Chemical composition and mixing-state of ice residuals sampled within mixed phase clouds

dc.bibliographicCitation.firstPage2805eng
dc.bibliographicCitation.issue6eng
dc.bibliographicCitation.lastPage2816eng
dc.bibliographicCitation.volume11
dc.contributor.authorEbert, M.
dc.contributor.authorWorringen, A.
dc.contributor.authorBenker, N.
dc.contributor.authorMertes, S.
dc.contributor.authorWeingartner, E.
dc.contributor.authorWeinbruch, S.
dc.date.accessioned2017-11-16T00:52:13Z
dc.date.available2019-06-26T17:18:06Z
dc.date.issued2011
dc.description.abstractDuring an intensive campaign at the high alpine research station Jungfraujoch, Switzerland, in February/March 2006 ice particle residuals within mixed-phase clouds were sampled using the Ice-counterflow virtual impactor (Ice-CVI). Size, morphology, chemical composition, mineralogy and mixing state of the ice residual and the interstitial (i.e., non-activated) aerosol particles were analyzed by scanning and transmission electron microscopy. Ice nuclei (IN) were identified from the significant enrichment of particle groups in the ice residual (IR) samples relative to the interstitial aerosol. In terms of number lead-bearing particles are enriched by a factor of approximately 25, complex internal mixtures with silicates or metal oxides as major components by a factor of 11, and mixtures of secondary aerosol and carbonaceous material (C-O-S particles) by a factor of 2. Other particle groups (sulfates, sea salt, Ca-rich particles, external silicates) observed in the ice-residual samples cannot be assigned unambiguously as IN. Between 9 and 24% of all IR are Pb-bearing particles. Pb was found as major component in around 10% of these particles (PbO, PbCl2). In the other particles, Pb was found as some 100 nm sized agglomerates consisting of 3–8 nm sized primary particles (PbS, elemental Pb). C-O-S particles are present in the IR at an abundance of 17–27%. The soot component within these particles is strongly aged. Complex internal mixtures occur in the IR at an abundance of 9–15%. Most IN identified at the Jungfraujoch station are internal mixtures containing anthropogenic components (either as main or minor constituent), and it is concluded that admixture of the anthropogenic component is responsible for the increased IN efficiency within mixed phase clouds. The mixing state appears to be a key parameter for the ice nucleation behaviour that cannot be predicted from the sole knowledge of the main component of an individual particle.eng
dc.description.versionpublishedVersioneng
dc.formatapplication/pdf
dc.identifier.urihttps://doi.org/10.34657/832
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/516
dc.language.isoengeng
dc.publisherMünchen : European Geopyhsical Unioneng
dc.relation.doihttps://doi.org/10.5194/acp-11-2805-2011
dc.relation.ispartofseriesAtmospheric Chemistry and Physics, Volume 11, Issue 6, Page 2805-2816eng
dc.rights.licenseCC BY 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/eng
dc.subjectaerosol compositioneng
dc.subjectchemical compositioneng
dc.subjectcloud condensation nucleuseng
dc.subjectcloud microphysicseng
dc.subjectenrichmenteng
dc.subjectmixingeng
dc.subjectparticle sizeeng
dc.subject.ddc550eng
dc.titleChemical composition and mixing-state of ice residuals sampled within mixed phase cloudseng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleAtmospheric Chemistry and Physicseng
tib.accessRightsopenAccesseng
wgl.contributorTROPOSeng
wgl.subjectGeowissenschafteneng
wgl.typeZeitschriftenartikeleng
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