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MCrAlY coatings are usually adopted to improve the environmental resistance of Ni-based superalloy components of turbine engines against high-temperature oxidation and hot corrosion. In this work, CoNiCrAlYRe coatings were produced by atmospheric plasma spraying. The coatings exhibited relatively low oxygen content and porosity. X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy analyses revealed that the high-temperature exposure at 1383ﾠK (1110ﾠﾰC) promoted the growth of an oxide scale on the top surface being composed of a continuous and dense Al2O3 inner layer followed by an outer mixed layer (Cr2O3 and spinels). The oxide scale was mainly composed of Al2O3, while the formation of mixed oxides occurred at lesser extent. After high-temperature exposure, the formation of internal oxides in some areas reduced the inter-lamellar cohesion, so that a decrease in microhardness was found.

Polycrystalline, close-packed, homogeneous nanostructured ceria thin films were prepared by sol–gel process via dip-coating technique on soda-lime glass and (100)-oriented Si substrates. To produce the films, a sol was prepared using, as precursor, a home made cerium sec-butoxide dissolved in secondary butanol. The chemical composition, the microstructural/morphological characteristics and the optical properties of the coatings were investigated in detail. The experimental results clearly demonstrate that the ceria films are nanocrystalline (CeO2, cubic phase $$ {\text{Fm}}\bar{3}{\text{m}} $$ ) with an average grain size of about 2–3 nm for the samples grown on glass and of about 4–5 nm for the samples grown on silicon. The analyses of ceria layers grown on silicon show that the ceria coatings are free from organic residues and that a Si-oxide layer is formed at the film/substrate interface. The optical results evidence a red shift of the energy gap of about 0.5 eV that can be ascribed to conversion of relevant Ce4+ sites to Ce3+ sites and a consequent creation of oxygen vacancy at the surface of the ceria grains.

Nanocrystalline anatase titania thin films were prepared by using two different precursor solutions, a highly acid solution (Sol-1) and a polymer-like solution (Sol-2), via the dip-coating technique on different substrates (-Si wafer, fused silica and soda lime glass). The influence of the two sol-gel titania precursor solutions and of the substrate type on the film morphology, coating porosity, surface roughness, crystalline phases and grain size of the titania films were investigated. Our experimental results clearly indicate that the sol - composition and substrate type remarkably influence the microstructural/morphological properties of the titanium dioxide. They consequently modify the optical response and hydrophilic performances of the samples. The photocatalytic oxidations of the methylene blue in water of the samples grown on the glass substrate were monitored to investigate the influence of the sol-gel precursor solution on the photocatalytic activity of the titania coatings, and the results were put in relation with the hydrophilic and optical properties of the films. The outcome demonstrates that the optical properties and the hydrophilic and photocatalytic performances of nanocrystalline titania can be opportunely tailored tuning the size dimension of the crystalline domain according to the specific coating applications.

The study of sorption reactions of metal hydrides is the subject of numerous researches in connection with the development of a safe technology for hydrogen storage, and MgH2, in particular, is one of the most promising materials. Several efforts have been already carried out in order to understand the kinetic mechanisms involved in the MgH2 decomposition which is at the basis of H2 release. However, the role of additives and induced structural defects on the sorption cycles is not clear yet. With the purpose of supporting the reaction analysis we have developed an experimental protocol for the metallographic examination at high spatial resolution of partially desorbed MgH2 powders. In particular, this procedure allows cross-sectional analysis of powders embedded into conductive matrix, while the observation method produces a different contrast among metallic Mg, MgH2 and additive particles made of heavier materials.