Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation

Bibliographic Details
Main Author: Castanheiro, J
Publication Date: 2008
Other Authors: Guerreiro, L, Fonseca, I, Ramos, A, Vital, J
Format: Article
Language: por
Source: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Download full: http://hdl.handle.net/10174/6558
https://doi.org/10.1016/S0167-2991(08)80132-2
Summary: The methoxylation of a-pinene was studied over sulfonic acid-functionalized mesoporous silica (MCM-41, PMO) at 60ºC. The support functionalization was achieved by the introduction of 3-(mercaptopropyl)trimethoxysilane onto the surface of these materials either by grafting or by co-condensation. The thiol groups were oxidized to SO3H by treatment with H2O2. All the catalysts were active in the studied reaction being the PMO-SO3H-g the best one. Good values of selectivity to a-terpinyl methyl ether were obtained with these catalysts. Catalytic stability of the PMO-SO3H-g was evaluated by performing consecutive batch runs with the same catalyst sample. After the third batch it was observed a stabilisation of the activity.
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spelling Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylationPinenemethoxylationmesoporous silicasulfonic groupsThe methoxylation of a-pinene was studied over sulfonic acid-functionalized mesoporous silica (MCM-41, PMO) at 60ºC. The support functionalization was achieved by the introduction of 3-(mercaptopropyl)trimethoxysilane onto the surface of these materials either by grafting or by co-condensation. The thiol groups were oxidized to SO3H by treatment with H2O2. All the catalysts were active in the studied reaction being the PMO-SO3H-g the best one. Good values of selectivity to a-terpinyl methyl ether were obtained with these catalysts. Catalytic stability of the PMO-SO3H-g was evaluated by performing consecutive batch runs with the same catalyst sample. After the third batch it was observed a stabilisation of the activity.Elsevier2012-12-06T17:55:13Z2012-12-062008-09-02T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/6558http://hdl.handle.net/10174/6558https://doi.org/10.1016/S0167-2991(08)80132-2porStudies in Surface Science and Catalysis, 174 (2008) 1319-1322.Departamento de Químicajefc@uevora.ptndndndnd433Castanheiro, JGuerreiro, LFonseca, IRamos, AVital, Jinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-01-03T18:46:07Zoai:dspace.uevora.pt:10174/6558Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:01:19.767282Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation
title Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation
spellingShingle Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation
Castanheiro, J
Pinene
methoxylation
mesoporous silica
sulfonic groups
title_short Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation
title_full Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation
title_fullStr Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation
title_full_unstemmed Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation
title_sort Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation
author Castanheiro, J
author_facet Castanheiro, J
Guerreiro, L
Fonseca, I
Ramos, A
Vital, J
author_role author
author2 Guerreiro, L
Fonseca, I
Ramos, A
Vital, J
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Castanheiro, J
Guerreiro, L
Fonseca, I
Ramos, A
Vital, J
dc.subject.por.fl_str_mv Pinene
methoxylation
mesoporous silica
sulfonic groups
topic Pinene
methoxylation
mesoporous silica
sulfonic groups
description The methoxylation of a-pinene was studied over sulfonic acid-functionalized mesoporous silica (MCM-41, PMO) at 60ºC. The support functionalization was achieved by the introduction of 3-(mercaptopropyl)trimethoxysilane onto the surface of these materials either by grafting or by co-condensation. The thiol groups were oxidized to SO3H by treatment with H2O2. All the catalysts were active in the studied reaction being the PMO-SO3H-g the best one. Good values of selectivity to a-terpinyl methyl ether were obtained with these catalysts. Catalytic stability of the PMO-SO3H-g was evaluated by performing consecutive batch runs with the same catalyst sample. After the third batch it was observed a stabilisation of the activity.
publishDate 2008
dc.date.none.fl_str_mv 2008-09-02T00:00:00Z
2012-12-06T17:55:13Z
2012-12-06
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/10174/6558
http://hdl.handle.net/10174/6558
https://doi.org/10.1016/S0167-2991(08)80132-2
url http://hdl.handle.net/10174/6558
https://doi.org/10.1016/S0167-2991(08)80132-2
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Studies in Surface Science and Catalysis, 174 (2008) 1319-1322.
Departamento de Química
jefc@uevora.pt
nd
nd
nd
nd
433
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
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