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dc.contributor.author
Gómez, Leticia Ester
dc.contributor.author
Múnera Agudelo, John Fernando
dc.contributor.author
Boix, Alicia Viviana
dc.date.available
2023-01-23T13:49:25Z
dc.date.issued
2021-11
dc.identifier.citation
Gómez, Leticia Ester; Múnera Agudelo, John Fernando; Boix, Alicia Viviana; In Situ Raman Spectroscopic Study of Species in Co-MnCeOx Catalysts under COPrOx Reaction Conditions; American Chemical Society; Industrial & Engineering Chemical Research; 60; 51; 11-2021; 18640-18650
dc.identifier.issn
0888-5885
dc.identifier.uri
http://hdl.handle.net/11336/185258
dc.description.abstract
This work is focused on the study of Co-MnCeOx catalysts by in situ Raman spectroscopy, under COPrOx conditions, and aims to establish a correlation with the catalytic results of different catalytic formulations. Through XRD, the catalysts structures were explored, and the oxidation states and relative concentrations of surface species were analyzed by XPS. Catalysts were prepared with Co (10 wt %) and different Mn concentrations. The more active catalyst contains 2.5 wt % of Mn and Co/Ce ≈ 1 (CO conversion 99.5%, 150–180 °C). The Co-Mn2.5Ce catalyst is composed of Co3O4 spinel, Mn inserted in the CeO2 lattice, and probably MnOx dispersed, which remains stable up to 250 °C under reaction conditions. XRD results confirm the crystalline structure of Co3O4 spinel; however, there was no evidence of crystalline phases of MnOx oxides. A lower lattice parameter suggests the insertion of Mnn+ ions in the ceria framework. The catalytic surface is composed of Co3+-Co2+ belonging to Co3O4 and Ce4+ of ceria and Mn4+-Mn3+ species.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
American Chemical Society
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
IN SITU RAMAN
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COPROX REACTION
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OXIDES-BASED CATALYSTS
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Otras Ingeniería Química
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Ingeniería Química
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INGENIERÍAS Y TECNOLOGÍAS
dc.title
In Situ Raman Spectroscopic Study of Species in Co-MnCeOx Catalysts under COPrOx Reaction Conditions
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2022-09-21T23:26:48Z
dc.journal.volume
60
dc.journal.number
51
dc.journal.pagination
18640-18650
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Washington D.C
dc.description.fil
Fil: Gómez, Leticia Ester. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
dc.description.fil
Fil: Múnera Agudelo, John Fernando. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
dc.description.fil
Fil: Boix, Alicia Viviana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
dc.journal.title
Industrial & Engineering Chemical Research
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.iecr.1c02788
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1021/acs.iecr.1c02788
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