The present paper represents an extension of recent work that considered the partitioning response of binary solvents placed into contact with charged, expandable clays. Previous theoretical work yielded a model of partitioning by performing a thermodynamic analysis, involving the work of polarization, on a binary solvent, treated as a continuum and residing within the interlayer space of a layered aluminosilicate clay. Partitioning, or the tendency for sorbed and bulk phases to have different compositions, was shown to be sensitive to the dielectric properties of the 2 solvents of the binary mixture and to the surface charge density on the clay, among other factors. Although previous experimental work has helped to validate the theory, additional work is reported here that looks at hysteresis effects, the role of the exchangeable cation (usually organic), the prediction of adsorption isotherms and the contribution that partitioning, or sorption, makes to the disjoining pressure that develops in binary solvent systems. In this current study, 3 different organo-clays were considered: Cetyltrimethylammonium (CTMA), Isopropanolammonium (IPA), and Benzylammonium (BA) montmorillonite. Solvent systems under study included: acetone/chloroform (a-c), acetone/quadricyclane (a-q) and acetonitrile/chloroform (an-c). While partitioning of the a-c system on CTMA-clay follows theory quite well, theory tends to over-predict partitioning for the a-q system on the same clay and under-predict partitioning for the an-c system on all clays. Predicted adsorption isotherms range from highly nonlinear to nearly linear. Finally, the delamination and subsequent swelling processes of BA-clay in a water/acetonitrile binary solvent system are very sensitive to composition, a result that is directly linked to the partitioning process.

Electric potentials as a function of distance were calculated for a model of the double layer on clays in which a surface zone a few water molecules thick has a low dielectric constant. This zone is followed by bulk water with a normal dielectric constant. The double layer potentials were found to be lower than those obtained from the Gouy model, in which water has a normal dielectric constant throughout the double layer.

Ion-exchange modeling is used widely to describe and predict ion-adsorption data on clay minerals. Although the model parameters are usually optimized by curve fitting experimental data, this approach does not confirm the identity of the adsorption sites. The purpose of the present study was to extend to divalent cations a previous study on the retention of monovalent cations on Na-saturated montmorillonite (NaMnt) which optimized some of the model parameters using density functional theory (DFT) simulations. The adsorption strength of divalent cations increased in the order Mg2+ < Cd2+ < Ca2+ < Sr2+ < Ba2+. After adding adsorption of metal hydroxide species (MOH+), the three-site ion-exchange model was able to describe adsorption data over a wide pH range (pH 1–10) on NaMnt. X-ray diffraction (XRD) analyses were conducted to investigate the interlayer dimension of clay samples under various conditions. The cation retention strengths of divalent cations did not correlate with interlayer dimensions. The XRD analyses of the Mnt showed a d001 value of 19.6 Å when saturated with alkaline earth cations, 22.1 Å with Cd2+, 15.6 Å with Na+, and 15.2 Å with H+. In the case of Na+, the 15.6 Å peak decreased gradually and disappeared, and new peaks at 22.1 and 19.6 Å appeared when the percentages of Mg2+ and Ba2+ adsorbed increased on NaMnt. The peak shifted from 22.1 to 20.3 and 19.6 Å when the pH increased for all cations except Cd2+, which stayed constant at 22.1 Å. The coexistence of multiple d001 peaks in the XRD patterns suggested that the interlayer cations were segregated, and that the interlayer ion–ion interactions among different types of ions were minimized.

Various fractions, ranging in size from 5 to 0·05 μ of natural clays from Mexico and Wyoming, occurring as heterogeneous or multicomponent cationic systems, were studied under specific equilibrium conditions of salt concentrations in the range found in many drilling fluids and formation waters.

Glass electrodes were utilized in this study. A Tektite electrode was found to have specific sensitivity to divalent cations.

Alumina is produced from bauxite, which contains a mixture of various oxides, such as aluminum (Al), iron (Fe), silicon (Si), and titanium (Ti). Bauxite can also be considered a source of several other valuable metals, such as scandium (Sc), vanadium (V), and gallium (Ga). The composition and mineralogy of alumina determine their economic value, but their characteristics vary by locality. The physicochemical characteristics of bauxites can also be influenced largely by weathering processes, even within the same locality. For this reason, the present study was undertaken with the objective of comparing the characterization data of three bauxite samples collected, which will be referred to as D, E, and F, from the Cruz Alta do Pará plateau in northern Brazil. The samples were solubilized by multi-acid digestion and fusion with lithium metaborate to quantify their metal compositions by inductively coupled plasma optical emission spectrometry (ICP-OES). The mineralogical characterization was conducted by X-ray diffraction (XRD), and the phase changes of minerals in bauxite were detected by thermogravimetric analysis (TGA/DTG). The total organic carbon (TOC) technique was used to quantify the C in the samples, and the moisture content was also measured. Alumina was 30 wt.% on average for all samples, good for producing high-purity alumina by hydrometallurgical processes. The results, however, showed high (~20 at.%) silica concentrations in two samples and ~3 wt.% Fe in one sample, which can pose a challenge in the Bayer process. The X-ray diffraction (XRD) analysis showed that gibbsite (Gbs), kaolinite (Kln), anatase (Ant), and hematite (Hem) were the major mineral phases in these samples. The study showed that the samples from the same mine vary in their metal content, especially with regard to Si, and they, thus, need to be processed selectively to maximize their economic value.

