[1] In the Annals of Philosophy for November 1821 is a long article entitled “Electromagnetism” by Oersted, in which he gives a detailed account of his discovery. He had his thoughts turned to it as far back as 1813, but not until the 20th of July 1820 had he actually made his discovery. He seems to have been arranging a compass needle to observe any deflections during a storm, and placed near it a platinum wire through which a galvanic current was passed.
[2] See Trans. Soc. Arts, 1825, 43, p. 38, in which a figure of Sturgeon’s electromagnet is given as well as of other pieces of apparatus for which the Society granted him a premium and a silver medal.
[3] See S.P. Thompson, The Electromagnet (London, 1891); J.A. Fleming, A Handbook for the Electrical Laboratory and Testing Room, vol. 2 (London, 1903); J.A. Ewing, Magnetic Induction in Iron and other Metals (London, 1903, 3rd ed.).
ELECTROMETALLURGY. The present article, as explained under [Electrochemistry], treats only of those processes in which electricity is applied to the production of chemical reactions or molecular changes at furnace temperatures. In many of these the application of heat is necessary to bring the substances used into the liquid state for the purpose of electrolysis, aqueous solutions being unsuitable. Among the earliest experiments in this branch of the subject were those of Sir H. Davy, who in 1807 (Phil. Trans., 1808, p. 1), produced the alkali metals by passing an intense current of electricity from a platinum wire to a platinum dish, through a mass of fused caustic alkali. The action was started in the cold, the alkali being slightly moistened to render it a conductor; then, as the current passed, heat was produced and the alkali fused, the metal being deposited in the liquid condition. Later, A. Matthiessen (Quarterly Journ. Chem. Soc. viii. 30) obtained potassium by the electrolysis of a mixture of potassium and calcium chlorides fused over a lamp. There are here foreshadowed two types of electrolytic furnace-operations: (a) those in which external heating maintains the electrolyte in the fused condition, and (b) those in which a current-density is applied sufficiently high to develop the heat necessary to effect this object unaided. Much of the earlier electro-metallurgical work was done with furnaces of the (a) type, while nearly all the later developments have been with those of class (b). There is a third class of operations, exemplified by the manufacture of calcium carbide, in which electricity is employed solely as a heating agent; these are termed electrothermal, as distinguished from electrolytic. In certain electrothermal processes (e.g. calcium carbide production) the heat from the current is employed in raising mixtures of substances to the temperature at which a desired chemical reaction will take place between them, while in others (e.g. the production of graphite from coke or gas-carbon) the heat is applied solely to the production of molecular or physical changes. In ordinary electrolytic work only the continuous current may of course be used, but in electrothermal work an alternating current is equally available.
Electric Furnaces.—Independently of the question of the application of external heating, the furnaces used in electrometallurgy may be broadly classified into (i.) arc furnaces, in which the intense heat of the electric arc is utilized, and (ii.) resistance and incandescence furnaces, in which the heat is generated by an electric current overcoming the resistance of an inferior conductor.
Excepting such experimental arrangements as that of C.M. Despretz (C.R., 1849, 29) for use on a small scale in the laboratory, Pichou in France and J.H. Johnson in England appear, in 1853, to have introduced the earliest Arc furnaces. practical form of furnace. In these arrangements, which were similar if not identical, the furnace charge was crushed to a fine powder and passed through two or more electric arcs in succession. When used for ore smelting, the reduced metal and the accompanying slag were to be caught, after leaving the arc and while still liquid, in a hearth fired with ordinary fuel. Although this primitive furnace could be made to act, its efficiency was low, and the use of a separate fire was disadvantageous. In 1878 Sir William Siemens patented a form of furnace[1] which is the type of a very large number of those designed by later inventors.
In the best-known form a plumbago crucible was used with a hole cut in the bottom to receive a carbon rod, which was ground in so as to make a tight joint. This rod was connected with the positive pole of the dynamo or electric generator. The crucible was fitted with a cover in which were two holes; one at the side to serve at once as sight-hole and charging door, the other in the centre to allow a second carbon rod to pass freely (without touching) into the interior. This rod was connected with the negative pole of the generator, and was suspended from one arm of a balance-beam, while from the other end of the beam was suspended a vertical hollow iron cylinder, which could be moved into or out of a wire coil or solenoid joined as a shunt across the two carbon rods of the furnace. The solenoid was above the iron cylinder, the supporting rod of which passed through it as a core. When the furnace with this well-known regulating device was to be used, say, for the melting of metals or other conductors of electricity, the fragments of metal were placed in the crucible and the positive electrode was brought near them. Immediately the current passed through the solenoid it caused the iron cylinder to rise, and, by means of its supporting rod, forced the end of the balance beam upwards, so depressing the other end that the negative carbon rod was forced downwards into contact with the metal in the crucible. This action completed the furnace-circuit, and current passed freely from the positive carbon through the fragments of metal to the negative carbon, thereby reducing the current through the shunt. At once the attractive force of the solenoid on the iron cylinder was automatically reduced, and the falling of the latter caused the negative carbon to rise, starting an arc between it and the metal in the crucible. A counterpoise was placed on the solenoid end of the balance beam to act against the attraction of the solenoid, the position of the counterpoise determining the length of the arc in the crucible. Any change in the resistance of the arc, either by lengthening, due to the sinking of the charge in the crucible, or by the burning of the carbon, affected the proportion of current flowing in the two shunt circuits, and so altered the position of the iron cylinder in the solenoid that the length of arc was, within limits, automatically regulated. Were it not for the use of some such device the arc would be liable to constant fluctuation and to frequent extinction. The crucible was surrounded with a bad conductor of heat to minimize loss by radiation. The positive carbon was in some cases replaced by a water-cooled metal tube, or ferrule, closed, of course, at the end inserted in the crucible. Several modifications were proposed, in one of which, intended for the heating of non-conducting substances, the electrodes were passed horizontally through perforations in the upper part of the crucible walls, and the charge in the lower part of the crucible was heated by radiation.
