MOLASSE, is a sandstone belonging to the tertiary strata, employed under that name by the Swiss for building.

MOLASSES, is the brown viscid uncrystallizable liquor, which drains from cane sugar in the colonies. See [Sugar].

MOLYBDENUM (Molybdène, Fr.; Molybdan, Germ.); is a rare metal which occurs in nature sometimes as a sulphuret, sometimes as molybdic acid, and at others as molybdate of lead. Its reduction from the acid state by charcoal requires a very high heat, and affords not very satisfactory results. When reduced by passing hydrogen over the ignited acid, it appears as an ash-gray powder, susceptible of acquiring metallic lustre by being rubbed with a steel burnisher; when reduced and fused with charcoal, it possesses a silver white colour, is very brilliant, hard, brittle, of specific gravity 8·6; it melts in a powerful air-furnace, oxidizes with heat and air, burns at an intense heat into molybdic acid, dissolves in neither dilute sulphuric, muriatic, nor fluoric acids, but in the concentrated sulphuric and nitric.

The protoxide consists of 85·69 of metal, and 14·31 of oxygen; the deutoxide consists of 75 of metal, and 25 of oxygen; and the peroxide, or molybdic acid, of 66·6 of metal, and 33·4 of oxygen. These substances are too rare at present to be used in any manufacture.

MORDANT, in dyeing and calico-printing, denotes a body which, having a twofold attraction for organic fibres and colouring particles, serves as a bond of union between them, and thus gives fixity to dyes; or it signifies a substance which, by combining with colouring particles in the pores of textile filaments, renders them insoluble in hot soapy and weak alkaline solutions. In order properly to appreciate the utility and the true functions of mordants, we must bear in mind that colouring matters are peculiar compounds possessed of certain affinities, their distinctive characters being not to be either acid or alkaline, and yet to be capable of combining with many bodies, and especially with salifiable bases, and of receiving from each of them modifications in their colour, solubility, and alterability. Organic colouring substances, when pure, have a very energetic attraction for certain bodies, feeble for others, and none at all for some. Among these immediate products of animal or vegetable life, some are soluble in pure water, and others become so only through peculiar agents. We may thus readily conceive, that whenever a dye-stuff possesses a certain affinity for the organic fibre, it will be able to become fixed on it, or to dye it without the intervention of mordants, if it be insoluble by itself in water, which, in fact, is the case with the colouring matters of safflower, annotto, and indigo. The first two are soluble in alkalis; hence, in order to use them, they need only be dissolved in a weak alkaline lye, be thus applied to the stuffs, and then have their tinctorial substance precipitated within their pores, by abstracting their solvent alkali with an acid. The colouring matter, at the instant of ceasing to be liquid, is in an extremely divided state, and is in contact with the organic fibres for which it has a certain affinity. It therefore unites with them, and, being naturally insoluble in water, that is, having no affinity for this vehicle, the subsequent washings have no effect upon the dye. The same thing may be said of indigo, although its solubility in the dye-bath does not depend upon a similar cause, but is due to a modification of its constituent elements, in consequence of which it becomes soluble in alkalis. Stuffs plunged into this indigo bath get impregnated with the solution, so that when again exposed to the air, the dyeing substance resumes at once its primitive colour and insolubility, and washing can carry off only the portions in excess above the intimate combination, or which are merely deposited upon the surface of the stuff.

Such is the result with insoluble colouring matters; but for those which are soluble it should be quite the reverse, since they do not possess an affinity for the organic fibres which can counterbalance their affinity for water. In such circumstances, the dyer must have recourse to intermediate bodies, which add their affinity for the colouring matter to that possessed by the particles of the stuff, and increase by this twofold action the intimacy and the stability of the combination. These intermediate bodies are the true mordants.

Mordants are in general found among the metallic bases or oxides; whence they might be supposed to be very numerous, like the metals; but as they must unite the twofold condition of possessing a strong affinity for both the colouring matter and the organic fibre, and as the insoluble bases are almost the only ones fit to form insoluble combinations, we may thus perceive that their number may be very limited. It is well known, that although lime and magnesia, for example, have a considerable affinity for colouring particles, and form insoluble compounds with them, yet they cannot be employed as mordants, because they possess no affinity for the textile fibres.

Experience has proved, that of all the bases, those which succeed best as mordants are alumina, tin, and oxide of iron; the first two of which, being naturally white, are the only ones which can be employed for preserving to the colour its original tint, at least without much variation. But whenever the mordant is itself coloured, it will cause the dye to take a compound colour quite different from its own. If, as is usually said, the mordant enters into a real chemical union with the stuff to be dyed, the application of the mordant should obviously be made in such circumstances as are known to be most favourable to the combination taking place; and this is the principle of every day’s practice in the dyehouse.

In order that a combination may result between two bodies, they must not only be in contact, but they must be reduced to their ultimate molecules. The mordants that are to be united with stuffs are, as we have seen, insoluble of themselves, for which reason their particles must be divided by solution in an appropriate vehicle. Now this solvent or menstruum will exert in its own favour an affinity for the mordant, which will prove to that extent an obstacle to its attraction for the stuff. Hence we must select such solvents as have a weaker affinity for the mordants than the mordants have for the stuffs. Of all the acids which can be employed to dissolve alumina, for example, vinegar is the one which will retain it with least energy, for which reason the acetate of alumina is now generally substituted for alum, because the acetic acid gives up the alumina with such readiness, that mere elevation of temperature is sufficient to effect the separation of these two substances. Before this substitution of the acetate, alum alone was employed; but without knowing the true reason, all the French dyers preferred the alum of Rome, simply regarding it to be the purest; it is only within these few years that they have understood the real grounds of this preference. This alum has not, in fact, the same composition as the alums of France, England, and Germany, but it consists chiefly of cubic alum having a larger proportion of base. Now this extra portion of base is held by the sulphuric acid more feebly than the rest, and hence is more readily detached in the form of a mordant. Nay, when a solution of cubic alum is heated, this redundant alumina falls down in the state of a subsulphate, long before it reaches the boiling point. This difference had not, however, been recognised, because Roman alum, being usually soiled with ochre on the surface, gives a turbid solution, whereby the precipitate of subsulphate of alumina escaped observation. When the liquid was filtered, and crystallized afresh, common octahedral alum alone was obtained; whence it was most erroneously concluded, that the preference given to Roman alum was unjustifiable, and that its only superiority was in being freer from iron.