Overlooked formation of chlorinated coupling byproducts during phenol degradation with ferrate(VI) oxidation
Dan Tao1, Yuxin Zhou1, Laura Carter2
1College of Science, Nanjing Agricultural University, Nanjing 210095, China.
Abstract:
Currently, ferrate(VI) oxidation technology (FOT) has been regarded as one of the most promising options for the degradation of emerging organic pollutants. However, the role and transformation of chloride ions (Cl-) in FOT have not been well explored. The current study aims to investigate the formation of chlorinated phenolic byproducts upon ferrate(VI) oxidation processes. The obtained results indicate that chlorides suffering ferrate(VI) attack will be transformed to active chlorine species (ACS), which will subsequently lead to the formation of highly toxic aromatic chlorinated byproducts. The identified byproducts include common chlorinated phenolic derivatives, as well as complex chlorinated oligomer byproducts with ether structures (mainly dimers and trimers). While the formation of common chlorophenols can be ascribed to the electrophilic substitution reactions mediated by ACS, the oligomer byproducts are generated via coupling reactions between chlorinated phenoxy radicals. ECOSAR software predicts that the generated chlorinated oligomer byproducts exhibit high ecotoxicological effects. As a whole, the above findings shed light on the potential risk of FOT in real practice.
More Related Videos
08:23Analyzing the Photo-oxidation of 2-propanol at Indoor Air Level Concentrations Using Field Asymmetric Ion Mobility Spectrometry
Published on: June 14, 2018
11:44Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
Related Concept Videos
Oxidation of Phenols to Quinones
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
Hydrolysis of Chlorobenzene to Phenol: Dow Process
Benzene to Phenol via Cumene: Hock Process
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
