Search Results (75)

To enhance the strength and water stability of stabilized expansive soil, this study investigates the use of cement, montmorillonite adsorption modifier (MAM), and their composite system. Laboratory tests evaluated compaction characteristics, swell–shrink behavior, and mechanical performance. The results show that MAM more effectively regulates compaction by reducing optimum water content and increasing maximum dry density; 6% MAM increases maximum dry density by ≈0.04 g/cm³ and reduces optimum water content by ≈2%. In terms of swell–shrink behavior, MAM reduces both swelling and linear shrinkage more effectively than cement. The incorporation of 5% MAM reduces the free swelling ratio by 40% and the equilibrium moisture absorption by 2.7%, lowering the swelling classification to non-expansive. Furthermore, 5% MAM decreases the unloaded and loaded swelling ratio by 14.7% and 5%, respectively, while increasing MAM from 2% to 6% further reduces linear shrinkage by 1.12%. Cement significantly enhances compressive strength, with 7–28 d values reaching 2.2–2.7 times those of untreated soil at 9% content; however, its water stability under wet–dry cycles is limited. In contrast, the cement–MAM composite system achieves balanced improvement by simultaneously suppressing swelling and enhancing both strength and water stability. These findings provide a reference for the treatment and engineering application of expansive soils. Full article

The colloidal particles present in natural soil and groundwater systems possess distinctive properties that enable them to migrate across solid surfaces, thereby exerting a significant influence on the distribution of pollutants. While the attachment of colloidal particles to solid surfaces has been extensively investigated, the mechanisms governing their detachment under varying hydrochemical conditions remain largely unexplored. The common interaction between montmorillonite colloids and solid medium (Al₂O₃) in soil affects the fate of pollutants such as heavy metals. In our study, Al₂O₃ was used as solid medium to observe the adsorption and desorption behavior of montmorillonite colloids. It was found that the adsorption capacity of Al₂O₃ to montmorillonite colloids could reach 4.71 mg g⁻¹ (pH 5.0 and 10 mM NaCl concentration). X-ray photoelectron spectroscopy analysis shows that montmorillonite colloids react with the Al₂O₃ surface mainly through chemical groups with –O–Si bonds. Desorption experiments show that SDS drives desorption by neutralizing and reversing the surface charge of Al₂O₃, while CTAB directly modifies montmorillonite colloids and introduces steric hindrance to achieve desorption. These research data contribute to a comprehensive understanding of the migration behavior of montmorillonite colloids on solid phases. Full article

Among the naturally abundant clays in the Earth’s crust, montmorillonite (MMT), a member of the smectite group, stands out for its versatility. Its interesting properties can be further improved by chemical processing with inorganic acids and reaction temperatures close to boiling. In this study, a Brazilian polycationic MMT was treated with a low-concentration (2M) aqueous solution of hydrochloric acid at 60 and 70 °C for 5 h. The resulting modified clay was then employed in the purification of post-consumption oil (PCO), specifically soybean oil. The effect of the modification variables of the clay and also the purification parameters (time and temperature) were investigated, comparing the adsorptive and purification capacities of the modified MMT with those of the natural and a commercial clay sample. The characterization of the MMT (raw and modified) was carried out by bulk density, moisture content, plasticity limit, BET, SEM/EDS, XRD, and FTIR, whereas the characterization of the PCO, as-received and after purification, involved the analyses of apparent density, relative flow time, UV-Vis spectrophotometry, and acid value. The results show that light acid activation, especially at 70 °C, promoted a significant increase in the surface area up to 96% and the adsorption capacity of the clay. The oil purification showed good results in all tests, with the best condition being 70 °C for 24 h with the C70 clay. Thus, the satisfactory results represent an economy of time and energy. Full article

