Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts

Detalhes bibliográficos
Autor(a) principal: Souza,Guilherme de
Data de Publicação: 2014
Outros Autores: Marcilio,Nilson Romeu, Perez-Lopez,Oscar William
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Materials research (São Carlos. Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000400031
Resumo: M-Co-Al (M = Ca, La, Li or Mg) materials were synthesised by co-precipitation and investigated for dry reforming of methane. Thermogravimetry, temperature-programmed oxidation, reduction and CO2 desorption, specific area and X-ray diffraction were utilised for characterisation. Activity tests were conducted at atmospheric pressure, temperatures between 400-550ºC , CH4/CO2 molar ratio of 1 and GHSV of 6000 NmL CH4·g-1·h-1. The partial substitution of Co by a third element increased the area and changed the acid/base properties, reducibility and crystallinity of the oxides. These modifications resulted in higher activity for dry reforming of methane, mainly related to the decrease in the acidity of the promoted materials and, consequently, lower carbon formation. The Li-modified sample presented the lowest coke deposition due to the increase in stronger basic sites. The Mg-promoted catalyst exhibited the best activity performance. This depicts the enhancement in the reducibility and acid/base properties found in the MgCoAl sample.
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spelling Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalystsDry reforming of methaneCo-based catalystcarbon depositionprecipitation methodmixed oxideM-Co-Al (M = Ca, La, Li or Mg) materials were synthesised by co-precipitation and investigated for dry reforming of methane. Thermogravimetry, temperature-programmed oxidation, reduction and CO2 desorption, specific area and X-ray diffraction were utilised for characterisation. Activity tests were conducted at atmospheric pressure, temperatures between 400-550ºC , CH4/CO2 molar ratio of 1 and GHSV of 6000 NmL CH4·g-1·h-1. The partial substitution of Co by a third element increased the area and changed the acid/base properties, reducibility and crystallinity of the oxides. These modifications resulted in higher activity for dry reforming of methane, mainly related to the decrease in the acidity of the promoted materials and, consequently, lower carbon formation. The Li-modified sample presented the lowest coke deposition due to the increase in stronger basic sites. The Mg-promoted catalyst exhibited the best activity performance. This depicts the enhancement in the reducibility and acid/base properties found in the MgCoAl sample.ABM, ABC, ABPol2014-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000400031Materials Research v.17 n.4 2014reponame:Materials research (São Carlos. Online)instname:Universidade Federal de São Carlos (UFSCAR)instacron:ABM ABC ABPOL10.1590/1516-1439.269614info:eu-repo/semantics/openAccessSouza,Guilherme deMarcilio,Nilson RomeuPerez-Lopez,Oscar Williameng2014-09-16T00:00:00Zoai:scielo:S1516-14392014000400031Revistahttp://www.scielo.br/mrPUBhttps://old.scielo.br/oai/scielo-oai.phpdedz@power.ufscar.br1980-53731516-1439opendoar:2014-09-16T00:00Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR)false
dc.title.none.fl_str_mv Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
title Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
spellingShingle Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
Souza,Guilherme de
Dry reforming of methane
Co-based catalyst
carbon deposition
precipitation method
mixed oxide
title_short Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
title_full Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
title_fullStr Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
title_full_unstemmed Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
title_sort Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
author Souza,Guilherme de
author_facet Souza,Guilherme de
Marcilio,Nilson Romeu
Perez-Lopez,Oscar William
author_role author
author2 Marcilio,Nilson Romeu
Perez-Lopez,Oscar William
author2_role author
author
dc.contributor.author.fl_str_mv Souza,Guilherme de
Marcilio,Nilson Romeu
Perez-Lopez,Oscar William
dc.subject.por.fl_str_mv Dry reforming of methane
Co-based catalyst
carbon deposition
precipitation method
mixed oxide
topic Dry reforming of methane
Co-based catalyst
carbon deposition
precipitation method
mixed oxide
description M-Co-Al (M = Ca, La, Li or Mg) materials were synthesised by co-precipitation and investigated for dry reforming of methane. Thermogravimetry, temperature-programmed oxidation, reduction and CO2 desorption, specific area and X-ray diffraction were utilised for characterisation. Activity tests were conducted at atmospheric pressure, temperatures between 400-550ºC , CH4/CO2 molar ratio of 1 and GHSV of 6000 NmL CH4·g-1·h-1. The partial substitution of Co by a third element increased the area and changed the acid/base properties, reducibility and crystallinity of the oxides. These modifications resulted in higher activity for dry reforming of methane, mainly related to the decrease in the acidity of the promoted materials and, consequently, lower carbon formation. The Li-modified sample presented the lowest coke deposition due to the increase in stronger basic sites. The Mg-promoted catalyst exhibited the best activity performance. This depicts the enhancement in the reducibility and acid/base properties found in the MgCoAl sample.
publishDate 2014
dc.date.none.fl_str_mv 2014-08-01
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=S1516-14392014000400031
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000400031
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1516-1439.269614
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 ABM, ABC, ABPol
publisher.none.fl_str_mv ABM, ABC, ABPol
dc.source.none.fl_str_mv Materials Research v.17 n.4 2014
reponame:Materials research (São Carlos. Online)
instname:Universidade Federal de São Carlos (UFSCAR)
instacron:ABM ABC ABPOL
instname_str Universidade Federal de São Carlos (UFSCAR)
instacron_str ABM ABC ABPOL
institution ABM ABC ABPOL
reponame_str Materials research (São Carlos. Online)
collection Materials research (São Carlos. Online)
repository.name.fl_str_mv Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR)
repository.mail.fl_str_mv dedz@power.ufscar.br
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