Catalisadores heterogêneos aplicados à reação de Biginelli
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFG |
dARK ID: | ark:/38995/0013000008bsk |
Texto Completo: | http://repositorio.bc.ufg.br/tede/handle/tede/7110 |
Resumo: | The Biginelli reaction involves the cyclocondensation of three reagents in the presence of an acid catalyst to obtain dihydropyrimidinones (DHPMs).This compound and its analogues are widely known to possess various pharmacological properties, such as antibacterial, antiinflammatory, antifungal, antiviral, anticancer and antihypertensive. This reaction is usually carried out via homogeneous catalysis, which presents, however, some difficulties, such as regeneration of the catalyst and difficult separation of the final product, thus becoming an obstacle for industrial use. In the present work, it was proposed the use of two classes of heterogeneous catalysts, which are: metal oxides and acid carbons in order to achieve attractive characteristics in the Biginelli reaction, as a reduction of reaction time and increase in yield. The acidic carbons were prepared by carbonization by impregnation of agroindustrial residues with sulfuric acid at a temperature of 200 °C in the mass ratio of 1:10 (precursor: H2SO4) for 6 h. The pure HY-340 and Nb2O5 were both tested and chemically treated with a solution of 30% sulfuric acid. The catalysts were characterized by X-ray diffraction (XRD), infrared spectroscopy (FTIR), thermogravimetric (TG), differential thermal analysis (DTA), textural adsorption/desorption analysis of N2 at -196 °C and desorption of ammonia at programmed temperature (DTP-NH3), scanning electron microscopy (SEM) and X-ray Dispersive Energy Spectrometry (EDS). The contents of C, N, O and S present on the surface of the coals were quantified by Elementary Analysis (CHNS-O). Exploratory catalytic tests were carried out to define the best experimental conditions of solvent, temperature, molar ratio and amount of catalyst. The results obtained allowed to establish the best experimental conditions for the realization of the Biginelli reaction. Thus, the following parameters were adopted to evaluate the performance of the different catalysts. These are: 5% catalyst content (by mass), molar ratio of 1 Benzaldehyde: 1,5 Methyl acetoacetate: 1,5 Urea, without solvent and temperature of 130 °C. The best catalyst was Nb2O5 treated with sulfuric acid, whereby a yield of 94% of dihydropyrimidinones (DHPMs). |
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Alonso, Christian Gonçalveshttp://lattes.cnpq.br/7285754665946583Oliveira, Guilherme Roberto dehttp://lattes.cnpq.br/8239498431579015Alonso, Christian Gonçalveshttp://lattes.cnpq.br/7285754665946583Oliveira, Guilherme Roberto dehttp://lattes.cnpq.br/8239498431579015Andrade, Fabiano Molinos deArroyo, Pedro Augustohttp://lattes.cnpq.br/3262057595733430Nascimento, Letícia Gomes do2017-04-10T11:16:14Z2017-03-07NASCIMENTO, L. G. Catalisadores heterogêneos aplicados à reação de Biginelli. 2017. 88 f. Dissertação (Mestrado em Engenharia Química) - Universidade Federal de Goiás, Goiânia, 2017.http://repositorio.bc.ufg.br/tede/handle/tede/7110ark:/38995/0013000008bskThe Biginelli reaction involves the cyclocondensation of three reagents in the presence of an acid catalyst to obtain dihydropyrimidinones (DHPMs).This compound and its analogues are widely known to possess various pharmacological properties, such as antibacterial, antiinflammatory, antifungal, antiviral, anticancer and antihypertensive. This reaction is usually carried out via homogeneous catalysis, which presents, however, some difficulties, such as regeneration of the catalyst and difficult separation of the final product, thus becoming an obstacle for industrial use. In the present work, it was proposed the use of two classes of heterogeneous catalysts, which are: metal oxides and acid carbons in order to achieve attractive characteristics in the Biginelli reaction, as a reduction of reaction time and increase in yield. The acidic carbons were prepared by carbonization by impregnation of agroindustrial residues with sulfuric acid at a temperature of 200 °C in the mass ratio of 1:10 (precursor: H2SO4) for 6 h. The