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High purity hydrogen production via aqueous phase reforming of xylose over small Pt nanoparticles on a gamma-Al2O3 support

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dc.contributor.authorKim, Yoondo-
dc.contributor.authorKim, Minkyeong-
dc.contributor.authorJeong, Hyangsoo-
dc.contributor.authorKim, Yongmin-
dc.contributor.authorChoi, Sun Hee-
dc.contributor.authorHam, Hyung Chul-
dc.contributor.authorLee, Seung Woo-
dc.contributor.authorKim, Jin Young-
dc.contributor.authorSong, Kwang Ho-
dc.contributor.authorYoon, Chang Won-
dc.contributor.authorJo, Young Suk-
dc.contributor.authorSohn, Hyuntae-
dc.date.accessioned2021-08-30T23:38:06Z-
dc.date.available2021-08-30T23:38:06Z-
dc.date.created2021-06-19-
dc.date.issued2020-05-18-
dc.identifier.issn0360-3199-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/55666-
dc.description.abstractIn this study, aqueous phase reforming (APR) of xylose was conducted over highly dispersed Pt nanoparticles supported on a gamma-Al2O3 support (Pt-SNP). Formation of small Pt nanoparticles was confirmed by X-ray diffraction and transmission electron microscopy, which revealed that most of the particles ranged between 0.8 and 1.6 nm in size and the average particle size was 1.3 nm. Temperature-programmed reduction analysis indicated that these small Pt nanoparticles were highly reducible under the reducing environment compared to the commercial Pt/gamma-Al2O3 catalysts (Pt-commercial). The catalytic activities of both Pt-SNP and Pt-commercial catalysts were examined in a semi-batch autoclave reactor system for the APR of xylose. It was found that Pt-SNP showed higher carbon to gas conversion with high hydrogen selectivity than Pt-commercial. This was likely due to the increased density of edge sites in the Pt-SNP catalyst that facilitated the cleavage of the C-C bonds rather than the C-O bonds, leading to greater hydrogen production. Furthermore, the Pt-SNP catalyst showed better carbon deposit resistance as compared to Pt-commercial. The amount of carbon deposition on the Pt-SNP catalyst surface and the organic carbon species dissolved in the post-reaction xylose solution were significantly lower compared to that of Pt-commercial. Finally, high purity hydrogen production was achieved using a continuous fixed-bed hybrid reactor including an aqueous phase reformer and a home-made Pd/Ta dense metallic composite membrane. A stable hydrogen gas production (99.999%) was obtained over the Pt-SNP catalyst, which demonstrated the success of a potentially commercial APR reactor system that continuously converted the aqueous xylose solution to hydrogen with high purity. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectSUPERCRITICAL WATER GASIFICATION-
dc.subjectOXYGENATED HYDROCARBONS-
dc.subjectRENEWABLE HYDROGEN-
dc.subjectMETAL DISPERSION-
dc.subjectETHYLENE-GLYCOL-
dc.subjectSOL-GEL-
dc.subjectBIOMASS-
dc.subjectCATALYSTS-
dc.subjectCONVERSION-
dc.subjectOXIDATION-
dc.titleHigh purity hydrogen production via aqueous phase reforming of xylose over small Pt nanoparticles on a gamma-Al2O3 support-
dc.typeArticle-
dc.contributor.affiliatedAuthorSong, Kwang Ho-
dc.identifier.doi10.1016/j.ijhydene.2020.03.014-
dc.identifier.scopusid2-s2.0-85082736696-
dc.identifier.wosid000530094600008-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.45, no.27, pp.13848 - 13861-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF HYDROGEN ENERGY-
dc.citation.titleINTERNATIONAL JOURNAL OF HYDROGEN ENERGY-
dc.citation.volume45-
dc.citation.number27-
dc.citation.startPage13848-
dc.citation.endPage13861-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaEnergy & Fuels-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryEnergy & Fuels-
dc.subject.keywordPlusSUPERCRITICAL WATER GASIFICATION-
dc.subject.keywordPlusOXYGENATED HYDROCARBONS-
dc.subject.keywordPlusRENEWABLE HYDROGEN-
dc.subject.keywordPlusMETAL DISPERSION-
dc.subject.keywordPlusETHYLENE-GLYCOL-
dc.subject.keywordPlusSOL-GEL-
dc.subject.keywordPlusBIOMASS-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusCONVERSION-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordAuthorHydrogen-
dc.subject.keywordAuthorXylose-
dc.subject.keywordAuthorBiomass-
dc.subject.keywordAuthorAPR-
dc.subject.keywordAuthorAqueous phase reforming-
dc.subject.keywordAuthorPlatinum-
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