Hydrothermal microwave method was used as a new route to synthesize pure BaTiO3 (BT) nanoparticles at 140°C for 10 min under rapid reacting with stoichiometric Ba/Ti ratio. The crystalline products were characterized by X-ray powder diffraction (XRD) and the structure was refined by the Rietveld method from the tetragonal structure, which was supported by the Ti K-edge X-ray absorption near-edge structure (XANES). The pre-edge of Ti in the XANES spectra indicated that titanium ions are localized in a nonregular octahedron. Typical FT-Raman spectra for tetragonal BaTiO3 nanoparticles presented well-defined peaks, indicating a substantial short-range order in the system. However, a scattering peak at 810 cm−1 was attributed to the presence of lattice OH− groups, commonly found in materials obtained by hydrothermal process. Besides, the peak at 716 cm−1 can be related to eventual Ba2+ defects in the BaTiO3 lattice. BaTiO3 (BT) nanoparticles presented spherical morphology with a non-uniform distribution of particle sizes. An intense and broad photoluminescence band was observed around the green color emission at room temperature. By means of an excitation energy of 2.54 eV (488 nm), it was noted that the maximum profile emission (2.2 eV) is smaller than the forbidden band gap energy of BaTiO3, indicating that certain localized levels within the band gap must exist.

The emission of wide band photoluminescence showed a synergic effect on barium zirconate and barium titanate thin films in alternate multilayer system at room temperature by 488 nm exiting wavelength. The thin films obtained by spin-coating were annealed at 350, 450, and 550 degrees C for 2 h. The X-ray patterns revealed the complete separation among the BaTiO3 and BaZrO3 phases in the adjacent films. Visible and intense photoluminescence was governed by BaZrO3 thin films in the multilayer system. Quantum mechanics calculations were used in order to simulate ordered and disordered thin films structures. The disordered models, which were built by using the displacement of formers and modifier networks, showed a different symmetry in each system, which is in accordance with experimental photoluminescence emission, thus allowing to establish a correlation among the structural and optical properties of these multilayered systems.

The transesterification reaction used to produce biodiesel was monitored with 1H high-resolution nuclear magnetic resonance (HRNMR), conventional low-resolution NMR (LRNMR), and unilateral NMR (UNMR) spectroscopy. HRNMR was used as a standard method to compare with the methods of LRNMR and UNMR. A Carr–Purcell–Meiboom–Gill (CPMG) pulse sequence was used in both LRNMR and UNMR experiments. In LRNMR, the CPMG signal was used to measure the transverse relaxation time (T 2), which depended on sample viscosity; it showed a good correlation (R = 0.994) for the concentration of biodiesel in the oil/biodiesel mixture. These measurements could only be used when the samples contained less than 1% of methanol. In UNMR, the CPMG decay of the biodiesel/oil mixture strongly depended on molecular diffusion because of the intrinsic high magnet field gradient (G) associated with the magnetic. The T 2eff had a good and negative correlation (R = −0.997) with the biodiesel concentration in the biodiesel/oil mixture. The UNMR measurements were insensitive to the methanol contamination up to 50%, which was contrary to the LRNMR method. As methanol diffused rapidly, its magnetization lost coherency quickly in the presence of strong G and it was not fully refocused by the CPMG sequence. Therefore, the use of the fast, portable, and low cost UNMR sensor to monitor transesterification reactions was demonstrated ex situ. Now, the UNMR sensor has been adapted to monitor the transesterification reaction in situ, in a biodiesel pilot plant.

Electrical conductive textured LaNiO 3 / SrTiO 3 ͑100͒ thin films were successfully produced by the polymeric precursor method. A comparison between features of these films of LaNiO 3 ͑LNO͒ when heat treated in a conventional furnace ͑CF͒ and in a domestic microwave ͑MW͒ oven is presented. The x-ray diffraction data indicated good crystallinity and a structural orientation along the ͑h00͒ direction for both films. The surface images obtained by atomic force microscopy revealed similar roughness values, whereas films LNO-MW present slightly smaller average grain size ͑ϳ80 nm͒ than those observed for LNO-CF ͑60-150 nm͒. These grain size values were in good agreement with those evaluated from the x-ray data. The transport properties have been studied by temperature dependence of the electrical resistivity ͑T͒ which revealed for both films a metallic behavior in the entire temperature range studied. The behavior of ͑T͒ was investigated, allowing to a discussion of the transport mechanisms in these films.

The experimental use of poly (alcohol-vinyl) (PVA) as a skin curative is increasing widely. However, the use of this hydrogel is challenging due to its favorable properties for microbiota growth. The association with silver nanoparticles (AgNPs) as an antimicrobial agent turns the match for PVA as a dressing, as it focuses on creating a physical barrier to avoid wound dehydration. When associated with extracellular components, such as the collagen matrix, the device obtained can create the desired biological conditions to act as a skin substitute. This study aimed to analyze the anti-microbiological activity and the in vitro and in vivo responses of a bilaminar device of PVA containing AgNPs associated with a membrane of collagen–hyaluronic acid (col-HA). Additionally, mesenchymal stem cells were cultured in the device to evaluate in vitro responses and in vivo immunomodulatory and healing behavior. The device morphology revealed a porous pattern that favored water retention and in vitro cell adhesion. Controlled wounds in the dorsal back of rat skins revealed a striking skin remodeling with new epidermis fulfilling all previously injured areas after 14 and 28 days. No infections or significant inflammations were observed, despite increased angiogenesis, and no fibrosis-markers were identified as compared to controls. Although few antibacterial activities were obtained, the addition of AgNPs prevented fungal growth. All results demonstrated that the combination of the components used here as a dermal device, chosen according to previous miscellany studies of low/mid-cost biomaterials, can promote skin protection avoiding infections and dehydration, minimize the typical wound inflammatory responses, and favor the cellular healing responses, features that give rise to further clinical trials of the device here developed