Part 2 — INTRODUCTION. (continued 2)
Robert Kerr translation
Distillation is not sufficient for depriving this acid of all its unnecessary water; and, for this purpose, the best way is by exposing it to a degree of cold from 4° to 6° below the freezing point, from 19° to 23° of Fahrenheit; by this means the aqueous part becomes frozen, and leaves the acid in a liquid state, and considerably concentrated. In the usual temperature of the air, this acid can only exist in the gasseous form, and can only be retained by combination with a large proportion of water. There are other chemical processes for obtaining the acetous acid, which consist in oxygenating the tartarous, oxalic, or malic acids, by means of nitric acid; but there is reason to believe the proportions of the elements of the radical are changed during this process. Mr Hassenfratz is at present engaged in repeating the experiments by which these conversions are said to be produced.
The combinations of acetous acid with the various salifiable bases are very readily formed; but most of the resulting neutral salts are not cristallizable, whereas those produced by the tartarous and oxalic acids are, in general, hardly soluble. Tartarite and oxalat of lime are not soluble in any sensible degree: The malats are a medium between the oxalats and acetites, with respect to solubility, and the malic acid is in the middle degree of saturation between the oxalic and acetous acids. With this, as with all the acids, the metals require to be oxydated previous to solution.
The ancient chemists knew hardly any of the salts formed by the combinations of acetous acid with the salifiable bases, except the acetites of potash, soda, ammoniac, copper, and lead. Mr Cadet discovered the acetite of arsenic[47]; Mr Wenzel, the Dijon academicians Mr de Lassone, and Mr Proust, made us acquainted with the properties of the other acetites. From the property which acetite of potash possesses, of giving out ammoniac in distillation, there is some reason to suppose, that, besides charcoal and hydrogen, the acetous radical contains a small proportion of azote, though it is not impossible but the above production of ammoniac may be occasioned by the decomposition of the potash.
Table of the Combinations of Acetic Acid with the Salifiable Bases, in the order of affinity.
Bases.Neutral Salts.
Barytes Acetat ofbarytes.
Potash potash.
Soda soda.
Lime lime.
Magnesia magnesia.
Ammoniac ammoniac.
Oxyd ofzinc zinc.
manganese manganese.
iron iron.
lead lead.
tin tin.
cobalt cobalt.
copper copper.
nickel nickel.
arsenic arsenic.
bismuth bismuth.
mercury mercury.
antimony antimony.
silver silver.
gold gold.
platina platina.
Argill argill.
Note.—All these salts were unknown to the ancients; and even those chemists who are most versant in modern discoveries, are yet at a lose whether the greater part of the salts produced by the oxygenated acetic radical belong properly to the class of acetites, or to that of acetats.—A.
Sect. XXXIV.—Observations upon Acetic Acid, and its Combinations.
We have given to radical vinegar the name of acetic acid, from supposing that it consists of the same radical with that of the acetous acid, but more highly saturated with oxygen. According to this idea, acetic acid is the highest degree of oxygenation of which the hydro-carbonous radical is susceptible; but, although this circumstance be extremely probable, it requires to be confirmed by farther, and more decisive experiments, before it be adopted as an absolute chemical truth. We procure this acid as follows: Upon three parts acetite of potash or of copper, pour one part of concentrated sulphuric acid, and, by distillation, a very highly concentrated vinegar is obtained, which we call acetic acid, formerly named radical vinegar. It is not hitherto rigorously proved that this acid is more highly oxygenated than the acetous acid, nor that the difference between them may not consist in a different proportion between the elements of the radical or base.
Table of the Combinations of Succinic Acid with the Salifiable Bases, in the order of Affinity.
Bases.Neutral Salts.
Barytes Succinat ofbarytes.
Lime lime.
Potash potash.
Soda soda.
Ammoniac ammoniac.
Magnesia magnesia.
Argill argill.
