Robert Berger wrote:

> I would like to know why the people on this list feel the need to add
> H2O2 to EIS ???
>
>
> Because tests run by Brookes Bradley indicated an increase in
> effectiveness of between 500 and 1000% and those who have tried it
> have also reported a significant increase in effectiveness.
>   If you make the EIS correctly then the addition of H2O2 creats as
> T.E. that should not be there !!!
>
> Why do you say that?  It usually produces a week tyndall, normalizing
> all batches regardless of if the tyndall was initially very week or
> very strong.  I have no idea why you say it should not be there, if
> you have some level of particles which are very necessary, then there
> will be tyndall.
>
>   Switch to assymetrical electrodes as two othe people on this list
> have, and you like their product.
>
> What is the asymetrical electrode?
>  When I made their systems I asked them to not reveal it as i am not
> in the business of making EIS systems. When my booklet comes out in a
> couple of weeks it will detail the process, and why one should do
> somethings. Diagrams, data plots, T.E.M.s the whole nine yards, even
> and invitro comparison with the best.
>
>
> In vitro is amost meanless except for determining the effectiveness as
> a disinfectant, in vivo has to be done to determine effectiveness when
> taken internally.
>
> Marshall
>
>
>   "Ole Bob"
>
> Dan Nave <na...@comcast.net> wrote:
>
>      Did you add the H2O2 to the batches at the same rel! ative
>      time after the
>      CS had been made? In other words, did one batch cure longer
>      than the
>      other before you added the H2O2? Someone has indicated that
>      the
>      reaction of the CS to H2O2 is different depending on how
>      fresh the CS is
>      or how long the CS has cured.
>
>      On the new brew, perhaps try taking smaller batch quantities
>      and adding
>      H202 to these smaller quantities at different times relative
>      to when the
>      CS was made. EG, using the same brew:
>
>      Batch 1 has H2O2 added immediately after it has been made.
>
>      Batch 2 has H2O2 added 3 hours after it has been made.
>
>      Batch 3 has H2O2 added 6 hours after it has been made.
>
>      Batch 4 has H2O2 added 9 hours after it has been made.
>
>      Batch 4 has H2O2 added 12 hours after it has been made.
>
>      Batch 5 has H2O2 added 24 hours after it has been made.
>
>      and so on...
>
>      Dan
>
>
>      >
>      ------------------------------------------------------------------------
>
>      >
>      > Subject: CS>EIS and H2O2
>      > From: Marshall Dudley
>      > Date: Thu, 29 Dec 2005 19:44:02 -0500
>      > To: silver-list@eskimo.com
>      >
>      > To: silver-list@eskimo.com
>      >
>      >
>      > OK, I am totally buffaloed now. I have made two 5 gallon
>      batches and
>      > added H2O2 to them. Everything is as close to identical
>      between them as I
>      > can get, but the reactions were totally different.
>      >
>      > Batches were produced as follows:
>      >
>      > Initial pH of water = 6.8
>      > electrode area = 48 square inches each .999 silver plates
>      > current = 38 mA
>      > voltage ran typically 15-16 volts during making it
>      > continuous stirring, and polarity reversal at one minute
>      per half cycle.
>      > Silver content estimate from conductivity measurements 20
>      ppm
>      > both were crystal clear, and measured 16.5 uS.
>      > both batches made at about 62 degrees F.
>      > tyndall was faint
>      > did not measure pH bef! ore adding H2O2
>      >
>      > Added .5 teaspoon H2O2 per gallon, IE 2.5 teaspoons of 3%
>      to 5 gallons to
>      > give 17 ppm
>      > First batch tyndall stayed faint, maybe even became
>      fainter -
>      > conductivity measured 16 uS essentially unchanged
>      > Second batch tyndall became strong, EIS has a slightly
>      cloudy look, but
>      > no color, conductivity 9.5 uS approximately halved.
>      > Both batches measure a pH of about 7.6 after adding H2O2.
>      Adding H2O2 to
>      > distilled water gives a pH of 6.8 unchanged from plain DW.
>
>      >
>      > Taking samples of the second batch I did the following:
>      >
>      > Heated it, cloudiness and tyndall stayed the same,
>      indicating that it was
>      > no silver chloride or silver oxide precipitant since the
>      solution limit
>      > goes up when you heat it.
>      > Diluted it by 50%, tyndall approximately halved,
>      indicating once again
>      > that the cloudiness is NOT a silver compound with limited
>      solubility
>      > Added a! nother 50 or so ppm of H2O2, no change. Added 500
>      or more ppm of
>      > H2O2 and it cleared up. I have no idea what that means.
>      > Added ammonia (ammonium hydroxide), tyndall did not
>      change, proving that
>      > the cloudyness is from colloidal particles not from any
>      molecular
>      > compounds of silver precipitated.
>      > Checked for color, none noted, meaning that the particle
>      size is either
>      > very small, so the absorption is in the uv range, or very
>      big so the
>      > absorption is in the infrared range. Strong tyndall
>      implies large
>      > particles though. Will let sit for 24 hours and see if
>      anything
>      > precipitates out, if we have large particles I expect to
>      see it clear
>      > upon sitting.
>      >
>      > I am making another batch now. Before adding the H2O2 to
>      the entire
>      > batch, I plan on adding it to a few ounce a drop at a time
>      and try to
>      > figure out some more if the 3rd batch clouds up.
>      >
>      > Marshall
>      >
>      >
>      &g! t;
>
>
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>
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