Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups

Detalhes bibliográficos
Autor(a) principal: Pito, D
Data de Publicação: 2009
Outros Autores: Fonseca, I, Ramos, A, Vital, J, Castanheiro, José
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://hdl.handle.net/10174/6270
https://doi.org/10.1016/j.cej.2008.11.020
Resumo: The methoxylation of a -pinene was studied using poly(vinyl alcohol) (PVA) containing sulfonic acid groups as catalysts. These groupswere introduced by the direct reaction between –OH groups of PVA and sulfosuccinic acid (SSA). Poly(vinyl alcohol) catalysts were prepared using sulfosuccinic acid by varying the amount of SSA (5–40 mol%). It was observed that the amount of acid sites increases with amount of SSA. It was also observed that the diffusivity of a -pinene through the polymeric catalysts decreases with the increase of crosslinking degree. The conversion of a-pinene increases when the amount of sulfosuccinic acid used in the polymer crosslinking is increased from 5% to 40%. However, when the crosslinking degree increases from 20% to 40%, the conversion of a-pinene increases only slightly. Good values of selectivity to a -terpinyl methyl ether (about 60% near complete conversion) were obtained over poly(vinyl alcohol) with sulfonic acid groups. Catalytic stability of the PVA SSA20 was evaluated by performing consecutive batch runs with the same catalyst sample. After the third batch it was observed a stabilisation of the initial activity. A kinetic model was developed assuming that the a-pinene is consumed according to the parallel reaction network. Since the concentration profiles of the reagent and the products do not exhibit any pronounced initial inductive period, the external and internal diffusion of the reagents and products on the catalyst were not considered. It was observed that the kinetic model fits experimental concentration data quite well.
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spelling Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groupsMethoxylationPVASulfonic acid groupsa-pineneThe methoxylation of a -pinene was studied using poly(vinyl alcohol) (PVA) containing sulfonic acid groups as catalysts. These groupswere introduced by the direct reaction between –OH groups of PVA and sulfosuccinic acid (SSA). Poly(vinyl alcohol) catalysts were prepared using sulfosuccinic acid by varying the amount of SSA (5–40 mol%). It was observed that the amount of acid sites increases with amount of SSA. It was also observed that the diffusivity of a -pinene through the polymeric catalysts decreases with the increase of crosslinking degree. The conversion of a-pinene increases when the amount of sulfosuccinic acid used in the polymer crosslinking is increased from 5% to 40%. However, when the crosslinking degree increases from 20% to 40%, the conversion of a-pinene increases only slightly. Good values of selectivity to a -terpinyl methyl ether (about 60% near complete conversion) were obtained over poly(vinyl alcohol) with sulfonic acid groups. Catalytic stability of the PVA SSA20 was evaluated by performing consecutive batch runs with the same catalyst sample. After the third batch it was observed a stabilisation of the initial activity. A kinetic model was developed assuming that the a-pinene is consumed according to the parallel reaction network. Since the concentration profiles of the reagent and the products do not exhibit any pronounced initial inductive period, the external and internal diffusion of the reagents and products on the catalyst were not considered. It was observed that the kinetic model fits experimental concentration data quite well.Elsevier2012-12-03T22:49:33Z2012-12-032009-04-15T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/6270http://hdl.handle.net/10174/6270https://doi.org/10.1016/j.cej.2008.11.020porChemical Engineering Journal 147 (2009) 302–306Departamento de Químicandndndndjefc@uevora.pt433Pito, DFonseca, IRamos, AVital, JCastanheiro, Joséinfo: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:RCAAP2024-01-03T18:45:53Zoai:dspace.uevora.pt:10174/6270Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T11:56:04.937294Repositórios 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 Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups
title Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups
spellingShingle Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups
Pito, D
Methoxylation
PVA
Sulfonic acid groups
a-pinene
title_short Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups
title_full Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups
title_fullStr Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups
title_full_unstemmed Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups
title_sort Methoxylation of -pinene over poly(vinyl alcohol) containing sulfonic acid groups
author Pito, D
author_facet Pito, D
Fonseca, I
Ramos, A
Vital, J
Castanheiro, José
author_role author
author2 Fonseca, I
Ramos, A
Vital, J
Castanheiro, José
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Pito, D
Fonseca, I
Ramos, A
Vital, J
Castanheiro, José
dc.subject.por.fl_str_mv Methoxylation
PVA
Sulfonic acid groups
a-pinene
topic Methoxylation
PVA
Sulfonic acid groups
a-pinene
description The methoxylation of a -pinene was studied using poly(vinyl alcohol) (PVA) containing sulfonic acid groups as catalysts. These groupswere introduced by the direct reaction between –OH groups of PVA and sulfosuccinic acid (SSA). Poly(vinyl alcohol) catalysts were prepared using sulfosuccinic acid by varying the amount of SSA (5–40 mol%). It was observed that the amount of acid sites increases with amount of SSA. It was also observed that the diffusivity of a -pinene through the polymeric catalysts decreases with the increase of crosslinking degree. The conversion of a-pinene increases when the amount of sulfosuccinic acid used in the polymer crosslinking is increased from 5% to 40%. However, when the crosslinking degree increases from 20% to 40%, the conversion of a-pinene increases only slightly. Good values of selectivity to a -terpinyl methyl ether (about 60% near complete conversion) were obtained over poly(vinyl alcohol) with sulfonic acid groups. Catalytic stability of the PVA SSA20 was evaluated by performing consecutive batch runs with the same catalyst sample. After the third batch it was observed a stabilisation of the initial activity. A kinetic model was developed assuming that the a-pinene is consumed according to the parallel reaction network. Since the concentration profiles of the reagent and the products do not exhibit any pronounced initial inductive period, the external and internal diffusion of the reagents and products on the catalyst were not considered. It was observed that the kinetic model fits experimental concentration data quite well.
publishDate 2009
dc.date.none.fl_str_mv 2009-04-15T00:00:00Z
2012-12-03T22:49:33Z
2012-12-03
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/10174/6270
http://hdl.handle.net/10174/6270
https://doi.org/10.1016/j.cej.2008.11.020
url http://hdl.handle.net/10174/6270
https://doi.org/10.1016/j.cej.2008.11.020
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Chemical Engineering Journal 147 (2009) 302–306
Departamento de Química
nd
nd
nd
nd
jefc@uevora.pt
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
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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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