The most usual method of separating Copper from the Vitriolic Acid is by presenting to that Acid a metal with which it hath a greater affinity than with Copper. Iron being so qualified is consequently very fit to bring about this separation. When therefore plates of Iron well cleaned are laid in a solution of Blue Vitriol, the Acid soon begins to act upon them, and by degrees, as it dissolves them, deposites on their surfaces a quantity of Copper in proportion to the quantity of Iron it takes up. The Copper thus precipitated hath the appearance of small leaves or scales, exceeding thin, and of a beautiful copper-colour. Care must be taken to shake the Iron-plates now and then, to make the scales of Copper fall off, which will otherwise cover them entirely, hinder the Vitriolic Acid from attacking the Iron, and so put a stop to the precipitation of the remaining Copper.

When these scales of Copper cease to settle on the clean Iron plates, you may be sure all the Copper that was in the liquor is precipitated, and that this liquor, which was a solution of Copper before the precipitation, is a solution of Iron after it. So that here two operations are performed at one and the same time; to wit, the precipitation of the Copper, and the dissolution of the Iron.

The Copper thus precipitated requires only to be separated from the liquor by filtration, and melted with a little black flux, to become very fine malleable Copper.

The Copper may also be precipitated out of a solution of Blue Vitriol by the interposition of a Fixed Alkali. This precipitate is of a greenish blue colour, and requires a much greater quantity of the black flux to reduce it.

Copper dissolves in the Nitrous Acid, in the Marine Acid, and in Aqua regis; from all of which it may be separated by the same methods as are here ordered with regard to the Vitriolic Acid.


CHAP. IV.

Of Iron.

PROCESS I.

To separate Iron from its Ore.

Pound into a coarse powder the martial stones or earths out of which you design to extract the Iron: roast this powder in a test under the muffle for some minutes, and let your fire be brisk. Then let it cool, beat it very fine, and roast it a second time, keeping it under the muffle till it emit no more smell.

Then mix with this powder a flux composed of three parts of Nitre fixed with Tartar, one part of fusile glass, and half a part of Borax and charcoal-dust. The dose of this reducing flux must be thrice the weight of the ore.

Put this mixture into a good crucible; cover it with about half a finger thick of Sea-salt; over the crucible put its cover, and lute it on with Windsor-loam made into a paste with water. Having thus prepared your crucible, set it in a melting furnace, which you must fill up with charcoal. Light the fire, and let it kindle by gentle degrees, till the crucible become red-hot. When the decrepitation of the Sea-salt is over, raise your fire to the highest by the blast of a pair of perpetual bellows, or rather several. Keep up this intense degree of heat for three quarters of an hour, or an whole hour, taking care that during all this time the furnace be kept constantly filling up with fresh coals as the former consume. Then take your crucible out of the furnace; strike the pavement on which you set it several times with a hammer, and let it stand to cool: break it, and you will find therein a Regulus of Iron covered with slag.

OBSERVATIONS.

Iron ore, like all others, requires roasting, to separate from it, as much as possible, the volatile minerals, Sulphur and Arsenic, which being mixed with the Iron would render it unmalleable. Indeed it is so much the more necessary to roast these ores, as Iron is, of all metallic substances, that which has the greatest affinity with those volatile minerals; on which account no metallic substance whatever is capable of separating it from them by fusion and precipitation.

Fixed Alkalis, it is true, have a greater affinity than Iron with Sulphur; but then the composition which a Fixed Alkali forms with Sulphur is capable of dissolving all metals. Consequently, if you do not dissipate the Sulphur by roasting, but attempt to separate it from the Iron by melting the ore with a Fixed Alkali, the Liver of Sulphur formed in the operation will dissolve the martial part; so that after the fusion you will find little or no Regulus.

All Iron ores in general are refractory, and less fusible than any other; for which reason a much greater proportion of flux, and a much more violent degree of fire, is required to smelt them. One principal cause why these ores are so refractory is the property which Iron itself has of being extremely difficult to fuse, and of resisting the action of the fire so much the more as it is purer, and further removed from its mineral state. Among all the metallic substances it is the only one that is less fusible when combined with that portion of phlogiston which gives it the metalline form, than when it is deprived thereof, and in the form of a calx.

In smelting-houses Iron ore is fused amidst charcoal, the phlogiston of which combines with the martial earth, and gives it the metalline form. The Iron thus melted runs down to the bottom of the furnace, from whence it is let out into large moulds, in which it takes the shape of oblong blocks, called Pigs of Iron. This Iron is still very impure, and quite unmalleable. Its want of ductility after the first melting arises partly from hence, that, notwithstanding the previous roasting which the ore underwent, there still remains, after this first fusion, a considerable quantity of Sulphur or Arsenic combined with the metal.

A certain quantity of quick-lime, or of stones that will burn to lime, is frequently mixed with Iron ore on putting it into the smelting furnace. The lime being an absorbent earth, very apt to unite with Sulphur and Arsenic, is of use to separate those minerals from the Iron.

It is also of use to mix some such matters with the ore, when the stones or earths which naturally accompany it are very fusible; for, as the Iron is of difficult fusion, it may happen that the earthy matters mixed with the Iron shall melt as easily as the metal, or perhaps more easily. In such a case there is no separation of the earthy from the metalline part, both of which melt and precipitate together promiscuously; now quick-lime, being extremely refractory, serves on this occasion to check the melting of those matters which are too fusible.

Yet quick-lime, notwithstanding its refractory quality, may sometimes be of use as a flux for Iron. This is the case when the ore happens to be combined with substances which, being united with lime, render it fusible: such are all arsenical matters, and even some earthy matters, which being combined with quick-lime make a fusible compound.

When the ore of an Iron mine is found difficult to reduce, it is usually neglected even though it be rich: because Iron being very common, people chuse to work those mines only whose ores are smelted with the most ease, and require the least consumption of wood.

Yet refractory ores are not to be altogether rejected, when another Iron ore of a different quality is found near them. For it often happens, that two several Iron ores, which being worked separately are very difficult to manage, and yield at last but bad metal, become very tractable, and yield excellent Iron, when smelted together: and accordingly such mixtures are often made at Iron-works.

The Iron obtained from ores by the first fusion may be divided into two sorts. The one, when cold, resists the hammer, doth not easily break, and is in some measure extensible on the anvil; but, if struck with a hammer when red-hot, flies into many pieces: this sort of Iron hath always a mixture of Sulphur in it. The other sort, on the contrary, is brittle when cold, but somewhat ductile when red-hot. This Iron is not sulphurated, is naturally of a good quality, and its brittleness arises from its metalline parts not being sufficiently compacted together.

Iron abounds so much, and is so universally diffused through the earth, that it is difficult to find a body in which there is none at all: and this hath led several Chymists, even men of great fame, into the error of thinking that they had transmuted into Iron several sorts of earths in which they suspected no Iron, by combining them with an inflammable matter; whereas, in fact, all they did was to give the metalline form to a true martial earth which happened to be mixed with other earths.