The furnace used by Henri Moissan in his experiments on reactions at high temperatures, on the fusion and volatilization of refractory materials, and on the formation of carbides, silicides and borides of various metals, consisted, in its simplest form, of two superposed blocks of lime or of limestone with a central cavity cut in the lower block, and with a corresponding but much shallower inverted cavity in the upper block, which thus formed the lid of the furnace. Horizontal channels were cut on opposite walls, through which the carbon poles or electrodes were passed into the upper part of the cavity. Such a furnace, to take a current of 4 H.P. (say, of 60 amperes and 50 volts), measured externally about 6 by 6 by 7 in., and the electrodes were about 0.4 in. in diameter, while for a current of 100 H.P. (say, of 746 amperes and 100 volts) it measured about 14 by 12 by 14 in., and the electrodes were about 1.5 in. in diameter. In the latter case the crucible, which was placed in the cavity immediately beneath the arc, was about 3 in. in diameter (internally), and about 3½ in. in height. The fact that energy is being used at so high a rate as 100 H.P. on so small a charge of material sufficiently indicates that the furnace is only used for experimental work, or for the fusion of metals which, like tungsten or chromium, can only be melted at temperatures attainable by electrical means. Moissan succeeded in fusing about ¾ ℔ of either of these metals in 5 or 6 minutes in a furnace similar to that last described. He also arranged an experimental tube-furnace by passing a carbon tube horizontally beneath the arc in the cavity of the lime blocks. When prolonged heating is required at very high temperatures it is found necessary to line the furnace-cavity with alternate layers of magnesia and carbon, taking care that the lamina next to the lime is of magnesia; if this were not done the lime in contact with the carbon crucible would form calcium carbide and would slag down, but magnesia does not yield a carbide in this way. Chaplet has patented a muffle or tube furnace, similar in principle, for use on a larger scale, with a number of electrodes placed above and below the muffle-tube. The arc furnaces now widely used in the manufacture of calcium carbide on a large scale are chiefly developments of the Siemens furnace. But whereas, from its construction, the Siemens furnace was intermittent in operation, necessitating stoppage of the current while the contents of the crucible were poured out, many of the newer forms are specially designed either to minimize the time required in effecting the withdrawal of one charge and the introduction of the next, or to ensure absolute continuity of action, raw material being constantly charged in at the top and the finished substance and by-products (slag, &c.) withdrawn either continuously or at intervals, as sufficient quantity shall have accumulated. In the King furnace, for example, the crucible, or lowest part of the furnace, is made detachable, so that when full it may be removed and an empty crucible substituted. In the United States a revolving furnace is used which is quite continuous in action.
The class of furnaces heated by electrically incandescent materials has been divided by Borchers into two groups: (1) those in which the substance is heated by contact with a substance offering a high resistance to the Incandescence furnaces. current passing through it, and (2) those in which the substance to be heated itself affords the resistance to the passage of the current whereby electric energy is converted into heat. Practically the first of these furnaces was that of Despretz, in which the mixture to be heated was placed in a carbon tube rendered incandescent by the passage of a current through its substance from end to end. In 1880 W. Borchers introduced his resistance-furnace, which, in one sense, is the converse of the Despretz apparatus. A thin carbon pencil, forming a bridge between two stout carbon rods, is set in the midst of the mixture to be heated. On passing a current through the carbon the small rod is heated to incandescence, and imparts heat to the surrounding mass. On a larger scale several pencils are used to make the connexions between carbon blocks which form the end walls of the furnace, while the side walls are of fire-brick laid upon one another without mortar. Many of the furnaces now in constant use depend mainly on this principle, a core of granular carbon fragments stamped together in the direct line between the electrodes, as in Acheson’s carborundum furnace, being substituted for the carbon pencils. In other cases carbon fragments are mixed throughout the charge, as in E.H. and A.H. Cowles’s zinc-smelting retort. In practice, in these furnaces, it is possible for small local arcs to be temporarily set up by the shifting of the charge, and these would contribute to the heating of the mass. In the remaining class of furnace, in which the electrical resistance of the charge itself is utilized, are the continuous-current furnaces, such as are used for the smelting of aluminium, and those alternating-current furnaces, (e.g. for the production of calcium carbide) in which a portion of the charge is first actually fused, and then maintained in the molten condition by the current passing through it, while the reaction between further portions of the charge is proceeding.