132-9 Mineralogical Changes during Ferrihydrite Sulfidization and Its Impact on Metal Behavior

See more from this Division: Topical Sessions
See more from this Session: Environmental Mineralogy

Sunday, 5 October 2008: 10:00 AM
George R. Brown Convention Center, 320ABC

Y. Thomas He, John T. Wilson and Rick T. Wilkin, Groundwater and Ecosystems Restoration Division, U.S. Environmental Protection Agency, National Risk Management Research Laboratory, Ada, OK
Abstract:

            Iron sulfides are common minerals that have important roles in permeable reactive barriers (PRB) and anoxic soils. Previous investigations have examined the dissolution of iron oxides in H2S solutions, but these studies focused on sulfide oxidation and iron oxide dissolution kinetics. Mineral phase transformation in the Fe-O-S system has not been explored in detail. This study investigates mineralogical changes during sulfidization of ferrihydrite by hydrogen sulfide and its impact on heavy metal behavior in reducing environments. Preliminary results show that FeS and S0 formation occurs rapidly through reductive dissolution of ferrihydrite by H2S. FeS transformation to FeS2 is slow at 25°C. However, transformation of FeS to FeS2 is accelerated at 45°C. Sulfur partitioning results indicate that FeS and FeS2 are inversely correlated within 21d. XRD shows a decrease in S0 over time, and S0 begins to disappear after 14d, which is in agreement with the stabilization of FeS. This indicates that transformation of FeS to FeS2 is halted due to exhaustion of S0. The results suggest that FeS2 is formed through FeS transformation, instead of direct pyritization of ferrihydrite. Nickel (Ni) is used as an example in this study to demonstrate how sulfidization of iron oxides affects metal partitioning in reducing environments.

See more from this Division: Topical Sessions
See more from this Session: Environmental Mineralogy

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