Water and ion diffusion in partially-water saturated compacted kaolinite: Role played by vapor-phase diffusion in water mobility.

Diffusion is the main transport process of water and solutes in clay-rich porous media owing to their very low permeability, so they are widely used as barriers against contaminant spreading. However, the prediction of contaminant mobility can be very complicated when these media are partially water-saturated. We conducted diffusion experiments for water (HTO and HDO) and ions (22Na+ and 125I-) through partially water saturated compacted kaolinite, a weakly charged clay material, to quantify the distinct diffusive behavior of these species. The osmosis method was used to set kaolinite samples at 67, 86 and 100% saturation. The results showed that desaturation led to a sharp decrease in diffusive rates by factors of 6.5, 18 and 35 for HTO, 125I- and 22Na+, respectively, from 100 to 67% of the degree of saturation. Thus, to interpret water diffusivities, we proposed a model taking into account the diffusion of water in both gas and liquid phases, using diffusion data obtained for ions, considered as inert species. This model was capable of properly predicting water diffusive flux, especially at a low degree of saturation (67% saturation), for which the assumption made for the occurrence of air phase continuity throughout the sample appears to be more relevant than at 86% saturation.

Influence of the ionic strength and solid/solution ratio on Ca(II)-for-Na+ exchange on montmorillonite. Part 2: Understanding the effect of the m/V ratio. Implications for pore water composition and element transport in natural media.

The aim of the present paper is to clarify previous results showing that selectivity coefficients determined for the exchange of Na(+) for Ca(2+) in montmorillonite were dependent on the solid/solution ratio. The organization of montmorillonite suspensions upon Na(+)/Ca(II) exchange was analyzed by combining optical microscopy, small-angle X-ray scattering and X-ray diffraction. All samples displayed flocculated characteristics, eliminating the possibility of contrasting accessibility of sorption sites with the solid/solution ratio. Modeling of experimental X-ray diffraction patterns was used to quantify the relative proportions of interlayer Ca(2+) and Na(+) cations along the exchange isotherm. The results further confirmed the influence of the solid/solution ratio on the degree of interlayer Ca(II)-for-Na(+) exchange, and specific selectivity coefficients for interlayer sites were determined. The effect of the solid/solution ratio was finally interpreted by the resulting local changes in the solution chemistry. We demonstrated that by accounting for the Donnan effect, the different data can be interpreted using a single selectivity coefficient. The obtained Kc constant was successfully applied to interpret existing hydrogeochemical data on a natural aquitard. This most likely represents a more constrained and valid approach for the modeling of reactive element transport in natural media than does the poorly defined Kd parameter.

Influence of the ionic strength and solid/solution ratio on Ca(II)-for-Na+ exchange on montmorillonite. Part 1: Chemical measurements, thermodynamic modeling and potential implications for trace elements geochemistry.

Na/Ca ion-exchange isotherms were performed on a Na-saturated montmorillonite for different constant normalities of the aqueous chloride solution and at two solid/solution ratios. The experimental data suggest that the affinity of Na(+) for the solid increases with total normality and m/V ratio and that a significant proportion of CaCl(+) is also sorbed. A thermodynamic modeling procedure with one sorption site and three sorbed cations (Na(+), Ca(2+) and CaCl(+)) was applied to interpret the data. We show that by accounting for the activities of aqueous species, the experimental data obtained at different total normalities for a given solid/solution ratio can be fitted using a unique set of selectivity coefficient values. However, when the m/V ratio is decreased from 25 to 2.5 g/L, an increase in the log Kc(Na(+)/Ca(2+)) of up to 0.4 ± 0.05 was required to interpret the data with a constant log Kc(Na(+)/CaCl(+)) value. The same behavior concerning the increase in the log Kc(Na(+)/Ca(2+)) with a m/V ratio decrease was observed when using a multi-site model taking into account the specific sorption of H(+). The results clearly indicate that the Na(+)/Ca(2+) selectivity coefficients strongly depend on the solid/solution ratio but are independent of the exchanger composition and the total normality of the solution. Such findings provide possible pitfalls when using selectivity coefficients obtained in diluted suspension to assess the sorption in compacted clayrocks and allow a better prediction of the sorption of trace elements in competition with major cations.

Methodology to obtain exchange properties of the calcite surface--application to major and trace elements: Ca(II), HCO3-, and Zn(II).

Sorption of inorganic elements onto carbonate minerals has been intensively described in the literature by two reaction steps: (1) a first one rapid and completed within a few hours and (2) a second one slower, eventually irreversible, and occurring at a constant rate. The first step is often attributed to an ion-exchange process, but its reversibility is rarely investigated. Consequently, discrimination of the global sorption phenomenon into two different mechanisms is not always justified. In this study, we investigated, by batch experiments, both sorption and desorption of Ca(II), HCO(3)(-), and Zn(II), radiolabeled with isotopes (45)Ca(II), H(14)CO(3)(-), and (65)Zn(II), respectively, onto synthetic pure calcite. Solutions were preequilibrated with atmospheric p(CO2) and saturated with respect to calcite. Therefore, our purpose was to: (1) obtain experimental distribution coefficients of major elements (Ca(II) and HCO(3)(-)) and a trace element (Zn(II)) onto calcite from sorption and desorption experiments, (2) test the validity of a first-occurring ion-exchange process generally noted in the literature, by calculating distribution coefficients for the "sole" exchange process, and (3) quantify the amounts of Ca(II), HCO(3)(-), and Zn(II) sorbed on the calcite surface by the sole "exchange process" and compare them with surface crystallochemical data. Ca(II) or HCO(3)(-) sorption experimental data suggest that a significant fraction of these two elements was sorbed irreversibly onto or in the calcite. By using a method based on isotopic ratios, the Ca(II) or HCO(3)(-) concentrations, which are reversibly adsorbed on the calcite, have been quantified. These concentrations are respectively estimated at 4.0+/-2.0 x 10(-4) and 7.0+/-1.5 x 10(-4) mol/kg. The obtained Ca(II) surface concentration value is one order of magnitude lower than the one obtained from isotopic measurement by former authors [Geochim. Cosmochim. Acta 55 (1991) 1549; Geochim. Cosmochim. Acta 51 (1987) 1477; Geochim. Cosmochim. Acta 52 (1988) 2281] at the same pH. On the other hand, the kinetics of Zn(II) sorption onto calcite was followed over more than 1000 h. Sorption/desorption experimental results suggest that the sorption is totally reversible at least when total aqueous Zn concentration is less than 10(-6) mol/L and when experiments are performed in equilibrium with both calcite and p(CO2)=10(-3.5) atm. Under these conditions and at pH 8.3, the occupancy rate of Zn(II) onto the calcite surface is estimated to represent approximately 1% of the total surface-site density.