Please use this identifier to cite or link to this item: https://doi.org/10.1007/s10563-008-9048-2
DC FieldValue
dc.titleStructural and morphological control in the preparation of high surface area zirconia
dc.contributor.authorJaenicke, S.
dc.contributor.authorChuah, G.K.
dc.contributor.authorRaju, V.
dc.contributor.authorNie, Y.T.
dc.date.accessioned2014-10-16T08:49:30Z
dc.date.available2014-10-16T08:49:30Z
dc.date.issued2008-09
dc.identifier.citationJaenicke, S., Chuah, G.K., Raju, V., Nie, Y.T. (2008-09). Structural and morphological control in the preparation of high surface area zirconia. Catalysis Surveys from Asia 12 (3) : 153-169. ScholarBank@NUS Repository. https://doi.org/10.1007/s10563-008-9048-2
dc.identifier.issn15711013
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95578
dc.description.abstractThe methods for the formation of zirconia including precipitation from aqueous salts, sol-gel synthesis from zirconium alkoxides, and the templated synthesis using surfactants are described in this review. The surface areas obtained vary widely but invariably decrease upon prolonged calcination. Digestion of hydrous zirconia and incorporation of dopants such as lanthanum, yttrium, or sulfate ions can increase the surface area and thermal stability. However, these methods also affect the crystal phase of zirconia. The transformation from the metastable tetragonal to the monoclinic phase occurs during the cooling phase of calcination. Mechanisms for the stabilization of the tetragonal phase are discussed. Zirconia with well-ordered mesopores or in the form of hollow spheres can be prepared but lack thermal stability, unless doped with phosphates, silicates or sulfates. © Springer Science+Business Media, LLC 2008.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s10563-008-9048-2
dc.sourceScopus
dc.subjectAcid-base catalysis
dc.subjectDigestion
dc.subjectHigh surface area
dc.subjectMesoporous
dc.subjectSol-gel
dc.subjectZirconia
dc.typeReview
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1007/s10563-008-9048-2
dc.description.sourcetitleCatalysis Surveys from Asia
dc.description.volume12
dc.description.issue3
dc.description.page153-169
dc.identifier.isiut000259935600001
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