Articles | Volume 7, issue 1
Atmos. Chem. Phys., 7, 211–222, 2007

Special issue: Quantification of aerosol nucleation in the European boundary...

Atmos. Chem. Phys., 7, 211–222, 2007

  16 Jan 2007

16 Jan 2007

Hygroscopic properties of ultrafine aerosol particles in the boreal forest: diurnal variation, solubility and the influence of sulfuric acid

M. Ehn1, T. Petäjä1, H. Aufmhoff2, P. Aalto1, K. Hämeri1,3, F. Arnold2, A. Laaksonen4,5, and M. Kulmala1 M. Ehn et al.
  • 1Division of Atmospheric Sciences, Department of Physical Sciences, P.O. Box 64, 00014 University of Helsinki, Finland
  • 2Max-Planck Institute for Nuclear Physics (MPIK), Atmospheric Physics Division, P.O. Box 103980, 69029 Heidelberg, Germany
  • 3Finnish Institute of Occupational Health, Topeliuksenkatu 41 a A, 00250 Helsinki, Finland
  • 4Department of Applied Physics, University of Kuopio, P.O. Box 1627, 70211 Kuopio, Finland
  • 5Finnish Meteorological Institute, P.O. Box 503, 00101 Helsinki, Finland

Abstract. The hygroscopic growth of aerosol particles present in a boreal forest was measured at a relative humidity of 88%. Simultaneously the gas phase concentration of sulfuric acid, a very hygroscopic compound, was monitored. The focus was mainly on days with new particle formation by nucleation. The measured hygroscopic growth factors (GF) correlated positively with the gaseous phase sulfuric acid concentrations. The smaller the particles, the stronger the correlation, with r=0.20 for 50 nm and r=0.50 for 10 nm particles. The increase in GF due to condensing sulfuric acid is expected to be larger for particles with initially smaller masses. During new particle formation, the changes in solubility of the new particles were calculated during their growth to Aitken mode sizes. As the modal diameter increased, the solubility of the particles decreased. This indicated that the initial particle growth was due to more hygroscopic compounds, whereas the later growth during the evening and night was mainly caused by less hygroscopic or even hydrophobic compounds. For all the measured sizes, a diurnal variation in GF was observed both during days with and without particle formation. The GF was lowest at around midnight, with a mean value of 1.12–1.24 depending on particle size and if new particle formation occurred during the day, and increased to 1.25–1.34 around noon. This can be tentatively explained by day- and nighttime gas-phase chemistry; different vapors will be present depending on the time of day, and through condensation these compounds will alter the hygroscopic properties of the particles in different ways.

Final-revised paper