Re: Doubled HMTD
You can't make any new explosives from HMTD, but if you make HMTD you must have hexamine and here are some explosives you can make using hexamine:
11) C.T.M.T.N.A. (Cyclotrimethylenetrinitrosamine, R-salt)
This is R.D.X., but missing three oxygen atoms (one from each NO2 group). It uses no concentrated nitric acid. The only acid used is hydrochloric, and it doesn't even have to be very concentrated. This explosive is carcinogenic and toxic, contact should be avoided. However, thi is perhaps the best explosive to make at home since it is easy to produce and powerful. The reason it's not used militarily is the low yield of 30% (I have seen 50% stated, but this means that the weight yielded is 50% of the weight of hexamethylenetetramine used, e.g. 3.5 grams of C.T.M.T.N.A. from 7 grams of hexamethylenetetramine.) VoD is 7800 m/s at 1.57 g/cm3. Relative briscancy is 1.17. Lead block expansion is 370 cm3. At this density 2.5 grams of Mercury Fulminate will cause detonation, at 0.85 g/cm3 a mere 0.3 grams of Mercury Fulmiate will suffice!
You will need:
7g of hexamethylenetetramine, 60mL of 15% hydrochloric acid, 10.5g of sodium nitrite, Distilled water, 50mL of 10% sodium carbonate solution, 20mL of acetone, 1g of sodium carbonate, An ice bath, A 150mL beaker, A thermometer, A filter funnel, Three filter papers.
1) Dissolve the hexamine in 25mL of water and add the hydrochloric acid in the 150mL beaker. 2) Cool this to 0*C in the ice bath, and add a solution of the sodium nitrite in 50mL of water, while stirring. 3) Leave the solution to react overnight at 5*C, and then filter out the crystals. 4) Wash them with 200mL of water, then the sodium carbonate solution, then another 200mL of water. 5) Dissolve them in the acetone at around 40*C, add the 1 gram of sodium carbonate, and stir for 5 minutes. 6) Filter the solution 7) Dump the filtrate into 100mL of cold water in the other 150mL beaker to precipitate the crystals. 7) Filter them out, and leave them to dry in a warm, dry place in a thin layer.
6) Hexamethylenetetramine Dinitrate (no HNO3 needed)
I don't have much information on this explosive at the moment, but I'll keep looking... I think I heard that VoD was around 6000-7000 m/s, with a lead block expansion of 220 cm3, but I can't remember. I will find out. It is a similar sort of explosive to Urea Nitrate and M.M.A.N., i.e. it is a nitrate salt.
You will need:
5g of hexamethylenetetramine, 65mL of 15% hydrochloric acid, 10g of ammonium nitrate, A 150mL beaker, A filter funnel, A filter paper, A glass rod, A fridge.
1) Pour the hydrochloric acid into the beaker and add the ammonium nitrate. 2) Stir the solution with the glass rod until all the ammonium nitrate has dissolved. 3) Cool the solution to 5*C in the fridge. 4) Add the hexamethylenetetramine. Stir it with the glass rod until it has all dissolved. A white crystalline precipitate should form. 5) Quickly filter out the precipitate. 6) Leave it in a warm, dry place to dry fully
6)a) Hexamethylenetetramine Dinitrate (with HNO3, much better yield)
You will need:
14g of hexamethylenetetramine, 20mL of 70% nitric acid, Distilled water, Three 150mL beakers, A thermometer, A filter funnel, Filter papers, An ice bath, A fridge, Acetone.
1) Dissolve the hexamethylenetetramine in 100mL of water in one of the beakers (it will help if you heat it up, to around 80*C). Put it into the fridge after it's all dissolved, and cool it to around 5*C. 2) Measure out the nitric acid into another 150mL beaker. 3) Slowly, while stirring with the thermometer and keeping the temperature below 5*C (with the ice bath), add the nitric acid to the hexamethylenetetramine solution. 4) After the nitric acid has been added, cool the solution to 0*C. 5) Filter out the precipitate, and add it to 100mL of acetone in the third 150mL beaker. 6) Use the thermometer to crush it up and stir it around under the acetone. 7) Filter out the solid, and leave it to dry. Protect it from moisture.
and then there is always RDX, that is made from hexamine
|