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into the ice bath, and that the ice bath will not overflow into the beaker
when more materials are added to it. Be sure to have a large enough ice bath
container to add more ice. Bring the temperature of the acid down to about 20
degrees centigrade or less.
5) When the nitric acid is as cold as stated above, slowly and carefully add the
39 ml of concentrated sulfuric acid to the nitric acid. Mix the two acids
together, and cool the mixed acids to 10 degrees centigrade. It is a good
idea to start another ice bath to do this.
6) With the eyedropper, slowly put the glycerine into the mixed acids, one drop
at a time. Hold the thermometer along the top of the mixture where the mixed
acids and glycerine meet. DO NOT ALLOW THE TEMPERATURE TO GET ABOVE 30
DEGREES CENTIGRADE; IF THE TEMPERATURE RISES ABOVE THIS TEMPERATURE, RUN
LIKE HELL!!! The glycerine will start to nitrate immediately, and the
temperature will immediately begin to rise. Add glycerine until there is a
thin layer of glycerine on top of the mixed acids. It is always safest to
make any explosive in small quantities.
7) Stir the mixed acids and glycerine for the first ten minutes of nitration,
adding ice and salt to the ice bath to keep the temperature of the solution
in the 100 ml beaker well below 30 degrees centigrade. Usually, the
nitroglycerine will form on the top of the mixed acid solution, and the
concentrated sulfuric acid will absorb the water produced by the reaction.
8) When the reaction is over, and when the nitroglycerine is well below 30
degrees centigrade, slowly and carefully pour the solution of nitroglycerine
and mixed acid into the distilled water in the beaker in step 1. The
nitroglycerine should settle to the bottom of the beaker, and the water-acid
solution on top can be poured off and disposed of. Drain as much of the
acid-water solution as possible without disturbing the nitroglycerine.
9) Carefully remove the nitroglycerine with a clean eye-dropper, and place it
into the beaker in step 2. The sodium bicarbonate solution will eliminate
much of the acid, which will make the nitroglycerine more stable, and less
likely to explode for no reason, which it can do. Test the nitroglycerine
with the litmus paper until the litmus stays blue. Repeat this step if
necessary, and use new sodium bicarbonate solutions as in step 2.
10) When the nitroglycerine is as acid-free as possible, store it in a clean
container in a safe place. The best place to store nitroglycerine is
far away from anything living, or from anything of any value.
Nitroglycerine can explode for no apparent reason, even if it is stored
in a secure cool place.
3.14 PICRATES
Although the procedure for the production of picric acid, or
trinitrophenol has not yet been given, its salts are described first, since they
are extremely sensitive, and detonate on impact. By mixing picric acid with
metal hydroxides, such as sodium or potassium hydroxide, and evaporating the
water, metal picrates can be formed. Simply obtain picric acid, or produce it,
and mix it with a solution of (preferably) potassium hydroxide, of a mid range
molarity. (about 6-9 M) This material, potassium picrate, is impact-sensitive,
and can be used as an initiator for any type of high explosive.
3.2 LOW-ORDER EXPLOSIVES
There are many low-order explosives that can be purchased in stores
and used in explosive devices. However, it is possible that a wise gun store
owner would not sell these substances to a suspicious-looking individual. Such
an individual would then be forced to resort to making his own low-order
explosives.
3.21 BLACK POWDER
First made by the Chinese for use in fireworks, black powder was first
used in weapons and explosives in the 12th century. It is very simple to make,
but it is not very powerful or safe. Only about 50% of black powder is
converted to hot gasses when it is burned; the other half is mostly very fine
burned particles. Black powder has one major problem: it can be ignited by
static electricity. This is very bad, and it means that the material must be
made with wooden or clay tools. Anyway, a misguided individual could
manufacture black powder at home with the following procedure:
MATERIALS EQUIPMENT
_________ _________
potassium clay grinding bowl
nitrate (75 g) and clay grinder
or or
sodium wooden salad bowl
nitrate (75 g) and wooden spoon
sulfur (10 g) plastic bags (3)
charcoal (15 g) 300-500 ml beaker (1)
distilled water coffee pot or heat source
1) Place a small amount of the potassium or sodium nitrate in the grinding bowl
and grind it to a very fine powder. Do this to all of the potassium or
sodium nitrate, and store the ground powder in one of the plastic bags.
2) Do the same thing to the sulfur and charcoal, storing each chemical in a
separate plastic bag.
3) Place all of the finely ground potassium or sodium nitrate in the beaker, and
add just enough boiling water to the chemical to get it all wet.
4) Add the contents of the other plastic bags to the wet potassium or sodium
nitrate, and mix them well for several minutes. Do this until there is no
more visible sulfur or charcoal, or until the mixture is universally black.
5) On a warm sunny day, put the beaker outside in the direct sunlight. Sunlight
is really the best way to dry black powder, since it is never too hot, but it
is hot enough to evaporate the water.
6) Scrape the black powder out of the beaker, and store it in a safe container.
