MOBILE CLEAN ETERNAL CONSTANT FREE ENERGY TECHNOLOGIES (refresh in
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Lorris Harmlawf. Also see my Charter For Fair English Language
Commonwealth; model update to the new 2011 (2013) Charter Of The
TO SURVIVE WE MUST SHUT DOWN ALL NUCLEAR POWER STATIONS NOW! (If built should be 100m underground in complete containment chamber 200m above sea level with enough backup generators with backup batteries to be able to power cooling pumps long enough for emergency shutdown) Hysteria about carbon dioxide has distracted us from real toxic pollution. Mass adoption of fission nuclear has been infinitely more toxic to green environment than carbon dioxide plant food. At current rates of consumption for nuclear power uranium reserves will run out in 40 years.
Do NOT patent your device (free energy technologies have always been rejected or sequestered, patents were a total dead end waste of money, time and talent), just make one, sell at maximum price such as on Ebay (you might have to call it something like an ambient energy harvester for free energy generators), do not hide secrets, open proof of operation will significantly boost sales, (keep technologies used as weapons secret such as physical time travel; we do not want to have had ourselves deleted or created multiple virtual time lines, chronovision ok with gradual introduction of choice true images as will only create peace, prevent disasters and guide policy and innovation, will still require some controls on devices for privacy): grow organically, do not sell shares (control), do not take on debt, start as a charity to eliminate tax (you can convert to business later), if called insane claim welfare and convert to religion (so you pay your workers less or not at all as voluntary devotion does not disqualify from welfare as any paid work has, religious law overrides parliament legislation in Australian 1901 constitution), take donations, this will help you have maximum security, technological, production and financial advantage. Keshe Foundation is best example of this approach.
3% for the national budget (from 40% of all government revenue) should be for commission of teleporter for military, private local and national postal and freight delivery services after more than one hour time delay, and national customs and sorting centers for international freight as the national parliament shall authorize and determine. Anyone in the nation (subject to restrictions as the national parliament set) should be able and free to have and use own personal red teleporter postal boxes with GPS of location and certification of up to 50cm x 50cm x 100cm internal chamber area where only to teleport to and from the local post and freight depot. Local post and freight depot should have teleporter of any size such as for trans delivery from personal post boxes and to any personal postal box in the same nation and for shipping container after initial checking to and from locals and to and from customs comprehensive inspection, scanning and checking centers at remote secure locations deep underground for international freight. Military teleportation as our defense minister approves. Only the military should be able to do human teleportation to and from within the same nation only as the defense minister approves.
tech teleport. Limit to world parcel postal service for dramatically
faster, cheaper, cleaner parcel post delivery. Not for peoples homes
to prevent invaded by mass illegal migration. Also for military
mobile teleporter in submarine to crew and supply on demand plus in
big VTOL anti-gravity craft to deploy 1 ton remote + AI robot tanks,
small drones, compact trucks and troop carriers, supplies and
personnel quickly. Also for time travel. Uses a field of radiant
energy to open up a
tunnel in time-space then on closure, the teleportee lands on the
the location where the tunnel closes, this may be choice of
point in time relative on the duration of the tunnel opening
including the real current time. The stargate is a Tesla teleporter
that so concentrates the radiant energy from a
hologram so as to send
vast distances in time and location. In the
teleportee can see tunnel walls of rippling blue and white
holographic light and sometimes alien observers. Teleportee may
and location-space using
star-gates but as more time is spent in the vortal tunnel may have to
have oxygen tanks so as to be not asphyxiated. Our (Earth)
Father Pellegrino Ernetti (degree in quantum physics) / Father Augustino Gemelli / Father François Brune (Roman Catholic Church monastic monks) Plus 12 scientists including Enrico Fermi and Wernher von Braun / Vatican. Chronovisor (looking glass). Discovery from study of harmonic patterns in Gregorian chants at the Catholic University of Milan, the microphone in development able to pick up the sounds of events across time. Leading to development by the Vatican of the Chronovisor: A TV like screen for viewing events across time and location: a cathode tube, antennas using alloy of 3 metals to capture light and sound, controls, meters, and a sound and light sensor. The US government further developing the Chronovisor under DARPA US defense research projects contracts. Currently the viewer stands in a cubical chamber to see dense hologram light images using lensing effect to view events across time and location so the viewer can track specific individuals and events across time and location using residual sound and light signature to see, hear and explore events.
The helical magnetic fusion plasma confinement chamber is a creation from science of Dr. Stirling Colgate as president of the New Mexico Institute of Science and Technology and a physicist at the Los Alamos National Laboratories. It uses radioactive plasma to propagate a wormhole which the time traveler travels in order to be embed temporarily in a past event. When this local quantum field effect created around the chrononaut wears off, he experiences transitioning spontaneously back to his point of embarkation in the chamber without traveling via wormhole.
The Aeronautical Re-positioning Chamber (Jump Room such as to travel to Mars in 20 minutes) A joint venture between Parsons, Lockheed and CIA. Reverse engineering chamber in crashed craft from Alpha Centauri star.
51 with Zeta ET help (These greys are military model bio-controller
of our ET allies in addition the 90% fair modern human DNA human
beings from 60,000 years in our future): U.S.A
silent very big clean free energy VTOL TR-6 Telos Phoenix Class
and passenger colonization craft: Including of
1061c U.S.A. colony. With Dart combat drone space craft on board.
Would be perfect for very fast UK to Australia flights, safer than
the illegals problem. To cleanly, vertically, slowly and silently
land in city airports without fumes, noise, fog visibility dangers or
height restrictions on buildings.
ET and Area 51 copy of Zeta ET design with Zeta help: TR-3b
interstellar and superluminal time travel.
Keshe Foundation Magravs 3kw(40kw) off grid eternal power units by
Mehran Tavakoli Keshe: Copper coils with fire to nano wire fibre coat
then coat with mixture of CO2 Carbon dioxide as nano state powder,
ZnO Zinc oxide as nano state powder and CH3 Methyl as nano state
powder, With crystals plus monoatomic elements in centre. To create
field to protect from radiation and convert to electricity. Started a
bit dubious, first products did not work: Keshe Foundation Magravs
off-grid home plasma power units for sale from the Netherlands.
Currently in full production in several countries including Italy,
China and Ghana and will expand as able. I have one on order; Paid
AUD$2700 on 13feb17, with promise of 90 day delivery, plus our local
taxes on arrival, I have receipt for payment; slipped to vapourware
(pre-orders) July, at 150 days now; have update email- to change over
production to new superior design, hopefully testing will sort out
technical issues by arrive here in September to make these 100%
reliable), still well worth my contribution, exactly what my
contribution should be for. Recently Keshe focus was made 120 compact
EMP WMD. Keshe has unhealtherly associated with black Africans, as
you know have been notoriously 100% persistently scammed fair people,
blacks may have pressured Keshe to have put fair people last, or
caused to have switched focus to EMP weapons (much cleaner than
nuclear weapons, to make them redundant). So feel free to copy the
design and make your own generator as Keshe suggests, I think Keshe
is copying technology as well, which is ok. I would rather Keshe
focus on off-grid generators such as for 1kg AI drones would to be
far more beneficial approach so reduce radiation so save the world.
As would abolish other nuclear power which has proliferated nuclear
weapons, so progressively destroyed the planet. To test before
delivery to ensure will be 100% reliable. To evaluate soon when here.
Very compact ~1kg for 3kw continuous eternal power (maximum rating
for home electrical certification compliance, can actually produce
40kw spike) continuous eternal power so should have circuit breaker
to protect things. Available with USA (110V) and 230v 50hz model for
UK and Schuko F sockets (parts of Europe) so for Australia simply add
a good $20 adapter (I have a proper Korjo UK plug with 2x 2kw double
adapter to proper Australian sockets from Kogan Australia not cheap
multi-adapter). Would also be good to power all wireless towers (4G,
5G, broadband) and fuel pumps to work also during blackouts and
satellite, 1ton remote and AI tanks, submarines, drones and the like
for eternal endurance. Also multiple redundancy plug in units for
Mars missions to create field to protect crew from radiation and
convert to electricity such as for heating and recharge batteries for
lighting, computers and thrust. (Comparable performance solar and
battery systems have cost about 20x more) It is also portable so you
can take it with you, pack it in your backpack and take it camping
such as to power electric heating of sleeping bags and tent heating
and for lighting in Antarctica. To run air conditioner cooling and
heating all the time all year round even during blackouts or solar
storms for free and save $300/month on electricity. 100+ days to
deliver (with extensive reliability testing) from receipt of payment
(I think counting of orders at the end of each month to put in orders
to manufacturers to make to order over next month, then one month
reliability testing at full load feeding to the grid so ensure will
be 100% reliable, and then one month to deliver and extra spare time
to use as required)
Alekz Cells: Eternal 1.5v AAA, AA, C and D cells:
How to make 3kw (6kw) Keshe plasma eternal 1kg mobile power generator:
(from an open German page on the web Google translation plus my grammar edit and clarification).
Nanowires under the scanning electron microscope after the fire coating, source: Yuan et al. (2011, p.2492)
Fire-coating on copper under the scanning electron microscope (a) clearly shows the Cu2O layer and the CuO layer, and the nanowires forms thereon, (b) enlargement of the area in green square region of (a), source: Yuan et al. (2011, p.2493)
Single nanowire (NW): (a) from a transmission electron microscope (BF-TEM), the two sides of the nanowire are visible, (b) the high-resolution transmission electron microscopy (HRTEM) also shows the two layers and the crystalline structure, SAED (selection area electron diffraction) pattern of a nanowire, source: Yuan et al. (2011, p.2494)
The basic material to coat is copper, of any shape. Method 1; coat thermally by heating (gas burners). Method 2; coat chemically by etching with NaOH. In the course of the coating, gaps between the atoms form on the copper surface to form a layer, which again consist of small particles, which look like wires, so these people call "nanowires" being so small and this is why people call this coating nano-coating. These nanoscales have the property of growing in the course of the coatings.
The development of this thermal coating of copper involves many institutions and universities. Working on the nature of the copper, graphene "nanowires" formations on the surface at a certain temperature. The scientists, Yuan, Wang, Mema & Zhou (2011) from the Department of Mechanical Engineering & Multidisciplinary, State University of New York, are investigating these nanoparticles and layers in detail. The graphic shows a picture of the nanowires in the size of micrometer or nanometer (1 nanomillimeter is 1 millionth of a millimeter: 1 / 1,000,000). The individual wires (threads), which in random arrangement, are clearly visible. In this case, the copper is after repeat heating to 450 ° over a period of two hours. First treat copper substrate of 99.99% purity with hydrochloric acid (HCl) then use water (with no minerals) to clean the copper and remove the natural oxide layer.
The authors reiterate that the "nanowires" were not from "grain boundaries" (cracks on the surface from heating), these nanowires develop independently. In detail, a copper (I) oxide layer (Cu2O) forms on the surface during the course of the coating process, then a copper (II) oxide layer (CuO), and finally, the "nanowires" are grow from the CuO layer out. It is only when the CuO nanoscale is larger than 1 micrometer that the nanowires begin to grow. The optimum temperature for the growth of the nanowires is between 300 and 550C. During the coating process the copper (I) oxide is yellowish to red-gray and then becomes black when it is heated, then after cooling again takes the original color. If the coating was yellowish to reddish brown, you have had no CuO layer so had no "nanowires". Copper (II) oxide is black, so it is important that the coated wires are black and do not bear the Cu2O (yellowish to reddish brown) colors. This is why it is important to choose the correct temperature for the fire coat.
Furthermore, Yuan (2011) finds that the surface of the nanowires is a crystalline structure (was not hollow), each side of a nanowire is a crystal with a clear crystal lattice structure. In Figs. A and b, the two sides can be seen using transmission electron microscopy.
NaOH-coat copper coils for the making of GaNS, since the nanoscale layers wear less quickly using this method of coating. Also use the NaOH coating method for health applications, among reasons because you can incorporate herbs and nutrients into the coating layer during the course of the coating process. Magravs power generator coils use the flame method of nano-wire coating copper wire.
Of several procedures, here is the one from the teachings of the Keshe Foundation. In addition to this procedure, there is also a method by Peter Salocher, for more information, please visit https://www.youtube.com/watch?v=9p1QaBemVmA
Plastic container with lid (not too big)
Weights to weigh the lid
Copper coils, wires and plates
~ 100 grams of pure NaOH. As powder and bead will work (not drain cleaner as for the leaching of furniture)
~ 2 liters of water from steam steam distillation (by quantity of coils and size of the plastic tub)
Water boiler such as kettle and stove to heat the water
Preparation for vapor coating of coils (for production of gans only) Source: www.Plasma-Energie.org
This phase is about cleaning the coils of grease and other substances. Cover (sprinkle) the bottom of the small plastic container with a thin layer of the NaOH powder, then place the copper (coils) on the powder (may touch the powder). Then place the lid of the plastic container obliquely on (across) the container so that only 1 small inlet remains open. Into this inlet pour the hot (boiling) water so as to cover all of the coils. Caution; caustic soda steam, please wear protective goggles and protective gloves. Place the weight on the lid, so that not too much steam escapes and leave the vessel in this condition for 24 hours.
In a plastic container of the same size as in phase 1, place a zinc wire grid mesh on the bottom of the container, so that the coils do not lie directly on the plastic. Tension the wires (in a similar container). Thinly cover the bottom of the container with NaOH powder as in phase 1. Place the coils from the NaOH water from phase 1 onto the wire grid mesh. The coils should be about 2cm away from the ground and not touch the container walls and any additional coils. In the next step, place the lid of the plastic container obliquely on the container so that only 1 small inlet remains open. In this inlet, pour hot (boiling) water, this time only about 1 cm (so as not to submerge the coil/s). Close the lid as quickly as possible, weigh the lid with (small) weights and wait for about 2 days. (Use protective goggles and gloves as in phase 1).
Polarization of a coil with multi-meter, so adjust to Ohm Source: www.Plasma-Energie.org
Polarization will stimulate coating of the copper surface, organize, align and stabilize. Proceed as follows:
Place the still wet coils from the steaming container onto an insulating surface (wood, plastic, fabric, etc.)
Measure the resistance with a multi-meter, set to Ohm, place probes at both ends of the coil. The coil resistance in any case will be higher than 100 kilo ohms, usually it is in the mega-ohms range.
After the procedure, hang the coils back in the plastic containers.
"pulling off potential" means the process, where the "plasma" from the coils move and organize by the current of the multi-meter. Thus draws current from the coils to stimulate the system to produce new power. Proceed as follows:
Pour out most of the liquid from phase 2 from the plastic container, the coils and hang for the drying process.
When the coils are dry, remove the coils from the hanger and place on an iron plate.
With a multi-meter (set to volt), touch the iron plate with the minus pole probe, then place the positive pole probe on the coil to short for a few seconds (at the beginning, middle and end of the coil/s). Ignore the measurement values; may vary between + and - on the display of the multi-meter.
Repeat this procedure every 3-6 hours within the 3 day drying period.
Gas burner (gas lamp) with butane gas.
Fire nano-wire coat using butane gas as with to construct Magravs generator coils. In this type of nano-wire coating, skip polarization and drying (+ pull off) part. The temperature and direction in the fire coating process is decisive. The movement of the flame during the fire coating process must always be in the direction to be the flow of electrons in the wires, so as to never glow. If the wires have got a golden glow, move the gas burner further along.
After a few seconds the wires cool down, if were different colors, such as red, turquoise or blue, the temperature was too low, in this case just pass frame over again with flame higher and closer to the coils for a high temperature. If the wire has glowed, the temperature was too high. In this case simply turn the gas burner back and further away for a lower temperature and then re-coat. Over time, you will develop a flair for the fire coating process and everything will run properly.
Gas burner with butane gas (also propane / butane mixture will work)
Coils (after fully winding and wiring)
Fire-resistant fixture for hanging coils (metallic best)
Important: Do not coat in cold rooms, otherwise the coating layer will dissolve very easily from the copper wire. Also according to the quality of the copper wires, sometimes even in the "raw" state slight cracks have appeared on the surface.
Formation of GaNS. Source: Keshe Foundation SSI, 2015
GaNS is the abbreviation for "Gas As Nano State also applies to any material in this nano state". In the Keshe Foundation process you may extract carbon dioxide (CO2) from the air using simple means and convert into the solid nano state. Furthermore, in the Keshe Foundation process this GaNS, both dry and bound in water, will supply useful energy.
The process of the Keshe Foundation will make CO2 GaNS, and additional "GaNS species". The diagram shows schematically the making of GaNS. The basis is "raw" copper, you see depiction of the compact atomic structure. In the first step nano-wire coat the copper. The gaps between the atoms are from the coating of nanoscale layers of nano-wires (see chapter Coating). The copper with the nano-wire coating will produce the CO2-GaNS, which will settle on the bottom of the plastic container, from the reaction in the zinc plate in salt water.
GaNS are part of the Keshe Magravs generator. The coils have a GaNS coating and GaNS containers are in the middle of the coils. In the guidelines, three types of GaNS are used: these are CO2 (carbon dioxide) GaNS, CH3 (methyl) GaNS and CuO (copper II oxide) GaNS. In this case, all three species are in the copper nano-wire coating with various metals from the 10% salt sea water (dissolve 100 grams of sea salt in 1 liter of water from steam distillation). Therefore, things you need to make the GaNS:
Small plastic containers
Water from steam distillation
Natural sea salt (unrefined), also stone salt will work.
Copper wires with nano-wire coating to short-circuit the metals
Copper with nano-wire coating (may use coils - best)
Ordinary pure metal plate for the type of GaNS (such as zinc, copper, iron)
The following table provides an overview of the formation of various GaNS species using the appropriate metal:
Yield after 4 days. Source: www.Plasma-Energie.org
Washing CO2 GaNS under green LED shows better structure but far more slowly produces CO2 GaNS.
Yield after 1 day. Source: www.Plasma-Energie.org
CO2 GaNS with high zinc oxide content (done without LED short).
CO2-GaNS (had no LED shortwith double the NaOH amount by weight and hot water). Has high zinc oxide percentage content and "nanosize". Wash more than 5 times to extract the pure CO2 GaNS (usually was very little). Source: www.Plasma-Energie.org
Connection of a small LED, Please use a green LED! Note; the longer wire on the LED is the anode to connect to positive power source. Source: www.Plasma-Energie.org
The LED producing light when production of GaNS is running and when the coils are generating power! Source: www.Plasma-Energie.org
Produce this GaNS by immersion of zinc plates and copper coils with nano-wire coating into the salt water. Connect these two metals objects with copper wires between which mount the small green LED, the ends of the plates and coils should not touch the bottom of the plastic container. Dissolve 100 grams of sea salt into one liter of the water from steam distillation and pour the solution into the container. Ensure to have no residual lumps of salt in the vessel. Use electricity to make CH3 and CuO GaNS, (electricity not required to make CO2-GaNS production). Also, connect the green small LED between the two plates, to ensure approximately 90% on the GaNS to make will be of CO2 GaNS. (Done without the LED mainly zinc oxide was generated according to Keshe. Connect the LED anode (longer wire = positive pole) to the (copper) plate / coil with nano-wire coating, and the LED cathode (notch on the LED housing and shorter wire = negative pole) to the pure (zinc) plate. After a few hours, a white layer should begin to settle on the bottom of the vessel, (Remember for to make CO2-GaNS: NO POWER (no batteries or power supply) and use a green LED!!)
