electrons (and positrons) inside the atom.

Do not try to overlay the orbital theory of the atom, onto yogically observed
*real* atoms. You must recognize that while the orbital **model** explains a
great deal, it is, in the final analysis, only an analogy of reality, and like all
analogies, breaks down eventually. Comparing its artificial constructs to real
atoms can be confusing.

In reality, yogically observed atoms do not have electron orbitals. They are not
constructed as we were taught in school. They do not have a single central
nucleus. They have instead multiple "nuclear" concentrations within the atom,
and these move about rapidly. That is the basis for the nuclear orbitals which
Science has recently begun to appreciate. Atoms are built differently than current
theories predict; the forces which hold them together and maintain their shapes
are as yet little understood by modern science. However, Science *has*
observed, cataloged, measured, and named many of their component particles.

If you will study the drawings of the atoms in the two references cited at the
beginning of this article, you will see that the funnels and bars are formed by the
motions of the groups of anu inside them.

The atom is observed to be built from anu, and the quantized energy-particle flux
between anu. Even the anu are essentially made of these energy-particles.
(Leadbeater has described how this is only an approximately correct statement,
so I won't go into that; see OC 3rd ed, p.19-20). Each anu is composed of the
*equivalent* of 49 smaller particles, on the first level.

The lines of force between the anu, are also streams of tiny particles. These
particles are the equivalents of electrons and positrons of conventional physics.
The positrons are basically the reality behind the "holes" of conventional solid
state physics. Their presence and number within the atom comprises the total
mass of the atom, both as (by equivalency) sub-components of the anu and as
energy streams.

I hope it is clear that each funnel or bar does not represent a single electron, but
only a valence. The valency arises as a result of the algebraic sum of + & -
charges in them, and is much less than the total charge present. Hence sodium
does not have 11 electrons and lawrencium 103 (they do in modern theory, but
not in real atoms). They each have many thousands of electrons and positrons.
Those who wish to go into this further (the electron as the basis of 3 dimensional
atoms) might hunt down a book titled "The Electron Theory of Matter" by Owen
Richardson, published in 1914 by Cambridge University; 612 pages. Owen
shows quite elegantly how all atomic phenomena can be derived, based on only
electrons. Very good book. Pity no one reads it anymore.

(5) PARTIAL ORMES

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In my opinion, the ORMEs David Hudson and others are working with under the
blanket term "ORMEs", are predominantly partials of various levels, and in most
cases high order partials, >65% paired, with some 100% species also present.
This somewhat arbitrary division includes 4 partial levels of from 8-11 Cooper
pairs for dumbbells, and two levels of from 5-6 pairs for bars-family elements.

Partials rapidly become difficult to distinguish, using ordinary methods, from one
level of pairing to the next, and from completely paired ORMEs, as the pairing
complement increases. That is, they behave like 100% ORMEs under most
circumstances. So the behavior of 100% ORMEs is "typical" of the ORME mixes
David Hudson is working with, composed of mostly high order partial and 100%
ORMEs. I said the color (whether they are white or not), does not particularly
matter, because high order partials are also white (& fluffy, recalcitrant, etc.), and
are in most ways like 100% ORMEs. However, I remain concerned about the
potential for long term biological effects of certain partials, other than gold.

For your convenience, the following table may help to explain what is happening.
I have arranged bars element pairing to approximately match up or correspond to
pairing levels of the dumbbell family. This table simply depicts the paired to
unpaired funnel ratio, as a percentage.

Dumbbells (24 funnels) Bars (14 bars)

ORME ORME
# Pairs # Pairs
Percent Percent

12 100.0 % 7 100.0 %
ORME
11 91.7
^
10 83.3 6 85.7
^
9 75.0 5 71.4
^
8 66.7
^
7 58.3 4 57.1
^
6 50.0
^
5 41.7 3 42.9
^
4 33.3
^
3 25.0 2 28.6
^
2 16.7 1 14.3
^
1 8.3
^
0 0.0 0 0.0
Metal

This table should not be interpreted as describing the degree of manifestation of

ORME properties, which are usually not in proportion to pairing complement,
but are rather nonlinear for many properties. The table only shows ORMEs
structural stages.

With fewer pairing combinations, bars group elements are "lumpier" in their
partial steps, while dumbbells have a fairly fine gradation of partial ORME
stages or steps. There are also differences in behavior, for the same number of
pairs, depending on where the pairs are, relatively speaking, on a particular
partial ORME atomic specimen.

