Just to confirm phenomenon:

Ran a batch of CS up to 28 uS..magnetically coupled mechanical stirring. 1
ma on 6" exposed surface 12 gauge electrodes.
 Clear, colorless and very faint TE

 Seperated batch into three 2oz jiggers as soon as it was done.
1] Added one drop of H2O2.  Instant explosion of murky vaguely yellow/brown
stuff gradually clearing by about 50%. Formation of oxygen? bubbles on
sides of jigger as solution cleared somewhat and got less milky looking. On
average, white but somewhat grey cast where light penetrates high particle
density less well in the center.  Extreme fine grained and very heavy dense
TE.  Conductivity drops to 11.2 uS.   Nothing settled
It's apparent that mega quantites of particles formed and oxygen? was
released forming an emulsion in the water which condensed into about 50 or
so 1/8th inch diameter bubbles clinging to the sides of the jigger.

2] Control..nothing done to it. Conductivity after 2 days, 18.8 uS. Very
slight increase in TE. Still clear and colorless. No bubbles or anything.

3] One drop H2O2 added after 2 days. No apparent reaction. Looks identical
to control in all respects after 2 days. Conductivity 18.6 uS after another
day.

Conclusion:  There's a major difference between freshly made EIS and the
same EIS that has been stored and stabilised with time.

 H2O2 reacts violently with "new"? ions? but not "old" ones, forming
extreme numbers of probably small particles.  Since there is an obvious gas
release, obviously on a molecular level, that "might" be more than what one
drop of peroxide contains, it's not likely to be an oxide formation that
results but, perhaps, a breaking down of oxides or maybe silver hydroxides.
 [Could be both hydrogen and oxygen bubbles]

At any rate, [in purely scientific terms] a freeking lot of particles get
formed quite fast and conductivity drops like a rock when peroxide is added
to fresh EIS.
 Nothing noticable happens when the same thing is done to stabilized EIS.

Personal observation with no way to validate it:
 Swigging down a jigger of very fresh EIS results in a distinct energetic
'awake'  feeling that is not apparent after swigging down stabilized EIS.
 There is a possibility that something similar to the H2O2 reaction is
taking place 'in vivo'...maybe free radical scavenging and blood
oxygenation side effect?
 [Or a case of delusions]

 Since very good results on toe fungus was during a period of
experimentation where I was always swigging from fresh batches and fungus
"slowly" grew back after that period, it could be that very fresh EIS is
much more beneficial than stored. [Or, I selected out a silver resistant
strain of fungus..or something else.]

 Ode

At 10:49 AM 12/9/2004 -0500, you wrote:
>
>Stuff wrote:
>
>> At 03:08 PM 12/7/2004 -0500, you wrote:
>> >Can anyone find anything on how to produce AgO4???  I have struck out
>> >doing searches.
>> >
>> >Marshall
>>
>> Don't you mean Ag404?
>>
>> I too would like to know.
>
>You are correct. I have been searching for AgO4 without much luck.  I
thought it was silver tetraoxide, but it is
>apparently tetrasilver tetraoxide.  But the CAS calls it silver oxide. So
I am now really confused, my CRC handbook
>calls Ag2O silver oxide and AgO silver peroxide and does not even show
Ag4O4.  Hmmm, I wonder if this is what is
>produced when you add H2O2 to EIS, if so that would explain the increased
effectiveness perhaps.
>
>If I find anything I will post another message.
>
>Marshall
>
>
>
>
>
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