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Chemical characterization of submicron regional background aerosols in the western Mediterranean using an Aerosol Chemical Speciation Monitor
oleh: M. C. Minguillón, A. Ripoll, N. Pérez, A. S. H. Prévôt, F. Canonaco, X. Querol, A. Alastuey
| Format: | Article |
|---|---|
| Diterbitkan: | Copernicus Publications 2015-06-01 |
Deskripsi
An Aerosol Chemical Speciation Monitor (ACSM, Aerodyne Research Inc.) was deployed at the Montseny (MSY; 41° 46'46" N, 02° 21'29" E, 720 m a.s.l.) regional background site in the western Mediterranean, Spain, from June 2012 to July 2013 to measure real-time inorganic (nitrate, sulfate, ammonium and chloride) and organic submicron aerosol concentrations. Co-located measurements, including real-time submicron particulate matter (PM<sub>1</sub>) and black carbon (BC) concentrations, and off-line PM<sub>1</sub> chemical analysis were also carried out. This is one of the few studies that compare ACSM data with off-line PM<sub>1</sub> measurements, avoiding the tail of the coarse mode included in the PM<sub>2.5</sub> fraction. The ACSM + BC concentrations agreed with the PM<sub>1</sub> measurements, and a strong correlation was found between the concentrations of ACSM species and the off-line measurements, although some discrepancies remain unexplained. Results point to a current underestimation of the relative ionization efficiency (RIE) established for organic aerosol (OA), which should be revised in the future. The OA was the major component of submicron aerosol (53% of PM<sub>1</sub>), with a higher contribution in summer (58% of PM<sub>1</sub>) than in winter (45% of PM<sub>1</sub>). Source apportionment of OA was carried out by applying positive matrix factorization (PMF), using the multilinear engine (ME-2) to the organic mass spectral data matrix. Three sources were identified in summer: hydrocarbon-like OA (HOA), low-volatile oxygenated OA (LV-OOA), and semi-volatile oxygenated OA (SV-OOA). The secondary OA (SOA; 4.8 μg m<sup>−3</sup>, sum of LV-OOA and SV-OOA) accounted for 85% of the total OA, and its formation during daytime (mainly SV-OOA) was estimated to be 1.1 μg m<sup>−3</sup>. In winter, HOA was also identified (12% of OA), a contribution from biomass burning OA (BBOA) was included and it was not possible to differentiate between two different SOA factors, but a single oxygenated OA (OOA) factor was resolved. The OOA contribution represented 60% of the total OA, with a degree of oxidation higher than both OOA summer factors. An intense wildfire episode was studied, obtaining a region-specific BBOA profile.