Chemistry of the Salts of Silver.
The principal Salts of Silver employed in the Photographic processes are four in number, viz. Nitrate of Silver, Chloride of Silver, Iodide of Silver, and Bromide of Silver. In addition to these, it will be necessary to describe the Oxides of Silver.
THE PREPARATION AND PROPERTIES OF THE NITRATE OF SILVER.
Nitrate of Silver is prepared by dissolving metallic Silver in Nitric Acid. Nitric Acid is a powerfully acid and corrosive substance, containing two elementary bodies united in definite proportions. These are Nitrogen and Oxygen; the latter being present in greatest quantity.
Nitric Acid is a powerful solvent for the metallic bodies generally. To illustrate its action in that particular, as contrasted with other acids, place pieces of silver-foil in two test-tubes, the one containing dilute Sulphuric, the other dilute Nitric Acid; on the application of heat a violent action soon commences in the latter, but the former is unaffected. In order to understand this, it must be borne in mind that when a metallic substance dissolves in an acid, the nature of the solution is different from that of an aqueous solution of salt or sugar. If salt water be boiled down until the whole of the water has evaporated, the salt is recovered with properties the same as at first; but if a similar experiment be made with a solution of Silver in Nitric Acid, the result is different: in that case metallic Silver is not obtained on evaporation, but Silver combined with Oxygen and Nitric Acid, both of which are strongly retained, being in fact in a state of chemical combination with the metal.
If we closely examine the effects produced by treating Silver with Nitric Acid, we find them to be of the following nature:--first, a certain amount of Oxygen is imparted to the metal, so as to form an Oxide, which Oxide dissolves in another portion of the Nitric Acid, producing Nitrate of the Oxide, or, as it is shortly termed, Nitrate of Silver.
The preparation of Nitrate of Silver from the standard coin of the realm is described in Part III., Art. "Silver."
It is the instability of Nitric Acid therefore--its proneness to part with Oxygen--which renders it superior to the Sulphuric and to most acids in dissolving Silver and various other substances, both organic and inorganic.
Properties of Nitrate of Silver.--In preparing Nitrate of Silver, when the metal has dissolved, the solution is boiled down and set aside to crystallize. The salt however as so obtained is still acid to test-paper, and requires either re-crystallization, or careful heating to about 300° Fahrenheit. It is this retention of small quantities of Nitric Acid, and sometimes probably of Nitrous Acid, which renders much of the commercial Nitrate of Silver useless for Photography, until rendered neutral by fusion and a second crystallization.
Pure Nitrate of Silver occurs in the form of white crystalline plates, which are very heavy and dissolve readily in an equal weight of cold water. The solubility is much lessened by the presence of free Nitric Acid, and in the concentrated Nitric Acid the crystals are almost insoluble. Boiling Alcohol takes up about one-fourth part of its weight of the crystallized Nitrate, but deposits nearly the whole on cooling. Nitrate of Silver has an intensely bitter and nauseous taste; acting as a caustic, and corroding the skin by a prolonged application. Its aqueous solution does not redden blue litmus-paper.
Heated in a crucible the salt melts, and when poured into a mould and solidified, forms the white lunar caustic of commerce. At a still higher temperature it is decomposed, and bubbles of Oxygen Gas are evolved: the melted mass cooled and dissolved in water leaving behind a black powder, and yielding a solution, which is faintly alkaline to test-paper, from the presence of minute quantities of Nitrite or basic Nitrite of Silver.
Nitrite of Silver differs from the Nitrate in containing less Oxygen, and is formed from it by the abstraction of two atoms of that element; it is described in the vocabulary, Part III.
THE CHEMISTRY OF THE CHLORIDES OF SILVER.
Preparation of Protochloride of Silver.--The ordinary white Chloride of Silver may be prepared in two ways,--by the direct action of Chlorine upon metallic Silver, and by double decomposition between two salts.
If a plate of polished silver be exposed to a current of Chlorine Gas, it becomes after a short time coated on the surface with a superficial film of white powder. This powder is Chloride of Silver, containing the two elements Chlorine and Silver united in single equivalents.
For the properties of the element "Chlorine," see the third division of the Work.
Preparation of Chloride of Silver by double decomposition.--In order to illustrate this, take a solution in water of Chloride of Sodium or "common salt," and mix it with a solution containing Nitrate of Silver; immediately a dense, curdy, white precipitate falls, which is the substance in question.
In this reaction the elements change places; the Chlorine leaves the Sodium with which it was previously combined, and crosses over to the Silver; the Oxygen and Nitric Acid are released from the Silver, and unite with the Sodium; thus
Chloride of Sodium plus Nitrate of Silver equals Chloride of Silver plus Nitrate of Soda.
This interchange of elements is termed by chemists double decomposition; further illustrations of it, with the conditions necessary to the proper establishment of the process, are given in the first Chapter of Part III.
The essential requirements in two salts intended for the preparation of Chloride of Silver, are simply that the first should contain Chlorine, the second Silver, and that both should be soluble in water; hence the Chloride of Potassium or Ammonium may be substituted for the Chloride of Sodium, and the Sulphate or Acetate for the Nitrate of Silver.
In preparing Chloride of Silver by double decomposition, the white clotty masses which first form must be washed repeatedly with water, in order to free them from soluble Nitrate of Soda, the other product of the change. When this is done, the salt is in a pure state, and may be dried, etc., in the usual way.
