Force-Field-Based Computational Study of the Thermodynamics of a Large Set of Aqueous Alkanolamine Solvents for Post-Combustion CO2 Capture

• Published in: Journal of chemical information and modeling Vol. 61; no. 9; pp. 4497 - 4513
• Main Authors: Noroozi, Javad, Smith, William R
• Format: Journal Article
• Language: English
• Published: Washington American Chemical Society 27.09.2021
• Subjects: Alkanolamines; Amines; Aqueous solutions; Bicarbonates; Carbamates (tradename); Carbon dioxide; Carbon sequestration; Chemical equilibrium; Computational Chemistry; Data points; Enthalpy; Free energy; Heat of reaction; High temperature; Hybrid systems; Hydration; Hydronium ions; Ideal gas; Molecular dynamics; Monoethanolamine (MEA); Protonation; Quantum chemistry; Solvents; Steric effects; Thermodynamic properties
• ISSN: 1549-9596; 1549-960X
• DOI: 10.1021/acs.jcim.1c00718

The ability to predict the thermodynamic properties of amine species in CO2-loaded aqueous solutions, including their deprotonation (pK a) and carbamate to bicarbonate reversion (pK c) equilibrium constants and their corresponding standard reaction enthalpies, is of critical importance for the design of improved carbon capture solvents. In this study, we used isocoulombic forms of both reactions to determine these quantities for a large set of aqueous alkanolamine solvent systems. Our hybrid approach involves using classical molecular dynamics simulations with the general amber force field (GAFF) and semi-empirical AM1–BCC charges (GAFF/AM1–BCC) in the solution phase, combined with high-level composite quantum chemical ideal-gas calculations. We first determined a new force field (FF) for the hydronium ion (H3O+) by matching to the single experimental pK a data point for the well-known monoethanolamine system at 298.15 K. We then used this FF to predict the pK a values for 76 other amines at 298.15 K and for all 77 amines at elevated temperatures. Additionally, we indirectly relate the H3O+ hydration free energy to that of H+ and provide expressions for intrinsic hydration free energy and enthalpy of the proton. Using the derived H3O+ FF, we predicted the pK a values of a diverse set of alkanolamines with an overall average absolute deviation of less than 0.72 pK a units. Furthermore, the derived H3O+ FF is able to predict the protonation enthalpy of these amines when used with the GAFF. We also predicted the carbamate reversion constants of the primary and secondary amine species in the data set and their corresponding standard heats of reaction, which we compared with the scarcely available experimental data, which are often subject to significant uncertainty. Finally, we also described the influence of electronic and steric effects of different molecular fragments/groups on the stabilities of the carbamates.