Objectives:The polyoxometalates are a class of inorganic compounds with controllable shapes and sizes, and with excellent properties that make them attractive for various applications. This study is aimed at the comparative UV and IR spectra of Keggin type polyoxometalates. Methods: Compounds under (UV and IR) investigations were divided into several groups to highlight similarities between compounds or classes of compounds for the same category. There are four types of saturated Keggin structures and six lacunar compounds included in this study. The study begins with the UV investigations on aqueous solutions with 10 -5 M concentration for these compounds. IR spectra were recorded as KBr pressed pellets. Results: The UV spectras presents large strong peaks between 185-195 nm corresponding to W = Od bonds, between 251-268 nm for W-O-W bridge bonds, depending on heteroatom types (As, Sb). The unsaturated cryptand ligand having Co 2+ coordinated presents the most intense peak, due to the involvement of oxygen atoms from terminal W = Od coordinative bonds with high electronic densities in coordination of W-O-Co bond. The IR spectra present many peaks that are associated as follows: for terminal bonds W = Od, 955-970 cm -1 ; for W-O-W bridging bonds, 790-910 cm -1 ; for W-O-As/Sb bonds to heteroatom, 690-760 cm -1 . Vibrations of the bonds between heteroatoms and oxygen (As/Sb-O) appear around 620-660 cm -1 . Conclusions: Similarities appear from the recorded spectra, between compounds of the same class, by category association. Very fi ne displacements of peaks that occur explain the infl uence of heteroatoms, addenda atoms or coordinated cations.

Abstract. Present paper is an experimental study on mass and dimensional stability of components manufactured by additive technology of Fused Deposition Modeling (FDM) from PLA and ABS filaments, components to be subjected to the action of aqueous phosphate/fluoride solutions during the process of surface modification and TiO2 nanotubes development on the surface of titanium based materials by electrochemical anodization. Several specimens were printed with 30% and 100% fill density; we used control samples of PP, PLA and ABS in order to compare the results. The specimens and control samples were in contact with 1M H3PO4 + 0.5 wt% HF electrolyte, for 2 hours and 48 hours. Regarding mass stability we found that the specimens' mass is increasing after exposure to electrolyte, showing absorption on to the material, the mass gain being up to 0.2% from initial mass. Dimensional stability is also questionable; there are modifications of up to 0.05 mm after 48 hours exposure to electrolyte. All of our results lead to the conclusion that, even if FDM has certain advantages in terms of flexibility of design and short design to product time, drawbacks appear in terms of mass and dimensional stability when the printed components work in aqueous acid solutions, raising questions regarding their safe utilization over time.