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Sample records for albite

  1. Effects of Irradiation on Albite's Chemical Durability.

    Science.gov (United States)

    Hsiao, Yi-Hsuan; La Plante, Erika Callagon; Krishnan, N M Anoop; Le Pape, Yann; Neithalath, Narayanan; Bauchy, Mathieu; Sant, Gaurav

    2017-10-19

    Albite (NaAlSi 3 O 8 ), a framework silicate of the plagioclase feldspar family and a common constituent of felsic rocks, is often present in the siliceous mineral aggregates that compose concrete. When exposed to radiation (e.g., in the form of neutrons) in nuclear power plants, the crystal structure of albite can undergo significant alterations. These alterations may degrade its chemical durability. Indeed, careful examinations of Ar + -implanted albite carried out using Fourier transform infrared spectroscopy (FTIR) and molecular dynamics simulations show that albite's crystal structure, upon irradiation, undergoes progressive disordering, resulting in an expansion in its molar volume (i.e., a reduction of density) and a reduction in the connectivity of its atomic network. This loss of network connectivity (i.e., rigidity) results in an enhancement of the aqueous dissolution rate of albite-measured using vertical scanning interferometry (VSI) in alkaline environments-by a factor of 20. This enhancement in the dissolution rate (i.e., reduction in chemical durability) of albite following irradiation has significant impacts on the durability of felsic rocks and of concrete containing them upon their exposure to radiation in nuclear power plant (NPP) environments.

  2. Molecular dynamics simulation of albite twinning and pericline twinning in low albite

    International Nuclear Information System (INIS)

    Li, Bin; Knowles, Kevin M

    2013-01-01

    Two twinning laws, the albite law and the pericline law, are the predominant growth twinning modes in triclinic plagioclase feldspars such as low albite, NaAlSi 3 O 8 , in which the aluminum and silicon atoms are in an ordered arrangement on the tetrahedral sites of the aluminosilicate framework. In the terminology used formally to describe deformation twinning in a triclinic lattice, these twin laws can be described as Type I and Type II twin laws, respectively, with the pericline twin law being conjugate to the albite twin law. In this study, twin boundaries have been constructed for low albite according to these two twinning laws and studied by molecular dynamics simulation. The results show that suitably constructed twin boundary models are quite stable for both albite twinning and pericline twinning during molecular dynamics simulation. The calculated twin boundary energy of an albite twin is significantly lower than that of a pericline twin, in accord with the experimental observation that albite twinning is the more commonly observed mode seen in plagioclase feldspars. The results of the molecular dynamics simulations also agree with conclusions from the prior work of Starkey that glide twinning in low albite is not favoured energetically. (paper)

  3. Radioluminescence and thermoluminescence of albite at low temperature

    International Nuclear Information System (INIS)

    Can, N.; Garcia-Guinea, J.; Kibar, R.; Cetin, A.; Ayvacikli, M.; Townsend, P.D.

    2011-01-01

    Feldspar as an archaeological and geological natural material for dating and retrospective dosimetry is receiving more and more attention because of its useful luminescence properties. In this study, the 25-280 K thermoluminescence (TL) and radioluminescence (RL) spectra in albite, which is a component of the two main feldspar series, the alkali feldspar (Na, K)AlSi 3 O 8 and the plagioclases (NaAlSi 3 O 8 -CaAl 2 Si 2 O 8 ) have been presented for aliquots along (001) and (010) crystallographic orientations. There are four main emission bands that are considered to arise from complexes of intrinsic defects linked in larger complexes with impurities such as Na + , Mn 2+ or Fe 3+ ions. The consequence of their association is to produce different luminescence efficiencies that produce wavelength sensitive TL curves. Radioluminescence data at low temperature for albites is distorted by contributions from the TL sites, even when the RL is run in a cooling cycle. This indicates the potential for a far more general problem for analysis of low temperature RL in insulating materials. - Highlights: → TL and RL spectra in albite were presented for different orientations. → There are 4 emission bands that are considered to arise from complexes of intrinsic. → RL data at low temperature for albite is distorted by contributions from TL sites. → This indicates the potential problem for analysis of low temperature RL.

  4. Dating Metasomatism: Monazite and Zircon Growth during Amphibolite Facies Albitization

    Directory of Open Access Journals (Sweden)

    Cailey B. Condit

    2018-04-01

    Full Text Available We present coupled textural observations and trace element and geochronological data from metasomatic monazite and zircon, to constrain the timing of high-grade Na-metasomatism (albitization of an Archean orthogneiss in southwest Montana, USA. Field, mineral textures, and geochemical evidence indicate albitization occurred as a rind along the margin of a ~3.2 Ga granodioritic orthogneiss (Pl + Hbl + Kfs + Qz + Bt + Zrn exposed in the Northern Madison range. The metasomatic product is a weakly deformed albitite (Ab + Bt + OAm + Zrn + Mnz + Ap + Rt. Orthoamphibole and biotite grew synkinematically with the regional foliation fabric, which developed during metamorphism that locally peaked at upper amphibolite-facies during the 1800–1710 Ma Big Sky orogeny. Metasomatism resulted in an increase in Na, a decrease in Ca, K, Ba, Fe, and Sr, a complete transformation of plagioclase and K-feldspar into albite, and loss of quartz. In situ geochronology on zoned monazite and zircon indicate growth by dissolution–precipitation in both phases at ~1750–1735 Ma. Trace element geochemistry of rim domains in these phases are best explained by dissolution–reprecipitation in equilibrium with Na-rich fluid. Together, these data temporally and mechanistically link metasomatism with high-grade tectonism and prograde metamorphism during the Big Sky orogeny.

  5. Adsorption of N-tallow 1,3-propanediamine-dioleate collector on albite and quartz minerals, and selective flotation of albite from greek stefania feldspar ore.

    Science.gov (United States)

    Vidyadhar, A; Hanumantha Rao, K; Forssberg, K S E

    2002-04-01

    The adsorption behavior of tallow 1,3-propanediamine-dioleate (Duomeen TDO) collector on albite and quartz minerals is assessed through Hallimond flotation, zeta potential, and diffuse reflectance FTIR investigations, together with the species distribution of the collector. The collector performance on albite separation from a natural feldspar material is evaluated in bench scale flotation tests. The Hallimond flotation responses of the minerals as a function of pH and collector concentration indicate that albite can be selectively floated from quartz at pH 2 where the doubly positively charged collector species adsorb on albite but not on quartz. However, the zeta potential and infrared spectra reveal that the adsorption behavior of the collector is similar on both minerals. The discrepancy in the flotation and adsorption results is attributed to the coarse and fine particle size fractions, and the shorter and longer equilibration periods employed in these studies respectively. The comparable adsorption on fine particles of albite and quartz at pH 2 is explained by the interaction of ammonium ions on silanol groups by hydrogen bonding as well as electrostatic interactions. The changes in zeta potentials are in good agreement with the formation of ionic species and free molecular forms of the collector. The IR spectra show the coexistence of neutral oleic acid together with charged amine species at low pH values in accordance with the species distribution diagram. Selective flotation of albite is accomplished from a natural feldspar material with tallow diamine-dioleate collector at pH 2 using sulfuric acid, only when the feed is deslimed prior to the bench scale flotation tests. An albite recovery exceeding 85% is achieved from a feed material containing about 50% albite.

  6. Identification of different generations of albite through microchemical fingerprint by LA-ICP-MS

    Energy Technology Data Exchange (ETDEWEB)

    Amorim, Lucas E.D.; Rios, Francisco J.; Freitas, Monica E.; Palmieri, Helena E.L.; Geraldes, Mauro C.; Matos, Evando C. de, E-mail: ledamorim@cdtn.br, E-mail: javier@cdtn.br, E-mail: monicaef@gmail.com, E-mail: help@cdtn.br, E-mail: geraldes@uerj.br, E-mail: carele@inb.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil); Universidade Estadual do Rio de Janeiro (UERJ), Rio de Janeiro, RJ (Brazil); Indústrias Nucleares do Brasil (INB), Caetité, BA (Brazil)

    2017-07-01

    The Lagoa Real Uranium Province located in the south-central part of the Bahia-BR, in the central portion of the San Francisco Craton, is composed of an association of Paleoproterozoic metagranitoids, alkali-gneisses, and albitites (barren and mineralized). Intense action of metamorphic and metasomatic processes characterize this region. These processes culminated in the transformation of granites into gneisses, albitites and U mineralization in some albitites bodies. There are three types of metagranites, Lagoa do Barro (1,77Ga), Juazerinho (1,75Ga) and São Timóteo (1,74Ga). In view of this information, we aimed to verify if the albite formed by metamorphism in the metagranites has the same fingerprint of the albite present in the barren albitites. We used a LA-ICP-MS system for this. The results allowed the determination of albites fingerprint, allowing the differentiation of at least two generations. The Sr / U ratio allows characterizing these generations. The albitites have albite with minimal microchemical variation. The metagranites Lagoa do Barro and São Timóteo has similar generation of albite. The Juazerinho presents two generations of albite, one with similar to São Timóteo, Lagoa do Barro and albitites and another generation with distinctly higher concentrations of Sr and U. These results show that the same event that generated the albitite's albite interfered with the formation of the metagranite's albite, but another event culminated with the formation of the second generation of the albite in the Juazerinho. (author)

  7. Identification of different generations of albite through microchemical fingerprint by LA-ICP-MS

    International Nuclear Information System (INIS)

    Amorim, Lucas E.D.; Rios, Francisco J.; Freitas, Monica E.; Palmieri, Helena E.L.; Geraldes, Mauro C.; Matos, Evando C. de

    2017-01-01

    The Lagoa Real Uranium Province located in the south-central part of the Bahia-BR, in the central portion of the San Francisco Craton, is composed of an association of Paleoproterozoic metagranitoids, alkali-gneisses, and albitites (barren and mineralized). Intense action of metamorphic and metasomatic processes characterize this region. These processes culminated in the transformation of granites into gneisses, albitites and U mineralization in some albitites bodies. There are three types of metagranites, Lagoa do Barro (1,77Ga), Juazerinho (1,75Ga) and São Timóteo (1,74Ga). In view of this information, we aimed to verify if the albite formed by metamorphism in the metagranites has the same fingerprint of the albite present in the barren albitites. We used a LA-ICP-MS system for this. The results allowed the determination of albites fingerprint, allowing the differentiation of at least two generations. The Sr / U ratio allows characterizing these generations. The albitites have albite with minimal microchemical variation. The metagranites Lagoa do Barro and São Timóteo has similar generation of albite. The Juazerinho presents two generations of albite, one with similar to São Timóteo, Lagoa do Barro and albitites and another generation with distinctly higher concentrations of Sr and U. These results show that the same event that generated the albitite's albite interfered with the formation of the metagranite's albite, but another event culminated with the formation of the second generation of the albite in the Juazerinho. (author)

  8. Neptunium(V) sorption on quartz and albite in aqueous suspension

    International Nuclear Information System (INIS)

    Kohler, M.; Leckie, J.O.

    1991-10-01

    The behavior of neptunium in the subsurface environment is of interest since neptunium isotopes are included in nuclear waste. Previous work investigated the sorption behavior of Np onto α-Fe 2 O 3 (hematite), an accessory mineral of the Yucca Mountain repository. The work reported herein involves the much more abundant silicate minerals quartz and albite, and is a logical continuation of the ongoing task. In previous work increased sorption was observed in systems containing hematite and EDTA, a ligand which acts as a surrogate for organic complexing agents. In addition, increased partial pressures of CO 2 are common in many ground waters and the effects of carbonate on sorption of radionuclides have to be studied as well. At concentration levels of 10 -7 M, Np(V) does not adsorb strongly on quartz and albite up to pH values of approximately 9 at solid/solution ratios of 30 to 40 g/l. Significant adsorption (> 20%) occurs on both minerals only at pH > 9. Pretreatment of albite affects the sorption behavior of this mineral at pH > 9, possibly due to the formation of secondary mineral phases at the albite surface. EDTA does not adsorb on quartz at concentrations of 10 -6 M. In the presence of 50 μM EDTA, Np(V) sorption seems to be restricted. EDTA at the 10 -6 M level adsorbs onto albite to an appreciable degree at pH values 3 - is the predominant solution species

  9. Uranium deposits in the metamorphic basement of the Rouergue massif. Genesis and extension of related albitization processes

    International Nuclear Information System (INIS)

    Schmitt, J.M.

    1982-02-01

    Albitization processes in the Rouergue metamorphic basement, probably Permian aged is evidenced. Late development of uranium orebodies occured within albitized zones. The detection of the latter serves as a highly valuable indirect guide for prospecting this type of deposits in a metamorphic basement [fr

  10. Influence of the amount containing spodumene or albite on the sintering of a triaxial ceramic

    International Nuclear Information System (INIS)

    Oliveira, Camila Felippe de; Strecker, Kurt

    2012-01-01

    In this study, we investigated the properties of porcelain stoneware, made with albite or spodumene. The amount of the feldspar in the compositions ranged from 15 to 30% by weight. Specimens were pressed and sintered at 1000, 1100, 1200 and 1280 °C with an isotherm of 1 hour at the maximum temperature. The samples were characterized by analysis of the fracture surface using scanning electron microscopy and the vitrification curves, showing both the linear shrinkage and porosity in relation to the sintering temperature. The best results were obtained for samples containing 30% spodumene sintered at 1280 °C, with a linear shrinkage of 9.97% and porosity of 13.28%, while the corresponding results of samples containing 30% albite were 10.13% and 12.17%, respectively. It is concluded that the use of spodumene in the production of porcelain stoneware is viable, resulting in comparable properties. (author)

  11. Hydrothermal reaction of albite and a sodium aluminosilicate glass: A solid-state NMR study

    Science.gov (United States)

    Yang, Wang-hong Alex; Kirkpatrick, R. James

    1989-04-01

    We present here a solid-state NMR study of the structure and chemical composition of the products and mechanisms of the reaction of crystalline low albite and a glass of nearly albite composition with aqueous solutions of pH from 1 to 11 at 250°C. For the crystalline albite, there are no detectable bulk or surface structural changes due to aqueous attack, consistent with the idea that both cation exchange and disruption of the aluminosilicate framework occur only near the mineral/solution interface and that the hydrated surface layer, if it exists, is not more than about 30 Å thick. This reaction occurs by solution/reprecipitation, and its rate decreases with increasing solution pH, supporting the idea that the dissolution of feldspar is initiated by cation-exchange. For the glass, the reaction proceeds by cation exchange of protons for Na +, incorporation of molecular water into the bulk glass, and a small amount of depolymerization of the aluminosilicate framework in the interior of the glass. Cation exchange becomes less important with increasing solution pH. The incorporation of molecular water and cation-exchange cause structural changes in the glass via solidstate adjustment without dissolution/reprecipitation. The large cations in the hydrated glass (Na and K) probably have a shell of water molecules around them, with a maximum average coordination number of six. The secondary phases formed from both albite and the glass are often amorphous and can be well characterized by NMR. The compositional and structural variations of the amorphous phases are important factors in these reactions and cannot be ignored in theoretical models of aluminosilicate dissolution. As expected, the aluminum coordination in the secondary phases changes from six-fold to four-fold as the solution pH increases.

  12. Capacity of Albit® Plant Growth Stimulator for Mitigating Side-effects of Pesticides on Soil Microbial Respiration

    Directory of Open Access Journals (Sweden)

    Natalia N. Karpun

    2017-11-01

    Full Text Available Microorganisms give an early and integrated measure of soil functioning. In particular, soil microbial respiration is recommended for monitoring soil quality. The present study aims to determine the capacity of Albit® (poly-β-hydroxybutyrate, PHB to reduce the detrimental effects of pesticides on soil microbial respiration. The effects of three conventional pesticides (deltamethrin, dithianon, and difenoconazole on basal respiration (BR and substrate-induced respiration (SIR were assessed in the presence and absence of Albit®. The studied pesticides caused negative impacts on soil functioning, reducing BR and SIR. Applications of Albit® increased BR and SIR, and both BR and SIR were kept similar to the control when pesticides were applied with Albit®. PHB, an active ingredient of Albit®, is known to increase beneficial microflora in the rhizosphere due to its regulatory activity on indigenous microorganisms. Thus, more studies should be carried out under different edaphoclimatic conditions to study the benefits of Albit® applications along with pesticides in order to mitigate their side effects on soil microbial functioning.

  13. Preliminary studies on fluid inclusions in metasomatic albite grains from Lagoa Real, Caetite, Ba, Brazil

    International Nuclear Information System (INIS)

    Fuzikawa, K.

    1980-01-01

    Preliminary fluid inclusion studies in metasomatic albite grains from the Lagoa Real uranium deposit pointed out to mixing of strong brines (23 wt% NaCl equivalent) with low salinity fluids (2.3 wt% NaCl equivalent). Microthermometry and crushing tests indicated elevated pressures and the presence of hidrocarbons in larger amount than CO 2 . The remobilization of uranium as uranyl carbonate complexes and its precipitation, reducing U 6 + to U 4 + by CH 4 , is considered as a possibility. (Author) [pt

  14. Elaboration and characterization of mullite-anorthite-albite porous ceramics prepared from Algerian kaolin

    International Nuclear Information System (INIS)

    Rouabhia, F.; Nemamcha, A.; Moumeni, H.

    2018-01-01

    Mullite-anorthite-albite porous ceramic materials were successfully prepared by a solid-state reaction between kaolin clay and two different additives (CaCO 3 and Na 2 CO 3 ). The starting raw material was characterized by X-ray fluorescence, X-ray diffraction (XRD) and dynamic light scattering techniques. The effect of CaCO 3 and Na 2 CO 3 concentration (10 to 70 wt%) on structure, morphology and thermal properties of the obtained ceramics was investigated by XRD, scanning electron microscopy and differential scanning calorimetry (DSC) techniques. The XRD patterns showed that mullite (3Al 2 O 3 .2SiO 2 ), anorthite (CaO.Al 2 O 3 .2SiO 2 ) and albite (Na 2 O.Al 2 O 3 .6SiO 2 ) were the main crystalline phases present in the materials. The morphology investigation revealed the porous texture of obtained ceramics characterized by the presence of sponge-like structure mainly due to the additive decomposition at high temperatures. The DSC results confirm the presence of four temperature regions related to the kaolin thermal transformations and the formation of minerals. The temperature and enthalpy of mineral formation are additive concentration dependent. As a result, the optimal content of additives which allowed the coexistence of the three phases, a spongelike morphology, and high porosity without cracks corresponded to 15 wt% CaCO 3 , 15 wt% Na 2 CO 3 , and 70 wt% kaolin. (author)

  15. Study of corrosive-erosive wear behaviour of Al6061/albite composites

    International Nuclear Information System (INIS)

    Sharma, S.C.; Krishna, M.; Murthy, H.N. Narasimha; Tarachandra, R.; Satyamoorthy, M.; Bhattacharyya, D.

    2006-01-01

    This investigation analyses the influence of dispersed alumina particles on the wear behaviour of the Al/albite composites in a corrosive environment. The composites were prepared by modified pressure die-casting technique. The corrosive-erosive wear experiments were carried out on a proprietary corrosion-erosion wear tester to study the wear characteristics of the composites. The slurry was made up of water and alumina (size: 90-150 μm, proportion: 0-30 wt.%), while H 2 SO 4 (0.01, 0.1 and 1N) was added to create the corrosive conditions. Experiments were arranged to test the relationships among the corrosive-erosive wear rate, concentrations of H 2 SO 4 and alumina in the slurry, weight percent of albite in the composite, erosion speed and distance. Wear rate varies marginally at low speeds but sharply increases at higher speeds. The corrosive wear rate logarithmically increased with the increasing concentration of the corrosive medium. The effect of abrasive particles and corrosion medium on the wear behaviour of the composite is explained experimentally, theoretically and using scanning electron microscopy

  16. The carbonaceous matter in the uraniferous dequartzified and albitized leucogranite of Saraya (Senegal): an example of superimposed hydrothermal alterations

    International Nuclear Information System (INIS)

    Mouthier, B.

    1988-01-01

    Two superimposed early hydrothermal alterations have been recognized in the Proterozoic Saraya leucogranite. Successively are described a major dequartzification leading to an episyenite infilled with carbonaceous matter and sulfate during an interruption of the system, succeeded by a mobilization of U and other elements during an albitization. A dolomite filling up followed by a silicopotassic feed-back alteration, close down the system [fr

  17. Mid Carboniferous lamprophyres, Cobequid Fault Zone, eastern Canada, linked to sodic granites, voluminous gabbro, and albitization

    Science.gov (United States)

    Pe-Piper, Georgia; Piper, David J. W.; Papoutsa, Angeliki

    2018-01-01

    Major intra-continental shear zones developed during the later stages of continental collision in a back-arc setting are sites of prolonged magmatism. Mantle metasomatism results from both melting of subducted sediments and oceanic crust. In the Cobequid Fault Zone of the northern Appalachians, back-arc A-type granites and gabbros dated ca. 360 Ma are locally intruded by lamprophyric dykes dated ca. 335 Ma. All the lamprophyres are kersantites with biotite and albite, lesser ilmenite, titanite and fluorapatite, and minor magmatic calcite, allanite, pyrite, magnetite, quartz and K-feldspar in some samples. The lamprophyres show enrichment in Rb, Ba, K, Th and REE and classify as calc-alkaline lamprophyre on the basis of biotite and whole rock chemistry. Pb isotopes lie on a mixing line between normal mantle-derived gabbro and OIB magma. Nd isotopes range from 1.3-3.5 εNdt, a little lower than in local gabbro. Most lamprophyres have δ18O = 3.8-4.4‰. Country rock is cut by pyrite-(Mg)-chlorite veins with euhedral allanite crystals that resemble the lamprophyres mineralogically, with the Mg-chlorite representing chloritized glass. Early Carboniferous unenriched mafic dykes and minor volcanic rocks are widespread along the major active strike-slip fault zones. The lamprophyres are geographically restricted to within 10 km of a small granitoid pluton with some sodic amphibole and widespread albitization. This was displaced by early Carboniferous strike-slip faulting from its original position close to the large Wentworth Pluton, the site of mantle-derived sodic amphibole granite, a major late gabbro pluton, and a volcanic carapace several kilometres thick, previously demonstrated to be the site of mantle upwelling and metasomatism. The age of the lamprophyres implies that enriched source material in upper lithospheric mantle or lower crust was displaced 50 km by crustal scale strike-slip faulting after enrichment by the mantle upwelling before lamprophyre emplacement

  18. Geomorphological stability of Permo-Triassic albitized profiles - case study of the Montseny-Guilleries High (NE Iberia)

    Science.gov (United States)

    Parcerisa, D.; Casas, L.; Franke, C.; Gomez-Gras, D.; Lacasa, G.; Nunez, J. A.; Thiry, M.

    2010-05-01

    Massif paleoalteration profiles (≥ 200 m) occur in the upper parts of the Montseny-Guilleries High (NE Catalan Coastal Ranges). The profiles consist of hard albitized-chloritized-hematized facies in the lower part and softer kaolinized-hematized facies in the upper part of the section. Preliminary paleomagnetic data show Triassic ages for both, the albitized and the kaolinized parts, and point to a surficial formation altered under oxidising conditions. Similar paleoalteration profiles have already been described and dated to Triassic ages elsewhere in Europe [Schmitt, 1992; Ricordel et al., 2007; Parcerisa et al., 2009]. These Permian-Triassic alterations are following a succession of different mineral transformations from the top to the base of the profile: 1) Red facies are defined by an increase in the amount and size of haematite crystals leading to the red colour of the rocks. The increase on haematite content is pervasively affecting the whole rock and is accompanied by the kaolinitization of the feldspars. 2) Pink facies: here, the granite shows an uniform pink colouration, which is mainly due to the albitization of the primary Ca-bearing plagioclases, accompanied by a precipitation of minute haematite, sericite, and calcite crystals inside the albite. Additionally primary biotite is fully chloritized. The pink granites are much more resistant to the present-day weathering than the "unaltered" facies at the base of the profile. 3) Spotted facies is characterized by a partial alteration of the rock, which caused a pink-screened aspect to the rock. The alteration developed along the fractures and is less well developed or absent in the non-fractured zones. In the pink-screened facies, the plagioclases are partially albitized and contain numerous hematite inclusions. Biotites are usually almost entirely chloritized. 4) Unaltered facies: These granites are coloured white to greyish, containing plagioclase and K-feldspar that do not show any trace of

  19. Anisotropic surface physicochemical properties of spodumene and albite crystals: Implications for flotation separation

    Science.gov (United States)

    Xu, Longhua; Peng, Tiefeng; Tian, Jia; Lu, Zhongyuan; Hu, Yuehua; Sun, Wei

    2017-12-01

    Aluminosilicate minerals (e.g., spodumene, albite) have complex crystal structures and similar surface chemistries, but they have poor selectivity compared to traditional fatty acid collectors, making flotation separation difficult. Previous research has mainly considered the mineral crystal structure as a whole. In contrast, the surface characteristics at the atomic level and the effects of different crystal interfaces on the flotation behavior have rarely been investigated. This study focuses on investigating the surface anisotropy quantitatively, including the chemical bond characteristics, surface energies, and broken bond densities, using density functional theory and classical theoretical calculations. In addition, the anisotropy of the surface wettability and adsorption characteristics were examined using contact angle, zeta potential, and Fourier-transform infrared measurements. Finally, these surface anisotropies with different flotation behaviors were investigated and interpreted using molecular dynamics simulations, scanning electron microscopy, and X-ray photoelectron spectroscopy. This systematic research offers new ideas concerning the selective grinding and stage flotation of aluminosilicate minerals based on the crystal characteristics.

  20. Preliminary notes about the processes of uranium albitization at Lagoa Real (Bahia) and its comparation with the Russian and Sweden processes

    International Nuclear Information System (INIS)

    Stein, J.H.; Netto, A.M.; Drummond, D.; Angeiras, A.G.

    1980-10-01

    A brief description and interpretation of the development of the processes of albitization in Russia, Sweden and Brazil, is presented. Based on the comparison of similar characteristics, interpreted and suggested, in the light of present knowledge, it is proposed to set a place in time and space for the uranium mineralization at Lagoa Real. A zoning of the Sn, Cu, Ba, Pb and Zn with respect to the uranium mineralization is suggested. (Author) [pt

  1. Geochemical criteria for distinguishing magmatic and metasomatic albite-enrichment in granitoids — examples from the Ta-Li granite Yichun (China) and the Sn-W deposit Tikus (Indonesia)

    Science.gov (United States)

    Schwartz, M. O.

    1992-03-01

    Two examples of albite-rich granitoids of different genesis are discussed: the Ta-Li granite at Yichun (China) exhibits dominantly igneous textures, and the sodium-enrichment zone in biotite granite of the Sn-W deposit at Tikus is characterized by metasomatic textures. The Yichun stock shows a magmatic evolution from biotite-muscovite granite to lepidolite granite with an increase of Na2O and F concentrations and a decrease of CaO and Sr concentrations. The composition of the different granite phases is close to pseudoternary minima in the haplogranite-H2O(-Li-F) system. The composition of the F-rich albitization zone at Tikus deviates strongly from the pseudoternary minima and shows a tendency to become monomineralic (nearly pure albitite). CaO and Sr concentrations are increased or remain unchanged with respect to the unaltered biotite granite at Tikus. Albitization produced by fluid-rock interaction in F-rich systems is characterized by that CaO or Sr released by the breakdown of plagioclase in the granite protolith, are fixed in newly formed fluorite or albite, respectively.

  2. Mega-solubility of quartz resulting from highly alkaline fluids produced by dissolved albite in H2O at deep crustal conditions

    Science.gov (United States)

    Makhluf, A. R.; Manning, C. E.

    2017-12-01

    Models of H2O-rich fluids equilibrated with rocks at high P and T fail to predict the high solubilities observed experimentally, chiefly because thermodynamic data for the most abundant solutes is lacking. We investigated the effects of dissolved albite (Ab) on the solubility of quartz (Qz) at 1.0 GPa and 675-900 °C using a piston-cylinder apparatus to quantify possible mineral buffering or enhancement effects. We found a very large enhancement effect on the solubility of Qz when dissolved in dilute aqueous Ab solutions. SiO2 concentrations are similar to Qz solubility in strongly alkaline KOH solutions. At the highest temperature of 900 °C, we found that the solubility of Qz in 1.0 molal Ab solution increases by of factor of 4.5 over that in pure H2O, which corresponds to 10.7 molal SiO2. The nearly identical solubility of Qz in KOH(aq) and Ab solutions of the same concentration, P, and T, strongly suggest that NaOH(aq) liberated from NaAlSi3O8 in H2O fluids effects SiO2 solubility in a similar manner to that of KOH(aq). The deprotonated silica dimer was found to be a key species responsible for the high solubility of Qz in KOH(aq) and is likely responsible for the high solubility of Qz in Ab solutions. While the binaries Qz-H2O, Ab-H2O, and Qz-Ab are well known at 1.0 GPa, little data exists on the ternary system. The new results help quantify the ternary relations in the Ab-Qz-H2O system, which can be used as a simple model for liquid-vapor immiscibility granitic magmas. In addition, these highly alkaline solute-rich aqueous fluids suggest a mechanism for Ab-Qz metasomatism in subduction zones, such as in the Catalina schist (Bebout and Barton 1993), which provides an alternative to high P-T magmas. Our results show that subduction zone and metasomatic fluids may be much more alkaline and have significantly higher dissolving power than previously thought.

