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dc.contributor.authorKim, Yong Tae-
dc.contributor.authorJung, Kwang-Deog-
dc.contributor.authorPark, Eun Duck-
dc.date.accessioned2024-01-20T16:31:58Z-
dc.date.available2024-01-20T16:31:58Z-
dc.date.created2021-09-05-
dc.date.issued2011-08-31-
dc.identifier.issn0926-3373-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/130064-
dc.description.abstractThe gas-phase dehydration of glycerol was conducted over silica-alumina catalysts with different Si/Al molar ratios. For comparison, SiO2 and eta-Al2O3 were also examined. A variety of techniques. X-ray diffraction (XRD), temperature-programmed desorption of ammonia (NH3-TPD), temperature-programmed oxidation (TPO) with mass spectroscopy (MS), infrared spectroscopy (FT-IR) after the adsorption of pyridine or glycerol, solid-state Si-29 and Al-22 magic-angle spinning nuclear magnetic resonance (MAS/NMR) spectroscopy, Raman spectroscopy, and CHNS analysis, were employed to characterize the catalysts. The initial glycerol conversion at 315 degrees C was strongly dependent on the total amount of acid sites over the silica-aluminas. The acrolein yield was proportional to the concentration of the Bronsted acid sites, whereas the 1-hydroxyacetone yield was proportional to the concentration of the Lewis acid sites. Among the tested catalysts, Si0.8Al0.2Ox showed the highest acrolein selectivity during the initial 2 h of the reaction. As long as the molar ratio between water and glycerol was in the range 2-11, the acrolein selectivity increased significantly with the water content of the feed. (C) 2011 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER-
dc.subjectNITRATE NONAHYDRATE-
dc.subjectACID SITES-
dc.subjectACROLEIN-
dc.subjectPYRIDINE-
dc.subjectCONVERSION-
dc.subjectZEOLITE-
dc.subjectSPECTRA-
dc.titleGas-phase dehydration of glycerol over silica-alumina catalysts-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcatb.2011.07.011-
dc.description.journalClass1-
dc.identifier.bibliographicCitationAPPLIED CATALYSIS B-ENVIRONMENTAL, v.107, no.1-2, pp.177 - 187-
dc.citation.titleAPPLIED CATALYSIS B-ENVIRONMENTAL-
dc.citation.volume107-
dc.citation.number1-2-
dc.citation.startPage177-
dc.citation.endPage187-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000294883300022-
dc.identifier.scopusid2-s2.0-80051471783-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Environmental-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.type.docTypeArticle-
dc.subject.keywordPlusNITRATE NONAHYDRATE-
dc.subject.keywordPlusACID SITES-
dc.subject.keywordPlusACROLEIN-
dc.subject.keywordPlusPYRIDINE-
dc.subject.keywordPlusCONVERSION-
dc.subject.keywordPlusZEOLITE-
dc.subject.keywordPlusSPECTRA-
dc.subject.keywordAuthorDehydration-
dc.subject.keywordAuthorGlycerol-
dc.subject.keywordAuthorAcrolein-
dc.subject.keywordAuthorSilica-alumina-
dc.subject.keywordAuthorAcidity-
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