Hi Mike, Thanks for your previous post on inductive and other sources of (non)-interference with CS generators, I'll respond to that when I have a little more time. Meanwhile, regarding the presencc of headache producing mold and spores in your environment, have you tried using the common copper-based garden spray solutions (Kop-r-spray, Liqui-cop are ones around here)? They contain a "copper ammonium complex" resulting in a content of 8% copper expressed as metallic, and they are just plain effective. Their toxicity is low as far as I can tell including my own personal bio-assay (yes I tasted some of the properly diluted stuff years ago when I was -err - even dumber than I am now) and could detect no bad effects or even significant taste. I don't know what it would do to the color of laundered cloth, maybe I'll give it a try on my work clothes, but it should be ok on floors and such household surfaces. Please note that I haven't delved into what a "copper ammonium complex" is, these days, it may no longer be a simple inorganic (I know, I know) compound. Just an idea in hope it will help.
Take care,  Malcolm

At 07:13 AM 10/7/03 -0400, you wrote:

url: http://escribe.com/health/thesilverlist/m63086.html
Re: CS>Measuring very high ppms
From: Ode Coyote
Date: Mon, 6 Oct 2003 05:43:48

  > If the  PWT  ignores  oxides and there are  a  lot  of  oxides [or
  > metallic silver micro particles] then the PWT reading  equating uS
  > to PPM will not be at unity.

  > Hence, the fudge factors.

  > At 3 uS, it's almost certain that the CS is 99+% ionic and the PWT
  > will be very close to unity.

  > At 27  uS,  it's unlikely that the CS is more than  90%  ionic and
  > could be less than 80% ionic.

  > In some cases the PWT can read 13 uS and the suspension can exceed
  > 60% [even 80%?] non ionic silver content as an extremely  heavy TE
  > or display a lot of crud in the bottom or both.

  > Ode

  Hi Ken,

  I'm sorry  I have not been able to respond to  your  posts recently.
  They force me to think, and the headaches from the mold  spores made
  that impossible. So I tackled the easy ones, like solar flares:)

  I have been working with colloidal copper. It is tough to  make, but
  it is the only thing that has any effect on the spores. I  have been
  applying it  to all the clothing, and the spore  levels  are finally
  starting to decline.

  I just spent four glorious hours with no headache, and I know how to
  get rid  of  them  when  they  do  return.  I  also  took Marshall's
  suggestion and applied the cc to the floors. I didn't think it would
  work, but  it worked GREAT! I can go into the  bathroom  and kitchen
  without collapsing  from  the  headaches. It also  works  on  my lab
  floor.

  Thanks, Marshall! You are the man.

  Ken, you  are right about the oxides messing things up. The  goal is
  to minimize them, which is why your silverpuppy design is so good. I
  love your U-shaped electrodes.

  That solved  the  problem of hot spots at the  cut  end  of straight
  rods, increased  the  rigidity and stability of  the  alignment, and
  doubled the  wetted  area all at once. Such a  simple  idea,  and so
  elegant. I  don't  mind telling everyone I copied it  for  my mini-W
  generator.

  These advances allow pretty good ppm, and minimize the production of
  oxides.

  We are now left with the ions, and how to measure them.

  There really should be a correlation between ppm and uS. Conductance
  measures the number of ions, and ppm measures the mass of the ions.

  Since all  silver ions have the same mass,  measuring  one parameter
  should give  the other. (Unless there's something really  wrong with
  the process, but nobody adds salt to start their cs anymore:)

  The only  question left is what is the conversion factor  between uS
  and ppm?

  Trem had his cs analyzed and found the correlation factor  was unity
  for the ionic portion.

  Frank Key  measured the uS and ppm on some  commercial  products and
  posted the results at

    http://www.silver-colloids.com/Reports/reports.html

  He separated the ionic and particulate portions and gave their value
  separately. I ignored the particulate data.

  I selected  five products that seem to correlate well.  Here  is the
  list:

  Product Name      Conductivity  Ionic PPM  Ratio
  ~~~~~~~~~~~~      ~~~~~~~~~~~~  ~~~~~~~~~  ~~~~~
  Silver Lightning    3.3 uS/cm    3.71 ppm  0.889
  Mesosilver          3.9 uS/cm    3.9  ppm  1.0
  Sovereign Silver    9.7 uS/cm    9.22 ppm  1.052
  ASAP Solution      11.4 uS/cm   10.65 ppm  1.070
  ASAP Solution      20.1 uS/cm   19.59 ppm  1.026

  The average is

    0.889 + 1.0 + 1.052 + 1.070 + 1.026 = 5.037 / 5 = 1.0074

  Ivan posted  a table comparing uS and ppm. Note it  tracks  above 20
  ppm within 1 ppm of measurement error:

    20uS - 20ppm
    21uS - 21ppm
    25uS - 26ppm
    26uS - 27ppm

    http://escribe.com/health/thesilverlist/m14498.html

  I didn't  find  any information on how Ivan  measured  the  ppm, but
  since his data confirms and extends Frank's data, I assume Ivan also
  separated the ionic and particulate portions.

  The work by Trem, Frank, and Ivan firmly establishes  the conversion
  factor at 1 uS = 1 ppm. This is valid over a very wide  range, using
  many different  cs processes from HVAC to LVDC. So  that  problem is
  solved.

  Now for your second topic. You said:

  > Using Faradays equation should tell how much silver  was liberated
  > but won't say what happened to it.

  > "IF" nothing has settled or plated out, it should still be  in the
  > water in  whatever  form and should be  accurate  but  any visible
  > fallout/plate out  at  all  will amount  to  a  highly significant
  > percentage of  the total that won't be contributing to the  PPM in
  > the water.

  Yes, you are right. Faraday's equation only tells us how much silver
  was liberated.  We assume the current density is low enough  to keep
  the production  of oxygen at the anode minimal, and  the  dw doesn't
  have contaminants  that plate out at the anode. I  had  that problem
  recently, and it required changing suppliers.

  The Faraday equation doesn't say what happens to the silver after it
  leaves the  anode.  Our  job is to keep most  of  it  intact  and in
  solution where it does the most good.

  > Darn it. It just ain't easy.

  Sure it  is.

    The Hanna measures uS. We now know it correlates directly to ppm.

    The Faraday equations give the ppm liberated.

    The difference  between  them tells us how much  was  lost  in the
    process. This  give  us a target to  improve,  and troubleshooting
    information when something goes wrong.

    If something  goes wrong with the Hanna, the salt  test  will show
    it.

    We can  weigh  the  electrodes  to  confirm  how  much  silver was
    liberated. Mercury makes this calculation trivial. All we  need is
    a good scale.

  We now  have four simple ways that help determine  the concentration
  of silver ions in solution.

  They are cheap, quick, available to anyone, reliable, self-checking,
  and certainly accurate enough for our needs.

  What could be easier:)

  I'm also working on a fifth way to measure the ppm directly.  I hope
  to be  able to start working on it soon, as long as the  progress in
  killing spores continues.

Best Regards,

Mike Monett


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