RadiochemistryPub Date : 2024-10-06DOI: 10.1134/S1066362224040015
L. B. Serezhkina, M. S. Grigoriev, D. S. Mitinа, V. N. Serezhkin
{"title":"Crystal Structure of New Iodacetatouranylates R[UO2(CH2ICOO)3]2·2CH2ICOOH·4H2O (R = Sr or Ba)","authors":"L. B. Serezhkina, M. S. Grigoriev, D. S. Mitinа, V. N. Serezhkin","doi":"10.1134/S1066362224040015","DOIUrl":"10.1134/S1066362224040015","url":null,"abstract":"<p>Synthesis, IR spectroscopic, and X-ray diffraction studies of R[UO<sub>2</sub>(mia)<sub>3</sub>]<sub>2</sub>·2Hmia·4H<sub>2</sub>O crystals, where R = Sr<sup>2+</sup> (<b>I</b>) or Ba<sup>2+</sup> (<b>II</b>), and mia is the monoiodacetate ion CH<sub>2</sub>ICOO<sup>−</sup>, have been carried out. The [UO<sub>2</sub>(mia)<sub>3</sub>]<sup>–</sup> complexes correspond to the crystal chemical formula A(B<sup>01</sup>)<sub>3</sub>, where A = UO<sub>2</sub><sup>2+</sup>, B<sup>01</sup> = mia. It has been established that a common feature of <b>I</b> and <b>II</b> is the presence of trinuclear electrically neutral clusters {R[UO<sub>2</sub>(mia)<sub>3</sub>]<sub>2</sub>(Hmia)<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>}. At the centers of the clusters there are trigonal RO<sub>8</sub> dodecahedra; half of their oxygen atoms belong to four different mia anions of two [UO<sub>2</sub>(mia)<sub>3</sub>]<sup>–</sup> complexes. In addition, each R atom coordinates the oxygen atoms of two water molecules and the carbonyl oxygen atoms of two Hmia molecules. Using the method of molecular Voronoi–Dirichlet polyhedra, an analysis of noncovalent interactions in the structure of <b>I</b> was carried out.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 4","pages":"397 - 404"},"PeriodicalIF":0.9,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142410220","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-10-06DOI: 10.1134/S1066362224040052
A. N. Turanov, V. K. Karandashev, V. E. Baulin, D. V. Baulin
{"title":"Effect of Ionic Liquid on the Extraction of Lanthanides(III) from Nitric Acid Solutions with Phosphoryl-Containing Podands","authors":"A. N. Turanov, V. K. Karandashev, V. E. Baulin, D. V. Baulin","doi":"10.1134/S1066362224040052","DOIUrl":"10.1134/S1066362224040052","url":null,"abstract":"<p>The effect of the ionic liquid, 1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide, on the extraction of lanthanides(III) from nitric acid solutions with phosphoryl-containing podands (2-(2-diphenylphosphoryl)-4-ethylphenoxy)methyl)diphenylphosphine oxide (<b>1</b>), (2-(2-diphenylphosphoryl)-4-ethylphenoxy)ethyl)diphenylphosphine oxide (<b>2</b>), and 2-[2-(diphenylphosphoryl)-4-ethylphenoxy]-<i>N,N</i>-dioctylacetamide (<b>3</b>) was studied. The stoichiometry of the extracted complexes was determined. The efficiency of extraction of lanthanides(III) with solutions of compounds <b>1–3</b> in dichloroethane from nitric acid solutions increases in the order 3 < 2 < 1. It has been established that, when replacing dichloroethane with an ionic liquid as a diluent, the extraction efficiency enhances. The magnitude of this effect decreases in the series of compounds <b>3</b> > <b>2</b> > <b>1</b>. In the case of compound <b>1</b>, the replacement of dichloroethane with an ionic liquid as a solvent is accompanied by a decrease in the extraction of lanthanides(III) at [HNO<sub>3</sub>] > 1.5 M.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 4","pages":"438 - 443"},"PeriodicalIF":0.9,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142410265","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-10-06DOI: 10.1134/S1066362224040131
G. A. Badun, E. M. Zhidkova, M. G. Chernysheva, A. D. Enikeev, M. G. Yakubovskaya, E. A. Lesovaya
