The combined effects of nano titanium dioxide (TiO₂-N) and clove oil (CO) on the physico-chemical, biological and structural properties of chitosan (CH)/starch (ST) films were investigated by using a solvent casting method. Results indicated that the incorporation of TiO₂-N could improve the compactness of the film, increase the tensile strength (TS) and antioxidant activity, and decrease the water vapour permeability (WVP). As may be expected, the incorporation of CO into the film matrix decreased TS but increased the hydrophobicity as well as water vapour barrier antimicrobial and antioxidant properties. Fourier-transform infrared spectroscopy (FTIR) data supported intermolecular interactions between TiO₂-N, CO and the film matrix. Use of a scanning electron microscope (SEM) showed that TiO₂-N and CO were well dispersed and emulsified in the film network. Thermogravimetric (TG) and derivative thermogravimetric (DTG) curves demonstrated that TiO₂-N and CO were well embedded in the film matrix, hence this blend film system could provide new formulation options for food packaging materials in the future.

Chitosan microspheres modified by 2-pyridinecarboxaldehyde were prepared and used in the construction of a heterogeneous catalyst loaded with nano-Cu prepared by a reduction reaction. The chemical structure of the catalyst was investigated by Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), and X-ray Photoelectron Spectroscopy (XPS). Under mild conditions, such as no ligand at room temperature, the catalyst was successfully applied to catalyze the borylation of α,β-unsaturated receptors in a water-methanol medium, yielding 17%–100% of the corresponding β-hydroxy product. Even after repeated use five times, the catalyst still exhibited excellent catalytic activity.

The first example of an environmentally-benign chitosan supported copper catalyzed conjugate silylation of α,β-unsaturated acceptors was accomplished in water under mild conditions. This protocol provides an efficient pathway to achieve an important class of β-silyl carbonyl compounds and the desired products were obtained in good to excellent yields. Gram-scale synthesis and easy transformation of obtained β-silyl products were also been demonstrated. Remarkably, this chitosan supported copper catalyst can be easily recycled and reused six times without any significant decrease of catalytic activity. The advantages of this newly developed method include operational simplicity, good functional group tolerance, scale-up ability, ready availability, and easy recyclability of catalyst.

Deketoxime–type room–temperature vulcanized silicone rubber cable materials were prepared using α, ω–dihydroxy polydimethylsiloxane, carbon black, calcium carbonate, magnesium hydroxide, piperazine bis (diphenoxy phosphate) salt (PBDP), and melamine diphenoxy phosphate (MDP). The effects of carbon black and flame retardants on the mechanical properties, flame–retardant properties, and electrical insulation properties of silicone cable coatings were investigated. The research results showed that the products obtained had good mechanical and electrical insulation properties, with tensile strength greater than 3.0 MPa, dielectric strength greater than 22 kV/mm, and volume resistivity higher than 6.5 × 10¹⁴ Ω·cm. When 30 parts of Mg(OH)₂:MDP = 2:1 are added to 100 parts of resin, the flame–retardant performance of wire and cable materials can be significantly improved. Under the thermal radiation illumination of 50 kW/m², the ignition time (TTI) of the Mg(OH)₂/MDP coating increased by 16 s, and the maximum heat release rate (pkHRR) and total heat release rate (THR) decreased by 29.7% and 68.8%, respectively, compared with silicone rubber without flame retardant. The silicone rubber coatings prepared were flame retardant up to the FV–1 level.