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Hydroisomerization of n-decane over SAPO-11 catalysts synthesized with methylamine as co-template

Bibliographic Details
Main Author: Bertolo, Raquel
Publication Date: 2010
Other Authors: Fernandes, Auguste, Ribeiro, Filipa, Silva, João, Martins, Ângela, Ribeiro, Fernando Ramoa
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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spelling 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
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.21/743
url http://hdl.handle.net/10400.21/743
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1878-5190
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dc.publisher.none.fl_str_mv Springer
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