Cellulose nanofibers were obtained from microcrystalline cellulose (MCC) by the action of hydrodynamic forces associated with ultrasound. Nanofibers isolated from MCC by applying different ultrasonication conditions were characterized to elucidate their morpho-structural features by field emission scanning electron microscopy, atomic force microscopy, X-ray diffraction, and dynamic light scattering. Several differences were observed regarding the size of the nanofibers obtained in different ultrasonic conditions, but no significant changes in the crystalline structure of cellulose nanofibers were detected. The obtained cellulose fibers were used at low levels (1 to 5 wt.%) as reinforcements in a poly(vinyl alcohol) (PVA) matrix. The mechanical and thermal properties of the PVA/cellulose fibers nanocomposites films were determined. The tensile strength and modulus of the PVA film were significantly improved by the addition of cellulose nanofibers. Slightly higher onset degradation temperatures were obtained for PVA composites in comparison to neat PVA, showing an increase of the thermal stability caused by the addition of cellulose fibers.

Hybrid nanomaterials based on zinc oxide were synthesized via the sol–gel method, using different silane coupling agents: (3-glycidyloxypropyl)trimethoxysilane (GPTMS), phenyltriethoxysilane (PhTES), octyltriethoxysilane (OTES), and octadecyltriethoxysilane (ODTES). Morphological properties and the silane precursor type effect on the particle size were investigated using dynamic light scattering (DLS), environmental scanning electron microscopy (ESEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), and X-ray diffraction (XRD). The bonding characteristics of modified ZnO materials were investigated using Fourier transform infrared spectroscopy (FTIR). The final solutions were deposited on metallic substrate (aluminum) in order to realize coatings with various wettability and roughness. The morphological studies, obtained by ESEM and TEM analysis, showed that the sizes of the ZnO nanoparticles are changed as function of silane precursor used in synthesis. The thermal stability of modified ZnO materials showed that the degradation of the alkyl groups takes place in the 300–500 °C range. Water wettability study revealed a contact angle of 142 ± 5° for the surface covered with ZnO material modified with ODTES and showed that the water contact angle increases as the alkyl chain from the silica precursor increases. These modified ZnO materials, therefore, can be easily incorporated in coatings for various applications such as anti-corrosion and anti-icing.

Epoxy resins were reinforced with different ZnO nanofillers (commercial ZnO nanoparticles (ZnO NPs), recycled ZnO and functionalized ZnO NPs) in order to obtain ZnO–epoxy composites with suitable mechanical properties, high adhesion strength, and good resistance to corrosion. The final properties of ZnO–epoxy composites depend on several factors, such as the type and contents of nanofillers, the epoxy resin type, curing agent, and preparation methods. This paper aims to review the preparation methods, mechanical and anti-corrosion performance, and applications of ZnO–epoxy composites. The epoxy–ZnO composites are demonstrated to be valuable materials for a wide range of applications, including the development of anti-corrosion and UV-protective coatings, for adhesives and the chemical industry, or for use in building materials or electronics.

In this research work, silica nanoparticles and silica-gentamicin nanostructured solution were synthesized by using the microwave-assisted synthesis, in basic medium, using two silane precursors (tetraethylorthosilicate and octyltriethoxysilane) and the antibiotic (gentamicin sulfate). The prepared materials were characterized through Fourier transform infrared (FTIR) spectroscopy, TGA analysis, transmission electron microscopy (TEM), and atomic force microscopy (AFM) to investigate the morphology and structure. Antimicrobial studies of the silica-gentamicin nanostructured solution versus silica nanoparticles were performed against Pseudomonas aeruginosa, Staphylococcus aureus, and Escherichia coli. FTIR spectra showed that the gentamicin has been loaded to the silica nanoparticles. AFM analysis showed that the morphology of the silica-gentamicin nanostructured solution has changed, and agglomerations of particles are present at the surface. Antimicrobial testing, performed using the diffusion method through spot inoculation, indicates that the silica-gentamicin nanostructured solution exhibited activity against the resistant strain. The obtained silica-gentamicin solution can be used as biochemical agent for the prevention and treatment of microorganisms which are deposited on different surfaces (e.g., glass, plastic, ceramic).

Ultra-hydrophobic bilayer coatings on a glass surface were fabricated by sol–gel process using hexadecyltrimethoxysilane (C₁₆TMS) and tetramethoxysilane (TMOS) (1:4 molar ratio) as precursors. After coating, silica nanoparticles (SiO₂ NPs) functionalized with different mono-alkoxy derivatives (methoxytrimethylsilane, TMeMS; ethoxydimethylvinylsilane, DMeVES; ethoxydimethylphenylsilane, DMePhES; and methoxydimethyloctylsilane, DMeC₈MS) were added, assuring the microscale roughness on the glass surface. Influences of the functionalized SiO₂ NPs and surface morphology on the hydrophobicity of the hybrid films were discussed. The successful functionalization of SiO₂ NPs with hydrophobic alkyl groups were confirmed by Fourier transform infrared spectroscopy (FTIR). The thermal stability of hydrophobic SiO₂ NPs showed that the degradation of the alkyl groups takes place in the 200–400 °C range. Bilayer coating with C₁₆TMS/TMOS and SiO₂ NPs modified with alkoxysilane substituted with C₈ alkyl chain (SiO₂ NP-C₈) has micro/nano structure. Hydrophobicity of functionalized SiO₂ NPs-C₈ and its higher degree of nanometer-scale roughness gave rise to ultra-hydrophobicity performance for bilayer coating C₁₆TMS/TMOS + SiO₂ NPs-C₈ (145°), compared to other similar hybrid structures. Our synthesis method for the functionalization of SiO₂ NPs is useful for the modification of surface polarity and roughness.