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Rates and Mechanisms of Mineral Carbonation in Peridotite: Natural Processes and Recipes for Enhanced, in situ CO2 Capture and Storage

2011/03/02 by Peter B. Kelemen, P. B. Kelemen, Juerg Matter +6 · 6 citations
Earth and Planetary Sciences · Environmental Science · #CO2 Sequestration and Geologic Interactions #Geological and Geochemical Analysis #High-pressure geophysics and materials

paper · doi:10.1146/annurev-earth-092010-152509

openalex publication_date 2011/03/02 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/31

Abstract

Near-surface reaction of CO 2 -bearing fluids with silicate minerals in peridotite and basalt forms solid carbonate minerals. Such processes form abundant veins and travertine deposits, particularly in association with tectonically exposed mantle peridotite. This is important in the global carbon cycle, in weathering, and in understanding physical-chemical interaction during retrograde metamorphism. Enhancing the rate of such reactions is a proposed method for geologic CO 2 storage, and perhaps for direct capture of CO 2 from near-surface fluids. We review, synthesize, and extend inferences from a variety of sources. We include data from studies on natural peridotite carbonation processes, carbonation kinetics, feedback between permeability and volume change via reaction-driven cracking, and proposed methods for enhancing the rate of natural mineral carbonation via in situ processes (“at the outcrop”) rather than ex situ processes (“at the smokestack”).

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