Thin carbon films containing both amorphous and crystalline structures were produced by RF magnetron sputtering. The depositions of the carbon films were performed on Co buffer layers previously deposited on c-plane (0001) sapphire substrates. The thin carbon films were characterized by high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Raman spectroscopy, energy dispersive X-ray spectroscopy (EDS), and field emission scanning electron microscope (FEG-SEM). The Raman spectra confirmed the presence of amorphous and crystalline structures by the existence of an intense D band separated from the G band, indicating early stages of crystallization. The interplanar distance corresponding to the graphite structures was determined by using HRTEM micrographs.

This study compares a wound dressing based on bacterial cellulose/collagen (BC/COL) hydrogel in rat dorsum with commercial collagenase ointment and untreated wound. The hydrogel was characterized by Scanning Electron Microscopy (SEM), Thermogravimetric Analysis (TGA), Fourier transformed - Infrared spectroscopy (FT-IR) and X-ray diffraction (XRD). According to the In vivo test and macroscopic evaluation, BC/COL hydrogel showed a better repair of wounds and promoted statistically significant differences of tissue repair between treatments on the 7th day after surgery. Better quality, quantity and orientation evaluation of collagen fibers (p=0.0001) were observed in the BC/COL hydrogel and collagenase ointment groups in relation to the control group. The BC/COL hydrogel promoted better wound healing than collagenase and the control group, therefore, it can be considered a potential wound dressing for skin regeneration.

In recent years, the inappropriate disposal of polymeric materials has increased due to industrial development and increase of population consumption. This problem may be minimized by using biodegradable polymers, such as bacterial cellulose and poly(hydroxybutyrate), from renewable resources. This work was aimed at monitoring and evaluating degradation of bacterial cellulose, vegetable cellulose and poly(3-hydroxybutyrate) using Thermogravimetric Analysis and Scanning Electron Microscopy. Controlled mass polymer samples were buried in pots containing soil. Samples were removed in 30 day intervals up to 180 days. The results show that the mass of the polymer increased in the first month when in contact with the soil but then it was degraded as evidenced by mass loss and changes on the sample surface.

In this work, the effects of incorporating cellulose nanocrystals from soy hulls (WSH30) on the mechanical, thermal, and barrier properties of methylcellulose (MC) nanocomposites were evaluated. MC/WSH30 nanocomposite films with different filler levels (2, 4, 6, 8, and 10%) were prepared by casting. Compared to neat MC film, improvements in the mechanical and barrier properties were observed, while thermal stability was retained. The improved mechanical properties of nanocomposites prepared may be attributed to mechanical percolation of WSH30, formation of a continuous network of WSH30 linked by hydrogen interactions and a close association between filler and matrix.

Este trabalho descreve a preparação de eletrodo de pasta de carbono (EPC) em minicavidade de contato sólido e sua avaliação quando a pasta de carbono contém ou não partículas sub-micormétricas de SiO2(Eu3+ 2%) e SiO2(Eu3+ 2%)-lisina. Nestes estudos, medidas de voltametria cíclica e impedância eletroquímica foram realizadas em PBS (0,1 mol L-1 pH 7,4) contendo as espécies redox Fe(CN)6-3/-4. Os resultados de impedância foram interpretados baseados na reação de transferência de carga envolvendo as espécies Fe(CN)6-3/-4 e/ou oxigênio em frequências mais altas e, difusão das espécies eletroativas e características da pasta de carbono a baixas frequências. EPC-minicavidade é apropriado para eletroanálises usando pasta de carbono modificada.

This work describes the preparation of carbon paste electrode (EPC) in a solid-contact minicavity and its evaluation when containing carbon paste without and with SiO2(Eu3+ 2%) and SiO2(Eu3+ 2%)-lysine sub-micrometrics particles. For this study cyclic voltammetry and electrochemical impedance measurements were performed at pH 7.4 in 0.1 mol L-1 PBS containing Fe(CN)6-3/-4 redox species. The impedance results were interpretated based on a charge-transfer reaction involving Fe(CN)6-3/-4 species and/or oxygen at higher frequencies and, diffusion of the electroactive species and carbon paste characteristics at lower frequencies. EPC-minicavity is suitable for electroanalysis using modified carbon paste.

