Resumo em Inglês:

Abstract Carbon fiber/polyaniline composites (CF/PAni) were synthesized at three different deposition time of 30, 60 and 90 min by oxidative polymerization. The composite materials were morphologically and physically characterized by scanning electron microscopy and by Raman spectroscopy, respectively. Their electrochemical responses were analyzed by cyclic voltammetry, by galvanostatic test, and by electrochemical impedance spectroscopy. The influence of the PAni layer thickness deposited on carbon fibers for the composite formation as well as for their electrochemical properties was discussed. The CF/PAni-30 showed a nanometric thickness with more homogeneous morphology compared to those formed in deposition times of 60 and 90 min. It also showed, from the electrochemical impedance spectroscopy measurements, the lowest charge transfer resistance value associated to the its highest value for the double-layer capacitance of 180 Fg-1 making it a very strong candidate as a supercapacitor electrode.

Resumo em Inglês:

Abstract Pluronics® molecules self-assemble in aqueous solution providing a core/shell architecture that improves the solubility of hydrophobic drugs. Binary mixtures of Pluronics® have been studied as drug nanocarriers in order to combine their advantages, like high colloidal stability, small particle size and good solubilisation capacity (Scp). In this work we studied Pluronics® binary mixture, P123 and F127, as nanocarriers of the hydrophobic drug griseofulvin. P123 (E21P67E21) shows a relative good Scp, whereas F127 (E98P67E98) shows a good colloidal stability. According to data, these binary mixtures form stables nano-sized comicelles in aqueous solution. The Scp of the P123/F127 systems at 25 and 37 °C was monitored by UV/Visible spectroscopy, showing good results at both temperatures, as would be expected, since P123/F127 have similar length hydrophobic block. Hydrophobic-dependence and temperature-responsive of the systems were evaluated by CMC, particle size and colloidal stability. Hence, stables P123/F127 comicelles may have potencial as hydrophobic drug delivery.

Resumo em Inglês:

Abstract This research is focused on the effect of porosity on the friction-wear properties of automotive brake pads. Waste Tire Dust (WTD) was used as a new friction material in brake pads. Newly formulated brake pad materials with five different components have been produced by conventional techniques. In the experimental studies, the change of the friction coefficient, the temperature of the friction surface, the specific wear rate, and the hardness, density and porosity were measured. In addition, the micro-structural characterizations of brake pads are determined using Scanning Electron Microscopy (SEM). The mean coefficient of friction, porosity and specific wear are increased due to a WTD rate increases, on the other hand, hardness and density are decreased. As a result, WTD can be considered as an alternative to revalorize this kind of waste products in the brake pads and the amount of porosity of the brake pad affected the friction coefficient and wear behavior of the pad.

Resumo em Inglês:

Abstract A new Schiff base type of polyester containing 2,2-dimethyl-1,3-diaminopropane was prepared by solution polycondensation of 1,4-benzenedicarbonyl dichloride with Bis(4-hydroxybenzilaldehid)-2,2-dimethyl-1,3-propildiimine (H2HB2P) which is derived from a 2,2-dimethyl-1,3-diaminopropane Schiff base reacted with a 4-hydroxybenzaldehyde monomer. The monomer and the polyester were characterized by FTIR,1HNMR, and elemental analysis. The prepared polyester showed inherent viscosity of 0.29 dl/g in NMP at 25 °C, indicating their moderate molecular weight. The Polyester was completely soluble in aprotic polar solvents such asN -methylpyrolidone (NMP), dimethylformamide (DMF), Dimethyl Acetamid (DMAC), dimthylsulfoxide (DMSO). TGA determined the 10% weight loss temperature (T10) at 280 °C and residual weight at 600 °C ca. 41% under nitrogen atmosphere.

