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CHEMIST'S CORNER ARTICLE #1: EXPLOSIVES
BY ZAPHOD BEEBLEBROX/MPG
UPLOADED BY -THE TRIXTER-
THIS ARTICLE DEALS WITH THE INSTRUCTIONS FOR CREATING SOME DANGEROUS
EXPLOSIVES. IF YOU INTEND TO MAKE ANY OF THESE EXPLOSIVES, DO SO IN
SMALL AMOUNTS ONLY, AS THEY ARE ALL DANGEROUS AND COULD SERIOUSLY INJURE
OR KILL YOU IF DONE IN LARGER AMOUNTS. IF YOU DON'T KNOW ANYTHING ABOUT
CHEMISTRY, DON'T DO THESE EXPERIMENTS! I AM NOT JOKING IN GIVING THIS
WARNING. UNLESS YOU HAVE A DEATH WISH, YOU SHOULDN'T TRY ANY OF THE
FOLLOWING UNLESS YOU HAVE HAD PRIOR EXPERIENCE WITH CHEMICALS.
I AM NOT RESPONSIBLE FOR ANY INJURY OR DAMAGE CAUSED BY PEOPLE USING
THIS INFORMATION. IT IS PROVIDED FOR USE BY PEOPLE KNOWLEDGABLE IN
CHEMISTRY WHO ARE INTERESTED IN SUCH EXPERIMENTS AND CAN SAFELY HANDLE
SUCH EXPERIMENTS.
===============================================================================
I. COMMON "WEAK" EXPLOSIVES.
A. GUNPOWDER:
75% POTASSIUM NITRATE
15% CHARCOAL
10% SULFUR
THE CHEMICALS SHOULD BE GROUND INTO A FINE POWDER (SEPERATELY!) WITH
A MORTER & PESTLE. IF GUNPOWDER IS IGNITED IN THE OPEN, IT BURNS FIERCELY,
BUT IF IN A CLOSED SPACE IT BUILDS UP PRESSURE FROM THE RELEASED GASES AND
CAN EXPLODE THE CONTAINER. GUNPOWDER WORKS LIKE THIS: THE POTASSIUM NITRATE
OXIDIZES THE CHARCOAL AND SULFUR, WHICH THEN BURN FIERCELY. CARBON DIOXIDE
AND SULFUR DIOXIDE ARE THE GASES RELEASED.
B. AMMONAL:
AMMONAL IS A MIXTURE OF AMMONIUM NITRATE (A STRONG OXIDIZER) WITH
ALUMINUM POWDER (THE 'FUEL' IN THIS CASE). I AM NOT SURE OF THE %
COMPOSITION FOR AMMONAL, SO YOU MAY WANT TO EXPERIMENT A LITTLE USING
SMALL AMOUNTS.
C. CHEMICALLY IGNITED EXPLOSIVES:
1. A MIXTURE OF 1 PART POTASSIUM CHLORATE TO 3 PARTS TABLE SUGAR
(SUCROSE) BURNS FIERCELY AND BRIGHTLY (SIMILAR TO THE BURNING OF MAGNESIUM)
WHEN 1 DROP OF CONCENTRATED SULFURIC ACID IS PLACED ON IT. WHAT OCCURS IS
THIS: WHEN THE ACID IS ADDED IT REACTS WITH THE POTASSIUM CHLORATE TO FORM
CHLORINE DIOXIDE, WHICH EXPLODES ON FORMATION, BURNING THE SUGAR AS WELL.
2. USING VARIOUS CHEMICALS, I HAVE DEVELOPED A MIXTURE THAT WORKS VERY
WELL FOR IMITATING VOLCANIC ERUPTIONS. I HAVE GIVEN IT THE NAME
'MPG VOLCANITE' (TM).
HERE IT IS: POTASSIUM CHLORATE + POTASSIUM PERCHLORATE + AMMONIUM
NITRATE + AMMONIUM DICHROMATE + POTASSIUM NITRATE + SUGAR + SULFUR
+ IRON FILINGS + CHARCOAL + ZINC DUST + SOME COLORING AGENT.
