Light metals
Another important development of the late 19th century was the separation from their ores, on a substantial scale, of aluminum and magnesium. In the earlier part of the century, several scientists had made small quantities of these light metals, but the most successful was Henri-Étienne Sainte-Claire Deville, who by 1855 had developed a method by which cryolite, a double fluoride of aluminum and sodium, was reduced by sodium metal to aluminum and sodium fluoride. The process was very expensive, but cost was greatly reduced when the American chemist Hamilton Young Castner developed an electrolytic cell for producing cheaper sodium in 1886. At the same time, however, Charles M. Hall in the United States and Paul-Louis-Toussaint Héroult in France announced their essentially identical processes for aluminum extraction, which were also based on electrolysis. Use of the Hall-Héroult process on an industrial scale depended on the replacement of storage batteries by rotary power generators; it remains essentially unchanged to this day.
Welding
One of the most significant changes in the technology of metals fabrication has been the introduction of fusion welding during the 20th century. Before this, the main joining processes were riveting and forge welding. Both had limitations of scale, although they could be used to erect substantial structures. In 1895 Henry-Louis Le Chatelier stated that the temperature in an oxyacetylene flame was 3,500 °C (6,300 °F), some 1,000 °C higher than the oxyhydrogen flame already in use on a small scale for brazing and welding. The first practical oxyacetylene torch, drawing acetylene from cylinders containing acetylene dissolved in acetone, was produced in 1901. With the availability of oxygen at even lower cost, oxygen cutting and oxyacetylene welding became established procedures for the fabrication of structural steel components.
The metal in a join can also be melted by an electric arc, and a process using a carbon as a negative electrode and the workpiece as a positive first became of commercial interest about 1902. Striking an arc from a coated metal electrode, which melts into the join, was introduced in 1910. Although it was not widely used until some 20 years later, in its various forms it is now responsible for the bulk of fusion welds.
Metallography
The 20th century has seen metallurgy change progressively, from an art or craft to a scientific discipline and then to part of the wider discipline of materials science. In extractive metallurgy, there has been the application of chemical thermodynamics, kinetics, and chemical engineering, which has enabled a better understanding, control, and improvement of existing processes and the generation of new ones. In physical metallurgy, the study of relationships between macrostructure, microstructure, and atomic structure on the one hand and physical and mechanical properties on the other has broadened from metals to other materials such as ceramics, polymers, and composites.
This greater scientific understanding has come largely from a continuous improvement in microscopic techniques for metallography, the examination of metal structure. The first true metallographer was Henry Clifton Sorby of Sheffield, England, who in the 1860s applied light microscopy to the polished surfaces of materials such as rocks and meteorites. Sorby eventually succeeded in making photomicrographic records, and by 1885 the value of metallography was appreciated throughout Europe, with particular attention being paid to the structure of steel. For example, there was eventual acceptance, based on micrographic evidence and confirmed by the introduction of X-ray diffraction by William Henry and William Lawrence Bragg in 1913, of the allotropy of iron and its relationship to the hardening of steel. During subsequent years there were advances in the atomic theory of solids; this led to the concept that, in nonplastic materials such as glass, fracture takes place by the propagation of preexisting cracklike defects and that, in metals, deformation takes place by the movement of dislocations, or defects in the atomic arrangement, through the crystalline matrix. Proof of these concepts came with the invention and development of the electron microscope; even more powerful field ion microscopes and high-resolution electron microscopes now make it possible to detect the position of individual atoms.

Another example of the development of physical metallurgy is a discovery that revolutionized the use of aluminum in the 20th century. Originally, most aluminum was used in cast alloys, but the discovery of age hardening by Alfred Wilm in Berlin about 1906 yielded a material that was twice as strong with only a small change in weight. In Wilm’s process, a solute such as magnesium or copper is trapped in supersaturated solid solution, without being allowed to precipitate out, by quenching the aluminum from a higher temperature rather than slowly cooling it. The relatively soft aluminum alloy that results can be mechanically formed, but, when left at room temperature or heated at low temperatures, it hardens and strengthens. With copper as the solute, this type of material came to be known by the trade name Duralumin. The advances in metallography described above eventually provided the understanding that age hardening is caused by the dispersion of very fine precipitates from the supersaturated solid solution; this restricts the movement of the dislocations that are essential to crystal deformation and thus raises the strength of the metal. The principles of precipitation hardening have been applied to the strengthening of a large number of alloys.
Clarence H. Lorig James A. CharlesExtractive metallurgy
Following separation and concentration by mineral processing, metallic minerals are subjected to extractive metallurgy, in which their metallic elements are extracted from chemical compound form and refined of impurities.
