|
|
|
|||||||||||||||||
| JOURNAL HOME | HELP | CONTACT PUBLISHER | SUBSCRIBE | ARCHIVE | SEARCH | TABLE OF CONTENTS |
UMR-CNRS 6532 HydrASA, 40 ave du Recteur Pineau, 86022 Poitiers Cedex, France
* E-mail address of corresponding author: philippe.vieillard{at}hydrasa.Univ-poitiers.fr
The method for prediction of Gibbs free energies of formation, based on the parameter
GO=M z+(clay) characterizing the oxygen affinity of the cation M z+, on the smectites, considered as hydrated clay minerals, has been used for micas and brittle micas, and yielded underestimated values. This method of prediction can be improved by a new set of parameters
GO=M z+(clay), characterizing the electronegativity of a cation in a specific site (interlayer, octahedral, tetrahedral in the 10 Å minerals), determined by minimizing the difference between experimental Gibbs free energies and calculated Gibbs free energies of formation from constituent oxides. By considering the crystal structure of 10 Å and 14 Å minerals, and assuming the same electronegativity of cations,
GO=M z+(o), in the octahedral sheets, an attempt is made to determine the electronegativity of cations in the brucitic sheet,
GO=M z+(b). The results indicate that this prediction method compared to other determinations, gives values within 0.25% of the experimentally-estimated values. The relationships between
GO=M z+(clay) corresponding to the electronegativity of a cation in the interlayer, octahedral, tetrahedral or brucitic sites and known
GO=M z+(aq) were thus determined, allowing the determination of the electronegativity of transition metal ions and trivalent ions in each of the four sites and consequently contribute to the prediction of Gibbs free energies of formation of different micas and chlorites. Examples are given for low-Fe clinochlore whose solubility is measured experimentally and the results appear excellent when compared with experimental values.
Key Words: Amesite Bityite Chamosite Chlorites Clinochlore Clintonite Cookeite Cronstedtite Dombassite Gibbs Free Energies of Formation Hendricksite Kinoshitalite Lepidolite Micas Polylithionite Preiswerkite Ripidolite Sudoite Taeniolite Zinnwaldite
This article has been cited by other articles:
![]() |
C. Zhu Geochemical Modeling of Reaction Paths and Geochemical Reaction Networks Reviews in Mineralogy and Geochemistry, January 1, 2009; 70(1): 533 - 569. [Full Text] [PDF] |
||||
![]() |
A. Decarreau, S. Petit, F. Martin, F. Farges, P. Vieillard, and E. Joussein HYDROTHERMAL SYNTHESIS, BETWEEN 75 AND 150{degrees}C, OF HIGH-CHARGE, FERRIC NONTRONITES Clays and Clay Minerals, June 1, 2008; 56(3): 322 - 337. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. KISTER, P. VIEILLARD, M. CUNEY, D. QUIRT, and E. LAVERRET Thermodynamic constraints on the mineralogical and fluid composition evolution in a clastic sedimentary basin: the Athabasca Basin (Saskatchewan, Canada) European Journal of Mineralogy, April 1, 2005; 17(2): 325 - 342. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. DECARREAU, S. PETIT, P. VIEILLARD, and N. DABERT Hydrothermal synthesis of aegirine at 200{degrees}C European Journal of Mineralogy, February 1, 2004; 16(1): 85 - 90. [Abstract] [Full Text] [PDF] |
||||
| JOURNAL HOME | HELP | CONTACT PUBLISHER | SUBSCRIBE | ARCHIVE | SEARCH | TABLE OF CONTENTS |