<p>Ferronickel (FeNi) slag can be used to sequestrate CO<sub>2</sub> by performing an alkaline pretreatment process using NaOH to obtain porous MgO-rich materials (MgO obtained from FeNi slag, MgO-FS). CO<sub>2</sub> is mineralized by porous MgO-FS in the form of MgCO<sub>3</sub>. This study aimed to investigate the overall carbonation reaction kinetics of porous MgO-FS. The carbonation process was performed in an autoclave reactor under controlled CO<sub>2</sub> pressure by continuously supplying CO<sub>2</sub> throughout the experiment. The carbonation reaction kinetics of MgO-FS were investigated by varying the CO<sub>2</sub> partial pressure (3–12&#xa0;bar) and reaction temperature (120–150&#xa0;°C). The surface coverage model fitted the experimental data well. This means that the carbonation product (MgCO<sub>3</sub>) was continuously deposited on the surface of the particles. The MgCO<sub>3</sub> crystals formed on the particle surface were clearly observed by scanning electron microscopy. The diffusion in the MgCO<sub>3</sub> surface covering the MgO-FS particles is the rate-controlling step, preventing the contact and diffusion between the solution and the free surface of the particles. By stirring at 500&#xa0;rpm, both the maximum degree of carbonation and overall reaction rate significantly improved because stirring reduces the formation of large particle agglomerates. Under the conditions of 150&#xa0;°C, CO<sub>2</sub> partial pressure of 12&#xa0;bar, duration of 1&#xa0;h, and liquid/solid ratio of 10&#xa0;mL/g without stirring, the degree of carbonation and overall reaction rate constant were only 51.1% and 0.48 × 10<sup>−6</sup>&#xa0;mol&#xa0;s<sup>−1</sup>&#xa0;m<sup>−2</sup>, but they increased to 73.3% and 2.25 × 10<sup>−6</sup>&#xa0;mol&#xa0;s<sup>−1</sup>&#xa0;m<sup>−2</sup> by stirring at 500&#xa0;rpm.</p>

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Kinetic evaluation of the CO2 sequestration process of MgO-rich materials derived from ferronickel slag

  • F. Abdul,
  • K. Adachi,
  • H.J. Ho,
  • A. Iizuka,
  • E. Shibata

摘要

Ferronickel (FeNi) slag can be used to sequestrate CO2 by performing an alkaline pretreatment process using NaOH to obtain porous MgO-rich materials (MgO obtained from FeNi slag, MgO-FS). CO2 is mineralized by porous MgO-FS in the form of MgCO3. This study aimed to investigate the overall carbonation reaction kinetics of porous MgO-FS. The carbonation process was performed in an autoclave reactor under controlled CO2 pressure by continuously supplying CO2 throughout the experiment. The carbonation reaction kinetics of MgO-FS were investigated by varying the CO2 partial pressure (3–12 bar) and reaction temperature (120–150 °C). The surface coverage model fitted the experimental data well. This means that the carbonation product (MgCO3) was continuously deposited on the surface of the particles. The MgCO3 crystals formed on the particle surface were clearly observed by scanning electron microscopy. The diffusion in the MgCO3 surface covering the MgO-FS particles is the rate-controlling step, preventing the contact and diffusion between the solution and the free surface of the particles. By stirring at 500 rpm, both the maximum degree of carbonation and overall reaction rate significantly improved because stirring reduces the formation of large particle agglomerates. Under the conditions of 150 °C, CO2 partial pressure of 12 bar, duration of 1 h, and liquid/solid ratio of 10 mL/g without stirring, the degree of carbonation and overall reaction rate constant were only 51.1% and 0.48 × 10−6 mol s−1 m−2, but they increased to 73.3% and 2.25 × 10−6 mol s−1 m−2 by stirring at 500 rpm.