Fe₂As has been studied in situ by synchrotron powder X-ray diffraction (PXRD) over the range of temperatures 25–850 °C and under a neutral atmosphere to understand its thermal behavior, which is potentially important for gold extraction. For the first time, incongruent high-temperature reactions of Fe₂As are observed as it breaks down and the existence of a previously undiscovered high-temperature FeAs phase with an NiAs-type structure has been determined experimentally. No evidence has been found for the existence of the high-temperature Fe₃As₂ phase. Hence, the previously published phase diagram for the Fe–As system has to be modified accordingly.

With "easy" ores becoming diminished, extractive industries are now shifting towards difficult deposits. In the future, gold-arsenic-bearing refractory ores will represent a prime example of the type of ores that may become more typical sourse for global gold recovery operations. Mining and beneficiation of As-bearing ores inevitably produce As-bearing wastes, which exacerbate any natural As mobilization. The mobility of As is governed by the interplay of redox reactions, adsorption/desorption, ion exchange, precipitation/dissolution, and biotransformation. The dominant processes depend on local biogeochemical conditions of the media, such as pH, Eh, chemical composition, as well as the presence and intensity of biological activity. This article provides an overview of current research on arsenic contamination of the environment caused by mineralization, mining and extraction of gold on the example of specific gold deposits.

This paper presents a modern spectroscopic characterization of the synthetic oil from oil sands of Beke, Munaily-Mola, and Dongeleksor. The pyrolysis process was carried out at temperatures up to 580 °C with a controlled heating rate, and the products obtained were analyzed using Fourier transform infrared spectroscopy (FTIR), gas chromatography–mass spectrometry (GC–MSD), and nuclear magnetic resonance (NMR) spectroscopy. The FTIR spectra showed a predominance of aliphatic hydrocarbons in the sample from Munaily-Mola synthetic oil, while the content of aromatic compounds was higher in the sample from Beke. GC–MSD analysis revealed significant differences in the distribution of hydrocarbons between the samples, with the Munaily-Mola sample containing a higher proportion of heavy hydrocarbons. NMR spectroscopy provided additional information about the structural composition of the extracted oil. The results indicate the potential of pyrolysis as an effective method for processing oil sands, while the composition of the product varies depending on the geological origin of the raw materials. These findings provide valuable information for optimizing oil sands processing technologies and improving the efficiency of synthetic oil production.

Zeolite-based composite nanomaterials represent a versatile and mechanistically rich platform for the removal of organic micropollutants (OMPs)—including pharmaceuticals, endocrine-disrupting compounds, pesticides, and per- and polyfluoroalkyl substances (PFAS)—from contaminated water systems. Although pristine zeolite frameworks provide well-defined microporous architectures, tunable Si/Al ratios, and ion-exchange capacity, their intrinsic hydrophilicity restricts interaction diversity and limits performance toward the structurally heterogeneous OMPs prevalent in real aquatic environments. Composite integration with carbonaceous nanophases, functional polymers and surfactants, and catalytically active metal oxide nanoparticles substantially extends this interaction repertoire, yielding multifunctional materials whose adsorption performance exceeds that of the individual components. Drawing on a systematic survey of peer-reviewed literature published between 2016 and 2026, this review develops a mechanism-oriented, structure–property–performance framework examining five dominant adsorption mechanisms—electrostatic attraction, π–π stacking, hydrogen bonding, hydrophobic partitioning, and micropore confinement—in relation to composite nanoarchitecture, surface chemistry, and structural parameters. The modulating influence of realistic water matrix conditions on adsorption efficiency is critically assessed, alongside challenges of regeneration, long-term stability, metal leaching, and the persistent gap between laboratory-scale synthesis and scalable deployment. Priority research directions are identified, including standardized performance evaluation under environmentally representative conditions and rational design of hierarchical multifunctional nanocomposites from earth-abundant and waste-derived precursors.

The physicochemical and adsorption properties of granular sorbents based on natural bentonite and modified sorbents based on it have been studied. It was found that modification of natural bentonite with iron (III) polyhydroxocations (mod. 1_Fe_5 GA) and aluminum (III) (mod. 1_Al_5 GA) by the “co-precipitation” method leads to a change in their chemical composition, structure, and sorption properties. It is shown that modified sorbents based on natural bentonite are finely porous (nanostructured) objects with a predominance of pores measuring 1.5–8.0 nm, with a specific surface area of 55–65 m²/g. Modification of bentonite with iron (III) and aluminum compounds by the “co-precipitation” method also leads to an increase in the sorption capacity of the obtained sorbents with respect to bichromate and arsenate anions and nickel cations by 5-10 times compared with natural bentonite. The obtained sorption isotherms were classified as Langmuir type isotherms. Kinetic analysis showed that at the initial stage the sorption process is controlled by an external diffusion factor, i.e. refers to the diffusion of sorbent from solution into a liquid film on the surface of the sorbent. Then the sorption process begins to proceed in a mixed diffusion mode, when it limits both the external diffusion factor and the internal diffusion factor (the diffusion of the sorbent to the active centers through the system of pores and capillaries). To determine the contribution of the chemical stage to the rate of adsorption of bichromate and arsenate anions and nickel(II) cations with the studied granular sorbents, kinetic curves were processed using the equations of chemical kinetics (pseudo-second-order model). As a result, it was found that the adsorption of the studied anions by modified sorbents based on natural bentonite is best described by a pseudo-second-order kinetic model. It is shown that the use of natural bentonite for the development of technology for the production of granular sorbents based on it has an undeniable advantage, firstly, in terms of its chemical and structural properties, it is easily and effectively modified, and secondly, having astringent properties, granules are easily made on its basis, which turn into ceramics during high-temperature firing. The result is a granular sorbent with high physical and mechanical properties. Since bentonite is an environmentally friendly product, the technology of recycling spent sorbents is also greatly simplified.