100% ORMEs are definitely scarcer in Nature, and in man-made processes

designed to create them, than are their less-perfect partial relatives. Perfection is
certainly not unheard of in Nature, but it is comparatively rare. It is the pinnacle
of achievement, not the rule or the norm. How could it be otherwise? 100%
ORMEs do not constitute anything like a majority fraction in Nature's stores of
these elements, though they certainly are an important fraction, whose magnitude
varies from element to element, and which Science will soon quantify, once it
learns how to detect them.
With understanding of how statistical processes function, and recognizing how
parallel thermal rate functions (referring here to internal geologic processes) of
association and dissociation work, as I describe elsewhere in this article, it seems
hard for me to see how someone could draw any other conclusion.

Though I believe David Hudson and company are certainly screening out (e.g. by
acid dissolutions, etc) most of the lower order, more metallic-like partial species,
and this increases the relative concentration of 100% ORMEs (and high order
partials) in their preparations. But again, remember that acid solubilities of
partials cannot be categorically defined, based on pairing alone, since it depends
strongly on the energy flowing in the paired valence circuits. More energy flux
brings out their ORME-ishness, and increasingly screens their remaining
chemical and metallic properties.

If the association and dissociation processes were symmetrical throughout the

ORMEs pairing range, this would result in a gaussian distribution, or a bell
curve, centered around 50% pairing, as the highest incidence of occurrence. But
there are non-lineraities that perturb this.

David Hudson's comments notwithstanding, it is noteworthy that partials

participate in metal clusters. They fit a bit awkwardly into the lattice, but they
still behave (partly) as metals, depending on their pairing levels. That is why
Hudson found that commercially prepared metal standards have a second
spectroscopic reading, which shows up late in the long burn, just like his native
ORMEs.

David Hudson has stated that ORMEs don't form metal-metal bonds, yet offers
no explanation for phenomena like this, other than pointing out the obvious
implication, that it is due to the presence of ORMEs. Many low order partials
exist in and among metals, rather than as monatomics. They might be termed
partial-ORME-to-metal alloys. They can markedly alter the properties of the
metal, when present in significant amounts. When partial ORMEs are
understood, their occurrence and effects in metals should come as no surprise.

An individual, free mon-atom may drop to a 0% ORME state (by any of a

number of mechanisms), so that it technically becomes an ordinary
metal/chemical atom. But unless it joins an aggregate of metal atoms, it remains
susceptible to collisions and other events, which now in all probability would
knock it back into some level of ORME state. Joining a metal cluster is an
unlikely event, since it has been existing as a free and independent mon-atom,
and is not likely to be close to a metallic cluster. So being a mon-atom is,
statistically, a hard habit to kick.
It is more likely that a metal atom will get knocked off its cluster, and become a
mon-atom (ORME or otherwise), than the chance that a metallic mon-atom will
get attached *to* the cluster. That is because mon-atoms are free, and subject to
dispersive forces, so concentrations of them tend not to develop. So there is a
distinct statistical bias, moving metallics into the ORME state. The rates of these
opposite processes (in Nature) only equalize when there are substantially more
ORMEs than metal in the region around a state system interface at which such
processes are active.

Within an ORME population, where all the members are monatomic (including
0% paired metal atoms), there are also important non-linearities. For internal
geophysical processes, the process rates that drive population distributions are
**typically** such that the rate of Cooper pair formation and the rate of Cooper
pair loss, do not balance until a population average above 50% pairing is reached.
There is at least one identifiable factor at work accounting for this. It is that
pairings, once formed, are not only stable (referring only to dumbbell and bars
elements), but tend to increase in stability as a result of energy subsequently
building up and increasing, flowing through the closed valence circuits. So it
typically takes less collision energy to form a pair, than to break it apart, once it
has existed for a while. In breaking apart, the acquired energy of stability is
sometimes all released, or may be absorbed to varying degrees by other circuits
that may be present.

A second factor is that, once an atom has been knocked into a high spin state and
some pairs have been formed, these tend to be (obviously enough) on opposite
ends, so the bar or dumbbell is more elongated in aspect than it was before. This
increases the likelihood that a subsequent collision will knock it into a spin on the
same spin plane again. This is particularly true for dumbbells, which tend to have
their population peak at a higher number of pairs than do bars elements.

In Nature, populations of most geothermally formed ORMEs elements peak at 8-

10 pairs for members of the dumbbell group, and 4-5 pairs for elements in the
bars family. Common ORME configurations for many bars elements, is for the
ORME to have two pairs on each end, ie roughly opposite each other as head and
tail, and 6 free valence bars sticking out in between, around the "waist"; or else
three pairs on one end, two on the other, and 4 free valence bars in between.

