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Mn-Catalyzed Oxidation Of Naphthalenediol, G. Whelan, Ronald C. Sims
Mn-Catalyzed Oxidation Of Naphthalenediol, G. Whelan, Ronald C. Sims
Biological Engineering Faculty Publications
This study investigates the effects that manganese(IV) dioxide particles have on 2,3-naphthalenediol at varying pH levels (i.e., initial pH of 4.58, 5.85, and 8.75) and under different organic concentration conditions (4×10−3, 4×10−4, and 4×10−5 M), and assesses the importance of Mn oxides on abiotic catalysis of the multiple-ringed aromatic compound. Proton concentration affected the rates of reductive dissolution; as the pH values increased, the rate of reductive dissolution decreased, as predicted by theory. Also, as the concentration of naphthalenediol increased, the rate of reductive dissolution increased, although not proportionally; thus indicating that a majority of …
Mn-Catalyzed Oxidation Of Multiple-Ringed Aromatics, G. Whelan, Ronald C. Sims
Mn-Catalyzed Oxidation Of Multiple-Ringed Aromatics, G. Whelan, Ronald C. Sims
Biological Engineering Faculty Publications
The role of manganese (Mn) oxides in catalyzing the abiotic oxidation of polynuclear aromatic compounds (PNAs) has been investigated by monitoring the oxidation of dihydrodiol and dione PNAs and corresponding reduction of Mn in an aqueous environment. 1,4-, 1,3-, and 2,3-naphthalenediol, 1,4-naphthoquinone, and l,4-dihydroxy-9,10-anthracenedione (Quinizarin) were oxidized in an oxic, aqueous environment, where each of these organic compounds is soluble in water, except Quinizarin. A mathematical model is presented, which describes the redox reactions, and suggests that electron transfer/organic release from the oxide surface is rate limiting with the reaction apparently proceeding through a free-radical formation. Results indicate significant oxidation …