Here some math based on Meyer and Puharich..they both say the RC time is 5kHz...this doesnt mean to pulse the circuit at 5kHz, this is just the RC time. Using the RC formula RC= 1/(2pi*f*C) we can find the pulsing frequency to fully charge the WFC. We know that the RC time is 5kHz and the cell used had a capacitance of 1.6nF, 3" single tube cell. So it breaks down like this:
RC = 1/(2pi*f*C)
5kHz = 1/(2pi*f*1.6nF)
f = (1/(2pi*1.6nF)) / 5kHz
f = 19904.46Hz
Now we have to take 19904.46Hz and divide it by 5, the reason we divide by 5 is because the 19904.46Hz is the RC total which equals to 5 Time Constants, 5TC.
19904.46Hz / 5 = 3980.89Hz
This 3980.89 Hz is the frequency that the circuit should be pulsed at. This number should look familiar because Puharich states this frequency in his water splitter patent!!!
-Tony Woodside-
http://www.globalkast.com
I will try to make a picture collage this weekend of all pictures I think could be useful to explain my ideas. Pictures explain best.
What do you mean when talking about resonance. Resonance of what? H2O, H2+O, H2, H H, H+? In my opinion we have two major tasks for H2 dissociation.
- H2O -> H2 + O via pulsed electric fields. Maybe even H2 -> H H
- H2 -> H H or -> H+ via photo dissociation.
Getting H2 could be enough though.
I just started to work myself into this topic and am still gathering informations. Until today I thought everything could be done by electric fields but when I read about photo dissociation I thought this could be useful too, especialy for the H2 -> HH part.
So I found this Document. http://www.freidok.uni-freiburg.de/volltexte/33/pdf/33_1.pdf The diagrams and schematics of the experiment set-up had some interesting informations.
They used a laser with 400nm and a laser with 800nm whereas the 800nm laser created most ions. Red laser pointers have about 650nm so I think I will experiment with that. I don't know how fast it's possible to puls them but even as a continues photon source it could be useful. They also used piezo pumps and shot at the H2 in an rectangular angle, like Meyer did.
@TonyWoodside: Your Youtube videos showed that you were successful in replicating Meyer's electronics. What do you want to improve or on what are you working now? Have you tried to measure how many Watts you need for a liter?
I am going to attempt to explain how Stan split the water molecule with low currents. Ok first thing, basic electrolysis uses current to slit water by using electron collision. In Stan's system he only wanted to use voltage and no current, which we all know by now. Well I've been digging deep into what Stan says in his lectures and memos. This is what I've come up with and it all make sense with what Stan says. Stan talks about the molecule and its "Ground State". Theground state of a system is its lowest-energy state. The energy of the ground state is known as the zero-point energy of the system. Basically the ground state refers to the electrons being in their correct orbit making them stable. Well Stan's talks about taking the molecule from ground state to excited state. Excitation is an elevation in energy level above an arbitrary baseline energy state. In physics there is a specific technical definition for energy level which is often associated with an atom being excited to an excited state. This means to make the electrons go from their correct orbit up to the next orbit. Like in the water molecule you have 2 orbital shells and the 1st orbit is the "K" shell and the 2nd orbit is the "L" shell. So to make the molecule go from ground state to exited state, the "L" shell electrons will be ejected to what is know in electronics as the conduction band, which is just an imaginary location outside the orbit of the molecule. Once you have less than 8 electrons occupying the "L", you will then have the 2 electrons from the "K" orbit jumping into the "L" orbit. This will continue till all electrons are in the conduction band and the "K" and "L" orbits are empty. Once the orbits are empty there is obviously no covalent bonding between the Hydrogen and Oxygen atoms at this point.
Now I will explain how this can be achieved. The key to Stan's system is Harmonic Oscillation. The LC circuit has to be made to give a specific Harmonic Oscillation Wave Function. This wave function will mimic a particle equal to that of the electrons. When the electrons are hit will this wave function signal, they will go from ground state into excitation state. If you stop the signal, after a short time period the electrons will emit photons and then return to ground state. This is why Stan say pulse for X amount of time and then gate and gas will be produces for another X time period. The gate will allow the photon energy to be released and this photon energy will continue to produce more gas and allow the water to go back to ground state.