  3. Dissolution and time-dependent compaction of albite sand: experiments at 100°C and 160°C in pH-buffered organic acids and distilled water

    Science.gov (United States)

    Hajash, Andrew; Carpenter, Thomas D.; Dewers, Thomas A.

    1998-09-01

    Aqueous fluids are important in the diagenesis and deformation of crustal rocks. Both chemical and physical interactions are involved and often they are strongly coupled. For example, pore waters not only dissolve, transport, and precipitate chemical species, but they also substantially affect the mechanical behavior of the rocks that contain them. Stresses magnified at grain contacts by differences in pore-fluid pressure ( Pp) and confining pressure ( Pc) can, in turn, influence the rate and extent of chemical exchange. To begin investigation of these coupled systems, compaction experiments were conducted using albite sand (250-500 μm) and distilled water (pH 5.8), 0.07 M acetate (pH 4.7), and 0.07 M acetate + 0.005 M citrate (pH 4.4) solutions in a hydrothermal flow-through system at conditions that simulate diagenesis. Pore-fluid chemistry and pore-volume loss were monitored to quantify the effects of organic acids on time-dependent compaction rates. The effects of stress and fluid chemistry on the dissolution kinetics were also examined. Albite dissolution rates, monitored by steady-state fluid chemistry, increased when an effective pressure ( Pe= Pc- Pp) was applied, probably due to increases in total surface area caused by grain breakage at contacts. These effects were transient in distilled water, however, Si and Al concentrations remained elevated in the acetate pore fluid. The average Si-based release rates indicate ≈35% increase in reactive surface area by application of Pe=34.5 MPa. At 100°C with Pe=34.5 MPa, steady-state Si concentrations were ≈2.3 times higher in 0.07 M acetate and 5.8 times higher in 0.07 M acetate + 0.005 M citrate than in distilled water. Al increased by even larger factors (3× in the acetate buffer and 10× in the citrate solution). These changes in fluid chemistry are attributed to both pH and ligand-enhanced reactions. Albite dissolution appears to be controlled by surface complexation reactions at Al sites. Rapid

  4. High-pressure phase relations in the composition of albite NaAlSi3O8 constrained by an ab initio and quasi-harmonic Debye model, and their implications

    Science.gov (United States)

    Deng, L.; Liu, X.; Liu, H.; Dong, J.

    2010-12-01

    The high pressure physical-chemical behaviors of feldspar in subducted slab are very important to the geodynamic process in the deep interior of the Earth. Albite (NaAlSi3O8;Ab) is one of the few end members in the feldspar family, and its high-P behavior is obviously a prerequisite to the full understanding of the physical-chemical properties of feldspar at high pressures. So far it has been well accepted that Ab breaks down to the phase assemblage of Jadeite+Stishovite(NaAlSi2O6; Jd, SiO2; St,JS hereafter) at ~9-10 GPa. The JS phase assemblage might be stable up to ~23 GPa, and eventually directly change into the phase assemblage of calcium-ferrite type NaAlSiO4 (Cf) +2St (CS hereafter). However, some independent researches suggest there is an intermediate phase Na-hollandite (Na-Hall; a phase with the composition of NaAlSi3O8 and the structure of hollandite) between JS phase assemblage transition into CS phase assemblage (Liu 1978; Tutti 2007; Sekine and Ahrens, 1992; Beck et al., 2004). Whether Na-Hall is a thermodynamic stable phase under high P-T conditions remains unknown. In this work, phase relations in the composition of albite NaAlSi3O8 at pressures up to 40 GPa were constrained by a theoretical method that combines the ab initio calculation and quasi-harmonic Debyemodel. First, the P-T dependence of the thermodynamic potentials of the individual phase, St, Cf, Jd and the hypothetical Na-Holl were derived. Our results are generally in consistent agreement with available experimental data and previous theoretical predictions. Second, the Gibbs free energy of the hypothetical Na-Holl phase was compared with that of the phase assemblages JS and CS. Our results show that the Na-Holl phase is not a thermodynamically stable phase over the studied P-T conditions of 0-40 GPa and 100-600 K, which rules it out as a possible intermediate phase along the transition path from the JS phase assemblage to CS phase assemblage. Our calculations have predicted that the JS

  5. Rational calculation of migrated component amount for metasomatically altered rocks--taking albitized trachyte at uranium deposit No.470 as an sample

    International Nuclear Information System (INIS)

    Liu Dezheng

    2006-01-01

    On the basis of overall confirming the reasonableness of available method for calculating migrated component amount, the author has further improved the true constant component fixed calculation method proposed by the author in 2000, i.e, the calculation of actual true migrated mass and atomic number of metasomatically atered rocks, by using two method of measuring rock density. (authors)

  6. Thermo-optical properties of optically stimulated luminescence in feldspars

    DEFF Research Database (Denmark)

    Poolton, N.R.J.; Bøtter-Jensen, L.; Johnsen, O.

    1995-01-01

    Optically stimulated luminescence processes in feldspars are subject to competing thermal enhancement and quenching processes: this article describes the thermal enhancement effects for orthoclase, albite and plagioclase feldspars. It is demonstrated that certain lattice vibrational modes can be ...

  7. A note on incipient spilitisation of central Indian basin basalts

    Digital Repository Service at National Institute of Oceanography (India)

    Karisiddaiah, S.M.; Iyer, S.D.

    Rocks dredged in the vicinity of the 79 degrees E fracture zone, in the Central Indian Basin, are sub-alkaline basalts, which are regarded as precursors to spilites. The minerals identified are mainly albitic plagioclase, augite, olivine, and less...

  8. Sodium storage in deep paleoweathering profiles beneath the Paleozoic-Triassic unconformity

    Science.gov (United States)

    Thiry, M.; Parcerisa, D.; Ricordel-Prognon, C.; Schmitt, J.-M.

    2009-04-01

    A major sodium accumulation has been recognized for long and by numerous authors in the Permo-Triassic salt deposits (Hay et al., 2006). Beside these basinal deposits, important masses of sodium were stored on the continents within deep palaeoweathering profiles in form of albite. Indeed, wide surfaces and huge volumes of granito-gneissic basements of the Hercynian massifs are albitized from North-Africa up to Scandinavia. These albitized rocks have usually been considered as related to tardi-magmatic metasomatic processes (Cathelineau 1986; Petersson and Eliasson 1997). Geometrical arrangement and dating of these alterations point out that these albitizations, or at least a part of them, developed under low temperature subsurface conditions in relation with the Triassic palaeosurface (Ricordel et al., 2007; Parcerisa et al., 2009). Petrology The albitized igneous rocks show a strong alteration with pseudomorphic replacement of the primary plagioclases into albite, replacement of primary biotite by chlorite and minor precipitation of neogenic minerals like albite, chlorite, apatite, haematite, calcite and titanite. Albitized rocks are characterized by their pink coloration due to the presence of minute haematite inclusions in the albite. The development and distribution of the albitization and related alterations above the unaltered basement occurs in three steps that define a vertical profile, up to 100-150 m depth. 1) In the lower part of the profile, albitization occurs within pink-colored patches in the unaltered rock, giving a pink-spotted aspect to the rock. 2) In the middle part of the profile, rocks have an overall pink coloration due to the albitization of the primary Ca-bearing igneous plagioclases. Usually, this facies develops in a pervasive manner, affecting the whole rock, but it may also be restricted to joints, giving a sharp-pink coloration to the fracture wall. 3) Finally, the top of the profile is defined by the same mineral paragenesis as in the

  9. Petrology of blueschist facies metamorphic rocks of the Meliata Unit

    Directory of Open Access Journals (Sweden)

    Faryad Shah Wali

    1997-06-01

    Full Text Available Meliata blueschists originated from basalts, limestones, pelites, psammitic and amphibolite facies basement rocks. Compositionally, the metabasalts have a geochemical signature mostly indicative of a transitional arc-MORB origin, but some mafic rocks having affinity with within plate basalts also present. The mafic blueschists consist of blue amphibole, epidote and albite, rarely also garnet, Na-pyroxene and chloritoid. Apart from phengite and quartz the metapelites and metapsammites contain one or more of the minerals: chloritoid, paragonite, glaucophane, albite, chlorite, occasionally also Na-pyroxene and garnet. Amphibolite facies rocks contain relic garnet, plagioclase and hornblende, the latter two replaced by albite and blue amphibole, respectively. The zoning patterns of blue amphibole, garnet and chloritoid suggest their formation during prograde stage of metamorphism. P-T conditions of meta-morphism are estimated to be about 350-460 oC and 10-12 kbar.

  10. Integration of geophysical and geological data for delimitation of mineralized zones in Um Naggat area, Central Eastern Desert, Egypt

    Directory of Open Access Journals (Sweden)

    Ibrahim Gaafar

    2015-06-01

    Interpretations of the aeromagnetic maps delineated four regional structural trends oriented due NNW, NW, ENE and E–W directions. They are identified as strike-slip faults, which coincide well with field observations, where NW-trending faults cut and displace right laterally ENE-trending older ones. The interaction between these two strike-slip fault systems confining the albite granite is easily identified on the regional data presenting longer wavelength anomalies, implying deep-seated structures. They could represent potential pathways for migration of enriched mineralized fluids. Geochemically, albite granites of peraluminous characteristics that had suffered extensive post-magmatic metasomatic reworking, resulted into development of (Zr, Hf, Nb, Ta, U, Th, Sn and albite-enriched and greisenized granite body of about 600 m thick, and more than 3 km in strike length. The albite granite is characterized by sharp increase in average rare metal content: Zr (830 ppm, Hf (51 ppm, Nb (340 ppm, Ta (44 ppm, and U (90 ppm. Thorite, uranothorite, uraninite and zircon are the main uranium-bearing minerals of magmatic origin within the enclosing granite. However, with respect to Zr, Nb, and Ta, the albitized granite can be categorized as rare metal granite. The integration of airborne geophysical (magnetic and γ-ray spectrometric, geological, geochemical and mineralogical data succeeded in assigning the albite granite of Um Naggat pluton as a mineralized zone. This zone is characterized by its high thorium and uranium of hydrothermal origin as indicated by its low Th/U ratio, with rare metals mineralization controlled by two main structural trends in the NW- and ENE-directions.

  11. Uruguay geology contributions no. 4

    International Nuclear Information System (INIS)

    Preciozzi, F.

    1989-01-01

    Sedimentary facies: the metasiltites and mela sandstones develop granoblastic textures. The present lepidoblastic textures in flexured bands of seri cite and/or chlorite, a fine qranoblastic matrix made by quartz-feldespaths. The carbonates develop mosaic textures with big crystals of calcites and dolomite, generally elongated following metamorphic foliation (seri cite/chlorite). The quartzites develop qranoblastic textures, with few minerals. Volcanics facies: the basic volcanics presents doleritic intersect al textural, that exist saussuritized plagioclase and albitic diabasa with diopside-augite beaches. Usually the pyroxenes develop poiquilitic textural. Present amphiboles of the acti note series and frequently sphene. Others basic rocks are microlitio porfiric, in intersect al or fluidal matrix, with albite microliters in epi dote-chlorite-acti note criploerislalline ground.The stability relationships of the diferents types of basic metavulcanites show low metamorphic facies, with temperatures under 530-550 grades C, being the most Irequenl association: albite+actinote+chlorite+epidote+opaques- opaques.The clastic faciest are integrated by monogenic breccia with elements of varied vulcanites and porfiric rnicrolitic texture. The matrix is made of line quartz and epidote aggregate. The basic volcanism present hyalo-porfiric textures with saussuritized plagiodase pheno crystals, and quartz in a micro lo criptocrystalline ground. Were also defined rocks with porfiric texture in a piromeritic ground as well as rocks with vacuolar microlitic texture.The clastic facies are made by breccias with sharp elements, with rare cement, integrated by pyroclastic products, The volcanics rocks present retrometamorphism of the phenocrystals and devitrification. The plagioclase are traslormated in fine aggregates of albite epidote. The regional metamorphism minerals are represented by the para genesis: quartz+albite+chlorite+epidote+(seri cite-actinole), subfacies quartz albite

  12. Triassic regolithization: A major stage of pre-enrichment in the formation of unconformity related deposits in Southern France

    International Nuclear Information System (INIS)

    Schmitt, J.M.; Clement, J.Y.

    1989-01-01

    The formation of unconformity related uranium deposits in Canada and Australia is currently thought to have involved some stage of preconcentration within the Proterozoic regolith. Uranium deposits in the southern Massif central (France) are spatially linked to the Mesozoic unconformity. Under this unconformity, rocks of the Hercynian basement as well as Permo-Carboniferous sediments show a regolithic alteration dating back to the Late Permian to Late Triassic period. On the elevated parts of the Triassic landscape, 30 to 50 m deep weathering profiles are preserved. Three main zones can be distinguished: a lower pink coloured zone, showing partly albitized and chloritized rocks: a middle bleached zone with neogenic clays; and an upper reddish zone with Fe-Mn oxyhydroxides. Towards the Triassic basin, much deeper (200-300 m) alteration profiles are observed on Permo-Carboniferous sediments. The two upper regolithic zones are present, but the lower albitized one is very developed with two subzones: analcite/albite at the top, and K-feldspar/albite at the bottom. Geochemical data show that potassium is fixed in the uppermost horizons of the regolith, whereas sodium is transported towards the lower horizons and basin areas and fixed in analcite/albite zones. Uranium, vanadium, copper and less mobile elements such as titanium and zirconium are strongly leached from the weathering profiles in elevated parts of the landscape but are enriched in basin zones of albitization up to 5-15 times. Thus, solutions generated from the weathering profiles have brought about a major redistribution of uranium in the Triassic landscape. The remarkable applanation and tectonic stability of the area as well as a subarid climate seem to have favoured this 'regolithization' process. In southern France, geochemical differentiation during the Triassic has thus given rise to important uranium pre-enrichment, and the regolith is a major control for later uranium deposits. (author). 16 refs, 8

  13. Uruguay geology contributions no. 4; Contribuciones a la geologia del Uruguay no. 4

    Energy Technology Data Exchange (ETDEWEB)

    Preciozzi, F [Ministerio de Industria Energia y Mineria, Direccion Nacional de Mineria y Geologia, Montevideo (Uruguay)

    1989-07-01

    Sedimentary facies: the metasiltites and mela sandstones develop granoblastic textures. The present lepidoblastic textures in flexured bands of seri cite and/or chlorite, a fine qranoblastic matrix made by quartz-feldespaths. The carbonates develop mosaic textures with big crystals of calcites and dolomite, generally elongated following metamorphic foliation (seri cite/chlorite). The quartzites develop qranoblastic textures, with few minerals. Volcanics facies: the basic volcanics presents doleritic intersect al textural, that exist saussuritized plagioclase and albitic diabasa with diopside-augite beaches. Usually the pyroxenes develop poiquilitic textural. Present amphiboles of the acti note series and frequently sphene. Others basic rocks are microlitio porfiric, in intersect al or fluidal matrix, with albite microliters in epi dote-chlorite-acti note criploerislalline ground.The stability relationships of the diferents types of basic metavulcanites show low metamorphic facies, with temperatures under 530-550 grades C, being the most Irequenl association: albite+actinote+chlorite+epidote+opaques- opaques.The clastic faciest are integrated by monogenic breccia with elements of varied vulcanites and porfiric rnicrolitic texture. The matrix is made of line quartz and epidote aggregate. The basic volcanism present hyalo-porfiric textures with saussuritized plagiodase pheno crystals, and quartz in a micro lo criptocrystalline ground. Were also defined rocks with porfiric texture in a piromeritic ground as well as rocks with vacuolar microlitic texture.The clastic facies are made by breccias with sharp elements, with rare cement, integrated by pyroclastic products, The volcanics rocks present retrometamorphism of the phenocrystals and devitrification. The plagioclase are traslormated in fine aggregates of albite epidote. The regional metamorphism minerals are represented by the para genesis: quartz+albite+chlorite+epidote+(seri cite-actinole), subfacies quartz albite

  14. Thermoluminescence studies having applications to geology and archaeometry

    International Nuclear Information System (INIS)

    Levy, P.N.

    1978-01-01

    Mineral thermoluminescence (TL) studies, undertaken as geophysics investigations, appear to have archaeometric applications. Measurements were made with equipment which records TL emission spectra at closely spaced temperatures. Carbonate rock containing lead-zinc deposits exhibit radiation induced TL against distance-from-ore patterns useful for mineral exploration and locating worked-out deposits. The feldspar albite has second-order TL kinetics, which can introduce dating errors. Heat induced changes in the albite TL emission spectra could be used as a paleotemperature indicator. Quartz remembers previous exposure to radiation, a property influencing TL intensity against dose curves but useful for uranium exploration

  15. Report on the vitrification and devitrification of Hanford, Washington soil. Final report

    International Nuclear Information System (INIS)

    King, J.A.; SubbaRao, S.C.

    1983-01-01

    This study as focused principally on the effects of melting or vitrification and recrystallization or devitrification on soil from the Hanford Reservation in Washington State. The fusion properties of soil are important because the containment of nuclear material in in-situ vitrified soil is a possible requirement. An understanding of the physical and chemical properties of the soil is important in determinaing how the soil can contain the nuclear material. The soil itself is composed of a plagioclastic feldspar, quartz, and hematite. The feldspar is made up of albite and anorthite. When the soil is heated, the first mineral to melt is the albite between 1100 0 C and 1200 0 C. The mineral anorthite melts above 1310 0 C and hematite below 1700 0 C. The quartz does not melt until the temperature exceeds 1715 0 C. The albite in the glass is sodium aluminosilicate. When the albite melts, microscopic spheres of non-crystalline, low-melting sodium silicate form. This indicates that the aluminosilicate matrix decomposes when heated. When crystals, which were previously fused, are heated: crystals begin to reform above 900 0 C. The minerals which crystallize are feldspar and magnetite, an iron oxide. Recrystallization should begin at a temperature 250 0 C below the liquidus point. The leaching of sodium, copper, calcium, and aluminum decreased with increasing fusion temperature, while the leaching of iron and barium increased with increasing fusion temperature

  16. U–Pb zircon and biostratigraphic data of high‐pressure/ low‐temperature metamorphic rocks of the Talea Ori : tracking the Paleotethys suture in central Crete, Greece

    NARCIS (Netherlands)

    Zulauf, G.; Dörr, W.; Krahl, J.; Lahaye, Y.; Chatzaras, V.; Xypolias, P.

    2016-01-01

    Inherited deformation microfabrics of detrital quartz grains and U–Pb (Laser ablation (LA)-ICPMS and ID TIMS) ages of detrital zircons separated from the Phyllite–Quartzite Unit s.l. of the Talea Ori, central Crete, suggest strikingly different source rocks. Albite gneiss of the lower Rogdia Beds

  17. Basement to surface expressions and critical factors in the genesis of unconformity-related deposits

    International Nuclear Information System (INIS)

    Potter, Eric

    2014-01-01

    Two subprojects: 1) Basement to surface expressions of deep mineralization and refinement of critical factors leading to the genesis of unconformity-related uranium deposits; and 2) Recognition of uranium ore system alteration signatures in complex terranes: IOCG vs albite-hosted uranium vs volcanic-hosted uranium.

  18. Chemical and mineralogical characterization and ceramic suitability ...

    African Journals Online (AJOL)

    The chemical and mineralogical characterization of raw feldspathic materials from Dschang (Cameroon) was realized by means of X-ray diffraction, differential thermal analyses, optical and scanning electron microscopies, and analytical techniques. It was found that these materials consist of albite (43 ± 3 wt.%), microcline ...

  19. Susceptibility of Granite Rock to scCO2/Water at 200 degrees C and 250 degrees C

    Energy Technology Data Exchange (ETDEWEB)

    Sugama, T.; Gill, S., Ecker, L., Butcher, T., Warren, J.

    2011-01-01

    Granite rock comprising anorthoclase-type albite and quartz as its major phases and biotite mica as the minor one was exposed to supercritical carbon dioxide (scCO{sub 2})/water at 250 C and 13.78 MPa pressure for 104 hours. For comparison purpose, four other rocks, albite, hornblende, diorite, and quartz, also were exposed. During the exposure of granite, ionic carbonic acid, known as the wet carbonation reactant, preferentially reacted with anorthoclase-type albite and biotite, rather than with quartz. The susceptibility of biotite to wet carbonation was higher than that of anorthoclase-type albite. All the carbonation by-products of anorthoclase-type albite were amorphous phases including Na- and K-carbonates, a kaolinite clay-like compound, and silicon dioxide, while wet carbonation converted biotite into potassium aluminum silicate, siderite, and magnesite in crystalline phases and hydrogen fluoride (HF). Three of these reaction by-products, Na- and K-carbonates and HF, were highly soluble in water. Correspondingly, the carbonated top surface layer, about 1.27 mm thick as carbonation depth, developed porous microstructure with numerous large voids, some of which have a size of {>=} 10 {mu}m, reflecting the erosion of granite by the leaching of these water-soluble reaction by-products. Comparing with this carbonation depth, its depth of other minerals was considerable lower, particularly, for hornblende and diorite with 0.07 and 0.02 mm, while no carbonate compound was detected in quartz. The major factor governing these low carbonation depths in these rocks was the formation of water-insensitive scale-like carbonate by-products such as calcite (CaCO{sub 3}), siderite (FeCO{sub 3}), and magnesite (MgCO{sub 3}). Their formation within the superficial layer of these minerals served as protective barrier layer that inhibits and retards further carbonation of fresh underlying minerals, even if the exposure time was extended. Thus, the coverage by this barrier layer

  20. Fluid inclusions in minerals associated to uranium mineralization in Jazida do Engenho (anomaly 09), Lagoa Real uranium province - Bahia, Brazil; Inclusoes fluidas nos minerais associados a mineralizacao uranifera da Jazida do Engenho (Anomalia 09), provincia uranifera de Lagoa Real, BA

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Aurelio da Silva de

    2009-07-01

    The Engenho deposit (anomaly 09) is south-eastern from Cachoeira Mine (anomaly 13), in the northern part of the Province. The uranium mineralization is associated to 'albitites' (over 70% of albite/oligoclase). Epidosites with uranium may also occur. The 'albitite' main minerals are pyroxene, gamet, albite/oligoclase feldspar, amphibole and biotite. Pyroxene, gamet, plagioclase, titanite and epidote are the minerals associated to the uranium mineralization. The fluids related to pyroxene, gamet and epidote are aqueous-saline, primary and with no carbonic phases and are constant, with small variations. They all present medium to high salinity (14 to 18wt% NaCl eq.), the higher values being related to pyroxene and the lower ones related to gamet and epidote. The fluids associated to albite/oligoclase, although aqua-saline and with no carbonic phases, show salinities much lower than in pyroxene, gamet and epidote, suggesting a intense dilution process indicating dilution toward the later minerals phases. The data suggest the pyroxene formation process occurring under a 3,5 kbar pressure condition which corresponds to approximately 10km depth. The dispersion on Th in albites, due probably to the overheating and non elastic increase in volume, precluded a reliable pressure calculation. The IF's microscopy m plagioclase gneiss (albitites host-rocks) suggests the probability of primary carbonic fluids associated to these minerals. The fluids with CO{sub 2} showed in the gneiss maybe also be present in the albitites, probably as late or intergranular fluids. This assumption is based on the fact that signs of carbonic gases were shown during crushing tests. These tendencies suggest the occurrence of two albitization phases in this Lagoa Real area: one associated to a fluid composed by H{sub 2}O + CO{sub 2} + salts (in the gneiss host) and another (in the albitite) formed by an aqueous-saline phase. The data indicate the Brasiliano event as a thermal

  1. Fluid inclusions in minerals associated to uranium mineralization in Jazida do Engenho (anomaly 09), Lagoa Real uranium province - Bahia, Brazil

    International Nuclear Information System (INIS)

    Souza, Aurelio da Silva de

    2009-01-01

    The Engenho deposit (anomaly 09) is south-eastern from Cachoeira Mine (anomaly 13), in the northern part of the Province. The uranium mineralization is associated to 'albitites' (over 70% of albite/oligoclase). Epidosites with uranium may also occur. The 'albitite' main minerals are pyroxene, gamet, albite/oligoclase feldspar, amphibole and biotite. Pyroxene, gamet, plagioclase, titanite and epidote are the minerals associated to the uranium mineralization. The fluids related to pyroxene, gamet and epidote are aqueous-saline, primary and with no carbonic phases and are constant, with small variations. They all present medium to high salinity (14 to 18wt% NaCl eq.), the higher values being related to pyroxene and the lower ones related to gamet and epidote. The fluids associated to albite/oligoclase, although aqua-saline and with no carbonic phases, show salinities much lower than in pyroxene, gamet and epidote, suggesting a intense dilution process indicating dilution toward the later minerals phases. The data suggest the pyroxene formation process occurring under a 3,5 kbar pressure condition which corresponds to approximately 10km depth. The dispersion on Th in albites, due probably to the overheating and non elastic increase in volume, precluded a reliable pressure calculation. The IF's microscopy m plagioclase gneiss (albitites host-rocks) suggests the probability of primary carbonic fluids associated to these minerals. The fluids with CO 2 showed in the gneiss maybe also be present in the albitites, probably as late or intergranular fluids. This assumption is based on the fact that signs of carbonic gases were shown during crushing tests. These tendencies suggest the occurrence of two albitization phases in this Lagoa Real area: one associated to a fluid composed by H 2 O + CO 2 + salts (in the gneiss host) and another (in the albitite) formed by an aqueous-saline phase. The data indicate the Brasiliano event as a thermal event without a predominant fluid

  2. Carboniferous-Permian tectonic transition envisaged in two magmatic episodes at the Kuruer Cu-Au deposit, Western Tianshan (NW China)

    Science.gov (United States)

    Yu, Jie; Li, Nuo; Qi, Nan; Guo, Jian-Ping; Chen, Yan-Jing

    2018-03-01

    The Western Tianshan in NW China is one of the most important gold provinces in the Central Asian Orogenic Belt (CAOB). The recently discovered Kuruer Cu-Au deposit has been interpreted to represent a transition from high-sulfidation epithermal to porphyry mineralization system. In this study, we present new LA-ICP-MS zircon U-Pb ages for the many magmatic rock types at Kuruer, including the Dahalajunshan Formation andesitic tuff (333.2 ± 1.6 Ma), diorite porphyry (269.7 ± 2.0 Ma), slightly-altered (264.4 ± 2.6 Ma) and intensively-altered (270.5 ± 2.5 Ma) albite porphyry. These ages reveal two distinct magmatic episodes: The Early Carboniferous Dahalajunshan Formation (wall rocks) andesitic tuff samples contain narrow ranges of SiO2 (60.29-61.28 wt.%), TiO2 (0.96-0.98 wt.%), Al2O3 (16.55-16.57 wt.%) and Fe2O3T (5.36-5.57 wt.%). The tuff is characterized by LREE enrichment and HFSE depletion, as well as LREE/HREE enrichment ((La/Yb)N = 8.31-8.76) and negative Eu anomalies (δEu = 0.64-0.76). Zircon εHf (t) values are 5.4-8.2, and two-stage Hf model ages (TDM2) are 821-1016 Ma, indicating partial melting of a moderately depleted mantle wedge with Precambrian continental crustal input. The ore-forming Middle Permian diorite porphyry and (quartz) albite porphyry have variable major oxide compositions (e.g., SiO2 = 53.09-53.12 wt.% for the diorite porphyry, 70.84-78.03 wt.% for the albite porphyry, and 74.07-75.03 wt.% for the quartz albite porphyry) but similar chondrite-normalized REE and primitive mantle-normalized multi-element patterns. These porphyries display LREE enrichment and HFSE depletion, as well as elevated LREE/HREE enrichment and negative Eu anomalies. The positive zircon εHf(t) values (11.7-15.9 for the diorite porphyry, 8.9-14.9 for the albite porphyry) and young two-stage Hf model ages (TDM2) (282-542 Ma for the diorite porphyry, 337-717 Ma for the albite porphyry) indicate a major juvenile continental crustal involvement. We propose that the

  3. Utilization of plastic detectors in autoradiographic studies of radioactive minerals from the Lagoa Real uranium Province, state of Bahia, Brazil

    International Nuclear Information System (INIS)

    Brandao, P.M.C.

