Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRN |
Texto Completo: | https://repositorio.ufrn.br/jspui/handle/123456789/29636 |
Resumo: | The effect of the chemical nature of the oxide support on the performance of cobalt Fischer–Tropsch catalysts is investigated. A series of supports is synthesized via monolayer coverage of porous γ-Al2O3 with various oxides representative of a wide range of Lewis acid–base character, as quantified by UV–vis spectroscopy coupled to alizarin adsorption. Incorporation of cobalt (20 wt %) results in model catalysts with identical porosities and similar Co particle sizes (>10 nm), allowing the study of support effects without overlap from diffusional or particle size factors. Under realistic reaction conditions, the initial TOF scales with the acidity of the oxide support, whereas the cobalt time yield and selectivity to industrially relevant C13+ hydrocarbons show a volcano dependence, with a maximum at an intermediate acid–base character. As inferred from in situ CO-FTIR, “selective” blockage of a few cobalt sites, though crucial for CO hydrogenation, by atoms from basic oxides and “unselective” site blockage via decoration of Co nanoparticles (strong metal–support interaction) with acidic, reducible oxides cause a decrease in reaction rate for supports with pronounced alkaline and acidic character, respectively. The extent of secondary isomerization reactions of α-olefin products, of relevance for chain reinsertion processes and product selectivity, also correlates with the support acidity. For a TiOx/Al2O3 as support, a remarkable C13+ productivity exceeding 0.09 molC gCo–1 h–1 is achieved, owing to the combination of optimal activity and selectivity. These results provide a unifying view of the support effects over a considerably broad study space and delineate a blueprint toward advanced Fischer–Tropsch catalysts. |
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Prieto, GonzaloMello, Mariele I. S. deConcepción, PatriciaMurciano, RaúlPergher, Sibele Berenice CastellãMartı́nez, Agustı́n2020-07-15T02:25:19Z2020-07-15T02:25:19Z2015-04-20PRIETO, Gonzalo; MELLO, Mariele I. S. de; CONCEPCIÓN, Patricia; MURCIANO, Raúl; PERGHER, Sibele Berenice Castellã; MARTÍNEZ, Agustı́n. Cobalt-Catalyzed Fischer–Tropsch Synthesis: chemical nature of the oxide support as a performance descriptor. Acs Catalysis, [s.l.], v. 5, n. 6, p. 3323-3335, 20 abr. 2015. ISSN 2155-5435 versão online. Disponível em: https://pubs.acs.org/doi/10.1021/acscatal.5b00057. Acesso em 14 jul. 2020. https://doi.org/10.1021/acscatal.5b000572155-5435 (online)https://repositorio.ufrn.br/jspui/handle/123456789/2963610.1021/acscatal.5b00057American Chemical SocietyAttribution-NonCommercial-NoDerivs 3.0 Brazilhttp://creativecommons.org/licenses/by-nc-nd/3.0/br/info:eu-repo/semantics/openAccessFischer−Tropsch synthesisModel catalystsSupport effectsLewis acidityStructure−performance relationshipsTurnover frequencyCO-FTIR spectroscopyCobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptorinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleThe effect of the chemical nature of the oxide support on the performance of cobalt Fischer–Tropsch catalysts is investigated. A series of supports is synthesized via monolayer coverage of porous γ-Al2O3 with various oxides representative of a wide range of Lewis acid–base character, as quantified by UV–vis spectroscopy coupled to alizarin adsorption. Incorporation of cobalt (20 wt %) results in model catalysts with identical porosities and similar Co particle sizes (>10 nm), allowing the study of support effects without overlap from diffusional or particle size factors. Under realistic reaction conditions, the initial TOF scales with the acidity of the oxide support, whereas the cobalt time yield and selectivity to industrially relevant C13+ hydrocarbons show a volcano dependence, with a maximum at an intermediate acid–base character. As inferred from in situ CO-FTIR, “selective” blockage of a few cobalt sites, though crucial for CO hydrogenation, by atoms from basic oxides and “unselective” site blockage via decoration of Co nanoparticles (strong metal–support interaction) with acidic, reducible oxides cause a decrease in reaction rate for supports with pronounced alkaline and acidic character, respectively. The extent of secondary isomerization reactions of α-olefin products, of relevance for chain reinsertion processes and product selectivity, also correlates with the support acidity. For a TiOx/Al2O3 as support, a remarkable C13+ productivity exceeding 0.09 molC gCo–1 h–1 is achieved, owing to the combination of optimal activity and selectivity. These results provide a unifying view of the support effects over a considerably broad study space and delineate a blueprint toward advanced Fischer–Tropsch catalysts.engreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNORIGINALCobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdfCobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdfapplication/pdf7010641https://repositorio.ufrn.br/bitstream/123456789/29636/1/Cobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdfb2f39fef1669eae54b83194d58f4470eMD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8811https://repositorio.ufrn.br/bitstream/123456789/29636/2/license_rdfe39d27027a6cc9cb039ad269a5db8e34MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81484https://repositorio.ufrn.br/bitstream/123456789/29636/3/license.txte9597aa2854d128fd968be5edc8a28d9MD53TEXTCobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdf.txtCobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdf.txtExtracted texttext/plain74230https://repositorio.ufrn.br/bitstream/123456789/29636/4/Cobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdf.txt7ad1dc9267a157ec8b18ff6534f03191MD54THUMBNAILCobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdf.jpgCobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdf.jpgGenerated Thumbnailimage/jpeg1922https://repositorio.ufrn.br/bitstream/123456789/29636/5/Cobalt-CatalyzedFischer-TropschSynthesis_Pergher_2015.pdf.jpga8af05abe10c9df39f491e8296adc1ccMD55123456789/296362021-02-15 15:36:29.201oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2021-02-15T18:36:29Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false |
