POTENTIAL MINING WASTE FROM AU-PORPHYRY DEPOSIT BIELY VRCH (SLOVAKIA)

Author(s):  
Peter Sottnik
2019 ◽  
Vol 5 (10) ◽  
pp. 153-158
Author(s):  
E.I. Khabarova ◽  
◽  
E.S. Zarubina ◽  
Keyword(s):  

2019 ◽  
Vol 12 ◽  
pp. 114-126 ◽  
Author(s):  
V.I. Usikov ◽  
◽  
L.N. Lipina ◽  
A.V. Alexandrov ◽  
S.I. Korneeva ◽  
...  

2018 ◽  
Vol 8 ◽  
pp. 200-207 ◽  
Author(s):  
N.N. Melnikov ◽  
◽  
V.M. Busyrev ◽  
O.E. Churkin ◽  
◽  
...  
Keyword(s):  

2019 ◽  
Author(s):  
Alec J. Martin ◽  
◽  
Jeffrey D. Keith ◽  
Eric H. Christiansen ◽  
Bart J. Kowallis ◽  
...  

2021 ◽  
Vol 2 (1) ◽  
Author(s):  
Lawrence C. Carter ◽  
Ben J. Williamson ◽  
Simon R. Tapster ◽  
Catia Costa ◽  
Geoffrey W. Grime ◽  
...  

AbstractPorphyry-type deposits are the world’s main source of copper and molybdenum and provide a large proportion of gold and other metals. However, the mechanism by which mineralising fluids are extracted from source magmas and transported upwards into the ore-forming environment is not clearly understood. Here we use field, micro-textural and geochemical techniques to investigate field relationships and samples from a circa 8 km deep cross-section through the archetypal Yerington porphyry district, Nevada. We identify an interconnected network of relatively low-temperature hydrothermal quartz that is connected to mineralised miarolitic cavities within aplite dykes. We propose that porphyry-deposit-forming fluids migrated from evolved, more water-rich internal regions of the underlying Luhr Hill granite via these aplite dykes which contained a permeable magmatic crystal mush of feldspar and quartz. The textures we describe provide petrographic evidence for the transport of fluids through crystal mush dykes. We suggest that this process should be considered in future models for the formation of porphyry- and similar-type deposits.


2020 ◽  
Vol 12 (1) ◽  
pp. 764-790
Author(s):  
Amin Allah Kamali ◽  
Mohsen Moayyed ◽  
Nasir Amel ◽  
Fadaeian Mohammad ◽  
Marco Brenna ◽  
...  

AbstractThe Sungun copper–molybdenum porphyry deposit is located in the north of Varzaghan, northwestern Iran. The Sungun quartz-monzonite is the oldest mineralized intrusive body in the region and was emplaced during the Early Miocene. Eight categories of the late and unmineralized dykes, which include quartz diorite, gabbrodiorite, diorite, dacite, microdiorite and lamprophyre (LAM), intrude the ore deposit. The main mineral phases in the dykes include plagioclase, amphibole and biotite, with minor quartz and apatite and secondary chlorite, epidote, muscovite and sericite. The composition of plagioclase in the quartz diorite dykes (DK1a, DK1b and DK1c) varies from albite-oligoclase to andesine and oligoclase to andesine; in the diorite, it varies from andesine to labradorite; in the LAM, from albite to oligoclase; and in the microdiorite (MDI), it occurs as albite. Amphibole compositions are consistent with classification as hornblende or calcic amphibole. Based on their AlIV value (less than 1.5), amphibole compositions are consistent with an active continental margin affinity. The average percentage of pistacite (Ps) in epidotes formed from alteration of plagioclase and ferromagnesian minerals is 27–23% and 25–30%, respectively. Thermobarometric studies based on amphibole and biotite indicate approximate dyke crystallization temperature of 850–750℃, pressure of 231–336 MPa and high fO2 (>nickel-nickel-oxide buffer). The range of mineral compositions in the postmineralization dyke suite is consistent with a genetic relationship with the subduction of the Neotethys oceanic crust beneath the continental crust of the northwest part of the Central Iranian Structural Zone. Despite the change from calc-alkaline to alkaline magmatism, the dykes are likely related to the late stages of magmatic activity in the subduction system that also generated the porphyry deposit.


2021 ◽  
Vol 13 (4) ◽  
pp. 1866
Author(s):  
Noor Allesya Alis Ramli ◽  
Faradiella Mohd Kusin ◽  
Verma Loretta M. Molahid

Mining waste may contain potential minerals that can act as essential feedstock for long-term carbon sequestration through a mineral carbonation process. This study attempts to identify the mineralogical and chemical composition of iron ore mining waste alongside the effects of particle size, temperature, and pH on carbonation efficiency. The samples were found to be alkaline in nature (pH of 6.9–7.5) and contained small-sized particles of clay and silt, thus indicating their suitability for mineral carbonation reactions. Samples were composed of important silicate minerals needed for the formation of carbonates such as wollastonite, anorthite, diopside, perovskite, johannsenite, and magnesium aluminum silicate, and the Fe-bearing mineral magnetite. The presence of Fe2O3 (39.6–62.9%) and CaO (7.2–15.2%) indicated the potential of the waste to sequester carbon dioxide because these oxides are important divalent cations for mineral carbonation. The use of small-sized mine-waste particles enables the enhancement of carbonation efficiency, i.e., particles of <38 µm showed a greater extent of Fe and Ca carbonation efficiency (between 1.6–6.7%) compared to particles of <63 µm (0.9–5.7%) and 75 µm (0.7–6.0%). Increasing the reaction temperature from 80 °C to 150–200 °C resulted in a higher Fe and Ca carbonation efficiency of some samples between 0.9–5.8% and 0.8–4.0%, respectively. The effect of increasing the pH from 8–12 was notably observed in Fe carbonation efficiency of between 0.7–5.9% (pH 12) compared to 0.6–3.3% (pH 8). Ca carbonation efficiency was moderately observed (0.7–5.5%) as with the increasing pH between 8–10. Therefore, it has been evidenced that mineralogical and chemical composition were of great importance for the mineral carbonation process, and that the effects of particle size, pH, and temperature of iron mining waste were influential in determining carbonation efficiency. Findings would be beneficial for sustaining the mining industry while taking into account the issue of waste production in tackling the global carbon emission concerns.


Author(s):  
Gustavo Ramos Dantés dos Reis ◽  
José Carlos de Oliveira ◽  
Marcus Vinicius Abrahão Porto Silva

2021 ◽  
Vol 771 ◽  
pp. 138482
Author(s):  
Daiane R.S. Cruz ◽  
Iris A.A. Silva ◽  
Rhayza V.M. Oliveira ◽  
Marco A.P. Buzinaro ◽  
Benilde F.O. Costa ◽  
...  

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