    1984-01-01

    A short account on an autoradiographic technique using plastic detectors, it's methodology, application and results is presented. With this technique the distribution of radioactive minerals in rocks can be studied in detail. As radioactive source for this study, samples mineralized in uraninite and/or pitchblende were used. The utilized detectors were the CR-39 (a polymer plate) and films of celulose nitrate: CA-80-15 and CN-85. The mineralization is associated to mafics (amphibole, pyroxene, biotite, garnet, etc.) and to plagioclase (albite or albite-oligoclase), occurring as small inclusions and also in microfractures, cleavages and grain boundaries, mainly among plagioclase crystals which occur close to or practically touching mafic minerals. (Author) [pt

  4. Effect of pressure on the short-range structure and speciation of carbon in alkali silicate and aluminosilicate glasses and melts at high pressure up to 8 GPa: 13C, 27Al, 17O and 29Si solid-state NMR study

    Science.gov (United States)

    Kim, Eun Jeong; Fei, Yingwei; Lee, Sung Keun

    2018-03-01

    Despite the pioneering efforts to explore the nature of carbon in carbon-bearing silicate melts under compression, experimental data for the speciation and the solubility of carbon in silicate melts above 4 GPa have not been reported. Here, we explore the speciation of carbon and pressure-induced changes in network structures of carbon-bearing silicate (Na2O-3SiO2, NS3) and sodium aluminosilicate (NaAlSi3O8, albite) glasses quenched from melts at high pressure up to 8 GPa using multi-nuclear solid-state NMR. The 27Al triple quantum (3Q) MAS NMR spectra for carbon-bearing albite melts revealed the pressure-induced increase in the topological disorder around 4 coordinated Al ([4]Al) without forming [5,6]Al. These structural changes are similar to those in volatile-free albite melts at high pressure, indicating that the addition of CO2 in silicate melts may not induce any additional increase in the topological disorder around Al at high pressure. 13C MAS NMR spectra for carbon-bearing albite melts show multiple carbonate species, including [4]Si(CO3)[4]Si, [4]Si(CO3)[4]Al, [4]Al(CO3)[4]Al, and free CO32-. The fraction of [4]Si(CO3)[4]Al increases with increasing pressure, while those of other bridging carbonate species decrease, indicating that the addition of CO2 may enhance mixing of Si and Al at high pressure. A noticeable change is not observed for 29Si NMR spectra for the carbon-bearing albite glasses with varying pressure at 1.5-6 GPa. These NMR results confirm that the densification mechanisms established for fluid-free, polymerized aluminosilicate melts can be applied to the carbon-bearing albite melts at high pressure. In contrast, the 29Si MAS NMR spectra for partially depolymerized, carbon-bearing NS3 glasses show that the fraction of [5,6]Si increases with increasing pressure at the expense of Q3 species ([4]Si species with one non-bridging oxygen as the nearest neighbor). The pressure-induced increase in topological disorder around Si is evident from an

  5. Structural controls and evolution of gold-, silver-, and REE-bearing copper-cobalt ore deposits, Blackbird district, east-central Idaho: Epigenetic origins

    Science.gov (United States)

    Lund, K.; Tysdal, Russell G.; Evans, Karl V.; Kunk, Michael J.; Pillers, Renee M.

    2011-01-01

    The Cu-Co ± Au (± Ag ± Ni ± REE) ore deposits of the Blackbird district, east-central Idaho, have previously been classified as Besshi-type VMS, sedex, and IOCG deposits within an intact stratigraphic section. New studies indicate that, across the district, mineralization was introduced into the country rocks as a series of structurally controlled vein and alteration systems. Quartz-rich and biotite-rich veins (and alteration zones) and minor albite and siderite veinlets maintain consistent order and sulfide mineral associations across the district. Both early and late quartz veins contain chalcopyrite and pyrite, whereas intermediate-stage tourmaline-biotite veins host the cobaltite. Barren early and late albite and late carbonate (generally siderite) form veins or are included in the quartz veins. REE minerals, principally monazite, allanite, and xenotime, are associated with both tourmaline-biotite and late quartz veins. The veins are in mineralized intervals along axial planar cleavage, intrafolial foliation, and shears.

  6. Blueschist metamorphism and its tectonic implication of Late Paleozoic-Early Mesozoic metabasites in the mélange zones, central Inner Mongolia, China

    Science.gov (United States)

    Zhang, Jinrui; Wei, Chunjing; Chu, Hang

    2015-01-01

    Blueschists in central Inner Mongolia are distributed as layers and blocks in mélanges including the southern zone in Ondor Sum area and the northern zone in Manghete and Naomuhunni areas. They have been attributed to the subduction of Early Paleozoic oceanic crust. Blueschists from Ondor Sum and Naomuhunni are characterized by occurrence of sodic amphibole coexisting with epidote, albite, chlorite, calcic amphibole (in Ondor Sum) and muscovite (in Naomuhunni). Blueschists in Manghete contain porphyroblastic albite with inclusions of garnet and epidote in a matrix dominated by calcic-sodic amphibole, epidote, chlorite, albite and muscovite. Phase equilibria modeling for three blueschist samples using pseudosection suggest that the AlM2 contents in sodic amphibole can be used as a good barometer in the limited assemblage involving sodic amphibole + actinolite + epidote + chlorite + albite + quartz under pressures 7-10 kbar. In the sodic amphibole-bearing assemblages, the NaM4 contents in sodic amphibole mainly decrease as temperature rises, being a potential thermometry. The calculated pseudosections constrain the P-T conditions of blueschists to be 3.2-4.2 kbar/355-415 °C in Ondor Sum, 8.2-9.0 kbar/455 °C-495 °C in Manghete and 6.6-8.1 kbar/420-470 °C in Naomuhunni. These P-T estimates indicate a rather high geothermal gradient of 18-25 °C/km for the blueschist metamorphism, being of intermediate P/T facies series. Available zircon U-Pb age data suggests that the protoliths of blueschists were formed later than Late Paleozoic-Early Mesozoic and metamorphosed soon afterwards. An alternative interpretation for the tectonic implication of blueschists in central Inner Mongolia is that they may be a new type attributed to closure of limited ocean basins and do not represent a tectonic regime occurred in conventional subduction setting.

  7. The study of the mineralogy and rare earth elements behavior in the hydrothermal alteration zones of the Astaneh granitoid massif (SW Arak, Markazi province, Iran)

    International Nuclear Information System (INIS)

    Esmaeily, D.; Afshooni, S. Z.; Valizadeh, M. V.

    2009-01-01

    The Astaneh granitoid massif is located about 40 km to Arak city, central Iran, is a part of Sanandaj-Sirjan structural zone. These intrusive rocks which are mainly composed of gronodioritic rocks, widely affected under hydrothermal alteration. The alteration zones, on the basis of field studies and mineralogy as well as the study of the REE behavior, are investigated in this paper. Eight alteration zones including phyllic (sericitic) with quartz, sericite and pyrite; chloritic with quartz, sericite and chlorite; propylitic with chlorite, epidot, calcite and albite; argillic with clay minerals (chlorite and illite); silicic with abundant quartz; albitic with albite, chlorite and quartz; hematitisation with hematite, Fe-carbonates (ankerite and siderite) and tourmalinisation with tourmaline (dravite) are identified. The results demonstrate notable differences in the REE behavior in the different alteration zones. Accordingly, comparison with the fresh rocks, in the phyllic (sericitic) alteration, LREE are enriched, but HREE, except Yb which enriched, unchanged. Also in chloritic alteration zone, LREEs are depleted, but HREEs represent different behaviors. In the argillic and propylitic alteration zones, all REE are depleted, but compared with HREE, the LREE represent more depletion. In the silicic and hematitisation alteration zones, compared with HREE, the LREE are enriched. Finally, in the albitic and tourmalinisation alteration zones all REE are depleted. These features indicate that the behavior of REE in the hydrothermal alteration zones of the Astaneh granitoid rocks is mainly controlled by p H, availability of complexing ions in the fluid as well as the presence of secondary phases as host REE minerals

  8. Journal of Earth System Science | Indian Academy of Sciences

    Indian Academy of Sciences (India)

    The Bijli Rhyolite can be recognized as a poorly sorted pyroclastic deposit, and comprises of phenocrystic K-feldspar + albite ± anorthoclase set in fine-grained micro-fragmental matrix of quartz-feldsparsericite- chlorite-iron-oxide ± calcite. The rocks are largely metaluminous with high SiO2, Na2O+ KO, Fe/Mg, Ga/Al, Zr, Ta, ...

  9. Caracterización geoquímica y estudio comparativo de plagiogranitos de las Zonas Surportuguesa y Ossa-Morena (SO del Macizo Ibérico, España)

    OpenAIRE

    Bellido, F.; Díez-Montes, A.; Sánchez-García, T.

    2010-01-01

    Plagiogranites and albitic rocks belonging to contrasted magmatic associations of different ages and geodynamic environments outcrop in Ossa-Morena (OMZ) and Surportuguese (SPZ) Zones. OMZ plagiogranites are related with Cambrian-Ordovician rifting and represent a part of the felsic members of a bimodal magmatic suite and show oceanic plagiogranites affinities. SPZ plagiogranites are related with a Carboniferous volcano-plutonic calc-alkaline suite related with Variscan Orogeny. Both plagiogr...

  10. Characterization of Mongolian Natural Minerals and Their Application for Heavy Metal Adsorbent

    OpenAIRE

    Dolgormaa, Munkhbat; Shiomori, Koichiro; Bayanjargal, Ochirkhuyag

    2016-01-01

    In this study, the structural characteristic and the adsorption properties of heavy metals on Mongolian natural minerals were investigated. The natural samples were confirmed as Heulandite group of Clinoptilolite type zeolite and clay sample that contains albite and quartz by X-ray diffraction analysis. According to BET surface analysis, natural zeolites have mesoporous type of pore. The results of adsorption study showed that adsorption ability of natural zeolite is high effective for lead i...

  11. A-thermal elastic behavior of silicate glasses.

    Science.gov (United States)

    Rabia, Mohammed Kamel; Degioanni, Simon; Martinet, Christine; Le Brusq, Jacques; Champagnon, Bernard; Vouagner, Dominique

    2016-02-24

    Depending on the composition of silicate glasses, their elastic moduli can increase or decrease as function of the temperature. Studying the Brillouin frequency shift of these glasses versus temperature allows the a-thermal composition corresponding to an intermediate glass to be determined. In an intermediate glass, the elastic moduli are independent of the temperature over a large temperature range. For sodium alumino-silicate glasses, the a-thermal composition is close to the albite glass (NaAlSi3O8). The structural origin of this property is studied by in situ high temperature Raman scattering. The structure of the intermediate albite glass and of silica are compared at different temperatures between room temperature and 600 °C. When the temperature increases, it is shown that the high frequency shift of the main band at 440 cm(-1) in silica is a consequence of the cristobalite-like alpha-beta transformation of 6-membered rings. This effect is stronger in silica than bond elongation (anharmonic effects). As a consequence, the elastic moduli of silica increase as the temperature increases. In the albite glass, the substitution of 25% of Si(4+) ions by Al(3+) and Na(+) ions decreases the proportion of SiO2 6-membered rings responsible for the silica anomaly. The effects of the silica anomaly balance the anharmonicity in albite glass and give rise to an intermediate a-thermal glass. Different networks, formers or modifiers, can be added to produce different a-thermal glasses with useful mechanical or chemical properties.

  12. Mid-crustal uranium and rare metal mineralisation in the Mount Isa Inlier: a genetic model for formation of orogenic uranium deposits

    OpenAIRE

    McGloin, Matthew

    2017-01-01

    Uranium mineralisation near Mount Isa in northwest Queensland, Australia, is widespread yet poorly understood. Within this region in the Western Fold Belt, one hundred and ninety uranium-rare metal occurrences are known. This uranium mineralisation is similar to worldwide examples of albitite-hosted or sodium-metasomatic uranium deposits, which host albite-carbonate ore zones enriched in incompatible elements. Various metal sources and ore-forming processes have been sugg...

  13. Influence of feldspar containing lithium in the sintering of triaxial ceramics

    International Nuclear Information System (INIS)

    Oliveira, Camila Felippe de; Strecker, Kurt

    2011-01-01

    In this work, the properties of a ceramic material based on a triaxial mass composed of clay, quartz and 15 to 30% feldspar, albite or spodumene, has been investigated. Specimen were prepared by uniaxial pressing under 28.5MPa and sintering at temperatures of 1000, 1100 and 1200 deg C, for 1h. The samples were characterized by their linear shrinkage, apparent porosity, apparent density and flexural strength, as well as analysis of the microstructure. The best results were obtained for samples prepared with 30% spodumene and sintered at 1200 deg C, with a shrinkage of 6.4%, density of 2.01g/cm 3 , porosity of 14.3% and flexural strength of 13.4MPa, while samples prepared with albite exhibited shrinkage of 5.8%, density of 1.9g/cm 3 , porosity of 18.9% and strength of 9.8MPa. Therefore, by the substitution of albite by spodumene in the ceramic triaxial mass, lower sintering temperatures may be employed, thus reducing production costs by the lesser energy consumption. (author)(

  14. Effects of heat-flow and hydrothermal fluids from volcanic intrusions on authigenic mineralization in sandstone formations

    Directory of Open Access Journals (Sweden)

    Wolela Ahmed

    2002-06-01

    Full Text Available Volcanic intrusions and hydrothermal activity have modified the diagenetic minerals. In the Ulster Basin, UK, most of the authigenic mineralization in the Permo-Triassic sandstones pre-dated tertiary volcanic intrusions. The hydrothermal fluids and heat-flow from the volcanic intrusions did not affect quartz and feldspar overgrowths. However, clay mineral-transformation, illite-smectite to illite and chlorite was documented near the volcanic intrusions. Abundant actinolite, illite, chlorite, albite and laumontite cementation of the sand grains were also documented near the volcanic intrusions. The abundance of these cementing minerals decreases away from the volcanic intrusions.In the Hartford Basin, USA, the emplacement of the volcanic intrusions took place simultaneous with sedimentation. The heat-flow from the volcanic intrusions and hydrothermal activity related to the volcanics modified the texture of authigenic minerals. Microcrystalline mosaic albite and quartz developed rather than overgrowths and crystals near the intrusions. Chlorite clumps and masses were also documented with microcrystalline mosaic albite and quartz. These features are localized near the basaltic intrusions. Laumontite is also documented near the volcanic intrusions. The reservoir characteristics of the studied sandstone formations are highly affected by the volcanic and hydrothermal fluids in the Hartford and the Ulster Basin. The porosity dropped from 27.4 to zero percent and permeability from 1350 mD to 1 mD.

  15. Mineral-solution equilibria—III. The system Na 2OAl 2O 3SiO 2H 2OHCl

    Science.gov (United States)

    Popp, Robert K.; Frantz, John D.

    1980-07-01

    Chemical equilibrium between sodium-aluminum silicate minerals and chloride bearing fluid has been experimentally determined in the range 500-700°C at 1 kbar, using rapid-quench hydrothermal methods and two modifications of the Ag + AgCl acid buffer technique. The temperature dependence of the thermodynamic equilibrium constant ( K) for the reaction NaAlSi 3O 8 + HCl o = NaCl o + 1/2Al 2SiO 5, + 5/2SiO 2 + 1/2H 2O Albite Andalusite Qtz. K = (a NaCl o) /(a H 2O ) 1/2/(a HCl o) can be described by the following equation: log k = -4.437 + 5205.6/ T( K) The data from this study are consistent with experimental results reported by MONTOYA and HEMLEY (1975) for lower temperature equilibria defined by the assemblages albite + paragonite + quartz + fluid and paragonite + andalusite + quartz + fluid. Values of the equilibrium constants for the above reactions were used to estimate the difference in Gibbs free energy of formation between NaCl o and HCl o in the range 400-700°C and 1-2 kbar. Similar calculations using data from phase equilibrium studies reported in the literature were made to determine the difference in Gibbs free energy of formation between KCl o and HCl o. These data permit modelling of the chemical interaction between muscovite + kspar + paragonite + albite + quartz assemblages and chloride-bearing hydrothermal fluids.

  16. Laser ablation - inductive coupled plasma - mass spectrometer (LA-ICP-MS) geochemistry characterization of albitites associated to uranium in Lagoa da Rabicha deposit, Lagoa Real, BA (Brazil)

    International Nuclear Information System (INIS)

    Oliveira, Lucilia A. Ramos de; Rios, Francisco Javier; Amorim, Lucas Eustaquio Dias; Souza, Aurelio da Silva; Prates, Sonia Pinto; Yardley, Bruce; Matos, Evando Carele

    2009-01-01

    The LA-ICP-MS technique is a good tool for mineral geochemical characterization. The technique has high spatial resolution, elevated sensibility, low detection limits and multi-elementary analysis possibility. Almost all chemistry elements can be analyzed by this methodology. Briefly, this methodology consists in vaporize the sample by Laser Ablation, which is dragged by argon into the Plasma where are created and accelerated the ions. They are separated by their mass/charge ratio into the Mass Spectrometer, being conveyed to a detector that convert the signals in specters. In this work LA-ICP-MS analyses were performed in two albitites thin sections, a mineralized and a non mineralized sample. Both samples are from the Lagoa da Rabicha Deposit, Uranium Lagoa Real Province, BA. From these analysis it was possible to chemically characterize the minerals present in the samples and better understand the trace elements on them. The results for plagioclase in both samples show that it is albite (NaAlSi 3 O 8 ). The albite from sample 200907-20 shows traces of strontium, lanthanum, cerium, neodymium, samarium and thorium in one crystal. The albite from sample 200907-23 has strontium with uranium, yttrium and lead in smaller quantities. The results obtained in this work are very important and contribute to a better understanding of the uranium origin in Lagoa Real deposits. (author)

  17. A mineralogical investigation of samples from the Eenzaamheid cobalt-molybdenum deposit

    International Nuclear Information System (INIS)

    De Nooy, C.D.

    1987-01-01

    The cobalt-molybdenum deposit on the farm Eenzaamheid, near Balmoral, is situated in gabbroic dykes in the higly altered quartzites and shales of the Pretoria beds in the Transvaal Supergroup. The mineralogy of both unmineralized and mineralized samples from the deposit was studied. The main minerals in the host rock are tremolite, albite, quartz and prehnite. Safflorite and molybdenite are the main ore minerals, with minor cobaltite, niccolite, and gersdorffite. The mineralization is associated with quartz- and albite-rich host rocks, whereas the tremolite- and albite-rich rocks are usually unmineralized. A cobalt content of 1,76 per cent and a molybdenum content of 0,20 per cent were determined by the chemical analysis of a representative sample. Owing to the coarse-grained and interstitial nature of the ore minerals, the ore should be free milling, and liberation is expected at a fairly coarse grain size (about 0,5 mm). The cobalt minerals and the molybdenite should be easily concentrated by gravity methods and flotation methods respectively. 18 figs., 4 tabs., 3 refs

  18. Hydrothermal alteration and diagenesis of terrestrial lacustrine pillow basalts: Coordination of hyperspectral imaging with laboratory measurements

    Science.gov (United States)

    Greenberger, Rebecca N.; Mustard, John F.; Cloutis, Edward A.; Mann, Paul; Wilson, Janette H.; Flemming, Roberta L.; Robertson, Kevin M.; Salvatore, Mark R.; Edwards, Christopher S.

    2015-12-01

    We investigate an outcrop of ∼187 Ma lacustrine pillow basalts of the Talcott Formation exposed in Meriden, Connecticut, USA, focusing on coordinated analyses of one pillow lava to characterize the aqueous history of these basalts in the Hartford Basin. This work uses a suite of multidisciplinary measurements, including hyperspectral imaging, other spectroscopic techniques, and chemical and mineralogical analyses, from the microscopic scale up to the scale of an outcrop. The phases identified in the sample are albite, large iron oxides, and titanite throughout; calcite in vesicles; calcic clinopyroxene, aegirine, and Fe/Mg-bearing clay in the rind; and fine-grained hematite and pyroxenes in the interior. Using imaging spectroscopy, the chemistry and mineralogy results extend to the hand sample and larger outcrop. From all of the analyses, we suggest that the pillow basalts were altered initially after emplacement, either by heated lake water or magmatic fluids, at temperatures of at least 400-600 °C, and the calcic clinopyroxenes and aegirine identified in the rind are a preserved record of that alteration. As the hydrothermal system cooled to slightly lower temperatures, clays formed in the rind, and, during this alteration, the sample oxidized to form hematite in the matrix of the interior and Fe3+ in the pyroxenes in the rind. During the waning stages of the hydrothermal system, calcite precipitated in vesicles within the rind. Later, diagenetic processes albitized the sample, with albite replacing plagioclase, lining vesicles, and accreting onto the exterior of the sample. This albitization or Na-metasomatism occurred when the lake within the Hartford Basin evaporated during a drier past climatic era, resulting in Na-rich brines. As Ca-rich plagioclase altered to albite, Ca was released into solution, eventually precipitating as calcite in previously-unfilled vesicles, dominantly in the interior of the pillow. Coordinated analyses of this sample permit

  19. Hydrothermal alteration and mass exchange in the hornblende latite porphyry, Rico, Colorado

    Science.gov (United States)

    Larson, P.B.; Cunningham, C.G.; Naeser, C.W.

    1994-01-01

    The Rico paleothermal anomaly, southwestern Colorado, records the effects of a large hydrothermal system that was active at 4 Ma. This hydrothermal system produced the deep Silver Creek stockwork Mo deposit, which formed above the anomaly's heat source, and shallower base and precious-metal vein and replacement deposits. A 65 Ma hornblende latite porphyry is present as widespread sills throughout the area and provided a homogenous material that recorded the effects of the hydrothermal system up to 8 km from the center. Hydrothermal alteration in the latite can be divided into a proximal facies which consists of two assemblages, quartz-illite-calcite and chlorite-epidote, and a distal facies which consists of a distinct propylitic assemblage. Temperatures were gradational vertically and laterally in the anomaly, and decreased away from the centra heat source. A convective hydrothermal plume, 3 km wide and at least 2 km high, was present above the stock-work molybdenum deposit and consisted of upwelling, high-temperature fluids that produced the proximal alteration facies. Distal facies alteration was produced by shallower cooler fluids. The most important shallow base and precious-metal vein deposits in the Rico district are at or close to the boundary of the thermal plume. Latite within the plume had a large loss of Na2O, large addition of CaO, and variable SiO2 exchante. Distal propylitized latite samples lost small amounts of Na2O and CaO and exchanged minor variable amounts of SiO2. The edge of the plume is marked by steep Na2O exchange gradients. Na2O exchange throughout the paleothermal anomaly was controlled by the reaction of the albite components in primary plagioclase and alkali feldspars. Initial feldspar alteration in the distal facies was dominated by reaction of the plagioclase, and the initial molar ratio of reactants (alkali feldspar albite component to plagioclase albite component) was 0.35. This ratio of the moles of plagioclase to alkali feldspar

  20. Microchemistry, geochemistry and geochronology of the Lagoa Real Uranium Province (BA) magmatic association: petrological and evolutionary significance

    International Nuclear Information System (INIS)

    Amorim, Lucas Eustaquio Dias

    2016-01-01

    The Lagoa Real Uranium Province (PULR) is located in the center-south of the Bahia State, in the central part of Sao Francisco Craton and consists of an association of Paleoproterozoic meta-granites, alkali-gneiss, albitites, meta-leucodiorite and charnockites. This work has as objective the studies of the magmatic association, trying to understand its petrological and evolutionary meaning. For this purpose, representative bodies were sampled in order to develop unpublished studies of litogeochemistry, isotopes, geochronology and mineral chemistry. These analyzes were performed in: different preserved granitoid facies (Lagoa do Barro, Sao Timoteo, Juazeirinho and late pegmatitic phases), the meta-leucodiorites and charnockite. The data obtained using several modern methodologies, such as geochronology and mineral chemistry by LA-ICP-MS, provided results that allowed the characterization of two magmatic lithologies not described in the literature (Juazeirinho granite e late pegmatitic phases), and also a lithology preliminarily described (Lagoa do Barro granite). Moreover, these data contributed to elucidate the origin and meaning of the leucodiorite and charnoquito varieties, and made it possible to verify new compositional and mineral chemistry tendencies of Sao Timoteo granite. The data presented show that the studied granites were affected by albititization events (tardi or post-magmatic), which have different micro-chemical characteristics from the processes of albite formation related to the non-mineralized albitites bodies. Three albititization events were identified: a) An event that affected the granites characterized by the formation of albite with Rb and U, (b) Another event related to fluids associated with late pegmatitic bodies that formed albite with high levels of U, Rb and Ba, and partially affected the granites of the next pegmatoids portions; and (c) a final albititization event that caused the formation of the albite gneiss bodies, with albite

  1. Origen de arcillas alumínicas en horizontes de alteración de materiales graníticos del borde sur de la sierra de Guadarrama

    Directory of Open Access Journals (Sweden)

    Martín Patino, M. T.

    1988-08-01

    Full Text Available Three weathering profiles of granitic rocks and two arkoses in the NW of Madrid Province have been studied. Rocks are granodiorites and adamellites with albites showing variable degrees of sericitization, and no-weathered potassic feldspars. Clay fraction in the weathered horizons from these rocks displays high content in beidellite, and minor amounts of illite and 7 Ǻ-halloysite. On the other hand, beidellite, illite and well crystallized kaolinite are clay minerals in the arkosic rocks. Microfabric characteristics from SEM studies show abundant weathered albites with clean surfaces and formation of beidellite in all areas of the samples. Moreover, spatial relations between albite and beidellite are not observed. In pedochemical weathering of albite, sodium from this mineral should be exchanged with protons from soil solution with very quick kinetics. This initial alkalinization produces an increase in the silica solubility released from albite network. In these environments, a continued contact between weathering solution and albite causes a silica and alumina enrichment and beidellite or 7 Ǻ-halloysite precipitation. Microclimatic variations in weathering environment may cause fluctuations in silica and alumina activities with resultant pH changes. So, when silica activities are high, beidellite neoformation is favoured; on the contrary, 7 Ǻ-halloysite is precipitated.Se han estudiado tres perfiles de alteración de rocas graníticas y dos muestras de arcosas en la zona NO de la provincia de Madrid. Las rocas, clasificadas como granodioritas y adamellitas, presentan albitas con sericitización variable, y escasos feldespatos potásicos muy poco alterados. La fracción arcilla de los horizontes de alteración de estas rocas presenta un alto contenido en beidellita, así como porcentajes menores de ilita y haloisita-7Ǻ. Por otra parte, los minerales de la arcilla presentes en las arcosas son ilita, beidellita y caolinita bien

  2. Complex layering of the Orange Mountain Basalt: New Jersey, USA

    Science.gov (United States)

    Puffer, John H.; Block, Karin A.; Steiner, Jeffrey C.; Laskowich, Chris

    2018-06-01

    The Orange Mountain Basalt of New Jersey is a Mesozoic formation consisting of three units: a single lower inflated sheet lobe about 70 m thick (OMB1), a middle pillow basalt about 10 to 20 m thick (OMB2), and an upper compound pahoehoe flow about 20 to 40 m thick (OMB3). The Orange Mountain Basalt is part of the Central Atlantic Magmatic Province. Quarry and road-cut exposures of OMB1 near Paterson, New Jersey, display some unusual layering that is the focus of this study. OMB1 exposures displays the typical upper crust, core, and basal crust layers of sheet lobes but throughout the Patterson area also display distinct light gray layers of microvesicular basalt mineralized with albite directly over the basal crust and under the upper crust. The lower microvesicular layer is associated with mega-vesicular diapirs. We propose that the upper and lower microvesicular layers were composed of viscous crust that was suddenly quenched before it could devolatilize immediately before the solidification of the core. During initial cooling, the bottom of the basal layer was mineralized with high concentrations of calcite and albite during a high-temperature hydrothermal event. Subsequent albitization, as well as zeolite, prehnite, and calcite precipitation events, occurred during burial and circulation of basin brine heated by recurring Palisades magmatism below the Orange Mountain Basalt. Some of the events experienced by the Orange Mountain Basalt are unusual and place constraints on the fluid dynamics of thick flood basalt flows in general. The late penetration of vesicular diapirs through the entire thickness of the flow interior constrains its viscosity and solidification history.