PROCESS II.

To render Pig-iron and brittle Iron malleable.

Into an earthen vessel widening upwards put some charcoal-dust, and thereon lay the Pig-iron which you propose to render ductile; cover it all over with a quantity of charcoal; excite the fire violently with a pair, or more, of perpetual bellows till the Iron melt. If it do not readily flow and form a great deal of slag on its surface, add some flux, such as a very fusible sand.

When the matter is in fusion keep stirring it from time to time, that all the parts thereof may be equally acted on by the air and the fire. On the surface of the melted Iron scoriƦ will be formed, which must be taken off as they appear. At the same time you will see a great many sparkles darted up from the surface of the metal, which will form a sort of fiery shower. By degrees, as the Iron grows purer, the number of these sparkles diminishes, though they never vanish entirely. When but few sparkles appear, remove the coals which cover the Iron, and let the slag run out of the vessel; whereupon the metal will grow solid in a moment. Take it out while it is still red-hot, and give it a few strokes with a hammer, to try if it be ductile. If it be not yet malleable, repeat the operation a second time, in the same manner as before. Lastly, when it is thus sufficiently purified by the fire, work it for a long time on the anvil, extending it different ways, and making it red-hot as often as there is occasion. Iron thus brought to the necessary degree of ductility, so as to yield to the hammer, and suffer itself to be extended every way, either hot or cold, without breaking to bits, or even cracking in the least, is very good and very pure. If it cannot be brought to this degree by the method here prescribed, it is a proof that the ore from which this Iron was extracted ought to be mixed with other ores; but it frequently requires a great number of trials to obtain an exact knowledge of the quality and proportion of those other ores with which it is to be mixed.

OBSERVATIONS.

The brittleness and shortness of Pig-iron arises from the heterogeneous parts which it contains, and which could not be separated from it by the first fusion. These extraneous matters are usually Sulphur, Arsenic, and unmetallic earth, and also a ferruginous earth; but such as could not be combined with the phlogiston as it ought to be, in order to have the properties of a metal, and must therefore be considered as heterogeneous, with respect to the other well-conditioned martial particles.

The Pig-iron, by undergoing repeated fusions, is freed from those heterogeneous matters; those which are volatile, such as Sulphur and Arsenic, being dissipated, and the unmetallic matters being scorified. As to the ferruginous earth, which did not at first acquire the metalline form, it becomes true Iron at last; because, among the coals with which it is encompassed, it meets with a sufficient quantity of phlogiston to reduce it to metal. Charcoal is also necessary on this occasion, that it may continually furnish phlogiston to the Iron, which would otherways be converted into a calx.

Hammering the red-hot Iron, after each fusion, serves to force out from amongst the martial parts such earthy matters as may happen to remain there, and so bring into closer contact the metalline parts which were separated before by the interposition of those heterogeneous matters.

PROCESS III.

To convert Iron into Steel.

Take small bars of the best Iron; that is, of such as is malleable both hot and cold; set them on their ends in a cylindrical earthen vessel, whose depth is equal to the length of the bars, and in such a manner that they may be an inch distant from each other, and from the sides of the crucible. Fill the vessel with a cement compounded of two parts of charcoal, one part of bones burnt in a close vessel till they become very black, and one half part of the ashes of green wood; having first pulverized and thoroughly mixed the whole together. Take care to lift up the Iron bars a little, to the end that the cement may cover the bottom of the vessel, and so that there be about the depth of half an inch thereof under every bar: cover the crucible and lute on the cover.

Set the crucible thus prepared in a furnace, so contrived that the crucible may be surrounded with coals from top to bottom: for eight or ten hours keep up such a degree of fire that the vessel may be moderately red; after this take it out of the furnace; plunge your little Iron bars into cold water, and you will find them converted into Steel.

OBSERVATIONS.

The principal difference between Iron and Steel consists in this, that the latter is combined with a greater quantity of phlogiston than the former.

It appears by this experiment, that, to make Iron unite with an inflammable matter, it is not necessary it should be in fusion; it is sufficient that it be so red-hot as to be opened and softened by the fire.

Every kind of charcoal is fit to be an ingredient in the composition of the cement employed to make Steel, provided it contain no Vitriolic Acid. However, it hath been observed, that animal coals produce a speedier effect than others: for which reason it is proper to mix something of that kind with charcoal-dust, as above directed.

The following signs shew that the operation hath succeeded, and that the Iron is changed into good Steel.

This metal being quenched in cold water, as proposed above, acquires such an extraordinary degree of hardness, that it will by no means yield to any impression of the file or hammer, and will sooner break in pieces than stretch upon the anvil. And here it is proper to observe, that the hardness of Steel varies with the manner in which it is quenched. The general rule is, that the hotter the Steel is when quenched, and the colder the water is in which you quench it, the harder it becomes. It may be deprived of the temper thus acquired, by making it red-hot, and letting it cool slowly; for it is thereby softened, rendered malleable, and the file will bite upon it. For this reason the artisans who work in Steel begin with untempering it, that they may with more ease shape it into the tool they intend to make. They afterwards new-temper the tool when finished, and by this second temper the Steel recovers the same degree of hardness it had acquired by the first temper.

The colour of Steel is not so white as that of Iron, but darker, and the grains, facets, or fibres, which appear on breaking it, are finer than those observed in Iron.

If the bars of Iron thus cemented in order to convert them into Steel be too thick, or not kept long enough in cementation, they will not be turned into Steel throughout their whole thickness: their surfaces only will be Steel to a certain depth, and the center will be mere Iron; because the phlogiston will not have thoroughly penetrated them. On breaking a bar of this sort, the difference in colour and grain between the Steel and the Iron is very visible.

It is easy to deprive Steel of the superabundant quantity of phlogiston which constitutes it Steel, and thereby reduce it to Iron. For this purpose it need only be kept red-hot some time, observing that no matter approach it all the while that is capable of refunding to it the phlogiston which the fire carries off. The same end is still sooner obtained by cementing it with meagre hungry matters, capable of absorbing the phlogiston; such as bones calcined to whiteness, and cretaceous earths.

Steel may also be made by fusion; or Pig-iron may be converted into Steel. For this purpose the same method must be employed as was above directed for reducing Pig-iron into malleable Iron; with this difference, that, as Steel requires more phlogiston than is necessary to Iron, all the means must be made use of that are capable of introducing into the Iron a great deal of phlogiston; such as melting but a small quantity of Iron at a time, and keeping it constantly encompassed with abundance of charcoal; reiterating the fusions; taking care that the blast of the bellows directed along the surface of the metal do not remove the coals that cover it, &c. And here it must be observed, that there are some sorts of Pig-iron which it is very difficult to convert into Steel by this method, and that there are others which succeed very readily, and with scarce any trouble at all. The ores which yield the last-mentioned sort of Pig-iron are called Steel Ores. Steel made by this means must be tempered in the same manner as that made by cementation[8].

