Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates.
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFOP |
Texto Completo: | http://www.repositorio.ufop.br/handle/123456789/5091 https://doi.org/10.1016/j.apcata.2011.09.032 |
Resumo: | Silica supported H3PW12O40 (PW), the strongest heteropoly acid in the Keggin series, is an active and environmentally friendly solid acid catalyst for liquid-phase esterification of camphene, a renewable biomass-based substrate, with C2, C4 and C6 short-chain fatty acids. The reaction provides isobornyl carboxylates, useful as fragrances, in virtually 100% selectivity and 80–90% yield. The reaction is equilibrium-controlled and occurs under mild conditions with a catalyst turnover number of up to 3000. The use of hydrocarbon solvent prevents PW from leaching to allow easy catalyst recovery. The catalyst can be reused several times without loss of activity and selectivity. |
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Meireles, Augusto Luís Pereira deRocha, Kelly Alessandra da SilvaKozhevnikov, Ivan V.Gusevskaya, Elena Vitalievna2015-04-14T17:57:47Z2015-04-14T17:57:47Z2011MEIRELES, A. L. P. de et al. Esterification of camphene over heterogeneous heteropoly acid catalysts: synthesis of isobornyl carboxylates. Applied Catalysis. A, General, v. 409-410, p. 82-86, 2011. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0926860X11005692>. Acesso em: 02 fev. 2015.0926-860Xhttp://www.repositorio.ufop.br/handle/123456789/5091https://doi.org/10.1016/j.apcata.2011.09.032Silica supported H3PW12O40 (PW), the strongest heteropoly acid in the Keggin series, is an active and environmentally friendly solid acid catalyst for liquid-phase esterification of camphene, a renewable biomass-based substrate, with C2, C4 and C6 short-chain fatty acids. The reaction provides isobornyl carboxylates, useful as fragrances, in virtually 100% selectivity and 80–90% yield. The reaction is equilibrium-controlled and occurs under mild conditions with a catalyst turnover number of up to 3000. The use of hydrocarbon solvent prevents PW from leaching to allow easy catalyst recovery. The catalyst can be reused several times without loss of activity and selectivity.Biomass-based feedstockEsterificationCampheneHeterogeneous acid catalysisHeteropoly acidEsterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleO periódico Applied Catalysis A: General concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 3581340583167.info:eu-repo/semantics/openAccessengreponame:Repositório Institucional da UFOPinstname:Universidade Federal de Ouro Preto (UFOP)instacron:UFOPLICENSElicense.txtlicense.txttext/plain; charset=utf-82636http://www.repositorio.ufop.br/bitstream/123456789/5091/2/license.txtc2ffdd99e58acf69202dff00d361f23aMD52ORIGINALARTIGO_EsterificatioCampheneOver.pdfARTIGO_EsterificatioCampheneOver.pdfapplication/pdf218826http://www.repositorio.ufop.br/bitstream/123456789/5091/1/ARTIGO_EsterificatioCampheneOver.pdffd5e06d557b6b96f72160746c64ea04cMD51123456789/50912019-07-11 09:19:09.466oai:localhost: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Repositório InstitucionalPUBhttp://www.repositorio.ufop.br/oai/requestrepositorio@ufop.edu.bropendoar:32332019-07-11T13:19:09Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP)false |
dc.title.pt_BR.fl_str_mv |
Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates. |
title |
Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates. |
spellingShingle |
Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates. Meireles, Augusto Luís Pereira de Biomass-based feedstock Esterification Camphene Heterogeneous acid catalysis Heteropoly acid |
title_short |
Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates. |
title_full |
Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates. |
title_fullStr |
Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates. |
title_full_unstemmed |
Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates. |
title_sort |
Esterification of camphene over heterogeneous heteropoly acid catalysts : synthesis of isobornyl carboxylates. |
author |
Meireles, Augusto Luís Pereira de |
author_facet |
Meireles, Augusto Luís Pereira de Rocha, Kelly Alessandra da Silva Kozhevnikov, Ivan V. Gusevskaya, Elena Vitalievna |
author_role |
author |
author2 |
Rocha, Kelly Alessandra da Silva Kozhevnikov, Ivan V. Gusevskaya, Elena Vitalievna |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Meireles, Augusto Luís Pereira de Rocha, Kelly Alessandra da Silva Kozhevnikov, Ivan V. Gusevskaya, Elena Vitalievna |
dc.subject.por.fl_str_mv |
Biomass-based feedstock Esterification Camphene Heterogeneous acid catalysis Heteropoly acid |
topic |
Biomass-based feedstock Esterification Camphene Heterogeneous acid catalysis Heteropoly acid |
description |
Silica supported H3PW12O40 (PW), the strongest heteropoly acid in the Keggin series, is an active and environmentally friendly solid acid catalyst for liquid-phase esterification of camphene, a renewable biomass-based substrate, with C2, C4 and C6 short-chain fatty acids. The reaction provides isobornyl carboxylates, useful as fragrances, in virtually 100% selectivity and 80–90% yield. The reaction is equilibrium-controlled and occurs under mild conditions with a catalyst turnover number of up to 3000. The use of hydrocarbon solvent prevents PW from leaching to allow easy catalyst recovery. The catalyst can be reused several times without loss of activity and selectivity. |
publishDate |
2011 |
dc.date.issued.fl_str_mv |
2011 |
dc.date.accessioned.fl_str_mv |
2015-04-14T17:57:47Z |
dc.date.available.fl_str_mv |
2015-04-14T17:57:47Z |
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.citation.fl_str_mv |
MEIRELES, A. L. P. de et al. Esterification of camphene over heterogeneous heteropoly acid catalysts: synthesis of isobornyl carboxylates. Applied Catalysis. A, General, v. 409-410, p. 82-86, 2011. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0926860X11005692>. Acesso em: 02 fev. 2015. |
dc.identifier.uri.fl_str_mv |
http://www.repositorio.ufop.br/handle/123456789/5091 |
dc.identifier.issn.none.fl_str_mv |
0926-860X |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1016/j.apcata.2011.09.032 |
identifier_str_mv |
MEIRELES, A. L. P. de et al. Esterification of camphene over heterogeneous heteropoly acid catalysts: synthesis of isobornyl carboxylates. Applied Catalysis. A, General, v. 409-410, p. 82-86, 2011. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0926860X11005692>. Acesso em: 02 fev. 2015. 0926-860X |
url |
http://www.repositorio.ufop.br/handle/123456789/5091 https://doi.org/10.1016/j.apcata.2011.09.032 |
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eng |
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eng |
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