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dc.contributor.authorEndah, Yohana Kurnia-
dc.contributor.authorHan, Sang Hoon-
dc.contributor.authorKim, Jae Hoon-
dc.contributor.authorKim, Nak-Kyoon-
dc.contributor.authorKim, Woo Nyon-
dc.contributor.authorLee, Hong-Shik-
dc.contributor.authorLee, Hyunjoo-
dc.date.accessioned2024-01-20T04:04:12Z-
dc.date.available2024-01-20T04:04:12Z-
dc.date.created2021-09-05-
dc.date.issued2016-05-10-
dc.identifier.issn0021-8995-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/124070-
dc.description.abstract2,5-Furandicarboxylic acid (FDCA) is a promising biobased alternative material to terephthalic acid. In this study, three types of poly(butylene adipamide) (PA-4,6) containing 10, 20, and 30 mol % of poly(butylene-2,5-furandicarboxylamide) (PA-4,F) were synthesized through consecutive prepolymerization and solid-state polymerization (SSP). The incorporation of a 10 mol % PA-4,F component into PA-4,6 resulted in slight increases in the intrinsic viscosity (IV) and glass-transition temperature (T-g) after 12 h of SSP at 220 degrees C. When the SSP temperature and reaction time increased, IV increased proportionally. The highest IV value of 0.75 was obtained by 48 h of SSP at 240 degrees C, whereas increases in the PA-4,F content to 20 and 30 mol % gave rise to decreases in IV, T-g, and melting temperature; this interrupted the increase in SSP temperature. The thermal decomposition temperature of the PA-4,F-incorporated polyamide was lower than that with PA-4,6 because of the lower thermal stability of the FDCA component. (c) 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 43391.-
dc.languageEnglish-
dc.publisherWILEY-BLACKWELL-
dc.subjectMOLECULAR-WEIGHT-
dc.subjectRENEWABLE RESOURCES-
dc.subjectREACTION-KINETICS-
dc.subjectSWEEP FLUID-
dc.subjectCARBONATE)-
dc.subjectPOLY(BISPHENOL-
dc.subjectPOLY(ETHYLENE-TEREPHTHALATE)-
dc.subjectTEREPHTHALATE)-
dc.subjectPOLYAMIDES-
dc.subjectNYLON-4,T-
dc.titleSolid-state polymerization and characterization of a copolyamide based on adipic acid, 1,4-butanediamine, and 2,5-furandicarboxylic acid-
dc.typeArticle-
dc.identifier.doi10.1002/app.43391-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF APPLIED POLYMER SCIENCE, v.133, no.18-
dc.citation.titleJOURNAL OF APPLIED POLYMER SCIENCE-
dc.citation.volume133-
dc.citation.number18-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000369996600021-
dc.identifier.scopusid2-s2.0-84968324801-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.relation.journalResearchAreaPolymer Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusMOLECULAR-WEIGHT-
dc.subject.keywordPlusRENEWABLE RESOURCES-
dc.subject.keywordPlusREACTION-KINETICS-
dc.subject.keywordPlusSWEEP FLUID-
dc.subject.keywordPlusCARBONATE)-
dc.subject.keywordPlusPOLY(BISPHENOL-
dc.subject.keywordPlusPOLY(ETHYLENE-TEREPHTHALATE)-
dc.subject.keywordPlusTEREPHTHALATE)-
dc.subject.keywordPlusPOLYAMIDES-
dc.subject.keywordPlusNYLON-4,T-
dc.subject.keywordAuthorbiopolymers and renewable polymers-
dc.subject.keywordAuthorsynthesis and processing-
dc.subject.keywordAuthorthermal properties-
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