PROCESS IV.

The Calcination of Iron. Sundry Saffrons of Mars.

Take filings of Iron, in what quantity you please; put them into a broad unglazed earthen vessel; set it under the muffle of a cupelling furnace; make it red-hot; stir the filings frequently; and keep up the same degree of fire till the Iron be wholly turned into a red powder.

OBSERVATIONS.

Iron easily loses its phlogiston by the action of fire. The calx that remains after its calcination is exceeding red; which makes this be thought the natural colour of the earth of that metal. It hath accordingly been observed, that all the earths and stones which either are naturally red, or acquire that colour by calcination, are ferruginous.

The yellowish red colour which every calx of Iron hath, in whatever manner it be prepared, hath procured the name of Crocus or Saffron to every preparation of this kind. That made in the manner above directed is called in Medicine Crocus Martis astringens.

The rust produced on the surface of Iron is a sort of calx of Iron made by way of dissolution. The moisture of the air acts upon the metal, dissolves it, and robs it of some of its phlogiston. This rust is called in Medicine Crocus Martis Aperiens; because it is thought that the saline parts, by means whereof the humidity dissolves the Iron, remain united with the metal after its dissolution, and give it an aperitive virtue. The Apothecaries prepare this sort of Saffron of Mars by exposing Iron filings to the dew, till they be turned entirely to rust: which is then called Saffron of Mars by dew.

Another Saffron of Mars is also prepared in a much shorter manner, by mixing filings of Iron with pulverized Sulphur, and moistening the mixture, which after some time ferments and grows hot. It is then set on the fire; the Sulphur burns away, and the mass is kept stirring till it become a red matter. This Saffron is nothing but Iron dissolved by the Acid of Sulphur, which is known to be of the same nature with that of Vitriol; and consequently this Saffron of Mars is no way differing from Vitriol calcined to redness.

PROCESS V.

Iron dissolved by the mineral Acids.

Put any mineral Acid whatever into a matrass with some water; set the matrass on a sand-bath gently heated; drop into the vessel some filings of Iron: the phenomena which usually accompany metalline dissolutions will immediately appear. Add more filings, till you observe the Acid hath lost all sensible action upon them: then remove your matrass from the sand-bath; you will find in it a solution of Iron.

OBSERVATIONS.

Iron is very easily dissolved by all the Acids. If you make use of the Vitriolic Acid, care must be taken to weaken it with water, in case it be concentrated; because the dissolution will succeed the better. The vapours that rise on this occasion are inflammable; and if a lighted paper be held to the mouth of the matrass, especially after keeping it stopt for some time and shaking the whole gently, the sulphureous vapours take fire with such rapidity as to produce a considerable explosion; which is sometimes strong enough to burst the vessel into a thousand pieces. This solution hath a green colour, and is in fact a fluid Green Vitriol, which wants nothing but rest to make it shoot into crystals.

If you make use of the Nitrous Acid, you must cease adding more filings when the liquor, after standing still some moments, becomes turbid; for, when this Acid is impregnated with Iron to a certain degree, it lets fall some of that which it had dissolved, and becomes capable of taking up fresh filings. Thus, by constantly adding new supplies of Iron, this Acid may be made to dissolve a much greater quantity thereof than is necessary to saturate it entirely. This solution is of a russet colour, and doth not crystallize.

If the weather be not extremely cold, and the Acids have a proper degree of strength, the sand-bath is unnecessary, as the dissolution will succeed very well without it.

Iron dissolved by Acids may be separated therefrom, like all other metallic substances in the same circumstances, either by the action of fire, which carries off the Acid and leaves the Martial Earth, or by the interposition of substances which have a greater affinity than metallic substances have with Acids; that is, by Absorbent Earths and Alkaline Salts. By whatever means you separate Iron from an Acid solvent, it constantly appears, after the separation, in the form of a yellowish red powder; because it is then deprived of most of the phlogiston to which it owed its metalline form; whence it is reasonable to think, that this is the proper colour of Martial earth.

All these precipitates of Iron are true Saffrons of Mars, which, as well as those prepared by calcination, are so much the further removed from the nature of a metal, the more they are deprived of their phlogiston. Thence it comes that they are more or less soluble by Acids, and more or less attracted by the magnet: as no ferruginous earth, perfectly deprived of all inflammable matter, is at all attracted by the magnet, or soluble by Acids.


CHAP. V.

Of Tin.

PROCESS I.

To extract Tin from its Ore.

Break your Tin ore into a coarse powder, and by washing carefully separate from it all the heterogeneous matters, and ores of a different kind, that may be mixed therewith. Then dry it, and roast it in a strong degree of fire, till no more Arsenical vapour rise from it. When the ore is roasted, reduce it to a fine powder, and mix it thoroughly with twice its weight of the black flux well dried, a fourth part of its weight of clean iron filings, together with as much borax and pitch; put the mixture into a crucible; over all put Sea-salt to the thickness of four fingers, and cover the crucible close.

Set the crucible thus prepared in a melting furnace: apply at first a moderate and slow degree of fire, till the flame of the pitch, which will escape through the joint of the cover, disappear entirely. Then suddenly raise your fire, and urge it with rapidity to the degree necessary for melting the whole mixture. As soon as the whole is in fusion take the crucible out of the furnace, and separate the Regulus from the scoria.

OBSERVATIONS.

All Tin ores contain a considerable quantity of Arsenic, and no Sulphur at all, or at most very little. Hence it comes that, though Tin be the lightest of all metals, its ore is nevertheless much heavier than any other; Arsenic being much heavier than Sulphur, of which the ores of every other kind always contain a pretty large proportion. This ore is moreover very hard, and is not brought to a fine powder with so much ease as the rest.

These properties of Tin ore furnish us with the means of separating it easily by lotion, not only from earthy and stony parts, but even from the other ores which may be mixed with it. And this is of the greater advantage on two accounts, viz. because Tin cannot endure, without the destruction of a great part thereof, the degree of fire necessary to scorify the refractory matters which accompany its ore; and again because this metal unites so easily with Iron and Copper, the ores of which are pretty commonly blended with Tin ore, that, after the reduction, it would be found adulterated with a mixture of these two metals, if they were not separated from it before the fusion.

But sometimes the Iron ore confounded with that of Tin is very heavy, and is not easily pulverized; whence it comes to pass that it cannot be separated therefrom by washing only. In that case the magnet must be employed to separate it, after the ore hath been roasted.

Roasting is moreover necessary for Tin ore, in order to dissipate the Arsenic which volatilizes, calcines, or destroys one part of the Tin, and reduces the rest to a short, brittle substance, like a Semi-metal. The ore is known to be sufficiently roasted when no more fumes rise from it; when it has lost the smell of garlic; and when it does not whiten a clean plate of Iron held over it.

