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of soda in powder. Only part of the salt will be dissolved, even after being agitated some time. Apply heat, and the whole of the salt will disappear. When the liquor cools, a portion of salt will separate again in a regular form or in crystals. This last appearance affords an instance of crystallization.

To this law, however, there are several exceptions; for many salts, among which is muriate of soda, or common salt, are equally, or nearly equally, soluble in cold as in hot water. (See the table of solubility of salts in water, in the Appendix.) Hence, a hot, and saturated solution of muriate of soda does not, like the sulphate, deposit crystals on cooling. To obtain crystals of the muriate, and of other salts which observe a similar law as to solubility, it is necessary to evaporate a portion of the water; and the salt will then be deposited, even while the liquor remains hot. In general, the more slow the cooling, or evaporation, of saline solutions, the larger and more regular are the crystals.

V. A very minute division of bodies is effected by solution.— Dissolve two grains of sulphate of iron in a quart of water, and add a few drops of this solution to a wine-glassful of water, into which a few drops of tincture of galls have been stirred. The dilute infusion of galls will speedily assume a purplish hue. This shows that every drop of the quart of water, in which the sulphate of iron was dissolved, contains a notable portion of the salt.

VI. Some bodies dissolve much more readily and copiously than others. Thus, an ounce measure of distilled water will dissolve half its weight of sulphate of ammonia, one third its weight of sulphate of soda, one sixteenth of sulphate of potash, and only one five-hundredth its weight of sulphate of lime.

VII. Mechanical agitation facilitates solution.-Into a wineglassful of water, tinged blue with the infusion of litmus, let fall a small lump of solid tartaric acid. The acid, if left at rest, even during some hours, will only change to red that portion of the infusion which is in immediate contact with it. Stir the liquor, and the whole will immediately become red. VIII. Bodies do not act on each other, unless either one or both be in a state of solution, or at least contain water.-1. Mix some

dry tartaric acid with dry bi-carbonate of soda, and grind them together in a mortar. No combination will ensue till water is added, which, acting the part of a solvent, promotes the union of the acid and alkali, as appears from a violent effervescence. It has been shown by Link,* that the water of crystallization, existing in certain salts, acts as free water in occasioning chemical action. For example, acetate of lead and sulphate of copper, both in crystals, become green when triturated together, a proof of the mutual decomposition of those two salts.

2. Spread thinly, on a piece of tinfoil, three or four inches square, some dry nitrate of copper, and wrap it up. No effect will follow. Unfold the tinfoil, and having sprinkled the nitrate of copper with the smallest possible quantity of water, wrap the tinfoil up again as quickly as possible, pressing down the edges closely. Considerable heat, attended with fumes, will now be excited; and, if the experiment has been dexterously managed, even light will be evolved. This shows that nitrate of copper has no action on tin, unless in a state of solution.

IX. Bodies, even when in a state of solution, do not act on each other at perceptible distances; in other words, contiguity is essential to the action of chemical affinity. Thus, when two fluids of different specific gravities, and which have a strong affinity for each other, are separated by a thin stratum of a third, which exerts no remarkable action on either, no combination ensues between the uppermost and lowest stratum. Into a glass jar, or deep ale glass, pour two ounce-measures of a solution of subcarbonate of potash, containing, in that quantity, two drachms of common salt of tartar. Under this introduce, very carefully, half an ounce-measure of water, holding in solution a drachm of common salt; and again, under both these, two ounce-measures of sulphuric acid, which has been diluted with an equal weight of water, and allowed

Thomson's Annals, vii. 426.

↑ To prepare nitrate of copper, dissolve the filings or turnings of that metal in a mixture of one part nitrous acid and three parts water; decant the liquor when it has ceased to emit fumes: and evaporate it to dryness, in a copper or earthen dish. The dry mass must be kept in a bottle.

to become cool. The introduction of a second and third liquid beneath the first, is best effected, by filling, with the liquid to be introduced, the dropping tube, fig. 15. pl. i. which may be done by the action of the mouth. The finger is then pressed on the upper orifice of the tube; and the lower orifice, being brought to the bottom of the vessel containing the liquid, the finger is withdrawn, and the liquid descends from the tube, without mingling with the upper strátum. When a solution of carbonate of potash is thus separated from diluted sulphuric acid, for which it has a powerful affinity, by the intervention of a thin stratum of brine, the two fluids will remain distinct and inefficient on each other; but, on stirring the mixture, a violent effervescence ensues, in consequence of the action of the sulphuric acid on the potash.

