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SOME REGULARITIES OF THE INTERRELATION OF THE GENESIS AND MINERALS DISTRIBUTION IN THE BOWELS 肠内成因与矿物分布相互关系的一些规律
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.04.022
V. Pavlyshyn, D. Chernysh, H. Kulchytska, O. Matkovskyi
Some regularities of the interrelation of the genesis and minerals distribution in the bowels based on the analysis of information on the temporal and spatial distribution of minerals in geological complexes, primarily in Ukraine, were revealed. The distribution of minerals in magmatic complexes, pegmatites, hydrothermalites and metamorphites was studied. The relationship between tectonics and the distribution of minerals is noted. There is a clear direction of the geological development of the earth's crust: the pacification of tectonic processes — the growth of platforms — the differentiation of mineral matter. The number of formed mineral species increased rapidly from Archean to Phanerozoic complexes, from "basaltic" to "crustal" mineral formation, from ultrabasic rocks to acid ones. The Pre-Greenstone crust of Ukrainian Shield (USh) is predominantly represented by plagioclases and pyroxenes; with the development of granitoids, quartz and alkali feldspars joined them. From early to late stages of USh development, the number of species increased by an order of magnitude. Near-Azov megablock is in the first place. Maximum species formation is associated with alkaline magmatism and processes involving volatile components, in particular pegmatite formation. The number of minerals in pegmatites reaches hundreds of species. Mountain building led to the destruction of igneous rocks and the formation of new minerals. The appearance of free oxygen became a powerful factor in mineral formation. Superimposed processes with the supplying of deep fluids contributed to the transformation and redistribution of minerals and the formation of polygenic ores. The distribution of minerals makes it possible to detect typomorphic species for certain processes, which can be used to determine the criteria of mineralization, its scale, and the erosion section of ore bodies. The distribution of various mineral species, and the same species with identified macro- and microdefects, as a result of the conditions of mineral formation, is of practical importance.
通过对以乌克兰为主的地质复合体矿物时空分布资料的分析,揭示了成矿与肠道内矿物分布相互关系的一些规律。研究了岩浆杂岩、伟晶岩、热液岩和变质岩中的矿物分布。指出了构造与矿物分布的关系。地壳的地质发展有一个明确的方向:构造过程的缓和-台地的生长-矿物的分化。从太古宙到显生宙杂岩,从“玄武岩”到“地壳”矿物形成,从超基性岩到酸性岩,形成的矿物种类迅速增加。乌克兰地盾(USh)前绿岩壳以斜长石和辉石为主;随着花岗岩类的发育,石英和碱长石加入其中。从USh发育的早期到后期,物种数量增加了一个数量级。亚速附近的超级大锁排在第一位。大多数物种的形成与碱性岩浆作用和涉及挥发性成分的过程有关,特别是伟晶岩的形成。伟晶岩中的矿物可达数百种。造山导致了火成岩的破坏和新矿物的形成。游离氧的出现成为矿物形成的一个重要因素。深部流体供给的叠加作用促进了矿物的转化和再分配,形成了多成因矿石。矿物的分布使探测某些过程的标型物种成为可能,可用于确定矿化标准、矿化规模和矿体的侵蚀剖面。由于矿物形成的条件,各种矿物的分布,以及具有确定的宏观和微观缺陷的同种矿物的分布,具有重要的实际意义。
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引用次数: 0
NEW DATA ON THE CRYSTAL-CHEMISTRY OF METAMICT MINERALS FROM THE VELYKA VYSKA SYENITE MASSIF (UKRAINIAN SHIELD) 乌克兰盾区velyka vyska正长岩体变质矿物晶体化学新数据
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.04.003
E. Grechanovskaya, I.M. Lunova, S. Kurylo, V. Belskyi
The structural properties and composition of metamict minerals, namely allanite, chevkinite, and britholite, occurring as inclusions in allanite from feldspar syenites of the Velyka Vyska massif (Korsun-Novomyrgorod pluton, Ukrainian Shield) were investigated by X-ray diffraction and electron probe microanalysis (EPMA). The age of the syenites is 1.7-1.8 Ga, which corresponds to their formation ages within the Ukrainian Shield. X-ray analysis shows that of the original samples of chevkinite and allanite give a broad diffraction peak between 16—28° 2Θ as well as Bragg reflections in the region of the most intense reflections of semimetamict allanite and britholite, indicating the metamict state of chevkinite and the semimetamict state of allanite. The content of radioactive Th found in the chevkinite (0.25-0.33 apfu) is higher compared to its amount in allanite (0.024-0.033 apfu). Calculated unit-cell parameters of the chevkinite and allanite samples showed that their structures underwent significant changes after annealing. There is a slight distortion of the chevkinite unit cell related to a decrease in the a and an increase in b and c edges. A decrease in b and the increase in c in the allanite is caused by a redistribution of cations in the structure and an oxidation of iron, Fe2+ → Fe3+, during heating. Thereby the stability of the allanite structure decreases and it ultimately breaks down. The structural sites A and A2 in chevkinite and allanite are mainly occupied by REEs of the cerium group. The amount of Y is minor. The substitution mechanism А2(REE)3+ + М3М2+ → А2Са2+ + М3М3+(allanite) and M2Fe3+ + M3,4Ti4+↔ M2Fe2+ + M3,4Nb5+ (chevkinite) occur. The M2 site in the structure of chevkinite and M3 in allanite contain more Fe2+ than Fe3+. This leads to a weakening of the bonds in their structures, and a stepwise breakdown and partial or total metamictization of their structures. The britholite inclusions in allanite belong to the Y variety. They were probably formed much later than allanite and chevkinite in the Velyka Vyska massif. According to the EPMA results, namely BSE-images and REE content determinations, allanite and chevkinite formed almost simultaneously.
