Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose

Detalhes bibliográficos
Autor(a) principal: Scolari, Eduardo
Data de Publicação: 2019
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFSCAR
Texto Completo: https://repositorio.ufscar.br/handle/ufscar/11376
Resumo: The 5-hydroximethilfurfural (5-HMF) is a platform molecule that has great potential to originate a wide range of compounds with potential interest in biorefinery, as well as compounds currently produced exclusively from non-renewable carbon sources. The 5-HMF can be obtained via dehydration of hexoses, but with low selectivity (< 30%). On the other hand, fructose, a glucose isomer, can be dehydrated to 5-HMF with high selectivity (> 70%). Recently it has been discovered that using a combination of Lewis acids and Brønsted acids, in the right proportion, allows the direct conversion of glucose into 5-HMF with selectivities higher than 60%. In this process, the Lewis acid isomerizes the glucose to fructose, which is subsequently dehydrated by the Brønsted acid. While several brønsted acid catalysts are known to be efficient in the dehydration of fructose, Sn-Beta zeolite appears almost exclusively as a heterogeneous Lewis acid catalyst for glucose isomerization. However, Sn-Beta has a long, complicated synthesis with questionable reproducibility. Thus, in this study, we proposed the use of mesoporous amorphous stannosilicates as catalysts of glucose isomerization. The effects of the synthesis parameters of mesoporous stannosilicates Sn-MCM-41 and Sn-SBA-15 were evaluated, in the face of its textural, structural and catalytic properties in the isomerization of glucose. The characteristic structures were obtained for all silicates, although the use of an organic base and higher concentrations of acid decreased the ordering respectively for samples MCM-41 and SBA-15. It was observed the presence of tetrahedral tin, indicating insertion in the framework, besides penta and hexacoordinated tin species. The isotherms obtained are as expected for these materials. Changes in pH and Si:Sn ratio didn’t present great effects on the MCM-41 cell parameters and wall thickness, although thermal treatment reduced the last. Variations in synthesis parameters have more visible effects for SBA-15 silicates. The materials in general showed values of selectivity for fructose above 75%, which can be considered very good. It is worth mentioning MCM-41 synthesized with TMAOH showed these values even with larger conversions. The most promising materials (TMAOH 12.9-3% Sn-25 ° C; NH4OH 12.9-3%-50 ° C and SBA15-0.07-3%) were studied more deeply in relation to their catalytic properties. The kinetic tests and indicated that in general the reaction goes into equilibrium at 110 minutes. Only exchange of the organic solvent GVL and THF (polar aprotic) to methanol (polar protic) resulted in significant changes in the behavior of the rates of glucose conversion and selectivity, being GVL the most interesting solvent.
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spelling Scolari, EduardoGallo, Jean Marcel Ribeirohttp://lattes.cnpq.br/3485408327490746http://lattes.cnpq.br/1209001063337177477930b6-a617-4486-995f-e1d105f6e3652019-05-07T12:39:44Z2019-05-07T12:39:44Z2019-02-18SCOLARI, Eduardo. Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose. 2019. Dissertação (Mestrado em Química) – Universidade Federal de São Carlos, São Carlos, 2019. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11376.https://repositorio.ufscar.br/handle/ufscar/11376The 5-hydroximethilfurfural (5-HMF) is a platform molecule that has great potential to originate a wide range of compounds with potential interest in biorefinery, as well as compounds currently produced exclusively from non-renewable carbon sources. The 5-HMF can be obtained via dehydration of hexoses, but with low selectivity (< 30%). On the other hand, fructose, a glucose isomer, can be dehydrated to 5-HMF with high selectivity (> 70%). Recently it has been discovered that using a combination of Lewis acids and Brønsted acids, in the right proportion, allows the direct conversion of glucose into 5-HMF with selectivities higher than 60%. In this process, the Lewis acid isomerizes the glucose to fructose, which is subsequently dehydrated by the Brønsted acid. While