Plastic tub such as drink bottle with top cut-off.
Pure zinc plate
Copper coil with nano-wires coating.
Small green LED (light emitting diode)
100 grams of natural sea salt (not refined)
1 liter of water from steam distillation.
Put the salt in a bucket with water from steam distillation and dissolve completely (after about 1 day), Remove the brine (the salt water). So produce fresh brine; always use fresh 15% salt water brine. Source: www.Plasma-Energie.org
Schematic design of CH3-GaNS production without current, instead of the short circuit connect to DC, source: Keshe Foundation
Produce this GaNS using pure iron plate and a copper coil with nano-wire coating in sea water. Connect the two metals together with a copper wire. (In contrast to the CO2-GaNS generation) You may use a small current and the air from a simple aquarium pump to speed up the process. For this purpose, use a conventional, controllable DC (DC) power supply, to produces an approximate current of 15mA between the two plates (instead of connecting together with the copper wire), clamp the negative pole (black) aligator clip to the (copper) material (coil) with the nano-wires coating and the positive pole (red) aligator clup to the pure (iron) material (plate, not-coated). As soon as you apply electricity add oxygen bubbler as well such as from of an aquarium pump. After a few hours, a red-brown layer will begin to deposit on the bottom of the vessel, this is the CH3-GaNS.
Pure iron plate
Copper coil/s with nano-wire coating.
100 grams of sea salt
1 liter of distilled water
Optional DC power supply, aquarium pump and plastic tubing.
Turquoise CuO GaNS before filling yet to settle down. Source: www.Plasma-Energie.org
To make this GaNS use a copper coil (a plate will also work) and a second copper coil (plate) in sea water. Connect the two copper objects together with a copper wire. As with to make CH3. Again you may apply a low power, and bubble air using a simple aquarium pump here as well to speed up the process. You may use a conventional, controllable DC (direct current) power supply to generate an approximate flow of 15mA (.015A) between the two plates (removing the copper wire), clamp the negative pole (from the black terminal wire with an alligator clip) on to the copper material with the nano-wires coating and clamp the positive pole (from the red terminal wire with an aligator clip) on to the pure copper material (that was not coated with nano-wire layer). Then as soon as you apply the 15mA power, add oxygen bubbles such as from of an aquarium pump. After several hours, a turquoise layer at the bottom of the vessel will begin to settle, this will be CuO GaNS.
Copper (such as from coil and plate)
Copper coil with nano-wires coating (from using caustic soda).
100 grams of sea salt
1 litre water from steam distillation.
Optional adjustable DC power supply, aquarium air bubler pump and plastic tubing.
The GaNS sediment is useful in a variety of states, the paste, for example, for the production of capacitors, and to filling the container in the middle of the Magravs generator and as a powder to make the plasma power cells. When the sediment is dry the plasma will be stronger and so the production of powder. However first a few steps to take:
Here drying on a radiator to obtain the dry GaNS sediment powder. Source: www.Plasma-Energie.org
Before beginning the gentle drying process, wash the GaNS sediment to reduce the salt content, do this with the following steps:
Before drying the GaNS, put the GaNS liquid and sediment into the highest possible quality glass container and let settle for a day and a night.
Then with a syringe (suction pump) suck the water from on top of the GaNS sediment.
Refill the glass container with pure water (from steam distillation)
Leave to settle again for a day and a night to seperate again and so repeat this process 3 to 6 times, then you will have the GaNS sediment without the salt.
Option: Drying out of GaNS with fan. Source: www.Plasma-Energie.org
The aim of the drying is the gentle removal of the water, this drying may be by gentle heating such as on a fire and a hot plate, the more natural the drying, the better. You may accelerate the drying by putting on a radiator and by turning on a heat lamp near the GaNS sediment container. If the sediment has formed crystals during drying, then the GaNS sediment did not get enough washing (cryrtals were from salt left behind). Over time, you will obtain GaNS paste and after more time drying GaNS powder.
With the production of GaNS powder oxide, it is possible to then mix the GaNS sediment powder with NaOH powder (1/3 GaNS sediment powder with 2/3 NaOH powder) and hot water then clean and dry to make nano GaNS in a very pure form.
Magravs plasma energy for homes and apartmentments, using plastic pipe. Source: www.Plasma-Energie.org
To make a Keshe Magravs generator for home first successfully produce the dry GaNS sediment powders. Here are the additional steps to then build a Magravs generator:
Each of the 3 pairs of coils consist of four individual coils, With coils from winding around 6mm rod inside coils from winding around 10mm rod for both the 2 longer coils and the concentrically nesting 2 shorter coils. With a sum total of 12 coils in each Magravs generator. For these coils use copper wire with a cross-section of 2.5mm² , so a diameter of about 1.8mm. Since this copper cable been difficult to obtain in naked form, you can use insulated copper wire such as for electric cables and remove the external insulation. Ideally the electric cable should be on a cable reels of 100+ meters as from any hardware store. The shorter coils having 81 turns, and the longer coils having 144 turns. To make the inside coils bend the copper wire around a rod with a diameter of 6 mm and for the outside coils bend the copper wire around a rod having a diameter of 10 mm. You may make the coils by clamping a drill and rod end to a bench to bend the wire coils around the rod, so run the drill in counterclockwise rotation from the perspective of a normal drill user. With a special apparatus may stripp and bend the copper wire into a coil around the rod in one step, which may be easier when several people together help. Have an approximately 1.4 mm wide gap between each windings. Make sure to count the turns.
about 50 meters of copper wire : 2.5mm²
Optional: Drill with counter-clockwise rotation to mount on wood and counter and device for winding of copper wire and stripping of insulation simultaneously
Here how to connect the inner, outer, shorter and longer coils forming each of the 3 layers; bottom, middle and top in each Magravs generator. Source: Keshe Foundation Research Group, 2015
After winding the coils while creating a distance between the turns, insert the thin coils inside the thick coils before bending the wire ends (you may then bend eyelets, preferably with pliers with no grooves so not damaged copper wire, to connect together easily through the eyelets, and the main reason for the eyelets are so plasma is not spread in all directions, eyelets are so as to not to lose plasma energy from the MAGRAVS generator system. Eylets on the ends of the wire will turn back the plasma energy which flows mainly on the surface of the wire (in the nano-coating), so feed back into the Magravs generator system.
Fully wired coil, already hanging ready to fire nano wire coat. Source: www.Plasma-Energie.org
Fire nano coating the coils after wiring together: Note direction of transition of the flame during coating process! Source: www.Plasma-Energie.org
Completely wire connect together the Magrav coils then add the nano-wire layer coating, so only two loose wire ends (the negative pole and the positive pole), proceed as follows:
Attach the Magrav coil to a metal support using one of the loose wire ends
Start the flame nano-wire coating at the far end of the wire that leads to the small coil, with the loose end of the inner coil on the right side.
After the copper wire changes color to golden yellow, move the gas burner flame slowly, you can observe the coating after natural cooling of the nano-wire for a few seconds, this should be brownish to gray with black inking.
Move the flame from the top of the shorter coil right and clockwise (as in the picture) around the central shorter coil.
Then do the longer coil counter-clockwise from the ends of the coils and moving to the left around to the ends of the longer coil.
Turn over the Magrav coils (careful as hot) and go to the second side.
Continue the flame nano-wire coating starting with the shorter central coil at the top ends of the wires leading between the coils, left counter-clockwise to the end of the shorter central coil, and then fire nano coat the longer copper coil starting at the top at the ends and move right in the clockwise direction around the longer coil to the wire ends
Let the coils cool after the coating of both sides for more than half an hour (you can fire coat the next coils set during this time)
REPEAT this entire process so to nano coat each copper coil set more than 3 times.
After flame nano-wire coating the coil sets inserted into GaNS and water solution. (If painted with GaNS paste the winding were glued togeter so reduced the performance of the Magravs energy system). Mix GaNS (after washing) of equal parts CO2, CH3 and CuO GaNS together in water (from steam distillation), (you may use water from your last GaNS washing) and pour this GaNS mixture water solution into a flat container in which a coil set may fit. Place each coils successively into the GaNS mixture water solution, so as to cover the coil sets. Then after this dipping the coil set in the GaNS water solution remove the coil set and hang to dry for more than 24 hours. Then to the next process.
This involves flame nano-wire coating external and internal capacitor parts
Note in this picture the flame direction during the nano-wire coating process after assembly! Source: www.Plasma-Energie.org
These condenser coils consist of the following parts:
Inner part: the strait copper wire with fire nano-wire coating
Outer part: coil of 2.5mm² cross section copper wire with 18 turns
For these condenser coils use a couple of feet of the 2.5 mm² copper wire for the production of 4 condenser. For each of the inner condenser strait wire part cut a length of about 15 cm of this wire and bend the ends of this each of these lengths of wire into eyelets. For each external condenser coil part cut length of the copper wire of about 45 cm and wind around 6mm rod such as screwdriver so to have 18 turns and bend the ends back into eyelets. Wind together the long ends of these four individual capacitors condensor coils to form one paralel unit as in the image. Then go to the next step and nono-wire coat these capacitor condensor coil parts.
Here flame nano wire coating the capacitors in parallel after first winding long ends together. Source: www.Plasma-Energie.org
Hang the capacitors and the wires for the capacitors on a wire. As with Magrav coils, it is important here the flame transition so also electron flow direction during coating only from top wire section where the coils join together downward over the bottom coil section. For these capacitors always use in the 4-way parallel cofiguration, After turning the 4 long wire ends into eyelets with pliers and turning together with each having an equal length of wire for a total length of about 10cm. As with all Magrav copper wire parts, always shape into the coils, wind together at top and then fire nano-wire coat. Repeat the flame nano-wire coating of these capacitor condenser units so do more than 3 times!
Diagram of 2 plasma capacitor separator components. Source: www.Plasma-Energie.org
Make the separator for the 4 capacitors units from thin hard foam boards, You can easily cut these with a Stanley knife. Fix the separator components between the four capacitors, then you may be encase this unit with materials such as shrink tubing. You need:
Rigid thin foam plastic sheet
Insulation pipe clamp
Wide cable ties
The 4 parallel capacitor unit after coating by flame with nano-wire layer
Cut out the thin rigid foam plastic parts with a (Stanley) knife, according to the adjacent plan and insert the parts into the 4 capacitor condenser unit together. Then push the 4 capacitor condenser unit into the external insulating 5cm diameter tube shell.
Here diagram with dimensions of baking paper. Source: www.Plasma-Energie.org
Next, create the internal capacitor parts. You need:
Refractory material such as baking paper
GaNS mixture of equal parts CO2, CH3, CuO GaNS, plus some silver GaNS to improve capacity
Copper wire with fire nano-wire coating
Place the baking paper on the table and spread on a thin layer of the GaNS mixture as a paste (with a small amount of water from steam distillation). Leave about 1cm at end edges free of the GaNS paste, Next, lay the copper wire with fire nano-wire coating along one the side end of the baking paper and wrap the parchment paper as narrow and as tight as possible around the copper wire with fire nano-coating. Do not squeeze this component too much. Then insert this new condenser inner part through the front of the condenser coils and pull this inner part gently out of the rear. Repeat this for all 4 coil parts of the capacitor unit.
Structure and polarity of a plasma capacitor. Source: Keshe Foundation, 2015. Source: www.Plasma-Energie.org
Insert the internal wire with nano-wire, GaNS paste and baking paper layers part into each of the capacitor coils, and secure with a cable tie to the insulation tube, then twist these long wire ends together as well, as you can see in the image. Sometimes the GaNS / baking paper layers have been damaged by assembly, so be careful, do again if failed. You may flame nano wire coat the unit, making sure not to melt or ignite the foam plastic separators, for example by using a metal shield to protect these rigid foam plastic parts.
Make the external shell from 150mm diameter plastic tube and ~500mm+ (square) sheet of rigid foam plastic, such as you can purchase at hardware stores. You need:
2 end stoppers with sleeve for 150mm PVC pipe
1 sleeve connector for joining 150mm PVC pipe
15 cm long length of 150mm diameter PVC tube
1 PVC plug
1 PVC coupling
2m 3core copper cable 1.5mm²
Laboratory test tubes with stopper, about 90mm long and diameter of about 14mm
Rigid thin foam plastic sheet of about 500x500mm
The inner plates serve to fix the Magravs shell, there are needed three interior plates, diameters and distances can be found in the accompanying drawing. The inner plate of small slits in the middle is the lowest internal plate.
Lower internal plate. Source: www.Plasma-Energie.org
Middle and upper inner plate. Source: www.Plasma-Energie.org
Stayers, go through through the inner plate. Source: www.Plasma-Energie.org
Lower internal plate with glued uprights. Source: www.Plasma-Energie.org
Lower internal plate with glued uprights. Source: www.Plasma-Energie.org
Dimensions lower inner plate. Source: www.Plasma-Energie.org
Dimensions middle and upper inner plate. Source: www.Plasma-Energie.org
Dimensions Stayers, a total of 6 pieces. Source: www.Plasma-Energie.org
Diagram, installation of capacitors. In this version, only the capacitors were installed parallel to the Magrav coils, however, it is also recommended to install those between neutral and phase. Source: Keshe Foundation, 2015
Connection of the coils together. Source: Keshe Foundation, 2015
According to the recommendation of the Foundation Keshe the height (H) to the diameter of the inner coil (D) to correspond to. In our case this 6cm (2 x 3cm spacers) are. Source: Keshe Foundation, 2015
. Source: www.Plasma-Energie.org
The components now integrate gradually into the housing. The design is so construction takes place from bottom to top. In this version, we have only one capacitor unit, with location parallel to the coils. In the first step drill and mill elongate hole for the lower stopper into which the two cables will fit. Then insert the cables through this slot and strip 4-5 cm of outer coating ends. Isolate the active phase (brown) from neutral phase (blue), both neutral and grounding straps may be the same are connected to terminal strips. When using multi-strand wire, wind and solder together both ground (green) wire ends and attach wire end ferrules. However keep active and neutral phases with natural wire strands end!
Here drilling holes and milling together to make the long hole for the cables with stopper. Source: www.Plasma-Energie.org
Here pulling the two cables through the long hole. Source: www.Plasma-Energie.org
Here connecting solder together both earth wires (green), Also wind together both neutral wires (blue) and both active hot wires (brown) for terminal block. Source: www.Plasma-Energie.org
Here parallel production so identical steps for to make more than one Magravs generator. Source: www.Plasma-Energie.org
Here fixing the first lower Magrav coils onto the lower plate. Source: www.Plasma-Energie.org
Here doing as with first Magrav coil with all the Magravs in production. Source: www.Plasma-Energie.org
Here in the Magravs pod; Twist together the "minus pole" of the capacitors (external coils winding together into centerpiece) and the incoming (active brown wire) phase together with the "negative" from Magravs first inner coil, Then twist together the "positive pole " of the capacitors (inner wire twisting together externally) to the outgoing neutral phase (blue insulation copper wire) and positive “plus-pole” 15cm wire from the Magravs final outer coil. Source: www.Plasma-Energie.org
Here; place the lower plate on the stopper, and invert a ring (3 cm wide, cut from a tube) as a spacer and the next plate above. Pull the positive pole of the lower coil and the loose coated copper wires through the cutouts to above. Quelle by: www.Plasma-Energie.org
Perform the same steps with coil 2 and three. Source: www.Plasma-Energie.org
You may fire nano coat connections to coils with gas burners, note the direction of exhaust. Source: www.Plasma-Energie.org
In total position two 3cm spacers above each other. Source: www.Plasma-Energie.org
Fill the tube with mixture of CH 3, CuO and CO2 nano state powder, close the tube with stopper and seal, best to use heat shrink tube. Source: www.Plasma-Energie.org
Slide the Goose tubes gently through the holes in each plate and center by this between the three coils. Source: www.Plasma-Energie.org
Over the last reel, you can not attach a smaller plate. (In the plan from Evert overlap sleeve) Source: www.Plasma-Energie.org
Place the cap on top with seals inside and fix, then clean for photo. Then your personal Magravs type unit will be ready to test! Source: www.Plasma-Energie.org
For your home.
One of five Rhinestone Magravs type power units. Source: www.Plasma-Energie.org
Key upgrades from V1:
Installation of split capacitors
Replacement of the GaNS powder test tube in the middle with a rock crystal with a 9cm bore
Additional aluminum GaNS powder in the capacitors for better storage efficiency
Use of better quality copper.
The two capacitor units with larger outer coil inner inner diameter for easier construction and better installation between active and neutral.
The following is the same as V1:
The complete housing with connectors, cables and spacers
Immersing the coils in a CO2, CuO and CH3 mixture
The number of turns of the coils (144/81) and capacitors (18)
The Coatingart, namely Feuercoaten
As crystals mountain crystals were used in these rock crystals, a 9cm deep hole with a diameter of 10 mm was drilled in the center. To realize this, we can make ourselves a diamond-coated special hollow drill. About two centimeters were cut from the lower crystal and then the hole was drilled. Pictures, you see below.
Cutting the crystal. Source: www.Plasma-Energie.org
Diamond Hohlborer. 9cm long with 1 cm diameter. Source: www.Plasma-Energie.org
Speed: 820 to 840. Source: www.Plasma-Energie.org
Clamping the crystal. Source: www.Plasma-Energie.org
Borehole. Source: www.Plasma-Energie.org
The finished crystal. Source: www.Plasma-Energie.org
And now ready for cleaning. Source: www.Plasma-Energie.org
We have placed all of the crystals in CO2 Goose Water, a shot Echinacea (Spagyrik) and purified with planetary singing bowls. Then allow to dry for several days and started to fill them. We have "nonosiert" CO2 goose. (Pour powder and the same amount of NaOH (by weight) with boiling water, let dry CO2 and wash as set goose is washed).
Echinacea from the garden. Ashed and combined again. Source: www.Plasma-Energie.org
The crystals in CO2 goose water. Source: www.Plasma-Energie.org
The crystals of the frequencies of the planetary sonicated. Source: www.Plasma-Energie.org
After cleaning. Source: www.Plasma-Energie.org
Preparation of dry CO2 Nano-goose. Source: www.Plasma-Energie.org
We mixed 30% crystal powder with 70% CO2 Nano-goose. Source: www.Plasma-Energie.org
9cm filled with goose. Source: www.Plasma-Energie.org
To above stuffed, so that the Gans is enclosed by the coil 3 on the floors. Source: www.Plasma-Energie.org
The cut "foot" again touched down with special glue and let dry. Source: www.Plasma-Energie.org
Magrav coil terminal Source: www.keshefoundation.org
Magrav coil terminal Source: www.keshefoundation.org
The split capacitors we have made with 9 turns and a 2,5q copper wire.
