Lateritic bauxites (silicate bauxites) are distinguished from karst bauxite ores (carbonate bauxites). The carbonate bauxites occur predominantly in Europe and Jamaica above carbonate rocks (limestone and dolomite), where they were formed by lateritic weathering and residual accumulation of intercalated clay layers – dispersed clays which were concentrated as the enclosing limestones gradually dissolved during chemical weathering.
The lateritic bauxites are found mostly in the countries of the tropics. They were formed by lateritization of various silicate rocks such as granite, gneiss, basalt, syenite, and shale. In comparison with the iron-rich laterites, the formation of bauxites depends even more on intense weathering conditions in a location with very good drainage. This enables the dissolution of the kaolinite and the precipitation of the gibbsite. Zones with highest aluminium content are frequently located below a ferruginous surface layer. The aluminium hydroxide in the lateritic bauxite deposits is almost exclusively gibbsite.
In the case of Jamaica, recent analysis of the soils showed elevated levels of cadmium, suggesting that the bauxite originates from recent Mioceneash deposits from episodes of significant volcanism in Central America.
In 2009, Australia was the top producer of bauxite with almost one-third of the world's production, followed by China, Brazil, India, and Guinea. Although aluminium demand is rapidly increasing, known reserves of its bauxite ore are sufficient to meet the worldwide demands for aluminium for many centuries. Increased aluminium recycling, which has the advantage of lowering the cost in electric power in producing aluminium, will considerably extend the world's bauxite reserves.
Numbers for 2010's total proven bauxite reserves x1,000 tonne
Bauxite being digested by washing with a hot solution of sodium hydroxide at 175°C under pressure at National Aluminium Company, Nalconagar, India.
Bauxite is usually strip mined because it is almost always found near the surface of the terrain, with little or no overburden. Approximately 70% to 80% of the world's dry bauxite production is processed first into alumina, and then into aluminium by electrolysis as of 2010. Bauxite rocks are typically classified according to their intended commercial application: metallurgical, abrasive, cement, chemical, and refractory.
Usually, bauxite ore is heated in a pressure vessel along with a sodium hydroxide solution at a temperature of 150 to 200 °C. At these temperatures, the aluminium is dissolved as sodium aluminate (the Bayer process). The aluminium compounds in the bauxite may be present as gibbsite(Al(OH)3), boehmite(AlOOH) or diaspore(AlOOH); the different forms of the aluminium component will dictate the extraction conditions. The undissolved waste, bauxite tailings, after the aluminium compounds are extracted contains iron oxides, silica, calcia, titania and some un-reacted alumina. After separation of the residue by filtering, pure gibbsite is precipitated when the liquid is cooled, and then seeded with fine-grained aluminium hydroxide. The gibbsite is usually converted into aluminium oxide, Al2O3, by heating in rotary kilns or fluid flash calciners to a temperature in excess of 1000oC. This aluminium oxide is dissolved at a temperature of about 960 °C in molten cryolite. Next, this molten substance can yield metallic aluminium by passing an electric current through it in the process of electrolysis, which is called the Hall–Héroult process, named after its American and French discoverers.
Prior to the invention of this process in 1886, elemental aluminium was made by heating ore along with elemental sodium or potassium in a vacuum. The method was complicated and consumed materials that were themselves expensive at that time. This made early elemental aluminium more expensive than gold.
In 1847, in the cumulative index of volume 3 of his series, Traité de minéralogie, French mineralogist Armand Dufrénoy listed the hydrated alumina from Les Beaux as "beauxite". (See: A. Dufrénoy, Traité de minéralogie, volume 3 (Paris, France: Carilian-Goeury et Vor Dalmont, 1847), p. 799.)