Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos

Detalhes bibliográficos
Autor(a) principal: Soares, João Carlos Serpa
Data de Publicação: 2019
Outros Autores: jcserpa@hotmail.com
Tipo de documento: Tese
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UERJ
Texto Completo: http://www.bdtd.uerj.br/handle/1/18891
Resumo: The aim of this work was to study the production of adipic acid from the oxidation of cyclohexene using H2O2 as oxidizing agent and heterogeneous Keggin type polyoxometalate catalysts. KPW-600, KPMo-600, CsPW-600 and CsPMo-600, were synthesized by ion exchange from the respective heteropolyacids (HPMo-200 and HPW-200) and cesium and potassium carbonates. During the synthesis and in the study of the properties of the catalysts, techniques such as SEM-EDS, XRF, XRD, FTIR, Raman, textural analysis, acid-base titration, TGA and XPS were used. The catalytic tests were performed in a batch type reactor under autogenous pressure at 75°C and magnetic stirring with a catalyst/cyclohexene mass ratio of 0.105 w/w. The Raman and XRD results showed that the Keggin structure of the polyoxometalates can be successfully obtained for both heteropolyacids and heteropolysalts. The XRF results confirmed the insertion of the cations (Cs and K) into the heteropolysalt structure. The acid-base titration proved to be adequate for determining the density of total acid sites, since it was performed in an aqueous environment similar to that of the reaction system. All catalysts completely converted cyclohexene within 24 h of reaction, and all catalysts were selective to adipic acid, yielding the following order of adipic acid yield: KPW-600>KPMo-600>CsPW-600>CsPMo-600. The KPW-600 reuse was performed twice consecutively without affecting the adipic acid yield, even though it was calcined at 600°C in muffle after each test. The heteropolysal KPW-600 presented higher acidity and higher concentration of surface species (W-O-W)/W, fundamental parameters for the oxidation reaction of cyclohexene to adipic acid under the conditions of the catalytic tests performed in this work. A reaction scheme was proposed based on the observations of this work and the literature, considering the main path of adipic acid formation from the cyclohexene epoxide, as well as the undesirable parallel reactions of diol rearrangement and allylic oxidation.
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spelling Araujo, Lucia Regina Raddi dehttp://lattes.cnpq.br/1592062469734844Zotin, Fatima Maria Zanonhttp://lattes.cnpq.br/2398224913573093Santos, Luz Amparo Palaciohttp://lattes.cnpq.br/2277031732030434Henriques, Cristiane Assumpçãohttp://lattes.cnpq.br/8669668633454299Appel, Lúcia Gorenstinhttp://lattes.cnpq.br/0171183220606416Rabello, Carlos René Klotzhttp://lattes.cnpq.br/0876810882404934Borges, Luiz Eduardo Pizarrohttp://lattes.cnpq.br/8756886156388456http://lattes.cnpq.br/3708838349183919Soares, João Carlos Serpajcserpa@hotmail.com2023-01-16T16:58:48Z2019-05-29SOARES, João Carlos Serpa. Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos. 2019. 152 f. Tese (Doutorado em Engenharia Química) - Faculdade de Química, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2019.http://www.bdtd.uerj.br/handle/1/18891The aim of this work was to study the production of adipic acid from the oxidation of cyclohexene using H2O2 as oxidizing agent and heterogeneous Keggin type polyoxometalate catalysts. KPW-600, KPMo-600, CsPW-600 and CsPMo-600, were synthesized by ion exchange from the respective heteropolyacids (HPMo-200 and HPW-200) and cesium and potassium carbonates. During the synthesis and in the study of the properties of the catalysts, techniques such