Feuercoaten from the pin to the coil 9 turns and a pin length of about 10-17cm (the longer be processed at the level 3). Source: www.Plasma-Energie.org
Level one: 2 left and 3 right. Two pins on the wound, the goose paper and pushed into the capacitors in the construction. Source: www.Plasma-Energie.org
Level two: two on the left and four on the right. The right of the pin is always a little longer, as the capacitors always be a more. Source: www.Plasma-Energie.org
Level three: two left and 5 right. This is where the right pin with goose-paper should be longer because it must by 5 capacitors. Source: www.Plasma-Energie.org
Wiring the coils as in Magrav V1 (version 1). Source: www.Plasma-Energie.org
Here we have wrapped the first capacitor from the left Magrav coil. Source: www.Plasma-Energie.org
links the second left it. Source: www.Plasma-Energie.org
Wiring the split capacitors. Source: www.Plasma-Energie.org
Feuercoaten the Magrav coils as usual. The capacitors are then coated to the turns out. Source: www.Plasma-Energie.org
Finished coated Magrav coil with its capacitors. Source: www.Plasma-Energie.org
Finished first level. Source: www.plasma-energie.org
Rinse the Magrav coils with CH3, CO2 and CUO and allow to dry 24 hours. Source: www.Plasma-Energie.org
Diesemal we need an aluminum goose. Produced as CH3 or CUO with an aluminum plate. Source: www.Plasma-Energie.org
Finished aluminum paste for our split capacitors. Source: www.Plasma-Energie.org
A mixture of: CH 3, CuO, CO2 and aluminum paste. Source: www.Plasma-Energie.org
Winding the split capacitors inside bars before installation. Source: www.Plasma-Energie.org
Feuercoaten the wires of connectors. Source: www.Plasma-Energie.org
Twisting the capacitors as Magrav Version1. Source: www.Plasma-Energie.org
Twisting the capacitors as Magrav Version1. Source: www.Plasma-Energie.org
Pushing of the crystal in the center hole adapted so that it is surrounded by the first coil. Source: www.Plasma-Energie.org
Finished second level. Source: www.plasma-energie.org
As we have also made the frame made entirely of copper pipes is our unit there like a tree in the plasma we then the coils as leaves on the "tree" hanging. We can first "steam" two weeks in a NaOH copper frame and then Feuergecoatet (sketch of the coating direction follows). The lengths of copper pipe as a guide and template you can read below. For the stand we have taken pipes with a diameter of 2oomm. In this work we use ONLY CO2 goose. In all parts.
For the basic framework you need:
14 meters of copper tubing 200mm
T-20 intermediate pieces
12 sheets of 90 degrees
Copper screws (200 pieces in Pk)
Material that you need for the frame. Source: www.Plasma-Energie.org
The lengths and quantities of copper pipes. Source: www.Plasma-Energie.org
Sketch of the lengths of tubes for the finished frame Source: www.Plasma-Energie.org
Sketch of bends and tees. Source: www.Plasma-Energie.org
Copper screws. Source: www.Plasma-Energie.org
Screw the pre-drill using a small drill and copper screws. Source: www.Plasma-Energie.org
screw together on the arches and tees, NOT solder. Source: www.Plasma-Energie.org
With the Flex the protruding screw tips sodas abflexen creates a smooth surface. Source: www.Plasma-Energie.org
In the bag there is a container with a NaOH solution. Daily with a pressure sprayer (plant) via a hole in the bag moisten the frame with NaOH solution and keep warm. Source: www.Plasma-Energie.org
We made an inspection window to check how far the coating is. Then the fire of the Red was the first not held on the tube, we decided the frame preprocess way. Better it would have been before the screw together all Dampfzucoaten. Source: www.Plasma-Energie.org
After 14 days NaOH fire red now holds very well. Since this pre-negotiation has been replaced by any coating / soiling. Source: www.Plasma-Energie.org
We have taken Plexiglas for the hanger of the coils. Better would be a plate made of polycarbonate, as it can be Coating better. We have just learned and we give so on. Since we wanted to make our unit variable and adjustable we made individual holders for 2 coils. In our case, there are five "slots" for each page. So 20 total coils.
Template for the Plexiglas for Spuleneinhängung. Source: www.Plasma-Energie.org
For the holder you need:
10 plexiglass windows (in our case 57cmx15cm)
20 sets of coils
70cm black hose diameter 12-15mm for attaching the coils (depending on the coil thickness)
Heisluftpistole for fixing
According stencil and a drill crop the Plexiglas. Source: www.Plasma-Energie.org
to gain more responsibility for the positions of 1cm long hoses roughening of the glass (in this case with a Dreml). Black tube about á 1 cm x 3 per coil. Source: www.Plasma-Energie.org
That's a total of 60 suspensions for 10 Plexiplatten. Source: www.Plasma-Energie.org
So it would be provided that it keeps the coils Source: www.Plasma-Energie.org
Here the coils are twisted differently for comparison Magrav. But since the Feuercoaten would go faster is not the stability of the coating layer is like the Noah-coating, we decided to take our time and the more complex type to use. The coils are not as soft as the fire. Although it is a lot of work because you need to subtract the potential and make the slow drying the alignment. For our Healt Unit, we have 20 sets of coils wound (20 Large us 20 Small)
Twisting the coils for Healing Unit. Source: http://www.keshefoundation.org
Here the twist loudly left the drawing opposite. Source: www.Plasma-Energie.org
Daily inspection and spraying the coils. Source: www.Plasma-Energie.org
Heat source is very useful here, and we put them in a room which was specially heated. Source: www.Plasma-Energie.org
Here you have caoten everything, even paper and aluminum (which is why we have taken Grill cups, foil would dissolve) and the plastic.
At these batteries a device for plasma-food is already provided. Source: http://www.keshefoundation.org
For 10 batteries you'll need:
1.5Q copper wire
Bond paper 20x 30cm (10 Units)
Aluminum (foil or grill cup)
2,5q uninsulated copper wire
CO2 goose paste
20cm tube (of 10)
2 holders (20)
1.5Q with a copper wire 9 turns and a length of about 10-12 cm long rod. 50 pieces. Source: www.Plasma-Energie.org
NaOH coated, aligned and subtracted potential. slowly dried and ready for processing. Source: www.Plasma-Energie.org
The "heart" is the negative pole with a 2,5q not stripped copper wire. peel the ends, turn ends and leave long Coating. 5 coil, paper and CO2 goose. Alustück about 6x8cm. Source: www.Plasma-Energie.org
The paper coating, drying and betreichen complete with CO2 paste. Let dry and strictly encase the 20 cm long copper wire. At one end wrap the aluminum and the coils (see instructions) about drag. Source: www.Plasma-Energie.org
Pull on the aluminum only two coils (please note the direction of insertion) if the coil over the aluminum to be nearly cut a little aluminum. But the aluminum MUST even wrap the paper completely. Source: www.Plasma-Energie.org
The wiring. The middle coil remains here once unnoticed for food to feed. Source: www.Plasma-Energie.org
Now the tube cut lengthwise and insert the battery. Source: www.Plasma-Energie.org
Finished Plasmabatterie.Quelle: www.Plasma-Energie.org
stick with the brackets 2 to the Plexiglas with the coil. Source: www.Plasma-Energie.org
The text is still under construction, .... Please be patient!
Schematic of the coils. Source: http://www.keshefoundation.org
16 pieces plug (2,5q cable) for connecting the coils. Source: www.Plasma-Energie.org
constant clean current free energy charger on market is 250watt
with 12v smart charger from Auroratek for about US$600 when
available: (in my opinion Auroratek should auction each new charger
starting at US$1200 on Ebay). C
taking orders for GoPowerUP 100 Suitcase 100 Watt version for sales
demonstrations ( for evaluation ). Includes: Harden plastic carrying
suitcase, Two USB charging ports, One 120VAC 100 W outlet, To order,
call Aurora in USA at 480-474-4388 Price: USD$1200.00 (Includes tax
Quantum Energy Generator (SmartPak) by William S. Alek. A technology
that can "flip" the Phase property of an Electron. Thus,
transforming a Time-Forward Electron into a Time-Reversed Electron.
The Mass of the Electron becomes Negative; however, the Charge
remains the same. The magnetic field produced by the Electron current
flow through the Spin-Zero Core forces the same Electron to phase
change or rotate from the positive dimension to negative dimension
causing the real observable magnetic portion of the field to almost
completely vanish. The remaining field engages the negative portion
The time dimension in reverse and negative energy dimensions:
magnetic flux, electricity, heat and gravity convert in turn to
negative flux negative electricity taking ambient energy by cooling
to induce superconductor with secondary feedback to create graviton
for anti-gravity expansion, to then time reverse the craft when
than the speed of light to arrive at destination before leaving
origin. Therefore, very large power gains exceeding 1,000 to 1
between the output and input are measured. This permits the
construction of self-sustainable FREE Energy / Over-unity devices
with phenomenally large observable power gains. As a superconductor
is a perfect diamagnet since there is no electrical resistance to the
forming of the current loops and fully expels internal magnetic
fields when cooled below a characteristic critical temperature. The
QEG is a parametric oscillator. There are two observations in regards
to the operation of this device. The first is the step-down
transformer configuration. This is essential to maximize
electric current output from the device. This ratio can be expressed
as 3100 turns to 350 turns or almost 10:1. In other words, the tank
circuit voltage oscillates at about 10 times the output voltage.
AuroraTek is developing a breakthrough technology that can “Quantum
Tunnel” through this barrier and transform NEGATIVE Energy into
usable energy that can safely and efficiently power our world. The
Quantum Tunneling process begins by setting up opposing forces in
magnetic material, which in turn, creates Cooper Pairing between
copper wire coils. As long as the phase angle is less than 90 degrees
for a traditional transformer, the resulting efficiency will always
be a positive number and less than 100%. This is NOT the case for the
Split-Flux [dual doughnut] Transformer (SFT) used by the SmartPAK
system. Given a special condition where the SFT output is shorted,
the input phase angle can and does exceed 90 degrees! When you
compute the cosine of this angle, the resulting value is NEGATIVE and
this is how we get a NEGATIVE Efficiency. What this means is the SFT
is acting as a source of power, sending power back to the generator.
A key observation in this article about Superconductivity is the
following "... the crucial realization
that superconductivity is associated with a bound pair of electrons,
each having equal but opposite spin and angular momentum, traveling
the metal ..." This is also known as "Cooper Pairing."
The key is opposite spin and angular momentum! Because of opposite
spin and angular momentum, the spin and angular momentum of the pair
CANCEL. The pair loses it's inertia and effectively DECOUPLEs from
the inertial field - the pair moves in the metal with NO resistance.
In other words, the metal has NO electrical resistance and becomes an
"ideal conductor" of electricity. An almost identical
effect occurs in the SFT or Split-Flux Transformer with one important
difference. The SFT becomes a Superconductor at ROOM TEMPERATURE!
This is how its done: In the SFT or Split-Flux Transformer, because
there are two output coils wired in a bifilar [An electromagnetic
coil winding of two closely spaced, parallel filament strands]
configuration, identical output current flows, but in opposite
direction. An opposing magneto-motive force is created causing
"Cooper Pairs" to form as shown above. This phenomenon
occurs below, at or above room-temperature. The SFT effectively
becomes a Superconductor at any temperature! How do we know this
phenomena is occurring? Because the primary input coil becomes an
"Ideal Inductor." In other words, the phase angle between
the voltage and current approaches 90 degrees. I can easily
demonstrate this phenomena. NO practical transformer on Earth can do
this except the SFT!!! What this means is the SFT driving a REAL load
consumes NO REAL power, or Pin -> 0 Watts! The ultimate overall
efficiency of the SFT is nearly infinite! This is critical for
understanding gravity and how this device interacts with gravity due
to the inertia-less reaction of "Cooper Pairs."
Counter-rotating opposing magnetic fields is the KEY towards building
anti-gravity technologies. The craft is essentially a macroscopic
"Cooper Pair," DECOUPLED from the inertial field. FREE
Energy is a by-product of the process.
generator with most potential: simple Quanta Magnetics PowerCells
able to survive extreme electromagnetic storms (my December 2016 6
plate module cost A$2600 (plus taxes) a
on the pricy side, a good introduction price for hand fabrication on
has become obsolete, so worth my payment to assist further
development. Buying eternal free energy products is probably the best
way to invest and help development as it exercises everything from
the science to production to promotion. Evaluation of my Quanta
Magnetics 6 plate unit: Each plate is ~31cm square. Actual output
more on hot days = 2volts x each plate varies from .1amps to .35 amps
x 6 = 2watts reducing slowly until having time to self recharge.
17C day 6 plates in parallel = 1.7volts x
falls after a while down to 25milliamps = ~.2
series = 10volts at 20milliamps = ~.2watts
I am currently using 4 plates to try and trickle charge the 4x
1.2Volt to 1.5Volt d-cell rechargeable batteries (5-7volts) of my
DAB+ radio. Quanta Magnetics new ThinFilm silicon crystal power cell
(6v) more amps and much smaller. My
2016) Quanta Magnetics 6 plate unit is about the same power as a home
made plain Hutchison (eternal) crystal power cell which you can make
at home for $100 with a copper cup and things from your local
supermarket with some extras from eBay apparently (maybe I will make
one some day). Apparently
the QM unit
best with capacitors (batteries) and QM pulse motor. The new 6v
ThinFilm PowerCells would be great for e-ink remote auto-update price
tags, mobile phones, radios, watches and a lot of
Magnetics: silicon crystal graphite PowerCell eternal charge. Sodium
Silicate gel with 10dopants between hard layers of graphite and
sodium silicate crystals I think.
plate module (the current model uses
carbide and has 10-100+ x more power with pulsing apparently)
state of the art compact 5V (6V) ThinFilm Silicon Crystal Graphite
PowerCells more powerful than each individual plate of above module.
(disappeared from QM web-page maybe a big deal to be in mobile
phones). Would also be great for internet of things such as shop
e-ink e-tags with
such as for
discount. Would also work in cars and submarines on a larger scale.
Very robust, will actually work better during solar storms,
electromagnetic pulse and higher
(Also works to some extent
the freezer). No fried circuits.
Elfe torch with eternal charger also for sale for A$99 from Australia
by Russian migrants and technology (paused production and
availability for model and technology upgrade). Harvests energy from
Schumann resonances and from Earth's magnetic field.
“ADGEX ENERGY STARTS TESTS OF GPA TECHNOLOGY FOR GENERATION OF ELECTRICITY FROM TERRESTRIAL FIELD AND PERTINENT SCIENTIFIC DISCOVERIES IN ENERGY DOMAIN: #ADGEX is glad to wish you a Blessing New Year and Merry Christmas! We’d like you to have much happiness and a wealth of smiles throughout the all upcoming year! May the world become greener and more kind! We have to make our Planet the better and greener place to live! We must be committed to the heritage and culture we will hand over to our kids and the next generation!
Forthcoming 2017 year for ADGEX will mostly become the year of entering targeted markets and rollout of such advanced green and high-effective projects as single crystals growth, MSW treatment and Energy.
Today we are making official announcement of developments in our Energy sector, particularly in regard to finalization of GPA program (Gravity Power Amplifier). This technology has been developing for several years, representing new era of electric current generators, powered by the principle of electricity amplification concentrated in terrestrial field. GPA technology is ecologically responsible and inflict no harm on biological and energy balance of Earth. GPA technology is in the sphere of renewable energy. The energy used by devices powered by GPA principle are brought back into environmental energy circulation: the taken energy amount will be always returned back.
Based on unified theory of physics of Dr Dzhabrail Kharunovich Baziev, who discovered electron neutrino, ADGEX ENERGY has developed new electrophysics where all elements are of material nature: magnetic and electric fields, as well as electric current itself. We understood the essence of gravitation and the way how we can use it as a carrier of infinite energy. ADGEX ENERGY has mastered the creation method of nonlinear systems “ground – atmosphere” and the technology of special electric pump, capable of extracting energy from Earth and transforming it into useful yield, like power, light, heat etc. The most important revelation we made and proved in practice on test benches and first prototypes was that all aspects in such systems can be forecasted based on calculations.
Drying inventing and developing of GPA, ADGEX ENERGY faced a pile of unknown problems and tasks, which had to be solved at the earliest. The most serious task to settle (despite its absurdity) was capability to repeat produced devices during mass production. For a long time, it was unclear for us why a flashlight works stable, and another one produced under the same scheme – unstable, or simply doesn’t work at all. After numerous experiments, seeking solutions and new inventions, we have come to know the key factor: highly accurate selection of materials, used for production of GPA generator core must be done. Generator core is the major part of the device, giving additional gain in electric power in complete electrical circuit.
Resulting from a long and meticulous work such selection of material was done and stable generation effect on different sources was achieved. At the same time ADGEX ENERGY has made several scientific discoveries in the following application domains: • Spontaneous noninductive generation of bridges on field transistors; • The essence of EMF (Electromotive force) and BEMF (Back electromotive force) and capability to freely control it; • Soliton electronics – discovery of solitons in impulse phenomena of electric current, which in classical physics are deemed parasitic; • Materiality of electric current, magnetic and electric fields; • The essence of generation and discharge of terrestrial field energy under the scheme Gravitation – Material (Ferro-resonance) – Electric current.
For today we have neared the next step – ADGEX ENERGY have to make and conduct testing program to make sure GPA devices operate stable as well to understand their dependence of geographical place of exploitation, light conditions, seasons and weather-climatic factors. Once the testing is over, from April 2017 we are planning to release the first readymade devices based on GPA technology, including the 2nd generation of ELFE flashlights, TACHYON Power Banks and Independent lighting systems OFF-THE-GRID.
ADGEX Company would like to apologize to all our customers for the delay in release of ELFE 2 flashlights. Unfortunately, the process of the product upgrade and transformation into the end commercial device took more time and efforts than primarily expected. We will endeavor to enter the market with readymade product by the end of the 1st quarter of 2017.
ADGEX wishes all people of our wonderful Planet for 2017 to have light and heat in your homes generated by GPA devices.”
Elfe torch. A$99.
L. Smith 400kw device is the simplest and has the highest power for
size by far but the inventor who died of old age inventions have been
mostly forgotten because of own secrecy.
Lee Smith simple construction compact 6kg (40cm x 37cm x 25.5cm)
400kw 1000v generator for cheap reliable robo-taxi and road vehicles,
Would also work in cheap electrical propeller aircraft and boats.