These pairing level distributions are sufficient to give those elements "ghost
gold" properties, making them somewhat detectable, though not recoverable as
metals by ordinary methods, since they won't coalesce into the metal lattices,
characteristic of their respective elements. That is about the level (coming
straight from natural materials) that Hudson experienced, when his dore' button
would shatter like glass when hit with a hammer. As solids, their abnormal
valence structures don't produce a regular symmetrical lattice, and that is why
they seem like ceramics. Low order partials are essentially glassy or amorphous
in their micro-structure.

So 100% ORMEs (within natural monatomic populations) are not as rare as

metal mon-atoms, but still by no means dominant.

As I have mentioned, there are ways of precisely separating each pairing species
from one another, and also similarly paired species of related elements. David
Hudson and company are presently unable to do this. Actually, hardly anyone
working with ORMEs at this point even understands or admits partial pairing
exists as a feature of atomic structure, and so experimenters don't even know
there is anything **to** separate.

The potential hazards of partial ORMEs should not be under-estimated. Low

order partials are inherently dangerous when taken indiscriminately, by those
oblivious to the very real effects of their remaining metallic factors. Gold, even
when metallic (let alone in its partial forms), is non-toxic, so less caution is
necessary. However, when someone is suffering from a life-threatening
condition, then it is sometimes necessary to take extraordinary measures, and to
weigh relative risks.

(6) SUPERCONDUCTIVITY AND ORMES

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While I have previously referred to ORMEs as exhibiting type II super-

conductivity, this is only superficially correct, and ORMEs (in my opinion)
deserve to be given a separate, distinct classification, such as type III.

In conventional type II Superconductors (SCs), for temperatures within their

superconducting regime, as the external field is increased, the Meissner-
generating currents flowing through the SC (necessary to expel the external flux)
reach a level at which superconductivity in the sample can no longer be
sustained, and superconductivity is destroyed. I have described this event as a
wholesale rupturing of bonds between valence funnels of adjacent atoms in the
lattice. Removing the external field (and hence the current) results in reforming
the Cooper pair bonds, and restoration of superconductivity (assuming the
sample temperature hasn't changed).
However, in the case of ORMEs, superconductivity (transmittance across the
sample body) occurs through Meissner field linkages between individual ORMEs
atoms - an entirely different mechanism. This is true whether the ORMEs are a
continuous body, like an ORMEs glass (small ORMEs-glass particles are merely
small examples of continuous bodies), or an aqueous dispersion. (Of course,
observing superconductivity in aqueous phase dispersions is not even a
possibility for other SC materials, because they are cryogenic.)

At Hc2 (Hc2 is the energy field level at which superconductivity ceases) for
ORMEs, the external Hc2 field only succeeds in establishing itself *between* the
ORMEs atoms, suppressing, or causing their individual atomic-level Meissner
fields to withdraw or be pushed back sufficiently so that the Meissner-mediated
energy transfer between atoms is blocked, interrupting macro-current flow in the
sample. To restate this, the macro Meissner-generating currents, which act to
expel an external flux from an ORMEs body, flow *between* ORMEs, not
*within* individual ORMEs. The function or role of the ORME atom is to
establish the macro-current *path* (via a continuous chain of Meissner fields),
not to produce the expelling current itself. It is, in fact, a DOUBLE-NESTED
system of superconductors: the macro body superconducts via Meissner field
linkages, and within that the individual ORMEs each superconduct on an atomic
level through their individual closed Cooper pair circuits.

An individual ORME atom in such a population is not much affected by the

presence of an Hc2 field, even despite its stopping of macro-current flow in the
sample body. The ORME atoms' own Meissner fields are only moderately
changed at best; they only must scrunch up a bit, so as to make room for the
external Hc2 field, which is now passing between them. The currents in the
ORMEs atomic circuits thus do not change very appreciably, since most of the
external flux passes around (between) them.

This leads one to the conclusion that Hc2 for ORMEs is not a constant (though
unlike type IIs, it does not depend on temperature). Instead, for each element, it
depends (primarily) upon the energy contained in the Meissner fields of the
individual ORMEs (I am also assuming the ORMEs as being arranged at their
preferred atomic spacings). The strength of these individual atomic fields
ultimately determines how much external field will be required to force them
apart, and supplant them from their inter-atomic connections. If the Meissner
fields are pumped up (or conversely, drained down) and the Hc2 measurement
experiment is tried again, a different value for Hc2 will be found.

