I'm not a technical person, but are you saying that the peroxide breaks up the 
particles?
 
Is is then a better form of CS to take?    (I'm concerned about the possibility 
of getting argyria.)
 
Sally

Ode Coyote <[email protected]> wrote:
While making charts to compare voltage drop with constant current to
conductivity, I ran two 8 oz batches up to 30 uS..the point at which the
chart was becoming irrevevant due to the voltage line flattening out for
some unknown reason.
They both turned deep deep yellow after a day or so and i just let them
sit around open before dumping them.
They evaporated by about 50% before I got around to them with some black
oxide dust in the bottom..not much, just a trace.
Just for grins and giggles, I poured them together, metered them at 85.5
uS, hit em with the laser pen to see a very heavy medium fine TE then added
6 drops of 3% H2O2.
2 days later...crystal clear CS with a very heavy and uniformly fine
grained TE. [Has a soft fuzzy quality rather than bright points of light
quality..which would be finer than than stars in a cloudy sky quality from
electrode crud sparklies that would eventually settle out]
Tastes like rocket fuel. [but not like Peroxide mad dog face flavor]
No precipitation visable.
86.6 uS

If allowing for a meager 15% non conducting particulate, this stuff should
be at 100 PPM or better and looks very nice.

Ode


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