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Introduction
Most would agree that the pinnacle of ORMUS production techniques would have
to be the classic sodium burn method, introduced to us by an individual whom, for
purposes of the Internet, prefers to remain known only as The Essene. The sodium
burn method is quite effective at disaggregating metals, but it unfortunately
requires the experimenter to handle a fairly spirited if not downright dangerous
substance - namely elemental sodium metal. Sodium metal itself is both caustic
and toxic, but much more problematic is the fact that elemental Sodium
spontaneously breaks down water into its component parts, Hydrogen and Oxygen,
immediately upon contact. This reaction occurs so quickly and so violently that it
produces a great quantity of heat, which more often than not ignites the highly
flammable Hydrogen gas, and that Hydrogen gas then burns even more fiercely
due to the presence of all that free Oxygen. If a large enough quantity of sodium
metal is involved, sufficient heat may be generated by these burning gases to reach
a temperature where the sodium metal itself may then ignite - and now you've got
some serious fireworks on your hands!
While elemental sodium metal can be safely handled with the use of a little
common sense, it is possible to attain results rivaling those of a sodium burn, by
utilizing a much tamer substance - namely the hydroxide of sodium, more
commonly known as lye. This process has come to be known as a "lye fusion" or
lye burn. It works well with black volcanic sand and it works very well with
copper metal. Unfortunately it has not proven very effective with gold metal,
however when you consider that the cost of a pound of sodium metal is roughly
$150 vs. an 18 oz. container of lye at three dollars and change - it makes pretty
good sense to save the sodium metal for use with gold or other precious metals.
It has been stated that Red Devil brand lye is almost as pure as reagent-grade
sodium hydroxide. Others claim that it contains contaminates. The author knows of
at least a dozen people who have been using Red Devil lye in their alchemical
Workings and ingesting the end products for years, and they are all still alive and
kicking - but if you are a perfectionist and worried about every part per gazillion of
contaminates, lab-grade sodium hydroxide is readily available, of course at a
significantly higher cost.
Perhaps this is also a good time to mention another controversy: that of glass
vessels vs. boiling lye. For all of you self-proclaimed scientific geniuses out there
who are so fond of pointing out that boiling lye reacts with glass, the author has
used the same Pyrex glass boiling crucible at least 25 times now with no
appreciable signs of attack other than a fine white film on the inner surface of the
crucible, and that is only in some spots. The ancient alchemist had no such
advantage as corrosion-resistant borosilicate glassware to work with, yet somehow
they got the job done without perishing. It is this author's opinion that, especially
for a beginner, the advantages of being able to see and more precisely control the
boiling process far outweigh any "danger of contamination" from lye attacking the
glass.
Many inexpensive small cooking pots have an aluminum-filled base plate attached
to the bottom of the pan to assist in evenly distributing the heat when used at
normal cook stove temperatures. Try to avoid using this type of pot. When used as
a crucible, the aluminum layer will melt and ooze out of the cracks around the
bottom of the pot. While this may not seem all that problematic at first glance,
keeping those blobs of melted aluminum from reacting with the lye solution just
makes one more thing to have to deal with unnecessarily when you already have
enough to keep you busy.
If you are unsure of the composition of your crucible - do a dry run in the fire first
and see how it reacts. Better to find out you've got a problem with an empty
crucible, instead of a pot full of valuable prima materia. Heating the crucible to red
heat will also remove any traces of oils, waxes or chemicals that may be present.
Down to Business
Aside from the monetary savings, another big advantage to using lye is that it is a
finely divided material, generally present as small beads or granules. The small
grains mix more intimately with the materia than large, jaggedly-cut, hurriedly-
arranged chunks of sodium metal. If you intend to do a burn using Copper or other
metal, take a thin sheet (foil is best) of your metal about 5 inches square and
hammer it out as thin as you can with a ball peen hammer. You may not notice
much happening with metals that are harder and less malleable than gold, but
hammer it out anyway - since you are putting a little of yourself and your intent
into the Work this way. Next, using a sturdy pair of scissors, cut the hammered
sheet into strips about 1/8th of an inch wide. Then take 3 or 4 strips at a time in
hand and cut them off into the smallest flakes you can make. The flakes should be
no larger than this letter "X."
If you are going to do a burn of black volcanic sand, put about 1/4 cup of your sand
into your prepared crucible and place it on the stove at the very lowest heat setting,
uncovered, for about 10-15 minutes to drive out any moisture. When you think the
sand is dry enough, place the cover on the crucible and set it aside to cool. When
the crucible is cool enough to hold in your hand, remove the top and add about 1 to
1-1/2 cups (8 to 12 oz.) of lye. Put the cover back on and shake thoroughly to mix
the lye and the sand together well. For metal flakes, a swirling motion works best
for this.
