Iron(II) oxide
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IUPAC name
Iron(II) oxide
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Other names
Ferrous oxide,iron monoxide
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.014.292 |
13590 | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
FeO | |
Molar mass | 71.844 g/mol |
Appearance | black crystals |
Density | 5.745 g/cm3 |
Melting point | 1,377 °C (2,511 °F; 1,650 K)[1] |
Boiling point | 3,414 °C (6,177 °F; 3,687 K) |
Insoluble | |
Solubility | insoluble in alkali, alcohol dissolves in acid |
+7200·10−6 cm3/mol | |
Refractive index (nD)
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2.23 |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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can be pyrophoric |
NFPA 704 (fire diamond) | |
variable | |
Safety data sheet (SDS) | ICSC 0793 |
Related compounds | |
Other anions
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iron(II) fluoride, iron(II) sulfide, iron(II) selenide, iron(II) telluride |
Other cations
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manganese(II) oxide, cobalt(II) oxide |
Related compounds
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Iron(III) oxide, Iron(II,III) 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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Iron(II) oxide or ferrous oxide is the inorganic compound with the formula FeO. Its mineral form is known as wüstite. One of several iron oxides, it is a black-colored powder that is sometimes confused with rust, the latter of which consists of hydrated iron(III) oxide (ferric oxide). Iron(II) oxide also refers to a family of related non-stoichiometric compounds, which are typically iron deficient with compositions ranging from Fe0.84O to Fe0.95O.[2]
Preparation
FeO can be prepared by the thermal decomposition of iron(II) oxalate.
- FeC2O4 → FeO + CO2 + CO
The procedure is conducted under an inert atmosphere to avoid the formation of ferric oxide. A similar procedure can also be used for the synthesis of manganous oxide and stannous oxide.[3][4]
Stoichiometric FeO can be prepared by heating Fe0.95O with metallic iron at 770 °C and 36 kbar.[5]
Reactions
FeO is thermodynamically unstable below 575 °C, tending to disproportionate to metal and Fe3O4:[2]
- 4FeO → Fe + Fe3O4
Structure
Iron(II) oxide adopts the cubic, rock salt structure, where iron atoms are octahedrally coordinated by oxygen atoms and the oxygen atoms octahedrally coordinated by iron atoms. The non-stoichiometry occurs because of the ease of oxidation of FeII to FeIII effectively replacing a small portion of FeII with two thirds their number of FeIII, which take up tetrahedral positions in the close packed oxide lattice.[5]
Below 200 K there is a minor change to the structure which changes the symmetry to rhombohedral and samples become antiferromagnetic.[5]
Occurrence in nature
Iron(II) oxide makes up approximately 9% of the Earth's mantle. Within the mantle, it may be electrically conductive, which is a possible explanation for perturbations in Earth's rotation not accounted for by accepted models of the mantle's properties.[6]
Iron dissolved in groundwater is in the reduced iron II form. If this groundwater comes in contact with oxygen at the surface, e.g. in natural springs, iron II is oxidised to iron III and forms insoluble hydroxides in water.[7]
Uses
Iron(II) oxide is used as a pigment. It is FDA-approved for use in cosmetics and it is used in some tattoo inks. It can also be used as a phosphate remover from home aquaria.
References
- ^ Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8
- ^ a b Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
- ^ H. Lux "Iron (II) Oxide" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 1497.
- ^ Practical Chemistry for Advanced Students, Arthur Sutcliffe, 1930 (1949 Ed.), John Murray - London
- ^ a b c Wells A.F. (1984) Structural Inorganic Chemistry 5th edition Oxford University Press ISBN 0-19-855370-6
- ^ Science Jan 2012 Archived January 24, 2012, at the Wayback Machine
- ^ lenntech.com