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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/242175

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network_name_str CONICET Digital (CONICET)
spelling 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
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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