Properties of Chloride of Silver.--Chloride of Silver differs in appearance from the Nitrate of Silver. It is not usually crystalline, but forms a soft white powder resembling common chalk or whiting. It is tasteless and insoluble in water; unaffected by boiling with the strongest Nitric Acid, but sparingly dissolved by concentrated Hydrochloric Acid.
Ammonia dissolves Chloride of Silver freely, as do solutions of Hyposulphite of Soda and Cyanide of Potassium. Concentrated solutions of alkaline Chlorides, Iodides, and Bromides are likewise solvents of Chloride of Silver, but to a limited extent, as will be more fully shown in Chapter IV., when treating of the modes of fixing the Photographic proofs.
Dry Chloride of Silver carefully heated to redness fuses, and concretes on cooling into a tough and semi-transparent substance, which has been termed horn silver or luna cornea.
Placed in contact with metallic Zinc or Iron acidified with dilute Sulphuric Acid, Chloride of Silver is reduced to the metallic state, the Chlorine passing to the other metal under the decomposing influence of the galvanic current which is established.
Preparation and Properties of the Subchloride of Silver.--If a plate of polished Silver be dipped in solution of Perchloride of Iron, or of Bichloride of Mercury, a black stain is produced, the Iron or Mercury Salt losing a portion of Chlorine, which passes to the Silver and converts it superficially into Subchloride of Silver. This compound differs from the white Chloride of Silver in containing less Chlorine; the composition of the latter being represented by the formula AgCl, that of the former may perhaps be written as Ag{2}Cl(?).
Subchloride of Silver is interesting to the Photographer as corresponding in properties and composition with the ordinary Chloride of Silver blackened by light. It is a pulverulent substance of a bluish-black colour not easily affected by Nitric Acid but decomposed by fixing agents such as Ammonia, Hyposulphite of Soda, or Cyanide of Potassium, into Chloride of Silver which dissolves, and insoluble metallic Silver.
THE CHEMISTRY OF IODIDE OF SILVER.
The properties of Iodine are described in the third division of the Work: they are analogous to those of Chlorine and Bromine, the Silver Salts formed by these elements bearing also a strong resemblance to each other.
Preparation and Properties of Iodide of Silver.--Iodide of Silver may be formed in an analogous manner to the Chloride, viz. by the direct action of the vapour of Iodine upon metallic Silver, or by double decomposition, between solutions of Iodide of Potassium and Nitrate of Silver.
When prepared by the latter mode it forms an impalpable powder, the colour of which varies slightly with the manner of precipitation. If the Iodide of Potassium be in excess, the Iodide of Silver falls to the bottom of the vessel nearly white; but with an excess of Nitrate of Silver it is of a straw-yellow tint. This point may be noticed, because the yellow salt is the one adapted for Photographic use, the other being insensible to the influence of light.
Iodide of Silver is tasteless and inodorous; insoluble in water and in dilute Nitric Acid. It is scarcely dissolved by Ammonia, which serves to distinguish it from the Chloride of Silver, freely soluble in that liquid. Hyposulphite of Soda and Cyanide of Potassium both dissolve Iodide of Silver; it is also soluble in solutions of the alkaline Bromides and Iodides, as will be further explained in Chapter IV.
Iodide of Silver is reduced by Metallic Zinc in the same manner as the Chloride of Silver, forming soluble Iodide of Zinc and leaving a black powder.
THE PREPARATION AND PROPERTIES OF BROMIDE OF SILVER.
This substance so closely resembles the corresponding salts containing Chlorine and Iodine, that a short notice of it will suffice.
Bromide of Silver is prepared by exposing a silvered plate to the vapour of Bromine, or by adding solution of Bromide of Potassium to Nitrate of Silver. It is an insoluble substance, slightly yellow in colour, and distinguished from Iodide of Silver by dissolving in strong Ammonia and in Chloride of Ammonium. It is freely soluble in Hyposulphite of Soda and in Cyanide of Potassium.
The properties of the element Bromine are described in Part III.
CHEMISTRY OF THE OXIDES OF SILVER.
The Protoxide of Silver (Ag O).--If a little Potash or Ammonia be added to solution of Nitrate of Silver, an olive-brown substance is formed, which, on standing, collects at the bottom of the vessel. This is Oxide of Silver, displaced from its previous state of combination with Nitric Acid by the stronger oxide. Potash. Oxide of Silver is soluble to a very minute extent in pure water, the solution possessing an alkaline reaction to Litmus; it is easily dissolved by Nitric or Acetic Acid, forming a neutral Nitrate or Acetate; also soluble in Ammonia (Ammonio-Nitrate of Silver), and in Nitrate of Ammonia, Hyposulphite of Soda, and Cyanide of Potassium. Long exposure to light converts it into a black substance, which is probably a Suboxide.
The Suboxide of Silver (Ag{2}O?)--This substance was obtained by Faraday on exposing a solution of the Ammonio-Nitrate of Silver to the action of the air. It bears a relation to the ordinary brown Protoxide of Silver similar to that which the Subchloride bears to Protochloride of Silver.
Suboxide of Silver is a black or grey powder, which assumes the metallic lustre on rubbing, and when treated with dilute Acids is resolved into Protoxide of Silver which dissolves, and metallic Silver.
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