The Harmonic Oscillation Wave Function is very similar to an AM signal. The signal has to be the correct band of frequencies in order to split the water molecule. Puharich gives these specific frequency bands ( 3.98kHz, 7.96kHz, 15.95kHz, and 31.84kHz, which these frequencies are all sub-harmonics of 63.68kHz ) need to split the molecule. I've noticed in Stan's setup he uses chokes in around 1H each and if you calculate the capacitance of a single tube it will be around 1.6nF, by using L= 1H and C= 1.6nF, the resonant frequency will be 3.98kHz....is this just coincidence? I think NOT. Research Meyer and Puharich's system and you will see that these two system are very much alike. Here are some references on what I've just explained, research it and you will see that this is the way it was done.
http://dev.physicslab.org/asp/applets/javaphysmath/java/atomphoton/default.asp (http://dev.physicslab.org/asp/applets/javaphysmath/java/atomphoton/default.asp)
http://en.wikipedia.org/wiki/Harmonic_oscillator (http://en.wikipedia.org/wiki/Harmonic_oscillator)
http://en.wikipedia.org/wiki/Matter_wave (http://en.wikipedia.org/wiki/Matter_wave)
http://www.brightstorm.com/science/physics/the-atom-and-quantum-physics/matter-wave-de-broglie-wavelength (http://www.brightstorm.com/science/physics/the-atom-and-quantum-physics/matter-wave-de-broglie-wavelength)
http://www.lsbu.ac.uk/water/vibrat.html (http://www.lsbu.ac.uk/water/vibrat.html)
http://en.wikipedia.org/wiki/Morse_potential (http://en.wikipedia.org/wiki/Morse_potential)
http://en.wikipedia.org/wiki/Quantum_harmonic_oscillator (http://en.wikipedia.org/wiki/Quantum_harmonic_oscillator)
http://en.wikipedia.org/wiki/Molecular_vibration (http://en.wikipedia.org/wiki/Molecular_vibration)
http://butane.chem.uiuc.edu/pshapley/GenChem2/A7/1.html (http://butane.chem.uiuc.edu/pshapley/GenChem2/A7/1.html)
http://www.thefullwiki.org/Nuclear_magnetic_resonance (http://www.thefullwiki.org/Nuclear_magnetic_resonance)
http://gregegan.customer.netspace.net.au/ORTHOGONAL/07/QM.html (http://gregegan.customer.netspace.net.au/ORTHOGONAL/07/QM.html)
http://www.absoluteastronomy.com/topics/Quantum_LC_circuit (http://www.absoluteastronomy.com/topics/Quantum_LC_circuit)
http://centros.edu.xunta.es/iesames/webantiga/webfq/EUSECTSUSO/chem_phys_bac/Chemistry_2/chemical_bonding.htm (http://centros.edu.xunta.es/iesames/webantiga/webfq/EUSECTSUSO/chem_phys_bac/Chemistry_2/chemical_bonding.htm)
http://universe-review.ca/F12-molecule.htm (http://universe-review.ca/F12-molecule.htm)
Hope This info sheds some light on this process and how it works.
Thanks,
Tony Woodside
I made a quick drawing with power point.
The laser beam gets reflected many times in this pipe increasing the amount of photons colliding with elektrons. The diameter of the pipe can be larger than the diameter of the hose to slow down the gas through the pipe and increasing the duration of the gas in the pipe -> more collisions -> more HH, H+.
