Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/6975
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dc.contributorDepartment of Civil and Environmental Engineering-
dc.creatorRodríguez, S-
dc.creatorDingenen, RV-
dc.creatorPutaud, JP-
dc.creatorDell'Acqua, A-
dc.creatorPey, J-
dc.creatorQuerol, X-
dc.creatorAlastuey, A-
dc.creatorChenery, S-
dc.creatorHo, KF-
dc.creatorHarrison, R-
dc.creatorTardivo, R-
dc.creatorScarnato, B-
dc.creatorGemelli, V-
dc.date.accessioned2014-12-11T08:29:16Z-
dc.date.available2014-12-11T08:29:16Z-
dc.identifier.issn1680-7316-
dc.identifier.urihttp://hdl.handle.net/10397/6975-
dc.language.isoenen_US
dc.publisherCopernicus GmbHen_US
dc.rights© Author(s) 2007. This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 2.5 License.en_US
dc.subjectAerosol compositionen_US
dc.subjectAmmonium nitrateen_US
dc.subjectAtmospheric pollutionen_US
dc.subjectBlack carbonen_US
dc.subjectCondensationen_US
dc.subjectParticle sizeen_US
dc.subjectParticulate organic matteren_US
dc.subjectPhysicochemical propertyen_US
dc.subjectSize distributionen_US
dc.subjectTraffic emissionen_US
dc.subjectUrban atmosphereen_US
dc.titleA study on the relationship between mass concentrations, chemistry and number size distribution of urban fine aerosols in Milan, Barcelona and Londonen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage2217-
dc.identifier.epage2232-
dc.identifier.volume7-
dc.identifier.issue9-
dc.identifier.doi10.5194/acp-7-2217-2007-
dcterms.abstractA physicochemical characterization, including aerosol number size distribution, chemical composition and mass concentrations, of the urban fine aerosol captured in MILAN, BARCELONA and LONDON is presented in this article. The objective is to obtain a comprehensive picture of the microphysical processes involved in aerosol dynamics during the: 1) regular evolution of the urban aerosol (daily, weekly and seasonal basis) and in the day-to-day variations (from clean-air to pollution-events), and 2) the link between "aerosol chemistry and mass concentrations" with the "number size distribution".-
dcterms.abstractThe mass concentrations of the fine PM₂.₅ aerosol exhibit a high correlation with the number concentration of >100 nm particles N>100 (nm) ("accumulation mode particles") which only account for <20% of the total number concentration N of fine aerosols; but do not correlate with the number of <100 nm particles ("ultrafine particles"), which accounts for >80% of fine particles number concentration. Organic matter and black-carbon are the only aerosol components showing a significant correlation with the ultrafine particles, attributed to vehicles exhausts emissions; whereas ammonium-nitrate, ammonium-sulphate and also organic matter and black-carbon correlate with N>100 (nm) and attributed to condensation mechanisms, other particle growth processes and some primary emissions. Time series of the aerosol DpN diameter (dN/dlogD mode), mass PM₂.₅ concentrations and number N>100 (nm) concentrations exhibit correlated day-to-day variations, which point to a significant involvement of condensation of semi-volatile compounds during urban pollution events. This agrees with the observation that ammonium-nitrate is the component exhibiting the highest increases from mid-to-high pollution episodes, when the highest DpN increases are observed. The results indicates that "fine PM₂.₅ particles urban pollution events" tend to occur when condensation processes have made particles grow large enough to produce significant number concentrations of N>100 (nm) ("accumulation mode particles"). In contrast, because the low contribution of ultrafine particles to the fine aerosol mass concentrations, high "ultrafine particles N<100(nm) events" frequently occurs under low PM₂.₅ conditions. The results of this study demonstrate that vehicles exhausts emissions are strongly involved in this ultrafine particles aerosol pollution.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationAtmospheric chemistry and physics, 3 May 2007, v. 7, no. 9, p. 2217-2232-
dcterms.isPartOfAtmospheric chemistry and physics-
dcterms.issued2007-05-03-
dc.identifier.isiWOS:000246456100006-
dc.identifier.scopus2-s2.0-34248171927-
dc.identifier.eissn1680-7324-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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