Hi Tom,

It would be a real boon to have some sort of standard quantitative 
analysis of silver content which could be done in a home lab/kitchen. a 
titration method maybe? which would involve simple reagents and 
glassware.  I think another way would be a colorimetric method or 
turbidity meter kind of thing which would involve test slides or a 
photometer of some sort. 

Do you , or anyone have any thoughts on this?

In the sticks,
Tony

On 22 Feb 2010 at 20:11, poast wrote about : Subject : Re: CS>Which layer 
of skin for silv  

> Hello Marshall,
> 
> I only did the reduction to 60 uS once just to see what happened.  While
> the solution was basically clear, you didn't need a laser to observe the
> Tyndall effect.  A pen light worked fine.  As I recall, I had a few larger
> sparkle particles in the solution.
> 
> I didn't keep it very long because I was using it in some soap. 
> Overnight, there was no residue settling on the bottom of the jar, but
> that was as long as it sat.
> 
> I regularly reduce a 10 uS solution to a 20 uS solution.  This also shows
> a strong Tyndall effect, is clear, and everything remains in suspension.
> 
> The main problem I have is not having the equipment to translate uS to
> PPM.
> 
> Tom
> 
> 
> ----- Original Message ----- 
> From: "Marshall Dudley" <[email protected]>
> To: <[email protected]>
> Sent: Monday, February 22, 2010 8:01 AM
> Subject: Re: CS>Which layer of skin for silver deposit?
> 
> 
> > Thus part I don't understand.  The ionic portion of EIS is silver oxide
> > and silver hydroxide, each with a solubility of only 13 ppm, so combined
> > they have a solubility of 26 ppm. (Actually since they continually
> > convert from one to the other, and theoretically the hydroxide should be
> > much more soluble than the oxide, I believer that what really happens is
> > that with it continually converting from one to the other and back again
> > when dissolved, the the less soluble one really sets the limit for
> > both). So just what IS the compound that is forming the 60 uS part. Is
> > it from carbon dioxide that is absorbed into the air forming silver
> > chloride?  Or if an analysis I made earlier where the silver particles
> > get cemented together by silver oxide particles produces an ionic form
> > which increases conduction?  I find it curious that the conductivity
> > increases.
> >
> > Marshall
> >
> >
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