Names | |
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IUPAC name
Cadmium oxide
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Other names
Cadmium(II) oxide,
Cadmium monoxide |
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Identifiers | |
1306-19-0 | |
3D model (Jmol) | Interactive image |
ChemSpider | 14099 |
ECHA InfoCard | 100.013.770 |
EC Number | 215-146-2 |
PubChem | 14782 |
RTECS number | EV1925000 |
UN number | 2570 |
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Properties | |
CdO | |
Molar mass | 128.41 g·mol−1 |
Appearance | colorless powder (alpha form) red-brown crystal (beta form) |
Odor | odorless |
Density | 8.15 g/cm3(crystalline), 6.95 g/cm3 (amorphous) solid. |
Melting point | 900–1,000 °C (1,650–1,830 °F; 1,170–1,270 K) decomposition of amorphous form |
Boiling point | 1,559 °C (2,838 °F; 1,832 K) sublimation |
4.8 mg/L (18 °C) | |
Solubility | soluble in dilute acid slowly soluble in ammonium salts insoluble in alkalies |
Vapor pressure | 0.13 kPa (1000 °C) 2.62 kPa (1200 °C) 61.4 kPa (1500 °C) |
Band gap | 2.18 eV |
Electron mobility | 531 cm2/V·s |
-3.0·10−5</sup cm3/mol | |
Thermal conductivity | 0.7 W/m·K |
Refractive index (nD)
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2.49 |
Structure | |
cubic, cF8 | |
Fm3m, No. 225 | |
a = 4.6958 Å
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Thermochemistry | |
43.64 J/mol·K | |
Std molar
entropy (S |
55 J/mol·K |
Std enthalpy of
formation (ΔfH |
−258 kJ/mol |
Gibbs free energy (ΔfG˚)
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-229.3 kJ/mol |
Hazards | |
Safety data sheet | [1] |
GHS pictograms | |
GHS signal word | Danger |
H330, H341, H350, H361, H372, H410 | |
P201, P260, P273, P281, P284, P310 | |
EU classification (DSD)
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T+ N Carc. Cat. 2 Muta. Cat. 3 Repr. Cat. 3 |
R-phrases | R45, R26, R48/23/25, R62, R63, R68, R50/53 |
S-phrases | S53, S45, S60, S61 |
NFPA 704 | |
Flash point | Non-flammable |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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72 mg/kg (oral, rat) 72 mg/kg (oral, mouse) |
LC50 (median concentration)
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500 mg/m3 (rat, 10 min) 2500 mg/m3 (rabbit, 10 min) 3500 mg/m3 (guinea pig, 10 min) 4000 mg/m3 (dog, 10 min) 780 mg/m3 (rat, 10 min) 340 mg/m3 (mouse, 10 min) 3000 mg/m3 (rabbit, 15 min) 3000 mg/m3 (guinea pig, 15 min) 400 mg/m3 (dog, 10 min) |
US health exposure limits (NIOSH): | |
PEL (Permissible)
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[1910.1027] TWA 0.005 mg/m3 (as Cd) |
REL (Recommended)
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Ca |
IDLH (Immediate danger)
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Ca [9 mg/m3 (as Cd)] |
Related compounds | |
Other anions
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Cadmium sulfide Cadmium selenide Cadmium telluride |
Other cations
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Zinc oxide Mercury 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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what is ?) | (|
Infobox references | |
Cadmium oxide is an inorganic compound with the formula CdO. It is one of the main precursors to other cadmium compounds. It crystallizes in a cubic rocksalt lattice like sodium chloride, with octahedral cation and anion centers. It occurs naturally as the rare mineral monteponite. Cadmium oxide can be found as a colorless amorphous powder or as brown or red crystals. Cadmium oxide is an n-type semiconductor with a band gap of 2.18 eV (2.31 eV) at room temperature (298 K).
Since cadmium compounds are often found in association with zinc ores, cadmium oxide is a common by-product of zinc refining. It is produced by burning elemental cadmium in air. Pyrolysis of other cadmium compounds, such as the nitrate or the carbonate, also affords this oxide. When pure, it is red, but CdO is unusual in being available in many differing colours due to its tendency to form defect structures resulting from anion vacancies. Cadmium oxide is prepared commercially by oxidizing cadmium vapor in air.
Cadmium oxide is used in cadmium plating baths, electrodes for storage batteries, cadmium salts, catalyst, ceramic glazes, phosphors, and nematocide. Major uses for cadmium oxide are as an ingredient for electroplating baths, and in pigments.
CdO is used as a transparent conductive material, which was prepared as a transparent conducting film as early as 1907 by Karl Baedeker. Cadmium oxide in the form of thin films has been used in applications such as photodiodes, phototransistors, photovoltaic cells, transparent electrodes, liquid crystal displays, IR detectors, and anti reflection coatings. CdO microparticles undergo bandgap excitation when exposed to UV-A light and is also selective in phenol photodegradation.