The bulk of research in carbon capture involves high CO concentrations. This work instead describes the kinetics of CaO carbonation in mixtures with CO between 0.38 and 2.70 vol % and at temperatures between 400 and 650 °C. The reaction was studied in a bed of SiO fluidized at flow rates corresponding to of ∼4. Lower concentrations of CO connected to the rates of mass transfer of CO 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 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 sorption and desorption being equilibrated, with the overall capture dominated mainly by slow kinetics of chemical reactions.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11586902 | PMC |
http://dx.doi.org/10.1021/acs.energyfuels.4c03770 | DOI Listing |
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