Metallic compounds are frequently rather complex mixtures (those treated commercially are for the most part sulfides, oxides, carbonates, arsenides, or silicates), and they are not often types that permit extraction of the metal by simple, economical processes. Consequently, before extractive metallurgy can effect the separation of metallic elements from the other constituents of a compound, it must often convert the compound into a type that can be more readily treated. Common practice is to convert metallic sulfides to oxides, sulfates, or chlorides; oxides to sulfates or chlorides; and carbonates to oxides. The processes that accomplish all this can be categorized as either pyrometallurgy or hydrometallurgy. Pyrometallurgy involves heating operations such as roasting, in which compounds are converted at temperatures just below their melting points, and smelting, in which all the constituents of an ore or concentrate are completely melted and separated into two liquid layers, one containing the valuable metals and the other the waste rock. Hydrometallurgy consists of such operations as leaching, in which metallic compounds are selectively dissolved from an ore by an aqueous solvent, and electrowinning, in which metallic ions are deposited onto an electrode by an electric current passed through the solution.
Extraction is often followed by refining, in which the level of impurities is brought lower or controlled by pyrometallurgical, electrolytic, or chemical means. Pyrometallurgical refining usually consists of the oxidizing of impurities in a high-temperature liquid bath. Electrolysis is the dissolving of metal from one electrode of an electrolytic cell and its deposition in a purer form onto the other electrode. Chemical refining involves either the condensation of metal from a vapour or the selective precipitation of metal from an aqueous solution.
The processes to be used in extraction and refining are selected to fit into an overall pattern, with the product from the first process becoming the feed material of the second process, and so on. It is quite common for hydrometallurgical, pyrometallurgical, and electrolytic processes to be used one after another in the treatment of a single metal. The choices depend on several conditions. One of these is that certain types of metallic compounds lend themselves to easiest extraction by certain methods; for example, oxides and sulfates are readily dissolved in leach solutions, while sulfides are only slightly soluble. Another condition is the degree of purity, which can vary from one type of extraction to another. Zinc production illustrates this, in that zinc metal produced by pyrometallurgical retort or blast-furnace operations is 98 percent pure, with traces of lead, iron, and cadmium. This is adequate for galvanizing, but the preferred purity for die-casting (99.99 percent) must be obtained hydrometallurgically, from the electrolysis of a zinc sulfate solution. Also to be considered in choosing a processing method is the recovery of particular impurities that may have value themselves as by-products. One example is copper refining: the pyrometallurgical refining of blister copper removes many impurities, but it does not recover or remove silver or gold; the precious metals are recovered, however, by subsequent electrolytic refining.
Pyrometallurgy
Two of the most common pyrometallurgical processes, in both extraction and refining, are oxidation and reduction. In oxidation, metals having a great affinity for oxygen selectively combine with it to form metallic oxides; these can be treated further in order to obtain a pure metal or can be separated and discarded as a waste product. Reduction can be viewed as the reverse of oxidation. In this process, a metallic oxide compound is fed into a furnace along with a reducing agent such as carbon. The metal releases its combined oxygen, which recombines with the carbon to form a new carbonaceous oxide and leaves the metal in an uncombined form.
Oxidation and reduction reactions are either exothermic (energy-releasing) or endothermic (energy-absorbing). One example of an exothermic reaction is the oxidation of iron sulfide (FeS) to form iron oxide (FeO) and sulfur dioxide (SO2) gas:
This process gives off large quantities of heat beyond that required to initiate the reaction. One endothermic reaction is the smelting reduction of zinc oxide (ZnO) by carbon monoxide (CO) to yield zinc (Zn) metal and carbon dioxide (CO2):
For this reaction to proceed at a reasonable rate, external heat must be supplied to maintain the temperature at 1,300 to 1,350 °C (2,375 to 2,450 °F).
Roasting
As stated above, for those instances in which a metal-bearing compound is not in a chemical form that permits the metal to be easily and economically removed, it is necessary first to change it into some other compound. The preliminary treatment that is commonly used to do this is roasting.
Processes
There are several different types of roast, each one intended to produce a specific reaction and to yield a roasted product (or calcine) suitable for the particular processing operation to follow. The roasting procedures are:
1. Oxidizing roasts, which remove all or part of the sulfur from sulfide metal compounds, replacing the sulfides with oxides. (The sulfur removed goes off as sulfur dioxide gas.) Oxidizing roasts are exothermic.
2. Sulfatizing roasts, which convert certain metals from sulfides to sulfates. Sulfatizing roasts are exothermic.
3. Reducing roasts, which lower the oxide state or even completely reduce an oxide to a metal. Reducing roasts are exothermic.
4. Chloridizing roasts, or chlorination, which change metallic oxides to chlorides by heating with a chlorine source such as chlorine gas, hydrochloric acid gas, ammonium chloride, or sodium chloride. These reactions are exothermic.
5. Volatilizing roasts, which eliminate easily volatilized oxides by converting them to gases.
6. Calcination, in which solid material is heated to drive off either carbon dioxide or chemically combined water. Calcination is an endothermic reaction.