Atmospheric Chemical Reactions of Monoethanolamine Initiated by OH Radical: Mechanistic and Kinetic Study

Monoethanolamine (MEA) is a benchmark and widely utilized solvent in amine-based postcombustion CO2 capture (PCCC), a leading technology for reducing CO2 emission from fossil fuel power plants. The large-scale implementation of PCCC would lead to inevitable discharges of amines to the atmosphere. Therefore, understanding the kinetics and mechanisms of the transformation of representative amine MEA in the atmosphere is of great significance for risk assessment of the amine-based PCCC. In this study, the H-abstraction reaction of MEA with center dot OH, and ensuing reactions of produced MEA-radicals, including isomerization, dissociation, and bimolecular reaction MEA-radicals+O-2, were investigated by quantum chemical calculation [M06-2X/aug-cc-pVTZ//M06-2X/6-311++G(d,p)] and kinetic modeling. The calculated overall rate constant [(7.27 x 10(-11)) cm(3) molecule(-1) s(-1)] for H-abstraction is in excellent agreement with the experimental value [(7.02 +/- 0.46) X 10(-11) cm(3) molecule(-1) s(-1)]. The results show that the product branching ratio of NH2CH2 center dot CHOH (MEA-beta) (43%) is higher than that of NH2 center dot CHCH2OH (MEA-alpha) (39%), clarifying that MEA-alpha is not an exclusive product. On the basis of the unveiled reaction mechanisms of MEA-radicals + O-2, the proton transfer reaction mass spectrometry signal (m/z 60.044), not recognized in the experiment, was identified.