Resumo em Inglês:

Abstract In this work, the rheological, mechanical and morphological behavior of immiscible blend poly (methyl methacrylate) with elastomeric particles (PMMAelast) and post-consumer poly (ethylene terephthalate) (PET) with and without the use of the interfacial compatibilizer poly (methyl methacrylate-co-glycidyl methacrylate-co-ethyl acrylate) (MGE) was studied. The significant increase in torque presented in rheological analyses has shown a indication of chemical reactions between the epoxy group of MGE with end groups of PET chains and also with the elastomeric phase of PMMAelast. The increased concentration of PET yielded an increase in maximum strength and elasticity modulus and a decrease in elongation at break. The PMMAelast/PET binary blend (50/50 wt%) and PMMAelast/PET/MGE compatibilized blend (65/30/5 wt%) showed pronounced results in elongation at break compared to PMMAelast, whereas, in the first results were due to the evidence of a co-continuous morphological structure and in the second, due to the efficiency of the dual reactive interfacial compatibilization of PMMAelast/PET blends. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses showed that PMMAelast/PET/MGE blends exhibit complex phase morphology due to the presence of elastomeric particles in the PMMAelast copolymer and in the use of MGE terpolymer.

Resumo em Inglês:

Abstract To recycle post-consumer HDPE contaminated with waste lubricating oils, companies include prior washing and drying in the process. This consumes large amounts of water and energy, generates significant effluent requiring treatment. This study assesses lubricating oil influence on HDPE properties to evaluate the feasibility of its direct mechanical recycling without washing. The current lubricating oil packaging reverse logistics in Rio de Janeiro municipality is also analyzed. HDPE bottle samples were processed with seven oil contents ranging from 1.6-29.4 (wt%). The results indicated the possibility to reprocess the polymer with oily residue not exceeding 3.2%. At higher levels, the external oil lubricating action affects the plastic matrix processing in the extruder and injection, and the recycled material has a burnt oil odor and free oil on the surface. Small residual oil amounts retain the plastic properties comparable to the washed recycled polymer and exhibited benefits associated with the oil plasticizer action. However, oil presence above 7.7% significantly changes the properties and reduces the elasticity and flexural modulus and the plastic matrix crystallinity.

Resumo em Inglês:

Abstract An efficient recycling of end-of-life products is of crucial interest from an economical and ecological point of view. However, the near infrared spectroscopy often used for the optic sorting processes is limited because of the absorption of carbon black present in black plastics and as it only sorts as a function of chemical formulas. The tracing technology developed in this study is based on the dispersion of lanthanide complexes particles into polymers to give them a code that can be related to their formulation and viscosity that are important parameters for their re-processing. As the success of this technology is conditioned by achieving a fine dispersion of the tracer particles, we also focus on accomplishing a fine dispersion of tracer particles by using a high shear process. Processing under high shear rate (N= 800 rpm) has proved to play a determining role in dispersing finely and homogenously tracer particles within PP matrix. Thanks to the good quality of dispersion, the detection of three tracers at a level of 0.1 wt% has been successfully achieved, even in black matrices for an acquisition time of 10 ms.

Resumo em Inglês:

Abstract Nanocomposite based on high density polyethylene (HDPE) and layered zirconium phosphate organically modified with octadecylamine (ZrPOct) was obtained through melt processing. The ZrPOct was synthesized by precipitation and modified by suspension and sonication procedures. The initial and maximum degradation temperatures (Tonset and Tmax) were increased. A slight decrease of crystallinity degree was detected. Reduction of elastic modulus and elongation at break were noticed. The lamellar spacing was increased (3.3 times higher). The storage modulus decreased and low field nuclear magnetic resonance (LFNMR) revealed an increasing of molecular mobility. The presence of octadecylamine enhanced the entrance of HDPE in the ZrPOct galleries. Several characteristics of HDPE were changed indicating that intercalation was successful. All results indicated that partially intercalated and/or exfoliated nanocomposite was achieved.

Resumo em Português:

Resumo Este trabalho teve como objetivo preparar e avaliar filmes PHB/vermiculita natural e modificada nas quantidades em peso de 1%, 3% e 6% através dos métodos intercalação por fusão e intercalação por solução. Os bionanocompósitos obtidos pelo método intercalação por fusão foram preparados em uma extrusora monorosca e posteriormente os filmes foram moldados via compressão. Na preparação dos filmes por solução, os sistemas foram submetidos à agitação e aquecimento a 80 °C. Os sistemas foram avaliados por difração de raios-X e o comportamento de biodegradação foi avaliado de acordo com a norma ASTM G 160-03. O acompanhamento da biodegradação foi realizado por meio de inspeção visual e perda de massa. Observou-se que o percentual de argila e o método de obtenção dos filmes influenciaram na estrutura formada e na biodegradação dos sistemas.

