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dc.contributor.authorPhillips, Gavin J.*
dc.contributor.authorThieser, Jim*
dc.contributor.authorTang, Mingjin*
dc.contributor.authorSobanski, Nicolas*
dc.contributor.authorFachinger, Johannes*
dc.contributor.authorDrewnick, Frank*
dc.contributor.authorLelieveld, Jos*
dc.contributor.authorCrowley, John N.*
dc.date.accessioned2015-03-02T13:02:49Z
dc.date.available2015-03-02T13:02:49Z
dc.date.issued2015-02-25
dc.identifier.citationPhillips et al. (2015). Geophysical Research Abstracts, 2015, 17, EGU2015-10435.en
dc.identifier.urihttp://hdl.handle.net/10034/345822
dc.descriptionOral presentation abstract given at EGU General Assembly 2015.en
dc.description.abstractWe present estimates of the uptake coefficient of N2O5 using ambient measurements of the trace gases N2O5 and ClNO2 and particle composition and surface area at the Kleiner Feldberg observatory, near Frankfurt, SW Germany, during the PARADE campaign (summer 2011). Three methods used to extract gamma(N2O5) from the datasets were found to be in reasonable agreement, generating values between 0.001 and 0.4. Gamma (N2O5) displayed a significant dependence on relative humidity (RH), the largest values obtained, as expected, at high RH. No significant dependence of gamma(N2O5) on particle organic content or sulphate-to-organic ratio was observed. The variability in gamma(N2O5) is however large, indicating that humidity is not the sole factor determining the uptake coefficient. There is also an indication that the yield of ClNO2 with respect to N2O5 uptake is larger with lower concentrations of PM1 total organics. Our results will be compared to existing uptake coefficients from laboratory studies and those derived from field observations.
dc.description.sponsorshipMax Planck Societyen
dc.language.isoenen
dc.publisherCopernicus Publicationsen
dc.relation.urlhttps://www.geophysical-research-abstracts.net/egu2015.htmlen
dc.relation.urlhttp://meetingorganizer.copernicus.org/EGU2015/EGU2015-10435.pdfen
dc.subjectatmospheric chemistryen
dc.subjectreactive nitrogenen
dc.subjectair pollutionen
dc.titleClNO2 and nitrate formation via N2O5 uptake to particles: Derivation of N2O5 uptake coefficients from ambient datasetsen
dc.typeConference Contributionen
dc.identifier.eissn1607-7962
dc.contributor.departmentMax Planck Institute for Chemistry; University of Chesteren
dc.identifier.journalGeophysical Research Abstracts
html.description.abstractWe present estimates of the uptake coefficient of N2O5 using ambient measurements of the trace gases N2O5 and ClNO2 and particle composition and surface area at the Kleiner Feldberg observatory, near Frankfurt, SW Germany, during the PARADE campaign (summer 2011). Three methods used to extract gamma(N2O5) from the datasets were found to be in reasonable agreement, generating values between 0.001 and 0.4. Gamma (N2O5) displayed a significant dependence on relative humidity (RH), the largest values obtained, as expected, at high RH. No significant dependence of gamma(N2O5) on particle organic content or sulphate-to-organic ratio was observed. The variability in gamma(N2O5) is however large, indicating that humidity is not the sole factor determining the uptake coefficient. There is also an indication that the yield of ClNO2 with respect to N2O5 uptake is larger with lower concentrations of PM1 total organics. Our results will be compared to existing uptake coefficients from laboratory studies and those derived from field observations.
rioxxterms.publicationdate2015-02-25
dc.date.deposited2015-03-02


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