Please use this identifier to cite or link to this item: https://doi.org/10.1039/b819993k
DC FieldValue
dc.titleCation-anion double hydrolysis derived mesoporous γ-Al 2O3 as an environmentally friendly and efficient aldol reaction catalyst
dc.contributor.authorBai, P.
dc.contributor.authorWu, P.
dc.contributor.authorYan, Z.
dc.contributor.authorZhao, X.S.
dc.date.accessioned2014-12-02T08:05:24Z
dc.date.available2014-12-02T08:05:24Z
dc.date.issued2009
dc.identifier.citationBai, P., Wu, P., Yan, Z., Zhao, X.S. (2009). Cation-anion double hydrolysis derived mesoporous γ-Al 2O3 as an environmentally friendly and efficient aldol reaction catalyst. Journal of Materials Chemistry 19 (11) : 1554-1563. ScholarBank@NUS Repository. https://doi.org/10.1039/b819993k
dc.identifier.issn09599428
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/114493
dc.description.abstractParameters, such as crystallization temperature, pH, P123 content and aluminium source in the synthesis of mesoporous aluminas using the cation-anion double hydrolysis method (P. Bai, P. Wu, G. Zhao, Z. Yan and X. S. Zhao, J. Mater. Chem., 2008, 18, 74) were examined. With the assistance of characterization techniques, such as N2 adsorption, X-ray diffraction (XRD), transmission electronic microscopy (TEM), selected area electron diffraction (SAED) and 27Al magic-angle spinning (MAS) nuclear magnetic resonance (NMR), it was found that the parameters studied all have an influence on both the textural properties and the crystalline structure of the resultant solid materials. Dependence of the catalytic activity of the mesoporous alumina materials on the synthesis parameters was observed. The observed remarkably high catalytic activity of the mesoporous alumina materials is attributed to the high surface area, surface basicity, pure γ-Al 2O3 phase and absence of anion residues, such as SO 4 2-. © 2009 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b819993k
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1039/b819993k
dc.description.sourcetitleJournal of Materials Chemistry
dc.description.volume19
dc.description.issue11
dc.description.page1554-1563
dc.description.codenJMACE
dc.identifier.isiut000263843400006
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