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Overunity Machines Forum



Ibpointless2 Crystal Cells

Started by ibpointless2, November 02, 2011, 02:54:15 PM

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0 Members and 7 Guests are viewing this topic.

Peanutbutter29

All nighter, yay!  So pardon me if something seems odd with me' writing.

Done a couple dozen tests on various electrolytes and electrodes (standard electrolytes and; Al, Mg, Cu, Pb, Ag and Carbon for electrodes)  That's all the metals I have sitting there, though they are all pure.  I could try Iron or Tin, but I doubt there would be anything new, plus Iron and chloride and sulfate will prolly bind.

the 2 Glue cells will probably take a couple days to dry 1/4" thick (used plates not wire), but it's doing fine.

I was able to isolate a couple more compounds from precipitates in my first round of tests (with the liquid mushy) Copper Chloride(+4) and the "other color substance" from the borax is "most likely" Magnesium Diboride.  Kinda got a laugh when I found that out, both for what it does and how accidentally I made it. heh.  Totally not pure o' course.

I've made a new 4 equal part superheated version again that's cooling.  I was able to reach and maintain a higher temp, so more Diboride.  I fully expect 0v without moisture though.

Also I've got a PhiCell (sort of) drying as well.  Using plaster of paris (ends up gypsum);  as well I only used Alum and Substitute, so trying kinda re-create that cell.

**Question for PHI<<  I've noticed, with this mix (since its' liquid when mixed) that the Cathode always bubbles.....how are you getting around this while your cells are drying?  or are you adding the Electrodes after it solidifies?   
I can't think of any other way to eliminate electrolysis while setting

Lastly I made a Gelcoat cell (drying) to see what's up there, though it's interesting already.  I used the "mix" I adopted from the tests (mentioned first) and coated it all (mixed) with just enough resin to cover all the particles.  It was placed in the form and is setting and its' gonna take a while too (darn hygroscopic salts)  At any rate, two odd notables.  Every grain is separate and visible (not joined or melted), since they are all coated.  Also having both electrodes in....I get no bubbling!  Could be good or bad though, lol;  it does however prove that gelcoat does in fact prevent hydrolysis very well.  I'm interested to see if there's Volts or current (salts were left hydrated).

So I guess I'm in wait mode now, with 5 cells prepping.  Maybe sleep heh...we'll see.

Oh Btw, I'm adopting Mg and Carbon for electrodes as a result of testing ;) Don't think that combo has been used yet.

Thanks

Edit took a couple pics at least.  One overview and a couple of close-ups.

First an overview
http://i615.photobucket.com/albums/tt239/billmckraken/Crystal%20Cell%20Stuff/SDC10632.jpg

From description: On left the metals. Bottom Glue Cells. Larger circle top mid is superheated and some diboride to the lower left of it. To the right of the larger superheated, we have the gel Cell, gypsum cell to the right and Mg and C pieces on far right

Next is a 100x magnification close up of the gel cell.  Turned out well and you can see the resin glaze and tight salt spacing
http://i615.photobucket.com/albums/tt239/billmckraken/Crystal%20Cell%20Stuff/PIC019.jpg

Last is a 100x magnification close up of the Gypsum cell.  Not the best but you can see the structure and distant spacing of salts
http://i615.photobucket.com/albums/tt239/billmckraken/Crystal%20Cell%20Stuff/PIC020.jpg


EDIT 2:

Decided to test the superheated cell (#2) to see.  Dry, anhydrous, no moisture like the first. Voltage test 2mv (I'm impressed! that means something....however tiny, lol).  Added 4 drops (n,s,e,w) away from Mg and re-tested....25mv.  Hmm a bit different than the first (it jumped right up) but this one did heat most of the borax, so is SHOULD be anhydrous and insoluble mostly.  Added 4 more drops (at 45's to the first) and re-tested....25mv, odd.  So I added 1ml and checked 1.46V...testing current through meter 4ma.  So this, being more insoluble, has less volts and a LOT less current (first was 1.6v and 900ma wet).  I can hear a faint crackling, so its' not totally insoluble, but much less so than the first attempt. 
Note: I can smell tiny bit of hydrogen sulfide, most likely from Boron Sulfide reacting to water.  So that's another end compound (if you use borax)
I'll let this sit a while and check later

triffid

My buttermilk/vitamin C cells are too wet today to do anything but look at them.The black copper oxide is being reduced back to red copper metal.triffid

triffid

I have a couple of ideas too.

It seems to me that we are making cells with casimir plates too close to each other.If we could make them with plates 100 times farther apart
Then we could get 100x the power that we do.There is plenty of power to be had without destroying the dipole.Afterall the energy compares to nuclear fusion.Or so I have heard from a lecture series I posted earlier in this thread.


to do this we may have to add something else to the epsom salts.


or charge the cells as they are drying (at different freqs maybe).


I am think of adding more silica to the epsom salts.

triffid

My other idea is to make a 100 volt or more cell.This might be done by making the pos electrode the size of a 55 gallon drum and the neg electrode the size of a double AA battery.from this you would maybe get lots of voltage.You make the cell big enough you could live in it.Always have power.Make a spaceship based on it and have power to go anywhere in the universe.triffid

triffid

Some body powders contain silica.
triffid