利用x射线衍射和电子探针显微分析(EPMA)研究了乌克兰盾区korson - novmyrgorod岩体长石正长岩中allanite、chevkinite和britholite等变质矿物的结构特征和组成。正长岩年龄为1.7 ~ 1.8 Ga,与它们在乌克兰地盾内的形成年龄相符。x射线分析表明,在原样品中,chevkinite和allanite在16-28°2Θ之间有一个较宽的衍射峰,并且在半异晶allanite和brithite反射最强烈的区域有Bragg反射,表明chevkinite和allanite处于异晶状态。放射性钍的含量(0.25 ~ 0.33 apfu)高于褐纹石(0.024 ~ 0.033 apfu)。计算得到的chevkinite和allanite样品的单胞参数表明,退火后它们的结构发生了显著的变化。由于a边的减少和b边和c边的增加,chevkinite单细胞有轻微的畸变。在加热过程中,由于结构中阳离子的重新分配和铁的氧化(Fe2+→Fe3+),引起了丙烯体中b的减少和c的增加。从而降低了allanite结构的稳定性,最终破坏。雪斑岩和allanite的结构位A和A2主要由铈族稀土元素占据。Y的量很小。出现了А2(REE)3+ + М3М2+→А2Са2+ + М3М3+(allanite)和M2Fe3+ + M3,4Ti4+ (chevkinite)的替代机制。chevkinite结构中的M2位点和allanite结构中的M3位点含Fe2+多于Fe3+。这导致其结构中化学键的减弱,并导致其结构的逐步破坏和部分或全部的甲基化。褐纹岩包裹体属Y型。它们的形成时间可能比Velyka - Vyska地块的allanite和chevkinite晚得多。根据EPMA结果,即bse图像和REE含量测定,allanite和chevkinite几乎同时形成。
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引用次数: 0
FEATURES OF THE FLUID REGIME OF POSTSEDIMENTOGENIC PROCESSES DURING THE FORMATION OF GAS CAPACITY OF THE TRANSCARPATHIAN BASIN (WITHIN THE LIMITS OF UKRAINE) 喀尔巴阡盆地(乌克兰境内)天然气形成过程中沉积后过程的流体体系特征
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.03.099
I. Naumko, M. Pavlyuk, A. Loktiev, Yu.V. Khokha, В.E. Sakhno, Yu.A. Belеts’ka, N. Sava
Gases in migrating paleofluids of the Transcarpathian Basin in Ukraine proper were investigated. Their properties were analyzed using fluid inclusions in minerals and fluids occurring in closed pores of promising gas-bearing rocks. Samples were taken from wells drilled within the Mukachevo (1-Borodivsk-Novosilsk) and Solotvyno (1-Bushtyno, 4-Hrushovo, 1-Danylovo, 28-Solotvyno) depressions. According to the data from mass-spectrometric chemical analysis, methane and its homologues and carbon dioxide were found in the composition of volatile compounds, which coincides with the identified advantage of methane and its homologues, on the one hand, and carbon dioxide, on the other hand, in the natural gases of fields of the Transcarpathian gas-bearing area. Methane (98.2 vol. %), ethane (1.2 vol. %) and propane (0.6 vol. %) are found in fluid inclusions in calcite of veinlet in the rock from the well 28 of the Solotvyno structure, which includes the Solotvyno natural gas field. Only methane is found in closed rock pores. Natural gases of the Solotvyno gas field contain methane (53.86%), ethane (2.65%) and propane + butane (1.34-0.32%). СО2 contents as high as 97.3 vol. % occur in fluid inclusions in calcite of veinlets in rocks of the well 1 at Ruski Komarivtsi of the Mukachevo depression and 100 % in fluid inclusions in zeolite (?) from impregnates in rocks of the well 1 at Bushtyno of the Solotvyno depression. This can be explained by the activity of two different composition paleofluids, namely reduced or oxidating types present in bowels of the Transcarpathian Basin. They are associated with significant amount of reduced compounds (methane and its homologues) or a high concentration of oxidized compounds for their (mainly СО2). This was determined by differences in the composition of the primary high-energy abiogenic deep fluid: hydrocarbon-containing or carbon dioxide-containing. The gas composition of paleofluids indicates that two types of natural gas deposits may exist, mainly hydrocarbon or mainly carbon dioxide rich and, accordingly, the discovery