Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.

Autores
Juárez , Juliana María; Rivoira , Lorena Paola; Gómez Costa, Marcos Bruno; Anunziata , Oscar Alfredo; Beltramone , Andrea Raquel; Anunziata , Oscar Alfredo; Rivoira , Lorena Paola
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión aceptada
Descripción
A nanostructured Carbon CMK-3 modified with Fe by using different sources of Fe, were used in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. Ordered mesoporous carbon CMK-3 was synthesized via a two-step impregnation of the SBA-15 silica mesonanopores with a solution of sucrose using an incipient wetness method. The sucrose–silica composite was heated at 1173 K for 4 h under nitrogen flow. The silica template was dissolved in 5 wt.% hydrofluoric acid in order to remove the silica. The template-free carbon product thus obtained was filtered, washed with deionized water and ethanol and dried. Fe-CMK-3 was prepared by wetness impregnation using FeCl3.6H2O and FeNO3.9H2O as different sources of Fe. A solution of FeCl3.6H2O/ FeNO3.9H2O in ethanol was mixed with the carbon solution at room temperature. The solution was placed in a rotary evaporator to remove excess of ethanol at about 333 K and 60 rpm. Afterwards, the sample was dried at 373 K for 18 h and was thermally treated in a dynamic inert (N2) atmosphere. The percentage of Fe has been 2 wt.% with respect to carbon in the final FeCl3-CMK-3 and FeNO3-CMK 3 material. Porous carbon CMK-3 and the samples modified with Fe were characterized by XRD, FTIR, XPS, BET, TEM and SEM. These studies indicated that it was possible to obtain a CMK-3 replica successfully from SBA-15, using sucrose as a carbon precursor. Wide angle XRD pattern of the sample modified with FeCl3.6H2O implies the formation of the magnetite phase in the silica channels. The surface areas were 1320 m2/g for the CMK-3 and 1240 m2/g and 609 m2/g for FeCl3- CMK-3 and FeNO3-CMK-3, respectively. While the nanomaterial area is significantly smaller with the incorporation of the metal, CMK-3`s characteristic structure is maintained after the metal is within the host, in agreement with the XRD studies. The catalytic activity was improved when the nanoporous carbon was modified with Fe. The sample modified with FeCl3.6H2O was the most active catalyst for ODS of DBT, using hydrogen peroxide (H2O2) as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at a short time in mild conditions.
Fil: Juárez, Juliana María. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Rivoira, Lorena Paola . Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Gómez Costa, Marcos Bruno. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Anunziata, Oscar Alfredo. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Beltramone, Andrea Raquel. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Materia
CMK-3
Iron
ODS of DBT
Nivel de accesibilidad
acceso abierto
Condiciones de uso
Attribution-NonCommercial-NoDerivatives 4.0 International
Repositorio
Repositorio Institucional Abierto (UTN)
Institución
Universidad Tecnológica Nacional
OAI Identificador
oai:ria.utn.edu.ar:20.500.12272/12539
Acceder
id RIAUTN_e153a2fd5f7c354f8aa6f577c6bbb8ac
oai_identifier_str oai:ria.utn.edu.ar:20.500.12272/12539
network_acronym_str RIAUTN
repository_id_str a
network_name_str Repositorio Institucional Abierto (UTN)
spelling Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.Juárez , Juliana MaríaRivoira , Lorena PaolaGómez Costa, Marcos BrunoAnunziata , Oscar AlfredoBeltramone , Andrea RaquelAnunziata , Oscar AlfredoRivoira , Lorena PaolaCMK-3IronODS of DBTA nanostructured Carbon CMK-3 modified with Fe by using different sources of Fe, were used in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. Ordered mesoporous carbon CMK-3 was synthesized via a two-step impregnation of the SBA-15 silica mesonanopores with a solution of sucrose using an incipient wetness method. The sucrose–silica composite was heated at 1173 K for 4 h under nitrogen flow. The silica template was dissolved in 5 wt.% hydrofluoric acid in order to remove the silica. The template-free carbon product thus obtained was filtered, washed with deionized water and ethanol and dried. Fe-CMK-3 was prepared by wetness impregnation using FeCl3.6H2O and FeNO3.9H2O as different sources of Fe. A solution of FeCl3.6H2O/ FeNO3.9H2O in ethanol was mixed with the carbon solution at room temperature. The solution was placed in a rotary evaporator to remove excess of ethanol at about 333 K and 60 rpm. Afterwards, the sample was dried at 373 K for 18 h and was thermally treated in a dynamic inert (N2) atmosphere. The percentage of Fe has been 2 wt.% with respect to carbon in the final FeCl3-CMK-3 and FeNO3-CMK 3 material. Porous carbon CMK-3 and the samples modified with Fe were characterized by XRD, FTIR, XPS, BET, TEM and SEM. These studies indicated that it was possible to obtain a CMK-3 replica successfully from SBA-15, using sucrose as a carbon precursor. Wide angle XRD pattern of the sample modified with FeCl3.6H2O implies the formation of the magnetite phase in the silica channels. The surface areas were 1320 m2/g for the CMK-3 and 1240 m2/g and 609 m2/g for FeCl3- CMK-3 and FeNO3-CMK-3, respectively. While the nanomaterial area is significantly smaller with the incorporation of the metal, CMK-3`s characteristic structure is maintained after the metal is within the host, in agreement with the XRD studies. The catalytic activity was improved when the nanoporous carbon was modified with Fe. The sample modified with FeCl3.6H2O was the most active catalyst for ODS of DBT, using hydrogen peroxide (H2O2) as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at a short time in mild conditions.Fil: Juárez, Juliana María. