In a message dated 9/30/2001 5:48:22 AM Eastern Daylight Time, [email protected] writes:
> Subj:Re: CS>Ions vs Particles > Date:9/30/2001 5:48:22 AM Eastern Daylight Time > From: [email protected] (Ode Coyote) > Reply-to: <A HREF="mailto:[email protected]";>[email protected]</A> > To: [email protected] > > > > > Thanks Frank > I think I get a clearer mental picture of what's happening now...in pure > water with a low energy electrolytic process. > And dissolved oxygen/ozone, some nitrates, CO2 and such are always present > to some small degree to account for being able to go over the limit a bit. > Ken > Ken: You said, "And dissolved oxygen/ozone, some nitrates, CO2 and such are always present to some small degree to account for being able to go over the limit a bit." My calculations clearly indicate that this conclusion is false. Professor Maass arrived at an incorrect conclusion because he initiated his calculations at an incorrect starting point. The CORRECT starting point is to ASSUME that a typical LVDC product is in equilibrium with air, and the pH of the CS product is representative of this TOTAL equilibrium (This is how I INITIATED my earlier calculations). THEN you set up your RELEVANT equations and solve them. I would love to conduct a tutorial about how to determine the solubility of ionic silver in a typical LVDC product. At the moment I feel totally frustrated that not one person on this list knows what the hell I'm talking about. Any thoughts about how I should proceed would be greatly appreciated. Roger