(SCARLET= STRONTIUM NITRATE, PURPLE= IODINE CRYSTALS, YELLOW= SODIUM
CHLORIDE, CRIMSON= CALCIUM CHLORIDE, ETC...). NOTE: THESE CHEMICALS GIVE
OFF A HAZARDOUS GAS WHEN IGNITED. STAY OUT OF THE SMOKE.
3. SO, DO YOU THINK WATER PUTS OUT FIRES? IN THIS ONE, IT STARTS IT. MIXTURE:
AMMONIUM NITRATE + AMMONIUM CHLORIDE + IODINE + ZINC DUST. WHEN A DROP OR TWO
OF WATER IS ADDED, THE AMMONIUM NITRATE FORMS NITRIC ACID WHICH REACTS WITH THE
ZINC TO PRODUCE HYDROGEN AND HEAT. THE HEAT VAPORIZES THE IODINE (GIVING OFF P
URPLE SMOKE) AND THE AMMONIUM CHLORIDE (BECOMES PURPLE WHEN MIXED WITH IODINE V
APOR). IT ALSO MAY IGNITE THE HYDROGEN AND BEGIN BURNING.
AMMONIUM NITRATE: 8 GRAMS
AMMONIUM CHORIDE: 1 GRAM
ZINC DUST: 8 GRAMS
IODINE CRYSTALS: 1 GRAM
4. POTASSIUM PERMANGANATE + GLYCERINE WHEN MIXED PRODUCES A PURPLE-COLORED FL
AME IN 30 SECS-1 MIN. WORKS BEST IF THE POTASSIUM PERMANGANATE IS FINELY GROUND
.
5. CALCIUM CARBIDE + WATER RELEASES ACETYLENE GAS (HIGHLY FLAMMABLE GAS USED
IN BLOW TORCHES...)
II. THERMITE REACTION.
THE THERMITE REACTION IS USED IN WELDING, BECAUSE IT GENERATES MOLTEN IRON AN
D TEMPERATURES OF 3500 C (6000F+). IT USES ONE OF THE PREVIOUS REACTIONS THAT I
TALKED ABOUT TO START IT!
STARTER=POTASSIUM CHLORATE + SUGAR
MAIN PT.= IRON (III) OXIDE + ALUMINUM POWDER (325 MESH OR FINER)
PUT THE POTASSIUM CHLORARE + SUGAR AROUND AND ON TOP OF THE MAIN PT. TO STA
RT THE REACTION, PLACE ONE DROP OF CONCENTRATED SULFURIC ACID ON TOP OF THE STA
RTER MIXTURE. STEP BACK! THE RATIOS ARE: 3 PARTS IRON(III) OXIDE TO 1 PART ALUM
INUM POWDER TO 1 PART POTASSIUM CHLORATE TO 1 PART SUGAR.
WHEN YOU FIRST DO IT, TRY 3G:1G:1G:1G!
ALSO, THERE IS AN ALTERNATIVE STARTER FOR THE THERMITE REACTION. THE ALTERNATI
VE IS POTASSIUM PERMANGANATE + GLYCERINE. AMOUNTS: 55G IRON(III) OXIDE, 15G ALU
MINUM POWDER, 25G POTASSIUM PERMANGANATE, 6ML GLYCERINE.
III. NITROGEN-CONTAINING HIGH EXPLOSIVES.
A. MERCURY(II) FULMINATE
TO PRODUCE MERCURY(II) FULMINATE, A VERY SENSITIVE SHOCK EXPLOSIVE, ONE M
IGHT ASSUME THAT IT COULD BE FORMED BY ADDING FULMINIC ACID TO MERCURY. THIS IS
SOMEWHAT DIFFICULT SINCE FULMINIC ACID IS VERY UNSTABLE AND CANNOT BE PURCHASE
D. I DID SOME RESEARCH AND FIGURED OUT A WAY TO MAKE IT WITHOUT FULMINIC ACID.
YOU ADD 2 PARTS NITRIC ACID TO 2 PARTS ALCOHOL TO 1 PART MERCURY. THIS IS THEOR
ETICAL (I HAVE NOT YET TRIED IT) SO PLEASE, IF YOU TRY THIS, DO IT IN VERY* SMA
LL AMOUNTS AND TELL ME THE RESULTS.