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Fil: Rivoira, Lorena Paola . Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Fil: Gómez Costa, Marcos Bruno. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Fil: Anunziata, Oscar Alfredo. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Fil: Beltramone, Andrea Raquel. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Univesidsad Tecnológica Nacional.2025-03-27T22:12:22Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articulopdfapplication/pdfXXV International Materials Research Congress.https://hdl.handle.net/20.500.12272/12539enginfo:eu-repo/semantics/openAccessAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/Juárez, Juliana María; Rivoira, Lorena Paola; Gómez Costa, Marcos Bruno; Anunziata, Oscar Alfredo; Beltramone, Andrea Raquel.https://creativecommons.org/licenses/by-nc-nd/4.0/reponame:Repositorio Institucional Abierto (UTN)instname:Universidad Tecnológica Nacional2026-09-24T12:45:53Zoai:ria.utn.edu.ar:20.500.12272/12539instacron:UTNInstitucionalhttp://ria.utn.edu.ar/Universidad públicaNo correspondehttp://ria.utn.edu.ar/oaigestionria@rec.utn.edu.ar; fsuarez@rec.utn.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:a2026-09-24 12:45:53.671Repositorio Institucional Abierto (UTN) - Universidad Tecnológica Nacionalfalse
dc.title.none.fl_str_mv Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
title Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
spellingShingle Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
Juárez , Juliana María
CMK-3
Iron
ODS of DBT
title_short Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
title_full Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
title_fullStr Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
title_full_unstemmed Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
title_sort Synthesis and characterization of a nanoporous carbon CMK-3 modified with iron for the ODS of DBT.
dc.creator.none.fl_str_mv Juárez , Juliana María
Rivoira , Lorena Paola
Gómez Costa, Marcos Bruno
Anunziata , Oscar Alfredo
Beltramone , Andrea Raquel
Anunziata , Oscar Alfredo
Rivoira , Lorena Paola
author Juárez , Juliana María
author_facet Juárez , Juliana María
Rivoira , Lorena Paola
Gómez Costa, Marcos Bruno
Anunziata , Oscar Alfredo
Beltramone , Andrea Raquel
author_role author
author2 Rivoira , Lorena Paola
Gómez Costa, Marcos Bruno
Anunziata , Oscar Alfredo
Beltramone , Andrea Raquel
author2_role author
author
author
author
dc.subject.none.fl_str_mv CMK-3
Iron
ODS of DBT
topic CMK-3
Iron
ODS of DBT
dc.description.none.fl_txt_mv A nanostructured Carbon CMK-3 modified with Fe by using different sources of Fe, were used in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. Ordered mesoporous carbon CMK-3 was synthesized via a two-step impregnation of the SBA-15 silica mesonanopores with a solution of sucrose using an incipient wetness method. The sucrose–silica composite was heated at 1173 K for 4 h under nitrogen flow. The silica template was dissolved in 5 wt.% hydrofluoric acid in order to remove the silica. The template-free carbon product thus obtained was filtered, washed with deionized water and ethanol and dried. Fe-CMK-3 was prepared by wetness impregnation using FeCl3.6H2O and FeNO3.9H2O as different sources of Fe. A solution of FeCl3.6H2O/ FeNO3.9H2O in ethanol was mixed with the carbon solution at room temperature. The solution was placed in a rotary evaporator to remove excess of ethanol at about 333 K and 60 rpm. Afterwards, the sample was dried at 373 K for 18 h and was thermally treated in a dynamic inert (N2) atmosphere. The percentage of Fe has been 2 wt.% with respect to carbon in the final FeCl3-CMK-3 and FeNO3-CMK 3 material. Porous carbon CMK-3 and the samples modified with Fe were characterized by XRD, FTIR, XPS, BET, TEM and SEM. These studies indicated that it was possible to obtain a CMK-3 replica successfully from SBA-15, using sucrose as a carbon precursor. Wide angle XRD pattern of the sample modified with FeCl3.6H2O implies the formation of the magnetite phase in the silica channels. The surface areas were 1320 m2/g for the CMK-3 and 1240 m2/g and 609 m2/g for FeCl3- CMK-3 and FeNO3-CMK-3, respectively. While the nanomaterial area is significantly smaller with the incorporation of the metal, CMK-3`s characteristic structure is maintained after the metal is within the host, in agreement with the XRD studies. The catalytic activity was improved when the nanoporous carbon was modified with Fe. The sample modified with FeCl3.6H2O was the most active catalyst for ODS of DBT, using hydrogen peroxide (H2O2) as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at a short time in mild conditions.
