Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes
- Autores
- Rivoira, Lorena Paola; Martinez, Maria Laura; Falcon, Horacio; Beltramone, Andrea Raquel; Campos-Martin, Jose M.; García Fierro, José Luis; Tartaj, Pedro
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Mesocrystals (basically nanostructures showing alignment of nanocrystals well beyond crystal size) are attracting considerable attention for modeling and optimization of functionalities. However, for surface-driven applications (heterogeneous catalysis), only those mesocrystals with excellent textural properties are expected to fulfill their potential. This is especially true for oxidative desulfuration of dibenzothiophenes (hard to desulfurize organosulfur compounds found in fossil fuels). Here, we probe the catalytic activity of anatases for the oxidative desulfuration of dibenzothiophenes under atmospheric pressure and mild temperatures. Specifically, for this study, we have taken advantage of the high stability of the (101) anatase surface to obtain a variety of uniform colloidal mesocrystals (approximately 50 nm) with adequate orientational order and good textural properties (pores around 3-4 nm and surface areas around 200 m2/g). Ultimately, this stability has allowed us to compare the catalytic activity of anatases that expose a high number of aligned single crystal-like surfaces while differing in controllable surface characteristics. Thus, we have established that the type of tetrahedral coordination observed in these anatase mesocrystals is not essential for oxidative desulfuration and that both elimination of sulfates and good textural properties significantly improve the catalytic activity. Furthermore, the most active mesocrystals have been used to model the catalytic reaction in three-(oil-solvent-catalyst) and two-phase (solvent-catalyst) systems. Thus, we have been able to observe that the transfer of DBT from the oil to the solvent phase partially limits the oxidative process and to estimate an apparent activation energy for the oxidative desulfuration reaction of approximately 40 kJ/mol in the two-phase system to avoid mass transfer limitations. Our results clearly establish that (101) anatase mesocrystals with excellent textural properties show adequate stability to withstand several post-treatments without losing their initial mesocrystalline character and therefore could serve as models for catalytic processes different from the one studied here.
Fil: Rivoira, Lorena Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigación y Tecnología Química. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química; Argentina
Fil: Martinez, Maria Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; Argentina
Fil: Falcon, Horacio. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina
Fil: Beltramone, Andrea Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; Argentina
Fil: Campos-Martin, Jose M.. Consejo Superior de Investigaciones Científicas; España
Fil: García Fierro, José Luis. Instituto de Catalisis y Petroleoquimica-csic; España
Fil: Tartaj, Pedro. Consejo Superior de Investigaciones Científicas. Instituto de Catálisis y Petroleoquímica; España - Materia
-
COLLOIDAL
ANATASE
DBT
ODS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/80893
Ver los metadatos del registro completo
id |
CONICETDig_32fc9ac0833557c4c5456cbd0ba3859f |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/80893 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenesRivoira, Lorena PaolaMartinez, Maria LauraFalcon, HoracioBeltramone, Andrea RaquelCampos-Martin, Jose M.García Fierro, José LuisTartaj, PedroCOLLOIDALANATASEDBTODShttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2Mesocrystals (basically nanostructures showing alignment of nanocrystals well beyond crystal size) are attracting considerable attention for modeling and optimization of functionalities. However, for surface-driven applications (heterogeneous catalysis), only those mesocrystals with excellent textural properties are expected to fulfill their potential. This is especially true for oxidative desulfuration of dibenzothiophenes (hard to desulfurize organosulfur compounds found in fossil fuels). Here, we probe the catalytic activity of anatases for the oxidative desulfuration of dibenzothiophenes under atmospheric pressure and mild temperatures. Specifically, for this study, we have taken advantage of the high stability of the (101) anatase surface to obtain a variety of uniform colloidal mesocrystals (approximately 50 nm) with adequate orientational order and good textural properties (pores around 3-4 nm and surface areas around 200 m2/g). Ultimately, this stability has allowed us to compare the catalytic activity of anatases that expose a high number of aligned single crystal-like surfaces while differing in controllable surface characteristics. Thus, we have established that the type of tetrahedral coordination observed in these