Mineral–organic matter (OM) associations play an important role in determining the long-term retention of OM in soils. However, the retention mechanisms of OM in cation–mineral–OM systems remain unclear. Taking into account the dominance of montmorillonite (Mnt) in the soil of the temperate zone, we investigated the stability of humic substances (HSs) in the Fe(III)–Mnt–HS system using thermal analysis. The HS degradation started at ~387°C in the Fe(III)–Mnt–HS system, which was higher than that of the Fe(III)–HS system (290°C). The formed ferrihydrite (Fhy) mainly contributed to the enhanced labile OM retention through adsorption and/or co-precipitation, whereas Mnt inhibited the initial formation and subsequent transformation of Fhy, thus improving the stability of OM. These results suggest that the HS stability in Fe(III)–clay–HS systems depends on the Fe speciation affected by clay minerals, and this finding provides insights into OM–mineral interactions in temperate-zone soils.

Polymers maintain colloidal stability by adsorbing onto the surface of sepiolite particles, and changes in temperature and salinity can affect this process. We chose three typical polymers to investigate their interactions with sepiolite under high-salinity (15 wt.% NaCl) conditions at >180°C. Sepiolite samples were characterized using infrared testing, X-ray diffraction testing, contact angle testing, thermogravimetric testing, filtration loss testing and rheological testing. The experimental results showed that the desorption of the polymers under high-temperature and high-salinity conditions reduces the stability and filtration control of the suspension significantly. Adding polymers to sepiolite suspensions can maintain good stability even after thermal ageing at 240°C. In terms of drilling fluid regulation, sepiolite can play a role in regulating rheological properties, and the interactions between various polymers and sepiolite can be utilized to maintain the stable colloidal state of the drilling fluid. Studying the adsorption behaviour of various types of polymers on the surface of sepiolite under high-temperature and high-salinity conditions has important implications for the design and selection of sepiolite drilling fluid treatment agents.

We obtained natural red soil (RS), rich in iron, from the region of Palotina in the state of Paraná, Brazil. The RS sample was purified by suspension in water and sieved to remove plant particulates. It was then treated thermally at 800°C to remove organic volatiles; this sample was called RS800. The samples were characterized using X-ray diffraction, X-ray fluorescence, infrared and electronic spectroscopy, ζ-potential analysis and scanning electron microscopy. Colorimetric studies were performed according to the CIEL*a*b* system. Tests have shown that RS800 has the ability to remove methylene blue (MB) dye from wastewater. Thus, it was used as an adsorbent at various temperatures (25, 35, 45°C). According to the Langmuir model, the maximum adsorption capacity (qmax) was 23.256 mg g–1 (25°C). Unexpectedly, increasing temperature reduced qmax to 21.659 mg g–1 at 35°C and to 21.186 mg g–1 at 45°C. Therefore, RS800 must be used at room temperature (25°C), making its application in large-scale wastewater treatment feasible. After using RS800 as an adsorbent, the solids were filtered, dried, pulverized, and used as hybrid pigments in commercial white paints. Pigmented paints were used to paint a plaster specimen and colorimetric measurement was performed. These paints were tested for colour stability in acidic and alkaline environments. The results indicate that RS800 is efficient in the treatment of water contaminated with cationic dyes and can be reused as a hybrid pigment.

The adsorption mechanisms of hazardous gas molecules such as NH3, H2S and SO2 on sepiolite have not yet been elucidated. Therefore, molecular dynamics (MD) simulations were employed to investigate the adsorption behaviour of sepiolite towards NH3, H2S and SO2. A calculation model for sepiolite containing structural and zeolitic water molecules was constructed in this study. The adsorption sites and molecular configurations of the hazardous gases in the sepiolite channels were studied. The radial distribution function was employed to evaluate the interactions between the gas molecules and sepiolite. The results show that the order of adsorption capacity of sepiolite for the gases is as follows: SO2 > H2S > NH3. These three types of gas molecules absorbed in the channel nanopores of sepiolite exhibit different atomic configurations. The diffusion coefficients of the gas molecules in the channels decreased in the following order: NH3 > H2S > SO2. In addition, the diffusion coefficients were affected significantly by the ratio of the number of gas/water molecules. This study provides new perspectives for understanding the molecular processes responsible for the adsorption properties of sepiolite.

