Surfactant-modified clay minerals are known for their good sorption properties of both organic and inorganic compounds from aqueous solutions. However, the current knowledge regarding the effect of both cationic and nonionic surfactants on the properties of bentonite is still insufficient. Bentonite, with montmorillonite as the base clay, was modified with hexadecethyltrimethylammonium bromide (a cationic surfactant) in the amount of 1.0 cation exchange capacity (CEC) of bentonite and varying concentrations of t-octylphenoxypolyethoxyethanol (Triton X-100, a nonionic surfactant). We aimed to improve the understanding of the effect of nonionic and cationic surfactants on clay minerals. The modified bentonites were characterized by X-ray diffraction (XRD), thermogravimetric analysis/differential thermal analysis (TG/DTA), Fourier transform infrared spectrometry (FTIR), field emission scanning electron microscopy (SEM) and specific surface area and pore volume (BET). According to our results, the presence of a cationic surfactant significantly increased the amount of the adsorbed nonionic surfactant. Moreover, an increase in the concentration of nonionic surfactants is also associated with an increase in the effectiveness of the modification process. Our results indicate that the amount of nonionic surfactant used has a significant effect on the properties of the obtained hybrid material. Modification of bentonite with a nonionic surfactant did not cause an expansion of the interlayer space of smectite, regardless of the presence of a cationic surfactant. The modification process was found to significantly decrease the specific surface area of bentonite. Improvement of hydrophobic properties and thermal stability was also observed.

Pesticides are pollutants found in wastewater due to increasing agricultural activities over the years. Inappropriate dosing of pesticides results in the dispersal of active ingredients in the environment. The complete removal of pesticides from wastewater is an immediate concern due to their high toxicity and mobility. At present, adsorption is one of the most widely used methods for pesticide removal, in which synthetic zeolites and mesoporous silica materials are extensively applied. This article presents a systematic and comparative review of the applications and comparison of these adsorbents, based on the data reported in the literature. The paper summarizes the information collected from various studies, including the type of adsorbents and pesticides used, experimental conditions, and results of each work. The studies analyzed were laboratory-based and show potential advantages for the treatment of pesticide-bearing waters using functionalized and unfunctionalized synthetic zeolites and mesoporous silica materials. As a whole, functionalized materials are reported to exhibit better removal performance for different pesticides than conventional materials. It is expected that the results of this review will help researchers to establish a powerful strategy for the abatement of pesticides in wastewater.

Heavy metal contamination in soils has become one of the most critical environmental issues. The most efficient in-situ remediation technique is chemical immobilization that uses cost-effective soil amendments such as phosphate compounds to decrease Pb, Cd and Zn accessibility in the contaminated soils. The present study examined the effectiveness of KH₂PO₄ in immobilizing Pb, Cd and Zn in three samples of contaminated soils collected from ZGH “Bolesław” (Mining and Smelting Plant “Bolesław”). Effectiveness was evaluated using the following methods: a toxicity characteristic leaching procedure (TCLP)-based experiment, sequential extraction, X-ray diffraction analyses (XRD), and scanning electron microscopy–energy dispersive spectroscopy (SEM–EDS). The most efficient percentage reduction of total leachable metal concentration assessed by TCLP was observed for lead (50%–80%), and the least reduction was observed for zinc (1%–17%). The most effective immobilization of stable compounds assessed by sequential extraction was noted for lead, while the weakest immobilization was noted for cadmium. New insoluble mineral phases were identified by SEM-EDS analysis. Cd, Zn, and Pb formed new stable mineral substances with phosphates. The predominant crystal forms were dripstones and groups of needles, which were easily formed by dissolved carbon rock surfaces containing zinc ions. The alkaline nature of the soil and a large number of carbonates mainly influenced the formation of new structures.