anatase mesocrystals is not essential for oxidative desulfuration and that both elimination of sulfates and good textural properties significantly improve the catalytic activity. Furthermore, the most active mesocrystals have been used to model the catalytic reaction in three-(oil-solvent-catalyst) and two-phase (solvent-catalyst) systems. Thus, we have been able to observe that the transfer of DBT from the oil to the solvent phase partially limits the oxidative process and to estimate an apparent activation energy for the oxidative desulfuration reaction of approximately 40 kJ/mol in the two-phase system to avoid mass transfer limitations. Our results clearly establish that (101) anatase mesocrystals with excellent textural properties show adequate stability to withstand several post-treatments without losing their initial mesocrystalline character and therefore could serve as models for catalytic processes different from the one studied here.Fil: Rivoira, Lorena Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigación y Tecnología Química. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química; ArgentinaFil: Martinez, Maria Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; ArgentinaFil: Falcon, Horacio. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaFil: Beltramone, Andrea Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; ArgentinaFil: Campos-Martin, Jose M.. Consejo Superior de Investigaciones Científicas; EspañaFil: García Fierro, José Luis. Instituto de Catalisis y Petroleoquimica-csic; EspañaFil: Tartaj, Pedro. Consejo Superior de Investigaciones Científicas. Instituto de Catálisis y Petroleoquímica; EspañaAmerican Chemical Society2017-05-26info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/80893Rivoira, Lorena Paola; Martinez, Maria Laura; Falcon, Horacio; Beltramone, Andrea Raquel; Campos-Martin, Jose M.; et al.; Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes; American Chemical Society; ACS Omega; 2; 5; 26-5-2017; 2351-23592470-1343CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acsomega.7b00307info:eu-repo/semantics/altIdentifier/doi/10.1021/acsomega.7b00307info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:10:03Zoai:ri.conicet.gov.ar:11336/80893instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:10:03.633CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes |
title |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes |
spellingShingle |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes Rivoira, Lorena Paola COLLOIDAL ANATASE DBT ODS |
title_short |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes |
title_full |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes |
title_fullStr |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes |
title_full_unstemmed |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes |
title_sort |
Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes |
dc.creator.none.fl_str_mv |
Rivoira, Lorena Paola Martinez, Maria Laura Falcon, Horacio Beltramone, Andrea Raquel Campos-Martin, Jose M. García Fierro, José Luis Tartaj, Pedro |
author |
Rivoira, Lorena Paola |
author_facet |
Rivoira, Lorena Paola Martinez, Maria Laura Falcon, Horacio Beltramone, Andrea Raquel Campos-Martin, Jose M. García Fierro, José Luis Tartaj, Pedro |
author_role |
author |
author2 |
Martinez, Maria Laura Falcon, Horacio Beltramone, Andrea Raquel Campos-Martin, Jose M. García Fierro, José Luis Tartaj, Pedro |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
COLLOIDAL ANATASE DBT ODS |
topic |
COLLOIDAL ANATASE DBT ODS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.4 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
Mesocrystals (basically nanostructures showing alignment of nanocrystals well beyond crystal size) are attracting considerable attention for modeling and optimization of functionalities. However, for surface-driven applications (heterogeneous catalysis), only those mesocrystals with excellent textural properties are expected to fulfill their potential. This is especially true for oxidative desulfuration of dibenzothiophenes (hard to desulfurize organosulfur compounds found in fossil fuels). Here, we probe the catalytic activity of anatases for the oxidative desulfuration of dibenzothiophenes under atmospheric pressure and mild temperatures. Specifically, for this study, we have taken advantage of the high stability of the (101) anatase surface to obtain a variety of uniform colloidal mesocrystals (approximately 50 nm) with adequate orientational order and good textural properties (pores around 3-4 nm and surface areas around 200 m2/g). Ultimately, this stability has allowed us to compare the catalytic activity of anatases that expose a high number of aligned single crystal-like surfaces while differing in controllable surface characteristics. Thus, we have established that the type of tetrahedral coordination observed in these anatase mesocrystals is not essential for