The global problem of microplastics in the environment is “inspiring” scientists to find environmentally friendly and economically viable methods to remove these pollutants from the environment. Advanced oxidation processes are among the most promising methods. In this work, the potential of Fenton, photo-Fenton, and Fenton-like processes for the degradation of microplastics from low-density polyethylene (LDPE), polypropylene (PP), and poly(vinyl chloride) (PVC) in water suspensions was investigated. The influence of three parameters on the efficiency of the degradation process was tested: the pH of the medium (3–7), the mass of added iron (10–50 times less than the mass of microplastics), and the mass of added H₂O₂ (5–25 times more than the mass of added iron). The effectiveness of the treatment was monitored by FTIR-ATR spectroscopy. After 60-min treatments, the PP microparticles were found to be insensitive. In the Fenton treatment of PVC and the photo-Fenton treatment of LDPE and PVC, changes in the FTIR spectra related to the degradation of the microplastics were observed. In these three cases, the treatment parameters were optimized. It was found that a low pH (3) and a high iron mass (optimal values were 1/12 and 1/10 of the mass of the microplastics for LDPE and PVC, respectively) favored all three. The degradation of LDPE by the photo-Fenton treatment was favored by high H₂O₂ concentrations (25 times higher than the mass of iron), while these concentrations were significantly lower for PVC (11 and 15 times for the Fenton and photo-Fenton treatment, respectively), suggesting that scavenging activity occurs.

The unique properties of nanostructures, such as their high surface-to-volume ratio, tunable physical and chemical characteristics, and enhanced sensitivity, are critical for advancing gas detection technologies. Therefore, this comprehensive review explores the recent advancements in nanostructured materials, emphasizing their pivotal role in enhancing gas sensing performance. A key focus of this review is metal oxide-based gas sensors, and the impact of synthesis methods and (micro)structural properties on sensor performance is thoroughly examined. By segmenting the discussion into 1D nanostructured materials, including different metal oxides, the review provides a broad yet detailed perspective on how different functional materials contribute to gas sensing efficiency. From a performance standpoint, this review highlights critical sensing parameters, including gas detection mechanisms, response times, selectivity, stability, and operating conditions. High-end detection values may reach around a few ppb for most gases. Beyond evaluating current advancements, this review also addresses existing challenges and future research directions, particularly in scalability, long-term sensor stability, low-temperature operation, and integration into real-world applications. By providing a comprehensive and up-to-date analysis, this review serves as a valuable resource for researchers and engineers, offering insights that can drive the next generation of high-performance, reliable, and selective gas sensors.

In this research, an emerging, non-metallic photocatalyst was prepared by the thermal polymerization method from three different precursors: urea, melamine, and three mixtures of melamine and cyanuric acid. Graphitic carbon nitride (g-C₃N₄) samples from urea and melamine were synthesized in a muffle furnace at three different temperatures: 450°, 500°, and 550 °C for 2 h, while the samples made of a mixture of melamine and cyanuric acid (with mass ratios of 1:1, 1:2, and 2:1) were synthesized at 550 °C for 2 h. All the samples were characterized in order to determine their chemical and physical properties, such as crystallite size and structure, and phase composition by the following techniques: Fourier transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), and scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDS). Nitrogen adsorption/desorption isotherms were used to investigate the Brunauer, Emmett, and Teller (BET) specific surface area and Barrett–Joyner–Halenda (BJH) pore size distribution. Band gap values were determined by diffuse reflectance spectroscopy (DRS). Furthermore, adsorption and photocatalytic degradation of the local anesthetic drug procaine were monitored under UV-A, visible, and simulated solar irradiation in a batch reactor. Kinetic parameters, as well as photocatalytic mechanisms using scavengers, were determined and analyzed. The results of the photocatalysis experiments were compared to the benchmark TiO₂ Evonik Aeroxide P25. The results indicated that the g-C₃N₄ sample synthesized from urea at 500 °C for 2 h exhibited the highest degradation rate of procaine under visible light.

Necessary advancements in the area of organic photovoltaic (OPV) devices include the upgrade of power conversion efficiencies (PCE) and stability. One answer to these demands lies in the research into new absorbers. Here, we focus on the development of new small molecule absorbers from the group of squaraines (SQs). These modular absorbers can be applied as donors in organic solar cells and have the ability to utilize a broad range of solar radiation if blended with suitable acceptors. In order to allow for the compatibility and favorable organization of donor and acceptor in the absorber layer, we intend to optimize the structure of the SQ by varying the groups attached to the squaric acid core. For that purpose, we accordingly developed a well-suited synthesis route. The novel alkyl- and benzyl-substituted aryl aminosquaraines were synthesized through an improved and eco-friendly procedure. Special emphasis was placed on optimizing the amination reaction to obtain initial precursors in the synthesis of squaraine, avoiding hitherto common catalytic processes. All SQ precursors and SQ products were completely described. The derived SQs were additionally characterized in thin-film configuration using cyclic voltammetry and UV-VIS spectroscopy and then processed to prepare self-standing bulk heterojunction (BHJ) thin films in conjunction with fullerene-based electron acceptors, which were characterized via profilometry. The comparison between SQ and BHJ solutions and thin films, using atomic force microscopy and UV-VIS spectroscopy, revealed differences in susceptibility for the organization and orientation of the constituting domains.

Bio-aerogels have emerged as promising materials for energy storage, providing a sustainable alternative to conventional aerogels. This review addresses their syntheses, properties, and characterization challenges for use in energy storage devices such as rechargeable batteries, supercapacitors, and fuel cells. Derived from renewable sources (such as cellulose, lignin, and chitosan), bio-based aerogels exhibit mesoporosity, high specific surface area, biocompatibility, and biodegradability, making them advantageous for environmental sustainability. Bio-based aerogels serve as electrodes and separators in energy storage systems, offering desirable properties such as high specific surface area, porosity, and good electrical conductivity, enhancing the energy density, power density, and cycle life of devices. Recent advancements highlight their potential as anode materials for lithium-ion batteries, replacing non-renewable carbon materials. Studies have shown excellent cycling stability and rate performance for bio-aerogels in supercapacitors and fuel cells. The yield properties of these materials, primarily porosity and transport phenomena, demand advanced characterization methods, and their synthesis and processing methods significantly influence their production, e.g., sol–gel and advanced drying. Bio-aerogels represent a sustainable solution for advancing energy storage technologies, despite challenges such as scalability, standardization, and cost-effectiveness. Future research aims to improve synthesis methods and explore novel applications. Bio-aerogels, in general, provide a healthier path to technological progress.

Currently used organic coatings for the protection of bronze sculptures have a relatively short lifespan as a consequence of strict requirements of conservation ethics, which limit the selection of coatings. For that reason, enhancement of the corrosion protection level and durability of appropriate coatings is needed. The aim of this work was to examine if corrosion protection of bronze by selected acrylic and polyurethane coatings could be improved by using two phosphonic acids, 16-phosphonohexadecanoic acid (COOH-PA) and 12-aminododecylphosphonic acid (NH₂-PA). Electrochemical measurements (linear polarization and electrochemical impedance spectroscopy, EIS) were performed to gain an insight into the influence of these phosphonic acids on the performance of the coatings during a two-week exposure to artificial acid rain and a three-month outdoor exposure. Besides the influence on the corrosion protection level, the influence on the coating adhesion was examined as well. A pull-off test clearly confirmed that the studied phosphonic acids act as adhesion promoters of both polyurethane and acrylic coatings, while electrochemical studies revealed improvements in corrosion protection levels, especially in the case of the acrylic coating Paraloid B72.