Discoveries and Inventions of the Nineteenth Century

it was obtained by distilling indigo with potash, and hence received its present name from anil, the Portuguese for indigo. The quantity of aniline contained in the tar is quite insignificant. Aniline is prepared from nitro-benzol on the large scale by heating it with acetic acid and iron filings or iron borings, a process which rapidly changes the nitro-benzol into aniline. The equation representing the change is— C6H5NO2 + H6 = C6H5H2N + 2H2O. Nitro-benzol. Hydrogen. Aniline. Water. The operation is effected in the apparatus represented in Fig. 355. It consists of a large iron cylinder, within which works a paddle on a vertical revolving spindle, which, being hollow, is also a pipe to convey high pressure steam within the apparatus. Fig. 356 is a section of the hollow spindle, in which f is the pivot at the bottom of the cylinder on which it turns; d is the stirring paddle; e is an aperture admitting the steam from the pipe, c, forming the shaft of the paddle, which is made to revolve by the bevil-wheel. The steams enters by the elbow-pipe, which has a nozzle ground to fit the head of the vertical revolving pipe, upon which it is pressed down by the screw. When the materials have been introduced into the cylinder, the stirrer is set in motion, and superheated steam is sent down the pipe; the aniline is volatilized and passes with the steam through the pipe, which is connected with a worm surrounded by cold water. The aniline is purified by another distillation over lime or soda. When pure, aniline is a colourless, somewhat oily-looking liquid, of a feeble aromatic odour. Under the influence of light and air it becomes of a brownish tint, in which condition it usually presents itself in commerce. It scarcely dissolves in water, but is readily soluble in alcohol, ether, &c. Fig. 356.—Section of Hollow Spindle,—Aniline Apparatus. It was Mr. Perkin who, in 1856, first obtained from aniline a substance 788practically available for dyeing. Let it be noticed that when Mr. Perkin discovered aniline purple, he was not engaged in searching for dye-stuffs, but was carrying on a purely scientific investigation as to the possibility of artificially preparing quinine. With this view, having selected a substance into the composition of which nitrogen, hydrogen, and carbon enter in exactly the same proportions as they occur in quinine, but differing from it by containing no oxygen, he thought it not improbable that by oxidizing this body he might obtain quinine. In this he was disappointed, for the result was a dirty reddish-brown powder. Being desirous, however, of understanding more fully the nature of this reddish powder, he proceeded to try the effects of oxidation on other similarly constituted but more simple bodies. For this purpose he fortunately selected aniline, which, when treated with sulphuric acid and bichromate of potash, he found to yield a perfectly black product. Persevering in his experiments by examining this black substance, he obtained, by digesting it with spirits of wine, the now well-known “aniline purple.” Mr. Perkin, having determined to make the aniline purple on the large scale, patented his process, and succeeded in overcoming the many obstacles incident to the establishment of a new manufacture requiring as its raw material products not at that time met with as commercial articles. The process is now carried on the large scale by mixing sulphuric acid and aniline in the proportions in which they combine to form the sulphate of aniline, and dissolving by boiling with water in a large vat. Bichromate of potash is dissolved in water in another large vat. When both solutions are cold, they are mixed together in a still larger vessel and allowed to stand a day or two. A fine black powder settles on the bottom of the vessel in large quantities; this is collected in filters, washed with water, and dried. This powder is not aniline purple alone, but a mixture of this with other products, presenting a very unpromising appearance; but when it has been digested for some time with diluted methylated spirit, all the colouring matter is dissolved out, and is obtained from the solution by placing the latter in a still, where the spirit is distilled off and collected for future use, while all the colouring matter remains behind, held in solution by the water. From this aqueous solution the mauve is thrown down by adding caustic soda. It is collected, washed, and drained until of a pasty consistence, in which condition it is sent into the market. It can be obtained in crystals, but the commercial article is seldom required in this form, as the additional expense is not compensated by any superiority in the practical applications of the colour. Mauve is readily soluble in spirits of wine, but not very soluble in water. Its tinctorial power is so great that one-tenth of a grain suffices to impart quite a deep colour to a gallon of water. Silk and woollen fabrics have an extraordinary attraction for this colouring matter, which attaches itself very firmly to their fibres. If some white wool is dipped into even a very dilute solution, the colour is quickly absorbed. Mauve is more permanent than any other coal-tar colour, being little affected by the prolonged action of light. Mauve is chemically a salt of a base which has been termed “mauveine.” Mauveine itself is a nearly black crystalline powder, which forms solutions of a dull blue-violet tint, but when an acid is added to such a solution the tint is at once changed to purple. Mauveine is a powerful base, displacing ammonia from its compounds. The commercial crystallized mauve is the acetate of mauveine. The process by which Mr. Perkin originally obtained mauve from aniline evidently depends upon the well-known oxidizing property of bichromate 789of potash, and experiments were accordingly made with other, oxidizing bodies and aniline; in fact, patents were taken out for the use of nearly every known oxidizing chemical. Three years after Mr. Perkin’s