In this study, for the first time to the best of our knowledge, the new garnets Y_3−xNa_xAl₅O₁₂, Y_3−xK_xAl₅O₁₂, Y₃Al_5−yV_yO_12, and Y_3−xNa_xAl_5−yV_yO₁₂ with various stoichiometric compositions were successfully synthesized by the aqueous sol-gel method. All obtained samples were characterized by X-ray diffraction (XRD) analysis, Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). It was determined from the XRD results that the formation of monophasic Y_3−xNa_xAl₅O₁₂, Y_3−xK_xAl₅O₁₂, Y₃Al_5−yV_yO₁₂, and Y_3−xNa_xAl_5−yV_yO₁₂ garnets is possible only at limited doping levels. The highest substitutional level of doped metal was observed for the YAG doped with sodium (x = 1), and the lowest substitutional level was observed for the YAG doped with vanadium (y = 0.05). Furthermore, the obtained FTIR spectroscopy results were in good agreement with the XRD analysis data, i.e., they confirmed that the YAG is the main crystalline phase in the end products. The SEM was used to study the morphology of the garnets, and the results obtained showed that all synthesized samples were composed of nano-sized agglomerated crystallites.

In the present work, iron–sillenite (Bi₂₅FeO₄₀) was synthesized using a simple solid-state reaction method and characterized. The effects of the synthesis conditions on the phase purity of Bi₂O₃/Fe₃O₄, morphological features, and possible application as an XRD/MRI dual-contrast agent were investigated. For the synthesis, the stoichiometric amounts of Bi₂O₃ and Fe₃O₄ were mixed and subsequently milled in a planetary ball mill for 10 min with a speed of 300 rpm. The milled mixture was calcined at various temperatures (550 $°$C, 700 $°$C, 750 $°$C, 800 $°$C, and 850 $°$C) for 1 h in air at a heating rate of 5 °C/min. For phase identification, powder X-ray diffraction (XRD) analysis was performed and infrared (FTIR) spectra were recorded. The surface morphology of synthesized samples was studied by field-emission scanning electron microscopy (FE-SEM). For the radiopacity measurements, iron–sillenite specimens were synthesized at different temperatures and mixed with different amounts of BaSO₄ and Laponite solution. It was demonstrated that iron–sillenite Bi₂₅FeO₄₀ possessed sufficient radiopacity and could be a potential candidate to meet the requirements of its application as an XRD/MRI dual-contrast agent.