The aim of this study was to characterize calcium phosphate ceramics with different Ca/P ratios and evaluate cell response of these materials for use as a bone substitute. Bioceramics consisting of mixtures of hydroxyapatite (HAp) and β-tricalcium phosphate (β-TCP) powders in different proportions were pressed and sintered. The physical and chemical properties of these bioceramics were then characterized. Characterization of the biological properties of these materials was based on analysis of cell response using cultured fibroblasts. The number of cells attached to the samples was counted from SEM images of samples exposed to cell culture solution for different periods. These data were compared by analysis of variance (ANOVA) complemented by the Tukey's test. The TCP sample had higher surface roughness and lower density. The adherence and growth of FMM1 cells on samples from all groups was studied. Even though the different calcium based ceramics exhibited properties which made them suitable as bone substitutes, those with higher levels of β-TCP revealed improved cell growth on their surfaces. These observations indicated two-phase calcium phosphate based materials with a β-TCP surface layer to be a promising bone substitute.

Silicon nitride based ceramics have been widely used as structural ceramics, due mainly to their thermo-mechanical properties such as high density, high thermal shock resistance, corrosion resistance and chemical stability. The aim of this study was to determine the influence of rare earth and aluminum oxide additions as sintering aids on densification, microstructure and mechanical properties of silicon nitride. Silicon nitride mixtures with 91 wt. (%) Si3N4 and 9% wt. (%) additives were prepared and sintered. The density, microstructure and mechanical properties of the sintered specimens of these mixtures were determined. In most specimens, scanning electron microscopic examination and X ray diffraction analysis revealed elongated grains of β-Si3N4 with aspect ratio of about 2.0 and dispersed in a glassy phase. The density of the sintered specimens was higher than 94% of the theoretical density (td) and specimens with La2O3 and Al2O3 additions exhibited the highest value. The results of this investigation indicate that the rare earth ion size influences densification of silicon nitride, but this correlation was not observed in specimens containing two different rare earth oxides. The hardness values varied in direct proportion to the density of the specimens and the fracture toughness values were influenced by the composition of the intergranular glassy phase.

Cr3C2-Ni20Cr coatings have been used for corrosion and wear resistant applications. However, one of the shortcomings of these coatings is its low hardness, and consequent low wear resistance, for long term high temperature applications. Nanostructured coatings of many materials have exhibited higher hardness and strength compared with conventional coatings of the same material. Consequently, nanostructured coatings of other materials, including Cr3C2-Ni20Cr have been attempted to enhance overall performance. In this study the effects of high energy milling parameters on Cr3C2-25(Ni20Cr) powder characteristics as well as the microstructure and mechanical properties of nanostructured Cr3C2-25(Ni20Cr) coatings formed by high velocity oxygen fuel (HVOF) spraying have been evaluated. The average particle size and crystallite size of milled Cr3C2-25(Ni20Cr) powders decreased with increase in milling time and this decrease was more pronounced in nitrogen compared to that in hexane. This difference has been attributed to a cushioning effect in the latter medium. The coatings prepared with milled Cr3C2-25(Ni20Cr) powders had a more uniform microstructure, were harder and had higher relative fracture toughness compared with coatings prepared with as-received powders.

Silicon nitride based ceramics are promising candidates for biomedical applications due to their chemical and dimensional stability associated to suitable mechanical strength and relatively high fracture toughness. However, the bioinert characteristics of these ceramics limit their application to situations where the formation of chemical bonds between the material and the tissue are not essential. A way to broaden the application field of these ceramics in medicine is promoting their bioactivity by means of a hydroxyapatite coating. Therefore, in this paper, samples of silicon nitride were coated with apatite using the biomimetic method. The treated silicon nitride surface was characterized by diffuse reflectance infrared Fourier transformed, X ray diffraction and scanning electron microscopy. The results showed that a layer of hydroxyapatite could be deposited by this method on silicon nitride samples surface.

In many 'in-vivo' and 'in-vitro' studies, the behavior of calcium phosphate ceramics like beta - tricalcium phosphate in biological environments has been reported to be predictive and positive. In terms of bone tissue growth, these ceramics are attractive biomaterials due to their porous microstructures. To obtain biomaterial quality ceramics, in this investigationbeta- TCP porous ceramics were prepared by a special consolidation method with albumin as a foam generating agent. This technique enables a variety of formats with complex geometries to be prepared. To obtain porous samples using albumin, heat had to be introduced into the system during the consolidation stage. After consolidation, the samples were sintered at 1250 °C for 30 minutes and characterized using X ray diffractometry, scanning electron microscopy and mercury porosimetry. The foams that were obtained by this method exhibited spherical and interconnected pores, characteristics desirable in biomedical implants.

Research in the preparation of ceramics from polymeric precursors is giving rise to increased interest in ceramic technology because it allows the use of several promising polymer forming techniques. In this work ceramic composite pieces were obtained by pyrolysis of a compacted mixture of a polysiloxane resin and alumina/silicon powder. The mixture consists of 60 vol% of the polymer phase and 40 vol% of the filler in a 1:1 ratio for alumina/silicon, which was hot pressed to crosslink the polymer, thus forming a compact body. This green body was trimmed into different geometries and pyrolised in nitrogen atmosphere at temperatures up to 1600 °C. X-ray diffraction analysis indicated the formation of phases such as mullite and Si2ON2 during pyrolysis, that result from reactions between fillers, polymer decomposition products and nitrogen atmosphere. The porosity was found to be less than 20% and the mass loss around 10%. The complex geometry was maintained after pyrolysis and shrinkage was approximately 8%, proving pyrolisis to be a suitable process to form near-net-shaped bulk ceramic components.

Silicon carbide is an important structural ceramic and finds applications as abrasives, as a refractory and in automotive engine components. This material can attain high densities during liquid phase sintering if suitable additives are used. Silicon carbides containing silica, alumina and rare earth oxides have suitable characteristics to promote liquid phase sintering. In this paper, the sintering behavior of silicon carbide ceramics with additives based on the (SiO2-RE2O3-Al2O3) system (RE = Y, Dy) has been studied. Samples with different compositions and containing 90 vol.% SiC were sintered in a dilatometer at 1950 °C/1h and in a graphite resistance furnace from 1500 °C/1h up to 1950 °C/1h. The shrinkage behavior as a function of rare earth oxide used and additive composition was also studied. The sintered materials were characterized by density and weight loss measurements. The crystalline phases were identified by X-ray diffraction analysis. The sintering kinetics of these materials can be related to the formation of secondary crystalline phases.