Motor driven resistance-less rotating disc to alternate magnetic
shield flux between permanent magnets in coils. Robust supply able to
continue operating if war or coronal mass ejection solar flare
disrupted supply of foreign oil or grid. Plus correct balance of
national international trade accounts. The physics works: instead of
using counter rotating magnetic resistance to create flux (electrical
potential) this generator uses rotating alternating magnetic
shielding so no physical resistance. (Technique1: Sprinkling glue on
vinyl record with alternating neodynium powder 2: glue alternating
magnetic shielding foil to vinyl record)
Effect (SEG Magnetics) free energy anti-gravity (flying saucer)
technology. ~100ton cargo military and to space infinite range (Mars)
launcher lifter, lander and return craft. Able to revolutionise
space, military and air transport. Free to run: no fuel required;
will convert all ambient energies and forces into electron flow for
collection as electricity starting with positive magnetic flux then
ambient heat and then after this causes super cooling
superconductivity negative flux convert gravity (the entire positive
and negative energy radiation spectrum) to electron flow for
collection as electricity (after ~5 minutes from start up) so cause
negative mass so as to lift any load within the field and as causes
expansion of universe, a month of anti-gravity effect acceleration in
space will propel craft to light speed.Generators can range in size
from soon again 15Kw, 100kw to power cars, up to power stations rated
producing hundreds of Megawatts. All materials and proportions of all
components of a Searl Effect Generator (SEG) are a product of a
precise law of squares. The SEG consists of three concentric layers
of equal weight to form rings and rollers each made of four different
materials in concentric attachment to each other. The layers
typically consist of (from inner layer) non aligned random magnetic
particle polarisation Neodymium, Teflon, Permanent magnet in polar
alignment such as ceramic and neodymium boron magnet, and outer most
is OFHC copper. The three rings are fixed to a base. Surrounding each
of the rings, and free to rotate around them, are rollers - typically
10 on the first ring, 25 on the next and 35 on the outer ring.
Surrounding the rollers on the outer ring are coils which are
connected in various configurations to supply either AC or DC current
at a variety of voltages. Imprint magnetic multiple poles in wave
formation onto rings and rollers to form frictionless magnetic
bearings. These also arrange the static charge into opposing charge
clusters which cause the rollers to rotate around the circumference
of the ring. When the SEG rollers are brought into close proximity to
the SEG Ring, the magnetic field causes negative ions and electrons
to be drawn to accelerate through the machine. This process is
assisted by the highly electron-attracting rare earth metal
neodymium. A SEG is 3 stage step up rotary transformer, increasing
final output to a very high voltage. The output windings collection
coils to step down to 240 volts at 15KW. Can provide electrical, and
anti-gravity output, in which case the SEG can propel the space
vehicle directly. Produces an anti-gravity effect strong enough to
cheaply and safely launch satellite, cargo, and people for less than
10% of the development and launch costs of obsolete dangerous
expensive rocketry technology. May produce artificial gravity such as
to live in space. Because a SEG is self-reliant will operate in
remote locations without liquid fuel. Quiet: little aircraft noise.
Searl Magnetics now SEG Magnetics in the USA will do on going
research and development with the discoverer John Searl. The first
experimental free energy generator with unexpected anti-gravity
effect, broke free, lifted the roof, flew off into space and was
lost. Our founder John Searl and company can control the anti-gravity
effect. Gave a remote control device to USA Edwards Air Force Base
For evaluation, but they were unable to make use of it as it or was
deemed theoretically impossible even when actually in flight, was
useless to the Air force in the then raw small configuration. John
Searl and company spent several million dollars of science
foundation, government and private donations to build several Levity
Discs and global guidance network in the 1960s. John Searl's unmanned
anti-gravity craft made 200 orbits of the earth at low altitude and
high speed. Our John Searl produced another small device in New
Zealand, and began work on a larger vehicle able to carry a
passenger. John Searl used the small machine as a household and
workshop power source. John Searl then persistently refused to pay
for the connection of electricity to his property, which at that time
was illegal in NZ, and was subsequently sent to prison, for destroyed
meter. During this period in prison someone set fire to John Searl's
workshop, the fire destroyed the large anti gravity vehicle with all
of his notes. It was not known what became of the small generator but
it was also lost or destroyed. John Searl and SEG Magnetics will
reconstruct plans and measurements, experiment with modern materials,
trial making some components, publish technical books (1000 page
engineers manual) so anyone with deep pockets will be able to build
Searl Levity Disk (saucer) and the Searl effect web page on the
device, and try to raise enough money to develop, build, and
manufacture more devices. Workshop has been constrained by shoestring
budget of less than $10,000/month for several years. I suggest John
Searl should make the technology more available for success one way
or another, including pending sale of saucer to China and eventual
construction in China. John Searl now wants to abandon any attempt to
gain a patent and void any attempt by others to steal and control
rights to his technology by open sourcing all of his Searl Effect
Generator Inverse Gravity Vehicle technology. John Searl is now about
80 years of age, and coming to the conclusion the only remaining
opportunity for manufacture of his invention and personal success is
to helps any maker with deeper pockets construct this invention. John
Searl should and would still like to be paid a prize and royalties
and gain credit for this work to lead to the construction of new
copies of this invention. Insufficient funds prevented the existence
of any currant demonstration device. I suggest PayPal subscriber
regular donations crowd funding for rights to portion of future
revenues (not shares to comply with SEC). $5,000,000 should be
sufficient to equip a workshop to construct a working demo model by
SEG Magnetics, Once having the equipment the manufacturing cost of
each precision Searl Effect device would be minimal above the cost of
materials. From then on each device would cost $5,000 to $10,000 to
construct. A Russian team have a part duplication single stage device
[ instead of the three stage Searl device ] and reproduce a small 35%
reduction in weight and free electricity. The first Searl Effect
products are envisioned to be 1-A compact 15 kW generator unit,
measuring approximately 46 x 61 x 12 cm, to provide DC or AC single
or three phase electricity at a variety of voltages, typically 12 to
240 V Each unit would deliver 60,000 KW hours before requiring
remagnetization on an exchange unit basis,. and 2-A flying craft
called an Inverse-G-Vehicle or (IGV). The Searl effect is verified by
partial duplication in Russia by Roschin and Godin. Institute for
High Temperatures, Russian Academy of Science ; "A 1 meter
diameter disc at 600 rpm obtains a 35% reduction in weight while
generating 7 KW of excess electric power." "There has been
a great interest in examining non linear effects in the system of
rotating magnetic fields. Such effects have been observed in the
device called Searl's generator or SEG (SEG, Searl Effect Generator)
A SEG consists of a series of three rings and rollers that go around
those rings. The rollers revolve around the plates that form the
rings, but they do not touch them," "All the results we
obtained are extremely unusual and require some theoretical
explanation. Unfortunately the interpretation of results within the
framework of the conventional physical theory cannot explain all the
observed phenomena and first of all the change of weight. The change
of weight is possible to interpret as a local change of gravity force
or as an occurrence of propulsion force by repelling from its own
field" Searl technology superior to top secret extra-terrestrial
technology exchange program anti gravity that required elements or
difficult expensive construction techniques not within Earth
resources or unsafe nuclear reactions such as for megawatt power
supply for Biefeld Brown technologies and because of ease of mass
production (has had high initial tooling costs) precise complete
system design, high power, no dangerous polluting toxic elements or
compounds (red mercury TR-3b and TR-6 having only 89% weight
reduction plus thrusters for superluminal speeds to travel forward in
time also back somehow) or nuclear reactions (element 115
ununpentium) so environmentally clean and infinite range as would
allow humans very fast travel (possibly faster than light) to and
return from Mars. Possibly the best combination of technologies would
be to use the Biefeld Brown principle for instant take off from
charging capacitor for instant ion wind away from and thrust towards
the sharp electrode with the surplus electricity and delayed extra
thrust for time travel speeds in space using the Searl effect. Montok
time travel experiments were limited because required huge power
input as were not self powering. To contribute to the Searl project:
Hutchison Crystal Power Cell:
Normal voltage 1.5Vx.2A.
#8 My convergence of several designs into a basic build process to make your own Crystal Plasma Power Cells. Someone should build this at home, this may work; Safety: Wear eye protection, gloves and air filter (I glue a snorkel mouthpiece into the best replacement filter component from a face mask type one for better seal). Items: Carbon graphite crucible and magnesium wire with carbon nano-wire coating possibilities as conductive + pole electrode (anode) core. Zinc and Copper cups with carbon nano-wire coating options as conductive – pole electrode (cathode) shell also stainless steel and aluminium pop drink cans additional options. Crystal diode electrolyte: blend dry (to prevent limited acid alkaline chemical reaction) powders, Hutchison method melts together just salt crystal components and dopants at about 200 degrees Celsius. Can also add just crystal and dopants mix to copper cup with magnesium core and non conductive heat resistant spacer in bottom then heat over flame to melt together, not boil solid. Dry crystal powder mix (without having to melt together) seems to work nearly as well and a lot easier. +Maybe with optional binder to make more durable of equal parts poly-vinyl-alcohol (PVA wood glue) to react with potassium hydroxide to create super capacitor and polyethylene terephthalate (PET polyester resin in styrene base to make solid) also as a capacitor? (may skip and use just dry powder mix so components will be upgradable and reusable for testing): +Powders to mix together and dehydrate in food dehydrator. (no water powders: so no limited acid alkaline to salt battery reaction). 50% Keshe gans mix. (Convert radiation to electricity as in Keshe units and as for Tepco Fukushima radiation cleanup) (note; possibly a drop of liver of sulphur in the sea water would help oxidization?) Such as; Dry carbon-dioxide gans (white) and zinc-oxide (cream yellow) Keshe gans powder; Use copper with nano wire coating, to coat wash then steam with water solution with 4% pure sodium hydroxide caustic soda, 1% pure potassium hydroxide, 1% silver nitrate (to create silver nano fibres) and a drop of liver of sulphur. Then neutralise alkalinity of caustic soda on plate with citric acid (lemon juice) to reduce toxicity and rinse with pure water while not touching or rubbing plate surface so protect nanowires structure. Also place carbon graphite rods in plastic food container to charge with ~3v such as from 10cm square solar panel. Also zinc plate in sea water if desperate, better to have in pure water from steam distillation 1.5% pure sodium chloride, 1.5% potassium chloride, 1.5% sodium silicate and 1.5% silicon dioxide solution I think (the main thing is the right salinity without contamination), Connect together plates with wires and normal green LED. NO power between the copper plate with black nano wire coating and pure zinc plate. (remove green LED for more zinc oxide). Add 2 separate carbon graphite rods and connect rods to (3V .5A/litre) charge such as from 10cm square solar panel to release carbon for the carbon dioxide gans. Let run for a week. Let settle for 2 days then pour off water on top so leave gans sedimentation on bottom, repeat 4 times then dry reduce in sun and may warm in Pyrex glass on stove if was too cold weather. Dry CH3 methyl Keshe gans (orange powder – use copper with nano wire coating from caustic soda (carbon graphite rod just as good) and stainless steel (iron + chromium) plate in sea water (10% sea salt for sodium chloride and silica). Dry titanium dioxide Keshe gans (white – use copper with nano wire coating from caustic soda and titanium plate in sea water (10% sea salt) connect together with resister and LED, apply 3V x .02A/litre to plates using adjustable power supply with negative black wire to copper with nanocoating with carbon graphite rod just as good). Dry copper oxide Keshe gans (turquoise powder – use copper plate with nano wire coating from caustic soda and copper plate in sea water (10% sea salt), aerate with aquarium oxygenation pump and bubbler, apply (1.9V .8A/litre) Dry nickel gans (blue turquoise), use copper with nano wire coating from caustic soda and nickel plate such as .999 nickel coins in sea water (10% sea salt), apply 1.9V x .005A/litre through resistor to + on nickel and – to copper plate with nano wire coating. Dry mix of Keshe ganses of each of the dopants in the dopants section (using same process), also possibly Ganses of copper and gold. 40% equal parts the following dry crystal salt powders and things – diode dielectric electrolyte: Dry silicon carbide powder (uses; abrasives, sandpaper, armour) Dry sodium hydrogen carbonate powder - (Bicarbonate Baking Soda / sodium carbonate) (alkaline - salt) Dry potassium hydrogen tartrate powder- Cream of tartar – (acidic - salt) Dry potassium chloride powder - common salt substitute and also as water softener. (acidic - salt) Dry potassium sodium tartrate tetrahydrate crystal powder - Rochelle salt. (alkaline - salt) Dry hydrated potassium aluminium sulphate powder / aluminium ammonium sulfate (alum). (acidic - salt) Dry sodium tetraborate powder - commonly known as 20 mule team Borax. (alkaline - salt) Dry magnesium sulfate powder - commonly known as epsom salt. (neutral – salt salt) Dry sodium silicate powder – (alkaline - salt) Dry perovskite crystal powder. (in solar cells to convert sunlight to electricity) 10% equal mix of additional crystal salts and electrets: Dry amethyst crystal powder. Dry cobalt chloride powder. Dry carbamide crystal powder – urea. Dry sodium hydroxide alkaline crystal powder – caustic soda. Dry potassium hydroxide. Dry fluoropolymers powder – electret polymer (do not burn). Dry polypropylene powder – electret polymer (do not burn). Dry polyethyleneterephthalate powder – electret polymer (do not burn). Dry potassium iodide crystal salt powder – as for radiation poisoning converts radiation to electricity. Dry zinc sulphide crystal powder – radiant energy collector in Thomas Moray power generator. Dry quartz crystal powder. Dry bath salts. (Dead Sea Mineral Bath Salts) Dry magnesium chloride. Dry sodium hypochlorite powder (swimming pool chlorine). Dry calcium carbonate crystal powder – chalk. Dry barium silicon oxide. Dry glucose sugar crystal powder; C6H12O6 Dry Ca3Co4O9 crystal powder. (heat to electricity) Dry barium titinate crystal powder – super capacitor also ptc thermistor current limiter to induce internal electrical resistance if hot to prevent burn out. Doping: To .01% Dry germanium powder - in resonance quantum tunnel diodes with negative resistance, frequency conversion and so amps x volts = constant current (watts). To .01% Dry silver nitrate powder. To .01% Dry iron pyrite crystal powder – fools gold. To .01% Dry galena - Lead sulphide crystal powder. Optional (Breath through air filter to limit lead poisoning) Radio wave collector and converter to electricity. To .01% Dry gallium arsenide powder – in resonance quantum tunnel diodes convert to single voltage. To .01% Dry tin powder – in quantum tunnel diode. To .01% Dry yttrium powder. To .01% Dry iridium powder. To .01% Dry terbium powder – heat to electricity.
To .01% Dry boron powder (as in solar cells).
To .01% Dry phosphorous powder (as in solar cells). Prime polarity of cell by application of 12 volts to cell then diode while hardening.
(you may have to reduce the portions of conductor metals and increase portion of resin to get the right conductivity in this semiconductor medium so not short internally)
Version 1: Zinc cup for electron donor cathode – pole. Wash and steam internal area in caustic soda. Let dry in sun to remove water. In bottom of cup put electrical insulator disc spacer. (For electron attraction anode + pole terminal to use carbon graphite crucible with Au+Pt (monoatomic gold and platinum) powder in it in shop bottle comes in and fill to top with pure water from steam distillation (from grocer) and shake (others used Pb (lead) gans powder in center but that was too toxic). In the gap around the crucible to place 3 tubes unit to join at silver coin (to go under crucible), to nano wire coat in entirety (before adding heat shrink tubing to each coil)); make tubes unit from 3 copper coil, each with an exterior coil and an interior coil with fire nano-coating of exterior of each before putting in heat shrink tubing; The coils wind the same way when looking from where join together at top at the top winding down a clockwise direction for 18 turns; the outer coil terminating so bending back into an eye ring, the second inner copper coil in heat shrink tubing to insulate from the (each) outer coil so to return through the middle of each outer coil to the bottom, then this inner coil to connect with normal copper power wire (in insulation) to the 1oz silver coin (to be the conductor at bottom of carbon graphite crucible which is also an electrical conductor); then fire nano wire coat the connections (such as with stove lighter flame) and then dip this entire coil tube unit including coin in caustic solution then steam in the caustic solution to nano wire coat everything; When dry seal each of the 3 (exterior) coils (with interior coils inside) exterior with heat shrink tubing with flame and seal bottom where to the copper wire to extend to the coin, so make 3 water proof tubular cup containers open at the top; fill each of these 3 copper coil tubular containers individually so as to have in clockwise order; one with CUO (copper oxide) gans in pure water from distillation slurry, one with CH3 (methyl) gans in pure water slurry, and one with CO2 (carbon dioxide) gans in pure water slurry, then seal the top above these coils by heating the top heat shrink tubing with stove lighter flame so completely seal without contaminated gans slurries. (An additional model has these 3 coil sets in series with junctions connecting to silver coin at base) Place 3 coil tubes and coin unit with nano wire coating below the carbon graphite crucible. Blend dry crystal powders and electret polymers mix, Keshe dry gans mix and dry dopants mix then put between the carbon graphite crucible, the copper coil tubes and the zinc cup shell (may use polyester resin to make more durable and fix copper tubes in place). Use edge of zinc cup for negative terminal. Use crystal plasma power cells to enhance power and polarize. (Be careful; do not electrocute yourself)
Version 2: 120mm-150mm cube plastic food container. Wash and steam 100cm x 100cm copper and silicon carbide graphite layers in pure 100% sodium hydroxide caustic soda. Let dry in sun. Place 100mm x 100mm x 1mm copper layer in bottom of container. Drill hole through copper layer and bottom of food container for conductor bolt, washers and nut to use as negative terminal (cathode). Then add 10mm layer mix of crystal salt powders, electret polymers, 3 Keshe gans and dopants to form 10mm powder layers (powder mix so maintain natural crystal structures). Then add 100mm x 100mm x 1mm carbon graphite layer. Then add second 100mm x 100mm x 1mm zinc layer. Then second 10mm layer of crystal salts, electret polymers, Keshe gans and dopants mix. Then second carbide graphite layer, and so on. Bolt top carbon graphite layer to lid for positive (anode) terminal. Place on side so powder mix will connect all plates.
Version 3: Wash and steam zinc layers and carbon graphite layers with water in 5% pure sodium hydroxide caustic soda and let dry in sun. Make layer of crystals and polymers and dopants mix together equal parts polyester resin with crystal powders, polymer electret powders, 3 Keshe gans powders and dopants mix and paste to both sides plus with hardener to make 3mm gel layer of consistent thickness harden around 110mm x 110mm thin layer of polyester fabric separator to ensure insulation between conductor plates of 100mm x 100mm x 1mm silicon carbide graphite and 100mm x 100mm x 1mm copper layer to bind together when set. Connect wire with black insulation to copper plate to be cathode negative terminal. Connect wire with red insulation to silicon carbide graphite layer to be anode positive terminal. Optional to boost as may produce more than enough electricity anywhere; adhere these tiles to reverse side of solar panels to collect and convert ambient heat or radiation into electricity. Version 4: With perovskites crystal powder in crystal powders mix and for anode use cheap transparent conductor film of zinc-oxide with aluminium and gallium dopants on PET (polyester substrate) to be actual solar cells as well.
