Iron(II) oxide
Names | |
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IUPAC name
Iron(II) oxide | |
Other names
Ferrous oxide,iron monoxide | |
Identifiers | |
1345-25-1 | |
ChEBI | CHEBI:50820 |
ChemSpider | 14237 |
Jmol interactive 3D | Image |
PubChem | 14945 |
UNII | G7036X8B5H |
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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 |
Refractive index (nD) |
2.23 |
Hazards | |
Main hazards | can be pyrophoric |
Safety data sheet | ICSC 0793 |
NFPA 704 | |
variable | |
Related compounds | |
Other anions |
iron(II) fluoride, iron(II) sulfide, iron(II) selenide, iron(II) telluride |
Other cations |
manganese(II) oxide, cobalt(II) oxide |
Related compounds |
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). | |
verify (what is ?) | |
Infobox references | |
Iron(II) 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, 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]
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 for filtering phosphates from home aquaria.
References
- ↑ Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8
- 1 2 Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 0-08-037941-9.
- ↑ 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
- 1 2 3 Wells A.F. (1984) Structural Inorganic Chemistry 5th edition Oxford University Press ISBN 0-19-855370-6
- ↑ Science Jan 2012
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