Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts

Autores
Busto, Mariana; Vera, Carlos Roman; Grau, Javier Mario
Año de publicación
2011
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
An assessment of the process conditions for the isomerization-cracking of long-chain n-paraffins over commercial Pt/SO42--ZrO 2 catalysts was made. Pretreatment and reaction conditions were optimized with a focus on the maximization of the yield of short, high octane branched paraffins for the gasoline pool. While selectivity was an important issue attention was also paid to the reduction of the yield to gases (C 1-C4). Therefore cracking had to be modulated to produce the correct molecular size adjustment without scission to too much smaller fragments. Skeletal isomerization was to be maximized. The activity in both acid-catalyzed reactions had to be tuned while keeping a stable activity level. The only pretreatment condition assessed was the calcination temperature (screened in the 600-800 °C range). Calcination at 600 °C produced the highest activity level while 700 °C was convenient from the point of view of selectivity. The optimum temperature coincided with the production of the highest concentration of Brönsted acid sites. Regarding the reaction conditions, increasing temperature values augmented the conversion but also increased the cracking. Therefore optimum values were found at a moderate temperature, 225 °C, given the high reactivity of the feed. Space velocity values were analyzed with attention to the liquid C5+ yield, the selectivity to branched isomers and the stability of the catalysts. Best yields to branched naphtha products were obtained at WHSV = 18 h- 1. The H2/hydrocarbon molar ratio was a function of the catalyst coking rate. A value of 10 was enough to attain a stable conversion value. The values of liquid yield as a function of pressure displayed a volcano pattern that was rationalized in terms of a non-classical bifunctional mechanism of reaction. High pressure values increased the concentration of Brönsted acid sites and hence the activity while high pressures enhanced hydrocracking and decreased the liquid yield. The optimal pressure value was 20 atm.
Fil: Busto, Mariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Vera, Carlos Roman. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Grau, Javier Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Materia
CRACKING
GASOLINE
ISOMERIZATION
N-HEXADECANE
REACTION CONDITIONS
SULFATE-ZIRCONIA
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:11336/100839

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network_name_str CONICET Digital (CONICET)
spelling Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalystsBusto, MarianaVera, Carlos RomanGrau, Javier MarioCRACKINGGASOLINEISOMERIZATIONN-HEXADECANEREACTION CONDITIONSSULFATE-ZIRCONIAhttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2An assessment of the process conditions for the isomerization-cracking of long-chain n-paraffins over commercial Pt/SO42--ZrO 2 catalysts was made. Pretreatment and reaction conditions were optimized with a focus on the maximization of the yield of short, high octane branched paraffins for the gasoline pool. While selectivity was an important issue attention was also paid to the reduction of the yield to gases (C 1-C4). Therefore cracking had to be modulated to produce the correct molecular size adjustment without scission to too much smaller fragments. Skeletal isomerization was to be maximized. The activity in both acid-catalyzed reactions had to be tuned while keeping a stable activity level. The only pretreatment condition assessed was the calcination temperature (screened in the 600-800 °C range). Calcination at 600 °C produced the highest activity level while 700 °C was convenient from the point of view of selectivity. The optimum temperature coincided with the production of the highest concentration of Brönsted acid sites. Regarding the reaction conditions, increasing temperature values augmented the conversion but also increased the cracking. Therefore optimum values were found at a moderate temperature, 225 °C, given the high reactivity of the feed. Space velocity values were analyzed with attention to the liquid C5+ yield, the selectivity to branched isomers and the stability of the catalysts. Best yields to branched naphtha products were obtained at WHSV = 18 h- 1. The H2/hydrocarbon molar ratio was a function of the catalyst coking rate. A value of 10 was enough to attain a stable conversion value. The values of liquid yield as a function of pressure displayed a volcano pattern that was rationalized in terms of a non-classical bifunctional mechanism of reaction. High pressure values increased the concentration of Brönsted acid sites and hence the activity while high pressures enhanced hydrocracking and decreased the liquid yield. The optimal pressure value was 20 atm.Fil: Busto, Mariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; ArgentinaFil: Vera, Carlos Roman. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; ArgentinaFil: Grau, Javier Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; ArgentinaElsevier Science2011-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/100839Busto, Mariana; Vera, Carlos Roman; Grau, Javier Mario; Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts; Elsevier Science; Fuel Processing Technology; 92; 9; 9-2011; 1675-16840378-3820CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0378382011001317info:eu-repo/semantics/altIdentifier/doi/10.1016/j.fuproc.2011.04.010info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:47:28Zoai:ri.conicet.gov.ar:11336/100839instacron: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 09:47:28.661CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts
title Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts
spellingShingle Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts
Busto, Mariana
CRACKING
GASOLINE
ISOMERIZATION
N-HEXADECANE
REACTION CONDITIONS
SULFATE-ZIRCONIA
title_short Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts
