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1.
ACS Omega ; 4(7): 11532-11539, 2019 Jul 31.
Artigo em Inglês | MEDLINE | ID: mdl-31460259

RESUMO

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 CO2 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-CO2 - 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 13C NMR, as well as with cross-peaks obtained by 1H-15N HSQC measurements at ca. 84 and 6.6 ppm verified the formation of RR'N-CO2 - Na+ products upon the chemical fixation of CO2. The CO2 sorption capacity of the examined biomaterials was evaluated volumetrically, with a maximum value of 8.18 mmol CO2·g-1 sorbent (36.0 (w/w)%, including both chemisorption and physisorption), for 5 (w/v)% solutions measured at 5 bar CO2 and 25 °C, for TYR and PEA. DFT calculations indicated that the intramolecular hydrogen bonding within the structural motif of EPN-N-CO2 - Na+ adduct provides an exceptional stability compared to monoethanolamine and other structurally related model compounds.

2.
Chem Commun (Camb) ; 55(24): 3449-3452, 2019 Mar 19.
Artigo em Inglês | MEDLINE | ID: mdl-30747173

RESUMO

Bio-renewables are emerging as potential materials for CO2 sorption. Epinephrine is employed as a green scrubbing agent for CO2 capturing through the formation of a metal carbamate as proved by 1H, 13C and 1H-15N NMR and ex situ ATR-FTIR spectroscopy, as well as supported by quantum-chemical calculations.


Assuntos
Carbamatos/química , Dióxido de Carbono/isolamento & purificação , Epinefrina/química , Química Verde/métodos , Agentes Molhantes/química , Dióxido de Carbono/química , Modelos Moleculares
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