as SEM-EDS, XRF, XRD, FTIR, Raman, textural analysis, acid-base titration, TGA and XPS were used. The catalytic tests were performed in a batch type reactor under autogenous pressure at 75°C and magnetic stirring with a catalyst/cyclohexene mass ratio of 0.105 w/w. The Raman and XRD results showed that the Keggin structure of the polyoxometalates can be successfully obtained for both heteropolyacids and heteropolysalts. The XRF results confirmed the insertion of the cations (Cs and K) into the heteropolysalt structure. The acid-base titration proved to be adequate for determining the density of total acid sites, since it was performed in an aqueous environment similar to that of the reaction system. All catalysts completely converted cyclohexene within 24 h of reaction, and all catalysts were selective to adipic acid, yielding the following order of adipic acid yield: KPW-600>KPMo-600>CsPW-600>CsPMo-600. The KPW-600 reuse was performed twice consecutively without affecting the adipic acid yield, even though it was calcined at 600°C in muffle after each test. The heteropolysal KPW-600 presented higher acidity and higher concentration of surface species (W-O-W)/W, fundamental parameters for the oxidation reaction of cyclohexene to adipic acid under the conditions of the catalytic tests performed in this work. A reaction scheme was proposed based on the observations of this work and the literature, considering the main path of adipic acid formation from the cyclohexene epoxide, as well as the undesirable parallel reactions of diol rearrangement and allylic oxidation.O objetivo deste trabalho foi estudar a produção de ácido adípico a partir da oxidação do cicloexeno utilizando H2O2 como agente oxidante e polioxometalatos do tipo Keggin como catalisadores heterogêneos. Sais de heteropoliácidos (heteropolissais), denominados KPW-600, KPMo-600, CsPW-600 e CsPMo-600, foram sintetizados por troca iônica a partir dos respectivos heteropoliácidos (HPMo-200 e HPW-200) e carbonatos de césio e potássio. Durante a síntese e no estudo das propriedades dos catalisadores, foram utilizadas técnicas como MEV-EDS, FRX, DRX, FTIR, Raman, análise textural, titulação ácido-base, TGA e XPS. Os testes catalíticos foram realizados em um reator do tipo batelada sob pressão autógena, a 75 ºC e agitação magnética, com uma razão mássica catalisador/cicloexeno de 0,105 m/m. Os resultados de Raman e DRX mostraram que a estrutura de Keggin dos polioxometalatos pode ser obtida com sucesso, tanto para os heteropoliácidos quanto para os heteropolissais. Os resultados de FRX confirmaram a inserção dos cátions (Cs e K) na estrutura dos heteropolissais. A titulação ácido-base mostrou-se adequada para a determinação da densidade de sítios ácidos totais, visto que ela foi realizada em ambiente aquoso, semelhante ao do sistema reacional. Todos os catalisadores converteram completamente o cicloexeno em 24 h de reação, e todos os catalisadores foram seletivos ao ácido adípico, obtendo-se a seguinte ordem de rendimento em ácido adípico: KPW-600 > KPMo-600 > CsPW-600 > CsPMo-600. O reuso do KPW foi realizado duas vezes consecutivas sem afetar o rendimento em ácido adípico, mesmo ele sendo calcinado a 600 ºC, em mufla, após cada teste. O heteropolissal KPW-600 apresentou maior acidez e maior concentração de espécies superficiais (W-O-W)/W, parâmetros fundamentais para a reação de oxidação do cicloexeno a ácido adípico nas condições dos testes catalíticos realizados neste trabalho. Um esquema de reação foi proposto baseado nas observações deste trabalho e da literatura, contemplando a rota principal de formação do ácido adípico a partir do epóxido de cicloexeno, bem como as reações