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Thermochemistry of Rare Earth Perovskites

Published online by Cambridge University Press:  30 June 2016

Dawei Feng
Affiliation:
Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California, Davis, One Shields Avenue, Davis, CA 95616, United States
Alexandra Navrotsky*
Affiliation:
Peter A. Rock Thermochemistry Laboratory and NEAT ORU, University of California, Davis, One Shields Avenue, Davis, CA 95616, United States
*
*Corresponding author email address: [email protected] (A. Navrotsky). Tel.: (530) 752-3292; fax: (530) 752-9307
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Abstract

The rare earth (RE) mineral loparite with the chemical composition (RE, Na, Sr, Ca)(Ti, Nb, Ta, Fe+3)O3 is the principal ore of the light rare earth elements (LREE) as well as niobium and tantalum. The enthalpies of formation of RE0.67-xNa3xTiO3 (RE = La, Ce) and Ca1-2xNaxLaxTiO3 from oxides and elements of lanthanum and cerium perovskites and their solid solutions have been obtained using high temperature oxide melt solution calorimetry. RE0.67-xNa3xTiO3 (RE = La, Ce) perovskites become more stable relative to oxide components as sodium content increases. Na0.5Ce0.5TiO3 and Na0.5La0.5TiO3 can be considered stable endmembers in natural loparite minerals. For perovskite solid solutions Ca1-2xNaxLaxTiO3, the enthalpies of formation from the constituent oxides $\Delta {\rm{H}}_{{\rm{f}},\,{\rm{ox}}}^^\circ$ become more exothermic with increasing Na+La content, suggesting a stabilizing effect of the substitution 2Ca2+ → Na+ + La3+ on the perovskite structure. The trend of increasing thermodynamic stability with decreasing structural distortion is similar to that seen in many other ABO3 perovskites.

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Articles
Copyright
Copyright © Materials Research Society 2016 

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