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Improving performance of a five-zone simulated moving bed chromatography for ternary separation by simultaneous use of partial-feeding and partial-closing of the product port in charge of collecting the intermediate-affinity solute molecules

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dc.contributor.authorMun, Sungyong-
dc.date.accessioned2022-07-16T18:24:35Z-
dc.date.available2022-07-16T18:24:35Z-
dc.date.issued2011-11-
dc.identifier.issn0021-9673-
dc.identifier.issn1873-3778-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/167255-
dc.description.abstractThe performance of a five-zone simulated moving bed (SMB) chromatographic process for ternary separation has been improved to a certain extent in previous researches by applying either a partial-feeding (PF) or a partial-closing of the extract-2 port (PCE(2)) to its operation. To make a further improvement, the strategy of applying both PF and PCE(2) simultaneously to the five-zone SMB operation was proposed in this study. The results from both equilibrium-theory analysis and detailed simulation proved that the proposed strategy, which was called PF-PCE(2) in this article, had the benefit of a synergy between the individual merits of PF and PCE(2) in the five-zone SMB performance. As a consequence, the PF-PCE(2) mode could surpass the PF and the PCE(2) modes by a wide margin and the standard mode by a much wider margin in the aspects of ternary-separation performance and throughput. For the separation system considered, the PF-PCE(2) mode was found to achieve more than 100% improvement, compared to the standard mode. Furthermore, such advantage of the PF-PCE(2) over all the other modes was greater as the selectivity between the intermediate-affinity and the highest-affinity components was reduced.-
dc.format.extent15-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleImproving performance of a five-zone simulated moving bed chromatography for ternary separation by simultaneous use of partial-feeding and partial-closing of the product port in charge of collecting the intermediate-affinity solute molecules-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.chroma.2011.09.015-
dc.identifier.scopusid2-s2.0-80054003892-
dc.identifier.wosid000296549000018-
dc.identifier.bibliographicCitationJournal of Chromatography A, v.1218, no.44, pp 8060 - 8074-
dc.citation.titleJournal of Chromatography A-
dc.citation.volume1218-
dc.citation.number44-
dc.citation.startPage8060-
dc.citation.endPage8074-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.subject.keywordPlusSTANDING-WAVE DESIGN-
dc.subject.keywordPlusMULTIOBJECTIVE OPTIMIZATION-
dc.subject.keywordPlusGENETIC ALGORITHM-
dc.subject.keywordPlusMULTICOMPONENT SEPARATION-
dc.subject.keywordPlusSMB-
dc.subject.keywordPlusOPERATION-
dc.subject.keywordPlusMIXTURES-
dc.subject.keywordPlusSYSTEMS-
dc.subject.keywordPlusSTRATEGY-
dc.subject.keywordPlusGLUCOSE-
dc.subject.keywordAuthorSimulated moving bed chromatography-
dc.subject.keywordAuthorTernary separation-
dc.subject.keywordAuthorContinuous separation process-
dc.subject.keywordAuthorFive-zone SMB-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S002196731101363X?via%3Dihub-
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