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Trace Metal Source Terms in Carbon Sequestration Environments

Journal Article · · Environmental Science and Technology
DOI:https://doi.org/10.1021/es304832m· OSTI ID:1129482

Carbon dioxide sequestration in deep saline and depleted oil geologic formations is feasible and promising, however, possible CO₂ or CO₂-saturated brine leakage to overlying aquifers may pose environmental and health impacts. The purpose of this study was to experimentally define trace metal source terms from the reaction of supercritical CO₂, storage reservoir brines, reservoir and cap rocks. Storage reservoir source terms for trace metals are needed to evaluate the impact of brines leaking into overlying drinking water aquifers. The trace metal release was measured from sandstones, shales, carbonates, evaporites, basalts and cements from the Frio, In Salah, Illinois Basin – Decatur, Lower Tuscaloosa, Weyburn-Midale, Bass Islands and Grand Ronde carbon sequestration geologic formations. Trace metal dissolution is tracked by measuring solution concentrations over time under conditions (e.g. pressures, temperatures, and initial brine compositions) specific to the sequestration projects. Existing metrics for Maximum Contaminant Levels (MCLs) for drinking water as defined by the U.S. Environmental Protection Agency (U.S. EPA) were used to categorize the relative significance of metal concentration changes in storage environments due to the presence of CO₂. Results indicate that Cr and Pb released from sandstone reservoir and shale cap rock exceed the MCLs by an order of magnitude while Cd and Cu were at or below drinking water thresholds. In carbonate reservoirs As exceeds the MCLs by an order of magnitude, while Cd, Cu, and Pb were at or below drinking water standards. Results from this study can be used as a reasonable estimate of the reservoir and caprock source term to further evaluate the impact of leakage on groundwater quality.

Research Organization:
National Energy Technology Laboratory - In-house Research
Sponsoring Organization:
USDOE Office of Fossil Energy (FE)
DOE Contract Number:
FE0004000
OSTI ID:
1129482
Report Number(s):
A-UNIV-PUB-024
Journal Information:
Environmental Science and Technology, Journal Name: Environmental Science and Technology Journal Issue: 1 Vol. 47; ISSN 0013-936X
Publisher:
American Chemical Society (ACS)
Country of Publication:
United States
Language:
English

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