B. NITROGEN TRIIODIDE
NITROGEN TRIIODIDE IS A VERY POWERFUL AND VERY SHOCK SENSITIVE EXPLOSIVE.
NEVER STORE IT AND BE CARFUL WHEN YOU'RE AROUND IT- SOUND, AIR MOVEMENTS, AND
OTHER TINY THINGS COULD SET IT OFF.
MATERIALS-
2-3G IODINE
15ML CONC. AMMONIA
8 SHEETS FILTER PAPER
50ML BEAKER
FEATHER MOUNTED ON A TWO METER POLE
EAR PLUGS
TAPE
SPATULA
STIRRING ROD
ADD 2-3G IODINE TO 15ML AMMONIA IN THE 50ML BEAKER. STIR, LET STAND FOR 5 MIN
UTES.
DO THE FOLLOWING WITHIN 5 MINUTES!
RETAIN THE SOLID, DECANT THE LIQUID (POUR OFF THE LIQUID BUT KEEP THE BROWN
SOLID...). SCAPE THE BROWN RESIDUE OF NITROGEN TRIIODIDE ONTO A STACK OF FOUR S
HEETS OF FILTER PAPER. DIVIDE SOLID INTO FOUR PARTS, PUTTING EACH ON A SEPERATE
SHEET OF DRY FILTER PAPER. TAPE IN POSITION, LEAVE TO DRY UNDISTURBED FOR AT L
EAST 30 MINUTES (PREFERRABLY LONGER). TO DETONATE, TOUCH WITH FEATHER. (WEAR EA
R PLUGS WHEN DETONATING OR COVER EARS- IT IS VERY LOUD!)
C. CELLULOSE NITRATE (GUNCOTTON)
COMMONLY KNOWN AS SMOKELESS POWDER, NITROCELLULOSE IS EXACTLY THAT- IT D
OES NOT GIVE OFF SMOKE WHEN IT BURNS.
MATERIALS-
70ML CONCENTRATED SULFURIC ACID
30ML CONCENTRATED NITRIC ACID
5G ABSORBENT COTTON
250ML 1M SODIUM BICARBONATE
250ML BEAKER
ICE BATH
TONGS
PAPER TOWELS
PLACE 250ML BEAKER IN THE ICE BATH, ADD 70ML SULFURIC ACID, 30 ML NITRIC ACI
D. DIVIDE COTTON INTO .7G PIECES. WITH TONGS, IMMERSE EACH PIECE IN THE ACID SO
LUTION FOR 1 MINUTE. NEXT, RINSE EACH PIECE IN 3 SUCCESSIVE BATHS OF 500ML WATE
R. USE FRESH WATER FOR EACH PIECE. THEN IMMERSE IN 250ML 1M SODIUM BICARBONATE.
IF IT BUBBLES, RINSE IN WATER ONCE MORE UNTIL NO BUBBLING OCCURS. SQUEEZE DRY
AND SPREAD ON PAPER TOWELS TO DRY OVERNIGHT.
D. NITROGLYCERINE
NITROGLYCERINE IS A *VERY* DANGEROUS SHOCK SENSITIVE EXPLOSIVE. IT IS USED
IN MAKING DYNAMITE, AMONG OTHER THINGS.
I AM NOT SURE AS TO THE PROPORTIONS AND AMOUNTS OF CHEMICALS TO BE USED, SO
I SHALL USE ESTIMATES.
