In this work the solid-phase reduction of iron from the Suroyam titanomagnetite ore was studied during metallization in a rotary kiln. The technique of preparation of the ore and reducing agent for metallization and the process of continuous processing of materials in a rotary kiln were described in detail. For metallization the temperature was chosen 1150°C, due to low melting point of apatite from one of the components. The results of the electron microscope analysis of the initial ore and samples subjected to metallization for 1-hour reduction time were presented. The reduction of iron occurred despite absence of pores and contact with a reducing agent in the grains of titanomagnetite. Iron in the grains of titanomagnetite surrounded by apatite was reduced to wustite; whereas, iron surrounded by clinopyroxene was reduced to metallic iron. This indicated the effect of composition of the gangue materials on the reduction process.

Issues with existing vanadium beneficiation stimulate the development of new technologies for wasteless production of vanadium. The present work investigates a possibility of beneficiation of vanadium and titanium oxides in a low-titanium magnetite concentrate by using selective reduction and extraction of iron. Iron was selectively reduced by coal without melting and separated from the oxide (slag) phase during further smelting operation. After the liquid-phase separation vanadium and titanium oxides were accumulated in a slag phase. The following products were produced: slag, containing vanadium and titanium oxides, and iron with relatively low carbon content. The content of vanadium and titanium in a final product has increased in comparison to the initial concentrate.

The direct reduction of metals from a complex oxide with low iron content by solid carbon and indirect reduction by CO gas were studied in a vertical laboratory resistance furnace at 1300 °C for an hour reduction time. The experimental results were described from the point of view of the electrochemical nature of the metal reduction process, that involves the interaction of ions and electrons in the oxide lattice. The technique was developed by using the two different software programs for the quantitative estimation of the areas, average size and number of the metal forming in a complex oxide with extensive fields of vision. The obtained results of the quantitative characteristics of the metal forming during solid-phase carbo-thermal reduction were presented. The processes of reduction by solid carbon and CO gas based on the areas occupied by metal particles were quantitatively compared. The experimental results and the prospects for further experimental work were assessed and outlined.

The possibility of joint solid-phase reduction of iron and phosphorus from ferromanganese ore has been experimentally confirmed. Solid-phase reduction was performed at a temperature of 1000°C and exposure time of 2-5 hours, in a CO atmosphere, also produced the separation of the reduction products by melting. The distribution of iron and phosphorus was studied using an electron scanning microscope. The phase analysis of the samples was studied using a Rigaku Ultima IV X-ray diffractometer. The results were processed using the "Match" software. Reducing roasting in a CO atmosphere provides a transition from the oxide phase to the metallic phase of only iron and phosphorus without loss of manganese, thus increasing the concentration of MnO oxide in the residual oxide phase of the ore.