Composites made from fiber-reinforced polymers (FRPs) are a crucial and highly adaptable category of materials widely utilized in numerous fields. Their flexibility and the range of criteria for classification enable the creation of tailored solutions to address distinct requirements in sectors such as civil engineering, aerospace, automotive, and marine, among others. The distinguishing characteristics of FRP composites include the type of reinforcing fiber used, the composition of the matrix material, the employed manufacturing process, the orientation of the fibers, and the specific end-use application. These classification variables offer engineers a versatile structure to determine and select the most appropriate materials and production techniques for their specific needs. Furthermore, the present study aims to reunite the criteria of classification for FRPs and specific manufacturing technologies of FRPs, such as conventional ones (matched die molding, contact molding), automated ones (filament winding, tape lay-up, and fiber placement), and advanced ones (electrospinning and additive manufacturing),with the chronological development of FRPs, insights on material characteristics, and comprehensive design guidelines based on their behavior in different environments of use.

Synthetic organic pigments like xanthene and azo dyes from the direct discharge of textile effluents are considered colossal global issues and attract the concern of scholars. Photocatalysis continues to be a very valuable pollution control method for industrial wastewater. Incorporations of metal oxide catalysts such as zinc oxide (ZnO) on mesoporous Santa Barbara Armophous-15 (SBA-15) support to improve catalyst thermo-mechanical stability have been comprehensively reported. However, charge separation efficiency and light absorption of ZnO/SBA-15 continue to be limiting its photocatalytic activity. Herein, we report a successful preparation of Ruthenium-induced ZnO/SBA-15 composite via conventional incipient wetness impregnation technique with the aim of boosting the photocatalytic activity of the incorporated ZnO. Physicochemical properties of the SBA-15 support, ZnO/SBA-15, and Ru-ZnO/SBA-15 composites were characterized by X-ray diffraction (XRD), N₂ physisorption isotherms at 77 K, Fourier-transform infrared (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray (EDS), and transmission electron microscopy (TEM). The characterization outcomes exhibited that ZnO and ruthenium species have been successfully embedded into SBA-15 support, andtheSBA-15 support maintains its structured hexagonal mesoscopic ordering in both ZnO/SBA-15 and Ru-ZnO/SBA-15 composites. The photocatalytic activity of the composite was assessed through photo-assisted mineralization of aqueous MB solution, and the process was optimized for initial dye concentration and catalyst dosage. 50 mg catalyst exhibited significant degradation efficiency of 97.96% after 120 min, surpassing the efficiencies of 77% and 81% displayed by 10 and 30 mg of the as-synthesized catalyst. The photodegradation rate was found to decrease with an increase in the initial dye concentration. The superior photocatalytic activity of Ru-ZnO/SBA-15 over the binary ZnO/SBA-15 may be attributed to the slower recombination rate of photogenerated charges on the ZnO surface with the addition of ruthenium.

A sol–gel synthesis technique was employed for the preparation of anatase phase {001}-TiO₂/Au hybrid nanocomposites (NCs). The scalable, schematic, and cost-efficient method was successfully modified using HF and NH₄OH capping agents. The photocatalytic activity of the as-synthesized {001}-TiO₂/Au NCs were tested over 2-cycle degradation of methylene blue (MB) dye and pharmaceutical active compounds (PhACs) of ibuprofen and naproxen under direct sunlight illumination at 35 °C and 44,000 lx. Transmission electron microscopy (TEM), high resolution transmission electron microscopy (HR-TEM), fast Fourier transform (FFT), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDS), and ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis DRS) were employed for the characterization of the as-prepared sample. The characterization results from the TEM, XPS, and XRD studies established both the distribution of Au colloids on the surface of TiO₂ material, and the presence of the highly crystalline structure of anatase {001}-TiO₂/Au NCs. Photodegradation results from the visible light irradiation of MB indicate an enhanced photocatalytic performance of Au/TiO₂ NCs over TiO₂. The results from the photocatalytic activity test performed under direct sunlight exposure exhibited promising photodegradation efficiencies. In the first cycle, the sol–gel synthesized material exhibited relatively better efficiencies (91%) with the MB dye and ibuprofen, while the highest degradation efficiency for the second cycle was 79% for the MB dye. Pseudo first-order photodegradation rates from the first cycle were determined to be comparatively slower than those from the second degradation cycle.