Water pollution by hexavalent chromium (Cr(VI)) is widespread and problematic. As a result, more research into economic Cr(VI) removal is needed. In this study, we created and employed an adsorption–reduction mechanism to remove Cr(VI). Magnetically reduced graphene oxide bentonite (MrGO-BT) is acid resistant and can undergo magnetic separation. The hydroxyl group of chitosan (CS) condensed with the functional groups on the surface of bentonite (BT), and the MrGO-BT sandwich has been fabricated and constructed from an Fe3O4 core layer sandwiched by reduced graphene oxide (rGO) and a BT shell, with CS acting as a crosslinker. Cr(VI) elimination by MrGO-BT was exothermic and spontaneous according to thermodynamic analyses. The adsorption kinetics and adsorption isotherms were characterized by the pseudo-second order kinetic theory and the Langmuir model, respectively. Regarding the elimination of Cr(VI), the greatest adsorption ability for Cr(VI) elimination achieved was 91.5 mg g–1. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy suggested that Cr(VI) was reduced by C–O–H on MrGO-BT to produce Cr(III) and H–C=O, and that Cr(III) chelated with amino groups or exchanged with BT after intercalation. In addition, the introduction of Cu2+ increased the positive charge of MrGO-BT and amplified the electrostatic interaction between Cr2O72− and HCrO4–, which is what caused Cr(VI) to be eliminated. Cu2+ and reduced Cr(III) combined with -NH2 on the surface of MrGO-BT to form -NH-Cr(III) or -NH-Cu2+, and Cr(VI) elimination via chelation and ion exchange was confirmed. MrGO-BT is shown to be an adsorbent with high acid resistance and good magnetic responsiveness and stability.

In the petroleum industry, one of the most important functions fluids must perform is to carry cuttings efficiently. In this context, the contamination of drilling fluids represents a challenge to the industry because it alters the properties of these fluids. This work compares two drilling fluids (one palygorskite-based and the other polymer-based), evaluating the effects of contaminants on these drilling fluids and their ability to carry cuttings. A contaminant is considered to be any material that causes undesirable changes in the properties of the drilling fluid. Contamination of an aqueous drilling fluid by calcium hydroxide (Ca(OH)2) and brine can increase the filtrate volume, decrease the perforation rate and alter the rheological properties of the fluid. This work analyses the effects of contamination by Ca(OH)2 and brine on the properties of salted water-based drilling fluids viscosified with palygorskite. For comparison, tests were performed with a polymeric drilling fluid. The cutting-carrying capacity of these fluids was verified using the empirical correlations of Moore (1974), Chien (1994) and Walker & Mayes (1975). The results show that the drilling fluid with palygorskite is resistant to contamination with Ca(OH)2 and brine, presenting low filtrate volume values. The drilling fluid with palygorskite presented greater slip velocities than the polymeric drilling fluid. Regarding the cutting-carrying capacity, the drilling fluid with palygorskite presented positive transport ratio values (>0), making it suitable for carrying rock cuttings. However, the polymeric drilling fluid showed better performance in terms of cutting-carrying capacity.

Adsorption of nanoparticles on minerals affects the fate and transport of nanoparticles directly and is of great significance to many fields, including research into ore deposits, geochemistry, the environment and mineral materials. Whereas many previous studies have been conducted under the equilibrium pH and low solid (mineral) to liquid (nanoparticle suspension) ratio conditions, adsorption processes under initial pH and high solid/liquid ratio conditions may represent many important yet underexamined complex scenarios. To fill in this research gap, the adsorption of gold nanoparticles on illite was investigated experimentally at a relatively high solid/liquid ratio of 5 g L–1 and the effects of initial pH, ionic strength, citrate concentration, temperature and illite particle size were evaluated. The adsorbed amount of gold nanoparticles (from <5% to nearly 100%) increased with increasing ionic strength, temperature and citrate concentration and decreased with increasing pH and illite particle size. The presence of illite resulted in the dynamic evolution of the pH of the suspension, which, along with solution chemistry parameters, controlled the electrostatic interaction of illite and gold nanoparticles. The adsorption results, scanning electron microscopy observations and surface properties of illite suggest that the negatively charged gold nanoparticles were adsorbed predominantly on the positive illite edges through electrostatic interaction. The electrostatic attraction between illite and gold nanoparticles appeared to be strong, supported by the minor amount of desorption. These research findings are expected to provide a valuable reference regarding many critical issues in the geosciences as well as for industrial applications.

