In modern energy, various technologies for absorbing carbon dioxide from the atmosphere are being considered, including photosynthetic microalgae. An important task is to obtain maximum productivity at high concentrations of CO₂ in gas–air mixtures. In this regard, the aim of the investigation is to study the effect of light intensity on the biomass growth and biochemical composition of five different microalgae strains: Arthrospira platensis, Chlorella ellipsoidea, Chlorella vulgaris, Gloeotila pulchra, and Elliptochloris subsphaerica. To assess the viability of microalgae cells, the method of cytochemical staining with methylene blue, which enables identifying dead cells during microscopy, was used. The microalgae were cultivated at 6% CO₂ and five different intensities: 80, 120, 160, 200, and 245 μmol quanta·m⁻²·s⁻¹. The maximum growth rate among all strains was obtained for C. vulgaris (0.78 g·L⁻¹·d⁻¹) at an illumination intensity of 245 µmol quanta·m⁻²·s⁻¹. For E. subsphaerica and A. platensis, similar results (approximately 0.59 and 0.25 g·L⁻¹·d⁻¹ for each strain) were obtained at an illumination intensity of 160 and 245 µmol quanta·m⁻²·s⁻¹. A decrease in protein content with an increase in illumination was noted for C. vulgaris (from 61.0 to 46.6%) and A. platensis (from 43.8 to 33.6%), and a slight increase in lipid content was shown by A. platensis (from 17.8 to 21.4%). The possibility of increasing microalgae biomass productivity by increasing illumination has been demonstrated. This result can also be considered as showing potential for enhanced lipid microalgae production for biodiesel applications.

Ball-milled hydroreactive powders of Mg-Al scrap with 20 wt.% additive (Wood’s alloy, KCl, and their mixture) and with no additives were manufactured. Their hydrogen yields and reaction rates in a 3.5 wt.% NaCl aqueous solution at 15–35 °C were compared. In the beginning of the reaction, samples with KCl (20 wt.%) and Wood’s alloy (10 wt.%) with KCl (10 wt.%) provided the highest and second-highest reaction rates, respectively. However, their hydrogen yields after 4 h were correspondingly the lowest and second-lowest percentages—(45.6 ± 4.4)% and (56.0 ± 1.2)% at 35 °C. At the same temperature, samples with 20 wt.% Wood’s alloy and with no additives demonstrated the highest hydrogen yields of (73.5 ± 10.0)% and (70.6 ± 2.5)%, correspondingly, while their respective maximum reaction rates were the lowest and second-lowest. The variations in reaction kinetics for the powders can be explained by the difference in their particle sizes (apparently affecting specific surface area), the crystal lattice defects accumulated during ball milling, favoring pitting corrosion, the morphology of the solid reaction product covering the particles, and the contradicting effects from the potential formation of reaction-enhancing microgalvanic cells intended to induce anodic dissolution of Mg in conductive media and reaction-hindering crystal-grain-screening compounds of the alloy and metal scrap components.

In this investigation, composite materials were manufactured of mixed scrap of Mg-based alloys and low melting point Sn–Pb eutectic by high energy ball milling, and their hydrogen generation performance was tested in NaCl solution. The effects of the ball milling duration and additive content on their microstructure and reactivity were investigated. Scanning electron microscopy (SEM) analysis indicated notable structural transformations of the particles during ball milling, and X-ray diffraction analysis (XRD) proved the formation of new intermetallic phases Mg₂Sn and Mg₂Pb, which were aimed to augment galvanic corrosion of the base metal. The dependency of the material’s reactivity on the activation time and additive content occurred to be non-monotonic. For all tested samples ball milling during the 1 h provided, the highest hydrogen generation rates and yields as compared to 0.5 and 2 h and compositions with 5 wt.% of the Sn–Pb alloy, demonstrated higher reactivity than those with 0, 2.5, and 10 wt.%.

This study is devoted to the hydrothermal oxidation of aluminum—the exothermic process in which hydrogen and aluminum oxide (or hydroxide) are produced. In this work, the influence of the chemical purity of aluminum on the conversion degree of coarse aluminum at hydrothermal oxidation was studied. Distilled water and coarse granules of aluminum with an average size of ~7–10 mm and three different aluminum purities—99.7, 99.9, and 99.99%—were used in the experiments. The oxidation experiments were carried out inside a 5 liter autoclave in an isothermal mode at temperatures from 200 to 280 °C, with a step of 20 °C. The holding time at the set temperature varied from 4 to 10 h. It was shown that the chemical purity of aluminum considerably influences the oxidation kinetics. More chemically pure aluminum oxidizes much faster, e.g., at a temperature of 280 °C and a holding time of 10 h, the conversion degree of granules with a chemical purity of 99.9% and 99.7% was less than 2%, while 99.99% aluminum was almost fully oxidized. The conversion degree of 99.99% aluminum decreased with the reduction in temperature and holding time, to 66–68% at 280 °C, 4 h, and 2–3% at 200 °C, 10 h.

The process of advanced aluminum-alumina powders production for selective laser melting was studied. The economically effective method of obtaining aluminum-alumina powdery composites for further selective laser melting was comprehensively studied. The aluminum powders with 10–20 wt. % alumina content were obtained by oxidation of aluminum in water. Aluminum oxidation was carried out at ≤200 °C. The oxidized powders were further dried at 120 °C and calcined at 600 °C. Four oxidation modes with different process temperatures (120–200 °C) and pressures (0.15–1.80 MPa) were investigated. Parameters of aluminum powders oxidation to obtain composites with 10.0, 14.5, 17.4, and 20.0 wt. % alumina have been determined. The alumina content, particle morphology, and particle size distribution for the obtained aluminum-alumina powdery composites were studied by XRD, SEM, laser diffraction, and volumetric methods. According to the obtained characteristics of aluminum-alumina powdery composites, they are suitable for the SLM process.