Hc2 for ORMEs is still defined as the external field which destroys super-
conductivity in the macro-body of the sample. On the surface it seems the same
as the definition for type II SCs, despite entirely different mechanisms at work,
and despite ORMEs' temperature independence. Furthermore, like type II SCs,
removing the external field restores superconductivity in ORMEs bodies. (The
ORMEs themselves never lost their atomic-level ORMEs circuits; if they had,
removing the external field would not result in a resumption of
superconductivity, which it does). Because of these similarities, it can be seen
how ORMEs could easily be mistaken as a type II material, and how casual
reference to it as such is even reasonably accurate for some purposes...

So these are laws at work behind the observed phenomena by which ORMEs
particles may sometimes flee the approach of a magnet or hand; first act inertly
when in an intense magnetic field and then resume their flightiness when it is
withdrawn; and so on.

Hopefully, the superficiality of the similarities between type II and ORMEs

behavior are now clear. The following few statements summarize these
conclusions about ORMEs.

1 ORMEs superconductivity is essentially temperature independent.

2 Macro currents are transmitted by inter-atomic Meissner field linkages through

an ORMEs body.

3 Hc2 is the level at which macro-currents in the ORMEs body cease.

4 The Hc2 level for an ORMEs body is a function of Meissner field strengths of
the individual ORMEs.

5 The atomic-level Meissner fields of individual ORMEs are distinct and largely
independent of the macro Meissner field of the ORMEs body, and only
moderately increase at Hc2.

6 Cooper pairs of the ORMEs themselves are typically unaffected by Hc2 field
levels, unless the ORMEs Cooper pair circuits are already carrying flux at or near
their critical capacity.

ORMEs are somewhat hydrophilic, and tend also to be hygroscopic. How much
so is in a proportion to how strongly their fields are charged. In "solution", the
Meissner field of each ORME is capable of controlling a significant number of
water molecules; how many, again depends on the ORME's charge. In such a
solution of ORMEs, the separation between ORMEs, specifically, the distance at
which energy normalization can occur between them is extended by the presence
of the water molecules, for a given strength of Meissner field. It is similar to how
inserting a dielectric material increases the capacitance between two plates. The
plates may be much more widely separated when the intervening space is filled
with a material of hi-dielectric constant, than without it, for the same capacitance.
Likewise, the ORMEs can be further apart in water, and still communicate
energy between one another.

The effect of the Meissner fields in such a situation is to artificially increase the
apparent viscosity of the water. It produces a "stiffness" or pseudo-viscosity
which is a function of the concentration of ORMEs, and of the field strength. The
field strengths naturally normalize between ORMEs under such conditions, so all
individuals within the population come to an equivalence in energy level
(assuming mixed species), or to an identical energy level between identical
species. This is the explanation behind the slimy, gelatinous consistency of
aqueous ORMEs dispersions.

The "viscosity" of the suspension may be altered drastically and dramatically, as

a function or cause of anything which affects the Meissner fields. For example,
placing a sample drop in a magnetic field, well in excess of Hc2, will suppress
the extent or range of the individual Meissner fields and (unless other field types,
as I alluded to elsewhere, are operative) the viscosity may be observed to
diminish, particularly if any macro-currents were present.

The possibility of achieving high-temperature superconductivity with Tc>300K

was predicted over 30 years ago by W.A. Little [Phys Rev A 1964, vol. 134, p
1416]. You may also be interested in reading D.M. Eagle's paper in Physica C
[1994, vol. 225 p 222-234] on observed room temperature superconductivity, and
other discussions of same delivered at Brookhaven National Laboratory in April
1994. This is related to the earlier work by LN Grigorov, et al.

THOUGHT EXPERIMENT ON
SUPERCONDUCTIVITY
Lets suppose that a small pile of lumpy and granulated ORMEs powder and
particles are the sample of an experiment. Let us also presume that these ORMEs
are only weakly or minimally charged, so that Hc2 for them is considerably
below the field strength of a test magnet, at a distance of a few centimeters. What
will happen then...when the magnet is brought near?

In their initial states, the weakly charged ORME atoms are fixed in position and
orientation, within the solid particle they are a part of. For individual ORME
atoms, sufficiently dispersed in a matrix of other ORMEs or non-ferrous
material, with the ORMEs being sufficiently low in atomic-level Meissner field
strength so as to not be in Meissner linkage with one another, they may be seen
to be capable of something superficially approximating ferromagnetic behavior.
Due to the atomic-level circuits each ORME atom possesses, some flux will
always be present (whenever there are closed valence circuits), and this will
result in a small, net magnetic moment; this is what I am referring to when I
assume they are only weakly charged. Another way of saying it is that this means
a tiny magnetic field is associated with each ORMEs atom, because of their
individual circuit flows.

