This paper presents the results of examinations of the structure and crystallinity of polyamide (PA6) modified with fly ash from biomass combustion in a fluidized-bed boiler. Composites based on a PA6 matrix were examined. They contained 5, 10, and 15 wt% fly ash. Fourier-transform infrared with attenuated total reflectance spectroscopy (FTIR-ATR) was used to identify the characteristic functional groups present in the chemical structure of polyamide and composites based on its matrix. Structural analysis was performed using a differential scanning calorimeter (DSC) and microscopic examinations. Analysis of the values of thermal effects determined using the DSC technique allowed for the evaluation of the degree of crystallinity of the materials studied. Polyamide is usually considered to be a two-phase system consisting of crystalline and amorphous regions. The addition of the filler in the form of fly ash reduced the degree of crystallinity of the studied specimens. Based on the FTIR-ATR spectra and the recorded DSC curves, it was found that the α-phase was the dominant crystalline phase in the studied materials. Microscopic examinations were conducted to analyze the microstructure of the materials, providing information on the distribution and shape of the filler particles. Most of the particles ranged in size from a few to tens of micrometers. Furthermore, the use of scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDS) allowed for the analysis of the distribution of chemical elements in selected filler particles.

The structure and properties of the glass can be modified by introducing appropriate additives. Dolomite is one of the primary raw materials modifying the properties of glass, in which the essential component is calcium-magnesium double carbonate CaCO₃∙MgCO₃. The paper presents the research results on glasses obtained by smelting pure amphibolite and amphibolite modified with 10 and 20% dolomite additives. The raw material used was mined in the Poland region of Lower Silesia. The glass melting process was carried out in an electric furnace at 1450 °C for 2 h. The structure and properties of the glasses and crystallization products were determined by Differential Scanning Calorimetry (DSC), X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy—Energy Dispersive Spectroscopy (SEM-EDS). Viscosity and Vickers microhardness were also measured. It was found that the modification of amphibolite glass by adding dolomite affects the glasses’ properties and structure. The research results determined the effect of dolomite addition on the properties of alumino-silicate glasses in terms of the mineral fibre products used in the construction industry.

This paper presents the results of the research on the structure and thermal properties of materials made from fly ash based on high-density polyethylene (HDPE). Composites based on a polyethylene matrix with 5, 10, and 15 wt% fly ash from hard coal combustion content were examined. Fourier transform infrared spectroscopy with attenuated total reflectance (FTIR-ATR) was used to identify characteristic functional groups present in the chemical structure of polyethylene and the composites based on its matrix. Structural analysis was performed using X-ray diffraction (XRD), a differential scanning calorimeter (DSC), and microscopic examinations. Mechanical properties were also examined. Analysis of the thermal effect values determined by the DSC technique, XRD, and FTIR-ATR allowed the evaluation of the crystallinity of the tested materials. Polyethylene is generally considered to be a two-phase system consisting of crystalline and amorphous regions and is a plastic characterized by a significant crystalline phase content. Based on the FTIR-ATR spectra, DSC curves, and XRD, the effect of the filler and the changes occurring in the materials studied resulted in a decrease in the degree of crystallinity and a change in the melting point and crystallization temperature of the polymer matrix were established. Microscopic examinations were carried out to analyze the microstructure of the composites to collect information on the distribution and shape of the filler particles, indicating their size and distribution in the polymer matrix. Furthermore, the use of scanning electron microscopy combined with energy-dispersive X-ray spectroscopy (SEM-EDS) allowed for the microanalysis of the chemical composition of the filler particles.

Environmental contamination with microplastics and trace pharmaceuticals is an increasing ecological and health concern. This study aimed to investigate the effects of low-temperature cold plasma on polyethylene (PE) microplastic particles and to assess the potential for degradation of pharmaceuticals adsorbed onto their surfaces. Two types of PE samples were prepared: suspended in distilled water and in treated wastewater. All samples were exposed to cold plasma. In the second stage, PE particles were saturated with selected pharmaceuticals (diclofenac, sulfamethoxazole, trimethoprim) and then subjected to plasma treatment. Pharmaceutical concentrations were measured using high-performance liquid chromatography (HPLC). Particle morphology was analyzed via light microscopy (after Nile red staining) and scanning electron microscopy (SEM). The results showed that cold plasma treatment leads to agglomeration of PE particles, with the extent increasing with longer plasma exposure time. Pharmaceuticals adsorbed to the PE surface in the range of 20–70% of the applied dose. Cold plasma demonstrated the ability to remove pharmaceutical contaminants, particularly diclofenac (>98%), sulfamethoxazole (99.99%) and trimethoprim (>98%). These findings indicate that cold plasma has promising potential as a supportive technology for removing both microplastics and pharmaceutical residues from wastewater and aquatic environments.

The presence of pharmaceuticals in treated wastewater has become an environmental concern due to their persistence, biological activity, and incomplete removal in conventional wastewater treatment systems. In this study, a g-C₃N₄/rGO nanocomposite was synthesized via thermal polycondensation of melamine in the presence of reduced graphene oxide and evaluated as a photocatalyst for the degradation of selected pharmaceuticals in membrane bioreactor (MBR)-treated wastewater. The obtained materials were characterized using Fourier-transform infrared spectroscopy (FTIR–ATR), X-ray diffraction (XRD), nitrogen adsorption–desorption measurements (BET), Raman spectroscopy, scanning electron microscopy (SEM), and UV–Vis spectroscopy to evaluate their chemical structure, crystallinity, textural properties, morphology, and optical characteristics. Photocatalytic experiments were performed under UV irradiation using real wastewater spiked with carbamazepine, diclofenac, ibuprofen, and sulfamethoxazole at an initial concentration of 50 mg/L, selected to ensure reliable quantification under laboratory conditions. The complete removal of diclofenac and sulfamethoxazole was achieved within 30 min of treatment, while the presence of the nanocomposite enhanced the degradation efficiency of ibuprofen and carbamazepine by approximately 19% and 13%, respectively, compared to UV irradiation alone. The obtained results demonstrate the applicability of the investigated g-C₃N₄/rGO system for pharmaceutical degradation in real wastewater matrices and indicate its potential as a preliminary photocatalytic post-treatment approach.