510941 Iron Oxide Impregnated Membrane for Sulfate Radical-Based Oxidation of Trichloroethene

Sam Thompson, Chemical and Materials Engineering, University of Kentucky, Lexington, KY, Ashish Aher, Chemical and Material Engineering, University of Kentucky, Lexington, KY and Dibakar Bhattacharyya, Department of Chemical and Materials Engineering, University of Kentucky, Lexington, KY

This study investigates an iron-activated oxidative reaction with sulfate radicals to degrade trichloroethene (TCE) using a composite membrane. The optimization of this degradation pathway was conducted by comparing three different oxidation states of iron (Fe3+, Fe2+, and Fe0), which are possible to incorporate in a variety of Fe nanoparticles. Performance of Fe-NPs was determined by measuring TCE degradation in a solution phase. The membranes consisted of polyacrylic acid (PAA) and graphene oxide (GO), deposited onto a polyvinyl difluoride (PVDF) backing. Diluted acrylic acid was polymerized using a UV initiator. Two types of membranes were made: a “mix” membrane where PAA and GO are deposited simultaneously, and a “sandwich” membrane where PAA is deposited between two GO layers, creating a substrate layer capable of iron deposition. Membrane characterization included permeability, contact angle, salt rejection (NaSO4 and CaSO4), pH responsiveness, and persulfate oxidation. Fe(III) systems showed 0.3 mol Cl- generated per 1mol S2O82-, which is a measure of TCE degradation efficiency. Efficiencies for systems with iron oxide and zero-valent iron were calculated, but require further analysis. When persulfate was passed through the “mix” membrane and “sandwich” membrane, persulfate concentration was reduced by 22.73% and 26.5%, respectively. In a control experiment, a GO only membrane reduced the concentration by 14.63%. This study demonstrates the successful use of impregnated membranes as a medium for the oxidative sulfate radical-based degradation pathway. This research was supported by NSF KY EPSCoR program and by NIH-NIEHS-SRP.

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