title_full Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts
title_fullStr Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts
title_full_unstemmed Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts
title_sort Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts
dc.creator.none.fl_str_mv Busto, Mariana
Vera, Carlos Roman
Grau, Javier Mario
author Busto, Mariana
author_facet Busto, Mariana
Vera, Carlos Roman
Grau, Javier Mario
author_role author
author2 Vera, Carlos Roman
Grau, Javier Mario
author2_role author
author
dc.subject.none.fl_str_mv CRACKING
GASOLINE
ISOMERIZATION
N-HEXADECANE
REACTION CONDITIONS
SULFATE-ZIRCONIA
topic CRACKING
GASOLINE
ISOMERIZATION
N-HEXADECANE
REACTION CONDITIONS
SULFATE-ZIRCONIA
purl_subject.fl_str_mv https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv An assessment of the process conditions for the isomerization-cracking of long-chain n-paraffins over commercial Pt/SO42--ZrO 2 catalysts was made. Pretreatment and reaction conditions were optimized with a focus on the maximization of the yield of short, high octane branched paraffins for the gasoline pool. While selectivity was an important issue attention was also paid to the reduction of the yield to gases (C 1-C4). Therefore cracking had to be modulated to produce the correct molecular size adjustment without scission to too much smaller fragments. Skeletal isomerization was to be maximized. The activity in both acid-catalyzed reactions had to be tuned while keeping a stable activity level. The only pretreatment condition assessed was the calcination temperature (screened in the 600-800 °C range). Calcination at 600 °C produced the highest activity level while 700 °C was convenient from the point of view of selectivity. The optimum temperature coincided with the production of the highest concentration of Brönsted acid sites. Regarding the reaction conditions, increasing temperature values augmented the conversion but also increased the cracking. Therefore optimum values were found at a moderate temperature, 225 °C, given the high reactivity of the feed. Space velocity values were analyzed with attention to the liquid C5+ yield, the selectivity to branched isomers and the stability of the catalysts. Best yields to branched naphtha products were obtained at WHSV = 18 h- 1. The H2/hydrocarbon molar ratio was a function of the catalyst coking rate. A value of 10 was enough to attain a stable conversion value. The values of liquid yield as a function of pressure displayed a volcano pattern that was rationalized in terms of a non-classical bifunctional mechanism of reaction. High pressure values increased the concentration of Brönsted acid sites and hence the activity while high pressures enhanced hydrocracking and decreased the liquid yield. The optimal pressure value was 20 atm.
Fil: Busto, Mariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Vera, Carlos Roman. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Grau, Javier Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
description An assessment of the process conditions for the isomerization-cracking of long-chain n-paraffins over commercial Pt/SO42--ZrO 2 catalysts was made. Pretreatment and reaction conditions were optimized with a focus on the maximization of the yield of short, high octane branched paraffins for the gasoline pool. While selectivity was an important issue attention was also paid to the reduction of the yield to gases (C 1-C4). Therefore cracking had to be modulated to produce the correct molecular size adjustment without scission to too much smaller fragments. Skeletal isomerization was to be maximized. The activity in both acid-catalyzed reactions had to be tuned while keeping a stable activity level. The only pretreatment condition assessed was the calcination temperature (screened in the 600-800 °C range). Calcination at 600 °C produced the highest activity level while 700 °C was convenient from the point of view of selectivity. The optimum temperature coincided with the production of the highest concentration of Brönsted acid sites. Regarding the reaction conditions, increasing temperature values augmented the conversion but also increased the cracking. Therefore optimum values were found at a moderate temperature, 225 °C, given the high reactivity of the feed. Space velocity values were analyzed with attention to the liquid C5+ yield, the selectivity to branched isomers and the stability of the catalysts. Best yields to branched naphtha products were obtained at WHSV = 18 h- 1. The H2/hydrocarbon molar ratio was a function of the catalyst coking rate. A value of 10 was enough to attain a stable conversion value. The values of liquid yield as a function of pressure displayed a volcano pattern that was rationalized in terms of a non-classical bifunctional mechanism of reaction. High pressure values increased the concentration of Brönsted acid sites and hence the activity while high pressures enhanced hydrocracking and decreased the liquid yield. The optimal pressure value was 20 atm.
publishDate 2011
dc.date.none.fl_str_mv 2011-09
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/11336/100839
Busto, Mariana; Vera, Carlos Roman; Grau, Javier Mario; Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts; Elsevier Science; Fuel Processing Technology; 92; 9; 9-2011; 1675-1684
0378-3820
CONICET Digital
CONICET
url http://hdl.handle.net/11336/100839
identifier_str_mv Busto, Mariana; Vera, Carlos Roman; Grau, Javier Mario; Optimal process conditions for the isomerization-cracking of long-chain n-paraffins to high octane isomerizate gasoline over Pt/SO4 2--ZrO2 catalysts; Elsevier Science; Fuel Processing Technology; 92; 9; 9-2011; 1675-1684
0378-3820
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0378382011001317
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.fuproc.2011.04.010
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 Elsevier Science
publisher.none.fl_str_mv Elsevier Science
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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