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7428733 
Journal Article 
Kinetics and mechanism of carbamate formation from CO2(aq), carbonate species, and monoethanolamine in aqueous solution 
Mccann, N; Phan, D; Wang, X; Conway, W; Burns, R; Attalla, M; Puxty, G; Maeder, M; , 
2009 
Journal of Physical Chemistry A
ISSN: 1089-5639
EISSN: 1520-5215 
AMER CHEMICAL SOC 
WASHINGTON 
113 
17 
5022-5029 
English 
Removal of carbon dioxide from fossil-based power generation is a potentially useful technique for the reduction of greenhouse gas emissions. Reversible interaction with aqueous amine solutions is most promising. In this process, the formation of carbamates is an important reaction of carbon dioxide. In this contribution, a detailed molecular reaction mechanism for the carbamate formation between MEA (monoethanolamine) and dissolved CO(2) as well as carbonate species in aqueous solution is presented. There are three parallel, reversible reactions of the free amine with CO(2), carbonic acid, and the bicarbonate ion; the relative importance of the three paths is strongly pH dependent. Kinetic and equilibrium measurements are based on (1)H NMR and stopped-flow measurements with rate constants, equilibrium constants, and protonation constants being reported. 
Amine solutions; Aqueous solutions; Carbonate species; Carbonic acids; Equilibrium measurements; Free amines; Kinetics and mechanism; Molecular reactions; Monoethanolamine; PH-dependent; Protonation constants; Relative importance; Reversible interactions; Reversible reaction; Stopped-flow measurements; Amines; Carbon dioxide; Complexation; Dissolution; Gas emissions; Global warming; Greenhouse gases; Leakage (fluid); Metal casting; Organic acids; Rate constants; Solutions; Equilibrium constants; carbamic acid derivative; carbon dioxide; carbonic acid derivative; ethanolamine; water; article; chemistry; kinetics; nuclear magnetic resonance spectroscopy; solution and solubility; synthesis; Carbamates; Carbon Dioxide; Carbonates; Ethanolamine; Kinetics; Magnetic Resonance Spectroscopy; Solutions; Water 
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