Esferas de poliestireno foram obtidas através da polimerização do estireno sem a presença de emulsificante. A suspensão foi caracterizada por Espalhamento de Luz e Microscopia Eletrônica de Transmissão apresentando monodispersidade com tamanho em torno de 463 nm. O método de deposição vertical foi utilizado para preparar filmes em substratos de vidro a partir da suspensão de esferas. Filmes de opalas de alta qualidade foram obtidos e caracterizados por Espectroscopia de Reflectância, Microscopia Eletrônica de Varredura e Microscopia Óptica.

Polystyrene latex spheres were obtained by free-emulsifier polymerization of styrene. Suspension was characterized by Photon Correlation Spectroscopy (PCS) and Transmission Electron Microscopy (TEM) and were observed to be monodisperse with sizes around 463 nm. A vertical deposition method was used in order to prepare films deposited on glass slides from the spheres suspension. High-quality opal-like films were obtained and characterized by Reflectance Spectroscopy, Scanning Electron Microscopy (SEM) and Optical Microscopy.

The assembly of a photochemical reactor with six fluorescent lamps, used for photopolymerizations is described. This chamber presents a mobile support, allowing the placement of samples at different heights and a safety lock that interrupts the radiation, if it is opened during operation. The mirrored internal walls avoid the dispersion and non-uniform distribution of light. There is no high heating because the own character of the used lamps. All parts could be purchased in commerce with less than U$ 150,00. This reactor was successfully used for monolithic stationary phase photopolymerization.

In this work we report some aspects of the chemistry involved in the preparation of modified silicon oxide by the sol-gel process. Europium III compounds were used as luminescent probe. An organic-inorganic hybrid was obtained by hydrolysis of tetraethylorthosilicate (TEOS) and 3-aminopropyltriethoxysilane (APTS). The Eu III compounds were added in different ways. In the first, silica was prepared in the presence of Eu III, and in the second, Eu III was added on the silica surface. These materials were studied by luminescence, infrared spectroscopy and termogravimetric analysis. The results obtained for the hybrid material show different behavior for Eu III emission, which could be excited by the antenna effect and the influence of the surrounding in the luminescence quenching. The thermogravimetric data present different mass loss in samples to range temperature 50 - 150 °C. Thermogravimetric and infrared spectra showed that inorganic polymers incorporated the organic part.

Er-doped SnO2 thin films and xerogels are obtained by sol-gel technique. In order to understand the Er³+ rare-earth ion activity in SnO2 matrix, a characterization of Er incorporation is done through emission and excitation spectra of xerogels, besides thin film electrical characterization. Effects to grain dimensions are also analyzed based on X-ray diffraction data showing the particle growth with annealing temperature and inhibition of this growth by Er doping. Electrical characterization results suggest that Er³+ has an acceptor-like character in SnO2, and that codoping with Yb³+ allows an energy transfer process Yb³+ -> Er³+.

Some aspects of the chemistry involved in the preparation and characterization of functionalized silicon oxide by sol-gel method are considered in this work. The synthesis was performed with different silicon alcoxide precursors and the influence of the acid and basic catalyst was investigated. Characterization was performed by infrared absorption spectroscopy, elemental analysis and 29Si NMR. Infrared data show Si-C and -CH2- vibrational modes at 1250 to 1280 and 2920 to 2940 cm-1, respectively. The elemental analysis confirmed the presence of organic groups in the inorganic silica network. 29Si NMR results show different hydrolisys depending on the acid or base catalysis.

Neste trabalho, usando o processo de coacervação, foi estudado o sistema NaPO3/AgNO3/H2O. Determinou-se o domínio de coacervação a partir de diferentes concentrações de NaPO3 e AgNO3 e a influência do pH na estabilização do coacervato foi determinada. Os coacervatos obtidos em pH ~ 5 apresentam maior região de estabilidade.

In this work, using coacervation process, the influence of the pH in the stability of the coacervates of the NaPO3/AgNO3/H2O system was studied. The coacervate domain was established using different concentrations of NaPO3 and AgNO3 and the influence of the pH in the stability of the coacervate was putfoward. The coacervates obtained at pH ~ 5 present highest stability.