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The Principles of Chemistry, Volume II

Note 17 — Chapter XXII · IRON, COBALT, AND NICKEL

George Kamensky translation

Iron vitriol or green vitriol, sulphate of iron or ferrous sulphate, generally crystallises from solutions, like magnesium sulphate, with seven molecules of water, FeSO4,7H2O. This salt is not only formed by the action of iron on sulphuric acid, but also by the action of moisture and air on iron pyrites, especially when previously roasted (FeS2 + O2 = FeS + SO2), and in this condition it easily absorbs the oxygen of damp air (FeS + O4 = FeSO4). Green vitriol is obtained in many processes as a by-product. Ferrous sulphate, like all the ferrous salts, has a pale greenish colour hardly perceptible in solution. If it be desired to preserve it without change—that is, so as not to contain ferric compounds—it is necessary to keep it hermetically sealed. This is best done by expelling the air by means of sulphurous anhydride or ether; sulphurous anhydride, SO2, removes oxygen from ferric compounds, which might be formed, and is itself changed into sulphuric acid, and hence the oxidation of the ferrous compound does not take place in its presence. Unless these precautions are taken, green vitriol turns brown, partly changing into the ferric salt. When turned brown, it is not completely soluble in water, because during its oxidation a certain amount of free insoluble ferric oxide is formed: 6FeSO4 + O3 = 2Fe2(SO4)3 + Fe2O3. In order to cleanse such mixed green vitriol from the oxide, it is necessary to add some sulphuric acid and iron and boil the mixture; the ferric salt is then transformed into the ferrous state: Fe2(SO4)3 + Fe = 3FeSO4.

Green vitriol is used for the manufacture of Nordhausen sulphuric acid (Chapter XX.), for preparing ferric oxide, in many dye works (for preparing the indigo vats and reducing blue indigo to white), and in many other processes; it is also a very good disinfectant, and is the cheapest salt from which other compounds of iron may be obtained.

The other ferrous salts (excepting the yellow prussiate, which will be mentioned later) are but little used, and it is therefore unnecessary to dwell upon them. We will only mention ferrous chloride, which, in the crystalline state, has the composition FeCl2,4H2O. It is easily prepared; for instance, by the action of hydrochloric acid on iron, and in the anhydrous state by the action of hydrochloric acid gas on metallic iron at a red heat. The anhydrous ferrous chloride then volatilises in the form of colourless cubic crystals. Ferrous oxalate (or the double potassium salt) acts as a powerful reducing agent, and is frequently employed in photography (as a developer).

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