> Hi Mike,

  > Thank you for your mail.

  > Would the  ULV  method you are trialing  be  feasible  with larger
  > batches, just taking a longer time?

  I'm pretty  sure  the key is to keep the  current  density  low, and
  provide a means to stabilize the current. It also seems to work best
  with equal area for the anode and cathode.

  You could  increase the silver wetted area by adding more  rods. The
  brew time would be inversely proportional to the wetted area.

  > I brew  with  1 liter, of room temp water, and 2  x  12g  rods, 7"
  > looped. I  run  it  at 23v until it  reaches  1mA,  then  drop the
  > voltage to 18v until it again reaches 1mA, drop again to 15v until
  > 1mA, until eventually 7v. Run for a total of 5hrs.

  5 hrs  at 1 mA is 5 * 3600 * 1e-3 = 18 Coulombs. Running at  0.25 mA
  would take 20 hrs.

  If you  are using 1 liter per day, you could simply run for  24 hrs,
  pour the  cs  into another container, and  start  another  batch. It
  would be slightly stronger.

  > I then  have a PWT reading in the vicinity of 18ppm.  The  brew is
  > very clear,  no  build  up, no mess, but  I  do  use  a mechanical
  > stirrer. I  am  curious  as   to   your  findings  of  the stirrer
  > inhibiting the brew. Could you please (in very simple  terms) help
  > me to  understand.  Only when and if you find you  have  the time.
  > Thank you for taking the time to read this.

  I'm not sure of the reason for the reduced biological  activity with
  stirring.

  Perhaps the  high  ion density still causes particles  to  form, but
  they are too small to cause any visible effects.

  This would reduce the number of silver ions available to kill bugs.

  > Best wishes, Margaret.

Best Regards,

Mike Monett


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