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R. Meyer J. Köhler A. Homburg Explosives

R. Meyer J. Köhler A. Homburg Explosives

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47 Butanetriol Trinitrate<br />

Butanediol Dinitrate<br />

1,3-Butylenglykoldinitrat; dinitrate de butyléneglycol<br />

colorless liquid<br />

empirical formula: C4N8N2O6<br />

molecular weight: 180.1<br />

oxygen balance: –53.3%<br />

nitrogen content: 15.56%<br />

density: 1.32 g/cm3 lead block test: 370 cm3 /10 g<br />

Butanetriol dinitrate is insoluble in water, but is soluble in solvents for<br />

nitroglycerine; it is more volatile than nitroglycerine. Soluble guncotton<br />

is readily gelatinized. The nitrate is formed by reaction of butylene<br />

glycol with a nitric acid-sulfuric acid mixture as in the nitroglycerine<br />

synthesis, but the product is very easily destroyed by oxidation; the<br />

reaction mixture decomposes generating heat and nitrous gases. The<br />

product cannot be obtained under industrial conditions and has not<br />

found practical application for this reason.<br />

Butanetriol Trinitrate<br />

1,2,4-Butantrioltrinitrat; trinitrate de butanetriol<br />

pale yellow liquid<br />

empirical formula: C4H7N3O9<br />

molecular weight: 241.1<br />

energy of formation: –379.2 kcal/kg = –1586.4 kJ/kg<br />

enthalpy of formation: – 402.5 kcal/kg = –1683.9 kJ/kg<br />

oxygen balance: –16.6%<br />

nitrogen content: 17.43%<br />

refractive index: nD 20 = 1.4738<br />

volume of explosion gases: 836 l/kg

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