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Ambient particulate matter source apportionment using receptor modelling in European and Central Asia urban areas.
Almeida, S M; Manousakas, M; Diapouli, E; Kertesz, Z; Samek, L; Hristova, E; Sega, K; Alvarez, R Padilla; Belis, C A; Eleftheriadis, K.
Affiliation
  • Almeida SM; Centro de Ciências e Tecnologias Nucleares, Instituto Superior Técnico, Universidade de Lisboa, Estrada Nacional 10, 2695-066, Bobadela-LRS, Portugal. Electronic address: smarta@ctn.tecnico.ulisboa.pt.
  • Manousakas M; Environmental Radioactivity Laboratory, INRaSTES, National Centre for Scientific Research "Demokritos", Patriarhou Gregoriou E' and Neapoleos, Agia Paraskevi, 15341, Athens, Greece; Laboratory of Atmospheric Chemistry, Paul Scherrer Institute (PSI), 5232, Villigen-PSI, Switzerland.
  • Diapouli E; Environmental Radioactivity Laboratory, INRaSTES, National Centre for Scientific Research "Demokritos", Patriarhou Gregoriou E' and Neapoleos, Agia Paraskevi, 15341, Athens, Greece.
  • Kertesz Z; ICER Centre, Institute for Nuclear Research, Bem ter 18C, 4026, Debrecen, Hungary.
  • Samek L; AGH University of Science and Technology, Faculty of Physics and Applied Computer Science, ul. Mickiewicza 30, 30-059, Krakow, Poland.
  • Hristova E; National Institute of Meteorology and Hydrology Bulgarian Academy of Sciences, 66 Tzarigradko Chaussee, 1784, Sofia, Bulgaria.
  • Sega K; Environmental Hygiene Unit, Institute for Medical Research and Occupational Health (IMROH), Ksaverska cesta 2, P.O. Box 291, 10001, Zagreb, Croatia.
  • Alvarez RP; International Atomic Energy Agency, Department of Nuclear Sciences and Applications, Division of Physical and Chemical Sciences, Physics Section, Nuclear Science and Instrumentation Laboratory, Vienna International Centre, Wagramer strasse 5, P.O. Box 100, 1400, Vienna, Austria.
  • Belis CA; European Commission, Joint Research Centre, Directorate Energy, Transport and Climate, Via Enrico Fermi 2749, Ispra (VA), 21027, Italy.
  • Eleftheriadis K; Environmental Radioactivity Laboratory, INRaSTES, National Centre for Scientific Research "Demokritos", Patriarhou Gregoriou E' and Neapoleos, Agia Paraskevi, 15341, Athens, Greece.
Environ Pollut ; 266(Pt 3): 115199, 2020 Nov.
Article in En | MEDLINE | ID: mdl-32777678
ABSTRACT
This work presents the results of a PM2.5 source apportionment study conducted in urban background sites from 16 European and Asian countries. For some Eastern Europe and Central Asia cities this was the first time that quantitative information on pollution source contributions to ambient particulate matter (PM) has been performed. More than 2200 filters were sampled and analyzed by X-Ray Fluorescence (XRF), Particle-Induced X-Ray Emission (PIXE), and Inductively Coupled Plasma Mass Spectrometry (ICP-MS) to measure the concentrations of chemical elements in fine particles. Samples were also analyzed for the contents of black carbon, elemental carbon, organic carbon, and water-soluble ions. The Positive Matrix Factorization receptor model (EPA PMF 5.0) was used to characterize similarities and heterogeneities in PM2.5 sources and respective contributions in the cities that the number of collected samples exceeded 75. At the end source apportionment was performed in 11 out of the 16 participating cities. Nine major sources were identified to have contributed to PM2.5 biomass burning, secondary sulfates, traffic, fuel oil combustion, industry, coal combustion, soil, salt and "other sources". From the averages of sources contributions, considering 11 cities 16% of PM2.5 was attributed to biomass burning, 15% to secondary sulfates, 13% to traffic, 12% to soil, 8.0% to fuel oil combustion, 5.5% to coal combustion, 1.9% to salt, 0.8% to industry emissions, 5.1% to "other sources" and 23% to unaccounted mass. Characteristic seasonal patterns were identified for each PM2.5 source. Biomass burning in all cities, coal combustion in Krakow/POL, and oil combustion in Belgrade/SRB and Banja Luka/BIH increased in Winter due to the impact of domestic heating, whereas in most cities secondary sulfates reached higher levels in Summer as a consequence of the enhanced photochemical activity. During high pollution days the largest sources of fine particles were biomass burning, traffic and secondary sulfates.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Air Pollutants / Particulate Matter Type of study: Prognostic_studies Country/Region as subject: Asia / Europa Language: En Journal: Environ Pollut Journal subject: SAUDE AMBIENTAL Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Air Pollutants / Particulate Matter Type of study: Prognostic_studies Country/Region as subject: Asia / Europa Language: En Journal: Environ Pollut Journal subject: SAUDE AMBIENTAL Year: 2020 Document type: Article