The pigments containing lead, copper, mercury and bismuth are extremely susceptible to the action of sulphuretted hydrogen, by the action of which they form black compounds. Since colours which contain these metals are not permanent, but darken considerably, endeavours have been made for a long time to replace them by others not susceptible to the action of sulphuretted hydrogen. Thus it is desirable to manufacture only colours free from metals forming black compounds with sulphuretted hydrogen. For the same reason pigments which contain sulphur should not be mixed with those containing metals which form black sulphur compounds.

The rules laid down in the preceding paragraphs are of the greatest importance for the artist, for by following them he will succeed in composing a “permanent palette,” that is, containing only such colours as will not, by their composition, bring about the speedy ruin of the painting.

Although the majority of the compounds of the heavy metals are poisonous, some possess this property in an eminent degree. These are chiefly colours which contain arsenic, antimony, copper and lead. So far as it is possible, these colours should be dispensed with and harmless pigments sold in their place, though this is not always possible, since several poisonous colours cannot be replaced by innocuous ones.

Compounds of the Heavy Metals.

Zinc Compounds.—Zinc oxide, ZnO, and zinc sulphate, ZnSO₄.7H₂O, are the compounds of this metal used in the colour industry. Zinc oxide, which is used as a white pigment, is a powder which turns yellow when heated, and is not acted upon by sulphuretted hydrogen. Zinc sulphate (white vitriol) occurs as colourless crystals, or more frequently as greyish white crystalline masses. The freedom of zinc sulphate from iron is of particular importance; the commercial article is seldom satisfactory in this respect. In order to free commercial zinc sulphate from iron, the property of zinc hydroxide of precipitating iron oxide from neutral solutions may be employed. The zinc sulphate is dissolved in water, and ammonia added in small quantities until the precipitate of zinc hydroxide remains on stirring. When the liquid is left in contact with the precipitate and stirred up once or twice a day, if iron is present the precipitate will turn yellowish brown, owing to the separation of ferric hydroxide, and in the course of a few days all the iron will be removed from solution. The liquid should then give no blue colouration with yellow prussiate of potash.

Zinc oxide is used as a white pigment, zinc chromate as a yellow, and zinc cobalt compounds as green colours.

Cadmium Compounds.—Cadmium is a metal which possesses great similarity to zinc, with which it occurs in nature. In the preparation of cadmium compounds the metal is generally used. This is dissolved in dilute sulphuric acid, hydrogen is evolved, and a solution of cadmium sulphate obtained.

Cadmium is used in colour making only for the preparation of the beautiful cadmium yellows.

Iron Compounds.—These are of the greatest importance to the colour maker. Several, in which iron alone is the colour principle, are very valuable: ochre, rouge, Venetian red, sienna and umber, for example. Iron compounds are also used in the preparation of many colours. The most important is:—

Ferrous Sulphate (Green Vitriol, Copperas), FeSO₄.7H₂0.—This substance, which occurs commercially in a form of great purity at a very low price, is generally the starting point in the preparation of iron pigments. When pure, it forms fine sea-green crystals, with an astringent metallic taste, which are not poisonous and are easily soluble in water. After long exposure to the air, ferrous sulphate becomes covered with an ochre-coloured crust, consisting of basic ferric sulphate. The ferrous oxide contained in the green vitriol has united with oxygen and been converted into ferric oxide. The latter requires a larger quantity of acid than ferrous oxide for the formation of soluble salts, so that an insoluble basic salt is separated. The same thing occurs when a solution of ferrous sulphate is exposed to the air.