Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template
Main Author: | |
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Publication Date: | 2010 |
Other Authors: | , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10400.21/743 |
Summary: | The present work deals with preliminary studies concerning a new synthesis approach to prepare SAPO materials with AEL structure and evaluate their catalytic behavior in the hydroisomerization of long paraffins. The new SAPO-11 catalysts were synthesized with the help of a small amine (methylamine, MA) added during the preparation of the initial gel. As MA incorporates into the structure of the final materials, it contributes, together with DPA (dipropylamine), to an increase in Si incorporation as isolated species, which results in Bronsted acid sites. Thus, this new and original synthesis strategy allows to obtain materials with enhanced Bronsted acidity when compared with free MA materials. The catalysts were tested in n-decane hydroisomerization (n-decane was used as a model molecule) and confirmed the effect of MA on the acidic properties of the catalysts. The samples synthesized with MA present a higher number of acid sites that increase the catalytic conversion but have a negative effect in the isomerization selectivity, i.e. a more significant amount of cracking products is formed. |
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Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-templaten-Decane hydroisomerizationSAPO-11AcidityMethylamineThe present work deals with preliminary studies concerning a new synthesis approach to prepare SAPO materials with AEL structure and evaluate their catalytic behavior in the hydroisomerization of long paraffins. The new SAPO-11 catalysts were synthesized with the help of a small amine (methylamine, MA) added during the preparation of the initial gel. As MA incorporates into the structure of the final materials, it contributes, together with DPA (dipropylamine), to an increase in Si incorporation as isolated species, which results in Bronsted acid sites. Thus, this new and original synthesis strategy allows to obtain materials with enhanced Bronsted acidity when compared with free MA materials. The catalysts were tested in n-decane hydroisomerization (n-decane was used as a model molecule) and confirmed the effect of MA on the acidic properties of the catalysts. The samples synthesized with MA present a higher number of acid sites that increase the catalytic conversion but have a negative effect in the isomerization selectivity, i.e. a more significant amount of cracking products is formed.SpringerRCIPLBertolo, RaquelFernandes, AugusteRibeiro, FilipaSilva, JoãoMartins, ÂngelaRibeiro, Fernando Ramoa2011-11-30T11:45:10Z2010-022010-02-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.21/743eng1878-5190info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-12T07:13:43Zoai:repositorio.ipl.pt:10400.21/743Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T19:48:03.970922Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template |
title |
Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template |
spellingShingle |
Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template Bertolo, Raquel n-Decane hydroisomerization SAPO-11 Acidity Methylamine |
title_short |
Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template |
title_full |
Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template |
title_fullStr |
Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template |
title_full_unstemmed |
Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template |
title_sort |
Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template |
author |
Bertolo, Raquel |
author_facet |
Bertolo, Raquel Fernandes, Auguste Ribeiro, Filipa Silva, João Martins, Ângela Ribeiro, Fernando Ramoa |
author_role |
author |
author2 |
Fernandes, Auguste Ribeiro, Filipa Silva, João Martins, Ângela Ribeiro, Fernando Ramoa |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
RCIPL |
dc.contributor.author.fl_str_mv |
Bertolo, Raquel Fernandes, Auguste Ribeiro, Filipa Silva, João Martins, Ângela Ribeiro, Fernando Ramoa |
dc.subject.por.fl_str_mv |
n-Decane hydroisomerization SAPO-11 Acidity Methylamine |
topic |
n-Decane hydroisomerization SAPO-11 Acidity Methylamine |
description |
The present work deals with preliminary studies concerning a new synthesis approach to prepare SAPO materials with AEL structure and evaluate their catalytic behavior in the hydroisomerization of long paraffins. The new SAPO-11 catalysts were synthesized with the help of a small amine (methylamine, MA) added during the preparation of the initial gel. As MA incorporates into the structure of the final materials, it contributes, together with DPA (dipropylamine), to an increase in Si incorporation as isolated species, which results in Bronsted acid sites. Thus, this new and original synthesis strategy allows to obtain materials with enhanced Bronsted acidity when compared with free MA materials. The catalysts were tested in n-decane hydroisomerization (n-decane was used as a model molecule) and confirmed the effect of MA on the acidic properties of the catalysts. The samples synthesized with MA present a higher number of acid sites that increase the catalytic conversion but have a negative effect in the isomerization selectivity, i.e. a more significant amount of cracking products is formed. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-02 2010-02-01T00:00:00Z 2011-11-30T11:45:10Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.21/743 |
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http://hdl.handle.net/10400.21/743 |
dc.language.iso.fl_str_mv |
eng |
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eng |
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1878-5190 |
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openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Springer |
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Springer |
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