The present study aimed to prepare experimental adhesives (EAs): 5 wt.% titanium dioxide (TiO2) adhesive; and 5 wt.% zirconium oxide (ZrO2) adhesive; and analyze their impact on bond integrity of fiber posts to root dentin, and viscosity. The EA was composed of: bisphenol A glycol dimethacrylate (BisGMA); triethylene glycol dimethacrylate (TEGDMA); 2-hydroxyethyl methacrylate (HEMA); and ethyl 4-dimethylamino benzoate and camphorquinone. TiO2 and ZrO2 particles were individually incorporated into the EA at 5 wt.%, to form two groups (5% TiO2 and 5% ZrO2). The adhesives, with particles, were characterized using scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) spectroscopy. The bonded interface was evaluated for adhesive–dentin penetration at the interface, using SEM. The study adhesive groups (EA, 5% TiO2 and 5% ZrO2) were analyzed for rheology and push-out bond strength of the fiber post to root dentin. Data were analyzed using analysis of variance and post hoc comparison. Both TiO2 and ZrO2 particles had irregular, non-uniform shapes. The EDX mapping showed the elemental presence of Ti (TiO2), Zr (ZrO2) and oxygen in formulated adhesives. The 5% TiO2 and 5% ZrO2 adhesives showed a decrease in viscosity, compared with the EA. Bond strength among the 5% TiO2 and 5% ZrO2 adhesives was statistically comparable (p > 0.05), but higher than the control group (10.57 ± 1.45 MPa) (p < 0.05). Reinforcement of the experimental dentin adhesive with 5% TiO2 or 5% ZrO2 increased the push-out bond strength of the fiber post to root dentin, in comparison with the EA. Particle-incorporated adhesives (5% TiO2 and 5% ZrO2) displayed decreased viscosity, compared with the EA (without particles).
Nanocomposites of silica gel (SG) and multiwalled carbon nanotubes (MWCNTs) of relatively low concentrations (0.25, 0.50, and 0.75 wt%) were characterized before and after annealing. Adsorption is a surface phenomenon, and based on this, the morphology of the composites was investigated by scanning electron microscopy (SEM). The produced images show that the MWCNTs were embedded into the silica gel base material. Fourier transform infrared (FTIR) transmittance spectroscopy showed that MWCNTs were not functionalized within the matrix of silica gel and MWCNT composites. However, after annealing the composites at 400 °C for 4 h in air, evidence of activation was observed in the FTIR spectrum. The effects of the embedding of MWCNTs on porosity, specific surface area, and pore size distribution were studied using Raman spectroscopy. The Raman spectra of the prepared composites were mainly dominated by characteristic sharp scattering peaks of the silica gel at 480, 780, and 990 cm−1 and a broad band centered at 2100 cm−1. The scattering peaks of MWCNTs were not well pronounced, as the homogeneity of the composite is always questionable. Nanosizer analysis showed that at 0.25 wt%, the distribution of MWCNTs within the silica gel was optimal. Vickers hardness measurements showed that the hardness increased with the increasing weight percent of MWCNTs within the composite matrix, while annealing enhanced the mechanical properties of the composites. Further studies are required to investigate the pore structure of silica gel within the matrix of MWCNTs to be deployed for efficient cooling and water purification applications.
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