Be advised: If you want to be able to attain cherry-red heat outdoors, even in very
cold ambient temperatures, you are going to need a BIG burner. It is also a good
idea to set up some sort of a wind-break around your burner. CBS blocks or bricks
are the best bet, but wood may also be used if sufficiently insulated by facing it
with foil-backed insulation or sheet metal on 1/4" standoffs.
A suitable wind-break helps to conserve heat.
Place your crucible and its contents onto the burner platform and place a 2-3 lb.
weight on the lid. A metal barbell weight works well for this. If nothing else, find a
good-sized rock or a brick. Avoid using concrete, as concrete tends to "explode"
when heated rapidly due to the expansion of trapped internal moisture. Try to get
your crucible centered over the burner as best you can. Some re-positioning of the
crucible may be necessary once you fire it up, so have some sort of implement
ready. Fireplace tongs work nicely for this, and it also wouldn't hurt to have a good
pair of welders gloves handy. Fire up the burner and try to get the crucible
completely engulfed in the flame so it is heated as evenly as possible.
There are generally no pyrotechnic flare-ups with lye, like you occasionally have
with a sodium burn, but there are still plenty of toxic vapors coming off of the
mixture so stay upwind of the burner. Ideally, your crucible should get red-hot, at
least the lower 1/3 of it. Once the crucible reaches glowing red heat, time the burn
for at least 30 minutes. You can let it go for an hour if you want to, but the author
has obtained good results at 30 minutes with both volcanic sand and Copper metal.
When you think your mixture has cooked sufficiently, cut the heat off and take a
break.
Bubble, bubble...
Remove the weight from the lid of the crucible as soon as you turn off the flame -
since this will usually take much longer to cool than the crucible itself and it's
entire contents. When the crucible is cool to the touch, remove the lid. It may be
necessary to tap the cover of the crucible gently around its circumference with a
small hammer to get it to loosen up and come off.
The contents of the crucible should now look kind of like solidified oatmeal.
Unlike a sodium burn, the material in the pan is still very water soluble after a lye
burn! Anyone who has ever spent a few hours with their hands stuck in a plastic
bag, chipping and smashing chunks of caustic sodium-metal "cement" loose from
the bottom of a steel pan will definitely appreciate this point. Set the crucible down
into the bottom of a large plastic bucket and SLOWLY add distilled water to it,
stirring with a large plastic or stainless-steel spoon. When no more of the burned
material will dissolve into that batch of distilled water, dump the water out into
another plastic bucket and add some more fresh distilled water. Continue this
procedure until the crucible is empty.
Pour the dissolved material, and any leftover sand, metal, or what-have-you into a
2 quart stainless-steel pot (or Pyrex casserole) with a well-fitting lid. Add more 1:8
lye solution [16 oz. lye to 1 gallon distilled water] if necessary to bring the level up
to within an inch of the rim of the pot. Again, it is a good idea to put a weight on
the lid to keep as much steam from escaping as possible. Bring the solution to a
GENTLE ROLLING BOIL over a GAS flame, and boil for 4 - 6 hours, adding
more pre-heated distilled water periodically as needed to keep the level constant.
[Note: When a lye menstruum such as this begins to boil, it boils ALL AT ONCE,
and it will immediately boil over if the flame is set anywhere above a bare
minimum. Trust me - this makes a hell of a mess, not to mention the hazard to
people, pets, etc. If you start out with a medium flame to "get it going" - STAY
RIGHT THERE WITH IT UNTIL IT BEGINS TO BOIL and immediately reduce
the flame to a minimum to keep it from boiling over. If you do not heed this
advice, you will sorely wish that you had.]
Filter Time
Allow the solution sufficient time to cool and settle. Unfortunately, this might take
an entire day...or longer. If you have ever done anything that has anything at all to
do with Alchemy, then you know it takes a lot of PATIENCE. Nothing will come
of this procedure that will make anything happen in a hurry. We're not baking a
cake here. This isn't moonshine we're brewing. In most cases, the effects of M-state
materials take months and years to manifest, so WHAT'S YOUR HURRY? If you
allow sufficient time for the material to settle, your menstruum will be almost
crystal-clear and it will filter quite quickly and easily. If you rush it - you will clog
your filter paper and it will wind up taking even longer to get the job done.
