Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-

Detalhes bibliográficos
Autor(a) principal: Trabuco, Elizeu [UNESP]
Data de Publicação: 1997
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0100-40421997000300002
http://hdl.handle.net/11449/22289
Resumo: The hydrocarbonylation reaction of ethanol with a CO/H2 mixture assisted by Ru(acac)3/iodide was investigated. Bronsted and Lewis acids and iodides salt were used as homogeneous promoters. The etherification reaction was the main reaction under typical acidic conditions of the catalytic system. When a hydrocarbon solvent (toluene) was added to the initial reaction, the alcohol conversion and the carbonylation products were increased. The catalytic activity of the Bronsted acids (conv. EtOH = 71-92%) was higher than that of the Lewis acids promoters (conv. EtOH = 65-85%). The salt present the lower catalytic activity among the promoters used. The long time reaction carried out with ethanol showed an increase of the product selectivity of the homologation and carbonylation reactions while the etherification reaction selectivity decreased. The recycled ether led to 60-65% ethanol conversion to C5 and C6 products. The main catalytic species are H+[Ru(CO)3I3]-, [HRu3(CO)11]- and [HRu(CO)4]-. The first one is active in the carbonylation and homologation reactions of alcohols while the two others take part only in the homologation reaction.
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spelling Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-Ethanol, reactions with co/h2 in the presence of the ru(acac)3/i- catalytic systemEthanolhydrocarbonylationrutheniumcatalysisThe hydrocarbonylation reaction of ethanol with a CO/H2 mixture assisted by Ru(acac)3/iodide was investigated. Bronsted and Lewis acids and iodides salt were used as homogeneous promoters. The etherification reaction was the main reaction under typical acidic conditions of the catalytic system. When a hydrocarbon solvent (toluene) was added to the initial reaction, the alcohol conversion and the carbonylation products were increased. The catalytic activity of the Bronsted acids (conv. EtOH = 71-92%) was higher than that of the Lewis acids promoters (conv. EtOH = 65-85%). The salt present the lower catalytic activity among the promoters used. The long time reaction carried out with ethanol showed an increase of the product selectivity of the homologation and carbonylation reactions while the etherification reaction selectivity decreased. The recycled ether led to 60-65% ethanol conversion to C5 and C6 products. The main catalytic species are H+[Ru(CO)3I3]-, [HRu3(CO)11]- and [HRu(CO)4]-. The first one is active in the carbonylation and homologation reactions of alcohols while the two others take part only in the homologation reaction.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)UNESP IBILCE Depto. de Química e GeociênciasUNESP IBILCE Depto. de Química e GeociênciasSociedade Brasileira de QuímicaUniversidade Estadual Paulista (Unesp)Trabuco, Elizeu [UNESP]2014-05-20T14:03:16Z2014-05-20T14:03:16Z1997-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article233-237application/pdfhttp://dx.doi.org/10.1590/S0100-40421997000300002Química Nova. Sociedade Brasileira de Química, v. 20, n. 3, p. 233-237, 1997.0100-4042http://hdl.handle.net/11449/2228910.1590/S0100-40421997000300002S0100-40421997000300002S0100-40421997000300002.pdf6947341745767693SciELOreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporQuímica Nova0.6460,255info:eu-repo/semantics/openAccess2023-11-11T06:15:41Zoai:repositorio.unesp.br:11449/22289Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-11-11T06:15:41Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-
Ethanol, reactions with co/h2 in the presence of the ru(acac)3/i- catalytic system
title Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-
spellingShingle Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-
Trabuco, Elizeu [UNESP]
Ethanol
hydrocarbonylation
ruthenium
catalysis
title_short Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-
title_full Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-
title_fullStr Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-
title_full_unstemmed Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-
title_sort Reações de Etanol com CO/H2 na Presença do Sistema Catalítico Ru(acac)3/I-
author Trabuco, Elizeu [UNESP]
author_facet Trabuco, Elizeu [UNESP]
author_role author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Trabuco, Elizeu [UNESP]
dc.subject.por.fl_str_mv Ethanol
hydrocarbonylation
ruthenium
catalysis
topic Ethanol
hydrocarbonylation
ruthenium
catalysis
description The hydrocarbonylation reaction of ethanol with a CO/H2 mixture assisted by Ru(acac)3/iodide was investigated. Bronsted and Lewis acids and iodides salt were used as homogeneous promoters. The etherification reaction was the main reaction under typical acidic conditions of the catalytic system. When a hydrocarbon solvent (toluene) was added to the initial reaction, the alcohol conversion and the carbonylation products were increased. The catalytic activity of the Bronsted acids (conv. EtOH = 71-92%) was higher than that of the Lewis acids promoters (conv. EtOH = 65-85%). The salt present the lower catalytic activity among the promoters used. The long time reaction carried out with ethanol showed an increase of the product selectivity of the homologation and carbonylation reactions while the etherification reaction selectivity decreased. The recycled ether led to 60-65% ethanol conversion to C5 and C6 products. The main catalytic species are H+[Ru(CO)3I3]-, [HRu3(CO)11]- and [HRu(CO)4]-. The first one is active in the carbonylation and homologation reactions of alcohols while the two others take part only in the homologation reaction.
publishDate 1997
dc.date.none.fl_str_mv 1997-06-01
2014-05-20T14:03:16Z
2014-05-20T14:03:16Z
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://dx.doi.org/10.1590/S0100-40421997000300002
Química Nova. Sociedade Brasileira de Química, v. 20, n. 3, p. 233-237, 1997.
0100-4042
http://hdl.handle.net/11449/22289
10.1590/S0100-40421997000300002
S0100-40421997000300002
S0100-40421997000300002.pdf
6947341745767693
url http://dx.doi.org/10.1590/S0100-40421997000300002
http://hdl.handle.net/11449/22289
identifier_str_mv Química Nova. Sociedade Brasileira de Química, v. 20, n. 3, p. 233-237, 1997.
0100-4042
10.1590/S0100-40421997000300002
S0100-40421997000300002
S0100-40421997000300002.pdf
6947341745767693
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Química Nova
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0,255
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 233-237
application/pdf
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv SciELO
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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