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
First, the Reduction of the Oxide of Silver will be taken, as the most
simple illustration; then that of Salts of Silver formed by Oxygen-acids;
and lastly, of the Chloride, Iodide, and Bromide of Silver containing no
Oxygen.
_Reduction of Oxide of Silver._--To illustrate this conveniently, the
Oxide of Silver should be in a state of solution; water dissolves Oxide
of Silver very sparingly, but it is freely soluble in Ammonia, forming
the liquid known as Ammonio-Nitrate of Silver. If, therefore, a little of
the Ammonio-Nitrate of Silver be placed in a test-tube, and solution of
Sulphate of Iron be added to it, immediately it becomes discoloured, and a
deposit settles to the bottom.
This deposit is metallic Silver, produced by the reducing agent
appropriating to itself the Oxygen previously combined with the metal. As
metallic Silver does not dissolve in Ammonia, the liquid becomes turbid,
and the metal subsides in the form of a bulky precipitate.
_Reduction of the Oxyacid Salts of Silver._--The term _Oxyacid_ includes
those salts which contain the Oxide of Silver intimately combined with
Oxygen-acids; as _e. g._ the Nitrate of Silver, the Sulphate, the Acetate
of Silver, etc.
These salts, soluble in water, are reduced by developing agents in the
same manner as Oxide of Silver, but more slowly. The presence of an
acid united with the base is a hindrance to the process and tends to
keep the oxide in solution, especially when that acid is powerful in
its affinities. To illustrate the effect of the acid constituent of the
salt in retarding reduction, take two test-tubes, the one containing
Ammonio-Nitrate, and the other ordinary Nitrate of Silver--a single drop
of solution of Sulphate of Iron added to each will indicate an evident
difference in the rapidity of deposition.
The precipitate of metallic Silver obtained by the action of reducing
agents upon the Nitrate, varies much in colour and in general appearance.
If Gallic or Pyrogallic Acid be employed, it is a black powder;[8] whilst
the salts of Iron, and especially the same with free Nitric Acid added,
produce a sparkling precipitate, resembling what is termed _frosted
silver_. Grape Sugar and many of the essential oils, such as the Oil of
Cloves, etc., separate the metal from Ammonio-Nitrate of Silver in the
form of a brilliant mirror film, and are often employed in silvering glass.
[8] Silver precipitated by Gallic or Pyrogallic Acid does not appear to be
free from organic matter, and probably contains also a small proportion of
Oxygen.
In remarking upon these peculiarities in the molecular condition of
precipitated Silver, it should be observed that the appearance of a metal
whilst in mass is no indication of its colour when in the state of fine
powder. Platinum and Iron, both bright metals, and susceptible of a high
polish, are dull and intensely black when in a fine state of division;
Gold is of a purple or yellowish brown; Mercury a dirty grey.
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