The nature of the magnetic field of a single ORME atom (although I am using
"atom", I am doing so loosely, so keep in mind that these are diatoms) depends
on which element it is (specifically, what its elemental atomic shape or form is),
how many closed valence circuits it has, and (for partial ORMEs) where these
circuits are located on it, among the possible pairing locations. The resulting field
shapes are not simple dipoles, but are complex multi-polarizations, depending on
the permutations of these several factors. Nevertheless, in many cases, there will
be some net dipolar or quasi-dipole component, which will be particularly
apparent and dominant in near-field aspect. The net effect of these tiny ORMEs
dipoles generally will produce a gross dipole of some degree in a particular
sample particle, though it is also possible that the sample particle will also
display a more complex field.

The degree to which the net dipoles of the individual ORMEs in a given particle
are aligned to form a gross dipole obviously depends on the history of the
particle, such as what aligning conditions were present at the time the ORMEs
became solidified and fixed into their matrix, and what other relevant influences
were present at the time. They usually tend to align, individually relative to their
neighbor's influences, and as a group relative to external influences.

When an ORMEs body is placed within an external magnetic field, only three
things may happen, as regards the flux of this field. It may pass around the body,
it may pass through the body, or it may terminate on a pole or poles associated
with the body; each magnetic flux line originates from, and eventually terminates
on, a pole, and these are the only possibilities (which I shall discuss) that will
satisfy this, as far as the ORMEs body is concerned.

As the test magnet approaches, under a watchful eye, two main things happen.

The first thing is, some of the magnet's flux engages, and terminates on, the
pseudo-dipoles of the ORMEs atoms (those that are aligned attractively with the
external field), whose fields then become continuations or a nexus for it. While
the individual ORMEs do not move about or flip, fixed as they are within the
solid, the particle as a whole may move to orient itself, under action of the
magnetic forces, so that it is aligned most attractively with this external field,
according to its gross dipole or the net disposition of the ORMEs within it, and
that will be its natural inclination, in seeking a condition of lowest potential
energy. This results *initially* in an apparent ferromagnetic attraction of the
gross ORMEs particle to the magnet. They start to line up in whiskers as if they
were iron filings, mapping the local field of the test magnet.

The second thing that happens is, some of the magnet's flux penetrates
*between* the individual ORMEs atoms (I don't mean between the particles of
powder, but actually between the atoms in each particle), separating the atoms
and cutting off any inter-atomic Meissner linkages which might have been
present. (Remember, I have assumed that the ORMEs were weakly charged, so
Hc2 is below the magnet's strength, allowing this penetration to occur.)

In penetrating the particle, the field attempts to pass through where the ORMEs
atoms themselves are also, and in doing so it tries to scrunch their tiny atomic
fields up, close to the atoms. This latter mentioned action, by induction, causes a
current in the superconducting ORMEs valence circuits, opposing the magnet's
encroaching field, and forcing it back, away from the atom. The superconducting
valence circuits act as a perfect inductive mirror.

If it were only one atom that we were talking about here, that is where things
would stop, but that is not the case. There is a community of atoms, and the atom
has other atom neighbors, on every side of it, and above and below, in a 3-
dimensional arrangement. Consequently, while the first atom is excluding the
field from near itself, it has several neighbors which are each doing the same
thing. As these neighbor atoms exclude the field, they are at the same time
pushing the unwanted flux toward the first atom again, just as the first atom is
pushing it towards them. It is a case of everybody saying "Not in my
neighborhood!", all at the same time.

This is the source, nature, and mechanism of the field amplification, within the
ORMEs population, that would be needed in order for the ORMEs to behave as
has been observed, in levitating in the earth's half gauss field, note also that type
II SCs do this.

The squeezing of the external field between the ORME atoms greatly increases
the local strength (flux density) of the external field, as seen from the viewpoint
of each individual ORME atom. (The actual degree of flux compression (field
strength amplification) that takes place in this inter-atomic flux pinch depends in
part on the separation between the ORME atoms, but is very, very great, and may
certainly exceed the factor of 10^6 that is required. The evidence that it does is
plainly obvious to anyone, in that ORMEs *do* levitate.

As the field compression progresses, each ORME atom continues, in this

runaway induction, to increase the strength of the Meissner-generating currents
which flow in its superconducting closed valence circuits until a state of
equilibrium is reached, as the flux compression function runs into an asymptotic
wall. From the standpoint of each ORME atom, it looks as though a wall of flux
surrounding it is increasing almost without limit (a near approximation to the
hypothetical... Irresistible Force), when all they are really doing is pushing
against each other with the external flux trapped in between, like a veneer. The
magnet's flux that succeeded in penetrating the particle is now trapped in the
inter-atomic spaces it intruded into. The particle is (for the moment) something
like a bead strung on the lines of external flux.