pure HY-340 and Nb2O5 were both tested and chemically treated with a solution of 30% sulfuric acid. The catalysts were characterized by X-ray diffraction (XRD), infrared spectroscopy (FTIR), thermogravimetric (TG), differential thermal analysis (DTA), textural adsorption/desorption analysis of N2 at -196 °C and desorption of ammonia at programmed temperature (DTP-NH3), scanning electron microscopy (SEM) and X-ray Dispersive Energy Spectrometry (EDS). The contents of C, N, O and S present on the surface of the coals were quantified by Elementary Analysis (CHNS-O). Exploratory catalytic tests were carried out to define the best experimental conditions of solvent, temperature, molar ratio and amount of catalyst. The results obtained allowed to establish the best experimental conditions for the realization of the Biginelli reaction. Thus, the following parameters were adopted to evaluate the performance of the different catalysts. These are: 5% catalyst content (by mass), molar ratio of 1 Benzaldehyde: 1,5 Methyl acetoacetate: 1,5 Urea, without solvent and temperature of 130 °C. The best catalyst was Nb2O5 treated with sulfuric acid, whereby a yield of 94% of dihydropyrimidinones (DHPMs).A reação de Biginelli envolve a ciclocondensação de três reagentes na presença de um catalisador ácido para a obtenção de Dihidropirimidinonas (DHPMs). Este composto e seus derivados são amplamente conhecidos por possuir diversas propriedades farmacológicas e terapêuticas. Esta reação é geralmente realizada via catálise homogênea, que apresentam, no entanto, algumas dificuldades, como regeneração do catalisador e difícil separação do produto final, tornando-se dessa forma um obstáculo para utilização industrial. O presente trabalho teve como objetivo geral avaliar diferentes catalisadores ácidos heterogêneos na produção de dihidropirimidinonas, como óxidos de nióbio sulfonados e carvões sulfonados produzidos a partir de resíduos agroindustriais (casca de arroz e bagaço de tomate). Os carvões ácidos foram preparados por carbonização, por meio da impregnação de resíduos agroindustriais com ácido sulfúrico a uma temperatura de 200 °C na proporção mássica de 1:10 (precursor: H2SO4), por 6 h. Testou-se, também, o ácido nióbico (HY-340) e Nb2O5 ambos puros e tratados quimicamente com uma solução de 30% de ácido sulfúrico. Os catalisadores foram caracterizados por Difração de Raios X (DRX), Espectroscopia no Infravermelho (IV), Termogravimetria (TG), Análise Térmica Diferencial (DTA), Análise Textural por Adsorção/Dessorção de N2 a -196 °C, Dessorção de Amônia a Temperatura Programada (DTP-NH3), Microscopia Eletrônica de Varredura (MEV) e Espectrometria de Energia Dispersiva de Raios X (EDS). Os teores de C, N, O e S presentes na superfície dos carvões foram quantificados por Análise Elementar (CHNS-O). Foram realizados testes catalíticos exploratórios para definir melhores condições experimentais de solvente, temperatura, razão molar e quantidade de catalisador. Os resultados obtidos permitiram estabelecer as melhores condições experimentais para a realização da reação de Biginelli. Desse modo, adotaram-se os seguintes parâmetros para avaliar o desempenho dos diferentes catalisadores. São estes: teor de 5% de catalisador (em massa), razão molar de 1 Benzaldeído: 1,5 Acetoacetato de metila: 1,5 Ureia, sem solvente e temperatura de 130 °C. O melhor catalisador foi o Nb2O5 tratado com ácido sulfúrico, em que obteve-se um rendimento de 94% de dihidropirimidinonas (DHPMs).Submitted by JÚLIO HEBER SILVA (julioheber@yahoo.com.br) on 2017-04-07T20:19:45Z No. of bitstreams: 2 Dissertação - Letícia Gomes do Nascimento - 2017.pdf: 6868423 bytes, checksum: 7a54ea8b28095c4c81126f3998e87c13 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2017-04-10T11:16:14Z (GMT) No. of bitstreams: 2 Dissertação - Letícia Gomes do Nascimento - 2017.pdf: 6868423 bytes, checksum: 7a54ea8b28095c4c81126f3998e87c13 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5)Made available in DSpace on 2017-04-10T11:16:14Z (GMT). No. of bitstreams: 2 Dissertação - Letícia Gomes do Nascimento - 2017.pdf: 6868423 bytes, checksum: 7a54ea8b28095c4c81126f3998e87c13 (MD5) license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Previous