The triaxial testing can be carried out according to the ASTM procedures D4767 [
74] and D7181 [
75] or other standards (e.g., CEN/ISO). The current paper aims to portray an undemanding procedure that could be easily implemented and accessible to any academic or commercial geotechnical laboratory. The test procedures recommended in this section seek to increase the accuracy and simplicity in the techniques used to define the CSL. Test methods will generally focus on the creation of loose cohesionless specimens taking advantage of the improved components in the triaxial apparatus. The soil specimens remoulded for such conditions tend to show contractile behaviour, which allows a reliable measurement of the CSL.
5.1. Soil Preparation
One of the features that guarantee the representativeness of the CSL regards the material that is used to reconstitute the soil specimens in the laboratory. The material must not be reused between tests since the soil can present grain changes or transitional behaviour, which should be verified as described before. Therefore, all samples should be remoulded with original material.
In addition, it is crucial to guarantee the homogeneity between the soil specimens used to define the CSL. If the material is in a wet condition, it should be dried first to facilitate user handling. Moreover, if the material has a high fines content (i.e., clods of silt and clay throughout the specimen), they must be carefully unbound without crushing the soil particles and mixed up. Afterwards, the sample can be divided and reduced to testing size using the quartering technique (e.g., standard testing procedure ASTM C702 [
76]), which minimises the variations between the different fractions. All portions are stored and oven-dried before remoulding the sample. These steps ensure the homogeneity and the representativeness of the material used to assess the CSL. However, additional procedures may be needed if the soil contains dissolved solids or chemical products that may influence the soil behaviour during testing.
5.2. Remoulding of Soil Specimens
The adopted procedure for specimen remoulding is described in this section. It follows the moist tamping technique combined with the undercompaction method, previously described, adapted for six layers. The number of layers to be used in the preparation of the specimen may vary accordingly to the specimen diameter and the required dry unit weight; however, the maximum thickness of the layers should not exceed 25 mm. The gravimetric water content to be used in the compaction process may differ according to the studied soil (e.g., 5% for sands or 15% for silty mining tailings). Ultimately, the definition of depends on the user sensibility to adopt a water content that can effortlessly achieve the pursued loose state. The same applies to the value of , which can fluctuate according to the target void ratio (from 0% on dense samples to 15% on very loose samples) or to high values of specific gravity (as the material self-weight can aggravate the densification of the lower layers).
The adopted procedure for remoulding soil specimens ensures a more uniform density distribution within the specimen. The exact internal variation in initial density seen in a particular sample is likely to depend both on the number of layers and on the undercompaction ratio used. However, regardless of the exact initial distribution of internal sample void ratio, Thomson and Wong [
77] showed that there is a tendency for each zone to tend towards a unique CSL. For this reason, the undercompaction ratio, number of layers and water content selected when compacting a sample will not influence the CSL parameters. It is noteworthy that this statement is only valid when testing the ultimate state in loose samples, as these remoulding conditions will influence the soil behaviour (e.g., compressibility parameters, stress/strain shearing paths and even cyclic or dynamic testing response).
The process starts with the preparation of the material and equipment. This phase covers the preparation of the lubricated ends platens, the positioning of filter paper and the adjusting of the latex membrane to the bottom platen using two O-rings. Afterwards, the split mould is assembled and 50 kPa vacuum is applied to draw the membrane with the mould, as previously illustrated in
Figure 9a. Meanwhile, the soil is prepared. Knowing the amount of material needed, the weight distribution by layers and the water content to be used in the sample preparation, the soil can be properly mixed with de-aired water to obtain the moist content intended. Each material will require the use of a certain pore water, from tap water to distilled water or even deionised water if no particular liquid is specified (which is commonly the case with marine sediments or mining tailings). The wet material must be saved in a sealed recipient during the compaction process to avoid air drying. The real water content of the soil specimen is estimated by taking two samples of that mixture, one before placing the first layer and the second after finishing the compaction. The average moisture value corresponds to
of the soil.
Figure 11 illustrates the remoulding procedure using the undercompaction moist tamping technique.
The first portion of soil is poured into the mould and distributed around the base with a spoon (
Figure 11a). The layer is lightly tamped using the compaction hammer until the tamper hits the stopping point in every simple stroke (
Figure 11b). Before tamping, the height adjuster is regulated so that the compaction foot tamps exactly at the top of the layer, avoiding an over compaction of the soil. To avoid planar surfaces between layers, the tamped layer must be superficially scratched. Both layer deposition and tamping process are repeated for all layers until fully remoulding the soil specimen.