several brønsted acid catalysts are known to be efficient in the dehydration of fructose, Sn-Beta zeolite appears almost exclusively as a heterogeneous Lewis acid catalyst for glucose isomerization. However, Sn-Beta has a long, complicated synthesis with questionable reproducibility. Thus, in this study, we proposed the use of mesoporous amorphous stannosilicates as catalysts of glucose isomerization. The effects of the synthesis parameters of mesoporous stannosilicates Sn-MCM-41 and Sn-SBA-15 were evaluated, in the face of its textural, structural and catalytic properties in the isomerization of glucose. The characteristic structures were obtained for all silicates, although the use of an organic base and higher concentrations of acid decreased the ordering respectively for samples MCM-41 and SBA-15. It was observed the presence of tetrahedral tin, indicating insertion in the framework, besides penta and hexacoordinated tin species. The isotherms obtained are as expected for these materials. Changes in pH and Si:Sn ratio didn’t present great effects on the MCM-41 cell parameters and wall thickness, although thermal treatment reduced the last. Variations in synthesis parameters have more visible effects for SBA-15 silicates. The materials in general showed values of selectivity for fructose above 75%, which can be considered very good. It is worth mentioning MCM-41 synthesized with TMAOH showed these values even with larger conversions. The most promising materials (TMAOH 12.9-3% Sn-25 ° C; NH4OH 12.9-3%-50 ° C and SBA15-0.07-3%) were studied more deeply in relation to their catalytic properties. The kinetic tests and indicated that in general the reaction goes into equilibrium at 110 minutes. Only exchange of the organic solvent GVL and THF (polar aprotic) to methanol (polar protic) resulted in significant changes in the behavior of the rates of glucose conversion and selectivity, being GVL the most interesting solvent.O 5-hidroximetilfurfural (5-HMF) é uma molécula plataforma que apresenta grande potencial de originar uma grande gama de compostos com potencial interesse na biorrefinaria, bem como compostos atualmente produzidos exclusivamente de fontes de carbono não-renováveis. O 5-HMF pode ser obtido via desidratação de hexoses, porém com baixa seletividade ( <30 %). Por outro lado, a frutose, um isômero da glicose, pode ser desidratada a 5-HMF com alta seletividade (> 70 %). Recentemente, descobriu-se a utilização de uma combinação de ácido de Lewis e ácido Brønsted na proporção correta permite a conversão direta da glicose em 5-HMF com seletividades superiores a 60 %. Nesse processo, o ácido de Lewis isomeriza a glicose a frutose, a qual é subsequentemente desidratada pelo ácido de Brønsted. Enquanto são conhecidos diversos catalisadores ácidos de Brønsted eficientes na desidratação da frutose, a Zeolita Sn-Beta aparece quase que exclusivamente como catalisador ácido de Lewis para a isomerização da glicose. Porém, a Sn-beta tem uma síntese longa, complicada e com reprodutibilidade questionável. Dessa forma, neste trabalho propusemos o uso de estanossílicas amorfas mesoporosas como catalisadores da isomerização da glicose. Foram avaliados os efeitos dos parâmetros de síntese de estanossilicatos mesoporosos Sn-MCM-41 e Sn-SBA-15, frente suas propriedades texturais, estruturais e catalíticas na isomerização de glicose. Obtiveram-se as estruturas características para todos os silicatos, embora o uso de uma base orgânica e concentrações e mais elevadas de ácido tenham diminuído o ordenamento respectivamente para amostras MCM-41 e SBA-15. Observou-se a presença de estanho tetraédrico, indicando inserção na rede, além de espécies penta e hexacoordenadas. As Isotermas obtidas estão conforme esperadas para estes materiais. Alterações de pH e razão Si:Sn não apresentaram grandes efeitos nas MCM-41 nos paramentos de cela e espessura das paredes, embora tratamento térmico tenha reduzido a última. As variações de parâmetros de síntese apresentam efeitos mais visíveis para os silicatos SBA-15. Os materiais em geral apresentaram valores de seletividade para frutose acima de 75 %, que podem ser considerados muito bons. Cabe ressaltar que MCM-41 sintetizadas com TMAOH mostraram estes valores mesmo com conversões maiores. Os Materiais mais promissores (TMAOH 12,9-3%Sn-25°C; NH4OH 12,9-3%-50°C e SBA15-0,07-3%) foram estudados mais a fundo em relação a suas propriedades catalíticas. Os testes cinéticos apontaram que em geral a reação entra em equilíbrio aos 110 minutos. Apenas troca do solvente orgânico GVL e THF (polares aproticos) ao pôr metanol (polar prótico) acarretou significantes mudanças de comportamento nas taxas de conversão de glicose e seletividade, sendo GVL o solvente mais interessante.