In this work, we analyze artificial heavy-metal solutions with ferrite nanoparticles. Measurements of adsorption effectiveness of different kinds of particles, pure magnetite or magnetite doped with calcium, cobalt, manganese, or nickel ions, were carried out. A dependence of the adsorption efficiency on the composition of the inorganic core has been observed. Ferrites surfaces were modified by phthalic anhydride (PA), succinic anhydride (SA), acetic anhydride (AA), 3-phosphonopropionic acid (3-PPA), or 16-phosphohexadecanoic acid (16-PHDA) to compare the adsorption capability of the heavy metals Cd, Cu and Pb. The obtained nanoparticles were structurally characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Mössbauer spectroscopy. The amounts of Cd, Cu and Pb were measured out by atomic absorption spectroscopy (AAS) and energy dispersive X-ray (EDX) as comparative techniques. The performed study shows that SA linker appears to be the most effective in the adsorption of heavy metals. Moreover, regarding the influence of the composition of the inorganic core on the detection ability, the most effective ferrite Mn0.5Fe2.5O4 was selected for discussion. The highest heavy-metal adsorption capability and universality was observed for SA as a surface modifier.
This paper refers to research based on tests completed on the adsorption of heavy metal ions (Pb2+, Cu2+, Cd2+) from selected natural liquid samples such as apple, tomato, and potato juices using surface-functionalized Mn ferrite nanoparticles (Mn0.2Fe2.8O4). To determine the most efficient adsorption conditions of these heavy metals, the nanoparticles’ surfaces were modified with five different ligands (phthalic anhydride, succinic anhydride, acetic anhydride, 3-phosphonopropionic acid, and 16-phosphonohexadecanoic acid). To evaluate the success of the adsorption process, the resultant liquid samples were examined for the amount of residuals using the flame atomic absorption spectroscopy method. The Mn ferrite particles selected for these tests were first characterized physicochemically by the following methods: transmission electron microscopy, scanning electron microscopy, X-ray diffraction, IR spectroscopy, Mössbauer spectroscopy.
The Mössbauer spectroscopy was used for the characterization of room temperature magnetic properties of magnetite/maghemite nanoparticles, in respect of surfactant. The studied nanoparticles were obtained using various types of surface stabilizers in order to see if the application of different surfaces substances has an influence on the magnetic response of nanoparticles core. Nanostructures were fabricated by co-precipitation of iron(II) and (III) chlorides in ammonia solution. Five types of organic acids were used for the stabilization of nanoparticles. Obtained nanoparticles were structurally characterized by transmission electron microscopy and X-ray diffraction. Room temperature magnetic behavior was analyzed on the base of conventional and in field (1.3 T) Mössbauer spectroscopy.
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