Names | |
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IUPAC name Iron(II) hydroxide | |
Other names Ferrous hydroxide, green rust | |
Identifiers | |
3D model (JSmol) | |
ChemSpider | |
ECHA InfoCard | 100.038.581 |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
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Properties | |
Fe(OH)2 | |
Molar mass | 89.86 g/mol |
Appearance | green solid |
Density | 3.4 g/cm3 [1] |
0.000052 g/100 g water (20 °C, pH 7) [2] | |
Solubility product (Ksp) | 8.0 x 10−16 [3] |
Acidity (pKa) | 17 [4] |
Hazards | |
Flash point | Non-flammable |
Related compounds | |
Related compounds | Iron(II) oxide Iron(III) hydroxide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Iron(II) hydroxide or ferrous hydroxide is an inorganic compound with the formula Fe(OH)2. It is produced when iron(II) salts, from a compound such as iron(II) sulfate, are treated with hydroxide ions. Iron(II) hydroxide is a white solid, but even traces of oxygen impart a greenish tinge. The air-oxidised solid is sometimes known as "green rust".
Iron(II) hydroxide is poorly soluble in water (1.43 × 10−3 g/L), or 1.59 × 10−5 mol/L. It precipitates from the reaction of iron(II) and hydroxide salts: [5]
If the solution is not deoxygenated and iron not totally reduced in Fe(II), the precipitate can vary in colour starting from green to reddish brown depending on the iron(III) content. Iron(II) ions are easily substituted by iron(III) ions produced by its progressive oxidation.
It is also easily formed as a by-product of other reactions, a.o., in the synthesis of siderite, an iron carbonate (FeCO3), if the crystal growth conditions are imperfectly controlled.
Fe(OH)2 adopts the brucite structure, i.e. the arrangement of the atoms in the crystal are the same as the arrangement of the atoms in Mg(OH)2. The Fe(II) centers are bonded to six hydroxide ligands. Each hydroxide ligand bridges to three Fe(II) sites. The O-H bonds are perpendicular to the planes defined by the oxygen atoms, projecting above and below these layers. [6]
Under anaerobic conditions, the iron(II) hydroxide can be oxidised by the protons of water to form magnetite (iron(II,III) oxide) and molecular hydrogen. This process is described by the Schikorr reaction:
Anions such as selenite and selenate can be easily adsorbed on the positively charged surface of iron(II) hydroxide, where they are subsequently reduced by Fe2+. The resulting products are poorly soluble (Se0, FeSe, or FeSe2).
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] The natural analogue of iron(II) hydroxide compound is the very rare mineral amakinite, (Fe,Mg)(OH)2. [8] [9]
Iron(II) hydroxide has also been investigated as an agent for the removal of toxic selenate and selenite ions from water systems such as wetlands. The iron(II) hydroxide reduces these ions to elemental selenium, which is insoluble in water and precipitates out. [10]
In a basic solution iron(II) hydroxide is the electrochemically active material of the negative electrode of the nickel-iron battery.
Hydroxide is a diatomic anion with chemical formula OH−. It consists of an oxygen and hydrogen atom held together by a single covalent bond, and carries a negative electric charge. It is an important but usually minor constituent of water. It functions as a base, a ligand, a nucleophile, and a catalyst. The hydroxide ion forms salts, some of which dissociate in aqueous solution, liberating solvated hydroxide ions. Sodium hydroxide is a multi-million-ton per annum commodity chemical. The corresponding electrically neutral compound HO• is the hydroxyl radical. The corresponding covalently bound group –OH of atoms is the hydroxy group. Both the hydroxide ion and hydroxy group are nucleophiles and can act as catalysts in organic chemistry.
In chemistry, iron(III) or ferric refers to the element iron in its +3 oxidation state. Ferric chloride is an alternative name for iron(III) chloride (FeCl3). The adjective ferrous is used instead for iron(II) salts, containing the cation Fe2+. The word ferric is derived from the Latin word ferrum, meaning "iron".
In chemistry, iron(II) refers to the element iron in its +2 oxidation state. The adjective ferrous or the prefix ferro- is often used to specify such compounds, as in ferrous chloride for iron(II) chloride (FeCl2). The adjective ferric is used instead for iron(III) salts, containing the cation Fe3+. The word ferrous is derived from the Latin word ferrum, meaning "iron".
Classical qualitative inorganic analysis is a method of analytical chemistry which seeks to find the elemental composition of inorganic compounds. It is mainly focused on detecting ions in an aqueous solution, therefore materials in other forms may need to be brought to this state before using standard methods. The solution is then treated with various reagents to test for reactions characteristic of certain ions, which may cause color change, precipitation and other visible changes.
Selenic acid is the inorganic compound with the formula H2SeO4. It is an oxoacid of selenium, and its structure is more accurately described as O2Se(OH)2. It is a colorless compound. Although it has few uses, one of its salts, sodium selenate is used in the production of glass and animal feeds.
Sodium selenite is the inorganic compound with the formula Na2SeO3. This salt is a colourless solid. The pentahydrate Na2SeO3(H2O)5 is the most common water-soluble selenium compound.
