The following has been gleaned from multiple (surprisingly consistent)
sources - I've pointed out where there are differences of opinion.  I'm
sorry that it's not strictly narrative, but hopefully I've covered most of
the ground.

The aims of JC water pretreatment are getting the stuff that we don't want
out of the liquid, and getting the orgone in (I'll continue to use the 'O'
word, where it makes sense in this context ;-).  These aims are achieved
through judicious application of electrical potential and/or power, either
within the cell itself, or in a larger 'charging vat'.

As with many things JC related, there are different opinions on how to
pretreat your cell water.  However, the basic objective is to take the water
to what's known as 'stage 3'.  Stages 1, 2 and 3 are expanded on in the
extract from Schiffer, further down this post.

The pretreatment will not necessarily follow sequentially through the 3
stages - a cell may 'start' at stage 3 or, conversely, never make it that
far.

Once at stage 3, a cell will stay clean - both the water and the cell
itself - and should neither produce any precipitate nor surface scum.

Nobody has ever publicly provided an analysis of stage 3 water.  I've
personally cajoled a number of people who appear to have reached it, but
have always received a reply that was one or more of (1) analysis would cost
too much, (2) they don't buy into 'this science thing' or (3) claimed fear
of my motives, MIB etc.

However, the observable properties of stage 3 water are well documented, and
may give us a clue as to what is going on.  This treated water is (sometimes
very) redox negative, and has a soapy feel and altered surface tension
(ringing any bells?).  This water can also be poured from one container to
another without losing its 'charge'.  The main thing that folks aim at to
determine arrival at stage 3 is the type of bubbles produced when the cell
is powered into electrolysis - masses of pure white bubbles that sit on the
cell surface for hours after it's powered off.

pH has been suggested as another indicator of cell status.  However, as the
orgonites believe that it's possible to construct either acid or alkali
cells, we're probably better off ignoring it.

Water height should be to the top of the inner cylinders, *not* over them.

Many (but not all) sources suggest that a cell being charged should be
electrically insulated from ground.

The electrical supply should be linear DC.

The consensus of opinion amongst the 'old timers' is to start with 1 amp
from a 12 volt supply through the cell during charging, when both electrodes
are connected.  Alex Schiffer recommends using electrolyte to get to this
ratio; others either don't worry too much about it or ratchet up the voltage
as required.

Schiffer's methodology calls for brief current flow through the cell
followed by long periods of 'resting', repeated over many days.

Stevens is very insistent on the power of 'negative electricity'.  The
cathode is connected to the power source for a duration.  The anode is then
also briefly connected, before being removed.  Finally, the cathode is
disconnected.  He believes something important is going on when only the
cathode is connected.

An alternative approach originated with Bernie Heere - he suggests 'cooking'
the cell.  People following his advice typically connect their 110v/240v
mains straight to the cell via a FWBR, speeding up the process somewhat!
This method obviously causes vigorous electrolysis whereas, in the slower
versions, electrolysis is claimed to not be a particularly important aspect
of the charging process.

As suggested above, there are several treatment regimes that have been
proposed by different individuals.  All supposedly lead to the same result,
but vary greatly in effort and time - and possibly in the end result, as we
only know about the *observable* aspects of stage 3 water...

I make no apologies for reproducing the lengthy quotes below.  The foregoing
is only my take on the main points - what follows is "from the horse's
mouth".



Peter Stevens has recently restated his methodology thus:

---quote---
You can use water out of the tap as long as you largely clear it of the
chemicals put in there by the water company (alum, chlorine, flourides
etc.}. To do this you can use a cell.

Put your tap water in the cell then do the procedure described above under
“Applying Electricity” [PV - redundant comment]. Put the negative of your
12volt battery, battery charger or 12 volt dc supply on for between 2 and 20
minutes at the base of the cell, then put on the positive at the top of the
cell’s outer cylinder for between 2 and 3 minutes leaving the negative in
place, then take off the positive and leave negative on for up to an hour.
Pour the water into a glass container or plastic bucket. Repeat. After 24
hours what will happen is the chemicals in the water in the bucket will have
become solids; some will have dropped to the bottom and some will have risen
to the top, depending on what charge they acquired in the process. Pour off
the solids at the top, then pour the middle (clean) water into your cell,
then throw away the stuff in the bottom.

