Re: ppm measurement techniques?

1998-07-29 Thread Frank Matzka
Great and creative ways to seperate the silver from water, but why not
just
weigh the solution? 1 litre of pure water weighs 1 Kg so anything over
1000gms is silver. 

Better yet! You could weigh the electrodes before and after(dried). 
Anybody got any ideas on how to build a scale sensitive enough to
register the small amounts? Is a beam type scale practical?

Just a couple thoughts.

Regards...Frank

M. G. Devour wrote:

 We could save some money and get quicker results if some of us could
 do our own ppm testing. Here's a couple of ideas I'd like to discuss
 and, hopefully, refine enough to make work.

 The first idea is to evaporate a quantity of CS to be tested, say
 100 ml (1/10th of a liter), and weigh the residue. 100 ml of a 20 ppm
 CS will leave 2 milligrams of residue. To get resolution to 1 ppm
 would require sensitivity to 1/10th of a milligram.

 So, ideally, you'll need access to an analytic balance sensitive to
 tenths of milligrams. This is a cut above your most common lab
 balances which will only handle milligrams. This type will typically
 have the measuring pan in a glass enclosure to stop drafts from
 effecting it. Otherwise you'd have to evaporate a much larger sample.

 I see putting the CS in a bag, bottle or funnel and allowing it to
 drip slowly onto a piece of absorbent paper. The paper would be held
 with clips over a heatlamp or hot air blower to evaporate the water.

 If you can get hold of some IV drip fittings you'd have the ideal
 setup, but I assume we could kludge up something with more common
 materials as well.

 The paper would need to be weighed before and after, and the results
 would be the difference between the weights.

 Now, right off, there are problems with this method. One is taking
 care that body oils and dust don't contaminate the paper and cause
 it to weigh more than it is supposed to. You can take care to handle
 the paper with gloves or tweezers, and perhaps enclose everything to
 minimize accumulation of dust.

 Another problem is knowing the exact state the silver is in when
 you're weighing it. Is it pure silver? Silver oxide?

 We could try using a few drops of nitric acid to digest the silver
 to form silver nitrate, which is one of the few silver compounds
 that is readily soluble in water.

 Now of course, we'd have to find out how the left over acid reacted
 with the paper. It would be easy to do a test with just the nitric
 acid in distilled water, and see how much weight the paper gained, if
 any. If all the nitrate hangs around then we *might* just be able to
 subtract it out and call the balance silver. The chemistry could
 prove to be more complicated, however.

 Which brings us to the *other* possibility, which is an entirely
 chemical assay that uses pH or some other characteristic with
 reagents and an indicator to standardize and visualize the reaction
 and allow you to measure the silver present by quantity required.

 If anyone knows a chemist who could help us with that it could save
 us a lot of effort.

 So here are some ideas. If I've convinced you an in-house ppm test
 would be useful, I hope you'll help me get one of these ideas
 working, or suggest another.

 Be well,

 Mike D.
 [Mike Devour, Citizen, Patriot, Libertarian]
 [mdev...@mail.id.net   ]
 [Speaking only for myself...  ]

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Re: Off topic (chorella)

1998-07-29 Thread Frank Matzka
I heard the same one. I also wondered if it was possible to do it at home. If
you find out let me/us know.

Regards...Frank



Harvey Flatbush wrote:

 Hi List,

 Is there anyone on the list that knows how to grow their own Chlorella as
 mentioned by Ed Dames on the Art Bell talk show several months ago?

 Thanks much,

 Harvey
 Harvey Flatbush  
  ha...@iomet.com
http://www.iomet.com
 Ione, Washington 

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Plans for stovetop distiller please?

1998-06-11 Thread Frank Matzka
Apparently a couple of months ago someone posted some plans or instructions
for stovetop distilling. Does anyone still have a copy of these posts? I
must have joined just after and Imissed them.

If anyone finds them could you either repost them or email them to me
please?

Thanks in advance...Frank




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CS and digestive bacteria

1998-06-01 Thread Frank Matzka
Thanks to all who contributed to this thread.

Since I wrote in I have received a little more info on Yakult and there 
is a web site here in Oz, www.yakult.com.au. But it's under construction 
so I'll have to wait and see what they include as they go along.

The Lactobacillus casei Shirota strain apparently survives gastric and
bile acids to actually get to the small intestine. It's cultured at 37C 
(body temp) and fermented for 6 days (all my favorite things are
fermented)and then has added citrus fruit flavours.

This is slightly different to yoghurt, certainly longer in the making,
and I was hoping to find someone who had made up their own. I'll give it
a try myself and come back with any meaningful results if I have any.

Regards...Frank


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Re: Finally - My first attempt ! How did I do ?