paralelas indesejáveis de rearranjo do diol e oxidação alílica.Submitted by Ana Rachel CTC/Q (ana.teles@uerj.br) on 2023-01-16T16:58:48Z No. of bitstreams: 1 Tese - João Carlos Serpa Soares - 2019 - Completa.pdf: 3156113 bytes, checksum: 9ed285dc8fc220f706bbe9c8f9b26ee0 (MD5)Made available in DSpace on 2023-01-16T16:58:48Z (GMT). No. of bitstreams: 1 Tese - João Carlos Serpa Soares - 2019 - Completa.pdf: 3156113 bytes, checksum: 9ed285dc8fc220f706bbe9c8f9b26ee0 (MD5) Previous issue date: 2019-05-29Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade do Estado do Rio de JaneiroPrograma de Pós-Graduação em Engenharia QuímicaUERJBrasilCentro de Tecnologia e Ciências::Instituto de QuímicaCyclohexene oxidationPolyoxometalatesHeteropolisaltsCatalisadoresCatálise heterogeneaOxidaçãoOxidação de cicloexenoPolioxometalatosHeteropolissaisENGENHARIAS::ENGENHARIA QUIMICA::TECNOLOGIA QUIMICASíntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatosSynthesis of adipic acid via heterogeneous catalysis: application of polyoxometalatesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UERJinstname:Universidade do Estado do Rio de Janeiro (UERJ)instacron:UERJORIGINALTese - João Carlos Serpa Soares - 2019 - Completa.pdfTese - João Carlos Serpa Soares - 2019 - Completa.pdfapplication/pdf3156113http://www.bdtd.uerj.br/bitstream/1/18891/2/Tese+-+Jo%C3%A3o+Carlos+Serpa+Soares+-+2019+-+Completa.pdf9ed285dc8fc220f706bbe9c8f9b26ee0MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-82123http://www.bdtd.uerj.br/bitstream/1/18891/1/license.txte5502652da718045d7fcd832b79fca29MD511/188912024-02-27 15:35:57.091oai:www.bdtd.uerj.br:1/18891Tk9UQTogTElDRU7Dh0EgUkVERSBTSVJJVVMKRXN0YSBsaWNlbsOnYSBkZSBleGVtcGxvIMOpIGZvcm5lY2lkYSBhcGVuYXMgcGFyYSBmaW5zIGluZm9ybWF0aXZvcy4KCkxJQ0VOw4dBIERFIERJU1RSSUJVScOHw4NPIE7Dg08tRVhDTFVTSVZBCgpDb20gYSBhcHJlc2VudGHDp8OjbyBkZXN0YSBsaWNlbsOnYSwgdm9jw6ogKG8gYXV0b3IgKGVzKSBvdSBvIHRpdHVsYXIgZG9zIGRpcmVpdG9zIGRlIGF1dG9yKSBjb25jZWRlIMOgIFVuaXZlcnNpZGFkZSAKZG8gRXN0YWRvIGRvIFJpbyBkZSBKYW5laXJvIChVRVJKKSBvIGRpcmVpdG8gbsOjby1leGNsdXNpdm8gZGUgcmVwcm9kdXppciwgIHRyYWR1emlyIChjb25mb3JtZSBkZWZpbmlkbyBhYmFpeG8pLCBlL291IApkaXN0cmlidWlyIGEgc3VhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbyAoaW5jbHVpbmRvIG8gcmVzdW1vKSBwb3IgdG9kbyBvIG11bmRvIG5vIGZvcm1hdG8gaW1wcmVzc28gZSBlbGV0csO0bmljbyBlIAplbSBxdWFscXVlciBtZWlvLCBpbmNsdWluZG8gb3MgZm9ybWF0b3Mgw6F1ZGlvIG91IHbDrWRlby4KClZvY8OqIGNvbmNvcmRhIHF1ZSBhIFVFUkogcG9kZSwgc2VtIGFsdGVyYXIgbyBjb250ZcO6ZG8sIHRyYW5zcG9yIGEgc3VhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbyAKcGFyYSBxdWFscXVlciBtZWlvIG91IGZvcm1hdG8gcGFyYSBmaW5zIGRlIHByZXNlcnZhw6fDo28uCgpWb2PDqiB0YW1iw6ltIGNvbmNvcmRhIHF1ZSBhIFVFUkogcG9kZSBtYW50ZXIgbWFpcyBkZSB1bWEgY8OzcGlhIGEgc3VhIHRlc2Ugb3UgCmRpc3NlcnRhw6fDo28gcGFyYSBmaW5zIGRlIHNlZ3VyYW7Dp2EsIGJhY2stdXAgZSBwcmVzZXJ2YcOnw6NvLgoKVm9jw6ogZGVjbGFyYSBxdWUgYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YcOnw6NvIMOpIG9yaWdpbmFsIGUgcXVlIHZvY8OqIHRlbSBvIHBvZGVyIGRlIGNvbmNlZGVyIG9zIGRpcmVpdG9zIGNvbnRpZG9zIApuZXN0YSBsaWNlbsOnYS4gVm9jw6ogdGFtYsOpbSBkZWNsYXJhIHF1ZSBvIGRlcMOzc2l0byBkYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YcOnw6NvIG7Do28sIHF1ZSBzZWphIGRlIHNldSAKY29uaGVjaW1lbnRvLCBpbmZyaW5nZSBkaXJlaXRvcyBhdXRvcmFpcyBkZSBuaW5ndcOpbS4KCkNhc28gYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YcOnw6NvIGNvbnRlbmhhIG1hdGVyaWFsIHF1ZSB2b2PDqiBuw6NvIHBvc3N1aSBhIHRpdHVsYXJpZGFkZSBkb3MgZGlyZWl0b3MgYXV0b3JhaXMsIHZvY8OqIApkZWNsYXJhIHF1ZSBvYnRldmUgYSBwZXJtaXNzw6NvIGlycmVzdHJpdGEgZG8gZGV0ZW50b3IgZG9zIGRpcmVpdG9zIGF1dG9yYWlzIHBhcmEgY29uY2VkZXIgw6AgVUVSSiBvcyBkaXJlaXRvcyBhcHJlc2VudGFkb3MgbmVzdGEgbGljZW7Dp2EsIGUgcXVlIGVzc2UgbWF0ZXJpYWwgZGUgcHJvcHJpZWRhZGUgZGUgdGVyY2Vpcm9zIGVzdMOhIGNsYXJhbWVudGUgCmlkZW50aWZpY2FkbyBlIHJlY29uaGVjaWRvIG5vIHRleHRvIG91IG5vIGNvbnRlw7pkbyBkYSB0ZXNlIG91IGRpc3NlcnRhw6fDo28gb3JhIGRlcG9zaXRhZGEuCgpDQVNPIEEgVEVTRSBPVSBESVNTRVJUQcOHw4NPIE9SQSBERVBPU0lUQURBIFRFTkhBIFNJRE8gUkVTVUxUQURPIERFIFVNIFBBVFJPQ8ONTklPIE9VIApBUE9JTyBERSBVTUEgQUfDik5DSUEgREUgRk9NRU5UTyBPVSBPVVRSTyBPUkdBTklTTU8gUVVFIE7Dg08gU0VKQSBFU1RBClVOSVZFUlNJREFERSwgVk9Dw4ogREVDTEFSQSBRVUUgUkVTUEVJVE9VIFRPRE9TIEUgUVVBSVNRVUVSIERJUkVJVE9TIERFIFJFVklTw4NPIENPTU8gClRBTULDiU0gQVMgREVNQUlTIE9CUklHQcOHw5VFUyBFWElHSURBUyBQT1IgQ09OVFJBVE8gT1UgQUNPUkRPLgoKQSBVbml2ZXJzaWRhZGUgZG8gRXN0YWRvIGRvIFJpbyBkZSBKYW5laXJvIChVRVJKKSBzZSBjb21wcm9tZXRlIGEgaWRlbnRpZmljYXIgY2xhcmFtZW50ZSBvIHNldSBub21lIChzKSBvdSBvKHMpIG5vbWUocykgZG8ocykgCmRldGVudG9yKGVzKSBkb3MgZGlyZWl0b3MgYXV0b3JhaXMgZGEgdGVzZSBvdSBkaXNzZXJ0YcOnw6NvLCBlIG7Do28gZmFyw6EgcXVhbHF1ZXIgYWx0ZXJhw6fDo28sIGFsw6ltIGRhcXVlbGFzIApjb25jZWRpZGFzIHBvciBlc3RhIGxpY2Vuw6dhLgo=Biblioteca Digital de Teses e Dissertaçõeshttp://www.bdtd.uerj.br/PUBhttps://www.bdtd.uerj.br:8443/oai/requestbdtd.suporte@uerj.bropendoar:29032024-02-27T18:35:57Biblioteca Digital de Teses e Dissertações da UERJ - Universidade do Estado do Rio de Janeiro (UERJ)false
dc.title.por.fl_str_mv Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos
dc.title.alternative.eng.fl_str_mv Synthesis of adipic acid via heterogeneous catalysis: application of polyoxometalates
title Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos
spellingShingle Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos
Soares, João Carlos Serpa
Cyclohexene oxidation
Polyoxometalates
Heteropolisalts
Catalisadores
Catálise heterogenea
Oxidação
Oxidação de cicloexeno
Polioxometalatos
Heteropolissais
ENGENHARIAS::ENGENHARIA QUIMICA::TECNOLOGIA QUIMICA
title_short Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos
title_full Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos
title_fullStr Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos
title_full_unstemmed Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos
title_sort Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos
author Soares, João Carlos Serpa
author_facet Soares, João Carlos Serpa
jcserpa@hotmail.com
author_role author
author2 jcserpa@hotmail.com
author2_role author
dc.contributor.advisor1.fl_str_mv Araujo, Lucia Regina Raddi de
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/1592062469734844
dc.contributor.advisor2.fl_str_mv Zotin, Fatima Maria Zanon
dc.contributor.advisor2Lattes.fl_str_mv http://lattes.cnpq.br/2398224913573093
dc.contributor.referee1.fl_str_mv Santos, Luz Amparo Palacio
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/2277031732030434
dc.contributor.referee2.fl_str_mv Henriques, Cristiane Assumpção
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/8669668633454299
dc.contributor.referee3.fl_str_mv Appel, Lúcia Gorenstin
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/0171183220606416
dc.contributor.referee4.fl_str_mv Rabello, Carlos René Klotz
dc.contributor.referee4Lattes.fl_str_mv http://lattes.cnpq.br/0876810882404934
dc.contributor.referee5.fl_str_mv Borges, Luiz Eduardo Pizarro
dc.contributor.referee5Lattes.fl_str_mv http://lattes.cnpq.br/8756886156388456
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/3708838349183919
dc.contributor.author.fl_str_mv Soares, João Carlos Serpa
jcserpa@hotmail.com
contributor_str_mv Araujo, Lucia Regina Raddi de
Zotin, Fatima Maria Zanon
Santos, Luz Amparo Palacio
Henriques, Cristiane Assumpção
Appel, Lúcia Gorenstin
Rabello, Carlos René Klotz
Borges, Luiz Eduardo Pizarro
dc.subject.eng.fl_str_mv Cyclohexene oxidation
Polyoxometalates
Heteropolisalts
topic Cyclohexene oxidation
Polyoxometalates
Heteropolisalts
