American Geophysical Union Become an AGU Member
Subscribe to AGU Journals
AGU Home AGU Publications

Read Full Article (file size: 558256 bytes)    Cited by

JOURNAL OF GEOPHYSICAL RESEARCH, VOL. 107, NO. D22, 8193, doi:10.1029/2001JD001292, 2002

Urban and rural aerosol characterization of summer smog events during the PIPAPO field campaign in Milan, Italy

U. Baltensperger

Paul Scherrer Institute, Villigen, Switzerland


N. Streit

Paul Scherrer Institute, Villigen, Switzerland


E. Weingartner

Paul Scherrer Institute, Villigen, Switzerland


S. Nyeki

Paul Scherrer Institute, Villigen, Switzerland


A. S. H. Prévôt

Paul Scherrer Institute, Villigen, Switzerland


R. Van Dingenen

Joint Research Centre, Environmental Institute, Ispra, Italy


A. Virkkula

Joint Research Centre, Environmental Institute, Ispra, Italy


J.-P. Putaud

Joint Research Centre, Environmental Institute, Ispra, Italy


A. Even

ECN, Netherlands Energy Research Foundation (ECN), Petten, Netherlands


H. ten Brink

ECN, Netherlands Energy Research Foundation (ECN), Petten, Netherlands


A. Blatter

Swiss Federal Research Station for Agro-Ecology and Agriculture, Institute of Environmental Protection and Agriculture, Bern, Switzerland


A. Neftel

Swiss Federal Research Station for Agro-Ecology and Agriculture, Institute of Environmental Protection and Agriculture, Bern, Switzerland


H. W. Gäggeler

Paul Scherrer Institute, Villigen, Switzerland
Department of Chemistry and Biochemistry, University of Bern, Bern, Switzerland


Abstract

A comprehensive range of aerosol parameters was measured at an urban and a rural site in the Milan, Italy metropolitan region during summer smog events in summer 1998. Measurements were performed as part of the Pianura Padana Produzione di Ozono (PIPAPO) field campaign to determine the sensitivity of O3 production to NOX and volatile organic carbon concentrations at several ground stations. Primary aerosol parameters (i.e., direct emissions) such as aerosol black carbon showed a distinct diurnal variation with maxima at about 0000 and 0800 central European summer time (CEST), in contrast to secondary aerosol parameters such as sulfate and nitrate. Aerosol number size distributions were measured under ambient conditions as well as after conditioning with volatility and hygroscopicity systems. A mode at d = 20–30 nm in the number concentration was found at 0800 CEST and exhibited high volatility at 110°C (∼80% volume lost upon heating) but no hygroscopic behavior. Based on these measurements, small particles (d < 40 nm) are thought to consist mainly of hydrophobic particulate organic matter, rather than soot or H2SO4 aerosols. Two distinct hygroscopic modes with average growth factors d/d0 ∼ 1.02 and 1.21–1.28 were found for particles with dry (relative humidity of <30%) diameters d0 = 50–200 nm. Submicrometer aerosols exhibited lower volatility at the rural than at the urban site, which is attributed to additional particulate mass produced by secondary particle formation.

Published 24 October 2002.

Index Terms: 0305 Atmospheric Composition and Structure: Aerosols and particles (0345, 4801); 0345 Atmospheric Composition and Structure: Pollution—urban and regional (0305); 0365 Atmospheric Composition and Structure: Troposphere—composition and chemistry; 0322 Atmospheric Composition and Structure: Constituent sources and sinks.


Read Full Article (file size: 558256 bytes)    Cited by

Citation: Baltensperger, U., et al. (2002), Urban and rural aerosol characterization of summer smog events during the PIPAPO field campaign in Milan, Italy, J. Geophys. Res., 107(D22), 8193, doi:10.1029/2001JD001292.