Preparation of Pt-loaded hydrogen selective membranes for methanol reforming

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dc.contributor.authorLee, Dong-Wookko
dc.contributor.authorNam, Seung-Eunko
dc.contributor.authorSea, Bongkukko
dc.contributor.authorIhm, Son Kiko
dc.contributor.authorLee, Kew-Hoko
dc.date.accessioned2008-03-29T08:16:07Z-
dc.date.available2008-03-29T08:16:07Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2006-10-
dc.identifier.citationCATALYSIS TODAY, v.118, no.1-2, pp.198 - 204-
dc.identifier.issn0920-5861-
dc.identifier.urihttp://hdl.handle.net/10203/3561-
dc.description.abstractWe prepared Pt-included microporous silica membranes (SiO2/gamma-AI(2)O(3)/Pt-SiO2/porous stainless steel (SUS)) to improve CO removal efficiency in a methanol reforming membrane reactor. The permeation test of an H-2 (99%)/CO(1%) mixture between 25 and 200 degrees C was conducted to observe the effect of the Pt intermediate layer included in the membrane on CO removal efficiency. A mesoporous membrane with the Pt intermediate layer (gamma-Al2O3/Pt-SiO2/SUS) showed a remarkable H-2/CO separation factor of 5.22-7.03, exceeding the Knudsen-dominated transport characteristics expected from a mesoporous gamma-Al2O3 layer. After coating a microporous silica skin layer on the Pt-included gamma-Al2O3 membrane, CO was not detected in the permeate side of the membrane by the corona ionization detector (CID). When the Pt-included microporous silica membrane was used in the methanol reforming membrane reactor, methanol conversion at 200 degrees C (methanol/water feed flow rate = 0.004 ml/min) was improved from 73.2% to 93.2% in comparison with the case of a conventional reactor, and CO in the produced gas mixture was efficiently rejected through the Pt-included silica composite membrane. The introduction of the Pt catalyst into the intermediate layer of the composite membrane contributed to the improvement in CO removal efficiency. The dilution of CH3OH/H2O feed led to an increase in the extent of methanol conversion improvement (a difference of methanol conversion between a membrane reactor and a conventional reactor) due to an increase in the hydrogen recovery. (c) 2006 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherElsevier Science Bv-
dc.subjectSILICA MCM-48 MEMBRANE-
dc.subjectFUEL-CELLS-
dc.subjectCOMPOSITE MEMBRANES-
dc.subjectCERAMIC MEMBRANES-
dc.subjectPERMEATION-
dc.subjectSEPARATION-
dc.subjectSTABILITY-
dc.subjectVEHICLES-
dc.subjectCO-
dc.titlePreparation of Pt-loaded hydrogen selective membranes for methanol reforming-
dc.typeArticle-
dc.identifier.wosid000241489700028-
dc.identifier.scopusid2-s2.0-33748980063-
dc.type.rimsART-
dc.citation.volume118-
dc.citation.issue1-2-
dc.citation.beginningpage198-
dc.citation.endingpage204-
dc.citation.publicationnameCATALYSIS TODAY-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorIhm, Son Ki-
dc.contributor.nonIdAuthorLee, Dong-Wook-
dc.contributor.nonIdAuthorNam, Seung-Eun-
dc.contributor.nonIdAuthorSea, Bongkuk-
dc.contributor.nonIdAuthorLee, Kew-Ho-
dc.type.journalArticleArticle; Proceedings Paper-
dc.subject.keywordAuthormethanol reforming-
dc.subject.keywordAuthorCO removal-
dc.subject.keywordAuthormembrane reactor-
dc.subject.keywordPlusSILICA MCM-48 MEMBRANE-
dc.subject.keywordPlusFUEL-CELLS-
dc.subject.keywordPlusCOMPOSITE MEMBRANES-
dc.subject.keywordPlusCERAMIC MEMBRANES-
dc.subject.keywordPlusPERMEATION-
dc.subject.keywordPlusSEPARATION-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusVEHICLES-
dc.subject.keywordPlusCO-
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