The discovery of oxygen by Priestley and by Scheele in 1774, and the explanation of its functions by Lavoisier during the following ten years, gave their true meaning to these phenomena. It was then recognized that combustion was union with oxygen; that an “earth” or “calx” was to be regarded as the compound of a metal with oxygen; that when a metal becomes tarnished, and converted into such an earthy powder, it is being oxidized; that this oxide, on ignition with charcoal or carbon, or with compounds such as coal, flour, or wood, of which carbon is a constituent, gives up its oxygen to the carbon, forming an oxide of carbon, carbonic oxide on the one hand, or carbonic “acid” on the other, while the metal is reproduced in its “reguline” or metallic condition, and that the true elements are metals, carbon, sulphur, phosphorus, and similar bodies, and not the products of their oxidation.

The discovery that air is in the main a mixture of nitrogen, an inert gas, and oxygen, an active one, together with a small proportion of carbonic “acid” (or, as it is now termed, anhydride)—a discovery perfected by Rutherford, Black, and Cavendish—and that water is a compound with oxygen of hydrogen, previously known as inflammable air, by Cavendish and by Watt, finally overthrew the theory of phlogiston; but at the beginning of this century it still lingered on, and was defended by Priestley until his death in 1804. Such, in brief, was the condition of chemical thought in the year 1800. Scheele had died in 1786, at the early age of forty-four; Lavoisier was one of the victims of the French Revolution, having been guillotined in 1794; Cavendish had ceased to work at chemical problems, and was devoting his extraordinary abilities to physical problems of the highest importance, while living the life of an eccentric recluse, and Priestley, driven by religious persecution from England to the more tolerant shores of America, was enjoying a peaceful old age, enlivened by occasional incursions into the region of sectarian controversy.

The first striking discovery of our century was that of the compound nature of the alkalies and of the alkaline earths. This discovery was made by Humphry Davy. Born in Cornwall in 1778, he began the study of chemistry, self-taught, in 1796; and in 1799 he became director of the “Pneumatic Institution,” an undertaking founded by Dr. Beddoes, at Bristol, for the purpose of experiments on the curative effects of gases in general. Here he at once made his mark by the discovery of the remarkable properties of “laughing gas,” or nitrous oxide. At the same time he constructed a galvanic battery, and began to perform experiments with it in attempting to decompose chemical compounds by its means. In 1801 Davy was appointed professor of chemistry at the Royal Institution, a society or club which had been founded a few years previously by Benjamin Thompson, Count Rumford, for the purpose of instructing and amusing its members with recent discoveries in chemistry and natural philosophy. In 1807 Davy applied his galvanic battery to the decomposition of damp caustic potash and soda, using platinum poles. He was rewarded by seeing globules of metal, resembling mercury in appearance, at the negative pole; and he subsequently proved that these globules, when burned, reproduced the alkali from which they had been derived. They also combined with “oxymuriatic acid,” as chlorine (discovered by Scheele) was then termed, forming ordinary salt, if sodium be employed, and the analogous salt, “muriate of potash,” if the allied metal, potassium, were subjected to combustion. By using mercury as the negative pole, and passing a current through a strong solution of the chloride of calcium, strontium, or barium, Davy succeeded in procuring mixtures with mercury or “amalgams” of their metals, to which he gave the names calcium, strontium, and barium. Distillation removed most of the mercury, and the metal was left behind in a state of comparative purity. The alkali metals, potassium and sodium, were found to attack glass, liberating “the basis of the silex,” to which the name silicon has since been given.

Thus nearly the last of the “earths” had been decomposed. It was proved that not merely were the “calces” of iron, copper, lead, and other well-known metals compounds of the respective metals with oxygen, but Davy showed that lime, and its allies, strontia and baryta, and even silica or flint, were to be regarded as oxides of elements of metallic appearance. To complete our review of this part of the subject, suffice it to say that aluminum, a metal now produced on an industrial scale, was prepared for the first time in 1827 by Wöhler, professor of chemistry at Göttingen, by the action of potassium on its chloride, and alumina, the earthy basis of clay, was shown to be the oxide of the metal aluminum. Indeed, the preparation of this metal in quantity is now carried out at Schoffhausen-on-the-Rhine and at the Falls of Foyers, in Scotland, by electrolysis of the oxide dissolved in melted cryolite, a mineral consisting of the fluorides of sodium and aluminum, by a method differing only in scale from that by means of which Davy isolated sodium and potassium in 1806.

