Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst
- Autores
- Beltramone, Andrea Raquel; Resasco, D. E.; Alvarez, W. E.; Choudhary, T. V.
- Año de publicación
- 2008
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Hydrogenation of six model feeds containing three-, two- and one-ring aromatic compounds was investigated to gain insights into the aromatic hydrogenation reaction chemistry over a commercial NiMo catalyst under practical reaction conditions. The hydrogenation reactivity of the aromatic compounds followed the following order: phenanthrene ~ two-ring aromatics >> one-ring aromatic. Comparison with previous studies revealed that the relative reactivity of the aromatic compounds is strongly influenced by the nature of the catalyst. Multiple component feed studies showed that phenanthrene and naphthalene strongly inhibited the tetralin hydrogenation rate, however naphthalene and tetralin had no appreciable effect on phenanthrene conversion. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics with physically meaningful and well identified parameter values. The inhibition was attributed to competitive adsorption and was described in the kinetic model by adsorption terms which were obtained from the multicomponent feed experiments.
Fil: Beltramone, Andrea Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina
Fil: Resasco, D. E.. Oklahoma State University; Estados Unidos
Fil: Alvarez, W. E.. No especifíca;
Fil: Choudhary, T. V.. No especifíca; - Materia
-
Simultaneous Hydrogenation
Multiring Aromatic Compounds
NiMo Catalyst - 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:11336/242175
Ver los metadatos del registro completo
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Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo CatalystBeltramone, Andrea RaquelResasco, D. E.Alvarez, W. E.Choudhary, T. V.Simultaneous HydrogenationMultiring Aromatic CompoundsNiMo Catalysthttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2Hydrogenation of six model feeds containing three-, two- and one-ring aromatic compounds was investigated to gain insights into the aromatic hydrogenation reaction chemistry over a commercial NiMo catalyst under practical reaction conditions. The hydrogenation reactivity of the aromatic compounds followed the following order: phenanthrene ~ two-ring aromatics >> one-ring aromatic. Comparison with previous studies revealed that the relative reactivity of the aromatic compounds is strongly influenced by the nature of the catalyst. Multiple component feed studies showed that phenanthrene and naphthalene strongly inhibited the tetralin hydrogenation rate, however naphthalene and tetralin had no appreciable effect on phenanthrene conversion. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics with physically meaningful and well identified parameter values. The inhibition was attributed to competitive adsorption and was described in the kinetic model by adsorption terms which were obtained from the multicomponent feed experiments.Fil: Beltramone, Andrea Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; ArgentinaFil: Resasco, D. E.. Oklahoma State University; Estados UnidosFil: Alvarez, W. E.. No especifíca;Fil: Choudhary, T. V.. No especifíca;American Chemical Society2008-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/242175Beltramone, Andrea Raquel; Resasco, D. E.; Alvarez, W. E.; Choudhary, T. V.; Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst; American Chemical Society; Industrial & Engineering Chemical Research; 47; 19; 8-2008; 7161-71660888-5885CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/ie8004258info:eu-repo/semantics/altIdentifier/doi/10.1021/ie8004258info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:40:51Zoai:ri.conicet.gov.ar:11336/242175instacron: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:34982025-10-15 14:40:51.651CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst |
title |
Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst |
spellingShingle |
Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst Beltramone, Andrea Raquel Simultaneous Hydrogenation Multiring Aromatic Compounds NiMo Catalyst |
title_short |
Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst |
title_full |
Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst |
title_fullStr |
Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst |
title_full_unstemmed |
Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst |
title_sort |
Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst |
dc.creator.none.fl_str_mv |
Beltramone, Andrea Raquel Resasco, D. E. Alvarez, W. E. Choudhary, T. V. |
author |
Beltramone, Andrea Raquel |
author_facet |
Beltramone, Andrea Raquel Resasco, D. E. Alvarez, W. E. Choudhary, T. V. |
author_role |
author |
author2 |
Resasco, D. E. Alvarez, W. E. Choudhary, T. V. |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Simultaneous Hydrogenation Multiring Aromatic Compounds NiMo Catalyst |
topic |
Simultaneous Hydrogenation Multiring Aromatic Compounds NiMo Catalyst |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.4 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
Hydrogenation of six model feeds containing three-, two- and one-ring aromatic compounds was investigated to gain insights into the aromatic hydrogenation reaction chemistry over a commercial NiMo catalyst under practical reaction conditions. The hydrogenation reactivity of the aromatic compounds followed the following order: phenanthrene ~ two-ring aromatics >> one-ring aromatic. Comparison with previous studies revealed that the relative reactivity of the aromatic compounds is strongly influenced by the nature of the catalyst. Multiple component feed studies showed that phenanthrene and naphthalene strongly inhibited the tetralin hydrogenation rate, however naphthalene and tetralin had no appreciable effect on phenanthrene conversion. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics with physically meaningful and well identified parameter values. The inhibition was attributed to competitive adsorption and was described in the kinetic model by adsorption terms which were obtained from the multicomponent feed experiments. Fil: Beltramone, Andrea Raquel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba; Argentina Fil: Resasco, D. E.. Oklahoma State University; Estados Unidos Fil: Alvarez, W. E.. No especifíca; Fil: Choudhary, T. V.. No especifíca; |
description |
Hydrogenation of six model feeds containing three-, two- and one-ring aromatic compounds was investigated to gain insights into the aromatic hydrogenation reaction chemistry over a commercial NiMo catalyst under practical reaction conditions. The hydrogenation reactivity of the aromatic compounds followed the following order: phenanthrene ~ two-ring aromatics >> one-ring aromatic. Comparison with previous studies revealed that the relative reactivity of the aromatic compounds is strongly influenced by the nature of the catalyst. Multiple component feed studies showed that phenanthrene and naphthalene strongly inhibited the tetralin hydrogenation rate, however naphthalene and tetralin had no appreciable effect on phenanthrene conversion. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics with physically meaningful and well identified parameter values. The inhibition was attributed to competitive adsorption and was described in the kinetic model by adsorption terms which were obtained from the multicomponent feed experiments. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-08 |
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/11336/242175 Beltramone, Andrea Raquel; Resasco, D. E.; Alvarez, W. E.; Choudhary, T. V.; Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst; American Chemical Society; Industrial & Engineering Chemical Research; 47; 19; 8-2008; 7161-7166 0888-5885 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/242175 |
identifier_str_mv |
Beltramone, Andrea Raquel; Resasco, D. E.; Alvarez, W. E.; Choudhary, T. V.; Simultaneous Hydrogenation of Multiring Aromatic Compounds over NiMo Catalyst; American Chemical Society; Industrial & Engineering Chemical Research; 47; 19; 8-2008; 7161-7166 0888-5885 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/ie8004258 info:eu-repo/semantics/altIdentifier/doi/10.1021/ie8004258 |
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 |
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 |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
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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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13.22299 |