In response to the requirements of wellbore plugging and lost circulation control, this study designed and prepared a new type of thixotropic polymer gel system. The optimal formula was obtained through systematic screening of the types and concentrations of high molecular polymers, cross-linking agents, flow pattern regulators, and resin curing agents. Comprehensive characterization of the gel’s gelling performance, thixotropic properties, high-temperature stability, shear resistance, and plugging capacity was conducted using methods such as the Sydansk bottle test, rheological testing, high-temperature aging experiments, plugging performance evaluation, as well as infrared spectroscopy, nuclear magnetic resonance, and thermogravimetric analysis, and its mechanism of action was revealed. The results show that the optimal formula is 1.2% AM-AA-AMPS terpolymer + 0.5% hydroquinone + 0.6% S-Trioxane + 0.8% modified montmorillonite + 14% modified phenolic resin. This gel system has a gelling time of 6 h, a gel strength reaching grade H, and a storage modulus of 62 Pa. It exhibits significant shear thinning characteristics in the shear rate range of 0.1~1000 s⁻¹, with a viscosity recovery rate of 97.7% and a thixotropic recovery rate of 90% after shearing. It forms a complete gel at a high temperature of 160 °C, with a dehydration rate of only 8.5% and a storage modulus retention rate of 80% after aging at 140 °C for 7 days. Under water flooding conditions at 120 °C, the converted pressure-bearing capacity per 100 m reaches 24.0 MPa. Mechanism analysis confirms that the system forms a stable composite network through the synergistic effect of “covalent cross-linking—hydrogen bonding—physical adsorption”, providing a high-performance material solution for wellbore plugging in high-temperature and high-salt environments. Full article

Water pollution by organic dyes poses serious environmental and health challenges, demanding efficient and selective remediation methods. In this study, we engineered tailored organo-clay nanocomposites by modifying montmorillonite with hexadecyltrimethylammonium bromide (HTAB) and intercalating polyethylene glycol (PEG) chains of two distinct molecular weights (PEG200 and PEG4000). Comprehensive characterization techniques (XRD, FTIR, SEM, zeta potential, and TGA) confirmed the successful modification of the composites. Notably, PEG4000 promoted significant interlayer expansion, as evidenced by the shift of the (00l) reflection corresponding to the basal spacing d, indicating an increase in basal spacing. This expansion contributed to the formation of a well-ordered porous framework with uniformly distributed pores. In contrast, PEG200 produced smaller pores with a more uniform distribution but induced less pronounced interlayer expansion. Adsorption tests demonstrated rapid kinetics, achieving equilibrium in under 15 min, and impressive capacities: 420 mg/g of methylene blue (MB) adsorbed on PEG200/MMT@HTAB, and 385 mg/g of Congo red (CR) on PEG4000/MMT@HTAB. The crucial role of PEG chain length in adsorption selectivity was assessed, showing that shorter PEG chains favored methylene blue adsorption by producing narrower pores and faster kinetics, while longer PEG chains enhanced CR uptake via a stable, interconnected pore network that facilitates diffusion of larger dye molecules. Thermodynamic and Dubinin–Radushkevich analyses confirmed that the adsorption was spontaneous, exothermic, and predominantly driven by physical adsorption mechanisms involving weak van der Waals and dipole interactions. These findings highlight the potential of PEG-modified montmorillonite nanocomposites as cost-effective, efficient, and tunable adsorbents for rapid and selective removal of organic dyes in wastewater treatment. Full article

This study explores the adsorption and catalytic degradation of 2,4,6-trinitrotoluene (TNT) from aqueous solutions, using montmorillonite-based catalysts. Commercially, montmorillonite K10 was modified through aluminum pillaring (K10-Al-PILC), followed by vanadium intercalation (K10-Al-PILC-V) and ozone activation. A novel aspect of this work is the use of naturally contaminated water as the TNT source. The selected sample, collected from the Plaiul Arșiței–Cireșu–Leșunț region (Oituz, Bacau, Romania), originated from an area historically exposed to explosive residues, where TNT traces were previously identified. The adsorption performance of the materials was evaluated by varying adsorbent dosage, contact time, and solution pH. Catalytic ozonation experiments were conducted under different catalyst masses, ozone concentrations, and reaction times to assess degradation efficiency. The results demonstrated that aluminum pillaring significantly enhanced the adsorption capacity of the clay, while vanadium incorporation further improved both adsorption and catalytic activity. The vanadium-modified material exhibited superior performance in TNT removal, both through adsorption and oxidative degradation. Additionally, the catalytic ozonation process led to the formation of degradation products with reduced toxicity, confirming the potential of these materials for environmental remediation of nitroaromatic pollutants in real water systems. Full article

