ACIDS.
455
the name of fusible spar, fluor spar, false amethyst, &c.
was confounded with spar, till the miners, in consequence
of their practice, distinguished it by its useful property of
serving as a flux to the most refractory ores.
Marggraf was the first who examined fusible spar, and
selenitic spar. He determined their different characters,
and that an earthy sublimate may yield in distilling this spar
with oil of vitriol.
Priestley first observed, that an acid gas was disengaged
in the distillation of this spar with sulphuric acid, which
communicated to water, as soon as it came into contact
with it, a strong acidity, and covered the surface of the
water with a stony crust.
Scheele, in 1771, assigned it the rank it was entitled to
among the mineral acids.
When the fluor acid is obtained from a mixture of fluor
spar and sulphuric acid in a glass retort, it is rendered
impure, for it is saturated with the silica it has dissolved
from the retort, and it is mixed with sulphuric and sulphurous ¬
acids. The presence of these is immediately shewn
by the acetate of barytes. To obtain the pure fluor acid,
the mixture must be distilled in lead or tin vessels, and the
inside of the receiver lined with a coat of wax.
The distillation of a mixture of four ounces of fluor spar,
and twelve ounces of sulphuric acid, in this way, is sufficient ¬
to render eight ounces of water very-strongly acid.
The acetate of barytes does not then discover any mixture
of sulphuric acid, though the acid obtained by the distillation ¬
is strong enough to dissolve calcareous earth with
effervescence.
This acid must be kept in flint-glass bottles, coated internally ¬
with a mixture of wax and oil.
The acid, when obtained this way, is, however, not qu’te
pure. It is mixed with a small quantity of oxide of lead
or of tin, according to the retort made use of.
Two ounces of vitriolic acid, and half an ounce of fluor
spar, were distilled in a small retort of lead, in a water bath.
The retort weighed eleven ounces eight drams. In the
first distillation, it lost one dram and a half ; in the second,
one dram ; and in the third, fifty-eight grains. The acid
obtained was whitish, and had a strong smell of liver of
sulphur. The fluor acid alone cannot dissolve tin or lead ;
but, during the distillation, the superabundant sulphuric
acid dissolves the metal, which is taken from it by the
fluor acid, and deprived of its oxygen. In this distillation,