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a b s t r a c tInvestigations into the surface modification of a Ti-15Mo alloy via plasma electrolytic oxidation are reported. The oxidation process was conducted in a solution containing Ca(H 2 PO 2 ) 2 , H 3 PO 4 , or (HCOO) 2 Ca. Anodisation was performed at voltages in the range of 100-400 V. The morphology of the sample surface did not change during alloy oxidation at lower voltages. Higher voltages led to the incorporation of calcium and phosphorus or of calcium only into the formed oxide layer and to significant modification of the surface morphology. Based on the SEM and EDX analysis results, a set of samples was selected for further investigations. To study the surface of the Ti-Mo alloy after anodic oxidation, we used scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), thin-layer X-ray diffraction (TL-XRD), and X-ray photoelectron spectroscopy (XPS). The electrochemical characteristics of the modified alloy in Ringer's solution were determined. Anodisation results in a considerable increase in the corrosion resistance of the Ti-15Mo alloy.

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The electronic components mounted on the printed circuit boards (PCBs) of mobile phones represent a resource that is rich in metals, and after separation from the boards, these components could be considered secondary raw materials. The concentrations of the valuable metals are insignificant when compared with those of complete PCBs; however, they could be significantly higher in a fraction formed from the separated components. This study focused on the analysis of Ag, Au, Cu, Nd, Nb, Ni, Pb, Pd, Sn, and Ta in fractions produced by the separation of all the components mounted on PCBs from several types of mobile phones. Atomic absorption spectrometry, atomic emission spectrometry, and mass spectrometry techniques were utilized, and a comparison of five older models of “brick” phones and five modern smartphones was conducted. Additionally, 50 kg of PCBs from the current recycling market were analyzed in the same way to create a summary of the current recycling stream.