Thiophene conversion under mild conditions over a ZSM-5 catalyst
- Autores
- Jaimes, Lisette; Ferreira, María Luján; de Lasa, Hugo
- Año de publicación
- 2009
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Refiners are nowadays actively considering the post-treating FCC gasoline processes as a viable and less costly approach for meeting sulfur environmental regulations. Most promising catalytic desulfurization processes do not require hydrogen addition, including between others the use of zeolites as adsorbents/catalysts. This type of desulfurization leads to the formation of significant amounts of coke, requiring keeping high catalyst activity a continuous twin fluidized bed system (fluidized-bed reactor, fluidized bed regenerator). This study evaluates the catalytic conversion of thiophene and/or thiophene in n-octane mixtures. Catalytic experiments are carried out in the CREC riser simulator under mild conditions, using H-ZSM5 zeolite dispersed in a silica matrix. The experimental results obtained demonstrate a higher selective conversion of thiophene over n-octane. It is shown that thiophene conversion proceeds via ring opening and alkylation yielding H2S, alkyl-thiophenes, benzothiophene, and coke, with no measurable thiophene saturation or dimerization reactions observed. The experimental results are also supported with an extensive thermodynamic analysis that includes all the possible thiophene conversion pathways over zeolites. On this basis and using as a reference the observable measurable species, a reaction network is proposed to represent the thiophene catalytic conversion under the suggested gasoline post treatment conditions.
Fil: Jaimes, Lisette. University of Western Ontario; Canadá
Fil: Ferreira, María Luján. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; Argentina
Fil: de Lasa, Hugo. University of Western Ontario; Canadá - Materia
-
Thiophene
Catalyst Selectivity
Zeolites
Zsm5 - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/42339
Ver los metadatos del registro completo
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Thiophene conversion under mild conditions over a ZSM-5 catalystJaimes, LisetteFerreira, María Lujánde Lasa, HugoThiopheneCatalyst SelectivityZeolitesZsm5https://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2Refiners are nowadays actively considering the post-treating FCC gasoline processes as a viable and less costly approach for meeting sulfur environmental regulations. Most promising catalytic desulfurization processes do not require hydrogen addition, including between others the use of zeolites as adsorbents/catalysts. This type of desulfurization leads to the formation of significant amounts of coke, requiring keeping high catalyst activity a continuous twin fluidized bed system (fluidized-bed reactor, fluidized bed regenerator). This study evaluates the catalytic conversion of thiophene and/or thiophene in n-octane mixtures. Catalytic experiments are carried out in the CREC riser simulator under mild conditions, using H-ZSM5 zeolite dispersed in a silica matrix. The experimental results obtained demonstrate a higher selective conversion of thiophene over n-octane. It is shown that thiophene conversion proceeds via ring opening and alkylation yielding H2S, alkyl-thiophenes, benzothiophene, and coke, with no measurable thiophene saturation or dimerization reactions observed. The experimental results are also supported with an extensive thermodynamic analysis that includes all the possible thiophene conversion pathways over zeolites. On this basis and using as a reference the observable measurable species, a reaction network is proposed to represent the thiophene catalytic conversion under the suggested gasoline post treatment conditions.Fil: Jaimes, Lisette. University of Western Ontario; CanadáFil: Ferreira, María Luján. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; ArgentinaFil: de Lasa, Hugo. University of Western Ontario; CanadáPergamon-Elsevier Science Ltd2009-06-24info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/42339Jaimes, Lisette; Ferreira, María Luján; de Lasa, Hugo; Thiophene conversion under mild conditions over a ZSM-5 catalyst; Pergamon-Elsevier Science Ltd; Chemical Engineering Science; 64; 11; 24-6-2009; 2539-25610009-2509CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.ces.2009.01.070info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0009250909001079info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:10:08Zoai:ri.conicet.gov.ar:11336/42339instacron: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 10:10:08.606CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Thiophene conversion under mild conditions over a ZSM-5 catalyst |
title |
Thiophene conversion under mild conditions over a ZSM-5 catalyst |
spellingShingle |
Thiophene conversion under mild conditions over a ZSM-5 catalyst Jaimes, Lisette Thiophene Catalyst Selectivity Zeolites Zsm5 |
title_short |
Thiophene conversion under mild conditions over a ZSM-5 catalyst |
title_full |
