The aim of this study is to investigate the impact of mechanical recycling on the physical and mechanical properties of recycled polyamide 6 (PA6) and polyamide 66 (PA66) in relation to their microstructures. Both PA6 and PA66 raw materials were reprocessed six times, and the changes in their properties were investigated as a function of recycling number. Until the sixth round of recycling, slight changes in the mechanical properties were detected, except for the percentage of elongation. For the physical properties, the change in both flexural strength and Young’s modulus followed a decreasing trend, while the trend in terms of elongation showed an increase. Microscopic analysis was performed on virgin and recycled specimens, showing that imperfections in the crystalline regions of polyamide 6 increased as the number of cycles increased.

This work presents the influences of glass fiber content on the mechanical and physical characteristics of polybutylene terephthalate (PBT) reinforced with glass fibers (GF). For the mechanical characterization of the composites depending on the GF reinforcement rate, tensile tests are carried out. The results show that increasing the GF content in the polymer matrix leads to an increase in the stiffness of the composite but also to an increase in its brittleness. Scanning Electron Microscope analysis is performed, highlighting the multi-scale dependency on types of damage and macroscopic behavior of the composites. Furthermore, flammability tests were performed. They permit certifying the flame retardancy capacity of the electrical composite part. Additionally, fluidity tests are carried out to identify the flow behavior of the melted composite during the polymer injection process. Finally, the cracking resistance is assessed by riveting tests performed on the considered electrical parts produced from composites with different GF reinforcement. The riveting test stems directly from the manufacturing process. Therefore, its results accurately reflect the fragility of the material used.

The lack of knowledge on the link between the manufacturing process and performance constitutes a major issue in brake lining development. The manufacturing process of organic brake friction composite materials includes several steps (mixing, preforming, hot molding and post-curing), which define their final microstructure, properties and performances. This study focuses on the effect of mixing duration on the microstructure, properties and tribological behavior of organic friction composite materials. The adopted methodology is based on simplified formulations effective in limiting synergistic effects by reducing the number and size distribution of constituents. Two simplified materials are here developed according to the mixing duration of the constituent introduction sequence. The microstructural characteristics are studied using 2D and 3D analyses, and then correlated with the thermophysical and mechanical properties. Wear mechanisms and tribological behavior are studied in relation to the microstructure and properties of the materials. The results show the effect of mixing duration as regards particle distribution and fiber arrangement. The distribution and size of fiber entanglements contribute to the formation of carbonaceous particle clusters, which create bulk bridges improving thermal conductivity. Moreover, the arrangement of rock fibers affects density, porosity and thermo-physical properties. In addition, the mixing disrupts the cohesion of fiber bundles with the matrix, affecting compressive modulus and wear behavior. This microstructural defect also fosters abundant third-body source flow, which disturbs the tribological circuit and behavior. Porosities induced by fiber entanglements, having a large and irregular size and distribution on the frictional surface, result in low wear resistance and alter the frictional stability.

ZnO:Er³⁺,Yb³⁺ thin films with a hexagonal wurtzite structure were successfully deposited on Si (111) substrates at 430 °C by an aerosol-assisted chemical vapor deposition (AACVD) atmospheric pressure process. The films were deposited with fixed 3 mol% erbium concentration and various ytterbium concentrations of 6, 8, 9 and 10 mol%. The annealing treatment at 1000 °C was found to enhance the crystallinity and the upconversion (UC) emission of the films. UC emissions were investigated under 980 nm excitation, and the ZnO:Er³⁺,Yb³⁺ films exhibited the intense red 665 nm upconverted emissions of Er³⁺ ions originating from an efficient Yb–Er energy transfer process. The absolute upconversion Quantum Yield (UC-QY) of each film was measured for the UC emissions centered at 410, 540 and 665 nm at varying excitation power densities. UC-QY analysis has revealed that the ZnO:3 mol% Er,9 mol% Yb thin film possesses the highest total quantum yield of 5.59 ± 0.1% with a power density of 19.3 ± 3 W cm⁻². These results show that this film is promising as an efficient upconversion layer suitable for many photonic applications.