Tungsten trioxide
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IUPAC name
Tungsten trioxide
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Other names
Tungstic anhydride
Tungsten(VI) oxide Tungstic oxide | |
Identifiers | |
3D model (
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ECHA InfoCard
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100.013.848 |
PubChem CID
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RTECS number
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UNII | |
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Properties | |
WO3 | |
Molar mass | 231.84 g/mol |
Appearance | Canary yellow powder |
Density | 7.16 g/cm3 |
Melting point | 1,473 °C (2,683 °F; 1,746 K) |
Boiling point | 1,700 °C (3,090 °F; 1,970 K) approximation |
insoluble | |
Solubility | slightly soluble in HF |
−15.8·10−6 cm3/mol | |
Structure | |
Monoclinic, mP32
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P121/n1, No. 14 | |
Octahedral (WVI) Trigonal planar (O2– ) | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Irritant |
Flash point | Non-flammable |
Safety data sheet (SDS) | External MSDS |
Related compounds | |
Other anions
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Tungsten trisulfide |
Other cations
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Chromium trioxide Molybdenum trioxide |
Tungsten(III) oxide Tungsten(IV) oxide | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tungsten(VI) oxide, also known as tungsten trioxide is a chemical compound of oxygen and the transition metal tungsten, with formula WO3. The compound is also called tungstic anhydride, reflecting its relation to tungstic acid H2WO4. It is a light yellow crystalline solid.[1]
Tungsten(VI) oxide occurs naturally in the form of hydrates, which include minerals: tungstite WO3·H2O, meymacite WO3·2H2O and hydrotungstite (of the same composition as meymacite, however sometimes written as H2WO4). These minerals are rare to very rare secondary tungsten minerals.
History
In 1841, a chemist named Robert Oxland gave the first procedures for preparing tungsten trioxide and sodium tungstate.[2] He was granted patents for his work soon after, and is considered to be the founder of systematic tungsten chemistry.[2]
Structure and properties
The crystal structure of tungsten trioxide is temperature dependent. It is
The pure compound is an electric insulator, but oxygen-deficient varieties, such as WO2.90 = W20O58, are dark blue to purple in color and conduct electricity. They can be prepared by combining the trioxide and the
Possible signs of superconductivity with critical temperatures Tc = 80–90 K were claimed in sodium-doped and oxygen-deficient WO3 crystals. If confirmed, these would be the first superconducting materials containing no copper, with Tc higher than the boiling point of liquid nitrogen at normal pressure. [5][4]
Preparation
Industrial
Tungsten trioxide is obtained as an intermediate in the recovery of tungsten from its minerals.
- CaWO4 + 2 HCl → CaCl2 + H2WO4
- H2WO4 → H2O + WO3
Laboratory
Another common way to synthesize WO3 is by calcination of ammonium paratungstate (APT) under oxidizing conditions:[2]
Reactions
Tungsten trioxide can be reduced with carbon or hydrogen gas yielding the pure metal.[citation needed]
- 2 WO3 + 3 C → 2 W + 3 CO2 (high temperature)
- WO3 + 3 H2 → W + 3 H2O (550–850 °C)
Uses
Tungsten trioxide is a starting material for the synthesis of
- Fireproofing fabrics[7]
- Ceramic glazes where it gives a rich yellow color.[6][1]
- Photocatalytic water splitting.[11][12][13][14]
- Substrate for surface-enhanced Raman spectroscopy replacing noble metals.[15][16][17][18]
References
- ^ a b c d e f J. Christian, R.P. Singh Gaur, T. Wolfe and J. R. L. Trasorras (2011): Tungsten Chemicals and their Applications. Brochure by International Tungsten Industry Association.
- ^ ISBN 978-0-306-45053-2.
- ^
- S2CID 121476634
- ^ ISBN 978-0-07-049439-8. Retrieved 2009-06-06.
- ^ Merck (2006): "Tungsten trioxide." The Merck Index, volume 14.
- S2CID 98302697.
- ^ K. J. Patel, M. S. Desai, C. J. Panchal, H. N. Deota, and U. B. Trivedi (2013): "All-Solid-Thin Film Electrochromic Devices Consisting of Layers ITO / NiO / ZrO2 / WO3 / ITO". Journal of Nano-Electronics and Physics, volume 5, issue 2, article 02023.
- PMID 29615620.
- .
- S2CID 49716355.
- S2CID 201278374.