Thiophene conversion under mild conditions over a ZSM-5 catalyst |
title_fullStr |
Thiophene conversion under mild conditions over a ZSM-5 catalyst |
title_full_unstemmed |
Thiophene conversion under mild conditions over a ZSM-5 catalyst |
title_sort |
Thiophene conversion under mild conditions over a ZSM-5 catalyst |
dc.creator.none.fl_str_mv |
Jaimes, Lisette Ferreira, María Luján de Lasa, Hugo |
author |
Jaimes, Lisette |
author_facet |
Jaimes, Lisette Ferreira, María Luján de Lasa, Hugo |
author_role |
author |
author2 |
Ferreira, María Luján de Lasa, Hugo |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Thiophene Catalyst Selectivity Zeolites Zsm5 |
topic |
Thiophene Catalyst Selectivity Zeolites Zsm5 |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.4 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
Refiners are nowadays actively considering the post-treating FCC gasoline processes as a viable and less costly approach for meeting sulfur environmental regulations. Most promising catalytic desulfurization processes do not require hydrogen addition, including between others the use of zeolites as adsorbents/catalysts. This type of desulfurization leads to the formation of significant amounts of coke, requiring keeping high catalyst activity a continuous twin fluidized bed system (fluidized-bed reactor, fluidized bed regenerator). This study evaluates the catalytic conversion of thiophene and/or thiophene in n-octane mixtures. Catalytic experiments are carried out in the CREC riser simulator under mild conditions, using H-ZSM5 zeolite dispersed in a silica matrix. The experimental results obtained demonstrate a higher selective conversion of thiophene over n-octane. It is shown that thiophene conversion proceeds via ring opening and alkylation yielding H2S, alkyl-thiophenes, benzothiophene, and coke, with no measurable thiophene saturation or dimerization reactions observed. The experimental results are also supported with an extensive thermodynamic analysis that includes all the possible thiophene conversion pathways over zeolites. On this basis and using as a reference the observable measurable species, a reaction network is proposed to represent the thiophene catalytic conversion under the suggested gasoline post treatment conditions. Fil: Jaimes, Lisette. University of Western Ontario; Canadá Fil: Ferreira, María Luján. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; Argentina Fil: de Lasa, Hugo. University of Western Ontario; Canadá |
description |
Refiners are nowadays actively considering the post-treating FCC gasoline processes as a viable and less costly approach for meeting sulfur environmental regulations. Most promising catalytic desulfurization processes do not require hydrogen addition, including between others the use of zeolites as adsorbents/catalysts. This type of desulfurization leads to the formation of significant amounts of coke, requiring keeping high catalyst activity a continuous twin fluidized bed system (fluidized-bed reactor, fluidized bed regenerator). This study evaluates the catalytic conversion of thiophene and/or thiophene in n-octane mixtures. Catalytic experiments are carried out in the CREC riser simulator under mild conditions, using H-ZSM5 zeolite dispersed in a silica matrix. The experimental results obtained demonstrate a higher selective conversion of thiophene over n-octane. It is shown that thiophene conversion proceeds via ring opening and alkylation yielding H2S, alkyl-thiophenes, benzothiophene, and coke, with no measurable thiophene saturation or dimerization reactions observed. The experimental results are also supported with an extensive thermodynamic analysis that includes all the possible thiophene conversion pathways over zeolites. On this basis and using as a reference the observable measurable species, a reaction network is proposed to represent the thiophene catalytic conversion under the suggested gasoline post treatment conditions. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-06-24 |
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/11336/42339 Jaimes, Lisette; Ferreira, María Luján; de Lasa, Hugo; Thiophene conversion under mild conditions over a ZSM-5 catalyst; Pergamon-Elsevier Science Ltd; Chemical Engineering Science; 64; 11; 24-6-2009; 2539-2561 0009-2509 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/42339 |
identifier_str_mv |
Jaimes, Lisette; Ferreira, María Luján; de Lasa, Hugo; Thiophene conversion under mild conditions over a ZSM-5 catalyst; Pergamon-Elsevier Science Ltd; Chemical Engineering Science; 64; 11; 24-6-2009; 2539-2561 0009-2509 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ces.2009.01.070 info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0009250909001079 |
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 |
Pergamon-Elsevier Science Ltd |
publisher.none.fl_str_mv |
Pergamon-Elsevier Science Ltd |
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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1842270107912372224 |
score |
13.13397 |