Andre Sampaio Mexias

Quantification of porosity evolution from unaltered to propylitic-altered granites: the 14C-PMMA method applied on the hydrothermal system of Lavras do Sul, Brazil

This work is an application of the 14 C-Polymethylmethacrylate method to compare the porosity evolution between unaltered and propylitic-altered granites, using samples from Lavras do Sul region, Brazil. This method, when coupled with optical and electronic petrography has the advantage over other methods to provide the quantification and identification of total and local porosity of rocks. From petrographic observations, different kinds of porous zones were identified and quantified (microfractures, grain boundaries, alteration of minerals, etc). Results show that unaltered granites have 0.5 to 0.6% porosity and propylitic-altered ones have 1.7 to 1.8% porosity, even between samples with different textures. Porosity of altered rocks increases mainly due to higher porosity of neoformed chlorite, calcite, sericite and microfractures. Field observations show that later phyllic alteration halos are wider in equigranular than in porphyritic granites, which could not be explained by different original porosity between those rocks. The observed differences of phyllic halos diffusion were controlled by structural and fluid/rock ratio variations between the equigranular and porphyritic granitic facies during the later hydrothermal stage.

SPATIAL AND TEMPORAL EVOLUTION OF HYDROTHERMAL ALTERATION AT LAVRAS DO SUL, BRAZIL: EVIDENCE FROM DIOCTAHEDRAL CLAY MINERALS

TheAu-Cu (±Pb, Zn, Ag) prospects of Lavras do Sul, southernmost Brazil, arehosted in Neoproterozoic granitic and volcanogenic rocks. Mineralization occurs in structurally controlled N40°W to E-W quartz veins; sericite (±chlorite) and sulfides are the main secondary minerals in associated wall rocks.In the present contribution we use petrography (optical microscopy and scanning electron microscopy (SEM)), mineralogy (X-ray diffraction (XRD) with polytypes, FWHM, decomposition of diffraction patterns), and crystal chemistry of samples from several prospects to document the spatial and temporal evolution of sericitic alteration of veins and wall rocks associated with gold.Hexagonal, coarse-grained 2M1 phengite-rich alteration (± illite) is best developed with coarse-grained primary growth (comb) quartz + pyrite ± Au veins and altered wall rock from the western portion of the granitic complex (phyllic alteration). Pure phengite was recognized by narrow XRD profiles (FWHM ⩽ 0.2°2θ CuKα) of the <5 µm particle-size fraction, non-expandable d001 X-ray reflections and interlayer charge (IC) >0.9 per O10(OH)2.Towards the eastern zones of the granitic complex and in the volcanogenic rocks, wider XRD profiles (FWHM values ⩾ 0.2°2θ CuKα) were decomposed. They contain mixtures of coarse- to fine-grained, lath-like crystals of both 2M1 and 1M illite (non-expandable d001 X-ray reflections, IC between 0.85 and 0.89 per O10(OH)2) with expandable d001 reflections associated with lath-like, fine-grained crystals of ordered (R ⩾ 1) illite-rich I-S (80–90% of illite; IC of ∼0.8 per O10(OH)2), and minor amounts of regularly ordered (R = 1), illite-rich I-S mixed layers (75% of illite; IC of ∼0.74 per O10(OH)2). The dioctahedral clay association of illite + illite-rich I-S mixed layers (intermediate argillic alteration) is best developed in quartz + pyrite ± Au veins, breccias, and wall-rock alteration from the eastern portion of the granitic complex and in the volcanic area. Quartz from veins and breccias has fine-grained primary growth, recrystallization, and replacement textures, similar to those in epithermal deposits.The overall distribution of the dioctahedral clays indicates that the study area represents a fracture-controlled, tilted, porphyry to epithermal deposit, with telescoping alteration features observed in the east of the mining district. Deeper levels of exposure of a large hydrothermal system are observed in the west of the mining district, as shown by higher-rank dioctahedral minerals (phengite) that crystallize at relatively high temperatures (Tphe ≈ 300°C, phyllic alteration) associated with coarse-grained, primary-growth quartz veins, similar to those observed in porphyry deposits. On the other hand, shallower levels of exposure are observed in the east of the study area, associated with abundant, lower-rank dioctahedral clay minerals (illite + illite-rich I-S mixed layers, intermediate argillic alteration) that crystallize at relatively lower temperatures (TI-S ≈ 120–200°C).Available data show that gold is associated with phengite, but that lower-rank, overprinting alteration characterized by illite-I-S may have locally modified the original gold grades.

