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Mineralogy of uranium and thorium
\"For students of geology, this book offers a systematic overview of uranium and thorium minerals, which are known for their intense ultraviolet fluorescence and are critically important as our source of nuclear energy. Learn about the geochemical conditions that produce significant ore deposits and view more than 600 maps, structure diagrams, color photos, and electron micrographs. A web link allows readers to view the more than 130 crystal structures in three dimensions for a richer appreciation of their details. The minerals are arranged to emphasize how they fit into chemical groups, and a thorough description is provided for each mineral. Major occurrences of interest to mineral collectors are arranged geographically, with maps showing the important deposits in uranium-producing countries. With the resurgence of interest in nuclear power, this book will be invaluable to mineral collectors and exploration geologists as well as to nuclear scientists and engineers interested in radioactive deposits.\" --Book jacket.
Book
A stable isotope (S, C and O) study of metamorphosed polymetallic sulphide deposits in the Bergslagen district, Sweden: The Stollberg example
The Paleoproterozoic Stollberg Zn-Pb-Ag plus magnetite ore field contains SVALS-type stratabound, limestone-skarn hosted sulphide deposits within volcanic (bimodal felsic and mafic rocks)/volcaniclastic rocks metamorphosed to the amphibolite facies. The sulphide ores consist of semi-massive to disseminated to vein-network sphalerite-galena and pyrrhotite (with subordinate pyrite, chalcopyrite, arsenopyrite and magnetite). Thermochemical considerations and stabilities of minerals in the systems K-Al-Si-O-H and Fe-S-O and sulphur isotope values for sulphides of δ34SVCDT = +1.12 to +5.71 ‰ suggest that sulphur most likely formed by inorganic reduction of seawater sulphate that was carried in hydrothermally modified seawater fluid under the following approximate physicochemical conditions: T = 250o–350 oC, δ34SΣS = +3 ‰, I = ∼1 m NaCl and a total dissolved S content of ∼0.01 to 0.1 moles/kg H2O. However, a magmatic contribution of sulphur cannot be discounted. Carbon and oxygen isotope compositions of calcite in altered rocks spatially associated with mineralisation show values of δ13CVPDB = −2.3 to −0.8 ‰ and δ18OVSMOW = +9.5 to +11.2 ‰, with one anomalous sample exhibiting values of δ13CVPDB = −0.1 ‰ and δ18OVSMOW = +10.9 ‰. Most carbonates in ore show lighter C and O isotope values than those of Proterozoic (Orosirian) limestones and are likely the result of premetamorphic hydrothermal alteration involving modified seawater followed by decarbonation during regional metamorphism. The isotopically light C and O isotope values are consistent with those for carbonates spatially associated with other SVALS-type deposits in the Bergslagen ore district and suggest that such values may be used for exploration purposes.
Journal Article
Wills' Mineral Processing Technology - An Introduction to the Practical Aspects of Ore Treatment and Mineral Recovery (8th Edition)
This book has been the definitive reference for the mineral processing industry for over thirty years. This industry standard reference provides practicing engineers and students of mineral processing, metallurgy, and mining with practical information on all the common techniques used in modern processing installations. Each chapter is dedicated to a major processing procedure-from underlying principles and technologies to the latest developments in strategies and equipment for processing increasingly complex refractory ores. The 8th Edition of this classic reference enhances coverage of practical applications via the inclusion of new material focused on meeting the pressing demand for ever greater operational efficiency, while addressing the pivotal challenges of waste disposal and environmental remediation. Advances in automated mineralogy and analysis and high-pressure grinding rolls are given dedicated coverage. The new edition also contains more detailed discussions of comminution efficiency, classification, modeling, flocculation, reagents, liquid-solid separations, and beneficiation of phosphate, and industrial materials.
