1. Scheele's first paper was published by Retzius, in 1770; it gives a method of obtaining pure tartaric acid: the process was to decompose cream of tartar by means of chalk. One half of the tartaric acid unites to the lime, and falls down in the state of a white insoluble powder, being tartrate of lime. The cream of tartar, thus deprived of half its acid, is converted into the neutral salt formerly distinguished by the name of soluble tartar, from its great solubility in water: it dissolves, and may be obtained in crystals, by the usual method of crystallizing salts. The tartrate of lime is washed with water, and then mixed with a quantity of dilute sulphuric acid, just capable of saturating the lime contained in the tartrate of lime; the mixture is digested for some time; the sulphuric acid displaces the tartaric acid, and combines with the lime; and, as the sulphate of lime is but very little soluble in water, the greatest part of it precipitates, and the clear liquor is drawn off: it consists of tartaric acid, held in solution by water, but not quite free from sulphate of lime. By repeated concentrations, all the sulphate of lime falls down, and at last the tartaric acid itself is obtained in large crystals. This process is still followed by the manufacturers of this country; for tartaric acid is used to a very considerable extent by the calico-printers, in various processes; for example, it is applied, thickened with gum, to different parts of cloth dyed Turkey red; the cloth is then passed through water containing the requisite quantity of chloride of lime: the tartaric acid, uniting with the lime, sets the chlorine at liberty, which immediately destroys the red colour wherever the tartaric acid has been applied, but leaves all the other parts of the cloth unchanged.

2. The paper on fluoric acid appeared in the Memoirs of the Stockholm Academy, for 1771, when Scheele was in Scharenberg's apothecary's shop in Stockholm, where, doubtless, the experiments were made. Three years before, Margraaf had attempted an analysis of fluor spar, but had discovered nothing. Scheele demonstrated that it is a compound of lime and a peculiar acid, to which he gave the name of fluoric acid. This acid he obtained in solution in water; it was separated from the fluor spar by sulphuric, muriatic, nitric, and phosphoric acids. When the fluoric acid came in contact with water, a white crust was formed, which proved, on examination, to be silica. Scheele at first thought that this silica was a compound of fluoric acid and water; but it was afterwards proved by Weigleb and by Meyer, that this notion is inaccurate, and that the silica was corroded from the retort into which the fluor spar and sulphuric acid were put. Bergman, who had adopted Scheele's theory of the nature of silica, was so satisfied by these experiments, that he gave it up, as Scheele himself did soon after.

Scheele did not obtain fluoric acid in a state of purity, put only fluosilicic acid; nor were chemists acquainted with the properties of fluoric acid till Gay-Lussac and Thenard published their Recherches Physico-chimiques, in 1811.

3. Scheele's experiments on manganese were undertaken at the request of Bergman, and occupied him three years; they were published in the Memoirs of the Stockholm Academy, for 1774, and constitute the most memorable and important of all his essays, since they contain the discovery of two new bodies, which have since acted so conspicuous a part, both in promoting the progress of the science, and in improving the manufactures of Europe. These two substances are chlorine and barytes, the first account of both of which occur in this paper.

The ore of manganese employed in these experiments was the black oxide, or deutoxide, of manganese, as it is now called. Scheele's method of proceeding was to try the effect of all the different reagents on it. It dissolved in sulphurous and nitrous acids, and the solution was colourless. Dilute sulphuric acid did not act upon it, nor nitric acid; but concentrated sulphuric acid dissolved it by the assistance of heat. The solution of sulphate of manganese in water was colourless and crystallized in very oblique rhomboidal prisms, having a bitter taste. Muriatic acid effervesced with it, when assisted by heat, and the elastic fluid that passed off had a yellowish colour, and the smell of aqua regia. He collected quantities of this elastic fluid (chlorine) in bladders, and determined some of its most remarkable properties: it destroyed colours, and tinged the bladder yellow, as nitric acid does. This elastic fluid, in Scheele's opinion, was muriatic acid deprived of phlogiston. By phlogiston Scheele meant, in this place, hydrogen gas. He considered muriatic acid as a compound of chlorine and hydrogen. Now this is the very theory that was established by Davy in consequence of his own experiments and those of Gay-Lussac and Thenard. Scheele's mode of collecting chlorine gas in a bladder, did not enable him to determine its characters with so much precision as was afterwards done. But his accuracy was so great, that every thing which he stated respecting it was correct so far as it went.

Most of the specimens of manganese ore which Scheele examined, contained more or less barytes, as has since been determined, in combination with the oxide. He separated this barytes, and determined its peculiar properties. It dissolved in nitric and muriatic acids, and formed salts capable of crystallizing, and permanent in the air. Neither potash, soda, nor lime, nor any base whatever, was capable of precipitating it from these acids. But the alkaline carbonates threw it down in the state of a white powder, which dissolved with effervescence in acids. Sulphuric acid and all the sulphates threw it down in the state of a white powder, which was insoluble in water and in acids. This sulphate cannot be decomposed by any acid or base whatever. The only practicable mode of proceeding is to convert the sulphuric acid into sulphur, by heating the salt with charcoal powder, along with a sufficient quantity of potash, to bring the whole into fusion. The fused mass, edulcorated, is soluble in nitric or muriatic acid, and thus may be freed from charcoal, and the barytes obtained in a state of purity. Scheele detected barytes, also, in the potash made from trees or other smaller vegetables; but at that time he was unacquainted with sulphate of barytes, which is so common in various parts of the earth, especially in lead-mines.

To point out all the new facts contained in this admirable essay, it would be necessary to transcribe the whole of it. He shows the remarkable analogy between manganese and metallic oxides. Bergman, in an appendix affixed to Scheele's paper, states his reasons for being satisfied that it is really a metallic oxide. Some years afterwards, Assessor Gahn succeeded in reducing it to the metallic state, and thus dissipating all remaining doubts on the subject.

4. In 1775 he gave a new method of obtaining benzoic acid from benzoin. His method was, to digest the benzoin with pounded chalk and water, till the whole of the acid had combined with lime, and dissolved in the water. It is requisite to take care to prevent the benzoin from running into clots. The liquid thus containing benzoate of lime in solution is filtered, and muriatic acid added in sufficient quantity to saturate the lime. The benzoic acid is separated in white flocks, which may be easily collected and washed. This method, though sufficiently easy, is not followed by practical chemists, at least in this country. The acid when procured by precipitation is not so beautiful as what is procured by sublimation; nor is the process so cheap or so rapid. For these reasons, Scheele's process has not come into general use.

5. During the same year, 1775, his essay on arsenic and its acid was also published in the Memoirs of the Stockholm Academy. In this essay he shows various processes, by means of which white arsenic may be converted into an acid, having a very sour taste, and very soluble in water. This is the acid to which the name of arsenic acid has been since given. Scheele describes the properties of this acid, and the salts which it forms, with the different bases. He examines, also, the action of white arsenic upon different bodies, and throws light upon the arsenical salt of Macquer.

6. The object of the little paper on silica, clay, and alum, published in the Memoirs of the Stockholm Academy, for 1776, is to prove that alumina and silica are two perfectly distinct bodies, possessed of different properties. This he does with his usual felicity of experiment. He shows, also, that alumina and lime are capable of combining together.