Destruction of a Carbon Tetrachloride Dense Nonaqueous Phase Liquid by Modified Fenton’s Reagent |
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Authors: | Richard J Watts Jimmy Howsawkeng Amy L Teel |
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Affiliation: | 1Professor, Dept. of Civil and Environmental Engineering, Washington State Univ., Pullman, WA 99164-2910 (corresponding author), E-mail: rjwatts@wsu.edu 2Graduate Student, Dept. of Civil and Environmental Engineering, Washington State Univ., Pullman, WA 99164-2910; mailing address: Brown & Caldwell, 501 Great Circle Rd., Nashville, TN 37228. 3Research Scientist, Dept. of Civil and Environmental Engineering, Washington State Univ., Pullman, WA 99164-2910.
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Abstract: | Destruction of a dense nonaqueous phase liquid (DNAPL) by soluble iron (III)-catalyzed and pyrolusite (β-MnO2)-catalyzed Fenton’s reactions (hydrogen peroxide and transition metal catalysts) was investigated using carbon tetrachloride (CT) as a model contaminant. In the system amended with 5 mM soluble iron (III), 24% of the CT DNAPL was destroyed after 3 h while CT dissolution in parallel fill-and-draw systems was minimal, indicating that CT was degraded more rapidly than it dissolved into the aqueous phase. Fenton’s reactions catalyzed by the naturally occurring manganese oxide pyrolusite were even more effective in destroying CT DNAPLs, with 53% degradation after 3 h. Although Fenton’s reactions are characterized by hydroxyl radical generation, carbon tetrachloride is unreactive with hydroxyl radicals; therefore, a transient oxygen species other than hydroxyl radicals formed through Fenton’s propagation reactions was likely responsible for CT destruction. These results demonstrate that Fenton-like reactions in which nonhydroxyl radical species are generated may provide an effective method for the in situ treatment of DNAPLs. |
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Keywords: | Nonaqueous phase liquids Ground-water pollution Manganese Oxidation Chemical treatment Organic chemicals |
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