issue date: 2017-03-07Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade Federal de GoiásPrograma de Pós-graduação em Engenharia Química (IQ)UFGBrasilInstituto de Química - IQ (RG)http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessCatálise heterogêneaDihidropirimidinonasReação de BiginelliCarvões sulfonadosÓxidos de nióbioHeterogeneous catalysisDihydropyrimidinonesBiginelli reactionSulfonated carbonsNiobium oxidesQUIMICA::QUIMICA ANALITICACatalisadores heterogêneos aplicados à reação de BiginelliHeterogeneous catalysts applied to the Biginelli reactioninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis34814965011584600786006006006007826066743741197278-86616021054614395492075167498588264571reponame:Repositório Institucional da UFGinstname:Universidade Federal de Goiás (UFG)instacron:UFGLICENSElicense.txtlicense.txttext/plain; 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dc.title.por.fl_str_mv |
Catalisadores heterogêneos aplicados à reação de Biginelli |
dc.title.alternative.eng.fl_str_mv |
Heterogeneous catalysts applied to the Biginelli reaction |
title |
Catalisadores heterogêneos aplicados à reação de Biginelli |
spellingShingle |
Catalisadores heterogêneos aplicados à reação de Biginelli Nascimento, Letícia Gomes do Catálise heterogênea Dihidropirimidinonas Reação de Biginelli Carvões sulfonados Óxidos de nióbio Heterogeneous catalysis Dihydropyrimidinones Biginelli reaction Sulfonated carbons Niobium oxides QUIMICA::QUIMICA ANALITICA |
title_short |
Catalisadores heterogêneos aplicados à reação de Biginelli |
title_full |
Catalisadores heterogêneos aplicados à reação de Biginelli |
title_fullStr |
Catalisadores heterogêneos aplicados à reação de Biginelli |
title_full_unstemmed |
Catalisadores heterogêneos aplicados à reação de Biginelli |
title_sort |
Catalisadores heterogêneos aplicados à reação de Biginelli |
author |
Nascimento, Letícia Gomes do |
author_facet |
Nascimento, Letícia Gomes do |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Alonso, Christian Gonçalves |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/7285754665946583 |
dc.contributor.advisor-co1.fl_str_mv |
Oliveira, Guilherme Roberto de |
dc.contributor.advisor-co1Lattes.fl_str_mv |
http://lattes.cnpq.br/8239498431579015 |
dc.contributor.referee1.fl_str_mv |
Alonso, Christian Gonçalves |
dc.contributor.referee1Lattes.fl_str_mv |
http://lattes.cnpq.br/7285754665946583 |
dc.contributor.referee2.fl_str_mv |
Oliveira, Guilherme Roberto de |
dc.contributor.referee2Lattes.fl_str_mv |
http://lattes.cnpq.br/8239498431579015 |
dc.contributor.referee3.fl_str_mv |
Andrade, Fabiano Molinos de |
dc.contributor.referee4.fl_str_mv |
Arroyo, Pedro Augusto |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/3262057595733430 |
dc.contributor.author.fl_str_mv |
Nascimento, Letícia Gomes do |
contributor_str_mv |
Alonso, Christian Gonçalves Oliveira, Guilherme Roberto de Alonso, Christian Gonçalves Oliveira, Guilherme Roberto de Andrade, Fabiano Molinos de Arroyo, Pedro Augusto |
dc.subject.por.fl_str_mv |
Catálise heterogênea Dihidropirimidinonas Reação de Biginelli Carvões sulfonados Óxidos de nióbio |
topic |
Catálise heterogênea Dihidropirimidinonas Reação de Biginelli Carvões sulfonados Óxidos de nióbio Heterogeneous catalysis Dihydropyrimidinones Biginelli reaction Sulfonated carbons Niobium oxides QUIMICA::QUIMICA ANALITICA |
dc.subject.eng.fl_str_mv |
Heterogeneous catalysis Dihydropyrimidinones Biginelli reaction Sulfonated carbons Niobium oxides |
dc.subject.cnpq.fl_str_mv |
QUIMICA::QUIMICA ANALITICA |
description |
