The refining operations which can be applied to ores after they have undergone preliminary concentration processes, depend en tirely upon the nature of the concentrate, and upon the facilities available in the locality where the work is to be done. Although the changes to be brought about are essentially of a chemical na ture, the methods which can be applied depend to some extent on the physical characteristics of the substance in question. Thus a finely-divided material cannot be treated in blast furnaces, while a strongly sintered product is not so well suited as a finely divided material to treatment with aqueous solvents or "leaching." Reduction Methods.—Broadly the reduction methods appli cable to ores may be divided into two groups involving respec tively furnace treatment and wet processes. Processes involving the use of mercury for "amalgamation" are allied to the true "wet" methods. The furnace methods depend upon chemical changes which occur at high temperatures ; these may involve the oxidation of impurities which it is desired to eliminate and the oxygen for this purpose may be derived from the air or from oxidised compounds which may be added to the ore or slag dur ing or prior to the treatment. There are also reduction processes,
in which oxygen is removed from the ore either partially or com pletely. Here the oxygen is removed, i.e., the oxides in the ore are "reduced," by the action of such agents as carbon, hydrogen, hydrocarbons or even other metals. It is a frequent sequence to find that at an early stage of a process the actions which take place involve oxidation and that reducing actions, which finally result in the production of the metal itself, are subsequently applied. The heat required for these operations may either be supplied by the combustion of fuel which may be mixed with the ore or burnt separately, or the heat may be generated by the combustion of such substances as sulphur or carbon already present in the ore or intermediate product.
Another method of metal production which is intermediate between the typical furnace processes and the wet-way electrolytic methods is that of "fusion electrolysis." Here the purified metal liferous substance is brought into a state of fusion, usually by admixture with some other substance which serves as flux—i.e., has the function of rendering the mixture much more fusible- while itself remaining as nearly as possible neutral. The "solu tion" of oxide of aluminium in molten cryolite is perhaps the most important example of this kind. The fused mixture then serves as electrolyte and the pure metal is separated at the cathode exactly as in wet-way electrolysis, except that the re duced metal is frequently formed in the liquid state and is run off periodically into suitable moulds. In other cases—as in the production of magnesium, calcium and other light metals the deposited metal is solid and is formed as a stick on a cathode rod which is steadily withdrawn from the bath. These processes find their application to metals which it is difficult or impossible to reduce satisfactorily by ordinary furnace methods and which cannot be produced by wet-way electrolysis because they react vigorously with water.
The wet methods of ore reduction afford a similarly large variety. In some few cases it is possible to extract the desired mineral direct from the mine by a leaching process. In the majority of cases, however, the solvent solution is applied to the ore after it has been removed from the mine and subjected to preliminary concentration, as, for example, by flotation. In other cases preliminary roasting, either purely oxidising or "chlor idising"—in which chlorides are added to the ore with a view to converting the mineral into an easily-attacked chloride—is em ployed before leaching is applied. In some cases, in fact, the ore is reduced to a crude form of the metal before it is subjected to wet-way (electrolytic) refining.