1998-05-24 Thread Frank Matzka
To save multiple messages I've replied to a few in this one message.


M. G. Devour wrote:

 Sounds like you got everything together just great...

  There was absolutely no reaction and I had to toss in
  about 10 ml 0.9% sodium chloride solution (irrigation sachet from
  pharmacy) and it roared off.

 I you'd have waited as much as a half hour, you'd have seen the
 reaction begin. It just takes longer without salt. The reaction
 actually was getting going, but too slowly to see.

I'll try that with the next batch and see how I go

Cisco wrote:

 Frank,

 Ditto.salt, if any impurity exists in the H20 will cause a
 undesired
 reaction and possibly a toxic effect.if I could in my limited
 abilities suggest somethingleave salt, of any type, out of your
 base.

 Cisco

That seems to be the consensus. Next batch I won't be so impatient and
just let it go without and see what happens.

Dean Woodward wrote:

 I don't know why no one I have read after ever mentioned the artistic beauty
 of the filmy, diaphanous web of particles which comes off the cathode when
 things really get going. I am going to try to create some art from this.


Yes, post them when you get some good ones


It's not me wrote:

 I haven't had much success with just rubbing the CS in topically.
 What
 usually works is to saturate something with CS and leave it in contact
 with
 the infected sight for some time.  Cold sores get about 10 min. and
 other
 nastier infections get overnight or several days.  I would think that
 with
 Mastitis, you would want the CS in contact at least overnight.


There was a recipe for gelling CS somewhere I'll chase it up and perhaps
try that.

As for a progress report: my wife says that although not much better
(yet) it hasn't got worse. It was fluctuating between worse and better
when it first started but it is now consistent at the lower end.

Thanks all.

Regards...Frank
===





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Finally - My first attempt ! How did I do ?

1998-05-21 Thread Frank Matzka
Well, after lurking for ages and humming and hahing, I finally got around to
making not only the generator but a first batch ! Tonight.

My generator is based on Tom Miller's design, 24 VAC rectified and using 20 Ma.

I  have 2.5mm fine silver wire electrodes. I decided on using the same on both
trodes figuring I would simply alternate which was the anode. That way I have
double the electrode life without worrying about whether a different metal
cathode would affect the quality of my brew. I had 6 cms (almost 2 1/2)
immersed into 250 ml (8 oz) of distilled water.

I haven't got around to making my own distilled water yet (not sure which way
to go) so I bought some bottled stuff from the supermarket. There was
absolutely no reaction and I had to toss in about 10 ml 0.9% sodium chloride
solution (irrigation sachet from pharmacy) and it roared off. I used the
irrigation sachet because I assumed that being pharmaceutical grade it HAD to
be pure NaCl and better than table salt.

So I let it brew for 10 mins. There were reasonable quantities of small bubbles
coming from one electrode and there was a slight milky haze around the other
with it slowly building up a whitish/creamy surface. Towards the end a milky
tail was starting to drop down underneath it.

The solution itself, when completed, had a slight white opaque appearance to
it. I tasted it and there was a floury taste to it. Not unpleasant or bitey,
just  -  something! The residue on the cathode was a creamy white on the outer
surface to an almost grey close to the metal. It came off easily just by
rubbing my fingers over the wire.

My wife is uncomfortable with a bit of mastitis at the moment and I remembered
reading something somewhere that it helps. But wouldn't you know it ! I
couldn't remember whether you had to drink it or rub it in. So being the caring
husband that I am, I wanted to make sure I helped so I insisted on both
drinking and topical application. Naturally I volunteered to put it on. And
folks, I'm convinced this CS stuff must work because I feel better already
after putting it on for her! But I'll let you know later whether she does.

So what do you think? Am I off and running or did I just get a cheap thrill?

Regards...Frank




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Position of electrodes ?

1998-05-06 Thread Frank Matzka
Is there a minimum distance from the sides of the glass jar that the electrodes
should be?

And is there an optimum or recommended distance between the electrodes? How
does the seperation distance have any effect on the production of CS?

Thanks in advance...Frank


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Re: Voltage Current.

1998-04-30 Thread Frank Matzka


Christian von Wechmar wrote:

 Hi there Frank and list,

  Another article states that the smaller the particles
 the lighter the colour. Clear for  best/smallest, light  yellow for
 acceptable, then onto to brown, green and gray for much bigger
 particles.

 I made some clear HVAC CS with a huge particle size (0.114 micron). My
 light yellow CS made with 30VDC has a particle size smaller than 0.026 micron.

How did you check the particle sizes ?
Is the HVAC unit commercial or did you make it yourself and what voltage does it
run at?

Regards..Frank




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Re: Replacing/renewing the silver electrodes

1998-04-30 Thread Frank Matzka


Dean Woodward wrote:

 I must be missing something here. Is there something wrong with solder, or
 is it just inconvenient??

