Crystal Cell Research

[plengo]

Today I had opportunity to see a pattern on my cells. Previously (In some of my videos #35 or so) I demonstrated the capability of the cell to have its own energy re-generated at any time at any rate, it is limited in that particular experiment but it is there and I can not kill it. Only by destruction of the whole physical cell.


They do present to have an ability to extract energy from some place and use that for their own benefit, crystal grow and in doing that they provide extra power for us to extract.


I was extracting very little for the, our desires, but nonetheless they do present free energy so to speak. IN  large scale I can easily see fruitful applications for it, but first we must learn and than learn in how to do it.


So little power that I almost desired a new direction or other more intense project but than I realized the same test under a totally different combination of metals. I was working with Lead/Alum before, now I decide to test against Alum/Magnesium, not in the sense of my carbon/sand/alum/Mg cells. They are working very well btw, I have many all over the house illuminating my favorite spots, all I do is remember them and give water, like plants.


Tell your wife, honey I have a plant too - it's a crystal cell in front of the pictures of the kids that every night I see and remember why I am working on this field AFTER my professional day pay with no pay for this extra work of mine.


With the Magnesium/Alum/MnO2/Epson Salts cell, under starving condition, meaning, little water, very little, they are ALSO presenting that same effect of the Lead/Alum never extinguishing  In the exact same manner, same response to switching from "UnderLoad to Resting", and repeat this to infinity.


They are presenting the same free energy effect, still in small scale, but much higher density, now in 8 ma at 0.05 v under short load (resistor less than 2 ohm - the wire).


Small quantity of water, means much less corrosion, whatever left that still corrodes. The cell returns a substantial usable amount of power to light LEDs now, not much, but much better than before and I say, much, much better.


If I apply this technique to my existing 8 months and 1+ year old cells, they will provide much more power.


The pattern is the same: Voltage goes UP as the cell rests, longer time doing that, higher voltage she reaches.  Many short "times" of rest, but more frequently ALSO work, and works with an accelerated effect. Current diminishes as voltage goes higher. Current diminishes in a much SLOWER rate than normally used without interruption, so much slower that I would say they are giving even more current over time that she could possibly give. Overall integration of power output IS big if given enough time and considering no input energy used.


With Magnesium cell and the same process, I am having a few orders of magnitude of improvement over my previous experiment. Off course Mg is much more sensitive to corrosion, but also improves the performance of the cell, controlling the water content of that precious surface is a must, a secret that I am uncovering in how to do it.


It is not about stopping 100% the contact with H20 and Mg, it is about extracting as much as possible of the "free energy" part that those cells give.


If I can find a combination of metals that would give me 12 volts difference when combined, what do you think I would do next? Now, imagine this cell under a controlled circuit that DOES give a very high input of voltage source to this cell, without allow any current to pass? The cell will give an enormous amount of current from non-where, since there is no current, no galvanic reaction of ANY kind (for a case where the whole electrolyte and metals used do not corrode each other without an agent - like Sulfuric acid and Lead for example), but now, I am passing over myself.


The cell is giving me 8 ma at .05v without loosing the amount of corrosion caused by one drop of water. The metal is very dry or very little humid, very little corrosion if any. And turning it on and off many times, the voltage of the cell INCREASES until current stops of existing which I could not find yet, that end.


Adding water AGAIN repeats the whole process again until 10 days have passed. One more drop of water and there she goes, another 10 days or more giving me that energy with the cost of 2 drops of water now. And so on.


Why the voltage increases like that? That is a strong electric field that must be moving something or causing something to move, I think, current would be one, and than, she stores that current somewhere, Where? in the crystals themselves. That's why they grow, energy storage, so silly me.


They are breathing capacitors and the longs muscles (Pulmonary) are the environment.


They don't like to be in series and neither in parallel BUT they perform very well when in parallel with parallel Loads. They do add voltage linearly but their internal resistance are limiting to the allowed current over all of the cells, which limits their series topology to high power usage and becomes very useful at small devices.