To solve the problem of the leakage of phase-change materials and expand the application of clay minerals in the field of phase-change materials, illite and paraffin wax were used for the first time as a new binary hybrid core material with silica as the wall material. Phase-change microcapsules were prepared using the sol–gel method and successfully applied in silicone rubber foams. Differential scanning calorimetry showed that the microcapsules had a melting temperature of 62.99°C and a latent heat capacity of 98.24 J g–1, indicating their good heat-storage capacity. Furthermore, the effectiveness of using illite as a filler for preventing paraffin leakage was demonstrated through 200 thermal cycling tests, which demonstrated a leakage rate of only 2.6% compared to 3.2% exhibited by microcapsules without illite.

Three clay materials (codded MY3, KG and KK) from western Cameroon were selected and investigated for the production of refractory bricks. Samples MY3 and KG are kaolinite-rich materials, having clay mineral contents of 88% and 72%, respectively, whereas KK is a sand-rich material with a total clay content of 44%. Chamottes were prepared using each clay, and the ground chamottes were later used in the refractory formulation, with each raw clay used as a binding phase. After firing, the X-ray diffraction analyses of all of the refractory bricks indicated the same mineral assemblage made of quartz, cristobalite and mullite. The cristobalite is due to high-temperature conversion of quartz, whereas the mullite is due to clay mineral conversion. The evaluation of the linear shrinkage, physical properties (including bulk density and open porosity) and mechanical testing through refractoriness under load and compressive strength indicates that all of these clays could be used as raw materials for standard clay refractory materials. These results stand as a proof for the potential for these locally available materials to be used as raw materials for refractories that could be locally produced to reduce the cost of access to refractory raw materials faced by industries located in Cameroon.

Various approaches have been used for the preparation of heterostructured materials based on clay minerals, with numerous potential applications offered by the resulting functional materials. In this study, a fibrous clay mineral (palygorskite) and a tetraethyl orthosilicate reagent were used to obtain silica–palygorskite heterostructures. The aim was to highlight the influence of two factors during the preparation process: the effect of acid activation pre-treatment of the palygorskite with HCl and the effect of varying the length of the amine chains used – dodecylamine and butylamine – on the formation and development of silica nanoparticles on the surface of the palygorskite fibres. The silica–palygorskite heterostructures were obtained after the removal of the organic templates by calcination at 500°C. The textural and structural properties of the silica–palygorskite heterostructured samples were determined using various experimental characterization techniques, such as X-ray diffraction, transmission electron microscopy, gas adsorption and Fourier-transform infrared spectroscopy. The experimental variables targeted in this study appeared to have a significant effect on the textural properties of the silica–palygorskite heterostructure obtained. The great specific surface area and the mesoporous, microporous and ultramicroporous volumes as determined using nitrogen and/or carbon dioxide gas adsorption confirm the benefit of combining the acid activation pre-treatment of the fibrous clay mineral with the use of a long-chain amine co-surfactant (dodecylamine). The resulting silica–palygorskite heterostucture has a great specific surface area (628 m2 g–1) and a well-developed total pore network (VN2 = 0.24 cm3 g–1; Vultra (CO2) = 0.18 cm3 g–1). This material will be tested for the removal of volatile organic compounds at low concentrations.

The effects of chemical treatment on the radiation-shielding properties of Philippine natural zeolites were investigated using EpiXS following the EPICS2017 library. The zeolites were studied using X-ray diffraction and energy-dispersive X-ray spectroscopy. The acid treatment eliminated Fe and Ca, having a negative impact on the cross-section of the HCl-modified zeolite. The mass attenuation coefficients of the raw, NaOH- and HCl-modified zeolites at 1332 keV were 0.0545, 0.0544 and 0.0548 cm2 g–1, respectively. At 100–10,000 keV, the linear attenuation coefficient depends on the density and increases in the order HCl-modified > NaOH-modified > raw zeolite. In the energy range of 100–16,000 keV, the mean free path and half-value layer values are in the order of HCl-modified < NaOH-modified < raw zeolite. The raw and NaOH-modified zeolites have comparable effective atomic numbers, whereas the HCl-treated zeolite has significantly lower such values.