{"title":"Preparation of Tritium Labeled Dexamethasone Phosphate and Its Application to Assess the Affinity of Ligands for Glucocorticoid Receptors","authors":"G. A. Badun, E. M. Zhidkova, M. G. Chernysheva, A. D. Enikeev, M. G. Yakubovskaya, E. A. Lesovaya","doi":"10.1134/S1066362224040131","DOIUrl":"10.1134/S1066362224040131","url":null,"abstract":"<p>The possibility of introducing tritium into dexamethasone and dexamethasone phosphate using the thermal activation method was demonstrated. The affinity of ligands for glucocorticoid receptors has been successfully assessed using labeled compounds.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 4","pages":"514 - 521"},"PeriodicalIF":0.9,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142410299","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-10-06DOI: 10.1134/S1066362224040167
N. P. Starovoitov, P. V. Kozlov, I. G. Tananaev, E. S. Braichun, N. A. Stakanova, M. B. Remizov, V. A. Dudkin, V. A. Kazakov, S. V. Korenev, E. V. Polyakov, N. V. Glushkova, E. A. Kinev, S. S. Zyryanov, M. N. Sarychev, A. V. Vasil’ev
{"title":"Evaluation of the Effect of External and Internal Irradiation on the Properties of Vitrified HLW to Substantiate the Safety of Their Environmental Impact","authors":"N. P. Starovoitov, P. V. Kozlov, I. G. Tananaev, E. S. Braichun, N. A. Stakanova, M. B. Remizov, V. A. Dudkin, V. A. Kazakov, S. V. Korenev, E. V. Polyakov, N. V. Glushkova, E. A. Kinev, S. S. Zyryanov, M. N. Sarychev, A. V. Vasil’ev","doi":"10.1134/S1066362224040167","DOIUrl":"10.1134/S1066362224040167","url":null,"abstract":"<p>The results obtained in the initial step of studying the effect of external proton irradiation on the properties and structure of simulated borosilicate and aluminophosphate glasses and of internal irradiation on the active glass arranged in the repository of the radiochemical plant of the Mayak Production Association are reported. These results show that the glass melting technologies used at the Mayak Production Association can reliably ensure the environmental safety of the glass incorporating the high-level waste.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 4","pages":"542 - 556"},"PeriodicalIF":0.9,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142410226","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-10-06DOI: 10.1134/S1066362224040155
L. Y. Jabbarova, I. I. Mustafaev, A. S. Mirzaeva, N. A. Ibadov
{"title":"Influence of Ionizıng Radiation on Physicochemical and Operational Properties of Diesel Fuel with Added Toluene","authors":"L. Y. Jabbarova, I. I. Mustafaev, A. S. Mirzaeva, N. A. Ibadov","doi":"10.1134/S1066362224040155","DOIUrl":"10.1134/S1066362224040155","url":null,"abstract":"<p>Radiation resistance of diesel fuel with the addition of various percentages of toluene was studied. The experiments were carried out for a long time to study the postpolymerization processes. The kinetics of processes during irradiation of pure diesel fuel was studied at the temperature <i>T</i> = 20°C and dose rate <i>P</i> = 0.07 Gy/s in the range of absorbed doses <i>D</i> = 15–150 kGy, and a mixture of toluene with diesel fuel was irradiated within the absorbed dose range <i>D</i> = 24–90 kGy at a toluene concentration of 1, 3, and 5 vol %. Analysis by gas chromatography–mass spectrometric (GC/MS) was performed, and the density, viscosity, and iodine number of the diesel fuel before and after irradiation at various absorbed doses were determined. The kinetics of postpolymerization processes after the end of irradiation shows that the rate of the process and its share in the total polymerization depend on the irradiation time, initial mixture density, and dose. By adding additives (antirads), one can choose the composition of diesel fuel that will better withstand radiation exposure. It is necessary to find the optimal concentration of toluene in the composition of diesel fuel, at which the viscosity and density will not change with an increase in the absorbed dose.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 4","pages":"531 - 541"},"PeriodicalIF":0.9,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142410227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-10-06DOI: 10.1134/S1066362224040064
M. N. Kouraim
