Understanding of the decisive role of non-isothermal treatment on the interaction mechanism and kinetics of the MoO₃-CuO-Mg-C system is highly relevant for the elaboration of optimal conditions at obtaining Mo-Cu composite powder in the combustion processes. The reduction pathway of copper and molybdenum oxides with combined Mg + C reducing agents at high heating rates from 100 to 5200 K min⁻¹ was delivered. In particular the sequence of the reactions in all the studied binary, ternary and quaternary systems contemporaneously demonstrating the effect of the heating rate on products’ phase composition and microstructure was elucidated. The combination of two highly exothermic and speedy reactions (MoO₃ + 3Mg and CuO + Mg vs. MoO₃ + CuO + 4Mg) led to a slow interaction with weak self-heating (dysynergistic effect) due to a change in the reaction mechanism. Furthermore, it has been shown that upon the simultaneous utilization of the Mg and C reducing agents, the process initiates exclusively with carbothermic reduction, and at relatively high temperatures it continues with magnesiothermic reaction. The effective activation energy values of the magnesiothermic stages of the studied reactions were determined by Kissinger isoconversional method.

The influence of mechano-ultrasonic activation (MUA) and nano-additives (carbon nanotubes-CNT) on the interaction pathway of nickel–aluminum powder mixture at high heating rates was investigated. The optimum conditions of the mechano-ultrasonic activation, along with the phase and structure formation peculiarities of nickel–aluminum and nickel–aluminum–carbon nanotubes mixtures by thermal analysis method, the so-called high-speed temperature scanner (HSTS), were found out. The optimum duration of mechanical and ultrasonic activation aiming to achieve homogeneous distribution in the agitated mixtures was determined. A shift in characteristic temperatures of MUA mixtures by the influence of both heating rate and ultrasound on the Ni + Al interaction pathway for the mechano-activated (1, 3, 5 min) and 1 wt% CNT containing mixtures was observed. The formation patterns of NiAl + Ni₃Al mixture or pure NiAl phase was manifested according to the interaction mechanism (depending on solid–liquid or solid–solid state of intermediates). The effective activation energy values for the Ni + Al exothermic reactions of all studied systems were determined by the isoconversional method of Kissinger.

Understanding of the decisive role of the interaction mechanism and kinetics in the combustion processes is highly relevant for the elaboration of optimal conditions for obtaining Mo-Cu composite powders. From this perspective, the efficient delivery of the reduction mechanism of copper and molybdenum oxides with combined Mg + C reducing agents at high heating rates is crucial to develop a valuable approach for the combustion synthesis of Mo-Cu composite powders. Herein, we shed light on the mechanism of the reactions in all the studied binary, ternary and quaternary systems contemporaneously demonstrating the effect of the heating rate on the conversion degree. The combination of two highly exothermic and speedy reactions (MoO3+3Mg and CuO+Mg vs MoO3+CuO+4Mg) led to a slow interaction with weak self-heating (dysynergistic effect) due to a change in the reaction mechanism. On the other hand, it has been shown that during the simultaneous utilization of the Mg and C reducing agents, the process begins exclusively with carbothermic reduction, and at relatively high temperatures it continues with magnesiothermic one. The effective activation energy values of the magnesiothermic stages of the studied reactions were determined by Kissinger isoconversional method.

Silicon carbide whiskers and fiber-like structures are of keen interest because of their useful mechanical properties at high temperatures, as well as their reinforcing ability in metal and ceramic matrix composites. An interestingly unique approach has been taken in the current work to grow whiskers of silicon carbide-based composite through simultaneous utilization of solution combustion synthesis (SCS) and high-speed temperature scanner (HSTS). In particular, a homogeneous mixture of silicon oxide, carbon and alumina was firstly produced by combustion synthesis of alumina impregnated solution of silicon dioxide gel and alanine in the presence of ammonium nitrate as an auxiliary oxidant. By the next step, the pellet obtained from the SCS product was heated up to 1600^oC by HSTS setup leading to the formation of silicon carbide whiskers in the alumina matrix.

High-entropy refractory alloys (HERA) were synthesized by self-propagating high-temperature synthesis (SHS) using aluminothermic reduction. The amount of reduce

The Ti–6Al–4V alloy was prepared by self-propagating high-temperature synthesis (SHS) through aluminothermic reduction of V2O5. Guided by therm