Transformation of methylcyclohexane on an FCC catalyst

Detalhes bibliográficos
Autor(a) principal: Rabeharitsara,A.
Data de Publicação: 2003
Outros Autores: Cerqueira,H.S., Magnoux,P., Guisnet,M., Costa,A.F., Sousa-Aguiar,E.F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Chemical Engineering
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322003000200003
Resumo: The transformation of methylcyclohexane at 723 K over on a USHY sample and on an FCC catalyst composed of 30% USHY and 70% matrix containing 25% Al2O3 was studied. With both samples, C2-C7 alkenes and alkanes, cyclopentane and methylcyclopentane (cracking products), dimethylcyclopentanes and ethylcyclopentane (isomers) and aromatics appeared as primary products. The activity and selectivity of fresh samples as well as the influence of coke deposits on porosity and selectivity are discussed.
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spelling Transformation of methylcyclohexane on an FCC catalystUSHY zeoliteFCC catalystmethylcyclohexanecokedeactivationThe transformation of methylcyclohexane at 723 K over on a USHY sample and on an FCC catalyst composed of 30% USHY and 70% matrix containing 25% Al2O3 was studied. With both samples, C2-C7 alkenes and alkanes, cyclopentane and methylcyclopentane (cracking products), dimethylcyclopentanes and ethylcyclopentane (isomers) and aromatics appeared as primary products. The activity and selectivity of fresh samples as well as the influence of coke deposits on porosity and selectivity are discussed.Brazilian Society of Chemical Engineering2003-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322003000200003Brazilian Journal of Chemical Engineering v.20 n.2 2003reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/S0104-66322003000200003info:eu-repo/semantics/openAccessRabeharitsara,A.Cerqueira,H.S.Magnoux,P.Guisnet,M.Costa,A.F.Sousa-Aguiar,E.F.eng2003-06-25T00:00:00Zoai:scielo:S0104-66322003000200003Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2003-06-25T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false
dc.title.none.fl_str_mv Transformation of methylcyclohexane on an FCC catalyst
title Transformation of methylcyclohexane on an FCC catalyst
spellingShingle Transformation of methylcyclohexane on an FCC catalyst
Rabeharitsara,A.
USHY zeolite
FCC catalyst
methylcyclohexane
coke
deactivation
title_short Transformation of methylcyclohexane on an FCC catalyst
title_full Transformation of methylcyclohexane on an FCC catalyst
title_fullStr Transformation of methylcyclohexane on an FCC catalyst
title_full_unstemmed Transformation of methylcyclohexane on an FCC catalyst
title_sort Transformation of methylcyclohexane on an FCC catalyst
author Rabeharitsara,A.
author_facet Rabeharitsara,A.
Cerqueira,H.S.
Magnoux,P.
Guisnet,M.
Costa,A.F.
Sousa-Aguiar,E.F.
author_role author
author2 Cerqueira,H.S.
Magnoux,P.
Guisnet,M.
Costa,A.F.
Sousa-Aguiar,E.F.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Rabeharitsara,A.
Cerqueira,H.S.
Magnoux,P.
Guisnet,M.
Costa,A.F.
Sousa-Aguiar,E.F.
dc.subject.por.fl_str_mv USHY zeolite
FCC catalyst
methylcyclohexane
coke
deactivation
topic USHY zeolite
FCC catalyst
methylcyclohexane
coke
deactivation
description The transformation of methylcyclohexane at 723 K over on a USHY sample and on an FCC catalyst composed of 30% USHY and 70% matrix containing 25% Al2O3 was studied. With both samples, C2-C7 alkenes and alkanes, cyclopentane and methylcyclopentane (cracking products), dimethylcyclopentanes and ethylcyclopentane (isomers) and aromatics appeared as primary products. The activity and selectivity of fresh samples as well as the influence of coke deposits on porosity and selectivity are discussed.
publishDate 2003
dc.date.none.fl_str_mv 2003-06-01
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=S0104-66322003000200003
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322003000200003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0104-66322003000200003
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 Brazilian Society of Chemical Engineering
publisher.none.fl_str_mv Brazilian Society of Chemical Engineering
dc.source.none.fl_str_mv Brazilian Journal of Chemical Engineering v.20 n.2 2003
reponame:Brazilian Journal of Chemical Engineering
instname:Associação Brasileira de Engenharia Química (ABEQ)
instacron:ABEQ
instname_str Associação Brasileira de Engenharia Química (ABEQ)
instacron_str ABEQ
institution ABEQ
reponame_str Brazilian Journal of Chemical Engineering
collection Brazilian Journal of Chemical Engineering
repository.name.fl_str_mv Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)
repository.mail.fl_str_mv rgiudici@usp.br||rgiudici@usp.br
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