13.08.2013 Views

The Chemistry of Powder and Explosives - Sciencemadness Dot Org

The Chemistry of Powder and Explosives - Sciencemadness Dot Org

The Chemistry of Powder and Explosives - Sciencemadness Dot Org

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

436 PRIMARY EXPLOSIVES, DETONATORS, AND PRIMERS<br />

must be manufactured in such a way that they are effectively<br />

sealed.<br />

Kast <strong>and</strong> Haid have determined the temperatures at which<br />

cyanuric triazide <strong>and</strong> certain other initiators explode spontaneously,<br />

both by raising the temperature <strong>of</strong> the samples at a constant<br />

rate <strong>and</strong> by keeping the samples at constant temperatures<br />

<strong>and</strong> noting the times which elapsed before they exploded. When<br />

no measurable time elapsed, the temperature was "the temperature<br />

<strong>of</strong> instantaneous explosion." <strong>The</strong>ir data are especially interesting<br />

because they show the rate <strong>of</strong> deterioration <strong>of</strong> the materials<br />

at various temperatures. 44<br />

Trinitrotrlazidobenzene<br />

l,3,5-Trinitro-2,4,6-triazidobenzene 45 is prepared from aniline<br />

by the reactions indicated below.<br />

T<br />

Trlnitro*<br />

trlazldobenzene<br />

ci<br />

Aniline is chlorinated to form trichloroanilinc. <strong>The</strong> amino group<br />

is eliminated from this substance by means <strong>of</strong> the diazo reaction,<br />

<strong>and</strong> the resulting sj/m-trichlorobenzene is nitrated. <strong>The</strong> nitration,<br />

as described by Turek, is carried out by dissolving the material<br />

in warm 32% oleum, adding strong nitric acid, <strong>and</strong> heating at<br />

140-150° until no more trinitrotrichlorobenzene, m.p. 187°, precipitates<br />

out. <strong>The</strong> chlorine atoms <strong>of</strong> this substance arc then<br />

replaced by azido groups. This is accomplished by adding an<br />

acetone solution <strong>of</strong> the trinitrotrichlorobenzene, or better, the<br />

powdered substance alone, to an actively stirred solution <strong>of</strong> sodium<br />

azide in moist alcohol. <strong>The</strong> precipitated trinitrotriazidobenzene<br />

is filtered <strong>of</strong>f, washed with alcohol <strong>and</strong> with water, <strong>and</strong>, after<br />

drying, is sufficiently pure for technical purposes. It may be<br />

45 Turek, Chimie et industrie, 26, 781 (1931); Ger. Pat. 498,050; Brit.<br />

Pat. 298,981. Muraour, Mem. artillerie jrang., 18, 895 (1939).

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!