Leonardo Pelcastre

Hot stamping is a forming process widely used in the manufacturing of structural components in automobiles. It is a versatile process that enables the fabrication of complex-shaped components with high strength. It also facilitates the manufacturing of components that incorporate high-strength sections and high-ductility sections, by controlling the cooling rate. The process is versatile in terms of the microstructures and mechanical properties that can be obtained. This versatility, however, puts high demands on the materials pertaining their stability, wear resistance, costs, etc. This study has focused on understanding the effect of temperature on the tribological response of different tool materials when these are exposed to high temperatures. The results show that friction significantly stabilises with increased temperature for most tool steels. One tool steel behaves more unstably at high temperature, and this is attributed to the presence of Cr₇C₃, MoO₃, and VO and severe wear on the workpiece material. The most severe wear on the workpiece is caused by a partially melted interdiffusion layer, which facilitates the detachment of the Al-Si coating and subsequent transfer onto the tool; this effect is maximised at the highest temperatures of the workpiece. An important finding is that friction and material transfer severity decrease as the workpiece temperature decreases, and friction is stabilised as tool temperature increases without minimising wear or the average friction coefficient.

In hot stamping of aluminium, the need for efficient methods to evaluate, compare, and rank lubricants based on their tribological performance is critical in the early stages of selection. Pilot and simulative testing can be costly, time-consuming, and complex, making it inefficient for initial benchmarking. This work aims to develop a test methodology to assess lubricant performance for hot stamping under key operating conditions without fully simulating the forming process. The proposed method distinguishes the impact of temperature on lubricant degradation, friction, wear response, and cleanability. The tests utilised a conventional hot work tool steel and a 6010S aluminium alloy with two commercially available lubricants: a polymeric lubricant and a lubricant containing graphite. The tribological tests involved a reciprocating, sliding flat-on-flat configuration at two temperatures (100 °C and 300 °C). The methodology showed that the graphite-containing lubricant exhibited over a four times lower friction coefficient than the polymer-based lubricant at 10 wt.% concentration and 300 °C. At 100 °C, both lubricants provide lubrication and can be cleaned, but increasing temperature led to a significant decline of both aspects. The observed temperature range where the lubricants degrade was between 120 °C and 170 °C.

Two 4,4′-(hexafluoroisopropylidene)diphthalic anhydride-based thermosetting polyimide formulations with varied amounts of crosslinking sites were compared to understand the influence of crosslinking density on fracture toughness, glass transition temperature and thermal oxidative stability. The thermal and mechanical properties of both materials were investigated through a series of single-edge notched beams, differential scanning calorimetry, dilatometry, weight loss, light optical microscopy and nanoindentation experiments. It was found out that the reduced crosslinking resulted in slightly increased fracture toughness but decreased the Tg of the material. No significant difference could be observed in the thermal oxidative stability with the experimental techniques considered.

The Ni-TiO₂ and Ni-CeO₂ composite coatings with varying hydrophilic/hydrophobic characteristics were fabricated by the electrodeposition method from a tartrate electrolyte at ambient temperature. To meet the requirements of tight regulation by the European Chemicals Agency classifying H₃BO₃ as a substance of very high concern, Rochelle salt was utilized as a buffer solution instead. The novelty of this study was to implement a simple one-step galvanostatic electrodeposition from the low-temperature electrolyte based on a greener buffer compared to traditionally used, aiming to obtain new types of soft-matrix Ni, Ni-CeO₂, and Ni-TiO₂ coatings onto steel or copper substrates. The surface characteristics of electrodeposited nickel composites were evaluated by SEM, EDS, surface contact angle measurements, and XPS. Physiochemical properties of pure Ni, Ni-CeO_2, and Ni-TiO₂ composites, namely, wear resistance, microhardness, microroughness, and photocatalytic activity, were studied. Potentiodynamic polarization, EIS, and ICP-MS analyses were employed to study the long-term corrosion behavior of coatings in a 0.5 M NaCl solution. Superior photocatalytic degradation of methylene blue, 96.2% after 6 h of illumination, was achieved in the case of Ni-TiO₂ composite, while no substantial change in the photocatalytic behavior of the Ni-CeO₂ compared to pure Ni was observed. Both composites demonstrated higher hardness and wear resistance than pure Ni. This study investigates the feasibility of utilizing TiO₂ as a photocatalytic hydrophilicity promoter in the fabrication of composite coatings for various applications.

The present research addresses the effect of surface condition on oxide scale formation at high temperatures such as those experienced during secondary cooling in Continuous Casting. Tests were carried out in clean, as-cast and surfaces covered with casting powder to replicate the oxidation/re-oxidation after the mould. Specimens oxidized at 1000, 1100 and 1200 °C under dry air and water-vapour conditions revealed that the oxide scale formation is strongly influenced by temperature, environmental and surface conditions. The oxide scale thickness increases with temperature alterations in the surface (e.g., as-cast and covered with powder) where oxides and carbonates from the casting powder accelerate oxidation kinetics leading to thick and unstable scales. A high amount of carbon is present on surfaces covered with casting powder where it diffuses through the oxide scale forming CO and CO₂ which lead to stress accumulation that makes scales prone to defects such as pores, voids and micro-cracks. Ultimately, if wüstite remains attached to the steel surface or inside oscillation marks, it may disturb heat transfer during secondary cooling which has deep industrial implications for crack formation and overall casting yield. Therefore, accurate insights on scale type and growth mechanisms could lead to accurate control of its formation during casting.

The findings in this work enhance the understanding of oxidation mechanisms and scale growth at high temperatures of a high strength low alloy (HSLA) steel for improving surface quality during continuous casting. The oxidation phenomenon was investigated under dry air and water vapor atmospheres by heating specimens at 1000, 1100, and 1200 °C at different holding times. Temperature and time had great effects on the kinetics, where faster (i.e., parabolic) oxidation rates were present under water vapor when compared with the dry air condition. Temperature strongly influenced the number of defects, such as pores, voids, gaps and micro-cracks, formed in the oxide scale. A phase analysis confirmed the presence of FeO as the first phase formed at the steel surface, Fe₃O₄ as the middle and thicker phase, and Fe₂O₃ as the last phase formed in the oxide/air interface. The micromechanics of the oxides demonstrated that a combination of phases with high (wüstite) and low plasticity (magnetite and hematite) could also have been the reason for the uneven cooling during Continuous Casting (CC) that resulted in the undesired surface quality of the steel slabs. This work gives a good look at the oxide scale effect on the surface quality of steel slabs through an understanding the kinetics during oxidation.