I guess the risk of the solder becoming immersed in the solution giving you
colloidal lead and whatever else is mixed in with the solder !

Regards...Frank






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Re: Voltage Current.

1998-04-28 Thread Frank Matzka
Sorry Dean,

He changed it to http://www.bioelectrifier.com/silver.htm I didn't know till
your message (almost straight away).

Whenever a link doesn't work, always try going backward to check where it went.

And I'll check that it works b4 I post :)

Dean Woodward wrote:

 I am unable to access the Thomas Millar article cited here. It must have
 been removed from the Infocom server. Does anyone have a copy I can borrow??

 Dean

 -Original Message-
 From:   Frank Matzka [mailto:fmat...@senet.com.au]
 Sent:   Tuesday, April 28, 1998 4:37 AM
 To: silver-list@eskimo.com
 Subject:Voltage  Current.

 I know there was a couple of articles recently about how much silver
 is in a CS solution based on calculations relating to current in the
 production process. These articles referred to current but not
 voltage. Can we assume that voltage is not relevant in any way to the
 production. (sorry for my electrical ignorance). I ask this because
 I've seen various devices described running from 1 X 9 volt battery, 3
 X 9volt batteries, plug packs supplying 30 volts etc.

 The Thomas Millar article (http://www.infocom/~thomil/silver.htm)
 suggests that the particles are produced by mechanical action, the
 current knocking off small particles of silver as it passes through
 the solution. If so then presumably the higher the current the bigger
 the particles. And this is where the colour comes into it
 (apparently). Another article states that the smaller the particles
 the lighter the colour. Clear for  best/smallest, light  yellow for
 acceptable, then onto to brown, green and gray for much bigger
 particles.

 However. Thomas Millar says that the longer you take to produce a
 solution, the more likely you are to form chemical compounds with any
 of the impurities or salts in the solution.  As I understand it pure
 distilled water is not conductive and at least a tiny amount of sodium
 chloride is required to allow current to pass thru it. So there will
 always be at least some silver chloride in with the colloidal.
 Apparently most silver compounds are described as being a pale yellow
 colour so I suppose it's hard to destinguish between optimum silver
 particle size and the amount of impurity in any given solution.

 I also presume that a larger electrode surface area would produce any
 given ppm concentration faster than a smaller one. eg a 1cm strip of
 silver would be faster than a 12 guage wire. Is this correct? And if
 so how can we calculate the difference?

 Does the conductivity of the solution change as the  ppm goes up? I
 ask this because Bob Lee mentioned in one of his posts that his
 current starts low and slowly rises as it goes along.

 Sorry to barge in with so many questions without so much as an intro
 from me :) But you guys have convinced me CS is worth a go and I'll be
 building a generator as soon as I clear up the above.

 Best regards ... Frank

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Voltage Current.

1998-04-28 Thread Frank Matzka
I know there was a couple of articles recently about how much silver
is in a CS solution based on calculations relating to current in the
production process. These articles referred to current but not
voltage. Can we assume that voltage is not relevant in any way to the
production. (sorry for my electrical ignorance). I ask this because
I've seen various devices described running from 1 X 9 volt battery, 3
X 9volt batteries, plug packs supplying 30 volts etc.

The Thomas Millar article (http://www.infocom/~thomil/silver.htm)
suggests that the particles are produced by mechanical action, the
current knocking off small particles of silver as it passes through
the solution. If so then presumably the higher the current the bigger
the particles. And this is where the colour comes into it
(apparently). Another article states that the smaller the particles
the lighter the colour. Clear for  best/smallest, light  yellow for
acceptable, then onto to brown, green and gray for much bigger
particles.

However. Thomas Millar says that the longer you take to produce a
solution, the more likely you are to form chemical compounds with any
of the impurities or salts in the solution.  As I understand it pure
distilled water is not conductive and at least a tiny amount of sodium
chloride is required to allow current to pass thru it. So there will
always be at least some silver chloride in with the colloidal.
Apparently most silver compounds are described as being a pale yellow
colour so I suppose it's hard to destinguish between optimum silver
particle size and the amount of impurity in any given solution.

I also presume that a larger electrode surface area would produce any
given ppm concentration faster than a smaller one. eg a 1cm strip of
silver would be faster than a 12 guage wire. Is this correct? And if
so how can we calculate the difference? 

Does the conductivity of the solution change as the  ppm goes up? I
ask this because Bob Lee mentioned in one of his posts that his
current starts low and slowly rises as it goes along.

Sorry to barge in with so many questions without so much as an intro
from me :) But you guys have convinced me CS is worth a go and I'll be
building a generator as soon as I clear up the above.

Best regards ... Frank


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