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The Chemistry of Powder and Explosives - Sciencemadness Dot Org

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NITROSTARCH 273<br />

At the beginning <strong>of</strong> an analysis, the reaction bulb <strong>and</strong> the measuring<br />

bulb <strong>and</strong> the capillary tubes at the tops <strong>of</strong> the bulbs are completely<br />

filled with mercury. A sample <strong>of</strong> about 1 gram <strong>of</strong> nitrocellulose is<br />

weighed in a small weighing bottle, dried for an hour <strong>and</strong> a half at<br />

100°, cooled in a desiccator, <strong>and</strong> weighed accurately. A little 95% sulfuric<br />

acid is poured onto the nitrocellulose <strong>and</strong> the whole is washed<br />

into the reaction bulb. <strong>The</strong> weighing bottle is rinsed out with several<br />

small portions <strong>of</strong> sulfuric acid, the same acid is used for rinsing the<br />

cup <strong>and</strong> is finally introduced into the reaction bulb, until altogether<br />

about 20 cc. <strong>of</strong> acid has been used, care being taken that no air is<br />

introduced. <strong>The</strong> mercury reservoir is lowered to give a reduced pressure<br />

in the reaction bulb <strong>and</strong> the bulb is shaken gently, the stopcock<br />

at its bottom being open, until the generation <strong>of</strong> gas has practically<br />

ceased. <strong>The</strong> bulb is then raised until the level <strong>of</strong> the mercury drops<br />

nearly to its lower shoulder, the stopcock is closed, <strong>and</strong> the bulb is<br />

shaken vigorously for 3 minutes. <strong>The</strong> cock is opened <strong>and</strong> the apparatus<br />

is allowed to st<strong>and</strong> for several minutes. <strong>The</strong> mercury level is then adjusted<br />

as before, the cock is closed, <strong>and</strong> the shaking is repeated for<br />

another 3 minutes. Finally the gas is transferred to the measuring bulb<br />

<strong>and</strong> allowed to st<strong>and</strong> for about 20 minutes. <strong>The</strong> measuring bulb <strong>and</strong><br />

the compensating bulb are then adjusted in such fashion that the<br />

mercury in both st<strong>and</strong>s at the same level <strong>and</strong> that the mercury in<br />

the compensating bulb st<strong>and</strong>s at the point indicated by the paper strip.<br />

<strong>The</strong> volume in the measuring bulb is then read. After each determination<br />

the reaction bulb is rinsed out twice with concentrated sulfuric<br />

acid.<br />

In practice it is convenient to st<strong>and</strong>ardize the nitrometer from time<br />

to time by means <strong>of</strong> a sample <strong>of</strong> pure potassium nitrate (13.85% N)<br />

or <strong>of</strong> nitrocellulose <strong>of</strong> known nitrogen content.<br />

<strong>The</strong> nitrometer is dangerous to one who does not underst<strong>and</strong> it fully.<br />

<strong>The</strong> closing at the wrong time <strong>of</strong> the stopcock at the bottom <strong>of</strong> the<br />

reaction bulb may result in the explosion <strong>of</strong> that vessel <strong>and</strong> the throwing<br />

about <strong>of</strong> glass <strong>and</strong> <strong>of</strong> acid.<br />

Nitrostarch<br />

Nitrostarch 105 is manufactured <strong>and</strong> used in the United States,<br />

but has not found favor in other countries. In all the early attempts<br />

to manufacture nitrostarch, the starch was dissolved in<br />

strong nitric acid <strong>and</strong> the nitric ester was precipitated by mixing<br />

the solution with sulfuric acid or with the spent acid from some<br />

105 <strong>The</strong> article by Urbanski <strong>and</strong> Hackel in Z. ges. Schiess- u. Sprengst<strong>of</strong>fw.,<br />

30, 98 (1935), is accompanied by an extensive bibliography.

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