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CO<sub>2</sub> Capture in Ionic Liquids Based on Amino Acid Anions With Protic Side Chains: a Computational Assessment of Kinetically Efficient Reaction Mechanisms

Stefano Onofri, Henry Adenusi, Andrea Le Donne, Enrico Bodo

2020ChemistryOpen20 citationsDOIOpen Access PDF

Abstract

Abstract Absorption and capture of CO 2 directly from sources represents one of the major tools to reduce its emission in the troposphere. One of the possibilities is to incorporate CO 2 inside a liquid exploiting its propensity to react with amino groups to yield carbamic acid or carbamates. A particular class of ionic liquids, based on amino acids, appear to represent a possible efficient medium for CO 2 capture because, at difference with current industrial setups, they have the appeal of a biocompatible and environmentally benign solution. We have investigated, by means of highly accurate computations, the feasibility of the reaction that incorporates CO 2 in an amino acid anion with a protic side chain and ultimately transforms it into a carbamate derivative. Through an extensive exploration of the possible reaction mechanisms, we have found that different prototypes of amino acid anions present barrierless reaction mechanisms toward CO 2 absorption.

Topics & Concepts

Carbamic acidIonic liquidChemistrySide chainAmino acidAbsorption (acoustics)Yield (engineering)Combinatorial chemistryDerivative (finance)Organic chemistryComputational chemistryCatalysisMaterials sciencePolymerComposite materialBiochemistryEconomicsMetallurgyFinancial economicsIonic liquids properties and applicationsCarbon Dioxide Capture TechnologiesCarbon dioxide utilization in catalysis
CO<sub>2</sub> Capture in Ionic Liquids Based on Amino Acid Anions With Protic Side Chains: a Computational Assessment of Kinetically Efficient Reaction Mechanisms | Litcius