MATERIALS-
70ML CONC. SULFURIC ACID
30ML CONC. NITRIC ACID
10 ML GLYCERINE
ICE BATH
150ML BEAKER
PUT THE 150ML BEAKER IN THE ICE BATH AND MAKE SURE THAT IT IS VERY COLD. SLO
WLY ADD THE 70ML SULFURIC AND 30ML NITRIC ACIDS TO THE BEAKER, TRYING TO MAINTA
IN A LOW TEMPERATURE. WHEN THE TEMPERATURE STARTS TO LEVEL OFF, ADD ABOUT 10ML
GLYCERINE. IF IT TURNS BROWN OR LOOKS FUNNY, **RUN LIKE HELL**. WHEN NITROGLYCE
RINE TURNS BROWN, THAT MEANS IT'S READY TO EXPLODE... IF IT STAYS CLEAR AND ALL
WORKS WELL, KEEP THE TEMPERATURE AS LOW AS YOU CAN AND LET IT SIT FOR A FEW HO
URS. YOU THEN SHOULD HAVE SOME NITROGLYCERINE, PROBABLY MIXED WITH NITRIC AND S
ULFURIC ACIDS. WHEN YOU SET IT OFF, YOU MUST NOT BE NEARBY. NITROGLYCERINE CAN
FILL 10,000 TIMES ITS ORIGINAL AREA WITH EXPANDING GASES. THIS MEANS THAT IF YO
U HAVE 10ML'S OF NITROGLYCERINE IN THERE, IT WILL PRODUCE SOME 100,000ML'S OF G
ASES.
TO MAKE IT INTO DYNAMITE, THE NITROGLYCERINE MUST BE ABSORBED INTO SOMETHING
LIKE WOOD PULP OR DIAMAECEOUS EARTH (SPELLED SOMETHING LIKE THAT).
REMEMBER: THIS STUFF IS EXTREMELY SENSITIVE TO CORRECT TEMPERATURES.
IV. OTHER STUFF
A. PEROXYACETONE
PEROXYACETONE IS EXTREMELY FLAMMABLE AND HAS BEEN REPORTED TO BE SHOCK SENSI
TIVE.
MATERIALS-
4ML ACETONE
4ML 30% HYDROGEN PEROXIDE
4 DROPS CONC. HYDROCHLORIC ACID
150MM TEST TUBE
ADD 4ML ACETONE AND 4ML HYDROGEN PEROXIDE TO THE TEST TUBE. THEN ADD 4 DROPS C
ONCENTRATED HYDROCHLORIC ACID. IN 10-20 MINUTES A WHITE SOLID SHOULD BEGIN TO A
PPEAR. IF NO CHANGE IS OBSERVED, WARM THE TEST TUBE IN A WATER BATH AT 40 CELSI
US. ALLOW THE REACTION TO CONTINUE FOR TWO HOURS. SWIRL THE SLURRY AND FILTER I
T. LEAVE OUT ON FILTER PAPER TO DRY FOR AT LEAST TWO HOURS. TO IGNITE, LIGHT A
CANDLE TIED TO A METER STICK AND LIGHT IT (WHILE STAYING AT LEAST A METER AWAY)
.
B. SMOKE SMOKE SMOKE...
THE FOLLOWING REACTION SHOULD PRODUCE A FAIR AMOUNT OF SMOKE. SINCE THIS REA
CTION IS NOT ALL THAT DANGEROUS YOU CAN USE LARGER AMOUNTS IF NECESSARY FOR LAR
GER AMOUNTS OF SMOKE.
6G ZINC POWDER
1G SULFUR POWDER
INSERT A RED HOT WIRE INTO THE PILE, STEP BACK. A LOT OF SMOKE SHOULD BE CR
EATED.
THERE ARE MANY OTHER EXPERIMENTS I COULD HAVE INCLUDED, BUT I WILL SAVE THEM F
OR THE NEXT CHEMIST'S CORNER ARTICLE. UPCOMING ARTICLES WILL INCLUDE GLOW-IN-TH
E-DARK REACTIONS, 'PARTY' REACTIONS, THINGS YOU CAN DO WITH HOUSEHOLD CHEMICALS
, AND MORE...
I WOULD LIKE TO GIVE CREDIT TO A BOOK BY SHAKASHARI ENTITLED "CHEMICAL DEMONST
RATIONS" FOR A FEW OF THE PRECISE AMOUNTS OF CHEMICALS IN SOME EXPERIMENTS.
THIS IS IT FOR CHEMIST'S CORNER #1... LOOK FOR CHEMIST'S CORNER #2: WHAT TO DO
WITH HOUSEHOLD CHEMICALS...
