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  • American Ceramics Society  (3)
  • American Chemical Society  (1)
  • 1995-1999  (4)
  • 1960-1964
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  • 1
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A composition-graded solid electrolyte has been used to determine the standard Gibbs free energy of formation of lanthanum zirconate (La2Zr2O7) from the component oxides lanthana (La2O3) (A-rare earth) and zirconia (ZrO2) (monoclinic) in the temperature range of 870–1240 K. The cell used for measurement can be represented as Pt, O2, CaO + CaF2∥ CaF2| (LaF3)x(CaF2)1-x∥LaF3+ La2Zr2O7+ ZrO2, O2, Pt x=0 x=0.32 A composition-graded electrolyte has been introduced to compensate the solubility effects of the electrode material (lanthanum fluoride, LaF3) in the solid electrolyte (calcium fluoride, CaF2). The ability of the graded electrolyte to gen-erate a Nernstian response is demonstrated, using electrodes with known fluorine chemical potentials. For the reaction La2O3 (A-rare earth) + 2ZrO2 (monoclinic) → La2Zr2O7 (pyrochlore), the Gibbs free energy change (ΔG°f,ox) is given by the formula −133800 −10.32T (±4500) (in units of J/mol). The enthalpy and entropy of formation of La2Zr2O7 obtained in this study are in good agreement with calorimetric data. The “third-law” enthalpy of formation of La2Zr2O7, from the component oxides at 298.15 K, is −133.8 ± 5 kJ/mol.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Solid-state miscibility gap in the pseudo-binary calcium oxide-strontium oxide (CaO-SrO) system is delineated by X-ray diffractometry studies on samples equilibrated either under vacuum or in a flowing inert-gas atmosphere at temperatures of 973-1273 K. For the CaxSr1−xO solid solution, an asymmetric phase boundary that is characterized by a critical temperature of 1173 (±3) K and a composition of x= 0.53 (±0.01) is obtained. The excess Gibbs energy of mixing of the solid solution, which is derived from the experimental phase-boundary compositions and temperatures, can be represented by the expression ΔGE=x (1−x)[(27040 − 5.82 T) x+ (24915 − 5.34 T)(1 −x)] (in units of J/mol). It is necessary to include excess entropy terms to obtain a good fit to the experimental data. The chemical spinodal curve is computed from the thermodynamic parameters. The results obtained in this study are compared with phase-diagram and calorimetric information that is available in the literature.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The standard Gibbs energy of formation of the spinel MgAl2O4 from component oxides, MgO and α-Al2O3, has been determined in the temperature range 900 to 1250 K using a solid-state cell incorporating single-crystal CaF2 as the solid electrolyte. The cell can be represented as—Pt,O2,MgO+MgF2|CaF2|MgF2+MgAl2O4+α-Al2O3,O2,Pt—The standard Gibbs energy of formation from binary oxides, computed from the reversible emf, can be represented by the expression—capdeltaG°f,ox=−23600 − 5.91T(±150) J/mol—The ‘second-law’ enthalpy of formation of MgAl2O4 obtained in this study is in good agreement with high-temperature solution calorimetric studies reported in the literature.
    Type of Medium: Electronic Resource
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  • 4
    Publication Date: 1998-04-29
    Print ISSN: 0020-1669
    Electronic ISSN: 1520-510X
    Topics: Chemistry and Pharmacology
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