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Abstract To assess the nature of the post-ore behaviour of uranium in the Namaru deposit (Khiagda ore field), U–Pb isotope systems and the isotopic composition of uranium (234U/238U and 238U/235U) were studied. The studied samples represent different ore zones of the deposit and were collected along cross-sections both vertically and horizontally. Wide variations in the isotopic composition of uranium and U–Pb isotopic age have been established. Deviations of the 234U/238U ratio from equilibrium values, which for some samples exceed 50%, along with significant variations in the isotopic age, indicate that permafrost layer, which covered the catchment areas of paleovalleys with meteoric oxygen-containing waters ca. 2.5 Ma ago, did not lead to preserving uranium ores at the deposit. Uranium migration took place during the Quaternary period. The effective combining the U–Pb dating and 234U/238U data in assessing the post-ore redistribution of uranium made it possible to recognize: removal of uranium from some zones of the ore body and its accompanying redeposition in others. Wide variations in the 238U/235U (137.484–137.851) ratios throughout the entire studied cross-sections can be explained by the different locations of samples relatively to the ore deposition front and change in redox conditions as this front advanced. Depletion of the light isotope 235U in the lower zone of the ore body may be associated with the influence of ascending carbonic waters established in the regional basement. The effect of such waters on uranium-bearing rocks causes predominant leaching of light 235U.

The trend fractionation of the 238U and 235U isotopes and the extent of this process at the oxidative weathering of uranium minerals were evaluated by studying the variations in the U isotope composition of rocks, minerals, and fracture waters sampled in the quarry of the broadly known Tulukuevskoe uranium deposit in the Streltsovskoe ore field, eastern Transbaikalia. In the rock block in question, fine uranium minerals disseminated in the rocks were weathered under the effect of oxidizing fracture waters. Uranium isotope composition was measured in 22 water samples, eleven samples of the mineralized rocks, and eight uranium minerals. High-precision (±0.07‰, 2SD) measurements of the 238U/235U were carried out by MC-ICP-MS, using a 233U–236U double spike. The results involve the 238U/235U and 234U/238U ratios and the overall range of the δ238U variations determined in the rocks and waters (from –0.13 to –1.0‰ and from –0.22 to –0.59‰, respectively). Interaction between the waters and rocks induces U(IV) → U(VI) oxidation, U(VI) transfer into the aqueous phase, and 0.15–0.28‰ enrichment of U dissolved in the water in the 235U isotope. When the pitchblende is replaced by U(VI) minerals, the 238U and 235U isotopes also fractionate with ~0.3‰ enrichment of the younger U(VI) mineral phases in the light 235U isotope. The 238U/235U and 234U/238U ratios are proved to correlate, and hence, the fractionation of the 238U and 235U isotopes and the enrichment of the aqueous phase in the light 235U isotope proceed simultaneously with the well known shift in equilibrium the 238U–234U system with the accumulation of excess amounts of the 234U in the aqueous phase. Uranium leaching from uranium minerals, which is associated with the enrichment of the aqueous phase in excess amounts of the 234U isotope, can be viewed as a process that controls isotope fractionation in the 238U–235U system. This should be taken into account in describing the fractionation mechanism of the 238U and 235U isotopes at U(IV) → U(VI) oxidation. The fractionation of the 238U and 235U isotopes, which results in the isotopic "lightening" of U in the aqueous phase, largely controlled the complicated distribution pattern of the 238U/235U ratio in the quarry. In addition to isotope fractionation, this distribution was likely also affected by isotope exchange between uranium dissolved in the water and uranium in the finely dispersed minerals. The isotopically light uranium of the water could participate in forming U(VI) minerals at lower levels of the quarry.

The production of SC CO2 extracts from different types of biologically active raw materials growing in different soil and climatic conditions has been studied and continues to be studied. The object of this study was the bones of a wild medlar (Mespilus germanica L.) growing in Azerbaijan. The purpose of this study was to determine the optimal technological parameters of extraction. The experimental part of the work included obtaining oil from medlar seeds by supercritical fluid extraction with carbon dioxide at the extraction plant of the company “SITEC” Switzerland at different technological parameters and determining the content of fatty acids by gas-liquid chromatography with mass-selective detection (GC-MS). Data were obtained characterizing the oil yield in a wide range of temperatures (40 …80°C) and pressures (100 …280 bar), as well as its physico-chemical parameters and fatty acid profile. It has been established that the optimal parameters for the extraction process are a pressure of 150-250 bar (preferably 200 bar), a temperature of 40°C, a time of 1 - 1.5 h. The data obtained allow us to get a more complete picture of the biotechnological potential of the local medlar as a raw material for processing by modern extraction methods.

Three groups of industrial uranium deposits that differ in the distribution of lanthanides in U oxides have been recognized. A dependence of the REE distribution type on the Yttrium content and Yttrium index YI = (La + Ce)/Y that controls the formation of REE phases capable of selective accumulation of lanthanides has been discovered. This indicates the important role of crystal–chemical fractionation in the distribution of lanthanides. Preferable accumulation of Sm–Gd by U oxides has been found to occur at relatively low contents of Y. In Proterozoic uranium deposits, the yttrium specialization of oxides predominates, while in most Phanerozoic deposits the lanthanum–cerium specialization is typical. These results extend the possibilities of using REEs in ores for purposes of study of the genesis of various uranium deposits.

The uneven character of the distribution of 18O/16O and 234U/238U values was established in the vertical cross section of the productive sequence of the Dybryn uranium deposit (Vitim uranium-ore region, Buryatia). Both a deficiency and an excess of 234U in relation to the equilibrium 234U/238U ratio in the vertical sequence may provide evidence for the extremely low rate of the infiltration water flow. The behavior of oxygen isotope characteristics for different size fractions of terrigenous rocks provides evidence for active uranium redistribution and openness of the isotope system of this element during interaction of terrigenous–sedimentary rocks with infiltration waters.

The variations in 238U/235U values accompanying mobilization of U by fracture waters from uranium-bearing rocks, in which U occurs as a fine impregnation of oxides and silicates, were studied by the high-precision (±0.07‰) MC–ICP–MS method. Transition of U into the aqueous phase in the oxidized state U(VI) is accompanied by its isotope fractionation with enrichment of dissolved U(VI) in the heavy isotope 238U up to 0.32‰ in relation to the composition of the solid phases. According to the sign, this effect is consistent with the tendency of the behavior of 238U and 235U upon interaction of river waters with rocks of the catchment areas [11] and with the effect observed during oxidation of uraninite by the oxygen-bearing NaHCO3 solution [12].

Isotopic analysis of hydrogen and oxygen was performed using the DeltaPlus mass spectrometer (ThermoQuest, Finnigan). Gaseous hydrogen from water samples was obtained by the decomposition of water on hot powder of metallic chrome at 800 ° C. Determination of the oxygen isotopic composition was based on the method of isotopic balance of water with ee 2 [5]. The δ D and δ 18 e values were determined accurate to 0.3 and 0.2 ‰, respectively. We used the following MAGATE reference samples: OH-1, OH-2, OH-3, and OH-4. All results presented in Figs. 1 and 2 are shown relative to the international standard V-SMOW.

The search for new materials with special optical properties, including luminophores, is basically performed empirically. At the same time on the basis of crystallochemical representations by variation of the anionic and cationic compositions of the phases, purposeful synthesis of compounds with a given structure and physicochemical characteristics can be performed. In this direction a low-temperature modification of calcium orthophosphate [i], which is related to the structural type of the natural mineral whitlockite is of definite interest [2].

Experimental and theoretical investigations have made it possible to define more exactly some features of ice formation on solid surfaces