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Article: Incorporating organic polymer into silica walls: A novel strategy for synthesis of templated mesoporous silica with tunable pore structure

TitleIncorporating organic polymer into silica walls: A novel strategy for synthesis of templated mesoporous silica with tunable pore structure
Authors
KeywordsCo-polymerization
Furfuryl alcohol
Mesoporous silica
Templating synthesis
Triblock copolymer
Issue Date2005
PublisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/micromeso
Citation
Microporous And Mesoporous Materials, 2005, v. 82 n. 1-2, p. 183-189 How to Cite?
AbstractThis paper presents a novel approach to the synthesis of mesoporous silicas with tunable pore size, pore volume and pore structure. Organic poly(furfuryl alcohol) (PFA) was incorporated into silica walls by co-polymerization of furfuryl alcohol (FA) and silica source such as tetraethyl orthosilicate during the triblock copolymer P123 templating process. Mesoporous silicas with wormhole pore structure were obtained by completely burning off organic polymers P123 and PFA from the silica-P123-PFA nanocomposites, and their pore size and pore volume were increased by simply adding a certian amount of FA. TGA, N 2 sorption, SEM, TEM and FT-IR were used to characterize the silica-P123 and silica-P123-PFA nanocomposites, and their final calcined mesoporous silicas. It is suggested that the P123 templating mechanism is not changed by the addition of FA under our experimental conditions, which is evidenced by the similar pore structure and pore size in the carbonized silica-PFA nanocomposites prepared with the addition of different amount of FA. When the large amount of FA (2.12FA:1SiO2 by mole) was used in the synthesis, the pore size was expanded from 3.4 nm to 7.4 nm, and the pore volume was increased from 0.46 cm3/g to 1.37 cm3/g. At the same time, the pore size distribution was broadened. The BET surface area of the mesporous silicas was measured to be 632-728 m2/g. As a result, the strategy reported here is simple and effective for tailoring pore size and pore structure of mesoporous silicas in the templating synthesis. © 2005 Elsevier Inc. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/69473
ISSN
2023 Impact Factor: 4.8
2023 SCImago Journal Rankings: 0.941
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorYao, Jen_HK
dc.contributor.authorWang, Hen_HK
dc.contributor.authorChan, KYen_HK
dc.contributor.authorZhang, Len_HK
dc.contributor.authorXu, Nen_HK
dc.date.accessioned2010-09-06T06:13:59Z-
dc.date.available2010-09-06T06:13:59Z-
dc.date.issued2005en_HK
dc.identifier.citationMicroporous And Mesoporous Materials, 2005, v. 82 n. 1-2, p. 183-189en_HK
dc.identifier.issn1387-1811en_HK
dc.identifier.urihttp://hdl.handle.net/10722/69473-
dc.description.abstractThis paper presents a novel approach to the synthesis of mesoporous silicas with tunable pore size, pore volume and pore structure. Organic poly(furfuryl alcohol) (PFA) was incorporated into silica walls by co-polymerization of furfuryl alcohol (FA) and silica source such as tetraethyl orthosilicate during the triblock copolymer P123 templating process. Mesoporous silicas with wormhole pore structure were obtained by completely burning off organic polymers P123 and PFA from the silica-P123-PFA nanocomposites, and their pore size and pore volume were increased by simply adding a certian amount of FA. TGA, N 2 sorption, SEM, TEM and FT-IR were used to characterize the silica-P123 and silica-P123-PFA nanocomposites, and their final calcined mesoporous silicas. It is suggested that the P123 templating mechanism is not changed by the addition of FA under our experimental conditions, which is evidenced by the similar pore structure and pore size in the carbonized silica-PFA nanocomposites prepared with the addition of different amount of FA. When the large amount of FA (2.12FA:1SiO2 by mole) was used in the synthesis, the pore size was expanded from 3.4 nm to 7.4 nm, and the pore volume was increased from 0.46 cm3/g to 1.37 cm3/g. At the same time, the pore size distribution was broadened. The BET surface area of the mesporous silicas was measured to be 632-728 m2/g. As a result, the strategy reported here is simple and effective for tailoring pore size and pore structure of mesoporous silicas in the templating synthesis. © 2005 Elsevier Inc. All rights reserved.en_HK
dc.languageengen_HK
dc.publisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/micromesoen_HK
dc.relation.ispartofMicroporous and Mesoporous Materialsen_HK
dc.rightsMicroporous and Mesoporous Materials. Copyright © Elsevier BV.en_HK
dc.subjectCo-polymerizationen_HK
dc.subjectFurfuryl alcoholen_HK
dc.subjectMesoporous silicaen_HK
dc.subjectTemplating synthesisen_HK
dc.subjectTriblock copolymeren_HK
dc.titleIncorporating organic polymer into silica walls: A novel strategy for synthesis of templated mesoporous silica with tunable pore structureen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1387-1811&volume=82&spage=183&epage=189&date=2005&atitle=Incorporating+organic+polymer+into+silica+walls:+A+novel+strategy+for+synthesis+of+templated+mesoporous+silica+with+tunable+pore+structureen_HK
dc.identifier.emailChan, KY:hrsccky@hku.hken_HK
dc.identifier.authorityChan, KY=rp00662en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.micromeso.2005.03.012en_HK
dc.identifier.scopuseid_2-s2.0-20144368866en_HK
dc.identifier.hkuros106518en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-20144368866&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume82en_HK
dc.identifier.issue1-2en_HK
dc.identifier.spage183en_HK
dc.identifier.epage189en_HK
dc.identifier.isiWOS:000230274200014-
dc.publisher.placeNetherlandsen_HK
dc.identifier.scopusauthoridYao, J=8902683600en_HK
dc.identifier.scopusauthoridWang, H=8393378100en_HK
dc.identifier.scopusauthoridChan, KY=7406034142en_HK
dc.identifier.scopusauthoridZhang, L=10639549900en_HK
dc.identifier.scopusauthoridXu, N=7202694866en_HK
dc.identifier.issnl1387-1811-

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