The more I Study Water the more it behaves like a Semiconducor!
So instead of treating it like a dielectric. I will start to treat it like a Semicondutor.
Here is the plan...
#1 how can one change the characterisitics in a semicoductor?
in the industry this process is called "Doping"
#2 So I will Start "Doping" Water.
Becouse of internal parrallel path and "Ez Zone" there exist leakage that the capacitor does not maintiane charge for longer periods.
by doping the dielectric we can extend the charge capacty of water...
The question is what material can we add to the water that does not involve chemical reaction?
Here is the answer and run with it yes fly:
Option number #1 Silica Dioxide Carefull not to breath.
Option number #2 Crushed Quartz crystal
Option number #3 Crushed Glass, fine powder.
What do they have in common?
[{(sand...Silicone) Same material used in semicondutors!}]
Yes
They all have a resistive carachteristic to current and do not bond chemicaly to the water.
https://en.wikipedia.org/wiki/Silicic_acid
"Silicic acid is the general name for a family of chemical compounds containing the element silicon attached to oxide and hydroxyl groups."
So the moment you put current to the water and start generating hydroxyl ions (OH-), you'll be generating silicic acid, which will carry the current, destroying your hopes of high voltage, low current dissociation.
Pure water acts as a dielectric because the molecules are highly polar. In fact, the water molecule is so polar that it'll rotate in an electric field to align itself with that electric field. Use that fact to align the water molecules properly to make dissociating them easier, then hit them with some other form of energy (x-rays would be the most efficient, given the resonant frequency of the water molecule is in the hard x-ray range) at such an angle that you have a wider cross-section of energy absorption (higher barn).
You can hit it with sub-harmonic frequencies, but between each "pulse" of that sub-harmonic, the proton will 'spin down' a bit... so the lower the sub-harmonic frequency you use, the harder it is to keep the proton 'spun up' to the point that it deprotonates. X-ray frequency will spin it up so quickly that it'll deprotonate immediately, with no spin-down.
Water Radiolysis - Dissociating Water with Radio Waves
"Guenther and Holzapfel irradiated water with X-rays in contact with a large free volume in a vacuum system and found large continuing yields of hydrogen gas."
How to generate the x-rays? Well, you can "amplify" the light from an LED until it's in the x-ray range:
Miniaturized high-speed modulated x-ray source
"A miniaturized high-speed modulated X-ray source (MXS) device and a method for rapidly and arbitrarily varying with time the output X-ray photon intensities and energies."
That's an x-ray source that essentially is an electron "amplifier", taking the light from an LED and adding energy to it until it's in the x-ray range. The good thing about this device is you can tune its wavelength from 120 eV (10.332 nm) to 120 KeV (0.010332 nm).
From my E-F posts, reverse engineering the resonant frequency of water:
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http://www.energeticforum.com/water-fuel/19877-molecular-distances-corresponding-frequencies.html
According to:
Hydrogen Bonding And Orbital Models
In ambient atmosphere the O—O in the water dimer is 2.985 angstrom (calculated by JMW); the short O—H bond is 0.948 angstrom and the long bond is 2.037 angstrom.
That's .2985 nm, .0948 nm and .2037 nm.
FREQUENCY & WAVELENGTH CALCULATOR
2.037 angstrom corresponds to a frequency of 1.4717e+18 Hz or 1.4717351890034363270 ExaHertz. X-ray range.
2.985 angstrom corresponds to a frequency of 1.0043e+18 Hz or 1.0043298425460636160 ExaHertz. X-ray range.
0.948 angstrom corresponds to a frequency of 3.1624e+18 Hz or 3.1623677004219407360 ExaHertz. X-ray range.
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Keep in mind that you'll want to target the short O-H bond, since the long O-H bond is so close in frequency to the inter-molecule O--O dimer bond that hitting it without stressing the dimer bond is near impossible. And if you stress that dimer bond, you also make it harder to cleave the O-H bond.
Also keep in mind that as you stress the short O-H bond, you'll need to 'blue-shift' your frequency (increase the frequency) to account for the change in O-H bond length as you stress it. I think that's why Meyer's waveform stepped up like it did.