Resumo em Inglês:

Abstract This study aimed to prepare and to evaluate natural and modified PHB /vermiculite films in quantities of 1%, 3% and 6% by weight, through melt intercalation and solution intercalation methods. The bionanocomposites in the form of thin films, obtained by the melt intercalation method, were prepared in a single screw extruder and then molded via compression. In the preparation of the films by solution method, the systems were stirred and heated at 80 °C in the presence of the chloroform solvent. The systems were evaluated by X-ray diffraction and the degradation behavior was evaluated according to ASTM G 160-03, by visual inspection and through weight loss. It was observed that the percentage of clay and the method of obtaining of the films influenced in the structure and biodegradability of the systems.

Resumo em Português:

Resumo Zeólitas foram submetidas à troca iônica ou impregnação com prata e posteriormente adicionadas em filmes de quitosana para a confecção de curativos para queimaduras. As zeólitas foram avaliadas por Ressonância magnética nuclear (RMN), Fluorescência de raios X por reflexão total (TXRF), Microscopia eletrônica de varredura (MEV). Os filmes poliméricos foram analisados com relação às suas propriedades mecânicas, permeabilidade ao vapor d’água (PVA) e liberação de prata. Observou-se que o procedimento de troca iônica não alterou a morfologia das zeólitas de partida. Grumos de zeólita foram observados nas micrografias dos filmes e estes influenciaram nas propriedades mecânicas devido à desorganizaçao local no empacotamento das cadeiras poliméricas da quitosana. A metodologia de troca iônica ou impregnação influenciou diretamente na quantidade de prata presente superficialmente na zeólita e consequentemente alterou o perfil de liberação de prata em uma solução simulada de exudato de ferida. Os modelos cinéticos sugeriram que a liberação da prata não foi essencialmente regulada pela lei de difusão de Fick.

Resumo em Inglês:

Abstract Zeolites were subjected to ion exchange or impregnation with silver and added to chitosan films for producing burns dressings. Zeolites were characterized by nuclear magnetic resonance (NMR), total reflection X-ray fluorescence (TXRF), scanning electron microscopy (SEM). The polymer films were analyzed with respect to their mechanical properties, water vapor permeability (WVP), and release of silver. It was observed that the ion exchange did not modify the morphology of the starting zeolite. Clusters of zeolite were observed in the micrographs of the films and they influenced the mechanical properties due to local disruption in the packing of the polymer chains of chitosan. The methodology of ion exchange or impregnation directly influenced the amount of silver present in the zeolite surface and consequently changed the silver release profile in an of simulated exudate fluid. The kinetic models suggested that the release of the silver was not primarily governed by Fick's law of diffusion.

Resumo em Inglês:

Abstract A novel monomer of S-2-mercaptoethyl 2-(thiophen-3-yl)ethanethioate (MTE) were synthesized via esterification reaction between 2-(thiophen-3-yl)acetic and ethane-1,2-dithiol in the presence of dicyclohexyl-carbodiimide (DCC) and N,N’-dimethylpyridin-4-amine (4-DMAP) as catalytic system. The structure of monomer was characterized via MS, 1H-NMR and 13C-NMR spectroscopies. The electrochemical polymerization of MTE monomer was performed in acetonitrile using lithium perchlorate (LiClO4) as electrolyte agent. The obtained polymer film (PMTE) was characterized via cyclic voltammetry and it exhibited the main oxidation peaks centered at +2V.

Resumo em Inglês:

Abstract This research studies influence of the flow pattern at annular die entrance through the inside of annular die flow channel of capillary rheometer on the swell behavior of NR compound. The annular die used in this research was specifically designed to create the specific pattern of Vortex Flow at Die Entrance (VFE) of NR compound. Results of the study showed that the thickness swell ratio was higher than diameter swell ratio by an average of 20% at every die gap size. It was also found that the VFE flow pattern had direct significant influence on the swell behavior of NR compound while extrudating through annular die. Results from the study of the flow pattern could be used to explain why the thickness swell ratio is higher than the diameter swell ratio in every test condition.