Version 5: Buy new zinc-carbon D-cells. Remove external coverings and end plates and insulator ring (wear gloves and eye protection). Carefully remove carbon graphite rod anode with pliers, dig out manganese dioxide, Wash carbon graphite rod and zinc can then with mix of water from steam distillation plus pure caustic soda in water solution. Add to water to make 4% by weight pure sodium hydroxide (caustic soda) and 1% pure potassium hydroxide to internally wet zinc cans and seal with end plate and tape and place opening down in sun for 1+days depending on temperature and repeat 5 times; should turn black inside with nano-wire coating (do not touch inside so not damage nano-wire coating), then open and dry completely to harden nano coating while connecting with alligator clips to multi meter on 200millivolt range to bleed electrical charge from zinc can. Fill bottom of each zinc can with dry ganses, crystal salts, electret polymers and dopants powders mix, set carbon graphite rod in middle so no short to zinc can fill to top with powder mix. Have thin tubes of CH3 (methyl) gans and nano particles? in H20 so water tight with seal at ends to place between carbon graphite rod core and zinc can shell and so as to not short out cell? Reassemble insulator ring and end plates (scrape away center of top plate to have good electrical connection with carbon graphite rod) seal such as with heat glue gun and in brown heat shrink tubing. D-cell battery charge should then be eternal. May require voltage converter and regulator which you may install inside your device such as a DAB+ radio. May also power charger, LED light, aerators and hydroponics pump eternally. May have in parallel and series and add DC-DC smart charger to direct charge batteries in line interactive uninterruptible power supply so use the UPS inverter to power home appliances.
Who known how this works; no complicated physics graffiti, just a lot of observations, convergence and basic principles.
Version 6: de sulphur lead acid battery for a week with electric de sulphur pulse unit, drain lead acid battery (wear gloves and goggles and be careful as acid was very corrosively dangerous), rinse battery with baking soda in water from distillation, nano wire coat battery plates with caustic soda so not short somehow, rinse with lemon juice, dry, and then fill with dry crystal salts, gans, electrets, capacitor and dopants powder mix, Can also add powders to resin and hardener to pour into battery so set solid so make indestructible and add capacitor for spike surge capability. Apparently this also works as rechargeable battery with water from distillation with full original amperage, voltage and about 50% of amp hours.
#9 InfinitySav Free Energy Device. Start with a normal 1.5v AA battery for under 1 second. Then the device works by its self and produces clean portable electricity free. Silent operation and perpetual. Feedback mechanism with 700% efficiency. Also will be possible to produce higher power such as 30W-2MW. The device works on the resonance frequencies 2-7Khz. Generates 12V DC and 220V AC reliable free electricity anywhere.
ERR Flux Generator by Noah's Ark Research Foundation. Inventor, James
B. Schwartz of the Philippines. For small electrical: Toaster, Lawn
mower, Vacuum cleaner. Small version for electronics. A suit case
sized device containing 4kg of components puts out six kilowatts of
electricity drawn from the surroundings, using a solid state with
solid state aluminum-bismuth layers of "left-handed materials"
Aluminum and Bismuth and interwoven coils. Tapping into Earth
radiation frequencies. Undergoing testing and refinement, new left
hand materials may produce an 8x improvement in power output per unit
of weight. Based on similar technology by Moray, Tesla, and Tom
Bearden except that it doesn't need an external power supply to
switch the magnetic fields. It uses a very powerful magnet with a
special circuit board that contains a new hi-tech chip to switch the
magnetic fields. It also contains ultra-thin graphite sheets called
graphene. Using a very sensitive technique to separate the individual
sheets of carbon atoms that are layered on top of one another in
graphite. These layers are electrically conducting because they
contain electrons that are free to roam across each layer. In the
graphene, the charge carrying particles act as if they're without
mass, or weight. In this respect they are more like photon particles
that convey light than like electrons. Progress is being made and
arrangements are in place to move toward the realisation of genuine
usable power production, but there are still steps ahead that must
not be rushed to ensure the success of this technology (Aug 8, 2009).
In one device three plates have a solid plate of aluminum on one
side, [followed by] a sheet of bismuth, [followed by] another
aluminium plate with six cut-outs which contain coils; covered by
another sheet of bismuth, another aluminium plate with cut outs for
more coils on top of that, then another sheet of bismuth, then
another solid plate of aluminium, form 1 panel. The activator causes
alternating frequencies in these plates to produce electrons. The
device hones into the correct frequencies to interact with the plates
interaction with the earths radiation fields. Other research teams
around the world are doing similar experiments that also backup this
theory. This device uses materials that support this type of effect
for light and other electromagnetic waves. The experimental Flux
Power Station uses A special frequency generator to induce a series
of alternating frequencies to create a flow of electrons when
activating the magnetic flux field. The theory is still in the
experimental stages which requires a lot of research and testing for
safety and other factors. The secret is in the material used, the
size of the wire and the number of turns plus the frequency and how
you alternate that frequency. There are many combinations that will
allow you to get small amounts of electrons to flow. A 160,000 watt
power station being built. A smaller model worked very well so bigger
one should work when built and tested. This ERR Flux Power Station is
designed to run a large house or you can add more Flux Power Vaults
each of 10,000 watts if you need more power. First prototype in the
basement of house in the Philippines. In an airtight chamber a
special gas is pressurised to 1.5 psi. Each of 10 chambers will be
produce 10 to 18,000 Watts DC power. The new Flux Power Plates should
be maintenance free for many years. As newer Power Plates are
developed the older Plates can be easily replaced by shutting down
one chamber at a time. After the frequency generator is shut down to
go into the chamber. The chamber holds ten Flux Power Plates that are
48” X 48” X 4” to produce 1,000 to as high 8,000
watts each depending on the Plates. As newer left-handed materials
that support electromagnetic wave propagation are made power output
may increase. Any oxygen in the chamber has caused flash burns
between the plates. Each inner aluminium plates has 144 slots that
are cut to 10 ½ X 2 ½ cm where 144 special coils are
inserted. Noah’s Ark Research facility planning to move from
Japan to Arizona to join the new Ranch Project of Bill Alek. Also
planning to put Noah’s Ark Research facilities in India and the
Fiji Islands with partner Company: New Ark Power. This inventor
produced 20,000 working devices for sale but all were confiscated by
the Japanese government for because many operating in close
to each other [ within 50 meters ] caused TV and radio interference.
Orbo on-board eternal charger cell: solid state for eternal use of
device without plugging in to recharge (no need for external cable
input). Between 2 sheets of different conductor metal possibly p-type
and n-type, a thin black electret gel compound (synthetic
Create electret by after heating it above its melting temperature
slowly cooling the
within a strong static electric field of several kilovolts/cm., To
hold charge potential when cool with voltage relative to sheet area
by slowing down magnetic field also gathers ambient fields into
electricity. (An electret is a stable dielectric material with a
quasi-permanently embedded static electric charge (which, due to the
high resistance of the material, will not decay for time periods of
up to hundreds of years) and/or a quasi-permanently oriented dipole
polarization. Electrets are made by first melting a suitable
dielectric material such as a polymer or wax that contains polar
molecules, and then allowing it to re-solidify in a powerful
electrostatic field. The polar molecules of the dielectric align
themselves to the direction of the electrostatic field, producing a
dipole electret with a permanent electrostatic 'bias'. Modern
electrets are usually made by embedding excess charges into a highly
insulating dielectric, by means of an electron beam, a corona
discharge, injection from an electron, electric breakdown across a
gap or a dielectric barrier. Electrets, like magnets, are dipoles.
Another similarity is the radiant fields: They produce an
electrostatic field (as opposed to a magnetic field) around their
perimeter. When a magnet and an electret are near one another, a
rather unusual phenomenon occurs: while stationary, neither has any
effect on one another. However, when an electret is moved with
respect to a magnetic pole, a force is felt which acts perpendicular
to the magnetic field, pushing the electret along a path 90 degrees
to the expected direction of 'push' as would be felt with another
a type of condenser microphone that eliminates the need for a power
supply by using a permanently charged material. ) Roll 3 (2 metal)
sheets into (1.4 volt) AA cell. Set to revolutionise cordless
electronics: light bulbs with auto darkness, infra red with
temperature adjustment and movement sensor and torches (remote
village lighting), mobile phones (eternal remote banking), portable
laptop computers (reliable remote research writing and submission),
radios (remote access to information), TVs (remote education),
Light Power (Blacklight Power): uses semi-nuclear reaction of
abundant water to create solar light for high intensity solar panels.
hydrogen (water) into
electricity and hydrinos (dark matter). Possible use as fuel and
energy for android able to survive in the wild, grid power stations,
also road, rail, ships and (military) submarine.
#14 Water as fuel: Stanley A. Meyer. Patent now expired so anyone can copy it all and use without restriction or royalty payment :
Process and apparatus for the production of fuel gas and the enhanced release of thermal energy from such gas US 5149407 A
Abstract: Water molecules are broken down into hydrogen and oxygen gas atoms in a capacitive cell by a polarization and resonance process dependent upon the dielectric properties of water and water molecules. The gas atoms are thereafter ionized or otherwise energized and thermally combusted to release a degree of energy greater than that of combustion of the gas in ambient air.
BRIEF DESCRIPTION OF THE DRAWINGS
FIGS. 1A through 1F are illustrations depicting the theoretical bases for phenomena encountered during operation of the fuel gas production stage of the invention herein.
FIG. 2 illustrates a circuit useful in the fuel gas generation process.
FIG. 3 shows a perspective of a "water capacitor" element used in the fuel cell circuit.
FIG. 4 illustrates a staged arrangement of apparatus useful in the process, beginning with a water inlet and culminating in the production of thermal explosive energy.
FIG. 5A shows a cross-section of a circular gas resonant cavity used in the final stage assembly of FIG. 4.
FIG. 5B shows an alternative final stage injection system useful in the apparatus of FIG. 4.
FIG. 5C shows an optical thermal lens assembly for use with either final stage of FIG. 5A or FIG. 5B.
FIGS. 6A, 6B, 6C and 6D are illustrations depicting various theoretical bases for atomic phenomena expected to occur during operation of the invention herein.
FIG. 7 is an electrical schematic of the voltage source for the gas resonant cavity.
FIGS. 8A and 8B, respectively, show (A) an electron extractor grid used in the injector assemblies of FIG. 5A and FIG. 5B, and (B) the electronic control circuit for the extractor grid.
FIG. 9 shows an alternate electrical circuit useful in providing a pulsating waveform to the apparatus.
What is claimed is:
1. In an apparatus for obtaining the release of a gas mixture including hydrogen and other dissolved gases entrapped in water, from water, the improvement consisting of a resonant electronic circuit in operative relationship with the water in which the dielectric property of water determines the resonance of the circuit.
2. The apparatus of claim 1 in which the resonant circuit includes a resonant charging choke.
3. The apparatus of claim 1 in which water is included as a dielectric between conductive members that form a capacitor in the resonant circuit.
4. A method of obtaining thermal energy from water, consisting of:
(A) providing a capacitor, within which water is included as a dielectric, in a resonant charging choke circuit that includes an inductance in series with the capacitor;
(B) subjecting the capacitor to a pulsating, unipolar electric field in which the polarity does not pass beyond an arbitrary ground, whereby the water molecules within the capacitor are subjected to a charge of the same polarity;
(C) further subjecting the water in said capacitor to said pulsating electric field to achieve a pulse frequency such that the pulsating electric field induces a resonance within the water molecule;
(D) continuing the application of the pulsing frequency to the capacitor after resonance occurs so that the energy level within the molecule is increased in cascading incremental steps in proportion to the number of pulses;
(E) maintaining the charge of said capacitor during the application of the pulsing field, whereby the co-valent electrical bonding of the hydrogen and oxygen atoms within said molecules is destabilized, such that the force of the electrical field applied within the molecule exceeds the bonding force of the molecule, and hydrogen and oxygen atoms are liberated from the molecule as elemental gases;
(F) collecting said hydrogen and oxygen gases, and any other gases that were formerly dissolved within the water
(G) subjecting the collected gas mixture to a pulsating, polar electric field whereby electrons of the gas atoms are distended in their orbital fields by reason of their subjection to electrical polar forces, at a frequency such that the pulsating electric field includes a resonance with respect to an electron of the gas atom;
(H) cascading said gas atoms with respect to the pulsating electric field such that the energy level of the resonant electron is increased in cascading incremental steps;
(I) ionizing said gas atoms;
(J) subjecting the ionized gas atoms to electromagnetic wave energy having a predetermined frequency to induce a further election resonance in the ion, whereby the energy level of the electron is successively increased;
(K) extracting further electrons from the resonating ions while such ions are in an increased energy state to destabilize the nuclear and electron configuration of said ions; and
(L) subjecting the destabilized ions to thermal ignition.
5. The apparatus of claim 2 in which water is included as a dielectric between conductive members that form a capacitor in the resonant circuit.
6. An apparatus in accordance with claim 1 or claim 2 or claim 3 or claim 5 in which the gas mixture released is collected and utilized as a source of thermal energy, and including further successively interconnected:
(A) means for collecting the gas mixture released in the apparatus;
(B) means for providing a pulsating, polar electric field to the gas mixture, whereby electrons of the gas atoms are distended in their orbital fields by reason of their subjection to electrical polar forces, at a frequency such that the pulsating electric field induces a resonance with respect to an electron of the gas atom; and the energy level of the resonant electron is increased in cascading, incremental steps; and
(C) means for providing a further electric field to ionize said gas atoms;
said further means being connected to an electromagnetic wave energy source for subjecting the ionized gas atoms to wave energy of a predetermined frequency to induce a further election resonance in the ion, whereby the energy level of the electron is further successively increased; and
(D) an electron sink for extracting electrons from the resonanting ions while such ions are in an increased energy state to destabilize the nuclear and electron configuration of said ions;
(E) a control means for directing particle flow in a continuous manner through the electric fields, wave energy source and electron sink to a final orifice at which the destabilized ions exit from the apparatus; and
(F) a terminal orifice at which the said ions exit from the apparatus.
7. An apparatus in accordance with claim 1 or claim 2 or claim 3 or claim 5 including means for collecting the gas mixture released from the water.
8. An apparatus in accordance with claim 7 including means for directing the gas mixture to a combustion locus.
9. The apparatus of claim 8 in which a flame is produced at the combustion locus.
10. The apparatus of claim 8 in which an explosion is produced at the combustion locus.
11. The apparatus of claim 8 in which the combustion locus is in an automobile.
12. The apparatus of claim 8 in which the combustion locus is in a jet engine.
FIELD OF THE INVENTION
This invention relates to a method of and apparatus for obtaining the release of a fuel gas mixture including hydrogen and oxygen from water and to a method of and apparatus for obtaining the further release of energy from such a fuel gas mixture. Charged ions derived from the fuel gas are stimulated to an activated state, and then passed through a resonant cavity, where successively increasing energy levels are achieved, and finally passed to an outlet orifice to produce thermal explosive energy.
OBJECTS OF THE INVENTION
A first object of the invention is to provide a fuel cell and a process in which molecules of water are broken down into hydrogen and oxygen gases, and a fuel gas mixture including hydrogen, oxygen and other gasses formerly dissolved within the water is produced. A further object of the invention is to realize significant energy-yield from a fuel gas derived from water (H2 O) molecules. Molecules of water are broken down into hydrogen and oxygen gases. Electrically charged hydrogen and oxygen ions of opposite electrical polarity are activated by electromagnetic wave energy and exposed to a high temperature thermal zone. Significant amounts of thermal energy with explosive force beyond the gas burning stage are released.
An explosive thermal energy under a controlled state is produced. The process and apparatus provide a heat energy source useful for power generation, aircraft, rocket engines, or space stations.
DESCRIPTION OF THE PREFERRED EMBODIMENT
A fuel gas is produced by a hydrogen fracturing process that follows the sequence of steps shown in the following Table I. Beginning with water molecules, the molecule is subjected to successively increasing electrical, wave energy and thermal forces. In the succession of forces, radomly oriented water molecules are aligned with respect to molecular polar orientation and themselves polarized and "elongated" by the application of an electric potential to the extent that covalent bonding of the water molecule is so weakened that the atoms disassociate and the molecule breaks down into hydrogen and oxygen elemental components. The released atomic gases are next ionized and electrically charged in a vessel while being subjected to a further energy source that promotes inter-particle impact in the gas at an increased overall energy level. Finally, the atomic particles in the excited gas, having achieved successively higher energy levels, are subjected to a laser or electromagnetic wave energy source that produces atomic destabilization and the final release of thermal explosive energy. Engineering design parameters based on known theoretical principles of atomic physics determine the incremental levels of electrical and wave energy input required to produce resonance in each stage of the system. Instead of a dampening effect, a resonant energization of the molecule, atom or ion provides a compounding energy interaction resulting in the final energy release.
Table 1: PROCESS STEPS LEADING TO IGNITION: RELATIVE STATE OF WATER MOLECULE AND ORHYDROGEN, OXYGEN and OTHER ATOMS.
1st Stage: RANDOM (AMBIENT STATE): Water to Gas ALIGNMENT OF POLAR FIELDS, POLARIZATION OF MOLECULES, MOLECULAR ELONGATION, ATOM LIBERATION BY BREAKDOWN OF COVALENT BOND.
2nd Stage: RELEASE OF GASES : Gas Ionization, LIQUID TO GAS IONIZATION, ELECTRICAL CHARGING EFFECT PARTICLE IMPACT.
3rd Stage: ELECTROMAGNETIC WAVE : LASER Priming / PHOTON INJECTION ELECTRON EXTRACTION ATOMIC DESTABILIZATION.
Final Stage: THERMAL IGNITION: Ignition.
In brief, in the first stage a gas mixture including hydrogen and oxygen and other dissolved gases formerly entrapped in water is obtained, from water. In general, the method used in the first stage consists of: (A) providing a capacitor, in which the water is included as a dielectric liquid between capacitor plates, in a resonant charging choke circuit that includes an inductance in series with the capacitor; (B) subjecting the capacitor to a pulsating, unipolar electric voltage field in which the polarity does not pass beyond an arbitrary ground, whereby the water molecules within the capacitor are subjected to a charge of the same polarity and the water molecules are distended by their subjection to electrical polar forces; (C) further subjecting the water in said capacitor to said pulsating electric field to achieve a pulse frequency such that the pulsating electric field induces a resonance within the water molecule; (D) continuing the application of the pulsing frequency to the capacitor cell after resonance occurs so that the energy level within the molecule is increased in cascading incremental steps in proportion to the number of pulses; (E) maintaining the charge of said capacitor during the application of the pulsing field, whereby the co-valent electrical bonding of the hydrogen and oxygen atoms within said molecules is destabilized such that the force of the electrical field applied, as the force is effective within the molecule, exceeds the bonding force of the molecule, and hydrogen and oxygen atoms are liberated from the molecule as elemental gases; and (F) collecting said hydrogen and oxygen gases, and any other gases that were formerly dissolved within the water, and discharging the collected gases as a fuel gas mixture.