You can use pulsed dc for this, but flat dc is better because it works
faster. You can do the same process as above with a charging vat but you
will wind up with a good deal more water and no need to fiddle about with
repeating your charge procedure. In passing, and while we are talking about
charging vats, those cones that you see in The Experimenters Guide to the
Joe Cell come from milk/cream separators as used in dairies [PV - Joe
originally used multiple nested cones as electrodes for charging].  No
electrolyte should be added.
---ends---



An even lengthier process is suggested by Alex Schiffer, which can take
weeks.  I've quoted an extensive portion here, as some of the notes
reinforce what I've said earlier:

---quote---
The charging process is separated in three distinct stages that I call Stage
1, 2 and 3.

These stages have some obvious differences and also some subtle ones . With
experience you will know immediately if the cell is charged, but in your
early attempts you will have to rely on my photographs and description or
visit someone with a working cell. Do not listen to armchair scientists. One
look is worth a thousand words.

For the rest of your charging process, you will be only connecting your
power source to the cell for a maximum of 5 minutes at a time. As Orgone
lags electricity by about 30 seconds, you will know the state of the cell in
less than a minute. Do not be tempted to leave the power connected to the
cell for long periods! Yes, I know that you are in a hurry and more is
better, but in this case you only generate heat, steam, waste power and
overheat the cell. You can pick the failures by seeing their cells running
non-stop for days with 20 or more amps turning the water to steam, etching
the cylinders and ending up with a barrel full of scum. What else would you
expect? After all, electrolysis is time and current related. If you have had
the misfortune of having your cell left on for a long period with high
current, you have probably destroyed your cylinders. You cannot polish this
etching or plating out. Yes, you throw the cell away and start again. I bet
you don't do it next time!

DANGER! Do not charge any cell that is totally sealed! The cell will
explode, with all the related consequences. Always remove the lid or unplug
the car cell before doing any charging. I repeat, an airtight seal IS NOT
REQUIRED! At no stage do I prescribe any form of airtight container.

Stage 1. This stage is plain old electrolysis. Due to us passing a direct
current through a liquid that contains ions, chemical changes will occur. In
our case, you will see small bubbles and a cloud of activity that is greater
nearest the outside of the inner negative cylinder. The important
observation points are that the activity is greatest nearest the central
cylinder and gets progressively less as we move outward via the different
chambers formed by the rest of the cylinders. Additionally, within a short
period of turning the power off, all activity stops, the water becomes clear
and the bubbles disappear.

Summary stage 1. Every fool and his dog gets to this stage. The secret is
not to increase the electrolyte and thus the current and/or leaving the cell
on for days on end. Be patient, leave the cell on for no longer than 5
minutes, turn the power source off, remove the leads to the cell, and put
the top on the test cell, or partially block off the exit of the car cell.
It does not have to be airtight! Go and do something else. It is like
waiting for a tree to grow from the seed. Do this on a daily basis for days
or a week or longer until you get to stage 2. You will find that the more
"alive" the water is , the quicker is the seeding of the cell. I have found
that the storage, age, and source of the water all affect the seeding speed.
I have also found that by changing the structure of the water by various
means e.g., vortexing, shaking, filtering, etc., you can greatly enhance the
water quality to make it more " alive ".

Stage 2. You will now notice on your initial powering up of the cell, that
the bubbles are getting larger and the white cloud of tiny bubbles in the
water are much smaller or more transparent. Also in stage 1, you had the
action occurring mainly in the proximity of the central cylinder. Now the
bubbles form in a regular fashion irrespective of location in the cell. More
importantly, on turning the power off from the cell, the bubbles do not go
away immediately but stay there for minutes rather than seconds as in stage
1. Also, the top of the water assumes a glazed look and the meniscus is
higher due to a change in the surface tension of the water. At this stage
you may have some brownish material amongst your bubbles. Don't panic. It is
only the impurities being removed from the cell. I find that if I wipe the
top surface of the water with a paper towel, the bubbles and the deposit
will adhere to the paper and can easily be removed. Top up the cell, if
required, after the above cleaning, so that again, only the top-edges of the
cylinders are just showing.

Note. All topping up of the cell at any stage is done with plain juvenile
water only. No more electrolyte is added!

In cleaning the top of the cell as described, it has been observed that some
people react unfavorably with the cell. If so, keep that person away, or if
it is you, try changing your hand, i.e., use your right instead of your left
or vice verse. If the presence of your hand seems to collapse the surface
bubbles, I would suggest you have a friend do the work for you.

