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SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene

Bibliographic Details
Main Author: Machado, J
Publication Date: 2012
Other Authors: Castanheiro, J, Matos, I, Ramos, A, Vital, J, Fonseca, I
Format: Article
Language: por
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10174/7225
https://doi.org/10.1016/j.micromeso.2012.07.028
Summary: The acetoxylation of a-pinene was carried out over SBA-15 with sulfonic acid groups. The products of acetoxylation of a-pinene are acetates (a-terpinyl acetate, bornyl acetate and b-fenchyl acetate) and hydrocarbons (camphene, tricyclene, limonene, g-terpinene, terpinolene and a-terpinene). Catalysts with different amount of sulfonic acid groups were prepared. It was observed that the activity increases with increase of the surface area and porous volume. Catalytic stability of the sample that showed the highest activity (C1) was evaluated by performing consecutive batch runs with the same catalyst sample. After the fifth batch, the catalyst exhibited a good initial activity.
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spelling SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pineneAcetoxylationa-pineneSulfonic acid groupsSBA-15The acetoxylation of a-pinene was carried out over SBA-15 with sulfonic acid groups. The products of acetoxylation of a-pinene are acetates (a-terpinyl acetate, bornyl acetate and b-fenchyl acetate) and hydrocarbons (camphene, tricyclene, limonene, g-terpinene, terpinolene and a-terpinene). Catalysts with different amount of sulfonic acid groups were prepared. It was observed that the activity increases with increase of the surface area and porous volume. Catalytic stability of the sample that showed the highest activity (C1) was evaluated by performing consecutive batch runs with the same catalyst sample. After the fifth batch, the catalyst exhibited a good initial activity.Elsevier2013-01-14T10:22:24Z2013-01-142012-11-15T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/7225http://hdl.handle.net/10174/7225https://doi.org/10.1016/j.micromeso.2012.07.028porMicroporous and Mesoporous Materials 163 (2012) 237–242Departamento de Químicandjefc@uevora.ptndndndnd433Machado, JCastanheiro, JMatos, IRamos, AVital, JFonseca, Iinfo: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:RCAAP2024-01-03T18:47:20Zoai:dspace.uevora.pt:10174/7225Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T11:57:09.174543Repositórios 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 SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene
title SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene
spellingShingle SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene
Machado, J
Acetoxylation
a-pinene
Sulfonic acid groups
SBA-15
title_short SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene
title_full SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene
title_fullStr SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene
title_full_unstemmed SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene
title_sort SBA-15 with sulfonic acid groups as a Green Catalyst for the acetoxylation of α-pinene
author Machado, J
author_facet Machado, J
Castanheiro, J
Matos, I
Ramos, A
Vital, J
Fonseca, I
author_role author
author2 Castanheiro, J
Matos, I
Ramos, A
Vital, J
Fonseca, I
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Machado, J
Castanheiro, J
Matos, I
Ramos, A
Vital, J
Fonseca, I
dc.subject.por.fl_str_mv Acetoxylation
a-pinene
Sulfonic acid groups
SBA-15
topic Acetoxylation
a-pinene
Sulfonic acid groups
SBA-15
description The acetoxylation of a-pinene was carried out over SBA-15 with sulfonic acid groups. The products of acetoxylation of a-pinene are acetates (a-terpinyl acetate, bornyl acetate and b-fenchyl acetate) and hydrocarbons (camphene, tricyclene, limonene, g-terpinene, terpinolene and a-terpinene). Catalysts with different amount of sulfonic acid groups were prepared. It was observed that the activity increases with increase of the surface area and porous volume. Catalytic stability of the sample that showed the highest activity (C1) was evaluated by performing consecutive batch runs with the same catalyst sample. After the fifth batch, the catalyst exhibited a good initial activity.
publishDate 2012
dc.date.none.fl_str_mv 2012-11-15T00:00:00Z
2013-01-14T10:22:24Z
2013-01-14
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/10174/7225
http://hdl.handle.net/10174/7225
https://doi.org/10.1016/j.micromeso.2012.07.028
url http://hdl.handle.net/10174/7225
https://doi.org/10.1016/j.micromeso.2012.07.028
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Microporous and Mesoporous Materials 163 (2012) 237–242
Departamento de Química
nd
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:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron:RCAAP
instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron_str RCAAP
institution RCAAP
reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
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