(http://www.ionizationx.com/index.php?action=dlattach;topic=2121.0;attach=9137)
Well, you could read Meyers patents in regards to EGR and Gas Processor and then read the PDF I wrote located in Reply #35 - page 8, that should help you understand what it is.hmm you are right Iontruster. This might not be the right place to post this "method" for photo dissociation but neither I think that it's fits to "water injector" or "ambient air-gas processor". I understood your quoted post in that thread as if the purpose of the ambient air gas processor is to add ambient air to the h2 to produce some kind auf natural gas (eureka). My post is rather a general suggestion on how to produce HH or H+ (if it works). And photo dissociation was one point Tony Woodside mentioned. Well never mind.
I made a quick drawing with power point.
The laser beam gets reflected many times in this pipe increasing the amount of photons colliding with elektrons. The diameter of the pipe can be larger than the diameter of the hose to slow down the gas through the pipe and increasing the duration of the gas in the pipe -> more collisions -> more HH, H+.
(http://www.ionizationx.com/index.php?action=dlattach;topic=2121.0;attach=9137)
Yes sir, in his earlier setup he used a variable inductor in the -Ve of the LC circuit. Now do you know why he used this?
Yes sir, in his earlier setup he used a variable inductor in the -Ve of the LC circuit. Now do you know why he used this?
Variable choke because Meyer's early setup was stuck at 10, 100, 10k, 100k hz frequency.
Variable inductor-----Possibly to match the resistance of the water between the tube sets to the inductor.
In my opinion it probably functions as a filter to only let through a certain frequency band.
Regards,
Sharky
Variable inductor-----Possibly to match the resistance of the water between the tube sets to the inductor.
not really...think about it guys...u need to know about an inductor and capacitor being used together, what does it form?
I'm thinking about 'side bands' and center frequency.
The L2 choke has opposite phase of L1 and can be adjusted to give a proper side bands to set resonance of the protons and electrons.
There is a resonance in the side bands at GHz frequencies...
Also what about the air-gap of the resonant cell? Puharich talks about 22.3GHz(wave length water resonance) found 20..40GHz EM in the sidebands and talks about 14mm gap. Thats full wavelength so 1/4 wavelength has still 3.36mm air-gap???
Did SM used a harmonic?
Br,
Webmug
give me a break, you don't know how I learn and your attitude is something I'm familiar with....
I took up this meyer thing up four years ago to learn electronics, something I always wanted to know more about, simple as that, I used it as a vehicle of sorts....
it has been said that the genius Einstein was a brilliant man yet he could not speak spanish, even the little kids in mexico know spanish and speak it well, to them he is a bit slow, however, I don't believe they would suggest he learn it in the fashion you proscribe for some of us who ask a question or two
sheesh again
kb
NOTE: The gap is smaller than 2.413mm, 0.0625 inch = 1.5875 millimeters! What I read it is 1.5mm thick 0.75inch outer diameter, 2.75inch length. I want to use a 20mm outer diameter and 2mm thick 2.75inch length tube to get 1.65mm air-gap!I'm thinking about 'side bands' and center frequency.
The L2 choke has opposite phase of L1 and can be adjusted to give a proper side bands to set resonance of the protons and electrons.
There is a resonance in the side bands at GHz frequencies...
Also what about the air-gap of the resonant cell? Puharich talks about 22.3GHz(wave length water resonance) found 20..40GHz EM in the sidebands and talks about 14mm gap. Thats full wavelength so 1/4 wavelength has still 3.36mm air-gap???
Did SM used a harmonic?
Br,
Webmug
Yes, Stan used harmonics. You are getting very close to what I'm looking for :) Do you know why Stan had to make the L2 choke out of phase?
Yeah Puharich's cell was 9" long and had a gap of 14mm....Stan's resonant cavity tubes had an effective capacitance length of 2.75" and a gap of 2.413mm.
The L2 coil is out of phase from the L1 coil so that it will make square wave pulses act like that of an AC signal. Meyer's was doing the same as Puharich and he had to use pulsed DC and configure the coils to this arrangement so he could generate a signal similar to a sine wave so that he could get around Puharich's patent and could patent it as his own.Puharich said that "a unipolar pulsed DC will be formed when a AC wave (AM?) signal is going into a tubular resonant cavity."
close... hand grenades and horseshoes?Make sense to me, he used the famous KISS method 8)
speedymetals 304
0.68 id versus 0.69 with a 0.35 thickness versus a 0.30 thus leaves a gap of .090 versus the .095 as you suggested based on 4" inner and 2.75" outer
perhaps meyer was using commercially available stock?
