Surface engineering of magnesium alloys requires adequate strategies, processes and materials permitting corrosion protection. Liquid formulations containing corrosion inhibitors often are to be optimized according to the demands of the respective substrate and following the service conditions during its application. As an interdisciplinary approach, a combination of several techniques for instantly monitoring or elaborately analyzing the surface state of magnesium was accomplished in order to characterize the performance of new adsorbing sustainable amphiphilic polymers which recently were developed to facilitate a multi-metal corrosion protection approach. The application of established techniques like Contact Angle measurements and X-ray Photoelectron Spectroscopy investigations was supplemented by introducing related and yet faster online-capable and larger-scale techniques like Aerosol Wetting Test and Optically Stimulated Electron Emission. Moreover, an inexpensive setup was configured for scaling the inset and the extent of degradation processes which occur at local electrochemical circuits and lead to hydrogen bubble formation. Using these analytical tools, changes of the surface state of emeried AM50 samples were investigated. Even in contact with water, being a moderate corrosive medium, the online techniques facilitated detecting surface degradation of the unprotected magnesium alloy within * Corresponding author. L. M. G. Gonçalves et al. 283 some seconds. In contrast, following contact with a 1 weight% formulation of a polymeric corrosion inhibitor, surface monitoring indicated a delay of the onset of degradation processes by approximately two orders of magnitude in time. Mainly based on the spectroscopic investigations, the corrosion inhibiting effects of the investigated polymer are attributed to the adsorption of a primary polymer layer with a thickness of a few nanometers which occurs within some seconds. Immersion of magnesium for several hours brings up a protective film with around ten nanometers thickness.

Poly (lactic acid) (PLA) was submitted up to five cycles of extrusion in order to evaluate the effect of mechanical recycling. The material was evaluated under two conditions, thoroughly dried before processing and without drying. The changes in the molecular weight, acidity, thermal properties and coloring were assessed after each extrusion, and with this information, mechanisms of degradation were purposed. Molecular weight was reduced at a maximum of 30% after the most aggressive condition; five cycles without drying, which caused also an increase in acidity due to hydrolysis. Thermal properties were not significantly altered, which in combination to the molecular weight decrease allow to infer the recyclability of PLA. However, the most degraded samples had developed strong yellowing, particularly for samples without drying, which could be a problem for final products.

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