Nitramine and nitrosamine formation is a minor pathway in the atmospheric oxidation of methylamine: A theoretical kinetic study of the CH3NH + O-2 reaction
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2019-09-01
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International Journal of Chemical Kinetics
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Wiley
Melbourne Authors
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Chemical and Biomolecular Engineering
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Journal Article
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Alam, M. A., Ren, Z. & da Silva, G. (2019). Nitramine and nitrosamine formation is a minor pathway in the atmospheric oxidation of methylamine: A theoretical kinetic study of the CH3NH + O-2 reaction. International Journal of Chemical Kinetics, 51 (9), pp.723-728. https://doi.org/10.1002/kin.21303.
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Abstract
The atmospheric oxidation of amines proceeds via initial radical attack at C–H or N–H bonds to form carbon‐ and nitrogen‐centered radicals, respectively. It is conventionally assumed that nitrogen‐centered aminyl radicals react slowly with oxygen in the troposphere and associate predominantly with the radicals •NO and NO2• to form toxic nitrosamines and nitramines. We have used theoretical kinetic modeling techniques to study the prototypical CH3N•H + O2 reaction and have shown that it proceeds to CH2NH + HO2• under tropospheric conditions with a rate coefficient of 3.6 × 10−17 cm3 molecule−1 s−1. Although this value is low compared to the competing NOx reactions (∼10−11 cm3 molecule−1 s−1), the much higher concentration of O2 versus NOx in air makes it the dominant process in the atmospheric oxidation of methylamine for NOx concentrations below 100 ppb. The mechanism identified here is available to amines with primary, secondary, and tertiary α carbons and suggests that they may be less likely to form nitramines and nitrosamines than is currently thought.