{"title":"Treatment of Crude Phosphoric Acid Using Activated Carbon-Based Nanocomposites Integrated with Catalytic Wet Peroxide Oxidation","authors":"M. N. Kouraim","doi":"10.1134/S1066362224040064","DOIUrl":"10.1134/S1066362224040064","url":null,"abstract":"<p>Activated carbon (AC) decorated by silver (Ag/AC) and silica (Ag-Si/AC) nanoparticles was used in the treatment of crude phosphoric acid to remove some inorganic and organic impurities. The effect of time, solid/liquid ratio, temperature, and hydrogen peroxide dose on the phosphoric acid treatment was examined. The catalytic activity and uranium uptake efficiency are improved when carbon structures contain Ag and Si nanoparticles. Uranium and organic matter are removed from crude phosphoric acid more efficiently when crude phosphoric acid is treated with activated carbon decorated by silver (Ag/AC) and silica (Ag-Si/AC) nanoparticles with catalytic wet peroxide oxidation, compared to the treatment with activated carbon only, and at high acid concentration (8 M) and solid/liquid mass ratios (0.001), using unsurpassed H<sub>2</sub>O<sub>2</sub>. The higher removal efficiencies of uranium and organic matter (OM) were attributed to the increased adsorptive interactions between the AC-based adsorbent surfaces and the OM and uranium species.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 4","pages":"444 - 453"},"PeriodicalIF":0.9,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142410260","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-10-06DOI: 10.1134/S1066362224040180
N. A. Bakunov, A. O. Aksenov
{"title":"Determination of 239,240Pu in Caspian Sea Water Using the Sorption–Diffusion Model of the Radionuclide Uptake by Bottom Sediments","authors":"N. A. Bakunov, A. O. Aksenov","doi":"10.1134/S1066362224040180","DOIUrl":"10.1134/S1066362224040180","url":null,"abstract":"<p>The content of global <sup>239,240</sup>Pu in Caspian sea water (1996–2056) was calculated using the sorption–diffusion model of the radionuclide uptake by bottom sediments with the distribution coefficient <i>K</i><sub>d</sub> = 50 × 10<sup>3</sup> and diffusion coefficient <i>D</i> = 0.1 × 10<sup>–7</sup> cm<sup>2</sup>/s. The <sup>239,240</sup>Pu global fallout on the sea was assumed to be equal to the experimental value for the mid-latitude belt of Russia, 60 Bq/m<sup>2</sup>. At the plutonium fallout density on the sea surface of 58 Bq/m<sup>2</sup>, its inventory in the sea <i>Q</i> as of the year 1964 is 21.9 TBq. In 1996, the experimentally determined <sup>239,240</sup>Pu concentration in Caspian sea water was ~20 μBq/L, and the calculation by the model gives 17.8 μBq/L. During the ~30-year migration of global <sup>239,240</sup>Pu, about 93% of the radionuclide passed from the aqueous phase to bottom soils. According to the calculations, the <sup>239,240</sup>Pu concentration in the seawater in the period 1996–2056 will decrease from 17.8 to 10.5 μBq/L, and the <sup>239,240</sup>Pu inventory in the seawater, from 6.3 to 3.7%, of the fallout value. The results were verified using an independent method for <sup>90</sup>Sr monitoring in Caspian sea water and determining the <sup>239,240</sup>Pu/<sup>90</sup>Sr concentration ratio in the water. The results of estimating the <sup>239,240</sup>Pu concentrations in the seawater (2017–2020) by these two methods reasonably agree with each other.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 4","pages":"570 - 575"},"PeriodicalIF":0.9,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142410261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-10-06DOI: 10.1134/S1066362224040118
A. V. Voronina, A. K. Suetina
