26.2.11

A Dictionary of Arts: Borax.


A Dictionary of Arts, Manufactures, and Mines; containing A Clear Exposition of Their Principles and Practice

by Andrew Ure, M. D.;
F. R. S. M. G. S. Lond.: M. Acad. M. S. Philad.; S. PH. DOC. N. GERM. Ranow.; Mulh. Etc. Etc.

Illustrated with nearly fifteen hundred engravings on wood
Eleventh American, From The Last London Edition.
To which is appended, a Supplement of Recent Improvements to The Present Time.

New York: D Appleton & company, 200 Broadway. Philadelphia: George S. Appleton, 148 Chestnut St.
MDCCCXLVII

1847


BORAX. A native saline compound of boacic 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 oer cent. of water; and Arvredeon, 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 brasiers in their soldering processes.

Borax has a sweetish, somewhat lixivial taste, and affects vegetable colors 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 puled up to the height of 12 inches, and washed with small quantities that the resulting solutions 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 coloring 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 begun the business, they sold the crystals at the same price as the Dutch, viz., 7 francs the kilogramme (2 1/8 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 favor 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 matks 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 thu 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 liquoe 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 oxydes at a high temperature, in a very remarkable manner, melting and vitrifying them into beautiful colored glasses. On this account, it is a most useful reagent for the blowpipe. Oxyde of xchrome tinges it of an emeral green; oxyde of cobalt, an intense blue; oxyde of copper, a pale green; oxyde of tin, opal; oxyde of iron, bottle-green and yellow; oxyde of manganese, violet; oxyde of nickel, pale emerald green, The white oxydes impart no color to it by themselves. In the fusion of metals, borax protects their surface from oxydezement, and even dissolves away any oxydes formed upon them; by which twofold agency it becomes an excellent flux, invaluable to the goldsmith in soldering the precious metals, and to be brasier 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 strenght 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.

When mixed with shellac-lac in the proportion of one part to five, borax renders that resinous body soluble in water, and forms with it a species of varnish.

Boracic acid is a compound of 31*19 of boron, and 68*81 oxygen, in 100 parts. Its prime equivalent referred to oxygen 100, is 871*96.

The following process for refining the native Indian borax or tincal, has been published by MM. Robiwuet and Marchand: -

It is put into large tabs, covered with water for 3 or 4 inches above its surface, and stirred through it several times during six hours. For 400 pounds of the tincal, there must bow be added one pound of quicklime diffused through two quarts of water. Next day the whole is thrown upon a sieve, to drain off the water with the impurities, consisting, in some measure, of the fatty matter combined with lime, as an insoluble soap. The borax, so far purified, is to be dissolved in 2½ times its weight of boiling water, and eight pounds of muriate of lime are to be added for the above quantity of borax. The liquor is now filtered, evaporated to the density of 18° or 20° B. (1*14 to 1*16 sp. grav.), and set to crystallize in vessels shaped like inverted pyramids, and lined with lead. At the end of a few days, the crystallization being completed, the mother waters are drawn off, the crystals are detached and dried. The loss of weight in this operation is about 20 per cent.

The quantity of borax imported into the United Kingdom in 1835 was 335,224 pounds; whereof 122,022 pounds were exported. The duty is 10s. upon the refined, and 4s unrefined.

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