Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al

Detalhes bibliográficos
Autor(a) principal: Silva, Renan Antunes Silvestre da
Data de Publicação: 2021
Outros Autores: renan.antunes.silva@gmail.com
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Biblioteca Digital de Teses e Dissertações da UERJ
Texto Completo: http://www.bdtd.uerj.br/handle/1/17717
Resumo: In this work, catalysts based on hydrotalcite-like precursors were synthesized with nominal formula Zn1-x(FeyAl1-y)x(OH)2(CO3)x/2, in order to be evaluated in oxidative dehydrogenation of propane (ODHP). The precursors were prepared by two methods, coprecipitation at low supersaturation and titration, with different contents of metals. The catalysts were prepared by calcination of the precursors at 550 ˚C. The precursors were characterized by XRD, ICP- OES, TGA and FTIR. The catalysts were characterized by XRD, N2 adsorption and tested in the ODHP. The chemical analysis indicated that all metal used was introduced in the solid phase, except for the series trivalent molar fractions equal to 0.22 (series X22), which had a significant Zn fraction in the liquid phase. The XRD shows that the desired phase (hydrotalcite-like phase) was obtained in all synthesis containing Al, series X20 and X25 (trivalent molar fractions equal to 0.2 and 0.25 respectively), but ZnO and Zn(OH)2 have also been found. The size of the unit cell calculated with those results confirms the presence of carbonate as the compensation anion. Moreover, in the X20 series, the unit cell size a reached a maximum value that could be related to a possible incorporation limit of either Fe or Zn in the desired structure. The presence of Fe2+ can also be considered and associated to the elimination of Zn of the desired structure. The series X22 resulted in amorphous materials and the series X33 (trivalent molar fraction equal to 0.33), in crystalline ZnO, Zn(OH)2 and amorphous material. The infrared characterization corroborated the presence of carbonate in all precursors but, in some cases, nitrate was found in small quantities. The XRD showed that the catalysts are composed of ZnO and magnetite (Fe2.962O4). The propene yields in the ODHP were very similar among all catalysts with the maximum value being around 3 % which is probably related to low selectivity observed (< 10%). The selectivity increased with the temperature which is uncommon in this type of reactions and could mean that the direct dehydrogenation is taking place instead of the oxidative one. The catalysts with the highest surface area and with the highest iron content exhibited the best yields.
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spelling Santos , Luz Amparo Palaciohttp://lattes.cnpq.br/2277031732030434Faro Júnior, Arnaldo da Costahttp://lattes.cnpq.br/4814996962747257Araújo, Lucia Regina Raddi dehttp://lattes.cnpq.br/1592062469734844Zotin, Fatima Maria Zanonhttp://lattes.cnpq.br/2398224913573093Pacheco Filho, Jose Geraldo de Andradehttp://lattes.cnpq.br/6315186407922891http://lattes.cnpq.br/6764610011834353Silva, Renan Antunes Silvestre darenan.antunes.silva@gmail.com2022-05-11T14:31:51Z2021-08-30SILVA, Renan Antunes Silvestre da. Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al. 2021. 91 f. Dissertação (Mestrado em Engenharia Química) - Faculdade de Química, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2021.http://www.bdtd.uerj.br/handle/1/17717In this work, catalysts based on hydrotalcite-like precursors were synthesized with nominal formula Zn1-x(FeyAl1-y)x(OH)2(CO3)x/2, in order to be evaluated in oxidative dehydrogenation of propane (ODHP). The precursors were prepared by two methods, coprecipitation at low supersaturation and titration, with different contents of metals. The catalysts were prepared by calcination of the precursors at 550 ˚C. The precursors were characterized by XRD, ICP- OES, TGA and FTIR. The catalysts were characterized by XRD, N2 adsorption and tested in the ODHP. The chemical analysis indicated that all metal used was introduced in the solid phase, except for the series trivalent molar fractions equal to 0.22 (series X22), which had a significant Zn fraction in the liquid phase. The XRD shows that the desired phase (hydrotalcite-like phase) was obtained in all synthesis containing Al, series X20 and X25 (trivalent molar fractions equal to 0.2 and 0.25 respectively), but ZnO and Zn(OH)2 have also been found. The size of the unit cell calculated with those results confirms the presence of carbonate as the compensation anion. Moreover, in the X20 series, the unit cell size a reached a maximum value that could be related to a possible incorporation limit of either Fe or Zn in the desired structure. The presence of Fe2+ can also be considered and associated to the elimination of Zn of the desired structure. The series X22 resulted in amorphous materials and the series X33 (trivalent molar fraction equal to 0.33), in crystalline ZnO, Zn(OH)2 and amorphous material. The infrared characterization corroborated the presence of carbonate in all precursors but, in some cases, nitrate was found in small quantities. The XRD showed that the catalysts are composed of ZnO and magnetite (Fe2.962O4). The propene yields in