--- william meyer <wme...@clarityconnect.com> wrote: > hi all > why can't we get other metals and make ionic water > with our silver machines? > -- > best > william meyer Gold is also made for a health solution, some say it's a spiritual side. We really need the chemistry experts here to say what metals dissolve as colloids. Supposedly certain grades of stainless steel as used for electrolysis plates do not corrode, thus we do not expect colloids. A possibility of a magnetic nickel colloid intrigues me, which made from Canadian coins might impregnate a dielectric solution of water so that both electric and magnetic fields could interact on the sample. In fact, an experimental effort was made with regard to using silver electrodes to arc to a water surface, to deduce the no. of strikes to the water surface per 60 hz cycle, by scope monitoring of coils on surface SrFe magnets, brought close to the high voltage AC source used to cause AC arcing to water. Of particular reference here is that I also use "vibrating magnets", as a three in SrFe layer wafers underneath the 10,000 volt AC resonant voltage process. The vibration from those magnets is contained by 36 windings, shunted to a common line where the current then goes through a series neon/ high BPS arc gap system to the end connection of a large aluminum foil connection, where my patient with back boils then leans against: thereby adding the polar capacity of his body to the circuit,which brightens the neon discharge considerably. This same coil system providing high voltage rise by bipolar series resonant voltage rise of 1000 ohm coils of 23 gauge wire: 60 henries indivually tuned for mutual induction at 60 hz resonance; yeilding a 24 fold voltage rise across a water silver/glass barrier, can have a "high freq. component" added if we futher add air as a barrier between the potentials so that an arc occurs to the water surface. An arc skimming the water surface is also possible from the system by immersing the opposite electrode on the edge of the glass container, as shown at teslafy homepage. But as happenstance would have it: this same high voltage resonant voltage rise system becomes a lion tamed down to a lamb when used for TWO electrode conductions. After inserting a 6 AMP full wave rectifier diode system (just grabbed what was handy)with silver coins in distilled water I had a current limited system, based on the impedance of the pathways: which for these 60 henry coils exhibiting 20,000 ohms impedance on either side of the DC made across the coins, functioned most efficiently as a 40,000 ohm impedance value in series; whereby then for a 13 oz sample, typically the starting current was already 95% or better then the final derived current limiting value set by variac. For a single cell like this, typically a 10 volt AC variac goes to process to enable a 1 ma short conduction, and when the actual conduction is initially read it shows .97-.98 ma conductions. A system set like this can run 12 hours for a good final conductivity 3.5 - 4 times more conductive then starting measurements.
This same system was expanded to incorporate 5 cells in parallel, using larger silver bar type conductors: produced a unique observation, the loss of high voltage effects from the system comes into play because the "short" as a diode made load "impedance", (current limited by the variance of 40,000 ohms outer impedance in series): this condition of having 5 times more current asked for from the resonant system dictates that the laws of internal resistance of the supply, vs the resistance of the load now start coming into play. Since formerly a 10 volt input enabled a 1 ma short conduction, we now find the non linear relationship where now it takes 100 volts to enable about 4.9 ma short. The second batch run this way for 14 hours showed a five fold conductivity from start! Excellant results! But to make a long story short, since I had two processes doing two diffferent things,I finally got into the habit of routinely making the CS over a north magnetic pole. When I did this for a single cell, I used the 3 layer magnet winding wafers already present. But for the 5 cell in parallel version, this called for making a 3 magnet holder, for the 5 glasses in a row. These I made on a common platform , and after a day or so I noticed I could touch the front magnets with the CS glasses removed during the high voltage process, and I observed I could feel vibration from the magnets by hand touch.. Next I put coils over these vibrating magnets, and found high freq. signals corresponding to expectations. In the the rife neon treatment I use large copper bars for an arc gap, and these create very high BPS, (Bursts per second) arcings. The coils over those magnets showed that, along with a finger of the subject that can better show the same signal 4 times over if he had been the influence for the coil. So the vibration of the polar capacity of the biological exceeds the magnets 4/1. In these High BPS conditions, 20 rf bursts per 60 hz cycle are common. Having seen this remarkable phenomenon whereby the AC excitation of a 3 magnet wafer could excite surrouding magnets, I tried a different version without the presence of a biological in series with neon/arc gap, and the remedy here was to make the arc go to water. Here I found tremendous differences found with previous experiments using a needle to make the arcing. In that case the arcing is very rapid. But here, because of the mass and size of used silver electrodes, what commonly happens is that the water will form a sort of cone, and then withdraw itself, where the arcing to water then resumes itself. Then the water will come again making a short: where in this case the reaction of the arc hitting the water/ MOVES THE WATER/ so suffiently that if creates a wave that bounces back between air gap/ and direct water contact/ although the bottom of the glass is still present making this not a "true short". Thus with large electrodes of size, not having a sharp point as would a needle: the attraction of the water becomes a problem. This water by nitrous oxides made by surface water arcing, naturally took on a different coloring than the 1 ma low voltage C.L process. So to conclude if nickel coins were made in high voltage arcing to surface/opposite wave of conduction, we should also expect the nickel to deposit something..., making a version of industrial magnetic water, not for drinking purposes obviously... ===== Tesla Research Group; Pioneering the Applications of Interphasal Resonances http://groups.yahoo.com/group/teslafy/ __________________________________ Do you Yahoo!? The New Yahoo! Search - Faster. Easier. Bingo. http://search.yahoo.com -- The silver-list is a moderated forum for discussion of colloidal silver. Instructions for unsubscribing may be found at: http://silverlist.org To post, address your message to: silver-list@eskimo.com Silver-list archive: http://escribe.com/health/thesilverlist/index.html List maintainer: Mike Devour <mdev...@eskimo.com>