A uniform density profile is intended; however, because the tamping compaction is more effective on the upper part of the layer, the specimen can present a ‘zig-zag’ pattern [
78] due to higher densities near the top of each layer.
Figure 12 shows a clear ‘zig-zag’ pattern of a soil specimen in the triaxial equipment compared to a regular one. Thomson and Wong [
77] showed that these samples’ uniformity improved significantly during shearing, allowing a reliable estimation of the CSL. However, this effect is an important concern for the triaxial testing because the area correction method used in this approach (further described) considers the sample as a right cylinder. Even though the ‘zig-zag’ effect does not influence the shearing behaviour, it can introduce a miscalculation on the volume changes during triaxial stages if the pattern is pronounced.
After compacting all layers, the upper platen (also lubricated and using filter paper) is placed, and the membrane is attached to the top cap using 2 O-rings (
Figure 11c). Once the sample is isolated, the mould can be removed by applying vacuum (≈
kPa) to the soil specimen through the drainage lines to help the soil specimen to keep its shape and then its density (
Figure 11d). The height and diameter of the sample are measured using a caliper rule to estimate the initial density, allowing the membrane thickness to be deduced.
At this point, the isolation and seal of the latex membrane can be verified. For this purpose, the drainage lines are closed, and if the specimen starts losing its suction, this may imply that the membrane was punctured or ripped during the reconstitution process. If the membrane is in good condition, the test may begin; otherwise, the sample must be disassembled because it will not reproduce the right behaviour in the forthcoming stages. If the conditions are appropriate for testing, the remainder of the triaxial cell is then assembled, filled with de-aired water, and a cell pressure of 10 kPa is applied in order to remove the vacuum.
5.3. Sample Saturation
The saturation process is fundamental for a proper assessment of the CSL, as the constant volume (or undrained) conditions cannot be assumed unless the soil is fully saturated. In drained tests, the volume change is estimated by measuring the amount of water entering or leaving the saturated soil specimen. The importance of the full saturation of soil is more pronounced in undrained tests since the development of pore-water pressure strongly depends on the stiffness of the pore fluid. Considering that the compressibility of water and air are significantly different, a small amount of air can have a large effect on the soil response. Hence, the saturation of the samples is fundamental to provide reliable values of pore water pressure and volume change during testing.
5.3.1. Carbon Dioxide Method
The use of carbon dioxide (CO
) before the water flushing significantly aids the full saturation of the soil specimen, since this inert gas is more soluble in water than air is. After the sample preparation, the CO
is introduced with low pressure (≈3 kPa) from the bottom drainage line, forcing the air to circulate upwards in the soil specimen. A tube connected to the top drainage line, which is open and submerged under water, allows for monitoring the bubbling velocity and the percolated volume of CO
. During this phase, it is important to monitor the gas pressure, to avoid any pore pressure build-up that could reduce the mean effective stress and to prevent the CO
from piping or flowing up in preferential pathways rather than displacing the air. Note that CO
is denser and less compressible than air. To ensure complete replacement of the air, the flushing of CO
is done for about 60 minutes or until the equivalent of one litre of the gas is displaced. The main advantage of using CO
is to achieve the full saturation condition of cohesionless soils faster than other saturation methods [
7,
44].
5.3.2. Water Flushing
Since this procedure aims to achieve a full saturation condition, the use of de-aired water inside the specimen is essential, as most of the dissolved gas (mixture of air and CO
) present in the fluid was already removed. However, if the material tested contains some dissolved solids (such as salt), deionised water should be used instead to avoid any pore fluid chemistry issues affecting the CSL definition [
73].
5.3.3. Backpressure Increment
Small air bubbles may remain attached to the soil grains after water percolation and can be difficult to flush out. The full saturation condition is then achieved by applying high pressures to the pore fluid to cause the pore air to dissolve completely into the pore water. The backpressure is gradually increased to high values while keeping a low effective stress (approximately 10 kPa). In the authors’ experience, a backpressure equal to 300 kPa together with the use of CO
and water flushing provides a full saturation condition. Currently, some commercial triaxial chambers are designed for pressures up to 1700 kPa, and some controllers can apply 2000 kPa of pressure, which allows for implementing other backpressure values during soil saturation. However, for some plastic or fine soils, additional techniques to achieve full saturation may be needed, namely the double vacuum during water flushing [
79], and the increment of backpressure to even higher values or a percolation under pressure. These topics will be further discussed.