the ODHP were very similar among all catalysts with the maximum value being around 3 % which is probably related to low selectivity observed (< 10%). The selectivity increased with the temperature which is uncommon in this type of reactions and could mean that the direct dehydrogenation is taking place instead of the oxidative one. The catalysts with the highest surface area and with the highest iron content exhibited the best yields.Neste trabalho foram sintetizados catalisadores oriundos de compostos de tipo hidrotalcita, com fórmula nominal Zn1-x(FeyAl1-y)x(OH)2(CO3)x/2, para avaliação catalítica na reação de desidrogenação oxidativa do propano (DHOP). Os precursores foram preparados por dois métodos, coprecipitação a baixa supersaturação e titulação, contendo diferentes teores de metais. Os catalisadores foram preparados pela calcinação dos precursores a 550 ˚C. Os precursores foram caracterizados por DRX, ICP-OES, TGA e FTIR. Os catalisadores foram caracterizados por DRX, adsorção de N2, e testados na reação de DHOP. A análise química indicou que todos os metais utilizados foram inseridos na fase sólida com exceção dos precursores cuja fração molar do metal trivalente foi igual a 0,22 (série X22), que tiveram uma parcela de Zn significativa na fase líquida. A DRX indicou que se obteve a fase desejada (fase tipo hidrotalcita) em todos os precursores contendo Al, série X20 e X25 ( fração molar de trivalentes igual a 0,20 e 0,25 respectivamente), mas ZnO e Zn(OH)2 também foram identificados. O tamanho da célula unitária calculado a partir desses resultados confirma a presença do carbonato como ânion de compensação na fase hidrotalcita. Além disso, nota-se na série X20 que o tamanho da célula unitária a atingiu um valor máximo que pode ser decorrente de um limite da incorporação de Fe ou de Zn na estrutura almejada. A presença de Fe+2 também pode ser considerada e associada à eliminação de Zn da estrutura da hidrotalcita. A série X22 resultou em materiais amorfos e a série X33 (de fração molar de trivalentes igual a 0,33) em ZnO, Zn(OH)2 cristalinos mais material amorfo. A caracterização por infravermelho corroborou a presença de carbonato em todos os precursores, mas em alguns casos nitrato, em quantidades pequenas, foi identificado. A DRX mostrou que catalisadores são compostos de ZnO e magnetita (Fe2.962O4). O rendimento a propeno na reação de DHOP foi muito similar em todos os catalisadores, sendo o valor máximo em torno de 3% o que muito provavelmente está associado à baixa seletividade observada (< 10%). A seletividade cresceu com o aumento da temperatura o que é incomum para este tipo de reações e pode significar que a desidrogenação direta esteja ocorrendo ao invés da oxidativa. Os catalisadores com maior área e maior quantidade de ferro foram os que exibiram os rendimentos mais altos.Submitted by Ana Rachel CTC/Q (ana.teles@uerj.br) on 2022-05-11T14:31:51Z No. of bitstreams: 1 Dissertação - Renan Antunes Silvestre da Silva - 2021 - Completa.pdf: 2530267 bytes, checksum: f29cc5c21f787ad627b9b752326935fc (MD5)Made available in DSpace on 2022-05-11T14:31:51Z (GMT). No. of bitstreams: 1 Dissertação - Renan Antunes Silvestre da Silva - 2021 - Completa.pdf: 2530267 bytes, checksum: f29cc5c21f787ad627b9b752326935fc (MD5) Previous issue date: 2021-08-30Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro - FAPERJapplication/pdfporUniversidade do Estado do Rio de JaneiroPrograma de Pós-Graduação em Engenharia QuímicaUERJBrasilCentro de Tecnologia e Ciências::Instituto de QuímicaHydrotalciteOxidative dehydrogenationHidrotalcitaZn-Fe-AlDesidrogenação oxidativaPropanoPropenoCatalisadoresPropanePropeneENGENHARIAS::ENGENHARIA QUIMICA::TECNOLOGIA QUIMICASíntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-AlSynthesis of catalysts for propane oxidative dehydrogenation based on hydrotalcite-like precursors of the system Zn-Fe-Alinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UERJinstname:Universidade do Estado do Rio de Janeiro (UERJ)instacron:UERJORIGINALDissertação - Renan Antunes Silvestre da Silva - 2021 - Completa.pdfDissertação - Renan Antunes Silvestre da Silva - 2021 - Completa.pdfapplication/pdf2530267http://www.bdtd.uerj.br/bitstream/1/17717/2/Disserta%C3%A7%C3%A3o+-+Renan+Antunes+Silvestre+da+Silva+-+2021+-+Completa.pdff29cc5c21f787ad627b9b752326935fcMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-82123http://www.bdtd.uerj.br/bitstream/1/17717/1/license.txte5502652da718045d7fcd832b79fca29MD511/177172024-02-27 15:35:57.711oai:www.bdtd.uerj.br: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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 catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al
dc.title.alternative.eng.fl_str_mv Synthesis of catalysts for propane oxidative dehydrogenation based on hydrotalcite-like precursors of the system Zn-Fe-Al
title Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al
spellingShingle Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al
Silva, Renan Antunes Silvestre da
Hydrotalcite
Oxidative dehydrogenation
Hidrotalcita
Zn-Fe-Al
Desidrogenação oxidativa
Propano
Propeno
Catalisadores
Propane
Propene
ENGENHARIAS::ENGENHARIA QUIMICA::TECNOLOGIA QUIMICA
