Mesoporous molecular sieve MCM-41 synthesis from fluoride media

Detalhes bibliográficos
Autor(a) principal: Bastos,F. S.
Data de Publicação: 2011
Outros Autores: Lima,O. A., Raymundo Filho,C., Fernandes,L. D.
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=S0104-66322011000400010
Resumo: A study of the synthesis of MCM-41 mesoporous molecular sieves in fluoride media, having no alkaline metal ions, was performed by changing the gel composition and crystallization temperature and time. X-ray diffraction and nitrogen adsorption analyses showed that highly ordered MCM-41 samples were obtained from gels with a NH4OH/SiO2 molar ratio in the 3.25-4.3 range (room temperature synthesis) or in the 4.3-20 range (24 hours at 373 K). During calcination, unit cell shrinkage, caused by high temperature polycondensation of the SiOH groups, was observed for all samples. The samples synthesized at high temperature (373 K) or using low pH gels (7.5) underwent lower unit cell shrinkage than those obtained at room temperature or high pH (9.0), indicating that the former samples had lower SiOH groups content than the latter. These highly-ordered samples showed large surface area (ca. 1100 m²/g) and pore volume (ca. 0.80 cm³/g), also presenting a narrow pore size distribution. Due to higher silicate polycondensation and a thicker pore wall, the samples synthesized at 373 K were more hydrothermally stable than those obtained at room temperature.
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spelling Mesoporous molecular sieve MCM-41 synthesis from fluoride mediaMesoporous silicaMCM-41Fluoride mediumMesoporous molecular sievesM41SA study of the synthesis of MCM-41 mesoporous molecular sieves in fluoride media, having no alkaline metal ions, was performed by changing the gel composition and crystallization temperature and time. X-ray diffraction and nitrogen adsorption analyses showed that highly ordered MCM-41 samples were obtained from gels with a NH4OH/SiO2 molar ratio in the 3.25-4.3 range (room temperature synthesis) or in the 4.3-20 range (24 hours at 373 K). During calcination, unit cell shrinkage, caused by high temperature polycondensation of the SiOH groups, was observed for all samples. The samples synthesized at high temperature (373 K) or using low pH gels (7.5) underwent lower unit cell shrinkage than those obtained at room temperature or high pH (9.0), indicating that the former samples had lower SiOH groups content than the latter. These highly-ordered samples showed large surface area (ca. 1100 m²/g) and pore volume (ca. 0.80 cm³/g), also presenting a narrow pore size distribution. Due to higher silicate polycondensation and a thicker pore wall, the samples synthesized at 373 K were more hydrothermally stable than those obtained at room temperature.Brazilian Society of Chemical Engineering2011-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322011000400010Brazilian Journal of Chemical Engineering v.28 n.4 2011reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/S0104-66322011000400010info:eu-repo/semantics/openAccessBastos,F. S.Lima,O. A.Raymundo Filho,C.Fernandes,L. D.eng2011-11-24T00:00:00Zoai:scielo:S0104-66322011000400010Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:2011-11-24T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false
dc.title.none.fl_str_mv Mesoporous molecular sieve MCM-41 synthesis from fluoride media
title Mesoporous molecular sieve MCM-41 synthesis from fluoride media
spellingShingle Mesoporous molecular sieve MCM-41 synthesis from fluoride media
Bastos,F. S.
Mesoporous silica
MCM-41
Fluoride medium
Mesoporous molecular sieves
M41S
title_short Mesoporous molecular sieve MCM-41 synthesis from fluoride media
title_full Mesoporous molecular sieve MCM-41 synthesis from fluoride media
title_fullStr Mesoporous molecular sieve MCM-41 synthesis from fluoride media
title_full_unstemmed Mesoporous molecular sieve MCM-41 synthesis from fluoride media
title_sort Mesoporous molecular sieve MCM-41 synthesis from fluoride media
author Bastos,F. S.
author_facet Bastos,F. S.
Lima,O. A.
Raymundo Filho,C.
Fernandes,L. D.
author_role author
author2 Lima,O. A.
Raymundo Filho,C.
Fernandes,L. D.
author2_role author
author
author
dc.contributor.author.fl_str_mv Bastos,F. S.
Lima,O. A.
Raymundo Filho,C.
Fernandes,L. D.
dc.subject.por.fl_str_mv Mesoporous silica
MCM-41
Fluoride medium
Mesoporous molecular sieves
M41S
topic Mesoporous silica
MCM-41
Fluoride medium
Mesoporous molecular sieves
M41S
description A study of the synthesis of MCM-41 mesoporous molecular sieves in fluoride media, having no alkaline metal ions, was performed by changing the gel composition and crystallization temperature and time. X-ray diffraction and nitrogen adsorption analyses showed that highly ordered MCM-41 samples were obtained from gels with a NH4OH/SiO2 molar ratio in the 3.25-4.3 range (room temperature synthesis) or in the 4.3-20 range (24 hours at 373 K). During calcination, unit cell shrinkage, caused by high temperature polycondensation of the SiOH groups, was observed for all samples. The samples synthesized at high temperature (373 K) or using low pH gels (7.5) underwent lower unit cell shrinkage than those obtained at room temperature or high pH (9.0), indicating that the former samples had lower SiOH groups content than the latter. These highly-ordered samples showed large surface area (ca. 1100 m²/g) and pore volume (ca. 0.80 cm³/g), also presenting a narrow pore size distribution. Due to higher silicate polycondensation and a thicker pore wall, the samples synthesized at 373 K were more hydrothermally stable than those obtained at room temperature.
publishDate 2011
dc.date.none.fl_str_mv 2011-12-01
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=S0104-66322011000400010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66322011000400010
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0104-66322011000400010
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.28 n.4 2011
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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