...ZAPHOD BEEBLEBROX/MPG!
---------------------------------------
THE CHEMIST'S CORNER
ARTICLE #2: HOUSEHOLD CHEMICALS
BY ZAPHOD BEEBLEBROX/MPG
THIS ARTICLE DEALS WITH INSTRUCTIONS ON HOW TO DO SOME INTERESTING EXPERIMENTS
WITH COMMON HOUSEHOLD CHEMICALS. SOME MAY OR MAY NOT WORK DEPENDING ON THE CON
CENTRATION OF CERTAIN CHEMICALS IN DIFFERENT AREAS AND BRANDS. I WOULD SUGGEST
THAT THE PERSON DOING THESE EXPERIMENTS HAVE SOME KNOWLEDGE OF CHEMISTRY, ESPEC
IALLY FOR THE MORE DANGEROUS EXPERIMENTS.
I AM NOT RESPONSIBLE FOR ANY INJURY OR DAMAGE CAUSED BY PEOPLE USING THIS INFO
RMATION. IT IS PROVIDED FOR USE BY PEOPLE KNOWLEDGABLE IN CHEMISTRY WHO ARE INT
ERESTED IN SUCH EXPERIMENTS AND CAN SAFELY HANDLE SUCH EXPERIMENTS.
===============================================================================
I. A LIST OF HOUSEHOLD CHEMICALS AND THEIR COMPOSITION
VINEGAR: 3-5% ACETIC ACID
BAKING SODA: SODIUM BICARBONATE
DRAIN CLEANERS: SODIUM HYDROXIDE
SANI-FLUSH: 75% SODIUM BISULFATE
AMMONIA WATER: AMMONIUM HYDROXIDE
CITRUS FRUIT: CITRIC ACID
TABLE SALT: SODIUM CHLORIDE
SUGAR: SUCROSE
MILK OF MAGNESIA- MAGNESIUM HYDROXIDE
TINCTURE OF IODINE- 47% ALCOHOL, 4% IODINE
RUBBING ALCOHOL- 70 OR 99% (DEPENDS ON BRAND) ISOPROPYL ALCOHOL (DO NOT DRINK!)
ETC...
EXP #1: YE OLD FIZZ EXPERIMENT
MIX VINEGAR WITH BAKING SODA. IT PRODUCES SODIUM ACETATE AND CARBONIC ACID. CA
RBONIC ACID QUICKLY DECOMPOSES INTO CARBON DIOXIDE AND WATER, RESULTING IN THE
"FIZZ".
THIS SIMPLE REACTION CAN BE CONTAINED IN A SMALL BOTTLE OR SOMETHING, AND WHEN
ENOUGH PRESSURE BUILDS UP IT WILL BREAK OPEN. I SINCERELY DOUBT THAT IT WILL B
LOW "ALL FOUR WALLS OFF THE HOUSE" AS SOME LOSER WROTE IN HIS SAFEHOUSE ARTICLE
. THE SAME BASIC THING CAN BE DONE WITH DRY ICE & WATER, BAKING POWDER & WATER,
CITRIC ACID & BAKING SODA, AND MANY OTHER COMBINATIONS.
EXP #2: A FRUITY BATTERY
IF YOU'RE EVER IN NEED OF A LITTLE POWER, GET YOUR HANDS ON THESE:
A CITRUS FRUIT (LEMON, ORANGE, ETC)
A SMALL ZINC STRIP
A SMALL COPPER STRIP
JUST STICK THE ZINC STRIP IN ONE END OF A LEMON AND A COPPER STRIP IN THE OTH
ER. YOU NOW HAVE A 1.5 VOLT BATTERY! JUST ATTACH THE WIRES TO THE COPPER & ZINC
STRIPS...
EXP #3: GENERATING CHLORINE GAS
THIS IS MUCH MORE DANGEROUS THAN THE OTHER TWO EXPERIMENTS, SO YOU SHOUILD
KNOW WHAT YOU'RE DOING BEFORE YOU TRY THIS...
