Gênese dos corpos de sulfeto maciço hidrotermal e platinóides associados no depósito de Fortaleza de Minas (MG)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

The fortaleza de minas nickel, copper and platinoids deposit: ore types, tectonics and volcanological aspects

Pós-graduação em Geologia Regional - IGCE

The Ni-Cu-PGE sulfide ores of the komatiite-hosted Fortaleza de Minas deposit, Brazil: Evidence of hydrothermal remobilization

The Fortaleza de Minas Ni-Cu-PGE sulfide deposit is hosted by Archean komatiitic rocks of the Morro do Ferro greenstone belt, near the southwestern margin of the Sa (aFrancisco) over tildeo Francisco craton, Minas Gerais state, Brazil. The deposit contains 6 million tonnes of ore with an average grade of 2.2 wt% Ni, 0.4% Cu, 0.05% Co and 1.2 ppm PGE+Au, and comprises (i) a main orebody, which is metamorphosed, deformed and transposed along a regional shear zone, consisting mainly of disseminated, brecciated and stringer sulfide ores that are interpreted to be of early magmatic origin, and (ii) PGE-rich discordant veins that are hosted in N-S- and NE-SW-trending late faults that cross-cut the main orebody. The discordant PGE-rich ore (up to 4 ppm total PGE) is characterized by thin, discontinuous and irregular veins and lenses of massive sulfides hosted by serpentinite and talc schist, and is relatively undeformed if compared with the early types of ore. It is composed mainly of pyrrhotite, pentlandite, chalcopyrite, magnetite, carbonates, and amphiboles, with minor cobaltite-gersdorffite, sphalerite, ilmenite, and quartz, and rarely maucherite (Ni11Asg), tellurides and platinum-group minerals (PGM). Omeeite, irarsite, sperrylite, and Ni-bearing merenskyite are the main PGM, followed by minor amounts of testibiopalladite and an unknown phase containing Ru, Te, and As. The PGM occur either included in, or at the margins of, sulfides, sulfarsenides, silicates and oxides, or filling fractures in pyrrhotite, pentlandite, and chalcopyrite, suggesting that they started to precipitate with these minerals and continued to precipitate after the sulfides were formed. The mantle-normalized metal distribution of the two samples of discordant veins shows distinct patterns: one richer in Ni-Pd-Ir-Rh-Ru-Os and another with higher amounts of Cu-Pt-Bi. Both are strongly depleted in Cr if compared with the metamorphosed magmatic ore of this deposit, which follows the general Kambalda-type magmatic trend. on the basis of structural, mineralogical and geochemical evidence, we propose that the PGE-rich discordant ore may have formed by remobilization of metals from the deformed, metamorphosed magmatic orebody (which shows a depleted pattern in these elements) by reduced (pyrrhotite - pentlandite - pyrite are stable), neutral to alkaline and carbonic fluids (carbonate-stable). The PGE may have been transported as bisulfide complexes, and precipitated as tellurides (mainly Pd) and arsenides (Pt, Rh, Ru, Os, Ir) in the late N-S and NE-SW-trending faults owing to a decrease in the activity of S caused by the precipitation of sulfides in the veins.

Evolução petrogenética das rochas máficas / ultramáficas na área ao sul do craton São Francisco, entre as cidades de Fortaleza de Minas e Jacuí - MG

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Modelo estrutural da jazida de sulfetos de NI-CU-CO e MGP, Fortaleza de Minas, MG

Pós-graduação em Geologia Regional - IGCE

Evolução geoquímica e mineralógica em perfis de alteração sobre rochas serpentinizadas no sudoeste de Minas Gerais

Estudou-se a evolução geoquímica e mineralógica em três perfis distintos de alteração de rochas serpentinizadas que ocorrem nas imediações dos municípios de Alpinópolis e Fortaleza de Minas, no sudoeste do Estado de Minas Gerais, sob regimes de umidade e de temperatura údico e térmico, respectivamente. Nas condições atuais, o grau de evolução química e mineralógica é moderado em relação ao desenvolvido sobre outros tipos de rochas básicas e ultrabásicas da mesma área, caracterizando-se por uma importante perda de Na e Mg e, em menor proporção, de Ca e Si. O Al (localmente também o Fe) é o elemento menos móvel dos sistemas. O K é escasso no material de origem e nas zonas de alteração, e ocorre enriquecimento desse elemento nos horizontes superficiais por aporte externo. Os minerais primários mais facilmente intemperizáveis, como o talco, a tremolita e a clorita trioctaédrica, são abundantes ainda na fração argila desses solos tropicais com composição mineralógica pouco comum, mas são todos termodinamicamente instáveis. do ponto de vista geoquímico, o processo de alteração atual pode ser definido como uma bissialitização, que pode coincidir com ferruginização, com formação de minerais trioctaédricos secundários por transformação direta de estrutura e também por neoformação, todos coexistindo com os minerais primários residuais. No entanto, as fases de maior evolução, em volumes com drenagem mais eficiente, tendem à monossialitização, com formação de caulinitas de diferentes graus de cristalinidade. A assembléia mineralógica existente evidencia a metaestabilidade e o caráter incipiente do sistema pedogenético.