I'll be looking around some more
kb
T & all
observations
I've found that good inductance from the coil at resonance will show much higher peaks like your scope shot when a substantial capacitance is added parallel to the plates. I put all the high voltage capacitors that I had on hand plus a couple of hefty tinfoil/waxed paper rolled capacitors that I made and produced almost twice the peak to peak voltage.
Lets see... 8x385v-330uf plus two 65v-50,000uf plus six 200v-1000uf plus one 150v-1400uf plus my two tinfoil caps... a bit of added parallel capacitance wouldn't you agree?
A slight frequency adjustment to bring it all back into the highest voltage peak to peak output and you'll end just about doubling the peak to peak voltage at the same input voltage
this was obtained with a three inch bifliiar wound composite core toroid at about 10khz with 20 volts and 250ma.... 2100v ptp
kb
Two resonances are taking place here. 1) The smaller AM signals are to match the resonance of the electrons of the molecule. 2) The larger and slower AM signal modulates the smaller AM signals to higher voltages and what this does is setup the resonance of the Nuclear Magnetic Relaxation (NMR) cycle of the proton water which is approximately 3 secs. You can also use subharmonics of the NMR cycle which would be around 0.5 Hz & 0.25 Hz@Tony
If the capacitance value changes, then the scanning circuit will lock back on to the resonant frequency. There's a certain ratio for the inductors, so if the resonant frequency does change, the sidebands will stay constant due to the ratio. Puharich gives this ratio in his book as the 12th root of 2 ( 1.059463094 ). I've calculate Stan's inductors based on this ratio and for his capacitance of 67nF, the resonant frequency is 547 Hz with L1 = 1263.5mH and L2 = 1125.7mH....This will make the two frequencies at the cell be 547 Hz and 579.5263124 Hz....579.5263124/547 = 1.059463094. For example, say the capacitance changes from 67nF to 60nF, the resonant frequency will now be 578 Hz... so the two frequencies will be changed to 578 Hz and 612.71 Hz....578/612.71..Hz = 1.059463094...So the ratio for the sidebands will stay constant.So if we use this 12th root of 2 ratio between chokes we can always "tune in" the structure of the water molecule (phonon vibrations between four vertices) because of the side band results on the center frequency.
@Tony,
What frequency are you going for?
Keely:
"In molecular dissociation one fork of 620 is used, setting the chords on the first octave.
Go for resonance frequency 620Hz and ratio 2^(1/12) = 656.8Hz; C=52.141nF; L1=1263.5mH and L2=1125.7mH
What is the bandwidth for molecular dissociation (620Hz)
Puharich calculated 657.4Hz and called it "beat" effect. I assume it depends on what type of water is used.
Also can you elaborate how the AM signal is generated for the first resonance (PULSE and GATE).
Is the gate frequency adjusted on 3sec time that corresponds to the nuclear spin relaxation time, tau/sec, of the water?
Br,
Webmug
I`m confused here! how did you guys came up with the 67n 60n 52n. They all seem to be very high values for the water capacitor we are using. Are you assuming this value for only one 3inch tube set?
hm
I`m confused here! how did you guys came up with the 67n 60n 52n. They all seem to be very high values for the water capacitor we are using. Are you assuming this value for only one 3inch tube set?
hm
The calculated value for the cell will be much different from the actual measured value. Like for Stan's resonant cavity, the tubes calculated capacitance is around 877pF, but the measured value for a single tube with distilled water is 670nF. Since Meyer had 10 tubes wired in series you will have a capacitance of around 67nF, but you can get the value lower by circulating the water through the tubes.