5.3.4. Evaluation of the Degree of Saturation
The saturation of the soil specimen can be determined by measuring the value of the pore pressure coefficient B, as defined by Skempton [
80], where an increment in the cell pressure (
) is applied under undrained conditions, and the corresponding increment of pore pressure (
) is measured. In fully saturated conditions,
, and the B-value is of about 1.0. However, a high B-value does not always guarantee full saturation for every type of soil [
44], which is particularly important when undrained tests are preformed and especially when liquefaction susceptibility is studied. For sandy soils, the B-value at full saturation condition varies from 0.90 to 0.99, but it can be lower than such a range in stiff and coarser geomaterials [
81,
82].
However, P-wave velocity (
) better indicates the full saturation of soil since it increases harshly from 90% to 100% degree of saturation [
83]. Due to this unreliability of the B-value, a correlation of this parameter with the P-wave velocity (
) provides a theoretical framework to validate the full saturation condition of the soil. In triaxial tests, the propagation time of the P-wave is measured by using bender/extender elements, which are embedded in the platens of the triaxial chamber [
84,
85] or simply bender elements if a proper analysis is conducted, as presented by Ferreira et al. [
85]. However, the authors do not recommend using bender/extender elements when the end-of-test soil freezing is adopted, due to possible damages in the piezoelectric transducers.
For granular soils, a B-value of higher than 0.97 is recommended to indicate the full saturation condition. This recommendation of B-value
is based on comparisons between such a parameter against the P-wave velocity (
). In saturated soils, the
values are higher than 1482 m/s since the wave propagation is commanded by water [
86]. Theoretical models for describing the evolution of Vp and B-value as a function of the degree of saturation (
) have been presented by [
87,
88,
89,
90,
91]. All
, B-value and
relations are based on continuum mechanics [
92,
93].
Figure 13 presents the evolution of both
and B-value as a function of the degree of saturation, together with the calibration of the B-value with
by applying the wave propagation theory in fluid-saturated porous media. Additionally, experimental data obtained from TP-Lisbon sand—soil characterisation details in [
94]—to contrast and corroborate the theoretical model are also presented in
Figure 13. From this figure, it can be observed that the full saturation condition (i.e.,
m/s) is achieved for a B-value of about 0.97, which is consistent with that observed by [
81,
83]. These findings allow for validating a proper consideration of the B-value, and then guaranteeing the full saturation conditions of the soil specimens that will define the CSL.
5.3.5. Percolation under Pressure
In case the full saturation is not reached after the backpressure increment, an efficient saturation procedure is to impose percolation under pressure. Different pressures are applied at the ends of the sample, higher at the base than on the top, forcing the water to seep through and in and out of the specimen. The differential pressure must respect the internal equilibrium of the pore pressure ( kPa) and maintain the effective confinement of 10 kPa to avoid an overconsolidation of the sample (e.g., cell pressure ≈ 310 kPa, bottom backpressure ≈ 303 kPa and top-pressure ≈ 297 kPa). For low permeability soils, the pressure difference between the drainage ports can be increased. From the authors’ experience, this process involves the flushing of at least 100 cm and must be repeated until the full saturation condition is achieve. If needed, an additional back pressure increment (usually up to 500 kPa) will speed up the saturation process, provided that the post-consolidation stresses are compatible with the equipment capacity. In addition, extra time under high backpressure can increase the degree of saturation.
5.4. Consolidation Phase
Laboratory testing aims at simulating the field stress conditions as close as possible; the applied consolidation pressures should correspond to a likely stress state on the field or defined by the project for specific purposes before shearing. The reference effective confining pressure and the previous stress history of the soil establish all aspects of its behaviour. For that reason, different initial stress states are required to define the CSL of any soil. However, for CSL definition, large ranges of confining pressures can be tested as long as the limitations of such studies are recognised (such as flow instability or evolution in grain size distribution or morphology).