of natural gas fields such as Solotvyno and carbon dioxide – such as Martovo. Hydrocarbon formation over a wide range of conditions and primary material ("oil polygenesis") allows the assessment of oil and gas resources of the region. A polygenetic approach for understanding hydrocarbon formation processes requires a changes in exploration strategy. More geochemical and thermobarometric research as well thermodynamic study of mineral-forming fluids is needed in promising geologic structures of the Transcarpathian gas-bearing area. This necessary, in order to predict possible occurrence of high-energy gas deposits and to determine areas for exploration.
研究了乌克兰境内外喀尔巴阡盆地迁移古流体中的气体。利用矿物中的流体包裹体和有前途的含气岩石封闭孔隙中的流体分析了它们的性质。样品取自Mukachevo (1-Borodivsk-Novosilsk)和Solotvyno (1-Bushtyno, 4-Hrushovo, 1-Danylovo, 28-Solotvyno)凹陷的井。质谱化学分析数据表明,在挥发性化合物组成中发现了甲烷及其同系物和二氧化碳,这与喀尔巴阡盆地外含气区气田天然气中甲烷及其同系物和二氧化碳的优势相吻合。Solotvyno构造(包括Solotvyno气田)28井岩石脉口方解石中的流体包裹体中含有甲烷(98.2% vol. %)、乙烷(1.2 vol. %)和丙烷(0.6 vol. %)。只有甲烷存在于封闭的岩石孔隙中。Solotvyno气田天然气主要含甲烷(53.86%)、乙烷(2.65%)和丙烷+丁烷(1.34-0.32%)。在穆卡切沃凹陷Ruski Komarivtsi 1井岩石中细脉方解石流体包裹体中СО2含量高达97.3%,在Solotvyno凹陷Bushtyno 1井岩石中浸染物沸石流体包裹体中СО2含量高达100%。这可以用两种不同成分古流体的活动来解释,即喀尔巴阡盆地内部存在的还原型或氧化型古流体。它们与大量的还原化合物(甲烷及其同系物)或高浓度的氧化化合物有关(主要是СО2)。这是由主要高能非生物成因深层流体组成的差异决定的:含碳氢化合物或含二氧化碳。古流体气体组成表明可能存在两种类型的天然气矿床,以烃类为主或以富含二氧化碳为主,因此发现了Solotvyno等天然气田和Martovo等二氧化碳气田。油气形成的条件和主要物质范围很广(“石油多成因”),这使得人们可以对该地区的油气资源进行评估。用多成因的方法来理解油气形成过程需要改变勘探策略。在喀尔巴阡外含气区有前景的地质构造中,需要进行更多的地球化学和热压学研究以及成矿流体的热力学研究。这是必要的,以便预测可能出现的高能气体矿床和确定勘探区域。
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引用次数: 0
CHEMICAL COMPOSITION OF WATER FROM THE SOURCES OF THE CARPATHIAN BIOSPHERE RESERVE 喀尔巴阡山脉生物圈保护区水源水的化学成分
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.04.061
N. Kryuchenko, P.S. Paparуga, O. Zhuk, M. Kuhar
The results of research into the sources of carbon dioxide underground water within the Carpathian Biosphere Reserve (CBR) are presented. According to the results of statistical processing of the results of the analysis of the chemical composition of water, the limits of the content of the components of the salt composition — SO42–, Cl–, Ca2+, Mg2+, HCO3–, Na++K+, mineralization, pH value, temperature, as well as СО2 and a comparison with known mineral carbon dioxide were established the waters of the Caucasus — Arzni, Narzan, Borjomi. Possible sources of carbon dioxide inflow into groundwater are given. It has been established that the source of the Kveliv forestry of the Chornohirsky massif of the CBR is similar to the carbonated mineral waters of the Narzan type, the sources of the tracts of Hoverla, Piddil and Krasne Pleso are similar to the carbonated mineral spring of the Borjomi type. The microcomponent composition (As, Pb, Zn, Cd, Cu, V, Cr, F) of the sources of carbonated waters of the CBR was determined, the median content and concentration coefficients were calculated, on the basis of which the source located in the Hoverla tract (the village of Lugi, Chornohirsky massif) was singled out CBR) has a content of cadmium, 20 times, lead — 9 times, and arsenic and chromium — 5 times higher than background. The possibility of enrichment of spring waters with microcomponents due to their inflow into underground waters from polymetallic ore deposits is considered.