Yes webmug, this is the reason for the train of impulses. Each pulse adds to the force field... And when the field collapses particle impact generate energy. The frequency is directly related to the voltage.Does this AM also work to make the "steam resonator" but on different frequency as the "resonant wfc"?
Why did SM build all the 11 VIC coils and circuits if he used 1 VIC and circuit and 10 wfc cells in series?
QT = Q1 = Q2 = Q3 .... ETCIn the following circuit, capacitors, C1, C2 and C3 are all connected together in a series branch between point A and B
VAB = VC1 + VC2 + VC3 = 12VKirchoff's Voltage Law (KVL)
VAB = VC1 + VC2 + VC3 = 12V
VC1 = QT /C1 - VC2 = QT / C2 - VC3 = QT / C3
VAB = QT/CT = QT/C1 + QT/C2 + QT/C3
Series Capacitance Equation
CT = (1/C1) + (1/C2) + (1/C3) + ... etc
here is a video I made that explains the process. Please read the video description. http://www.youtube.com/watch?v=rP7k6sG1NXQ (http://www.youtube.com/watch?v=rP7k6sG1NXQ)Thanks for sharing this video of the effect, Tony!!! :)
Getting back to the 12th root of 2 ratio, ... do you guys know that in music the 12th root of 2 ratio is exactly the difference between two notes! E.g., an A has a frequency of 440Hz, the next higher note is the Ais which is 466.16 Hz, the difference between that is exactly the 12th root of 2 or 1,05946309. This is the same for all subsequent notes. So does this mean that it has to do something with the sound wave created in the cavity as well?It all has to do with sound waves "vibrations" in the cavity.
Sharky
(http://www.globalkast.com/images/tonywoodside/AP_Overtones.PNG)I'm not a musician so my knowledge is limited.
According to Don's messurement, the electrode distance is 2,413 (or 0.095") mm for the latest cell. Frequensy responce is 3610.5263Hz (3,61kHz) at that distance - to match the 3.98kHz from Puharich, we need the electrode distance to be 0.086" or 2.1844 mm electrode distance.How did you calculate this, can you elaborate? Isn't that water-gap in the GHz frequency range?
How did you calculate this, can you elaborate? Isn't that water-gap in the GHz frequency range?
Also the value of 0.090" showed up in the patents.
Br,
Webmug
Okay, here is a question. Stanley used a solid rod as a cathode, and so far, we've narrowed it down that that the harmonic frequency are related to the chokes and also the electrode gap - a match in the electrode gap and chokes = resonance as long as you start of with the correct input. Now, during all these years that I've been working on this, sometimes someone pops up and say - hey, you need the tubes to ring at the resonance frequency and you need to tune them.. hmm, well, yes, for the old system yes. It should be quite clear by now that what Stanley did was TUNING in his old system, that is why he built them. I recon he had a fairly good understanding of what he needed (if we look at the system from the start till the end) and all he did was tune and adjust, and that is the reason for all the versions.What I think: the Rod is a KISS approach, mechanical solution for fixing it in a Delrin cavity.
So, now we are @ the last 3" cell (well, its actually 2,5") and remarks about the 0.095" gap was made. Which got me thinking, so back to the cathode.
We have voltage that perform work and we want to isolate this area, so we insulate the capacitor. We then have resonance that stretch the molecule, you create a Rydberg Molecule (partial ionization) and this is happening with sound waves within the medium. All of this is doable. First of all - the charge is on the electrode surface and in the medium, essentially making the material good for two things 1) Transport the current to the surface. 2) Transport the harmonic oscillation frequency's to the charging medium. It seams like its not used - anymore - as the oscillator itself (the electrodes). Now, correct me if I am wrong or you have another theory, that is why we are all here. So, as I said, all of this got me thinking.
The electrodes now got a dedicated job, and stainless is used to prevent oxidation. But why do we need a solid metal rod as the cathode? We know that we do not want or need water there, but could we not simply go for a solution where the cathode also is a tube and close it off, lets say with a Delrin or Teflon rod? Or is a solid metal rod needed in the sense that it actually is part of the harmonic frequency creation ??
