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Paper No. 10
Presentation Time: 11:00 AM

GROUNDWATER QUALITY CHANGES IN RESPONSE TO CO2 LEAKAGE FROM DEEP GEOLOGICAL STORAGE


BIRKHOLZER, Jens T.1, ZHENG, Liange1, SPYCHER, Nicolas1, VARADHARAJAN, Charuleka1 and NICO, Peter S.2, (1)Earth Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, MS 90-1116, Berkeley, CA 94720, (2)Earth Sciences Division, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, JTBirkholzer@lbl.gov

CO2 sequestration into deep reservoirs needs to ensure the safety of overlying groundwater resources. Questions exist whether groundwater could become contaminated by leakage and upward migration of CO2. The formation of carbonic acid in response to elevated levels of dissolved CO2 and the resulting decrease in groundwater pH could cause toxic metals to be mobilized through several pathways that include ion exchange, desorption from surface sites, and mineral dissolution. Additional effects could be caused by the transport of co-injected H2S and/or organic compounds mobilized by supercritical CO2 at depth. This paper touches on these various questions and discusses results from reactive transport simulations conducted for both hypothetical scenarios as well as for a CO2 controlled-release field experiment. Model predictions and experimental results suggest that CO2 dissolution into shallow groundwater can trigger the dissolution of minerals and sorption/exchange reactions, possibly mobilizing trace elements. The leakage of co-injected H2S into groundwater could exacerbate such potential impacts. Preliminary simulations also suggest that any volatile organic species present in CO2 storage formations could be readily dissolved by supercritical CO2 and mobilized to be transported into shallower groundwater.
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