Tin being one of those metals which are most easily calcined, it is necessary in reducing its ore to employ such matters as may furnish it with phlogiston. In order to defend it from the contact of the air, which always accelerates the calcination of metallic substances, the mixture is to be covered with Sea salt; and the addition of pitch helps to increase the quantity of phlogiston.

PROCESS II.

The Calcination of Tin.

Into an unglazed earthen dish put the quantity of Tin you intend to calcine; melt it, and keep stirring it from time to time. Its surface will be covered with a greyish white powder: continue the calcination till all your Tin be converted into such a powder, which is the Calx of Tin.

OBSERVATIONS.

Though the calcination of metalline substances is promoted by exposing them, in powder, or in filings, to the action of fire, and by ordering it so that they may not melt, because they present a much smaller surface when melted than when unmelted; yet we have not directed this precaution to be used in calcining Tin. The reason is, this metal is so fusible that it cannot endure the degree of fire requisite to destroy its phlogiston without melting, and of course, though Tin calcines easily, the operation is nevertheless tedious, because the melted metal presents but a small surface to be acted on by the fire and the air. This inconvenience may be partly remedied, and the operation greatly expedited, by dividing the quantity of Tin to be calcined into several small parcels, and exposing them to the fire in separate vessels, so that they may not re-unite when melted, and form one single mass.

Leaf Tin cast on Nitre in actual fusion causes it to deflagrate and fulminate; and from this mixture there rises a white vapour, which is converted into flowers when it meets with any obstacle to impede its flying off entirely.

Mr. Geoffroy, who went through a course of experiments on Tin, an account whereof may be seen in the Memoirs of the Academy of Sciences, found that from the colour of the calx of that metal a judgment may be formed of its degree of purity, and nearly of the quantity and quality of the metallic substances with which it is alloyed. The experiments tried on this subject by that eminent Chymist are very curious.

He performed the calcination in a crucible, which he heated to a cherry-red, and kept up the same degree of fire from the beginning to the end of the operation. The calx which formed upon his metal, in that degree of heat, appeared like small white scales, a little reddish on the under side. He pushed it to one side as it formed, to the end that it might not cover the surface of the metal, which, like all others, requires the contact of the air to turn it into a calx.

"While he was making these calcinations, he had an opportunity of observing a curious fact, of which no body before him had ever taken notice; probably because no body had ever calcined Tin by the same method. The fact is, that during the calcination of the Tin, whether you break the pellicle which forms on the surface of the metal while in red-hot fusion, or whether you let it remain without touching it, you perceive in several places a small swell of a certain matter, which bursts and makes its way through the pellicle. This matter puffs up, grows red, at the same instant takes fire, and darts out a small whitish flame, as vivid and as brilliant as that of Zinc, when urged by a fire strong enough to sublime it into flowers. The vividness of this flame may be further compared to that of several small grains of phosphorus of urine fired and gently dropped on boiling water. From this bright flame a white vapour exhales; after which the swelled mass partly crumbles down, and turns to a light white powder, sometimes spotted with red, according to the force of the fire. After this momentary ignition, there arise stronger, more numerous, or more frequent heavings of matter, out of which issues a good deal of white fume, that may be intercepted by a cover of tin-plate or copper fitted to the crucible, and appears to be the flowers of Tin, which in some measure corrode these metals. Hence Mr. Geoffroy conjectures, with a great deal of probability, that their sublimation is promoted by a portion of Arsenic. When the crust formed by this calx comes to be too thick, or in too great a quantity, to be pushed on one side, so as to leave part of the metal uncovered, Mr. Geoffroy puts out the fire, because no more calx would be formed: the communication of the external air with the Tin in fusion being absolutely necessary thereto, as hath been already said. In this operation it is to be observed that, if the fire be too slow, neither the inflammation of the sulphureous particles, nor the white fumes that rise, will be so distinctly perceived, as when the fire is of the degree requisite to keep the crucible just of a cherry-red heat.

"Mr. Geoffroy having taken off this first calx began the calcination anew. In this second heat the buddings or heavings were more considerable, and shot up in the form of cauli-flowers; but were still composed of little scales. The thoroughly calcined portion of this vegetation was likewise white and red; and the inferior surfaces of some little bits thereof were wholly red. When these calcinations are continued, sulphureous vapours rise seemingly of another kind than those which appeared in the beginning; for all the calx made by the first heat was perfectly white: whereas in the second it begins to be spotted here and there with a tinge of black. Mr. Geoffroy was obliged to go through a course of twelve several calcinations before he could convert two ounces of Tin into a calx. He had the opportunity, during these several calcinations, to observe that after the fourth, and sometimes after the third, the red spots of the calx decrease, and the black increase; that the germinations cease; that the crust of the calx remains flat; that in the twelfth fire the Tin yields no more of this scaly crust; that towards the end the undulations of the fused metal appear no longer; and that the small remainder of calx is mixed with several very minute grains of metal, which seem much harder than Tin. Mr. Geoffroy could not collect a sufficient quantity thereof to cupel them, and satisfy himself whether or no they were Silver."

Though Tin, and all the imperfect metals in general, seem converted to a calx, and lose the metalline form, by one single calcination, and that a slight one; yet they are not wholly deprived of their phlogiston: for if the calx of Tin, for instance, prepared according to the process above delivered, be cast upon Nitre in fusion, it will make that salt deflagrate very perceptibly; a convincing proof that it still contains much inflammable matter. If therefore a calx be required absolutely free from phlogiston, this first calx must be recalcined by a more violent fire, and the calcination continued till all the phlogiston be dissipated.

"Mr. Geoffroy, being desirous of having his calx of Tin very pure and perfectly calcined, exposed once more to the action of fire the twelve portions of calx obtained by his former calcinations. But, as it would have been too tedious to re-calcine them all separately, he made four parcels of the whole, each consisting of three taken according to the order in which they were first calcined; and gave to each a fire sufficiently strong, and long enough continued, to calcine them as thoroughly as was possible. After this second calcination he found them all of a most beautiful white, except the first parcel: as that consisted of the portions obtained by the three first heats, in all of which there were scales tinged with red, it still retained a stain of carnation, though hardly perceptible. Agreeably to the general rule, the two ounces of Tin gained in weight by being thus calcined; and the increase was two drams and fifty seven grains.

"Mr. Geoffroy observes, that no Tin, but what is absolutely pure, will yield a perfectly white calx. He calcined in this manner several other parcels of Tin that were impure and variously alloyed; each of which produced a calx differently coloured, according to the nature and quantity of its alloy: whence he justly concludes, that calcination is a very good method of trying the fineness of Tin, or its degree of purity." The particulars of Mr. Geoffroy's experiments on this subject, which are very curious, may be seen in the Memoirs of the Academy for 1738.

It is proper to take notice that a man should be very cautious how he exposes himself to the vapours of Tin, because they are dangerous; this metal being very justly suspected by Chymists of containing something Arsenical.

PROCESS III.

