Additive manufacturing opens new possibilities for designing light-weight structures using aluminium alloys. The microstructure of two Al alloys and their corrosion resistance in NaCl and natural seawater environments were investigated. The newly designed Al-Mn-Cr-Zr based alloy showed a higher corrosion resistance than reference AlSi10Mg alloy in both environments in as printed and heat-treated conditions. The corrosion initiated in the Al matrix along the precipitates in the alloys where the Volta potential difference was found the highest. The coarser microstructure and precipitate composition of the new Al-alloy led to the formation of a resistant passive film which extended the passivity region of the Al-Mn-Cr-Zr alloy compared to the AlSi10Mg alloy. The effect of heat treatment could be seen in the microstructure as more precipitates were found in between the melt pool boundaries, which affected the corrosion initiation and slightly the pitting resistance. Overall, this study shows that a newly designed Al-alloy for additive manufacturing has a suitable corrosion resistance for applications in marine environments.

Direct microscopic observation of the isothermal bainite evolution in terms of nucleation events, the location of the nuclei, as well as their growth is very valuable for the refinement of models predicting the kinetics of bainite transformation. To this aim, the microstructural evolution in a Fe-0.2C-1.5Mn-2.0Cr alloy during isothermal bainite formation at temperatures between 723 K and 923 K is monitored in situ using high temperature laser scanning confocal microscopy (LSCM). Both the nucleation and the growth kinetics of the bainitic plates are analyzed quantitatively. Bainitic plates are observed to nucleate on three different types of locations in the grain: at austenitic grain boundaries, on newly-formed bainite plates and at unspecific sites within the austenite grains. Grain boundary nucleation is observed to be the dominant nucleation mode at all transformation temperatures. The rate of nucleation is found to vary markedly between different austenite grains. The temperature dependence of the average bainite nucleation rate is in qualitative agreement with the classical nucleation theory. Analysis of plate growth reveals that also the lengthening rates of bainite plates differ strongly between different grains. However, the lengthening rates do not seem to be related to the type of nucleation site. Analysis of the temperature dependence of the growth rate shows that the lengthening rates at high temperatures are in line with a diffusional model when a growth barrier of 400 J mol⁻¹ is considered.

Corrosion inhibiting conversion coating formation is triggered by the activity of micro-galvanic couples in the microstructure and subsequent local increase in pH at cathodic sites, which in the case of aluminium alloys are usually intermetallics. Ceria coatings are formed spontaneously upon immersion of aluminium alloys in a cerium conversion coating solution, the high pH gradient in the vicinity of intermetallics drives the local precipitation of ceria conversion compounds. Cu-rich intermetallics demonstrate a highly cathodic nature and have shown the local precipitation reaction to occur readily. Fe-rich intermetallics are, however, weaker cathodes and have shown varied extents of localized deposits and are in focus in the current work. Model cast Al-7wt.%Si alloys have been designed with 1 wt.% Fe, solidified at different cooling rates to achieve two different microstructures, with big and small intermetallics, respectively. Upon subjecting the two microstructures to the same conversion coating treatment (immersion in a 0.1 M CeCl₃ solution) for a short period of 2 h, preferential heavy deposition on the boundaries of the big intermetallics and light deposition on the small intermetallics was observed. Based on these observations, a mechanism of localized coating initiation at these Fe-rich intermetallic particles (IM) is proposed.

An approach involving the quantification of microstructure characterized by different techniques such as SEM, EDS, and SKPFM is statistically treated to provide a deeper insight into the influence of recycling AA6063 on localized corrosion susceptibility. Particularly, the intermetallic particles and the two forms of localized corrosion – pitting and intergranular corrosion are systematically documented, measured, and analyzed. Even trace amounts of Cu and Zn introduced into the alloy from recycling had a remarkable effect on the localized corrosion susceptibility. The study found that the initiation and early evolution of the two localized corrosions are in competition, and the predominance of one over the other is closely linked to the composition of the alloy, and microstructure. Recycled variants with higher trace Cu made the alloy more susceptible to pitting attack whereas higher trace Zn is linked with greater IGC susceptibility. The trace amount of higher Zn addition has a particularly beneficial effect on pitting susceptibility as it reduces the likelihood of pitting even in alloys with a higher trace Cu content. The SKPFM results obtained in this study provided a basis for the circumferential pitting susceptibility around intermetallic particles, as a higher volta potential difference (∆V) implied a higher driving force for corrosion. ∆V differences between the different variants were further explained based on trace recycled element distribution in the microstructure.

In Al–Si–Cu–Fe alloys, localized cerium conversion coating (CeCC) deposition on intermetallic (IM) particles is strongly influenced by surface preparation. Here, we investigate how single-step etching (NaOH only) and multi-step etching and pickling (NaOH + HNO₃​) preparation times affect CeCC nucleation and growth on Cu-rich θ-Al₂Cu and Fe-rich β-Al₅FeSi IMs in directionally solidified Al-7Si-2Cu-1Fe and Al-7Si-1Fe alloys. The reactivity of surface was characterized with AFM–SKPFM and surface coverage of CeCC deposits characterized with SEM. A quantitative analysis was performed to discern the effects of different surface preparation procedures on CeCC deposition. Single-step NaOH activates both IMs but leaves substantial Al(OH)₃​ smut on θ-containing alloys, which elevates local pH yet introduces variability in coating coverage. In contrast, multi-step etching removes smut, ensuring more consistent CeCC on θ-Al₂Cu driven primarily by cathodic activity of the IMs. Fe-rich β-Al₅FeSi IMs exhibit nearly 100% coverage even after a short 30 s NaOH etch and 0.5 h CeCC treatment, whereas Cu-rich θ-Al₂Cu requires 120 s NaOH etching plus HNO₃​ pickling for reliable coverage. Prolonged CeCC times promote lateral deposit growth on both IM types when using single-step NaOH, but such growth is absent for θ-Al₂Cu in multi-step samples. These findings reveal that Al(OH)₃​ smut, coupled with local Volta potential and alkaline microenvironments, governs IM reactivity during conversion coating formation. Accordingly, single-step NaOH is sufficient for Fe-rich alloys, while multi-step etching is recommended for Cu-rich alloys. This work provides insights into optimizing surface preparation for improved and predictable CeCC deposition on distinct intermetallic phases.