Iron(III) oxide-hydroxide or ferric oxyhydroxide[2] is the chemical compound of iron, oxygen, and hydrogen with formula FeO(OH).

Quick Facts Names, Identifiers ...
Iron(III) oxide-hydroxide
Thumb
Names
IUPAC name
Iron(III) oxide-hydroxide
Other names
Metaferric acid
Ferric oxyhydroxide
Goethite
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.039.754 Edit this at Wikidata
EC Number
  • 215-176-6
MeSH Goethite
UNII
  • InChI=1S/Fe.H2O.O/h;1H2;/q+1;;/p-1 checkY
    Key: AEIXRCIKZIZYPM-UHFFFAOYSA-M checkY
  • O=[Fe]O
Properties
FeO(OH)
Appearance Vivid, dark orange, opaque crystals
Odor odorless
Density 4.25 g/cm3
insoluble at pH 7
2.79×10−39 for Fe(OH)3[1]
Hazards
NFPA 704 (fire diamond)
ThumbHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
0
0
Pharmacology
B03AB04 (WHO)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The compound is often encountered as one of its hydrates, FeO(OH)·nH
2
O
[rust]. The monohydrate FeO(OH)·H
2
O
is often referred to as iron(III) hydroxide Fe(OH)
3
,[3] hydrated iron oxide, yellow iron oxide, or Pigment Yellow 42.[3]

Natural occurrences

Minerals

Anhydrous ferric hydroxide occurs in the nature as the exceedingly rare mineral bernalite, Fe(OH)3·nH2O (n = 0.0–0.25).[4][5] Iron oxyhydroxides, FeOOH, are much more common and occur naturally as structurally different minerals (polymorphs) denoted by the Greek letters α, β, γ and δ.

  • Goethite, α-FeO(OH), has been used as an ochre pigment since prehistoric times.
  • Akaganeite is the β polymorph,[6] formed by weathering and noted for its presence in some meteorites and the lunar surface. However, recently it has been determined that it must contain some chloride ions to stabilize its structure, so that its more accurate formula is FeO
    0.833
    (OH)
    1.167
    Cl
    0.167
    or Fe
    6
    O
    5
    (OH)
    7
    Cl
    .[7]
  • Lepidocrocite, the γ polymorph, is commonly encountered as rust on the inside of steel water pipes and tanks.
  • Feroxyhyte (δ) is formed under the high pressure conditions of sea and ocean floors, being thermodynamically unstable with respect to the α polymorph (goethite) at surface conditions.

Non-mineral

Goethite and lepidocrocite, both crystallizing in orthorhombic system, are the most common forms of iron(III) oxyhydroxide and the most important mineral carriers of iron in soils.

Mineraloids

Iron(III) oxyhydroxide is the main component of other minerals and mineraloids:

  • Ferrihydrite is an amorphous or nanocrystalline hydrated mineral, officially FeOOH·1.8H
    2
    O
    but with widely variable hydration.

Properties

The color of iron(III) oxyhydroxide ranges from yellow through dark-brown to black, depending on the degree of hydration, particle size and shape, and crystal structure.

Structure

The crystal structure of β-FeOOH (akaganeite) is that of hollandite or BaMn
8
O
16
. The unit cell is tetragonal with a = 1.048 and c = 0.3023 nm, and contains eight formula units of FeOOH. Its dimensions are about 500 × 50 × 50 nm. Twinning often produces particles with the shape of hexagonal stars. [2]

Chemistry

On heating, β-FeOOH decomposes and recrystallizes as α-Fe
2
O
3
(hematite).[2]

Uses

Limonite, a mixture of various hydrates and polymorphs of ferric oxyhydroxide, is one of the three major iron ores, having been used since at least 2500 BC.[8][9]

Yellow iron oxide, or Pigment Yellow 42, is Food and Drug Administration (FDA) approved for use in cosmetics and is used in some tattoo inks.

Iron oxide-hydroxide is also used in aquarium water treatment as a phosphate binder.[10]

Iron oxide-hydroxide nanoparticles have been studied as possible adsorbents for lead removal from aquatic media.[11]

Medication

Iron polymaltose is used in treatment of iron-deficiency anemia.

Production

Iron(III) oxyhydroxide precipitates from solutions of iron(III) salts at pH between 6.5 and 8.[12] Thus the oxyhydroxide can be obtained in the lab by reacting an iron(III) salt, such as ferric chloride or ferric nitrate, with sodium hydroxide:[13]

FeCl
3
+ 3 NaOH → Fe(OH)
3
+ 3 NaCl
Fe(NO
3
)
3
+ 3 NaOH → Fe(OH)
3
+ 3 NaNO
3

In fact, when dissolved in water, pure FeCl
3
will hydrolyze to some extent, yielding the oxyhydroxide and making the solution acidic:[12]

FeCl
3
+ 2 H
2
O
FeOOH + 3 HCl

Therefore, the compound can also be obtained by the decomposition of acidic solutions of iron(III) chloride held near the boiling point for days or weeks:[14]

FeCl
3
+ 2 H
2
O
FeOOH(s) + 3 HCl(g)

(The same process applied to iron(III) nitrate Fe(NO
3
)
3
or perchlorate Fe(ClO
4
)
3
solutions yields instead particles of α-Fe
2
O
3
.[14])

Another similar route is the decomposition of iron(III) nitrate dissolved in stearic acid at about 120 °C.[15]

The oxyhydroxide prepared from ferric chloride is usually the β polymorph (akaganeite), often in the form of thin needles.[14][16]

The oxyhydroxide can also be produced by a solid-state transformation from iron(II) chloride tetrahydrate FeCl
2
·4H
2
O
.[6]

The compound also readily forms when iron(II) hydroxide is exposed to air:

4Fe(OH)
2
+ O
2
→ 4 FeOOH + 2 H
2
O

The iron(II) hydroxide can also be oxidized by hydrogen peroxide in the presence of an acid:

2Fe(OH)
2
+ H
2
O
2
→ 2 Fe(OH)
3

See also

References

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