As environmental regulations become stricter, weight- and cost-effective fiber-reinforced polymer composites are being considered as alternative materials in the automobile industry. Rapidly impregnating resin into the reinforcing fibers is critical during liquid composite molding, and the optimization of resin impregnation is related to the cycle time and quality of the products. In this review, various resins capable of rapid impregnation, including thermoset and thermoplastic resins, are discussed for manufacturing fiber-reinforced composites used in the automobile industry, along with their advantages and disadvantages. Finally, vital factors and perspectives for developing rapidly impregnated resin-based fiber-reinforced composites for automobile applications are discussed.

In this study, Y₂O₃/TiO₂-loaded polyester fabric was prepared to improve the catalytic activity of the TiO₂ and to increase its reuse efficiency. The samples were systematically characterized by scanning electron microscopy (SEM), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), and infrared spectroscopy (FT-IR). Furthermore, the degradation performance of methyl orange in the presence of simulated visible light irradiation was also investigated. The results showed that the TiO₂ in the Y₂O₃/TiO₂ composite photocatalyst was suitably anatase. In addition, Y₂O₃/TiO₂-loaded polyester fabric had higher photocatalytic performance than that of pure polyester fabric under visible light and the degradation rate reached 83% after 120 min of light exposure but remained above 50% after repeated exposure (three times). Compared to the pure polyester fabric, Y₂O₃/TiO₂-loaded polyester fabric had self-cleaning effects in methyl blue and soy sauce solutions under visible light.

Graphene oxide (GO) and multiwalled carbon nanotubes with silver particles (MWNT-Ag) of different concentrations were used as nanofillers to prepare poly(lactic acid) (PLA) nanoparticle films through the solvent casting method. In this study, the effects of nanoparticles on the crystallization behavior, relationships between the dispersion and electrical properties, and hydrolytic degradation behaviors were investigated for the PLA/MWNT-Ag and PLA/rGO films. Differential scanning calorimetry was used to evaluate the crystallization behaviors of the PLA/MWNT-Ag and PLA/reduced GO (rGO) films. Electron probe microanalysis was performed to characterize the dispersion of MWNT-Ag, and X-ray diffraction and Raman spectroscopy were used to determine the degree of dispersion of rGO in the PLA matrix. The results showed that nanoparticles enhanced the crystallization kinetics of PLA as well as the hydrolytic degradation rate. From the measurement of electrical properties, the electrical conductivity of PLA/MWNT-Ag 1.0 wt% was much higher than that of the pure PLA and PLA/rGO films, showing that MANT and Ag nanoparticles contribute greatly to enhancing the electrical conductivity of the PLA/MWNT-Ag films.

An eco-friendly approach for improvement of antibacterial properties of polylactic acid (PLA) nonwoven fabrics was obtained by in situ reduction of silver nanoparticles (Ag NPs) on dielectric barrier discharge (DBD) plasma-induced chitosan grafted (DBD-CS-Ag NPs) PLA nonwoven fabrics. The surface morphology, surface element composition and the chemical state of silver of the PLA surfaces after the treatment were evaluated through scanning electron microscopy (SEM), energy dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), respectively. The antibacterial activity of DBD-CS-Ag NPs treated PLA against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) was tested. The uniform dispersion of silver nanoparticles on the DBD-CS-Ag NPs treated PLA surface were confirmed by SEM images. The results of XPS and XRD showed that the concentration of silver element on the surface of PLA nonwoven fabrics was significantly improved after DBD-CS-Ag NPs treatment. The DBD-CS-Ag NPs treated PLA nonwoven fabrics also exhibited excellent antibacterial properties.

Nanoparticle delivery of functional molecules or vaccines is an effective method for the treatment of many diseases. This study aims to design ginsenoside Rh2-conjugated O-carboxymethyl chitosan (O-CMC/Rh2) as a drug delivery system and explore its anti-nociceptive effects. O-CMC/Rh2 was synthesized with an esterification reaction, and its chemical composition and morphology were evaluated using proton nuclear magnetic resonance (¹H NMR), the attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, and scanning electron microscopy (SEM). In addition, the in vitro cumulative release of Rh2 from the O-CMC/Rh2 was also evaluated under different pH conditions. The results showed that the ginsenoside Rh2 was successfully conjugated to the O-CMC matrix and exhibited a highly porous structure after conjugation, facilitating the release of Rh2 from O-CMC. Complete Freund’s adjuvant (CFA) and burn injury-induced pain models were used to evaluate the anti-nociceptive effects of O-CMC/Rh2 on inflammatory pain. O-CMC/Rh2 reduced CFA-induced pain hypersensitivity in a dose-dependent manner and had a longer analgesic effect than Rh2. In addition, O-CMC/Rh2 also relieved the chronic pain induced by bury injury. These results indicated that O-CMC/Rh2 could be useful in reducing inflammatory pain, thus possessing a potential medicinal application in pain therapy.

Heavy metal ion contamination in aquatic systems presents substantial environmental and public health challenges, demanding innovative remediation solutions. This study reports the synthesis of phosphorylated cellulose (PC) monoliths via thermally induced phase separation (TIPS) as a sustainable solution for heavy metal removal. Through systematic optimization of phosphorylation degree (ranging from 16.3% to 49.5%) and pore architecture, we developed materials with exceptional adsorption capacity and flow characteristics. Comprehensive characterization (SEM, FTIR, and elemental analysis) confirmed the successful incorporation of the phosphate group while revealing tunable three-dimensional porous structures controlled by cellulose acetate concentration (80–120 mg mL⁻¹) and phosphorylation parameters. Optimal Cu²⁺ adsorption occurs at 43.9% phosphorylation, coupled with stable permeability, under continuous flow conditions. The monolith effectively removes heavy metal ions (e.g., Cu²⁺, Ni²⁺, Cd²⁺) across a wide pH range, driven by electrostatic and hard-soft acid-base interactions. Additionally, the material maintains an absorption capacity of over 90% after multiple regeneration cycles. These findings highlight the potential of PC monoliths as cost-effective, scalable, and environmentally friendly adsorbents for heavy metal ion removal in water treatment applications.