Global production of antimony(III) oxide in 2012 was 130,000 tonnes, an increase from 112,600 tonnes in 2002. China produces the largest share followed by US/Mexico, Europe, Japan and South Africa and other countries (2%). As of 2010, antimony(III) oxide was produced at four sites in the EU. It is produced via two routes, re-volatilizing of crude antimony(III) oxide and by oxidation of antimony metal. Oxidation of antimony metal dominates in Europe. Several processes for the production of crude antimony(III) oxide or metallic antimony from virgin material. The choice of process depends on the composition of the ore and other factors. Typical steps include mining, crushing and grinding of ore, sometimes followed by
froth flotation and separation of the metal using pyrometallurgical processes (smelting or roasting) or in a few cases (e.g. when the ore is rich in precious metals) by hydrometallurgical processes. These steps do not take place in the EU but closer to the mining location.
Re-volatilizing of crude antimony(III) oxide Step 1) Crude stibnite is oxidized to crude antimony(III) oxide using furnaces operating at approximately 500 to 1,000 °C. The reaction is the following: :2 Sb2S3 + 9 O2 → 2 Sb2O3 + 6 SO2 Step 2) The crude antimony(III) oxide is purified by
sublimation.
Oxidation of antimony metal Antimony metal is oxidized to antimony(III) oxide in furnaces. The reaction is exothermic. Antimony(III) oxide is formed through sublimation and recovered in bag filters. The size of the formed particles is controlled by process conditions in furnace and gas flow. The reaction can be schematically described by: :4 Sb + 3 O2 → 2 Sb2O3
Properties Antimony(III) oxide is an
amphoteric oxide. It dissolves in aqueous
sodium hydroxide solution to give the meta-antimonite NaSbO2, which can be isolated as the trihydrate. Antimony(III) oxide also dissolves in concentrated
mineral acids to give the corresponding salts, which hydrolyzes upon dilution with water. With
nitric acid, the trioxide is oxidized to
antimony(V) oxide. When heated with
carbon, the oxide is reduced to
antimony metal. With other reducing agents such as
sodium borohydride or
lithium aluminium hydride, the unstable and very toxic gas
stibine is produced. When heated with
potassium bitartrate, a complex salt
potassium antimony tartrate, KSb(OH)2·C4H2O6, is formed. ==Structure==