BEFORE I GET A SLEW OF REPLIES ABOUT THE DANGERS HERE, PLEASE UNDERSTAND THAT I AM NOT MAKING THIS FOR HUMAN CONSUMPTION!
If we look at some of the expertise on this list, we find that the "experts" are out there. Particularly relevant here is a simple question of electrochemistry. Are there certain metals that do not easily form water colloids? in the Gold colloidal thread, people have noted that the typical DC low voltage DC method does not seem effective. Notes from a nickel colloidal trial also indicate that the low voltage DC method is also not effective, but that it does work to a limited degree. First let me indicate WHY I need colloidal nickel water. This is because I am doing experiments at higher source AC frequencies from a converted AC alternator, where water can be used as the capacitor in resonance, when a large induction coil is employed at 480 hz AC resonance. The water capacity is made axially by means of a copper pipe inserted into a poly container with a foil connection on the outside: these serve as the two polarity connections of the water capacitor. Now because of the sizings of these two resonators, in this situation it becomes possible to insert the water capacitor inside the core of the magnetic field of the coil. Thus we should have created a self reacting resonance, because we have created a situation of crossing moving electric and magnetic fields in space, and on the third remaining angle, a lorentz force will exist to also do work to move charges. It is supposed that in this scenario that a set of plates inserted into the water at that correct third angle of field interaction,: when an electrolysis reaction is tried between those plates, the efficiency of operation might be enhanced by the issue that the process is taking place in the spatial vicinty of these moving electric and magnetic fields obtained by resonance. The very real concern becomes the fact that the energy input to make these magnetic and electric fields exist practically for free, where the fields in a resonance represent borrowed and returned energy from the generator, where the swing of these energy manifestations takes place kinetically as a magnetic field, and potentially as an electric field. The nickel colloidal water idea is to use an agent that might amplify that magnetic field, beyond what the air core inductor can supply. In the final emobiment of these scheme, TWO 90 degree phases of resonance made from two phases of the alternator are used so that the fields of these resonances can be juxtaposed in each others space, thereby procurring a predicted DC pulsing by Lorentz force across said interaction electrolysis plates. Now the sizing requirements for making all these possibilities are very problematic. If we could make the water appear slightly magnetic, smaller inductors could be used. Hence making a colloid from magnetic Canadian nickel quarters to use for that water in reaction sounds like something that should be tried. But the essential issue on the whole idea being manifested into reality: is that of using the borrowed and returned energies in resonance to procure ACTUAL work from that field oscillation by being orthogonally spatially reacted in volumes of space, and thus this should enhance the efficiency of a water electrolysis process made in the correct angle of those field interactions. In the first trial, a 1.25 ma current limited by rectified current limited transformer was used. Two Canadian nickels were used for each polarity. In the normal situation of making silver colloids with this regimen, a ~ tripling of conductivity is made in 4 hours. For the nickel trial this did not occur at that rate at all. After some 10 hours, the conductivity had increased only 50%. Start for a 19 volt battery test showed it enabling 1.87 ma. Finish of tests showed the same battery source making 18.7 volts enabling 2.85 ma, only a 50% increase of conductivity. The water has a small whitish tint, so some kind of interaction seems to have been made. No kind of coin residue appears, except for a very light dark tint on the negative coins. Perhaps because I am dealing with nickel, much higher voltages are needed for colloid formation? I will try the next trial at higher DC voltages. In this trial the initial voltage procurred from the current limited system was 12 volts, where near ending just over 6 volts was present. For the equivalent silver colloid testing a 10 volt drop in starting and finishing voltages is common. I would suppose that some kind of high voltage AC method might proove more useful for making nickel colloids, since this apparently is used for gold, possibly another metal which might not make colloids as easily? Sincerely HDN ===== Tesla Research Group; Pioneering the Applications of Interphasal Resonances http://groups.yahoo.com/group/teslafy/ __________________________________ Do you Yahoo!? Yahoo! SiteBuilder - Free, easy-to-use web site design software http://sitebuilder.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: [email protected] Silver-list archive: http://escribe.com/health/thesilverlist/index.html List maintainer: Mike Devour <[email protected]>