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)CAPES: 1600947porUniversidade Federal de São CarlosCâmpus São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarGlicoseIsomerizaçãoEstanosilicatosGlucoseCIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA::DETERMINACAO DE ESTRUTURA DE COMPOSTOS INORGANICOSCIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA::FISICO QUIMICA INORGANICAEstudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicoseStudy of the effect of the synthesis parameters of Sn-MCM-41 and Sn-SBA-15 on their structural, textural and catalytic properties in the isomerization of glucoseinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisOnline60060055f26ad6-4e1e-4727-9713-0fe8011516bfinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINALdissertação V13 _Final.pdfdissertação V13 _Final.pdfapplication/pdf1181672https://repositorio.ufscar.br/bitstream/ufscar/11376/1/disserta%c3%a7%c3%a3o%20V13%20_Final.pdf60ce4506902522064b61ced4cec6adf0MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81957https://repositorio.ufscar.br/bitstream/ufscar/11376/3/license.txtae0398b6f8b235e40ad82cba6c50031dMD53TEXTdissertação V13 _Final.pdf.txtdissertação V13 _Final.pdf.txtExtracted texttext/plain127063https://repositorio.ufscar.br/bitstream/ufscar/11376/4/disserta%c3%a7%c3%a3o%20V13%20_Final.pdf.txt374bec9c86502d7512d095df0d7ccf41MD54THUMBNAILdissertação V13 _Final.pdf.jpgdissertação V13 _Final.pdf.jpgIM Thumbnailimage/jpeg9382https://repositorio.ufscar.br/bitstream/ufscar/11376/5/disserta%c3%a7%c3%a3o%20V13%20_Final.pdf.jpg63fe0bcdf74973ee6ef8473de9618c8cMD55ufscar/113762023-09-18 18:31:25.881oai:repositorio.ufscar.br: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Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-09-18T18:31:25Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose
dc.title.alternative.eng.fl_str_mv Study of the effect of the synthesis parameters of Sn-MCM-41 and Sn-SBA-15 on their structural, textural and catalytic properties in the isomerization of glucose
title Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose
spellingShingle Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose
Scolari, Eduardo
Glicose
Isomerização
Estanosilicatos
Glucose
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA::DETERMINACAO DE ESTRUTURA DE COMPOSTOS INORGANICOS
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA::FISICO QUIMICA INORGANICA
title_short Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose
title_full Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose
title_fullStr Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose
title_full_unstemmed Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose
title_sort Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose
author Scolari, Eduardo
author_facet Scolari, Eduardo
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/1209001063337177
dc.contributor.author.fl_str_mv Scolari, Eduardo
dc.contributor.advisor1.fl_str_mv Gallo, Jean Marcel Ribeiro
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/3485408327490746
dc.contributor.authorID.fl_str_mv 477930b6-a617-4486-995f-e1d105f6e365
contributor_str_mv Gallo, Jean Marcel Ribeiro
dc.subject.por.fl_str_mv Glicose
Isomerização
Estanosilicatos
topic Glicose
Isomerização
Estanosilicatos
Glucose
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA::DETERMINACAO DE ESTRUTURA DE COMPOSTOS INORGANICOS
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA::FISICO QUIMICA INORGANICA
dc.subject.eng.fl_str_mv Glucose
dc.subject.cnpq.fl_str_mv CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA::DETERMINACAO DE ESTRUTURA DE COMPOSTOS INORGANICOS
CIENCIAS EXATAS E DA TERRA::QUIMICA::QUIMICA INORGANICA::FISICO QUIMICA INORGANICA