Just about the same time as this is going on, something else happens. As the
external magnet's flux becomes more and more confined, and the Meissner fields
of the individual ORMEs atoms become increasingly powerful, they are also
forming increasingly efficient field linkages between themselves. The atoms
begin to become capable of (more and more efficiently) transferring energy with
one another, which is another way of saying that the Hc2 value for the system is
increasing.

As this inter-atomic coupling begins to develop, macro "currents" begin to flow

(only in small localized regions of the particle at first). These localized effects
begin expelling the external flux from their area. As the atoms come into
communication with each other, and external flux continues to be expelled, this
sort of cascades and the whole population transitions into a superconducting state
as contiguous, extended particle body.

In other words, the first thing they do when linkages form is to promptly develop
Meissner-field-generating currents in the macro-particle, to exclude the external
magnet's flux that has, just before, become trapped between the ORME atoms.
As the flux is expelled, the growing diamagnetic field opposes that of the test
magnet's field, and the particle's attraction changes to being repelled from it.

The rate of development of diamagnetism (or repulsive force) starts slow, as

inter-atomic linkages begin to form for the most closely spaced atoms, increases
as more linkages form and larger currents are possible, and then finally levels off,
as nearly all interatomic linkages which are possible within a given particle have
formed, even for the more widely spaced ORMEs atomic neighbors. At that point
the diamagnetic field stops growing further.

It takes a certain amount of time for the ORME atoms, working cooperatively, to
move the embedded external field's lines from being inside to being out of the
particle. Its like when you see somebody being passed across the room, above the
heads of the audience at a rock concert, by everyone's arms gradually handing
them from person to person. But eventually the lines get expelled from the
particle. This migration time (which depends on several factors) causes a delay
before significant repulsion begins to become apparent.

In finally flying away from the magnet, the particle then obeys kinematic laws
(a=f/m) as the acceleration (integrating into velocity) is determined by the
instantaneous repulsive force, as a function of instantaneous field strengths (etc.).

So the particles first appear to ferromagnetically attract, but before long change
their minds and fly away in diamagnetic repulsion. Please allow me to point out,
that all these behavioral phenomena are consequences (as put forth in the
inductive reasoning of the foregoing explanation) only of the fact that ORMEs
have closed valence circuits. Showing in a compelling way that the same
observed behaviors are required by theoretical atomic concepts or models, which
do not admit to or include closed Cooper pair valence circuits, may be very
difficult indeed, and certainly not as compelling, I would say.

(7) OTHER MEISSNER RELATED PROPERTIES

back

Zero point coupling is also related to ORMEs' ability to interact with water,
producing the pseudo-viscosity discussed in the previously. The electromagnetic
zero point in these phenomena is an important mechanism by which energy
moves to and from the vacuum energy field, and out of or into our own space-
time.

There exist many zero point doublets, within reach of our experience (ie,
associated with matter and energy phenomena we are capable of manipulating).
They are points where physical and transcendental resonances occur
simultaneously, ie, highly non-linear natural interactions between matter, energy,
and space-time. Each of these zero points represents a point of communication,
through which energy may enter (or exit) our 3 dimensional world from higher
dimensions, the ultimate source of the vacuum energy.
The important thing to understand, is, that it is not necessary for a particular
wave's frequency to "match" the mid-frequency of a particular zero point doublet,
to experience this sort of transition. It is only necessary that coupling exist
between energy (or matter, or both) in our dimensions (for example) and a zero
point resonator. The presence of the appropriate coupling circumstances with a
zero point notch or doublet results in the entrainment or discharge of energy, by
means of coupling transfer. It is the coupling to the doublet resonator (e.g. a
water molecule, ORME, etc.) which is important. The frequency "shift" of the
coupled energy occurs as a natural consequence of this, due to topological
properties associated with the zero points themselves. The zero points are not
merely the specific frequencies they happen to fall on, within the electromagnetic
spectrum, but are the result of the trans-dimensional resonator, which just
happens to have whatever frequency it has; tuning the 'right' frequency without or
apart from a zero point resonator does not constitute a zero point.

Meissner effects may also affect taste. Strongly charged ORMEs might be
masked in their metallic properties by the Meissner fields. The manna of the
Israelites was described as tasting like "honey" (Exodus 16:31), or "fresh oil"
(Num 11:8). In making it into cakes, the Hebrews, of course, had to add water to
it. Both honey and oil are viscous substances, and these terms may also give us
an indication of the amount of charge present for those allusions in the account,
with perceived taste varying according to charge.

