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Environmental variables such as temperature, matric suction and pore fluid composition are well known to influence the hydro-mechanical behavior of clays and shales. The type and the relevance of this influence depends on the mineralogical composition and on the fabric of the material. Soil activity is an engineering proxy for mineralogical composition which can be used for a preliminary characterization of the expected type of behaviour under chemical actions, if those do not imply very significant cation exchange or pH variations. Very large chemo-mechanical effects occur in highly active soils used in engineering works such as barriers for nuclear waste or landfills, however concentration changes also impact on the mechanical behavior of non – active soils and rocks, such as illitic or natural blends of clays. Such materials are widely distributed in nature and their mechanical response upon chemical changes can be problematic in many cases. Examples of engineering relevance include vast slope instabilities promoted by fabric changes due to desalinization in Scandinavian quick clays, and instability or convergence issues for boreholes drilled in shales exposed to muds with a different chemical composition from the one of the pore fluid. An elastoplastic model is formulated to simulate the volumetric behaviour of such materials along chemical and mechanical loads. In addition to the parameters of the Modified Cam Clay, it requires defining the dependency of the elasto-plastic compliance and reference void ratio on pore fluid salinity. The model performs well against experiments from literature where complex chemo-mechanical histories were imposed.

Cement bentonite mixtures are often used to build slurry walls for the containment of both aqueous and non aqueous pollutants, due to their quite low hydraulic conductivity and relatively high ductility and strength. Although their hydro-mechanical behaviour in saturated conditions has been studied in the past, a part of the slurry wall is expected to rest above the groundwater level. The hydraulic characterization in unsaturated conditions is then particularly relevant to evaluate the performance of the barrier, especially when it is aimed at containing non aqueous pollutant liquids which are lighter than water (LNAPL). These non wetting fluids rest above the water table and their penetration is possible just if the barrier is unsaturated. This paper presents some preliminary results of a laboratory characterization of the water retention behaviour of three different cement bentonite mixtures. The mixtures, prepared at cement – bentonite mass ratios ranging from 4:1 to 6:1, were immersed in water and cured for 28 days. Their water retention behaviour was then determined along drying and wetting paths through different techniques, namely axis translation, filter paper and vapour equilibrium. In the high suction range, the water content – suction relationship was found to be independent of cement-bentonite ratio. In the low suction range, the water content at a given suction was found to decrease for increasing cement bentonite ratios.

Upon drying, matter and energy are exchanged between the atmosphere and porous media through evaporation, which is a coupled process that involves the simultaneous transport of liquid water, water vapour and heat. At shallow depths, evaporation controls the water content and suction of both natural soils and earthworks, affecting their hydraulic response. This impact is particularly relevant when the earthworks are aimed at the containment of aqueous or non-aqueous pollutants, as in the case of cement bentonite cut-off walls. A coupled model for the transport of liquid water, water vapour and heat through cement bentonite mixtures upon evaporation was formulated. The model considers flow of water driven by both total suction and temperature gradients. Model predictions were compared to experimental results obtained in the laboratory on samples having different sizes and imposed boundary conditions. A good agreement between predicted and measured volumetric water contents was obtained, once defined a suitable dependency of the relative permeability of the mixture on degree of saturation. The results suggest that the proposed formulation correctly accounts for the underlying physical processes, and that it might be used to model the real scale behaviour of cut-off walls.

Cement bentonite slurry cutoff walls are used to encapsulate pollutants within contaminated areas, so avoiding their spreading in the environment. In both temperate and arid climates, at shallow depths, slurry walls are exposed to interaction with the atmosphere and thus to relative humidity values which might induce desaturation and significant shrinkage. This note presents the main results of a study aimed at investigating the impact of drying processes on the integrity and the hydraulic performance of cement bentonite slurry walls. Cement bentonite samples were cured under water for different times (1 months, 2 months and 4 months) and then dried naturally by exposing them to the laboratory environment (T = 21 °C, relative humidity approximately 38%). Once dried, the bottom of the samples was placed in contact with a thin layer of water to induce wetting. The distribution of the electrical conductivity within these samples was evaluated through Electrical Resistivity Tomography measurements, and electrical conductivity maps were converted then into maps of water contents on basis of a phenomenological relationship. The reconstructed water contents compared very well to the measured ones. Drying induced a limited cracking of the samples, which might affect to some extent the hydraulic performance of the barriers.