The water molecules are subjected to increasing electrical forces. In an ambient state, randomly oriented water molecules are aligned with respect to a molecular polar orientation. They are next, themselves polarized and "elongated" by the application of an electric potential to the extent that covalent bonding of the water molecule is so weakened that the atoms disassociate and the molecule breaks down into hydrogen and oxygen elemental components. In the process, the point of optimum gas release is reached at a circuit resonance. Water in the fuel cell is subjected to a pulsating, polar electric field produced by the electrical circuit whereby the water molecules are distended by reason of their subjection to electrical polar forces of the capacitor plates. The polar pulsating frequency applied is such that the pulsating electric field induces a resonance in the molecule. A cascade effect occurs and the overall energy level of specific water molecules is increased in cascading, incremental steps. The hydrogen and oxygen atomic gases, and other gas components formerly entrapped as dissolved gases in water, are released when the resonant energy exceeds the co-valent bonding force of the water molecule. A preferred construction material for the capacitor plates is a stainless steel T-304 which is non-chemically reactive with water, hydrogen, or oxygen. An electrically conductive material which is inert in the fluid environment is a desirable material of construction for the electric field plates of the "water capacitor" employed in the circuit.
Once triggered, the gas output is controllable by the attenuation of operational parameters. Thus, once the frequency of resonance is identified, by varying the applied pulse voltage to the water fuel cell assembly, gas output is varied. By varying the pulse shape and/or amplitude or pulse train sequence of the initial pulsing wave source, final gas output is varied. Attenuation of the voltage field frequency in the form of OFF and ON pulses likewise affects output.
The overall apparatus thus includes an electrical circuit in which a water capacitor having a known dielectric property is an element. The fuel gases are obtained from the water by the disassociation of the water molecule. The water molecules are split into component atomic elements (hydrogen and oxygen gases) by a voltage stimulation process called the electrical polarization process which also releases dissolved gases entrapped in the water.
From the outline of physical phenomena associated with the first stage of the process described in Table 1, the theoretical basis of the invention considers the respective states of molecules and gases and ions derived from liquid water. Before voltage stimulation, water molecules are randomly dispersed throughout water within a container. When a unipolar voltage pulse train such as shown in FIGS. 1B through 1F is applied to positive and negative capacitor plates, an increasing voltage potential is induced in the molecules in a linear, step-like charging effect. The electrical field of the particles within a volume of water including the electrical field plates increases from a low energy state to a high energy state successively in a step manner following each pulse-train as illustrated figuratively in the depictions of FIGS. 1A through 1F. The increasing voltage potential is always positive in direct relationship to negative ground potential during each pulse. The voltage polarity on the plates which create the voltage fields remains constant although the voltage charge increases. Positive and negative voltage "zones" are thus formed simultaneously in the electrical field of the capacitor plates.
In the first stage of the process describe in Table 1, because the water molecule naturally exhibits opposite electrical fields in a relatively polar configuration (the two hydrogen atoms are positively electrically charged relative to the negative electrically charged oxygen atom), the voltage pulse causes initially randomly oriented water molecules in the liquid state to spin and orient themselves with reference to positive and negative poles of the voltage fields applied. The positive electrically charged hydrogen atoms of said water molecule are attracted to a negative voltage field; while, at the same time, the negative electrically charged oxygen atoms of the same water molecule are attracted to a positive voltage field. Even a slight potential difference applied to inert, conductive plates of a containment chamber which forms a capacitor will initiate polar atomic orientation within the water molecule based on polarity differences.
When the potential difference applied causes the orientated water molecules to align themselves between the conductive plates, pulsing causes the voltage field intensity to be increased in accordance with FIG. 1B. As further molecular alignment occurs, molecular movement is hindered. Because the positively charged hydrogen atoms of said aligned molecules are attracted in a direction opposite to the negatively charged oxygen atoms, a polar charge alignment or distribution occurs within the molecules between said voltage zones, as shown in FIG. 1B. And as the energy level of the atoms subjected to resonant pulsing increases, the stationary water molecules become elongated as shown in FIGS. 1C and 1D. Electrically charged nuclei and electrons are attracted toward opposite electrically charged voltage zones--disrupting the mass and charge equilibrium of the water molecule.
As the water molecule is further exposed to an increasing potential difference resulting from the step charging of the capacitor, the electrical force of attraction of the atoms within the molecule to the capacitor plates of the chamber also increases in strength. As a result, the co-valent bonding between atoms which form the molecule is weakened--and ultimately terminated. The negatively charged electron is attracted toward the positively charged hydrogen atoms, while at the same time, the negatively charged oxygen atoms repel electrons.
In a more specific explanation of the "sub-atomic" action that occurs in the water cell that provides a fuel gas for the subsequent stages, it is known that natural water is a liquid which has a dielectric constant of 78.54 at 20° C. and 1 atm pressure. [Handbook of Chemistry and Physics, 68th ed., CRC Press (Boca Raton, Fla. (1987-88)), Section E-50, H2 O (water)].
When a volume of water is isolated and electrically conductive plates, that are chemically inert in water and are separated by a distance, are immersed in the water, a capacitor is formed, having a capacitance determined by the surface area of the plates, the distance of their separation and the dielectric constant of water.
When water molecules are exposed to voltage at a restricted current, water takes on an electrical charge. By the laws of electrical attraction, molecules align according to positive and negative polarity fields of the molecule and the alignment field. The plates of a capacitor constitute such an alignment field when a voltage is applied.
When a charge is applied to a capacitor, the electrical charge of the capacitor equals the applied voltage charge; in a water capacitor, the dielectric property of water resists the flow of amps in the circuit, and the water molecule itself, because it has polarity fields formed by the relationship of hydrogen and oxygen in the covalent bond, and an intrinsic dielectric property, becomes part of the electrical circuit, analogous to a "microcapacitor" within the capacitor defined by the plates.
In the Example of a fuel cell circuit of FIG. 2, a water capacitor is included. The step-up coil is formed on a conventional torroidal core formed of a compressed ferromagnetic powdered material that will not itself become permanently magnetized, such as the trademarked "Ferramic 06# "Permag" powder as described in Siemens Ferrites Catalog, CG-2000-002-121, (Cleveland, Ohio) No. F626-1205. The core is 1.50 inch in diameter and 0.25 inch in thickness. A primary coil of 200 turns of 24 gauge cooper wire is provided and a coil of 600 turns of 36 gauge wire comprises the secondary winding. Other primary/secondary coil winding ratios may be conventionally determined.
An alternate coil arrangement using a conventional M27 iron transformer core is shown in FIG. 9. The coil wrap is always in one direction only.
In the circuit of FIG. 2, the diode is a 1N1198 diode which acts as a blocking diode and an electric switch that allows voltage flow in one direction only. Thus, the capacitor is never subjected to a pulse of reverse polarity.
The primary coil of the torroid is subject to a 50% duty cycle pulse. The torroidal pulsing coil provides a voltage step-up from the pulse generator in excess of five times, although the relative amount of step-up is determined by pre-selected criteria for a particular application. As the stepped-up pulse enters first inductor (formed from 100 turns of 24 gauge wire 1 inch in diameter), an electromagnetic field is formed around the inductor, voltage is switched off when the pulse ends, and the field collapses and produces another pulse of the same polarity; i.e., another positive pulse is formed where the 50% duty cycle was terminated. Thus, a double pulse frequency is produced; however, in a pulse train of unipolar pulses, there is a brief time when pulses are not present.
By being so subjected to electrical pulses in the circuit of FIG. 2, water confined in the volume that includes the capacitor plates takes on an electrical charge that is increased by a step charging phenomenon occurring in the water capacitor. Voltage continually increases (to about 1000 volts and more) and the water molecules starts to elongate.
The pulse train is then switched off; the voltage across the water capacitor drops to the amount of charge that the water molecules have taken on, i.e. voltage is maintained across the charged capacitor. The pulse train is then reapplied.
Because a voltage potential applied to a capacitor can perform work, the higher the voltage potential, the more work is performed by a given capacitor. In an optimum capacitor that is wholly non-conductive, zero (0) current flow will occur across the capacitor. Thus, in view of an idealized capacitor circuit, the object of the water capacitor circuit is to prevent electron flow through the circuit, i.e. such as occurs by electron flow or leakage through a resistive element that produces heat. Electrical leakage in water will occur, however, because of some residual conductivity and impurities or ions that may be otherwise present in the water. Thus, the water capacitor is preferably chemically inert. An electrolyte is not added to the water.
In the isolated water bath, the water molecule takes on charge, and the charge increases. The object of the process is to switch off the co-valent bonding of the water molecule and interrupt the sub-atomic force, i.e. the electrical force or electromagnetic force, that binds the hydrogen and oxygen atoms to form a molecule so that the hydrogen and oxygen separate.
Because an electron will only occupy a certain electron shell (the shells are well known) the voltage applied to the capacitor affects the electrical forces inherent in the co-valent bond. As a result of the charge applied by the plates, the applied force becomes greater than the force of the co-valent bonds between the atoms of the water molecule; and the water molecule becomes elongated. When this happens, the time share ratio of the electrons between the atoms and the electron shells is modified.
In the process, electrons are extracted from the water bath; electrons are not consumed nor are electrons introduced into the water bath by the circuit as electrons are conventionally introduced in an electrolysis process. There may nevertheless occur a leakage current through the water. Those hydrogen atoms missing electrons become neutralized; and atoms are liberated from the water. The charged atoms and electrons are attracted to opposite polarity voltage zones created between the capacitor plates. The electrons formerly shared by atoms in the water co-valent bond are re-allocated such that neutral elemental gases are liberated.
In the process, the electrical resonance may be reached at all levels of voltage potential. The overall circuit is characterized as a "resonant charging choke" circuit which is an inductor in series with a capacitor that produces a resonant circuit. [SAMS Modern Dictionary of Electronics, Rudolff Garff, ©1984, Howard W. Sams & Co. (Indianapolis, Ind.), p. 859.] Such a resonant charging choke is on each side of the capacitor. In the circuit, the diode acts as a switch that allows the magnetic field produced in the inductor to collapse, thereby doubling the pulse frequency and preventing the capacitor from discharging. In this manner a continuous voltage is produced across the capacitor plates in the water bath; and the capacitor does not discharge. The water molecules are thus subjected to a continuously charged field until the breakdown of the co-valent bond occurs.
As noted initially, the capacitance depends on the dielectric properties of the water and the size and separation of the conductive elements forming the water capacitor.
In an example of the circuit of FIG. 2 (in which other circuit element specifications are provided above), two concentric cylinders 4 inches long formed the water capacitor of the fuel cell in the volume of water. The outside cylinder was 0.75 inch in outside diameter; the inner cylinder was 0.5 inch in outside diameter. Spacing from the outside of the inner cylinder to the inner surface of the outside cylinder was 0.0625 inch. Reasonance in the circuit was achieved at a 26 volt applied pulse to the primary coil of the torroid at 10 KHz, and the water molecules disassociated into elemental hydrogen and oxygen and the gas released from the fuel cell comprised a mixture of hydrogen, oxygen from the water molecule, and gases formerly dissolved in the water such as the atmospheric gases or oxygen, nitrogen, and argon.
In achieving resonance in any circuit, as the pulse frequency is adjusted, the flow of amps is minimized and voltage is maximized to a peak. Calculation of the resonance frequency of an overall circuit is determined by known means; different cavities have a different frequency of resonance dependent on parameters of the water dielectric, plate size, configuration and distance, circuit inductors, and the like. Control of the production of fuel gas is determined by variation of the period of time between a train of pulses, pulse amplitude and capacitor plate size and configuration, with corresponding value adjustments to other circuit components.
The wiper arm on the second inductor tunes the circuit and accommodates to contaminants in water so that the charge is always applied to the capacitor. The voltage applied determines the rate of breakdown of the molecule into its atomic components. As water in the cell is consumed, it is replaced by any appropriate means or control system.
Thus in the first stage, which is of itself independently useful, a fuel gas mixture is produced having, in general, the components of elemental hydrogen and oxygen as well as formerly dissolved entrapped atmospheric gases such as nitrogen, argon, and the like. The fuel gas is itself combustible in a conventional manner.
After the first stage the gas atoms become elongated during electron removal as the atoms are ionized. Laser, or light wave energy of a predetermined frequency is injected into a containment vessel in a gas ionization process. The light energy absorbed by voltage stimulated gas nuclei causes destabilization of gas ions still further. The absorbed laser energy causes the gas nuclei to increase in energy state, which, in turn, causes electron deflection to a higher orbital shell.
The electrically charged and laser primed combustible gas ions from a gas resonant cavity may be directed into an optical thermal lens assembly for triggering. Before entry into the optimal thermal lens, however, electrons are stripped from the ions and the atom is destabilized. The destabilized gas ions which are electrically and mass unbalanced atoms having highly energized nuclei are pressurized during spark ignition. The unbalanced, destablized atomic components thermally interact; the energized and unstable hydrogen gas nuclei collide with highly energized and unstable oxygen gas nuclei, causing and producing thermal explosive energy beyond the gas burning stage. The ambient air gas components in the initial mixture aid the thermal explosive process under a controlled state.
In the process, the point of optimum energy-yield is reached when the electron deficient oxygen atoms (having less than a normal number of electrons) lock onto and capture a hydrogen atom electron prior to or during thermal combustion of the hydrogen/oxygen mixture. Atomic decay results in the release of energy.
After the first stage, the gas mixture is subjected to a pulsating, polar electric field whereby electrons of the gas atoms are distended in their orbital fields by reason of their subjection to electrical polar forces The polar pulsating frequency applied is such that the pulsating electric field induces a resonance with respect to an electron of the gas atom. A cascade effect results and the energy level of specific resonating electron is increased in cascading, incremental steps.
Next, the gas atoms are ionized and subjected to electro-magnetic wave energy having a predetermined frequency to induce a further election resonance in the ion, whereby the energy level of the election is successively increased. Electrons are extracted from the resonating ions while such ions are in an increased energy state to destabilize the nuclear electron configuration of said ions; and the gas mixture of destabilized ions is thermally ignited.
In the apparatus shown in FIG. 4, water is introduced at inlet 1 into a first stage water fracturing module 2, such as the water fuel cell described above, in which water molecules are broken down into hydrogen, oxygen and released entrapped gas components. The released atomic gases and other gas components formerly entrapped as dissolved gases in water may be introduced to a successive stage 3 or other number of like resonant cavities, which are arranged in either a series of parallel combined array. The successive energization of the gas atoms provides a cascading effect, successively increasing the voltage stimulation level of the released gasses as they sequentially pass through cavities 2, 3, etc. In a final stage, an injector system 4, of a configuration of the type shown in FIGS. 5A or 5B, receives energized atomic and gas particles where the particles are subjected to further energy input, electrical excitation and thermal stimulation, whereby thermal explosive energy results 5, which may be directed thru a lens assembly of the type shown in FIG. 5C to provide a controlled thermal energy output.
A single cell, or a battery of cells such as shown in FIG. 3, provides a fuel gas source for stages after the first stage. The fuel gas is activated by electromagnetic waves, and electrically charged gas ions of hydrogen and oxygen (of opposite polarity) are expelled from the cascaded cells 2, 3, etc. shown in FIG. 4. The circuit of FIG. 9 may be utilized as a source of ionizing energy for the gases. The effect of cascading successively increases the voltage stimulation level of the released gases, which then are directed to the final injector assembly 4. In the injector assembly, gas ions are stimulated to a yet higher energy level. The gases are continually exposed to a pulsating laser or other electromagnetic wave energy source together with a high intensity oscillating voltage field that occurs within the cell between electrodes or conductive plates of opposite electrical polarity. A preferred construction material for the plates is a stainless steel T-304 which is non-chemically reactive with water, hydrogen, or oxygen. An electrically conductive material which is insert in the fluid environment is a desirable material of construction for the electrical field producing plates, through which field the gas stream of activated particles passes. Gas ions of opposite electrical charges reach and maintain a critical energy level state. The gas ions are oppositely electrically charged and subjected to oscillating voltage fields of opposite polarity and are also subjected to a pulsating electromagnetic wave energy source. Immediately after reaching critical energy, the excited gas ions are exposed to a high temperature thermal zone in the injection cell, 4, that causes the excited gas ions to undergo gas combustion. The gas ignition triggers atomic decay and releases thermal energy, 5, with explosive force.
Once triggered, the thermal explosive energy output is controllable by the attenuation of operational parameters. With reference to FIG. 6A, for example, once the frequency of resonance is identified, by varying applied pulse voltage to the initial water fuel cell assemblies, 2, 3, the ultimate explosive energy output is likewise varied. By varying the pulse shape and/or amplitude or pulse train sequence of the electromagnetic wave energy source, final output is varied. Attenuation of the voltage field frequency in the form of OFF and ON pulses likewise affects output of the staged apparatus. Each control mechanism can be used separately, grouped in sections, or systematically arranged in a sequential manner.
A complete system in accordance with the present application thus includes a water fuel cell for providing a first fuel gas mixture consisting of at least a portion of hydrogen and oxygen gas. An electrical circuit of the type shown in FIG. 7 provides a pulsating, polar electric field to the gas mixture as illustrated in FIG. 6A, whereby electrons of the gas atoms are distended in their orbital fields by reason of their subjection to electrical polar forces, changing from the state conceptually illustrated by FIG. 6B to that of FIG. 6C, at a frequency such that the pulsating electric field induces a resonance with respect to electrons of the gas atoms. The energy level of the resonant electrons is thereby increased in cascading, incremental steps. A further electric field to ionize said gas atoms is applied and an electromagnetic wave energy source for subjecting the ionized gas atoms to wave energy of a predetermined frequency to induce a further electron resonance in the ion, whereby the energy level of the election is successively increased is an additional element of the apparatus as shown in FIG. 6D.
An electron sink, which may be in the form of the grid element shown in FIG. 8A, extracts further electrons from the resonating ions while such ions are in an increased energy state and destabilizes the nuclear electron configuration of the ions. The "extraction" of electrons by the sink means is coordinated with the pulsating electrical field of the resonant cavity produced by the circuit of FIG. 7, by means of an interconnected synchronization circuit, such as shown in FIG. 8B. A nozzle, 10 in FIG. 5B, or thermal lens assembly, FIG. 5C, provides the directing means in which the destabilized ions are finally thermally ignited.
As previously noted, to reach and trigger the ultimate atomic decay of the fuel cell gases at the final stage, sequential steps are taken. First, water molecules are slit into component atomic elements (hydrogen and oxygen gases) by a voltage stimulation process which also releases dissolve gases entrapped in the water. In the injector assembly, a laser produced light wave or other form of coherent electromagnetic wave energy capable of stimulating a resonance within the atomic components is absorbed by the mixture of gases (hydrogen/oxygen/ambient air gases) released by the polarization process. At this point, as shown in FIG. 6B, the individual atoms are subjected to an electric field to begin an ionization process.