Oxydof zinc zinc.
iron iron.
manganese manganese.
cobalt cobalt.
nickel nickel.
lead lead.
tin tin.
copper copper.
bismuth bismuth.
antimony antimony.
arsenic arsenic.
mercury mercury.
silver silver.
gold gold.
platina platina.
Note.—All the succinats were unknown to the ancient chemists.—A.
Sect. XXXV.—Observations upon Succinic Acid, and its Combinations.
The succinic acid is drawn from amber by sublimation in a gentle heat, and rises in a concrete form into the neck of the subliming vessel. The operation must not be pushed too far, or by too strong a fire, otherwise the oil of the amber rises alongst with the acid. The salt is dried upon blotting paper, and purified by repeated solution and crystallization.
This acid is soluble in twenty-four times its weight of cold water, and in a much smaller quantity of hot water. It possesses the qualities of an acid in a very small degree, and only affects the blue vegetable colours very slightly. The affinities of this acid, with the salifiable bases, are taken from Mr de Morveau, who is the first chemist that has endeavoured to ascertain them.
Sect. XXXVI.—Observations upon Benzoic Acid, and its Combinations with Salifiable Bases[48].
This acid was known to the ancient chemists under the name of Flowers of Benjamin, or of Benzoin, and was procured, by sublimation, from the gum or resin called Benzoin: The means of procuring it, via humida, was discovered by Mr Geoffroy, and perfected by Mr Scheele. Upon benzoin, reduced to powder, pour strong lime-water, having rather an excess of lime; keep the mixture continually stirring, and, after half an hour's digestion, pour off the liquor, and use fresh portions of lime-water in the same manner, so long as there is any appearance of neutralization. Join all the decanted liquors, and evaporate, as far as possible, without occasioning cristallization, and, when the liquor is cold, drop in muriatic acid till no more precipitate is formed. By the former part of the process a benzoat of lime is formed, and, by the latter, the muriatic acid combines with the lime, forming muriat of lime, which remains dissolved, while the benzoic acid, being insoluble, precipitates in a concrete state.
Sect. XXXVII.—Observations upon Camphoric Acid, and its Combinations with Salifiable Bases[49].
Camphor is a concrete essential oil, obtained, by sublimation, from a species of laurus which grows in China and Japan. By distilling nitric acid eight times from camphor, Mr Kosegarten converted it into an acid analogous to the oxalic; but, as it differs from that acid in some circumstances, we have thought necessary to give it a particular name, till its nature be more completely ascertained by farther experiment.
As camphor is a carbono-hydrous or hydro-carbonous radical, it is easily conceived, that, by oxygenation, it should form oxalic, malic, and several other vegetable acids: This conjecture is rendered not improbable by the experiments of Mr Kosegarten; and the principal phenomena exhibited in the combinations of camphoric acid with the salifiable bases, being very similar to those of the oxalic and malic acids, lead me to believe that it consists of a mixture of these two acids.
Sect. XXXVIII.—Observations upon Gallic Acid, and its Combinations with Salifiable Bases[50].
The Gallic acid, formerly called Principle of Astringency, is obtained from gall nuts, either by infusion or decoction with water, or by distillation with a very gentle heat. This acid has only been attended to within these few years. The Committee of the Dijon Academy have followed it through all its combinations, and give the best account of it hitherto produced. Its acid properties are very weak; it reddens the tincture of turnsol, decomposes sulphurets, and unites to all the metals when they have been previously dissolved in some other acid. Iron, by this combination, is precipitated of a very deep blue or violet colour. The radical of this acid, if it deserves the name of one, is hitherto entirely unknown; it is contained in oak willow, marsh iris, the strawberry, nymphea, Peruvian bark, the flowers and bark of pomgranate, and in many other woods and barks.
Sect. XXXIX.—Observations upon Lactic Acid, and its Combinations with Salifiable Bases[51].
