The production of high performance metal matrix composites depends on a proper design of the surface of the reinforcing phase, ensuring a good contact with a metal phase. In the present work, two Ag decorating procedures to modify the surface of multi-walled carbon nanotubes (MWCNT) were evaluated for further production of aluminum matrix composites. The procedures consisted in a two steps route based on acid oxidation of carbon nanotubes (CNT) followed by suspension in an Ag ion solution; and a single step route, based on the effect of n-dimethylformamide (DMF) as an activation agent of CNT surface, in presence of Ag ions. Transmission and scanning-transmission electron microscopy, Raman and Fourier-transformed infrared spectroscopy were employed in order to characterize the results. The two steps route resulted in Ag nano-particles homogeneously deposited over the CNT surface. The mechanism for the deposition is based on carboxyl and probably hydroxyl functional groups formed in the first step, acting as nucleation sites for Ag precipitation in the second step. The single step route resulted in the formation of sub-micrometric Ag particles heterogeneously mixed to CNT bundles.

An aluminium matrix composite was prepared by mixing commercial aluminium powders and 15 vol % of FeAlCr powders and consolidation by hot extrusion. The extruded composite was subjected to severe plastic deformation by equal channel angular pressing (ECAP) at room temperature and at 150°C. The extruded composite presents a uniform distribution of particles although some defects are observed such as residual pores and particle agglomerates. The particle distribution does not show a significant change due to ECAP. The extruded composite exhibits a relatively fine grain size of the order of 1-2 μm that was refined to 550 nm after three ECAP passes at room temperature by route A and to 636 nm after four passes at 150°C by route Bc. The yield stress of the composites was increased by 140 to 180% after ECAP as compared with the extruded condition.

The austenitic stainless steel 316L is the most used metallic biomaterials in orthopedics applications, especially in the manufacture of articulated prostheses and as structural elements in fracture fixation, since it has high mechanical strength. However, because it is biologically inactive, it does not form chemical bond with bone tissue, it is fixed only by morphology. The development of biocomposites of stainless steel with a bioactive material, such as hydroxyapatite - HA, is presented as an alternative to improve the response in the tissue-implant interface. However significant reductions in mechanical properties of the biocomposite can occur. Different compositions of the biocomposite stainless steel 316L/HA (5, 20 and 50 wt. (%) HA) were prepared by mechanical alloying. After milling the powders for 10 hours, the different compositions of the biocomposite were compacted isostatically and sintered at 1200 ºC for 2 hours. The mechanical properties of the biocomposites were analyzed by compression tests. The powders and the sintered composites were analyzed by scanning electron microscopy (SEM) and X-ray diffraction (XRD).

In order to obtain quasicrystalline (QC) phase by mechanical alloying (MA) in the Al-Cu-Fe system, mixtures of elementary Al, Cu and Fe in the proportion of 65-20-15 (at. %) were produced by high energy ball milling (HEBM). A very high energy type mill (spex) and short milling times (up to 5 hours) were employed. The resulting powders were characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). QC phase was not directly formed by milling under the conditions employed in this work. However, phase transformations identified by DSC analysis reveals that annealing after HEBM possibly results in the formation of the ψ QC phase.

Interest in laser beam welding for aerospace applications is continuously growing, mainly for aluminum alloys. The joints quality is usually assessed by non-destructive inspection (NDI). In this work, bead on plate laser welds on 1.6 mm thick AA6013 alloy sheets, using a 2 kW Yb-fiber laser were obtained and inspected by pulse/echo ultrasonic phased-array technique. Good and poor quality welds were inspected in order to verify the limits of inspection, comparing also to X-ray radiography and metallographic inspections. The results showed that ultrasonic phased array technique was able to identify the presence of grouped porosity, through the attenuation of the amplitude of the echo signal. This attenuation is attributed to the scattering of the waves caused by micro pores, with individual size below the resolution limit of the equipment, but when grouped, can cause a perceptive effect on the reflection spectra.

Porous 316L austenitic stainless steel was synthesized by powder metallurgy with relative density of 0.50 and 0.30 using 15 and 30 wt. (%) respectively of ammonium carbonate and ammonium bicarbonate as foaming agents. The powders were mixed in a planetary ball mill at 60 rpm for 10 minutes. The samples were uniaxially pressed at 287 MPa and subsequently vacuum heat treated in two stages, the first one at 200 ºC for 5 hours to decompose the carbonate and the second one at 1150 ºC for 2 hours to sinter the steel. The sintered samples had a close porous structure and a multimodal pore size distribution that varied with the foaming agent and its concentration. The samples obtained by addition of 30 wt. (%) of foaming agents had a more homogeneous porous structure than that obtained with 15 wt. (%). The MTT cytotoxicity test (3-[4,5-dimethylthiazol]-2,5-diphenyltetrazolium bromide) was used to evaluate the mitochondrial activity of L929 cells with samples for periods of 24, 48, and 72 hours. The cytotoxicity test showed that the steel foams were not toxic to fibroblast culture. The sample with the best cellular growth, therefore the most suitable for biomedical applications among those studied in this work, was produced with 30 wt. (%) ammonium carbonate. In this sample, cell development was observed after 48 hours of incubation, and there was adhesion and spreading on the material after 72 hours. Electrochemical experiments using a chloride-containing medium were performed on steel foams and compared to massive steel. The massive steel had a better corrosion performance than the foams as the porosity contributes to increase the surface area exposed to the corrosive medium.

In this work, solution heat treatments at different temperatures were performed in a commercial based AA7050 aluminium alloy, with and without titanium addition, produced by mechanical alloying and hot extrusion with the aim to investigate the effect of titanium addition and mechanical alloying in the precipitates stability. The same heat treatment conditions were used in a reference sample obtained from a commercial AA7050 alloy. Solution heat treated samples were characterised by differential scanning calorimetry (DSC), optical microscopy and hardness test. Once the better temperature for the solution treatment of modified alloys was defined, the ageing curve at 120 °C was obtained to verify the effect of milling and Ti addition in the precipitation and in the maximum values of hardness obtained for the alloys.