Jump to content

Thallium(III) oxide

From Wikipedia, the free encyclopedia
Thallium(III) oxide
Thallium(III) oxide
Names
Other names
thallium trioxide, thallium sesquioxide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.013.846Edit this at Wikidata
EC Number
  • 215-229-3
UNII
  • InChI=1S/3O.2Tl/q3*-2;2*+3checkY
    Key: LPHBARMWKLYWRA-UHFFFAOYSA-NcheckY
  • [O-2].[O-2].[O-2].[Tl+3].[Tl+3]
Properties[1]
Tl2O3
Molar mass 456.76 g/mol
Appearance dark brown solid
Density 10.19 g/cm3,solid (22 °C)
Melting point 717 °C (1,323 °F; 990 K)
Boiling point 875 °C (1,607 °F; 1,148 K) (decomposes)
insoluble
+76.0·10−6cm3/mol
Structure
Cubic,(Bixbyite)cI80[2]
Ia3(No. 206)
Hazards
GHSlabelling:[3]
GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard
Danger
H300+H330,H373,H411
P273,P301+P310+P330,P304+P340+P310,P314
NFPA 704(fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
4
0
0
Lethal doseor concentration (LD, LC):
44 mg/kg (oral, rat)
Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).

Thallium(III) oxide,also known asthallic oxide,is a chemical compound ofthalliumandoxygen.It occurs in nature as the rare mineralavicennite.[4]Its structure is related to that of Mn2O3which has abixbyitelike structure. Tl2O3is metallic with high conductivity and is a degenerate n-typesemiconductorwhich may have potential use insolar cells.[5]A method of producing Tl2O3byMOCVDis known.[6]Any practical use of thallium(III) oxide will always have to take account of thallium's poisonous nature. Contact withmoistureandacidsmay form poisonous thallium compounds.

Production

[edit]

It is produced by the reaction of thallium with oxygen orhydrogen peroxidein an alkaline thallium(I) solution. Alternatively, it can be created by the oxidation ofthallium(I) nitrateby chlorine in an aqueouspotassium hydroxidesolution.[7]

References

[edit]
  1. ^Weast, Robert C., ed. (1981).CRC Handbook of Chemistry and Physics(62nd ed.). Boca Raton, FL: CRC Press. p. B156.ISBN0-8493-0462-8..
  2. ^Otto H.H.; Baltrasch R.; Brandt H.J. (1993). "Further evidence for Tl3+ in Tl-based superconductors from improved bond strength parameters involving new structural data of cubic Tl2O3".Physica C.215(1–2): 205.doi:10.1016/0921-4534(93)90382-Z.
  3. ^GHS:Sigma-Aldrich 204617
  4. ^http://www.handbookofmineralogy.org/pdfs/avicennite.pdfHandbook of Mineralogy
  5. ^Phillips R. J.; Shane M. J.; Switzer J. A. (1989). "Electrochemical and photoelectrochemical deposition of Thallium(III) Oxide thin films".Journal of Materials Research.4(4): 923.Bibcode:1989JMatR...4..923P.doi:10.1557/JMR.1989.0923.S2CID96808351.
  6. ^D. Berry; R. T. Holm; R. L. Mowery; N. H. Turner & M. Fatemi (1991). "Thallium(III) Oxide by Organometallic Chemical Vapor Deposition".Chemistry of Materials.3(1): 72–77.doi:10.1021/cm00013a019.
  7. ^Georg Brauer; Handbuch der präparativen anorganischen Chemie, Band 2, S.884;ISBN3-432-87813-3(in German)