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Synthesis methods of K2CO3 based adsorbents

sol gel; impregnation; physical mixing

https://doi.org/10.1016/j.ccst.2021.100011

“Yang et al. prepared carbon aerogels (CAs) using the sol-gel method, and they loaded K2CO3 on the mesoporous supports to prepare the CA-potassium carbonate (KC) nanocomposites. The 7CA-KC adsorbent with good textural properties exhibited a high CO2 uptake of 2.68 mmol CO2/g and a declined regeneration temperature (Yang et al., 2016). This was because the sol-gel and impregnation method had enabled the K2CO3 nanocrystals being embedded in the nanopores of the CAs, and the incorporated K2CO3 nanocrystals exhibited higher reactivity than bulk K2CO3 (Yang et al., 2016). Guo et al. reported that the sol-gel and impregnation method had benefited the silica-alumina aerogel and silica aerogel supported K2CO3 adsorbents developed microstructure and good morphology for enhanced CO2 uptakes (1.32-1.86 mmol CO2/g) (Guo, B. et al., 2020aGuo, B. et al., 2020cGuo et al., 2018b). For silica aerogel supported K2CO3 adsorbents (KSGs), the dispersion of K2CO3 would be affected by the different solvents employed in the impregnation process. Instead of deionized water, ethanol as solvent or dispersing agent would bestow the KSGs adsorbents with uniform dispersion of K2CO3 (Guo et al., 2015c, d; Guo et al., 2018b). It is well known that K2CO3/Al2O3 would suffer deactivation in repeated cycles due to the formation of byproduct of KAl(CO3)(OH)2. Given this, a novel K2CO3/Al2O3 adsorbent was synthesized by CO2 thermal treatment of the impregnated K2CO3 on porous δ-Al2O3 support. CO2 thermal treatment played an important role in inhibiting the formation of KAl(CO3)(OH)2 byproduct, and therefore had endowed the new K2CO3/Al2O3 adsorbent with stable CO2 adsorption capacity (∼3.09 mmol CO2/g) over multiple cycles (Jo et al., 2016). Efforts had also been made to construct core/shell-structured potassium-based adsorbents by employing γ-alumina and boehmite (γ-AlOOH) as cores and titanium propoxide, tetra ethyl ortho silicate, and zirconium butoxide as shells. By creating a layer between K2CO3 and alumina, the core-shell technique had weakened the interactions between the two phases, and the formation of KAl(CO3)(OH)2 byproduct could be inhibited. Therefore, the core-shell-structured potassium-based adsorbent retained a high CO2 uptake (3.31 mmol CO2/g) and good working stability (Bararpour et al., 2020). It was reported that K2CO3/Al2O3 prepared by the single-step impregnation (SI) method suffered evident pore structure blockage and limited K2CO3 utilization. The multi-step impregnation (MI) method was proposed to promote the dispersion of K2CO3 in the broad macropores, and the CO2 adsorption capacity of the adsorbent prepared via the MI method had been significantly improved from 1.93 to 3.12 mmol CO2/g (Sengupta et al., 2014a). Bararpour et al. prepared K2CO3/alumina adsorbents by the physical mixing method and incipient wetness impregnation method, respectively, and the adsorbent synthesized by the physical mixing method showed a higher CO2 capture capacity (2.75 mmol CO2/g) (Bararpour et al., 2018).”

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