Fil: Juárez, Juliana María. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Rivoira, Lorena Paola . Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Gómez Costa, Marcos Bruno. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Anunziata, Oscar Alfredo. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Beltramone, Andrea Raquel. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
description A nanostructured Carbon CMK-3 modified with Fe by using different sources of Fe, were used in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. Ordered mesoporous carbon CMK-3 was synthesized via a two-step impregnation of the SBA-15 silica mesonanopores with a solution of sucrose using an incipient wetness method. The sucrose–silica composite was heated at 1173 K for 4 h under nitrogen flow. The silica template was dissolved in 5 wt.% hydrofluoric acid in order to remove the silica. The template-free carbon product thus obtained was filtered, washed with deionized water and ethanol and dried. Fe-CMK-3 was prepared by wetness impregnation using FeCl3.6H2O and FeNO3.9H2O as different sources of Fe. A solution of FeCl3.6H2O/ FeNO3.9H2O in ethanol was mixed with the carbon solution at room temperature. The solution was placed in a rotary evaporator to remove excess of ethanol at about 333 K and 60 rpm. Afterwards, the sample was dried at 373 K for 18 h and was thermally treated in a dynamic inert (N2) atmosphere. The percentage of Fe has been 2 wt.% with respect to carbon in the final FeCl3-CMK-3 and FeNO3-CMK 3 material. Porous carbon CMK-3 and the samples modified with Fe were characterized by XRD, FTIR, XPS, BET, TEM and SEM. These studies indicated that it was possible to obtain a CMK-3 replica successfully from SBA-15, using sucrose as a carbon precursor. Wide angle XRD pattern of the sample modified with FeCl3.6H2O implies the formation of the magnetite phase in the silica channels. The surface areas were 1320 m2/g for the CMK-3 and 1240 m2/g and 609 m2/g for FeCl3- CMK-3 and FeNO3-CMK-3, respectively. While the nanomaterial area is significantly smaller with the incorporation of the metal, CMK-3`s characteristic structure is maintained after the metal is within the host, in agreement with the XRD studies. The catalytic activity was improved when the nanoporous carbon was modified with Fe. The sample modified with FeCl3.6H2O was the most active catalyst for ODS of DBT, using hydrogen peroxide (H2O2) as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at a short time in mild conditions.
publishDate 2017
dc.date.none.fl_str_mv 2017
2025-03-27T22:12:22Z
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str acceptedVersion
dc.identifier.none.fl_str_mv XXV International Materials Research Congress.
https://hdl.handle.net/20.500.12272/12539
identifier_str_mv XXV International Materials Research Congress.
url https://hdl.handle.net/20.500.12272/12539
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
Juárez, Juliana María; Rivoira, Lorena Paola; Gómez Costa, Marcos Bruno; Anunziata, Oscar Alfredo; Beltramone, Andrea Raquel.
https://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
Juárez, Juliana María; Rivoira, Lorena Paola; Gómez Costa, Marcos Bruno; Anunziata, Oscar Alfredo; Beltramone, Andrea Raquel.
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.format.none.fl_str_mv pdf
application/pdf
dc.publisher.none.fl_str_mv Univesidsad Tecnológica Nacional.
publisher.none.fl_str_mv Univesidsad Tecnológica Nacional.
dc.source.none.fl_str_mv reponame:Repositorio Institucional Abierto (UTN)
instname:Universidad Tecnológica Nacional
reponame_str Repositorio Institucional Abierto (UTN)
collection Repositorio Institucional Abierto (UTN)
instname_str Universidad Tecnológica Nacional
repository.name.fl_str_mv Repositorio Institucional Abierto (UTN) - Universidad Tecnológica Nacional
repository.mail.fl_str_mv gestionria@rec.utn.edu.ar; fsuarez@rec.utn.edu.ar
_version_ 1877230911131484160
score 13.265058

Publicaciones similares