本文介绍了喀尔巴阡山脉生物圈保护区(CBR)地下水二氧化碳来源的研究结果。根据对水化学成分分析结果的统计处理结果,确定了高加索- Arzni、Narzan、Borjomi水的盐组成成分- SO42 -、Cl -、Ca2+、Mg2+、HCO3 -、Na++K+、矿化度、pH值、温度以及СО2的限量,并与已知矿物二氧化碳进行了比较。给出了二氧化碳流入地下水的可能来源。研究表明,CBR的Chornohirsky地块Kveliv森林的来源与Narzan型碳酸矿泉水相似,Hoverla、Piddil和Krasne Pleso地块的来源与Borjomi型碳酸矿泉水相似。测定了CBR碳酸水源的微量元素组成(As、Pb、Zn、Cd、Cu、V、Cr、F),计算了中位数含量和浓度系数,在此基础上筛选出位于Hoverla地区(Chornohirsky地块Lugi村)的CBR源镉含量为本底的20倍,铅含量为本底的9倍,砷和铬含量为本底的5倍。考虑了多金属矿床注入地下水的微量成分在泉水中富集的可能性。
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引用次数: 2
THE CHEMICAL AND MINERAL COMPOSITION OF NATURAL ZEOLITES AND THEIR SORPTION PROPERTIES DURING OZONATION WITH DRAIN WATER FROM NUCLEAR POWER PLANTS 天然沸石的化学和矿物组成及其在核电厂污水臭氧化过程中的吸附性能
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.04.084
B. Shabalin, K. Yaroshenko, O. Lavrynenko, O. Pavlenko
The article reveals the regularities of the overall process of ozonolytic destruction of organic components of model drain water from nuclear power plants and sorption of imitators of the main dose-forming radionuclides (Cs — with the isotopic 137Cs label; stable isotopes of Co, Sr, Mn salts) by natural zeolite of the Sokyrnytsky deposit and sorption-reagent compounds — salts of ferrous and manganese (II). The chemical composition of the main elements of zeolite after ozonation with the addition of iron and manganese salts practically does not differ from the composition of natural zeolite. Its phase composition in the ozonation process in the presence of ferrum salts is represented by the main rock-forming mineral clinoptilolite and the secondary mineral — quartz. The main ferrum-containing phase on the zeolite surface is goethite. Secondary phases include Fe(II)-Fe(III) layered double hydroxides (Green Rust) and lepidocrocite, but their relative content is insignificant. For zeolites, after ozonation with the addition of both ferrous and manganese (II) salts, the main phases are clinoptilolite and quartz. Manganese-containing phases on the zeolite surface are represented by hausmannite Mn3O4, manganese (II) oxide, and manganese oxyhydroxide MnO(OH)2. The iron- and manganese-containing phases deposited on the surface of the zeolite in the process of ozonation are mainly characterized by a weakly crystallized or amorphized structure. The main sorbent of dose-forming radionuclides is zeolite, not the iron- and manganese-containing compounds that formed on its surface during ozonolysis. The maximum degree of sorption of 137Cs by zeolite is up to 90% when the concentration of Fe2+ is increased to 50 mg/dm3 or Mn2+ to 100 mg/dm3. The degree of cobalt sorption is 97.5% at the initial typical concentration of competing cations (Fe2+ — 5 mg/dm3; Mn2+ — 10 mg/dm3) and when Mn2+ concentration increases to 100 mg/dm3. The maximum degree of extraction of Sr2+ and Mn2+ is 99.4% and 99.9%, respectively. For effective extraction of 137Cs and Co2+ by zeolite in the ozonation process, an increase in the concentration of competing Fe2+ cations is permissible — 50 mg/dm3; Mn2+ — 100 mg/dm3 in solutions. The efficiency of extraction of Sr2+ and Mn2+ practically does not depend on the concentration of competing cations (Fe2+, Mn2+) in the drain water solutions.
