Iron(III) chloride | |
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IUPAC name | Iron(III) chloride |
Other names | ferric chloride iron trichloride molysite (mineral) Flores martis |
Identifiers | |
CAS number | 7705-08-0, hexahydrate: [ ] |
RTECS number | LJ9100000 |
Properties | |
Molecular formula | FeCl3 |
Molar mass | 162.2 g·mol-1 hexahydrate: 270.3 g·mol−1 |
Appearance | green-black by reflected light; purple-red by transmitted light hexahydrate: yellow solid aq. solutions: brown |
Density | 2.80 g·cm−3 40% solution: 1.4 g·ml−1 |
Melting point |
306 °C, 579 K, 583 °F |
Boiling point |
315 °C, 588 K, 599 °F (partial decomposition to FeCl2+Cl2) |
Solubility in water | 92 g/100 ml (20 °C) |
Solubility in acetone Methanol Ethanol Diethyl ether |
63 g/100 ml (18 °C) highly soluble 83 g/100 ml highly soluble |
Viscosity | 40% solution: 12 cP |
Structure | |
Crystal structure | hexagonal |
Coordination geometry |
octahedral |
Hazards | |
Main hazards | Very corrosive |
NFPA 704 |
0
3
1
|
R-phrases | R22, R34 |
S-phrases | S26, S28 |
Related compounds | |
Other anions | Iron(III) fluoride Iron(III) bromide |
Other cations | Iron(II) chloride Manganese(II) chloride Cobalt(II) chloride Ruthenium(III) chloride |
Related coagulants | Iron(II) sulfate Polyaluminium chloride |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references |
Iron(III) chloride, generically called ferric chloride, is an industrial scale commodity chemical compound, with the formula FeCl3. The colour of iron(III) chloride crystals depends on the viewing angle: by reflected light the crystals appear dark green, but by transmitted light they appear purple-red. Anhydrous iron(III) chloride is deliquescent, forming hydrated hydrogen chloride mists in moist air. It is rarely observed in its natural form, mineral molysite, known mainly from some fumaroles.
When dissolved in water, iron(III) chloride undergoes hydrolysis and gives off heat in an exothermic reaction. The resulting brown, acidic, and corrosive solution is used as a coagulant in sewage treatment and drinking water production, and as an etchant for copper-based metals in printed circuit boards. Anhydrous iron(III) chloride is a fairly strong Lewis acid, and it is used as a catalyst in organic synthesis.
Contents |
Iron(III) chloride has a relatively low melting point and boils at around 315 °C. The vapour consists of the dimer Fe2Cl6 (compare aluminium chloride) which increasingly dissociates into the monomeric FeCl3 (D3h point group molecular symmetry) at higher temperature, in competition with its reversible decomposition to give iron(II) chloride and chlorine gas.[1]
Iron(III) chloride is a moderately strong Lewis acid, forming adducts with Lewis bases such as triphenylphosphine oxide, e.g. FeCl3(OPPh3)2 where Ph = phenyl.
Iron(III) chloride reacts with other chloride salts to give the yellow tetrahedral FeCl4− ion. Salts of FeCl4− in hydrochloric acid can be extracted into diethyl ether.
When heated with iron(III) oxide at 350 °C, iron(III) chloride gives iron oxychloride, a layered solid and intercalation host.
In the presence of base, alkali metal alkoxides react to give the dimeric complexes:
Oxalates react rapidly with aqueous iron(III) chloride to give [Fe(C2O4)3]3−. Other carboxylate salts form complexes, e.g. citrate and tartrate.
Iron(III) chloride is a mild oxidising agent, for example capable of oxidising copper(I) chloride to copper(II) chloride. Reducing agents such as hydrazine convert iron(III) chloride to complexes of iron(II).
Iron(III) chloride adopts the BiI3 structure, which features octahedral Fe(III) centres interconnected by two-coordinate chloride ligands.
Anhydrous iron(III) chloride may be prepared by union of the elements:[2]
Solutions of iron(III) chloride are produced industrially both from iron and from ore, in a closed-loop process.
Alternatively, iron(II) chloride can be oxidised with sulfur dioxide:
Like many other hydrated metal chlorides, hydrated iron(III) chloride can be converted to the anhydrous salt by refluxing with thionyl chloride.[3] The hydrate cannot be converted to anhydrous iron(III) chloride by only heat, as instead HCl is evolved and iron oxychloride forms.
In industrial application, iron(III) chloride is used in sewage treatment and drinking water production.[4] In this application, FeCl3 in slightly basic water reacts with the hydroxide ion to form a floc of iron(III) hydroxide, or more precisely formulated as FeO(OH)-, that can remove suspended materials.
It is also used as a leaching agent in chloride hydrometallurgy, [5] for example in the production of Si from FeSi. (Silgrain process)[6]
Another important application of iron(III) chloride is etching copper in two-step redox reaction to copper(I) chloride and then to copper(II) chloride in the production of printed circuit boards.[7]
Iron(III) chloride is used as catalyst for the reaction of ethylene with chlorine, forming ethylene dichloride (1,2-dichloroethane), an important commodity chemical, which is mainly used for the industrial production of vinyl chloride, the monomer for making PVC.
In the laboratory iron(III) chloride is commonly employed as a Lewis acid for catalysing reactions such as chlorination of aromatic compounds and Friedel-Crafts reaction of aromatics. It is less powerful than aluminium chloride, but in some cases this mildness leads to higher yields, for example in the alkylation of benzene:
The ferric chloride test is a traditional colorimetric test for phenols, which uses a 1% iron(III) chloride solution that has been neutralised with sodium hydroxide until a slight precipitate of FeO(OH) is formed.[8] The mixture is filtered before use. The organic substance is dissolved in water, methanol or ethanol, then the neutralised iron(III) chloride solution is added—a transient or permanent coloration (usually purple, green or blue) indicates the presence of a phenol or enol.
Iron(III) chloride is toxic, highly corrosive and acidic. The anhydrous material is a powerful dehydrating agent.