This study examined the incorporation of benzalkonium chloride into palygorskite and montmorillonite, assessing their potential as drug carriers. The aim was to evaluate the use of both clay minerals as viable options for antibacterial drug delivery. Various amounts (0.5, 1.0 and 2.0 times the cation-exchange capacity) of benzalkonium chloride were incorporated into both clay minerals, and the resulting materials were characterized using Fourier-transform infrared spectroscopy, thermogravimetric analysis, X-ray diffraction and elemental analysis using both CHNS-O elemental analysis and energy-dispersive X-ray spectroscopy. The Fourier-transform infrared spectroscopy and elemental analysis results indicate that benzalkonium chloride was incorporated successfully into the clay minerals. The X-ray diffraction traces of organo-montmorillonite indicate that the d-value increased as benzalkonium chloride content increased, confirming the intercalation of benzalkonium chloride within the montmorillonite interlayer space. By contrast, this behaviour was not observed for palygorskite. For the benzalkonium chloride-release studies, an initial burst release was found within the first 5 h, followed by a sustained release of benzalkonium chloride during the remaining testing time (24 h). Drug-release profiles were similar for modified palygorskite or montmorillonite during the testing time (24 h). Both clay minerals modified with benzalkonium chloride are promising materials for use as antibacterial fillers for several applications, including in the dental care industry.

The retreat of the Dead Sea and the lowering of the base level in recent decades have led to the exposure of the littoral clay sediments on the shore, the occurrence of exposed mudflats and the development of ground subsidence along strips (‘subsidence strips’) and clustered sinkholes. Based on field observations and laboratory analyses, the present study characterizes the clayey sediments in the environment of the exposed mudflats on the western Dead Sea shore. The clayey sediments of the exposed mudflats (‘mudflat sediments’) consist of fine-grained laminated calcareous clays. The mineral composition of the bulk mudflat sediments consists of clay and carbonate minerals (calcite, aragonite and dolomite) with some quartz and feldspar, and frequently gypsum and halite. The clay mineral composition of these samples is smectitic illite–smectite and kaolinite with some discrete illite and palygorskite. The smectitic illite–smectite is randomly interstratified (1.7 nm illite–smectite type R = 0). Although the detrital smectitic illite–smectite in the mudflat sediments is situated in the saline environment of the Dead Sea shore, no significant illitization is observed in the depositional detrital clay. Subsidence strips with clustered sinkholes were formed in the exposed mudflats as part of the adjustment of the Dead Sea periphery to the lowering of the base level as a result of the retreat. The field observations in the studied area reveal that the subsiding of mudflat sediments in the formation of the subsidence strips usually involves mud sagging of wet clayey sediments in the subsurface and sediment collapse of dry clayey sediments near the surface.

Fast drying (~60 min) is useful for optimizing production processes by increasing productivity and reducing costs and environmental impacts, especially in red ceramic industries in Brazil. However, suitable clays are necessary and, currently, studies focused on the plastic behaviour of clays with compositions suitable for extrusion, especially for fast drying, are scarce. Therefore, in this study, three different clays from the same mineral deposit were studied for producing clay-based structural products via fast drying. The clays were characterized according to their chemical, mineralogical and thermal properties, particle size, cation-exchange capacity, specific surface area and open pore volume distribution. Ten formulations were developed using a simplex-centroid mixture design of experiments and their plasticity index (PI) values were determined. The response surfaces of the formulations were evaluated according to their PI, while the formation characteristics were determined according to their extrusion workability factor values. Formulations F5 (50.0 wt.% yellow clay and 50.0 wt.% green clay) and F8 (66.6 wt.% yellow clay, 16.7 wt.% grey clay and 16.7 wt.% green clay; PI = 15.5–16.6%) displayed optimal extrusion properties, followed by formulations F7 (33.3 wt.% yellow clay, 33.3 wt.% grey clay and 33.3 wt.% green clay) and F10 (16.7 wt.% yellow clay, 16.7 wt.% grey clay and 66.6 wt.% green clay; PI = 13.8–14.2%), which are within acceptable extrusion index values. Thus, the chosen formulations have significant potential for use in the manufacture of fast-drying red ceramics.

