The microcalorimetric hydrogen titration technique combined with conventional volumetric measurements has been used to reveal peculiarities of the hydrogenation of the single-phase TiZrVNbTa equiatomic high-entropy alloy. The alloy has been produced in the form of microfibers by the pendent drop melt extraction technique. Palladium coating of the fibers has been applied to enable first hydrogenation at room temperature without additional activation. An analysis of the obtained data allows us to evaluate the dependence of hydrogenation enthalpy on the hydrogen concentration in the alloy. Three concentration ranges, presumably related to the formation of the hydrogen solid solution, monohydride and dihydride phases, have been identified, and the corresponding ΔH values of about −100, −80 and −60 kJ/mol H₂, respectively, have been determined.

In this work, composites based on a hydride-forming fiber of a multi-principal-component (MPC) Ti₂₀Zr₂₀Nb₂₀V₂₀Hf₂₀ alloy, carbosil, dicumylperoxide and nitrile butadiene rubber (NBR) matrix were obtained. The composites were prepared in a three-stage process including the mixing of elastomeric compounds via a rubber mixing mill and low-temperature vulcanization by heat pressing. Using dynamical mechanical analysis (DMA) and differential scanning calorimetry (DSC) the effect of the metallic filler on the process of carbonization of the composite elastomeric matrix was studied. The microstructure and gas separation properties of the resulting composites were also studied. The results showed that the filler content increase in the elastomeric matrix leads to a noticeable and gradual decrease in the activation energy of the carbonization process, reduces the temperature of this process, and accelerates the growth of the elastic modulus during carbonization. It was shown that the finely dispersed fiber of the MPC acts as an activation center for the process of thermal-oxidative degradation in the elastomeric matrix accompanying the onset of carbonization. The gas permeability values were found to be relatively low and no visible correlation with the MPC alloy content in the composite membrane was observed.