Materials Science Forum Vols. 660-661

Abstract: Ion specimens can be incorporated in glasses or natural clays by ionic exchange process with different concentrations dependent of matrix´s type and of the ionic exchange parameters. In particular, the incorporation of silver ions presents high interest by its biocidal properties. A compound contending ion silver specimens presents bactericidal and fungicidal properties with effect proportional to ion concentration. This work presents results about application of the atomic absorption technical to determine the silver ion concentration incorporated in a glass matrix by ionic exchange process. The ionic exchange experiments were realized with different AgNO3 concentration and constant temperature. After ionic exchange process, the glass samples were submitted to characterization by Energy Dispersive X-Ray Spectroscopy and Atomic Absorption Techniques. The comparative results between different techniques showed that atomic absorption technical is adequate to determine ion silver concentration incorporated in the glass matrix after ionic exchange process.

Abstract: A considerable increase in the ceramic products demand occurred due to the evolution of dental restoration techniques and these materials must resist to the complex mouth environment. The pH of saliva can decrease significantly due to the ingestion of acidic foods and beverages and mainly due to reactions occurring during bacteria metabolism that lead to the formation of organic acids. Fluorides are also present in the mouth since fluorides are usually added in drinking water, mouth washes, tooth pastes and gels for the prevention of plaque and caries formation. The combination of low pH and presence of fluorides can lead to the formation of HF and HF2- which are detrimental to metallic and probably to ceramic devices. In this work, commercial blocks of ZrO2 ceramics (ProtMat Materiais Avançados® and Ivoclar®) were immersed in Fusayama artificial saliva of different pHs and fluoride concentrations. The properties of the as-produced ceramics (crystalline phases (XRD), microstructure (SEM), roughness (3D surface topography AFM) and mechanical resistance – Vickers hardness (Hv) and fracture toughness (KIC) were evaluated. Some of these properties were also determined after the immersion tests as well as the mass variation of the samples in order to evaluate the resistance of these ZrO2 ceramics to degradation under these conditions.

Abstract: Alumina ceramics have been used in dental prosthesis because it is inert, presents higher corrosion and shear resistance when compared to metals, excellent aesthetic, and mechanical resistance. In this work it was produced an infrastructure material for applications in dental crowns, obtained by glass infiltration in alumina preforms. Various oxides, among that, rare-earth oxide produced by Xenotime, were melted at 1450°C and heat treatment at 700°C to obtain the glass (RE-glass). The alumina was pre-sintered at 1100°C cut and machined to predetermine format (unidirectional indirect infiltration) and finally conducted to infiltration test. The alumina was characterized by porosity (Hg-porosity and density) and microstructure (SEM). The glass wettability in alumina was determined as function of temperature, and the contact angle presented a low value (<90º), showing that glass can be infiltrated spontaneously in alumina. The infiltration test was conducted at glass melting temperature, during 30, 60, 180, 360 minutes. After infiltration, the samples were cut in longitudinal section, ground and polished, and analyzed by XRD (crystalline phases), SEM (microstructure) and EDS (composition).The REglass presents higher infiltration height when compared to current processes (direct infiltration), and homogeneous microstructure, showing that it is a promising method used by prosthetics and dentists.

Abstract: The kaolin beneficiation industries produce waste that is rich in Al2O3 and SiO2, oxides that when sintered at high temperatures react to form mullite. Due to the rare occurrence of the mullite mineral in nature, the number of studies in order to obtain it has been growing in recent years due to its properties excellent. This study aims to examine the feasibility of the use of microwave energy as an alternative to synthesize mullite from kaolin residue, since the use of microwave energy in the synthesis of materials has gained importance for the speed and economy when compared to conventional methods. The compositions studied (residual kaolin + alumina) were established according to the stoichiometry of mullite. The samples were sintered in a microwave oven home changed, varying power and time. It was observed that with the increase of these variables the intensity of the peaks of the mullite phase increased.

Abstract: This work has for aim to synthesize CeO2 catalytic supports doped with Cu2+ by combustion reaction method. Thus were obtained catalytic supports with the composition Ce1-xCuxO2 and the effect caused by doped element in the structure of the CeO2 was evaluated. The concentration value (x) of the Cu doped took over the values of 0.0; 0.3 and 0.5 mol. The catalytic supports developed were submitted to the structural characterization by X-ray diffraction, morphologic analysis by SEM and textural analysis by means of adsorption-dessorption of N2 by BET method. The results showed that the doped element (Cu) was not completely incorporated in the CeO2 structure and was evidenced that how much larger the quantity of Cu larger maid the disorder of the atomic structure of the obtained material. The analyzed supports present mesoporous nature structure.