description The 5-hydroximethilfurfural (5-HMF) is a platform molecule that has great potential to originate a wide range of compounds with potential interest in biorefinery, as well as compounds currently produced exclusively from non-renewable carbon sources. The 5-HMF can be obtained via dehydration of hexoses, but with low selectivity (< 30%). On the other hand, fructose, a glucose isomer, can be dehydrated to 5-HMF with high selectivity (> 70%). Recently it has been discovered that using a combination of Lewis acids and Brønsted acids, in the right proportion, allows the direct conversion of glucose into 5-HMF with selectivities higher than 60%. In this process, the Lewis acid isomerizes the glucose to fructose, which is subsequently dehydrated by the Brønsted acid. While several brønsted acid catalysts are known to be efficient in the dehydration of fructose, Sn-Beta zeolite appears almost exclusively as a heterogeneous Lewis acid catalyst for glucose isomerization. However, Sn-Beta has a long, complicated synthesis with questionable reproducibility. Thus, in this study, we proposed the use of mesoporous amorphous stannosilicates as catalysts of glucose isomerization. The effects of the synthesis parameters of mesoporous stannosilicates Sn-MCM-41 and Sn-SBA-15 were evaluated, in the face of its textural, structural and catalytic properties in the isomerization of glucose. The characteristic structures were obtained for all silicates, although the use of an organic base and higher concentrations of acid decreased the ordering respectively for samples MCM-41 and SBA-15. It was observed the presence of tetrahedral tin, indicating insertion in the framework, besides penta and hexacoordinated tin species. The isotherms obtained are as expected for these materials. Changes in pH and Si:Sn ratio didn’t present great effects on the MCM-41 cell parameters and wall thickness, although thermal treatment reduced the last. Variations in synthesis parameters have more visible effects for SBA-15 silicates. The materials in general showed values of selectivity for fructose above 75%, which can be considered very good. It is worth mentioning MCM-41 synthesized with TMAOH showed these values even with larger conversions. The most promising materials (TMAOH 12.9-3% Sn-25 ° C; NH4OH 12.9-3%-50 ° C and SBA15-0.07-3%) were studied more deeply in relation to their catalytic properties. The kinetic tests and indicated that in general the reaction goes into equilibrium at 110 minutes. Only exchange of the organic solvent GVL and THF (polar aprotic) to methanol (polar protic) resulted in significant changes in the behavior of the rates of glucose conversion and selectivity, being GVL the most interesting solvent.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-05-07T12:39:44Z
dc.date.available.fl_str_mv 2019-05-07T12:39:44Z
dc.date.issued.fl_str_mv 2019-02-18
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.identifier.citation.fl_str_mv SCOLARI, Eduardo. Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose. 2019. Dissertação (Mestrado em Química) – Universidade Federal de São Carlos, São Carlos, 2019. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11376.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/ufscar/11376
identifier_str_mv SCOLARI, Eduardo. Estudo do efeito dos parâmetros de síntese da Sn-MCM-41 e Sn-SBA-15 em suas propriedades estruturais, texturais e catalíticas na isomerização da glicose. 2019. Dissertação (Mestrado em Química) – Universidade Federal de São Carlos, São Carlos, 2019. Disponível em: https://repositorio.ufscar.br/handle/ufscar/11376.
url https://repositorio.ufscar.br/handle/ufscar/11376
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language por
dc.relation.confidence.fl_str_mv 600
600
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dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Universidade Federal de São Carlos
Câmpus São Carlos
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química - PPGQ
dc.publisher.initials.fl_str_mv UFSCar
publisher.none.fl_str_mv Universidade Federal de São Carlos
Câmpus São Carlos
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instacron:UFSCAR
instname_str Universidade Federal de São Carlos (UFSCAR)
instacron_str UFSCAR
institution UFSCAR
reponame_str Repositório Institucional da UFSCAR
collection Repositório Institucional da UFSCAR
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