Summary stage 2. Very similar to stage 1, but now we have a more even bubble
distribution and an increase of surface tension and a longer presence of the
bubbles when the power is turned off. If you look in the bottom of your
glass test cell, you will have no scum and the water will be crystal clear.

At this stage the Orgone force has seeded the cell, but as yet, is not
breeding. With the right cell, water and operator, it is possible to go
straight to stage 2 on the first turn on of your new cell. I have this
occurring every time with modified juvenile water.

Stage 3. Not many people get to this stage, or what is worse, get here
incorrectly. If you get here following the above steps, your water is still
crystal clear with no deposits in the sump. If you get here by brute force,
you will have stripped appreciable amounts of material from the cylinders
and this material will now deposit on the insulators and hang around as a
colloid and finally form in the sump as a deposit. The low resistance
insulators and the metallic colloid will create a more leaky cell that will
cause endless mysterious car stoppages or refusal of the car to start, etc.

Right, the miracle of Nature is now breeding in your cell. Upon turning your
power on to the cell, within 30 seconds copious beautiful white bubbles will
rise from all the surface area of the cell. Before these bubbles cover the
water surface, you will notice a slowly rotating and pulsing front in all
cylinders, that is synchronized and has a regular rhythm of about 2 pulses
per second and a clockwise rotation speed of about 1 revolution every 2
seconds. These effects are very hard to observe for a first time viewer that
does not know what to look for. I find it easier to watch these effects with
the aid of a fluorescent light, as the 100 cycles per second pulsations of
the light "strobe" the water surface and help the observation.

The bubbles may overflow the container and show great surface tension. But
one of the definite proofs that the cell is breeding is that, on turning the
power source off and coming back the next day, most of the bubbles will
still be on top of the water as opposed to stage 1 or stage 2 where they
disappeared in minutes. Please have a look at my photo sequence.

Summary stage 3. There is no way that you can mistake this stage once you
have seen it. Some lucky people can feel the living energy and can react
with it, Reich's " Y factor ". For the rest of you normal people, the signs
are radically different. The bubbles are larger and pure white, the surface
tension is greater, the bubbles are pulsating and most importantly the
surface tension remains days after the power has been removed.

Additional note for the desperate electronically inclined individual. Please
note. I do not recommend any additional tests or measurements, your eyes and
brains should suffice, but if you are in trouble, you may measure the
voltage across the cell after it has been left standing with the power off
for at least 24 hours. A live cell will have a residual voltage, or more
correctly, a self generated voltage of around 1 Volt. A stage 1 cell
measured under similar conditions will read .1 to .2 of a Volt. Remember,
that unless you know what you are doing, these voltage measurements can be
very misleading due to probe materials and battery effects that can easily
mask your true measurement. As the cell reaches the maximum density of
Orgone that it can hold, the result of the breeding process is the
conversion of this excess Orgone into the formation of electricity. As such,
electrical measurement with the correct instruments is a very valuable
method in the verification of the efficiency of the cell. If you are
conversant with Reich's work, you may care to make an Orgone meter and thus
remove all guesswork. This meter is fully described on a few web sites as
mentioned in my bibliography.
---ends---



Recently, and possibly as a reaction against the effort involved
(particularly using Schiffer's method), a 'quick and dirty' approach has
been devised by Bernie Heere.  Again, it does produce the same stage 3
observable artifacts:

---quote---
Now that interest in the cells is once again at a high level and many new
people are  assembling cells, I’ve been trying to come up with charging
techniques to help all  these new cellers get their cells to stage 3, and
not have this interest all die off  because of frustration.

That being said, I’d like to first do some myth debunking.

1. Stage 3 water is ultra pure. This one is easy – Pure water is an
insulator. It is  impossible to get current through pure water. What stage 3
water really is in fact,  is water with all the anions and cat ions
precipitated out. That is all elements with  a net charge in solution. The
remaining ions are electrically neutral in solution.  I’m suggesting that
the water used by our Aussie friends is loaded with neutral  elements, since
they can apparently get 1 amp of current through their cells with  only 12
volts.

In other words, I’m suggesting that stage 3 water will have a neutral PH of
close to  7. When current is applied the PH of the water in the inner ring
will shift to  slightly acidic, and the outer ring will shift toward the
alkaline. This is once  again caused by the fact that the remaining
non-neutral elements in the water will  still be attracted to the different
potentials. I’m not positive of this PH  conjecture, but after much reading
of other’s opinions, and my own experiments, I  think this is true.

