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Improving arsenopyrite oxidation rate laws: implications for arsenic mobilization during aquifer storage and recovery
Chelsea W Neil1, M Jason Todd2,3, Y Jeffrey Yang4
1Office of Research and Development, National Risk Management Research Laboratory, U.S. Environmental Protection Agency, 26 W. Martin Luther King Dr., Cincinnati, OH, 45268, USA. neil.chelsea@epa.gov.
Abstract:
Aquifer storage and recovery (ASR) and aquifer recharge (AR) provide technical solutions to address water supply deficits and growing future water demands. Unfortunately, the mobilization of naturally present arsenic due to ASR/AR operations has undermined its application on a larger scale. Predicting arsenic mobility in the subsurface during ASR/AR is further complicated by site-specific factors, including the arsenic mobilization mechanisms, groundwater flow conditions, and multi-phase geochemical interactions. In order to ensure safe and sustainable ASR/AR operation, a better understanding of these factors is needed. The current study thus aims to better characterize and model arsenic remobilization at ASR/AR sites by compiling and analyzing available kinetic data on arsenic mobilization from arsenopyrite under different aqueous conditions. More robust and widely applicable rate laws are developed for geochemical conditions relevant to ASR/AR. Sensitivity analysis of these new rate laws gives further insight into the controlling geochemical factors for arsenic mobilization. When improved rate laws are incorporated as the inputs for reactive transport modeling, arsenic mobilization in ASR/AR operations can be predicted with an improved accuracy. The outcomes will be used to guide groundwater monitoring and specify ASR/AR operational parameters, including water pretreatment requirements prior to injection.
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