Phase II of poly(2, 6-oxynaphthoate)

Kaszonyiová, Martina; Rybnikář, František; Geil, Phillip H.

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