Back to Search Start Over

Speciation of organic fractions does matter for aerosol source apportionment. Part 3: Combining off-line and on-line measurements

Authors :
Yunjiang Zhang
Nicolas Bonnaire
Olivier Favez
Uwayemi Sofowote
Eric Villenave
Philip K. Hopke
Valérie Gros
Alexandre Albinet
Emilie Perraudin
Deepchandra Srivastava
Jean-Eudes Petit
Institut National de l'Environnement Industriel et des Risques (INERIS)
Environnements et Paléoenvironnements OCéaniques (EPOC)
Observatoire aquitain des sciences de l'univers (OASU)
Université Sciences et Technologies - Bordeaux 1 (UB)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Sciences et Technologies - Bordeaux 1 (UB)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-École Pratique des Hautes Études (EPHE)
Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)
Laboratoire des Sciences du Climat et de l'Environnement [Gif-sur-Yvette] (LSCE)
Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)
Ontario Ministry of the Environment and Climate Change
Center for Air Resources Engineering and Science, Clarkson University, Potsdam, NY, USA
Department of Public Health Sciences, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA
European Project: 654109,H2020,H2020-INFRAIA-2014-2015,ACTRIS-2(2015)
UMR 5805 Environnements et Paléoenvironnements Océaniques et Continentaux (EPOC)
Université Sciences et Technologies - Bordeaux 1-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Sciences et Technologies - Bordeaux 1-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-École pratique des hautes études (EPHE)
Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
Source :
Science of the Total Environment, Science of the Total Environment, 2019, 690, pp.944-955. ⟨10.1016/j.scitotenv.2019.06.378⟩, Science of the Total Environment, Elsevier, 2019, 690, pp.944-955. ⟨10.1016/j.scitotenv.2019.06.378⟩
Publication Year :
2019

Abstract

International audience; he present study proposes an advanced methodology to refine the source apportionment of organic aerosol (OA). This methodology is based on the combination of offline and online datasets in a single Positive Matrix Factorization (PMF) analysis using the multilinear engine (ME-2) algorithm and a customized time synchronization procedure. It has been applied to data from measurements conducted in the Paris region (France) during a PM pollution event in March 2015. Measurements included OA ACSM (Aerosol Chemical Speciation Monitor) mass spectra and specific primary and secondary organic molecular markers from PM10 filters on their original time resolution (30 min for ACSM and 4 h for PM10 filters). Comparison with the conventional PMF analysis of the ACSM OA dataset (PMF-ACSM) showed very good agreement for the discrimination between primary and secondary OA fractions with about 75% of the OA mass of secondary origin. Furthermore, the use of the combined datasets allowed the deconvolution of 3 primary OA (POA) factors and 7 secondary OA (SOA) factors. A clear identification of the source/origin of 54% of the total SOA mass could be achieved thanks to specific molecular markers. Specifically, 28% of that fraction was linked to combustion sources (biomass burning and traffic emissions). A clear identification of primary traffic OA was also obtained using the PMF-combined analysis while PMF-ACSM only gave a proxy for this OA source in the form of total hydrocarbon-like OA (HOA) mass concentrations. In addition, the primary biomass burning-related OA source was explained by two OA factors, BBOA and OPOA-like BBOA. This new approach has showed undeniable advantages over the conventional approaches by providing valuable insights into the processes involved in SOA formation and their sources. However, the origins of highly oxidized SOA could not be fully identified due to the lack of specific molecular markers for such aged SOA.

Details

ISSN :
18791026 and 00489697
Volume :
690
Database :
OpenAIRE
Journal :
The Science of the total environment
Accession number :
edsair.doi.dedup.....85738cd25d08aea6fc953dccf013c117