Pyrophyllite is an important layered phyllosilicate material that is used in many fields due to its beneficial physicochemical and mechanical properties. Due to the presence of multiple defects in pyrophyllite, an in-depth investigation was conducted using density functional theory to explore the effects of Na(I), K(I), Mg(II), Ca(II) and Fe(II) doping on the atomic structure, electronic properties and mechanical characteristics of pyrophyllite. The results demonstrated that, among the studied defects, K(I) doping had the most pronounced effects on the lattice constants and bonding lengths of pyrophyllite, while the least significant effects were observed in the case of Fe(II) doping. Moreover, the partial and total densities of states and band structures of the five kinds of doped pyrophyllite also changed significantly due to the redistribution of electrons. Finally, the elastic constants of the doped pyrophyllite were lower than that of the undoped pyrophyllite. Doping with Na(I), K(I), Mg(II), Ca(II) and Fe(II) reduced the deformation resistance, stiffness and elastic wave velocity but increased the degree of anisotropy in pyrophyllite. The observed effects on the mechanical properties of pyrophyllite followed the order: Mg(II) > Fe(II) > Ca(II) >K(I) > Na(I).

Clay minerals are effective adsorbents used for the remediation of toxic heavy metals from wastewater due to their large surface areas and great cation-exchange capacities. In this study, the removal of lead ions from aqueous solutions via adsorption was investigated using raw and iron-modified Turkish sepiolite. The aim of this study was to examine the effects of modification and environmental conditions on the sorptive properties of sepiolite samples. Initially, the raw sepiolite (Sep) and magnetic sepiolite/Fe2O3 composite (MagSep) prepared using the co-precipitation method were characterized via mineralogical and petrographical means and the physicochemical properties were determined. Then, the batch adsorption of lead (Pb2+) ions on the sepiolite samples was examined under various conditions (solution pH, adsorbent dosage, contact time, initial Pb2+ ion concentration, temperature, shaking rate). The adsorption capacity of MagSep was found to be greater than that of Sep under all experimental conditions. The results showed that the adsorption process followed a pseudo-second-order kinetic model, and the Langmuir isotherm best correlated with the experimental data. The maximum adsorption capacities were found to be 60.6 and 90.1 mg g–1 for Sep and MagSep, respectively. The characterization of the Pb-adsorbed sepiolite samples showed that lead formed covalent bonds with the sepiolite samples and attached to the sepiolite surface mainly through ion exchange. MagSep can be used efficiently in the field of wastewater treatment for the removal of Pb2+ ions as it does not release any toxic pollutants and can be separated easily with the use of a magnetic field.

The Palaeocene–Eocene Thermal Maximum (PETM) was a global extreme climatic event, but it is relatively unknown from lower latitudes or equatorial regions in comparison to mid- and high latitudes. The present study provides the first clay mineralogical evidence of the PETM and subsequent hyperthermal events in a near-equatorial region represented by the Akli Formation in the Barmer Basin, India. The 32 m-thick succession of the Akli Formation shows abrupt changes in smectite and kaolin abundances preceding, during and succeeding the PETM event. Within the studied section, the kaolin content increases from 5–8% pre-PETM to 30–35% during the PETM, and then again decreases to 5–6% during the post-PETM period. The smectite, however, is marked by a corresponding decrease and its transformation into kaolin in acid weathering conditions. The transformation of the smectite is first marked by hydroxy interlayering and then transformation into kaolin during the PETM. The transformation of smectite into kaolin also resulted in extensive precipitation of iron oxide in sediments. The clay mineralogical changes in the Palaeocene–Eocene transition sediments of the Akli Formation were caused by 3–5°C warming and a 25–50% increase in rainfall during the hyperthermal events. Unusually high charcoal (~20%) fragments during the Palaeocene–Eocene transition also suggest warming and widespread biomass burning during the PETM in the lower latitudes.