The dissolution of Tin by Acids, The Smoking Liquor of Libavius.

Put into a glass vessel what quantity you please of fine Tin cut into little bits. Pour on it thrice as much aqua regis, compounded of two parts aqua fortis weakened with an equal quantity of very pure water, and one part Spirit of Salt. An ebullition will arise, and the Tin will be very rapidly dissolved; especially if the quantities of metal and of aqua regis be considerable.

OBSERVATIONS.

Tin is soluble by all the Acids; but aqua regis dissolves it best of any. Yet in this dissolution it comes to pass that part of the dissolved Tin precipitates of its own accord to the bottom of the vessel, in the form of a white powder. This solution of Tin is very fit for preparing the purple-coloured precipitate of Gold. For this purpose the solution of Tin must be let fall, drop by drop, into a solution of Gold. Spirit of Nitre dissolves Tin nearly as aqua regis does; but it occasions a greater quantity of calx.

If two or three parts of Oil of Vitriol be poured on one part of Tin, and if the vessel in which the mixture is made be exposed to such a degree of heat as to evaporate all the moisture, there will remain a tenacious matter sticking to the sides of the vessel. If water be poured on this matter, and it be then exposed a second time to the fire, it will dissolve entirely, excepting a small portion of a glutinous substance, which also may be dissolved in fresh Oil of Vitriol.

The Acid of Sea-salt may be combined with Tin by the following process. Mix perfectly, by trituration in a marble mortar, an amalgam of two ounces of fine Tin, and two ounces and a half of Quick-silver, with as much Corrosive Sublimate. As soon as the mixture is completed, put it into a glass retort, and distil with the same precautions as we directed to be used in preparing concentrated and smoking Acids. There will first come over into the receiver some drops of a limpid liquor, which will be soon followed by an elastic spirit that will issue out with impetuosity. At last some flowers, and a saline tenacious matter, will rise into the neck of the retort. Then stop your distillation, and pour into a glass bottle the liquor you will find in the receiver. This liquor continually exhales a considerable quantity of dense, white fumes, as long as it is allowed to have a free communication with the air.

The product of this distillation is a combination of the Acid of Sea-salt with Tin. As the affinity of Tin with this Acid is greater than that of Mercury, the Acid contained in the Corrosive Sublimate quits the Mercury, wherewith it was united, to join the Tin; which it volatilizes so as to make it rise with itself in a limpid form. We make use of the amalgam of Tin with Quick-silver, because we are thereby enabled to mix the Corrosive Sublimate perfectly therewith, as the success of the operation requires it should be.

In this experiment the Tin is volatilized, and the Acid of Sea-salt, which is exceedingly concentrated, flies off incessantly in the form of white vapours. This compound is known in Chymistry by the name of Smoking Liquor of Libavius; a name derived from its quality, and from its Inventor. Tin dissolved by Acids is easily separated from them by Alkalis. It always precipitates in the form of a white calx.


CHAP. VI.

Of Lead.

PROCESS I.

To extract Lead from its Ore.

Having roasted your Lead ore reduce it to a fine powder; mix it with twice its weight of the black flux, and one fourth of its weight of clean iron filings and borax; put the whole into a crucible capable of containing at least thrice as much; over all put Sea-salt four fingers thick; cover the crucible; lute the juncture; dry the whole with a gentle heat, and set it in a melting furnace.

Make the crucible moderately red: you will hear the Sea-salt decrepitate, and after the decrepitation a small hissing in the crucible. Keep up the same degree of fire till that be over.

Then throw in as many coals as are necessary to complete the operation entirely, and raise the fire suddenly, so as to bring the whole mixture into perfect fusion. Keep up this degree of fire for a quarter of an hour, which is time sufficient for the precipitation of the Regulus.

When the operation is finished, which may be known by the quietness of the matter in the crucible, and by a bright vivid flame that will rise from it, take the crucible out of the furnace, and separate the Regulus from the scoria.

OBSERVATIONS.

All Lead ore contains a good deal of Sulphur, which must be first separated from it by roasting: and as this kind of ore is apt to fly when first exposed to the fire, it is proper to keep it covered till it be thoroughly heated. Another precaution to be used, in roasting this ore, is not to give it too great a heat, but to keep the vessel which contains it just moderately red; because it easily turns clammy, which occasions it to stick to the vessel.

The Iron that is added, and mixed with the flux, absorbs the Sulphur which may happen to remain, even after roasting: it helps also to separate from the Lead some portions of semi-metal, especially of Antimony, which are frequently mixed with this ore.

There is no fear least the Iron mix with the Lead in fusion, and adulterate it: for these two metals are incapable of contracting any union together, when each has its metalline form.

Nor is there any reason to apprehend lest the Iron should, by its refractory quality, obstruct the fusion of the mixture; for though this metal be not fusible when alone, yet, by the union it contracts with the matters it is designed to absorb, it becomes so to such a degree as in some measure to perform, on this occasion, the office of a flux.

The government of the fire is a point of great consequence in this operation. It is necessary to apply but a moderate degree of heat at first: for, when the metallic earth of the Lead, combining with the phlogiston, acquires the metalline form, it swells up in such an extraordinary manner, that there is great danger least the matter should overflow, and run all out of the containing vessel. With a view therefore to avoid this inconvenience, we direct a very large crucible to be used. This heaving of the Lead, at the instant of its reduction, is attended with a noise like the whistling of wind.

Notwithstanding all the precautions that can be used to prevent the reduction from taking place too hastily, and so occasioning the effusion of the matter, it often happens that, on raising the fire in order to bring the mixture into fusion, the hissing suddenly begins again, and is very loud. In that case all the apertures of the furnace must immediately be shut close, in order to choak and suffocate the fire: for, if this be neglected, the matter in the crucible will swell up, make its way through the luting of the juncture, nay, push up the cover, and run over. This accident is to be apprehended during the first five or six minutes after you raise the fire in order to melt the mixture. This effusion of the matter is accompanied with a dull flame, a thick, grey and yellow smoke, and a noise like that of some boiling liquor. When you observe these several phenomena you may be sure the matter is run out of the crucible, either in the manner above described, or by making its way through some cracks in the vessel, and consequently that the operation is spoiled.

Moreover, this event infallibly follows whenever a bit of coal happens to fall into the crucible; and this is one reason why it is necessary to cover it.

You may be certain that the operation hath succeeded if the scoria be smooth when cold, and have not in part escaped through the lute; if the Lead be not dispersed in globules through the whole mass of the matter contained in the crucible, but is, on the contrary, collected at the bottom, in the form of a solid Regulus, not very shining, but of a blueish cast, and ductile. Moreover, the scoria ought, in the present case, to be hard and black, and should not appear full of holes like a sieve, except only in that part which was contiguous to the Salt.

Here it is proper to observe, that the Sea-salt doth not mix with the scoria, but floats upon it. After the operation it is black; which colour it gets, no doubt, from the charred parts of the flux. The absence of these signs shews the operation to have miscarried.