This current study assessed the impacts of morphology adjustment of perovskite BiFeO₃ (BFO) on the construction and photocatalytic activity of P-infused g-C₃N₄/U-BiFeO₃ (U-BFO/PCN) heterostructured composite photocatalysts. Favorable formation of U-BFO/PCN composites was attained via urea-aided morphology-controlled hydrothermal synthesis of BFO followed by solvosonication-mediated fusion with already synthesized P-g-C₃N₄ to form U-BFO/PCN composites. The prepared bare and composite photocatalysts’ morphological, textural, structural, optical, and photocatalytic performance were meticulously examined through various analytical characterization techniques and photodegradation of aqueous rhodamine B (RhB). Ellipsoids and flakes morphological structures were obtained for U-BFO and BFO, and their effects on the successful fabrication of the heterojunctions were also established. The U-BFO/PCN composite exhibits 99.2% efficiency within 20 min of visible-light irradiation, surpassing BFO/PCN (88.5%), PCN (66.8%), and U-BFO (26.1%). The pseudo-first-order kinetics of U-BFO/PCN composites is 2.41 × 10⁻¹ min⁻¹, equivalent to 2.2 times, 57 times, and 4.3 times of BFO/PCN (1.08 × 10⁻¹ min⁻¹), U-BFO, (4.20 × 10⁻³ min⁻¹), and PCN, (5.60 × 10⁻² min⁻¹), respectively. The recyclability test demonstrates an outstanding photostability for U-BFO/PCN after four cyclic runs. This improved photocatalytic activity exhibited by the composites can be attributed to enhanced visible-light utilization and additional accessible active sites due to surface and electronic band modification of CN via P-doping and effective charge separation achieved via successful composites formation.

Purely siliceous MCM-41, MCM-48, SBA-15, and Ni-containing molecular sieves were synthesized by the sol–gel method. The impact of the Ni loaded by incorporation and impregnation in the framework of molecular sieves on the textural and morphological characteristics of the solids was comprehensively investigated. The incorporation method proved to be more effective in terms of textural and morphological properties; therefore, we also investigated the influence of Ni incorporation on the structure of MCM-41 at different loadings (3, 6 and 9 wt.%). Moreover, all solids were characterized by FT-IR, TGA, XRD, SEM-EDS, and N₂ adsorption. The resulting mesoporous materials exhibit a porous structure with well-defined pore sizes of about 2.0–5.0 nm and high specific surface areas (634 m²g⁻¹ for SBA-15, 1592 m²g⁻¹ for MCM-48, and 1769 m²g⁻¹ for MCM-41) alongside uniform pore size distributions. The MCM-41 structure remained unchanged after loading of Ni; however, its surface area and pore diameter decreased due to pore blockage.

Synthetic organic pigments from the direct discharge of textile effluents are considered as colossal global concern and attract the attention of scholars. The efficient construction of heterojunction systems involving precious metal co-catalysis is an effective strategy for obtaining highly efficient photocatalytic materials. Herein, we report the construction of a Pt-doped BiFeO₃/O-g-C₃N₄ (Pt@BFO/O-CN) S-scheme heterojunction system for photocatalytic degradation of aqueous rhodamine B (RhB) under visible-light irradiation. The photocatalytic performances of Pt@BFO/O-CN and BFO/O-CN composites and pristine BiFeO₃ and O-g-C₃N₄ were compared, and the photocatalytic process of the Pt@BFO/O-CN system was optimized. The results exhibit that the S-scheme Pt@BFO/O-CN heterojunction has superior photocatalytic performance compared to its fellow catalysts, which is due to the asymmetric nature of the as-constructed heterojunction. The as-constructed Pt@BFO/O-CN heterojunction reveals high performance in photocatalytic degradation of RhB with a degradation efficiency of 100% achieved after 50 min of visible-light irradiation. The photodegradation fitted well with pseudo-first-order kinetics proceeding with a rate constant of 4.63 × 10⁻² min⁻¹. The radical trapping test reveals that h⁺ and ^•O₂⁻ take the leading role in the reaction, while the stability test reveals a 98% efficiency after the fourth cycle. As established from various interpretations, the considerably enhanced photocatalytic performance of the heterojunction system can be attributed to the promoted charge carrier separation and transfer of photoexcited carriers, as well as the strong photo-redox ability established. Hence, the S-scheme Pt@BFO/O-CN heterojunction is a good candidate in the treatment of industrial wastewater for the mineralization of organic micropollutants, which pose a grievous threat to the environment.