X. Two bodies, having no affinity for each other, unite by the intervention of a third. Thus, the oil and water which, in Experiment I., could not, by agitation, be brought into union, unite immediately on adding a solution of caustic potash. The alkali, in this case, acts as an intermedium. The fact, indeed, admits of being explained by the supposition, that the oil and alkali form, in the first instance, a compound which is soluble

in water.

XI. Saturation and neutralization illustrated.-Water, after having taken up as much common salt as it can dissolve, is said to be saturated with salt. Muriatic acid, when it has ceased to act any longer on lime, is said to be neutralized, as is also the lime.

XII. The properties characterizing bodies, when separate, are destroyed by chemical combination, and new properties appear in the compound. Thus, muriatic acid and lime, which, in a separate state, have each a most corrosive taste, lose this entirely when mutually saturated; the compound is extremely soluble, though lime itself is very difficult of solution; the acid no longer reddens syrup of violets; nor does the lime change it, as before, to green. The resulting compound, also, muriate of lime, exhibits new properties. It has an intensely bitter taste; is susceptible of a crystallized form; and the crystals, when mixed with snow or ice, generate a degree of cold sufficient to freeze quicksilver.

XIII. Single elective affinity illustrated.-1. Add to the combination of oil with alkali, formed in Experiment X., a little diluted sulphuric acid. The acid will seize the alkali, and set the oil at liberty, which will rise to the top. In this instance, the affinity of alkali for acid is greater than that of alkali for oil. 2. To a dilute solution of muriate of lime (prepared in Experiment II.), add a little of the solution of pure potash. The potash will seize the muriatic acid, and the lime will fall down, or be precipitated.

XIV. In every instance, in comparing the affinities of two bodies for a third, a weaker affinity, in one of the two compared, will be found to be compensated by increasing its quantity.—It is not easy to offer clear and unequivocal examples of this law, and such as the student may submit to the test of experiment. The following, however, may illustrate the proposition sufficiently: Mingle together, in a mortar, one part of muriate of soda (common salt) with half a part of red oxide of lead (litharge, or red lead), and add sufficient water to form a thin paste. The oxide of lead, on examining the mixture after twenty-four hours, will be found not to have detached the muriatic acid from the soda; for the strong taste of that alkali will not be apparent. Increase the weight of the oxide of lead to three or four times that of the salt; and, after the same interval, the mixture will exhibit, by its taste, marks of uncombined soda. This proves, that the larger quantity of the oxide must have detached a considerable portion of muriatic acid from the soda, though the oxide has a weaker affinity for that acid than the soda possesses.

Another illustration of the same general principle has been suggested by Berzelius. It is necessary to premise, that the colour of the compound of sulphuric acid with oxide of copper is blue, and that of muriatic acid with the same oxide, green. To a saturated solution of sulphate of copper in water, add by degrees concentrated muriatic acid. Every addition will render the colour of the liquid more distinctly green, showing an increased production of muriate of copper; the oxide of copper being divided between the sulphuric and muriatic acids, in proportion to the quantity of each acid that is present.

XV. Double elective affinity exemplified.-In a watery solution of sulphate of zinc, immerse a thin sheet of lead: the lead will remain unaltered, as also will the sulphate of zinc, because zinc attracts sulphuric acid more strongly than lead. But let a solution of acetate of lead be mixed with one of sulphate of zinc; the lead will then go over to the sulphuric acid, while the zinc passes to the acetic. The sulphate of lead being insoluble, will fall down in the state of a white powder; but the acetate of zinc will remain in solution. The changes that occur in this experiment will be better understood from the following scheme:

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The vertical brackets include the original compounds, viz. sulphate of zinc, and acetate of lead; and the horizontal line and bracket point out the new ones, viz. acetate of zinc and sulphate of lead. By the upper horizontal line, it is denoted, that the acetate of zinc remains in solution; and, by the point of the lower bracket being directed downwards, it is meant to express, that the sulphate of lead falls down, or is precipitated.

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