To address the challenges of friction and wear in mechanical systems, two functionalized montmorillonite (MMT) nanolubricants were developed through mechanochemistry, namely 3-sulfotetradecyldimethyl betaine-modified MMT (BS-MMT) and coconut amide propyl betaine-modified MMT (CAB-MMT) lubricants. The modification significantly expanded MMT’s interlayer spacing, with CAB-MMT exhibiting superior delamination and dispersion stability due to its coconut fatty amide groups. Tribological tests demonstrated that 0.5% CAB-MMT reduced the friction coefficient by 71.4% (to 0.08) and wear scar diameter by 58.8%, while maintaining stable performance under high loads (392 N) and speeds (1450 rpm). The exceptional performance stems from a synergistic mechanism involving the physical adsorption of MMT nanosheets, chemical adhesion via Fe-N/C-N⁺ bonds, and dynamic repair by friction-induced oxides. This work presents an eco-friendly, high-performance water-based nano-lubricant with broad industrial application potential. Full article

This study examines the formation of the clay mineral simonkolleite (Skl) in bentonites contaminated with zinc(II) chloride (ZnCl₂), a process that has been little documented in heterogeneous systems such as contaminated bentonites. We explain the contamination mechanisms and provide new insights into the mineralogical, structural, and physicochemical transformations occurring within these materials. The objective, explored for the first time, was to assess how the ZnCl₂-induced mineral phase formation influences the properties of bentonites used as sealing materials, particularly regarding changes in specific surface area and porosity. Three bentonites were analyzed: Ca-bentonite from Texas (STx-1b), Na-bentonite from Wyoming (SWy-3), and Ca-bentonite from Jelsovy Potok, Slovakia (BSvk). Treatment with ZnCl₂ solution led to ion exchange and the formation of up to ~30% simonkolleite, accompanied by a concurrent decrease in montmorillonite content by 9–30%. A suite of analytical techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), X-ray fluorescence (XRF), and energy-dispersive X-ray spectroscopy (EDS), was employed to characterize these transformations. The contamination mechanism of ZnCl₂ involves an ion exchange of Zn²⁺ within the montmorillonite structure, the partial degradation of specific montmorillonite phases, and the formation of a secondary phase, simonkolleite. These transformations caused a ~50% decrease in specific surface area and porosity as measured by the Brunauer–Emmett–Teller (BET) nitrogen adsorption and Barrett–Joyner–Halenda (BJH) methods. The findings raise concerns regarding the long-term performance of bentonite-based barriers. Further research should evaluate hydraulic conductivity, mechanical strength, and the design of modified bentonite materials with improved resistance to Zn-induced alterations. Full article

The development of antimicrobial and antioxidant packaging materials is critical for improving food safety and extending shelf life. This study aimed to design and characterize low-density polyethylene (LDPE) and poly(ethylene-co-vinyl acetate) (EVA) films incorporating organically modified montmorillonite (OMt) nanocarriers loaded with carvacrol (C) and thymol (T) essential oil components. The incorporation of carvacrol and thymol into OMt was conducted through an evaporation/adsorption method without the use of organic solvents. In the next step, LDPE, EVA and OMtC or OMtT were melt-compounded in order to obtain films. Characterization of the bioactive nanocarriers and films was performed through X-ray diffraction (XRD), tensile testing, oxygen permeability measurements (OTR) and antioxidant assays. Films LDPE/EVA/OMtC and LDPE/EVA/OMtT showed improved mechanical strength and antioxidant activity, with IC₅₀ values between 0.32 and 0.52 mg/mL. Film with component weight ratio LDPE/EVA/OMtC equal to 80/10/10 also demonstrated enhanced barrier properties and significantly inhibited fungal growth on baguette bread for up to 60 days. These findings highlight the potential of these bioactive films to improve the microbial safety and shelf life of bakery products. Full article