Estudo geofísico em um depósito de manganês supergênico no município de Itapira - SP

The mining research is a complex activity, which should preferably involve the combination of direct and indirect techniques of geological research. The increasing demand for base metals in domestic and international markets provide the revaluation of mineral occurrences, which can be converted into deposits and mines. This paper presents the results of the application of geophysical methods of electric resistivity and induced polarization in main foliation parallel to the arrangement of the area, in a deposit of oxides and hydroxides in massive and disseminated ores, docked in gneisses and quartzites, located in the municipality of Itapira, in the North of the State of São Paulo in Brazil. Inversion models indicate the predominance of high cargabilidade that partially coincide with low resistivity values. Integration of geophysical data made possible the drafting of sections of electric walking with cross-checking distance x depth, for detailing your target. The integrated analysis of geophysical and geological structural data leads to the conclusion that the primary mining suffers structural control with the regional foliation in ores

Caracterização petrográfica das zonas de alteração hidrotermais no alvo Arex, do depósito polimetálico de Aripuanã, MT

The Roosevelt-Domain Aripuanã that by Filho et al 2004 is characterized by a metavolcanic sedimentary sequence, containing acidic to interemediary metavolcanic rocks and clastic and chemical sediments, deformed and metamorphosed at low grade, with U-Pb age of 1.743 +- 4 Ma, (by Granito Zé do Torno), and circumscribed bodies of granites late to post-orogenic (Aripuanã)...

Geologia do depósito de ouro do alvo guarda-mor, na sequência Jaupaci (Israelândia - GO)

The study area of the Guarda-Mor target (Israelândia-GO) contextualizes the terrains of the estaern portion of the Arenópolis Magmatic Arc, more accurately, the Neoproterozoic associations inserted in the field of the Jaupaci volcano-sedimentary sequence. The mapped area is located in the central-western of Goiás state. The presente paper has as main objective to characterize the structural, petrographic and litogeochemistry of the target rocks beyond to compare these factors with the Mina Bacilândia rocks (Fazenda Nova-GO) in order to assess the genetic similarity of volcano-sedimentary units and deposits associated. The Guarda-Mor target is represented by the Jaupaci metavolcanic rocks sequence presenting bimodal volcanism. This sequence consists in metafelsic rocks like sericite/muscovite quartz schist, phyllite and metarriolites and/or metariodacites with calc-alkaline geochemical signature and metamafic rocks with tholeiitic character formed by actinolite - chlorite schist and chlorite - quartz schist. Besides the package of supracrustal rocks also can be observed the occurrence of a local intrusion syn- to late - tectonic named Granito Subvulcânico. In the study area beyond the marked volcanism also seen an event of crustal melting granitogênese evidenced by the presence of 2 granites at the east and the west of the map, Granito Israelândia and Granito Iporá respectively. Structural analysis both at the macro and micro have identified 3 deformation phases. The types of rock on the region record features in the metamorphic facies top and down. These features were subdivided into 3 metamorphic areas: the east and West areas show thermal metamorphism due to intrusion of adjacente granites while the central domain displays features of regional metamorphism. Gold mineralization of the Guarda –Mor deposit target suggests a possible structural control beyond pronounced the hydrothermal alteration. The mineralization may also be...

Diseño y construcción del vertedero para el depósito del material de excavación del túnel del Espiño (Orense)

El presente documento presenta la definición de las obras e instalaciones necesarias para dar cobertura a unos niveles de producción de material de excavación proveniente del túnel del Espiño, para lo cual se decide construir el Vertedero del Espiño. Dicho vertedero cumple con la normativa ambiental, una vez finalizadas las actividades dentro del túnel el vertedero se clausura, sella y recupera medioambientalmente la zona afectada. Para ello se incluyen todos los documentos necesarios para la definición, justificación y valoración de las obras. This paper presents the definition of works and facilities needed to cover production levels of material from tunnel excavation Espiño, for which it is decided to build the weir Espiño. This landfill complies with environmental regulations, once finalized the activities inside the tunnel the landfill closes, environmentally sealed and recovers the affected area. To do all the necessary documents for the definition, justification and evaluation of the works included

Diccionario de artes y manufacturas, de agricultura, de minas, etc. : descripción de todos los procedimientos industriales y fabriles.

