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1 Department of Geology, Moscow State University, Vorobyevy Gory, Moscow 119899, Russia
2 Thermochemistry Facility, Department of Chemical Engineering and Materials Science, University of California at Davis, Davis, California 95616, U.S.A.
3 Institute of Mineralogy and Petrography, Academy of Sciences, Novosibirsk 630090, Russia
Correspondence: * E-mail: anavrotsky{at}ucdavis.edu
Calorimetric measurements were made on natural samples of heulandite having the composition Ca0.86Na0.37K0.06Al2.14Si6.86O18·6.1H2O and stilbite Ca1.01Na0.12Al2.12Si6.88O18·7.27H2O both from the same locality (Nidym River, E. Siberia, Russia). Enthalpies of formation and hydration were studied by calorimetry in lead borate solvent at 975 K. The enthalpies of formation from oxides and elements at 298 K of heulandite are: 238.7 ± 4.9 kJ/mol, and 10656.3 ± 8.6 kJ/mol, and of stilbite are 232.0 ± 8.3 kJ/mol and 11017.9 ± 10.9 kJ/mol respectively. The integral hydration enthalpies including the enthalpies of phase transitions during heulandite and stilbite dehydration are 209.4 ± 5.9 kJ/mol and 229.2 ± 7.4 kJ/mol at 298 K, respectively. The molar Gibbs free energies of formation for idealized calcium-sodium and pure calcium heulandites and stilbites were calculated by combining these new calorimetric data with thermodynamic quantities from the literature. Equilibrium temperatures for the reaction: Ca-stilbite = Ca-heulandite + H2O, calculated on the basis of these thermodynamic data, agree with experimental phase equilibria.
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