Hi ya'all,

I hope that I can shed some light on the problem between Mike's work and
mine.

Mike is working in the low voltage (<v6) and at low current, so that
little or no oxygen is liberated at the anode and hence it stays clean
and the work function for silver remains at 3.09. While I am working in
the 27 to 36 volt range and the anode blackens very quickly and its work
function approaches 4.31. I very seldom clean the anode but always wipe
the cathode. In addition I always use mechanical stirring.

A review of "electrolysis" where they use cylindrical anode and
concentric cylindrical cathode with constant stirring to measure the
plate out of a metal ion from a solution, (in the book "Instrumental
Methods of Analysis" by Willard, Merrirr, and Dean, I find the statement
that "the mass transfer coefficient is dependent on the rate of
stirring, cell and electrode geometries, diffusion coefficient of the
electroactive species, and the like."

While this is not electroplating (CS process) the admonishments should
not be ignored. It would tend to indicate that for several people to get
the same results then identical setups may well be required.

In trying to nail down the conductivity question, yesterday I made a new
conductivity cell based on 1" x 1" x 1" which would give results in
uS/inch instead of uS/cm. When first immersed in the tank of CS the
conductance reading for clean silver electrodes was 86 uS/inch. After
about 2 hours the reading had slowly change as the electrodes blackened
and stabilized at 92 uS/inch. My standard 1 cm x 1 cm x 1 cm probe gave
a reading of 36 uS/cm. One would expect the reading to closely follow
the ratio of cm to inch and it does ! The ration is 92/36 = 2.55 rather
than 2.54. This can well be due to assembly or parts fabrication errors.

The only thing left for me to do is find a laboratory that has a good
conductivity to cross check my results.

I will find the answer !!!!!!

"Ole Bob"


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