EVER WONDER WHY AMMONIA BOTTLES ALWAYS SAY 'DO NOT MIX WITH CHLORINE BLEACH',
AND VISA-VERSA? THAT'S BECAUSE IF YOU MIX AMMONIA WATER WITH AJAX OR SOMETHING
LIKE IT, IT WILL GIVE OFF CHLORINE GAS. TO CAPTURE IT, GET A LARGE BOTTLE AND P
UT AJAX IN THE BOTTOM. THEN POUR SOME AMMONIA DOWN INTO THE BOTTLE. SINCE THE C
HLORINE IS HEAVIER THAN AIR, IT WILL STAY DOWN IN THERE UNLESS YOU USE LARGE AM
OUNTS OF EITHER AJAX OR AMMONIA (DON'T!). FOR SOMETHING FUN TO DO WITH CHLORINE
STAY TUNED.... INHALING CHLORINE GAS CAN KILL YOU.
EXP #4: CHLORINE + TURPENTINE
TAKE A SMALL CLOTH OR RAG AND SOAK IT IN TURPENTINE. QUICKLY DROP IT INTO THE
BOTTLE OF CHLORINE. IT SHOULD GIVE OFF A LOT OF BLACK SMOKE AND PROBABLY START
BURNING...
EXP #5: GENERATING HYDROGEN GAS
TO GENERATE HYDROGEN, ALL YOU NEED IS AN ACID AND A METAL THAT WILL REACT WITH
THAT ACID. TRY VINEGAR (ACETIC ACID) WITH ZINC, ALUMINUM, MAGNESIUM, ETC. YOU
CAN COLLECT HYDROGEN IN SOMETHING IF YOU NOTE THAT IT IS LIGHTER THAN AIR.... L
IGHT A SMALL AMOUNT AND IT BURNS WITH A SMALL *POP*.
ANOTHER WAY OF CREATING HYDROGEN IS BY THE ELECTROLYSIS OF WATER. THIS INVOLVE
S SEPERATING WATER (H2O) INTO HYDROGEN AND OXYGEN BY AN ELECTRIC CURRENT. TO DO
THIS, YOU NEED A 6-12 VOLT BATTERY, TWO TEST TUBES, A LARGE BOWL, TWO CARBON E
LECTRODES (TAKE THEM OUT OF AN UNWORKING 6-12 VOLT BATTERY), AND TABLE SALT. DI
SSOLVE THE SALT IN A LARGE BOWL FULL OF WATER. SUBMERGE THE TWO TEST TUBES IN T
HE WATER AND PUT THE ELECTRODES INSIDE THEM, WITH THE MOUTH OF THE TUBE AIMING
DOWN. CONNECT THE BATTERY TO SOME WIRE GOING DOWN TO THE ELECTRODES. THIS WILL
WORK FOR A WHILE, BUT CHLORINE WILL BE GENERATED ALONG WITH THE OXYGEN WHICH WI
LL UNDOUBTEDLY CORRODE YOUR COPPER WIRES LEADING TO THE CARBON ELECTRODES... (T
HE TABLE SALT IS BROKEN UP INTO CHLORINE AND SODIUM IONS, THE CHLORINE COMES OF
F AS A GAS WITH OXYGEN WHILE SODIUM REACTS WITH THE WATER TO FORM SODIUM HYDROX
IDE....). THEREFORE, IF YOU CAN GET YOUR HANDS ON SOME SULFURIC ACID, USE IT IN
STEAD. IT WILL NOT AFFECT THE REACTION OTHER THAN MAKING THE WATER CONDUCT ELEC
TRICITY.
EXP #6: HYRDOGEN + CHLORINE
TAKE THE TEST TUBE OF HYDROGEN AND COVER THE MOUTH WITH YOUR THUMB. KEEP IT IN
VERTED, AND BRING IT NEAR THE BOTTLE OF CHLORINE (NOT ONE THAT HAS REACTED WITH
TURPENTINE). SAY "GOODBYE TEST TUBE", AND DROP IT INTO THE BOTTLE. THE HYDROGE
N AND CHLORINE SHOULD REACT AND POSSIBLY EXPLODE (DEPENDING ON PURITY AND AMOUN
T OF EACH GAS). AN INTERESTING THING ABOUT THIS IS THEY WILL NOT REACT IF IT IS
DARK AND NO HEAT OR OTHER ENERGY IS AROUND. WHEN A LIGHT IS TURNED ON, ENOUGH
ENERGY IS PRESENT TO CAUSE THEM TO REACT...
