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dc.contributor.authorKuk, YM-
dc.contributor.authorLee, BC-
dc.contributor.authorLee, YW-
dc.contributor.authorLim, JS-
dc.date.accessioned2024-01-21T12:01:20Z-
dc.date.available2024-01-21T12:01:20Z-
dc.date.created2021-09-04-
dc.date.issued2001-09-
dc.identifier.issn0021-9568-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/140226-
dc.description.abstractPhase behavior data are presented for biodegradable polymers in high-pressure dimethyl ether (DME) and in supercritical mixtures of DME and carbon dioxide (CO2). The cloud point curves of poly(D,L-lactide) MW = 30000) in DME were measured at polymer concentrations up to similar to 15 mass % and at temperatures to 373.15 K and pressures to 14 MPa using a variable-volume view cell apparatus. This system exhibited the characteristics of a lower critical solution temperature phase behavior and showed the pressure-polymer concentration isotherms with the maximum cloud point pressure at the polymer concentration of similar to5 mass %. The cloud point pressure increased with increasing molecular weight of the poly(D,L-lactide). For poly(D,L-lactide-co-glycolide) copolymers in DME, decreasing the D,L-lactide content in the copolymer caused the single-phase region to shrink and changed the cloud point curve from a lower critical solution temperature behavior to an upper critical solution temperature behavior. The cloud points of poly(D,L-lactide) in the solvent mixtures of DME and CO2 were measured at various CO2 Compositions up to similar to 73 mass % (on a polymer-free basis) and at temperatures up to similar to 373.15 K. As the CO2 Composition in the mixed solvent increased, the cloud point pressure at a fixed temperature increased significantly. Addition Of CO2 to DME caused a lowering of the dissolving power of the mixed solvent due to the decrease of the solvent polarity.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectCHLORODIFLUOROMETHANE-
dc.subjectPARTICLES-
dc.titlePhase behavior of biodegradable polymers in dimethyl ether and dimethyl ether plus carbon dioxide-
dc.typeArticle-
dc.identifier.doi10.1021/je010056o-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF CHEMICAL AND ENGINEERING DATA, v.46, no.5, pp.1344 - 1348-
dc.citation.titleJOURNAL OF CHEMICAL AND ENGINEERING DATA-
dc.citation.volume46-
dc.citation.number5-
dc.citation.startPage1344-
dc.citation.endPage1348-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000171213400074-
dc.identifier.scopusid2-s2.0-0035437814-
dc.relation.journalWebOfScienceCategoryThermodynamics-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalResearchAreaThermodynamics-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.type.docTypeArticle-
dc.subject.keywordPlusCHLORODIFLUOROMETHANE-
dc.subject.keywordPlusPARTICLES-
dc.subject.keywordAuthorsupercritical-
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