Linda Pastero

CO2 sorption–desorption cycles with a methyldiethanolamine (MDEA)/piperazine (PZ) blend have been performed with a rotoevaporator. Similar to other CO2 separation technologies, the heating involved in MDEA/PZ solvent regeneration is the most energy-intensive step in the overall CO2 separation process. Thus, this study investigated the desorption kinetics under low-pressure (<200 mbar) and low-temperature conditions in the range from 308 to 363 K with the aim of reducing costs. The CO2 desorption time to unload the samples from ~2.35 mol/kg to below the threshold of 1 mol/kg was reduced from 500 s at 333 K to 90 s at 363 K. The Avrami–Erofoyev model was found to fit the experimental kinetic data accurately. The Arrhenius law calculations provided an activation energy of the CO2 desorption process equal to 76.39 kJ/mol. It was demonstrated that the combination of a pressure reduction and the increase in temperature resulted in an enhancement of the desorption kinetics, especially at low temperatures. The combined effect of these two factors resulted in higher desorption kinetics compared to the individual effects of either factor alone. Solvent regeneration at a low temperature was demonstrated to be a valid option when coupled with pressure reduction.