Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction

Detalhes bibliográficos
Autor(a) principal: Florindo,Bianca R.
Data de Publicação: 2021
Outros Autores: Catuzo,Gabriel L., Martins,Leandro
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021000501051
Resumo: The pore size of the chabazite structure is exceptionally suitable for the methanol to olefins (MTO) reaction. The reaction has an induction period required for the formation of a hydrocarbon pool (HP), usually composed of aromatic compounds of different sizes. HP is alkylated by methanol and afterward cracked, leading to the formation of olefins. Despite the importance of HP, its formation and growth in size are exceedingly dependent on the porosity of the catalyst. The ideal is that the formed HP remains stable throughout the reaction because the growth in its size causes blockage of the small catalyst pores, decreasing its capacity. Herein we studied chabazite zeolites with different porosity and structure, caused by variation in the particle size and pores’ volume. Porosity influenced the formation of HP species in quantity (as revealed by thermogravimetric analysis (TGA)) and polymerization degree (gas chromatography coupled with mass spectrometer (GC-MS) analysis) and, consequently, the MTO reaction’s performance.
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spelling Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins ReactionMTO reactionCHA zeoliteporosity of catalystidentification of cokeThe pore size of the chabazite structure is exceptionally suitable for the methanol to olefins (MTO) reaction. The reaction has an induction period required for the formation of a hydrocarbon pool (HP), usually composed of aromatic compounds of different sizes. HP is alkylated by methanol and afterward cracked, leading to the formation of olefins. Despite the importance of HP, its formation and growth in size are exceedingly dependent on the porosity of the catalyst. The ideal is that the formed HP remains stable throughout the reaction because the growth in its size causes blockage of the small catalyst pores, decreasing its capacity. Herein we studied chabazite zeolites with different porosity and structure, caused by variation in the particle size and pores’ volume. Porosity influenced the formation of HP species in quantity (as revealed by thermogravimetric analysis (TGA)) and polymerization degree (gas chromatography coupled with mass spectrometer (GC-MS) analysis) and, consequently, the MTO reaction’s performance.Sociedade Brasileira de Química2021-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021000501051Journal of the Brazilian Chemical Society v.32 n.5 2021reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20210008info:eu-repo/semantics/openAccessFlorindo,Bianca R.Catuzo,Gabriel L.Martins,Leandroeng2021-04-28T00:00:00Zoai:scielo:S0103-50532021000501051Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2021-04-28T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction
title Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction
spellingShingle Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction
Florindo,Bianca R.
MTO reaction
CHA zeolite
porosity of catalyst
identification of coke
title_short Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction
title_full Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction
title_fullStr Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction
title_full_unstemmed Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction
title_sort Porosity of CHA Zeolite Driving the Formation of Polyaromatic Coke Species in the Methanol to Olefins Reaction
author Florindo,Bianca R.
author_facet Florindo,Bianca R.
Catuzo,Gabriel L.
Martins,Leandro
author_role author
author2 Catuzo,Gabriel L.
Martins,Leandro
author2_role author
author
dc.contributor.author.fl_str_mv Florindo,Bianca R.
Catuzo,Gabriel L.
Martins,Leandro
dc.subject.por.fl_str_mv MTO reaction
CHA zeolite
porosity of catalyst
identification of coke
topic MTO reaction
CHA zeolite
porosity of catalyst
identification of coke
description The pore size of the chabazite structure is exceptionally suitable for the methanol to olefins (MTO) reaction. The reaction has an induction period required for the formation of a hydrocarbon pool (HP), usually composed of aromatic compounds of different sizes. HP is alkylated by methanol and afterward cracked, leading to the formation of olefins. Despite the importance of HP, its formation and growth in size are exceedingly dependent on the porosity of the catalyst. The ideal is that the formed HP remains stable throughout the reaction because the growth in its size causes blockage of the small catalyst pores, decreasing its capacity. Herein we studied chabazite zeolites with different porosity and structure, caused by variation in the particle size and pores’ volume. Porosity influenced the formation of HP species in quantity (as revealed by thermogravimetric analysis (TGA)) and polymerization degree (gas chromatography coupled with mass spectrometer (GC-MS) analysis) and, consequently, the MTO reaction’s performance.
publishDate 2021
dc.date.none.fl_str_mv 2021-05-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021000501051
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021000501051
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20210008
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.32 n.5 2021
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
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reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
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