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Hydrogen production via methane partial oxidation over SBA-15-coated cordierite monolithic NiO catalysts: Synergistic effects of CeO2 and ZrO2 doping

dc.contributor.authorBayraktar, Ilke Ilicak
dc.contributor.authorFigen, Halit Eren
dc.date.accessioned2026-06-27T15:19:53Z
dc.date.issued2025
dc.description.abstractThis study investigates the effect of mesoporous silica (SBA-15) combined with nickel and metal oxides on hydrogen production. Metal, metal oxide and SBA-15 solutions were successfully coated on the surface of cordierite monolith using the wash coating method. The characterization results confirmed the structural and chemical properties of the synthesized catalysts. SEM-EDS analysis demonstrated the uniform distribution of active components within the monolithic framework, ensuring effective metal dispersion. XPS spectra identified the binding states of Ni, Ce, and Zr, elucidating the active metal species responsible for catalytic activity. BET analysis revealed that alumina-supported catalysts exhibited a pore size range of 9-13 nm along with an enhanced surface area. XRD analysis confirmed the high crystallinity of the cordierite structure and the presence of NiO, CeO2, and ZrO2 phases. TPR analysis provided insights into metal-support interactions, highlighting the reducibility of NiO species and the temperature range at which reduction occurs. The catalytic performance of the synthesized monolithic catalysts was assessed in the partial oxidation of methane at reaction temperatures of 750, 800, and 850 degrees C under GHSV conditions of 10,000 and 20,000 h-1. The results indicated that decreasing the GHSV to 10,000 h-1 significantly improved methane conversion due to prolonged gas-catalyst contact time, thereby enhancing reaction efficiency. Among the catalysts, SBA-15/ZrO2/Ni exhibited the highest CH4 conversion and stability, maintaining a conversion of 95.6% at 800 degrees C after 10 h, while demonstrating minimal coke accumulation (0.22 mg C/gsupported catalyst). Although alumina-containing catalysts initially achieved higher CH4 conversion and H2 selectivity, they exhibited greater susceptibility to coke deposition over time, which affected their long-term stability.en
dc.description.sponsorshipTUBITAK [1003, 213M368]
dc.description.urihttps://doi.org/10.1016/j.ijhydene.2025.02.376
dc.identifier.doi10.1016/j.ijhydene.2025.02.376
dc.identifier.eissn1879-3487
dc.identifier.endpage712
dc.identifier.issn0360-3199
dc.identifier.startpage697
dc.identifier.urihttps://hdl.handle.net/20.500.14981/69812
dc.identifier.volume144
dc.identifier.wos001518660400010
dc.language.isoeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.relation.ispartofINTERNATIONAL JOURNAL OF HYDROGEN ENERGY
dc.subjectSBA-15
dc.subjectPartial oxidation of methane
dc.subjectHydrogen production
dc.subjectSupported catalyst
dc.subjectSYNTHESIS GAS
dc.subjectCARBON
dc.subjectSYNGAS
dc.subjectSURFACE
dc.subjectFUEL
dc.subjectTRANSITION
dc.subjectDEPOSITION
dc.subjectSUPPORT
dc.subjectCOKING
dc.subjectChemistry
dc.subjectElectrochemistry
dc.subjectEnergy & Fuels
dc.titleHydrogen production via methane partial oxidation over SBA-15-coated cordierite monolithic NiO catalysts: Synergistic effects of CeO2 and ZrO2 doping
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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