A Manual of Photographic Chemistry, Including the Practice of the Collodion Process — John Shaqi
A Manual of Photographic Chemistry, Including the Practice of the Collodion ProcessHardwich, T. Frederick
Science
A Manual of Photographic Chemistry, Including the Practice of the Collodion Process
Hardwich, T. Frederick
Photographic chemistry; Photography
The Proto- and Persalts of Iron do not resemble each other in their
physical and chemical properties. The former are usually of an apple-green
colour, and the aqueous solutions almost colourless, if not highly
concentrated. The latter, on the other hand, are dark, and give a yellow
or even blood-red solution.
The Protosalts of Iron are alone useful in Photography; but the following
experiment will serve to illustrate the properties of both classes of
salts:--Take a crystal of Protosulphate of Iron, and, having reduced
it to powder, pour a little Nitric Acid upon it in a test-tube. On the
application of heat, abundance of fumes will be given off, and a red
solution obtained. The Nitric Acid in this reaction imparts Oxygen, and
converts the _Proto_sulphate entirely into a _Per_sulphate of Iron. It is
this feature, viz. the tendency to absorb Oxygen, and to pass into the
state of Persalts, which makes the Protosalts of Iron useful as developers.
There are two Protosalts of Iron commonly employed by Photographers: the
Protosulphate and the Protonitrate of Iron.
a. _Protosulphate of Iron._--This salt, often termed _Copperas_ or _Green
Vitriol_, is an abundant substance, and used for a variety of purposes in
the arts. Commercial Sulphate of Iron however, being prepared on a large
scale, requires re-crystallization to render it sufficiently pure for
Photographic purposes.
Pure Sulphate of Iron occurs in the form of large transparent, prismatic
crystals, of a delicate green colour: by exposure to the air they
gradually absorb Oxygen and become rusty on the surface. Solution of
Sulphate of Iron, colourless at first, afterwards changes to a red tint,
and deposits a brown powder; this powder is a _basic_ Persulphate of Iron,
that is, a Persulphate containing an excess of the oxide or _base_. By the
addition of Sulphuric or Acetic Acid to the solution, the formation of a
deposit is prevented, the brown powder being soluble in acid liquids.
The Crystals of Sulphate of Iron include a large quantity of water of
crystallization, a part of which they lose by exposure to dry air. By a
higher temperature, the salt may be rendered perfectly _anhydrous_, in
which state it forms a white powder.
b. _Protonitrate of Iron._--This salt is prepared by double decomposition
between Nitrate of Baryta or of Lead and Protosulphate of Iron. It is an
unstable substance and crystallizes with great difficulty; its aqueous
solution is pale green at first, but very prone to decomposition, even
more so than the corresponding Sulphate of Iron.
SECTION II.
_The Reduction of Salts of Silver by Developing Agents._
The general theory of the reduction of metallic oxides having been
explained, it may be desirable to enter more minutely into the exact
nature of the process as applied to the compounds of Silver.
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