  3. Geochemistry of Hydrothermal Alteration Associated with Cenozoic Intrusion-Hosted Cu-Pb-Zn Mineralization at Tavşanlı Area, Kütahya, NW Turkey

    Directory of Open Access Journals (Sweden)

    Mustafa Kumral

    2016-02-01

    Full Text Available The Miocene magmatic intrusion in the Tavşanlı zone of the Kütahya-Bolkardağ Belt (KBB in the northwestern region of Turkey is represented by the Eğrigöz granitoids. This paper studies the petrology and geochemistry of hydrothermal alterations associated with the vein-type Cu-Pb-Zn mineralization hosted by this pluton, focusing on the determination of the mass gains and losses of chemical components, which reflect the chemical exchanges between the host rocks and hydrothermal fluids. Vein-type Cu-Pb-Zn mineralization is closely associated with intense hydrothermal alterations within the brecciation, quartz stockwork veining, and brittle fracture zones that are controlled by NW-SE trending faults cutting through the Eğrigöz granitoids. Paragenetic relationships reveal three stages of mineralization: pre-ore, ore, and supergene. The ore mineralogy typically includes hypogene chalcopyrite, sphalerite, galena, and pyrite, with locally supergene covellite, malachite, and azurite. Wall-rock hypogene hydrothermal alterations include pervasive silicification, sulfidation, sericitization, and selective carbonatization and albitization. These are distributed in three main alteration zones (zone 1: silicified/iron carbonatized alterations ± albite, zone 2: argillic-silicic alterations, and zone 3: phyllic alterations. Based on the gains and losses of mass and volume (calculated by the GEOISO-Windows™ program, zone 1 has a higher mass and volume gain than zones 2 and 3. Non-systematic zonal distributions of alterations are observed in which the silicic-carbonate alterations +/− albitization appeared in zone 1 in the center and the phyllic-argillic alterations appeared in zones 2 and 3, with an increase in base metals (Cu-Pb-Zn in the zone from Cu, Cu-Pb, to Cu-Pb-Zn moving outwards.

  4. Formation of albitite-hosted uranium within IOCG systems: the Southern Breccia, Great Bear magmatic zone, Northwest Territories, Canada

    Science.gov (United States)

    Montreuil, Jean-François; Corriveau, Louise; Potter, Eric G.

    2015-03-01

    Uranium and polymetallic U mineralization hosted within brecciated albitites occurs one kilometer south of the magnetite-rich Au-Co-Bi-Cu NICO deposit in the southern Great Bear magmatic zone (GBMZ), Canada. Concentrations up to 1 wt% U are distributed throughout a 3 by 0.5 km albitization corridor defined as the Southern Breccia zone. Two distinct U mineralization events are observed. Primary uraninite precipitated with or without pyrite-chalcopyrite ± molybdenite within magnetite-ilmenite-biotite-K-feldspar-altered breccias during high-temperature potassic-iron alteration. Subsequently, pitchblende precipitated in earthy hematite-specular hematite-chlorite veins associated with a low-temperature iron-magnesium alteration. The uraninite-bearing mineralization postdates sodic (albite) and more localized high-temperature potassic-iron (biotite-magnetite ± K-feldspar) alteration yet predates potassic (K-feldspar), boron (tourmaline) and potassic-iron-magnesium (hematite ± K-feldspar ± chlorite) alteration. The Southern Breccia zone shares attributes of the Valhalla (Australia) and Lagoa Real (Brazil) albitite-hosted U deposits but contains greater iron oxide contents and lower contents of riebeckite and carbonates. Potassium, Ni, and Th are also enriched whereas Zr and Sr are depleted with respect to the aforementioned albitite-hosted U deposits. Field relationships, geochemical signatures and available U-Pb dates on pre-, syn- and post-mineralization intrusions place the development of the Southern Breccia and the NICO deposit as part of a single iron oxide alkali-altered (IOAA) system. In addition, this case example illustrates that albitite-hosted U deposits can form in albitization zones that predate base and precious metal ore zones in a single IOAA system and become traps for U and multiple metals once the tectonic regime favors fluid mixing and oxidation-reduction reactions.

  5. Origin of the Okrouhlá Radouň episyenite-hosted uranium deposit, Bohemian Massif, Czech Republic: fluid inclusion and stable isotope constraints

    Science.gov (United States)

    Dolníček, Zdeněk; René, Miloš; Hermannová, Sylvie; Prochaska, Walter

    2014-04-01

    The Okrouhlá Radouň shear zone hosted uranium deposit is developed along the contact of Variscan granites and high-grade metasedimentary rocks of the Moldanubian Zone of the Bohemian Massif. The pre-ore pervasive alteration of wall rocks is characterized by chloritization of mafic minerals, followed by albitization of feldspars and dissolution of quartz giving rise to episyenites. The subsequent fluid circulation led to precipitation of disseminated uraninite and coffinite, and later on, post-ore quartz and carbonate mineralization containing base metal sulfides. The fluid inclusion and stable isotope data suggest low homogenization temperatures (˜50-140 °C during pre-ore albitization and post-ore carbonatization, up to 230 °C during pre-ore chloritization), variable fluid salinities (0-25 wt.% NaCl eq.), low fluid δ18O values (-10 to +2 ‰ V-SMOW), low fluid δ13C values (-9 to -15 ‰ V-PDB), and highly variable ionic composition of the aqueous fluids (especially Na/Ca, Br/Cl, I/Cl, SO4/Cl, NO3/Cl ratios). The available data suggest participation of three fluid endmembers of primarily surficial origin during alteration and mineralization at the deposit: (1) local meteoric water, (2) Na-Ca-Cl basinal brines or shield brines, (3) SO4-NO3-Cl-(H)CO3 playa-like fluids. Pre-ore albitization was caused by circulation of alkaline, oxidized, and Na-rich playa fluids, whereas basinal/shield brines and meteoric water were more important during the post-ore stage of alteration.

  6. Phanerozoic extensional faulting and alteration control on uranium mineralization in trachytes of the Central Eastern Desert of Egypt

    Science.gov (United States)

    Hamdy, Mohamed M.; Waheeb, Anton G.; Aly, Samir M.; Farag, Nagdy M.; Sadek, Adel F.

    2017-12-01

    The Gabal Nasb El Atshan Upper Carboniferous-Lower Permian altered trachytes include uranium up to 3165 ppm. The paleostress and resolved shear stress analyses of the deformation systems in Gabal Nasb El Atshan area indicate that the trachyte was subjected to WNW-ESE to E-W tensile shear stress directed extensional regimes. The low-stress regions in the vicinity of extensional faults and their associated joints were favorable locations for fluid flow and the consequence alteration and U-mineralization. This occurred more extensively along the contacts between the sills of trachyte and the Hammamat sedimentary rocks; where the latter acted as a physical barrier for the alteration fluids migration outward. Alteration styles include albitization, aegirinization, arfvedsonization, chloritization and ferruginisation. The albitization is the most common sodic metasomatism, giving sanidine from Or98.8Ab0.7 to Or62.3Ab37.6, anorthoclase from Or51.4Ab48.0 to Or12.2Ab87.6 and albite from Or11.0Ab89.0 to Or0.8Ab99.2. Aegirine and arfvedsonite formed due to decreasing sodium activity in the metasomatic fluids. Sodic metasomatism may be the source of uranium-enrichment, taking place during the late magmatic to deuteric processes. This was followed by a retrograde alteration of chloritization between 175 and 42 °C toward precipitation of Fe-oxides and alteration of primary uranium. Surficial low-temperature alteration remobilized and redistributed the produced uranylhydroxides and ferruginisation caused the reduction and adsorption of U forming betafite, uranophane, soddyite, umohoite, uranotile and uranopilite.

  7. Laboratory and in situ determination of the migration processes of actinide complexes and colloids in a fissured granitic environment. El Berrocal project (preliminary activities - phase 0)

    International Nuclear Information System (INIS)

    Astudillo, J.; Del Olmo, C.; Commission of the European Communities, Ispra

    1993-01-01

    The experimental site of El Berrocal has been chosen for a study of the migration of natural radionuclides in a fractured granitic environment. The granite is classified as an alkaline feldspar-rich quartz granite with two micas. The fresh granite is affected by hydrothermal alteration processes related to fractures, which has led to a strong sericitization of albite, and the precipitation of secondary chlorites and carbonates. The most important U-bearing and Th-bearing accessory minerals are uraninite, thorite-auerlite, monazite, anatase, apatite and zircon. Approximately 65% of the total of U in the rock is held as uraninite. In the altered granite, most of the U is held as autunite. Hydrogeochemical data show that Co 2 /H 2 CO 3 is the dominant system, followed by the silica-silicate system. Based on their stability analyses, two zones can be defined: (i) waters north of the dyke and from deep zones where calcite is in equilibrium and albite and gibbsite precipitate, and (ii) surface waters, south of the dyke, subsaturated in relation to calcite, producing the alteration of albite and the precipitation of montmorillonite. The size distribution of the colloids varies, depending on the treatment given to the water samples. The particles are mainly composed of K-feldspars and clay minerals (smectite) and occasionally by quartz, mica, calcite and pollen. The El Berrocal groundwaters have a very low amount of organic matter. Column migration tests have been carried out and were performed with intact granitic cores and with crushed granite. Np proved to be an adequate radionuclide for these experiments. Under oxic conditions and in the absence of organic matter, it was completely retained in both types of columns, whereas in the presence of organic matter a more rapid breakthrough was observed. Under anoxic conditions, and with or without organic matter, Np was found to move faster than under oxic conditions. (author). 13 refs., 46 figs., 23 tabs

  8. The Petäjäskoski Formation, a new lithostratigraphic unit in the Paleoproterozoic Peräpohja Belt, northern Finland

    Directory of Open Access Journals (Sweden)

    Markus Kyläkoski

    2012-12-01

    Full Text Available This paper gives the first description of a newly-recognized, basin-wide metasedimentary unit in the Paleoproterozoic (~2.4–1.9 Ga Peräpohja Belt, northern Finland. The unit, which is named the Petäjäskoski Formation (PFm after the single location where the rocks are known to be exposed, is situated stratigraphically in the middle part of the Kivalo Group between the quartzites of the>2.22 Ga Palokivalo Formation and the mafic volcanic rocks of the ~2.1 Ga Jouttiaapa Formation.The bulk of the PFm comprises phlogopitic-sericitic and albitic schists with abundant hematite as a diagnostic feature. Quartzite and dolomite interbeds are common. Based on drillcore and geophysical data, the succession is several hundreds of meters thick. The unit has prograde, chiefly lower greenschist facies mineral assemblages and, though being commonly intensely deformed, shows well-preserved sedimentary structures that imply deposition in shallow-water tosubaerial environments. Based on the original lithological features, the Petäjäskoski Formation can be defined as a claystone-siltstone-sandstone-dolostone association. On the geochemical and stratigraphic basis, the albite schists likely represent albitized equivalents of the micaceous claystones and siltstones. They are intercalated with stratabound collapse breccias, up to tens of meters in thickness, with clasts composed mainly of bordering albite schist. A mafic sill intruding the Petäjäskoski Formation yielded a U-Pb zircon age of 2140 ± 11 Ma. The older, c. 2220 Ma, differentiated sills are not known to reach the stratigraphic level of thePetäjäskoski Formation and hence, the depositional age of the PFm sediments can be bracketed between c. 2220 and 2140 Ma. Detrital zircon grains dated from a quartzitic sample from the PFmshow an Archean (c. 2650–3470 Ma provenance.The moderate to high MgO (~6–13 wt.%, K2O (~3–8 wt.% and FeOtot(8–15 wt.% contents, low CaO and Na2O contents, and abundant

  9. A study on mineralization U,REE and related processes in anomaly No.6 Khoshomy area central Iran

    International Nuclear Information System (INIS)

    Heidaryan, F.

    2005-01-01

    Uranium mineralization in Khoshomy prospect, located in central. part of Iran, with 303-15000 (cps) and 14 to 4000 (ppm) released, The main rock types include: gneiss, granite, pegmatite and migmatite, that influenced by pegmatite-albitic vines (quartz-heldespatic). Acidic and basic dykes, granodioritic, units and dolomite and marble have been seen. The alteration associated with the mineralization is potassic, argillic, propylitic, carbonization, silisificaition and hematitizaition. Uranium mineralization occurred in a hydrothermal phase with Cu, Mo, Ni and Au elements. Uranium primary minerals include pitchblende, coffinite, uraninite; and uranium secondary minerals include uranophane and . boltwoodite. REE mineralization occurred by the potassic phase in peginatitization process

  10. Mueilha rare metals granite, Eastern Desert of Egypt: An example of a magmatic-hydrothermal system in the Arabian-Nubian Shield

    Science.gov (United States)

    Abu El-Rus, Mohamed A.; Mohamed, Mohamed A.; Lindh, Anders

    2017-12-01

    The Mueilha granite pluton is one of the rare-metals bearing peraluminous granitic plutons in the Arabian-Nubian Shield. It represents the apical part of a highly evolved magma chamber emplaced at a shallow level subsequent to the post Pan-African orogeny. The pluton can be seen as a highly leucocratic medium-grained albite/oligoclase framework infilled with quartz, K-feldspar and muscovite that are variably overgrown by K-feldspar, muscovite, quartz and topaz megacrysts. The increasing number and size of the K-feldspar megacrysts at the expense of the whitened albite/oligoclase framework imparts variably red color to the Mueilha granite. Contacts between the milky white and red granites are usually gradational, but may be locally sharp or may form narrow transition zones resulting from abrupt variations in texture and lithology. Textural relations indicate an initial stage of hydrothermal albitization of magmatic plagioclase and crystallization of topaz megacrysts resulting from infiltration of Na-rich fluorine bearing fluids. A subsequent stage of metasomatic enrichment is characterized by extensive growth of large K-feldspar, quartz and muscovite megacrysts at the expense of the albite/oligoclase crystals as a result of infiltration of K-Si rich hydrous fluids. Post-magmatic infiltration of hydrous fluids along the fault planes is shown by the intense replacement of alkali feldspar megacrysts by quartz, development of myrmekitic intergrowth pockets along the K-feldspar megacrysts and sealing of the micro-fractures by cryptocrystalline mixtures of clay minerals, iron oxides, sericite and chlorite. Compositionally, the red granitic rocks have higher SiO2, Fe2O3total, K2O/Na2O, Σ REE, Y, Th, U, Zr and Zn and lower Al2O3, Ga, Ta, Nb and Mo compared to the milky white granites. LILE and Sn do not show clear variation trends throughout the Mueilha granite pluton, suggesting their immobility during hydrothermal alteration. Microthermometric measurements indicate that

  11. Preparation and Characterization of Microfiltration Ceramic Membranes Based on Natural Quartz Sand

    Directory of Open Access Journals (Sweden)

    Andrei Ivanets

    2017-06-01

    Full Text Available The effect of phase and chemical composition of natural quartz sand, binder and burnable additives was studied. The conditions of application of the membrane and biocide layers on the formation of porous ceramic and microfiltration membranes were investigated. It is shown that a crystalline oxide of Si(IV is determinant for obtaining the ceramic materials. The presence of carbonates (calcite, dolomite, aragonite, etc. and crystalline aluminosilicates (microcline, albite, phlogopit, etc. leads to a decrease in mechanical strength of ceramics. The biocide coating designed to protect the ceramic membrane surfaces from biofouling was applied and its anti-bacterial activity was shown.

  12. Knowledge-based time management in the planning of plant shut-downs; WISENT: Wissensbasiertes Zeitmanagement bei der Planung von Anlagenstillstaenden

    Energy Technology Data Exchange (ETDEWEB)

    Verweyen-Frank, H.

    1996-12-31

    At STEAG of Essen, an operator of hard-coal-fired power stations, the WISENT system distributes the necessary shut-down times in order to permit precautionary maintenance work to be carried out. This expert system, developed in cooperation with the company ALBIT, has a particular trait. It is not only based on ``if``-statements, as is typical of expert systems, but makes use also of fuzzy methods in order to optimize overall distribution. In other words, this system is the first to add to the strict yes-or-no logic a weighting component for each criterion of optimization. (orig.)

  13. Geology and age of the Lac a la Perdrix fenite, southern Gatineau district, Quebec

    Energy Technology Data Exchange (ETDEWEB)

    Hogarth, D D [Ottawa Univ., ON (Canada). Dept. of Geology; VanBreemen, O [Geological Survey of Canada, Ottawa, ON (Canada)

    1997-12-31

    The Lac a Ia Perdrix fenite lies in the Central Metasedimentary Belt of the Grenville Province. This 30 m wide fenite, adjacent to a narrow calciocarbonatite sill, replaces diopside-oligoclase gneiss and is composed of magnesio-arfvedsonite, aegirine, microcline, albite, and fluorapatite. Near the contact with carbonatite, it contains appreciable monazite and barite whereas aegirine virtually disappears. Fenitization probably took place early in the igneous stage of carbonatite development. A Pb/U monazite age of 1026 {+-} 2 Ma is thought to date fenite formation. Together with published data, this age shows that carbonatite intruded metamorphic rocks near the close of the Grenville Orogeny. (author). 33 refs., 4 tabs., 5 figs.

  14. Favourable environments for uranium occurences in Brazil

    International Nuclear Information System (INIS)

    Santos, L.C.S. dos

    1980-01-01

    Based on the present knowledge of Brazilian Precambrian geology, an attempt is made to divide Precambrian rocks into different regions according to their favourability criteria for uranium concentrations. Paleozoic and Mesozoic occurrences are also mentioned. They are mainly associated with large sedimentary basins. Brazilian uranium occurrences can be grouped into the following environments: (1) Metaconglomerates; (2) Metasomatic rocks (associated with albitization); (3) Vein type; (4) Sandstone type and (5) Intrusive alkalic rock. Upper Proterozoicas folding regions related to mobile belts and large Precambrian unconformities are good targets for uranium exploration in Brazil. (Author) [pt

  15. Paleozoic age of high-pressure metamorphic rocks of the Dakh salient, North-Western Caucasus: results of U-Pb-geochronological study

    International Nuclear Information System (INIS)

    Somin, M.L.; Levchenkov, O.A.; Kotov, A.B.; Makeev, A.F.; Komarov, A.N.; Ro, N.I.; Lavrishchev, V.A.; Lebedev, V.A.

    2007-01-01

    U-Pb geochronological studies of an ancient component of the Dakh salient, i.e. metaaplites, which are vein fine-grained rocks made up by albite, microcline, quartz and potash mica, were made. Besides, K-Ar dating of granodiorites breaking through metamorphic rocks was conducted. U-Pb dating of accessory zircons (353 mln. years) defines the lower age boundary of the Dakh salient rock metamorphism. Its upper boundary was identified by K-Ar dating (301 ± 10 mln. years) of hornfels blende of nonmetamophized granodiorites [ru

  16. Reconnaissance geochemical exploration of the plutons of quartz monzonite and granite in the Jabal Lababa and Ar Rayth areas, southern Asir, Kingdom of Saudi Arabia

    Science.gov (United States)

    Overstreet, W.C.; Assegaff, A.B.; Jambi, Mohammed; Hussain, M.A.; Selner, G.I.; Matzko, J.J.

    1985-01-01

    Geochemical reconnaissance for rare metals in plutons of albite-muscovite granite and quartz monzonite in the vicinity of Jabal Lababa disclosed positive geochemical anomalies for beryllium, tantalum, thorium, lanthanum, niobium, tin, yttrium, and zirconium. The low anomalous values for the rare metals in rocks and the short mechanical dispersion trains, seldom exceeding 4 km in length, of rare-metal-bearing heavy minerals, are interpreted to indicate that primary deposits of these metals are lacking, and any placers would be small and low in tenor.

  17. Southern complex: geology, geochemistry, mineralogy, and mineral chemistry of selected uranium- and thorium-rich granites

    International Nuclear Information System (INIS)

    Hoffman, M.A.

    1987-01-01

    Four major rock groups are defined in the Southern Complex: the Bell Creek Granite (BCG), the Clotted Granitoids (CGR), the Albite Granite (AGR), and the Migmatite Complex. Metatexites of the Migmatite Complex are the oldest rocks and include paleosome of a metasedimentary and metavolcanic protolith represented by Banded Iron Formation, Banded Amphibolite, and Banded Gneisses, and interlayered or crosscutting leucogranites. The CGR span the range from metatexite to diatexite and represent in-situ partial melting of metapelitic layers in the protolith during intrusion of the BCG. The BCG cuts the migmatites, is locally cut by the CGR, and was derived by partial melting of a dominantly metasedimentary protolith at some depth below the presently exposed migmatites during a regional tectonothermal event. The Albite Granite is a 2km diameter, muscovite-fluorite-columbite-bearing intrusive stock that cuts all other major units. The thorium history of the BCG is a function of the history of monazite. The thorium history of the CGR is also dominated by monazite but the thorium content of this unit cannot be entirely accounted for by original restite monazite. The uranium history of the BCG and CGR was dominated by magmatic differentiation and post magmatic, metamorphic and supergene redistributions and is largely independent of the thorium history. The thorium and uranium history of the AGR was dominated by magmatic/deuteric processes unlike the BCG and CGR

  18. Actinide sorption on granites and minerals as a function of pH and colloids/pseudocolloids

    International Nuclear Information System (INIS)

    Torstenfelt, B.; Rundberg, R.S.; Mitchell, A.J.

    1988-01-01

    The sorption of uranium, neptunium and plutonium was studied on three granites - Finnsjoe granite, Stripa granite and Westerly granite, and on six minerals - albite, anorthite, bentonite, hornblende, illite and microcline. The aqueous phase was a natural groundwater collected at the Nevada Test Site (NTS). This water is used as reference water for the U.S. Nevada Nuclear Waste Storage Investigations (NNWSI). At neutral pH there was only a minor difference in sorption between the different methods of separation. Below a pH resulting in hydrolysis of the nuclide, the sorption was low. Uranium and especially neptunium sorbed significantly more at high pH, as compared to the sorption at neutral pH. High pH had only little influence on the sorption of plutonium on the minerals with a high cation exchange capacity (CEC); hornblende, bentonite and illite, but on the feldspars albite, anorthite and microcline, with low CEC, there was a pronounced difference between neutral and high pH. For uranium at high pH, the sorption increased significantly with increasing centrifugal force, indicating that part of the uranium either exists as a colloid or as a polymer. This effect was only in a few cases observed for neptunium and plutonium. (orig./RB)

  19. Modelling of the evolution of ground waters in a granite system at low temperature: the Stripa ground waters, Sweden

    International Nuclear Information System (INIS)

    Grimaud, D.; Michard, G.; Beaucaire, C.

    1990-01-01

    From chemical data on the Stripa ground waters we have tried to model the evolution of the chemical composition of a ground water in a granitic system at low temperature. The existence of two end-member ground water compositions made it possible first, to test the conventional model of a geothermal system according to which an overall equilibrium between the waters and a given mineral assemblage can be defined, and then to show that such a model could be extended to low temperatures (10 o C). Conversely, if we know the mineral assemblage, the equilibration temperature and the charge of the mobile ions (in this case, Cl), the composition of the solution is entirely fixed. In our model of the Stripa ground waters, the existence of two end-member ground water compositions can be explained by an evolution from a ''kaolinite-albite-laumontite'' equilibrium to a ''prehnite-albite-laumontite'' equilibrium, the latter requiring less Al than the former. We have also emphasized the importance of the Cl ion concentrations of the ground waters, because they can be considered as indicators of the degree of reaction progress between rock and water, thus determining the degree of equilibration of the system. (author)

  20. Stable isotopic and mineralogical studies of hydrothermal alteration at Arima Spa, Southwest Japan

    International Nuclear Information System (INIS)

    Masuda, Harue; Osaka City Univ.; Sakai, Hitoshi; Chiba, Hitoshi; Matsuhisa, Yukihiro; Nakamura, Takeshi

    1986-01-01

    The waters of Arima Spa, Southwest Japan, have high salinity (Cl = 54 g/kg) and high isotopic ratios (deltaD = -32, and delta 18 O = +10 per mille), and issue from shallow wells drilled into altered rhyolitic pyroclastic rocks of Cretaceous age. Alteration of the host rocks occurred in two stages. The earlier regional alteration stage is characterized by the presence of 2M- and 1M-type muscovite, albite, chlorite, calcite and epidote, whereas muscovite and Fe-chlorite formation at the expense of partly albitized plagioclase and altered biotite or hornblende occurred in the following hydrothermal stage. Pyrite, sphalerite, galena and siderite are present in the central part of the hydrothermal alteration zone. Oxygen and hydrogen isotopic ratios of secondary muscovite show that regional alteration proceeded under the meteoric circulation, and that the hydrothermal fluid for the second stage had chemical and stable isotopic characteristics of non-meteoric origin similar to the present-day Arima brine. The oxygen and to a lesser extent the hydrogen isotopic ratios of the muscovite rapidly decrease with increasing distance from the central zone of hydrothermal alteration. The isotopic variation is best interpreted as reflecting rapidly decreasing fluid/rock ratios with increasing distance of fluid penetration from the narrow hydrothermal alteration zone into the surrounding area. The results are discussed. (author)

  1. Three-dimensional cooling pattern of a granitic pluton 2. The study of deuteric sub-solidus reactions in the Toki granite, Central Japan

    International Nuclear Information System (INIS)

    Yuguchi, Takashi; Tsuruta, Tadahiko; Nishiyama, Tadao

    2011-01-01

    Petrographical studies examining the development and variations of sub-solidus reactions recorded in the Toki granite represent the three-dimensional cooling pattern of this zoned pluton in Central Japan. Samples collected from 19 boreholes in the Toki granite show characteristics indicative of spatial variations in the extent of the sub-solidus reactions. Exsolution coarsening has produced microperthite, including albite-rich lamellae, in this pluton, while deuteric coarsening has resulted in the formation of patchperthite, myrmekite, and the reaction rim. The extent of the deuteric coarsening reactions can be evaluated from the width and spacing of the albite-rich patch in patchperthite and from the thickness of myrmekite and the reaction rim. The width, spacing, and thickness of these textural features increase systematically with elevation; they also increase gradually in the horizontal inward direction in the western part of the pluton but not in the eastern part of the pluton. The systematic variations in textural development indicate that the Toki granite cooled effectively from the roof and from the western margin during the deuteric coarsening stage. The deuteric coarsening may have occurred at temperatures below 500°C, as indicated by ternary feldspar thermometry. (author)

  2. Diffusion-controlled melting in granitic systems at 800-900degC and 100-200 MPa. Temperature and pressure dependence of the minimum diffusivity in granitic melts

    International Nuclear Information System (INIS)

    Yuguchi, Takashi; Yamaguchi, Takashi; Iwamoto, Manji-rou; Eguchi, Hibiki; Isobe, Hiroshi; Nishiyama, Tadao

    2012-01-01

    This paper presents the temperature and pressure dependence of the minimum binary diffusivity in granitic melts. The minimum diffusivities are determined by monitoring the temporal development of the diffusion-controlled melt layer(DCM) in granitic systems (albite (Ab)-quartz (Qtz)-H 2 O and orthoclase (Or)-Qtz-H 2 O) gathered during 31 melting experiments under conditions of 800-900degC and 100-200 MPa for durations of 19-72 h. The DCM is formed between single crystals (Ab or Or crystals) and powdered quartz in all runs and is characterized by a distinct concentration gradient. The maximum thickness of the DCM increases systematically with temperature, pressure, and run duration. Temporal development of the DCM obeys the parabolic growth rate law, using which the diffusivity can be estimated. Plots of concentrations along the diffusion paths in ternary diagrams (Na 2 O-Al 2 O 3 -SiO 2 diagram for the Ab-Qtz-H 2 O system and K 2 O-Al 2 O 3 -SiO 2 diagram for the Or-Qtz-H 2 O system) show linear trends rather than S-shaped trends, indicating that binary nature of diffusion occurs in these systems. Therefore, the diffusive component can be interpreted as an albite component or orthoclase and quartz components (SiO 2 ) rather than an oxide or a cation. (author)

  3. Pore Fluid Evolution Influenced by Volcanic Activities and Related Diagenetic Processes in a Rift Basin: Evidence from the Paleogene Medium-Deep Reservoirs of Huanghekou Sag, Bohai Bay Basin, China

    Directory of Open Access Journals (Sweden)

    Zhongheng Sun

    2017-01-01

    Full Text Available Volcanic activities exert a significant influence on pore fluid property and related diagenetic processes that substantially controlled reservoirs quality. Analysis of Paleogene medium-deep sandstones on the Huanghekou Sag provides insight into relating the diagenetic processes to pore fluid property evolution influenced by volcanic activities. Three distinct types of pore fluids were identified on the basis of an integrated and systematic analysis including core and thin section observation, XRD, SEM, CL, and trace element. Alkaline aqueous medium environment occurred in E2s1+2 where volcanic activities have insignificant influence on pore fluids, evidenced by typical alkaline diagenetic events such as K-feldspar albitization, quartz dissolution, feldspar dissolution, and carbonate cementation. During the deposition of E3d3, influx of terrestrial freshwater and alteration of ferromagnesian-rich pore water result in the formation of mixing aqueous medium environment through volcanic eruption dormancy causing zeolite dissolution, clay mineral transformation, and K-feldspar albitization. Ferromagnesian-rich aqueous medium environment developed resulting from the intensive hydrolysis of the unstable ferromagnesian minerals formed due to intense volcanic activities during E3d1+2 and corresponding predominant diagenetic processes were characterized by the precipitation and dissolution of low-silica zeolites. Therefore, the differential properties of pore fluids caused various diagenetic processes controlling reservoir quality.

