If you run an EIS geneator with just a touch of Hydrogen Peroxide in the
water, it will make a high particle count...most likely pure silver
particles [They aren't brown] by the reasoning following.
Too much H2O2 and conductivity never goes up and large mirror like silver
flakes form and settle out, later oxidized by the Peroxide into black balls
on the bottom of the container.
I recently ran a batch [using SWAP polarity switching] started with
leftovers of several other batches, one had been cleared up with H2O2 and I
forgot it had.
SO, a small amount of peroxide was there and the batch came out with a very
heavy milky white TE and virtually nothing settling out. [Why did it do
that, I asked me ?] OH !! That's when I remembered that peroxide treated
batch remnant tossed in there. [6 drops of 3% per quart with about 1/4 cup
of that in a half gallon of distilled]
Apparently, how much H2O2 used is key to controlling the particle size and
ratio to ionic content.
Reading several patents, the use of H2O2 is mentioned. [but not where, how
or how much, when ..which all make a difference in the results]
Particularly the patent for Tetrasilver Tetroxide [pure silver particles
with an oxide coating] and several copy cats who cannot use that term
without encountering patent infringement problems. [Like ABL American
Biotech Labs ]
The idea promoted is that the oxides ON the sliver aid in ion exchanges in
vivo.
If you add H2O2 to very fresh EIS, it will flash brown, an appearance like
Tetra Silver.
[ **IS** that Tetra Silver? I dunno. ]
Go right ahead and try this at home.
Now, if you have an ultra centrifuge to herd those brown particulates to
the outer regions where they can be scooped out to concentrate them ????
Reduced ionic content, increased particulate content.
An AA Spec only tells total silver content regardless of form.
..and no, it's not light being absorbed that makes the 'silver suspension'
look brown...it's the brown color of the oxide coating ON the silver,
absorbing light.
Pure Silver reflects light in virtually all the visible spectrum...that's
why it's used to make mirrors.
Finely divided silver dust appears white in white light...dry or in suspension.
Electro sputtering is done in a vacuum...hard to keep a liquid, liquid in a
vacuum...and the vacuum, a vacuum.
But, now you CAN buy [electro sputtered ? ] nano-silver dust [mostly made
in India for industrial applications ] from the same lab supply houses that
sell Mild Silver Protein [MSP] powder and Silver Nitrate.
http://www.mknano.com/
is a source
[Oddly, STRONG Silver protein powder has less silver content than the Mild ]
If I recall, the average particle size of nano-silver dust is around 5 to
40 nanometers. [.05 to .04 microns]
Ode
At 03:22 PM 11/29/2012 -0600, you wrote:
Hello all,
Thanks for the answers, it seems that most of the answers where addressing
why I should prefer IONs instead of PARTICLES.. to respond to those who
suggested that can somebody please explain me why Frank Key (owner of
MesoSilver and CS LAB) prefer particle based colloidal silver due to its
ability to be absorped by the blood stream AND at the same time avoid
being converted to silver chloride in the stomach as ION based does?
(Source: http://www.purestcolloids.com/notcs.php )
I appreciate the suggestion of adding a kind of acid to convert ionic to
particlem, but isnt there a way to generate it without adding this acid? I
dont think Mesosilver or Silvercillin who produce pure particle liquid add
such acids.. How do they do it?
Thanks guys.
Alex
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