Carbon Dioxide Sequestration By Direct Mineral Carbonation: Process Mineralogy Of Feed And Products

Society for Mining, Metallurgy & Exploration
W. K. O’Connor D. C. Dahlin G. E. Rush C. L. Dahlin W. K. Collins
Organization:
Society for Mining, Metallurgy & Exploration
Pages:
7
File Size:
539 KB
Publication Date:
Jan 1, 2003

Abstract

Direct mineral carbonation was investigated as a process to convert gaseous CO2, into a geologically stable final form. The process utilizes a slurry of water, with bicarbonate and salt additions, mixed with a mineral reactant, such as olivine (Mg2SiO4) or serpentine [Mg3Si2O5(OH)4]. Carbon dioxide is dissolved into this slurry, resulting in dissolution of the mineral and precipitation of magnesium carbonate (MgCO3). Optimum results were achieved using heat-pretreated serpentine feed material and a high partial pressure of CO2 (Pc02). Specific conditions include 155°C, PC02 = 185 atm and 15% solids. Under these conditions, a 78% conversion of the silicate to the carbonate was achieved in 30 minutes. Process mineralogy was utilized to investigate the appropriate feed characteristics, identify the process products and interpret the mineral dissolution and carbonate precipitation reaction paths. Key words: Mineral carbonation, Carbon dioxide sequestration, Carbonates
Citation

APA: W. K. O’Connor D. C. Dahlin G. E. Rush C. L. Dahlin W. K. Collins  (2003)  Carbon Dioxide Sequestration By Direct Mineral Carbonation: Process Mineralogy Of Feed And Products

MLA: W. K. O’Connor D. C. Dahlin G. E. Rush C. L. Dahlin W. K. Collins Carbon Dioxide Sequestration By Direct Mineral Carbonation: Process Mineralogy Of Feed And Products. Society for Mining, Metallurgy & Exploration, 2003.

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