To Davy, too, belongs the merit of having dethroned oxygen from its central position among the elements. Lavoisier gave to this important gas the name “oxygen,” because he imagined it to be the constituent of all acids. He renamed the common compounds of oxygen in such a manner that the term oxygen was not even represented in the name—only inferred. Thus a “nitrate” is a compound of an oxide of nitrogen and an oxide of a metal; a “sulphate,” of the oxide of a metal with one of the oxides of sulphur, and so on. Davy, by discovering the elementary nature of chlorine, showed, first, that it is not an oxide of hydrochloric acid (or muriatic acid as it was then called); and, second, that the latter acid is the compound of the element chlorine with hydrogen. This he did by passing chlorine over white-hot carbon—a substance eminently suited to deprive oxy-compounds of their oxygen—and proving that no oxide of carbon is thereby produced; by acting on certain chlorides, such as those of tin or phosphorus with ammonia, and showing that no oxide of tin or phosphorus is formed; and, lastly, by decomposing “muriatic acid gas” (gaseous hydrogen chloride) with sodium, and showing that the only product besides common salt is hydrogen. Instead, therefore, of the former theory that a chloride was a compound of the unknown basis of oxymuriatic acid with oxygen and the oxide of a metal, he introduced the simpler and correct view that a chloride is merely a compound of the element chlorine with a metal. In 1813 he established the similar nature of fluorine, pointing out that on the analogy of the chlorides it was a fair deduction that the fluorides are compounds of an undiscovered element, fluorine, with metals; and that hydrofluoric acid is the true analogue of hydrochloric acid. The truth of this forecast has been established of recent years by Henri Moissan, who isolated gaseous fluorine by subjecting a mixture of hydrofluoric acid and hydrogen potassium fluoride contained in a platinum U tube to the action of a powerful electric current. He has recently found that the tube may be equally well constructed of copper; and this may soon lead to the industrial application of the process. The difficulty of isolating fluorine is due to its extraordinary chemical energy; for there are few substances, elementary or compound, which resist the action of this pale yellow, suffocating gas. In 1811 iodine, separated by Courtois from the ashes of sea-plants, was shown by Davy to be an element analogous to chlorine. Gay-Lussac subsequently investigated it and prepared many of its compounds; and in 1826 the last of these elements, bromine, was discovered in the mother-liquor of sea-salt by Balard. The elements of this group have been termed “halogens,” or “salt producers.”

While Davy was pouring his researches into the astonished ears of the scientific and dilettante world, John Dalton, a Manchester school-master, conceived a theory that has proved of the utmost service to the science of chemistry, and which bids fair to outlast our day. It had been noticed by Wenzel, by Richter, by Wollaston, and by Cavendish, towards the end of the last century, that the same compounds contain the same constituents in the same proportions, or, as the phrase runs, “possess constant composition.” Wollaston, indeed, had gone one step farther, and had shown that when the vegetable acid, oxalic acid, is combined with potash, it forms two compounds, in one of which the acid is contained in twice as great an amount relatively to the potash as in the other. The names monoxalate and binoxalate of potash were applied to these compounds, to indicate the respective proportions of the ingredients. Dalton conceived the happy idea that by applying the ancient Greek conception of atoms to such facts the relative weights of the atoms could be determined. Illustrating his views with the two compounds of carbon with hydrogen, marsh gas and olefiant gas, and with the two acids of carbon, carbonic oxide, carbonic “acid,” he regarded the former as a compound of one atom of carbon and one of hydrogen, and the second as a compound of one atom of carbon and two of hydrogen, and similarly for the two oxides of carbon. Knowing the relative weights in which these elements enter into combination, we can deduce the relative weights of the atoms. Placing the relative weight of an atom of hydrogen equal to unity, we have:

Marsh
Gas		Olefiant
Gas		 Carbonic
Oxide		Carbonic
Acid
Carbon66Carbon56
Hydrogen12Oxygen816 

Thus the first compound, marsh gas, was regarded by Dalton as composed of an atom of carbon in union with an atom of hydrogen; or, to reproduce his symbols, as

; while the second, olefiant gas, on this hypothesis, was a compound of two atoms of hydrogen with one of carbon, or