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dc.contributor.authorDuarte, R.M.B.O.
dc.contributor.authorMatos, J.T.V.
dc.contributor.authorPaula, A.S.
dc.contributor.authorLopes, S.P.
dc.contributor.authorPereira, G.
dc.contributor.authorVasconcellos, P.
dc.contributor.authorGioda, A.
dc.contributor.authorCarreira, R.
dc.contributor.authorSilva, A.M.S
dc.contributor.authorDuarte, A.C.
dc.contributor.authorSmichowski, P.
dc.contributor.authorRojas, N.
dc.contributor.authorSánchez Ccoyllo, Odón
dc.date.accessioned2020-03-21T01:38:22Z
dc.date.available2020-03-21T01:38:22Z
dc.date.issued2017-08
dc.identifier.urihttps://hdl.handle.net/20.500.12542/290
dc.description.abstractThis study describes and compares the key structural units present in water-soluble organic carbon (WSOC) fraction of atmospheric aerosols collected in different South American (Colombia – Medellín and Bogotá, Peru – Lima, Argentina – Buenos Aires, and Brazil – Rio de Janeiro, São Paulo, and Porto Velho, during moderate (MBB) and intense (IBB) biomass burning) and Western European (Portugal – Aveiro and Lisbon) locations. Proton nuclear magnetic resonance (1H NMR) spectroscopy was employed to assess the relative distribution of non-exchangeable proton functional groups in aerosol WSOC of diverse origin, for the first time to the authors’ knowledge in South America. The relative contribution of the proton functional groups was in the order H-C > H–C–C= > H-C-O > Ar-H, except in Porto Velho during MBB, Medellín, Bogotá, and Buenos Aires, for which the relative contribution of H-C-O was higher than that of H-C-C=. The 1H NMR source attribution confirmed differences in aging processes or regional sources between the two geographic regions, allowing the differentiation between urban combustion-related aerosol and biological particles. The aerosol WSOC in Aveiro, Lisbon, and Rio de Janeiro during summer are more oxidized than those from the remaining locations, indicating the predominance of secondary organic aerosols. Fresh emissions, namely of smoke particles, becomes important during winter in Aveiro and São Paulo, and in Porto Velho during IBB. The biosphere is an important source altering the chemical composition of aerosol WSOC in South America locations. The source attribution in Medellín, Bogotá, Buenos Aires, and Lima confirmed the mixed contributions of biological material, secondary formation, as well as urban and biomass burning emissions. Overall, the information and knowledge acquired in this study provide important diagnostic tools for future studies aiming at understanding the water-soluble organic aerosol problem, their sources and impact at a wider geographic scale.en_US
dc.language.isoengen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofurn:issn:1873-6424
dc.relation.urihttps://www.sciencedirect.com/science/article/abs/pii/S0269749116320942
dc.rightsinfo:eu-repo/semantics/closedAccess*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourceRepositorio Institucional - SENAMHIen_US
dc.sourceServicio Nacional de Meteorología e Hidrología del Perúen_US
dc.subjectMedio Ambienteen_US
dc.subjectBiomasaen_US
dc.subjectCarbónen_US
dc.subjectCombustibleen_US
dc.subjectCompuesto Orgánicoen_US
dc.titleStructural signatures of water-soluble organic aerosols in contrasting environments in South America and Western Europeen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.identifier.isni0000 0001 0746 0446
dc.description.peerreviewPor pares
dc.identifier.doihttps://doi.org/10.1016/j.envpol.2017.05.011
dc.identifier.journalEnvironmental Pollution
dc.source.volume227
dc.source.initialpage513
dc.source.endpage525
dc.subject.ocdeContaminación Atmosférica
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#1.05.08


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