Nb2O5 is attacked by HF and dissolves in fused alkali.
Reduction to the metal The conversion of Nb2O5 is the main route for the industrial production of niobium metal. In the 1980s, about 15,000,000 kg of Nb2O5 were consumed annually for reduction to the metal. The main method is reduction of this oxide with
aluminium: :3 Nb2O5 + 10 Al → 6 Nb + 5 Al2O3 An alternative but less practiced route involves carbothermal reduction, which proceeds via reduction with carbon and forms the basis of the two stage Balke process: :Nb2O5 + 7 C → 2 NbC + 5 CO (heated under vacuum at 1800 °C) :5 NbC + Nb2O5 → 7 Nb + 5 CO
Conversion to halides Many methods are known for conversion of Nb2O5 to the halides. The main problem is incomplete reaction to give the oxyhalides. In the laboratory, the conversion can be effected with thionyl chloride: :Nb2O5 + 5 SOCl2 → 2 NbCl5 + 5 SO2 Nb2O5 reacts with
CCl4 to give
niobium oxychloride NbOCl3.
Conversion to niobates Treating Nb2O5 with aqueous
NaOH at 200 °C can give crystalline sodium niobate, NaNbO3 whereas the reaction with
KOH may yield soluble Lindqvist-type hexaniobates, .
Lithium niobates such as LiNbO3 and Li3NbO4 can be prepared by reaction
lithium carbonate and Nb2O5. :Nb2O5 + 3Nb → 5 NbO The burgundy-coloured niobium(III) oxide, one of the first superconducting oxides, can be prepared again by an comproportionation: :Li3NbO4 + 2 NbO → 3 LiNbO2 ==Uses==