ORMEs, having individual atomic-level Meissner fields, differ in behavior from

that of type II superconductors, when an ORMEs suspension is exposed to an
external magnetic field. The external magnetic field direction (earth's field),
which penetrates a water suspension of ORMEs is nearly horizontal. The reaction
of the ORMEs population is to exclude the magnetic field. But because the
ORMEs population in suspension is both mobile and discontinuous, some
interesting things occur. The ORMEs nullify and confine the penetrating field by
forming current vortices around each of the quantal lines of flux. This forms a
vortex field, that is, a field made up of a great number of tiny vortices, dispersed
uniformly through the solution when viewed in a direction parallel to the earth's
field lines.

Despite being discrete entities, these vortices mathematically sum into a single
peripheral vortex encircling the flux. Because of the mobility of the ORMEs in
suspension, the ORMEs themselves gradually flow towards an arrangement of
lower energy, which shall eventually exclude all the field lines from the
container. As they do this, these small vortices gradually coalesce into larger and
larger vortices, containing and enveloping the penetrating flux in larger and
larger clumps, till it is all lassoed into only one large bundle. This might look like
a solar prominence. A large ring current flowing through the arch (and continued
in a circuit through the material in the container), sufficient to exclude the flux
from it. If you broke the arch (physically), the ring current would be interrupted
and cease, and the arch would fall and collapse (no current left to sustain it, once
broken), and the flux trapped under it would escape out through the point of the
breach as the two limbs of the arch fell.

You can reach Fourth Millennium, or Z.A.P. by e-mail at [email protected] to

consult for examples of technology engineered to your specifications.

Contact Information

Fourth Millennium
[email protected]

(510) 761-4602
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 created on May 8, 2003 - JLN Labs - Last update October 18, 2007
Toutes les informations et schémas sont publiés gratuitement ( OpenSource ) et sont destinés à un usage
personnel et non commercial
All informations and diagrams are published free (OpenSource) and are intended for a private use and a non
commercial use.

 Full CFR replication at the

CNAM in Paris
 September 19,
2006 : Successful CFR replication by Ronald Hohls (South Africa)

 March 15,
2006 : Successful CFR replication at Boulder (Colorado, USA)

 Do It Yourself: The
APE experiment
 Interesting : Electrical
power from the plasma with APE ?

 Do It Yourself: The
basic CFR experiment
 Do It Yourself : The
Enhanced CFR experiment

The successful CFR replication by the CNAM has been presented at the 12th
International Conference
on Condensed Matter Nuclear Science (ICCF 12) at Yokohama (Japan) -
November 27 - December 2, 2005





Transmutation of metal in confined plasma in water by A.
Datillo, V.Iorio, D.Cirillo
Read the Full Test Report online by A. Datillo, V.Iorio, D.Cirillo
 CFR experiment, full
datas results

 Successfull CFR by
Morgan H. and Marissa C.

 Successfull CFR
replication by a French lab
 A Stirling engine
powered with the CFR

 CFR with a Palladium Cathode

 CFR v4.0 Test with a Power Meter
 CFR v4.0 - Radiations measurements
 Preliminary tests of the Big CFR v4.0
A FULL SCREEN MPEG VIDEO of the Enhanced CFR v4.0 in action...
 FULL TESTS of the CFR v4.0
 Tests of the CFR v3.3 with a New PS
 The Enhanced CFR v3.0
A FULL SCREEN MPEG VIDEO of the Enhanced CFR v3.0 in action...
 A NEW Power Supply for your CFR

The High Power CFR v2.1

 Tests of the CFR v2.0 at HIGH POWER

o A FULL SCREEN MPEG VIDEO of the High Power CFR v2.0 in action...
  The CFR v2.0 with K2CO3
 The CFR tests with K2CO3 and W cathode
 The Tiny-CFR tests with a 2x25 mm W cathode
 Power Input measurements with a Power-Meter
 CFR v1.4 tests with a 6x45 mm W cathode
o A FULL SCREEN MPEG VIDEO DEMO of the CFR v1.4 in action...
 CFR v1.3 tests with a 2x45 mm W cathode
o A FULL SCREEN MPEG VIDEO DEMO of the CFR v1.3 in action...
 CFR v1.1 tests with W and K2CO3
 The CFR v1.0
 The CFR for producing BingoFuel...
 A Simple Calibration test with the CFR

The CFR Experimenter's

corner

Interesting documents and references :

 Mizuno, T., et al., Production of Heat During Plasma Electrolysis. Jpn. J.

