Abstract Recent sea floor sulfide deposits form when seawater, heated within the oceanic crust, discharges to the sea floor. Upon mixing with cold seawater, sulfide-forming elements such as sulfur, iron, copper, and zinc are precipitated from the fluid. Actively forming sea floor massive sulfide deposits are found from different lithologic and tectonic environments varying from mid-ocean ridges to back-arc spreading centers. At a few localities, sulfide deposits are associated with turbiditic sediments that cover the axial valley of the spreading center. The southern part (Escanaba Trough) of the Gorda Ridge (NE Pacific) is one such example. At Escanaba Trough, massive sulfide deposits are associated with small sediment hills, which were uplifted by the intrusion of sills and laccoliths within the sediments. Hydrothermal deposits are dominated by pyrrhotite-rich massive sulfides, with subordinate amounts of sulfate-rich precipitates and polymetallic sulfides. Compared to deposits hosted by volcanites, Escanaba Trough sulfides contain relatively low amounts of copper and zinc. However, the average gold concentration is relatively high for a sediment-hosted deposit, and is comparable with other, Au-enriched, sea floor sulfide deposits. Despite the relatively high Au concentration in many volcanic-hosted sea floor sulfide deposits, discrete Au grains are rare. They occur mostly with sphalerite, pyrite, chalcopyrite and tetrahedrite-tennantite. Sixteen of the pyrrhotite-rich samples from Escanaba Trough were found to contain visible Au grains. They occur mostly with native Bi and various BiTe phases, and to lesser degree, with Fe-Co sulfarsenides. Transport of Au in sea floor hydrothermal systems is attributed to the presence of Au(HS)2- complex, which is destabilized when the fluid mixes with seawater. Hydrothermal fluids are generally undersaturated with respect to Au complexes and additional mechanisms, such as remobilizing earlier precipitated Au is required to explain the high Au concentrations encountered in many deposits. At Escanaba Trough the mechanism is attributed to early precipitation of Bi as melt droplets, at temperatures greater its melting temperature, as liquid Bi is capable of collecting Au even from an undersaturated fluid. Upon cooling Au is exsolved from the Bi host as native Au or maldonite (Au2Bi).

The Rävliden North deposit (Rävliden N) is a volcanogenic massive sulphide (VMS) deposit in the western part of the Skellefte district, northern Sweden. The district is one of Sweden’s major metallogenic provinces with a significant amount of VMS deposits. The Rävliden N deposit, discovered in 2011, contains copper, zinc, lead, silver and subordinate gold and occurs close to the largest VMS deposit in the district, the Kristineberg deposit, which has been mined for more than 70 years. The purpose of this master thesis is to study the composition, mineralogy and paragenetic relationships in different types of sulphide mineralization from the Rävliden N deposit. Emphasis is placed on characterizing the distribution and paragenetic relationships of silver-bearing minerals. The methods include core logging, sampling and mineralogical studies through light optical microscopy (LOM), scanning electron microscopy (SEM) and quantitative evaluation of mineralogy by scanning electron microscopy (QEMSCAN). Lastly, electron microprobe analysis (EMPA) was used to determine the chemical composition of silver-bearing minerals and sulphides. Mineralization types studied include 1: the main massive to semi-massive sulphide mineralization, 2: stratigraphically underlying stringer mineralization and 3: local, vein- and/or fault-hosted silver-rich mineralization in the stratigraphic hanging wall. The massive to semi-massive sulphide mineralization is dominated by sphalerite with lesser galena and pyrrhotite. In contrast, the stringer mineralization is dominated by chalcopyrite and pyrrhotite. The major minerals show evidence of a coeval formation and textural as well as structural evidence suggest that ductile deformation has affected the mineralization types. Notable evidence includes ball-ore textures, accumulation of minerals in pressure shadows and brittle fracturing of competent arsenopyrite and pyrite porphyroblasts and infilling by more incompetent sulphide minerals. The silver-bearing minerals