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dc.contributor.authorKarl, Matthias
dc.contributor.authorGross, A.
dc.contributor.authorPirjola, L.
dc.contributor.authorLeck, C.
dc.date.accessioned2020-04-14T13:10:42Z
dc.date.available2020-04-14T13:10:42Z
dc.date.created2011-12-29T20:07:31Z
dc.date.issued2011
dc.identifier.citationTellus. Series B, Chemical and physical meteorology. 2011, 63 (5), 1001-1025.en_US
dc.identifier.issn0280-6509
dc.identifier.urihttps://hdl.handle.net/11250/2651030
dc.description.abstractA new sectional aerosol dynamics model, MAFOR, was developed with the focus to study nucleation in the marine boundary layer. Novel aspects of the model are (1) flexibility in the treatment of gas phase chemistry, (2) treatment of liquid phase chemistry, which can be extended according to needs and (3) simultaneous calculation of number and mass concentration distributions of a multicomponent aerosol as functions of time. Comparison with well-documented aerosol models (MONO32 and AEROFOR), a comprehensive data set on gas phase compounds, aerosol size distribution and chemical composition obtained during theA OE-96 (Arctic Ocean Expedition, 1996)was used to evaluate the model. Dimethyl sulphide decay during advection of an air parcel over the Arctic pack ice was well captured by the applied models and predicted concentrations of gaseous sulphuric acid and methane sulphonic acid range up to 1.0 × 106 cm−3 and 1.8 × 106 cm−3, respectively. Different nucleation schemes were implemented in MAFOR which allow the simulation of new particle formation. Modelled nucleation rates from sulphuric acid nucleation via cluster activation were up to 0.21 cm−3 s−1 while those from ion-mediated nucleationwere below 10−2 cm−3 s−1. Classical homogeneous binary and ternary nucleation theories failed to predict nucleation over the central Arctic Ocean in summer.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleA new flexible multicomponent model for the study of aerosol dynamics in the marine boundary layeren_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2011 John Wiley & Sonsen_US
dc.source.pagenumber1001-1025en_US
dc.source.volume63en_US
dc.source.journalTellus. Series B, Chemical and physical meteorologyen_US
dc.source.issue5en_US
dc.identifier.doi10.1111/j.1600-0889.2011.00562.x
dc.identifier.cristin873761
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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