When the ore to be smelted is pyritose and refractory, it may be roasted at first with a much stronger degree of fire than is used for ores that are fusible; because the martial earth, and the unmetallic earth, which are always mixed in pyritose matters, hinder it from growing readily soft in the fire. Besides, such an ore requires a greater quantity of the black flux and of borax to be mixed with it, and a higher degree of fire to fuse it.

It is generally needless to mix iron filings with this sort of ore; because the martial earth, with which pyritose matters are always accompanied, is reduced during the operation by the help of the black flux, which for that purpose is mixed with it in a large proportion, and furnishes a quantity of iron sufficient to absorb the heterogeneous minerals mixed with the Lead.

Yet, if it should be observed that the pyrites which accompany the Lead ore are arsenical, then, as such pyrites contain but a small quantity of ferruginous earth, iron filings must be added; which are, on this occasion, so much the more necessary for absorbing the Arsenic, as this mineral remains in part confounded with the ore, is reduced to a Regulus during the operation, unites with the Lead, and destroys a great deal of it by procuring its vitrification.

The Lead obtained from such pyritose ores is commonly not very pure; it is blackish and scarce ductile; qualities communicated to it by a small mixture of Copper in the pyrites, which always contain more or less thereof. We shall presently shew the method of separating Lead from Copper.

Lead ore may also be reduced by melting it amidst coals. For that purpose first kindle a fire in the furnace in which you intend to melt your ore; then put a layer of your ore immediately upon the lighted coals, and cover it with another layer of coals.

Though the melting furnace used for this operation be capable of giving a considerable heat, yet it is necessary further to increase the force of the fire by the means of a good pair of perpetual bellows, which will produce an effect like that of a forge. The ore melts, the earth of the Lead unites with the phlogiston of the coals, and so is reduced to metal, which runs through the coals, and falls into an earthen vessel placed at the bottom of the furnace to receive it. Care must be taken to keep this vessel well filled with charcoal-dust, to the end that the Lead may be in no danger of calcination while it continues there; the charcoal-dust constantly furnishing it with phlogiston to preserve its metalline form.

The earthy and stony matters that accompany the ore are scorified by this fusion, just as they are by the other which is performed in a close vessel. With regard to the Sulphur and Arsenic, they are supposed to have been first accurately separated from the ore by roasting. This is the method commonly employed for smelting Lead ore at the works.

PROCESS II.

To separate Lead from Copper.

With luting earth and charcoal-dust make a flat vessel, widening upwards, and large enough to contain your metalline mass. Set it shelving downwards from the back towards the fore-part; and in the fore-part, at the bottom, make a little gutter communicating with another vessel of the same nature, placed near the former and a little lower. Let the mouth of the gutter within side the upper vessel be narrowed, by means of a small iron plate fixed across it, while the loam is yet soft; so as to leave a very small aperture, in the lower part of this canal, sufficient to discharge the Lead as it melts. Dry the whole by placing lighted coals around it.

When this apparatus is dry, put your mixed mass of Copper and Lead into the upper vessel: both in that, and in the other vessel, light a very gentle fire of wood or charcoal, so as not to exceed the degree of heat necessary to melt Lead. In such a degree of heat the Lead contained in the mixed mass will melt, and you will see it run out of the upper vessel into the lower; at the bottom of which it will unite into a Regulus. When in this degree of heat no more Lead flows, increase the fire a little, so as to make the vessel moderately red.

When no more will run, collect the Lead contained in the lower vessel. Melt it over again in an iron ladle, with a degree of fire sufficient to make the ladle red; throw into it a little tallow or pitch, and while it burns keep stirring the metal, in order to reduce any part of it that may be calcined. Remove the pellicle or thin crust which will form on the surface; squeeze out all the Lead it contains, and then put it to the mass of Copper left in the upper vessel. Check the fire, and in the same manner take off a second skin that will form on the surface of the Lead. Lastly, when the metal is ready to fix, take off the skin that will then appear on it. The Lead remaining after this will be very pure, and free from all alloy of Copper.

With regard to the Copper itself, you will find it in the upper vessel covered with a thin coat of Lead: and if the Lead mixed with it was in the proportion of a fourth or a fifth part only, and the fire applied was gentle and slow, it will retain nearly the same form after the operation that the mixed mass had before.

OBSERVATIONS.

Lead frequently remains mixed with Copper after the reduction of its ore, especially if the ore was pyritose. Though Copper be a much more beautiful and more ductile metal than Lead, yet the latter by being alloyed with the former is rendered eager and brittle. This bad quality is easily discovered by the eye on breaking it: for the surface of the broken part appears all granulated; whereas when it is pure it is more evenly, and resembles a congeries of solid angles. If the Lead be alloyed with a considerable quantity of Copper, its colour hath a yellowish cast.

Considering the bad qualities which Copper communicates to Lead, it is necessary to separate these two metals from each other. The method above laid down is the simplest and the best. It is founded on two properties belonging to Lead: the first is that of being much more fusible than Copper; so that it will melt and run in a degree of heat that is not capable of making the Copper even red-hot, which yet is very far from being able to melt it: the second is, that Lead, though it hath an affinity with Copper, and unites very perfectly therewith, yet is not able to dissolve it without a greater heat than the degree barely necessary to fuse Lead. Hence it comes that Lead may be melted in a Copper vessel, provided no greater degree of heat be applied than that purpose requires. But when the Lead becomes so hot as to be red, fume, and boil, it instantly begins to dissolve the Copper. For this reason, it is essential to the success of our operation that a moderate degree of heat only be applied, and no greater than is requisite to keep the Lead in fusion.

Charcoal-dust is made an ingredient in the composition of the vessels used on this occasion, in order to prevent the calcination of the Lead.

The iron plate, with which the entrance of the gutter within the upper vessel is narrowed, serves to prevent the larger pieces of Copper, which the Lead may carry along with it, from passing through: it stops them, and allows the Lead to run off alone.

But as these parcels of Copper may entirely choak the passage, care must be taken, when any happen to be stopt, to remove them from the entrance of the gutter, and push them back into the middle of the vessel. It is also necessary to observe whether or no the Lead fixes any where in the passage; and, if it does, the heat of that part must be increased, in order to melt it and make it run off.

Notwithstanding all the precautions that can be taken, to hinder the melted Lead from carrying off any Copper with it, it is impossible to prevent this inconvenience entirely; and therefore the Lead is melted over again, in order to separate the small portion of Copper with which it is still adulterated.

As Copper is much lighter than Lead, if these two metals happen to be so blended together that the Copper, without being in fusion and dissolved by the Lead, is only interposed between the parts of the melted Lead, so as to swim therein, it is then precisely in the case of a solid body plunged into a fluid heavier than itself, and must rise to the surface, like wood thrown into water. It is proper to burn some inflammable matter on this melted Lead, in order to reduce such parts thereof as are constantly calcining on its surface while it is in fusion; for without this precaution they would be taken off together with the Copper.

