dc.contributor.author
Khawaja, Nozair
dc.contributor.author
Hillier, Jon
dc.contributor.author
Klenner, Fabian
dc.contributor.author
Nölle, Lenz
dc.contributor.author
Zou, Zenghui
dc.contributor.author
Napoleoni, Maryse
dc.contributor.author
Reviol, Rene
dc.contributor.author
Postberg, Frank
dc.date.accessioned
2022-11-22T14:22:07Z
dc.date.available
2022-11-22T14:22:07Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/36985
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-36698
dc.description.abstract
Mass spectrometers on board spacecraft typically use either impact ionization or electron ionization (EI) as ion sources. Understanding the similarities and differences in the spectral signatures and fragmentation patterns produced by different techniques in mass spectrometry could elucidate the composition of organic compounds. Here we present a comparison between the mass spectra obtained through laser-induced liquid beam ion desorption (LILBID; proven to simulate the impact ionization mass spectra of ice grains) and EI mass spectra of pairs of low-mass, isomeric aldehydes and ketones. Our comparison confirms that EI produces more fragmentation of carbonyl compounds, particularly aldehydes, than LILBID. We find protonated molecular ions [M+H]+ in LILBID but molecular ions [M]+ in EI spectra. From the evaluated species, LILBID generally produces oxygen-carrying fragment ions (e.g., [CHO]+ and [C2H3O]+) in the mass ranges 26–30 and 39–44 u, while in EI, most ions in these ranges correspond to hydrocarbon fragments. The LILBID spectra additionally show mostly protonated oxygen-bearing fragments [CH3O]+ and [C2H5O]+ at m/z 31 and 45, less commonly observed in EI spectra. We observe a decrease in the relative intensities of cation fragment mass lines between m/z 26 and 33 and an increase between m/z 39 and 45, with an increasing carbon number for ketones and aldehydes with LILBID and EI, respectively. Our study provides a basis for complementary compositional analysis to identify the structural properties of organic species in a space environment using different spaceborne mass spectrometers (e.g., SUrface Dust Analyzer and MAss Spectrometer for Planetary EXploration) on board NASA’s future Europa Clipper space mission.
en
dc.format.extent
24 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
mass spectrometers
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::520 Astronomie::520 Astronomie und zugeordnete Wissenschaften
dc.title
Complementary Mass Spectral Analysis of Isomeric O-bearing Organic Compounds and Fragmentation Differences through Analog Techniques for Spaceborne Mass Spectrometers
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.3847/PSJ/ac97ed
dcterms.bibliographicCitation.journaltitle
The Planetary Science Journal
dcterms.bibliographicCitation.number
11
dcterms.bibliographicCitation.originalpublishername
The American Astronomical Society
dcterms.bibliographicCitation.volume
3
dcterms.bibliographicCitation.url
https://doi.org/10.3847/PSJ/ac97ed
refubium.affiliation
Geowissenschaften
refubium.affiliation.other
Institut für Geologische Wissenschaften / Fachrichtung Planetologie und Fernerkundung

refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
2632-3338
refubium.resourceType.provider
DeepGreen