Functional UV Blocking and Superhydrophobic Coatings Based on Functionalized CeO2 and Al2O3 Nanoparticles in a Polyurethane Nanocomposite.

Water repellency has significant potential in applications like self-cleaning coatings, anti-staining textiles, and electronics. This study introduces a novel nanocomposite system incorporating functionalized Al2O3 and CeO2 nanoparticles within a polyurethane matrix to achieve hydrophobic and UV-blocking properties. The nanoparticles were functionalized using an octadecyl phosphonic acid solution and characterized by FTIR and XPS, confirming non-covalent functionalization. Spin-coated polyurethane coatings with functionalized and non-functionalized Al2O3, CeO2, and binary Al2O3-CeO2 nanoparticles were analyzed. The three-layered Al2O3-CeO2-ODPA binary system achieved a contact angle of 166.4° and 85% transmittance in the visible range. Incorporating this binary functionalized system into a 0.4% w/v polyurethane solution resulted in a nanocomposite with 75% visible transmittance, 60% at 365 nm UV, and a 147.7° contact angle after three layers. These findings suggest that ODPA-functionalized nanoparticles, when combined with a polymer matrix, offer a promising approach to developing advanced hydrophobic and UV-protective coatings with potential applications across various industrial sectors.

Influence of silica nanocoating on stain susceptibility and superficial integrity of dimethacrylate-based composites.

The aim of this study was to investigate the ability of a novel silica (SiO2 )-based nanocoating approach to extend the superficial integrity of current composites. Cylindrical discs (7 × 2 mm) were produced from nanohybrid and nanofilled composites. Specimens in control groups were not coated, but SiO2 nanocoating was performed on specimens in experimental groups (n = 8). Specimens were stored for 24 h in distilled water at 37°C (baseline) and then artificially aged for 15, 90, or 180 d in a low-pH staining solution. Surface roughness (Ra) was measured using a profilometer, and a goniometer was used to determine surface free energy (SFE). Color change was evaluated by a reflectance spectrophotometer, applying the color distance metric, ΔE00 , according to the Commission Internationale de l'Eclairage (CIE) L*a*b* coordinates. Data were subjected to repeated-measures anova and the Tukey post-hoc test. Composites presented visually perceptible color changes (ΔE00  > 0.81) as early as 15 d of aging, with significantly higher ΔE00 values recorded over time. Nanocoating with SiO2 significantly reduced the SFE of composites at all storage times, and significantly lower Ra values were identified after aging. Nanohybrid and nanofilled composites were susceptible to substantial hydrolytic superficial degradation and staining, which was dramatically attenuated by the proposed SiO2 nanocoating approach. Nanocoating effectively lowered the SFE of composites, thus minimizing water-composite interactions, which contributed to reduced superficial deterioration and lower stain susceptibility over time.

Effect of an additional hydrophilic versus hydrophobic coat on the quality of dentinal sealing provided by two-step etchand-rinse adhesives

OBJECTIVE: To test the hypothesis that the quality of the dentinal sealing provided by two-step etch-and-rinse adhesives cannot be altered by the addition of an extra layer of the respective adhesive or the application of a more hydrophobic, non-solvated resin. MATERIAL AND METHODS: full-crown preparations were acid-etched with phosphoric acid for 15 s and bonded with Adper Single Bond (3M ESPE), Excite DSC (Ivoclar/Vivadent) or Prime & Bond NT (Dentsply). The adhesives were used according to the manufacturers' instructions (control groups) or after application to dentin they were a) covered with an extra coat of each respective system or b) coated with a non-solvated bonding agent (Adper Scotchbond Multi-Purpose Adhesive, 3M ESPE). Fluid flow rate was measured before and after dentin surfaces were acid-etched and bonded with adhesives. RESULTS: None of the adhesives or experimental treatments was capable to block completely the fluid transudation across the treated dentin. Application of an extra coat of the adhesive did not reduce the fluid flow rate of adhesive-bonded dentin (p>0.05). Conversely, the application of a more hydrophobic non-solvated resin resulted in significant reductions in the fluid flow rate (p<0.05) for all tested adhesives. CONCLUSIONS: The quality of the dentinal sealing provided by etch-and-rinse adhesives can be significantly improved by the application of a more hydrophobic, non-solvated bonding agent.