A thermodynamic model for the prediction of pore water composition of clayey rock at 25 and 80 °C - Comparison with results from hydrothermal alteration experiments

被引:27
作者
Beaucaire, C. [1 ]
Tertre, E. [2 ]
Ferrage, E. [2 ]
Grenut, B. [1 ]
Pronier, S. [2 ]
Made, B. [3 ]
机构
[1] CEA, Ctr Etud Saclay, DANS DPC SECR L3MR, F-91191 Gif Sur Yvette, France
[2] Univ Poitiers, CNRS, UMR 7285, IC2MP, F-86022 Poitiers, France
[3] ANDRA, DRD TR, F-92298 Chatenay Malabry, France
关键词
Hydrothermal alteration experiments; Clayey pore water chemistry; Thermodynamic model at 25 and 80 degrees C; X-ray diffraction profile modeling; X-RAY-DIFFRACTION; CALLOVIAN-OXFORDIAN FORMATION; SMECTITE HYDRATION PROPERTIES; CA(II)-FOR-NA+ EXCHANGE; SOLID/SOLUTION RATIO; DIAGENETIC SMECTITE; PHASE-RELATIONSHIPS; LAYERED STRUCTURES; ILLITE EQUILIBRIA; IONIC-STRENGTH;
D O I
10.1016/j.chemgeo.2012.09.040
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
This study proposes a thermodynamic model that is able to predict the pore water chemical composition of clayey rocks at temperatures up to 80 degrees C. The model is based on equilibrium with a quartz/kaolinite/calcite/dolomite/Mg-chlorite mineralogical buffer and accounts for the sorption properties of both the montmorillonite and illite phases. Hydrothermal alteration experiments were also performed at 80 degrees C on centimeter-sized samples from the Callovo-Oxfordian clay-rich formation (Paris Basin, France) to assess the validity of the proposed model at this temperature. The experiments were performed in both open and closed systems, and the initial CO2(g) partial pressure (p(CO2(g))) used in each system was fixed to log p(CO2(g)) = -0.4. After 15 months of alteration, the aqueous and gas phases were extracted at 80 degrees C and analyzed. The evolution of the clay mineralogy was also characterized using X-ray diffraction profile modeling of experimental patterns and transmission electron microscopy (TEM). The composition of the Callovo-Oxfordian pore water predicted by our model at 25 degrees C is in good agreement with that reported in the literature and measured in the geological formation. At 80 degrees C, experiments in open systems were used to assess the kinetics of alteration process and the time needed to reach equilibrium for several dissolution-precipitation mineral reactions. For the closed system, it is shown that the proposed model well predicts the chemical composition of the fluid extracted at 80 degrees C, considering the existing variability in the solubility constants for both Mg-chlorite and kaolinite minerals. Despite the need for additional alteration experiments to better constrain the temperature-dependence of the predicted p(CO2(g)) values, the proposed model provides reliable predictions of pore fluid composition at 80 degrees C, a temperature expected in the framework of radioactive waste storage. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:62 / 76
页数:15
相关论文
共 65 条
[1]   The stability of Fe-Mg chlorites in hydrothermal solutions - I. Results of experimental investigations [J].
Aja, SU ;
Dyar, MD .
APPLIED GEOCHEMISTRY, 2002, 17 (09) :1219-1239
[2]  
AJA SU, 1991, GEOCHIM COSMOCHIM AC, V55, P1365
[3]   ILLITE EQUILIBRIA IN SOLUTIONS .1. PHASE-RELATIONSHIPS IN THE SYSTEM K2O-AL2O3-SIO2-H2O BETWEEN 25 AND 250-DEGREES-C [J].
AJA, SU ;
ROSENBERG, PE ;
KITTRICK, JA .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1991, 55 (05) :1353-1364
[4]   Solubility of silica polymorphs in electrolyte solutions .2. Activity of aqueous silica and solid silica polymorphs in deep solutions from the sedimentary Paris Basin [J].
Azaroual, M ;
Fouillac, C ;
Matray, JM .
CHEMICAL GEOLOGY, 1997, 140 (3-4) :167-179
[5]  
Barany R., 1961, HEATS FREE ENERGIES, P5825
[6]   Kinetic constraints on illitization reactions and the effects of organic diagenesis in sandstone/shale sequences [J].
Berger, G ;
Lacharpagne, JC ;
Velde, B ;
Beaufort, D ;
Lanson, B .
APPLIED GEOCHEMISTRY, 1997, 12 (01) :23-35
[7]   Experimental dissolution of sanidine under hydrothermal conditions: Mechanism and rate [J].
Berger, G ;
Beaufort, D ;
Lacharpagne, JC .
AMERICAN JOURNAL OF SCIENCE, 2002, 302 (08) :663-685
[8]   INTERNALLY-CONSISTENT THERMODYNAMIC DATA FOR MINERALS IN THE SYSTEM NA2O-K2O-CAO-MGO-FEO-FE2O3-AL2O3-SIO2-TIO2-H2O-CO2 [J].
BERMAN, RG .
JOURNAL OF PETROLOGY, 1988, 29 (02) :445-522
[9]  
Blanc P., 2010, BRGMRP57798 FR
[10]   Clay minerals in the Meuse-Haute marne underground laboratory (France): Possible influence of organic matter on clay mineral evolution [J].
Claret, F ;
Sakharov, BA ;
Drits, VA ;
Velde, B ;
Meunier, A ;
Griffault, L ;
Lanson, B .
CLAYS AND CLAY MINERALS, 2004, 52 (05) :515-532