Pt-Pd-F/AI203catalyst applied in the HDT process.
- Autores
- Balangero, Gerardo Simón; Falcón , Horacio; Beltramone , Andrea Raquel
- Año de publicación
- 2015
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión aceptada
- Descripción
- The inhibiting effect of basic and non-basic nitrogen compounds on the hydrogenation of polyaromatic compounds and on the hydrodesulphurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6DMDBT), has been investigated on Pt-Pd-F/Al2O3 and compared with a commercial NiMo hydrotreating catalyst. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics accurately with physically meaningful and well identified parameter values. Model parameters were tuned by fitting experimental data obtained in a continuous flow reactor at 345°C, 1000 psi pressure and different contact times. Pt-Pd-F/Al2O3 was more active than NiMo catalyst and conversion remained constant during 24 h of TOS. The model was able to correctly interpret all the experimental data. Parameter estimation results showed that phenanthrene and naphthalene inhibited the tetralin hydrogenation rate, whereas naphthalene and tetralin had no appreciable effect on the rate of phenanthrene conversion. This inhibition could be explained by the competitive adsorption and was described in the kinetic model by adsorption terms obtained from the multicomponent experiments. The inhibiting effect of different nitrogen compounds on the polyaromatic hydrogenation was determined. The following nitrogen compounds were investigated in this study: quinoline, 1,2,3,4-tetrahydroquinoline, indole, and indoline. The degree of inhibition was expressed in terms of an apparent adsorption constant derived from the kinetics.The inhibiting effect on the HDS of DBT and 4,6 DBT followed the same trend
Fil: Balangero, Gerardo Simón. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Falcón, Horacio. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
Fil: Beltramone, Andrea Raquel. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina. - Materia
-
Pt-Pd-F/AI203
HDT process - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- Attribution-NonCommercial-NoDerivatives 4.0 International
- Repositorio
.jpg)
- Institución
- Universidad Tecnológica Nacional
- OAI Identificador
- oai:ria.utn.edu.ar:20.500.12272/12611
Ver los metadatos del registro completo
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Pt-Pd-F/AI203catalyst applied in the HDT process.Balangero, Gerardo SimónFalcón , HoracioBeltramone , Andrea RaquelPt-Pd-F/AI203HDT processThe inhibiting effect of basic and non-basic nitrogen compounds on the hydrogenation of polyaromatic compounds and on the hydrodesulphurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6DMDBT), has been investigated on Pt-Pd-F/Al2O3 and compared with a commercial NiMo hydrotreating catalyst. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics accurately with physically meaningful and well identified parameter values. Model parameters were tuned by fitting experimental data obtained in a continuous flow reactor at 345°C, 1000 psi pressure and different contact times. Pt-Pd-F/Al2O3 was more active than NiMo catalyst and conversion remained constant during 24 h of TOS. The model was able to correctly interpret all the experimental data. Parameter estimation results showed that phenanthrene and naphthalene inhibited the tetralin hydrogenation rate, whereas naphthalene and tetralin had no appreciable effect on the rate of phenanthrene conversion. This inhibition could be explained by the competitive adsorption and was described in the kinetic model by adsorption terms obtained from the multicomponent experiments. The inhibiting effect of different nitrogen compounds on the polyaromatic hydrogenation was determined. The following nitrogen compounds were investigated in this study: quinoline, 1,2,3,4-tetrahydroquinoline, indole, and indoline. The degree of inhibition was expressed in terms of an apparent adsorption constant derived from the kinetics.The inhibiting effect on the HDS of DBT and 4,6 DBT followed the same trendFil: Balangero, Gerardo Simón. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Fil: Falcón, Horacio. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Fil: Beltramone, Andrea Raquel. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.Univesidsad Tecnológica Nacional.2025-04-03T19:58:06Z2015info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articulopdfapplication/pdfIMMS-9,17-20 August 2015, Brisbane, Australia.https://hdl.handle.net/20.500.12272/12611enginfo:eu-repo/semantics/openAccessAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/Balangero, Gerardo Simón; Falcón, Horacio; Beltramone, Andrea Raquel.https://creativecommons.org/licenses/by-nc-nd/4.0/reponame:Repositorio Institucional Abierto (UTN)instname:Universidad Tecnológica Nacional2026-09-24T12:45:27Zoai:ria.utn.edu.ar:20.500.12272/12611instacron:UTNInstitucionalhttp://ria.utn.edu.ar/Universidad públicaNo correspondehttp://ria.utn.edu.ar/oaigestionria@rec.utn.edu.ar; fsuarez@rec.utn.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:a2026-09-24 12:45:27.895Repositorio Institucional Abierto (UTN) - Universidad Tecnológica Nacionalfalse |
| dc.title.none.fl_str_mv |
Pt-Pd-F/AI203catalyst applied in the HDT process. |
| title |
Pt-Pd-F/AI203catalyst applied in the HDT process. |
| spellingShingle |
Pt-Pd-F/AI203catalyst applied in the HDT process. Balangero, Gerardo Simón Pt-Pd-F/AI203 HDT process |
| title_short |
Pt-Pd-F/AI203catalyst applied in the HDT process. |
| title_full |
Pt-Pd-F/AI203catalyst applied in the HDT process. |
| title_fullStr |
