Hygroscopicity and volatility of 4–10 nm particles during summertime atmospheric nucleation events in urban Atlanta

American Geophysical Union (AGU) - Tập 110 Số D22 - 2005
Hiromu Sakurai1, Melissa A. Fink1, Peter H. McMurry1, L. Mauldin2, Katharine F. Moore3,2, James N. Smith2, F. L. Eisele2,4
1Department of Mechanical Engineering, University of Minnesota, Minneapolis, Minnesota, USA
2Atmospheric Chemistry Division, National Center for Atmospheric Research, Boulder, Colorado, USA
3Advanced Study Program National Center for Atmospheric Research Boulder Colorado USA
4Earth and Atmospheric Sciences Georgia Institute of Technology Atlanta Georgia USA

Tóm tắt

Continuous measurements of hygroscopicity and volatility of atmospheric aerosol particles of 4–10 nm diameter were conducted with a nanometer tandem differential mobility analyzer (Nano TDMA) during the Aerosol Nucleation and Real‐time Characterization Experiment (ANARChE), which took place in Atlanta in July and August 2002. In the Nano TDMA measurements, particles were exposed to either a high humidity (∼90% RH) or an elevated temperature (∼100°C) downstream of the first differential mobility analyzer (DMA) and were then resized by the second DMA to determine the change in size due to water uptake or evaporation. There were several days when nucleation occurred and high concentrations of sub‐20 nm particles were observed, and during those events, particles of 4–10 nm diameter were very hygroscopic and nonvolatile. These observations, together with parallel Thermal Desorption Chemical Ionization Mass Spectrometer (TDCIMS) measurements of sub‐20 nm particle composition, suggest that the particles were mostly composed of ammoniated sulfates. This finding strongly supports the hypothesis that the nucleation and subsequent growth of nanoparticles were driven by reactions involving sulfuric acid and ammonia during this study.

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