Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10174/7232 https://doi.org/10.1016/j.apcata.2012.06.036 |
Resumo: | The ring opening reaction of epoxides by alcohols and amines using mesoporous activated carbon as efficient and environmentally friendly heterogeneous catalyst is reported. Carbon xerogels were synthesized by polymerization of resorcinol and formaldehyde. The surface of the activated carbon was oxidized in liquid phase with HNO3 and then functionalized with H2SO4. Chemical and textural characterization by elemental analysis, pHPZC, TPD, BET and XPS indicates that oxidation in liquid phase is effective in the introduction of strong acid groups in the carbon surface. The functionalization with H2SO4 led to more acid functional groups, as expected. The activated carbons were tested in alcoholysis and aminolysis of epoxides, having been obtained excellent results of conversion and selectivity, both over 95%. |
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Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxidesRing openingMesoporous carbonAlcoholysis of epoxidesAminolysis of epoxidesThe ring opening reaction of epoxides by alcohols and amines using mesoporous activated carbon as efficient and environmentally friendly heterogeneous catalyst is reported. Carbon xerogels were synthesized by polymerization of resorcinol and formaldehyde. The surface of the activated carbon was oxidized in liquid phase with HNO3 and then functionalized with H2SO4. Chemical and textural characterization by elemental analysis, pHPZC, TPD, BET and XPS indicates that oxidation in liquid phase is effective in the introduction of strong acid groups in the carbon surface. The functionalization with H2SO4 led to more acid functional groups, as expected. The activated carbons were tested in alcoholysis and aminolysis of epoxides, having been obtained excellent results of conversion and selectivity, both over 95%.Elsevier2013-01-14T10:41:47Z2013-01-142012-10-10T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/7232http://hdl.handle.net/10174/7232https://doi.org/10.1016/j.apcata.2012.06.036porApplied Catalysis A: General, 439– 440 (2012) 24– 30.Departamento de Químicandndjefc@uevora.ptndndndndndnd433Matos, INeves, PCastanheiro, JPerez-Mayoral, EMartin-Aranda, RDuran-Valle, CVital, JBotelho do Rego, AFonseca, Iinfo: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:RCAAP2024-01-03T18:47:19Zoai:dspace.uevora.pt:10174/7232Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:01:49.431379Repositório 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 carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides |
title |
Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides |
spellingShingle |
Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides Matos, I Ring opening Mesoporous carbon Alcoholysis of epoxides Aminolysis of epoxides |
title_short |
Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides |
title_full |
Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides |
title_fullStr |
Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides |
title_full_unstemmed |
Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides |
title_sort |
Mesoporous carbon as an efficient catalyst for alcoholysis and aminolysis of epoxides |
author |
Matos, I |
author_facet |
Matos, I Neves, P Castanheiro, J Perez-Mayoral, E Martin-Aranda, R Duran-Valle, C Vital, J Botelho do Rego, A Fonseca, I |
author_role |
author |
author2 |
Neves, P Castanheiro, J Perez-Mayoral, E Martin-Aranda, R Duran-Valle, C Vital, J Botelho do Rego, A Fonseca, I |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Matos, I Neves, P Castanheiro, J Perez-Mayoral, E Martin-Aranda, R Duran-Valle, C Vital, J Botelho do Rego, A Fonseca, I |
dc.subject.por.fl_str_mv |
Ring opening Mesoporous carbon Alcoholysis of epoxides Aminolysis of epoxides |
topic |
Ring opening Mesoporous carbon Alcoholysis of epoxides Aminolysis of epoxides |
description |
The ring opening reaction of epoxides by alcohols and amines using mesoporous activated carbon as efficient and environmentally friendly heterogeneous catalyst is reported. Carbon xerogels were synthesized by polymerization of resorcinol and formaldehyde. The surface of the activated carbon was oxidized in liquid phase with HNO3 and then functionalized with H2SO4. Chemical and textural characterization by elemental analysis, pHPZC, TPD, BET and XPS indicates that oxidation in liquid phase is effective in the introduction of strong acid groups in the carbon surface. The functionalization with H2SO4 led to more acid functional groups, as expected. The activated carbons were tested in alcoholysis and aminolysis of epoxides, having been obtained excellent results of conversion and selectivity, both over 95%. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-10-10T00:00:00Z 2013-01-14T10:41:47Z 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/10174/7232 http://hdl.handle.net/10174/7232 https://doi.org/10.1016/j.apcata.2012.06.036 |
url |
http://hdl.handle.net/10174/7232 https://doi.org/10.1016/j.apcata.2012.06.036 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
Applied Catalysis A: General, 439– 440 (2012) 24– 30. Departamento de Química nd nd jefc@uevora.pt nd nd 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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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799136501703901184 |