Oxychlorination
In chemistry, oxychlorination is a process for generating the equivalent of chlorine gas (Cl2) from hydrogen chloride and oxygen.[1] This process is attractive industrially because hydrogen chloride is less expensive than chlorine.[2]
Mechanism
The reaction is usually initiated by
- CH2=CH2 + 2 CuCl2 → 2 CuCl + ClH2C-CH2Cl
The copper(II) chloride is regenerated by sequential reactions of the cuprous chloride with oxygen and then hydrogen chloride:
- ½ O2 + 2 CuCl → CuOCuCl2
- 2 HCl + CuOCuCl2 → 2 CuCl2 + H2O
Applications
Oxychlorination is employed in the conversion of ethylene into vinyl chloride. In the first step in this process, ethylene undergoes oxychlorination to give ethylene chloride:
- CH2=CH2 + 2 HCl + ½ O2 → ClCH2CH2Cl + H2O
Oxychlorination is of special importance in the making of 1,2-dichloroethane, which is then converted into vinyl chloride. As can be seen in the following reaction, 1,2-dichloroethane is cracked:
- ClCH2CH2Cl → CH2=CHCl + HCl
The HCl from this cracking process is recycled by oxychlorination in order to reduce the consumption of raw material HCl (or Cl2, if direct chlorination of ethylene is chosen as main way to produce 1,2-dichloroethane).[3]
Iron(III) chloride is produced commercially by oxychlorination (and other methods). For example, dissolution of iron ores in hydrochloric acid gives a mixture of ferrous and ferric chlorides:[4]
- Fe3O4 + 8 HCl → FeCl2 + 2 FeCl3 + 4 H2O
The iron(II) chloride is converted to the iron(III) derivative by treatment with oxygen and hydrochloric acid:
- 4 FeCl2 + O2 + 4 HCl → 4 FeCl3 + 2 H2O
References
- ISBN 978-3527306732.
- ^ Marshall, K. A. 2003. Chlorocarbons and Chlorohydrocarbons, Survey. Kirk-Othmer Encyclopedia of Chemical Technology
- ^ Chemistry of the Oxychlorination Catalyst: An In situ, Time-resolved, Dispersive XANES Study — ESRF - European Synchrotron Radiation Facility
- S2CID 105925459.