Pt-Pd-F/AI203catalyst applied in the HDT process. |
| title_full_unstemmed |
Pt-Pd-F/AI203catalyst applied in the HDT process. |
| title_sort |
Pt-Pd-F/AI203catalyst applied in the HDT process. |
| dc.creator.none.fl_str_mv |
Balangero, Gerardo Simón Falcón , Horacio Beltramone , Andrea Raquel |
| author |
Balangero, Gerardo Simón |
| author_facet |
Balangero, Gerardo Simón Falcón , Horacio Beltramone , Andrea Raquel |
| author_role |
author |
| author2 |
Falcón , Horacio Beltramone , Andrea Raquel |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
Pt-Pd-F/AI203 HDT process |
| topic |
Pt-Pd-F/AI203 HDT process |
| dc.description.none.fl_txt_mv |
The inhibiting effect of basic and non-basic nitrogen compounds on the hydrogenation of polyaromatic compounds and on the hydrodesulphurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6DMDBT), has been investigated on Pt-Pd-F/Al2O3 and compared with a commercial NiMo hydrotreating catalyst. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics accurately with physically meaningful and well identified parameter values. Model parameters were tuned by fitting experimental data obtained in a continuous flow reactor at 345°C, 1000 psi pressure and different contact times. Pt-Pd-F/Al2O3 was more active than NiMo catalyst and conversion remained constant during 24 h of TOS. The model was able to correctly interpret all the experimental data. Parameter estimation results showed that phenanthrene and naphthalene inhibited the tetralin hydrogenation rate, whereas naphthalene and tetralin had no appreciable effect on the rate of phenanthrene conversion. This inhibition could be explained by the competitive adsorption and was described in the kinetic model by adsorption terms obtained from the multicomponent experiments. The inhibiting effect of different nitrogen compounds on the polyaromatic hydrogenation was determined. The following nitrogen compounds were investigated in this study: quinoline, 1,2,3,4-tetrahydroquinoline, indole, and indoline. The degree of inhibition was expressed in terms of an apparent adsorption constant derived from the kinetics.The inhibiting effect on the HDS of DBT and 4,6 DBT followed the same trend Fil: Balangero, Gerardo Simón. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina. Fil: Falcón, Horacio. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina. Fil: Beltramone, Andrea Raquel. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina. |
| description |
The inhibiting effect of basic and non-basic nitrogen compounds on the hydrogenation of polyaromatic compounds and on the hydrodesulphurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6DMDBT), has been investigated on Pt-Pd-F/Al2O3 and compared with a commercial NiMo hydrotreating catalyst. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics accurately with physically meaningful and well identified parameter values. Model parameters were tuned by fitting experimental data obtained in a continuous flow reactor at 345°C, 1000 psi pressure and different contact times. Pt-Pd-F/Al2O3 was more active than NiMo catalyst and conversion remained constant during 24 h of TOS. The model was able to correctly interpret all the experimental data. Parameter estimation results showed that phenanthrene and naphthalene inhibited the tetralin hydrogenation rate, whereas naphthalene and tetralin had no appreciable effect on the rate of phenanthrene conversion. This inhibition could be explained by the competitive adsorption and was described in the kinetic model by adsorption terms obtained from the multicomponent experiments. The inhibiting effect of different nitrogen compounds on the polyaromatic hydrogenation was determined. The following nitrogen compounds were investigated in this study: quinoline, 1,2,3,4-tetrahydroquinoline, indole, and indoline. The degree of inhibition was expressed in terms of an apparent adsorption constant derived from the kinetics.The inhibiting effect on the HDS of DBT and 4,6 DBT followed the same trend |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015 2025-04-03T19:58:06Z |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
| format |
article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
IMMS-9,17-20 August 2015, Brisbane, Australia. https://hdl.handle.net/20.500.12272/12611 |
| identifier_str_mv |
IMMS-9,17-20 August 2015, Brisbane, Australia. |
| url |
https://hdl.handle.net/20.500.12272/12611 |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ Balangero, Gerardo Simón; Falcón, Horacio; Beltramone, Andrea Raquel. https://creativecommons.org/licenses/by-nc-nd/4.0/ |
| eu_rights_str_mv |
openAccess |
| rights_invalid_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ Balangero, Gerardo Simón; Falcón, Horacio; Beltramone, Andrea Raquel. https://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.format.none.fl_str_mv |
pdf application/pdf |
| dc.publisher.none.fl_str_mv |
Univesidsad Tecnológica Nacional. |
| publisher.none.fl_str_mv |
Univesidsad Tecnológica Nacional. |
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reponame:Repositorio Institucional Abierto (UTN) instname:Universidad Tecnológica Nacional |
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Repositorio Institucional Abierto (UTN) |
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Universidad Tecnológica Nacional |
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Repositorio Institucional Abierto (UTN) - Universidad Tecnológica Nacional |
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gestionria@rec.utn.edu.ar; fsuarez@rec.utn.edu.ar |
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13.265058 |