BORAX. A native saline compound of boracic acid and soda, found abundantly in Thibet and in South America. The crude product from the former locality was imported into Europe under the name of tincal, and was purified from some adhering fatty matter by a process kept a long time secret by the Venetians and the Dutch, and which consisted chiefly in boiling the substance in water with a little quicklime.
Gmelin found borax, in prismatic crystals, to contain 46·6 per cent. of water; and Arvredson, in the calcined state, to consist of 68·9 of acid and 31·1 soda, in 100 parts. M. Payen describes an octahedral borax, which contains only 30·64 per cent. of water, and is therefore preferred by the braziers in their soldering processes.
Borax has a sweetish, somewhat lixivial taste, and affects vegetable colours like an alkali; it is soluble in 12 parts of cold and 2 of boiling water. It effloresces and becomes opaque in a dry atmosphere, and appears luminous, by friction, in the dark. It melts at a heat a little above that of boiling water, and gives out its water of crystallization, after which it forms a spongy mass, called calcined borax. The octahedral borax, which is prepared by crystallization, in a solution of 1·256 sp. gr., kept up at 145° F., is not efflorescent. When borax is ignited, it fuses into a glassy-looking substance.
The following is the improved mode of purifying borax. The crude crystals are to be broken into small lumps, and spread upon a filter lined with a lead grating, under which a piece of cloth is stretched upon a wooden frame. The lumps are piled up to the height of 12 inches, and washed with small quantities of a caustic soda lye of 5° B. (sp. gr. 1·033) until the liquor comes off nearly colourless; they are then drained, and put into a large copper of boiling water, in such quantities that the resulting solution stands 20° B. (sp. gr. 1·160). Carbonate of soda, equivalent to 12 per cent. of the borax must now be added; the mixed solution is allowed to settle, and the clear liquid syphoned off into crystallizing vessels. Whenever the mother waters get foul, they must be evaporated to dryness in cast-iron pots, and roasted, to burn away the viscid colouring matter.
Borax is sometimes adulterated with alum and common salt: the former addition may be readily detected by a few drops of water of ammonia, which will throw down its alumina; and the latter by nitrate of silver, which will give with it a precipitate insoluble in nitric acid.
The native boracic acid obtained from the lakes of Tuscany, which has been manufactured in France into borax, has greatly lowered the price of this article of commerce. When MM. Payen and Cartier first began the business, they sold the crystals at the same price as the Dutch, viz. 7 francs the kilogramme (21⁄5 lbs. avoird.); but, in a few years, they could obtain only 2 francs and 60 centimes, in consequence of the market getting overstocked. The annual consumption of France in 1823 was 25,000 kilos., and the quantity produced in M. Payen’s works was 50,000. The mode of making borax from the acid is as follows:—The lake water is evaporated in graduation houses, and then concentrated in boilers till it crystallizes. In that state it is carried to Marseilles. About 500 kilogrammes of water are made to boil in a copper, and 600 kilogrammes of crystallized carbonate of soda are dissolved in it by successive additions of 20 kilogrammes. The solution being maintained at nearly the boiling point, 500 kilogrammes of the crystallized boracic acid of Tuscany are introduced, in successive portions. At each addition of about 10 kilogrammes, a lively effervescence ensues, on which account the copper should be of much greater capacity than is sufficient to contain the liquors. When the whole acid has been added, the fire must be damped by being covered up with moist ashes, and the copper must be covered with a tight lid and blankets, to preserve the temperature uniform. The whole is left in this state during 30 hours; the clear liquor is then drawn off into shallow crystallizing vessels of lead, in which it should stand no higher than 10 or 12 inches, to favour its rapid cooling. At the end of three days in winter, and four in summer, the crystallization is usually finished. The mother water is drawn off, and employed, instead of simple water, for the purpose of dissolving fresh crystals of soda. The above crystals are carefully detached with chisels, redissolved in boiling water, adding for each 100 kilos., 10 kilos. of carbonate of soda. This solution marks 20° B. (sp. gr. 1·160); and, at least, one ton (1000 kilos.) of borax should be dissolved at once, in order to obtain crystals of a marketable size. Whenever this solution has become boiling hot, it must be run off into large crystallizing lead chests of the form of inverted truncated pyramids, furnished with lids, enclosed in wooden frames, and surrounded with mats to confine the heat. For a continuous business there should be at least 18 vessels of this kind; as the solution takes a long time to complete its crystallization, by cooling to 30° C. (86° F.). The borax crystals are taken out with chisels, after the liquor has been drawn off, and the whole has become cold.
One hundred parts of the purest acid, usually extracted from the lakes of Tuscany, contain only fifty parts of the real boracic acid, and yield no more, at the utmost, than 140 or 150 of good borax.
Dry borax acts on the metallic oxides at a high temperature, in a very remarkable manner, melting and vitrifying them into beautiful coloured glasses. On this account it is a most useful reagent for the blowpipe. Oxide of chrome tinges it of an emerald green; oxide of cobalt, an intense blue; oxide of copper, a pale green; oxide of tin, opal; oxide of iron, bottle green and yellow; oxide of manganese, violet; oxide of nickel, pale emerald green. The white oxides impart no colour to it by themselves. In the fusion of metals borax protects their surface from oxidizement, and even dissolves away any oxides formed upon them; by which twofold agency it becomes an excellent flux, invaluable to the goldsmith in soldering the precious metals, and to the brazier in soldering copper and iron.
Borax absorbs muriatic and sulphurous acid gases, but no others, whereby it becomes, in this respect, a useful means of analysis.
The strength or purity of borax may be tested by the quantity of sulphuric acid requisite to neutralize a given weight of it, as indicated by tincture of litmus.