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NO3 radical, OH radical and O3-initiated secondary aerosol formation from aliphatic amines
- Tang, Xiaochen, Price, Derek, Praske, Eric, Lee, Su Anne, Shattuck, Morgan A., Purvis-Roberts, Kathleen, Silva, Philip J., Asa-Awuku, Akua, Cocker, David R.
- Atmospheric environment 2013 v.72 pp. 105
- aerosols, amines, ammonia, atmospheric chemistry, hydroxyl radicals, nitrates, ozone, photooxidation, relative humidity, water vapor
- Aliphatic amines enter the atmosphere from a variety of sources, and exist in both gas and particle phases in the atmosphere. Similar to ammonia, amines can form inorganic salts through acid–base reactions. However, the atmospheric behavior of amines with atmospheric oxidants (e.g. the nitrate radical (NO3), the hydroxyl radical (OH), O3) is still poorly understood. In this study, chamber experiments were conducted to explore the reaction between three aliphatic amines and HNO3/O3/NO3/OH. Effects of water vapor were also explored by conducting experiments under different relative humidity conditions (RH<0.1% to ∼40%). Results show that all three amines have a high potential to form secondary aerosol in reactions with NO3, and are affected by the presence of water vapor. DEA and BA are capable of forming a significant amount of stable inorganic salt at ppb level concentrations, while TMA tends to form mostly non-salt secondary organic aerosol under dry conditions. The OH photooxidation of amines has much lower secondary aerosol yield and is independent of relative humidity, while ozonolysis produced negligible amount of aerosol. Secondary aerosol from OH oxidation was composed of organic components only, due to the lack of acid source. This study shows that night time chemistry of aliphatic amines can produce secondary organic and inorganic aerosol mixtures, and the relative contribution of each component depends on the environment relative humidity.