Distribution of moist over the protected surface of Mg will be very important in future improvements. Ah I almost forgot, Mg gives a good power ratio output, Lead does but if you put energy in first, which other metals will have a better output ratio of energy? If you know, let me know please.


Crystals grow over the surface of Mg seams to be key in this relation of voltage and stored energy. Crystals grow dry, but I think the water is inside them when they "dry" and become hard like a rock. Why water ionize things? Is not that the culture?


but I can measure current in a rock of iron pyrite. I think water helps but it is not the necessary ingredient of providing a mean of energy flow. Where is the energy is coming from when they are starved of energy?


I am starting to see the crystal cells like capacitors with little wheels inside them spinning and creating energy that is stored in the capacitor itself. They are very small capacitors. Different crystals, different densities and relationship, more in parallel, less in series and different combinations of those in layers.


They have a difference of potential provided by the two electrodes, in my case now - Mg and Copper/Nickel, and so energy is attracted to them and they store it. When we close the loop, we extract it from the cells, and the cycle repeats to as long as we have the metals, electrolytes and water.


Fausto.

[plengo]

Today I had excellent progress with the dry cells. Using a different formula and iron pyrite I could make a cell increase voltage and current given as she forms from the moment of conception (been created and put together) to until hours later under load via switching technique.


It is very clear in the graph below that the cell is decreasing her output power up to middle point of the graph where she than start to present the voltage increase I mention in my videos and written. Even as she dries 100% she is already presenting the phenomena.


Time will tell if this behavior continues. Now she is giving under 100 ohm load, .380v (380 milivolts) at 3.5miliAmps. When I let her rest during the switching, her voltage is increasing, clearly shown by the end of the graph.


I think that as the cell drys under load and under relaxation (time I let her rest without any load) the crystal structure formed inside between the two electrodes grows with a certain disposition for allowing flow of electricity energy and at the same time static alignment that creates voltage, therefore, causing a following current too.

This is becoming a little weird concept to explain but I will try.  I think as the cell absorbs he water and converts it into energy available for external use, a change happens in the molecular level. One is the corrosion that we all know, other is solidification of its physical structure, another is the flow of energy caused by corrosion to flow through that physical structure that is solidifying.


When solidifying that structure presents a perfect flow habitat for energy to flow, after all, it was formed when the crystals could move to anywhere while energy passes (imagine a very resistor burning as current passes), the same with the cell but very small level.


This structure presents a voltage charge now freezing in time, literally, dipoles being formed and locked while the cell dries under load.

Relaxation helps simply because the "pressure" of the current is stopped and so the structure has time to adjust a little bit while drying and becoming even more effective for energy flow because of the released stress therefore less loss of strength. It is a little bit difficult to believe what I am saying but this simple theory is providing success in my research.


This new formula also has a much higher level of absorption of water than other and at the same type not liquefying in any shape but the opposite, becoming even harder. Very interesting.


Iron pyrite is an attempt to reduce internal resistance, extra protection of the magnesium and piezo properties and God knows what-else it does but it does.





Fausto.

[aaron5120]

Very interesting, Plengo. And good research work.
This cell may eventually power the LS JR crossover circuit, I hope.

[plengo]

This cell is performing better and better every day. As I add a tiny little bit of water, it produces 50ma at .15v easily and stay there for hours.


It is a total winner. It is not 100% dry but it is so little water that I don't even think the water really gets to the Magnesium.


Fausto.

[plengo]

I think my work is finally paying off. In this video (http://www.youtube.com/watch?v=CGatm42N6rA) I show the output power of this one cell.


You must let the cell be formed before start using it extensively. More you use it, more it gives to you back. The crystal growth is crucial and the protection of the Magnesium metal is essential.


This last formula is working better than the previous MnO2 although I still will use MnO2 in different ways. Water is the fuel, at least that is what I think.

Fausto.