Ferrate(VI) is the inorganic anion with the chemical formula [FeO4]2−. It is photosensitive, contributes a pale violet colour to compounds and solutions containing it and is one of the strongest water-stable oxidizing species known. Although it is classified as a weak base, concentrated solutions containing ferrate(VI) are corrosive and attack the skin and are only stable at high pH. It is similar to the somewhat more stable permanganate.
A nitrate test is a chemical test used to determine the presence of nitrate ion in solution. Testing for the presence of nitrate via wet chemistry is generally difficult compared with testing for other anions, as almost all nitrates are soluble in water. In contrast, many common ions give insoluble salts, e.g. halides precipitate with silver, and sulfate precipitate with barium.
Iron(III) nitrate, or ferric nitrate, is the name used for a series of inorganic compounds with the formula Fe(NO3)3.(H2O)n. Most common is the nonahydrate Fe(NO3)3.(H2O)9. The hydrates are all pale colored, water-soluble paramagnetic salts.
Iron shows the characteristic chemical properties of the transition metals, namely the ability to form variable oxidation states differing by steps of one and a very large coordination and organometallic chemistry: indeed, it was the discovery of an iron compound, ferrocene, that revolutionalized the latter field in the 1950s. Iron is sometimes considered as a prototype for the entire block of transition metals, due to its abundance and the immense role it has played in the technological progress of humanity. Its 26 electrons are arranged in the configuration [Ar]3d64s2, of which the 3d and 4s electrons are relatively close in energy, and thus it can lose a variable number of electrons and there is no clear point where further ionization becomes unprofitable.
Ferric acetate is the acetate salt of the coordination complex [Fe3O(OAc)6(H2O)3]+ (OAc− is CH3CO2−). Commonly the salt is known as "basic iron acetate". The formation of the red-brown complex was once used as a test for ferric ions.
Barium ferrate is the chemical compound of formula BaFeO4. This is a rare compound containing iron in the +6 oxidation state. The ferrate(VI) ion has two unpaired electrons, making it paramagnetic. It is isostructural with BaSO4, and contains the tetrahedral [FeO4]2− anion.
Cobalt(II) hydroxide or cobaltous hydroxide is the inorganic compound with the formula Co(OH)
2, consisting of divalent cobalt cations Co2+
and hydroxide anions OH−
. The pure compound, often called the "beta form" is a pink solid insoluble in water.
Sodium ferrioxalate are inorganic compounds with the formula Na3Fe(C2O4)3(H2O)n. The pentahydrate has been characterized by X-ray crystallography. In contrast the potassium, ammonium, and rubidium salts crystallize from water as their trihydrates.
The Schikorr reaction formally describes the conversion of the iron(II) hydroxide (Fe(OH)2) into iron(II,III) oxide (Fe3O4). This transformation reaction was first studied by Gerhard Schikorr. The global reaction follows:
Green rust is a generic name for various green crystalline chemical compounds containing iron(II) and iron(III) cations, the hydroxide (OH−
) anion, and another anion such as carbonate (CO2−
3), chloride (Cl−
), or sulfate (SO2−
4), in a layered double hydroxide (LDH) structure. The most studied varieties are the following:
Many compounds of thorium are known: this is because thorium and uranium are the most stable and accessible actinides and are the only actinides that can be studied safely and legally in bulk in a normal laboratory. As such, they have the best-known chemistry of the actinides, along with that of plutonium, as the self-heating and radiation from them is not enough to cause radiolysis of chemical bonds as it is for the other actinides. While the later actinides from americium onwards are predominantly trivalent and behave more similarly to the corresponding lanthanides, as one would expect from periodic trends, the early actinides up to plutonium have relativistically destabilised and hence delocalised 5f and 6d electrons that participate in chemistry in a similar way to the early transition metals of group 3 through 8: thus, all their valence electrons can participate in chemical reactions, although this is not common for neptunium and plutonium.
Manganese(II) hydroxide is the inorganic compound with the formula Mn(OH)2. It is a white solid although samples darken quickly upon exposure to air owing to oxidation. It is poorly soluble in water.
Iron(II) selenate (ferrous selenate) is an inorganic compound with the formula FeSeO4. It has anhydrous and several hydrate forms. The pentahydrate has the structure, [Fe(H2O)4]SeO4•H2O, isomorphous to the corresponding iron(II) sulfate. Heptahydrate is also known, in form of unstable green crystalline solid.
Gallium compounds are compounds containing the element gallium. These compounds are found primarily in the +3 oxidation state. The +1 oxidation state is also found in some compounds, although it is less common than it is for gallium's heavier congeners indium and thallium. For example, the very stable GaCl2 contains both gallium(I) and gallium(III) and can be formulated as GaIGaIIICl4; in contrast, the monochloride is unstable above 0 °C, disproportionating into elemental gallium and gallium(III) chloride. Compounds containing Ga–Ga bonds are true gallium(II) compounds, such as GaS (which can be formulated as Ga24+(S2−)2) and the dioxan complex Ga2Cl4(C4H8O2)2. There are also compounds of gallium with negative oxidation states, ranging from -5 to -1, most of these compounds being magnesium gallides (MgxGay).