In addition, isotropic consolidation is often used in practice, although the stress state in the field is commonly anisotropic. It is well known that in the laboratory, the anisotropic consolidation of soils requires advanced triaxial equipment, but the present work aims at an undemanding procedure that can be easily implemented and accessible to any academic or commercial geotechnical laboratory. Hence, isotropic consolidation is recommended to assess the critical state parameters due to the uniqueness of the CSL and independence of initial soil fabric [
5,
10,
29]. For both isotropic and anisotropic consolidations, the drainage valves are open to allow the drainage of the sample, avoiding the pore pressure excess. An automatic volume gauge instrumented with an electronic displacement transducer (e.g., LVDT transducers) monitors the drainage of soil. Moreover, a gradual pressure ramp is recommended to track the variation of void ratio.
5.5. Shear Phase
During triaxial testing, the specimens are loaded to failure by increasing the axial deformation while keeping the cell pressure constant. For drained conditions, shear loading by axial compression is imposed with an axial strain velocity compatible with the excess pore pressure dissipation rate that guarantees the effective stress. A suitable loading for ensuring the complete drainage of soil can be defined using the consolidation parameters—
or
[
95]. In undrained tests, the shearing velocity is not critical, but it should be low enough to secure equalisation of the pore pressure at failure.
The undrained shearing stage begins by closing the drainage valves before shear loading. As no drainage is allowed, the tendency of the soil to change volume is reflected by a variation in pore pressure. Because of the undrained condition, no volume changes in the fully saturated sample are induced. Therefore, the water content and void ratio at the end of the test are the same at the end of consolidation. In drained shearing, the drainage valves are open. The specimen will expel or absorb water to keep the effective stress of the consolidation stage. A soil specimen changes volume during shearing in a drained test. Hence, the water content, the void ratio and the dry density of the sample at the end of the test are distinct from the beginning of shearing.
During this stage, an automatic volume gauge measures the specimen volume changes, the axial displacement is quantified with an electronic displacement transducer and the load should be measured through a submersible internal load cell. Usually, the monotonic shearing is applied under strain control by increasing the deformation up to the ultimate or critical state. Following the end of the triaxial test, the specimen must be inspected for any localised shear band or other abnormalities that may affect the results and definition of CSL. The recommended procedures to measure the final void ratio are detailed below.
5.6. Data Correction
For a proper interpretation of the results during the shearing phase, it may be necessary to apply some corrections to the measured quantities. The corrections must be evaluated relative to their importance for the final values/results of the tests. Due to critical state testing generally implying large strains, an area correction method and the membrane effect should be quantified. When using lubricated end platens, the right circular cylinder (RCC) can be maintained for axial strains higher than 20%. Therefore, the reported stresses must be corrected in terms of the sample cross-section evolution since the specimen is compressed. Considering that the specimen deforms as a right cylinder, it can be assumed that the corrected area of the sample (
A) during shearing is given by
where
is the initial cross-section area of the sample at the start of the shear (end of consolidation).
The main stresses can also be influenced by the presence of the rubber membrane. For this reason, the data should be corrected considering two major effects: (i) membrane penetration and (ii) membrane stiffness. When a triaxial test is performed on a granular soil, the membrane enclosing the triaxial specimen tends to penetrate the voids between the particles at the interface, which can cause an experimental error. In a drained test, the measured is not only representative of the soil skeleton compression but also includes the volume of water that is forced out due to the membrane penetration. In undrained conditions, as the pore pressure increases, the water inside the sample tends to move to the lateral surface, refilling the voids. As a result, the measured is underestimated.
The membrane penetration effect depends mainly on the soil particle size but also on the specimen density and overall geometry, the range of effective confining stresses during a given test and the modulus and thickness of the latex membrane. According to Nicholson et al. [
96], membrane-compliance effects may be negligible for sands and silts tested in conventional 71 mm diameter samples, since even very thin membranes cannot penetrate significantly into the small surficial voids. Since this paper deals with granular soils (sandy, silty and non-plastic geomaterials), the membrane penetration effect was not taken into account. However, this effect must be considered for testing of gravels in large scale specimens—commonly used for the characterisation of geomaterials in transportation infrastructures [
97].