Per- and polyfluoroalkyl substances (PFASs) represent one of the most challenging classes of persistent organic pollutants, and adsorption is currently one of the most widely deployed method for their removal from water. However, the long-term sustainability of adsorption-based treatment depends on how adsorbents are regenerated, managed after exhaustion, and integrated into broader environmental and regulatory frameworks. This review synthesises recent advances in regeneration strategies for PFAS-saturated adsorbents, including thermal, solvent-based, chemical, hybrid, and emerging methods, and provides a targeted analysis of policy and regulatory frameworks governing PFAS management in water. Evidence from the literature is critically assessed with attention to regeneration efficiencies, adsorbent stability, secondary waste generation, and long-term reuse potential. Life cycle assessment (LCA) studies are also examined to evaluate the environmental and cost implications of different management options. The analysis highlights that while solvent and chemical regeneration achieve high short-term recovery, thermal processes offer partial destructive potential, and electrochemical methods are emerging as promising but unproven alternatives. Persistent challenges include incomplete PFAS desorption, performance decline over multiple cycles, energy intensity, and secondary waste burdens. Advancing sustainable PFAS treatment requires integrated evaluation frameworks linking technical performance with environmental impact and cost, supported by policy drivers that incentivize regeneration and safe end-of-life management.

The presence of pesticides in our environment is a consequence of intensive industrial and civilizational development, necessitating the search for effective and safe methods to remove them. We suggest utilizing zeolite X and a zeolite-carbon composite, obtained through the chemical transformation of fly ash, as pesticide sorbents. To increase the sorption efficiency of 2,4-dichlorophenoxyacetic acid (2,4-D), 2-methyl-4-chlorophenoxyacetic acid (MCPA), carbendazim, and simazine, we functionalized the zeolite materials with cationic (hexadecyltrimethylammonium) and nonionic (Triton X-100) surfactants. We used transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), thermogravimetric/differential thermal analysis (TG/DTA) and point of zero charge (pHpzc) analysis to characterize the functionalized sorbent materials. Our results indicate that cationic surfactants significantly enhance the adsorption of 2,4-D and MCPA. In contrast, carbendazim and simazine exhibit maximum sorption on the unmodified zeolite-carbon composite. The sorption mechanism is intricate, with physical sorption predominating, primarily due to electrostatic interactions between the protonated binding sites of the adsorbents and the negatively charged pesticide molecules. Regeneration tests demonstrated that ethanol is the most effective in regenerating zeolite-carbon composite with adsorbed MCPA and 2,4-D, while thermal regeneration was not possible. Adsorbents with simazine and carbendazim can be regenerated using both thermal and ethanol methods, but the thermal regeneration of zeolite with adsorbed simazine is more efficient. Utilizing functionalized zeolite materials obtained from industrial waste, such as fly ash, could provide an efficient way to remove pesticides from the environment.

Montmorillonite—the most popular mineral of the smectite group—has been recognized as a low-cost, easily available mineral sorbent of heavy metals and other organic and inorganic compounds that pollute water. The aim of this work was to determine the sorption mechanism and to identify the reaction products formed on the surface of montmorillonite and organo-montmorillonite after sorption of molybdates (Mo(VI)) and tungstates (W(VI)). Montmorillonites are often modified to generate a negative charge on the surface. The main objective of the study was to investigate and compare the features of Na-montmorillonite (Na-M), montmorillonite modified with dodecyl trimethyl ammonium bromide (DDTMA-M), and montmorillonite modified with didodecyl dimethyl ammonium bromide (DDDDMA-M) before and after sorption experiments. The material obtained after sorption was studied by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). The XRD pattern showed the presence of a new crystallic phase in the sample that was observed under an SEM as an accumulation of crystals. The FTIR spectra showed bands related to Mo–O and W–O vibration (840 and 940 cm⁻¹, respectively). The obtained results suggest that molybdenum(VI) and tungsten(VI) ions sorb onto the organo-montmorillonite in the form of alkylammonium molybdates and tungstates.