• journal_title：Clays and Clay Minerals
• Contributor：K. B. Rozov ; U. Berner ; D. A. Kulik ; L. W. Diamond
• Publisher：Clay Minerals Society
• Date：2011-
• Format：text/html
• Language：en
• Identifier：10.1346/CCMN.2011.0590301
• journal_abbrev：Clays and Clay Minerals
• issn：0009-8604
• volume：59
• issue：3
• firstpage：215
• section：Articles

The naturally occurring layered double hydroxides (LDH, or anionic clays) are of particular interest in environmental geochemistry because of their ability to retain hazardous cations and especially anions. However, incorporation of these minerals into predictive models of water–rock interaction in contaminant environments, including radioactive-waste repositories, is hampered by a lack of thermodynamic and stability data. To fill part of this gap the present authors have derived properties of one of the complex multicomponent solid solutions within the LDH family: the hydrotalcite–pyroaurite series, Mg₃(Al_1−xFe_x)(OH)₈(CO₃)_0.5·2.5H₂O.

Members of the hydrotalcite–pyroaurite series with fixed Mg^II/(Al^III+Fe^III) = 3 and various Fe^III/(Fe^III+Al^III) ratios were synthesized by co-precipitation and dissolved in long-term experiments at 23±2°C and pH = 11.40±0.03. The chemical compositions of co-existing solid and aqueous phases were determined by inductively coupled plasma-optical emission spectroscopy, thermogravimetric analysis, and liquid scintillation counting of ⁵⁵Fe tracers; X-ray diffraction and Raman were used to characterize the solids. Based on good evidence for reversible equilibrium in the experiments, the thermodynamic properties of the solid solution were examined using total-scale Lippmann solubility products, ∑Π_T. No significant difference was observed between values of ∑Π_T from co-precipitation and from dissolution experiments throughout the whole range of Fe/Al ratios. A simple ideal solid-solution model with similar end-member ∑Π_T values (a regular model with 0 < W_G < 2 kJ mol⁻¹) was sufficient to describe the full range of intermediate mineral compositions. In turn, this yielded the first estimate of the standard Gibbs free energy of the pyroaurite end member, G^o_298,Pyr = −3882.60±2.00 kJ/mol, consistent with G^o_298,Htlc = −4339.85 kJ/mol of the hydrotalcite end member, and with the whole range of solubilities of the mixed phases. The molar volumes of the solid-solution at standard conditions were derived from X-ray data. Finally, Helgeson’s method was used to extend the estimates of standard molar entropy and heat capacity of the end members over the pressure–temperature range 0–70°C and 1–100 bar.