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The Chemistry of Powder and Explosives - Sciencemadness Dot Org

The Chemistry of Powder and Explosives - Sciencemadness Dot Org

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NITROGLYCIDE 219<br />

oxide ring, <strong>and</strong> mononitroglycerin is formed. Nitroglycide was<br />

first prepared by Naoum 34 in 1907 by shaking dinitroglyccrin at<br />

room temperature with a 30% aqueous solution <strong>of</strong> sodium<br />

hydroxide. <strong>The</strong> clear solution presently deposited a colorless<br />

oil, <strong>and</strong> this, washed with water <strong>and</strong> dried in a desiccator, constituted<br />

a practically quantitative yield <strong>of</strong> nitroglycide.<br />

Nitroglycide is a very mobile liquid with a faint but pleasant<br />

aromatic odor, specific gravity 1.332 at 20°. It does not freeze<br />

at —20°. It boils at 94° at 20 mm., <strong>and</strong> with some decomposition<br />

at 174-175° at atmospheric pressure. It is not hygroscopic but is<br />

distinctly soluble in water, 5 grams in 100 cc. at 20°. Ether will<br />

extract nitroglycide from the cool aqueous solution; if the solution<br />

is boiled, however, the nitroglycide is hydrated to mononitroglycerin.<br />

Nitroglycide is miscible in all proportions with<br />

alcohol, ether, acetone, ethyl acetate, <strong>and</strong> nitroglyccrin. It gelatinizes<br />

collodion nitrocotton <strong>and</strong> even guncotton rapidly at ordinary<br />

temperature. It explodes in contact with concentrated sulfuric<br />

acid. If dissolved in dilute sulfuric acid <strong>and</strong> then treated<br />

with strong sulfuric acid, it gives <strong>of</strong>f nitric acid. It is converted<br />

into dinitroglycerin <strong>and</strong> nitroglycerin by the action <strong>of</strong> nitric acid.<br />

It dissolves in concentrated hydrochloric acid with the evolution<br />

<strong>of</strong> considerable heat, <strong>and</strong> the solution on dilution with water<br />

gives a precipitate <strong>of</strong> monochlorohydrin mononitratc. Nitroglycide<br />

reduces ammoniacal silver nitrate slowly on gentle warming;<br />

glycide reduces the same reagent in the cold.<br />

When heated rapidly in a test tube nitroglycide explodes with<br />

a sharp report at 195-200°. It is mure easily detonated than<br />

liquid nitroglycerin. Naoum believes that its great sensitivity<br />

results mainly from the easy propagation <strong>of</strong> the wave <strong>of</strong> detonation<br />

by a liquid <strong>of</strong> low viscosity. 33 He points out further that<br />

mononitroglycerin has 69.5% <strong>of</strong> the energy content (i.e., heat <strong>of</strong><br />

explosion) <strong>of</strong> nitroglycide, but as a crystal powder in the Trauzl<br />

test it gives only about 62 % as much net expansion, whence it is<br />

to be inferred that nitroglycide has the higher velocity <strong>of</strong> detonation.<br />

Nitroglycide has only 52% <strong>of</strong> the energy content (if nitroglycerin,<br />

but produces 72% as much effect in the Trauzl test. It<br />

is therefore "relatively more brisant than nitruglyecrin."<br />

id., p. 176.<br />

Sli lbid., p. 178.

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