Hi KD'C,

What strength H2O2 are you using, I would guess 3% as you put some in
your mouth without burning it!

I have posted experiments (along with others) in the past, using 50%
H2O2. If you care to check the archives, you may find the answers to
most of your questions there.

H2O2 does react with pure metallic silver, in fact passing high
concentration H2O2 through a silver mesh is a method used in DIY
rocket engines!

A small length (10mm) of new silver wire was left in 100mls of 50%
H2O2 for  a few days. A small stream of bubbles emanated from the
silver and the concentration of silver ions in the solution increased
from zero to well above 20ppm, as measured by Ion Selective Electrode
(ISE). There was no silver oxide.

A nasty brew of dirty grey (inclusion of large uncharged metallic
colloids, emanating from the cathode) CS was created, there was much
fallout on the bottom of the container. Some of this colloid was
taken, to which a few ml of 50% H2O2 was added. A great cloud of
minute bubbles formed immediately, which were so small that the
solution looked milky, and the Tyndal beam showed a shower of
sparklies.
Within a few hours the solution was completely clear, showing very
little Tyndal effect. The concentration of silver ions increased as
the solution cleared.
I concluded that the H2O2 oxidised the metallic silver particles as it
reduced to O2 gas and water, forming free silver ions and not silver
oxide.

You talk of the 'oxide load', what do you mean? Is this the build up
on the neg. cathode or pos. anode, fall out on the bottom of the
container or floaters on the solution surface, or colour in the
solution?

Regards
Ivan.

----- Original Message -----
From: "coyote" <coy...@alltel.net>
To: <silver-list@eskimo.com>
Sent: Sunday, 9 April 2000 00:46
Subject: Re: CS>hydrogen peroxide and CS production experiment [a
quicky]


> ###  Interestingly, it seems that the hydrogen peroxide does not
react
> with clean silver but only attacks the oxides wedged in the pits of
an old
> used electrode. Why? I have no clue.  I will now take a piece of new
silver
> and place it in h2o2 for several days and see what happens.
>
>  Another oddity: [current controlled to .8ma, starting voltage at
24.5v
> winding down to 6v in approx 2 hrs] The oxides seem to form more
vigerously
> at the beginning of the process and in cool water.  If the prods and
> container are cleaned about half way through, the oxide load seems
greatly
> reduced.
>  If fresh ozonated water is used with cool water, oxide load is
great.
> If the water is warmed to about 100 deg F, bubbles form [dissolved
ozygen?]
> and dissipate [bubbles off] and the subsequent process shows a
greatly
> reduced oxide load. But, running with warm water increases hydrogen
bubbles
> sticking to the other prod [Perhaps something to do with increased
vapor
> pressure forming bigger more stable bubbles and surface tension of
the
> water.] and silver gets trapped on or under the surface of the
hydrogen
> bubbles making a gray fur that clings to one prod.  When the prods
are
> removed, the bubbles break at the surface and some of this silver
transfers
> from the surface tension of the hydrogen bubbles to the surface
tension of
> the water and makes what I call a " gray floater".
>
>   Back to h2o2 and new silver... so far, no reaction whatsoever.
>
>   BTW, running the generator on straight h202 made a sour nasty
tasting
> somewhat milky liquid that foamed in the mouth.
>     Momentarily, a rabid looking coyote with a sour expression.   I
guess
> even with all that violent bubbling at the electrodes going on, the
o2
> content of the h202 was pretty much unchanged.
>
>
>  Getting small bubbles coming off the new silver now [20  minutes or
so]and
> some signs of gray/black tarnish and initial signs of slight
pitting.
>  Looks like h2o2 reacts somewhat violently with silver resulting in
oxides
> being blasted out of the pits? The rougher [more pitted]the silver,
the
> more surface area available, the more violent the reaction?
>  KD'C
>


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