The laser or electromagnetic wave energy is absorbed and causes gas atoms to lose electrons and form positively charged gas ions. The energized hydrogen atoms which, as ionized, are positively charged, now accept electrons liberated from the heavier gases and attract other negatively charged gas ions as conceptually illustrated in FIG. 6C. Positively and negatively charged gas ions are re-exposed to further pulsating energy sources to maintain random distribution of ionized atomic gas particles.
The gas ions within the wave energy chamber are subjected to an oscillating high intensity voltage field in a chamber 11 in FIGS. 5A and 5B formed within electrodes 12 and 13 in FIGS. 5A and 5B of opposite electrical polarity to produce a resonant cavity. The gas ions reach a critical energy state at a resonant state.
At this point, within the chamber, additional electrons are attracted to said positive electrode; whereas, positively charged ions or atomic nuclei are attracted to the negative electrode. The positive and negative attraction forces are co-ordinate and operate on said gas ions simultaneously; the attraction forces are non-reversible. The gas ions experience atomic component deflection approaching the point of electron separation. At this point electrons are extracted from the chamber by a grid system such as shown in FIG. 5A. The extracted electrons are consumed and prevented from re-entering the chamber by a circuit such as shown in FIG. 8B. The elongated gas ions are subjected to a thermal heat zone to cause gas ignition, releasing thermal energy with explosive force. During ionic gas combustion, highly energized and stimulated atoms and atom nuclei collide and explode during thermal excitation. The hydrogen fracturing process occurring sustains and maintains a thermal zone, at a temperature in excess of normal hydrogen/oxygen combustion temperature, to wit, in excess of 2500° F. To cause and maintain atomic elongation depicted in FIG. 6C before gas ignition, a voltage intensifier circuit such as shown in FIG. 7 is utilized as a current restricting voltage source to provide the excitation voltage applied to the resonant cavity. At the same time the interconnected electron extractor circuit, FIG. 8B, prevents the reintroduction of electrons back into the system. Depending on calculated design parameters, a predetermined voltage and frequency range may be designed for any particular application or physical configuration of the apparatus.
In the operation of the assembly, the pulse train source for the gas resonant cavity shown at 2 and 3 in FIG. 4 may be derived from a circuit such as shown in FIGS. 2, 7 or 9, and such cavity circuits may be in sequence to provide a cascading energy input. It is necessary in the final electron extraction that the frequency with which electrons are removed from the system by sequenced and synchronized with the pulsing of the gas resonant cavity. In the circuit of FIG. 8B, the coordination of synchronization of the circuit with the circuit of FIG. 7 may be achieved by interconnecting point "A" of the gate circuit of FIG. 8B to coordinate point "A" of the pulsing circuit of FIG. 7.
The circuit shown in FIG. 9 enhances the voltage potential across the resonant charging choke coils during pulsing operations and restricts amp flow by allowing an external electromagnetic pulsing field, F, derived from the primary coil A being energized to transverse the coil windings D and E being energized by the incoming pulse train Ha xxx Hn, through switching diode G. The external pulse field, F and the incoming pulse-train Ha xxx Hn, are sequentially the same, allowing resonant action to occur, restricting amp flow while allowing voltage intensity to increase to stimulate the electrical polarization process, the gas ionization process and the electron extraction process. The voltage intensifier circuit of FIG. 9 prevents electrons from entering into those processes.
Together, the hydrogen injector assembly 4 and the resonant cavity assemblies 2, 3 form a gas injector fuel cell which is compact, light in weight and design variable. For example, the hydrogen injector system is suited for automobiles and jet engines. Industrial applications require larger systems. For rocket engine applications, the hydrogen gas injector system is positioned at the top of each resonant cavity arranged in a parallel cluster array. If resonant cavities are sequentially combined in a parallel/series array, the hydrogen injection assembly is positioned after the exits of said resonant cavities are combined.
From the outline of physical phenomena associated with the process described in Table 1, the theoretical basis of the invention considers the respective states of molecules, gases and ions derived from liquid water. Before voltage stimulation, water molecules are randomly dispersed throughout water within a container. When a unipolar voltage pulse train such as shown in FIG. 6A (53a xxx 53n) is applied, an increasing voltage potential is induced in the molecules, gases and/or ions in a linear, step-like charging effect. The electrical field of the particles within a chamber including the electrical field plates increases from a low energy state (A) to a high energy state (J) in a step manner following each pulse-train as illustrated in FIG. 6A. The increasing voltage potential is always positive in direct relationship to negative ground potential during each pulse. The voltage polarity on the plates which create the voltage fields remains constant. Positive and negative voltage "zones" are thus formed simultaneously.
In the first stage of the process described in Table 1, because the water molecule naturally exhibits opposite electrical fields in a relatively polar configuration (the two hydrogen atoms are positively electrically charged relative to the negative electrically charged oxygen atom), the voltage pulse causes initially randomly oriented water molecules in the liquid state to spin and orient themselves with reference to positive and negative poles of the voltage fields applied. The positive electrically charged hydrogen atoms of said water molecule are attracted to a negative voltage field; while, at the same time, the negative electrically charged oxygen atoms of the same water molecule are attracted to a positive voltage field. Even a slight potential difference applied to the inert, conductive plates of a containment chamber will initiate polar atomic orientation within the water molecule based on polarity differences.
When the potential difference applied causes the orientated water molecules to align themselves between the conductive plates, pulsing causes the voltage field intensity to be increased in accordance with FIG. 6A. As further molecular alignment occurs, molecular movement is hindered. Because the positively charged hydrogen atoms of said aligned molecules are attracted in a direction opposite to the negatively charged oxygen atoms, a polar charge alignment or distribution occurs within the molecules between said voltage zones, as shown in FIG. 6B. And as the energy level of the atoms subjected to resonant pulsing increases, the stationary water molecules become elongated as shown in FIG. 6C. Electrically charged nuclei and electrons are attracted toward opposite electrically charged voltages zones--disrupting the mass equilibrium of the water molecule.
In the first stage, as the water molecule is further exposed to a potential difference, the electrical force of attraction of the atoms within the molecule to the electrodes of the chamber also increases in intensity. As a result, the covalent bonding between said atoms which forms the molecule is weakened and ultimately terminated. The negatively charged electron is attracted toward the positively charged hydrogen atoms, while at the same time, the negatively charged oxygen atoms repel electrons.
Once the applied resonant energy caused by pulsation of the electrical field in the cavities reaches a threshold level, the disassociated water molecules, now in the form of liberated hydrogen, oxygen, and ambient air gases begin to ionize and lose or gain electrons during the final stage in the injector assembly. Atom destabilization occurs and the electrical and mass equilibrium of the atoms is disrupted. Again, the positive field produced within the chamber or cavity that encompasses the gas stream attracts negatively charged ions while the positively charged ions (and/or hydrogen nuclei) are attracted to the negative field. Atom stabilization does not occur because the pulsating voltage applied is repetitive without polarity change. A potential of approximately several thousand volts triggers the ionization state.
As the ionized particles accumulate within said chamber, the electrical charging effect is again an incremental stepping effect that produces an accumulative increased potential while, at the same time, resonance occurs. The components of the atom begin to "vibrate" at a resonant frequency such that an atomic instability is created. As shown in k FIG. 6D, a high energy level is achieved, which then collapses resulting in the release of thermal explosive energy. Particle impact occurs when liberated ions in a gas are subjected to further voltage. A longitudinal cross section of a gas resonant cavity is shown in FIG. 5A. To promote gas ionization, electromagnetic wave energy such as a laser or photon energy source of a predetermined wave length and pulse-intensity is directed to and absorbed by the ions forming said gas. In the device of FIG. 5A, semiconductor optical lasers 20a-20p, 20xxx surround the gas flow path. In the device of FIG. 5B, photo energy 20 is injected into a separate absorption chamber 21. The incremental stimulation of nuclei to a more highly energized state by electromagnetic wave energy causes electron deflection to a higher orbital state. The pulse rate as well as intensity of the electromagnetic wage source is varied to match the absorption rate of ionized particles to produce the stepped incremental increase in energy. A single laser coupled by means of fiber optic light guides is an alternative to the plurality of lasers shown in FIG. 5B. Continued exposure of the gas ions to different forms of wave energy during voltage stimulation maintains individual atoms in a destabilized state and prevents atomic stabilization.
The highly energized gas ions are thermally ignited when said combustible gas ions pass from injector 4 and enter into and pass through a nozzle, 10 in FIG. 5B, or an optical thermal lens assembly such as shown in FIG. 5C. In FIG. 5C, the combustible gas ions are expelled through and beyond a quenching circuit, 30, and reflected by lenses, 31 and 32, back and forth through a thermal heat zone, 33, prior to atomic breakdown beyond exiting through a final port, 34. A quenching circuit is a restricted orifice through which the particle stream passes such that flashback does not occur. The deflection shield or lens, 31, superheats beyond 3,000° F. and the combustible gas ions passing through said exiting-ports are regulated to allow a gas pressure to form inside said thermal zone. The energy yield is controlled by varying the applied voltage, or pulse-train since said thermal-lens assembly is self-adjusting to the flow-rate of said ionized and primed gases. The combustible ionic gas mixture is composed of hydrogen, oxygen, and ambient air gases. The hydrogen gas provides the thermal explosive force, the oxygen atoms aid the gas thermal ignition, and the ambient air gases retard the gas thermal ignition process to a controllable state. As the combustible gas mixture is exposed to a voltage pulse train, the stepped increasing voltage potential cases said moving gas atoms to become ionized (losing or gaining electrons) and changes the electrical and mass equilibrium of said atoms. Gases that do not undergo the gas ionization process may accept the liberated electrons (electron entrapment) when exposed to light or photon stimulation. The electron extractor grid circuit, FIGS. 8A and 8B, is applied to the assembly of FIG. 5A or FIG. 5B, and restricts electron replacement. The extractor grid, 56, is applied adjacent to electric field producing members, 44 and 45, within the resonant cavity. The gas ions incrementally reach a critical-state which occurs after a high energy resonant state. At this point the atoms no longer tolerate the missing electrons, the unbalanced electrical field, and the energy stored in the nucleus. Immediate collapse of the system occurs and energy is released as the atoms decay into thermal explosive energy.
The repetitive application of a voltage pulse train (A through J of FIG. 6A) incrementally achieves the critical state of said gas ions. As the gas atoms or ions (1a xxx 1n) shown in FIG. 6C become elongated during electron removal, electromagnetic wave energy of a predetermined frequency and intensity is injected. The wave energy absorbed by the stimulated gas nuclei and electrons causes further destabilization of the ionic gas. The absorbed energy from all sources causes the gas nuclei to increase in energy state, and induces the ejection of electrons from the nuclei.
To further stimulate the electron entrapment process beyond the atomic level (capturing the liberated electrons during the hydrogen fracturing process) the electron extractor grid (as shown in FIG. 8A) is placed in spaced relationship to the gas resonant cavity structure shown in FIG. 5A. The electron extractor grid is attached to an electrical circuit (such as shown in FIG. 8B) that allows electrons to flow to an electrical load, 55, when a positive electrical potential is placed on the opposite side of said electrical load. The electrical load may be a typical power consuming device such as a light bulb or resistive heat producing device. As the positive electrical potential is switched on or pulse-applied, the negative charged electrons liberated in the gas resonant cavity are drawn away and enter into resistive load where they are consumed and released at heat or light energy. The consuming electrical circuit can be directly connected to the gas resonant cavity positive electrical voltage zone. The incoming positive wave form applied to resonant cavity voltage zone through a blocking diode is synchronized with the pulse train applied to the gas resonant cavity by the circuit of FIG. 7 via alternate gate circuit. As one pulse train is gated "ON", the other pulse train is switched "OFF." A blocking diode directs the electron flow to said electrical load while resistive wire prevents voltage leakage during pulse train "ON" time.
The electron extraction process is maintained during gas flow-rate change by varying the trigger pulse rate in relationship to applied voltage. The electron extraction process also prevents spark-ignition of the combustible gases traveling through the gas resonant cavity because electron build-up and potential sparking is prevented.
In an optical thermal lens assembly or thrust-nozzle, such as shown in FIG. 5C, destabilized gas ions (electrically and mass unbalanced gas atoms having highly energized nuclei) can be pressurized during spark-ignition. During thermal interaction, the highly energized and unstable hydrogen gas nuclei collide with the highly energized and unstable oxygen gas nuclei and produce thermal explosive energy beyond the gas burning stage. Other ambient air gases and ions not otherwise consumed limit the thermal explosive process.
Variations of the process and apparatus may be evident to those skilled in the art. }
Genepax water car:
USA Military water Hummer
power cells in general:
much more abundant and much safer than Uranium. Uranium nuclear was
pursued exclusively because it destroyed Japan, so politicians liked
it, that was what they were into, so they then destroyed the entire
planet 1000 times over to show off. Then they lied, murdered anyone
competing so robbed us all while they destroyed the planet and the
(100year half life) Carbon14 (5000year half life) + Diamond beta
+ Helium 3 fusion surplus particle decay energy reactor so not
produced dangerous radiation.
Weber, of Executive Engineering, is developing a nuclear accelerated
generator (NAG), for military uses such as night vision, field laptop
computers, and remote outposts and hospitals. His main breakthrough
is the direct conversion of small amounts of radioactive isotope
nuclear energy into electrical energy. Using radioactive isotopes in
regular production by the U.S. Department of Energy. NAG technology
utilizes beta-minus radiation (electrons) from isotopes such as
strontium-90 (Sr-90), nickle-63 (Ni-63), and promethium-147 (Pm-147).
Promethium-147 is the most desirable with a half life of 2.5 years it
decays into a stable element (inert promethium) within 30 years.
Weber stated that NAG technology uses a more efficient [60% to 80%
energy conversion] energy-recovery mechanism. 10 mg of Pm-147 would
enable the 10 Watts of power required by modern netbooks for a half
life of 2.62 years constant use. Costing 1 to 2 cents per kilowatt
hour about half the cost of coal. A potential candidate for DARPA
funding. Fuel for the NAG is plentiful and, since it consumes nuclear
waste, with no additional nuclear waste. With direct energy
conversion from nuclear waste the NAG produces 25 times more power
per unit of fuel than current thermal nuclear reactor technology. [3%
power conversion compared to a NAG atomic Battery conversion rate of
~75% efficiency. The cost of batteries is $20.00 per watt. The NAG is
capable of producing power at less cost than gasoline when gasoline
was selling for $2.25 per gallon. EENAG's are DC Atomic Battery
Systems. They consist of an Atomic Charging Core (Nuclear Accelerated
Generator) and a Lithium Battery; They are safe, pose no health
hazard and have no harmful radiation that can be detected outside the
battery. Potential uses would include sensors, cell phones, computers
or any other electronic and/or electrical equipment requiring
dependable, long-life batteries.
MPKCO Litroenergy Power Cells. Betavoltaic battery able to provide
constant power for 10 years [ half life of 12 years ] so no need for
external re-charger ever; Litroenergy Power Cells generate constant
electricity for 10 years with no waste byproduct. Litroenergy light
emitting micro particles (Litrospheres) and/or sheets are not
affected by heat or cold and produce constant light. Used in
combination with solar cells to create light weight, non-toxic,
non-radioactive, durable, solid-state long term low cost electrical
BetaBatt Direct Energy Conversion D Cells: is a Houston-based company
in the business of developing long-lasting reliable power sources.
The Company has researched and patented a novel 3D energy conversion
architecture named the DECTM Cell, based on nano-scale porous
silicon. The DECTM Cell is able to convert decay electrons to
electricity 10 times more efficiently than conventional 2D devices
using standard semiconductor manufacturing methods. The company's
first commercial product, a quarter size battery with a 12-20 year
lifespan and mission critical reliability, has performance
characteristics that address current problems faced by medical
implant, oil and gas, and remote sensing industries, as well as
military and space organizations. Going forward, BetaBatt intends to
apply its novel architecture to Micro-Electro Mechanical Systems
(MEMS), Mesh Networks, Smart Dust and other micro/nano architectures
requiring long-lasting reliable power sources. Semiconductor devices
based on Direct Energy Conversion (DECTM) technology will generate
electric current from a radioelement source. The efficiency of the
DECTM Cell stems from its single step capture-and-conversion method.
DECTM Cells use energy produced from the decay of a radioactive
isotope, not a chemical reaction. The Company's patented architecture
- based on the same physical principles that are employed in solar
cells - and the selection of beta emitters ensures a power source
that emits no radiation and is safer than chemical batteries for a
broad variety of industrial and medical applications. A key
innovation is the distribution of the beta emitter energy source
throughout the DECTM Cell volume. This means that the current
generation is not just a surface effect, but occurs everywhere within
the active volume. Thus, DECTM current sources are extremely
efficient, converting a large fraction of the available decay energy
into electric current. The first and second generations of
tritium-powered BetaBatteriesTM are expected to produce 50- and
125-micro-Watts per cubic centimeter of active device volume,
respectively. BetaBatteryTM current sources are long-lasting, based
on the selection of the beta source. Tritium has a half-life (T½)
equal to 12.3 years. This means that after 12.3 years, the current
output will be half its original value and a tenth of the original
after 40 years. This productive life is orders of magnitude longer
than chemical batteries. The decline in output for DECTM power cells
will be quite predictable and can be accommodated by appropriate
electronics design for each specific application. BetaBatteriesTM are
far more reliable than chemical batteries, and have significantly
longer life spans. They have about the same energy density as a
lithium battery, but last ten or more times longer. BetaBatteriesTM
can be stacked or scaled to meet application-specific requirements.
When compared to chemical batteries, BetaBatteries are strongly
differentiated by their intrinsic features: *Small or Big; MEMS to
"D" size. * High Efficiency From Direct Energy Conversion.
*Green And Safe No harmful radiation, leaching, or contamination. *
Long Life 12 - 100+ years (depending on energy source). * Scalable
Wide form factor variety. * Extreme Environments -100°C to
+150°C, shock tolerant. * Manufacturable, Well known
semiconductor techniques. BetaBatteriesTM may be used in two ways: *
In stand-alone mode for low current applications. * Paired with
chemical batteries for high current, limited duty cycle applications.
BetaBatteriesTM increase shelf life and ensure readiness by acting as
a trickle charger, thus enhancing capability, reliability and useful
life. The properties and performance characteristics of DECTM Cells
make them particularly suitable for applications which benefit from a
constant and sustained current and one or more of the following: *
Battery replacement is difficult, costly or high risk. *
Mission-critical reliability. * Size or form factor constraints. *
Performance in extreme or fluctuating environments (e.g., outer
space). A major advantage of DECTM power cells is their "always
on" capability. This means they would be ideal for permanent or
semi-permanent "install and forget" applications in remote
or inaccessible locations. Another advantage is that DECTM technology
is scalable. DECTM current sources could be used to power the
smallest realizations of MEMS devices and sensors. By selecting
appropriately-sized semiconductor wafers and connecting the resulting
DECTM Cells together, a very wide range of BetaBatteryTM power levels
can be delivered. Another advantage of DECTM technology is that the
high efficiency of energy conversion gives rise to a very small
amount of waste heat. This means that in the majority of applications
there will not need to be any extra design effort nor auxiliary
systems installed to remove excess heat. Space-worthy DECTM
technology has many advantages compared to Radioisotope Thermal
Generators (RTGs) including high efficiency, little waste heat, low
mass, no shielding requirements and a zero noise signature in all
energy regions important for astrophysical investigations.
