h i g h l i g h t sThe CA enzyme activity did not change noticeably with CO 2 loading in a PC solution. Absorption rate into CO 2 -rich PC with 3 g/L of CA were twice that into a rich 5 M MEA. Liquid-phase mass transfer resistance dominated in both the PC and MEA systems. Packing volume of IVCAP absorber with 10 g/L of CA was comparable with that of MEA. a b s t r a c t Development of enzyme-mediated solvents are regarded as a potential option to overcome the energy use disadvantages associated with the benchmark monoethanolamine (MEA) solvent for post-combustion CO 2 capture. In this work, the kinetics of CO 2 absorption into a 20 wt% potassium carbonate (PC) solution promoted with the enzyme carbonic anhydrase (CA) was investigated using a stirred tank reactor. Experimental results showed no noticeable change in the intrinsic activity of the CA enzyme with increasing CO 2 loading in PC solution. A rate-based mass transfer analysis was conducted using the enzymatic kinetics measured, and results revealed that in a packed-bed column, the CO 2 absorption rates into a lean and rich PC solution with 3 g L À1 CA were 50% lower and 2.2 times higher, respectively, than those into their 5 M MEA counterparts. The liquid-phase mass transfer resistance was dominant for both PC-and MEA-based systems. Modeling results revealed the effective packing volume of the absorber with PC in the presence of 10 g L À1 CA was only slightly larger than that with MEA for post-combustion CO 2 capture.