Nanocomposites with polymer matrix offer excellent opportunities to explore new functionalities beyond those of conventional materials. TiO₂, as a reinforcement agent in polymeric nanocomposites, is a viable strategy that significantly enhanced their mechanical properties. The size of the filler plays an essential role in determining the mechanical properties of the nanocomposite. A defining feature of polymer nanocomposites is that the small size of the fillers leads to an increase in the interfacial area compared to traditional composites. The interfacial area generates a significant volume fraction of interfacial polymer, with properties different from the bulk polymer even at low loadings of the nanofiller. This review aims to provide specific guidelines on the correlations between the structures of TiO₂ nanocomposites with polymeric matrix and their mechanical properties. The correlations will be established and explained based on interfaces realized between the polymer matrix and inorganic filler. The paper focuses on the influence of the composition parameters (type of polymeric matrix, TiO₂ filler with surface modified/unmodified, additives) and technological parameters (processing methods, temperature, time, pressure) on the mechanical strength of TiO₂ nanocomposites with the polymeric matrix.

The presence of toxic, non-biodegradable and harmful organic pollutants in soils, wastewater, and atmosphere has become an indisputable, and global fact as a significant environmental problem. The heterogeneous photocatalysis, an advanced oxidation process (AOP) using semiconductor materials as catalysts, is a topic of great interest considering the possibility of the pollutants removal from water. The photocatalytic degradation of organic contaminants (i.e., dyes, pesticides, phenolic compounds) present in water using semiconductor materials depends on a number of parameters such as: the bandgap energy, phase composition, crystallinity, morphology and surface area of catalyst, electron-hole recombination rate, intensity of light, and adsorption capacity of the dye on the photocatalyst surface. One of the important constraints related to the catalyst photocatalytic efficiency is the fast recombination of the photogenerated electrons and holes. Therefore, various strategies have been involved in promoting the charge separation, including the development of heterojunction between two semiconductor materials, by tailoring the photocatalysts properties. This mini-review deals with the recent developments on dyes photodegradation using as catalysts various heterojunctions based on copper sulfide nanostructures, such as copper sulfide/metal oxide, copper sulfide/metal sulfide, copper sulfide/graphene, copper sulfide/organic semiconductors etc. The effects of different parameters, such as synthesis parameters, particle size, bandgap energy, surface area, and morphology on the photocatalytic activity of copper sulfide heterojunctions for dyes degradation is also highlighted.

The direct or indirect discharge of toxic and non-biodegradable organic pollutants into water represents a huge threat that affects human health and the environment. Therefore, the treatment of wastewater, using sustainable technologies, is absolutely necessary for reusability. Photocatalysis is considered one of the most innovative advanced techniques used for pollutant removal from wastewater, due to its high efficiency, ease of process, low-cost, and the environmentally friendly secondary compounds that occur. The key of photocatalysis technology is the careful selection of catalysts, usually semiconductor materials with high absorption capacity for solar light, and conductivity for photogenerated charge carriers. Among copper sulfides, CuS (covellite), a semiconductor with different morphologies and bandgap values, is recognized as an important photocatalyst used for the removal of organic pollutants (dyes, pesticides, pharmaceutics etc.) from wastewater. This review deals with recent developments in organic pollutant photodegradation, using as catalysts various CuS nanostructures, consisting of CuS NPs, CuS QDs, and heterojunctions (CuS/ carbon-based materials, CuS/organic semiconductor, CuS/metal oxide). The effects of different synthesis parameters (Cu:S molar ratios, surfactant concentration etc.) and properties (particle size, morphology, bandgap energy, and surface properties) on the photocatalytic performance of CuS-based catalysts for the degradation of various organic pollutants are extensively discussed.

The development of new technologies using nanomaterials has allowed scientists to design advanced processes with many applications in environmental protection, energy production and storage, and medicinal bio-mediated processes. Due to their significant potential applications in different branches of science, the development of new polymer composites represents a priority, especially for nano-technological processes. Interest in polymeric composites was outlined by the synthesis of a large number of nano- or mezzo-scale materials with targeted functional properties for polymer matrix hybridization. The present mini review explores some of the most representative and recent papers reporting the photocatalytic activity of polymer composites toward different organic compounds (dyes, pharmaceutically active molecules, phenol, etc.). The polymer composites were divided based on their composition and photocatalytic activity. TiO₂- and ZnO-based polymeric composites have been described here in light of their photocatalytic activity toward different pollutants, such as rhodamine B, phenol, or methyl orange. Polymeric composites based on WO₃, Fe₂O₃, or Bi₂MoO₆ were also described. The influence of different polymeric composites and photocatalytic parameters (light spectra and intensity, pollutant molecule and concentration, irradiation time, and photocatalyst dosage) on the overall photocatalytic efficiency indicates that semiconductor (TiO₂, ZnO, etc.) insertion in the polymeric matrix can tune the photocatalytic activity without compromising the structural integrity. Future perspectives and limitations are outlined considering the systematic and targeted description of the reported results. Adopting green route synthesis and application can add economic and scientific value to the knowledgebase by promoting technological development based on photocatalytic designs.

The functionalization of polyethylene terephthalate (PET) from tire rubber–PET–high density polyethylene (HDPE) composites represents a key strategy for improving the composite properties. This is a practical and effective method to improve the interface between matrix (waste tire rubber) and fillers (waste PET and HDPE). By PET functionalization, adherence and surface properties of composite materials can be controlled. PET functionalization was performed with polyethylene glycol (PEG 400, 1%) and sodium dodecyl sulphate (SDS 1%). The characterization of the components and composite are discussed in terms of surface energy values (evaluated from water contact angle measurements) and surface morphology by using scanning electron microscopy (SEM). The structural and conformational changes were investigated by Fourier Transform Infrared (FTIR) Spectroscopy while the crystalline structure was studied by X-ray diffraction (XRD). The improved interfacial adhesion, thermal stability and mechanical properties (stress–strain, compression and impact resistance) of the composites are correlated with the PET functionalization, with non-ionic (PEG) and an anionic surfactant (SDS). The results proved that the interface properties are improved by functionalization of PET. The best mechanical properties were recorded at 30min moulding. The samples with 45% PET–SDS showed the best combination of mechanical properties: tensile strength (1.56N/mm2), impact strength (43.72kJ/m2) and compression (158.78N/mm2)