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R. Meyer J. Köhler A. Homburg Explosives

R. Meyer J. Köhler A. Homburg Explosives

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311 Tetryl<br />

Tetryl<br />

trinitro-2,4,6-phenylmethylnitramine; Tetryl; tétryl;<br />

Tetranitromethylanilin; pyronite; tetralita<br />

pale yellow crystals<br />

empirical formula: C7H5N5O8<br />

molecular weight: 287.1<br />

energy of formation: +35.3 kcal/kg = +147.6 kJ/kg<br />

enthalpy of formation: +16.7 kcal/kg<br />

= +69.7 kJ/kg<br />

oxygen balance: – 47.4%<br />

nitrogen content: 24.39%<br />

volume of explosion gases: 861 l/kg<br />

heat of explosion<br />

(H2O gas): 996 kcal/kg = 4166 kJ/kg calculated*)<br />

1021 kcal/kg = 4271 kJ/kg }<br />

(H2O liq.): { 1140 kcal/kg = 4773 kJ/kg experimental**)<br />

specific energy: 123 mt/kg = 1208 kJ/kg<br />

density: 1.73 g/cm 3<br />

melting point: 129.5 °C = 265 °F<br />

heat of fusion: 19.1 kcal/kg = 80 kJ/kg<br />

lead block test: 410 cm 3 /10 g<br />

detonation velocity, confined:<br />

7570 m/s = 24800 ft/s at r = 1.71 g/cm 3<br />

deflagration point: 185 °C = 365 °F<br />

impact sensitivity: 0.3 kp m = 3 N m<br />

friction sensitivity: 36 kp = 353 N<br />

pistil load reaction<br />

critical diameter of steel sleeve test: 6 mm<br />

Tetryl is poisonous; it is practically insoluble in water, sparingly soluble<br />

in alcohol, ether, and benzene, and is more readily soluble in acetone.<br />

It is obtained by dissolving mono- and dimethylaniline in sulfuric acid<br />

and pouring the solution into nitric acid, with cooling.<br />

Tetryl is a highly brisant, very powerful explosive, with a satisfactory<br />

initiating power which is used in the manufacture of primary and<br />

* computed by the “ICT-Thermodynamic-Code”.<br />

** value quoted from Brigitta M. Dobratz, Properties of Chemical <strong>Explosives</strong> and<br />

Explosive Simulants, University of California, Livermore.

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