Relating hygroscopicity and optical properties to chemical composition and structure of secondary organic aerosol particles generated from the ozonolysis of α-pinene

dc.bibliographicCitation.firstPage3339eng
dc.bibliographicCitation.issue6eng
dc.bibliographicCitation.lastPage3358eng
dc.bibliographicCitation.volume15
dc.contributor.authorDenjean, C.
dc.contributor.authorFormenti, P.
dc.contributor.authorPicquet-Varrault, B.
dc.contributor.authorPangui, E.
dc.contributor.authorZapf, P.
dc.contributor.authorKatrib, Y.
dc.contributor.authorGiorio, C.
dc.contributor.authorTapparo, A.
dc.contributor.authorMonod, A.
dc.contributor.authorTemime-Roussel, B.
dc.contributor.authorDecorse, P.
dc.contributor.authorMangeney, C.
dc.contributor.authorDoussin, J.F.
dc.date.accessioned2017-09-21T09:55:28Z
dc.date.available2019-06-26T17:17:14Z
dc.date.issued2015
dc.description.abstractSecondary organic aerosol (SOA) were generated from the ozonolysis of α-pinene in the CESAM (French acronym for Experimental Multiphasic Atmospheric Simulation Chamber) simulation chamber. The SOA formation and aging were studied by following their optical, hygroscopic and chemical properties. The optical properties were investigated by determining the particle complex refractive index (CRI). The hygroscopicity was quantified by measuring the effect of relative humidity (RH) on the particle size (size growth factor, GF) and on the scattering coefficient (scattering growth factor, f(RH)). The oxygen to carbon atomic ratios (O : C) of the particle surface and bulk were used as a sensitive parameter to correlate the changes in hygroscopic and optical properties of the SOA composition during their formation and aging in CESAM. The real CRI at 525 nm wavelength decreased from 1.43–1.60 (±0.02) to 1.32–1.38 (±0.02) during the SOA formation. The decrease in the real CRI correlated to the O : C decrease from 0.68 (±0.20) to 0.55 (±0.16). In contrast, the GF remained roughly constant over the reaction time, with values of 1.02–1.07 (±0.02) at 90% (±4.2%) RH. Simultaneous measurements of O : C of the particle surface revealed that the SOA was not composed of a homogeneous mixture, but contained less oxidised species at the surface which may limit water absorption. In addition, an apparent change in both mobility diameter and scattering coefficient with increasing RH from 0 to 30% was observed for SOA after 14 h of reaction. We postulate that this change could be due to a change in the viscosity of the SOA from a predominantly glassy state to a predominantly liquid state.
dc.description.versionpublishedVersioneng
dc.formatapplication/pdf
dc.identifier.urihttps://doi.org/10.34657/1218
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/337
dc.language.isoengeng
dc.publisherMünchen : European Geopyhsical Union
dc.relation.doihttps://doi.org/10.5194/acp-15-3339-2015
dc.relation.ispartofseriesAtmospheric Chemistry and Physics, Volume 15, Issue 6, Page 3339-3358eng
dc.rights.licenseCC BY 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/eng
dc.subjectaerosol formation
dc.subjectaerosol property
dc.subjectchemical composition
dc.subjecthygroscopicity
dc.subjectoptical property
dc.subjectorganic compound
dc.subjectparticle size
dc.subjectrefractive index
dc.subjectrelative humidity
dc.subject.ddc550
dc.titleRelating hygroscopicity and optical properties to chemical composition and structure of secondary organic aerosol particles generated from the ozonolysis of α-pinene
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleAtmospheric Chemistry and Physicseng
tib.accessRightsopenAccesseng
wgl.contributorTROPOSeng
wgl.subjectGeowissenschafteneng
wgl.typeZeitschriftenartikeleng
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