588 CHEMISTRY AND TECHNOLOGY OF EXPLOSIVES
also yields nitroform. Hantzsch and Rinckenberger [50] obtained its ammonium
salt by treating tetranitromethane with aqueous ammonia. This method is mostly
applied for the laboratory preparation of nitroform.
Nitroform can exist in two forms [50]: a nitro form (I) and an aci-form (II)
I II
The colourless form (I) exists in solution acidified with hydrochloric or sulph-
uric acid and also in anhydrous benzene, carbon disulphide and ether. Aqueous
and basic solutions are intensely yellow due to the presence of the form II. Solu-
tions in acetic acid are slightly yellow, which would indicate that the two forms exist
in equilibrium in this medium.
Most salts derive from the aci-form (II). However, the silver and mercuric salts
exist in two forms: colourless and yellow. This would indicate that two forms of
these salts - nitro and aci - can exist.
The explosive properties of nitroform have been proved by Shishkov [48].
Nitroform salts also exhibit explosive character.
Trinitromethane reacts with formaldehyde forming trinitroethyl alcohol (Hurd
and Starke [51]) :
CH(NO 2 ) 3 + CH 2 O -> C(NO 2 ) 3 .CH 2 OH (19)
The reaction is highly exothermic. It should be controlled, so as to prevent its
temperature exceeding 70-80°C. Trinitroethyl alcohol is an unstable, crystalline
compound, melting at 36-37°C (Ficheroulle and Gay-Lussac [52]). Its initiation
temperature is about 120°C.
Trinitroethyl alcohol may be esterified with acetic anhydride to the acetate,
which is much more stable than the alcohol itself and at temperatures of 120-140°C
shows no distinct signs of decomposition. Both alcohol and acetate are very good
solvents for nitrocellulose.
TETRANITROMETHANE
Tetranitromethane was first obtained by Shishkov [48] in 1857, but it was only
during the World War II that the Germans experimented with it on a large scale,
using mixtures of tetranitromethane with various combustible materials as rocket
propellants.
PHYSICAL PROPERTIES
Tetranitromethane, C(NO 2 ) 4 , is a heavy oily liquid (sp. gr. 1.65), which solidi-
fies at +3°C and boils at 126°C without decomposition. It is insoluble in water,
but it dissolves easily in alcohol and benzene. It is a volatile substance with a charac-
teristic smell, reminiscent of nitrogen oxides.
Menzies [53], later Nicholson [54] and Edwards [551 measured the vapour pres-
sures of tetranitromethane and obtained similar values.