Plastic is really the safest container, followed by paper. Never store black
powder in a plastic bag, since plastic bags are prone to generate static
electricity.
3.22 NITROCELLULOSE
Nitrocellulose is usually called "gunpowder" or "guncotton". It is more
stable than black powder, and it produces a much greater volume of hot gas. It
also burns much faster than black powder when it is in a confined space.
Finally, nitrocellulose is fairly easy to make, as outlined by the following
procedure:
MATERIALS EQUIPMENT
_________ _________
cotton (cellulose) two (2) 200-300 ml beakers
concentrated funnel and filter paper
nitric acid
blue litmus paper
concentrated
sulfuric acid
distilled water
1) Pour 10 cc of concentrated sulfuric acid into the beaker. Add to this
10 cc of concentrated nitric acid.
2) Immediately add 0.5 gm of cotton, and allow it to soak for exactly 3
minutes.
3) Remove the nitrocellulose and prepare water to wash it in.
4) Allow the material to dry, and then re-wash it.
5) After the cotton is neutral when tested with litmus paper, it is ready to
be dried and stored.
3.23 FUEL-OXODIZER MIXTURES
There are nearly an infinite number of fuel-oxodizer mixtures that can
be produced by a misguided individual in his own home. Some are very effective
and dangerous, while others are safer and less effective. A list of working
fuel-oxodizer mixtures will be presented, but the exact measurements of each
compound are debatable for maximum effectiveness. A rough estimate will be
given of the percentages of each fuel and oxodizer:
Oxodizer, % by weight Fuel, % by weight Speed # Notes
________________________________________________________________________________
potassium chlorate 67% sulfur 33% 5 friction/
impact sensitive
rather unstable
________________________________________________________________________________
potassium chlorate 50% sugar 35% 5 fairly slow
charcoal 15% burning;
unstable
________________________________________________________________________________
potassium chlorate 50% sulfur 25% 8 extremely
magnesium or unstable!
aluminum dust 25%
________________________________________________________________________________
potassium chlorate 67% magnesium or 8 unstable
aluminum dust 33%
________________________________________________________________________________
sodium nitrate 65% magnesium dust 30% ? unpredictable
sulfur 5% burn rate
________________________________________________________________________________
potassium permanganate 60% glycerine 40% 4 delay before
ignition depends
WARNING: IGNITES SPONTANEOUSLY WITH GLYCERINE!!! upon grain size
________________________________________________________________________________
potassium permanganate 67% sulfur 33% 5 unstable
________________________________________________________________________________
potassium permangenate 60% sulfur 20% 5 unstable
magnesium or
aluminum dust 20%
________________________________________________________________________________
potassium permanganate 50% sugar 50% 3 ?
________________________________________________________________________________
potassium nitrate 75% charcoal 15% 7 this is
sulfur 10% black powder!
________________________________________________________________________________
potassium nitrate 60% powdered iron 1 burns very hot
or
magnesium 40%
________________________________________________________________________________
potassium chlorate 75% phosphorus 8 used to make
sesquisulfide 25% strike-anywhere
matches
________________________________________________________________________________
ammonium perchlorate 70% aluminum dust 30% 6 solid fuel for
+ small amount of space shuttle
iron oxide
________________________________________________________________________________
potassium perchlorate 67% magnesium or 10 flash powder
(sodium perchlorate) aluminum dust 33%
________________________________________________________________________________
potassium perchlorate 60% magnesium or 8 alternate
(sodium perchlorate) aluminum dust 20% flash powder
sulfur 20%
________________________________________________________________________________
barium nitrate 30% aluminum dust 30% 9 alternate
potassium perchlorate 30% flash powder
________________________________________________________________________________
barium peroxide 90% magnesium dust 5% 10 alternate
aluminum dust 5% flash powder
________________________________________________________________________________
potassium perchlorate 50% sulfur 25% 8 slightly
magnesium or unstable
aluminum dust 25%
________________________________________________________________________________
potassium chlorate 67% red phosphorus 27% 7 very
calcium carbonate 3% sulfur 3% unstable!
impact sensitive
________________________________________________________________________________
potassium permanganate 50% powdered sugar 25% 7 unstable;
aluminum or ignites if
magnesium dust 25% it gets wet!
________________________________________________________________________________
potassium chlorate 75% charcoal dust 15% 6 unstable
sulfur 10%
________________________________________________________________________________
NOTE: Mixtures that uses substitutions of sodium perchlorate for potassium
perchlorate become moisture-absorbent and less stable.
The higher the speed number, the faster the fuel-oxodizer mixture burns
AFTER ignition. Also, as a rule, the finer the powder, the faster the rate of
burning.
As one can easily see, there is a wide variety of fuel-oxodizer mixtures
that can be made at home. By altering the amounts of fuel and oxodizer(s),
different burn rates can be achieved, but this also can change the sensitivity of
the mixture.
3.24 PERCHLORATES
As a rule, any oxidizable material that is treated with perchloric acid
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