The use of essential oil components as natural antifungal preservatives in the active packaging of bread is an innovative approach that leverages the antimicrobial properties of these compounds to extend the shelf life of bread and ensure its safety. The aim of the present work was the thorough investigation of the antioxidant properties and antifungal activity of low-density polyethylene (LDPE or PE) nanocomposite films with organically modified montmorillonite (O) loaded with carvacrol (C) or thymol (T) as a function of time, starting from 2 months and concluding at 12 months. The films PE_OC and PE_OT were prepared through the evaporation/adsorption method, a green methodology developed by our group compatible with food packaging. For a comprehensive analysis of the synthesized films’ oxygen permeability (OTR), measurements were employed, indicating that the incorporation of clay–bioactive nanocarriers into LDPE films reduced their oxygen permeability. A thorough analysis in terms of the antioxidant activity of the films was assessed at various intervals (2, 3, 6, and 12 months), showing high antioxidant activity for films PE_OC10 and PE_OT10 (polyethylene with 10% wt. organically modified montmorillonite loaded with carvacrol or thymol), even at 12 months. Based on the overall analysis, the PE_OC10 film was identified as the most effective option in the antifungal evaluation conducted using white bread, demonstrating substantial inhibition of fungal growth for up to six months. Full article

Natural gas hydrate (NGH) is a clean resource characterized by abundant potential reserves, clean combustion, and high energy density. Although significant progress has been made in the development of NGH resources all around the world, challenges still exist that hinder commercial exploitation, such as a low daily gas production rate and short steady production periods. One significant reason lies in the complex gas–liquid–solid phase transitions occurring within the formation during production, which lead to changes in flow capacity. Understanding the phase change mechanism of NGH reservoirs will help to further reveal the production increase mechanism. To address the phase transitions’ effect on production, this paper establishes a numerical simulation model for the depressurization exploitation of natural gas hydrates in order to investigate phase transition characteristics at the field scale. First, the phase equilibrium calculation method is presented and the phase equilibrium curve is modified by considering the capillary effect, soluble salt, and surface adsorption. Then, the phase transition model is successfully characterized in a simulation and the numerical simulation model is established based on the first test project parameters in the Shenhu area. The production characteristics of different sediment types (montmorillonite, South China Sea sediments, kaolin, and silt) are analyzed under the effects of water content and salinity. It is shown that lower initial water content and higher salinity result in higher gas production. The results provide a better understanding of the effects of phase transition parameters on NGH production at the field scale. Full article

The modification of the layered silicate with a structural type 2:1 montmorillonite by the cationic surfactant hexadecyltrimethylammonium bromide was carried out. The obtained organomontmorillonite was milled for 2–25 min in a high-energy planetary ball mill. The structural and physicochemical characteristics of the modified montmorillonite and the mechanochemically activated montmorillonite were investigated using various methods such as X-ray diffraction, thermal analysis, scanning electron microscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy, and determination of the specific surface area as well as the parameters of the porous structure by the low-temperature adsorption–desorption of nitrogen. The modification of montmorillonite with the quaternary ammonium salt led to a slowdown of deformation and subsequent amorphization of the montmorillonite structure during the high-energy milling. Mechanochemical activation of the modified montmorillonite increased its sorption capacity nine times, with the maximum uranium sorption achieved after mechanochemical treatment for 10 min. Full article

Clays have been exploited in the manufacture of diverse products from ceramics to paints, pharmaceuticals, plastics, cosmetics, and more. Thus, they can be used in many industrial applications, showing good adsorbent ability thanks to their lamellar structure, high cation exchange capacity, pore size distribution, and large surface area. For this reason, considerable attention has been paid to their in-depth characterization, for further integration in sectors such as biomedicine, construction, remediation, aerospace, and nanotechnology. For this aim, two samples of natural clays, ALO1 and PRE4, from the southeast part of Albania, were subject to a multi-methodological characterization, with the aim of addressing the use of such geomaterials in possible sensing applications. X-ray fluorescence analysis, morphological characterization of the samples, and energy-dispersive system spectroscopy pointed to an extreme mineralogical variety, with kaolinite in AL01 and montmorillonite in PRE4 as the most abundant phases. This fact was further confirmed by powder X-ray diffraction, showing a quartz content of 20%, a kaolinite content of 64%, and a muscovite content of 16% for ALO1; meanwhile, for PRE4, we found a content of quartz of 45%, a content of montmorillonite of 34.9%, and a content of clinochlore of 20%. Infrared spectroscopy and thermal analyses confirmed the presence of hydroxyl groups in both samples, suggesting a higher content in ALO1. Measurement of N₂ adsorption isotherms on the clay samples yields specific surface areas of 87 m²/g for PRE4 and 32 m²/g for ALO1, pore volumes of 0.721 cm³/g for PRE4 and 0.637 cm³/g for ALO1, and similar pore sizes in the range of 6–12 nm. Electrochemical analysis highlighted a good conductivity of ALO1 and PRE4 when used for the modification of commercial carbon-based screen-printed electrodes. In detail, higher currents were registered by differential pulse voltammetry for the electrodes modified with the clays with respect to bare electrodes, as well as good repeatability of the measurements. In addition, a comparative study with nanomaterials, known for their good conductivity, was achieved, using carbon black and gold nanoparticles as a reference, showing that the conductivity of the clays was lower than but not so different from those of the reference materials. Full article

