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Phase II of poly(2, 6-oxynaphthoate)

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dc.title Phase II of poly(2, 6-oxynaphthoate) en
dc.contributor.author Kaszonyiová, Martina
dc.contributor.author Rybnikář, František
dc.contributor.author Geil, Phillip H.
dc.relation.ispartof Journal of Macromolecular Science, Part B: Physics
dc.identifier.issn 0022-2348 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2012
utb.relation.volume 51
utb.relation.issue 4
dc.citation.spage 685
dc.citation.epage 697
dc.type article
dc.language.iso en
dc.identifier.doi 10.1080/00222348.2011.609791
dc.relation.uri http://www.tandfonline.com/doi/abs/10.1080/00222348.2011.609791
dc.subject DSC-melting en
dc.subject poly(2,6-oxynaphthoate) preparation en
dc.subject polymorphism en
dc.subject X-ray structure en
dc.description.abstract The bulk melt polycondensation of 2, 6-acetoxynaphthoic acid [poly (2, 6-oxynaphthoate) (P-ON)] at temperatures below 250C made it possible to prepare P-ON samples with phase II content approaching 100%. The structure, morphology, and melting behavior of P-ON phase II are described and compared with a similar liquid crystal polyester, poly (p-oxybenzoate). © 2012 Copyright Taylor and Francis Group, LLC. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1002847
utb.identifier.rivid RIV/70883521:28110/12:43868106!RIV13-MSM-28110___
utb.identifier.obdid 43868197
utb.identifier.scopus 2-s2.0-84861980118
utb.identifier.wok 000304422900008
utb.identifier.coden JMAPB
utb.source j-scopus
dc.date.accessioned 2012-06-25T14:29:02Z
dc.date.available 2012-06-25T14:29:02Z
utb.contributor.internalauthor Kaszonyiová, Martina
utb.contributor.internalauthor Rybnikář, František
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