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Hydration of selected divalent. beta. double prime -aluminas

Journal Article · · Chemistry of Materials; (USA)
OSTI ID:5562946
;  [1];  [2]
  1. Univ. of Pennsylvania, Philadelphia (USA)
  2. Univ. of Uppsala (Sweden)
The absorption and desorption of H{sub 2}O by Ca(II)-{beta}{double prime}-alumina, Ba(II)-{beta}{double prime}-alumina, and Ba(II)-{beta}{double prime}-ferrite were studied by thermogravimetry, differential scanning calorimetry, and evolved gas analysis, and the crystal structures of Ba{sub 0.83}Mg{sub 0.67}Al{sub 10.33}O{sub 17}{center dot}(H{sub 2}O){sub 0.64} and Ca{sub 0.83}Mg{sub 0.67}Al{sub 10.33}O{sub 17}{center dot}(H{sub 2}O){sub 1.0} were determined by the refinement of single-crystal X-ray diffraction data. The crystals are in the rhombohedral space group, R{bar 3}m, and have three formula units per hexagonal unit cell. The hexagonal cell dimensions for the hydrated Ba(II) isomorph area a = 5.617 (1) {angstrom}, c = 34.115 (8) {angstrom}, and V = 932.2 (4) {angstrom}{sup 3}, and for the hydrated Ca(II) isomorph are a = 5.628 (1) {angstrom}, c = 33.837 (11) {angstrom}, and V = 928.2 (4) {angstrom}{sup 3}. A comparison with previously reported data for other isomorphs indicates that in {beta}{double prime}-alumina-type compounds absorbed water appears to interact more strongly with the structural framework than with the mobile cations.
OSTI ID:
5562946
Journal Information:
Chemistry of Materials; (USA), Journal Name: Chemistry of Materials; (USA) Vol. 3:2; ISSN CMATE; ISSN 0897-4756
Country of Publication:
United States
Language:
English