The Copper remaining after this separation is, as we took notice before, still mixed with a little Lead. If you desire to separate it entirely therefrom, you must put it into a cupel, and expose it under the muffle to such a degree of fire as may convert all the Lead into litharge. This cannot be so done but that some of the Copper also will be scorified by the heat of the fire, and by the action of the Lead: but as there is a very great difference between the facility and readiness with which these two metals calcine, the portion of Copper that is calcined, while the whole Lead is turning into litharge, is scarce worth considering.

The Lead, though carefully separated from the Copper by the process here delivered, is not yet absolutely pure: sometimes it is alloyed with Gold, and almost always contains some Silver. If you would free the Lead as much as possible from any mixture of these two metals, you must convert it into glass, separate the remaining bead, and afterwards reduce this glass of Lead. But, as these two perfect metals are of no prejudice to the Lead, it is not usual to separate them from it, unless they be in a sufficient proportion to defray the charge, and produce some profit besides.

When we examine by the cupel the just proportion of Gold and Silver that an ore or a mixed metalline mass will yield, we make a previous assay of the Lead to be employed in the operation, and afterwards, in our estimate, deduct a proper allowance for the quantity of fine metal due to the Lead made use of.

PROCESS III.

The Calcination of Lead.

Take what quantity of Lead you please; melt it in one or more unglazed earthen pans: a dark grey powder will be found on its surface. Keep stirring the metal incessantly till it be wholly converted into such a powder, which is the Calx of Lead.

OBSERVATIONS.

As Lead is a very fusible metal, and in that respect greatly resembles Tin, most of the observations we made on the calcination of Tin may be applied here.

In the calcination of all metals, and particularly in this of Lead, there appears a singular phenomenon which is not easily accounted for. It is this: though these matters lose a great deal of their substance, either by the dissipation of their phlogiston, or because some of the metal, perhaps, exhales in vapours, yet when the calcination is over their calces are found to be increased in weight, and this increase is very considerable. An hundred pounds of Lead, for example, converted into Minium, which is nothing but a calx of Lead brought to a red colour by continuing the calcination, are found to gain ten pounds weight; so that for an hundred pounds of Lead we have one hundred and ten pounds of Minium: a prodigious and almost incredible augmentation, if it be considered that, far from adding any thing to the Lead, we have on the contrary dissipated part of it.

To account for this phenomenon Natural Philosophers and Chymists have invented several ingenious hypotheses, but none of them entirely satisfactory. As we have no established theory to proceed upon, we shall not undertake to explain this extraordinary fact.

PROCESS IV.

To prepare Glass of Lead.

Take two parts of Litharge, and one part of pure crystalline Sand; mingle them together as exactly as possible, adding a little Nitre and Sea-salt: put this mixture into a crucible of the most solid and most compact earth. Shut the crucible with a cover that may perfectly close it.

Set the crucible thus prepared in a melting furnace; fill the furnace with coals; light the fire gradually, so that the whole may be slowly heated: then raise the fire so as to make the crucible very red, and bring the matter it contains into fusion; keep it thus melted for a quarter of an hour.

Then take the crucible out of the furnace, and break it: in the bottom thereof you will most commonly find a small button of Lead, and over it a transparent Glass, of a yellow colour nearly resembling that of amber. Separate this Glass from the little button of metal, and from the saline matters which you will find above it.

OBSERVATIONS.

Pure Lead, being exposed to a strong fire without any additament, turns to Litharge; which is a scaly sort of substance, more or less yellowish, shining, and soft to the touch. This is the first advance to the Vitrification of Lead. The large refineries of Gold and Silver by the means of Lead furnish a great quantity of this material. It is sometimes whitish, and is then called Litharge of Silver; sometimes yellow, and then bears the name of Litharge of Gold. The difference of its colour depends on the degree of fire it hath undergone, and on the metalline substances vitrified with it.

Litharge alone is very fusible, and being exposed to the fire is easily converted into glass: but this Glass of Lead, made without additament, is so active, so penetrating, and so apt to swell, that it can scarcely be made use of when pure. We are obliged in some sort to clog it, by uniting it with some vitrifiable matter that is not so subtile, such as sand; and it is for this reason, not to render the mixture more fusible, that we have directed the addition of one third part of Sand to two thirds of Litharge.

The Nitre and Sea-salt, prescribed as ingredients in the mixture, are designed to procure an equal fusion of the whole. For, as the sand is lighter and less fusible than the Litharge, it will partly rise towards the upper part of the crucible when that matter first begins to flow; in consequence whereof the contents of the upper part will be much more difficult to melt, and form a Glass much more compact than that below: but the Nitre and Sea-salt possessing the upper part of the crucible, because they are still lighter than the Sand, and being in their own nature very efficacious fluxes, on account of their great fusibility, they quickly bring about the fusion of those particles of sand, which, having escaped the action of the Litharge, may have risen unvitrified to its surface.

The most difficult thing to procure, and yet the most necessary to the success of this operation, is a crucible of earth so firm and compact as not to be penetrated by the Glass of Lead, which corrodes and makes its way through every thing.

The precaution of chusing a crucible, that shall contain a good deal more than the matter to be vitrified, is a necessary one, because Litharge and Glass of Lead are very apt to swell.

The rule to keep the crucible close shut is also indispensably necessary, to prevent any bit of charcoal, or other inflammable matter, from falling into it: for when this happens it occasions a reduction of the Lead, which is always attended with a sort of effervescence, and such a considerable heaving, that commonly most of the mixture runs over the crucible. For the same reason it is very proper, before you expose the mixture to the fire, to examine whether or no it contains any matter capable of furnishing a phlogiston during the operation; and if it does, to remove that matter with great care.

The little button of Lead, found at the bottom of the crucible after the operation, comes from a small portion of Lead that is commonly left in Litharge, unless you prepare it carefully yourself, and do not take it from the fire till you are sure of having destroyed all the Lead. Besides, this small portion of Lead can be of no prejudice to the operation, because it cannot communicate its phlogiston to the rest of the matter.

The revivifying of Litharge, of the Calx, and of the Glass of Lead, may be obtained by the same processes as the reduction of its ore.

PROCESS V.

Lead dissolved by the Nitrous Acid.

Put into a matrass some aqua fortis precipitated like that used to dissolve Silver; weaken it by mixing therewith an equal quantity of common water; set the matrass in a hot sand-bath; throw into it, little by little, small bits of Lead, till you see that no more will dissolve. Aqua fortis thus lowered will dissolve about a fourth of its weight of Lead.

There is gradually formed upon the Lead, as it dissolves, first a grey powder, and afterwards a white crust, which at last hinder the solvent from acting on the remaining part of the metal; and therefore the liquor should be made to boil, and the vessel should be shaken to remove those impediments, by which means all the Lead will be dissolved.

OBSERVATIONS.