  4. Release of uranium through cataclastic deformation of Mansehra granite gneiss and its precipitation in the overlying intramontane basin in northern Pakistan

    International Nuclear Information System (INIS)

    Butt, K.A.

    1989-01-01

    The Mansehra pluton belongs to a discontinuous belt of two mica granites of the Lesser Himalayas. The Mansehra granite is generally foliated except in the area around Mansehra. Several phases of granitic activity have been reported from the Mansehra Complex. Shams and Rahman have demonstrated that the younger phases tend to be enriched in Na 2 O. Ashraf extensively studied minor bodies ranging from albitites through aplites to pegmatites and suggested a late stage albitization event. The northern edge of this sheet-like granitic mass has undergone extensive cataclastic deformation, resulting in the formation of shear zones, mylonites and cataclasites. A chemical comparison of crushed granite with granite outside the shear zone suggests little chemical reconstitution in terms of major elements during cataclastic deformation. A huge shear zone in albitized granite gneiss has yielded secondary uranium minerals at water seepages, suggesting a liberation of uranium. Hydrogeochemical surveys of the crushed granite and adjoining areas suggest that uranium from crushed granite was easily leachable in comparison with rocks outside the shear zone. The uranium thus liberated was trapped in a Pleistocene sequence of clays and unsorted fluviatile sand overlying the granite and country rock metamorphics. (author). 17 refs, 2 figs, 2 tabs

  5. Research on uranium and thorium elements exploration through the study of petrography, petrology and geophysical method in the Saghand Area (Central Iran) Islamic Republic of Iran

    International Nuclear Information System (INIS)

    Iranmanesh, J.; Fattahi, V.; Raziani, S.

    2014-01-01

    This study is a research on uranium and thorium exploration by use of the petrography, petrology and radiometric data in the Saghand area, Central Iran plateau. The lithologies of this area comprise of granite and metasomatized granite. As a result of metasomatic process, uranium and thorium bearing minerals such as davidite and alanite were formed. Sericitization and albitization are the main alterations detected in the study area and thorium mineralization is more common in albitization. By investigation of the chemical classification, non-radioactive specimens, rock types include: diorite and granodiorite, while radioactive specimens consist of gabbroic rocks (basalt). According to the magma source graphs, these rocks formed by calc-alkaline series magma. A scintillometer and spectrometer (MGS-150) were used for radiometric data acquisition. 1001 data points have been obtained from 11 profiles and total counts for, K, U, Th were measured. After primary data processing, data logarithms were calculated for normalizing, and the radiometric data show that uranium and thorium enrichment is more than potassium, while thorium and uranium enrichment are approximately equal. After data integration, two probable anomalies were determined in northwest and northeast parts of the study area. (author)

  6. Metamorphism, metasomatism and mineralization at Lagoa Real, Bahia, Brazil

    International Nuclear Information System (INIS)

    Lobato, L.M.

    1985-09-01

    Uranium deposits cumulatively in the 100,000 tonne U 3 O 8 range occur within ductile shear zones transecting Archean basement gneisses of the Sao Francisco Craton, at the Lagoa Real region of south-central Bahia, Brasil. The gneisses, dated at 2.6-3.0Ga, are at amphibolite and granulite facies and overlie to the west, the Proterozoic Espinhaco metasedimentary sequence along a thrust fault. Petrography and mineral chemistry show that in the zones of alteration/mineralization, the original K-feldspar + quartz + albite/oligoclase + hastingsite assemblage, is replaced by albite + aegirine - angite + andradite + hematite assemblages, with or without uraninite. This information along with oxygen isotope, whole rock geochemistry and fluid inclusion studies indicate that the alteration process involves removal of Si, K, Rb, Ba and addition of Na under oxidizing conditions. V, Pb and Sr were introduced along with U via interaction with saline SO 2 - rich, isotopically light fluids under varying water/rock ratios and at temperatures of 500 - 550 0 C. 87 Sr/ 86 Sr systematics suggest that it is unlikely that Sr, and by extension uranium, were introduced by fluids originating from the basement gneisses. Geological constraints and the general alteration pattern are consistent with the release of the mineralizing fluids in response to the overloading of the basement rocks onto the Sedimentary Espinhaco via a thrust mechanism. (Author) [pt

  7. Uranium mineralization at Lagoa Real, BA, Brazil: the role of fluids in its genesis

    International Nuclear Information System (INIS)

    Prates, Sonia Pinto; Neves, Jose Marques Correia; Fuzikawa, Kazuo

    2009-01-01

    The Lagoa Real uranium province is situated in the central-south of Bahia state . Brazil and it is presently by far the most important and best known uranium occurrence in Brazil. Nowadays 34 anomalies are known in a 30 Km long and 5 km wide area. An open pit mine was open in Cachoeira Mine, in the north portion of the area, and it is the only uranium mine in operation in Brazil and even in South America as well. The uranium mineralization in the Lagoa Real uranium province occurs in metamorphic rocks named albitites, due to their albite content (over 70%). Uraninite is the main uranium mineral, followed by pechblende, uranophane, torbernite and other uranyl minerals. Uraninite occurs as tiny round and irregular crystals (20 a 30 μm) included or associated to mafic minerals, mainly pyroxene and garnet, and also to amphibole and biotite and sometimes to albite. Some secondary minerals such as, for instance, uranophane, torbernite and tyuyamunite are also found. The main albitites minerals from the Cachoeira mine (plagioclase, garnet, biotite, pyroxene, amphibole and titanite) were studied by means of Infrared Spectroscopy Techniques. Good results were obtained from small quantities of material (around 2 mg) and allowed the minerals identification, and also to know their composition (from the peak position) and to detect the presence of water molecules, which indicates an aqueous phase during the uranium formation, probably rich in Fluorine. (author)

  8. Propiedades termoluminiscentes de una albita de minas Geraes (Brasil

    Directory of Open Access Journals (Sweden)

    García-Guinea, J.

    2004-04-01

    Full Text Available Albite sodium feldspar is studied by thermoluminescent methods using the blue region of the spectra (circa 400nm and the possible uses as a dosimeter are explored. The light emission of the spectra bands of natural and irradiated albite under X and gamma rays are determined using automated RISØ thermoluminescence equipment. Albite is a potential material to be used as retrospective dosimeter due to its good blue thermoluminescence characteristics in good agreement with the dosimetric requirements. It is sensitive to radiation, possesses a good linearity (0.06-8Gy, shows an acceptable stability in time, it is highly reproducible and can detect low levels of dose (60mGy. The TL glow curves emission exhibit a very complex structure associated to a continuous trap distribution. This behaviour could be explained as a consequence of a dynamic creation-annihilation of a [AlO4/alkali]+ and [AlO4]o centres.

    Se estudian las posibilidades dosimétricas de la albita (feldespato sódico por métodos termoluminiscentes utilizando la región espectral del azul (alrededor de los 400nm. Se registran las posiciones espectrales de emisión de luz de este material irradiado con rayos X y con radiación gamma en un equipo automático de termoluminiscencia Risø. La albita puede ser empleada potencialmente en el campo de la reconstrucción de dosis post-accidental ya que sus propiedades termoluminiscentes en la región espectral del azul presentan buenas características dosimétricas. Se observa que la albita es muy sensible a la radiación, presenta una excelente linealidad con la dosis (0.06-8Gy, muestra una gran estabilidad con el tiempo, tiene reproducibilidad aceptable y puede detectar bajos rangos de dosis (60mGy. Sus curvas de termoluminiscencia tienen una estructura compleja asociada a una distribución continua de trampas en todo el rango de temperaturas. Este comportamiento podría explicarse como consecuencia de la formación-aniquilación din

  9. High-Temperature Thermal Diffusivity Measurements of Silicate Glasses

    Science.gov (United States)

    Pertermann, M.; Hofmeister, A. M.; Whittington, A. G.; Spera, F. J.; Zayac, J.

    2005-12-01

    Transport of heat in geologically relevant materials is of great interest because of its key role in heat transport, magmatism and volcanic activity on Earth. To better understand the thermal properties of magmatic materials at high temperatures, we measured the thermal diffusivity of four synthetic end-member silicate glasses with the following compositions: albite (NaAlSi3O8), orthoclase (KAlSi3O8), anorthite (CaAl2Si2O8), and diopside (CaMgSi2O6). Thermal diffusivity measurements were conducted with the laser-flash technique and data were acquired from room temperature to a maximum temperature near 1100°C, depending on the glass transition temperature. The presence of sub-mm sized bubbles in one of the orthoclase samples had no discernable effect on measured diffusivities. At room temperature, the three feldspar-type glasses have thermal diffusivity (D) values of 0.58-0.61 mm2/s, whereas the diopside glass has 0.52 mm2/s. With increasing temperature, D decreases by 5-10% (relative) for all samples and becomes virtually constant at intermediate temperatures. At higher temperatures, the anorthite and diopside glasses exhibit significant drops in thermal diffusivity over a 50-100°C interval, correlating with previously published heat capacity changes near the glass transition for these compositions. For anorthite, D (in mm2/s) decreases from 0.48 at 750-860°C to 0.36 at 975-1075°C; for diopside, D changes from 0.42 at 630-750°C to 0.30 at 850-910°C, corresponding to relative drops of 24 and 29%, respectively. Albite and orthoclase glasses do not exhibit this change and also lack significant changes in heat capacity near the glass transition. Instead, D is constant at 400-800°C for albite, and for orthoclase values go through a minimum at 500-600°C before increasing slightly towards 1100°C but it never exceeds the room temperature D. Our data on thermal diffusivity correlate closely with other thermophysical properties. Thus, at least in case of simple

  10. Fault rocks and veins formation in the crystalline Palaeozoic basement of the N margin of the Littoral Chain (Catalan Coastal Ranges, NE Spain)

    Science.gov (United States)

    Alías, Gemma; Belmonte, Alba; Cantarero, Irene; Inglés, Montserrat; Travé, Anna

    2013-04-01

    The Littoral Chain corresponds to a horst of NE-SW direction formed during the Neogene extension which in the studied area (Collserola-Montnegre massif) is mainly composed by Paleozoic materials. At the northern margin the horst limits with the Vallès basin which is infilled by Miocene detrital materials. In the Forques Hill, two km to the est of Martorell, an excellent outcrop of Ordovician phyllites summarise an spread tectonic evolution from Hercynian to Neogene deformation. This work evaluates the behaviour of phyllites during the Hercynian ductile deformation and later during the fragile Mesozoic and Neogene tectonics. The weakness of these rocks together with the situation very close to the Vallès Fault favour that this area concentrates many deformation structures related to extensional tectonics, such as veins, cataclasites and gouges. Phyllites present a pervasive regional hercynian foliation oriented WNW-ESE and dipping moderately to the NNE; a huge amount of quartz veins, up to 20% of the rock volume, were injected during and immediately after the main foliation development. Two groups of fractures cutting the phyllites can be distinguished in the field according to the fault rock products, the vein infilling, the orientation and the geometry. The first one corresponds to Mesozoic fractures that have a NE-SW trend and dip indistinctly to the NW or SE, in a conjugate system. They are characterized by the formation of a broad zone of 0,2 m up to 1,5 m formed either by cataclasites or en echelon veins that indicate a normal movement. The cataclasites are cohesive greenish rocks, with 50% of clasts of wall rock from mm to dm in size. Neoformed minerals in the matrix are chlorite - albite - barite ± titanite and rutile. Veins are white to pinkish in colour and two types of infill have been identified: albite - chlorite - iron oxides± rutile and dolomite - chlorite. The second group belongs to Neogene fractures which although similar orientation than those

  11. Emplacement and deformation of the A-type Madeira granite (Amazonian Craton, Brazil)

    Science.gov (United States)

    Siachoque, Astrid; Salazar, Carlos Alejandro; Trindade, Ricardo

    2017-04-01

    The Madeira granite is one of the Paleoproterozoic (1.82 Ga) A-type granite intrusions in the Amazonian Craton. It is elongated in the NE-SW direction and is composed of four facies. Classical structural techniques and the anisotropy of magnetic susceptibility (AMS) method were applied to the study of its internal fabric. Magnetic susceptibility measurements, thermomagnetic curves, remanent coercivity spectra, optical microscopy and SEM (scanning electron microscopy) analyses were carried out on the earlier and later facies of the Madeira granite: the rapakivi granite (RG) and the albite granite (AG) respectively. The last one is subdivided into the border albite granite (BAG) and the core albite granite (CAG) subfacies. AMS fabric pattern is controlled by pure magnetite in all facies, despite significant amounts of hematite in the BAG subfacies. Microstructural observations show that in almost all sites, magnetic fabric correlates to magmatic state fabrics that are defined by a weak NE-SW orientation of mafic and felsic silicates. However, strain mechanisms in both subfacies of AG also exhibit evidence for solid-state deformation at high to moderate temperatures. Pegmatite dyke, strike slip fault (SFA-B-C), hydrothermal vein, normal fault (F1-2) and joint (J) structures were observed and their orientation and kinematics is consistent with the magmatic and solid-state structures. Dykes, SFA-C and F1, are usually orientated along the N70°E/40°N plane, which is nearly parallel to the strike of AMS and magmatic foliations. In contrast, veins, SFB, F2 and some J are oriented perpendicular to the N70°E trend. Kinematic analysis in these structures shows evidence for a dextral sense of movement in the system in the brittle regime. The coherent structural pattern for the three facies of Madeira granite suggests that the different facies form a nested pluton. The coherence in orientation and kinematics from magmatic to high-temperature solid-state, and into the brittle

  12. Thermal stabilization of uranium mill tailings

    International Nuclear Information System (INIS)

    Dreesen, D.R.; Williams, J.M.; Cokal, E.J.

    1981-01-01

    The sintering of tailings at high temperatures (1200 0 C) has shown promise as a conditioning approach that greatly reduces the 222 Rn emanation of uranium mill tailings. The structure of thermally stabilized tailings has been appreciably altered producing a material that will have minimal management requirements and will be applicable to on-site processing and disposal. The mineralogy of untreated tailings is presented to define the structure of the original materials. Quartz predominates in most tailings samples; however, appreciable quantities of gypsum, clay, illite, or albites are found in some tailings. Samples from the Durango and Shiprock sites have plagioclase-type aluminosilicates and non-aluminum silicates as major components. The iron-rich vanadium tailings from the Salt Lake City site contain appreciable quantities of α-hematite and chloroapatite. The reduction in radon emanation power and changes in mineralogy as a function of sintering temperature are presented

  13. Geochemistry and geochronology Rb-Sr, K-Ar and 40Ar/39Ar of the Pan-African granitic complexes of the Tamanrasset area (Algeria): relationships with the associated Sn-W mineralizations and tectonic evolution of Central Hoggar

    International Nuclear Information System (INIS)

    Bertrand, J.M.; Zimmermann, J.L.; Dautel, D.; Boullier, A.M.; Bouabsa, L.; Farrar, E.; Archibald, D.A.; Moulahoum, O.

    1992-01-01

    New field mapping, petrographic and mineralogic, geochemical and geochronological data allow us to distinguish two successive magmatic suites with contrasting geochemistry: (1) granites with subalkaline affinity between 615 Ma (Anfeg) and 576 Ma (Tifferkit); (2) peraluminous magmatism and Li-F specialized leucogranites with associated Sn-W mineralization between 539 and 525 Ma. Such a magmatic evolution is interpreted as resulting from thickening of the continental crust during the Pan-African collision. Earliest magmas show mantle contribution and were formed close to the crust-mantle boundary where synchronous crustal stacking developed in amphibolite facies conditions. Latest peraluminous magmatism of crustal derivation and albite-topaz leucogranites appear to be controlled by localized extensional structures, 80 Ma after the main tectono-metamorphic event

  14. Physicochemical study of ceramics from Pre classic of Cuicuilco 'C' Mexico, methodology to define origin of raw material

    International Nuclear Information System (INIS)

    Badillo S, A.; Sanchez P, S.; Perez C, M.A.; Jimenez D, G.; Aguilar F, M.; Zorrilla C, C.; Arenas A, J.A.

    2006-01-01

    Cuicuilco has been considered one of the most important centers during the Formative Period (1000 - 0 b. C.) in the south of Mexico Basin, mainly, due its dimensions. Because of the Xitle volcano eruption, its occupation decreases around 200 b. C. This paper presents the results of a multidisciplinary investigation about ceramic material from Cuicuilco 'C', located in the south of Mexico City, and sediments from different places near to it. The analysis was done by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS) and X- Ray Diffraction (XRD). Its results show the presence of Si, O, Fe and Al as majority elements, and crystalline phases as albite, hematite, quartz, maghemite and cristobalite. Chemical elements identified at ceramic samples has been submitted to an statistical analysis in order to be compared with the results of analyzed sediments, to determinate the raw material origin. (Author)

  15. Contributions to the mineralogy, petrography and metallogeny of the Itataia phosphorus-uranium deposit, state of Ceara, Brazil

    International Nuclear Information System (INIS)

    Netto, A.M.

    1984-01-01

    The phosphorus-uranium mineralization of the Itataia deposit is unique. Most of the uranium is contained in the collophane (uraniferous fluorapatite) obtained through the transformation of metamorphic apatite of the country rocks (Itataia Group). A graphite-rich pelitic metasediment origin for the uranium and phosphorus is suggested. Initially, the rocks were subjected to isoclinal and homoclinal folding associated with overthrusting and regional metamorphism of the high amphibolite facies with some migmatization. The mineralization is epigenetic and dominated by sodium-rich metasomatic fluids. The mobilized quartz-feldspathic migmatites were transformed into collophane-albite-episyenites. The considerably thick markbles provided the conditions favoring an increase in the fluids pH which caused the precipitation of collophane concentrated in pockets and stockworks. (Author) [pt

  16. MINERALOGIA E QUÍMICA DE SOLO DE VÁRZEA E SUAS SUSCEPTIBILIDADES NO PROCESSO DE TERRAS CAÍDAS NA COMUNIDADE DO DIVINO ESPÍRITO SANTO-AM / Mineralogy and chemistry of the lowland soil and its sensibilities in the process of lands falls in community Divino Espírito Santo (Amazonas, Brazil.

    Directory of Open Access Journals (Sweden)

    Regiane Campos Magalhães

    2013-12-01

    Full Text Available The study about the mineralogical and chemical lowland soils generate information to compose a current survey about the susceptibility of lowland soil to process Fallen Lands. With this purpose we studied five profiles the banks of the Solimões River, located in the municipality of Iranduba (AM. The information obtained allowed to determine the Neosoil Fluvic the study area has favorable conditions for cultivation with an average pH of 6.2, with high levels of Ca, Mg, K, P, micronutrients and zero Al content, with high levels of C and M. O. in the first layer and a decrease in depth. Thus, Neosoil Fluvic was characterized as Tb eutrophic, with base saturation above 50%, with good CTC. The mineralogy was homogeneous in all profiles, with a predominance of primary minerals: Quartz, Albite and rutile, with low proportions of clay minerals Muscovite, Kaolinite, Muscovite-Illite interstratified and Illite.

  17. Physicochemical study of ceramics from Pre classic of Cuicuilco 'C' Mexico, methodology to define origin of raw material; Estudio fisico-quimico de ceramica del Preclasico de Cuicuilco 'C' Mexico. Metodologia para definir procedencia de materia prima

    Energy Technology Data Exchange (ETDEWEB)

    Badillo S, A.; Sanchez P, S. [Escuela Nacional de Antropologia e Historia INAH, Periferico Sur y Zapote s/n, Col. Isidro Fabela, Delegacion Tlalpan, Mexico D.F. (Mexico); Perez C, M.A. [Proyecto Arqueologico de Cuicuilco, DEA-INAH, Lic. Verdad 3, Col. Centro (Mexico); Jimenez D, G. [Instituto de Investigaciones Antropologicas de la UNAM, Ciudad Universitaria, 04510 Mexico D.F. (Mexico); Aguilar F, M.; Zorrilla C, C.; Arenas A, J.A. [IFUNAM, Circuito de la Investigacion Cientifica s/n, Ciudad Universitaria, 04510, Mexico D.F. (Mexico)]. e-mail: alejandrabadillo_s@yahoo.mx

    2006-07-01

    Cuicuilco has been considered one of the most important centers during the Formative Period (1000 - 0 b. C.) in the south of Mexico Basin, mainly, due its dimensions. Because of the Xitle volcano eruption, its occupation decreases around 200 b. C. This paper presents the results of a multidisciplinary investigation about ceramic material from Cuicuilco 'C', located in the south of Mexico City, and sediments from different places near to it. The analysis was done by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS) and X- Ray Diffraction (XRD). Its results show the presence of Si, O, Fe and Al as majority elements, and crystalline phases as albite, hematite, quartz, maghemite and cristobalite. Chemical elements identified at ceramic samples has been submitted to an statistical analysis in order to be compared with the results of analyzed sediments, to determinate the raw material origin. (Author)

  18. Alkali based slagging: a case study from Leigh Creek

    Energy Technology Data Exchange (ETDEWEB)

    R.A. Creelman; J. Bamberry; L.A. Juniper; C. Ward [University of Western Sydney, Penrith South, NSW (Australia)

    2003-07-01

    A systematic study was undertaken at NRG Port Augusta Power station in South Australia to determine the cause of ash deposition (slagging) in the boilers. Conventional wisdom suggests that iron in the ash is generally a major player in furnace ash deposition; however, mineralogical and chemical analyses of the deposits showed that the binding phase was plagioclase feldspar, dominated by the sodic feldspar albite. The study resulted in recognition that the cause of the formation of ash deposits in the North Flinders furnaces was the result of the ingestion of sodium and calcium into the melt that bound the deposits. This finding was a breakthrough in understanding the deposition process within these furnaces, and emphasises that not all slagging is iron related and that systematic studies of deposits, coal and ash make fundamental contributions to understanding the ash deposition mechanisms. 9 refs., 5 figs., 2 tabs.

  19. THE ROLE OF DYNAMOMETAMORPHISM IN THE FORMATION OF THE MUKODEK GOLD FIELD (NORTH PRIBAIKALIE

    Directory of Open Access Journals (Sweden)

    V. A. Vanin

    2017-01-01

    Full Text Available The Mukodek gold field is discussed as an example proving that dynamometamorphism is a major factor in the formation of gold deposits in the Abchad fault zone. This deposit belongs to the gold‐silver‐ore zones of mylonitization and schistosity. The ore source is related to the original host rocks with an increased geochemical background concentration of Au. Due to dynamometamorphism processes, gold particles are abundant and mostly enlarged. From the primary rocks, the dynamometamorphites inherit a positive correlation between the number of particles and the concentrations of gold. The dynamometamorphic complex of the ore field developed in two stages, as a minimum. At the early stage (321.0±1.9 Ma, the host rocks were mechanochemically deformed and transformed into the gold‐ bearing mineralized dynamometamorphites containing sericite, chlorite, ankerite, albite, and quartz. In the second stage (280±15 Ma, the albite‐dolomite‐quartz ore veins were formed. Such veins have industrial gold contents.

  20. Synthetic multielement standards used for instrumental neutron activation analysis as rock imitations

    International Nuclear Information System (INIS)

    Leypunskaya, D.I.; Drynkin, V.I.; Belenky, B.V.; Kolomijtsev, M.A.; Dundera, V.Yu.; Pachulia, N.V.

    1975-01-01

    Complex (multielemental) standards representing microelement composition of standard rocks such as trap ST-1 (USSR), gabbrodiorite SGD-1 (USSR), albitized granite SG-1 (USSR), basalt BCR-1 (USA) and granodiorite GSP-1 (USA) have been synthesized. It has been shown that the concentration of each microelement in the synthetic standards can be given with a high precision. Comparative investigation has been carried out of the synthetic imitations and the above natural standard rocks. It has been found that the result of the instrumental neutron activation analysis using the synthetic standards is as good as in the case when natural standard rocks are used. The results obtained have been also used for substantiation of the versatility of the method used for standard preparation, i.e. a generalization has been made of a possibility of using this method for the preparation of synthetic standards representing the microelement composition of any natural rocks with various compositions and concentrations of microelements. (T.G.)

  1. Meta-evaporite in the Carajás mineral province, northern Brazil

    Science.gov (United States)

    Riehl, Walter; Cabral, Alexandre Raphael

    2018-05-01

    Evidence for connecting evaporite-sourced high-salinity fluids with iron-oxide-copper-gold (IOCG) deposits in the Carajás mineral province has solely been based on boron-isotope compositions of tourmaline. Presence of meta-evaporitic rocks remains unrecognised. Here, we report laminated albitite, tourmalinite and banded albite-phlogopite rock, intercepted by exploratory drilling in a clastic metasedimentary sequence. These rocks represent evaporite precursors. Their location in the copper-gold prospects Açaí and Angélica, in the westernmost part of the Carajás mineral province, indicates that (i) evaporite-sourced fluids were regional and (ii) evaporite-bearing metasedimentary sequences may have been an important source of high-salinity fluids and/or sulfur for the IOCG deposits of the Carajás mineral province.

  2. Dacite – siltstone peperite from Trlično at Rogatec, Eastern Slovenia

    Directory of Open Access Journals (Sweden)

    Polona Kralj

    2006-06-01

    Full Text Available Dacitic glassy lava flow at Trlično is surrounded by a dacite – siltstone peperite and peperitic breccia that underwent alteration, recognised in two, only a few metres thick zones. In the higher-temperature alteration zone, albite extensively replaces volcanic glass and primary plagioclases. The siltstone components are altered to microcrystalline quartz, iron oxides and interlayered illite/smectite clay minerals. This zone developed upon thermalmetamorphosis related to the transfer of heat from the cooling lava. In the lower temperature alteration zone, analcime occurs as the replacement of volcanic glass and pore- and fissure-filling, while the primary plagioclases and poorly lithified siltstone remained fairly unchanged. This zone developed under hydrothermal conditions related to the heating, circulation and reactions of pore waters in the sediment surrounding the lava flow.

  3. Geology and age of the Lac a la Perdrix fenite, southern Gatineau district, Quebec

    International Nuclear Information System (INIS)

    Hogarth, D.D.

    1996-01-01

    The Lac a Ia Perdrix fenite lies in the Central Metasedimentary Belt of the Grenville Province. This 30 m wide fenite, adjacent to a narrow calciocarbonatite sill, replaces diopside-oligoclase gneiss and is composed of magnesio-arfvedsonite, aegirine, microcline, albite, and fluorapatite. Near the contact with carbonatite, it contains appreciable monazite and barite whereas aegirine virtually disappears. Fenitization probably took place early in the igneous stage of carbonatite development. A Pb/U monazite age of 1026 ± 2 Ma is thought to date fenite formation. Together with published data, this age shows that carbonatite intruded metamorphic rocks near the close of the Grenville Orogeny. (author). 33 refs., 4 tabs., 5 figs

  4. Le volcanisme cambrien du Maroc central : implications géodynamiquesThe Central Morocco Cambrian volcanism: geodynamic implications

    Science.gov (United States)

    Ouali, Houssa; Briand, Bernard; Bouchardon, Jean-Luc; Capiez, Paul

    2003-05-01

    In southeastern Central Morocco, the Bou-Acila volcanic complex is considered of Cambrian age. In spite of low-grade metamorphic effect, initial volcanic texture and mineralogy can be recognized and volcanic rocks are dominated by dolerites and porphyric dolerites. The initial mineralogy is composed of plagioclases, pyroxenes and dark minerals. A secondary mineral assemblage is composed of albite, epidote, chlorite and calcite. According to their immobile elements compositions, the southeastern central Morocco metavolcanites are of within-plate continental tholeiites. This volcanism and those recognized in many other areas in Morocco confirm a Cambrian extensive episode within the Gondwana supercontinent. To cite this article: H. Ouali et al., C. R. Geoscience 335 (2003).To cite this article: H. Ouali et al., C. R. Geoscience 335 (2003).