Numerosos grab. tip. intercalados en el texto.

Evolução temporal do complexo vulcano sedimentar associado ao depósito de Neves-Corvo

Resumo alargado

The molecular structure of matioliite – NaMgAl5(PO4)4(OH)6·2(H2O) : a pegmatite mineral from Minas Gerais, Brazil

Detailed spectroscopic and chemical investigation of matioliite, including infrared and Raman spectroscopy, scanning electron microscopy and electron probe microanalysis has been carried out on homogeneous samples from the Gentil pegmatite, Mendes Pimentel, Minas Gerais, Brazil. The chemical composition is (wt.%): FeO 2.20, CaO 0.05, Na2O 1.28, MnO 0.06, Al2O3 39.82, P2O5 42.7, MgO 4.68, F 0.02 and H2O 9.19; total 100.00. The mineral crystallize in the monoclinic crystal system, C2/c space group, with a = 25.075(1) Å, b = 5.0470(3) Å, c = 13.4370(7) Å, β = 110.97(3)°, V = 1587.9(4) Å3, Z = 4. Raman spectroscopy coupled with infrared spectroscopy supports the concept of phosphate, hydrogen phosphate and dihydrogen phosphate units in the structure of matioliite. Infrared and Raman bands attributed to water and hydroxyl stretching modes are identified. Vibrational spectroscopy adds useful information to the molecular structure of matioliite.

Vibrational spectroscopy of the phosphate mineral lazulite – (Mg, Fe)Al2(PO4)2·(OH)2 found in the Minas Gerais, Brazil

This research was done on lazulite samples from the Gentil mine, a lithium bearing pegmatite located in the municipality of Mendes Pimentel, Minas Gerais, Brazil. Chemical analysis was carried out by electron microprobe analysis and indicated a magnesium rich phase with partial substitution of iron. Traces of Ca and Mn, (which partially replaced Mg) were found. The calculated chemical formula of the studied sample is: (Mg0.88, Fe0.11)Al1.87(PO4)2.08(OH)2.02. The Raman spectrum of lazulite is dominated by an intense sharp band at 1060 cm-1 assigned to PO stretching vibrations of of tetrahedral [PO4] clusters presents into the HPO2/4- units. Two Raman bands at 1102 and 1137 cm-1 are attributed to both the HOP and PO antisymmetric stretching vibrations. The two infrared bands at 997 and 1007 cm-1 are attributed to the m1 PO3/4- symmetric stretching modes. The intense bands at 1035, 1054, 1081, 1118 and 1154 cm-1 are assigned to the v3PO3/4- antisymmetric stretching modes from both the HOP and tetrahedral [PO4] clusters. A set of Raman bands at 605, 613, 633 and 648 cm-1 are assigned to the m4 out of plane bending modes of the PO4, HPO4 and H2PO4 units. Raman bands observed at 414, 425, 460, and 479 cm-1 are attributed to the m2 tetrahedral PO4 clusters, HPO4 and H2PO4 bending modes. The intense Raman band at 3402 and the infrared band at 3403 cm-1 are assigned to the stretching vibration of the OH units. A combination of Raman and infrared spectroscopy enabled aspects of the molecular structure of the mineral lazulite to be understood.

Assessment of the molecular structure of natrodufrénite – NaFe2+Fe3+5(PO4)4(OH)6•2(H2O), a secondary pegmatite phosphate mineral from Minas Gerais, Brazil

The mineral natrodufrénite a secondary pegmatite phosphate mineral from Minas Gerais, Brazil, has been studied by a combination of scanning electron microscopy and vibrational spectroscopic techniques. Electron probe analysis shows the formula of the studied mineral as (Na0.88Ca0.12)∑1.00(Mn0.11Mg0.08Ca0.04Zr0.01Cu0.01)∑0.97(Al0.02)∑4.91(PO4)3.96(OH6.15F0.07)6.22⋅2.05(H2O). Raman spectroscopy identifies an intense peak at 1003 cm−1 assigned to the ν1 symmetric stretching mode. Raman bands are observed at 1059 and 1118 cm−1 and are attributed to the ν3 antisymmetric stretching vibrations. A comparison is made with the spectral data of other hydrate hydroxy phosphate minerals including cyrilovite and wardite. Raman bands at 560, 582, 619 and 668 cm−1 are assigned to the ν4 bending modes and Raman bands at 425, 444, 477 and 507 cm−1 are due to the ν2 bending modes. Raman bands in the 2600–3800 cm−1 spectral range are attributed to water and OH stretching vibrations. Vibrational spectroscopy enables aspects of the molecular structure of natrodufrénite to be assessed.