EXP #7: PREPARATION OF OXYGEN
GET SOME HYDROGEN PEROXIDE (FROM A DRUG STORE) AND MANGANESE DIOXIDE (FROM A B
ATTERY- IT'S A BLACK POWDER). MIX THE TWO IN A BOTTLE, AND THEY GIVE OFF OXYGEN
. IF THE BOTTLE IS STOPPERED, PRESSURE WILL BUILD UP AND SHOOT IT OFF. TRY LIGH
TING A WOOD SPLINT AND STICKING IT (WHEN ONLY GLOWING) INTO THE BOTTLE. THE OXY
GEN WILL MAKE IT BURST INTO FLAME. EXPERIMENT WITH IT. THE OXYGEN WILL ALLOW TH
INGS TO BURN BETTER...
EXP #8: ALCOHOL
BUY SOME RUBBING ALCOHOL IN A DRUG STORE. USUALLY THIS IS EITHER 70% OR 99% AL
COHOL AND BURNS JUST GREAT. YOU CAN SOAK A TOWEL IN WATER AND THEN IN ACOHOL, L
IGHT THE TOWEL, AND WHEN IT FINISHES BURNING THE ALCOHOL, THE FLAME SHOULD GO O
UT AND LEAVE THE TOWEL UNHARMED. NICE FOR "PARTY TRICKS", ETC.
EXP #9: IODINE?
TINCTURE OF IODINE CONTAINS MAINLY ALCOHOL AND A LITTLE IODINE. TO SEPERATE TH
EM, PUT THE TINCTURE OF IODINE IN A METAL LID TO A BOTTLE AND HEAT IT OVER A CA
NDLE. HAVE A STAND HOLDING ANOTHER METAL LID DIRECTLY OVER THE TINCTURE (ABOUT
4-6 INCHES ABOVE IT) WITH ICE ON TOP OF IT. THE ALCOHOL SHOULD EVAPORATE, AND T
HE IODINE SHOULD SUBLIME, BUT SHOULD REFORM IODINE CRYSTALS ON THE COLD METAL L
ID DIRECTLY ABOVE. IF THIS WORKS (I HAVEN'T TRIED), YOU CAN USE THE IODINE ALON
G WITH HOUSEHOLD AMMONIA TO FORM NITROGEN TRIIODIDE (DISCUSSED IN ARTICLE #1).
EXP #10: GRAIN-ELEVATOR EXPLOSION!
WANT TO TRY YOUR OWN 'GRAIN-ELEVATOR EXPLOSION'? GET A CANDLE AND SOME FLOUR..
. LIGHT THE CANDLE AND PUT SOME FLOUR IN YOUR HAND. TRY VARIOUS WAYS OF GETTING
THE FLOUR TO LEAVE YOUR HAND AND BECOME DUST RIGHT OVER THE CANDLE FLAME. THE
ENORMOUS SURFACE AREA ALLOWS ALL THE TINY DUST PARTICLES TO BURN, WHICH THEY DO
AT ABOUT THE SAME TIME, COMBINING TO FORM A FIREBALL EFFECT. IN GRAIN ELEVATOR
S, MUCH THE SAME THING HAPPENS. IF YOU CAN GET YOUR HANDS ON SOME LYCOPODIUM PO
WDER, DO. THIS WILL WORK MUCH BETTER, CREATING HUGE FIREBALLS THAT ARE UNEXPECT
ED.
THAT'S ENOUGH FOR NOW... MORE TO COME IN LATER CHEMIST'S CORNER ARTICLES...
...ZAPHOD BEEBLEBROX/MPG!
TRIXS OF THE TRADE...APPLE-BOOTLEGGER
/-/-/-/-/-/-/-/-/-/-/-/-/-/-/-/-/-/-/-/
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