  5. Petrogenetic and geodynamic origin of the Neoarchean Doré Lake Complex, Abitibi subprovince, Superior Province, Canada

    DEFF Research Database (Denmark)

    Polat, Ali; Frei, Robert; Longstaffe, Fred J.

    2018-01-01

    Group, which is composed of two cycles of tholeiitic-to-calc-alkaline volcanic and volcaniclastic rocks, siliciclastic and chemical sedimentary rocks, and layered mafic-to-ultramafic sills. In this study, we report major and trace element results, and Nd, Sr, Pb and O isotope data for anorthosites......, leucogabbros, gabbros and mafic dykes from the Doré Lake Complex and spatially associated basalts and gabbros of the Obatogamau Formation to assess their petrogenetic origin and geodynamic setting. Field and petrographic observations indicate that the Doré Lake Complex and associated volcanic rocks underwent...... extensive metamorphic alteration under greenschist facies conditions, resulting in widespread epidotization (20–40%) and chloritization (10–40%) of many rock types. Plagioclase recrystallized mainly to anorthite and albite endmembers, erasing intermediate compositions. Metamorphic alteration also led...

  6. Petrography, mineral chemistry and lithochemistry of the albitite and granite-gneissics rocks of anomaly 35 from Lagoa Real uranium province; Petrografia, quimica mineral e litoquimica do albitito e das rochas granito-gnaissicas da anomalia 35, provincia uranifera de Lagoa Real

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Camila Marques dos

    2016-07-01

    albitites and gneisses are macroscopically gradational, however, in the garnet albitites replacement of granitic mineral facies by the albitite facies were observed petrographically, implying a granitic protolith for this rock. On the other hand, magnetite albitites do not have clear relationship with granites. Albitites usually have porphyroblastic texture with granoblastic polygonal matrix and chessboard texture in albite porphyroclasts. The garnet albitites comprise hedenbergite, hastingsite, garnet, magnetite and sphena. Magnetite albitites, in turn, have hedenbergite, Fe-edenite, biotite, martitized magnetite, allanite and sphene. The diopside+actinolite+eastonita association is late, and in these rocks, it is restricted to more deformed portions or filling voids. The biotite albitites comprise biotite, zircon and apatite hedenbergite (?). Mineralization occurs in magnetite albitites as thin lenses composed by sphene, magnetite, carbonate and zircon. The uranium mineral is the uraninite, which occurs filling spaces between crystals and sphene or albite granules. In comparison to granites, albitites have a higher content of Na{sub 2}O, MgO, V, W, Zr, Pb and Sr for and lower K{sub 2}O, SiO{sub 2} and F. They have a geochemical REE pattern that is identical to that of granite. The similarity between macroscopic granites and albitites, the presence of vazios, feldspar hematitization and sericitization causing macroscopical reddening in transitional portions and the replacement of potassic feldspar by albite and oligoclase are suggestive of episyenitization processes. The metasomatic perthites and presence of chessboard texture in porphyroclasts indicate successive albitization processes prior to deformation. The comparison between albitite samples of different drill cores and anomalies shows that there are differences in the formation and mineralization of these rocks. The V and Mg enrichment in some albitites suggests that these rocks may result from the interaction of

  7. Mineralogical characterization of quarry fines from Tracuateua city, state of Para, Brazil

    International Nuclear Information System (INIS)

    Costa, J.H.B. da; Negrao, R.C.; Angelica, R.S.; Universidade Federal do Para

    2011-01-01

    The aim of this study was to characterize the mineralogy quarry fines samples for its reuse and thus contributing to mitigate the environmental impact caused by this waste. In order to achieve the results, samples were collected and prepared for assays and identification of the mineralogical phases present in the quarry fines from the samples. X-ray diffraction and optical microscopy techniques were used. The quarry of fines characterization was based on qualitatively identification the minerals present in the samples. It was detected the presence of quartz, muscovite and feldspar (albite and microclinite) by x-ray diffraction technique and microscopic and macroscopic observations. Moreover, the size distribution was determined, and the samples presented a medium to fine size (ranging from 9,5 mm to 0,075 mm) and the grains presented an irregular and angular shapes. (author)

  8. The stibian mustard gold from the Kriván¿ Au deposit,Tatry Mts., Slovak Republic

    DEFF Research Database (Denmark)

    Makovicky, Emil; Martin, Chovan; František, Bakos

    2007-01-01

    The Kriván Au-Sb mineralization is hosted in several subhorizontal variscan mylonite zones located in granitoid rocks. Ore minerals occur in thin lens-shaped quartz veinlets. Albite, chlorite, calcite, muscovite and tourmaline are minor gangue minerals. Four mineral assemblages have been recognized...... - (1) pyrite-arsenopyrite-gold, (2) stibnite-sulfosalts-sphalerite, (3) tetrahedrite- chalcopyrite-electrum, (4) supergene minerals. Isometric and irregular grains of mustard gold are 0.X mm in size. In refl ected light it is isotropic with low refl ectivity and orange-red or brown-yellow color...... with pores more or less fi lled by oxidation products of Sb and Fe. Compositionally it does not conform with stibian mustard gold from Yakutia and Bolivia, approximately AuSb1.4O2.1, derived from decomposition of aurostibite, but it conforms with mustard gold from Krásná Hora, Czech Republic. For this type...

  9. Microstructural analysis from archaeological sculptures of the Olmeca culture

    International Nuclear Information System (INIS)

    Rodriguez L, V.; Mendoza A, D.; Espinosa P, M.; Martinez C, G.

    1999-01-01

    This work presents the results obtained from the characterization of a series of samples belonging to different monuments of the Olmec culture. These monuments are exhibited in the archaeological site of La Venta, Tabasco, Mexico. Scanning Electron Microscopy (SEM) and X-ray diffraction (XRD) were used to determine the crystalline phases that characterise the samples, these phases are associated to different morphology. The elemental analysis exhibits the presence mainly of such elements as C, Si, O, Al, Na, Ca and in less abundance Ti, K, Cr, Ni and Mn were determined. The morphology is characterized by the presence of plane tabular structures, schists, extended slates and clusters of irregular grain. Such crystal phases as anorthite, albite, sanidine, zinnwaldite and clinochlore were identified. These phases are associated with such type of materials as feldspars and mica. All the identified phases are noted for presenting near perfect exfoliation. (Author)

  10. International Uranium Resources Evaluation Project (IUREP) orientation phase mission summary report: Cameroon

    International Nuclear Information System (INIS)

    1985-01-01

    A report has recently been published which describes the findings of the International Uranium Resources Evaluation Project (IUREP) Mission to Cameroon. The IUREP Orientation Phase Mission to Cameroon estimates the Speculative Resources of that country to be in the order of 10 000 tonnes uranium for syenite-associated U-deposits in southern Cameroon, and in the order of 5 000 tonnes uranium for uranium deposits associated with albitized and desilicified late tectonic Panafrican granites (episyenite) and Paleozoic volcanics in northern Cameroon. No specific tonnage is given for Francevillian equivalents (DJA-Series) and for Mesozoic and Cenozoic sedimentary basins, which are thought to hold limited potential for sandstone hosted uranium. However the Douala basin, consisting of mixed marine and continental sequences merits some attention. No specific budget and programme for uranium exploration are proposed for Cameroon. Instead specific recommendations concerning specific potential environments and general recommendation concerning the methodology of exploration are made. (author)

  11. Mineralogy, geochemistry, porosity and redox properties of rocks from Forsmark. Compilation of data from the regional model volume for SR-Site

    Energy Technology Data Exchange (ETDEWEB)

    Sandstroem, Bjoern (WSP Sverige AB, Stockholm (Sweden)); Stephens, Michael B. (Geological Survey of Sweden, Uppsala (Sweden))

    2009-11-15

    This report is a compilation of the data acquired during the Forsmark site investigation programme on the mineralogy, geochemistry, redox properties and porosity of different rock types at Forsmark. The aim is to provide a final summary of the available data for use during the SR-Site modelling work. Data presented in this report represent the regional model volume and have previously been published in various SKB reports. The data have been extracted from the SKB database Sicada and are presented as calculated median values, data range and lower/upper quartile. The representativity of all samples used for the calculations have been evaluated and data from samples where there is insufficient control on the rock type have been omitted. Rock samples affected by alteration have been omitted from the unaltered samples and are presented separately based on type of alteration (e.g. oxidised or albitized rock)

  12. Analysis of deterioration of rocky material which conform the sculptured serpents of the Tenayuca pyramid

    International Nuclear Information System (INIS)

    Mendoza A, D.; Martinez C, G.; Rodriguez L, V.

    2004-01-01

    This work presents the results about the characterization of rocky materials samples proceeding from heads of snakes that adorn the pyramid of Tenayuca, Mexico. Analysis of these samples, that show deterioration presence was performance through Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS) and X-ray Diffraction (XRD). Several morphological structures such as granular, tubular, acicular growths and fibers were observed, some of they could be associate to salt migration. It was possible to identify different crystalline phases associated with albite (NaAlSi 3 O 8 ), anorthite [(Ca,Na)(Si,Al) 4 O 8 ], ferroactinolite [(Ca,Na,K) 2 Fe 5 Si 8 O 22 (OH) 2 ], gypsum (CaSO 4 2H 2 O), quartz (SiO 2 ) and thenardite (Na 2 SO 4 ). (Author) 10 refs., 2 tabs., 12 figs

  13. Petrography, mineral chemistry and lithochemistry of the albitite and granite-gneissics rocks of anomaly 35 from Lagoa Real uranium province

    International Nuclear Information System (INIS)

    Santos, Camila Marques dos

    2016-01-01

    albitites and gneisses are macroscopically gradational, however, in the garnet albitites replacement of granitic mineral facies by the albitite facies were observed petrographically, implying a granitic protolith for this rock. On the other hand, magnetite albitites do not have clear relationship with granites. Albitites usually have porphyroblastic texture with granoblastic polygonal matrix and chessboard texture in albite porphyroclasts. The garnet albitites comprise hedenbergite, hastingsite, garnet, magnetite and sphena. Magnetite albitites, in turn, have hedenbergite, Fe-edenite, biotite, martitized magnetite, allanite and sphene. The diopside+actinolite+eastonita association is late, and in these rocks, it is restricted to more deformed portions or filling voids. The biotite albitites comprise biotite, zircon and apatite hedenbergite (?). Mineralization occurs in magnetite albitites as thin lenses composed by sphene, magnetite, carbonate and zircon. The uranium mineral is the uraninite, which occurs filling spaces between crystals and sphene or albite granules. In comparison to granites, albitites have a higher content of Na 2 O, MgO, V, W, Zr, Pb and Sr for and lower K 2 O, SiO 2 and F. They have a geochemical REE pattern that is identical to that of granite. The similarity between macroscopic granites and albitites, the presence of vazios, feldspar hematitization and sericitization causing macroscopical reddening in transitional portions and the replacement of potassic feldspar by albite and oligoclase are suggestive of episyenitization processes. The metasomatic perthites and presence of chessboard texture in porphyroclasts indicate successive albitization processes prior to deformation. The comparison between albitite samples of different drill cores and anomalies shows that there are differences in the formation and mineralization of these rocks. The V and Mg enrichment in some albitites suggests that these rocks may result from the interaction of fluids with

  14. Geochemistry of the uranium mineralized Achala granitic complex, Argentina: Comparison with Hercynian peraluminous leucogranites of western Europe

    International Nuclear Information System (INIS)

    Cuney, M.; Leroy, J.; Valdiviezo, P.A.; Daziano, C.; Gamba, M.; Zarco, A.J.; Morello, O.; Ninci, C.; Molina, P.

    1989-01-01

    The Achala granitic complex belongs to the Sierras Pampeanas Hercynian belt, located west of the city of Cordoba, Argentina. This complex is very large (about 100 km N-S and 40 km E-W) and is composed of biotite, biotite with muscovite and muscovite with tourmaline granites intruded in amphibolite grade metamorphic rocks, along a main N 20 deg. E structural direction. Numerous uranium mineralizations are located within the granitic massif and tungsten mineralizations are present both in the enclosing metamorphic rocks and in the granite. The geochemistry of the granite has been studied in four test areas (Southern, Copina, Median and Don Vincente). Two test areas (Median and Don Vicente) present clear evidence of hydrothermal alteration: albitization and dequartzification similar to the French 'episyenites', silicification and argillic alteration. Potassic alteration is rare and weakly developed. The two test areas with hydrothermal alteration present a high uranium geochemical background (5-30 ppm). High thorium contents (up to 65 ppm) are essentially observed in the less differentiated granites of the Copina and Median areas. Thorium/uranium ratios are highly variable (1-10). Uranium minerals are related to different environments - (1) apatite-biotite enclave mineralized with uraninite and uranothorite, (2) gneiss from the contact metamorphism rim, (3) granite with incipient dequartzification, (4) granite associated with albitic episyenites and (5) silicified granite - but are all located in the two test areas presenting clear evidence of hydrothermal alteration. The three petrogenetic events are clearly related to very different mechanisms, separated from each other by several tens of millions of years in the west European Hercynian chain. In the same period the same succession of events leading to uranium deposits is observed in Argentina. 34 refs, 10 figs, 1 tab

  15. Characterization of pyroxenes associated with the uranium mineralization of the Jazida Cachoeira (Lagoa Real Uranium Province, Bahia State, Brazil

    International Nuclear Information System (INIS)

    Goncalves, Rhaine Matos

    2005-01-01

    This work has as objective to contribute for the knowledge about the genesis of the Cachoeira uranium deposit (Lagoa Real Uranium Province, Bahia State, Brazil), characterizing pyroxenes (with emphasis in those associated with the uranium mineralization and those hosting inclusions) of the deposit and their associated inclusions. In function of the accomplished analyses, steps that should be followed to obtain and interpret data from fluid inclusions (FI), in the D09B XRF X-Ray Fluorescence Beam Line of the National Synchrotron Light Laboratory, Campinas, Brazil, have been described. The analyzed pyroxenes are augites, diopsides and aegirine-augites, and intermediate terms, for example between augite and diopside, were detected. They presented two and three phases fluid inclusions being some, possible, primary ones. The three phases FI could present a birefringent solid phase. The pyroxenes presented, also, solid inclusions. The analysis of some solid inclusions revealed that they were albites. These albites are, probably, previous to the pyroxene host mineral. The obtained results indicated that the studied pyroxenes are associated to an important phase of caleic metasomatism. These pyroxenes are not totally associated to the precipitation of the uranium. In the petrographic study of the samples, two types of plagioclase were identified, one very altered and other less altered. Synchrotron light is a powerful tool for analyze FI. It was verified that care in the preparation of the sample, such as the selection of near-surface FI, are very important to obtain reliable data. In the studies with synchrotron light only the vanadium was detected in larger amount in the area that contained FI (in pyroxene), in relation to the control area, due, mainly, to experimental factors. The presence of this element it is not easy to interpret. Additional studies, on solid and fluid inclusion in pyroxene, and in other minerals, will be important to understand the Cachoeira uranium

  16. Mass change calculations of hydrothermal alterations within the volcanogenic metasediments hosted Cu-Pb (-Zn) mineralization at Halilar area, NW Turkey

    Science.gov (United States)

    Kiran Yildirim, Demet; Abdelnasser, Amr; Doner, Zeynep; Kumral, Mustafa

    2016-04-01

    The Halilar Cu-Pb (-Zn) mineralization that is formed in the volcanogenic metasediments of Bagcagiz Formation at Balikesir province, NW Turkey, represents locally vein-type deposit as well as restricted to fault gouge zone directed NE-SW along with the lower boundary of Bagcagiz Formation and Duztarla granitic intrusion in the study area. Furthermore, This granite is traversed by numerous mineralized sheeted vein systems, which locally transgress into the surrounding metasediments. Therefore, this mineralization closely associated with intense hydrothermal alteration within brecciation, and quartz stockwork veining. The ore mineral assemblage includes chalcopyrite, galena, and some sphalerite with covellite and goethite formed during three phases of mineralization (pre-ore, main ore, and supergene) within an abundant gangue of quartz and calcite. The geologic and field relationships, petrographic and mineralogical studies reveal two alteration zones occurred with the Cu-Pb (-Zn) mineralization along the contact between the Bagcagiz Formation and Duztarla granite; pervasive phyllic alteration (quartz, sericite, and pyrite), and selective propylitic alteration (albite, calcite, epidote, sericite and/or chlorite). This work, by using the mass balance calculations, reports the mass/volume changes (gain and loss) of the chemical components of the hydrothermal alteration zones associated with Halilar Cu-Pb (-Zn) mineralization at Balikesir area (Turkey). It revealed that the phyllic alteration has enrichments of Si, Fe, K, Ba, and LOI with depletion of Mg, Ca, and Na reflect sericitization of alkali feldspar and destruction of ferromagnesian minerals. This zone has high Cu and Pb with Zn contents represents the main mineralized zone. On the other hand, the propylitic zone is characterized by addition of Ca, Na, K, Ti, P, and Ba with LOI and Cu (lower content) referring to the replacement of plagioclase and ferromagnesian minerals by albite, calcite, epidote, and sericite

  17. Petrography and geochemistry of granitoids from the Samphire Pluton, South Australia: Implications for uranium mineralisation in overlying sediments

    Science.gov (United States)

    Domnick, Urs; Cook, Nigel J.; Bluck, Russel; Brown, Callan; Ciobanu, Cristiana L.

    2018-02-01

    The Blackbush uranium deposit (JORC Inferred Resource: 12,580 tonnes U), located on the north-eastern Eyre Peninsula, is currently the only sediment-hosted U deposit investigated in detail in the Gawler Craton. Uranium is hosted within Eocene sandstone of the Kanaka Beds, overlying Mesoproterozoic granites of the Samphire pluton, affiliated with the Hiltaba Intrusive Suite ( 1.6 Ga). These are considered the most probable source rocks for uranium mineralisation. By constraining the petrography and mineralogy of the granites, insights into the post-emplacement evolution can be gained, which may provide an exploration indicator for other sediment-hosted uranium systems. Three geochemically distinct granite types were identified in the Samphire Pluton and correspond to domains interpreted from geophysical data. All granites show complex alteration overprints and textures with increasing intensity closer to the deposit, as well as crosscutting veining. Alkali feldspar has been replaced by porous K-feldspar and albite, and plagioclase is overprinted by an assemblage of porous albite + sericite ± calc-silicates (prehnite, pumpellyite and epidote). This style of feldspar alteration is regionally widespread and known from Hiltaba-aged granites associated with iron-oxide copper-gold mineralisation at Olympic Dam and in the Moonta-Wallaroo region. In two granite types biotite is replaced by calcic garnet. Calc-silicates are indicative of Ca-metasomatism, sourced from the anorthite component of altered plagioclase. Minor clay alteration of feldspars is present in all samples. Mineral assemblages in veins include quartz + hematite, hematite + coffinite, fluorite + quartz, and clay minerals. Minor chlorite and sericite are found in all vein types. All granite types are anomalously rich in U (concentrations between 10 and 81 ppm). Highly variable Th/U ratios, as well as hydrothermal U minerals (mostly coffinite) in granites and veins, are clear evidence for U mobility. Uranium

  18. Thermoluminescence response of the poly mineral fraction from hibiscus sabdariffa L foodstuffs

    International Nuclear Information System (INIS)

    Cruz Z, E.; Guzman, S.; Brown, F.; Chernov, V.; Barboza F, M.

    2011-01-01

    Food processed by ionizing irradiation is a safe technology and has been recognized by the FAO/Who Codes Alimentarius Commission. It is an excellent method to prevent food spoilage and food borne diseases by inhibiting the growth of microorganisms and slowing down ripening. The widespread use of food irradiation treatments that include spices, dry vegetables, grains and fruits make relevant the developing of methods for identification and analyses of foodstuffs processed by irradiation. The present work focuses on the thermoluminescence property of Mexican Roselle flower previously irradiated for detection purposes. The poly mineral content of irradiated commercial Roselle flower (Hibiscus sabdariffa L.) was extracted and analyzed by thermoluminescence (Tl). The X-ray diffraction analyses showed that quartz and albite composition for the poly mineral fraction. Different grain sizes; 10, 53, 74 and 149 μm, were selected for the Tl analyses. The Tl glow curves depended on the grain sizes. The glow curves depicted two peaks around 92 and 120 C. The first peak was ascribed to quartz and the broad part of the glow curves (120-250 C) seems to correspond to the albite. Because the complex structure of the Tl glow curves from poly minerals the kinetic parameters were calculated by a fitting process using a deconvolution method based on a non-linear least-squares Levenberg-Ma quart. The values of the activation energy were found to be at 0.79-1.05 eV and 0.79-1.04 for 53 μm and 250 μm, respectively. The Tl properties of the samples were determined including dose response, reproducibly, fading and UV light bleaching. (Author)

  19. Thermoluminescence response of the poly mineral fraction from hibiscus sabdariffa L foodstuffs

    Energy Technology Data Exchange (ETDEWEB)

    Cruz Z, E.; Guzman, S. [UNAM, Instituto de Ciencias Nucleares, Apdo. Postal 70-543, 04510 Mexico D. F. (Mexico); Brown, F. [Universidad de Sonora, Departamento de Investigacion en Polimeros y Materiales, Apdo. Postal 130, 83000 Hermosillo, Sonora (Mexico); Chernov, V.; Barboza F, M., E-mail: ecruz@nucleares.unam.m [Universidad de Sonora, Departamento de Investigacion en Fisica, Apdo. Postal 5-088, 83190 Hermosillo, Sonora (Mexico)

    2011-02-15

    Food processed by ionizing irradiation is a safe technology and has been recognized by the FAO/Who Codes Alimentarius Commission. It is an excellent method to prevent food spoilage and food borne diseases by inhibiting the growth of microorganisms and slowing down ripening. The widespread use of food irradiation treatments that include spices, dry vegetables, grains and fruits make relevant the developing of methods for identification and analyses of foodstuffs processed by irradiation. The present work focuses on the thermoluminescence property of Mexican Roselle flower previously irradiated for detection purposes. The poly mineral content of irradiated commercial Roselle flower (Hibiscus sabdariffa L.) was extracted and analyzed by thermoluminescence (Tl). The X-ray diffraction analyses showed that quartz and albite composition for the poly mineral fraction. Different grain sizes; 10, 53, 74 and 149 {mu}m, were selected for the Tl analyses. The Tl glow curves depended on the grain sizes. The glow curves depicted two peaks around 92 and 120 C. The first peak was ascribed to quartz and the broad part of the glow curves (120-250 C) seems to correspond to the albite. Because the complex structure of the Tl glow curves from poly minerals the kinetic parameters were calculated by a fitting process using a deconvolution method based on a non-linear least-squares Levenberg-Ma quart. The values of the activation energy were found to be at 0.79-1.05 eV and 0.79-1.04 for 53 {mu}m and 250 {mu}m, respectively. The Tl properties of the samples were determined including dose response, reproducibly, fading and UV light bleaching. (Author)

  20. Further description of the petrology of the Topopah Spring member of the paintbrush tuff in drill holes UE25A-1 and USW-G1 and of the lithic-rich tuff in USW-G1, Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Carroll, P.I.; Caporuscio, F.A.; Bish, D.L.

    1981-11-01

    The Topopah Spring Member of the Paintbrush Tuff and the Lithic-rich tuff and two Tertiary volcanic units that occur in cores from drill holes UE25a-1 and USW-G1 at Yucca Mountain, Nevada. Recently they have been suggested as possibly suitable for the permanent storage of high-level radioactive waste. Earlier petrologic characterization of these units is augmented here. The Topopah Spring Member (approximately 350 m thick) has two compound cooling units. The upper, thinner unit is densely welded to vitrophyric. The lower unit ranges from nonwelded to vitrophyric, and its nonwelded base is extensively zeolitized to clinoptilolite and mordenite. Heulandite occurs as fracture fill in the overlying vitrophyric part, but zeolites are absent above that vitrophyre. Here primary devitrification plus vapor-phase crystallization dominate the mineralogy. Vapor-phase effects are especially prominent between the two vitrophyres in both cores and include numerous large lithophysal cavities throughout most of this moderately to densely welded tuff. The Lithic-rich tuff extends from 1203 to 1506 m in the USW-G1 drill core. It is nonwelded to partly welded but is well indurated due to pervasive intergrowths of authigenic minerals. These phases are analcime, albite, alkali feldspar, sericite, chlorite and quartz. The transition from analcime to secondary albite corresponds to Iijima's zeolite Zone IV boundary, and this boundary appears in USW-G1 at 1326 m. However, analcime remains as a prominent phase through most of the Lithic-rich tuff. Further work is necessary to assess the suitability of either of these horizons for a waste repository. In the Topopah Spring Member, both mechanical and hydrologic properties of thick lithophysal zone must be studied, as well as the complete sequence of fracture fill. For both units, zeolite and clay mineral stabilities need to be investigated

  1. The Lagoa Real subalkaline granitic complex (south Bahia, Brazil): a source for uranium mineralizations associated with Na-Ca metasomatism

    International Nuclear Information System (INIS)

    Maruejol, P.; Cuney, M.; Poty, B.; Neto, A.M.

    1987-01-01

    In the central zone of the Sao Francisco Craton (South Bahia), the lower Proterozoic Lagoa Real granites and orthogneisses overthrust to the West the younger Urandi and Espinhaco metamorphic series, probably a late Brazilian event. This thrust is related to the regional metamorphism (amphibolite facies) of the Lagoa Real granites and induces a reverse HP metamorphism in the over thrusted series. Undeformed granites (sao Timoeto type) present two feldspars, perthitic orthoclase largely predominant over plagioclase (oligoclase ≥ albite), blue quartz, Fe-rich amphibole and biotite ± clinopyroxene assemblages, ilmenite ≥ magnetite, zircon, apatite, allanite and Nb ± Ti-REE oxides and silicates. The crystallization of the granites begins at high temperature and under low fO 2 and P H2O conditions. Fractional crystallization of pyroxene and plagioclase leads to silica enrichment during magmatic differentiation. Increasing fO 2 and P H2O are observed during this evolution. Orthogneisses show strongly recrystallized paragenesis: equal abundance of non-perthitic microcline and plagioclase (oligoclase ≤ albite), quartz, more Al-rich amphibole and biotite, magnetite, sphene, zircon, allanite, Nb ± Ti-REE oxides and silicates, and ± apatite. HT Na and Ca metasomatism occurs 330 Ma later than granite emplacement and is synchronous with important uranium mineralizations. Major elements and trace-elements geochemistry of the granites and orthogneisses indicate subalkaline to alkaline typology. Incompatible behaviour of Th, REE, Y, Zr, Nb, and F points out a convergence with alkaline magmatism. CI, F, Th, Y, REE, NB enrichments and Ba, Sr depletions are also related to a late magmatic stage. U-Th-rich and metamict accessory minerals of the granites represent a favorabl source for the Lagoa Real uranium ore-deposits [pt

  2. Oxygen mobility in alkali feldspars; Etude de la mobilite de l'oxygene dans les feldspaths alcalins

    Energy Technology Data Exchange (ETDEWEB)

    Merigoux, H [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1968-03-15

    The oxygen mobility is shown from oxygen atoms exchange between potassic and sodic feldspars and 18 oxygen enriched water. Exchanges are carried out in autoclaves between 400 and 800 deg. C under a water pressure between 300 and 800 bars. The oxygen is extracted from silicate by a ClF{sub 3} attack. Two distinct mechanisms may be found. The first one is auto-diffusion; for adularia we have: D = 9.10{sup -7} exp(-32000/RT) (cm{sup 2}.s{sup -1}), for albite: D 4.5.10{sup -5} exp(-37000/RT) (cm{sup 2}.s{sup -1}). The second one, more rapid, is associated with alkali atoms exchanges. These results are applied to the order-disorder problem in feldspars and to the oxygen geochemistry. (author) [French] La mobilite de l'oxygene est mise en evidence a partir d'echanges d'atomes d'oxygene entre des feldspaths potassiques et sodiques en presence d'une eau enrichie en oxygene 18. Les echanges sont effectues en autoclave entre 400 et 800 deg. C sous des pressions de vapeur d'eau comprises entre 300 et 800 bars. L'oxygene est extrait du silicate par attaque au ClF{sub 3}. Deux mecanismes, bien distincts, peuvent se rencontrer. Le premier correspond a l'autodiffusion de l'oxygene; dans le domaine etudie on trouve pour l'adulaire: D = 9,10{sup -7} exp(-32000/RT) (cm{sup 2}.s{sup -1}), et pour l'albite: D 4,5.10{sup -5} exp(-37000/RT) (cm{sup 2}.s{sup -1}). Le second, beaucoup plus rapide, est associe a l'echange des atomes alcalins avec la solution. Ces resultats sont appliques au probleme du passage ordre-desordre dans les feldspaths et a la geochimie de l'oxygene. (auteur)

  3. Petrography, Gamma Radiation Measurements and Dose Rate, Northeastern Um Ara Area, South Eastern Desert, Egypt

    International Nuclear Information System (INIS)

    Moghazy, N.M.