本文用同位素137Cs标记揭示了核电厂模型排水中有机组分的臭氧破坏和主要剂量形成核素(Cs -)仿制品吸附的全过程规律;Sokyrnytsky矿床的天然沸石(Co, Sr, Mn盐的稳定同位素)和吸附试剂化合物-亚铁和锰盐(II)。添加铁和锰盐臭氧化后的沸石的主要元素的化学组成实际上与天然沸石的组成没有什么不同。在含铁盐的臭氧化过程中,其物相组成以主要造岩矿物斜沸石和次生矿物石英为代表。沸石表面主要含铁相为针铁矿。次生相包括Fe(II)-Fe(III)层状双氢氧化物(绿锈)和绢云母,但相对含量不显著。对于沸石,在加入亚铁盐和锰(II)盐的臭氧氧化后,沸石的主要相为斜沸石和石英。沸石表面的含锰相主要为豪斯曼锰矿Mn3O4、氧化锰(II)和氧化锰MnO(OH)2。臭氧化过程中沉积在沸石表面的含铁相和含锰相主要表现为弱结晶或非晶化结构。形成剂量的放射性核素的主要吸附剂是沸石,而不是臭氧分解过程中在沸石表面形成的含铁和含锰的化合物。当Fe2+浓度增加到50 mg/dm3或Mn2+浓度增加到100 mg/dm3时,沸石对137Cs的最大吸附度可达90%。在初始典型竞争阳离子浓度(Fe2+ - 5 mg/dm3;Mn2+ - 10 mg/dm3),当Mn2+浓度增加到100 mg/dm3时。Sr2+和Mn2+的最大萃取度分别为99.4%和99.9%。为了使沸石在臭氧化过程中有效地提取137Cs和Co2+,可以增加竞争Fe2+阳离子的浓度- 50 mg/dm3;溶液中Mn2+ - 100mg /dm3。Sr2+和Mn2+的萃取效率实际上不取决于排水溶液中竞争阳离子(Fe2+, Mn2+)的浓度。
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引用次数: 0
GENETIC SIGNIFICANCE OF VARIATIONS IN THE FACES OF THE SIMPLE FORMS OF TOPAZ CRYSTAL FROM CHAMBER PEGMATITES OF THE KOROSTEN PLUTON (UKRAINIAN SHIELD) 乌克兰盾构岩体室晶岩中黄玉晶面简单形态变异的遗传意义
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.03.040
O. Vovk, I. Naumko, V. Pavlyshyn
Topaz crystal morphology and habit distortion has been studied in various mineral-structural zones of chamber pegmatites of the Korosten pluton, which is located in north-western part of the Ukrainian Shield. It was assumed that the symmetry of the crystals obey the Curie principle. This means that only the symmetry elements common to the crystal and the medium in which it is formed will remain on real polyhedrons. The types of symmetry that contain the axes of infinite order are reduced to the following groups: 1) ∞L∞∞PC is a ball; 2) ∞L∞ is a ball filled with an optically active liquid; 3) L∞∞L2∞PПC is a cylinder; 4) L∞ПС is a rotating cylinder; 5) L∞∞P is a cone; 6) L∞∞L2 is a twisted cylinder; 7) L∞ is a rotating cone. Symmetry of the real fluid-dynamic situation of the mineral-forming medium of topaz-bearing parageneses often evolves in the following way: ∞L∞∞PC → L∞∞P → P. In this case, the flow of the mineral-forming fluid has the symmetry P. The resulting topaz crystals can have P symmetry if their symmetry plane coincides with the flow symmetry plane, otherwise they have no symmetry elements at all. In particular, it is shown for the first crystals that the upper faces grew faster, and their size is smaller than that of the lower ones. Growth was limited by the supply of the necessary fluid to the growing crystal faces. Hence, it follows that the fluid flow was in the direction from top to bottom. If the planes of symmetry of the fluid flow and of the polyhedron do not coincide, then visually triclinic crystals of the second type are formed. They are much more abundant than the ones of the first type. In addition to these two types, polyhedra with external symmetry L2 are found. It is difficult to imagine an environment with such symmetry because; it is unlikely that an attached crystal would grow between two fluid streams moving in opposite directions. Nevertheless, polyhedra flattened along the faces M {110} and less often along l {120} are frequent. That is, they grew in the environment in which the fluid flow moved in a direction parallel to the {110} faces (and less often {120}), in the direction from the smaller faces of a simple forms to the larger ones. The direction of fluid flow is more difficult to establish, with more or less the same development of the faces of the simple form of the topaz crystal.
