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Crystal Data for Two Molybdates MIV (MoO4)2 With MIV = Zr, Hf

Published online by Cambridge University Press:  28 October 2013

M. Auray
Affiliation:
Université Pierre et Marie Curie, Laboratoire de Chimie II, Tour 54, 4, Place Jussieu, 75230 Paris Cedex 05, France
M. Quarton
Affiliation:
Université Pierre et Marie Curie, Laboratorie de Chimie Minérals, CNRS-CRL85, Tour 54, 4, Place Jussieu, 75230 Paris Cedex 05, France
P. Tarte
Affiliation:
Université de Liêge, Institut de Chimie, B-4000 Sart-Tilman par Liêge 1, Belgium

Abstract

Two molybdates MIV (MoO4)2 (with MIV = Hf or Zr) were synthesized by solid state reaction between MIVO2 and MoO3. Zirconium molybdate undergoes a reversible phase transition at 952 K.

Hf(MoO4)2 and H.T. Zr(MoQ4)2, obtained as single crystals, are trigonal, space group with Z = 6; the cell dimensions are respectively a = 10.1005(3), c = 11.7230(5)Å; V = 1035.76(11)Å3; Dm(298 K) = 4.78(4), Dx = 4.792 Mg m−3 and a = 10.1409(3), c = 11.7097(5)Å; V = 1042.88(11)Å3; Dm (298 K) = 3.91(4), Dx = 3.926 Mg m−3.

L.T. Zr(MoO4)2, indexed by the Visser automatic indexing program (1969) was found to be monoclinic, possible space group P2, P21 or Pm with Z = 4; the cell dimensions are a = 9.7557(5), b = 7.9373(5), c = 7.4631(4)Å, β = 97.959°(5); V = 572.3(5)Å Dm(298 K) = 4.74(5), Dx = 4.770 Mg m−3. Powder diffraction data were obtained at 293 K on a counter diffractometer with Ni-filtered copper radiation ( = 1.5418 Å).

Type
Research Article
Copyright
Copyright © Cambridge University Press 1987

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References

Freundlich, W. & Thoret, J. (1967). C. R. Séances Acad. Sci. Ser. C265, 9698.Google Scholar
Rimsky, A., Thoret, J. & Freundlich, W. (1968). C. R. Séances Acad. Sci. Ser. C267, 14681470.Google Scholar
Smith, G. S. & Snyder, R. L. (1969). J. Appl. Crystallogr. 12, 6065.Google Scholar
Trunov, V. K. & Kovba, L. M. (1967). Russ. J. Inorg. Cham. (Engl. Transl.) 12, 1703.Google Scholar
Visser, J. W. (1969). J. Appl. Crystallogr. 2, 8995.Google Scholar
Williams, D. E. (1964). LCR-2: A Fortran Lattice-constant Refinement Program. U.S.A.E.C. Rep.Google Scholar