Abstract: CoFe2O4 powders were synthesized by combustion reaction using glycine as fuel, aiming obtaining nanosized and monophase powders. Thus, different conditions of external heating during the synthesis were investigated. The powders were prepared according to the propellants and explosives theory, using glycine as fuel in the stoichiometric proportion (Φe = 1). During the synthesis the flame temperature and time were measured. The resulting powders were characterized by X-rays diffraction and scanning electronic microscopy (SEM). The results show that the condition in which the synthesis was done it influences in the combustion flame temperature and time and contributes for the obtainment of powders with majority phase without secondary phases. Crystallite size varied of 33 to 50 nm. All powders presented morphology constituted by soft agglomerated formed by nanoparticles.

Abstract: This paper describes the synthesis of Ni-Zn nanoferrites by combustion reaction using microwave energy as a heating source, and evaluates the performance of these materials as absorbers of electromagnetic energy at frequencies between 4 - 12 GHz. The influence of the synthesis conditions on the structure, morphology and absorption characteristics was investigated. The powders were characterized by DRX, BET, AGM and reflectivity measurements in the frequency bands of 8 to 12 GHz. The XRD results show the formation of Ni-Zn ferrite phase and Fe2O3 and Ni as secondary phases. The crystallite sizes ranged from 32 to 42 nm. The parameters of exposure time and power of the microwave oven changed the final characteristics of the resulting powders. The morphology of all the powders consisted of soft nanoparticle agglomerates. The best saturation magnetization and attenuation results were 70 emu/g and -4.1 dB in the frequency of 10 GHZ.

Abstract: The aim of this work is to evaluate the catalytic activity of NiAl2O4 powders, prepared by combustion reaction with different glycine contents, for the steam reforming of methane. The NiAl2O4 powders were prepared according to the theory of propellants and explosives, using glycine reductant in stoichiometric ratio (Φe = 1) and in excess of 10% and 20% (Φe < 1). During the synthesis, parameters such as flame combustion temperature and time were measured. The samples were characterized by XRD, textural analysis by nitrogen adsorption (BET/BJH), TPR and evaluated as catalysts for the steam reforming of methane. The XRD results showed the presence of NiAl2O4 as major phase and traces of NiO and Ni in all the samples. The glycine content increase caused a decrease of crystallite size and an increase of surface area, from 29 to 39 m2/g. The TPR profiles showed reduction peaks of NiO species in weak interaction with the support, and reduction of nickel present in the NiAl2O4. It was observed that higher methane conversions were obtained in the presence of NiAl2O4 samples prepared using glycine excess. However, it was also observed a rapid deactivation of these catalysts due to high coke deposition onto the active surface phases.

Abstract: Composites consist of a mixture or combination of the two or more, micro or macro constituents that differ in shape and chemical composition and, in essence, are insoluble in one another. The polyamide is a polymer that presents dimensional stability, good resistance to impact without notch and excellent chemical resistance. Already the ferrites are absorbers of electromagnetic radiation and have versatility to be used as a composite of ferrites. The composite of polyamide6/ferrite was obtained by mixing 10 and 30wt.% of ferrite added to polyamide 6 in a Torque Rheometer Haake. The objective of this work was to develop of polyamide6/ferrite composites to be used as absorbers of electromagnetic radiation. The results were very promising and showed that occurs interaction between the ferrite and polyamide6.

Abstract: The alumina powder was obtained through a technique based on firing irradiated pseudoboehmites powder to study the radiation effects in the alumina properties. The electron beam radiation effect in a pseudoboehmite produced by sol-gel synthesis was investigated, using aluminum chloride and ammonium hydroxide as precursors. The addition of poly(vinyl alcohol) ([C2H3OH]n) solution (8 wt% in water) was also analyzed. The aluminum chloride solution was mixed with the polyvinyl alcohol and the mixture was dropped into an ammonium hydroxide solution. The work presents the effects of pseudoboehmite radiation in the structure of alumina. The alumina was obtained by pseudoboehmite calcinations. The milky-white colloidal pseudoboehmite precipitate obtained by sol-gel method was filtered, washed with distilled water, dried at 70°C, and powdered in a mortar. The sample acquired was calcined 4 hours at 1100oC, and after that X-ray powder diffraction was performed. The well defined α-alumina crystal was obtained from 1100oC treatment for some samples. The X-ray powder diffraction data shows that in some irradiated samples calcined at 1100o C for four hours presented θ-alumina and -alumina. The powder dried at 70o C was also examined by thermal analysis. The Thermo Gravimetric Analysis (TG) and Differential Thermal analysis (DTA) were used to evaluate mass loss and the pseudoboehmite endothermic and exothermic transformations. The samples were analyzed through scanning electron microscopy technique