The only accurate knowledge we have of this acid is from the works of Mr Scheele. It is contained in whey, united to a small quantity of earth, and is obtained as follows: Reduce whey to one eighth part of its bulk by evaporation, and filtrate, to separate all its cheesy matter; then add as much lime as is necessary to combine with the acid; the lime is afterwards disengaged by the addition of oxalic acid, which combines with it into an insoluble neutral salt. When the oxalat of lime has been separated by decantation, evaporate the remaining liquor to the consistence of honey; the lactic acid is dissolved by alkohol, which does not unite with the sugar of milk and other foreign matters; these are separated by filtration from the alkohol and acid; and the alkohol being evaporated, or distilled off, leaves the lactic acid behind.
This acid unites with all the salifiable bases forming salts which do not cristallize; and it seems considerably to resemble the acetous acid.
Table of the Combinations of Saccholactic Acid with the Salifiable Bases, in the Order of Affinity.
Bases.Neutral Salts.
Lime Saccholat oflime.
Barytes barytes.
Magnesia magnesia.
Potash potash.
Soda soda.
Ammoniac ammoniac.
Argill argill.
Oxydof zinc zinc.
manganese manganese.
iron iron.
lead lead.
tin tin.
cobalt cobalt.
copper copper.
nickel nickel.
arsenic arsenic.
bismuth bismuth.
mercury mercury.
antimony antimony.
silver silver.
Note.—All these were unknown to the ancient chemists.—A.
Sect. XL.—Observations upon Saccholactic Acid, and its Combinations.
A species of sugar may be extracted, by evaporation, from whey, which has long been known in pharmacy, and which has a considerable resemblance to that procured from sugar canes. This saccharine matter, like ordinary sugar, may be oxygenated by means of nitric acid: For this purpose, several portions of nitric acid are distilled from it; the remaining liquid is evaporated, and set to cristallize, by which means cristals of oxalic acid are procured; at the same time a very fine white powder precipitates, which is the saccholactic acid discovered by Scheele. It is susceptible of combining with the alkalies, ammoniac, the earths, and even with the metals: Its action upon the latter is hitherto but little known, except that, with them, it forms difficultly soluble salts. The order of affinity in the table is taken from Bergman.
Table of the Combinations of Formic Acid, with the Salifiable Bases, in the Order of Affinity.
Bases.Neutral Salts.
Barytes Formiat ofbarytes.
Potash potash.
Soda soda.
Lime lime.
Magnesia magnesia.
Ammoniac ammoniac.
Oxyd of
zinc zinc.
manganese manganese.
iron iron.
lead lead.
tin tin.
cobalt cobalt.
copper copper.
nickel nickel.
bismuth bismuth.
silver silver.
Argill argill.
Note.—All unknown to the ancient chemists.—A.
Sect. XLI.—Observations upon Formic Acid, and its Combinations.
This acid was first obtained by distillation from ants, in the last century, by Samuel Fisher. The subject was treated of by Margraff in 1749, and by Messrs Ardwisson and Ochrn of Leipsic in 1777. The formic acid is drawn from a large species of red ants, formica rufa, Lin. which form large ant hills in woody places. It is procured, either by distilling the ants with a gentle heat in a glass retort or an alembic; or, after having washed the ants in cold water, and dried them upon a cloth, by pouring on boiling water, which dissolves the acid; or the acid may be procured by gentle expression from the insects, in which case it is stronger than in any of the former ways. To obtain it pure, we must rectify, by means of distillation, which separates it from the uncombined oily and charry matter; and it may be concentrated by freezing, in the manner recommended for treating the acetous acid.
Sect. XLII.—Observations upon Bombic Acid, and its Combinations with Acidifiable Bases[52].
The juices of the silk worm seem to assume an acid quality when that insect changes from a larva to a chrysalis. At the moment of its escape from the latter to the butterfly form, it emits a reddish liquor which reddens blue paper, and which was first attentively observed by Mr Chaussier of the Dijon academy, who obtains the acid by infusing silk worm chrysalids in alkohol, which dissolves their acid without being charged with any of the gummy parts of the insect; and, by evaporating the alkohol, the acid remains tollerably pure. The properties and affinities of this acid are not hitherto ascertained with any precision; and we have reason to believe that analogous acids may be procured from other insects. The radical of this acid is probably, like that of the other acids from the animal kingdom, composed of charcoal, hydrogen, and azote, with the addition, perhaps, of phosphorus.
