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Redox cycling of CuFe2O4 supported on ZrO2 and CeO2 for two-step methane reforming/water splitting

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dc.contributor.authorKang, Kyoung-Soo-
dc.contributor.authorKim, Chang-Hee-
dc.contributor.authorBae, Ki-Kwang-
dc.contributor.authorCho, Won-Chul-
dc.contributor.authorKim, Woo-Jin-
dc.contributor.authorKim, Young-Ho-
dc.contributor.authorKim, Sung-Hyun-
dc.contributor.authorPark, Chu-Sik-
dc.date.accessioned2021-09-08T06:07:18Z-
dc.date.available2021-09-08T06:07:18Z-
dc.date.created2021-06-11-
dc.date.issued2010-01-
dc.identifier.issn0360-3199-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/117264-
dc.description.abstractCuFe2O4 supported on ZrO2 and CeO2 for two-step methane reforming was evaluated to determine if it could enhance the reactivity, CO selectivity and thermal stability of CuFe2O4. Two-step methane reforming consists of a syngas production step and a water splitting step. CuFe2O4 supported on ZrO2 and CeO2 was prepared using an aerial oxidation method. Non-isothermal methane reduction was carried out on TGA to compare the reactivity of CuFe2O4/ZrO2 and CuFe2O4/CeO2. In addition, a syngas production step was performed at 900 degrees C and water splitting was conducted at 800 degrees C alternatively five times to compare the methane conversion, CO selectivity, cycle ability and hydrogen production by water splitting in a fixed bed reactor. If the 1st syngas production step results are excluded due to over-oxidation, CuFe2O4/ZrO2 and CuFe2O4/CeO2 showed approximately 74.0-82.8% and 60.3-87.5% methane conversion, respectively, and 44.0-47.8% and 65.2-81.5% CO selectivity, respectively. Using CeO2 and ZrO2 as supports effectively improved the reactivity and methane conversion compared to CuFe2O4. CuFe2O4/ZrO2 showed high methane conversion due to the high phase stability and thermal stability of ZrO2 but the selectivity was not improved. After 5 successive cycles, the CeFeO3 phase was found on CuFe2O4/CeO2. Furthermore, methane conversion, CO selectivity and the amounts of hydrogen production of CuFe2O4/CeO2 increased with increasing number of cycles. Additional test up to the 11th cycle on CuFe2O4/CeO2 revealed that CeO2 is a better support that ZnO2 in terms of the reactivity and CO selectivity. (C) 2009 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectPARTIAL OXIDATION-
dc.subjectSYNTHESIS GAS-
dc.subjectCARBON-DIOXIDE-
dc.subjectSOLAR-
dc.subjectREDUCTION-
dc.subjectSYNGAS-
dc.subjectCATALYSTS-
dc.subjectHYDROGEN-
dc.subjectOXIDANT-
dc.subjectWATER-
dc.titleRedox cycling of CuFe2O4 supported on ZrO2 and CeO2 for two-step methane reforming/water splitting-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Sung-Hyun-
dc.identifier.doi10.1016/j.ijhydene.2009.10.099-
dc.identifier.scopusid2-s2.0-73749083640-
dc.identifier.wosid000274719800017-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF HYDROGEN ENERGY, v.35, no.2, pp.568 - 576-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF HYDROGEN ENERGY-
dc.citation.titleINTERNATIONAL JOURNAL OF HYDROGEN ENERGY-
dc.citation.volume35-
dc.citation.number2-
dc.citation.startPage568-
dc.citation.endPage576-
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.keywordPlusPARTIAL OXIDATION-
dc.subject.keywordPlusSYNTHESIS GAS-
dc.subject.keywordPlusCARBON-DIOXIDE-
dc.subject.keywordPlusSOLAR-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusSYNGAS-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusHYDROGEN-
dc.subject.keywordPlusOXIDANT-
dc.subject.keywordPlusWATER-
dc.subject.keywordAuthorTwo-step methane reforming-
dc.subject.keywordAuthorCuFe2O4-
dc.subject.keywordAuthorCO selectivity-
dc.subject.keywordAuthorWater splitting-
dc.subject.keywordAuthorSolar-
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