Fig. 5: Amine-CO2 reactions in nonaqueous solvents. | Nature Communications

Fig. 5: Amine-CO2 reactions in nonaqueous solvents.

From: Electrifying amine carbon capture with robust redox-tunable acids

Fig. 5

a Regeneration of carbamic acid adduct via 1H+−1CO2 pathway and carbamate adduct via 2H+−1CO2 pathway. b 1H NMR study of the amine-CO2 reaction pathways in DMSO as a factor of amine concentration, supporting salt, and CO2 partial pressure. Black, MEA (50 mM) under N2; red, MEA (50 mM), HTFSI (50 mM) under N2; blue, MEA (50 mM) saturated with 100% CO2; green, MEA (50 mM) in DMSO with LiTFSI (500 mM) saturated with 100% CO2; purple, MEA (500 mM) in DMSO with LiTFSI (500 mM) saturated with 100% CO2; yellow, MEA (500 mM) in DMSO with LiTFSI (500 mM) saturated with 10% CO2. c Illustration of the titration experiment setup. The solution was purged by a stream of 20% CO2 (balanced with N2) at a flow rate of 10 sccm. The CO2 level at the exit of the septum-capped vial was monitored by an IR-based CO2 sensor. For the CO2 absorption experiment, various amounts of MEA were added to the vial containing either neat DMSO or DMSO with 0.5 M LiTFSI. For the CO2 desorption experiment, a solution of MEA (500 mM) and LiTFSI (500 mM) in DMSO was saturated with 20% CO2 and then added with various amounts of TfOH. For both experiments, the CO2 level was allowed to return to 20% before the next addition. d CO2 absorption capacity at various MEA concentrations. Grey, pure DMSO solvent; red, DMSO with 500 mM LiTFSI as the supporting salt. e CO2 desorption capacity with various concentrations of TfOH added. Source data for Fig. 5 are provided as a Source Data file.

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