Organobentonites have been applied for the removal of two common non-steroidal anti-inflammatory drugs, ibuprofen (IBU) and diclofenac sodium (DS), from aqueous solutions. Two surfactants, one with and the other without benzyl group (octadecyldimethylbenzylammonium chloride, ODMBA, and hexadecyltrimethylammonium bromide, HDTMA), in amounts equivalent to 50, 75, and 100% of the cation exchange capacity of bentonite were used for the preparation of organobentonites. Successful modification of bentonite was confirmed by several methods: X-ray powder diffraction (XRPD), point of the zero charge (pH_PZC), determination of exchanged inorganic cations in bentonite, determination of textural properties, and scanning electron microscopy (SEM). Kinetic and thermodynamic data on the adsorption of IBU and DS showed that drug adsorption was controlled by the type and the amount of surfactant incorporated into the bentonite and by their arrangement in the interlayer space and at the surface of organobentonites. The adsorption of both drugs increased with an increase in the amount of both surfactants in organobentonites. The presence of the benzyl group in organobentonites enhanced the adsorption of IBU and DS and was more pronounced for IBU. Drug adsorption fits the pseudo-second-order kinetic model the best. The thermodynamic data revealed that the adsorption process was endothermic in nature and with increase of the amount of both surfactants drug adsorption processes were more spontaneous. The results obtained from this study revealed that adsorbents based on surfactants modified bentonite are promising candidates for IBU and DS removal from contaminated water.

Modified phillipsite samples were prepared with two different amounts (monolayer and bilayer coverage) of surfactants octadecyldimethylbenzylammonium chloride (O) and dodecylamine (D). Composites were characterized by Fourier transform infrared spectroscopy with attenuated total reflectance (FTIR–ATR), thermal analysis and determination of zeta potential, and subsequently tested for removal of diclofenac sodium (DCF). Drug adsorption experiments were performed under different initial DCF concentrations and different contact times. In order to investigate the influence of the chemical structure of surfactants used for modification of phillipsite on the preparation and properties of composites and DCF adsorption, experimental data were compared with previously published results on DCF adsorption by composites containing phillipsite and the same amounts of surfactants cetylpyridinium chloride (C) and Arquad^®2HT-75 (A). DCF adsorption isotherms for O and D composites showed a better fit with the Langmuir model with maximum adsorption capacities between 12.3 and 38.4 mg/g and are similar to those for C and A composites, while kinetics run followed a pseudo-second-order model. Composites containing either benzyl or pyridine functional groups showed higher adsorption of DCF, implying that surfactant structure has a significant impact on drug adsorption. Drug adsorption onto O, D, C and A composites was also confirmed by FTIR–ATR spectroscopy and zeta potential measurements.

The production route for cement clinker, including the clinkerization protocol and temperature, is highly dependent on the selection of raw materials. Natural resource reserves used in cement manufacturing are steadily declining due to rapid urbanization and the growing demand for building materials. Consequently, there is an urgent need to identify alternative resources, potentially from cost-effective primary raw materials or waste products. This study aims to evaluate the feasibility of incorporating recycled concrete as construction and demolition waste (C&DW) with unconventional clayey materials (bentonite and zeolite) into clinker synthesis at a reduced temperature of 1300 °C. The effect of mechanical pretreatment of the clinker raw meal, applied for durations of 10 to 30 min, was investigated. Mix designs combining traditional and alternative raw materials, along with different mechanical pretreatment durations, were systematically tested to assess their impact on raw meal clinkerization and the resulting cement mechanical properties. Despite variations in raw meal composition, the produced clinkers consistently exhibited phase compositions comprising C₃S, C₂S, C₃A, and C₄AF, as confirmed by XRD, FTIR, and SEM/EDS analyses. Among the studied raw materials, clayey components played a dominant role in controlling the formation of the main cement minerals, demonstrating that zeolite and bentonite can effectively substitute standard clays. Additionally, C&DW did not impede clinkerization; rather, it functioned as a silica source, replacing quartz sand. Short mechanical pretreatments (10 min) enhanced the content of cement minerals, whereas longer treatments adversely affected clinkerization. This study offers new insights into cement clinker production at reduced temperatures through the use of C&DW combined with unconventional clayey materials. The clinkerization temperature was reduced by approximately 100 °C from the conventional 1400–1450 °C, while still producing cements with mechanical performance comparable to ordinary Portland cement (OPC). The resulting zeolite- and bentonite-based cements, either mechanically untreated or subjected to short pretreatment, are potentially suitable for structural concrete applications, while cements produced with longer mechanical pretreatments may be more appropriate for lower-demand or non-structural uses.

In this study, natural kaolin was modified with hexadecyltrimethylammonium bromide (HDTMA-Br) at two levels corresponding to 50% and 90% of its cation exchange capacity. The resulting materials, designated as HKR-50 and HKR-90, were used as adsorbents for the mycotoxins ochratoxin A (OCHRA) and zearalenone (ZEN). The characterization of the HKRs with several methods (X-ray diffraction, DRIFT spectroscopy, thermal analysis (DTA/TG), SEM, zeta potential measurements, and the determination of the point of zero charge and textural properties) confirmed the presence of surfactant ions on the organokaolinites’ surfaces. The adsorption of ZEN and OCHRA by HKRs followed nonlinear adsorption isotherms, suggesting a complex adsorption mechanism. The adsorption capacities of ZEN and OCHRA were similar for HKR-50 and HKR-90 at pH 3, with higher adsorption observed for ZEN (~13.0 mg/g for HKR-50 and HKR-90 for ZEN and ~8.0 mg/g for HKR-50 and HKR-90 for OCHRA). At pH 7, the adsorption of ZEN and OCHRA was lower than at pH 3, especially for OCHRA, but slightly increased with increased amounts of surfactant on the kaolinite surface (8.5 mg/g for HKR-50 and 10.8 mg/g for HKR-90 for ZEN and 2.6 mg/g for HKR-50 and 4.1 mg/g for HKR-90 for OCHRA). Special attention was paid to the safety assessment of the natural kaolin and HKR-90, and toxicological tests confirmed the safety of both materials, as no adverse effects were observed in rats.

This study investigates the adsorption of ibuprofen (IBU) and diclofenac sodium (DS) using bentonite modified with varying amounts (50, 75, and 100% of cation exchange capacity—CEC) of two surfactants: octadecyl(dimethylbenzyl)ammonium (ODMBA) chloride and hexadecyltrimethylammonium (HDTMA) bromide. The resulting organobentonites were characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry/thermogravimetric analysis (DSC/TG), and zeta potential analysis. The results indicated that higher surfactant concentrations in organobentonites improved adsorption efficiencies for both drugs, while ODMBA-modified organobentonites exhibited notably larger adsorption capacities than HDTMA-modified samples. The adsorption isotherms fitted well to both the Langmuir and Freundlich models, with a better fit observed for the Freundlich model. The highest adsorption capacities were 102 mg/g for IBU and 160 mg/g for DS on sample OB-100 (organobentonite with 100% of ODMBA). Characterization of samples after drug adsorption, using FTIR, zeta potential and DSC/TG analysis, confirmed drug presence in organobentonites. Adsorption tests of DS in real river water (Danube and Sava rivers) showed that OB-100 demonstrated high removal capacity for DS. The findings suggest that organobentonites are low-cost adsorbents with potential for the removal of pharmaceutical contaminants from real aquatic environments.