Abstract
Over the past decade, the formation and growth of nanometer-size atmospheric aerosol particles have been observed at a number of sites around the world. Measurements of particle formation have been performed on different platforms (ground, ships, aircraft) and over different time periods (campaign or continuous-type measurements). The development during the 1990s of new instruments to measure nanoparticle size distributions and several gases that participate in nucleation have enabled these new discoveries. Measurements during nucleation episodes of evolving size distributions down to 3 nm can be used to calculate the apparent source rate of 3-nm particles and the particle growth rate. We have collected existing data from the literature and data banks (campaigns and continuous measurements), representing more than 100 individual investigations. We conclude that the formation rate of 3-nm particles is often in the range 0.01-10 cm-3 s-1 in the boundary layer. However, in urban areas formation rates are often higher than this (up to 100 cm-3 s-1), and rates as high as 104-10 5 cm-3 s-1 have been observed in coastal areas and industrial plumes. Typical particle growth rates are in the range 1-20 nm h-1 in mid-latitudes depending on the temperature and the availability of condensable vapours. Over polar areas the growth rate can be as low as 0.1 nm h-1. Because nucleation can lead to a significant increase in the number concentration of cloud condensation nuclei, global climate models will require reliable models for nucleation.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 143-176 |
| Number of pages | 34 |
| Journal | Journal of Aerosol Science |
| Volume | 35 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 2004 |
Bibliographical note
Funding Information:The authors are grateful to several groups collecting and publishing the data. Particularly we would like to thank Dr. E.D. Nilsson, Mrs. S.-P- Malvikko, Mr. M. Savimaa, Dr. I.K. Koponen and Mr. Pasi Aalto for their help. We acknowledge financial support by the Academy of Finland (Project No. 47668). WB acknowledges support by EU Marie Curie grant EKV4-CT-2000-50002. PHM acknowledges support from the U.S. DOE through Grant No. DE-FG02-98R62556 and EPA through Grant No. R829620, and the assistance of Hiromu Sakurai and Qian Shi in analysing the data from St. Louis. Although the research described in this article has been funded wholly or in part by the United States Environmental Protection Agency, it has not been subjected to the Agency's required peer and policy review and therefore does not necessarily reflect the views of the Agency and no official endorsement should be inferred.
Keywords
- Atmospheric aerosols
- Condensation growth
- Nucleation
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