identified are commonly spatially associated with galena and the major species is freibergite ((Ag,Cu,Fe)12(Sb,As)4S13), which also occur as inclusions in chalcopyrite mainly in the stringer mineralization. The stringer mineralization also contains notable amounts of hessite (Ag2Te). Notably, galena, pyrrhotite, freibergite and other sulphosalt minerals are commonly accumulated in pressure shadows near host rock fragments in the massive to semi-massive sulphide mineralization. The only gold-bearing mineral identified in this study is electrum (Au, Ag) in the stringer mineralization. The hanging wall mineralization locally comprises faulted and/or sheared massive sulphide mineralization which is compositionally similar to the main massive to semi-massive sulphide mineralization, besides a significantly higher content of freibergite. However, parts of the hanging wall mineralization are entirely dominated by sulphides and sulphosalts of silver, such as pyrargyrite (Ag3SbS3), pyrostilpnite (Ag3SbS3), argentopyrite (AgFe2S4), sternbergite (AgFe2S3) and stephanite (Ag5SbS4). These occur in structurally late settings, which along with consideration of their temperature stabilities suggest a late origin. Since the silver-bearing minerals in the massive to semi-massive sulphide mineralization and the two varieties of hanging wall mineralization contains the same metals, the mineralization in the hanging wall may have formed by late-stage remobilization of ore components from the underlying Rävliden N deposit. This negates the need for multiple mineralization events to explain the local silver-enriched zones in the hanging wall. The paragenetically late mineralization types contains high content of Ag-bearing minerals in relation to base metal sulphides. This suggests that remobilisation processes were important for locally upgrading the Ag-content.

Previous mineralogical investigations (QemSCAN) performed on all effluent flotation streams of Mimosa mine (Zimbabwe) indicated the presence of appreciable amounts of platinum group minerals (PGMs), which are not recovered. Most, generally in excess of 70%, of the liberated PGMs in these streams belonged to the Pt-Pd-Bi-Te class in all the samples investigated. In the first part of this work, electrochemical investigations, electrochemically-controlled contact angle measurements and Raman spectroscopy have been employed to investigate the interaction of ethyl xanthate with Pd-Bi-Te and PtAs2. Impedance measurements showed lower capacitance values in solutions containing KEX indicating the formation of a continuous surface layer. Anodic and cathodic polarization diagrams show the mixed potential to be higher than the reversible potential of the xanthate-dixanthogen equilibrium reaction, hence the formation of dixanthogen on the surface is possible. Electrochemically controlled in situ Raman spectroscopy has confirmed the co-presence of xanthate with dixanthogen indicating that xanthate retains its molecular integrity when it adsorbs on the surface of the Pd-Bi-Te. The result of this investigation has shown dixanthogen to be present on both the minerals (PtAs2 and Pd-Bi-Te) when the surfaces are anodically polarized. Chemisorbed xanthate could be identified within 120 seconds yielding a hydrophobic surface as indicated by electrochemically-controlled contact angle measurements. Maximum contact angles of 63o were measured in the case Pd-Bi-Te. As a result the mineral surface is expected to be hydrophobic and a lack of collector interaction with the mineral is not the reason for low PGM recoveries experienced. Secondly, the flotation recovery of synthetically prepared Pd-Bi-Te was compared with that of chalcopyrite (a typical fast-floating mineral) and pyrrhotite (a typical slow-floating mineral), with microflotation tests. These indicated Pd-Bi-Te to be a fast-floater with flotation rates exceeding that of chalcopyrite. Predicted flotation rate constants (from the Ralston model) were significantly lower for small particles (with diameters similar to those lost to the effluent streams) compared with those of particle with intermediate sizes. This supports the suggestion that losses to effluent streams are caused by particle size effects. / Thesis (PhD (Metallurgical Engineering))--University of Pretoria, 2006. / Materials Science and Metallurgical Engineering / unrestricted