Butanediols production from erythritol on Rh promoted catalyst

Autores
Virgilio, Emanuel Martin; Padro, Cristina; Sad, Maria Eugenia
Año de publicación
2020
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The C-O hydrogenolysis of Erythritol to Butanodiols was studied in aqueous solution at 473 K and 25 bar of H2 using Rh/ReOx/TiO2 and the monometallic Rh/TiO2 and ReOx/TiO2 catalysts. The solids were characterized by temperature programmed reduc-tion (TPR), TEM and XPS. TPR and XPS showed that ReOx species are close to Rh particles leading to reduction at lower temperature than Re on mono-metallic catalyst. However, some segregated Rhenium species were suspected by TPR profile for the bimetallic catalyst and detected by TEM. Re/TiO2 exhibited low activity forming only products from dehydration and epimerization. Although Rh/TiO2 showed high activity (total conversion at 14 h), was more selective to C-C cleavage leading to lower car-bon products. Rh/ReOx/TiO2, showed instead, a good activity and selectivity towards C-O hydrogenolysis route yielding 37.5% of Butanodiols. Activation en-ergy and reaction orders on ERY (0.58) and H2 (0.53) were estimated from experiences made at dif-ferent reaction conditions.
Fil: Virgilio, Emanuel Martin. 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
Fil: Padro, Cristina. 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
Fil: Sad, Maria Eugenia. 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
Materia
BUTANEDIOLS
ERYTHRITOL
HIDROGENOLYSIS
RHODIUM CATALYSTS
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/145732
Acceder
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oai_identifier_str oai:ri.conicet.gov.ar:11336/145732
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Butanediols production from erythritol on Rh promoted catalystVirgilio, Emanuel MartinPadro, CristinaSad, Maria EugeniaBUTANEDIOLSERYTHRITOLHIDROGENOLYSISRHODIUM CATALYSTShttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2The C-O hydrogenolysis of Erythritol to Butanodiols was studied in aqueous solution at 473 K and 25 bar of H2 using Rh/ReOx/TiO2 and the monometallic Rh/TiO2 and ReOx/TiO2 catalysts. The solids were characterized by temperature programmed reduc-tion (TPR), TEM and XPS. TPR and XPS showed that ReOx species are close to Rh particles leading to reduction at lower temperature than Re on mono-metallic catalyst. However, some segregated Rhenium species were suspected by TPR profile for the bimetallic catalyst and detected by TEM. Re/TiO2 exhibited low activity forming only products from dehydration and epimerization. Although Rh/TiO2 showed high activity (total conversion at 14 h), was more selective to C-C cleavage leading to lower car-bon products. Rh/ReOx/TiO2, showed instead, a good activity and selectivity towards C-O hydrogenolysis route yielding 37.5% of Butanodiols. Activation en-ergy and reaction orders on ERY (0.58) and H2 (0.53) were estimated from experiences made at dif-ferent reaction conditions.Fil: Virgilio, Emanuel Martin. 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"; ArgentinaFil: Padro, Cristina. 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"; ArgentinaFil: Sad, Maria Eugenia. 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"; ArgentinaPlanta Piloto de Ingeniería Química2020-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/145732Virgilio, Emanuel Martin; Padro, Cristina; Sad, Maria Eugenia; Butanediols production from erythritol on Rh promoted catalyst; Planta Piloto de Ingeniería Química; Latin American Applied Research; 50; 2; 4-2020; 89-940327-07931851-8796CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://laar.plapiqui.edu.ar/OJS/index.php/laar/article/view/353info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:45:18Zoai:ri.conicet.gov.ar:11336/145732instacron: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:34982025-10-22 11:45:18.628CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Butanediols production from erythritol on Rh promoted catalyst
title Butanediols production from erythritol on Rh promoted catalyst
spellingShingle Butanediols production from erythritol on Rh promoted catalyst
Virgilio, Emanuel Martin
BUTANEDIOLS
ERYTHRITOL
HIDROGENOLYSIS
RHODIUM CATALYSTS