{"title":"Determination of 137Cs in Natural Water and Waste Streams Using Ferrocyanide Sorbents Based on Various Supports: a Comparative Analysis","authors":"A. V. Voronina, A. K. Suetina","doi":"10.1134/S1066362224040118","DOIUrl":"10.1134/S1066362224040118","url":null,"abstract":"<p>The possibility of using ferrocyanide sorbents NPF-HTD, NPF-C, and T-35 for cesium concentration in the method of <sup>137</sup>Cs determination in natural and waste waters has been investigated. Differences in sorption characteristics of sorbents and conditions of cesium concentration to achieve a chemical yield of 98–99% in the concentrate have been revealed. A variable method for determination of <sup>137</sup>Cs in natural and waste waters has been developed, taking into account the ratio of sample volume and sorbent mass in the column, the efficiency of <sup>137</sup>Cs detection, and the time of concentrate measurement to achieve the minimum detectable activity of <sup>137</sup>Cs in the sample of 0.001–0.01 Bq/L. The method was tested for determination of <sup>137</sup>Cs in waters of natural reservoirs and rivers in the territories of Sverdlovsk oblast and Chelyabinsk oblast, as well as waters of monitoring wells in the territories of long-term storage and disposal of radioactive waste. The data on the composition of river and reservoir waters are presented, and the dependence of the cesium chemical yield into the concentrate on the concentration of macrocomponents in samples is shown.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 4","pages":"493 - 505"},"PeriodicalIF":0.9,"publicationDate":"2024-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142410325","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-07-16DOI: 10.1134/S1066362224030032
I. A. Charushnikova, M. S. Grigoriev, A.M. Fedoseev
{"title":"Neptunium(VI) Nitrate Complexes with Urea and Terpyridine Derivatives","authors":"I. A. Charushnikova, M. S. Grigoriev, A.M. Fedoseev","doi":"10.1134/S1066362224030032","DOIUrl":"10.1134/S1066362224030032","url":null,"abstract":"<p>Two new complex Np(VI) nitrates with carbamoylurea (biuret) and with a derivative of terpyridine (Ph-Terpy) of the composition [(NpO<sub>2</sub>)(biuret)(NO<sub>3</sub>)<sub>2</sub>] (<b>I</b>) and [H<sub>2</sub>(Ph-terpy)(NO<sub>3</sub>)]<sub>2</sub>[NpO<sub>2</sub>(NO<sub>3</sub>)<sub>4</sub>] (<b>II</b>) have been synthesized and structurally characterized. The coordination environment of Np atoms in compounds are distorted hexagonal bipyramids with “yl” oxygen atoms in apical positions. The equatorial plane of the bipyramid in complex <b>I</b> is formed by oxygen atoms of two bidentate NO<sub>3</sub><sup>–</sup> anions and an electroneutral ligand. The equatorial plane of the bipyramid in <b>II</b> is formed by oxygen atoms of two bidentate and two monodentate NO<sub>3</sub><sup>–</sup> anions. The twice protonated Ph-terpy is the basis of the complex cation [H<sub>2</sub>(Ph-terpy)(NO<sub>3</sub>)]<sup>+</sup>.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 3","pages":"310 - 320"},"PeriodicalIF":0.9,"publicationDate":"2024-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141719659","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
RadiochemistryPub Date : 2024-07-16DOI: 10.1134/S1066362224030020
V. N. Serezhkin, M. S. Grigoriev, D. S. Mitinа, V. Yu. Losev, L. B. Serezhkina
{"title":"Structure and IR Spectroscopic Study of Sodium Tris(monoiodacetato)uranilate","authors":"V. N. Serezhkin, M. S. Grigoriev, D. S. Mitinа, V. Yu. Losev, L. B. Serezhkina","doi":"10.1134/S1066362224030020","DOIUrl":"10.1134/S1066362224030020","url":null,"abstract":"<p>NaUO<sub>2</sub>(mia)<sub>3</sub> (<b>I</b>) crystals (mia: monoiodacetate ion CH<sub>2</sub>ICOO<sup>−</sup>) were synthesized and studied by X-ray diffraction and IR spectroscopic analyses. Uranyl-containing complexes [UO<sub>2</sub>(mia)<sub>3</sub>]<sup>–</sup> in the structure correspond to the crystal chemical formula A(B<sup>01</sup>)<sub>3</sub>, where A = UO<sub>2</sub><sup>2+</sup>, B<sup>01</sup> = mia. Using coordination sequences, we analyzed the features of the 3D framework, which is realized in the structure of crystals of <b>I</b> and contains 8 crystallographically nonequivalent U or Na atoms. A semiempirical calculation and comparison of the calculated and experimental vibration frequencies in the IR spectrum of <b>I</b> were performed.</p>","PeriodicalId":747,"journal":{"name":"Radiochemistry","volume":"66 3","pages":"301 - 309"},"PeriodicalIF":0.9,"publicationDate":"2024-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141722292","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}