Carbon sequestration via aqueous olivine mineral carbonation: Role of passivating layer formation

Hamdallah Béarat, Michael J. Mckelvy, Andrew Chizmeshya, Deirdre Gormley, Ryan Nunez, Ray Carpenter, Kyle Squires, George Wolf

Research output: Contribution to journalArticlepeer-review

301 Scopus citations


CO2 sequestration via carbonation of widely available low-cost minerals, such as olivine, can permanently dispose of CO2 in an environmentally benign and a geologically stable form. We report the results of studies of the mechanisms that limit aqueous olivine carbonation reactivity under the optimum sequestration reaction conditions observed to date: 1 M NaCl + 0.64 M NaHCO3 at T ≈ 185 °C and PCO2 ≈ 135 bar. A reaction limiting silica-rich passivating layer (PL) forms on the feedstock grains, slowing carbonate formation and raising process cost. The morphology and composition of the passivating layers are investigated using scanning and transmission electron microscopy and atomic level modeling. Postreaction analysis of feedstock particles, recovered from stirred autoclave experiments at 1500 rpm, provides unequivocal evidence of local mechanical removal (chipping) of PL material, suggesting particle abrasion. This is corroborated by our observation that carbonation increases dramatically with solid particle concentration in stirred experiments. Multiphase hydrodynamic calculations are combined with experiment to better understand the associated slurry-flow effects. Large-scale atomic-level simulations of the reaction zone suggest that the PL possesses a "glassy" but highly defective SiO2 structure that can permit diffusion of key reactants. Mitigating passivating layer effectiveness is critical to enhancing carbonation and lowering sequestration process cost.

Original languageEnglish (US)
Pages (from-to)4802-4808
Number of pages7
JournalEnvironmental Science and Technology
Issue number15
StatePublished - Aug 1 2006

ASJC Scopus subject areas

  • General Chemistry
  • Environmental Chemistry


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