title_short Butanediols production from erythritol on Rh promoted catalyst
title_full Butanediols production from erythritol on Rh promoted catalyst
title_fullStr Butanediols production from erythritol on Rh promoted catalyst
title_full_unstemmed Butanediols production from erythritol on Rh promoted catalyst
title_sort Butanediols production from erythritol on Rh promoted catalyst
dc.creator.none.fl_str_mv Virgilio, Emanuel Martin
Padro, Cristina
Sad, Maria Eugenia
author Virgilio, Emanuel Martin
author_facet Virgilio, Emanuel Martin
Padro, Cristina
Sad, Maria Eugenia
author_role author
author2 Padro, Cristina
Sad, Maria Eugenia
author2_role author
author
dc.subject.none.fl_str_mv BUTANEDIOLS
ERYTHRITOL
HIDROGENOLYSIS
RHODIUM CATALYSTS
topic BUTANEDIOLS
ERYTHRITOL
HIDROGENOLYSIS
RHODIUM CATALYSTS
purl_subject.fl_str_mv https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv The C-O hydrogenolysis of Erythritol to Butanodiols was studied in aqueous solution at 473 K and 25 bar of H2 using Rh/ReOx/TiO2 and the monometallic Rh/TiO2 and ReOx/TiO2 catalysts. The solids were characterized by temperature programmed reduc-tion (TPR), TEM and XPS. TPR and XPS showed that ReOx species are close to Rh particles leading to reduction at lower temperature than Re on mono-metallic catalyst. However, some segregated Rhenium species were suspected by TPR profile for the bimetallic catalyst and detected by TEM. Re/TiO2 exhibited low activity forming only products from dehydration and epimerization. Although Rh/TiO2 showed high activity (total conversion at 14 h), was more selective to C-C cleavage leading to lower car-bon products. Rh/ReOx/TiO2, showed instead, a good activity and selectivity towards C-O hydrogenolysis route yielding 37.5% of Butanodiols. Activation en-ergy and reaction orders on ERY (0.58) and H2 (0.53) were estimated from experiences made at dif-ferent reaction conditions.
Fil: Virgilio, Emanuel Martin. 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
Fil: Padro, Cristina. 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
Fil: Sad, Maria Eugenia. 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
description The C-O hydrogenolysis of Erythritol to Butanodiols was studied in aqueous solution at 473 K and 25 bar of H2 using Rh/ReOx/TiO2 and the monometallic Rh/TiO2 and ReOx/TiO2 catalysts. The solids were characterized by temperature programmed reduc-tion (TPR), TEM and XPS. TPR and XPS showed that ReOx species are close to Rh particles leading to reduction at lower temperature than Re on mono-metallic catalyst. However, some segregated Rhenium species were suspected by TPR profile for the bimetallic catalyst and detected by TEM. Re/TiO2 exhibited low activity forming only products from dehydration and epimerization. Although Rh/TiO2 showed high activity (total conversion at 14 h), was more selective to C-C cleavage leading to lower car-bon products. Rh/ReOx/TiO2, showed instead, a good activity and selectivity towards C-O hydrogenolysis route yielding 37.5% of Butanodiols. Activation en-ergy and reaction orders on ERY (0.58) and H2 (0.53) were estimated from experiences made at dif-ferent reaction conditions.
publishDate 2020
dc.date.none.fl_str_mv 2020-04
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/11336/145732
Virgilio, Emanuel Martin; Padro, Cristina; Sad, Maria Eugenia; Butanediols production from erythritol on Rh promoted catalyst; Planta Piloto de Ingeniería Química; Latin American Applied Research; 50; 2; 4-2020; 89-94
0327-0793
1851-8796
CONICET Digital
CONICET
url http://hdl.handle.net/11336/145732
identifier_str_mv Virgilio, Emanuel Martin; Padro, Cristina; Sad, Maria Eugenia; Butanediols production from erythritol on Rh promoted catalyst; Planta Piloto de Ingeniería Química; Latin American Applied Research; 50; 2; 4-2020; 89-94
0327-0793
1851-8796
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://laar.plapiqui.edu.ar/OJS/index.php/laar/article/view/353
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Planta Piloto de Ingeniería Química
publisher.none.fl_str_mv Planta Piloto de Ingeniería Química
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
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score 12.982451

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