Fundamental question.
Where is the *sulphur* coming from that makes the silver "tarnish" to start with ?

AgOH [Silver Hydroxide] isn't black..it's whitish to tan. [look it up]
AgO is formed when oxygen encounters a silver ion...and it is yellowish, to brown, to black depending on how dense the concentration of the pigment.
Oxygen gas is produced by electrolysis, as is Hydrogen gas.
We do see Hydrogen bubbles.
Why do we never see Oxygen bubbles? The Oxygen probably makes Silver Oxides out of some of the silver ions before they even form, ya think?

There are several configurations of silver oxides, either destroyed or made by exposure to H2O2.
One of them is a byproduct of electrolysis.
H2O2 will clean up a black electrode in just a few minutes, then turn it black again in several more, indicating 2 different forms of silver oxides

Equations don't change the eyeballs, but I suppose they can lead to tunnel vision.

Add in elements that aren't there [Sulphur?] or leave out a few that are...and equations can be made to prove any thing you want them to.

Ode


At 09:42 PM 9/14/2011 -0400, you wrote:

  Ode Coyote <odecoy...@windstream.net> wrote:

  > You can do the same thing by wrapping the electrodes in  foil with
  > a little salt water or vinegar...any conductive liquid.

  > What that  does is make a battery effect that strips  a  layer off
  > the silver by ionization and deposits it on the aluminum.

  > That's how  the  silver bandaids work...the  silver  ions released
  > sterilize the wound.

  > You don't need aluminum to reverse current clean electrodes.

  > I don't  know why sulphur would be a problem unless you  live down
  > wind of  a coal power plant or something and leave  your distilled
  > water, or electrodes open to the air for a long time.

  > The black  stuff  that forms on electrodes  is  silver  oxide, not
  > sulphur oxides "tarnish".

  > There is  no  need  to  do anything but  wipe  it  off  and switch
  > electrode positions to change the polarity now and then.

  >Ode

  Ode,

  1. We do not want to immerse the electrodes in a sodium solution. It
  will be very difficult to remove the ions.

  2. The galvanic series shows the electromotive force  when different
  metals are immersed in an electrolyte. One example is

  http://www.ssina.com/corrosion/galvanic.html

  This shows  aluminum is positive with respect to silver.  This means
  we can  eliminate  the  sodium ions and use  our  own  dc  supply to
  accomplish the same thing.

  3. The classical equations show that the sulfur is deposited  on the
  aluminum. However, this produces aluminum sulfide,  which decomposes
  in water. Please see

  http://en.wikipedia.org/wiki/Aluminium_sulfide

  In distilled water, the classical equations are incorrect or  do not
  apply.

  4. Instead of aluminum, you could use copper or zinc as the anode.

  However, metals other than aluminum release ions into  the solution,
  which would travel to the silver cathodes and contaminate them.

  5. The  typical  equations  posted on the  web  are  incorrect. They
  contain many fundamental flaws, such as mass and charge inbalance in
  the coefficients, and gross errors such as stating the sulfur ion is
  positive. It is not. The sulfur ion is S(2-), not S(2+)

  6. Aluminum  is  inert in this reaction. I have  posted  the correct
  equations to my Yahoo forum at

  http://health.groups.yahoo.com/group/silvercentral/message/20?l=1

  I made one small error. It is corrected at

  http://health.groups.yahoo.com/group/silvercentral/message/21?l=1

  7. The black stuff that forms on the electrodes is silver hydroxide,
  AgOH, not silver oxide, Ag2O.

  Your statement is incorrect.

  You cannot produce silver Oxide, Ag2O, by using electrolysis.

  8. Every silver surface tarnishes. You cannot wipe it off.  The film
  is invisible  at  the  beginning, but it  will  severely  impact the
  brewing process, and cause a significant reduction in the silver ion
  concentration in the 48 hours following the brew.

  9. The   reduction   in   ion   concentration   severly  reduces the
  effectiveness of  the colloidal silver. You may examine  my  post to
  sol to verify this:

  http://www.mail-archive.com/silver-list@eskimo.com/msg76134.html

  Please note that sol also remarked that a weak solution did not work
  as well.

  You cannot   remove   the   silver   tarnish   without  damaging the
  electrodes, except by the process I have described.

  When you  do, you may find your brew is much  stronger  than before,
  and much more effective.

  However, for  the  ultimate in colloidal  silver  generation, please
  visit my forum at

  http://health.groups.yahoo.com/group/silvercentral/messages

  Here you will find the most significant advance in  colloidal silver
  generators since the original 3 nines.

  Best Regards,

  Mike Monett
  Silvercentral


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