This work combines experimental and computational modeling studies for the preparation of a composite of metformin and an organoclay, examining the advantages of a Tunisian clay used for drug delivery applications. The clay mineral studied is a montmorillonite-like smectite (Sm-Na), and the organoclay derivative (HDTMA-Sm) was used as a drug carrier for metformin hydrochloride (MET). In order to assess the MET loading into the clays, these materials were characterized by means of cation exchange capacity assessment, specific surface area measurement, and with the techniques of X-ray diffraction (XRD), differential scanning calorimetry, X-ray fluorescence spectroscopy, and Fourier-transformed infrared spectroscopy. Computational molecular modeling studies showed the surface adsorption process, identifying the clay–drug interactions through hydrogen bonds, and assessing electrostatic interactions for the hybrid MET/Sm-Na and hydrophobic interactions and cation exchange for the hybrid MET/HDTMA-Sm. The results show that the clays (Sm-Na and HDTMA-Sm) are capable of adsorbing MET, reaching a maximum load of 12.42 and 21.97 %, respectively. The adsorption isotherms were fitted by the Freundlich model, indicating heterogeneous adsorption of the studied adsorbate–adsorbent system, and they followed pseudo-second-order kinetics. The calculations of ΔGº indicate the spontaneous and reversible nature of the adsorption. The calculation of ΔH° indicates physical adsorption for the purified clay (Sm-Na) and chemical adsorption for the modified clay (HDTMA-Sm). The release of intercalated MET was studied in media simulating gastric and intestinal fluids, revealing that the purified clay (Sm-Na) and the modified organoclay (HDTMA-Sm) can be used as carriers in controlled drug delivery in future clinical applications. The molecular modeling studies confirmed the experimental phenomena, showing that the main adsorption mechanism is the cation exchange process between proton and MET cations into the interlayer space. Full article

Modified clays with organic molecules have many applications, such as the adsorption of pollutants, catalysts, and drug delivery systems. Different methodologies for intercalating these structures with organic moieties can be found in the literature with many purposes. In this paper, a new methodology of modifying Sodium Montmorillonite clays (Na-Mt) with a faster drying time was investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), BET, and thermogravimetric analysis (TG and DTG). In the modification process, a mixture of ethyl alcohol, DMSO, and Na-Mt were kept under magnetic stirring for one hour. Statistical analysis was applied to evaluate the effects of the amount of DMSO, temperature, and sonication time on the modified clay (DMSO-SMAT) using a 2³-factorial design. XRD and FTIR analyses showed the DMSO intercalation into sodium montmorillonite Argel-T (SMAT). An average increase of 0.57 nm for the interplanar distance was found after swelling with DMSO intercalation. BET analysis revealed a decrease in the surface area (from 41.8933 m²/g to 2.1572 m²/g) of Na-Mt when modified with DMSO. The porosity increased from 1.74 (SMAT) to 1.87 nm (DMSO-SMAT) after the application of the methodology. Thermal analysis showed a thermal stability for the DMSO-SMAT material, and this was used to calculate the DMSO-SMAT formula of Na[Al₅Mg]Si₁₂O₃₀(OH)₆ · 0.54 DMSO. Statistical analysis showed that only the effect of the amount of DMSO was significant for increasing the interlayer space of DMSO-SMAT. In addition, at room temperature, the drying time of the sample using this methodology was 30 min. Full article