Abstract

Abstract. Studies on ultrafine particles (diameter < 100nm) and air quality have mostly focused on vehicle exhaust emissions and on new particle formation in "clean" ambient air. Here we present a study focused on the processes contributing to ultrafine particle concentrations in a city (Huelva, SW Spain) placed close to a coastal area where significant anthropogenic emissions of aerosol precursors occur. The overall data analysis shows that two processes predominantly contribute to the number of particles coarser than 2.5 nm: vehicle exhaust emissions and new particle formation due to photo-chemical activity. As typically occurs in urban areas, vehicle exhaust emissions result in high concentrations of black carbon (BC) and particles coarser than 2.5 nm (N) during the morning rush hours. The highest N concentrations were recorded during the 11:00–17:00 h period, under the sea breeze regime, when low BC concentrations were registered and photochemical activity resulted in high O3 levels and in new particle formation in the aerosol precursors' rich inland airflow. In this period, it is estimated that about 80% of the number of particles are linked to sulfur dioxide emissions. The contributions to N of "carbonaceous material and those compounds nucleating/condensing immediately after emission" and of the "new particle formation processes in air masses rich gaseous precursors (e.g. SO2)" were estimated by means of a relatively novel method based on simultaneous measurements of BC and N. A comparison with two recent studies suggests that the daily cycles of "new particle formation" during the inland sea breeze is blowing period seem to be a feature of ultrafine particles in coastal areas of South-west Europe.

Highlights

  • Urban air quality impairment by atmospheric nano-sized particles is becoming a topic of great interest in the atmospheric and environmental sciences

  • The overall data analysis shows that two processes predominantly contribute to the number of particles coarser than 2.5 nm: vehicle exhaust emissions and new particle formation due to photo-chemical activity

  • The specific aerosol absorption coefficient σ was determined by comparing the absorption coefficient σap measured by the Multi-Angle Absorption Photometer (MAAP) with the elemental carbon (EC) concentrations determined by the Sunset analysis of the PM10 samples

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Summary

Introduction

Urban air quality impairment by atmospheric nano-sized particles is becoming a topic of great interest in the atmospheric and environmental sciences. A growing volume of scientific evidences shows that exposure to ultrafine particles (diameter

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