The current study focuses on the production of biochars derived from aquatic plants, specifically red seaweed Ahnfeltia and seagrass Zostera and Ruppia, found in brackish lagoons in the Sea of Okhotsk, Sakhalin Island. These biochars were obtained through a stepwise pyrolysis process conducted at temperatures of 500 and 700 °C. The characteristics of the biochars, including their elemental composition, specific surface area, and particle size distribution, were found to be influenced by both the type of biomass used and the pyrolysis temperature. The primary objective of this research was to investigate the potential of these biochars to be used as negative electrodes for lithium ion batteries. Among the various samples we tested, the biochar derived from the macroalgae Ahnfeltia tobuchiensis, produced at 700 °C, exhibited the highest carbon content (70 at%) and nitrogen content (>5 at%). The reversible capacity of this particular biochar was measured to be 391 mAh g⁻¹ during the initial cycles and remained relatively stable at around 300 mAh g⁻¹ after 25 cycles. These findings suggest that biochars derived from aquatic plants have the potential to be utilized as effective electrode materials in lithium ion batteries. The specific properties of the biochar, such as its elemental composition and surface area, play a significant role in determining its electrochemical performance. Further research and optimization of the pyrolysis conditions may lead to the development of biochar-based electrodes with improved capacity and cycling stability, thereby contributing to the advancement of sustainable and environmentally friendly energy storage systems.

A series of sorption materials based on layered double hydroxides (Co-Fe LDH, Ni-Fe LDH, and Zn-Ti LDH) were obtained by a facile and environmentally friendly method of coprecipitation. A low particle size of no more than 10 µm was achieved. The use of transition metals makes it possible to obtain compounds that are mechanically and chemically stable in aggressive environments. XRD analysis revealed that the compounds have a highly organized crystalline structure. Using SEM, it was determined that Co-Fe LDH and Ni-Fe LDH had a loose, highly dispersed surface structure, while Zn-Ti LDH had a monolithic surface structure. U(VI) adsorption on the obtained materials in solutions containing Na₂CO₃, Na₂SO₄, KNO₃, NaCl, K₃PO₄, and NaHCO_3, was studied in batch mode. The degree of purification in the presence of these salts reached 99.9%, while the distribution coefficient K_d reached 10⁵ mL/g. Sorption capacity q_max and equilibrium adsorption constants K_f and K_L for U(VI) adsorption in batch mode (for 24 h) from distilled and seawater were determined using the Freundlich and Langmuir equations. The highest sorption capacity of 101.6 mg/g in seawater and 114.1 mg/g in distilled water was registered for Co-Fe-LDH. The presence of competing ions in seawater can reduce sorption efficiency by up to 40%. The provided research allowed us to conclude that the obtained materials, Co-Fe LDH, Ni-Fe LDH, and Zn-Ti LDH are promising for the sorption removal of U(VI) from aqueous media of medium salinity.