For the first time, new sorbents based on polyacrylonitrile (PAN) fiber and transition metal ferrocyanides were obtained. The main difference between the obtained sorbents and the existing ones is the stage of preliminary preparation of the initial support by converting it into the forms PAN-Fe(OH)₃ or PAN-MnO₂, due to which additional ion exchange groups (carboxyl, carbonyl, etc.) are formed, which increases the amount of ferrocyanide fixed to the support. The best components and conditions for the synthesis of new sorbents were determined (concentration (0.1–0.2 mol/L), as well as pH (1 for sorbents based on PAN-Fe(OH)₃, and 1–5—PAN-MnO₂) of potassium ferrocyanide solution, concentration of transition metal salts (0.02 mol/L), temperature conditions). The influence of the studied solution composition (pH, concentration of Na⁺, K⁺, NH₄⁺ ions) on the cesium distribution coefficients during its recovery by the obtained sorbents was assessed. The possibility of cesium recovery from solutions with pH 1–9 containing macro quantities of cations was demonstrated. The sorbents derived were characterized by modern structural methods such as infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy with EDS analysis. A study of the trace amount sorption of ¹³⁷Cs was carried out in comparison with commercially available highly efficient sorbents (FNS-10 and Termoksid-35), and it was shown that the resulting sorbents are not inferior to industrial ferrocyanide sorbents and can be used for ¹³⁷Cs selective sorption from technological solutions and natural waters.

To solve radioecological and oceanological problems (estimate the vertical transport, flows of particulate organic carbon, phosphorus biodynamics, submarine groundwater discharge, etc.), it is necessary to determine the natural values of the radionuclides’ activity in seawater and particulate matter. For the first time, the radionuclides’ sorption from seawater was studied using sorbents based on activated carbon modified with iron(III) ferrocyanide (FIC) and based on activated carbon modified with iron(III) hydroxide (FIC A—activated FIC) obtained by FIC sorbent treatment with sodium hydroxide solution. The possibility of trace amounts of phosphorus, beryllium, and cesium recovery in laboratory conditions has been investigated. Distribution coefficients, dynamic, and total dynamic exchange capacities were determined. The physicochemical regularities (isotherm and kinetics) of sorption have been studied. The results obtained are characterized via Langmuir, Freindlich, and Dubinin–Radushkevich isotherm equations, as well as pseudo-first and pseudo-second-order kinetic models, intraparticle diffusion, and the Elovich model. Under expeditionary conditions, the sorption efficiency of ¹³⁷Cs using FIC sorbent, ⁷Be, ³²P, and ³³P—using FIC A sorbent with a single-column method by adding a stable tracer, as well as the sorption efficiency of radionuclides ²¹⁰Pb and ²³⁴Th with their natural content by FIC A sorbent in a two-column mode from large volumes of seawater was assessed. High values of efficiency of their recovery by the studied sorbents were achieved.

Sorbents based on polyacrylonitrile fiber, containing ferrocyanides of transition metals and manganese oxides (CoMn-PAN and FeMn-PAN) or iron(III) hydroxide (CoFe-PAN) in their structure were obtained, as confirmed by the results of X-ray diffraction and energy-dispersive analyses. The selectivity of the obtained sorbents was investigated, along with their ability to sorb Cs, Ba (as an analog of Ra), P, and Be from various natural media, including river water and seawater with varying salinity of 18.2 and 33.8 ‰. The data show that the sorbents are universal for the recovery of artificial ¹³⁷Cs and natural radionuclides from the natural environments, including complex salt composition (seawater). Researching the obtained sorbents during marine expeditions confirmed the efficiency of the obtained materials based on transition metal ferrocyanides and manganese oxides (CoMn-PAN and FeMn-PAN) for the sorption of ¹³⁷Cs, ⁷Be, ²¹⁰Pb, ²¹⁰Po, ²²⁶Ra, ²²⁸Ra, and ²³⁴Th. Additionally, the sorbent based on transition metal ferrocyanides and iron(III) hydroxide (CoFe-PAN) was effective for the sorption of ¹³⁷Cs, ⁷Be, ³²P, ³³P, ²¹⁰Pb, ²¹⁰Po, and ²³⁴Th. Based on the obtained results, methods for comprehensively determining artificial ¹³⁷Cs and natural radionuclides using these sorbents were developed.

Sorbents based on polyacrylonitrile (PAN) fiber and transition metal ferrocyanides were obtained. The influence of the studied solution composition (pH, concentration of Na+, K+, NH4+ ions) on the cesium distribution coefficients during its recovery by the obtained sorbents was assessed. A study of the trace amount sorption of 137Cs was carried out in comparison with commercially available highly efficient sorbents (FNS-10 and Termoksid-35), and it was shown that the resulting sorbents are not inferior to industrial ferrocyanide sorbents.

During the 71st cruise of the R/V Akademik Oparin in the summer of 2024, we assessed the distributions of dissolved and particulate forms of ²¹⁰Pb and ²¹⁰Po in the Sea of Japan, the Sea of Okhotsk, and the northwestern Pacific Ocean. Quantitative estimates of vertical fluxes were derived based on measured concentrations of suspended particulate matter (SPM) and particulate organic carbon (POC). This study provides the first in situ measurements of these radionuclides and the first estimates of derived fluxes for the Sea of Okhotsk. The study confirmed the existence of two contrasting biogeochemical regimes: a sedimentation regime in the productive waters of the Sea of Okhotsk and a recycling regime in the oligotrophic waters of the open ocean, separated by the dynamic transition zone of the Kuril Islands. The calculated POC fluxes confirmed the high efficiency of the biological pump in the coastal seas. The identified anomalies in the distribution of radionuclides indicate a significant role of lateral transport and the sorption of organic carbon onto mineral particles in shaping vertical fluxes matter.