Microplastics (MPs) are one of the major threats to aquatic ecosystems. Surprisingly, our knowledge of its occurrence and its impact on the organisms that dwell in small water bodies is still scarce. The aim of this study was to investigate the occurrence and chemical composition of MPs in tadpoles of pond-breeding amphibians. In total, 201 tadpoles belonging to 5 species were collected from 8 ponds located in southwestern Poland. MPs were found in all examined sites and in all studied species. Among those tested, 53 (26%) tadpoles ingested a total of 71 MPs. IR-ATR analysis revealed that particles were of anthropogenic origin and included nylon, polyurethane, polyisoprene and 1,2 polybutadiene.

A literature review of the five main theories describing the interaction mechanisms in the bitumen/aggregate system was conducted: theory of weak boundary layers, mechanical theory, electrostatic theory, chemical bonding theory, and thermodynamic theory (adsorption theory). The adhesion assessment methods in the bitumen/aggregate system are described, which can be divided into three main groups: determination of adhesion forces for bitumen with different materials, determination of bitumen resistance to the exfoliating action of water with different materials, and determination of adhesion as a fundamental value (contact angle measurements, interfacial fracture energy, adsorption capacity and others). It is proposed to evaluate the quality of adhesive interaction in the bitumen/aggregate system in two stages. The authors recommend using the adhesion determination methods for these two stages from the second group of methods the determination of bitumen resistance to the exfoliating action of water with different materials. In the first stage, the adhesion in the bitumen/aggregate system is determined by an accelerated technique in which the used bitumen binder and mineral material are considered as test materials. After the first stage, there are positive results in the second tests on compacted mixtures (indirect tensile strength test, Modified Lottman indirect tension test, immersion-compression test, and Hamburg wheel tracking test).

Developing biodegradable complex fertilizers is crucial for sustainable agriculture to reduce the environmental impact of mineral fertilizers and enhance soil quality. This study evaluated chitosan-based hydrogel coatings for sodium alginate matrices encapsulating amino acid hydrolysates from mealworm larvae, known for their plant growth-promoting properties. The research aims to identify the potential of biopolymer matrices for producing biodegradable slow-release fertilizers and to outline future development pathways necessary for this technology to be usable in the fertilizer industry. Chitosan coatings prepared with citric acid and crosslinked with ascorbic acid optimized plant growth, while those using acetic acid negatively affected it. Water absorption and nutrient release tests showed that chitosan coatings reduced water uptake and slowed initial nutrient release compared to uncoated samples. Leaching assays confirmed controlled-release behavior, with an initial burst followed by stability, driven by alginate–chitosan interactions and ion exchange. The X-ray diffraction (XRD) analysis revealed that adding hydrolysate and chitosan increased amorphousness and reduced porosity, improving structural properties. Thermogravimetric analysis (TGA) and Fourier-transform infrared (FTIR) spectroscopy demonstrated enhanced homogeneity and the presence of chemical interactions, which led to improvements in the material’s thermal stability and chemical characteristics. Biodegradation tests indicated greater durability of chitosan-coated composites, although hydrolysate incorporation accelerated decomposition due to its acidic pH. Germination tests confirmed no phytotoxicity and highlighted the potential of biopolymeric matrices for slow nutrient release. These findings indicate the possibilities of chitosan-coated alginate matrices as sustainable fertilizers, emphasizing the importance of adjusting coating composition and hydrolysate pH for enhanced efficacy and environmental benefits. The main recommendation for future research focuses on optimizing the chitosan coating process by exploring whether adding hydrolysate to the chitosan solution can reduce diffusional losses. Additionally, investigating the use of glycerol in the alginate matrix to minimize pore size and subsequent losses during coating is suggested. Future studies should prioritize analyzing percentage losses during the crosslinking of the alginate matrix, chitosan coating, and final shell crosslinking. This pioneering research highlights the potential for encapsulating liquid fertilizers in biopolymer matrices, offering promising applications in modern sustainable agriculture, which has not been studied in other publications.

Hydrogels, versatile materials used in various applications such as medicine, possess properties crucial for their specific applications, significantly influenced by their preparation methods. This study synthesized 18 different types of hydrogels using sodium alginate (SA) and two molecular weights of polyvinyl alcohol (PVA). Crosslinking agents such as aqueous solutions of calcium (Ca²⁺) and copper (Cu²⁺) ions and solutions of these ions in boric acid were utilized. The hydrogels were subjected to compression strength tests and drying kinetics analysis. Additionally, six hydrogel variants containing larger PVA particles underwent Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) post-drying. Some samples were lyophilized, and their surface morphology was examined using scanning electron microscopy (SEM). The results indicate that the choice of crosslinking method significantly impacts the physicochemical properties of the hydrogels. Crosslinking in solutions with higher concentrations of crosslinking ions enhanced mechanical properties and thermal stability. Conversely, using copper ions instead of calcium resulted in slower drying kinetics and reduced thermal stability. Notably, employing boric acid as a crosslinking agent for hydrogels containing heavier PVA molecules led to considerable improvements in mechanical properties and thermal stability.

Antibiotic overuse and mass production have led to a global problem with the treatment of antibacterial infections. Thus, any possibility to limit the number of antibacterial drugs used will contribute to a decrease in the development of pathogenic bacterial resistance. In this study, the enhanced bacterial growth reduction of pharmaceutical activated carbon (PAC) material with adsorbed antimicrobial agents compared to the activity of pure antibacterial drugs was investigated. Sulfamethoxazole (SMZ) at a concentration of 1.1 mg/mL retained the growth of S. aureus and E. coli at 20.5% and 26.5%, respectively, whereas SMZ adsorbed on PAC increased the reduction of the tested bacteria in the range of 47–72%. The use of PAC with adsorbed gentamycin (G) over 24 h improved the effectiveness of E. coli growth reduction by 50% compared to the application of pure antibiotic (3.6 µg/mL). The increased reduction of S. aureus growth by 6% using G with PAC for a 24-h incubation time compared to the use of pure antibiotics at a concentration of 3.6 µg/mL was observed. The results provide proof-of-principle that the new approach of activated carbon with adsorbed antimicrobial agents could yield an attractive background with potential as a new starting material for S. aureus and E. coli pathogen elimination, e.g., in wound-healing treatment in the future.