Abstract

Tetraethylenepentamine (TEPA), consisting mainly of primary and secondary amines, exhibits a high CO2 sorption capacity; however, its poor thermal stability hampers practical utilization in the temperature swing adsorption process for CO2 capture. Here, a facile functionalization of TEPA with 1,2-epoxybutane (EB) substantially enhanced its thermal stability as well as the CO2 adsorption kinetics. Our careful analysis on the liquid-state 13C NMR disclosed the amine state distribution of EB-functionalized TEPA (EB-TEPA). Although the increase in tertiary amine portion induced by EB-functionalization reduced CO2 sorption capacity, the 0.64EB-TEPA (i.e., TEPA functionalized with EB with a TEPA/EB molar ratio of 1:3)/SiO2 showed an excellent long-term stability over the 10 consecutive cycles of adsorption/desorption processes with a CO2 swing capacity of 2.0 mmol CO2 g–1 under dry CO2/N2 (15/85 mol/mol) feed conditions. Also, the first-principles calculation identified the configuration of modified TEPA molecu...

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