Fe is a common substituent in palygorskites (Plg), but its effect on the microscopic properties is unclear. In the current study, molecular dynamics (MD) simulations were carried out to investigate the effect of Fe on the properties of the nano-pores in Plg. The structures and dynamics of water and Na+ ions in the pores were computed by analyzing the MD trajectories. The results revealed that for both Fe-containing and ordinary Plg, zeolitic water molecules can diffuse into the pores with very low mobility whereas Mg-coordinated water fails to escape. Na+ ions show no obvious diffusivity because they are fixed above the Si–Osix-membered rings. Detailed comparison indicates that Fe-substitution has no significant influence on the pore properties of Plg.

Extinction bend contours, observed in Cs-treated mica-vermiculites by transmission electron microscopy, give information on the morphology and crystal orientation and continuity in individual particles of clay size. Interlayer Cs apparently stretches that part of the silicate sheet in closest proximity and when exchange by Cs is incomplete, warping of the particle occurs. Warping favors the appearance of bend contours in transmission electron microscopic images of the particles. These contours terminate at crystal boundaries within a particle. A specimen tilting stage is useful in bringing the contours into view and in “exploring” individual particles.

Volcanic activity was important in Spain during the second half of the Cenozoic Era. It was closely related to the late kinematic and subsequent periods of the Alpidic orogenic cycle. Manifestations of the volcanic activity are seen in several parts of the Iberian Peninsula, but the main ones were confined to a few rather individualized zones. Cabo de Gata, Cartagena, and Mazarrón show a strong similarity, as does the Guelaya volcanic province, Morocco. The rocks (rhyolites, dacites and andesites) are clearly calcalkaline and, in many places, strong contamination processes have been demonstrated. The eruptions were, at least in part, fissural and fill important fractures, mainly northeast-southwest. They occurred just after the more important folding in the Betic-Riffien orogen. In these regions bentonite has formed by alteration of volcanic material.

The most important deposits are in Sierra of Nijar and Gata (Almería, Spain) and in the Monte Tidinit (Morocco). The Cabo de Gata bentonites are composed mainly of calcic and calcosodic montmorillonites. Palygorskite has been found in some places.

The bentonite of the Monte Tidinit is mainly calcium montmorillonite but some samples contain cristobalite. In Monte Maazza there is also a sedimentary deposit, consisting of a complex mixture of endellite, halloysite, gibbsite, montmorillonite and alunite—probably of hydrothermal origin. Halloysito is the main component: it is accompanied by gibbsite in the bottom layers and by montmorillonite and alunite in the top ones.

The ground clay, after processing by cation exchange or acid activation, is used for several industrial products, such as soaps and detergents, cosmetics and pharmacy; but the main use is for drilling muds, foundry molds, and clarification of mineral and vegetable oils.

All the bentonites are amenable to acid activation but the natural mixture of halloysite and montmorillonite from Monte Maazza gave the best results in tests on lubricating oils at a laboratory scale.

Research still in progress on the rheology of suspensions of the Almeréa bentonite contaminated with electrolytes gave interesting results using several thinner and filter oss control agents.

This paper presents a layer extraction method for obtaining a representative sample of clay-size material from a soil suspension. This method is especially advantageous in preparing a sample of relatively large size, and the procedure is simpler than that of the decantation method, a comparable method of extraction.

In the layer method, the position and the thickness of the layer to be extracted from a soil suspension can be varied and one or more extractions can be made. The effect of these variables on the size composition and the quantity of the extracted material is analyzed mathematically. Based upon such an analysis, the proper position and thickness of the layer and the desirable number of extractions can be determined to suit the requirements of a particular test.

The potential for structural failure of consolidated clay materials, which is of great importance in many applications, typically are assessed by measuring the localized strain bands that develop under anisotropic load stress. Most methods are precluded from providing a full understanding of the strain anisotropy because they only give two-dimensional information about the stressed clay blocks. The purpose of the present study was to investigate three-dimensional strain localization in a kaolinite matrix, caused by strain anisotropy due to a biaxial plane-strain test, using a relatively new method known as Anisotropy of Magnetic Susceptibility (AMS). This method involves induction of magnetism in an oriented sample in different directions and measurement of the induced magnetization in each direction. The AMS analyses were performed on core samples from different parts of the deformed kaolinite matrix. The degree of magnetic anisotropy (P′), which is a measure of the intensity of magnetic fabric and a gauge of strain intensity, was shown to be greater in cores containing shear bands than in those containing none. A threshold value for P′ for the deformed kaolinite matrix was identified, above which shear bands may develop. The comparison of the shape parameter (T), obtained from undeformed and deformed samples, illustrated a superimposition of prolate strain over the original oblate fabric of the kaolinite matrix. The orientation of the principal strain axis revealed that reorientation or rotation of the principal axis occurred along the shear bands.

Shales from six locations in Oklahoma were subjected to natural weathering for 2 yr. Simulated weathering of these shales was effected in the laboratory by subjecting them to ultrasonic treatment in a tank type device. Both treatments produced disaggregation. X-ray diffraction patterns for the ultrasoni-cally treated and weathered shales indicated no major changes in the types of clay minerals. However, natural weathering in the field produced degradation of the clay minerals in addition to disaggregation of the shales. Ultrasonic treatment appears to be a good predictive test for determining the durability and weatherability of the shales; however, it can simulate field weathering only so far as the engineering index properties of the shale are concerned. It is not a predictive test where the mineralogical characteristics are of significance.