Reaction path modeling of enhanced in situ CO2 mineralization for carbon sequestration in the peridotite of the Samail Ophiolite, Sultanate of Oman

Paukert, Amelia N., Matter, Jürg M., Kelemen, Peter B., Shock, Everett L. and Havig, Jeff R. (2012) Reaction path modeling of enhanced in situ CO2 mineralization for carbon sequestration in the peridotite of the Samail Ophiolite, Sultanate of Oman. Chemical Geology, 330-331, 86-100. (doi:10.1016/j.chemgeo.2012.08.013).

Abstract

The peridotite section of the Samail Ophiolite in the Sultanate of Oman offers insight into the feasibility of mineral carbonation for engineered, in situ geological CO2 storage in mantle peridotites. Naturally occurring CO2 sequestration via mineral carbonation is well-developed in the peridotite; however, the natural process captures and sequesters CO2 too slowly to significantly impact the concentration of CO2 in the atmosphere. A reaction path model was developed to simulate in situ CO2 mineralization through carbonation of fresh peridotite, with its composition based on that of mantle peridotite in the Samail Ophiolite and including dissolution kinetics for primary minerals. The model employs a two-stage technique, beginning with an open system and progressing to three different closed system scenarios- a natural system at 30 °C, an engineered CO2 injection scenario at 30 °C, and an engineered CO2 injection scenario at 90 °C. The natural system model reproduces measured aqueous solute concentrations in the target water, signifying the model is a close approximation of the natural process. Natural system model results suggest that the open system achieves steady state within a few decades, while the closed system may take up to 6,500 years to reach observed fluid compositions. The model also identifies the supply of dissolved inorganic carbon as the limiting factor for natural CO2 mineralization in the deep subsurface. Engineered system models indicate that injecting CO2 at depth could enhance the rate of CO2 mineralization by a factor of over 16,000. CO2 injection could also increase mineralization efficiency – kilograms of CO2 sequestered per kilogram of peridotite – by a factor of over 350. These model estimates do not include the effects of precipitation kinetics or changes in permeability and reactive surface area due to secondary mineral precipitation. Nonetheless, the faster rate of mineralization in the CO2 injection models implies that enhanced in situ peridotite carbonation could be a significant sink for atmospheric CO2.

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Contributors

Author: Jürg M. Matter

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