The novelty of this study consists in the formulation and characterization of three experimental dental composites (PM, P14M, P2S) for cervical dental lesion restoration compared to the commercial composites Enamel plus HRi® - En (Micerium S.p.A, Avengo, Ge, Italy), G-ænial Anterior® - Ge, (GC Europe N.V., Leuven, Belgium), Charisma® - Ch (Heraeus Kulzer, Berkshire, UK). The physio-chemical properties were studied, like the degree of conversion and the residual monomers in cured samples using FTIR-ATR (attenuated total reflectance) and HPLC-UV (ultraviolet detection), as well as the evaluation of the mechanical properties of the materials. The null hypothesis was that there would be no differences between experimental and commercial resin composites regarding the evaluated parameters. Statistical analysis revealed that water and saliva storage induced significant modifications of all mechanical parameters after three months for all tested materials, except for a few comparisons for each type of material. Storage medium seemed not to alter the values of mechanical parameters in comparison with the initial ones for: diametral tensile strength (DTS-saliva for Ge and PM, compressive strength (CS)-water for Ch, DTS-water and Young’s modulus YM-saliva for P14M and YM-water/ saliva for P2S (p > 0.05). Two of the experimental materials showed less than 1% residual monomers, which sustains good polymerization efficiency. Experimental resin composites have good mechanical properties, which makes them recommendable for the successful use in load-bearing surfaces of posterior teeth.

The clinical performances of dental materials depend on their mechanical profiles, determining their long-term deformation and wear resistance. This paper describes a study on the mechanical properties, water absorption and morphological properties of a polymethyl methacrylate (PMMA) resin enriched with graphene-silver nanoparticles (Gr-Ag). Two different concentrations—1 and 2 wt.%—of Gr-Ag were loaded into the PMMA material. For the mechanical characterization, the compression behavior, flexural strength and tensile strength were evaluated. Optical microscopy in polarized light and scanning electron microscopy were used for filler analysis. The filler addition led to an improvement in all mechanical properties, with slight changes being derived from the filler content variation. Gr-Ag use led to an increase in the applied maximum loads. Moreover, 1 wt.% Gr-Ag determined an increase of 174% in the modulus of rupture, which indicates high flexibility.

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Graphene/TiO 2 -Ag based composites having various quantities of TiO 2 -Ag nanoparticles (5, 10 or 15 wt%) were successfully prepared through a facile chemical-thermal route. The morphological and structural characteristics of the synthesized materials denoted GTA-5, GTA-10 and GTA-15 were investigated by TEM, XRD and FTIR techniques. The composites were used for the modification of three gold electrodes (Au/GTA-5, Au/GTA-10, Au/GTA-15) which were next employed in the electrochemical detection and degradation of amaranth (an azo dye model). The electrode with the best performance in terms of sensitivity was the Au/GTA-10 electrode. It had considerably larger sensitivity (24 mA/M), in comparison with that of Au/GTA-5 and Au/GTA-15 electrode (8 mA/M and 12 mA/M, respectively). The limit of detection was the same for all modified electrodes (LOD = 1 × 10 −7 M; S/N = 3). The Au/GTA-10 electrode was also tested at the electrochemical degradation of amaranth, from aqueous solutions. The degradation reaction followed a first order kinetics with a half-time of degradation of 203 minutes. The response characteristics of the proposed sensor made it a good candidate for integration in the Ubiquitous sensor's network for IOT.

Various powders of graphene oxide (GO), GO with silver (GO-Ag) and zinc oxide (GO-ZnO) were obtained. The powders were silanized with (3-aminopropyl) triethoxysilane (APTES) aiming to be used, in a future stage, as additives in the hydraulic lime mortars composition. The powders were characterized by Fourier Transform Infrared Spectrometry (FTIR) and Scanning Electron Microscopy (SEM) before and after the silanization process. GO, GO-Ag, GO-Ag-APTES, GO-ZnO and GO-ZnO-APTES powders were also investigated by Thermogravimetric Analysis (TG/DTA) and Ultraviolet–Visible Spectroscopy (UV-Vis). Likewise, the antibacterial effect of powders against five bacterial strains was evaluated. The peaks associated to the functional groups from GO, GO-APTES, GO-Ag, GO-Ag-APTES, GO-ZnO and GO-ZnO-APTES powders were identified by FTIR analysis. The mass losses of powders, analyzed by TG/DTA were lower than those recorded for GO. By UV-VIS analysis, maxima corresponding to the electronic π-π * and n-π * transitions were recorded. SEM images highlighted the lamellar and layered structure of GO, but also the presence of Ag and Zn nanoparticles on the surface of graphene sheets. All these results confirm the presence of Ag/ZnO/APTES on the GO. The antibacterial effect evaluated by recording the diameter of the inhibition zone ranged between 12–22 mm.

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