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Synthesis and characterization of a series of thermotropic liquid crystalline copolyester nanocomposites

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dc.contributor.authorChang, Jin-Hae-
dc.contributor.authorJu, Chul Ha-
dc.contributor.authorKim, Seong Hun-
dc.date.accessioned2022-12-21T12:13:19Z-
dc.date.available2022-12-21T12:13:19Z-
dc.date.issued2006-01-
dc.identifier.issn0887-6266-
dc.identifier.issn1099-0488-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181882-
dc.description.abstractA series of aromatic thermotropic liquid crystalline copolyester (TLCP) nanocomposites were prepared by the in situ intercalation polymerization of p-acetoxybenzoic acid (ABA), terephthalic acid (TPA), and diacetoxynaphthalene (DAN) isomers in the presence of the organoclay. The DAN isomers used in this study were 2,3- and 2,7-naphthylene. We examined the variation of the liquid crystallinity, morphology, and thermal properties of the nanocomposites with organoclay content in the range 0-10 wt %. All the polymer nanocomposites were fabricated with a molar ratio of ABA:TPA:DAN = 2:1:1; they were shown to consist of a nematic liquid crystalline phase for low organoclay contents (<= 5 wt %), whereas the hybrids with a higher concentration of organoclay (>= 10 wt %) were found not to be mesomorphic. By using transmission electron microscopy, the clay layers in the 2,3-DAN copolyester hybrids were found to be better dispersed in the matrix polymer than those in the 2,7-DAN copolyester hybrids. The introduction of an organoclay into the matrix polymer was found to improve the thermal properties of the 2,3-DAN copolyester hybrids. However, the thermal properties of the 2,7-DAN copolyester hybrids were found to be worse than those of the pure matrix polymer for all organoclay compositions tested. (c) 2005 Wiley Periodicals, Inc.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Inc.-
dc.titleSynthesis and characterization of a series of thermotropic liquid crystalline copolyester nanocomposites-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1002/polb.20609-
dc.identifier.scopusid2-s2.0-31344461261-
dc.identifier.wosid000234353600013-
dc.identifier.bibliographicCitationJournal of Polymer Science, Part B: Polymer Physics, v.44, no.2, pp 387 - 397-
dc.citation.titleJournal of Polymer Science, Part B: Polymer Physics-
dc.citation.volume44-
dc.citation.number2-
dc.citation.startPage387-
dc.citation.endPage397-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusTHERMOMECHANICAL PROPERTIES-
dc.subject.keywordPlusPOLYMER-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusEXFOLIATION-
dc.subject.keywordPlusPOLYESTERS-
dc.subject.keywordPlusORGANOCLAY-
dc.subject.keywordPlusSEQUENCE-
dc.subject.keywordPlusBLENDS-
dc.subject.keywordAuthornanocomposite-
dc.subject.keywordAuthornaphthylene unit-
dc.subject.keywordAuthororganoclay-
dc.subject.keywordAuthorthermotropic liquid crystalline copolyester-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/polb.20609-
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