Tony:"The speed of sound through water is 1482 m/s and with a gap of 0.095" = 614173.23 Hz."Still I have not a clue, how you came up with the gap frequency for 0.0950" in the kHz range?
Iontruster:"Frequency response is 3610.5263Hz (3,61kHz) at that distance"
Okay, here is a question. Stanley used a solid rod as a cathode, and so far, we've narrowed it down that that the harmonic frequency are related to the chokes and also the electrode gap - a match in the electrode gap and chokes = resonance as long as you start of with the correct input. Now, during all these years that I've been working on this, sometimes someone pops up and say - hey, you need the tubes to ring at the resonance frequency and you need to tune them.. hmm, well, yes, for the old system yes. It should be quite clear by now that what Stanley did was TUNING in his old system, that is why he built them. I recon he had a fairly good understanding of what he needed (if we look at the system from the start till the end) and all he did was tune and adjust, and that is the reason for all the versions.
So, now we are @ the last 3" cell (well, its actually 2,5") and remarks about the 0.095" gap was made. Which got me thinking, so back to the cathode.
We have voltage that perform work and we want to isolate this area, so we insulate the capacitor. We then have resonance that stretch the molecule, you create a Rydberg Molecule (partial ionization) and this is happening with sound waves within the medium. All of this is doable. First of all - the charge is on the electrode surface and in the medium, essentially making the material good for two things 1) Transport the current to the surface. 2) Transport the harmonic oscillation frequency's to the charging medium. It seams like its not used - anymore - as the oscillator itself (the electrodes). Now, correct me if I am wrong or you have another theory, that is why we are all here. So, as I said, all of this got me thinking.
The electrodes now got a dedicated job, and stainless is used to prevent oxidation. But why do we need a solid metal rod as the cathode? We know that we do not want or need water there, but could we not simply go for a solution where the cathode also is a tube and close it off, lets say with a Delrin or Teflon rod? Or is a solid metal rod needed in the sense that it actually is part of the harmonic frequency creation ??
Cool!(pun intended)
I do see where you are going with this Steve, and I think it could be a good view of it all. It could work with enough compression and heat. But with plain HHO, we have more of a problem of generating enough heat. How can we fix that problem? Pre-combustion fuel ionization?
You see, even with electrolysis, I always found it wasn't that hard to produce enough HHO to run a motor. It was never an issue of quantity, it was more about torque and power. Which keeps driving me back to why it is paramount that electrons are "extracted" from the fuel mixture. It blatantly seems obvious to me, that the only way this could be a possibilty, would be to harness the atomic energy of the atoms. Like snapping a tiny atomic rubber band!
So, could it be that simply making an "electron extraction" device could do the trick? Can we easily make the incoming air electron deficient? How will the the positively charged air react with HHO and water?
I just noticed something about a drawing I was looking at for an illustration. The way that it is drawn is confusing, making it look connected where it shouldn't be. I took the liberty of dividing the two, have a look...
According to Keely the molecule will maintain its integrity (steady state: state of relative harmony ratio 1:1:1) until the ratio of width to length exceeds 1:4 at which point the molecule disrupts or comes apart forming a dipole and a monopole particles. Implying the molecule can not separate into three distinct particles at one time. Because to do so would mean that as they got further and further apart approaching the 1:4 ratio its confines of ratio would be held in strict relativity - i.e., as the molecule stretched the ratios would remain relative to one another. This scenario is interesting in that a molecule could be made to stretch in all three directions artificially. Once it reached a point where all three diameters exceeded the original 1:4 ratio two frequencies could be quickly demodulated such that they instantly revert to the original rates thus leaving one of them at the 4+ ratio. The molecule would instantly disrupt with little apparent energy input. In other words, the molecule could be stimulated until it was in a state of maximum instability and then "nudged" into dissociation with a small tickle of force.