If I’m not mistaken, electrically neutral water is also good to drink – free
radicals  and all that.

2. You need a charging vat for serious cell work. Not necessarily true. I
think the  same ends can be achieved with 2 simple SS plates in a glass
container, or even in  any cell, for the reasons specified above.

3. You need to have a bottom bolt to introduce the negative into the cell.
While this is a proven way to go, it’s not really necessary, and adds
greatly to the  cost and complexity of a cell. Just get the negative
connected to the bottom of the  center cylinder any way you can. An
insulated SS wire or strap is fine. Just run it  up next to the container.
The same goes for the welded bottom. It’s nice, but it  complicates things,
and it forces the use of the bottom bolt to support the inner  cylinders.
Without the welded bottom all the cylinders can be supported with spacers.
It’s probably best to have an SS bottom on the cell but it can simply be
held there  with whatever means are convenient to the builder. I use PVC end
caps and o-rings,  which seem to work fine, until the unit is subjected to
vacuum. Than you need to back  the o-rings up with something like sikaflex
or other caulking. To prevent air leaks.

4. Stainless steel that is non-magnetic. This is probably necessary, even
for a cell  that is not used to charge water. The reason, I think, is
because the ferromagnetism  causes magnet fields to be built up when current
flows through the cell that directly  counter the desired magnetic fields.
This causes the charged ions to be repelled,  when we actually want them to
concentrate and precipitate out during the charging  process.

5. Short duration charging cycles. This is the key to the whole thing. As I’
ve  mentioned above, the charging involves getting rid of all the charged
elements. There  are 2 very obvious ways to do this. The first would be to
start with distilled water  and introduce only the desired impurities.
Anybody with any chemistry background  should be able to look at a chart of
the elements and come up with a good guess as to  what might work. The
second way is to force the undesirable elements to precipitate  out of the
water. This is the traditional way in the Joe Cell world, whether you use  a
charging vat, a cell, or some other esoteric means to charge the water.

All this is well and good, but what does it mean in the real world, or just
how do  you accomplish this. Here is a simple and effective technique that I
think will work  well. At least it has for me in a couple cells.

First you want to cook the cell. By that I mean simply charge it for a long
time.  What this does is concentrates the charged ions near the positive or
negative  (relatively speaking) plates. The ions will then cluster and
precipitate out of  solution. As far as how long to do this, my best guess
is until the water gets hot to  the touch. I think boiling the water would
be counter-productive because the  agitation would probably disperse the
clusters.

Once this stage is reached, immediately coarse filter the water into a glass
or SS  container using something like an old t-shirt. Try to avoid lint.

Now rinse any remaining sludge out of the cell. Tap water should be fine for
this.  Get as much of this undesirable water out of the cell as you can in a
short time by  simply inverting it and let it drain for a few minutes/

Now fine filter the water back into the cell. A couple thicknesses of paper
towel  should work fine. The water in the cell should now be very clear, but
it could have  some coloration. Not to worry, this is caused by the
desirable impurities in the  water.

Now just let the water cool to room temperature and try a normal charging
cycle. You  should see stage 3 bubbles start to form very quickly. If they
don’t, I think it  simply indicates that your starting water was very
contaminated and you need to  repeat the process to clear it some more.

The closer cylinder spacing of my test/charging cell really does this well.
The water becomes a really sludgy mess with a lot of precipitates. After one
pass  through this process the cell now really produces lots of stage three
bubbles.

For cells with the normal 1” spacing on the cylinders, this appears to be a
slower  process, and several passes will probably be required. I tried one
with 2,3,4, and 5”  cylinders, and it’s producing some stage 3 bubbles after
one pass. I think one more  cycle through the process will prep the water
enough to take it into a good stage 3.

Alex Schiffers was always pushing filtering, and now I think I understand
why it  helps. If you don’t filter after each charging cycle, a lot of the
undesired  materials simply get re-dissolved back into the water. The idea
of “cooking” the  water this way is really nothing new, just a way to speed
up the process and filter  off a lot with each cycle.

I don’t think the heat that builds up is a necessary part of this process,
so it’s  possible that by controlling the buildup with an ice pack might
allow for an even  longer charging cycle, and get larger cells to get the
water prepped to stage 3  levels in a single pass. Higher current should
speed up the process as well.
---ends---


I realise that there is a considerable amount of information above.  If any
clarifications are needed, please ask - I've an awful lot of JC docs
cluttering up my HD...

Patrick
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