Table of the Combinations of Sebacic Acid, with the Salifiable Bases, in the Order of Affinity.
Bases.Neutral Salts.
Barytes Sebat ofbarytes.
Potash potash.
Soda soda.
Lime lime.
Magnesia magnesia.
Ammoniac ammoniac.
Argill argill.
Oxyd of
zinc zinc.
manganese manganese.
iron iron.
lead lead.
tin tin.
cobalt cobalt.
copper copper.
nickel nickel.
arsenic arsenic.
bismuth bismuth.
mercury mercury.
antimony antimony.
silver silver.
Note.—All these were unknown to the ancient chemists.—A.
Sect. XLIII.—Observations upon Sebacid Acid, and its Combinations.
To obtain the sebacic acid, let some suet be melted in a skillet over the fire, alongst with some quick-lime in fine powder, and constantly stirred, raising the fire towards the end of the operation, and taking care to avoid the vapours, which are very offensive. By this process the sebacic acid unites with the lime into a sebat of lime, which is difficultly soluble in water; it is, however, separated from the fatty matters with which it is mixed by solution in a large quantity of boiling water. From this the neutral salt is separated by evaporation; and, to render it pure, is calcined, redissolved, and again cristallized. After this we pour on a proper quantity of sulphuric acid, and the sebacic acid passes over by distillation.
Sect. XLIV.—Observations upon the Lithic Acid, and its Combinations with the Salifiable Bases[53].
From the later experiments of Bergman and Scheele, the urinary calculus appears to be a species of salt with an earthy basis; it is slightly acidulous, and requires a large quantity of water for solution, three grains being scarcely soluble in a thousand grains of boiling water, and the greater part again cristallizes when cold. To this concrete acid, which Mr de Morveau calls Lithiasic Acid, we give the name of Lithic Acid, the nature and properties of which are hitherto very little known. There is some appearance that it is an acidulous neutral salt, or acid combined in excess with a salifiable base; and I have reason to believe that it really is an acidulous phosphat of lime; if so, it must be excluded from the class of peculiar acids.
Table of the Combinations of the Prussic Acid with the Salifiable Bases, in the order of affinity.
Bases.Neutral Salts.
Potash Prussiat ofpotash.
Soda soda.
Ammoniac ammoniac.
Lime lime.
Barytes barytes.
Magnesia magnesia.
Oxydof zinc zinc.
iron iron.
manganese manganese.
cobalt cobalt.
nickel nickel.
lead lead.
tin tin.
copper copper.
bismuth bismuth.
antimony antimony.
arsenic arsenic.
silver silver.
mercury mercury.
gold gold.
platina platina.
Note.—-All these were unknown to former chemists.—A.
Observations upon the Prussic Acid, and its Combinations.
As the experiments which have been made hitherto upon this acid seem still to leave a considerable degree of uncertainty with regard to its nature, I shall not enlarge upon its properties, and the means of procuring it pure and dissengaged from combination. It combines with iron, to which it communicates a blue colour, and is equally susceptible of entering into combination with most of the other metals, which are precipitated from it by the alkalies, ammoniac, and lime, in consequence of greater affinity. The Prussic radical, from the experiments of Scheele, and especially from those of Mr Berthollet, seems composed of charcoal and azote; hence it is an acid with a double base. The phosphorus which has been found combined with it appears, from the experiments of Mr Hassenfratz, to be only accidental.
Although this acid combines with alkalies, earths, and metals, in the same way with other acids, it possesses only some of the properties we have been in use to attribute to acids, and it may consequently be improperly ranked here in the class of acids; but, as I have already observed, it is difficult to form a decided opinion upon the nature of this substance until the subject has been farther elucidated by a greater number of experiments.