The best method is to siphon the top liquid off of the settled solids using a length
of vinyl tubing (like air tubing used with an aquarium). If, however, you are one of
those people that just never got the hang of starting a siphon, you can simply use a
ladle to scoop out the liquid slowly so as not to disturb the settled solids.
Whichever method you choose, when the liquid level gets low, removing the last
of it will be a little easier if you cant the vessel to one side by propping it up
underneath one edge with something.
The best method is of course is to vacuum filter the menstruum with a Buchner
funnel and a 1 micron glass filter, however this is not absolutely necessary. Even if
you plan to do a vacuum filtration, you will still need to pre-filter the material.
Shown below is a method of filtering that has proven to work well either as a
prelude to vacuum filtering or as an end in itself. Obtain some stainless steel
strainers (try a dollar store) and stack 5 coffee filters into each of three strainers.
Place 3 clothespins evenly spaced around the rim of the first strainer, and pre-wet
the filters with distilled water. Repeat with the second strainer, then place the
second strainer inside the first, resting it's clothespins directly on top of the first set
of clothespins. Repeat with the third strainer. Some juggling of the clothespins may
be necessary to get everything situated, but once everything is in place, the setup
will remain stable throughout the procedure.
If you do not have a large Pyrex beaker, find a suitable container like a wide-
mouthed gallon jug or a large bowl and position the strainers up above it as best
you can. Slowly add your menstruum until it all filters down into the container.
After filtering, the liquid should be as clear as vodka. If it is not, repeat the
procedure with fresh filters. (If your liquid is still cloudy after 30 coffee filters -
there's something wrong with your eyes, or your filters!)
Rock that pH!
For this portion of the process it is best to use a pH meter with decent resolution,
preferably one that has temperature compensation. Simple pH paper simply cannot
successfully be used for this. Why, you ask? Because unless you have eyes like an
oriental pearl sorter, it is impossible to discern a fraction of a pH point with pH
paper, not to mention the fact that you will need about 200 pieces of pH paper
every time that you do this. Practically every piece of lab equipment used in
Alchemy can be fudged with kitchenware or other common items, but not the pH
meter, sorry. If you are serious about alchemical Work, break down and buy a
decent meter, and I don't mean one of those $39 specials suitable only for checking
your salt-water aquarium. Get yourself a real pH meter. Probably the best-known
source for pH meters is Hanna Instrument Co. and their most economical, yet still
decent meter would be the HI8314.
Assuming that you have a decent pH meter, put a sufficient quantity of your
menstruum into a large beaker or other Pyrex glass container, position the meter
probe(s) and begin stirring the solution with a glass rod or nylon spoon. Be sure the
stirring tool is resistant to room-temperature acids and alkalis. Slowly drip in 20%
- 30% HCl into the menstruum while constantly stirring.
The goal here is to adjust the pH slowly, lowering it by no more than .1 pH point
per minute. Monitor the temperature of the solution while you are titrating it, and
do not allow the temperature to go above 45 degrees Centigrade (about 100 F). If
the temperature reaches 45 C, stop and let the solution cool. Go make a cup of tea
or something. - remember, we're not in any hurry here.
Bring the pH slowly down to 1.0 and stop. You may notice a characteristic
effervescence of the menstruum just before this point - this is quite normal. If the
temperature is still low enough, begin dripping in 1:8 lye solution, again while
constantly stirring. This time, the goal is now to RAISE the pH by no more than .1
pH point per minute. As before, do not allow the solution to heat above 45 degrees
C. When you get to about pH 7 or 8, depending on the temperature, you should see
a white precipitate beginning to form. If you are working with copper or black
volcanic sand, you can take the pH up to about 9.5 and stop.
If you were working with Copper metal, look very closely at the color of the
precipitate which forms. The precipitate MUST be white - any other color except
white is no good. If you should happen to get a blue or green precipitate, re-
dissolve it by once again dripping HCl into the menstruum slowly until the pH
goes back down to 1.0 and try again. This time work much, much more slowly.
When the solution has settled completely - again, this may take a day or longer -
pour or siphon off the top water until only precipitate remains in the cylinder and
add roughly 3 times the volume of the precipitate of distilled water and let it settle
again. When this has settled, taste a little bit of it with a plastic spoon. If it is still
too salty for you, wash it again. If you plan to carry any of the solution anywhere
by car, or send any of it to someone by mail, be sure to leave plenty of salt in it to
protect it from x-rays and EMF from scanners, etc.