Kinetics of CO<sub>2</sub> Capture with Calcium Oxide during Direct Air Capture in a Fluidized Bed

The bulk of research in carbon capture involves high CO<sub>2</sub> concentrations. This work instead describes the kinetics of CaO carbonation in mixtures with <i>p</i>CO<sub>2</sub> between 0.38 and 2.70 vol % and at temperatures between 400 and 650 °C. The reaction was studied in a bed of SiO<sub>2</sub> fluidized at flow rates corresponding to <i>U/U</i> <sub>mf</sub> of ∼4. Lower concentrations of CO<sub>2</sub> connected to the rates of mass transfer of CO<sub>2</sub> of the same order of magnitude as the rates of carbonation, thus, were eliminated from the kinetic analysis. The introduction of steam to the gas mixture (2 vol %) increased the rates of carbonation, demonstrating a pseudocatalytic effect, yet diminishing at higher temperatures. A rate expression generally accepted in the literature for high concentration CO<sub>2</sub> in CaO carbonation was assessed for its applicability at near-equilibrium conditions, demonstrating that the order of the rate expression changes between 0 and 1, increasing at higher temperatures. Using nonlinear regression, the experimental values were fitted to the Langmuir-Hinshelwood rate expression. The obtained parameters indicate CO<sub>2</sub> sorption and desorption being equilibrated, with the overall capture dominated mainly by slow kinetics of chemical reactions.

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Publication Details

Journal
Energy & Fuels
Published
2024-09-21
DOI
https://doi.org/10.1021/acs.energyfuels.4c03770
Citations
12
Primary Topic
Chemical Looping and Thermochemical Processes
Type
article
Field-Weighted Citation Impact
2.21

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article

Kinetics of CO2 Capture with Calcium Oxide during Direct Air Capture in a Fluidized Bed

Ewa Marek, Bryan Kean Hong Ooi
12 citations
Energy & Fuels
Chemical Looping and Thermochemical Processes
2.21
article

Kinetics of CO2 Capture with Calcium Oxide during Direct Air Capture in a Fluidized Bed

Ewa Marek, Bryan Kean Hong Ooi
article en
12 citations

Abstract

The bulk of research in carbon capture involves high CO<sub>2</sub> concentrations. This work instead describes the kinetics of CaO carbonation in mixtures with <i>p</i>CO<sub>2</sub> between 0.38 and 2.70 vol % and at temperatures between 400 and 650 °C. The reaction was studied in a bed of SiO<sub>2</sub> fluidized at flow rates corresponding to <i>U/U</i> <sub>mf</sub> of ∼4. Lower concentrations of CO<sub>2</sub> connected to the rates of mass transfer of CO<sub>2</sub> of the same order of magnitude as the rates of carbonation, thus, were eliminated from the kinetic analysis. The introduction of steam to the gas mixture (2 vol %) increased the rates of carbonation, demonstrating a pseudocatalytic effect, yet diminishing at higher temperatures. A rate expression generally accepted in the literature for high concentration CO<sub>2</sub> in CaO carbonation was assessed for its applicability at near-equilibrium conditions, demonstrating that the order of the rate expression changes between 0 and 1, increasing at higher temperatures. Using nonlinear regression, the experimental values were fitted to the Langmuir-Hinshelwood rate expression. The obtained parameters indicate CO<sub>2</sub> sorption and desorption being equilibrated, with the overall capture dominated mainly by slow kinetics of chemical reactions.

Energy & FuelsVol. 38(22)
University of Cambridge (GB)
Engineering and Physical Sciences Research Council
Openalex Percentile: Top 12%
Chemical Looping and Thermochemical Processes
2.21
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