Ferrous chloride
-chlorid01.png)
| |
| |
| Names | |
|---|---|
| IUPAC names
Iron(II) chloride
Iron dichloride | |
| Other names
Ferrous chloride,
Rokühnite | |
| Identifiers | |
3D model (JSmol)
|
|
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 879: attempt to index field 'wikibase' (a nil value). |
PubChem CID
|
|
| UNII | |
| |
| |
| Properties | |
| FeCl2 | |
| Molar mass | 126.751 g/mol (anhydrous) 198.8102 g/mol (tetrahydrate) |
| Hazards | |
| Related compounds | |
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) chloride, also known as ferrous chloride, is the chemical compound of formula FeCl2. It is a paramagnetic solid with a high melting point, and is usually obtained as an off-white solid. FeCl2 crystallizes from water as the greenish tetrahydrate, which is the form that is most commonly encountered in commerce and the laboratory. There is also a dihydrate. The compound is also soluble in water; aqueous solutions of FeCl2 are yellow.
Production
Hydrated forms of ferrous chloride are generated by treatment of wastes from steel production with hydrochloric acid. Such solutions are designated "spent acid," especially when the hydrochloric acid is not completely consumed:
The spent acid requires treatment before its disposal. It is also byproduct from titanium production, since some titanium ores contain iron.[2]
Laboratory preparation
Ferrous chloride is conveniently prepared by addition of iron powder to a solution of methanol and concentrated hydrochloric acid under an inert atmosphere. This reaction gives the methanol solvate, which upon heating in a vacuum at about 160 °C gives anhydrous FeCl2.[3] FeBr2 and FeI2 can be prepared analogously.
- Fe + 2HCl + 2CH3OH → FeCl2 + CH4 + H2O
An alternative laboratory synthesis of FeCl2 entails the reaction of FeCl3 with chlorobenzene:[4]
- 2 FeCl3 + C6H5Cl → 2 FeCl2 + C6H4Cl2 + HCl
FeCl2 exhibits convenient solubility in tetrahydrofuran (THF), a common solvent for chemical reactions. In one of two classic syntheses of ferrocene, Wilkinson generated FeCl2 by heating FeCl3 with iron powder in THF.[5] Ferric chloride decomposes to ferrous chloride at high temperatures.
Reactions
FeCl2 forms complexes with many ligands. It reacts with two molar equivalents of [(C2H5)4N]Cl to give the salt [(C2H5)4N]2[FeCl4]. Related compounds that can be prepared similarly include the [MnCl4]2−, [MnBr4]2−, [MnI4]2−, [FeBr4]2−, [CoCl4]2−, [CoBr4]2−, [NiCl4]2−, and [CuCl4]2− salts.[6]
Applications
Ferrous chloride has a variety of niche applications, but the related compounds ferrous sulfate and ferric chloride enjoy more applications. Aside from use in the laboratory synthesis of iron complexes, ferrous chloride serves as a reducing flocculating agent in wastewater treatment, especially for wastes containing chromate. It is the precursor to hydrated iron(III) oxides that are magnetic pigments.[2] Ferrous chloride is employed as a reducing agent in many organic synthesis reactions.
References
- ↑ Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, ISBN 0-07-049439-8
- ↑ 2.0 2.1 Egon Wildermuth, Hans Stark, Gabriele Friedrich, Franz Ludwig Ebenhöch, Brigitte Kühborth, Jack Silver, Rafael Rituper “Iron Compounds” in Ullmann’s Encyclopedia of Industrial Chemistry Wiley-VCH, Wienheim, 2005.
- ↑ G. Winter; Thompson, D. W.; Loehe, J. R. (1973). "Iron(II) Halides". Inorg. Synth. 14: 99–104. doi:10.1002/9780470132456.ch20.
- ↑ P. Kovacic and N. O. Brace (1960). "Iron(II) Chloride". Inorg. Synth. 6: 172. doi:10.1002/9780470132371.ch54.
- ↑ Template:OrgSynth
- ↑ N. S. Gill, F. B. Taylor (1967). "Tetrahalo Complexes of Dipositive Metals in the First Transition Series". Inorg. Synth. 9: 136–142. doi:10.1002/9780470132401.ch37.