This paper investigates the influence of Si content and Si particle morphology on the corrosion protection of anodized oxide layers on Al-Si alloys. Two Al alloys with low Si concentrations (2.43 wt-% and 5.45 wt-%, respectively) were studied and compared with 6082-T6 via electrochemical impedance spectroscopy (EIS) in 3 wt-% NaCl solution prior to oxide layer sealing. Si particles were also modified by the addition of Sr to study the influence of Si particle morphology on the corrosion protection of the oxide layer. The EIS showed that the corrosion protection provided by the oxide layer on Al-Si alloys is significantly affected by the presence of Si particles. Si particles make the oxide layer locally thinner and more defective in the eutectic region, thereby increasing the ease of substrate corrosion attack. However, the addition of Sr can improve the corrosion protection of anodized Al-Si alloys significantly. Furthermore, it was proved that higher Si level influences negatively the anodized oxide corrosion protection due to the higher amount of cracks and defects, but Sr modification is efficient in preventing this negative effect.

This paper aims to investigate the anodising behaviour of Al-Si components produced by rheocasting, to understand the effect of the surface liquid segregation (SLS) on the anodising response. The material investigated was EN AC 42000 Al-alloy with an addition of 150 ppm Sr. The component was rheocast and conventionally liquid cast for benchmarking. The RheoMetal^TM process was used to prepare slurry and subsequently cast using a vertical pressure die casting machine. Prior to anodising, mechanical grinding was used as pre-treatment method for selected samples as comparison with components in the as-cast state. Anodising was performed on the components using a constant controlled voltage at 25 V, in 1 M H₂SO₄, at room temperature. The duration of anodising was varied from 30 mins to 120 mins to examine the relationship between oxide layer thickness and the anodising time. The oxide layer was investigated and characterised. The results demonstrated that the presence of the SLS layer, which was enriched with alloying elements, had a significant influence on the anodising behaviour of the cast component. The oxide layer thickness of the components produced by rheocasting and fully liquid casting was measured and compared. The relations between the oxide layer thickness and anodising time, as well as the casting methods are presented and discussed in this paper.

Four-point bending fatigue tests were performed on semi-solid Al–7Si–Mg castings with varying magnesium contents and heat treatment conditions. Additionally, the effect of anodising on the fatigue resistance of semi-solid Al–7Si–Mg castings was evaluated. Fracture surface and microstructure analysis showed that fatigue crack initiation occurred mainly at the periphery of regions of positive macrosegregation at the casting surface, resulting most likely from exudation. The microstructure of these macrosegregation regions was mostly eutectic and was frequently found surrounded by a layer of oxides. This layer of oxides promoted weak bonding between the macrosegregation region and the surrounding material and acted as a crack initiation site. In this study, primary α-Al globule agglomerates at the casting surface and surrounded by a layer of oxides also promoted fatigue crack initiation. Fatigue resistance of semi-solid Al–7Si–Mg castings in the T5 and T6 conditions increased with the increase in the magnesium content of the alloy from 0.3 to 0.45 wt.% due to the higher precipitation hardening response. However, the increase in the magnesium content from 0.45 to 0.6 wt.% resulted in a slight decrease in the fatigue resistance. The oxide layer formed during anodising had no significant effect on the fatigue resistance of the semi-solid Al–7Si–Mg castings in this study due to the dominant effect of the macrosegregation regions on fatigue crack initiation.

To address the issues of high cutting temperature and insufficient heat dissipation during the machining of γ-TiAl alloys, this study systematically investigates the effects of three cooling strategies—dry cutting, flood cooling, and high-pressure cooling—on tool wear and surface integrity. The variations in tool wear, surface morphology, surface roughness, surface defects, microstructure, and microhardness were analyzed in detail. The experimental results indicate that adhesive wear is the dominant wear mechanism under all three cooling conditions. Owing to its superior penetration capability, high-pressure cooling significantly suppresses tool wear, although it may induce groove wear. In terms of surface integrity, high-pressure cooling significantly improves the machined surface quality while reducing surface defects, plastic deformation, and work hardening. Compared with dry cutting, the surface roughness decreases by approximately 9.1%–39.0%, the thickness of the plastically deformed layer is reduced by up to 50.74%, and the degree of work hardening decreases by approximately 11.5%–14.5%. With increasing cutting speed, the surface roughness, plastically deformed layer thickness, and degree of work hardening increase under all three cooling conditions; however, high-pressure cooling still maintains the best overall performance at high cutting speeds. These results indicate that high-pressure cooling effectively suppresses thermo-mechanical coupling in the cutting zone by enhancing coolant penetration and lubrication, thereby providing an efficient approach to reducing tool wear and improving the surface quality of machined γ-TiAl alloys.