Quite an interesting theory, Marshall. If it works, the generation time
is quite fast even using 9 volt batteries.
 - Steve N

-----Original Message-----
From: Marshall Dudley [mailto:[email protected]] 
Sent: Monday, December 07, 2009 1:36 PM
To: [email protected]
Subject: Re: CS>silver citrate -- Concentrated silver?

Norton, Steve wrote:
> Dick and Scott,
>
> I hope you don't mind me combining both of your questions into one
response since there is an overlap in subject matter.
>
> It is generally accepted that you cannot make a stable EIS solution
above 30 ppm. However, there is a method claimed to be able to make EIS
as high as 500 ppm. It will of course be a dark color but it is also
claimed that when sufficiently diluted, it will return to a light yellow
color.( I would assume that at that point you could add a little H2O2 to
produce a clear solution.) 
> See:
>
> http://www.silverceramicsystems.com/CS16-5-3.html
> Recent Success at Concentrated CS Production  
> Points Up Requirement of Very Pure, Distilled Water
>
>   

That fellow used to be a member of this list.  We all assisted him ( 
made suggestions ) on his silver impregnated filtering clay.  Anyway, 
the page is very interesting.  First from reading it it appears that one

could use high quality distilled water for both the double boiler and 
colloid water.  Realizing that this is for areas where labor is cheap, 
and equipment expensive, there are a number of ways one could reduce the

energy requirements, water requirements and labor requirements.

1. Use a timer to switch polarity as I presently do with my flow through

system
2. Use a thermistor and temperature controller to maintain the desired 
temperature of the colloid without using a double boiler arrangement (a 
thermometer and a temperature controlled heating base could do it.)

That said, I think I do understand what is happening.  Our limit of 20 
ppm, which includes the ionic silver primarily, is set by the solubility

of the ionic silver at room temperature.  Since that arrangement is 
heating the solution then two things happen.  First the solubility of 
the silver oxide goes up significantly, from about 13 ppm to over 50 
ppm.   In addition the Browning movement will increase tremendously.  
Now if you increase the ion concentration, the probability of a 
collision between oxide or hydroxide silver ions increases by the 
square, so that alone should cause the colloidal portion to go up by a 
factor of about 20 to 25, setting the limit to about 400 to 500 ppm. The

increase in Browning movement adds to this ability, especially of an ion

and colloidal particle banging into each other.  Not limiting the 
current also adds to the particle size thereby allowing a higher silver 
concentration.

Now the colloid turns red. That indicates that the particle size of the 
colloid is much higher than optimum.  Thus far it all makes pretty good 
sense.  However they say that if you dilute it down to 20 ppm or so, it 
returns back to a light yellow, indicating small near optimum particle 
size.  That does not make sense to me.

I only  have one theory as to how that is even possible.  This is just a

theory, and it could well be very very wrong.  At the increased 
concentration and temperature, we end up with silver oxide and/or silver

hydroxide ions colliding with silver particles, and they "stick" 
together. Once this happens, another silver particle can collide with 
the ion stuck to the first silver particle, making two particle stuck 
together with an oxygen or hydroxyl ion. This produces what appears to 
be a larger silver particle, although it is really made up of smaller 
particles stuck together by an oxygen or hydroxyl ions.  Think of a 
popcorn ball, where the popcorn is the silver particles, and the sugar 
is the oxygen or hydroxide ions.  Now, this is a stable arrangement, 
since the solution is at the solubility limit of silver 
oxide/hydroxide.  However if you dilute it, the silver oxide/hydroxide 
"glue" dissolves back into the water, unglueing the silver particles, 
which are now small.  Thus it will reconstitute back to good, but not 
necessarily excellent EIS equivalent.

I have GOT to try this.  This could be one of the most exciting 
discoveries in this field in years.

Marshall


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