Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol

Autores
Gatti, Martín Nicolás; Mizrahi, Martín D.; Ramallo López, José Martín; Pompeo, Francisco; Santori, Gerardo Fabián; Nichio, Nora N.
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
In previous studies, we prepared Ni catalysts supported on a silica-carbon composite which is selective for obtaining 1,2-propylene glycol (1,2-PG). In order to improve the activity levels of this catalyst, in the present work we propose to modify the catalyst formulation by means of two strategies: on the one hand, to modify the acidity of the catalyst through the functionalization of the carbon support and, on the other hand, to modify the metallic phase by the addition of Zn from a controlled preparation technique (Surface Organometallic Chemistry on Metals), which allows the selective addition of small amounts of modifier on the metallic particles. The functionalization of the SC support at 80 °C employing HNO3 at 60 wt% as oxidizing agent allowed increasing the number of surface acid sites that provide Lewis-type acidity without loss of specific surface area. The addition of 1.1–1.8 wt% of Zn (which corresponds to catalysts NiZn0.2/SC and NiZn0.32/SC) generates the formation of an active site composed of an α-NiZn alloy responsible for the increase in activity. When the addition of Zn is 2.8 wt% (which corresponds to catalyst NiZn0.5/SC), the generation of a new tetragonal phase of β1-NiZn would cause the decrease of catalytic activity. These results indicate that the Zn addition has a more significant effect upon the activity and selectivity on the CeO bond cleavage reactions than the effect of the support acidity upon the dehydration activity.
Facultad de Ciencias Exactas
Materia
Ciencias Exactas
NiZn catalysts, functionalization, bio-propylene glycol, glycerol
Glicerol
Zinc
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/74670

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spelling Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerolGatti, Martín NicolásMizrahi, Martín D.Ramallo López, José MartínPompeo, FranciscoSantori, Gerardo FabiánNichio, Nora N.Ciencias ExactasNiZn catalysts, functionalization, bio-propylene glycol, glycerolGlicerolZincIn previous studies, we prepared Ni catalysts supported on a silica-carbon composite which is selective for obtaining 1,2-propylene glycol (1,2-PG). In order to improve the activity levels of this catalyst, in the present work we propose to modify the catalyst formulation by means of two strategies: on the one hand, to modify the acidity of the catalyst through the functionalization of the carbon support and, on the other hand, to modify the metallic phase by the addition of Zn from a controlled preparation technique (Surface Organometallic Chemistry on Metals), which allows the selective addition of small amounts of modifier on the metallic particles. The functionalization of the SC support at 80 °C employing HNO3 at 60 wt% as oxidizing agent allowed increasing the number of surface acid sites that provide Lewis-type acidity without loss of specific surface area. The addition of 1.1–1.8 wt% of Zn (which corresponds to catalysts NiZn0.2/SC and NiZn0.32/SC) generates the formation of an active site composed of an α-NiZn alloy responsible for the increase in activity. When the addition of Zn is 2.8 wt% (which corresponds to catalyst NiZn0.5/SC), the generation of a new tetragonal phase of β1-NiZn would cause the decrease of catalytic activity. These results indicate that the Zn addition has a more significant effect upon the activity and selectivity on the CeO bond cleavage reactions than the effect of the support acidity upon the dehydration activity.Facultad de Ciencias Exactas2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf24-32http://sedici.unlp.edu.ar/handle/10915/74670enginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2017.08.037info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2026-05-27T11:07:03Zoai:sedici.unlp.edu.ar:10915/74670Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292026-05-27 11:07:04.174SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol
title Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol
spellingShingle Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol
Gatti, Martín Nicolás
Ciencias Exactas
NiZn catalysts, functionalization, bio-propylene glycol, glycerol
Glicerol
Zinc
title_short Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol
title_full Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol
title_fullStr Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol
title_full_unstemmed Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol
title_sort Improvement of the catalytic activity of Ni/SiO<SUB>2</SUB>-C by the modification of the support and Zn addition: Bio-propylene glycol from glycerol
dc.creator.none.fl_str_mv Gatti, Martín Nicolás
Mizrahi, Martín D.