对位于乌克兰地盾西北部的Korosten岩体室晶岩的不同矿物构造带的黄玉晶体形态和习性畸变进行了研究。假定晶体的对称性遵循居里原理。这意味着只有晶体和形成晶体的介质共有的对称元素才会保留在真正的多面体上。将包含无穷阶轴的对称类型简化为以下几类:1)∞L∞∞PC是一个球;2)∞L∞是一个充满光活性液体的球;3) L∞∞L2∞PПC为圆柱体;4) L∞ПС为旋转气缸;5) L∞∞P为锥;6) L∞∞L2为扭圆柱;7) L∞是一个旋转锥。含黄玉共生石的成矿介质的真实流体动力学情况的对称性往往演变为:∞L∞∞PC→L∞∞P→P。在这种情况下,形成的黄玉晶体具有P对称性,如果其对称面与流动对称面重合,则其晶体具有P对称性,否则根本没有对称元素。特别是,对于第一个晶体,上面的表面生长得更快,并且它们的尺寸比下面的小。生长受到生长晶面所需液体供应的限制。因此,可以得出流体的流动方向是自上而下的。如果流体流动的对称面和多面体的对称面不重合,则在视觉上形成第二种类型的三斜晶体。它们比第一种要丰富得多。除了这两种类型之外,还发现了具有外部对称L2的多面体。很难想象一个如此对称的环境,因为;在两个方向相反的流体流之间不太可能生长附着的晶体。然而,沿M{110}面变平的多面体和沿l{120}面变平的多面体是常见的。也就是说,它们生长的环境中,流体流动的方向与{110}面平行(较少情况下是{120}),从简单形状的小面流向大面。流体的流动方向很难确定,黄玉晶体的简单形态的面或多或少具有相同的发展。
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引用次数: 0
MINERAL COMPOSITION AND ADSORPTION CAPACITY OF PRECIPITATES FORMED DURING OZONATION OF RADIOACTIVELY CONTAMINATED WATER FROM NUCLEAR POWER PLANTS TOWARDS 137Cs 核电厂放射性污染水臭氧化沉淀对137Cs的矿物组成及吸附能力
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.02.060
B. Shabalin, K. Yaroshenko, O. Lavrynenko, N. Mitsiuk
The mineral composition and sorption properties of precipitates formed during ozonation of a model solution simulating nuclear power plant wastewater (total mineralization 7 g/dm3, pH = 11.5, T = 60°C, t = 2 hours) 137Cs were studied. The precipitate is represented by finely dispersed spherical particles of metal oxides ranging in size from 20 to 30 nm, forming microaggregates and their associates of various shapes. The composition of the precipitates, along with X-ray amorphous phases, includes Fe(II)-Fe(III) layered double hydroxides (Green Rust), as well as LDH of mixed composition, in particular Fe-Co, and iron oxyhydroxides — goethite and lepidocrocite. The precipitates also contain manganese-containing phases represented by manganese (IV) hydroxide and manganese (II) carbonate with an admixture of manganese oxides, such as Mn2O3∙H2O, MnO, Mn3O4 (gaussmanite). In the process of ozonation, organic compounds that are part of the solutions undergo destruction, co-precipitation with other components of the solution, which is accompanied by the sorption of 137Cs radionuclides on the surface of mineral particles. An increase in the concentration of Fe2+ and Mn2+ cations by 10 times (up to 50 and 100 mg/dm3, respectively) in wastewater reduces the concentration of 137Cs in the initial solution by 50.5%.