Natural tuff samples in western Anatolia (Türkiye) originating from Miocene rhyolitic–pyroclastic rocks with >80 wt.% heulandite/clinoptilolite zeolites were investigated for their surface characteristics determined according to nitrogen adsorption after degassing at 150°C (specific surface area, pore volume and pore diameter). Additionally, these surface characteristics were correlated with the cationic compositions of the heulandite/clinoptilolite group minerals. The examined samples were characterized by two main pore diameters that were not related to specific surface area and pore volume but were partially related to the types and occupancy of extra-framework cations. One set of samples has a pore diameter of ~24 Å, total cation content (Na + K + Ca + Mg) ranging from 3.46 to 4.40 and a (Na + K)/(Ca + Mg) ratio ranging from 0.34 to 0.92. The total cation contents and (Na + K)/(Ca + Mg) ratios of the remaining samples with a pore diameter of ~37 Å are 4.30–5.08 and 1.48–2.85, respectively. After degassing at 300°C, there is a slight difference in the pore diameters of these two sets of samples (~37 and 38 Å). The pore sizes of the samples with a (Na + K)/(Ca + Mg) ratio < 1 (heulandite composition) increased from 24 to 36–38 Å with increasing degassing temperature, whereas the pore sizes of the samples with a (Na + K)/(Ca + Mg) ratio > 1 (clinoptilolite composition) increased from 37 to only 38–39 Å. However, there is no correlation between the Si/Al ratios and the cation-exchange capacities of the samples and their surface characteristics obtained by degassing at the two temperatures.

The Clay Minerals Group (CMG), the first of the Special Interest Groups of the Mineralogical Society of the UK and Ireland, was inaugurated in January 1947. The CMG, together with its Belgian equivalent (originally the Comité Belge pour l'Etude des Argiles, later the Belgian Clay Group, now defunct), formed the world's first organizations dedicated to clay mineral research. The CMG celebrated its 75th anniversary in 2022. The Group's aims are to stimulate interest in clay mineralogy, to facilitate an exchange of information between members by providing facilities for reading and discussing papers on research on clay minerals (and allied topics) and to expedite their publication and to encourage practical applications of such research, and these have remained reassuringly the same throughout its history. A founder and active member of both the European Clay Groups Association and the Association Internationale Pour L'Etude des Argiles, the CMG has promoted clay science through the publication of the highly regarded journal Clay Minerals and a series of influential book titles, organizing international and national scientific conferences and meetings, the George Brown Lecture series, providing bursaries and grants to assist researchers and hosting the Images of Clay archive. The initial and sustained success of the CMG has been largely due to the labours of many officers and committee members, some of whom have been recognized for their science and service with awards from the Mineralogical Society of the UK and Ireland and elsewhere. By maintaining this effort, the evident, continuing demand for clay mineral research to assist with changing societal needs should ensure the relevance and health of the CMG for the foreseeable future.

Bentonites are proposed to be used as buffers in high-level radioactive waste repositories. The elevated temperatures in repositories may, however, affect bentonites’ desired properties. For instance, heating under dry conditions can cause cation fixation, potentially affecting swelling properties. The kinetics of mineral dissolution and precipitation reactions will equally be influenced by temperature. Redistributions of Ca-sulphates and -carbonates have been observed, as well as illitization of smectite. Illitization, however, has only been observed in laboratory experiments at large solution/solid ratios, whereas it has not yet been unambiguously identified in large-scale experiments. In many large-scale tests, cation exchange is the first observable geochemical reaction. In addition, an enrichment of Mg close to the heater is found in many such tests. The thermal gradient and (incongruent) smectite dissolution are suspected to play a role with respect to the Mg enrichment, but the underlying mechanism has not been unravelled so far. To predict the long-term performance of a bentonite buffer, numerical modelling is required in order to be able to simulate the reactions of all accompanying mineral phases. Smectites, which dominate the bentonite composition, are therefore particularly difficult to characterise, as their dissolution is often observed to be non-stoichiometric. Various model approaches exist to simulate smectite reactions, mostly based on kinetic rate reactions, ideally considering the effect of pH (congruent or incongruent dissolution), temperature and the degree of saturation of the solution. Reassessing and improving the thermodynamic/kinetic data of smectites are prerequisites for improving long-term buffer performance assessment.