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Cited 61 time in webofscience Cited 63 time in scopus
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dc.contributor.authorRyu, DY-
dc.contributor.authorJeong, U-
dc.contributor.authorLee, DH-
dc.contributor.authorKim, J-
dc.contributor.authorYoun, HS-
dc.contributor.authorKim, JK-
dc.date.accessioned2016-03-31T12:51:50Z-
dc.date.available2016-03-31T12:51:50Z-
dc.date.created2009-08-25-
dc.date.issued2003-04-22-
dc.identifier.issn0024-9297-
dc.identifier.other2003-OAK-0000003342-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/18574-
dc.description.abstractThe phase behavior of deuterated polystyrene-block-poly(n-pentyl methacrylate) copolymers (dPS-PnPMA) was investigated by using small-angle X-ray (SAXS) and neutron (SANS) scatterings and rheology. This block copolymer exhibited a closed-loop type of phase behavior as did hydrogenated PS-PnPMA copolymers. The closed loop consists of two transitions: lower disorder-to-order transition (LDOT) and upper order-to-disorder transition (UODT) occurring at a lower and higher temperature, respectively. The segmental interaction parameter (chi) between dPS and PnPMA blocks at various temperatures was obtained by fitting the incompressible random phase approximation theory to SANS results using a low molecular weight of dPS-PnPMA exhibiting a disordered homogeneous state over the entire temperature range. We found that at higher temperatures chi increased initially with increasing temperature (T), achieved a maximum, and then decreased. Such behavior is in keeping with polymer blends or block copolymers that would exhibit a closed-loop phase behavior. However, at temperatures below LDOT, chi did not decrease monotonically with decreasing T. Rather, with decreasing T, chi decreased initially, achieved a minimum, and then increased again. This strongly suggests that another transition of order-to-disorder transition (ODT) might be expected at lower temperatures.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfMACROMOLECULES-
dc.subjectORDER-DISORDER TRANSITION-
dc.subjectPOLYSTYRENE-BLOCK-POLYISOPRENE-
dc.subjectSOLUTION TEMPERATURE BEHAVIOR-
dc.subjectLATTICE CLUSTER THEORY-
dc.subjectDIBLOCK COPOLYMERS-
dc.subjectPOLYMER BLENDS-
dc.subjectMICROPHASE SEPARATION-
dc.subjectMOLECULAR-WEIGHT-
dc.subjectMELTS-
dc.subjectTHERMODYNAMICS-
dc.titlePhase behavior of deuterated polystyrene-block-poly(n-pentyl methaerylate) copolymers-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1021/MA026002G-
dc.author.googleRyu, DY-
dc.author.googleJeong, U-
dc.author.googleLee, DH-
dc.author.googleKim, J-
dc.author.googleYoun, HS-
dc.author.googleKim, JK-
dc.relation.volume36-
dc.relation.issue8-
dc.relation.startpage2894-
dc.relation.lastpage2902-
dc.contributor.id10076321-
dc.relation.journalMACROMOLECULES-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationMACROMOLECULES, v.36, no.8, pp.2894 - 2902-
dc.identifier.wosid000182361700049-
dc.date.tcdate2019-01-01-
dc.citation.endPage2902-
dc.citation.number8-
dc.citation.startPage2894-
dc.citation.titleMACROMOLECULES-
dc.citation.volume36-
dc.contributor.affiliatedAuthorKim, JK-
dc.identifier.scopusid2-s2.0-0037461408-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc57-
dc.type.docTypeArticle-
dc.subject.keywordPlusORDER-DISORDER TRANSITION-
dc.subject.keywordPlusPOLYSTYRENE-BLOCK-POLYISOPRENE-
dc.subject.keywordPlusSOLUTION TEMPERATURE BEHAVIOR-
dc.subject.keywordPlusLATTICE CLUSTER THEORY-
dc.subject.keywordPlusDIBLOCK COPOLYMERS-
dc.subject.keywordPlusPOLYMER BLENDS-
dc.subject.keywordPlusMICROPHASE SEPARATION-
dc.subject.keywordPlusMOLECULAR-WEIGHT-
dc.subject.keywordPlusMELTS-
dc.subject.keywordPlusTHERMODYNAMICS-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPolymer Science-

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김진곤KIM, JIN KON
Dept. of Chemical Enginrg
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