Metamorphism of uranium deposits and individual uranium minerals

1964 ◽  
Vol 16 (4) ◽  
pp. 404-415 ◽  
Author(s):  
A. I. Tugarinov ◽  
E. V. Bibikova ◽  
S. I. Zykov
Author(s):  
Wensheng Liao ◽  
Weimin Que ◽  
Liming Wang ◽  
Zhiming Du

Abstract In alkaline in-situ leaching uranium, oxygen is the most common oxidizer with bicarbonate as a complexing agent. For those sandstone uranium deposits with strongly reductive capacity or complicated hydrogeological environment, the oxidation by oxygen is low efficiency. An efficient leaching method, therefore, is needed for these uranium deposits. In this study, a typical sandstone uranium deposit which characterizes with high TDS and high chloride content in groundwater and intractable uranium leach is selected to investigate the effects of synergetic oxidation by a strong oxidant with oxygen. Based on the research on batch leach, pressure leach and field trials, the oxidants such as hydrogen peroxide, potassium permanganate and sodium dichloroisocyanurate (NaDCC) are tested. The results of pressure batch leach indicate that synergetic oxidization is achieved by NaDCC in oxygen leaching process. Leaching tests indicate that a minor oxidizer of NaDCC shows good synergetic oxidization with oxygen and leaching effects on uranium minerals. The results also demonstrate that hydrogen peroxide shows no oxidation effects when it is used as a single oxidant. While potassium permanganate shows good oxidation on uranium when it is used as a single oxidant, however, it leads inhibiting effects on oxygen oxidation on uranium minerals. The further field tests are conducted to study the synergetic effects of oxygen with and without sodium dichloroisocyanurate. The preliminary results indicate that a fast leach is observed by the composite oxidants in early stage while no synergetic leach is found after 200 days. Further studies should be conducted in laboratory experiments and pilot scale tests for its potential applications.


Clay Minerals ◽  
2016 ◽  
Vol 51 (4) ◽  
pp. 635-651 ◽  
Author(s):  
Sophie Billon ◽  
Patricia Patrier ◽  
Daniel Beaufort ◽  
Paul Sardini ◽  
Aurélia Wattinne-Morice

AbstractTosudite, a regularly interstratified chlorite-smectite, crystallizes as an alteration mineral of several preexisting Al-bearing silicates (feldspars, kaolin minerals, chlorites) present in arkosic sandstones hosted in uranium deposits in Niger. X-ray diffraction patterns show a sharp superstructure at 29–29.6 Å for an air-dried state and a peak at 30.8–31.6 Å following ethylene glycol solvation. The 060 reflection at 1.507–1.509 Å indicates an overall dioctahedral character, and the very low coefficient of variation of the d00l reflections for the solvated mineral (0.03–0.13) permits validation of the regular interstratification justifying its identification as tosudite. Microprobe analysis allowed specification of the component layers of this mixed-layer mineral. The chlorite is a di-trioctahedral type analogous to sudoite (Si3Al4Mg2(OH)8), and the smectite component is a low-charge montmorillonite type Tosudite is characterized by large Al2O3 and MgO contents and small Fe content; its composition corresponds approximately to the formula where octahedral occupancy is ∼7. Scanning electron microscope (SEM) observations show that tosudite is closely associated with some uranium minerals: tosudite crystallization occurred during a late alteration event which post-dates burial diagenesis and during which uranium was remobilized by Mg-rich oxidizing fluids.


