The work is devoted to developing a cost-efficient method for the processing of metallurgical wastes such as oiled mill scale formed upon the mechanical cl

In this work, a new two-stage scalable method for the synthesis of magnetite nanoparticles for biomedical applications is proposed. The influence of the milling time, medium, and surfactants on the formation of the structure, magnetic, and functional properties of magnetite nanoparticles has been studied. Comprehensive investigation of the formation of the structure and properties of magnetite nanoparticles has been carried out using X-ray diffraction analysis, scanning and transmission electron microscopy, Mössbauer spectroscopy, measurements of magnetic properties, specific loss power (SLP), and cytotoxicity. It was shown that the milling medium of water with the addition of trisodium citrate is a harsher milling condition compared to octadecene-1 with the addition of oleic acid. Continuous milling for 50 h allowed to obtain a fraction of colloidally stable nanoparticles at the level of 80–90%. Harsher milling conditions led to the formation of a larger fraction of superparamagnetic particles, which reduced the coercivity and SLP. The maximum SLP value of 1140 W/g was reached by large particles, while nanoparticles had decreased SLP values of 100–190 W/g, which was completely determined by the coercivity dependence. Different synthesis conditions allowed obtaining particles with different cytotoxicity against PC-3 cells.

A program for modeling the hysteretic behavior of permanent magnets based on Nd₂Fe₁₄B alloys and visualizing their domain structure was developed on the basis of a phenomenological approach to the elementary event of magnetization reversal of highly anisotropic uniaxial ferromagnets. It is shown that the magnetostatic interaction between microvolumes of the material leads to cooperative magnetization reversal of microvolumes with the formation of reverse-magnetization channels and interaction domains.