The Biginelli reaction involves the cyclocondensation of three reagents in the presence of an acid catalyst to obtain dihydropyrimidinones (DHPMs).This compound and its analogues are widely known to possess various pharmacological properties, such as antibacterial, antiinflammatory, antifungal, antiviral, anticancer and antihypertensive. This reaction is usually carried out via homogeneous catalysis, which presents, however, some difficulties, such as regeneration of the catalyst and difficult separation of the final product, thus becoming an obstacle for industrial use. In the present work, it was proposed the use of two classes of heterogeneous catalysts, which are: metal oxides and acid carbons in order to achieve attractive characteristics in the Biginelli reaction, as a reduction of reaction time and increase in yield. The acidic carbons were prepared by carbonization by impregnation of agroindustrial residues with sulfuric acid at a temperature of 200 °C in the mass ratio of 1:10 (precursor: H2SO4) for 6 h. The pure HY-340 and Nb2O5 were both tested and chemically treated with a solution of 30% sulfuric acid. The catalysts were characterized by X-ray diffraction (XRD), infrared spectroscopy (FTIR), thermogravimetric (TG), differential thermal analysis (DTA), textural adsorption/desorption analysis of N2 at -196 °C and desorption of ammonia at programmed temperature (DTP-NH3), scanning electron microscopy (SEM) and X-ray Dispersive Energy Spectrometry (EDS). The contents of C, N, O and S present on the surface of the coals were quantified by Elementary Analysis (CHNS-O). Exploratory catalytic tests were carried out to define the best experimental conditions of solvent, temperature, molar ratio and amount of catalyst. The results obtained allowed to establish the best experimental conditions for the realization of the Biginelli reaction. Thus, the following parameters were adopted to evaluate the performance of the different catalysts. These are: 5% catalyst content (by mass), molar ratio of 1 Benzaldehyde: 1,5 Methyl acetoacetate: 1,5 Urea, without solvent and temperature of 130 °C. The best catalyst was Nb2O5 treated with sulfuric acid, whereby a yield of 94% of dihydropyrimidinones (DHPMs). |
publishDate |
2017 |
dc.date.accessioned.fl_str_mv |
2017-04-10T11:16:14Z |
dc.date.issued.fl_str_mv |
2017-03-07 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
NASCIMENTO, L. G. Catalisadores heterogêneos aplicados à reação de Biginelli. 2017. 88 f. Dissertação (Mestrado em Engenharia Química) - Universidade Federal de Goiás, Goiânia, 2017. |
dc.identifier.uri.fl_str_mv |
http://repositorio.bc.ufg.br/tede/handle/tede/7110 |
dc.identifier.dark.fl_str_mv |
ark:/38995/0013000008bsk |
identifier_str_mv |
NASCIMENTO, L. G. Catalisadores heterogêneos aplicados à reação de Biginelli. 2017. 88 f. Dissertação (Mestrado em Engenharia Química) - Universidade Federal de Goiás, Goiânia, 2017. ark:/38995/0013000008bsk |
url |
http://repositorio.bc.ufg.br/tede/handle/tede/7110 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.program.fl_str_mv |
3481496501158460078 |
dc.relation.confidence.fl_str_mv |
600 600 600 600 |
dc.relation.department.fl_str_mv |
7826066743741197278 |
dc.relation.cnpq.fl_str_mv |
-8661602105461439549 |
dc.relation.sponsorship.fl_str_mv |
2075167498588264571 |
dc.rights.driver.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.publisher.program.fl_str_mv |
Programa de Pós-graduação em Engenharia Química (IQ) |
dc.publisher.initials.fl_str_mv |
UFG |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Instituto de Química - IQ (RG) |
publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFG instname:Universidade Federal de Goiás (UFG) instacron:UFG |
instname_str |
Universidade Federal de Goiás (UFG) |
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UFG |
institution |
UFG |
reponame_str |
Repositório Institucional da UFG |
collection |
Repositório Institucional da UFG |
bitstream.url.fl_str_mv |
http://repositorio.bc.ufg.br/tede/bitstreams/985d11d1-766b-4e00-91f2-2e8ec2cadd84/download http://repositorio.bc.ufg.br/tede/bitstreams/a00e9d65-41e8-48c5-8d6a-75dce8aed488/download http://repositorio.bc.ufg.br/tede/bitstreams/af76ab49-fc92-457d-aad8-c0f7229a5456/download http://repositorio.bc.ufg.br/tede/bitstreams/219f6f51-f2f9-4bc1-9ba5-816395c37c25/download http://repositorio.bc.ufg.br/tede/bitstreams/df83fac1-0673-4171-80c3-85fd956f9da6/download |
bitstream.checksum.fl_str_mv |
bd3efa91386c1718a7f26a329fdcb468 4afdbb8c545fd630ea7db775da747b2f d41d8cd98f00b204e9800998ecf8427e d41d8cd98f00b204e9800998ecf8427e 7a54ea8b28095c4c81126f3998e87c13 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFG - Universidade Federal de Goiás (UFG) |
repository.mail.fl_str_mv |
tasesdissertacoes.bc@ufg.br |
_version_ |
1815172599060103168 |