Biomaterials for CO2Harvesting: From Regulatory Functions to Wet Scrubbing Applications

A new series of 2-aminoethyl-benzene-based biomaterials, namely, dopamine (DOP), tyramine (TYR), phenylethylamine (PEA), and epinephrine (EPN), dissolved in dimethylsulfoxide (DMSO) have been investigated for CO 2 capture upon activatiing their hydhydrochloride salts  with a NaOH pellet. Spectroscopic measurements, including ex situ ATR-FTIR, 1D and 2D NMR experiments have been applied to verify the formation of the sodium carbamate adducts (RR'N-CO 2 - Na + ). The emergence of new peaks in the IR spectra ranging between 1702 and 1735 cm -1 together with the chemical shift within 157-158 ppm in the 13 C NMR, as well as with cross-peaks obtained by 1 H- 15 N HSQC measurements at ca. 84 and 6.6 ppm verified the formation of RR'N-CO 2 - Na + products upon the chemical fixation of CO 2 . The CO 2 sorption capacity of the examined biomaterials was evaluated volumetrically, with a maximum value of 8.18 mmol CO 2 ·g -1 sorbent (36.0 (w/w)%, including both chemisorption and physisorption), for 5 (w/v)% solutions measured at 5 bar CO 2 and 25 °C, for TYR and PEA. DFT calculations indicated that the intramolecular hydrogen bonding within the structural motif of EPN-N-CO 2 - Na + adduct provides an exceptional stability compared to monoethanolamine and other structurally related model compounds.