title_short Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al
title_full Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al
title_fullStr Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al
title_full_unstemmed Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al
title_sort Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al
author Silva, Renan Antunes Silvestre da
author_facet Silva, Renan Antunes Silvestre da
renan.antunes.silva@gmail.com
author_role author
author2 renan.antunes.silva@gmail.com
author2_role author
dc.contributor.advisor1.fl_str_mv Santos , Luz Amparo Palacio
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/2277031732030434
dc.contributor.advisor2.fl_str_mv Faro Júnior, Arnaldo da Costa
dc.contributor.advisor2Lattes.fl_str_mv http://lattes.cnpq.br/4814996962747257
dc.contributor.referee1.fl_str_mv Araújo, Lucia Regina Raddi de
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/1592062469734844
dc.contributor.referee2.fl_str_mv Zotin, Fatima Maria Zanon
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/2398224913573093
dc.contributor.referee3.fl_str_mv Pacheco Filho, Jose Geraldo de Andrade
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/6315186407922891
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/6764610011834353
dc.contributor.author.fl_str_mv Silva, Renan Antunes Silvestre da
renan.antunes.silva@gmail.com
contributor_str_mv Santos , Luz Amparo Palacio
Faro Júnior, Arnaldo da Costa
Araújo, Lucia Regina Raddi de
Zotin, Fatima Maria Zanon
Pacheco Filho, Jose Geraldo de Andrade
dc.subject.eng.fl_str_mv Hydrotalcite
Oxidative dehydrogenation
topic Hydrotalcite
Oxidative dehydrogenation
Hidrotalcita
Zn-Fe-Al
Desidrogenação oxidativa
Propano
Propeno
Catalisadores
Propane
Propene
ENGENHARIAS::ENGENHARIA QUIMICA::TECNOLOGIA QUIMICA
dc.subject.por.fl_str_mv Hidrotalcita
Zn-Fe-Al
Desidrogenação oxidativa
Propano
Propeno
Catalisadores
Propane
Propene
dc.subject.cnpq.fl_str_mv ENGENHARIAS::ENGENHARIA QUIMICA::TECNOLOGIA QUIMICA
description In this work, catalysts based on hydrotalcite-like precursors were synthesized with nominal formula Zn1-x(FeyAl1-y)x(OH)2(CO3)x/2, in order to be evaluated in oxidative dehydrogenation of propane (ODHP). The precursors were prepared by two methods, coprecipitation at low supersaturation and titration, with different contents of metals. The catalysts were prepared by calcination of the precursors at 550 ˚C. The precursors were characterized by XRD, ICP- OES, TGA and FTIR. The catalysts were characterized by XRD, N2 adsorption and tested in the ODHP. The chemical analysis indicated that all metal used was introduced in the solid phase, except for the series trivalent molar fractions equal to 0.22 (series X22), which had a significant Zn fraction in the liquid phase. The XRD shows that the desired phase (hydrotalcite-like phase) was obtained in all synthesis containing Al, series X20 and X25 (trivalent molar fractions equal to 0.2 and 0.25 respectively), but ZnO and Zn(OH)2 have also been found. The size of the unit cell calculated with those results confirms the presence of carbonate as the compensation anion. Moreover, in the X20 series, the unit cell size a reached a maximum value that could be related to a possible incorporation limit of either Fe or Zn in the desired structure. The presence of Fe2+ can also be considered and associated to the elimination of Zn of the desired structure. The series X22 resulted in amorphous materials and the series X33 (trivalent molar fraction equal to 0.33), in crystalline ZnO, Zn(OH)2 and amorphous material. The infrared characterization corroborated the presence of carbonate in all precursors but, in some cases, nitrate was found in small quantities. The XRD showed that the catalysts are composed of ZnO and magnetite (Fe2.962O4). The propene yields in the ODHP were very similar among all catalysts with the maximum value being around 3 % which is probably related to low selectivity observed (< 10%). The selectivity increased with the temperature which is uncommon in this type of reactions and could mean that the direct dehydrogenation is taking place instead of the oxidative one. The catalysts with the highest surface area and with the highest iron content exhibited the best yields.
publishDate 2021
dc.date.issued.fl_str_mv 2021-08-30
dc.date.accessioned.fl_str_mv 2022-05-11T14:31:51Z
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 SILVA, Renan Antunes Silvestre da. Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al. 2021. 91 f. Dissertação (Mestrado em Engenharia Química) - Faculdade de Química, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2021.
dc.identifier.uri.fl_str_mv http://www.bdtd.uerj.br/handle/1/17717
identifier_str_mv SILVA, Renan Antunes Silvestre da. Síntese de catalisadores para a desidrogenação oxidativa do propano a partir de precursores do tipo hidrotalcita no sistema Zn-Fe-Al. 2021. 91 f. Dissertação (Mestrado em Engenharia Química) - Faculdade de Química, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, 2021.
url http://www.bdtd.uerj.br/handle/1/17717
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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
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