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

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TLDR
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 as mentioned in this paper, and small particles (d < 40 nm) are thought to consist mainly of hydrophobic particulate organic matter, rather than soot or H2SO4 aerosols.
Abstract
[1] 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.

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Organic aerosol and global climate modelling: a review

TL;DR: In this article, the authors reviewed existing knowledge with regard to organic aerosol (OA) of importance for global climate modelling and defined critical gaps needed to reduce the involved uncertainties, and synthesized the information to provide a continuous analysis of the flow from the emitted material to the atmosphere up to the point of the climate impact of the produced organic aerosols.
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Atmospheric composition change – global and regional air quality

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TL;DR: A review of the state of scientific understanding in relation to global and regional air quality is outlined in this article, in terms of emissions, processing and transport of trace gases and aerosols.
References
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Atmospheric chemistry and physics: from air pollution to climate change.

TL;DR: In this article, the authors present a model for the chemistry of the Troposphere of the atmosphere and describe the properties of the Atmospheric Aqueous phase of single aerosol particles.
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Atmospheric Chemistry and Physics: From Air Pollution to Climate Change

TL;DR: In this paper, the authors present a model for the chemistry of the Troposphere of the atmosphere and describe the properties of the Atmospheric Aqueous phase of single aerosol particles.
Journal ArticleDOI

Heterogeneous and Multiphase Chemistry in the Troposphere

TL;DR: In this paper, the authors make a distinction between reactions on solids (heterogeneous reactions) and those occurring in liquid droplets (multiphase reactions) is convenient for understanding, describing, and including them in models of the troposphere.
Journal ArticleDOI

A new electromobility spectrometer for the measurement of aerosol size distributions in the size range from 1 to 1000 nm

TL;DR: The Electromobility Spectrometer as mentioned in this paper is an automated measurement system for the size analysis of fine and ultrafine aerosols using Differential Mobility Analysers (DMA) for the classification of particles and an electrical sensor for their detection.
Journal ArticleDOI

Hygroscopic properties of carbon and diesel soot particles

TL;DR: In this article, the hygroscopic properties of freshly produced carbon and diesel soot particles at subsaturations (i.e. at relative humidity < 100%) were investigated. And the results showed that freshly emitted combustion particles are unlikely to act as cloud condensation nuclei whereas an aging of the particles will enhance their nucleation ability.
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