Full metadata record

DC Field Value Language
dc.contributor.authorKim, Tae-Ho-
dc.contributor.authorGong, Gyeong-Taek-
dc.contributor.authorLee, Byung Gwon-
dc.contributor.authorLee, Kwan-Young-
dc.contributor.authorJeon, Hee-Young-
dc.contributor.authorShin, Chae-Ho-
dc.contributor.authorKim, Honggon-
dc.contributor.authorJung, Kwang-Deog-
dc.date.accessioned2024-01-21T03:04:07Z-
dc.date.available2024-01-21T03:04:07Z-
dc.date.created2021-09-01-
dc.date.issued2006-05-17-
dc.identifier.issn0926-860X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/135506-
dc.description.abstractThe iodine-sulfur (IS) cycle has been focused for hydrogen production by water splitting using a very high temperature nuclear reactor (VHTR) which is a high temperature heat source. The nuclear energy was absorbed at the temperature ranges of 750-900 degrees C by SO3 decomposition reaction to SO2 and O-2 in IS cycle. In this work, the activity of Fe/Al and Fe/Ti catalysts prepared by a co-precipitation was studied in an attempt to find some suitable catalysts for the decomposition of sulfur trioxide as the oxygen-generating reaction in the thermo-chemical water splitting process. The SO3 decomposition was performed in the temperature range of 750-950 degrees C at a space velocity of 72,000 cm(3)/g cat. h in a fixed bed reactor. The catalytic activity of Fe/Al and Fe/Ti catalysts increased with an increase in Fe loadings, indicating that the Fe component should be active. The mechanism for the SO3 decomposition on metal oxides can be described as follows: the metal sulfate formation (MO + SO3 -> MSO4) and the decomposition of metal sulfate (MSO4 -> MO2 + SO2 and MO2 -> MO + 1/2O(2)). (c) 2006 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectHYDROGEN-
dc.titleCatalytic decomposition of sulfur trioxide on the binary metal oxide catalysts of Fe/Al and Fe/Ti-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcata.2006.02.052-
dc.description.journalClass1-
dc.identifier.bibliographicCitationAPPLIED CATALYSIS A-GENERAL, v.305, no.1, pp.39 - 45-
dc.citation.titleAPPLIED CATALYSIS A-GENERAL-
dc.citation.volume305-
dc.citation.number1-
dc.citation.startPage39-
dc.citation.endPage45-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000237709300006-
dc.identifier.scopusid2-s2.0-33646487669-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.type.docTypeArticle-
dc.subject.keywordPlusHYDROGEN-
dc.subject.keywordAuthorIS cycle-
dc.subject.keywordAuthorSO3 decomposition-
dc.subject.keywordAuthormetal sulfate decomposition-
dc.subject.keywordAuthorhydrogen production-
Appears in Collections:
KIST Article > 2006
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE