Dry reforming of methane at moderate temperatures over modified Co-Al Co-precipitated catalysts
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , |
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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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 |
_version_ |
1754212665056559104 |