1979 ◽  
Vol 19 (06) ◽  
pp. 393-400 ◽  
Author(s):  
Paul M. Bommer ◽  
Robert S. Schechter

Abstract This paper presents the development and results of a computer model of in-situ uranium leaching. This model uses a streamline-concentration balance approach and is useful with a wide range of reservoirs. It can be used with any type of well system, in a reservoir with or without boundaries, and with any form of discriptive kinetics. The model also includes the effects of dispersion and consumption of oxidant by minerals other than uranium. The effects of well pattern, variable uranium concentrations, and the pattern, variable uranium concentrations, and the presence of oxidant consumers on uranium presence of oxidant consumers on uranium production are discussed. production are discussed. Introduction The sandstone uranium deposits of south Texas represent a possible major energy source. These deposits consist mainly of widely scattered roll fronts (pods) of unoxidized uranium minerals in loosely packed sands. It is thought that these deposits were packed sands. It is thought that these deposits were formed by the downdip migration of groundwater carrying oxidized uranium leached from the host rock, Catahoula Tuff. When the uranium-bearing waters reached a reducing zone, the uranium was precipitated, forming mainly the mineral uraninite, precipitated, forming mainly the mineral uraninite, UO2(). Much of the uranium ore in the area is low grade (less than 0.05% U3 O8) and is at depths of 100 to 1,500 ft.Since 1960, various companies have been mining some of the higher-grade deposits to depths of up to 200 ft, using conventional strip-mining techniques. The concomitant surface disruption is extensive, and the costs of mining and transporting, to a mill such large amounts of material prohibit the utilization of low-grade ore.A mining technique that may overcome these difficulties to some extent and ultimately make more of the south Texas uranium deposits amenable to recovery is in-situ solution mining. This technique consists of pumping through the ore body a chemical solution that will dissolve the uranium minerals so that they may be leached from the ore and recovered from the solution. For this process to be economically feasible, a low-cost solution must be available that will dissolve a large portion of the uranium present, the uranium must be easily recoverable from the leach solution, the physical attributes of the ore body must be such that the leach solution can be pumped through the ore without great loss to the surroundings, and environmental hazards must be avoided.The leaching process and its chemistry are basically simple. Uranium is generally found to have one of two oxidation states - oxidized, U (+6), or unoxidized, U (+4). In the oxidized +6 state, uranium forms many soluble ions, among them the uranyl ion UO2(), the uranyl dicarbonate ion UO2(CO3)(−2), and the uranyl tricarbonate ion UO2(CO3)3(−4). Hostetler and Garrels have investigated the equilibria of uranium minerals with natural solutions and found that under oxidizing conditions, stable soluble ions exist over a wide range of pH. The results suggest that to dissolve uranium minerals, one must provide an oxidizing agent to oxidize reduced uranium to the +6 state and a complexing agent that will form stable complex ions with U+6. A typical set of reactions is as follows:(1) (2) SPEJ P. 393


2020 ◽  
Vol 28 (2) ◽  
pp. 295-306
Author(s):  
Štefan Ferenc ◽  
Eva Hoppanová ◽  
Richard Kopáčik ◽  
Tomáš Mikuš ◽  
Šimon Budzák

Occurrence of infiltration, stratiform U-Cu mineralization Spišská Teplica - Vápenica-Vysová is located approximately 7.8 km SW from the district town Poprad and 4.3 km SW from the centre of Spišská Teplica village (Slovak Republic). Primary U-Cu mineralization is bound to arkosic sandstones with abundant coalified fragments of higher plants (Kravany Beds, Upper Permian, Hronicum Unit) and consists of uraninite and pyrite. The chalcopyrite and Cu-S mineral phase (digenite?, roxbyite?) form inclusions in clastic fluorapatite and zircon. Among supergene minerals, malachite and goethite are absolutely dominant, azurite, zálesíite and baryte are less represented. Phosphate, probably of the florencite group, and acanthite were only rarely found. Supergene uranyl minerals were not detected. Their lack, or their weak development in all uranium deposits in Kozie Chrbty Mts. can be explained as follows: during the weathering of primary ores, the cation UO22+ is released from uraninite and coffinite into supergene solutions (uranyl complexes). However, these solutions come into almost immediate contact with fragments of coalified flora (especially in the case of rich U ores), where UO22+ binds to the organic uranyl complexes (complexation). Only a relatively small part of uranyl cation escapes from this geochemical trap, and in that case supergene uranium minerals may precipitate.


Sign in / Sign up

Export Citation Format

Share Document