CO2 capture using in-situ polymerized amines into pore-expanded-SBA-15: Performance evaluation, kinetics, and adsorption isotherms

Abstract

Over the last decades, carbon dioxide capture has attracted lots of attention and different solution have been proposed, yet the global CO2 concentration is still increasing along with its environmental impacts. Covalently tethered amines were in-situ polymerized into mesoporous silica support, namely PE-SBA-15, for the reversible temperature swing CO2 adsorption. The in-situ polymerization approach shows high loadings of amines in comparison to the grafting technique which was confirmed via thermal decomposition and CHN elemental analysis. The covalent tethering of amines, evidenced by the characteristic absorption peaks via FTIR, resulted in good thermal stability of the sorbent and constant CO2 uptake during multicycle operation. Porosimetry analysis, pore volume and BET surface area, showed a noticeable decrease upon the functionalization of support indicating that most of the pores of the support are occupied by the amines. CO2 capture of the sorbent at different concentrations and temperatures, from 400 ppm for the direct air CO2 capture to 15 % CO2 for coal-powered plants showed good performance. A reduction in CO2 uptake was noticed upon the decrease in adsorption temperature with an optimum temperature of 25 °C. Adsorption kinetics were found to be best represented by a pseudo-second order model with significant adsorption rates. Dry adsorption isotherms of CO2 and N2 were studied at different temperatures and the CO2 isotherms were found to follow Langmuir dual site (LDS) model with a very high selectivity towards CO2. This study shows that in-situ polymerization is a key route for mitigating the continuous increase in atmospheric CO2 concentration.