Ramallo López, José Martín
Pompeo, Francisco
Santori, Gerardo Fabián
Nichio, Nora N.
author Gatti, Martín Nicolás
author_facet Gatti, Martín Nicolás
Mizrahi, Martín D.
Ramallo López, José Martín
Pompeo, Francisco
Santori, Gerardo Fabián
Nichio, Nora N.
author_role author
author2 Mizrahi, Martín D.
Ramallo López, José Martín
Pompeo, Francisco
Santori, Gerardo Fabián
Nichio, Nora N.
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
NiZn catalysts, functionalization, bio-propylene glycol, glycerol
Glicerol
Zinc
topic Ciencias Exactas
NiZn catalysts, functionalization, bio-propylene glycol, glycerol
Glicerol
Zinc
dc.description.none.fl_txt_mv In previous studies, we prepared Ni catalysts supported on a silica-carbon composite which is selective for obtaining 1,2-propylene glycol (1,2-PG). In order to improve the activity levels of this catalyst, in the present work we propose to modify the catalyst formulation by means of two strategies: on the one hand, to modify the acidity of the catalyst through the functionalization of the carbon support and, on the other hand, to modify the metallic phase by the addition of Zn from a controlled preparation technique (Surface Organometallic Chemistry on Metals), which allows the selective addition of small amounts of modifier on the metallic particles. The functionalization of the SC support at 80 °C employing HNO3 at 60 wt% as oxidizing agent allowed increasing the number of surface acid sites that provide Lewis-type acidity without loss of specific surface area. The addition of 1.1–1.8 wt% of Zn (which corresponds to catalysts NiZn0.2/SC and NiZn0.32/SC) generates the formation of an active site composed of an α-NiZn alloy responsible for the increase in activity. When the addition of Zn is 2.8 wt% (which corresponds to catalyst NiZn0.5/SC), the generation of a new tetragonal phase of β1-NiZn would cause the decrease of catalytic activity. These results indicate that the Zn addition has a more significant effect upon the activity and selectivity on the CeO bond cleavage reactions than the effect of the support acidity upon the dehydration activity.
Facultad de Ciencias Exactas
description In previous studies, we prepared Ni catalysts supported on a silica-carbon composite which is selective for obtaining 1,2-propylene glycol (1,2-PG). In order to improve the activity levels of this catalyst, in the present work we propose to modify the catalyst formulation by means of two strategies: on the one hand, to modify the acidity of the catalyst through the functionalization of the carbon support and, on the other hand, to modify the metallic phase by the addition of Zn from a controlled preparation technique (Surface Organometallic Chemistry on Metals), which allows the selective addition of small amounts of modifier on the metallic particles. The functionalization of the SC support at 80 °C employing HNO3 at 60 wt% as oxidizing agent allowed increasing the number of surface acid sites that provide Lewis-type acidity without loss of specific surface area. The addition of 1.1–1.8 wt% of Zn (which corresponds to catalysts NiZn0.2/SC and NiZn0.32/SC) generates the formation of an active site composed of an α-NiZn alloy responsible for the increase in activity. When the addition of Zn is 2.8 wt% (which corresponds to catalyst NiZn0.5/SC), the generation of a new tetragonal phase of β1-NiZn would cause the decrease of catalytic activity. These results indicate that the Zn addition has a more significant effect upon the activity and selectivity on the CeO bond cleavage reactions than the effect of the support acidity upon the dehydration activity.
publishDate 2017
dc.date.none.fl_str_mv 2017
dc.type.none.fl_str_mv info:eu-repo/semantics/article
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url http://sedici.unlp.edu.ar/handle/10915/74670
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2017.08.037
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
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