Paul Brown Nucell. A radioisotope electric power system developed by
inventor Paul Brown is a scientific breakthrough in nuclear power.
The battery utilizes the energy given off by decaying radioactive
material, converting it directly into a continuous AC electrical
current. Unlike conventional nuclear generating devices, the power
cell does not rely on a nuclear reaction or chemical process and does
not produce radioactive waste products. Brown's first prototype power
cell produced 100,000 times as much energy per gram of strontium-90
(the energy source) than the most powerful thermal nuclear battery
yet in existence. The Nucell battery yielded 7500 watts per gram of
strontium-90. Compare this to an advanced device recently developed
by the US Dept. of Energy Byproducts Utilization Program. Their
state-of-the-art thermal nuclear battery produced 0.063 watts per
gram of strontium-90. The key to the Nucell battery is Brown's
discovery of a method to harness the magnetic energy given off by the
alpha and beta particles inherent in nuclear material. Alpha and beta
particles are produced by the radioactive decay of certain naturally
occurring and man-made nuclear material (radionuclides). The electric
charges of the alpha and beta particles have been captured and
converted to electricity for existing nuclear batteries, but the
amount of power generated from such batteries has been very small.
Alpha and beta particles also possess kinetic energy by successive
collisions of the particles with air molecules or other molecules.
The bulk of the R&D of nuclear batteries in the past has been
concerned with this heat energy which is readily observable and
measurable. The magnetic energy given off by alpha and beta particles
is several orders of magnitude greater than either the kinetic energy
or the direct electric energy produced by these same particles.
However, the myriads of tiny magnetic fields existing at any tie
cannot be individually recognized or measured. This energy is not
captured locally in nature to produce heat or mechanical effects, but
instead the energy escapes undetected. Brown has invented a way to
"organize" these magnetic fields so the great amounts of
otherwise unobservable energy could be harnessed.
weight of the strontium-90 used to generate 75 watts of power in the
Nucell prototype is approximately the same as the weight of 2
millimeters of wire cut off the end of a small paper clip. Projected
sizes of the Nucell battery will range from the size of a soup can to
the size of a small barrel or waste can for a 50 kilowatt model. The
alpha and beta particles utilized in the Nucell battery have a
limited ability to penetrate matter; alpha particles can be contained
by a piece of paper; beta particles require 0.03" of aluminum.
The Nucell battery is housed in a stainless steel, high-vacuum
container, making it a safe, impermeable source of power.
Domestic power, calculators and watches: conventionalphotovoltaic and
battery systems. Best current option for appliance power including
nuclear process using nickel and hydrogen to produce copper. Best
option for domestic room heating in winter.
above options would best to survive 200year solar flare coronal mass
ejection grid failure and 100,000 year cyclical 90,000 year ice age
[we are at the very end of a cyclical 10,000 year life promoting
warming period. Ice age caused by the sun dimming and also less so by
changes in distance to the sun and carbon dioxide slight warming in
the context of 10 million years of ice ages because of carbon dioxide
deprivation are cancelling each other out so as to have average
temperature most stable 10,000 years in 10 million years]. Cooler
summers and warmer winters are also caused by the tilt of the Earth's
axis in relation to the Sun shift.
dioxide is the most starved for vital plant nutrient. Optimal levels
of 1% or 20 x current levels we would prevent the due 90,000 year ice
age and lead to explosive 10 fold growth in crop biomass. General
warming and forestation will create more water vaper and carbon
dioxide blanket affect will moderate temperatures, making weather
more comfortable for life. Carbon dioxide is not pollution. Life on
earth is most abundant when carbon dioxide levels are at 1% or 20
times current levels. Carbon dioxide levels are up 50% to .04% of
levels 200 years ago but have decreased 95% in the last 500million
years and so reduced the abundance of life on earth. Over the next
1000 years at current levels of carbon dioxide will be responsible
for 20% of climate change (warming), all greenhouse gasses including
water vaper feedback mechanism 20% (warming and moderating), and
100,000 year cyclical changes in the suns activity 40% (cooling) of
the cause of climate change. We are at very end of a cyclical 10,000
years of interglacial global warming as part of the 100,000 year suns
activity cycle. A 2 fold increase in carbon dioxide would prevent the
due 90,000 years ice age. We have had 20 deeper and deeper ice ages
in a regular 100,000 year cycle death spiral over the last 2,000,000
years. Information from wikipedia;
http://en.wikipedia.org/wiki/Ice_age )The politically motivated
funding conclusions which sed we have excessive carbon dioxide only
considered the last 200 years and were wrong in the longer
term(20million year)context. Ice ages have come into existence and
have become increasingly more extreme over the last 20 million years,
before ice ages the coolest extremes of global temperature were
warmer than the hottest global temperature today. Northern Eurasia
would benefit from some global warming. This unusual period of
warming is caused by sun activity and carbon dioxide. Also there is a
need to reduce urban combustion engine particulate air, noise
pollution, inconvenience, and cost of combustion fuels and to find an
alternative to uranium nuclear power stations to stop more countries
developing the capacity to have nuclear weapons. We should adapt by
growing timber forests to use instead of native forests and build
giant desal plants for water for irrigation. We should use whatever
energy source is cheapest and most abundant. Cars should not use
combustion fuels I hate the regular fuel up requirement, going to the
service station, paying for fuel, and brake down tendency. Better
than just battery electric cars the Blacklight Power electric
generator for electric motor would be more reliable, cheap or free to
run, easier to maintain and easier to repair. This would be pleasing.
The combustion engine is an obsolete technology. Newer solid state
nuclear battery technologies could be used In small devices where
safe and old large nuclear technologies should be phased out. If we
all converted to nuclear the resource would only last 40 years.
Nuclear betavoltaic batteries would have mobile phone run always on
for 20 years. It is becoming apparent that our public universities
academics have said that free energy technologies were impossible an
obsolete and incorrect dogma, that has contradicted real world
observations. Public university warming alarmists have lied about the
true facts to match the dogma, I engineer the theory to fit the true
image observable facts. Public universities should be privatised and
sponsored by a levy on payroll to develop free energy, anti-gravity
and other products for profit. Desalination may also use one of the
many free energy technologies that have fallen onto unfertile minds.
money: The billions of dollars spent replicating hot fusion in the
sun was a complete waste of money. Many working models for nuclear
energy already exist including room temperature fusion (decay).
Gravity in its self is free energy as powers the sun. Also matter as
a store of nuclear energy which can be released by nuclear decay of
left over subatomic particles after re-combination of subatomic
particles required by fission, fusion and electrolysis. Gravity
powers fusion in the sun. Fusion does not power the sun. Fusion is a
consumer of energy except when accompanied by greater nuclear decay
of atoms. Solar and wind has not reduced the need for base-load
constant power capacity. Money diverted from constant energy sources
has caused blackouts. Geothermal systems have caused earth quakes
except when using closed loop technologies. Uranium has only 100
years supply using old technologies and 1,000 using new travelling
wave technologies by which time if uranium was relied on the Earth
would have been made inhospitable at the rate of 1 large nuclear
accident be decade.
do want a replacement for combustion by car particulates, noise,
expense, maintenance, refueling, unreliability, aggression, limited
life waste when disposed of, In favour of cheap to run, reliable,
long range, calming, peaceful, prosperity bringing free energy
transport engines. For other battery powered electronic devices 10
year half life nuclear decay fusion batteries would improve
performance. We can make a start towards having a zero cost energy
fleet, even if we do not change over old vehicles until the old
combustion engine goes bung. I am for solar cooling and heating. I
believe their would be virtue in updating the theory of the
conservation of energy; that energy may never be created or destroyed
only transformed, into the Conservation Of Free Energy, energy is
created for free(gravity and magnetism)then never destroyed only
transformed. The repulsive force which keeps the universe expanding
seems to be created in a vacuum from nothing. Gravity seems to create
from nothing but the presence of elements heat and pressure in the
sun to convert through fusion atoms into heavier atom elements. The
strong and week atomic forces also seem to create energy from
nothing. Permanent magnets attract and repel without any consumption
of mass. All that is required to transform these forces into
electricity or directed motive force is a method of turning off and
on these forces. All energy is either free energy or an end product
of free energy. The sun is not powered by fusion, Fusion in the sun
is a by product of gravity, Gravity powers fusion in the sun and as a
by product the conversion of gravity into radiation. Fusion is
usually not a net producer but a consumer of energy. The massive
effort to create energy from hot fusion has been based on bad
physics. Monies should be directed into other new free energy
technologies which also harness ambient energy including heat,
gravity, and permanent magnets, conversion to electricity. Coal is
created from plant chemical energy, from photosynthesis, from
sunlight, from gravity. Where conservation of energy is correct is
that energy is not destroyed but transformed into elements or
dissipated throughout the universe. The conservation of energy theory
was developed in the 1850s only considering terrestrial phenomena,
and not the effect of gravity on fusion in the sun or permanent
magnets. Government scientists have been trained in ancient small
minded dogma of inversion of reality caused by odd number reflected
image by universities so to have made them mentally crippled and
rejected free energy even when the clear as day visual true evidence
is overwhelming making wrong mathematical algebra broken and useless
in the end. Truth has its own beauty independent of logic. Money
should be allocated to safe, pollution free energy technology prizes,
prize for the fastest transcontinental crossing of Australia by self
contained zero greenhouse emission vehicle, prizes for battery
technologies, For electronics, electric vehicles and utility scale
batteries, and for prizes for nuclear batteries able to provide
electrical energy for 10 to 30 years. The best way to decrease
electricity prices is to increase supply and the best way to increase
supply is not for government to own power stations, but for the
government to sell power stations then commission new power stations
with the proceeds. ]
to Einstein theories normal positive mass craft time rate will slow
down so the rest of the universe would seem to fast forward around
the craft at a higher rate of time the closer we get to the speed of
light, the craft would seem to move in slow motion from the rest of
the universe and move into the future of the rest of the universe at
what would seem a normal rate of time inside the craft. We have not
been able to travel into the future using anti-gravity negative mass.
Three methods for travelling into the future are application of
energy to teleport into future possibilities as in Montauk
experiments, stasis and contact with beings from the future
travelling back in time. Some aliens claim to be from the Earth in
the future who travel back in time by some how travelling vast
distances in space much faster than light for offset space negative
time divergence (time = speed x mass). The reason Einstein said we
could not travel faster than light was because normal craft would
require infinite energy and have infinite mass (black hole). Searl's
craft supercool superconductors to instead create infinite
negative-mass, infinite negative energy (supercooling) and infinite
acceleration through the speed of light repelling other mass such as
obstacles in space to then connect vast distance in space and reverse
time with the universe around the craft seemingly to be in reverse,
runaway time reversal able to send the craft back to the singularity
big bang at the beginning of time, to create space time expansion and
create vacuum quantum dark negative energy cooling anti-gravity with
expansion of the space time universe converting dark space vacuum
energy into gravitational dark matter (hydrinos) to collect together
with time travel seeds of the universe and vacuum gravitational
energies to fuse into atoms to build the entire physical universe.
The one true image to harness butterfly effect for telepathic
technology convergence universe is a single time-line, all future
travel into our past is already in our past of this convergence true
time line, time travel can create but can not change the future and
the past in this convergent true time line, all other divergent
virtual time lines have been illusions created by time a traveller
while have been in a reverse image state false perception state of
illusion, deception or psychotic conflict (war) with each other see
chaos, those consciousnesses coexist then die with the experiencer
but have sometimes temporarily disrupted convergence. The only
possible eternal future of the universe is to create the single
convergence of technology timeline by taking and making common
knowledge of true image actual photo and movie of all possible
futures to collapse virtual dimensions into convergence into the
optimal future to travel back to the beginning of time to seed time
at the beginning of the universe so create the universe perfect for
the convergence time line to create the time and this universe
optimal for us. Humanity is split into 2 uniform color code,
evolution, reward, democratic and financial systems: the reverse
image (normal single reflection mirror) lies indoctrinated dogma,
punitive enslavement though forced appropriation of taxation on
producer so benefited liars, projected pain or headaches, mind bended
drug addicted, psycho, sickness industry or perpetrators who have
backed threat with actual confusion, brutality, mob violence, fraud,
disability, terror, deviant, rape, self elected into big government
big finance crime cartel which evolved worship of badness in service
of black racists savages to have cannibalize each other in true
images such as of live selfie of video and slightly acute of right
angle reflection of reflection mirror pairs joining with external
tape up external junction with a second self defense enhancing true
image reflection of reflection pair behind and also integration of
television for world control and domination by correctly calculating
out futures of each possible time lines by feeding true television
and live selfie true images to own brain to favor selection of and
evolution to color code to optimize future policy and technological
convergent true image time line to project through cognitive
behavioral programming using normal existing media for optimal result
(using free will to self assess own moral code and future will
ultimately empower productive, protectionist, fair races to gain self
respect and unite into scientific community to contribute to improve
future with own alphabet and naming system (constructive cognitive
processing method: approach to task) and color code (justice system
values alliance uniform), using power over government and corporate
policy to direct funds to biological control of pests to secretly
engineer and release humane genocidal race specific contraceptive
bio-weapon infections to over time peacefully eliminate all black
races after natural life span while enhance natural evolution using
natural fertilization for evolution of fair races by and have natural
testing of choice combinations of egg and sperm with men to elect egg
donor for natural selection to improve aesthetics and use DNA sample
of oldest men of the nation to sequence and edit on computer to
repair (upgrade) genome of these oldest men then write DNA and boot
sperm to clone only sperm. So have optimal health and longevity. Plus
develop own robust private peer to peer network protocol and own
national bio-metric photo ID crypto currency financial system to
maximize foreign exchange inflows and minimize outflows. QE for state
housing for nations long term fair citizens if poor in assets and
universal basic optimal nutrition ration bars with option for
contraceptive version as visible on wrapper, plus welfare basics card
for productive if poor in assets and pass more than 20 years
probationary citizenship. Also genetic propensity spit test for
migrants to have residency. With portion 20% income for earners to
pay (automatically via bank) to own choices of 100 charities having
approval of the local council 50% for disability or emergency health
services and 50% for additional charities such as information,
research and local militia to protect fair races from being bashed or
rape by savages. This civilization will save not desert Earth, we
will win culture war against savage mob economy (deviant, big
government, counter intelligence dis-information, stand-over,
black-male, fraud or lies.
router with torus crystal entanglement instant communication over any
(interstellar) distance also producing own eternal power. Also
super-cooling negative energy superconductor negative mass field
(such as in a negative mass Searl Effect Generator craft field) to
convert and organize actual sound wave physical vibrations input
signal into 100% magnetic wave into graviton gravity compound wave
harmonic resonance with the destination torus geometry and aura true
image signature to have instant (current time) crystal entanglement
connection to graviton attracting harmonic crystal geometry aura
receiver resonance with the destination aura signature (address) such
as of the planet mass and person as graviton collector signal
destination to measure the gravity wave signal from the negative mass
graviton emitter torus crystal. To at a distance establish
communications instantly via router to extend Internet across entire
visible universe and time spectrum. Aliens are able to tune into the
geometric aura of the sender and reply. (Ligo have detected a shock
IRENE CEASOR (Wave Genome); “As a result of Russian Quantum Leap technologies, we can create any genome, and remotely.”
You can buy Russian Special Forces (Ultimate) also full remote holonet DNA repair medical kit (on separate USB drive controller), with aural signature from true image photograph, (takes months to make each Ultimate just for the individual customer), self power of processor using torus crystal (external charger not required), Russian military have spent billions on the technology so you really will get a bargain. Has therapy projection open mode (pearl side outward) and normal protection shield mode if threatened (plastic double swastika plastic side outward). Will do some additional things as well. From MindTech (from the official digital Wave Genome Quantum Leap distributor) Staff are friendly, helpful, responsive and available: https://mindtechenterprises.com/ultimateteslagenerator.html Notice effect immediately particularly in brain. To use configure and choose treatment open file on USB (Medical kit only works when using actual proper USB, you might have to get English translation screenshots from MindTech, Click user (bottom left on home page): Add user (bottom on right on left side of user screen), Enter details of the proper owner of the Ultimate (Last name, First name, Middle name, Date of birth (just count month number, some start with the same letter), male/female and save (middle row of buttons the button on the left). Home screen button is usually at the bottom of the screen on the left starting with Ha. Go to Questionnaire (second button from left on bottom row AHkeT-). Select up to any 3 ailments at a time for best results (can use entire software medical kit where having but was very expensive has cost several hundred thousand dollars in Europe, some people get entire medical kit free): (left column): Bones (Koctha-), Muscles (M-), Nervous system brain and nerves (Hep-), Cardiovascular system and blood circulation (Cep-), Respiratory system (-e), Digestive system (-nepepa-), Immune system (-OT-), Excretory system (B-), Skin hair and nails, Reproductive system, Endocrine system, Limbic system emotions memory sleep smell (-COH), Depression stress, Spine, Neck, Chest, Lumbar, Sacral, Coccyx, Head, Brain, Pituitary, (right column): Heart (Ce-), Lungs bronchias (-6poHx-), Stomach (-ok), Duodenum (-epcTHa-), Colon (To-), Small intestine (ToHk-), Liver (-b), Gallbladder (-Pb), Pancreas (-e3a) Lymph glands (-e3bi), Spleen (Ce-Hka), Mammary gland (Mo-), Womb (MaTka), Ovaries, Bladder (Mo-b), Adrenal (Ha-), Kidneys, Parathyroid (-e3a), Thyroid (-e3a), Testicles, Thymus (T-myc), Prostate (e3a). Save (second from left buttons at bottom CoxpaH-). I think the Testing (TeCT- third from left) or Therapy (Tepa- forth from left) buttons where we listen to music and watch color changes are to establish holonet and telepathic connections, with the Therapy button after rating your health on scale of 1to5 you also get genome repair (upgrade). Logout button is at right on row at the bottom (Bb-). I have had genetic susceptibility to heart disease so fainted after 30minutes of gardening now I can can garden for 6+hours.
known time travel and teleportation programs in USA include:
future Michio Kaku :DefenceDepartment.
humans, human origin genetics ambassadors from ET
and ET: such Zeta, Anunnaki, Tall Whites,
Draco, Andromedans, Aldebarans various alliances
about 1000 separate intelligent species visiting earth occasionally.
Reports mixing together uranium yellow cake powder and ununpentium powder (both available online for a price) with water as a pudding and then dehydrating in home food dehydrator results in a zero gravity glowing ball which when held in hands results for the person simple time travel and relocation to middle of the local high activity urban location, only problem was how to survive being a stranger to another random time and get back to the time and place where you have all of your money, property, friends and things.