DESTRUCTION OF CHLORINATED ORGANICS BY COBALT(III)-MEDIATED ELECTROCHEMICAL OXIDATION

被引:45
作者
FARMER, JC
WANG, FT
LEWIS, PR
SUMMERS, LJ
机构
[1] University of California, Lawrence Livermore National Laboratory, Livermore
关键词
chlorine compounds chemical reactors; electrolysis; organic compounds; oxidation; radioactive waste processing; reaction kinetics;
D O I
10.1149/1.2069027
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In the future, mediated electrochemical oxidation (MEO) may be used for the ambient temperature destruction of hazardous waste and for the conversion of mixed waste to low-level radioactive waste. We have studied the Co(III)-mediated electrochemical oxidation of ethylene glycol, 1,3-dichloro-2-propanol, 2-monochloro-1-propanol, and isopropanol in sulfuric acid. The electrochemical reactor had a rotating cylinder anode that was operated well below the limiting current for Co(III) generation. Rates of CO2 generation were measured and used to calculate both destruction and current efficiencies for the process. We found that electrode separators can be eliminated in MEO processes based upon Co(III) and sulfuric acid. Electrodes must be separated by ion exchange membranes in classical Ag(II)-based processes.
引用
收藏
页码:3025 / 3029
页数:5
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