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TitleEvolution of crystalline aluminates from hybrid gel-derived precursors studied by XRD and multinuclear solid state MAS NMR IV: Calcium dialuminate, CaAl4O7 and calcium hexaluminate, CaAl12O19
Publication TypeJournal Article
Year of Publication2000
AuthorsMackenzie, K.J.D., Schmücker M., Smith M.E., Poplett I.J.F., and Kemmitt T.
JournalThermochimica Acta
Volume363
Issue1-2
Pagination181 - 188
Date Published2000
ISSN00406031 (ISSN)
Keywordsaluminum derivative, article, calcium derivative, chemical composition, chemical structure, Crystallization, gel, nuclear magnetic resonance imaging, solid state, thermal analysis, X ray diffraction, X ray powder diffraction
AbstractX-ray amorphous calcium aluminate gels of dialuminate and hexaluminate composition were prepared, the former by two methods, and their thermal crystallisation was monitored by thermal analysis, X-ray powder diffraction and 27Al MAS NMR. Both gel compositions lose a large amount of solvent and organic by-products below 600°C, forming amorphous precursors with 27Al NMR spectra containing resonances corresponding to tetrahedral and octahedral sites, and another site with a peak at 36-39 ppm. The dialuminate gel crystallises abruptly at 900°C to the essentially phase-pure compound containing Al predominantly in two distorted tetrahedral environments. The hexaluminate gel crystallises exothermically at 900°C to γ-alumina spinel, containing only tetrahedral and octahedral Al. The magnetoplumbite structure of the hexaluminate phase appears in an exothermic reaction at 1160°C, this phase-pure reaction product containing Al atoms in one tetrahedral and two distinguishable octahedral sites. The first 43Ca MAS NMR spectra of the crystalline dialuminate and hexaluminate are also reported. (C) 2000 Elsevier Science B.V.
URLhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0034722607&partnerID=40&md5=9c494f648b4882b819b135dd2a2e682f
DOI10.1016/S0040-6031(00)00630-4

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