Environmental actions are known to induce relevant effects on the fabric of compacted active clays, which are successfully described by adopting a double porosity framework. In particular, the role of aggregate deformation has been recognized as fundamental to interpret the water retention behavior and the transport properties. These aspects are particularly relevant in the context of clay liners, being the material cast in place in unsaturated conditions and subjected to wetting process by pore fluids characterized by a chemical composition that is different from the one of compaction. Experimental data evidence that the water retention properties of active clays evolve as a function of pore water chemistry, since for a given matric suction the mass of stored water changes with water salinity. In this paper, a double porosity water retention model is proposed, capable of reproducing the variation of matric suction with water content accounting for the salinity of pore fluid. The role of salinity changes is accounted for by a suitable evolution law for aggregate deformation, which in turn affects the inter-aggregate porosity and thus the storage properties of the material.

Modelling the water retention behaviour requires proper understanding of all the processes which affect the amount of water stored in the pore network, depending on the soil state and the soil history. Traditionally, in many applications a single water content – suction curve is used. This approach limits the applicability of the retention data to practical cases, especially when fine grain soils are dealt with, when the deformability and activity of the clay fraction significantly affect the interaction with water. On the other side, water retention is being recognised more and more as a fundamental information in the description of the mechanical response of the soil, as it provides the key connection to the partial volumetric strains in a deformation process. With reference to the work performed at the Politecnico di Milano in the last years, a contribution on the understanding and modelling the coupled water retention- mechanical response in deformable soils is presented. The contribution aims to: (i) summarise the mechanisms which contribute to water retention; (ii) point out the role played by an evolving fabric and the fluid properties on water retention; and (iii) provide an overview on some of the consequences of evolving water retention properties on the mechanical behaviour.

Desiccation cracks are usually thought to start from the surface of an evaporating soil layer, and the available simplified models for crack initiation and propagation are based on this hypothesis. On the contrary, experimental results on a Dutch river clay showed that cracks in an evaporating soil layer may start and propagate below the surface, confirming earlier findings by other researchers. A simple one-dimensional model was set up to analyse the consequences of different hypotheses about the material behaviour on the crack onset in a homogenous soil layer undergoing surface drying. The results of the model show that dependence of the material behaviour on the rate of water content change is a necessary requirement for cracks to initiate below the surface. The conclusion suggests that, to properly understand cracking in an evaporating soil layer, an intrinsic time scale for the mechanical response must be accounted for, among all the other factors which were previously highlighted by other researchers. The key factor to predict crack onset below the surface is the dependence of the drying branch of the water retention curve of the compressible soil on the rate of drying, which would be justified by a rate dependent fabric evolution.

Changes in the chemistry of the pore fluid are known to have an impact on the hydro-mechanical behaviour of clays. Experimental evidence collected in recent decades has led to the formulation of constitutive chemo-mechanical models for expansive soils used in engineering practice for the containment of pollution, such as bentonite. Less attention has been paid to modelling the chemo-mechanical behaviour of non-expansive clays, which are less frequently used for geoenvironmental applications, but equally exposed to chemical changes. Key differences between the impact of salinity on the fabric of expansive and non-expansive clays are pointed out. At the macroscopic scale, an increase in salinity causes a translation of the normal compression line of non-expansive clays to higher void ratios, which in some cases is also accompanied by an increase in compressibility. The opposite occurs for expansive clays. Such experimental evidence provides the basis for a chemo-mechanical model formulated in the frame of elasto-plasticity with generalised hardening, whose yield surface expands with pore fluid concentration. The model is validated against experimental results, both original and from the literature. Simulation results compare very well with those of tests performed on reconstituted, compacted and intact samples. [ABSTRACT FROM AUTHOR]