"Ole Bob" and Ivan,

Thanks Bob for the information you have provided in this message and thanks
Ivan for the follow up message on the Tyndall.

I liked your item # 2 Bob about the IR light and size of particles. I did
produce CS with barely no Tyndall effect detected with my laser pointer and
I was wondering if the CS was good or not (even though the voltage plot was
ok - I have a current limiting set up). I was under the impression that we
must be able to detect very low Tyndall effect with a laser pointer to
ensure that we do have CS. But, I presume now that we can have good CS
without being able to detect Tyndall effect with a laser pointer as
mentionned in Ivan's message.

Pls correct me if  I am wrong.

Thanks again for all this information.

Gaston
=================================================
----- Original Message -----
From: "Robert L. Berger" <[email protected]>
To: "silver-list" <[email protected]>
Sent: Tuesday, August 08, 2000 5:10 AM
Subject: CS>Standardization


> Hi Ya'all,
>
> There are two general types of CS generators; constant voltage and
> constant current.
>
> 1.) with either method constant stirring reduces the agglomeration of
> silver ions, and should result in a weaker T.E. for a given PPM.  (first
> step)
>
> In any manufacturing operation the product made will have a distribution
> for a particular parameter. The distribution curve is generally a bell
> shaped curve. If the process is under control the center of the bell
> will be the desired parameter. The + or -
> three sigma limit is set by the equipment used. Poor equipment will have
> a very wide range and top notch equipment will have a narrow range. We
> never can realize the ideal of a single point.
>
> 2.) With the average IR laser the wavelength of the IR light is about
> 680 nanometers. If all CS particles were smaller than 680 nm then there
> would be no T.E. Since there is a distribution of particles in the CS
> then the brightness of the T.E. is a direct indication of particle
> sizes. Which could be correlated to bioavailability.
>
> 3.) The second step to standardization would be to meter the current in
> a constant voltage system or the cell voltage in a constant current
> system. In a constant voltage system the current will increase at an
> increasing rate up to a point. Then the rate of increase will stop and
> actually reverse. When the increasing rate starts to slow down (can be
> seem if data is plotted during the brew cycle) agglomeration has set in
> and the T.E. will start to get brighter.
>
> 4.) Step #3 is to plot the current or voltage with time to observe what
> is happening. As in #2 above.
>
> 5.) The initial cell current in a constant voltage system is your best
> measure of the water quality. If one will data plot then a history can
> be obtained for your process so as the water quality varies you will
> know when to shut off the system.
>
> 6.) If one measures with a Hanna type meter it will be found that the
> conductivity will change with time, so note the reading after brew and
> 24, and 48 hours later for data plotting. Then if one has an AA or
> spectrophotometer reading made for a stable product a bench mark has
> been reached to the standardization of your individual system, and then
> we can talk about relative ppm of CS with some degree of accuracy.
>
> This might seem to be a lot of work, but stop and consider the value of
> being able to talk intelligently about the results that one can get with
> ones CS.
>
> The work by Stephen Quinto shows a remarkable difference in "killing
> power" between 9 ppm (fair) and 12 ppm (very good)
> for Staph and Ecoli1 and Ecoli2.
>
> So having a reasonable knowledge of your product may mean the success or
> failure in what you are trying to accomplish.
>
> Sorry for the harangue.
>
> "Ole Bob"
>
>
>
>
>
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