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Powder X-ray data for the ammonium trioxalatoaluminate (III) and its hydrates: (NH4Al(C2O4)3·xH2O, x=0,2,3

Published online by Cambridge University Press:  10 January 2013

Mohamed Ezahri ,
Georges Coffy  and
Bernard F. Mentzen
Mohamed Ezahri
Affiliation:
Laboratoire de Physico-Chimie Minérale, URA n°. 116 du CNRS, Université Claude-Bernard, LYON 1, 43 Bd du 11 Novembre 1918, F-69622 Villeurbanne, Cedex, France
Georges Coffy
Affiliation:
Laboratoire de Physico-Chimie Minérale, URA n°. 116 du CNRS, Université Claude-Bernard, LYON 1, 43 Bd du 11 Novembre 1918, F-69622 Villeurbanne, Cedex, France
Bernard F. Mentzen
Affiliation:
Laboratoire de Physico-Chimie Minérale, URA n°. 116 du CNRS, Université Claude-Bernard, LYON 1, 43 Bd du 11 Novembre 1918, F-69622 Villeurbanne, Cedex, France
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Abstract

X-ray powder diffraction data are reported for the trihydrated (A3N), the dihydrated (A2N), and the anhydrous ammonium trioxalatoaluminate (III) (AN). A3N is triclinic with space group . A2N and AN are monoclinic with space groups P21/c and P21/n respectively. The stability domains are A3N: –7.8 to 86 °C; A2N: 86 to 102 °C; AN: 102 to 180 °C.

Keywords

ammonium trioxalatoaluminateshydratepowder diffraction data
Type
Research Article
Information
Powder Diffraction , Volume 10 , Issue 3 , September 1995 , pp. 195 - 197
Copyright
Copyright © Cambridge University Press 1995

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References

Bulc, N., Golic, L., and Siftar, J. (1984). “Structure of ammonium trisoxalato gallate(III) trihydrate, (I)(NH4)3Ga(C2O4)3·3H2O, and ammonium tris-oxalato aluminate (III) trihydrate (II)(NH4)3Al(C2O4)3·3H2O,” Acta Cryst. C 40, 1829–1832.Google Scholar
De Wolff, P. M. (1968). “A simplified criterion for the reliability of powder pattern indexing,” J. Appl. Crystallogr. 1, 108–109.CrossRefGoogle Scholar
Ezahri, M., Coffy, G., Chassagneux, F., and Mentzen, B. F. (1994). “Study of aqueous solubility and thermal behaviour of ammonium tris-oxalato aluminate(III) and its hydrates: (NH4)3Al(C2O4)3·xH2O, x = 0,2,3,” Eur. J. Solid State Inorg. Chem. 31, 391–399.Google Scholar
Mentzen, B. R., Favre, R., and Cauwet, F. (1994). “Characterization of guest molecules sorbed in zeolithes of known structures. Part VI— Localization of methanol at several pore fillings in a highly siliceous MFI silicalite material,” Mater. Res. Bull. 29, 587–594.CrossRefGoogle Scholar
Mentzen, B. F., and Sacerdote-Peronnet, M. (1993). “Flexibility of the framework structure in highly crystalline silicalite during the reversible monoclinic/orthorhombic solid state polymorphic phase transition,” Mater. Res. Bull. 28, 1017–1024.CrossRefGoogle Scholar
Merrachi, E. H., Cohen-Adad, R., Chassagneux, F., and Mentzen, B. F. (1987a). “Etude du diagramme ternaire H2O-(NH4)3Cr(C2O4)3-(NH4)3Fe(C2O4)3. Isothermes 25 et 70 °C,” Rev. Chim. Min. 24, 489–502.Google Scholar
Merrachi, E. H., Mentzen, B. F., and Chassagneux, F., (1987b). “Données cristallographiques sur le trioxalato-chromate(III) d'ammonium trihydrate: (NH4)3Cr(C2O4)3·3H2O,” Powder Diffr. 2, 104–105.CrossRefGoogle Scholar
Merrachi, E. H., Mentzen, B. F., and Chassagneux, F. (1988). “Données cristallographiques sur le trioxalato-ferrate(III) d'ammonium trihydraté: (NH4)3Fe(C2O4)3·3H2O,” Powder Diffr. 3, 96–97.CrossRefGoogle Scholar
Pâris, J. (1963). Ph. D. thesis, Lyon, France, no. 315.Google Scholar
Smith, G. S. and Snyder, R. L. (1979). “FN: a criterion for rating powder diffraction patterns and evaluating the reliability of powder-pattern indexing,” J. Appl. Crystallogr. 12, 60–65.CrossRefGoogle Scholar
Visser, J. W. (1969). “A fully automatic program for finding the unit cell from powder data,” J. Appl. Cryst. 2, 89–95.CrossRefGoogle Scholar