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dc.contributor
dc.contributor.author
Mahrt, Fabian
dc.contributor.author
Alpert, Peter A.
dc.contributor.author
Dou, Jing
dc.contributor.author
Grönquist, Philippe
dc.contributor.author
Corral Arroyo, Pablo
dc.contributor.author
Ammann, Markus
dc.contributor.author
Lohmann, Ulrike
dc.contributor.author
Kanji, Zamin A
dc.date.accessioned
2020-05-18T11:37:05Z
dc.date.available
2020-05-15T08:02:32Z
dc.date.available
2020-05-18T11:37:05Z
dc.date.issued
2020-04-01
dc.identifier.issn
2050-7887
dc.identifier.issn
2050-7895
dc.identifier.other
10.1039/c9em00525k
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/415007
dc.identifier.doi
10.3929/ethz-b-000415007
dc.description.abstract
Fresh soot particles are generally hydrophobic, however, particle hydrophilicity can be increased through atmospheric aging processes. At present little is known on how particle chemical composition and hydrophilicity change upon atmospheric aging and associated uncertainties governing the ice cloud formation potential of soot. Here we sampled two propane flame soots referred to as brown and black soot, characterized as organic carbon rich and poor, respectively. We investigated how the ice nucleation activity of these particles changed through aging in water and aqueous acidic solutions, using a continuous flow diffusion chamber operated at cirrus cloud temperatures (T ≤ 233 K). Single aggregates of both unaged and aged soot were chemically characterized by scanning transmission X-ray microscopy and near edge X-ray absorption fine structure (STXM/NEXAFS) measurements. Particle wettability was determined through water sorption measurements. Unaged black and brown soot particles exhibited significantly different ice nucleation activities. Our experiments revealed significantly enhanced ice nucleation activity of the aged soot particles compared to the fresh samples, lowering the required relative humidities at which ice formation can take place at T = 218 K by up to 15% with respect to water (ΔRHi ≈ 25%). We observed an enhanced water uptake capacity for the aged compared to the unaged samples, which was more pronounced for the black soot. From these measurements we concluded that there is a change in ice nucleation mechanism when aging brown soot. Comparison of the NEXAFS spectra of unaged soot samples revealed a unique spectral feature around 287.5 eV in the case of black soot that was absent for the brown soot, indicative of carbon with hydroxyl functionalities. Comparison of the NEXAFS spectra of unaged and aged soot particles indicates changes in organic functional groups, and the aged spectra were found to be largely similar across soot types, with the exception of the water aged brown soot. Overall, we conclude that atmospheric aging is important to representatively assess the ice cloud formation activity of soot particles.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Royal Society of Chemistry
en_US
dc.rights.uri
http://creativecommons.org/licenses/by-nc/3.0/
dc.title
Aging induced changes in ice nucleation activity of combustion aerosol as determined by near edge X-ray absorption fine structure (NEXAFS) spectroscopy
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution-NonCommercial 3.0 Unported
dc.date.published
2020-03-18
ethz.journal.title
Environmental Science: Processes & Impacts
ethz.journal.volume
22
en_US
ethz.journal.issue
4
en_US
ethz.journal.abbreviated
Environ Sci Process Impacts
ethz.pages.start
895
en_US
ethz.pages.end
907
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
Cambridge
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02350 - Dep. Umweltsystemwissenschaften / Dep. of Environmental Systems Science::02717 - Institut für Atmosphäre und Klima / Inst. Atmospheric and Climate Science::03690 - Lohmann, Ulrike / Lohmann, Ulrike
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02350 - Dep. Umweltsystemwissenschaften / Dep. of Environmental Systems Science::02717 - Institut für Atmosphäre und Klima / Inst. Atmospheric and Climate Science::03690 - Lohmann, Ulrike / Lohmann, Ulrike
ethz.date.deposited
2020-05-15T08:02:48Z
ethz.source
SCOPUS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2020-05-18T11:37:14Z
ethz.rosetta.lastUpdated
2024-02-02T10:54:30Z
ethz.rosetta.versionExported
true
ethz.COinS
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