eBook
Trace elements and Sr-Nd isotopes of scheelite; implications for the W-Cu-Mo polymetallic mineralization of the Shimensi Deposit, south China
The Shimensi deposit (South China) is a newly discovered W-Cu-Mo polymetallic deposit with a reserve of 0.76 million tones WO3, one of the largest tungsten deposits in the world. We report elemental and Sr-Nd isotopic data for scheelites from the giant deposit, to determine the source region and genesis of the deposit. Scheelite is the most important ore mineral in the Shimensi deposit. Trace elements (including REEs) and Nd-Sr isotopic compositions of scheelites were used to constrain the origin of the mineralizing fluids and metals. Our data reveal that the REEs of scheelite are mainly controlled by the substitution mechanism 3Ca2+ = 2REE3++ ∎Ca, where ∎Ca is a Ca-site vacancy. Scheelites from the Shimensi deposit show negative Eu anomalies in some samples, but positive Eu anomalies in others in the chondrite-normalized REE patterns. The variation of Eu anomalies recorded the ore-forming processes. Considering the close spatial and temporal relationship between the mineralization and porphyritic granite, we think the negative Eu anomalies were inherited from the porphyritic granite and the positive ones from destruction of plagioclase of country rock during fluid-rock interaction. The variation of cathodeluminescence (CL) color of a single scheelite from red to blue and to yellow was likely associated with the increase of REE contents. The scheelites hosted in the Mesozoic porphyritic granite with negative Eu anomalies formed in a primitive ore-forming fluid, whereas the scheelites hosted in Neoproterozoic granite with positive Eu anomalies precipitated in an evolved ore-forming fluid. The high Nb, Ta, LREE contents, and LREE-enriched REE patterns of scheelites from the Shimensi deposit reveal a close relationship with magmatic hydrothermal fluids. The scheelites from the Shimensi deposit are characterized by low εNd(t) values (-6.1 ∼ -8.1) and unusually high and varied initial 87Sr/86Sr ratios (0.7230∼0.7657). The εNd(t) values of scheelites are consistent with those of the Mesozoic porphyritic granite, but the Sr isotopic ratios are significantly higher than those of the granites, and importantly, beyond the Sr isotopic range of normal granites. This suggests that the ore-forming fluids and metals cannot be attributed to the Mesozoic porphyritic granites alone, the local Neoproterozoic Shuangqiaoshan Group schists/gneisses with high Rb/Sr ratios and thus radiogenic Sr isotopic compositions should have contributed to the ore-forming fluids and metals, particularly, in a later stage of ore-forming process, by intense fluid-rock interaction. This is different from a commonly accepted model that the ore-forming fluids and metals were exsolved exclusively from the granite plutons.
Journal Article
Uranium geology of the Middle East and North Africa : resources, exploration and development program
Uranium Geology of the Middle East and North Africa demonstrates mining potential in the MENA region, with a special interest given to Uranium. The formation and origin of uranium deposits is of interest for uranium exploration and is necessary for the long-term sustainability of nuclear energy production. The book proposes a new classification system built on earlier classification with detailed new maps, explanatory diagrams, cross sections, helpful satellite images, etc. In addition, it explains why the occurrences, depositional and geological environments of uranium in the Middle East and North Africa vary from one country to another. Using various related recognition criteria, the book reports the potential uranium provinces in the Middle East and North Africa countries. The definition of these provinces is based on the existing geologic and tectonic settings, along with geochronological sequences and geochemical characteristics.
