STRONG OXIDANTS FOR ORGANIC WASTE DESTRUCTION FROM OXIDATION OF MANGANESE HYDROXIDE

D.K. Cha* and S.-M. Park, Department of Chemistry, University of New Mexico, Albuquerque, NM, 87131


ABSTRACT The redox chemistry of Mn(OH)2 has been studied at manganese electrodes in 0.10 M KOH solutions employing transient electrochemical techniques in an effort to elucidate mechanisms involved. The charge transfer process is shown to be affected by the film formed on the electrode surface during redox processes. The Mn(0)/Mn(II) and Mn(II)/Mn(III) pairs, which have not been reported hitherto clearly in the literature, has been observed using techniques such as chronopotentiometry and differential pulse voltammetry. Electrode potentials for these redox processes, i.e., between Mn(OH)2 and higher valence oxides as well as the manganese metal, have been assigned. Diffusion coefficients of reactant molecules through the Mn(OH)2 film and exchange rate constants for redox processes are also reported.

KEYWORDS: manganese oxidation, redox potential, diffusion coefficient

This paper is from the Proceedings of the HSRC/WERC Joint Conference on the Environment, May 1996, published in hard copy and on the Web by the Great Plains/Rocky Mountain Hazardous Substance Research Center.


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