A nanocrystalline zeolite of Na-X type (CFAZ) was synthesized by ultrasonic-assisted double stage fusion-hydrothermal alkaline conversion of lignite coal fly ash. Modified CFAZ with magnetic nanoparticles (MNP-CFAZ) was obtained by adding presynthesized magnetic nanoparticles between the synthesis stages. CFAZs loaded by particles of copper (Cu-CFAZ) and cobalt (Co-CFAZ) oxides were prepared by postsynthesis modification of the parent CFAZ, applying a wet impregnation technique. The parent and modified CFAZs were examined for their phase composition by X-ray diffraction, morphology by scanning electron microscopy, and surface characteristics by N₂ physisorption. Comparative studies have been carried out on the adsorption capacity of the starting CFAZ and its derivatives with respect to Cd²⁺- and Pb²⁺-ions from aqueous solutions. Adsorption isotherms of Cd²⁺-ions on the studied samples were plotted and described by the adsorption equations of Langmuir, Freundlich, Langmuir–Freundlich, and Temkin. The best correlation between the experimental and model isotherms for the parent and modified CFAZ was found with the Langmuir linear model, assuming a monolayer adsorption mechanism. Parent and modified CFAZs were also studied as catalysts for heterogeneous thermal Fenton oxidation of methylene blue. At 90 °C, the higher catalytic activity exhibits the nonmodified sample, but with the decrease in temperature to 60 °C, the modified samples are more effective catalysts.

We demonstrated the deposition of the architecture of graphene oxide on stainless steel substrate and its potential environmental application. The synthesis and characterization of graphene oxide were described. The controlled formation of graphene oxide coatings in the form of the homogenous structure on stainless steel is demonstrated by scanning electron microscopy (SEM). The structure, morphology and properties of the material were assessed by Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, transmission electron microscopy (TEM) and atomic force microscopy (AFM). The morphology and stability of these structures are shown to be particularly related to the pre-treatment of stainless steel substrate before the electrophoretic deposition. This approach opens up a new route to the facile fabrication of advanced electrode coatings with potential use in environmental applications.

This contribution describes the preparation, coupled with detailed characterization, of Nb₂O₅ nanofibers and their application in lithium–sulfur batteries for the improvement of electrochemical performance. The utilization of reactive needle-less electrospinning allowed us to obtain, in a single step, amorphous pre-ceramic composite PAN/Nb₂O₅ fibers, which were transformed into porous ceramic Nb₂O₅ nanofibers via calcination. Thermogravimetric studies defined that calcination at 600 °C results in crystalline ceramic fibers without carbon residues. The fibrous morphology and mean diameter (614 ± 100 nm) of the ceramic nanofibers were analyzed via scanning and transmission electron microscopy. A surface area of 7.472 m²/g was determined through nitrogen adsorption measurements, while a combination of X-ray diffraction and Raman spectroscopy was used to show the crystallinity and composition of the fibers after calcination—single T-phase Nb₂O₅. Its performance in the cathode of lithium–sulfur batteries was defined through electrochemical tests, and the obtained results were compared to a similar blank electrode. The initial discharge capacity of 0.5 C reached a value of 570 mAh∙g⁻¹, while the reversible capacity of 406 mAh∙g⁻¹ was retained after 200 cycles, representing a capacity retention of 71.3%. The presence of Nb₂O₅ nanofibers in the carbon cathode inhibits the shuttle effect through polysulphide confinement, which originates from porosity and chemical trapping.

Microwave-activated carbons from walnut shells (ACMW) were impregnated with Ag and Se nanoparticles and with the Enoxil biologically active preparation, and the microbiological properties of the obtained composites were studied. To increase the functionality of the adsorbent, the activated carbon was oxidized with ozone, resulting in ACMWO containing aliphatic and aromatic carboxylic groups. There was a considerable decrease in the specific surface of the activated carbon after the oxidation process. Nitrogen adsorption was used to determine the structural parameters of the activated carbons. A simultaneous thermal analysis was used to study the thermal behavior of intact and oxidized activated carbons. Infrared spectroscopy was applied to analyze the surface chemistry of the adsorbents. The microbiological activity of the activated carbons was studied using Escherichia coli bacteria and Candida albicans fungi. The kinetic study of the microbiological activity allowed the estimation of the bactericidal/fungicidal action time of the activated carbons.

This study demonstrated the successful recovery of zinc, lead, and copper collective concentrates from historical metal-bearing mine tailings (sulfide–polymetallic ore with a composition of 7.38% Zn, 1.45% Pb, and 0.49% Cu) using froth flotation techniques, which were originally developed during uranium ore mining. Froth flotation techniques were used to justify suitability for recovering metals. The effects of a dosage of the foaming agent Polyethylene glycol (PEG 600) at 50 and 100 g t⁻¹, collector types Aerophine 3418A (AERO), Danafloat 067 (DF), and potassium ethyl xanthate (KEX) at 50 and 80 g t⁻¹, and a suspension density of 300 and 500 g L⁻¹ on froth flotation collective concentrates were investigated. The final collective concentrate achieved recoveries exceeding 91% for lead (Pb), 88% for copper (Cu), and 87% for zinc (Zn). The obtained concentrates were analyzed using Atomic Absorption Spectroscopy (AAS) and X-ray Fluorescence Spectrometry (XRF), while selected samples were further examined via Scanning Electron Microscopy (SEM) with Energy Dispersive X-ray Spectroscopy (EDS). The resulting sulfide concentrates can subsequently be treated using suitable hydrometallurgical techniques. The application of these concentrates in metal production would help reduce the environmental burden of mining activities.