Iron amendment and Fenton oxidation of MTBE-spent granular activated carbon |
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| Authors: | Scott G. Huling Sangchul Hwang |
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| Affiliation: | a U.S. Environmental Protection Agency, Office of Research and Development, National Risk Management Research Laboratory, Robert S. Kerr Environmental Research Center, P.O. Box 1198, Ada, OK 74820, USA
b Department of Civil Engineering and Surveying, University of Puerto Rico at Mayaguez, P.O. Box 9041, Mayaguez, PR 00681, USA |
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| Abstract: | Fenton-driven regeneration of methyl tert-butyl ether (MTBE)-spent granular activated carbon (GAC) involves an Fe amendment step to increase the Fe content and to enhance the extent of MTBE oxidation and GAC regeneration. Four forms of iron (ferric sulfate, ferric chloride, ferric nitrate, ferrous sulfate) were amended separately to GAC. Following Fe amendment, MTBE was adsorbed to the GAC followed by multiple applications of H2O2. Fe retention in GAC was high (83.8-99.9%) and decreased in the following order, FeSO4·7H2O > Fe2(SO4)3·9H2O > Fe(NO3)3·9H2O > FeCl3. A correlation was established between the post-sorption aqueous MTBE concentrations and Fe on the GAC for all forms of Fe investigated indicating that Fe amendment interfered with MTBE adsorption. However, the mass of MTBE adsorbed to the GAC was minimally affected by Fe loading. Relative to ferric iron amendments to GAC, ferrous iron amendment resulted in lower residual iron in solution, greater Fe immobilization in the GAC, and less interference with MTBE adsorption. MTBE oxidation was Fe limited and no clear trend was established between the counter-ion (SO42−, Cl−, NO3−) of the ferric Fe amended to GAC and H2O2 reaction, MTBE adsorption, or MTBE oxidation, suggesting these processes are anion independent. |
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| Keywords: | Iron Activated carbon Hydrogen peroxide Methyl tert-butyl ether Oxidation Anion |
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