oxidative desulfuration and that both elimination of sulfates and good textural properties significantly improve the catalytic activity. Furthermore, the most active mesocrystals have been used to model the catalytic reaction in three-(oil-solvent-catalyst) and two-phase (solvent-catalyst) systems. Thus, we have been able to observe that the transfer of DBT from the oil to the solvent phase partially limits the oxidative process and to estimate an apparent activation energy for the oxidative desulfuration reaction of approximately 40 kJ/mol in the two-phase system to avoid mass transfer limitations. Our results clearly establish that (101) anatase mesocrystals with excellent textural properties show adequate stability to withstand several post-treatments without losing their initial mesocrystalline character and therefore could serve as models for catalytic processes different from the one studied here. Fil: Rivoira, Lorena Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigación y Tecnología Química. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación y Tecnología Química; Argentina Fil: Martinez, Maria Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; Argentina Fil: Falcon, Horacio. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina Fil: Beltramone, Andrea Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación en Nanociencia y Nanotecnología; Argentina Fil: Campos-Martin, Jose M.. Consejo Superior de Investigaciones Científicas; España Fil: García Fierro, José Luis. Instituto de Catalisis y Petroleoquimica-csic; España Fil: Tartaj, Pedro. Consejo Superior de Investigaciones Científicas. Instituto de Catálisis y Petroleoquímica; España |
description |
Mesocrystals (basically nanostructures showing alignment of nanocrystals well beyond crystal size) are attracting considerable attention for modeling and optimization of functionalities. However, for surface-driven applications (heterogeneous catalysis), only those mesocrystals with excellent textural properties are expected to fulfill their potential. This is especially true for oxidative desulfuration of dibenzothiophenes (hard to desulfurize organosulfur compounds found in fossil fuels). Here, we probe the catalytic activity of anatases for the oxidative desulfuration of dibenzothiophenes under atmospheric pressure and mild temperatures. Specifically, for this study, we have taken advantage of the high stability of the (101) anatase surface to obtain a variety of uniform colloidal mesocrystals (approximately 50 nm) with adequate orientational order and good textural properties (pores around 3-4 nm and surface areas around 200 m2/g). Ultimately, this stability has allowed us to compare the catalytic activity of anatases that expose a high number of aligned single crystal-like surfaces while differing in controllable surface characteristics. Thus, we have established that the type of tetrahedral coordination observed in these anatase mesocrystals is not essential for oxidative desulfuration and that both elimination of sulfates and good textural properties significantly improve the catalytic activity. Furthermore, the most active mesocrystals have been used to model the catalytic reaction in three-(oil-solvent-catalyst) and two-phase (solvent-catalyst) systems. Thus, we have been able to observe that the transfer of DBT from the oil to the solvent phase partially limits the oxidative process and to estimate an apparent activation energy for the oxidative desulfuration reaction of approximately 40 kJ/mol in the two-phase system to avoid mass transfer limitations. Our results clearly establish that (101) anatase mesocrystals with excellent textural properties show adequate stability to withstand several post-treatments without losing their initial mesocrystalline character and therefore could serve as models for catalytic processes different from the one studied here. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-05-26 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/80893 Rivoira, Lorena Paola; Martinez, Maria Laura; Falcon, Horacio; Beltramone, Andrea Raquel; Campos-Martin, Jose M.; et al.; Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes; American Chemical Society; ACS Omega; 2; 5; 26-5-2017; 2351-2359 2470-1343 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/80893 |
identifier_str_mv |
Rivoira, Lorena Paola; Martinez, Maria Laura; Falcon, Horacio; Beltramone, Andrea Raquel; Campos-Martin, Jose M.; et al.; Probing the catalytic activity of sulfate-derived Pristine and post-treated porous TiO2(101) anatase mesocrystals by the oxidative desulfurization of dibenzothiophenes; American Chemical Society; ACS Omega; 2; 5; 26-5-2017; 2351-2359 2470-1343 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acsomega.7b00307 info:eu-repo/semantics/altIdentifier/doi/10.1021/acsomega.7b00307 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
_version_ |
1842270104457314304 |
score |
13.13397 |