Geochemical modeling of gold precipitation conditions in the Bloco do Butiá Mine, Lavras do Sul/Brazil

A geochemical modeling of gold deposition was performed using the EQ3/EQ6 software package using conditions inferred from geological, petrographic, geochemical and fluid inclusion data from the Bloco do Butiá gold mine, Lavras do Sul, RS. Gold in the mine occurs only in the pyrite structure (invisible gold). The pyrite occurs associated with white mica (phengite) in the zone of phyllic alteration. The process of gold deposition showed to be related to temperature and pH decrease. The pH decrease was fundamental to gold deposition by destabilization of sulfur species [Au(HS)2- , HAu(HS)2(0) and Au(HS)0] dissolved in the aqueous solution, being Au(HS)0 the main gold transporting complex. The addition of KCl is hard to accept as cause of gold precipitation because no Cl- was detected in phengite. However, the geochemical mass balance calculation resulted in the gain of some potassium in the zone of phyllic alteration. The precipitation of pyrite (+/- auriferous) may have been strongly influenced by iron availability resulting from dissolution of ferrous chlorites by the fluids responsible for phengite deposition. The low salinity in quartz grain fluid inclusions from the propylitized wall rock also indicates the little importance of chlorine as gold transporting agent. Sulfur, and not chlorine, compounds must have dominated the gold transporting complexes in the Bloco do Butiá gold area.

MINERALOGICAL CHARACTERIZATION OF Ni-BEARING SMECTITES FROM NIQUELÂNDIA, BRAZIL

Nickel-lateritic ore is the most common source of nickel in Brazil. The Niquelândia deposit, located in State of Goias, is one of the most famous deposits due to the large amounts of nickel associated with both oxidized and mainly silicated ores. The terms oxidized and silicated ores are used to specify two different ores formed exclusively by oxides and silicate (clay) minerals, respectively. The aim of the present study was to characterize thoroughly the silicated ore to identify the Ni-bearing clay minerals and their crystal chemistry in support of developing a better mineral-processing method or optimizing the current one to improve Ni recoveries. X-ray diffraction, chemical analyses, scanning electron microscopy, and Fourier transform infrared (FTIR) spectroscopy demonstrated that nickel is associated with Ni-rich stevensite and to a lesser extent with Fe-rich montmorillonite. The crystal chemistry performed by FTIR spectroscopy revealed that Ni is present in the octahedral positions, substituting for Mg or Fe, which results in significant chemical and layer-charge heterogeneity in the samples. This heterogeneity seems to be responsible for reduction in Ni recoveries during the hydrometallurgical process.

Caracterização dos argilominerais usados em matéria-prima cerâmica, da formação Rio do Rasto, Bacia do Paraná, no município de Turvo, SC

In the southeastern part of Santa Catarina state, Brazil, many mines of clays used as raw material for the ceramic industry are found. A detail study of this material was developed in a mine in activity. The exploitation of clays is held in sedimentary rocks of Rio do Rasto Formation (Upper Permian) in the Parana Basin. The outcrops are in hills testimonies. Fourteen samples were collected and represent the levels of this mine which consisted of argillites with intercalation of slim siltite layer. These samples were analyzed by X-ray diffraction using the powder method and in the fraction < 4 µm. The chemical composition was determined by X-ray fluorescence spectrometer. Petrographic observations in thin section were also performed. Scanning electron microscope images was obtained in samples fragments by secondary electron method. Electron microprobe microanalysis was performed in one thin section. The results showed large vertical variation in the mineralogy and it has been identified three different levels. Up to 2.00 m there is a predominance of smectite. Between 5.50 m 2.00 m the smectite is the main clay mineral, but with significant amounts of illite/mica and above 5.50 m occurs large increase in K-feldspar and detrital mica. Studies in detail by X-ray diffraction (determination of the b-parameter) and microanalysis by wavelength dispersive X-ray spectroscopy have identified montmorillonite clay mineral as the smectite mineral specie.