Chapter 11: The Telfer Gold-Copper Deposit, Paterson Province, Western Australia

2020 ◽  
pp. 227-249
Author(s):  
Alan J. Wilson ◽  
Nick Lisowiec ◽  
Cameron Switzer ◽  
Anthony C. Harris ◽  
Robert A. Creaser ◽  
...  

Abstract The giant (>20 Moz) Telfer Au-Cu deposit is located in the Paterson Province of Western Australia and is hosted by complexly deformed marine Neoproterozoic metasedimentary siltstones and quartz arenites. The Telfer district also contains magnetite- and ilmenite-series granitoids dated between ca. 645 and 600 Ma and a world-class W skarn deposit associated with the reduced, ~604 Ma O’Callaghans granite. Based on monazite and xenotime U-Pb geochronology, Telfer is estimated to be older than O’Callaghans, forming between 645 and 620 Ma. Au-Cu mineralization at Telfer is hosted in multistage, bedding-parallel quartz-dolomite-pyrite-chalcopyrite reefs and related discordant veins and stockworks of similar composition that were emplaced into two NW-striking doubly plunging anticlines or domes. Mineralization is late orogenic in timing, with hot (≤460°C), saline (<50 wt % NaCl equiv) ore fluids channeled into preexisting domes along a series of shallow, ENE-verging thrust faults and associated fault-propagated fold corridors. A combination of fault-propagated fold corridors acting as fluid conduits below the apex of the Telfer domes and the rheology and chemical contrast between interbedded siltstone and quartz arenite units within the dome are considered key parameters in the formation of the Telfer deposit. Based on the presence of the reduced Au-Cu-W-Bi-Te-Sn-Co-As assemblage, saline and carbonic, high-temperature hydrothermal fluids in Telfer ore, and widespread ilmenite-series granites locally associated with W skarn mineralization, Telfer is considered to be a distal, intrusion-related gold deposit, the high copper content of which may be explained by the predominance of highly saline, magmatic fluids in gangue assemblages cogenetic with ore.

2018 ◽  
Vol 29 (6) ◽  
pp. 1323-1330 ◽  
Author(s):  
Xiran Wang ◽  
Shizhong Wei ◽  
Liujie Xu ◽  
Jiwen Li ◽  
Xiuqing Li ◽  
...  

1998 ◽  
Vol 26 (5) ◽  
pp. 628-635 ◽  
Author(s):  
Anna Giovanetti ◽  
Luisa Rossi ◽  
Mariateresa Mancuso ◽  
Carmine C. Lombardi ◽  
Maria Rita Marasco ◽  
...  

Nanomaterials ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 1551 ◽  
Author(s):  
Torregrosa-Rivero ◽  
Moreno-Marcos ◽  
Albaladejo-Fuentes ◽  
Sánchez-Adsuar ◽  
Illán-Gómez

BaFe1-xCuxO3 perovskites (x = 0, 0.1, 0.3 and 0.4) have been synthetized, characterized and tested for soot oxidation in both Diesel and Gasoline Direct Injection (GDI) exhaust conditions. The catalysts have been characterized by BET, ICP-OES, SEM-EDX, XRD, XPS, H2-TPR and O2-TPD and the results indicate the incorporation of copper in the perovskite lattice which leads to: i) the deformation of the initial hexagonal perovskite structure for the catalyst with the lowest copper content (BFC1), ii) the modification to cubic from hexagonal structure for the high copper content catalysts (BFC3 and BFC4), iii) the creation of a minority segregated phase, BaOx-CuOx, in the highest copper content catalyst (BFC4), iv) the rise in the quantity of oxygen vacancies/defects for the catalysts BFC3 and BFC4, and v) the reduction in the amount of O2 released in the course of the O2-TPD tests as the copper content increases. The BaFe1-xCuxO3 perovskites catalyze both the NO2-assisted diesel soot oxidation (500 ppm NO, 5% O2) and, to a lesser extent, the soot oxidation under fuel cuts GDI operation conditions (1% O2). BFC0 is the most active catalysts as the activity seems to be mainly related with the amount of O2 evolved during an. O2-TPD, which decreases with copper content.


2005 ◽  
Vol 36 (2) ◽  
pp. 455-458 ◽  
Author(s):  
Gang Duan ◽  
Donghua Xu ◽  
William L. Johnson

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