Planck's constant, is a physical constant reflecting the sizes of quanta in quantum mechanics. The Planck constant was first described as the proportionality constant between the energy (E) of a photon and the frequency of its associated electromagnetic wave (?).
The Planck constant is a fixed amount of energy being the difference of energy quantities as measured from orbital shell to orbital shell or from one energy state to another. The Planck constant is the difference between the energy levels. This difference is the same as the interval as spoken of in music.
A semitone is the smallest change of pitch (frequency) used in conventional music and musical notation. Semitones correspond with the individual keys of a tuned piano. A semitone is defined as the "12th root of 2" (1.05946...). The Golden Ratio (1.61803...) when cubed, almost exactly equals 25 semitones. Therefore the 25th root of a cubed golden ratio (1.05945...) equals 0.99998... semitones. This difference, when accumulated over the entire range of human hearing (about 120 semitones) is less than 3.5/100 of one semitone, and is undetectable by the human ear.
It is assumed the natural progression of discord follows the following pattern of ratios from perfect harmony or equation of forces to the least harmonious or the point of disruption:
Harmony 1:1:1 / 1:1:2 / 1:2:2 / 1:2:3 / 1:3:5 Disruption
The above figures are the natural progression of the Fibonacci spiral and all other life activities resulting from a natural progression of events.
They are intimately connected with the golden ratio, for example the closest rational approximations to the ratio are 2/1, 3/2, 5/3, 8/5, ...
So the ratio Puharich found (also valid for water molecules) was "12th root of 2" and is tightly coupled to Keely's work.
Br,
Webmug
Now to the paper.
(Go to equation 4.)
Coulomb described the electrical force with his constants Q etc. and variable radius “r”. Znidarsic rearranged the constants in the form of the elastic energy of a spring.
together they equal a group constant K. The variable 1/r remains the same.
Amazingly, the new form revealed the classical radius of the electron “2rp”. However, that’s not nearly as important as what else he discovered… The mechanical elastic constant and displacement 2rp can be used to determine the velocity of sound within the electron.
You see, the strength of the electric field varies with distance r away from the electron and this is reflected in this variable elastic constant. The speed of sound also varies at different locations within the electron.
(Go to equation 4).
The velocity 1 million meters per second was then written in terms of a product of frequency and wavelength. Znidarsic assumed that this was the velocity of light within these experiments.
(Now onto eq. 10:)
The condition of the velocity of light (left side) was set equal to the condition produced by the velocity of sound (right side). The velocity of a wave in medium is determined by the stiffness of that medium. (Show waves going at different velocities). The greater the strength of the forces within the medium, the faster the wave propagates. This is why sound travels faster in steel than in water. In the case where all the waves are going at the same velocity the strength of the forces between the components is the same. This implies that the strength of the electromagnetic, gravitomagentic, and nuclear forces converge under this condition.
This discovery has important technical ramifications. It shows the conditions necessary to control the natural forces. As in, controlling Gravity and Nuclear Forces.
This idea does not end in the clouds, however, it can also be used to produce the structure of the hydrogen atom (in equation #12.) This has never been done before from a classical premise.
Not only that, but the structure was extended to produced the intensity of spectral emission.
Finally, if you set rx equal to the radius of the hydrogen atom. The elastic energy contained by an elastic discontinuity of displacement 2rp equals the zero point kinetic energy of the ground state electron. Frank suggests that the natural force fields are pinned into the structure of matter at this discontinuity. The transitional quantum state removes the discontinuity and releases the fields.
