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American Mineralogist; April 2004; v. 89; no. 4; p. 633-639
© 2004 Mineralogical Society of America
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Isothermal equation of state and compressional behavior of tetragonal edingtonite

Giacomo Diego Gatta1,*, Tiziana Boffa Ballaran1, Paola ComodI2 and Pier Francesco Zanazzi2

1 Bayerisches Geoinstitut, Universitaet Bayreuth, Universitaet Strasse 30, D-95447 Bayreuth, Germany
2 Dipartimento di Scienze della Terra, Università di Perugia, Piazza Università, I-06100 Perugia, Italy

Correspondence: * E-mail: diego.gatta{at}uni-bayreuth.de

The high-pressure (HP) structural evolution of a natural tetragonal edingtonite from Ice River, Canada, was investigated up to 5.1 GPa using in situ single-crystal X-ray diffraction and a diamondanvil cell. The isothermal equation of state was determined. The values of V0, KT0, and K' refined with a third-order Birch-Murnaghan equation of state (BM-EoS) are V0 = 601.6(3) Å3, KT0 = 59(2) GPa, and K' = 3.4(8). Under high-pressure conditions the main deformation mechanisms can be described by rotation/kinking of "rigid units," represented by the 4 = 1 secondary building unit (SBU), due to the tetrahedra tilting. The angle between the SBUs ({phi}) increased from 17.15(8)° at 0.0001 GPa to 20.03(9)° at 4.61 GPa.

The bulk structural compression results from the combination of the "soft" behavior of the not fully occupied channels [KT0 = 19(1) GPa for [100]-channels; KT0 = 21(1) GPa for [110]-channels] and of the rigid behavior of the tetrahedral framework.

The extra-framework cations do not increase in coordination number within the pressure range investigated. The barium occupancy factors for the Ba1 and Ba2 sites change with increasing pressure. For P > 2.3 GPa the Ba2 site is completely empty, and only the position Ba1 is occupied.




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