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The Transition States for CO 2 Capture by Substituted Ethanolamines
Author(s) -
Gangarapu Satesh,
Marcelis Antonius T. M.,
Alhamed Yahia A.,
Zuilhof Han
Publication year - 2015
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201500511
Subject(s) - steric effects , chemistry , bicarbonate , carbamate , ethanolamines , activation energy , transition state , solvent , inorganic chemistry , computational chemistry , organic chemistry , ethanolamine , catalysis
Quantum chemical studies are used to understand the electronic and steric effects on the mechanisms of the reaction of substituted ethanolamines with CO 2 . SCS‐MP2/6‐311+G(2d,2p) calculations are used to obtain the activation energy barriers and reaction energies for both the carbamate and bicarbonate formation. Implicit solvent effects are included with the universal solvation model SMD. Carbamate formation is more favorable than bicarbonate formation for monoethanolamine (MEA) both kinetically and thermodynamically. Increase of the steric hindrance on the C atoms around the N atom in substituted ethanolamines favors bicarbonate formation over carbamate formation with lower activation barriers and thereby higher reaction rates. In contrast, substitution by an N ‐methyl or N ‐ethyl group on MEA leads to a lower activation barrier for both carbamate formation and bicarbonate formation. As a result, higher reaction rates are expected as compared to MEA, and therefore these compounds have significant potential as industrial CO 2 capturing solvents.