In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane

Detalhes bibliográficos
Autor(a) principal: Toscani, Lucia M.
Data de Publicação: 2018
Outros Autores: Genoveva Zimicz, M., Martins, Tereza S. [UNIFESP], Lamas, Diego G., Larrondo, Susana A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://repositorio.unifesp.br/handle/11600/54318
http://dx.doi.org/10.1039/c8ra01528g
Resumo: In this work we analyze the effect of adding CuO to a NiO/Ce0.9Zr0.1O2 oxide by in situ X-ray absorption near-edge structure XANES technique in Ce L3, Ni K and Cu K absorption edges in terms of sample reducibility and catalytic activity. The oxidation states of Ce, Ni and Cu cations are followed up during temperature programmed reduction (TPR) experiments in diluted hydrogen and during catalytic tests for partial oxidation of methane (POM) reaction. Redox behavior was correlated to conventional fixed bed reactor results. The effect of firing temperature, crystallite size, CeO2-ZrO2 support and the presence of Cu and/or Ni as an active phase is also analyzed. Results showed a beneficial effect of CuO addition in terms of Ce and Ni reduction. A stronger interaction of NiO species with the support was revealed upon analysis of XANES reduction profiles in sample NiO/ZDC in contrast to bimetallic CuO-NiO/ZDC sample. Reduction onset temperature was found to depend on Ni crystallite size, being markedly promoted when samples exhibited low values of crystallite size both in supported and non-supported CuO-NiO species. In situ catalytic experiments for partial oxidation of methane showed a clear interplay between the redox behavior from the Ce in the CeO2-ZrO2 support and the Ni from the active phase. Sample NiO/ZDC exhibited a continuous reduction of Ce cations in CH4 : O-2 feed flow, carbon formation was detected in X-ray Powder Diffraction (XPD) patterns and Ni re-oxidation was found to take place, clear indications of catalyst deactivation. In contrast, sample CuO-NiO/Ce0.9Zr0.1O2 displayed a slight reoxidation of Ce and no re-oxidation of Ni altogether with the suppression of carbon formation.
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spelling Toscani, Lucia M.Genoveva Zimicz, M.Martins, Tereza S. [UNIFESP]Lamas, Diego G.Larrondo, Susana A.2020-07-08T13:09:57Z2020-07-08T13:09:57Z2018Rsc Advances. Cambridge, v. 8, n. 22, p. 12190-12203, 2018.2046-2069https://repositorio.unifesp.br/handle/11600/54318http://dx.doi.org/10.1039/c8ra01528gWOS000431976000036.pdf10.1039/c8ra01528gWOS:000431976000036In this work we analyze the effect of adding CuO to a NiO/Ce0.9Zr0.1O2 oxide by in situ X-ray absorption near-edge structure XANES technique in Ce L3, Ni K and Cu K absorption edges in terms of sample reducibility and catalytic activity. The oxidation states of Ce, Ni and Cu cations are followed up during temperature programmed reduction (TPR) experiments in diluted hydrogen and during catalytic tests for partial oxidation of methane (POM) reaction. Redox behavior was correlated to conventional fixed bed reactor results. The effect of firing temperature, crystallite size, CeO2-ZrO2 support and the presence of Cu and/or Ni as an active phase is also analyzed. Results showed a beneficial effect of CuO addition in terms of Ce and Ni reduction. A stronger interaction of NiO species with the support was revealed upon analysis of XANES reduction profiles in sample NiO/ZDC in contrast to bimetallic CuO-NiO/ZDC sample. Reduction onset temperature was found to depend on Ni crystallite size, being markedly promoted when samples exhibited low values of crystallite size both in supported and non-supported CuO-NiO species. In situ catalytic experiments for partial oxidation of methane showed a clear interplay between the redox behavior from the Ce in the CeO2-ZrO2 support and the Ni from the active phase. Sample NiO/ZDC exhibited a continuous reduction of Ce cations in CH4 : O-2 feed flow, carbon formation was detected in X-ray Powder Diffraction (XPD) patterns and Ni re-oxidation was found to take place, clear indications of catalyst deactivation. In contrast, sample CuO-NiO/Ce0.9Zr0.1O2 displayed a slight reoxidation of Ce and no re-oxidation of Ni altogether with the suppression of carbon formation.CONICETNational Synchrotron Light Laboratory (LNLS)ANPCyT-PICTConsejo Nacl Invest Cient & Tecn, MINDEF, UNIDEF, Dept Invest Solidos,CITEDEF, JB de La Salle 4397, RA-1603 Villa Martelli, Buenos Aires, ArgentinaUNSAM, Inst Invest & Ingn Ambiental, Campus Miguelete,25 Mayo & Francia, RA-1650 San Martin, Buenos Aires, ArgentinaUNS, CONICET, Inst Fis IFISUR, Dept Fis, Av Alem 1253, RA-8000 Bahia Blanca, Buenos Aires, ArgentinaUniv Fed Sao Paulo, UNIFESP, Dept Quim, Inst Ciencias Ambientais Quim & Farmaceut, Rua Sao Nicolau 210,2nd Floor, BR-09913030 Diadema, SP, BrazilUNSAM, CONICET, Escuela Ciencia & Tecnol, Campus Miguelete,25 Mayo & Francia, RA-1650 San