Catalisadores
Catálise heterogenea
Oxidação
Oxidação de cicloexeno
Polioxometalatos
Heteropolissais
ENGENHARIAS::ENGENHARIA QUIMICA::TECNOLOGIA QUIMICA
dc.subject.por.fl_str_mv Catalisadores
Catálise heterogenea
Oxidação
Oxidação de cicloexeno
Polioxometalatos
Heteropolissais
dc.subject.cnpq.fl_str_mv ENGENHARIAS::ENGENHARIA QUIMICA::TECNOLOGIA QUIMICA
description The aim of this work was to study the production of adipic acid from the oxidation of cyclohexene using H2O2 as oxidizing agent and heterogeneous Keggin type polyoxometalate catalysts. KPW-600, KPMo-600, CsPW-600 and CsPMo-600, were synthesized by ion exchange from the respective heteropolyacids (HPMo-200 and HPW-200) and cesium and potassium carbonates. During the synthesis and in the study of the properties of the catalysts, techniques such as SEM-EDS, XRF, XRD, FTIR, Raman, textural analysis, acid-base titration, TGA and XPS were used. The catalytic tests were performed in a batch type reactor under autogenous pressure at 75°C and magnetic stirring with a catalyst/cyclohexene mass ratio of 0.105 w/w. The Raman and XRD results showed that the Keggin structure of the polyoxometalates can be successfully obtained for both heteropolyacids and heteropolysalts. The XRF results confirmed the insertion of the cations (Cs and K) into the heteropolysalt structure. The acid-base titration proved to be adequate for determining the density of total acid sites, since it was performed in an aqueous environment similar to that of the reaction system. All catalysts completely converted cyclohexene within 24 h of reaction, and all catalysts were selective to adipic acid, yielding the following order of adipic acid yield: KPW-600>KPMo-600>CsPW-600>CsPMo-600. The KPW-600 reuse was performed twice consecutively without affecting the adipic acid yield, even though it was calcined at 600°C in muffle after each test. The heteropolysal KPW-600 presented higher acidity and higher concentration of surface species (W-O-W)/W, fundamental parameters for the oxidation reaction of cyclohexene to adipic acid under the conditions of the catalytic tests performed in this work. A reaction scheme was proposed based on the observations of this work and the literature, considering the main path of adipic acid formation from the cyclohexene epoxide, as well as the undesirable parallel reactions of diol rearrangement and allylic oxidation.
publishDate 2019
dc.date.issued.fl_str_mv 2019-05-29
dc.date.accessioned.fl_str_mv 2023-01-16T16:58:48Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv SOARES, João Carlos Serpa. Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos. 2019. 152 f. Tese (Doutorado em Engenharia Química) - Faculdade de Química, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2019.
dc.identifier.uri.fl_str_mv http://www.bdtd.uerj.br/handle/1/18891
identifier_str_mv SOARES, João Carlos Serpa. Síntese de ácido adípico via catálise heterogênea: aplicação de polioxometalatos. 2019. 152 f. Tese (Doutorado em Engenharia Química) - Faculdade de Química, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2019.
url http://www.bdtd.uerj.br/handle/1/18891
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language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Universidade do Estado do Rio de Janeiro
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Engenharia Química
dc.publisher.initials.fl_str_mv UERJ
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Centro de Tecnologia e Ciências::Instituto de Química
publisher.none.fl_str_mv Universidade do Estado do Rio de Janeiro
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da UERJ
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