MOVING BEYOND TRACERS: 13C INSIGHTS INTO CARBON SEQUESTRATION
Prediction of the subsurface behaviour of CO2 on a decadal time scale can be achieved through laboratory and field experiments in engineered systems and modeling. Understanding the fate of injected CO2 on the millennia time scale needed to assure reservoir competence and safety remains a challenge. A key unknown is the CO2 residence time and mobility once injected. Addressing this requires understanding how much CO2 ultimately reacts with the rock to form immobile carbonate rocks; how much remains in a near pure, but buoyant, CO2 gas phase; and how much is dissolved into the groundwater.
Traditional use of carbon isotope signatures in investigations of CO2 sequestration in saline aquifers and oil field brines focuses on injected tracer study approaches, are dependent on having a sufficiently different carbon isotopic signature between injected CO2 and background CO2 and dissolved inorganic carbon species (DIC) in the subsurface, and yield information on a timescale of years to decades. Recently the use of in situ carbon isotope studies in naturally occurring CO2-rich gas fields has shown the insights available on CO2 trapping mechanisms and water-rock interreactions over millenia from geologic analog sites worldwide.
[1] Shewrood Lollar, B. and Ballentine, C.J.. (2009) Nature Geoscience 2, 543-547.