dc.title.pt_BR.fl_str_mv |
Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor |
title |
Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor |
spellingShingle |
Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor Prieto, Gonzalo Fischer−Tropsch synthesis Model catalysts Support effects Lewis acidity Structure−performance relationships Turnover frequency CO-FTIR spectroscopy |
title_short |
Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor |
title_full |
Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor |
title_fullStr |
Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor |
title_full_unstemmed |
Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor |
title_sort |
Cobalt-catalyzed fischer–tropsch synthesis: chemical nature of the oxide support as a performance descriptor |
author |
Prieto, Gonzalo |
author_facet |
Prieto, Gonzalo Mello, Mariele I. S. de Concepción, Patricia Murciano, Raúl Pergher, Sibele Berenice Castellã Martı́nez, Agustı́n |
author_role |
author |
author2 |
Mello, Mariele I. S. de Concepción, Patricia Murciano, Raúl Pergher, Sibele Berenice Castellã Martı́nez, Agustı́n |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Prieto, Gonzalo Mello, Mariele I. S. de Concepción, Patricia Murciano, Raúl Pergher, Sibele Berenice Castellã Martı́nez, Agustı́n |
dc.subject.por.fl_str_mv |
Fischer−Tropsch synthesis Model catalysts Support effects Lewis acidity Structure−performance relationships Turnover frequency CO-FTIR spectroscopy |
topic |
Fischer−Tropsch synthesis Model catalysts Support effects Lewis acidity Structure−performance relationships Turnover frequency CO-FTIR spectroscopy |
description |
The effect of the chemical nature of the oxide support on the performance of cobalt Fischer–Tropsch catalysts is investigated. A series of supports is synthesized via monolayer coverage of porous γ-Al2O3 with various oxides representative of a wide range of Lewis acid–base character, as quantified by UV–vis spectroscopy coupled to alizarin adsorption. Incorporation of cobalt (20 wt %) results in model catalysts with identical porosities and similar Co particle sizes (>10 nm), allowing the study of support effects without overlap from diffusional or particle size factors. Under realistic reaction conditions, the initial TOF scales with the acidity of the oxide support, whereas the cobalt time yield and selectivity to industrially relevant C13+ hydrocarbons show a volcano dependence, with a maximum at an intermediate acid–base character. As inferred from in situ CO-FTIR, “selective” blockage of a few cobalt sites, though crucial for CO hydrogenation, by atoms from basic oxides and “unselective” site blockage via decoration of Co nanoparticles (strong metal–support interaction) with acidic, reducible oxides cause a decrease in reaction rate for supports with pronounced alkaline and acidic character, respectively. The extent of secondary isomerization reactions of α-olefin products, of relevance for chain reinsertion processes and product selectivity, also correlates with the support acidity. For a TiOx/Al2O3 as support, a remarkable C13+ productivity exceeding 0.09 molC gCo–1 h–1 is achieved, owing to the combination of optimal activity and selectivity. These results provide a unifying view of the support effects over a considerably broad study space and delineate a blueprint toward advanced Fischer–Tropsch catalysts. |
publishDate |
2015 |
dc.date.issued.fl_str_mv |
2015-04-20 |
dc.date.accessioned.fl_str_mv |
2020-07-15T02:25:19Z |
dc.date.available.fl_str_mv |
2020-07-15T02:25:19Z |
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 |
PRIETO, Gonzalo; MELLO, Mariele I. S. de; CONCEPCIÓN, Patricia; MURCIANO, Raúl; PERGHER, Sibele Berenice Castellã; MARTÍNEZ, Agustı́n. Cobalt-Catalyzed Fischer–Tropsch Synthesis: chemical nature of the oxide support as a performance descriptor. Acs Catalysis, [s.l.], v. 5, n. 6, p. 3323-3335, 20 abr. 2015. ISSN 2155-5435 versão online. Disponível em: https://pubs.acs.org/doi/10.1021/acscatal.5b00057. Acesso em 14 jul. 2020. https://doi.org/10.1021/acscatal.5b00057 |
dc.identifier.uri.fl_str_mv |
https://repositorio.ufrn.br/jspui/handle/123456789/29636 |
dc.identifier.issn.none.fl_str_mv |
2155-5435 (online) |
dc.identifier.doi.none.fl_str_mv |
10.1021/acscatal.5b00057 |
identifier_str_mv |
PRIETO, Gonzalo; MELLO, Mariele I. S. de; CONCEPCIÓN, Patricia; MURCIANO, Raúl; PERGHER, Sibele Berenice Castellã; MARTÍNEZ, Agustı́n. Cobalt-Catalyzed Fischer–Tropsch Synthesis: chemical nature of the oxide support as a performance descriptor. Acs Catalysis, [s.l.], v. 5, n. 6, p. 3323-3335, 20 abr. 2015. ISSN 2155-5435 versão online. Disponível em: https://pubs.acs.org/doi/10.1021/acscatal.5b00057. Acesso em 14 jul. 2020. https://doi.org/10.1021/acscatal.5b00057 2155-5435 (online) 10.1021/acscatal.5b00057 |
url |
https://repositorio.ufrn.br/jspui/handle/123456789/29636 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
Attribution-NonCommercial-NoDerivs 3.0 Brazil http://creativecommons.org/licenses/by-nc-nd/3.0/br/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Attribution-NonCommercial-NoDerivs 3.0 Brazil http://creativecommons.org/licenses/by-nc-nd/3.0/br/ |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFRN instname:Universidade Federal do Rio Grande do Norte (UFRN) instacron:UFRN |
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Universidade Federal do Rio Grande do Norte (UFRN) |
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UFRN |
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UFRN |
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Repositório Institucional da UFRN |
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Repositório Institucional da UFRN |
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