Lead very much resembles Silver, with respect to the phenomena which attend its dissolution in Acids. For example, the Nitrous Acid must be very pure and uncontaminated with the Vitriolic or Marine Acid, to qualify it for keeping the Lead in solution: for, if it be mixed with either the one or the other of these Acids, the Lead will precipitate in the form of a white powder as fast as it dissolves; which is just the case with Silver.

If the Vitriolic Acid be mixed with the Nitrous, the precipitate will be a combination of the Vitriolic Acid with Lead; that is, a Neutral Metallic Salt, or Vitriol of Lead. If the Acid of Sea-salt be mixed therewith, the precipitate will be a Plumbum corneum; that is, a Metallic Salt resembling the Luna cornea.

When all the Lead is dissolved as above described, the liquor appears milky. If it be kept warm over the fire till little crystals begin to appear on its surface, and afterwards left to stand quiet, in a certain time there will be found at the bottom a greyish powder, which being tried on Gold is Mercurial enough to whiten it. Little globules of Quick-silver are even discernible in it.

We owe this observation, together with this manner of proving the existence of Mercury in Lead, and of procuring it from thence, to M. Grosse, who hath given an account of his process in the Memoirs of the Academy of Sciences, from whence we have copied the description of the operation in hand.

The solution being quickly poured off by inclination from the grey mercurial precipitate is still milky, and deposites another white sediment. When this second precipitate falls the liquor becomes clear and limpid, and is then of a fine yellow colour, like a solution of Gold. On this gold-coloured solution, and on the two precipitates above-mentioned, M. Grosse made several observations, the chief of which we shall here insert.

The yellow liquor affects the tongue at first with a taste of sweetness; but afterwards vellicates it very smartly, and leaves on it a strong sensation of acrimony, which continues for a long time.

Alkalis precipitate the Lead suspended in this liquor, just as they do all other metals dissolved by Acids; and this precipitate of Lead is white.

Sea-salt, or Spirit of Salt, separates the Lead from its solvent, and precipitates it, as we observed before, into a Plumbum corneum: but this precipitate differs from the Luna cornea, as being very soluble in water; whereas the Luna cornea will not dissolve in it at all; or at least dissolves therein with great difficulty, and in a very small quantity. This Plumbum corneum dissolved in water is again precipitated by the Vitriolic Acid. M. Grosse observes, that this forms an exception to the eighth column of Mr. Geoffroy's Table of Affinities; in which the Acid of Sea-salt is marked as having a greater affinity than any other Acid with Metallic substances.

Our solution of Lead is also precipitated in a white powder by several Neutral Salts; such as Vitriolated Tartar, Alum, and common Vitriol. It is by the means of double affinities that these Neutral Salts effect this precipitation.

Even pure water alone is capable of precipitating the Lead of our solution, by weakening the Acid, and thereby disabling it from keeping the metal suspended.

Lastly, as all the solutions of metals in Acids are nothing but Neutral Metallic Salts in a fluid form, so if the solution of Lead be evaporated over the fire, it will shoot into very beautiful crystals, about the bigness of hemp-seed, shaped like regular pyramids having square bases. These crystals are yellowish, and have a sweet saccharine taste: but what is most singular in them is, that, as they consist of the Nitrous Acid combined with Lead, which manifestly contains a great deal of phlogiston, they constitute a Nitrous Metallic Salt, which has the property of deflagrating in a crucible, without the addition of any other inflammable matter. It is extremely hard to dissolve this Salt in water.

The grey mercurial precipitate which whitens Gold, and in which little globules of running Mercury are perceivable, is far from being pure Mercury. This metallic substance makes but a small part thereof: for it is an assemblage, 1. of little crystals of the same nature with those afforded by the evaporated solution; 2. of a portion of the white matter, or powder, which renders the solution milky; 3. of a grey powder, which M. Grosse considers as the only mercurial part; 4. and lastly, of little particles of Lead that have escaped the action of the solvent; especially if a little more Lead than the Acid is capable of dissolving were added with a view to saturate it entirely, as in the present process.

By means of motion and heat the small parcels of Mercury may be amalgamated with the Lead.

That Mercury should be found entire and in globules in the Spirit of Nitre, which very easily dissolves that metallic substance, will not be surprizing to those who reflect that, in the present case, the Acid is saturated with Lead, with which it has a greater affinity than with Mercury; as appears by M. Geoffroy's Table of Affinities, where, in the column that hath the Nitrous Acid at top, Lead is placed above Mercury. Agreeably to this, if Lead be presented to a solution of Mercury in Spirit of Nitre, the Lead will be dissolved, and as the dissolution thereof advances the Mercury will precipitate.

Hence it appears that, in order to find any Mercury in the spontaneous precipitate of Lead dissolved by the Nitrous Acid, it is necessary that the Acid be entirely saturated with Lead; or else that portion of the Acid which remains unsaturated will dissolve the Mercury.

With regard to the white powder that renders the solution milky, and afterwards precipitates, it is nothing but a portion of the Lead, which, not being intimately united with the Acid, falls in part of its own accord. It is a sort of calx of Lead, which being exposed to the fire becomes partly glass, and partly Lead, because it still retains some of its phlogiston.


CHAP. VII.

Of Mercury.

PROCESS I.

To extract Mercury from its Ore, or to revivify it from Cinabar.

Pulverize the Cinabar from which you would extract the Mercury; with this powder mix an equal part of clean iron filings; put the mixture into a retort of glass or iron, leaving at least one third part thereof empty. Set the retort thus prepared in a sand-bath, so that its body may be quite buried in the sand, and its neck decline considerably downwards: fit on a receiver half filled with water, and let the nose of the retort enter about half an inch into the water.

Heat the vessels so as to make the retort moderately red. The Mercury will rise in vapours, which will condense into little drops, and fall into the water in the receiver. When you see that nothing more comes over with this degree of heat, increase it, in order to raise what Mercury may still be left. When all the Mercury is thus brought over, take off the receiver, pour out the water contained in it, and collect the Mercury.

OBSERVATIONS.

Mercury is never mineralized in the bowels of the earth by any thing but Sulphur; with which it forms a compound of a brownish red colour, known by the name of Cinabar.

Sometimes it is only mixed with earthy and stony matters that contain no Sulphur; but, as this metallic substance is never destitute of its phlogiston, it then has its metalline form and properties. When it is found in this condition, nothing is more easy than to separate it from those heterogeneous matters. For that purpose no more is requisite than to distil the whole with a fire strong enough to raise the Mercury in vapours. This mineral is volatile; the earthy and stony matters are fixed; and a certain degree of heat will effect a complete separation of what is volatile from what is fixed.

This is not the case when Mercury is combined with Sulphur: for this latter mineral is volatile as well as Mercury; and the compound resulting from the union of them both is also volatile: so that if Cinabar were exposed to the fire in close vessels, as it must be to save the Mercury, it would be sublimed in substance, without being decomposed at all.