Articles | Volume 18, issue 2
https://doi.org/10.5194/acp-18-845-2018
https://doi.org/10.5194/acp-18-845-2018
Research article
 | 
23 Jan 2018
Research article |  | 23 Jan 2018

New particle formation in the sulfuric acid–dimethylamine–water system: reevaluation of CLOUD chamber measurements and comparison to an aerosol nucleation and growth model

Andreas Kürten, Chenxi Li, Federico Bianchi, Joachim Curtius, António Dias, Neil M. Donahue, Jonathan Duplissy, Richard C. Flagan, Jani Hakala, Tuija Jokinen, Jasper Kirkby, Markku Kulmala, Ari Laaksonen, Katrianne Lehtipalo, Vladimir Makhmutov, Antti Onnela, Matti P. Rissanen, Mario Simon, Mikko Sipilä, Yuri Stozhkov, Jasmin Tröstl, Penglin Ye, and Peter H. McMurry

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Cited articles

Ball, S. M., Hanson, D. R., Eisele, F. L., and McMurry, P. H.: Laboratory studies of particle nucleation: Initial results for H2SO4, H2O, and NH3 vapors, J. Geophys. Res.-Atmos., 104, 23709–23718, https://doi.org/10.1029/1999JD900411, 1999. 
Bergman, T., Laaksonen, A., Korhonen, H., Malila, J., Dunne, E. M., Mielonen, T., Lehtinen, K. E. J., Kühn, T., Arola, A., and Kokkola, H.: Geographical and diurnal features of amine-enhanced boundary layer nucleation, J. Geophys. Res.-Atmos., 120, 9606–9624, https://doi.org/10.1002/2015JD023181, 2015. 
Berndt, T., Sipilä, M., Stratmann, F., Petäjä, T., Vanhanen, J., Mikkilä, J., Patokoski, J., Taipale, R., Mauldin III, R. L., and Kulmala, M.: Enhancement of atmospheric H2SO4 H2O nucleation: organic oxidation products versus amines, Atmos. Chem. Phys., 14, 751–764, https://doi.org/10.5194/acp-14-751-2014, 2014. 
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A recent laboratory study (CLOUD) showed that new particles nucleate efficiently from sulfuric acid and dimethylamine (DMA). The reanalysis of previously published data reveals that the nucleation rates are even faster than previously assumed, i.e., nucleation can proceed at rates that are compatible with collision-controlled new particle formation for atmospheric conditions. This indicates that sulfuric acid–DMA nucleation is likely an important source of particles in the boundary layer.
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