Abstract A multi-methodical characterization of a sauconite (Zn-bearing trioctahedral smectite) specimen from the Skorpion ore deposit (Namibia) was performed by combining X-ray powder diffraction (XRPD), cation exchange capacity (CEC) analysis, differential thermal analysis (DTA), thermo-gravimetry (TG), Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM-HRTEM-AEM). The X-ray diffraction pattern exhibits the typical features of turbostratic stacking disorder with symmetrical basal 00l reflections and long-tailed hk bands, as confirmed by TEM observations. Besides sauconite, the sample contains minor amounts of kaolinite, dioctahedral smectite, and quartz. CEC analysis provides a total of Ca (~69%), Mg (~26%), Na (~4%), and K (0.7%) exchangeable cations. Therefore, Zn is located exclusively within the octahedral site of sauconite. TG analysis of the sample yields a total mass loss of about 17%. Three endothermic peaks can be observed in the DTA curve, associated with dehydration and dehydroxylation of the material. An exothermic peak at 820 °C is also present as a consequence of decomposition and recrystallization. The infrared spectrum shows the typical Zn3OH stretching signature at 3648 cm–1, whereas, in the OH/H2O stretching region two bands at 3585 and 3440 cm–1 can be attributed to stretching vibrations of the inner hydration sphere of the interlayer cations and to absorbed H2O stretching vibration, respectively. Diagnostic bands of kaolinite impurity at ~3698 and 3620 cm–1 are also found, whereas 2:1 dioctahedral layer silicates may contribute to the 3585 and 3620 cm–1 bands. Finally, using the one-layer supercell approach implemented in the BGMN software, a satisfactory XRPD profile fitting model for the Skorpion sauconite was obtained. These findings have implications not only for economic geology/recovery of critical metals but also, more generally, in the field of environmental sciences.
Zn-bearing phyllosilicates are common minerals in nonsulfide Zn deposits, but they seldom represent the prevailing economic species. However, even though the presence of Zn-bearing clays is considered as a disadvantage in mineral processing, their characteristics can give crucial information on the genesis of the oxidized mineralization. This research has been carried out on the Mina Grande and Cristal Zn-sulfide/nonsulfide deposits, which occur in the Bongará district (Northern Peru). In both of the deposits, Zn-bearing micas and clays occur as an accessory to the ore minerals. The XRD analyses and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS) investigations revealed that the Zn-bearing micas that are occurring in both deposits mostly consist of I/S mixed layers of detrital origin, which have been partly altered or overprinted by sauconite during the supergene alteration of sulfides. Sporadic hendricksite was also identified in the Cristal nonsulfide mineral assemblage, whereas at Mina Grande, the fraipontite-zaccagnaite (3R-polytype) association was detected. The identified zaccagnaite polytype suggests that both fraipontite and zaccagnaite are genetically related to weathering processes. The hendricksite detected at Cristal is a product of hydrothermal alteration, which is formed during the emplacement of sulfides. The complex nature of the identified phyllosilicates may be considered as evidence of the multiple processes (hydrothermal and supergene) that occurred in the Bongará district.
Abstract The Santa Fé Ni-Co deposit is a major undeveloped lateritic deposit located in the Goiás State of Central Brazil. The deposit comprises two properties that together have indicated resources of 35.7 million tonnes (Mt), grading 1.14% Ni and 0.083% Co, and inferred resources of 104.3 Mt at 1.03% Ni and 0.054% Co. The laterite was derived from Late Cretaceous alkaline ultramafic lithologies that experienced an initial silicification from Eocene to Oligocene, followed by lateritization and partial reworking in Miocene-Pliocene. The deposit is characterized both by oxide- and phyllosilicate-dominated ore zones. In the former, Ni- and Co-bearing hematite and goethite dominate the supergene mineralogical assemblage, while ore-bearing Mn oxyhydroxides occur as minor components. In the phyllosilicate-dominated horizons the major Ni-carrying phase is chlorite. Multivariate statistical analyses (factor analysis and principal components analysis) conducted on the drill core assay database (bulk-rock chemical analyses) showed that significant differences exist between Ni and Co distributions. The Ni distribution is not controlled by any clear geochemical correlation. This is because the highest Ni concentrations have been measured in the ferruginous and in the ochre saprolite zones, where Ni-bearing minerals (chlorite and goethite) are mostly associated with reworked material and only in a limited way, with zones affected by in situ ferrugination. Cobalt has an atypical statistical distribution at Santa Fé if compared with other laterites, correlated not only with Mn but also with Cr in the majority of the laterite facies. From microchemical analyses on several potential Co-bearing minerals, it was found that the Co-Cr association is related to elevated Co contents in residual spinels, representing unweathered phases of the original parent rock now included in the laterite. This element distribution is atypical for Ni-Co laterite deposits, where Co is normally associated with Mn in supergene oxyhydroxides. In the case of the Santa Fé laterite, the Co concentration in spinels is likely related to magmatic and postmagmatic processes that affected the original parent rock before lateritization, specifically (1) orthomagmatic enrichment of Co in chromite, due to its high affinity to spinels in alkaline melts, and (2) trace elements (i.e., Co, Mn, Ni, and Zn) redistribution during the hydrothermal alteration of chromite into ferritchromite. The Santa Fé deposit represents a good example of how the prelateritic evolution of a parent rock strongly affects the efficiency of Co mobilization and enrichment during supergene alteration. Based on the interpretation of metallurgical test work, a fraction of total Co between 20 and 50% is locked in spinels.
Zones of advanced argillic alteration with general low permeability (i.e., lithocaps) are common place in the shallow parts of porphyry and epithermal ore deposits and active geothermal systems. The study of structural control on alteration distributions is of paramount importance for exploitation purposes as it really influences the caprock efficiency. We present the results of a structural-mineralogical study carried out in the lithocap of the Allumiere-Tolfa epithermal system (Northern Apennines). We characterized the composition, textures and physical properties (i.e., in-situ permeability; relative rock strength) of alteration facies. We then integrated field structural analysis with analysis of a virtual outcrop model to reconstruct the geometry of principal fluid-corridors. It resulted that advanced argillic alteration was promoted by circulation of highly reactive fluid(s) along a complex network of NE- and NW-striking faults and fractures dissecting the acidic volcanic dome. Such structures likely developed in response to a local disturbance of the regional stress field due to the extrusion of the Tolfa dome, which controlled the syn-extensional mineralization of the Allumiere-Tolfa area.
Stable isotope (C–O) analysis was applied to smithsonites and cerussites from Zn(Pb) nonsulphide ores from Britain and Ireland, to determine the nature of the fluids responsible for the precipitation of secondary carbonates, and any relationship with palaeoclimatic conditions. The carbon isotope compositions of the Irish smithsonites show a major contribution of organic carbon whereas those of both Zn- and Pb-carbonates in the UK deposits indicate contribution of organic carbon and host-rock carbonates. δ 18 O VSMOW values for cerussite from both areas are about 13‰ lower than those of smithsonites, UK smithsonite δ 18 O VSMOW values are more variable than those for cerussites and the Irish smithsonites have unusually high values. Isoscape maps indicate that δ 18 O values for both carbonates are higher in the west and decrease toward the east. This trend correlates with a general decrease in the oxygen isotope compositions of rainwater moving eastward, and suggests that oxidation of sulphides occurred at temperatures of about 15–20°C, under climatic conditions warmer than today. Supplementary material: A comprehensive overview of the investigated sites, detailed data for the samples and SEM images are available at https://doi.org/10.6084/m9.figshare.c.4579535
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