研究了核电厂废水模拟模型溶液(总矿化7 g/dm3, pH = 11.5, T = 60℃,T = 2 h) 137Cs臭氧化过程中沉淀的矿物组成和吸附性能。析出物由细小分散的金属氧化物球形颗粒组成,尺寸从20到30纳米不等,形成微聚集体及其各种形状的伴生物。析出相的组成,连同x射线无定形相,包括Fe(II)-Fe(III)层状双氢氧化物(绿锈),以及混合组成的LDH,特别是Fe- co,铁氧氢氧化物-针铁矿和鳞石。析出相中还含有以氢氧化锰和碳酸锰为代表的含锰相,并掺杂Mn2O3∙H2O、MnO、Mn3O4(高锰矿)等锰氧化物。在臭氧化过程中,作为溶液一部分的有机化合物受到破坏,与溶液的其他组分共沉淀,同时伴随着矿物颗粒表面137Cs放射性核素的吸附。废水中Fe2+和Mn2+阳离子浓度增加10倍(分别达到50和100 mg/dm3),使初始溶液中的137Cs浓度降低50.5%。
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引用次数: 0
MOLYBDENUM MINERALIZATION OF BALKA ZOLOTA Au-Mo DEPOSIT (MIDDLE DNIPRO, UKRAINIAN SHIELD) 乌克兰盾中第聂伯罗BALKA ZOLOTA金钼矿床的钼矿化
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.04.125
V. Sukach, L. Riazantseva, S. Bondarenko, M.S. Kotenko
The Balka Zolota gold-molybdenum deposit is located in the central part of the Solone ore field in the southern part of the Sura greenstone structure of the Middle Dnipro megablock of the Ukrainian Shield. Molybdenum mineralization is confined to the eastern flank of the deposit and is termed as the Solone occurrence. Main questions are address in this study of thе occurrence: i) the discovery and study of the deposit, ii) the composition of wall rock complex, iii) the structural position and localization of molybdenum mineralization, iv) the morphology of ore-bearing zones and ore bodies, (v) the composition of the ores, (vi) the ore mineral associations and the sequence of their formation, (vii) morphological features of molybdenite and (viii) a general analysis on the genesis of molybdenum mineralization. Mining of molybdenum ore of Balka Zolota deposit is possible in the case of output, first of all, gold ores. It can be realized more realistically after the start of mining operations within the Serhiivka gold-molybdenum deposit. Further geological exploration focusing on the Balka Zolota deposit is needed to assess the resources and reserves potential of the gold and molybdenum mineralization, especially on the eastern flank of the deposit.
Balka Zolota金钼矿床位于乌克兰地盾中第聂伯罗巨型岩块苏拉绿岩构造南部的Solone矿田中部。钼矿化局限于矿床的东侧翼,称为索龙赋存。本产状研究的主要问题是:1)矿床的发现与研究,2)围岩复合体的组成,3)钼矿化的构造位置和定位,4)含矿带和矿体的形态,(5)矿石的组成,(6)矿石矿物组合及其形成顺序,(7)辉钼矿的形态特征,(8)钼矿化成因的一般分析。Balka Zolota矿床在产出的情况下可以开采钼矿,首先是金矿。在谢廖夫卡金钼矿床内开始采矿作业后,可以更加现实地实现。今后需要以Balka Zolota矿床为重点进行地质勘探,以评价金矿、钼矿化资源和储量潜力,特别是矿床东侧翼。
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引用次数: 0
GRANITOIDS OF THE ZACHATIVKA-FEDORIVKA ANTICLINE IN THE MANGUSH SYNCLINORIUM: GEOCHEMICAL FEATURES, ORIGIN, AND AGE (AZOV DOMAIN OF THE UKRAINIAN SHIELD) 曼古什向斜扎卡提夫卡-费多里夫卡背斜花岗岩类:地球化学特征、成因和年龄(乌克兰地脉亚速域)
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.01.048
G. Artemenko, L. Stepanyuk, L.S. Dovbysh, B. Borodynya
The Paleoproterozoic crust formation in the Azov domain remains underexplored. In the Neoarchean-Paleoproterozoic, the Azov segment of the Archean crust was fragmented by large rift structures. This stage is associated with the formation of Neoarchean-Paleoproterozoic sedimentary-volcanic complexes of the Central Azov Series (2.76-2.22 Ga) and extensive granitoid magmatism. The research aimed at studying granitoid intrusions in the Zachativka-Fedorivka anticline in the Mangush synclinorium of the Central Azov region from the geochemical perspective. Granitoids of the Zachativka-Fedorivka anticline in the Mangush synclinorium include granitoids and later pegmatoidal granites. Plagiogranitoids are moderate-potassium rocks of the K-Na series, with predominance of Na2O over K2O and low Rb/Sr ratio (0.03). They are divided into plagiogranites with low contents of HFS elements and positive europium anomalies and granodiorites with higher contents of HFS elements and predominantly negative europium anomalies. The U-Pb age of titanite from granodiorites is 2028±47 Ma. This age corresponds to the closure of the U-Pb isotope system of titanite and thus reflects the minimum age of granodiorite. The 207Pb/206Pb age of zircon from granites is 2.07-2.09 Ga. The formation of the Paleoproterozoic granitoids of the Central Azov may be related to the activization of the mantle beneath the Azov domain during the formation of the East Sarmatian orogen at ca. 2.1 Ga. They could have formed because of partial melting of the lower crust because of underplating of mafic melts. The 2.05 Ga old vein bodies of pegmatoidal subalkaline granites, were probably formed at the stage of collision of the Sarmatia and Volga-Ural continents.
