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Selective resonance enhanced multiphoton ionization of aromatic polymers in supersonic beam mass spectrometry

dc.contributor.authorLustig, David A.en_US
dc.contributor.authorLubman, David M.en_US
dc.date.accessioned2006-04-10T14:39:07Z
dc.date.available2006-04-10T14:39:07Z
dc.date.issued1991-07-15en_US
dc.identifier.citationLustig, David A., Lubman, David M. (1991/07/15)."Selective resonance enhanced multiphoton ionization of aromatic polymers in supersonic beam mass spectrometry." International Journal of Mass Spectrometry and Ion Processes 107(2): 265-280. <http://hdl.handle.net/2027.42/29225>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TG6-44W57N4-94/2/e6d2e25a76bf62737d6cf66b0cfe3317en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29225
dc.description.abstractVarious polymers have been studied using a pulsed laser evaporation method for volatilizing these species and entraining them into a supersonic jet expansion followed by resonance enhanced multiphoton ionization (REMPI) detection in a reflection time-of-flight mass spectrometer. In most cases the monomer is detected as the dominant ion, although sometimes smaller characteristic fragments are observed instead. Fragmentation of the monomer can also be produced for structural analysis. However, larger oligomers are rarely observed with any intensity unless the average molecular weight distribution is less than 1000. In addition, REMPI at 266 nm is shown to be a means of selectivity detecting absorbing aromatic polymers in polymer blends without interference from aliphatic or non-aromatic polymers. Among the polymers studied are polystyrene, EPON epoxy resins and various polyamides.en_US
dc.format.extent924932 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleSelective resonance enhanced multiphoton ionization of aromatic polymers in supersonic beam mass spectrometryen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, 930 N. University Ave., Ann Arbor, MI 48109 USAen_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, 930 N. University Ave., Ann Arbor, MI 48109 USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29225/1/0000280.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0168-1176(91)80063-Sen_US
dc.identifier.sourceInternational Journal of Mass Spectrometry and Ion Processesen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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