discovery of mauve, M. Verguin, of Lyons, obtained, by treating crude aniline with chloride of tin, the bright red colouring matter now known as magenta. It was found also that crude aniline, when treated with other metallic chlorides, nitrates, or other salts, which are oxidizing agents less powerful than bichromate of potash, yields this bright red colouring matter. A process patented by Medlock, in 1860, in which arsenic acid is the oxidizing agent, has almost entirely superseded, in England at least, all the others yet proposed for the manufacture of magenta. It is not a little remarkable that magenta would not have been discovered had M. Verguin and others operated on pure aniline instead of on the ordinary commercial article. For it was found subsequently by Dr. Hofman that pure aniline cannot be made to yield magenta: the presence of another body is necessary. A reference to the table of coal-tar constituents will show that there is a hydro-carbon named “toluol.” This substance is of a similar nature to benzol, and has a boiling-point so little above that of benzol, that in the rough methods of separation usually employed, a notable quantity of toluol is carried over with the benzol, and is always present in the commercial article. In the processes which benzol undergoes for conversion into aniline, the toluol accompanies it in a series of parallel transformations, resulting in the production of a base termed “toluidine”—similar to aniline—being, however, in its pure state a solid at ordinary temperatures. We write down the symbols representing the composition of the bodies formed in the two cases in order to clearly show this: Benzol C6H6 Nitro-benzol C6H5(NO2) Aniline C6H5NH2 Toluol C7H8 Nitro-toluol C7H7(NO2) Toluidine C7H7NH2 This aniline prepared from commercial benzol always contains some toluidine; and it is essential for the production of magenta that this substance should be operated on along with the aniline. Whether the presence of some toluidine is also necessary for the production of mauve and other colours is not yet known, but they are always prepared from commercial benzol. It is certain that pure aniline yields no magenta, neither does pure toluidine; but a mixture supplies it in abundance. For the preparation of magenta the best proportions for this mixture would be about three parts of aniline to one of toluidine; but, in practice, it is not necessary to obtain the two substances separately, as benzol, mixed with a sufficient quantity of toluol, may be obtained by regulating the distillation. The apparatus used in the production of magenta is shown in Fig. 352. It consists of a large iron pot set over a furnace in brickwork, and having a lid with a stuffing-box, through which passes a spindle carrying a stirrer. A bent tube rises from the lid, and is connected with a worm surrounded by cold water, for the purpose of condensing the aniline which is vapourized in the process. The aniline, containing a due amount of toluidine, is mixed in this apparatus with about one and a half times its weight of a saturated solution of arsenic acid (H3AsO4). The fire is lighted and kept up for several hours: water first, and lastly aniline, distil over. When the operation is ended, steam is blown through the apparatus, thus carrying off an additional portion of aniline. The crude product is then boiled with water, the solution filtered, 790and common salt added, which precipitates an impure magenta. This is afterwards dissolved and recrystallized several times. The crystals of this magenta—like those of many of the coal-colour products—have a peculiar greenish metallic lustre; they dissolve in warm water, forming a deep purplish-red solution. The chemical composition of magenta has been investigated by Dr. Hofman, who found it to be a salt of an organic base, to which he gave the name of “rosaniline.” This rosaniline is easily obtained from magenta by addition to its solution of an alkali. While all its salts are intensely coloured, rosaniline itself is a perfectly colourless substance, becoming reddened by exposure to the air, as it absorbs carbonic acid, thus passing to the condition of a salt. Rosaniline, then, displays its chromatic powers only when it is combined with an acid. This property is sometimes shown at lectures in a striking manner by dipping a piece of paper into a colourless solution of rosaniline, and exposing it to the air, when, as the rosaniline absorbs carbonic acid, the paper changes from white to red. A more elegant form of the same experiment is to dip a white rose into a solution of rosaniline containing a little ammonia. As the ammonia escapes, or is expelled by a current of warm air, the same kind of action occurs, and the white rose changes to red—as if by magic, the emblem of the House of York is transformed into the badge of Lancaster! The chemical nature of rosaniline is regarded as analogous to that of ammonia—it is, in fact, looked upon by chemists as a sort of ammonia, in each particle of which some atoms of hydrogen have been replaced by certain groups of carbon and hydrogen atoms—some of these groups being derived from the aniline and others from the toluidine. The particular salt of rosaniline which constitutes the crude product of the action on the aniline and toluidine, depends on the substance employed to effect the oxidation. If a chloride, the resulting product is chloride of rosaniline; if a nitrate, it is the nitrate; and so on. The magenta which is formed in the first instance by the process we have described is an arseniate of rosaniline; but in the subsequent processes, it is converted into the chloride—the salt usually sold as magenta. Other salts of rosaniline are made on the large scale—especially the acetate, the beautiful crystals of which have the advantage of being very soluble. Magenta attaches itself strongly to animal fibres, but the colour is somewhat fugacious under the action of sunlight. It is used not only as a dye, but more largely as the raw material from which a number of