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Concentrated hazardous organic waste destruction by electrochemical oxidation

Conference ·
OSTI ID:6739533
Concentrated organic compounds typical of major hazardous waste components were subjected to anodic electrochemical oxidation (ECO) in a continuous recycle mode in the presence of a molar nickel nitrate (Ni(II)) electron carrier in molar nitric acid. The catholyte comprised molar nitric acid. Chlorinated compounds such as chlorobenzene, chloroform, perchloro- and trichloroethylene were readily oxidized to a mixture of carbon dioxide and oxygen (the latter from water electrolysis). ECO conversion of phenol rapidly led to insoluble tar formation by a free radical coupling mechanism. The lack of water solubility of most of the compounds examined did not affect the oxidation per se, although it may have contributed to a lower oxidation rate than was previously observed for hexone (MIBK, methyl isobutyl ketone) in solution. A conceptual design for a commercial ECO-system is being developed based on these laboratory results, and work is continuing on the oxidation of mixtures of hazardous materials often found at waste sites. The technique offers promise as a low-temperature and pressure method for waste destruction, especially for concentrated organic wastes. 6 refs., 6 tabs.
Research Organization:
Pacific Northwest Lab., Richland, WA (USA)
DOE Contract Number:
AC06-76RL01830
OSTI ID:
6739533
Report Number(s):
PNL-SA-15883; CONF-881054-25; ON: DE89001705
Country of Publication:
United States
Language:
English