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

Author:

Kelemen Peter B.1,Matter Juerg1,Streit Elisabeth E.1,Rudge John F.2,Curry William B.3,Blusztajn Jerzy3

Affiliation:

1. Lamont Doherty Earth Observatory, Columbia University, Palisades, New York 10964;

2. Institute of Theoretical Geophysics, Bullard Laboratories, University of Cambridge, Cambridge, CB3 0EZ, United Kingdom

3. Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543

Abstract

Near-surface reaction of CO2-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 CO2 storage, and perhaps for direct capture of CO2 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”).

Publisher

Annual Reviews

Subject

Space and Planetary Science,Earth and Planetary Sciences (miscellaneous),Astronomy and Astrophysics

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