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Effect of high electric fields on the isotropic phase of a lyotropic liquid-crystalline system

dc.contributor.authorMenna, Todd J.en_US
dc.contributor.authorFilisko, Frank E.en_US
dc.date.accessioned2006-04-19T14:04:04Z
dc.date.available2006-04-19T14:04:04Z
dc.date.issued2004-11-15en_US
dc.identifier.citationMenna, T. J.; Filisko, F. E. (2004)."Effect of high electric fields on the isotropic phase of a lyotropic liquid-crystalline system." Journal of Polymer Science Part B: Polymer Physics 42(22): 4116-4125. <http://hdl.handle.net/2027.42/35008>en_US
dc.identifier.issn0887-6266en_US
dc.identifier.issn1099-0488en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/35008
dc.description.abstractThe effect of high (>1000 V/mm) electric fields on solutions of a lyotropic liquid-crystalline polymer, poly( n -hexyl isocyanate) in p-xylene, is presented. The concentrations are adjusted such that the solutions are strictly within the isotropic phase domain region, thus exhibiting no spontaneous liquid crystallinity. The effects of field strength, frequency, and concentration are varied and the morphological changes are noted. The results are analyzed with birefringence measurements via comparison with the optical Kerr effect. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 4116–4125, 2004en_US
dc.format.extent184408 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherChemistryen_US
dc.subject.otherPolymer and Materials Scienceen_US
dc.titleEffect of high electric fields on the isotropic phase of a lyotropic liquid-crystalline systemen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan, Materials Science and Engineering, Ann Arbor, Michigan 48109 ; University of Michigan, Materials Science and Engineering, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumUniversity of Michigan, Materials Science and Engineering, Ann Arbor, Michigan 48109en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/35008/1/20219_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/polb.20219en_US
dc.identifier.sourceJournal of Polymer Science Part B: Polymer Physicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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