    2016-01-01

    The northern part of Um Ara alkali feldspar micro granite has subjected to extensive post-magmatic metasomatic reworking resulting in development of amazonitized and albitized zones, reflecting K- and Na metasomatism leading to gross enrichment in U and Th towards the more evolved phases (e.g., albitized zones). Spectrometric survey data indicate that eU in Dokhan volcanics has the range of 2 to 42 ppm with an average value of 10 ppm and in monzogranites. It varies from 3 to 13 ppm with an average of 7 ppm while in alkali feldspar microgranites eU contents vary from 3 to 282 ppm with an average value of 30 ppm. The (eTh) contents in Dokhan volcanics ranges from 5-51 ppm with an average 18 ppm, in monzogranites their content was in the range of 11 to 47 ppm with an average value of 27 ppm where it ranges from 14 to 83 ppm with an average 46 ppm in alkali feldspar granite. The enhanced uranium content in altered zones was attributed to disseminated and fracture filling uranophane, autonite, in addition to other U and Th bearing minerals (such as columbite, zircon, monazite, xenotime and fluorite). Gamma-radiation dose rate and annual effective dose equivalents in mSv/y, Radium equivalent activity, external (H e x) and internal hazard index (H i n) and gamma activity index (Iγ) for all investigated samples were calculated to assess the potential radiation hazard for people living in dwellings made of the studied granites. Alkali feldspar granite activities would suggest that caution must be taken when using granites as building materials because they have radioactivity above the proposed acceptable level.

  4. Origin of convex tetrads in rare earth element patterns of hydrothermally altered siliceous igneous rocks from the Zinnwald Sn W deposit, Germany

    Science.gov (United States)

    Monecke, T.; Dulski, P.; Kempe, U.

    2007-01-01

    The chondrite-normalized rare earth element (REE) patterns of whole rock samples from evolved granitic systems hosting rare metal deposits sometimes show a split into four consecutive curved segments, referred to as tetrads. In the present contribution, a rigorous statistical method is proposed that can be used to test whether geological significance should be attributed to tetrads that are only of limited size. The method involves a detailed evaluation of element and sample specific random and systematic errors that are constrained on the basis of independent repeated preparations and analyses of sample and reference materials. Application of the proposed method to samples from the granite-hosted Zinnwald Sn-W deposit, Germany, revealed that at least two tetrads in normalized whole rock REE patterns have to be analytically significant to rule out that fractional crystallization led to the unusual behavior of the REEs. Based on the analysis of altered albite granite and greisen samples from the endocontact of the Zinnwald granite massif, it is demonstrated that the lanthanide tetrad effect is responsible for the formation of the convex tetrads. Geological and petrological evidence suggests that the tetrads in the samples developed prior to greisenization and related cassiterite precipitation. In contrast to the endocontact samples, the rhyolitic wall rocks are typified by normalized REE patterns having tetrads that are variable in size and frequently close to the limit of analytical significance. The sizes of the tetrads apparently correlate with the intensity of albitization, but show no relation to subsequent alteration processes including greisenization and low-temperature argillization. This observation proves that curved segments in normalized whole rock REE patterns can be introduced during hydrothermal fluid-rock interaction.

  5. Supra-subduction zone extensional magmatism in Vermont and adjacent Quebec: Implications for early Paleozoic Appalachian tectonics

    Science.gov (United States)

    Kim, J.; Coish, R.; Evans, M.; Dick, G.

    2003-01-01

    Metadiabasic intrusions of the Mount Norris Intrusive Suite occur in fault-bounded lithotectonic packages containing Stowe, Moretown, and Cram Hill Formation lithologies in the northern Vermont Rowe-Hawley belt, a proposed Ordovician arc-trench gap above an east-dipping subduction zone. Rocks of the Mount Norris Intrusive Suite are characteristically massive and weakly foliated, have chilled margins, contain xenoliths, and have sharp contacts that both crosscut and are parallel to early structural fabrics in the host metasedimentary rocks. Although the mineral assemblage of the Mount Norris Intrusive Suite is albite + actinolite + epidote + chlorite + calcite + quartz, intergrowths of albite + actinolite are probably pseudomorphs after plagioclase + clinopyroxene. The metadiabases are subalkaline, tholeiitic, hypabyssal basalts with preserved ophitic texture. A backarc-basin tectonic setting for the intrusive suite is suggested by its LREE (light rare earth element) enrichment, negative Nb-Ta anomalies, and Ta/Yb vs. Th/Yb trends. Although no direct isotopic age data are available, the intrusions are broadly Ordovician because their contacts are clearly folded by the earliest Acadian (Silurian-Devonian) folds. Field evidence and geochemical data suggest compelling along-strike correlations with the Coburn Hill Volcanics of northern Vermont and the Bolton Igneous Group of southern Quebec. Isotopic and stratigraphic age constraints for the Bolton Igneous Group bracket these backarc magmas to the 477-458 Ma interval. A tectonic model that begins with east-dipping subduction and progresses to outboard west-dipping subduction after a syncollisional polarity reversal best explains the intrusion of deformed metamorphosed metasedimentary rocks by backarc magmas.

  6. Radionuclide sorption in Yucca Mountain tuffs with J-13 well water: Neptunium, uranium, and plutonium. Yucca Mountain site characterization program milestone 3338

    International Nuclear Information System (INIS)

    Triay, I.R.; Cotter, C.R.; Kraus, S.M.; Huddleston, M.H.

    1996-08-01

    We studied the retardation of actinides (neptunium, uranium, and plutonium) by sorption as a function of radionuclide concentration in water from Well J-13 and of tuffs from Yucca Mountain. Three major tuff types were examined: devitrified, vitric, and zeolitic. To identify the sorbing minerals in the tuffs, we conducted batch sorption experiments with pure mineral separates. These experiments were performed with water from Well J-13 (a sodium bicarbonate groundwater) under oxidizing conditions in the pH range from 7 to 8.5. The results indicate that all actinides studied sorb strongly to synthetic hematite and also that Np(V) and U(VI) do not sorb appreciably to devitrified or vitric tuffs, albite, or quartz. The sorption of neptunium onto clinoptilolite-rich tuffs and pure clinoptilolite can be fitted with a sorption distribution coefficient in the concentration range from 1 X 10 -7 to 3 X 10 -5 M. The sorption of uranium onto clinoptilolite-rich tuffs and pure clinoptilolite is not linear in the concentration range from 8 X 10 -8 to 1 X 10 -4 M, and it can be fitted with nonlinear isotherm models (such as the Langmuir or the Freundlich Isotherms). The sorption of neptunium and uranium onto clinoptilolite in J-13 well water increases with decreasing pH in the range from 7 to 8.5. The sorption of plutonium (initially in the Pu(V) oxidation state) onto tuffs and pure mineral separates in J-13 well water at pH 7 is significant. Plutonium sorption decreases as a function of tuff type in the order: zeolitic > vitric > devitrified; and as a function of mineralogy in the order: hematite > clinoptilolite > albite > quartz

  7. Co-Cu-Au deposits in metasedimentary rocks-A preliminary report

    Science.gov (United States)

    Slack, J.F.; Causey, J.D.; Eppinger, R.G.; Gray, J.E.; Johnson, C.A.; Lund, K.I.; Schulz, K.J.

    2010-01-01

    A compilation of data on global Co-Cu-Au deposits in metasedimentary rocks refines previous descriptive models for their occurrence and provides important information for mineral resource assessments and exploration programs. This compilation forms the basis for a new classification of such deposits, which is speculative at this early stage of research. As defined herein, the Co-Cu-Au deposits contain 0.1 percent or more by weight of Co in ore or mineralized rock, comprising disseminated to semi-massive Co-bearing sulfide minerals with associated Fe- and Cu-bearing sulfides, and local gold, concentrated predominantly within rift-related, siliciclastic metasedimentary rocks of Proterozoic age. Some deposits have appreciable Ag ? Bi ? W ? Ni ? Y ? rare earth elements ? U. Deposit geometry includes stratabound and stratiform layers, lenses, and veins, and (or) discordant veins and breccias. The geometry of most deposits is controlled by stratigraphic layering, folds, axial-plane cleavage, shear zones, breccias, or faults. Ore minerals are mainly cobaltite, skutterudite, glaucodot, and chalcopyrite, with minor gold, arsenopyrite, pyrite, pyrrhotite, bismuthinite, and bismuth; some deposits have appreciable tetrahedrite, uraninite, monazite, allanite, xenotime, apatite, scheelite, or molybdenite. Magnetite can be abundant in breccias, veins, or stratabound lenses within ore or surrounding country rocks. Common gangue minerals include quartz, biotite, muscovite, K-feldspar, albite, chlorite, and scapolite; many deposits contain minor to major amounts of tourmaline. Altered wall rocks generally have abundant biotite or albite. Mesoproterozoic metasedimentary successions constitute the predominant geologic setting. Felsic and (or) mafic plutons are spatially associated with many deposits and at some localities may be contemporaneous with, and involved in, ore formation. Geoenvironmental data for the Blackbird mining district in central Idaho indicate that weathering of

  8. Compositional Variation of Tourmaline from the Paleoproterozoic Bhukia Gold Prospect of Aravalli Supergroup, Western India: Implications for the Provenance and Gold Metallogeny

    Science.gov (United States)

    Mukherjee, R.; Venkatesh, A. S.; Fareeduddin, F.

    2016-12-01

    Bhukia is a unique gold prospect in terms of its host lithologies such as albitite and carbonates with respect to greenstone hosted Archean gold deposits from India. Tourmaline occurs along with apatite, magnetite, graphite, chalcopyrite and gold-sulfide association in Bhukia gold prospect preserve geochemical record of changing physico-chemical conditions during its growth. Tourmalinization is one of the distinct hydrothermal alterations present in the study area. Chemical composition of two varieties of tourmalines presents as significant amounts within albitite and carbonate rocks from Bhukia gold prospect. EPMA analysis of two varieties of tourmalines viz. 1) rounded to sub-rounded, euhedral, green colored tourmalines and 2) elongated, zoned, brown colored tourmalines unlocks their chemical compositions as well as variations from core to rim. In some albitite litho-units, tourmaline occurs as major constituents (>15%), present as layers, termed as tourmalinites. Al-Fe-Mg and Na/ (Na+Ca) vs Fe/ (Fe+Mg) suggests that tourmalines from the Bhukia gold prospect are Mg-rich dravite to Fe-rich schrol in composition. Tourmalines present within the albitite rocks show variations in iron and sodium content from core to rim whereas similarity exist from core to rim in case of carbonate rocks. Presence of albite confirms the role of Na-rich fluids during the formation of tourmalines. Tourmalines present in Bhukia gold prospect is mainly influenced by boron influx and the source may be boron bearing hydrothermal fluid or boron bearing minerals. Dewatering of original un-metamorphosed rock during progressive metamorphism may remove boron from the metasedimentary rocks. Due to the mobile nature of boron, it dispersed and mixed with hydrothermal fluids and alumina that is required for the formation of the tourmaline might have been leached from metasedimentary rocks present in Bhukia gold prospect. Presence of hydrothermal alterations such as tourmalinization and albitization

  9. Geochronology and geochemistry of the granites from the Zhuxi W-Cu ore deposit in South China: Implication for petrogenesis, geodynamical setting and mineralization

    Science.gov (United States)

    Pan, Xiaofei; Hou, Zengqian; Zhao, Miao; Chen, Guohua; Rao, Jianfeng; Li, Yan; Wei, Jin; Ouyang, Yongpeng

    2018-04-01

    The giant Zhuxi tungsten deposit is located in the Taqian-Fuchun Ore Belt in northeastern Jiangxi province, and genetically associated with the Zhuxi granitic stocks and dykes. Three mineralization-related granites including granite porphyry dykes (GP), biotite granitic stocks (BG), and white granitic dykes (WG), were identified in the Zhuxi deposit. SHRIMP zircon U-Pb analysis for the three granitic rocks present ages ranging from 153.5 ± 1.0 Ma to 150.4 ± 1.0 Ma. The BG mainly contains quartz, microcline, albite, biotite and muscovite with minor accessory minerals including zircon, apatite, monazite, Ti/Fe oxides, and dolerite. However, the WG is mainly composed of quartz, microcline and albite with minor muscovite and accessory minerals. The GP is a medium-grained porphyritic granite and its phenocrysts include quartz, alkali feldspar, muscovite and plagioclase. All the Zhuxi granites have high SiO2 content (71.97 wt%-81.19 wt%) and total alkali (3.25 wt%-9.42 wt%), and their valid aluminum saturation index (ASI) values show a wide range of 1.03 to 2.49. High Rb/Sr ratios, low Sr content (data suggest that these highly fractionated I-S transform-type granites were originated from magmas which showed affinity with the Proterozoic continent and the Shuangqiaoshan Group and little mantle contribution was involved during the generation of Zhuxi granitic rocks. Extreme fractional crystallization resulted in further enrichment of tungsten in the evolved granitic magma. New data, presented together with previously published data, suggest that the Zhuxi granitic complex was likely to be formed during lithospheric compression setting during the late Jurassic to early Cretaceous. The biotite granite stock predominately contributed to the production of skarn alteration and mineralization, followed by the white granite dyke; the granite porphyry dykes have little effect.

  10. Genesis and petrology of Late Neoproterozoic pegmatites and aplites associated with the Taba metamorphic complex in southern Sinai, Egypt

    Energy Technology Data Exchange (ETDEWEB)

    Abdelfadil, K.M.; Asimow, P.D.; Azer, M.K.; Gahlan, H.A.

    2016-07-01

    We present new field, petrographical, mineralogical and geochemical data from late Neoproterozoic pegmatites and aplites in southern Sinai, Egypt, at the northernmost limit of the Arabian-Nubian Shield. The pegmatites cross-cut host rocks in the Taba Metamorphic Complex (TMC) with sharp contacts and are divided into massive and zoned pegmatites. Massive pegmatites are the most common and form veins, dykes and masses of variable dimensions; strikes range mainly from E-W through NW-SE to N-S. Mineralogically, the massive pegmatites are divided into K-feldspar-rich and albite-rich groups. Zoned pegmatites occur as lenses of variable dimensions, featuring a quartz core, an intermediate zone rich in K-feldspars and an outer finer-grained zone rich in albite. All compositions are highly evolved and display geochemical characteristics of post-collisional A-type granites: high SiO2, Na2O+K2O, FeO*/MgO, Ga/Al, Zr, Nb, Ga and Y alongside low CaO, MgO, Ba and Sr. They are rich in Rare Earth Elements (REE) and have extreme negative Eu anomalies (Eu/Eu*= 0.03–0.09). A genetic linkage between the pegmatites, aplites and alkali granite is confirmed by their common mild alkaline affinity and many other geochemical characteristics. These pegmatites and aplites represent the last small fraction of liquid remaining after extensive crystallization of granitic magma, injected along the foliation and into fractures of the host metamorphic rocks. The extensional tectonic regime and shallow depth of emplacement are consistent with a post-collisional environment. (Author)

  11. The blueschits from the Kopina Mt., West Sudetes, Poland - what do they tell us about accretion of the Variscides?

    Science.gov (United States)

    Majka, Jarosław; Mazur, Stanisław; Kośmińska, Karolina; Dudek, Krzysztof

    2015-04-01

    Blueschists are tracers of sutures, thus marking fossil subduction zones at convergent plate boundaries and providing important constraints on plate tectonic reconstructions. Their occurrences are scarce in the Variscan belt owing to a strong collisional overprint but just because of that each locality deserves particular attention. The Variscan blueschists must have formed during the early stage of the Variscan Orogeny and may represent a vestige of missing marginal basins fringing the Rheic Ocean at the onset of subduction. The studied rocks from the Kopina Mt. consist mainly of garnet, glaucophane, clinozoisite-epidote, chlorite-I, titanite, hematite and quartz. The original high-pressure assemblage is overprinted by later, lower pressure paragenesis, which comprises mostly Ca-amphiboles, chlorite-II, albite and K-feldspar. The latter occurs in polymineral inclusions in other phases together with albite and chlorite that are interpreted as phengite breakdown products. Garnet shows chemical compositional variation from Alm54Prp3Grs30Sps13 in the cores to Alm66Prp4Grs29Sps1 in the rims. The almandine zoning is bowl-shaped, whereas spessartine profiles show bell-shaped trends. The grossular and pyrope contents are generally constant throughout the grain. Rather gradual changes in the chemical zoning suggest a progressive, one-step garnet growth pattern. Glaucophane, although commonly well preserved, in some cases disintegrates to the albite-chlorite assemblage. The pressure-temperature (P-T) conditions were estimated using the phase equilibrium modelling in the NCKFMMnASHTO system using the PerpleX software. The compositional isopleths cross cut in the stability field of Grt+Gln+Ep+Chl+Pheng+Ttn+Hem+Q. P-T estimates indicate that the peak conditions occur at c. 14-17 kbar and 470-500°C, which corresponds to quite a low geothermal gradient in the range of 8-10°C/km. The P-T conditions estimated lie on a low temperature geotherm that is typical for a relatively

  12. Experimental Studies on the Interaction of scCO2 and scCO2-SO2 With Rock Forming Minerals at Conditions of Geologic Carbon Storages - First Results

    Science.gov (United States)

    Erzinger, J.; Wilke, F.; Wiersberg, T.; Vasquez Parra, M.

    2010-12-01

    Co-injection of SO2 (plus possibly NOx and O2) during CO2 storage in deep saline aquifers may cause stronger brine acidification than CO2 alone. Because of that, we investigate chemical corrosion of rocks and rock-forming minerals with impure supercritical CO2 (scCO2) at possible storage conditions of >73.7 bar and >31°C. Contaminates were chosen with respect to the composition of CO2 captured industrially from coal-fired power plants using the oxyfuel technology. The resulting data should build a base for the long-term prediction of the behavior of CO2 in geologic storage reservoirs. Experiments of up to 1000 hrs duration have been performed with 10 natural mineral concentrates (calcite, dolomite, siderite, anhydrite, hematite, albite, microcline, kaolinite, muscovite, biotite) in 3n NaCl solution and pure scCO2 or scCO2+SO2 (99.5+0.5 vol%). The NaCl reaction fluid resembles the average salinity of deep formation waters of the North German Basin and is not free of oxygen. To increase reaction rates all minerals were ground and the reagents agitated either by stirring or shaking in autoclaves of about one liter in volume. The autoclaves consist of Hastelloy™ or ferromagnetic stainless steel fully coated with PTFE. We used in average 15 g of solids, 700 ml liquid, and the vessels were pressurized up to 100 bars with CO2 or CO2-SO2 mixture. Experiments were run at temperatures up to 90°C. Before, during and after the experiments small amounts fluids were sampled and analyzed for dissolved constituents and pH. Solid phases were characterized by XRF, XRD, and EMPA before and after the experiments. Pure scCO2 corrodes all carbonates, reacts only slightly with anhydrite, albite, and microcline at a minimum pH of 4, and does not recognizably interact with the others. After the experiment, albite has gained in a, not yet fully identified, carbonate phase which might be dawsonite. Reaction fluids of the experiments with scCO2+SO2 have mostly lower pH than using scCO2

  13. Geology, mineralization, and fluid inclusion characteristics of the Skrytoe reduced-type W skarn and stockwork deposit, Sikhote-Alin, Russia

    Science.gov (United States)

    Soloviev, Serguei G.; Kryazhev, Sergey G.

    2017-08-01

    The Skrytoe deposit (>145 Kt WO3, average grade 0.449% WO3) in the Sikhote-Alin orogenic system (Eastern Russia) is situated in a metallogenic belt of W, Sn-W, Au, and Au-W deposits formed in a late to post-collisional tectonic environment after cessation of active subduction. It is localized within a mineralized district of reduced-type skarn W and veined Au (±W) deposits and occurrences related to the Early Cretaceous ilmenite-series plutonic suite. The deposit incorporates large stockworks of scheelite-bearing veinlets related to propylitic (amphibole, chlorite, quartz) and phyllic (quartz, sericite, albite, apatite, and carbonate) hydrothermal alteration. The stockwork cuts flat-lying mafic volcanic rocks and limestone partially replaced by pyroxene skarn that host the major W orebodies. Scheelite is associated with pyrrhotite and/or arsenopyrite, with minor chalcopyrite and other sulfide minerals; the late phyllic stage assemblages hosts Bi and Au mineralization. The fluid evolution included low-salinity moderate-temperature, moderate-pressure (˜370-390 °C, ˜800 bars) methane-dominated carbonic-aqueous fluids that formed post-skarn propylitic alteration assemblages. Then, at the phyllic stage, there has been an evolution from methane-dominated, moderate-temperature (330-360 °C), low-salinity (<12.3 wt% NaCl equiv.) fluids forming the early quartz-sericite-albite-arsenopyrite assemblage, through lower temperature (290-330 °C) methane-dominated, low-salinity (˜9-10 wt% NaCl equiv.) fluids forming the intermediate quartz-sericite-albite-scheelite-pyrrhotite assemblage, to yet lower temperature (245-320 °C) CO2-dominated carbonic-aqueous low-salinity (˜1-7 wt% NaCl equiv.) fluids forming the late quartz-sericite-sulfide-Bi-Au assemblage. Recurrent fluid immiscibility (phase separation) and cooling probably affected W solubility and promoted scheelite deposition. The stable isotope data support a sedimentary source of carbon (δ13Cfluid = ˜-21 to -10

  14. Rare earth element and yttrium geochemistry applied to the genetic study of cryolite ore at the Pitinga Mine (Amazon, Brazil

    Directory of Open Access Journals (Sweden)

    Orlando R.R. Minuzzi

    2008-12-01

    Full Text Available This work aims at the geochemical study of Pitinga cryolite mineralization through REE and Y analyses in disseminated and massive cryolite ore deposits, as well as in fluorite occurrences. REE signatures in fluorite and cryolite are similar to those in the Madeira albite granite. The highest ΣREE values are found in magmatic cryolite (677 to 1345 ppm; ΣREE is lower in massive cryolite. Average values for the different cryolite types are 10.3 ppm, 6.66 ppm and 8.38 ppm (for nucleated, caramel and white types, respectively. Disseminated fluorite displays higher ΣREE values (1708 and 1526ppm than fluorite in late veins(34.81ppm. Yttrium concentration is higher in disseminated fluorite and in magmatic cryolite. The evolution of several parameters (REEtotal, LREE/HREE, Y was followed throughout successive stages of evolution in albite granites and associated mineralization. At the end of the process, late cryolite was formed with low REEtotal content. REE data indicate that the MCD was formed by, and the disseminated ore enriched by (additional formation of hydrothermal disseminated cryolite, hydrothermal fluids, residual from albite granite. The presence of tetrads is poorly defined, although nucleated, caramel and white cryolite types show evidence for tetrad effect.Este trabalho enfoca a geoquímica de elementos terras raras (ETR e de Y no minério criolítico disseminado, no depósito criolítico maciço e na fluorita associada na mina Pitinga. As assinaturas de ETR na criolita e fluorita são similares àquelas do granito Madeira. Os maiores valores de SETR são encontrados na criolita magmática disseminada (677 a 1.345 ppm; SETR é menor na criolita maciça, com valores médios de 10,3 ppm, 6,66 ppm e 8,38 ppm, respectivamente, nos tipos de criolita nucleada, caramelo e branca. A fluorita magmática disseminada apresenta os valores mais altos de SETR (1.708 e 1.526 ppm, contrastando com a fluorita de veio tardio(34,81 ppm. A concentra

  15. Coordinated Analyses of Diverse Components in Whole Stardust Cometary Tracks

    Science.gov (United States)

    Nakamura-Messenger, K.; Keller, L. P.; Messenger, S. R.; Clemett, S. J.; Nguyen, L. N.; Frank, D.

    2011-12-01

    enstatite. Their O isotopic compositions are in the range of meteoritic materials, implying that they originated in the inner Solar System. Complex aromatic hydrocarbons are distributed along aerogel tracks and in TPs. These organics are likely cometary but were affected by shock heating. Three TPs of track #147 and two of track 168 have completely different mineralogy. TP2 of track #147 entirely consists of Fe-Ni alloy (5 at% Ni) and TP3 contains Fa28 with partial olivine-pyroxene intergrowth and minor albite. TP4 contains pentlandite, Fe-olivine, albite and high Ca pyroxene with Na and Cr (kosmochlor component). TP1 of #168 contains Fe-olivine, albite and pentlandite, and the concentric TP2 has a core of olivine grains with co-existing indigenous amorphous SiO2 surrounded by a carbon mantle, which in turn is surrounded by a layer of compressed aerogel. The TP of the carrot track #112 is a 16O-rich forsteritic olivine grain that likely formed in the inner Solar System. The track also contains submicron-sized diamond grains of likely Solar System origin.

  16. Mineral Replacement Reactions as a Precursor to Strain Localisation: an (HR-)EBSD approach

    Science.gov (United States)

    Gardner, J.; Wheeler, J.; Wallis, D.; Hansen, L. N.; Mariani, E.

    2017-12-01

    Much remains to be learned about the links between metamorphism and deformation. Our work investigates the behaviour of fluid-mediated mineral replacement reaction products when exposed to subsequent shear stresses. We focus on albite from a metagabbro that has experienced metamorphism and subsequent deformation at greenschist facies, resulting in a reduction in grain size and associated strain localisation. EBSD maps show that prior to grain size reduction, product grains are highly distorted, yet they formed, and subsequently deformed, at temperatures at which extensive dislocation creep is unlikely. The Weighted Burgers Vector can be used to quantitatively describe the types of Burgers vectors present in geometrically necessary dislocation (GND) populations derived from 2-D EBSD map data. Application of this technique to the distorted product grains reveals the prominence of, among others, dislocations with apparent [010] Burgers vectors. This supports (with some caveats) the idea that dislocation creep is not responsible for the observed lattice distortion, as there are no known slip systems in plagioclase with a [010] Burgers vector. Distortion in a replacement microstructure has also been attributed to the presence of nanoscale product grains, which share very similar, but not identical, orientations due to topotactic nucleation from adjacent sites on the same substrate. As a precipitate, the product grains should be expected to be largely free of elastic strain. However, high angular resolution EBSD results demonstrate that product grains contain both elastic strains (> 10-3) and residual stresses (several hundred MPa), as well as GND densities on the order of 1014-1015 m-2. Thus we suggest the observed distortion (elastic strain plus rotations) in the lattice is produced during the mineral replacement reaction by a lattice mismatch and volume change between parent and product. Stored strain energy then provides a driving force for recovery and

  17. Shear-hosted base metal mineralisation at the Dana Peaks, Murchison Mountains, Fiordland, New Zealand

    International Nuclear Information System (INIS)

    Allibone, A.; Ashley, P.; Craw, D.

