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To achieve low regeneration energy consumption and viscosity, a novel amino-functionalized ionic liquid TEPAH2-MI combined with organic solvents has been proposed for CO2 capture in this work. The results demonstrated that the absorption loading of TEPAH2-MI/N-propanol (NPA)/ethylene glycol (EG) was 1.72 mol·mol–1 (28 wt %, 257 g·L–1), which was much higher than that of monoethanolamine/water, and the regeneration efficiency was maintained at 90.7% after the fifth regeneration cycle. The viscosities of the solution were only 3.66 and 7.65 mPa·s before and after absorption, respectively, which were significantly lower than those of traditional nonaqueous absorbents. The reaction mechanism investigated via 13C NMR and quantum calculations summarized that CO2 first reacted with the amino group of TEPAH+ to form the carbamates through the zwitterion formation and protonation process, while CO2 reacted with the N atom of 2-MI− to directly form the carbamate. Then, some of them further reacted with NPA and EG to form the carbonates. Moreover, Nπ and Nτ tautomers of TEPAH2-MI could convert into each other continuously when CO2 was absorbed. During CO2 desorption, the carbamates and carbonates reacted with AFILH+ to decompose and released CO2 directly.
Liu et al. (Mon,) studied this question.