Niobium pentoxide

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Niobium pentoxide
Niobium-pentoxide-2D-dimensions.svg
Niobium-pentoxide-3D-balls.png
Niobium-pentoxide-3D-vdW.png
Kristallstruktur Niob(V)-oxid.png
Names
IUPAC name
Niobium(V) oxide
Other names
Niobium pentoxide
Identifiers
  • 1313-96-8 checkY
3D model (JSmol)
ECHA InfoCard 100.013.831 Edit this at Wikidata
UNII
Properties
Nb2O5
Molar mass 265.81 g/mol
Appearance white orthogonal solid
Density 4.60 g/cm3
Melting point 1,512 °C (2,754 °F; 1,785 K)
insoluble
Solubility soluble in HF
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N  (what is checkY☒N ?)
Infobox references

Niobium pentoxide is the inorganic compound with the formula Nb2O5. It is a colorless 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.[1]

Structure[]

It has many polymorphic forms all based largely on octahedrally coordinated niobium atoms.[2][3] The polymorphs are identified with a variety of prefixes.[2][3] 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.[4] 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.[5]

Molten niobium pentoxide has lower mean coordination numbers than the crystalline forms, with a structure comprising mostly NbO5 and NbO6 polyhedra.[6]

Production[]

Hydrolysis[]

Nb2O5 is prepared by hydrolysis of alkali-metal niobates, alkoxides or fluoride using base. Such ostensibly simple procedures afford hydrated oxides that can then be calcined. Pure Nb2O5 can also be prepared by hydrolysis of NbCl5:[7]

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 orthorhombic form,[2] T-Nb2O5.[8]

Oxidation[]

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.[9] The oxidation of niobium dioxide, NbO2 in air forms the polymorph, L-Nb2O5.[10]

Nano-sized niobium pentoxide particles have been synthesized by LiH reduction of NbCl5, followed by aerial oxidation as part of a synthesis of nano structured niobates.[citation needed]

Reactions[]

Nb2O5 is attacked by HF and dissolves in fused alkali.[5][9]

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.[11] 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:[12][13]

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:[14]

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, Nb
6O8−
19.[15] Lithium niobates such as LiNbO3 and Li3NbO4 can be prepared by reaction lithium carbonate and Nb2O5.[16][17]

Conversion to reduced niobium oxides[]

High temperature reduction with H2 gives NbO2:[9]

Nb2O5 + H2 → 2 NbO2 + H2O

Niobium monooxide arises from a comproportionation using an arc-furnace:[18]

Nb2O5 + 3Nb → 5 NbO

The burgundy-coloured niobium(III) oxide, one of the first superconducting oxides, can be prepared again by an comproportionation:[17]

Li3NbO4 + 2 NbO → 3 LiNbO2

Uses[]

Niobium pentoxide is used mainly in the production of niobium metal,[11] but specialized applications exist for lithium niobate and as a component of optical glass.[1]

Thin films of Nb2O5 form the dielectric layers in solid electrolyte capacitors.

External links[]

References[]

  1. ^ Jump up to: a b Francois Cardarelli (2008) Materials Handbook Springer London ISBN 978-1-84628-668-1
  2. ^ Jump up to: a b c C. Nico; et al. (2011). "Sintered NbO powders for electronic device applications". The Journal of Physical Chemistry C. 115 (11): 4879–4886. doi:10.1021/jp110672u.
  3. ^ Jump up to: a b Wells A.F. (1984) Structural Inorganic Chemistry 5th edition Oxford Science Publications ISBN 0-19-855370-6
  4. ^ The crystal structure of the high temperature form of niobium pentoxide B. M. Gatehouse and A. D. Wadsley Acta Crystallogr. (1964). 17, 1545-1554 doi:10.1107/S0365110X6400384X
  5. ^ Jump up to: a b D.A. Bayot and M.M. Devillers, Precursors routes for the preparation of Nb based multimetallic oxides in Progress in Solid State Chemistry Research, Arte M. Newman, Ronald W. Buckley, (2007),Nova Publishers, ISBN 1-60021-313-8
  6. ^ Alderman, O. L. G. Benmore, C. J. Neuefeind, J. C. Coillet, E Mermet, Alain Martinez, V. Tamalonis, A. Weber, J. K. R. (2018). "Amorphous tantala and its relationship with the molten state". Physical Review Materials. 2 (4): 043602.CS1 maint: multiple names: authors list (link)
  7. ^ Process for the manufacture of niobium pentoxide or tantalum pentoxide, Kern, Therwil, Jacob, Hooper (CIBA Switzerland), US Patent number: 3133788, (1964)
  8. ^ Sol-gel route to niobium pentoxide, P Griesmar, G Papin, C Sanchez, J Livage - Chem. Mater.; 1991; 3(2); 335-339 doi:10.1021/cm00014a026
  9. ^ Jump up to: a b c Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  10. ^ Electrical properties of NbO2 and Nb2O5 at elevated temperature in air and flowing argon, G. C. Vezzoli Phys. Rev. B 26, 3954 - 3957 (1982)doi:10.1103/PhysRevB.26.3954
  11. ^ Jump up to: a b Joachim Eckert, Hermann C. Starck "Niobium and Niobium Compounds" Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a17_251
  12. ^ Alan E. Comyns (1999) Encyclopedic Dictionary of Named Processes in Chemical Technology CRC Press, ISBN 0-8493-1205-1
  13. ^ U.S. Environmental Protection Agency, Development Document for Effluent Limitations, Guidelines and Standards for the Nonferrous Metals Manufacturing Point Source Category, Volume VIII, Office of Water Regulations and Standards, May 1989
  14. ^ D. Brown "Niobium(V) Chloride and Hexachloroniobates(V)" Inorganic Syntheses, 1957 Volume 9, pp. 88–92.doi:10.1002/9780470132401.ch24
  15. ^ Studies on the hydrothermal synthesis of niobium oxides, I.C. M. S. Santos, L. H. Loureiro, M. F. P. Silva and Ana M. V. Cavaleiro, Polyhedron, 21, 20, (2002), 2009-2015, doi:10.1016/S0277-5387(02)01136-1
  16. ^ US Patent 5482001 - Process for producing lithium niobate single crystal,1996, Katoono T., Tominaga H.,
  17. ^ Jump up to: a b Margret J. Geselbracht, Angelica M. Stacy, "Lithium Niobium Oxide: LiNbo2 and Superconducting LiXNbO2" Inorganic Syntheses 1995, Volume 30, Pages: 222–226.doi:10.1002/9780470132616.ch42
  18. ^ T. B. Reed, E. R. Pollard "Niobium Monoxide" Inorganic Syntheses, 1995 Volume 30, pp. 108–110, 2007. doi:10.1002/9780470132616.ch22
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