Martin, Buenos Aires, ArgentinaComis Nacl Energia Atom, Ctr Atom Constituyentes, Gerencia Invest & Aplicac, Dept Fis Mat Condensada, Av Gen Paz 1499, RA-1650 San Martin, Buenos Aires, ArgentinaUniv Fed Sao Paulo, UNIFESP, Dept Quim, Inst Ciencias Ambientais Quim & Farmaceut, Rua Sao Nicolau 210,2nd Floor, BR-09913030 Diadema, SP, BrazilLNLS: XAFS1-15329ANPCyT-PICT: 1587Web of Science12190-12203engRoyal Soc ChemistryRsc AdvancesIn situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methaneinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleCambridge822info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALWOS000431976000036.pdfapplication/pdf1343355${dspace.ui.url}/bitstream/11600/54318/1/WOS000431976000036.pdfd8dc3d77e2494c1fbce9e85320db9482MD51open accessTEXTWOS000431976000036.pdf.txtWOS000431976000036.pdf.txtExtracted texttext/plain68056${dspace.ui.url}/bitstream/11600/54318/8/WOS000431976000036.pdf.txtda04b1c060ad0aa4d8870de245daa8c8MD58open accessTHUMBNAILWOS000431976000036.pdf.jpgWOS000431976000036.pdf.jpgIM Thumbnailimage/jpeg7351${dspace.ui.url}/bitstream/11600/54318/10/WOS000431976000036.pdf.jpg509819596989647c160484d2fdf5f117MD510open access11600/543182023-06-05 19:24:54.205open accessoai:repositorio.unifesp.br:11600/54318Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-06-05T22:24:54Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane
title In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane
spellingShingle In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane
Toscani, Lucia M.
title_short In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane
title_full In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane
title_fullStr In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane
title_full_unstemmed In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane
title_sort In situ X-ray absorption spectroscopy study of CuO-NiO/CeO2-ZrO2 oxides: redox characterization and its effect in catalytic performance for partial oxidation of methane
author Toscani, Lucia M.
author_facet Toscani, Lucia M.
Genoveva Zimicz, M.
Martins, Tereza S. [UNIFESP]
Lamas, Diego G.
Larrondo, Susana A.
author_role author
author2 Genoveva Zimicz, M.
Martins, Tereza S. [UNIFESP]
Lamas, Diego G.
Larrondo, Susana A.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Toscani, Lucia M.
Genoveva Zimicz, M.
Martins, Tereza S. [UNIFESP]
Lamas, Diego G.
Larrondo, Susana A.
description In this work we analyze the effect of adding CuO to a NiO/Ce0.9Zr0.1O2 oxide by in situ X-ray absorption near-edge structure XANES technique in Ce L3, Ni K and Cu K absorption edges in terms of sample reducibility and catalytic activity. The oxidation states of Ce, Ni and Cu cations are followed up during temperature programmed reduction (TPR) experiments in diluted hydrogen and during catalytic tests for partial oxidation of methane (POM) reaction. Redox behavior was correlated to conventional fixed bed reactor results. The effect of firing temperature, crystallite size, CeO2-ZrO2 support and the presence of Cu and/or Ni as an active phase is also analyzed. Results showed a beneficial effect of CuO addition in terms of Ce and Ni reduction. A stronger interaction of NiO species with the support was revealed upon analysis of XANES reduction profiles in sample NiO/ZDC in contrast to bimetallic CuO-NiO/ZDC sample. Reduction onset temperature was found to depend on Ni crystallite size, being markedly promoted when samples exhibited low values of crystallite size both in supported and non-supported CuO-NiO species. In situ catalytic experiments for partial oxidation of methane showed a clear interplay between the redox behavior from the Ce in the CeO2-ZrO2 support and the Ni from the active phase. Sample NiO/ZDC exhibited a continuous reduction of Ce cations in CH4 : O-2 feed flow, carbon formation was detected in X-ray Powder Diffraction (XPD) patterns and Ni re-oxidation was found to take place, clear indications of catalyst deactivation. In contrast, sample CuO-NiO/Ce0.9Zr0.1O2 displayed a slight reoxidation of Ce and no re-oxidation of Ni altogether with the suppression of carbon formation.
publishDate 2018
dc.date.issued.fl_str_mv 2018
dc.date.accessioned.fl_str_mv 2020-07-08T13:09:57Z
dc.date.available.fl_str_mv 2020-07-08T13:09:57Z
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dc.identifier.citation.fl_str_mv Rsc Advances. Cambridge, v. 8, n. 22, p. 12190-12203, 2018.
dc.identifier.uri.fl_str_mv https://repositorio.unifesp.br/handle/11600/54318
http://dx.doi.org/10.1039/c8ra01528g
dc.identifier.issn.none.fl_str_mv 2046-2069
dc.identifier.file.none.fl_str_mv WOS000431976000036.pdf
dc.identifier.doi.none.fl_str_mv 10.1039/c8ra01528g
dc.identifier.wos.none.fl_str_mv WOS:000431976000036
identifier_str_mv Rsc Advances. Cambridge, v. 8, n. 22, p. 12190-12203, 2018.
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