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Organics in the Mix during SAPUSS M. Dall´Osto and the SAPUSS team CSIC, Barcelona, Spain manuel.dallosto@gmail.com
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“How can Europe control the composition of its atmosphere under a changing climate?”
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SAPUSS aims to identify sources of particles in the atmosphere and to understand the physical and chemical transformations occurring in them once emitted.
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SAPUSS studies the urban Mediterranean environment
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(1)Simultaneous off-line filter measurements at 12 hours resolution, concentrations of 36 neutral and polar organic compounds were obtained by GC-MS, classified by MCR-ALS. (2)Simultaneous single particle mixing state measurements with Aerosol Time Of Flight Mass Spectrometry (ATOFMS), classified by ART-2a algoritm. (3)Simultaneous measurements with High Resolution Aerosol Mass Spectrometry (HR-ToF-AMS) were taken; classified by PMF. To get close to the full picture of the source identification of particles you need to synergistically deploy a number of aerosol techniques
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Part 1:PM 1 (12 hours)
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Part 1. Off line in a nutshell (Marta Alier, Barend Van Drooge, ACP 2013) Six OA identified at both sites: two primary OA, three of SOA origin (60%), one not clearly defined. (1)POA from emissions of local anthropogenic activities (43% RS, 18% UB). (2)Biomass burning (BBOA - 7% RS; 12% UB), regional air mass circulation. (3) Isoprene oxidation (about 10% both sites), influence of inland air masses. (4) A SOA biogenic component attributed to α-pinene oxidation (SOA BIO PIN) did not impact the two monitoring site at the same level (about double at UB). (5)Aged anthropogenic and biogenic SOA, stagnant atmospheric conditions (about 15% both sites). (6) Component formed by C7-C9 dicarboxylic acids, detected mainly only during daytime (23% RS vs. 10% at UB). Air mass dependent, showing an enhancement under sulphate-rich North African air masses and a reduction under nitrate-rich stagnant regional air masses.
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Anti correlation between SOA ISO and SOA PIN during nucleation days Growth of urban NPF events linked with biogenic α-pinene oxidation products but inhibited by isoprene organic compounds. (Marta Alier, Barend Van Drooge, ACP 2013)
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Part 2: ATOFMS: UB and RS Birmingham ATOFMS (RS). Hit 1,042,331 particles; classified 890,873 Cork ATOFMS (UB) Hit 274,974; classified 218,657 RS UB
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2. ATOFMS a nutshell -Ten different particle types were detected at both locations -Four were related to amines (primary and secondary origin). Aminium salts were found related to coarse sulphate rich particle types, (heterogeneous reaction mechanisms?). -Four organic rich particles showed a complex single particle mixing state relationship between organic carbon and nitrate. The atmosphere in the Mediterranean urban areas has large variability in OA-nitrate mixing state.
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Part 3: HR-ToF-AMS Does it compare well with PM 1 filters? Overall, yes. However, OA presents lowest correlations… Both AMS shows same trends at both RS and UB
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AMS organic factors: HOA, OOA, SV-OOA, COA (conservative)
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Trying to push AMS-PMF into more factors to justify more than HOA,SV-OOA,OOA,COA by comparing it with other techniques. Receptor modeling applied to all results will simplify the organic aerosol source apportionment during SAPUSS. QUESTION: “How can Europe control the composition of its atmosphere under a changing climate?”
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