Book
The trace-element compositions of amphibole, magnetite and ilmenite as potential exploration guides to metamorphosed Proterozoic Cu-Zn±Pb±Au±Ag volcanogenic massive sulfide deposits in Colorado, USA
Orthoamphibole, clinoamphibole and magnetite are common minerals in altered rocks associated spatially with Palaeoproterozoic volcanogenic massive sulfide (VMS) deposits in Colorado, USA and metamorphosed to the amphibolite facies. These altered rocks are dominated by the assemblage orthoamphibole (anthophyllite/gedrite)-cordierite-magnetite±gahnite±sulfides. Magnetite also occurs in granitoids, banded iron formations, quartz garnetite, and in metallic mineralisation consisting of semi-massive pyrite, pyrrhotite, chalcopyrite, and sphalerite with subordinate galena, gahnite and magnetite; amphibole also occurs in amphibolite. The precursor to the anthophyllite/gedrite-cordierite assemblages was probably the assemblage quartz-chlorite formed from hydrothermal ore-bearing fluids (∼250° to 400°C) associated with the formation of metallic minerals in the massive sulfide deposits. Element-element variation diagrams for amphibole, magnetite and ilmenite based on LA-ICP-MS data and Principal Component Analysis (PCA) for orthoamphiboles and magnetite show a broad range of compositions which are primarily dependent upon the nature of the host rock associated spatially with the deposits. Although discrimination plots of Al/(Zn+Ca) vs Cu/(Si+Ca) and Sn/Ga vs Al/Co for magnetite do not indicate a VMS origin, the concentration of Al+Mn together with Ti+V and Sn vs Ti support a hydrothermal rather than a magmatic origin for magnetite. Principal Component Analyses also show that magnetite and orthoamphibole in metamorphosed altered rocks and sulfide zones have distinctive eigenvalues that allow them to be used as prospective pathfinders for VMS deposits in Colorado. This, in conjunction with the contents of Zn and Al in magnetite, Zn and Pb in amphibole, ilmenite and magnetite, the Cu content of orthoamphibole and ilmenite, and possibly the Ga and Sn concentrations of magnetite constitute effective exploration vectors.
Journal Article
Discrete Zr and REE mineralization of the Baerzhe rare-metal deposit, China
Although REE (lanthanides+Sc+Y) mineralization in alkaline silicate systems is commonly accompanied with Zr mineralization worldwide, our understanding of the relationship between Zr and REE mineralization is still incomplete. The Baerzhe deposit in Northeastern China is a reservoir of REE, Nb, Zr, and Be linked to the formation of an Early Cretaceous, silica-saturated, alkaline intrusive complex. In this study, we use in situ laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) analyses of zircon and monazite crystals to constrain the relationship between Zr and REE mineralization at Baerzhe. Three groups of zircon are identified and are differentiated based upon textural observations and compositional characteristics. Type Ia zircons display well-developed oscillatory zoning. Type Ib zircons are darker in cathodoluminescence images and have more irregular zoning and resorption features than type Ia zircons. In addition, type Ib zircons can locally occur as overgrowths on type Ia zircons. Type II zircons contain irregular but translucent cores and rims with oscillatory zoning that are murky brown in color and occur in aggregates. Textural features and compositional data suggest that types Ia and Ib zircon crystallized at the magmatic stage, with type Ia being least-altered and type Ib being strongly altered. Type II zircons, on the other hand, precipitated during the magmatic to magmatic-hydrothermal transition. Whereas the magnitude of the Eu anomaly is moderate in the barren alkaline granite, both magmatic and deuteric zircon exhibit pronounced negative anomalies. Such features are difficult to explain exclusively by feldspar fractionation and could indicate the presence of fluid induced modification of the rocks. Monazite crystals occur mostly through replacement of zircon and sodic amphibole; monazite clusters are also present. Textural and compositional evidence suggests that monazite at Baerzhe is hydrothermal. Types Ia and Ib magmatic zircon yield 207Pb-corrected 206Pb/238U ages of 127.2±1.3 and 125.4±0.7 Ma, respectively. Type II deuteric zircon precipitated at 124.9±0.6 Ma. The chronological data suggest that the magmatic stage of the highly evolved Baerzhe alkaline granite lasted less than two million years. Hydrothermal monazite records a REE mineralization event at 122.8±0.6 Ma, approximately 1 or 2 million years after Zr mineralization. We therefore propose a model in which parental magmas of the Baerzhe pluton underwent extensive magmatic differentiation while residual melts interacted with aqueous hydrothermal fluids. Deuteric zircon precipitated from a hydrosilicate liquid, and subsequent REE mineralization, exemplified by hydrothermal monazite, correlates with hydrothermal metasomatic alteration that postdated the hydrosilicate liquid event. Such interplay between magmatic and hydrothermal processes resulted in the formation of discrete Zr and REE mineralization at Baerzhe.
Journal Article