According to Keely the molecule will maintain its integrity (steady state: state of relative harmony ratio 1:1:1) until the ratio of width to length exceeds 1:4 at which point the molecule disrupts or comes apart forming a dipole and a monopole particles. Implying the molecule can not separate into three distinct particles at one time. Because to do so would mean that as they got further and further apart approaching the 1:4 ratio its confines of ratio would be held in strict relativity - i.e., as the molecule stretched the ratios would remain relative to one another. This scenario is interesting in that a molecule could be made to stretch in all three directions artificially. Once it reached a point where all three diameters exceeded the original 1:4 ratio two frequencies could be quickly demodulated such that they instantly revert to the original rates thus leaving one of them at the 4+ ratio. The molecule would instantly disrupt with little apparent energy input. In other words, the molecule could be stimulated until it was in a state of maximum instability and then "nudged" into dissociation with a small tickle of force.Keely gives frequencies for molecule manipulation and starting the oscillation of the molecule with three frequencies, called Thirds! Also he has more higher ones (Sixths, etc just like SM did for the gas-processor: Atomic Hydrogen etc.), but the Third is still a misery using SM setup for starting to grasp the electrical polarization process (molecular dissociation).
think of this LCL circuit as a Filter circuit. You have a resonant frequency for L1 and the Cell, that will be your driving frequency. This driving frequency will be the same at the output of the L1 inductor, but the driving frequency modified by the L2 inductor to give a higher frequency. For example, Lets use Stan inductor values: L1 = 1262.7 mH, L2 = 1138 mH, and the calculated value for the cell is around 877nF. So the resonant frequency for L1 and C = 4785 Hz. This will give rise to the HV's in the LC circuit, which will modulate the signal of L2. The L2 frequency with the driving frequency of 4785 Hz will be modified to a frequency of 5038 Hz. So now you have two frequencies being applied to the cell, 4.785kHz and 5.038kHz. These two frequencies will form a Modulated AM signal.Harmonic oscillator III: Forced oscillations
(http://www.globalkast.com/images/tonywoodside/Modulated_AM.png)
No feedback on this?think of this LCL circuit as a Filter circuit. You have a resonant frequency for L1 and the Cell, that will be your driving frequency. This driving frequency will be the same at the output of the L1 inductor, but the driving frequency modified by the L2 inductor to give a higher frequency. For example, Lets use Stan inductor values: L1 = 1262.7 mH, L2 = 1138 mH, and the calculated value for the cell is around 877nF. So the resonant frequency for L1 and C = 4785 Hz. This will give rise to the HV's in the LC circuit, which will modulate the signal of L2. The L2 frequency with the driving frequency of 4785 Hz will be modified to a frequency of 5038 Hz. So now you have two frequencies being applied to the cell, 4.785kHz and 5.038kHz. These two frequencies will form a Modulated AM signal.Harmonic oscillator III: Forced oscillations
(http://www.globalkast.com/images/tonywoodside/Modulated_AM.png)
http://nptel.iitm.ac.in/courses/Webcourse-contents/IIT-KANPUR/engg_mechanics/ui/Course_home_26.htm (http://nptel.iitm.ac.in/courses/Webcourse-contents/IIT-KANPUR/engg_mechanics/ui/Course_home_26.htm)
Br,
Webmug
Awesome, have you been selling a lot of them?
I've been working on my own design for a while,
and honestly If you guys look at the time and effort it
takes to design, build, test, redesign etc I think
it's cheaper just to buy one....i'll be buying one soon.
Awesome, have you been selling a lot of them?
I've been working on my own design for a while,
and honestly If you guys look at the time and effort it
takes to design, build, test, redesign etc I think
it's cheaper just to buy one....i'll be buying one soon.
Yea I started selling them back in July and sold out of them pretty quick. I have made so changes on the current ones that I am selling and they have been selling pretty good as well. I have a limited supply available and I also have kits available as well. It usually takes about 2 to 3 hours to complete one board. Yea you are right about the time and effort to build and design the boards. It took several months to back engineer this circuit and come up with the design.
You need to also remember that each resonant cavity and VIC transformer are matched. For example, lets say the coil will resonant at 3.5kHz, well the resonant cavity needs to also resonant at 3.5kHz. They have to be matched, just like a coil and antenna of a radio.More "Thoughts on how Meyer split water":
webmugFor more information what matter is you can read it here
I read almost all people toughts on how water molecule is affected by voltage/freq.but the are verry contradictory...can you make/give me a link with a 3d drawing of the process?1000toughts 1000confuses..if you understand..