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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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236 NITRIC ESTERS<br />

by dissolving erythrite in strong nitric acid with cooling, <strong>and</strong> then<br />

precipitating by the addition <strong>of</strong> concentrated sulfuric acid. 64 It<br />

crystallizes from alcohol in colorless plates, m.p. 61°. Its use as<br />

an addition to smokeless powder has been suggested, 65 but it is<br />

as powerful as nitroglycerin, <strong>and</strong> has the advantage over it that<br />

it is a solid, <strong>and</strong> it would be suitable, if it were cheaper, for the<br />

same uses as nitromannite.<br />

Nitromannite (Mannitol hexanitrate)<br />

NO2—O—CHj—(CH—ONO2)4—CH,!—ONO2<br />

d-Mannitol occurs fairly widely distributed in nature, particularly<br />

in the Fraxinus ornus, the sap <strong>of</strong> which is manna. It may<br />

also be procured by the reduction <strong>of</strong> d-mannose either electrolytically<br />

or by means <strong>of</strong> sodium amalgam, or along with d-sorbite<br />

by the reduction <strong>of</strong> d-fructose. It may be nitrated satisfactorily<br />

with the same mixed acid as is used for the nitration <strong>of</strong> glycerin,<br />

or more conveniently, because the mass <strong>of</strong> crystals is so voluminous,<br />

by dissolving in strong nitric acid <strong>and</strong> precipitating by the<br />

addition <strong>of</strong> concentrated sulfuric acid.<br />

Preparation <strong>of</strong> Nitromannite. Fifty grams <strong>of</strong> nitric acid (specific<br />

gravity 1.51) is cooled thoroughly in a 300-cc. Erlenmeyer pyrex flask<br />

immersed in a freezing mixture <strong>of</strong> ice <strong>and</strong> salt. Ten grams <strong>of</strong> mannite<br />

is then introduced in small portions at a time while the flask is tilted<br />

from side to side <strong>and</strong> the contents is stirred gently with a thermometer,<br />

care being taken that the temperature does not rise above 0°. After<br />

all is dissolved, 100 grams <strong>of</strong> sulfuric acid (specific gravity 1.84) is<br />

added slowly from a dropping funnel while the liquid is stirred <strong>and</strong> the<br />

temperature is maintained below 0°. <strong>The</strong> porridge-like mass is filtered<br />

on a sinter-glass filter, or on a Biichner funnel with a hardened filter<br />

paper, washed with water, then with dilute sodium bicarbonate solution,<br />

then finally again with water. <strong>The</strong> crude product is dissolved in<br />

boiling alcohol; the solution is filtered if need be, <strong>and</strong> on cooling deposits<br />

white needle crystals <strong>of</strong> nitromannite, m.p. 112-113°. A second<br />

crop <strong>of</strong> crystals may be obtained by warming the alcoholic mother<br />

liquors to boiling, adding water while still boiling until a turbidity<br />

appears, <strong>and</strong> allowing to cool. Total yield about 23 grams.<br />

Nitromannite is readily soluble in ether <strong>and</strong> in hot alcohol,<br />

only slightly soluble in cold alcohol, <strong>and</strong> insoluble in water.<br />

64 Stenhouse, Ann., 70, 226 (1849); 130, 302 (1864).<br />

«S5Ger. Pat. 110,289 (1898); Brit. Pat. 27,397 (1898).

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