4.5 Article

Mineral Carbonation of CO2

Journal

ELEMENTS
Volume 4, Issue 5, Pages 333-337

Publisher

MINERALOGICAL SOC AMER
DOI: 10.2113/gselements.4.5.333

Keywords

CO2 sequestration; mineral carbonation; mineralogic storage; basalt carbonation

Funding

  1. Centre National de la Recherche Scientifique
  2. Earth Institute at Columbia University
  3. Carb-Fix and two European Commission Marie Curie Grants [MEST-2005-012210, MRTN-2006-31482]

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A survey of the global carbon reservoirs suggests that the most stable, long-term storage mechanism for atmospheric CO, is the formation of carbonate minerals such as calcite, dolomite and magnesite. The feasibility Is demonstrated by the proportion of terrestrial carbon bound in these minerals: at least 40,000 times moire carbon Is present In carbonate rocks than In the atmosphere. Atmospheric carbon can be transformed Into carbonate minerals either ex situ, as part of an Industrial process, or In situ, by Injection Onto geological formations where the elements required for carbonate-mineral formation are present. Many challenges In mineral carbonation remain to be resolved. They Include overcoming the slow kinetics of mineral-fluid reactions, dealing with the large volume of source material required and reducing the energy needed to hasten the carbonation process. To address these challenges, several pilot studies have been launched, Including the CarbFix program in Iceland. The aim of CarbFix Is to inject CO, Into permeable basaltic rocks in an attempt to form carbonate minerals directly through a coupled dissolution-precipitation process.

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