Another implication inherent to samples that, during shearing, reach high levels of strains is due to the rubber membrane stiffness. As deformation occurs, the membrane tends to constrain the specimen laterally, making the radial stress truly applied higher than the one that is measured. Consequently, the axial stress is also influenced due to the load taken by the membrane. Therefore, the stresses acting on the specimen must be corrected considering the membrane stiffness. The literature presents many different correction methods; however, the authors recommend the expressions given by Duncan and Seed [
98,
99] because these corrections can be applied to a large number of criteria (large strains, drained and undrained conditions and compression and extension tests). This effect is more pronounced at lower stress levels [
44]. The corrections to the axial (
) and radial (
) stresses are the following:
where
is the initial thickness of the membrane,
the elastic modulus for the membrane and
the initial diameter of the specimen. Standard triaxial latex membranes with
mm and
MPa are used in UPorto.
5.7. Void Ratio Measurements
The measurement of the void ratio (
e) of samples in triaxial tests is one of the most important aspects in determining the CSL. Furthermore, it is one of the variables more subject to be miscalculated, particularly in loose samples. While it is relatively simple to estimate the initial void ratio through the initial sample dimensions, dry weight and water content, the volume changes during sample saturation (including sample flushing and back pressure increasing) can lead to significant errors if ignored, as exposed by Sladen and Handford [
23]. During saturation, samples experience deformations due to the soil collapse or changes during the stresses’ ramp application and the release of surface tension effects in moist samples. However, volume changes during saturation are particularly difficult to measure because of the air existence in the voids of the soil, the water lines and porous stones after water flushing. An accurate approach to overcome these challenges is to measure the sample volume at the end of the test and then calculate the volume change during saturation. Hence, the axial strain is estimated considering the direct measurements of the LVDT, while the radial strain is estimated by applying the relations of volumetric and axial strains for a perfect cylinder.
In this paper, the authors recommend the end-of-test soil freezing (EOTSF) technique proposed by Sladen and Handford [
23] because of its precision and simplicity of void ratio measurement through the final gravimetric water content (GWC). The final volume is used to calculate the void ratio at the ultimate state, and data processing is made from the end of the test to the beginning. This technique consists of freezing the specimen at the end of triaxial testing, ensuring that the final void ratio is accurately determined by keeping the water volume inside the specimen at the end of the shear stage. Thus, once the test is finished, the sample is isolated by closing the drainage valves (if not already done), the cell pressure is reduced to zero, the piston is unloaded and the cell chamber fluid is drained. The triaxial cell is disassembled as much as possible without breaking the ‘seal’ on the sample and placed in the freezer.
Once the sample is frozen, it can be removed intact and weighed without losing water or soil. The weight from the adherent items (membrane, filter papers and lubricated ends) is deducted, and the water content is determined from the oven-dried weight of the sample. Note that by the end of the shearing phase, especially in loose samples with low confining pressures under undrained conditions, the soil specimen is very unstable, as segregation occurs due to liquefaction, resulting in a challenging sample recovery. The handling of the sample is significantly improved by freezing it, which will allow for a reliable water content measurement.
This method cannot be used if the platens are set up with electronic equipment such as bender elements, as freezing will damage these components. In such cases, the void ratio can be determined through the direct measurement of end-of-test GWC, providing that during the sample removal no water or soil is lost. The same can be applied to denser samples, as they will remain quite stable after shearing and will be easier to handle.
The final volume is determined by assuming a non-loss of the water in the specimen voids, which is completely saturated using the relation , where is the specific gravity of the soil, is the water content and is the degree of saturation. With this final void ratio and the continuous measurements of volume changes, the void ratio is easily determined at the beginning of both consolidation and shear stages.
Moreover, during the percolation and saturation, the axial shortening of the sample can be measured using the top guided piston guidelines (see
Figure 7). The volume change during these stages can be estimated by assuming that the volumetric strain is isotropic—that is, the total volumetric strain is three times the axial strain. This volume can be included in additional approaches of void ratio measurement, as part of internal checks by the laboratory. The authors also recognise other methods for obtaining accurate void ratios, such as cell calibration and Verdugo and Ishihara’s [
36] methods. In the cell calibration method, the ‘corrected’ cell volume change is assumed to be equal to the sample volume change during saturation [
100], while Verdugo and Ishihara’s [
36] method covers, after shearing, the removing of additional water from the sample by increasing the cell pressure, allowing for an easier sample recovery. These methods, if used correctly, may be equally accurate to the EOTSF. However, they are complicated, time-consuming and depend on the operator expertise, which is not the intention of this paper.