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- ANARCHY 'N' EXPLOSIVES
- =====> VOLUME 3 <=====
-
- This is the MOST important or one of the most important volumes regarding
- the various mixtures of anarchy that I will be "publishing" to the "public".
- Also, it may as well be the MOST DANGEROUS to prepare, the substance we will
- be dealing with is Trinitrotoluene, or short - TNT. This high expolosive
- is a VERY DANGEROUS, slightly unstable substance. The crystalized crude TNT
- is about the color of brown sugar and feels greasy to the touch. It is
- suitable for many uses as a high-explosive, but not for the use in high-
- explosive shells. It is also highly reactive to many other chemical
- substances. It can be incorporated into dynamite and many other explosives
- that will be explained in further detail later, in other volumes of ANARCHY.
-
- WARNING:
- DO NOT ATTEMPT TO FINISH THIS PROJECT UNLESS YOU ARE FULLY CAPABLE SAFELY
- EXECUTING THE PROCESSES IN A SAFE ENVIRONMENT! IF YOU CHOOSE TO CONTINUE,
- READ THE INSTRUCTIONS COMPLETELY THROUGH BEFORE BEGINNING AND HAVE ALL
- MATERIALS AND TOOLS (INCLUDING SAFETY/EMERGENCY EQUIPTMENT) READY FOR USE
- WHEN OR IF THEY ARE NEEDED. THIS IS NOT A JOKE! USE AT YOUR OWN RISK!!!!!
-
- Preparation of Trinitrotoluene (Three Stages). A mixture of 294 grams
- of concentrated sulfuric acid (density 1.84) and 147 grams of nitric
- acid (density 1.42) is added slowly from a dropping funnel to 100
- grams of toluene in a tall 600-cc. beaker, while the liquid is stirred
- vigorously with an electric stirrer and it's temperature is maintained
- at 30 to 40 degrees celsius by running cold water in the vessel in
- which the beaker is standing. The addition of acid will require from an
- hour to an hour and a half. The stirring is then continued for half an
- hour longer without cooling; the mixture is allowed to stand over night
- in a separatory funnel; the lower layer of spent acid is drawn off; and
- the crude mononitrotoluene is weighed. One-half of it, corresponding to
- 50 grams of toluene, is taken for the dinitration.
- The mononitrotoluene (MNT) is dissolved in 109 grams of concentrated
- sulfuric acid (d. 1.84) while the mixture is cooled in running water.
- The solution in a tall beaker is warmed to 50 degrees
- and a mixed acid,
- composed of 54.5 grams each of nitric acid (d. 1.50) and sulfuric acid
- (d. 1.84), is added slowly drop by drop from a dropping funnel while
- the mixture is stirred mechanically. The heat generated by the reaction
- raises the temperature, and the rate of addition of the acid is regulated
- so that the temperature of the mixture lies always between 90 degrees
- and 100 degrees. The addition of the acid will require about 1 hour.
- After the acid has been added, the mixture is stirred for 2 hours longer
- at 90-100 degrees to complete the nitration. Two layers seperate on
- standing. The upper layer consists largely of dinitrotoluene (DNT), but
- probobly contains a certain amount of TNT. The trinitration in the
- laboratory is converniently carried out without separating the DNT from
- the spent acid.
-
- While the dinitration mixture is stirred actively at a temperature of
- about 90 degrees, 145 grams of fuming sulfuric aced (oleum containing
- 15% free SO3) is added slowly by pouring from a beaker. A mixed acid,
- composed of 72.5 grams each of nitric acid (d. 1.50) and the 15% oleum,
- is now added drop by drop with good agitation while the heat of the
- reaction maintains the temperature at 100-115 degrees. After about
- three-quarters of the acid has been added, it will be found necessary
- to apply external heat to maintain the temperature. After all the acid
- has been added (taking 1 1/2 to 2 hours), the heating and stirring are
- continued for 2 hours longer at 100-115 degrees. After the material has
- stood overnight, the upper TNT layer will be found to have solidified
- to a hard cake, and the lower layer of spent acid to be filled with
- cdata bstals. The acid is filtered through a Buchner funnel (without filter
- paper), and the cake is broken up and washed with water on the same
- filter to remove excess of acid. The spent acid contains considerable
- amounts of TNT in solution; this is precipitated by pouring the acid
- into a large volume of water, filtered off, rinsed with water, and added
- to the main batch. All the of the product is washed three or four times
- by agitating it vigorously with hot water under which it is melted.
- After the last washing, the TNT is granulated by allowing it to cool
- slowly under hot water while the stirring is continued. The product,
- filtered off and dried at ordinary room temperature, is equal to a good
- commercial sample of crude TNT. It may be purified by dissolving in warm
- alcohol at 60 degrees and allowing to cool slowly, or it may be purified
- by digesting with 5 times its weight of 5% sodium hydrogen sulfite
- solution at 90 degrees for half an hour with vigorous stirring, washing
- with hot water until the washings are colorless, and finally granulating
- as before. The product of this last treatment is equal to a good
- commercial sample of purified TNT. Pure ALPHA-TNT, melting point 80.8
- degrees, may be procured by recrystallizing this material once from
- nitric acid (d. 1.42) and once from alcohol.
-
- Well, that's it... AND REMEMBER MY WARNING!
-
- future editions of ANARCHY 'N' EXPLOSIVES comming soon.....
- (whenever I have time to type them up!)
-
-
-
- by Doctor Dissector of course!
-
-
-
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