Appl. Phys. A, 2000. 39: p. 6055.
 Mizuno, T., T. Akimoto, and T. Ohmori. Confirmation of anomalous
hydrogen generation by plasma electrolysis. in 4th Meeting of Japan CF
Research Society. 2003. Iwate, Japan: Iwate University.
 Infinite Energy Vol.4, No20, 1998
 Mizuno, T., Nuclear Transmutation: The Reality of Cold Fusion. 1998,
Concord, NH: Infinite Energy Press.
 Mizuno, T. Experimental Confirmation of the Nuclear Reaction at Low
Energy Caused by Electrolysis in the Electrolyte. in Proceedings for the
Symposium on Advanced Research in Energy Technology 2000. 2000.
Hokkaido University.
 COLD FUSION BY PLASMA ELECTROLYSIS OF WATER by Ph.M. Kanarev - The Kuban State
Agrarian University, Department of Theoretical Mechanics.
 Ph.M. Kanarev. Water is New Source of Energy. The Third Edition.
Krasnodar 2002.194p
 The LENR-CANR home page
 Full downloadable PDF documents about Cold Fusion researches at the
LEN-CANR web site
 The Atomic Hydrogen blowtorch invented by Irwing Langmuir in 1926
 Anomalous Heat from Atomic Hydrogen in contact with potassium
carbonate by R. M. Shaubach and N.J. Gernert from Thermacore, Inc

 Click here to download the full PDF document


 Click here to download the full PDF document

PATENT : WO0025320 : " Energy Generation " from Eccles Christopher

Robert ( GB ) - May 4, 2000

Abstact :
Methods and apparatus are described for releasing energy from hydrogen and/or
deuterium atoms. An electrolyte is provided which has a catalyst therein suitable for
initiating transitions of hydrogen and/or deuterium atoms in the electrolyte to a
 subground energy state. A plasma discharge is generated in the electrolyte to
release energy by fusing the atoms together.

Click here to download the Full Patent

PATENTS from MIZUNO TADAHIKO (JP) :

o JP2004059977 - METHOD AND APPARATUS FOR GENERATING

HYDROGEN GAS - February 26, 2004

Abstract : PROBLEM TO BE SOLVED: To provide a method for generating a

hydrogen gas with a high efficiency by continuously and directly pyrolyzing water
with a satisfactory controllability.
SOLUTION: This gas-generating method comprises a step of accommodating an
aqueous solution of an acid, an alkali or a metal salt in a reaction vessel, and
heating it to 70 deg.C or higher but less than 100 deg.C, a step of applying a
voltage of 100-2,000 V to the above heated solution with pulse widths of 0.1-10 s
and pulse intervals of 0.01-5 s to generate plasma, and a step of electrolyzing the
above aqueous solution with the above plasma.
Click here to download the Full Patent

o WO0126117 - THERMAL ENERGY EXTRACTION APPARATUS,

HOT-WATER SUPPLY, AND ELECTRIC GENERATOR - April 12,
2001

Abstract : A thermal energy extraction apparatus comprises an electrolyte bath (1),

electrolytic solution (4), electrodes (2, 3), an atomic nuclear fission means (11), and
a thermal energy extraction means (5, 6a, 6b, 13a-13e, 14, 23a, 23b). The
electrolytic solution (4) is kept inside the electrolyte bath (1) and contains at least
light water or heavy water. The electrodes (2, 3) are so arranged as to be in contact
with the electrolytic solution (4) and include an anode (3) and a cathode (3). The
atomic nuclear fission means (11) fissions atomic nuclei of the material constituting
the electrodes (2, 3) by applying a voltage and a current to the electrodes (2, 3).
The thermal energy extraction means (5, 6a, 6b, 13a-13e, 14, 23a, 23b) extracts
heat medium (18, 19, 21, 22a, 22b) heated by the thermal energy generated by the
fission of the atomic nuclei of the material constituting the electrodes (2, 3) to the
outside of the electrolyte bath (1).
Click here to download the Full Patent

o WO9949471 - REACTOR FOR PRODUCING ENERGY AND

NEUTRONS BY ELECTROLYTIC REACTION IN LIGHT- OR
HEAVY-WATER SOLUTION - September 30, 1999

Abstract : A reactor for producing energy and neutrons by electrolytic reaction in a

light- or heavy-water solution comprises a base made of a refractory metal and a
metal layer formed on the base and active against hydrogen. The reactor to serve
 as a cathode is immersed in an electrolyte together with an anode. Current is made
to flow between the cathode and anode to cause an electrolytic reaction. Thus,
thermal energy and neutrons are produced.
Click here to download the Full Patent

o JP5027062 : GENERATION OF ABNORMAL HEAT- February 5,

1993

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