亚速域的古元古代地壳形成仍未得到充分研究。在新太古代-古元古代,太古宙亚速段地壳被大型裂谷构造破碎。该阶段与中亚速系(2.76 ~ 2.22 Ga)新太古代—古元古代沉积—火山杂合体的形成和广泛的花岗岩类岩浆活动有关。本研究旨在从地球化学角度研究中亚速地区曼古什向斜Zachativka-Fedorivka背斜中的花岗岩类侵入岩。曼古什向斜中的扎卡蒂夫卡-费多里夫卡背斜的花岗岩类包括花岗类和后来的伟晶花岗岩。斜长花岗岩类为K-Na系列中钾岩石,Na2O优于K2O, Rb/Sr比值低(0.03)。它们分为HFS元素含量低、铕正异常的斜长花岗岩和HFS元素含量高、铕负异常为主的花岗闪长岩。花岗闪长岩中钛矿的U-Pb年龄为2028±47 Ma。该年龄对应于钛矿U-Pb同位素体系的闭合,反映了花岗闪长岩的最小年龄。花岗岩锆石207Pb/206Pb年龄为2.07 ~ 2.09 Ga。中亚速盆地古元古代花岗岩类的形成可能与约2.1 Ga时东萨尔马提亚造山带形成过程中亚速域地幔的活化有关。它们的形成可能是由于镁铁质熔体的下地壳部分融化。2.05 Ga年龄的伟晶状亚碱性花岗岩脉体,可能形成于萨尔马提亚大陆与伏尔加-乌拉尔大陆碰撞阶段。
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引用次数: 0
AGE AND DURATION OF CRYSTALS GROWTH IN CHAMBERS OF VOLYN PEGMATITES (UKRAINIAN SHIELD) volyn伟晶岩室中晶体生长的年龄和持续时间(乌克兰盾)
IF 0.2 Pub Date : 2022-01-01 DOI: 10.15407/mineraljournal.44.04.035
D. Voznyak, L. Stepanyuk, T. Dovbush, O. Vyshnevskyi
Formation of chamber pegmatites is associated with tectonomagmatic activation of the region of their distribution. It should be expected that the granitic chamber pegmatites of Volyn were formed by products of degassing of acidic magma. However, in the growth of quartz of the late generation, the beginning of crystallization of which was about 200ºC, CO2-fluids were involved. They are products of degassing of basic magma, which also took part in the growth of crystals at higher temperatures (˃573ºC). Crystallization of minerals in chambers was long: from 1.75±0.10 billion years (age of protogenetic inclusions of zircon and uraninite in topaz crystals) to 1.39 billion years (age of galena inclusions in late-generation quartz). So, for the first time, it was substantiated that the duration of crystal growth in the chambers of Volyn pegmatites was at least 360±100 million years. Therefore, it is assumed that the growth of crystals in chambers Volyn pegmatites lasted for quite a long time.
室状伟晶岩的形成与其分布区域的构造岩浆活化有关。可以推测,沃林花岗岩室伟晶岩是酸性岩浆脱气作用的产物。而在晚代石英的生长过程中,其结晶开始于200℃左右,涉及co2流体。它们是基性岩浆脱气的产物,这也参与了晶体在高温(573℃)下的生长。室内矿物的结晶时间较长,从黄玉晶体中锆石和铀矿的原生包裹体年龄(1.75±0.10亿年)到晚期石英中方铅矿包裹体年龄(13.9亿年)不等。因此,第一次证实了沃林伟晶岩室中晶体生长的持续时间至少为3.6±1亿年。因此,可以假设沃林伟晶岩室中晶体的生长持续了相当长的时间。
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引用次数: 0
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Mineralogical Journal-Ukraine
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