Surface Stoichiometry and Roughness of a Degraded A380 Alloy after Casting, Technical Cleaning and Packaging

The surface stoichiometry of the degraded surface of a commercial Al–Si casting was investigated. The die-cast component was previously stored in a sealed plastic envelope. After that, surface stains in the form of white layers were observed. X-ray photoelectron spectroscopy (XPS) was used to study these layers. For comparison, a seemingly unaffected area as well as a freshly cut surface of the casting were also analysed. In order to additionally assess the surface condition, surface roughnesses were measured. Based on the binding energies (BEs) of the Al and O in the XPS spectra, and the stoichiometric results, it was concluded that the surface layers of the degraded and undegraded samples consist mostly of aluminium oxide and aluminium hydroxide. Furthermore, sodium phosphate from the leftover detergent and silicon oxide were detected in both analysed areas. Analyses of the Al KLL Auger transition were used to corroborate this. The relative shares of Al oxide vs. hydroxide based on the elemental concentrations were determined. The chemical compositions and chemical states of the elements in the top layers were thus obtained. The combination of surface-sensitive analytical techniques was found to be a suitable tool for the ex-post identification of the source of defects

Surface Analysis of Biodegradable Mg-Alloys after Immersion in Simulated Body Fluid

Two binary biodegradable Mg-alloys and one ternary biodegradable Mg-alloy (Mg-0.3Ca, Mg-5Zn and Mg-5Zn-0.3Ca, all in wt%) were investigated. Surface-sensitive X-ray photoelectron spectroscopy analyses (XPS) of the alloy surfaces before and after immersion in simulated body fluid (SBF) were performed. The XPS analysis of the samples before the immersion in SBF revealed that the top layer of the alloy might have a non-homogeneous composition relative to the bulk. Degradation during the SBF immersion testing was monitored by measuring the evolution of H2. It was possible to evaluate the thickness of the sample degradation layers after the SBF immersion based on scanning electron microscopy (SEM) of the tilted sample. The thickness was in the order of 10-100 µm. The typical bio-corrosion products of all of the investigated alloys consisted of Mg, Ca, P and O, which suggests the formation of apatite (calcium phosphate hydroxide), magnesium hydrogen phosphate hydrate and magnesium hydroxide. The bioapplicability of the analyzed alloys with regard to surface composition and degradation kinetics is discussed