Affiliations 

  • 1 Department of Geoscience, Universiti Teknologi PETRONAS (UTP), 32610Seri Iskandar, Tronoh, Perak Darul Ridzuan, Malaysia
  • 2 Department of Natural Resources Engineering and Management, School of Science and Engineering, University of Kurdistan Hewlêr (UKH), Erbil 44001, Kurdistan Region, Iraq
  • 3 Department of Gas Sustainability Technology, PETRONAS Research Sdn Bhd, Kawasan Institusi Bangi, Kajang 43000, Selangor Darul Ehsan, Malaysia
  • 4 Department of Chemical and Petroleum Engineering, Sharif University of Technology, Tehran 11365-11155, Iran
ACS Omega, 2020 Nov 17;5(45):28942-28954.
PMID: 33225124 DOI: 10.1021/acsomega.0c02358

Abstract

The research presented here investigates the reaction mechanism of wollastonite in situ mineral carbonation for carbon dioxide (CO2) sequestration. Because wollastonite contains high calcium (Ca) content, it was considered as a suitable feedstock in the mineral carbonation process. To evaluate the reaction mechanism of wollastonite for geological CO2 sequestration (GCS), a series of carbonation experiments were performed at a range of temperatures from 35 to 90 °C, pressures from 1500 to 4000 psi, and salinities from 0 to 90,000 mg/L NaCl. The kinetics batch modeling results were validated with carbonation experiments at the specific pressure and temperature of 1500 psi and 65 °C, respectively. The results showed that the dissolution of calcium increases with increment in pressure and salinity from 1500 to 4000 psi and 0 to 90000 mg/L NaCl, respectively. However, the calcium concentration decreases by 49%, as the reaction temperature increases from 35 to 90 °C. Besides, it is clear from the findings that the carbonation efficiency only shows a small difference (i.e., ±2%) for changing the pressure and salinity, whereas the carbonation efficiency was shown to be enhanced by 62% with increment in the reaction temperature. These findings can provide information about CO2 mineralization of calcium silicate at the GCS condition, which may enable us to predict the fate of the injected CO2, and its subsurface geochemical evolution during the CO2-fluid-rock interaction.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.