The mechanical relations are to be found in the apparatus employed for wincing, siring, and pressing the goods, as we have described under [Calico Printing] and [Bandanna]. The hydraulic relations refer to the wash-wheels and other similar apparatus, of which an account is given under the same articles. The optical relations have been already considered. In the sequel of this article an automatic dyeing vat will be described.
The extracts of solutions of native dye-stuffs may be divided into two classes, in reference to their habitudes with the oxygen of the atmosphere; such as continue essentially unaltered in the air, and such as suffer oxidation, and thereby precipitate a determinate colouring matter. The dyes contained in the watery infusions of the different vegetable and animal substances which do not belong to the second class, are feebly attached to their solvents, and quit them readily for any other bodies that possess an attraction for them. On this principle, a decoction of cochineal, logwood, brazil wood, or a solution of sulphate of indigo, by digestion with powdered bone black, lose their colour, in consequence of the colouring particles combining by a kind of capillary attraction with the porous carbon, without undergoing any change. The same thing happens when well-scoured wool is steeped in such coloured liquids; and the colours which the wool assumes by its attraction for the dye, is, with regard to most of the above coloured solutions, but feeble and fugitive, since the dye may be again abstracted by copious washing with simple water, whose attractive force therefore overcomes that of the wool. The aid of a high temperature, indeed, is requisite for the abstraction of the colour from the wool and the bone-black, probably by enlarging the size of the pores, and increasing the solvent power of the water.
Those dye-baths, on the contrary, whose colouring matter is of the nature of extractive or apothème, form a faster combination with stuffs. Thus the yellow, fawn, and brown dyes, which contain tannin and extractive, become oxygenated by contact of air, and insoluble in water; by which means they can impart a durable dye. When wool is impregnated with decoctions of that kind, its pores get charged by capillarity, and when the liquid becomes oxygenated, they remain filled with a colour now become insoluble in water. A similar change to insolubility ensues when the yellow liquor of the indigo vat gets oxidized in the pores of cotton and wool, into which it had been introduced in a fluid state. The same change occurs when protosulphate of iron is converted into persulphate, with the deposition of an insoluble peroxide in the substance of the stuff. The change here effected by oxidation can, in other circumstances, be produced by acids which have the power of precipitating the dye-stuff in an insoluble state, as happens with decoction of fustic.
Hence we perceive that the dyeing of fast colours rests upon the principle, that the colours dissolved in the vat, during their union with the stuff, should suffer such a change as to become insoluble in their former menstruum. The more this dye, as altered in its union with the stuff, can resist other menstrua or agents, the faster it will be. This is the essential difference between dyeing and painting; or applying a coat of pigment devoid of any true affinity for the surface.
If we mix a clear infusion of a dye with a small quantity of a solution of an earthy or metallic salt, both in water, the limpid liquids soon become turbid, and there gradually subsides sooner or later, according to the nature of the mixture, a coloured precipitate, consisting of the altered dye united with a basic or subsalt. In this compound the colouring matter seems to act the part of an acid, which is saturated by a small quantity of the basis, or in its acid relationship is feeble, so that it can also combine with acids, being in reference to them a base. The decomposition of a salt, as alum, by dyes, is effected principally through the formation of an insoluble subsalt, with which the colour combines, while a supersalt remains in the bath, and modifies, by its solvent reaction, the shade of the dyed stuff. Dyed stuffs may be considered as composed of the fibrous body intimately associated with the colouring matter, the oxide, and acid, all three constituting a compound salt. Many persons have erroneously imagined, that dyed goods contained none of the acid employed in the dye bath; but they forget that even potash added to alum does not throw down the pure earthy basis, but a subsalt; and they should not ascribe to colouring matter a power of decomposition at all approaching to that of an alkali. Salts, containing strong acids, saturate a very large quantity of colouring matter, in proportion to their place in the scale of chemical equivalents. Mere bases, such as pure alumina, and pure oxide of tin, have no power of precipitating colouring matter; when they seem to do so, they always contain some acid.
Such salts, therefore, as have a tendency to pass readily into the basic state, are peculiarly adapted to act as mordants in dyeing, and to form coloured lakes. Magnesia affords as fine a white powder as alumina, and answers equally well to dilute lakes, but its soluble salts cannot be employed to form lakes, because they do not pass into the basic state. This illustration is calculated to throw much light upon dyeing processes in general.
The colour of the lake depends very much upon the nature of the acid, and the basis of the precipitating salt. If it be white, like alumina and oxide of tin, the lake will have, more or less, the colour of the dye, but brightened by the reflection of white light from the basis; while the difference of the acid occasions a difference in the hue. The coloured bases impart more or less of their colour to the lakes, not merely in virtue of their own tints, but of their chemical action upon the dye.
Upon these principles a crimson precipitate is obtained from infusions of cochineal by alum and salt of tin, which becomes scarlet by the addition of tartar; by acetate of lead, a violet blue precipitate is obtained, which is durable in the air; by muriate of lime, a pink brown precipitate falls, which soon becomes black, and at last dirty green; by the solution of a ferruginous salt, the precipitates are dark violet, and black; and, in like manner, all other salts with earthy or metallic bases, afford diversities of shade with cochineal. If this dye stuff be dissolved in weak water of ammonia, and be precipitated with acetate of lead, a green lake is obtained, which, after some time, will become green on the surface by contact of air, but violet and blue beneath. Hence it appears, that the shade of colour of a lake depends upon the degree of oxidation or change of the colour caused by the acid of the precipitating salt, upon the degree of oxidation or colour of the oxide which enters into union with the dye, and upon its quantity in reference to that of the colouring principle.
Such lakes are the difficultly soluble salts which constitute the dyeing materials of stuffs. Their particles, however, for the purposes of dyeing, must exist in a state of extremely fine division in the bath liquor, in order that they may penetrate along with it into the minute pores of textile fibres, and fill the cavities observed by means of the microscope in the filaments of wool, silk, cotton, and flax. I have examined these stuffs with an achromatic microscope, and find that when they are properly dyed with fast colours, the interior of their tubular texture is filled, or lined at least, with colouring matter. When the bath contains the colouring particles, so finely divided that they can pass through filtering paper, it is capable of dyeing; but if the infusion mixed with its mordant be flocculent and ready to subside, it is unfit for the purpose. In the latter case, the ingredients of the dye have already become aggregated into compounds too coherent and too gross for entering into combination with fibrous stuffs. Extractive matter and tannin are particularly liable to a change of this kind, by the prolonged action of heat in the bath. Hence also an alkaline solution of a colouring matter, affords no useful dye bath, when mixed with the solution of a salt having an earthy or metallic basis.
These circumstances, which are of frequent occurrence in the dye-house, render it necessary always to have the laky matter in a somewhat soluble condition, and to effect its precipitation within the pores of the stuffs, by previously impregnating them with the saline solutions by the aid of heat, which facilitates their introduction.