August's Process
by August
My gold is still boiling yellow, heres a pic, its been going for a couple of
weeks or more.....how crappin long does this take?
While bringing the gold to the green stage, a second
4000 ml flask was
processing iridium. the gold started its green color on 2/11 and the next
day the iridium went green. It was deep red chloride for a month.
The gold should turn just as dark green. Perhaps tonight when I salt it out.
Fresh gold chloride monatomic.
If it never gets to green it never gets to monatoms
Occlusion Sequence
The stuff was almost clear to start.
I was curious about the size of vapor and realized that water vapor was just excited H2O
molecules and then realized that monatoms of gold, either expelled by the EMF created by the electric
burner like some suggest, or simply small enough to float off with the water molecules might be coming off
the gold salting reductions as they boil away.
I wrote you all about this a week or so ago when I also followed up with an early evaluation stating that
there appeared to be no ppt in the titrated 6M HCl collected as vapor and condensed into liquid.
But I was curious. I thought maybe it was too fine to see and let the jar sit for a week. I
fine off white flocculant fell to the bottom of the jar. It can only be monatomic gold
Well, I think the following method is an excellent side extraction going on during salt reductions of
disolved transition metals.
1 do a fusion on gold using sodium peroxide and sodium hydroxide
2 melt the cake into 6M HCl and add more HCl and HClO4 and boil 6hrs
3 at the end of 6 hrs adjust pH to pH12 and boil 6 hrs
4 cool, filter, adjust filtrate to pH3
5 reduce filtrate to half the starting volume
6 on a spin table mix in 6M HCl (salting occurs immediately)
7 reduce to salt repeatedly in a 4L flask with a side nipple. Put a stopper in the top, attached a
automotive high temperature neoprene gasoline hose to
the flask neck side nipple and connect the other end to a condenser tube to cool the evaporating HCl
vapor.
8 collect the vapor and adjust pH to pH7
9 Let sit until the PPT falls to the bottom of the settling vessel
you won't get much each gallon, maybe 10 or 20 ml, but it is monatomic hydroxide.
wash it like regular precip
Yes, you can convert Gold to a white elemental non
reactive powder
If patience is a virtue, I must be loaded with virtue
And, I suppose I became an alchemist on 5-29-2002
Heres a picture of pure monatomic gold (Au+3) from a session on the scanning electron microscope at Caltech.
What you are seeing are bound state spheres of monatomic gold reagions electrostatically bound into the beautiful
material that it is.....
I have made a small amount of transparent gold, problem is, it's rather porous. It was made in a helium
atmosphere here on earth. I'm trying to work some of my old NASA contacts to see if I could get a ride up and
have in fact arranged for a canadian sonic furnace that is space rated from my CSA contacts in Ottowa if I can get
a spot. Know anyone with contacts in Russia and the 10M fee to ride to the station? Ha! yeah right.
I'm figuring that if I can try some various samples under other heavier enert gases like krypton or xenon it might
be more ordered.
But, yeah, the idea I came up with back in 1998 worked and I'm in testing to determine its qualities. Damn
but this stuff takes time with short development funds. The material is in testing to show if there is photon
capacitance. The original patent design is for a material to capture quanta at the resonant frequency of the
material. The material shields all frequencies but is transparent to the resonant frequency or those near it
in a small window of frequencies into the quantum matrix. Then the idea is to extract the frequencies by
tesla transmission.
Date: Mon, 05 Aug 2002 00:44:41 -0400
I thought everyone might like to see monatomic rhodium, iridium and gold refined powder.
The powder is kept in an argon atmosphere in sealed bottles.
I seem to be rather happy, perhaps its the month we are in.
Ha
august
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