Iron oxide: Difference between revisions

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** Fe<sub>5</sub>O<sub>7</sub><ref name = "oxides">{{cite journal| title = Structural complexity of simple Fe2O3 at high pressures and temperatures| journal = Nature Communications| volume = 7| pages = 10661| doi = 10.1038/ncomms10661| pmid = 26864300| pmc = 4753252| year = 2016| last1 = Bykova| first1 = E.| last2 = Dubrovinsky| first2 = L.| last3 = Dubrovinskaia| first3 = N.| last4 = Bykov| first4 = M.| last5 = McCammon| first5 = C.| last6 = Ovsyannikov| first6 = S. V.| last7 = Liermann| first7 = H. -P.| last8 = Kupenko| first8 = I.| last9 = Chumakov| first9 = A. I.| last10 = Rüffer| first10 = R.| last11 = Hanfland| first11 = M.| last12 = Prakapenka| first12 = V.| bibcode = 2016NatCo...710661B}}</ref>
** Fe<sub>5</sub>O<sub>7</sub><ref name = "oxides">{{cite journal| title = Structural complexity of simple Fe2O3 at high pressures and temperatures| journal = Nature Communications| volume = 7| pages = 10661| doi = 10.1038/ncomms10661| pmid = 26864300| pmc = 4753252| year = 2016| last1 = Bykova| first1 = E.| last2 = Dubrovinsky| first2 = L.| last3 = Dubrovinskaia| first3 = N.| last4 = Bykov| first4 = M.| last5 = McCammon| first5 = C.| last6 = Ovsyannikov| first6 = S. V.| last7 = Liermann| first7 = H. -P.| last8 = Kupenko| first8 = I.| last9 = Chumakov| first9 = A. I.| last10 = Rüffer| first10 = R.| last11 = Hanfland| first11 = M.| last12 = Prakapenka| first12 = V.| bibcode = 2016NatCo...710661B}}</ref>
** Fe<sub>25</sub>O<sub>32</sub><ref name="oxides" />
** Fe<sub>25</sub>O<sub>32</sub><ref name="oxides" />
**Fe<sub>13</sub>O<sub>19</sub><ref>{{cite journal| title = The crystal structures of Mg2Fe2C4O13, with tetrahedrally coordinated carbon, and Fe13O19, synthesized at deep mantle conditions| journal = American Mineralogist| volume = 100| issue = 8–9| pages = 2001–2004| doi = 10.2138/am-2015-5369| year = 2015| last1 = Merlini| first1 = Marco| last2 = Hanfland| first2 = Michael| last3 = Salamat| first3 = Ashkan| last4 = Petitgirard| first4 = Sylvain| last5 = Müller| first5 = Harald| bibcode = 2015AmMin.100.2001M| s2cid = 54496448}}</ref>
**Fe<sub>13</sub>O<sub>19</sub><ref>{{cite journal| title = The crystal structures of Mg2Fe2C4O13, with tetrahedrally coordinated carbon, and Fe13O19, synthesized at deep mantle conditions| journal = American Mineralogist| volume = 100| issue = 8–9| pages = 2001–2004| doi = 10.2138/am-2015-5369| year = 2015| last1 = Merlini| first1 = Marco| last2 = Hanfland| first2 = Michael| last3 = Salamat| first3 = Ashkan| last4 = Petitgirard| first4 = Sylvain| last5 = Müller| first5 = Harald| bibcode = 2015AmMin.100.2001M| s2cid = 54496448| doi-access = free}}</ref>
* Oxides of Fe<sup>III</sup>
* Oxides of Fe<sup>III</sup>
** Fe<sub>2</sub>O<sub>3</sub>: [[iron(III) oxide]]  
** Fe<sub>2</sub>O<sub>3</sub>: [[iron(III) oxide]]  

Latest revision as of 02:11, 24 June 2025

Template:Short description

File:Almindeligt rust - jernoxid.jpg
Electrochemically oxidized iron (rust)

An iron oxide is a chemical compound composed of iron and oxygen. Several iron oxides are recognized. Often they are non-stoichiometric. Ferric oxyhydroxides are a related class of compounds, perhaps the best known of which is rust.[1]

Iron oxides and oxyhydroxides are widespread in nature and play an important role in many geological and biological processes. They are used as iron ores, pigments, catalysts, and in thermite, and occur in hemoglobin. Iron oxides are inexpensive and durable pigments in paints, coatings and colored concretes. Colors commonly available are in the "earthy" end of the yellow/orange/red/brown/black range. When used as a food coloring, it has E number E172.

Stoichiometries

File:IronOxidePigmentUSGOV.jpg
Iron oxide pigment. The brown color indicates that iron is at the oxidation state +3.
File:Red and green iron oxides.jpg
Green and reddish brown stains on a limestone core sample, respectively corresponding to oxides/hydroxides of Fe2+ and Fe3+.

Iron oxides feature as ferrous (Fe(II)) or ferric (Fe(III)) or both. They adopt octahedral or tetrahedral coordination geometry. Only a few oxides are significant at the earth's surface, particularly wüstite, magnetite, and hematite.

Thermal expansion

Iron oxide CTE (× 10−6 °C−1)
Fe2O3 14.9[6]
Fe3O4 >9.2[6]
FeO 12.1[6]

Oxide-hydroxides

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Reactions

In blast furnaces and related factories, iron oxides are converted to the metal. Typical reducing agents are various forms of carbon. A representative reaction starts with ferric oxide:[9]

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In nature

Iron is stored in many organisms in the form of ferritin, which is a ferrous oxide encased in a solubilizing protein sheath.[10]

Species of bacteria, including Shewanella oneidensis, Geobacter sulfurreducens and Geobacter metallireducens, use iron oxides as terminal electron acceptors.[11]

Uses

Almost all iron ores are oxides, so in that sense these materials are important precursors to iron metal and its many alloys.

Iron oxides are important pigments, coming in a variety of colors (black, red, yellow). Among their many advantages, they are inexpensive, strongly colored, and nontoxic.[12]

Magnetite is a component of magnetic recording tapes.

See also

References

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External links

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Template:Iron compounds Template:Oxides

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