The manufacture of mineral and lake pigments : $b Containing directions for the manufacture of all artificial artists' and painters' colours, enamel colours, soot and metallic pigmentsBersch, Josef
Science
The manufacture of mineral and lake pigments : $b Containing directions for the manufacture of all artificial artists' and painters' colours, enamel colours, soot and metallic pigments
Bersch, Josef
Dyes and dyeing; Pigments
=Lead Chloride=, PbCl₂, is seldom used in making colours. It may
be prepared by stirring powdered litharge in common salt solution
until the powder appears white. This, when washed, constitutes basic
lead chloride. On adding hydrochloric acid to the washed mass until
the liquid remains acid, lead chloride is obtained in the form of
crystalline needles, which are very little soluble in cold, but more
easily in hot, water.
Like any other soluble lead salt, lead chloride may be used in the
precipitation of colours, but is seldom employed on account of its
small solubility. Basic lead chloride was, at one time, used as a white
pigment, and after melting, by which it is turned yellow, as a yellow
pigment; it is no longer in use for these purposes.
=Copper Compounds.=—These are generally green or blue, and have an
extended use in the production of colours. The metallic copper which
is used in the preparation of colours is of the ordinary commercial
quality. The impurities which it contains are generally so small in
quantity that they are without importance for our purpose.
=Copper Sulphate= (Bluestone, Blue Vitriol), CuSO₄.5H₂O.—This is the
commonest of the commercial copper salts, and on that account deserves
our especial attention. It forms large sky-blue crystals, which
effloresce slightly in the air, possess an unpleasant metallic taste,
and are poisonous, like all soluble copper compounds.
Copper sulphate comes into commerce in a very pure form, but some
qualities contain zinc sulphate or ferrous sulphate. The presence of
zinc may be detected most easily by boiling the solution with excess
of caustic soda, when copper oxide separates as a black powder, whilst
zinc oxide remains dissolved. When sulphuretted hydrogen is passed
through the liquid, a white precipitate of zinc sulphide is formed.
Iron is detected by passing sulphuretted hydrogen through the solution
so long as a precipitate is formed, allowing the liquid to stand in
a covered vessel, pouring it off from the precipitate, adding nitric
acid, boiling and adding a solution of potassium ferrocyanide; a blue
precipitate denotes the presence of iron.
Copper sulphate is rarely found which is quite free from iron and zinc.
If these impurities are present in but small quantity, the zinc not
exceeding 1 per cent. and the iron at most 0·5 per cent., the copper
sulphate may be regarded as sufficiently pure for our purposes.
It may be here remarked that copper sulphate obtained from mints is
generally of great purity, and hence particularly adapted for colour
making.
When copper sulphate and other copper salts are dissolved in water,
pale blue flocks of copper carbonate generally separate. This is due
to the carbonate of lime contained in the water. An addition of a few
drops of sulphuric, nitric or hydrochloric acid suffices to prevent
this separation.
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