|Jmol-3D images||Image 1|
|Molar mass||265.81 g/mol|
|Appearance||white orthogonal solid|
|Melting point||1,512 °C (2,754 °F; 1,785 K)|
|Solubility in water||insoluble|
|Solubility||soluble in HF|
|Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)|
|(what is: / ?)|
Niobium pentoxide is the inorganic compound with the formula Nb2O5. It is a colourless insoluble solid that is fairly unreactive. It is the main precursor to all materials made of niobium, the dominant application being alloys, but other specialized applications include capacitors, lithium niobate, and optical glasses.
It has many polymorphic forms all based largely on octahedrally coordinated niobium atoms. The polymorphs are identified with a variety of prefixes.   The form most commonly encountered is monoclinic H-Nb2O5 which has a complex structure, with a unit cell containing 28 niobium atoms and 70 oxygen, where 27 of the niobium atoms are octahedrally coordinated and one tetrahedrally. There is an uncharacterised solid hydrate, Nb2O5.nH2O, the so-called niobic acid (previously called columbic acid), which can be prepared by hydrolysis of a basic solution of niobium pentachloride or Nb2O5 dissolved in HF.
Nb2O5 is prepared by hydrolysis of alkali-metal niobates and alkoxides and the fluorides using base. Such ostensibly simple procedures afford hydrated oxides that are calcined.
Given that Nb2O5 is the most common and robust compound of niobium, many methods, both practical and esoteric, exist for its formation. The oxide for example, arises when niobium metal is oxidised in air. The oxidation of niobium dioxide, NbO2 in air forms the polymorph, L-Nb2O5. Pure Nb2O5 can be prepared by hydrolysis of NbCl5:
- 2 NbCl5 + 5 H2O → Nb2O5 + 10 HCl
A method of production via sol-gel techniques has been reported hydrolysing niobium alkoxides in the presence of acetic acid, followed by calcination of the gels to produce the polymorphic form, T-Nb2O5.
Nano-sized niobium pentoxide particles have been synthesised by LiH reduction of NbCl5, followed by aerial oxidation as part of a synthesis of nano structured niobates.
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
- 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
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, Nb
19. Lithium niobates such as LiNbO3 and Li3NbO4 can be prepared by reaction lithium carbonate and Nb2O5.
Conversion to reduced niobium oxides
High temperature reduction with H2 gives NbO2:
- Nb2O5 + H2 → 2 NbO2 + H2O
Niobium monooxide arises from a comproportionation using an arc-furnace:
- 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
- Basic Niobium Information and Research Data
- Thin films of Nb2O5 form the dielectric layers in solid electrolyte capacitors and these layers can be grown electrolytically on sintered bodies containing niobium monoxide.Katsuhiro Yoshida, Noriko Kuge (NEC Corporation), Sintered bodies based on niobium suboxide US patent 6215652, 2001.
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