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dc.contributor.authorKim, Hak-Min-
dc.contributor.authorOh, Kyeongseok-
dc.contributor.authorKyung, Daeseung-
dc.contributor.authorAhn, Han-geun-
dc.contributor.authorYoon, Inhwan-
dc.contributor.authorKwak, Soonjong-
dc.contributor.authorNah, In Wook-
dc.date.accessioned2024-01-19T11:32:52Z-
dc.date.available2024-01-19T11:32:52Z-
dc.date.created2022-01-10-
dc.date.issued2022-08-
dc.identifier.issn0008-4034-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/114856-
dc.description.abstractAn eco-friendly polyvinyl alcohol (PVA)-chitosan(CS)-NH4Br catalyst was prepared using a modified solution method. Although the amounts of PVA and CS were fixed, the amount of NH4Br was varied in the range 15-45 wt.%. The catalytic performance of PVA-CS-NH4Br was compared based on the carbonation performance in the presence of single-component catalysts (PVA, CS, and NH4Br) and dual component catalyst (PVA-CS). The catalytic activity of PVA-CS was inadequate and considerably less than that observed when either PVA or CS was exclusively loaded. The number of functional groups within the PVA-CS structure was presumed to have been reduced due to the interactions of the OH groups in PVA and CS. However, the PVA-CS-NH4Br catalyst distinctively exhibited its catalytic performance. It has been suggested that NH4Br aided in sustaining the innate functional groups that both PVA and CS have within the PVA-CS-NH4Br structure. These results indicate that the functional groups and nucleophiles within the PVA-CS-NH4Br structure more effectively participated in the carbonation of propylene oxide. Quantitatively, the addition of 30 wt.% NH4Br yielded the best performance. Characteristic analyses of the catalysts were performed using X-ray diffraction, thermogravimetric analysis, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy.-
dc.languageEnglish-
dc.publisherWILEY-
dc.titlePreparation of polyvinyl alcohol-chitosan-NH4Br catalyst and its application to cycloaddition of carbon dioxide to propylene oxide-
dc.typeArticle-
dc.identifier.doi10.1002/cjce.24275-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCANADIAN JOURNAL OF CHEMICAL ENGINEERING, v.100, no.8, pp.1755 - 1763-
dc.citation.titleCANADIAN JOURNAL OF CHEMICAL ENGINEERING-
dc.citation.volume100-
dc.citation.number8-
dc.citation.startPage1755-
dc.citation.endPage1763-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000687784100001-
dc.identifier.scopusid2-s2.0-85113807285-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalResearchAreaEngineering-
dc.type.docTypeArticle-
dc.subject.keywordPlusBIOPOLYMER-SUPPORTED CATALYST-
dc.subject.keywordPlusCYCLIC CARBONATES-
dc.subject.keywordPlusIONIC LIQUID-
dc.subject.keywordPlusQUATERNIZED CHITOSAN-
dc.subject.keywordPlusPOLYMER ELECTROLYTE-
dc.subject.keywordPlusCO2-
dc.subject.keywordPlusEPOXIDES-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusMEMBRANES-
dc.subject.keywordPlusFIXATION-
dc.subject.keywordAuthorcycloaddition reaction-
dc.subject.keywordAuthorfunctional group-
dc.subject.keywordAuthorNH4Br-
dc.subject.keywordAuthorpropylene oxide-
dc.subject.keywordAuthorPVA-chitosan-
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