    2010-01-01

    Darran Suite dioritic, tonalitic and granodioritic plutonic rocks and schistose Loch Burn Formation volcaniclastic rocks in the central Murchison Mountains at the Dana Peaks have been affected by widespread biotite-sericite-chlorite-albite-quartz-pyrite ± carbonate ± epidote/clinozoisite ± titanite/rutile ± actinolite alteration. More intense, paler coloured sericite-albite-quartz-pyrite ± carbonate alteration is concentrated along orange weathered shear zones. Alteration assemblages are transitional between those commonly referred to as propylitic, potassic and phyllic. Altered rocks contain anomalous concentrations of copper, lead, zinc and silver over an area of c. 2.56 km. Metal concentrations 2-5 times those typical of Darran Suite plutonic rocks and the Loch Burn Formation are commonly associated with more extensive weak to moderate intensity alteration. Higher metal grades up to c. 0.5% copper, 1% zinc, 1.3% lead and 30 ppm silver are concentrated in or adjacent to the 1-5 m wide, more intensely altered shear zones which contain entrained lenses of pyritised country rock, breccias and quartz ± K-feldspar ± chlorite ± carbonate ± hematite ± tourmaline veins. Some mineralised rocks also contain traces of tungsten (2-7 ppm), arsenic (<5-35 ppm) and tellurium (0.2-5.4 ppm). Most samples lack detectable molybdenum (<3 ppm), gold (<0.004 ppm) or bismuth (<0.2 ppm), with atypical higher values (40, 0.03 and 50 ppm, respectively) generally restricted to the most intensely altered and/or deformed rocks. The mineralised rocks show a close spatial and temporal relationship with several narrow ductile shear zones that probably developed in the Early Cretaceous between c. 128 and 110 Ma. Mineralised shear zones form minor splays off larger shear zones that are part of a major intra-arc fault system, active along or near the boundary between inboard and outboard parts of the Median Batholith at this time. Traces of similar lead mineralisation are present at the

  18. P-T composition and evolution of paleofluids in the Paleoproterozoic Mag Hill IOCG system, Contact Lake belt, Northwest Territories, Canada

    Science.gov (United States)

    Somarin, A. Karimzadeh; Mumin, A. Hamid

    2014-02-01

    The Echo Bay stratovolcano complex and Contact Lake Belt of the Great Bear Magmatic Zone, Northwest Territories, host a series of coalescing Paleoproterozoic hydrothermal systems that affected an area of several hundred square kilometers. They were caused by intrusion of synvolcanic diorite-monzodioritic plutons into andesitic host rocks, producing several characteristic hydrothermal assemblages. They include early and proximal albite, magnetite-actinolite-apatite, and potassic (K-feldspar) alteration, followed by more distal hematite, phyllic (quartz-sericite-pyrite), and propylitic (chlorite-epidote-carbonate±sericite±albite±quartz) alteration, and finally by late-stage polymetallic epithermal veins. These alteration types are characteristic of iron oxide copper-gold deposits, however, with distal and lower-temperature assemblages similar to porphyry Cu systems. Magnetite-actinolite-apatite alteration formed from high temperature (up to 560 °C) fluids with average salinity of 12.8 wt% NaCl equivalent. The prograde propylitic and phyllic alteration stages are associated with fluids with temperatures varying from 80 to 430 °C and a wide salinity range (0.5-45.6 wt% NaCl equivalent). Similarly, wide fluid temperature (104-450 °C) and salinity (4.2-46.1 wt% NaCl equivalent) ranges are recorded for the phyllic alteration. This was followed by Cu-Ag-U-Zn-Co-Pb sulfarsenide mineralization in late-stage epithermal veins formed at shallow depths and temperatures from 270 °C to as low as 105 °C. The polymetallic veins precipitated from high salinity (mean 30 wt% NaCl equivalent) dense fluids (1.14 g/cm3) with a vapor pressure of 3.8 bars, typical of epithermal conditions. Fluid inclusion evidence indicates that mixed fluids with evolving physicochemical properties were responsible for the formation of the alteration assemblages and mineralization at Mag Hill. An early high temperature, moderate salinity, and magmatic fluid was subsequently modified variably by

  19. Petrology, chronology and sequence of vein systems: Systematic magmatic and hydrothermal history of a major intracontinental shear zone, Canadian Appalachians

    Science.gov (United States)

    Pe-Piper, Georgia; Piper, David J. W.; McFarlane, Chris R. M.; Sangster, Chris; Zhang, Yuanyuan; Boucher, Brandon

    2018-04-01

    Intra-continental shear zones developed during continental collision may experience prolonged magmatism and mineralization. The Cobequid Shear Zone formed part of a NE-SW-trending, orogen-parallel shear system in the late Devonian-early Carboniferous, where syn-tectonic granite-gabbro plutons and volcanic rocks 4 km thick were progressively deformed. In late Carboniferous to Permian, Alleghanian collision of Africa with Laurentia formed the E-W trending Minas Fault Zone, reactivating parts of the Cobequid Shear Zone. The 50 Ma history of hydrothermal mineralization following pluton emplacement is difficult to resolve from field relationships of veins, but SEM study of thin sections provides clear detail on the sequence of mineralization. The general paragenesis is: albite ± quartz ± chlorite ± monazite → biotite → calcite, allanite, pyrite → Fe-carbonates, Fe-oxides, minor sulfides, calcite and synchysite. Chronology was determined from literature reports and new U-Pb LA-ICPMS dating of monazite and allanite in veins. Vein mineralization was closely linked to magmatic events. Vein emplacement occurred preferentially during fault movement recognised from basin-margin inversion, as a result of fractures opening in the damage zone of master faults. The sequence of mineralization, from ca. 355 Ma riebeckite and albite veins to ca. 327 (-305?) Ma siderite-magnetite and sulfide mineralization, resembles Precambrian iron-oxide-copper-gold (IOCG) systems in the literature. The abundant magmatic Na, halogens and CO2 in veins and some magmatic bodies, characteristic of IOCG systems, were derived from the deeply subducted Rheic Ocean slab with little terrigenous sediment. Regional extension of the Magdalen Basin caused asthenospheric upwelling and melting of the previously metasomatized sub-continental lithospheric mantle. Crustal scale strike-slip faulting facilitated the rise of magmas, resulting in high heat flow driving an active hydrothermal system. Table S2

  20. Thermoluminescent dependence with the particle size in ionized foods by radiation

    International Nuclear Information System (INIS)

    Teuffer Z, C.A.

    2005-01-01

    The influence of the particle size of poly minerals in the signals of the thermally stimulated luminescence (TL) is analysed. The poly minerals were extracted of Mexican spices such as Origanum vulgare L. (origanum) and Capsicum annum (Chilli guajillo), these underwent to an homogenization process to obtain four different particle sizes corresponding to 149, 74, 53 and 10 μ m, and later on to expose them to gamma radiation in an interval of 0.5- 45 kGy in the Gamma beam 651 PT of 60 Co irradiator of the Nuclear Sciences Institute, UNAM. The glow curves show a maximum of TL intensity for Capsicum annum to dose of 0.5- 10 kGy with particle size selected by means of a mesh of opening of 53 μ m, while for Origanum vulgare L., the more intense emission is observed with 149 μ m. In the interval of dose 12- 45 kGy the maximum in intensity emission it was presented in 53 μ m in both cases. For the case of 10 μ m, the TL emissions were of smaller intensity, and were achieved glow curves in a clear, defined way and an overlapping that allows to center the maximum of TL emission, in a defined temperature 126 C for Origanum vulgare L., and 166 C for Capsicum annum. The behavior before described is related with the composition of the samples. For Capsicum annum it was found Quartz (60%), Albite (30%) and Ortosa (10%), while Origanum vulgare stops L., Quartz (50%), Calcite (20%), Albite (20%) and Clay (10%). The homogenization of the samples is an important factor because exists high probability of avoiding as much as possible rests of organic matter traces that can contribute to the total signal of the glow curves. Likewise the defects that pollute from a natural way to each one of the minerals found in the samples, they play an outstanding role in the TL emissions. Although to the interacting the gamma radiation with the poly minerals of different particle sizes, there is a certain energy transfer that will be translated in the absorbed dose and this it will depend on the

  1. Experiment and simulation study on the effects of cement minerals on the water-rock-CO2 interaction during CO2 geological storage

    Science.gov (United States)

    Liu, N.; Cheng, J.

    2016-12-01

    The CO2 geological storage is one of the most promising technology to mitigate CO2 emission. The fate of CO2 underground is dramatically affected by the CO2-water-rock interaction, which are mainly dependent on the initial aquifer mineralogy and brine components. The cement minerals are common materials in sandstone reservoir but few attention has been paid for its effects on CO2-water-rock interaction. Five batch reactions, in which 5% cement minerals were assigned to be quartz, calcite, dolomite, chlorite and Ca-montmorillonite, respectively, were conducted to understanding the cement minerals behaviors and its corresponding effects on the matrix minerals alterations during CO2 geological storage. Pure mineral powders were selected to mix and assemble the 'sandstone rock' with different cement components meanwhile keeping the matrix minerals same for each group as 70% quartz, 20% K-feldspar and 5% albite. These `rock' reacted with 750ml deionized water and CO2 under 180° and 18MPa for 15 days, during which the water chemistry evolution and minerals surface micromorphology changes has been monitored. The minerals saturation indexes calculation and phase diagram as well as the kinetic models were made by PHREEQC to uncover the minerals reaction paths. The experiment results indicated that the quartz got less eroded, on the contrary, K-feldspar and albite continuously dissolved to favor the gibbsite and kaolinite precipitations. The carbonates cement minerals quickly dissolved to reach equilibrium with the pH buffered and in turn suppressed the alkali feldspar dissolutions. No carbonates minerals precipitations occurred until the end of reactions for all groups. The simulation results were basically consistent with the experiment record but failed to simulate the non-stoichiometric reactions and the minerals kinetic rates seemed underestimated at the early stage of reactions. The cement minerals significantly dominated the reaction paths during CO2 geological

  2. Late Paleozoic onset of subduction and exhumation at the western margin of Gondwana (Chilenia Terrane): Counterclockwise P-T paths and timing of metamorphism of deep-seated garnet-mica schist and amphibolite of Punta Sirena, Coastal Accretionary Complex, central Chile (34° S)

    Science.gov (United States)

    Hyppolito, T.; García-Casco, A.; Juliani, C.; Meira, V. T.; Hall, C.

    2014-10-01

    In this study, the Paleozoic albite-epidote-amphibolite occurring as meter-sized intercalations within garnet-mica schist at Punta Sirena beach (Pichilemu region, central Chile) is characterized for the first time. These rocks constitute an unusual exposure of subduction-related rocks within the Paleozoic Coastal Accretionary Complex of central Chile. Whereas high pressure (HP) greenschist and cofacial metasediments are the predominant rocks forming the regional metamorphic basement, the garnet-mica schist and amphibolite yield higher P-T conditions (albite-epidote amphibolite facies) and an older metamorphic age. Combining detailed mineral chemistry and textural information, P-T calculations and Ar-Ar ages, including previously published material from the Paleozoic Accretionary Complex of central Chile, we show that the garnet-mica schist and associated amphibolite (locally retrograded to greenschist) are vestiges of the earliest subducted material now forming exotic bodies within the younger HP units of the paleo-accretionary wedge. These rocks are interpreted as having been formed during the onset of subduction at the southwestern margin of Gondwana. However, we show that the garnet-mica schist formed at a slightly greater depth (ca. 40 km) than the amphibolite (ca. 30 km) along the same hot-subduction gradient developed during the onset of subduction. Both lithotypes reached their peak-P conditions at ca. 335-330 Ma and underwent near-isobaric cooling followed by cooling and decompression (i.e., counterclockwise P-T paths). The forced return flow of the garnet-mica schist from the subduction channel started at ca. 320 Ma and triggered the exhumation of fragments of shallower accreted oceanic crust (amphibolite). Cores of phengite (garnet-mica schist) and amphibole (amphibolite) grains have similar chemical compositions in both the S1 and S2 domains, indicating rotation of these grains during the transposition of the burial-related (prograde peak-T) foliation S1

  3. Thermoluminescent dependence with the particle size in ionized foods by radiation; Dependencia termoluminiscente con el tamano de particula en alimentos ionizados por radiacion

    Energy Technology Data Exchange (ETDEWEB)

    Teuffer Z, C.A

    2005-07-01

    The influence of the particle size of poly minerals in the signals of the thermally stimulated luminescence (TL) is analysed. The poly minerals were extracted of Mexican spices such as Origanum vulgare L. (origanum) and Capsicum annum (Chilli guajillo), these underwent to an homogenization process to obtain four different particle sizes corresponding to 149, 74, 53 and 10 {mu} m, and later on to expose them to gamma radiation in an interval of 0.5- 45 kGy in the Gamma beam 651 PT of {sup 60} Co irradiator of the Nuclear Sciences Institute, UNAM. The glow curves show a maximum of TL intensity for Capsicum annum to dose of 0.5- 10 kGy with particle size selected by means of a mesh of opening of 53 {mu} m, while for Origanum vulgare L., the more intense emission is observed with 149 {mu} m. In the interval of dose 12- 45 kGy the maximum in intensity emission it was presented in 53 {mu} m in both cases. For the case of 10 {mu} m, the TL emissions were of smaller intensity, and were achieved glow curves in a clear, defined way and an overlapping that allows to center the maximum of TL emission, in a defined temperature 126 C for Origanum vulgare L., and 166 C for Capsicum annum. The behavior before described is related with the composition of the samples. For Capsicum annum it was found Quartz (60%), Albite (30%) and Ortosa (10%), while Origanum vulgare stops L., Quartz (50%), Calcite (20%), Albite (20%) and Clay (10%). The homogenization of the samples is an important factor because exists high probability of avoiding as much as possible rests of organic matter traces that can contribute to the total signal of the glow curves. Likewise the defects that pollute from a natural way to each one of the minerals found in the samples, they play an outstanding role in the TL emissions. Although to the interacting the gamma radiation with the poly minerals of different particle sizes, there is a certain energy transfer that will be translated in the absorbed dose and this it

  4. Estimation of the reactive mineral surface area during CO2-rich fluid-rock interaction: the influence of neogenic phases

    Science.gov (United States)

    Scislewski, A.; Zuddas, P.

    2010-12-01

    Mineral dissolution and precipitation reactions actively participate to control fluid chemistry during water-rock interaction. It is however, difficult to estimate and well normalize bulk reaction rates if the mineral surface area exposed to the aqueous solution and effectively participating on the reactions is unknown. We evaluated the changing of the reactive mineral surface area during the interaction between CO2-rich fluids and Albitite/Granitoid rocks (similar mineralogy but different abundances), reacting under flow-through conditions. Our methodology, adopting an inverse modeling approach, is based on the estimation of dissolution rate and reactive surface area of the different minerals participating in the reactions by the reconstruction the chemical evolution of the interacting fluids. The irreversible mass-transfer processes is defined by a fractional degree of advancement, while calculations were carried out for Albite, Microcline, Biotite and Calcite assuming that the ion activity of dissolved silica and aluminium ions was limited by the equilibrium with quartz and kaolinite. Irrespective of the mineral abundance in granite and albitite, we found that mineral dissolution rates did not change significantly in the investigated range of time where output solution’s pH remained in the range between 6 and 8, indicating that the observed variation in fluid composition depends not on pH but rather on the variation of the parent mineral’s reactive surface area. We found that the reactive surface area of Albite varied by more than 2 orders of magnitude, while Microcline, Calcite and Biotite surface areas changed by 1-2 orders of magnitude. We propose that parent mineral chemical heterogeneity and, particularly, the stability of secondary mineral phases may explain the observed variation of the reactive surface area of the minerals. Formation of coatings at the dissolving parent mineral surfaces significantly reduced the amount of surface available to react

  5. Oxygen mobility in alkali feldspars; Etude de la mobilite de l'oxygene dans les feldspaths alcalins

    Energy Technology Data Exchange (ETDEWEB)

    Merigoux, H. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1968-03-15

    The oxygen mobility is shown from oxygen atoms exchange between potassic and sodic feldspars and 18 oxygen enriched water. Exchanges are carried out in autoclaves between 400 and 800 deg. C under a water pressure between 300 and 800 bars. The oxygen is extracted from silicate by a ClF{sub 3} attack. Two distinct mechanisms may be found. The first one is auto-diffusion; for adularia we have: D = 9.10{sup -7} exp(-32000/RT) (cm{sup 2}.s{sup -1}), for albite: D 4.5.10{sup -5} exp(-37000/RT) (cm{sup 2}.s{sup -1}). The second one, more rapid, is associated with alkali atoms exchanges. These results are applied to the order-disorder problem in feldspars and to the oxygen geochemistry. (author) [French] La mobilite de l'oxygene est mise en evidence a partir d'echanges d'atomes d'oxygene entre des feldspaths potassiques et sodiques en presence d'une eau enrichie en oxygene 18. Les echanges sont effectues en autoclave entre 400 et 800 deg. C sous des pressions de vapeur d'eau comprises entre 300 et 800 bars. L'oxygene est extrait du silicate par attaque au ClF{sub 3}. Deux mecanismes, bien distincts, peuvent se rencontrer. Le premier correspond a l'autodiffusion de l'oxygene; dans le domaine etudie on trouve pour l'adulaire: D = 9,10{sup -7} exp(-32000/RT) (cm{sup 2}.s{sup -1}), et pour l'albite: D 4,5.10{sup -5} exp(-37000/RT) (cm{sup 2}.s{sup -1}). Le second, beaucoup plus rapide, est associe a l'echange des atomes alcalins avec la solution. Ces resultats sont appliques au probleme du passage ordre-desordre dans les feldspaths et a la geochimie de l'oxygene. (auteur)

  6. Metallogenetic modeling for uranium exploration in rocks of the Abaira-Jussiape Anticlinal nucleus, Chapada Diamantina, Bahia; Modelagem metalogenetica para prospeccao de uranio nas rochas do nucleo da Anticlinal Abaira-Jussiape, Chapada Diamantina, Bahia

    Energy Technology Data Exchange (ETDEWEB)

    Santana, Jocilene dos Santos; Cruz, Simone Cerqueira Pereira; Barbosa, Johildo Salomao Figueiredo [Universidade Federal da Bahia (PPGG/UFBA), Salvador, BA (Brazil); Abram, Maisa Bastos; Martins, Adriano Alberto Marques, E-mail: jocilenesanttana@yahoo.com.br, E-mail: simonecruzufba@gmail.com, E-mail: johildo@cpgg.ufba.br, E-mail: maisa.abram@cprm.gov.br, E-mail: adriano1952@gmail.com [Companhia de Pesquisas de Recursos Minerais (CPRM), Salvador, BA (Brazil). Superintendencia Regional de Salvador. Servico Geologico do Brasil

    2011-06-15

    The NNW-SSE-trending Abaira-Jussiape Anticlinal is an antiformal culmination of folding and shearing in the Paramirim Corridor of the Western Chapada Diamantina. In its core paleoproterozoic, mylonitized Caraguatai Suite, tonalites-granodiorites, alkali-feldspar granites, syenites to quartz-syenites and Jussiape Suite granites crop out. Compressional and distensional stresses mark the structural geology of the area. The compressional structures are related to two distinct deformation phases, named D1a and D1b. The main compressional phase is ductile D1a, which is related to the nucleation of dextral to dextral-reverse shearing zones. Deformation and syn-D1a recrystallization involving plagioclase and the K-feldspar suggest deformation temperature conditions above 550 deg C. The following phase D2 is of ductilebrittle nature and culminates in reverse shearing zones. The distensional structures correspond to the D3 phase and are represented by frontal shear zones with normal movement. The petrographic study helped identify a pre-D1a hydrothermal alteration process related to albitization and potassification, syn-D1 oxidation process, and hydration and saussuritization related to phases D2 and D3. The integration of lithological, petrographic, structural and geophysical data by means of the logic Fuzzy, plus the existing information regarding structural and lithologic controls of the known uranium mineralization in the Paramirim Corridor, led us to identify two promising areas for radioactive element exploration in the nucleus of Abaira-Jussiape Anticlinal. (author)

  7. The Morro do Resende orthogneiss: mineralogy, petrography, geochemistry and geochronology; Ortognaisse Morro do Resende: mineralogia, petrografia, geoquimica e geocronologia

    Energy Technology Data Exchange (ETDEWEB)

    Vasconcelos, Fabiana Franco de; Avila, Ciro Alexandre; Bongiolo, Everton Marques; Camara, Beatriz de Oliveira; Menezes, Victor Hugo Riboura; Cunha, Fernanda Caetano de Mattos, E-mail: fma3003@globo.com, E-mail: avila@mn.ufrj.br, E-mail: ebongiolo@geologia.ufrj.br, E-mail: camara_b@hotmail.com, E-mail: vmenezes92@gmail.com, E-mail: fefemattos@gmail.com [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil); Neumann, Reiner, E-mail: reiner.neumann@gmail.com [Centro de Tecnologia Mineral (CETEM), Rio de Janeiro, RJ (Brazil); Teixeira, Wilson; Barbosa, Natali, E-mail: wteixeir@usp.br, E-mail: natali@usp.br [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil). Instituto de Geociencias

    2017-01-15

    The Morro do Resende orthogneiss is a hololeucocratic to leucocratic, fine-grained body with monzogranitic to granodioritic composition, cropping out near the Volta Grande mine in Nazareno County, State of Minas Gerais, Brazil. It bears xenoliths of metamafic rocks of the Rio das Mortes metavolcano-sedimentary sequence and yields a U-Pb SHRIMP crystallization age of 2174 ± 4 Ma, relating it to one of the magmatic pulses of the Mineiro Belt. The primary mineralogy includes quartz, albite, microcline, biotite, allanite, zircon, magnetite, titanite and apatite, while sericite, epidote, zoisite, clinozoisite, carbonate and chlorite are metamorphic minerals. Maghemite, barite, fluorite, monazite, xenotime, garnet and REE fluorides (possibly gagarinite) are hydrothermal, as they fill the fractures, intergrow or replace the primary and metamorphic minerals. Fluid interaction was not homogeneous throughout the body. Metamorphic paragenesis points to greenschist facies conditions, which could be related to the Paleoproterozoic II event of the Mineiro Belt, which lasted from 2131 to 2101 Ma. The Morro do Resende orthogneiss is distinguished by significant REE enrichment, as well as a negative Eu anomaly linked to the magmatic crystallization and a negative Ce anomaly related to oxidizing hydrothermal fluids circulation. (author)

  8. Na-metasomatism in the uranium fields of Singhbhum Shear zone, India

    International Nuclear Information System (INIS)

    Chaki, Anjan

    2013-01-01

    Singhbhum Shear Zone (SSZ) of eastern India hosts uranium, copper and apatite-magnetite mineralization, which occurs either independently or overlaps in space. SSZ is a nearly 200 km long, 1-5 km wide, intensely techtonized, northward-convex, arcuate mobile belt that separates the Archaean cratonic nucleus to its south from the Proterozoic North Singhbhum Fold Belt on the north. Except Bagjata mines in the eastern sector, majority of the known uranium deposits and mines (e.g. Jaduguda, Bhatin, Narwapahar, Banduhurang and Mohuldih) are situated in the central sector of the shear zone. All the deposits are of low grade (0.05% U 3 O 8 ) and low to medium tonnage. The common rock types of the SSZ are quartz-chlorite schists, quartzsericite schists, quartzite, metaconglomerate, soda granite, quartz-albite bearing schists/gneisses, granophyres and tourmalinite. The mineralization occur as lenticular to tabular bodies, which are (pene-) concordant with dominant planer structures, i.e. foliation parallel with the lithological layering (S 3 II S 0 ). Principal uranium mineral is uraninite with low thorium (UO 2 /ThO 2 =70-150), high lead (PbO =14-15%) and moderate REE contents with minor pitchblende and some secondary minerals near the surface. Many ore minerals, particularly the sulfide phases of Ni, Co, Mo, Cu and Fe are common

  9. Electrical conductivity of the plagioclase-NaCl-water system and its implication for the high conductivity anomalies in the mid-lower crust of Tibet Plateau

    Science.gov (United States)

    Li, Ping; Guo, Xinzhuan; Chen, Sibo; Wang, Chao; Yang, Junlong; Zhou, Xingfan

    2018-02-01

    In order to investigate the origin of the high conductivity anomalies geophysically observed in the mid-lower crust of Tibet Plateau, the electrical conductivity of plagioclase-NaCl-water system was measured at 1.2 GPa and 400-900 K. The relationship between electrical conductivity and temperature follows the Arrhenius law. The bulk conductivity increases with the fluid fraction and salinity, but is almost independent of temperature (activation enthalpy less than 0.1 eV). The conductivity of plagioclase-NaCl-water system is much lower than that of albite-NaCl-water system with similar fluid fraction and salinity, indicating a strong effect of the major mineral phase on the bulk conductivity of the brine-bearing system. The high conductivity anomalies of 10-1 and 100 S/m observed in the mid-lower crust of Tibet Plateau can be explained by the aqueous fluid with a volume fraction of 1 and 9%, respectively, if the fluid salinity is 25%. The anomaly value of 10-1 S/m can be explained by the aqueous fluid with a volume fraction of 6% if the salinity is 10%. In case of Southern Tibet where the heat flow is high, the model of a thin layer of brine-bearing aqueous fluid with a high salinity overlying a thick layer of partial melt is most likely to prevail.

  10. International Uranium Resources Evaluation Project (IUREP) national favourability studies: Italy

    International Nuclear Information System (INIS)

    1977-10-01

    The Italian Republic comprises a 1200 - Km - long peninsula ex- tending from southern Europe into the Mediterranean Sea, and a number of adjacent islands, among which the principals are Sicily and Sardinia. The total area is in excess of 300,000 Sq.Km, the islands account for some 50, 000 Sq.Km. From a physiographic and morphologic point of view, Italy mainly consists of the Alpine region and the Po valley to the North and of the Appennine range and small Coastal plains to the Centre and South. Plains occupied only 20% of the total area, hills and mountains, up to 4,810 m of elevation, contribute almost equally to the remaining 80%. The most promising uranium mineralizations have been found in the Bergamasc Alps, near the small town of Novazza. Pitchblende and minor sphalerite (formation temperature, 80 deg. - 100 deg. C) occur disseminated in volcanics of permian age. The host rocks at the Novazza uranium deposit, consist of an acid ignimbrite with cineritic texture. The rocks have been affected by metasomatism which brought abundant neo-formation minerals such as silica, sericite, carbonates and minor adularia, albite and muscovite. The reasonably assured resources of the Novazza deposit have been estimated to be 1,200 ton of U having a grade of 900 p.p.m. U. Estimated additional resources are 1,000 ton U. Production is scheduled to start in 1980

  11. A possible origin of EL6 chondrites from a high temperature-high pressure solar gas

    Energy Technology Data Exchange (ETDEWEB)

    Blander, M. [Argonne National Lab., IL (United States); Unger, L. [Purdue Univ., Westiville, IN (United States). Dept. of Chemistry; Pelton, A.; Eriksson, G. [Ecole Polytechnique, Montreal, PQ (Canada). Dept. of Metallurgy and Materials Engineering

    1994-05-01

    Condensates from a gas of ``solar`` composition were calculated to investigate the origins of EL6 chondrites using a free energy minimization program with a data base for the thermodynamic properties of multicomponent molten silicates as well as for other liquids solids, solid solutions and gaseous species. Because of high volatility of silicon and silica, the high silicon content of metal (2.6 mole %) can only be produced at pressures 10{sup {minus}2} atm at temperatures above 1475 K. At 100--500 atm, a liquid silicate phase crystallizes at a temperature where the silicon content of the metal, ferrosilite content of the enstatite and albite concentration in the plagioclase are close to measured values. In pyrometallurgy, liquid silicates are catalysts for reactions in which Si-O-Si bridging bonds are broken or formed. Thus, one attractive mode for freezing in the compositions of these three phases is disappearance of fluxing liquid. If the plagioclase can continue to react with the nebula without a liquid phase, lower pressures of 10{sup {minus}1} to 1 atm might be possible. Even if the nebula is more reducing than a solar gas, the measured properties of EL6 chondrites might be reconciled with only slightly lower pressures (less than 3X lower). The temperatures would be about the same as indicated in our calculations since the product of the silicon content of the metal and the square of the ferrosilite content of the enstatite constitute a cosmothermometer for the mineral assemblage in EL6 chondrites.

  12. Clay minerals in uraniferous deposit of Imouraren (Tim Mersoi basin, Niger): implications on genesis of deposit and on ore treatment process

    International Nuclear Information System (INIS)

    Billon, Sophie

    2014-01-01

    Nigerian uraniferous deposits are located in carboniferous and Jurassic formations of Tim Mersoi basin. AREVA is shareholder of 3 mine sites in this area: SOMAIR and COMINAK, both in exploitation since 1960's and IMOURAREN, 80 km further South, whose exploitation is planned for 2015. Mineralization of Imouraren deposit is included in the fluvial formation of Tchirezrine 2 (Jurassic), composed of channels and flood plains. Facies of channel in-fillings range from coarse sandstones to siltstones, while overflow facies are composed of analcimolites. Secondary mineralogy was acquired during 2 stages: 1- diagenesis, with formation of clay minerals, analcime, secondary quartz and albites, and 2- stage of fluids circulations, which induced alteration of detrital and diagenetic minerals, formation of new phases and uranium deposition. A mineralogical zoning, at the scale of deposit resulted from this alteration. The heterogeneity of Tchirezrine 2, at the level of both facies and mineralogy, is also evidenced during ore treatment, as ore reacts differently depending on its source, with sometimes problems of U recovery. Ore treatment tests showed that analcimes and chlorites were both penalizing minerals, because of 1- the sequestration of U-bearing minerals into analcimes, 2- their dissolution which trends to move away from U solubilization conditions (pH and Eh) and to form numerous sulfates, and 3- problems of percolation. A detection method of analcime-rich ores, based on infrared spectroscopy, was developed in order to optimize ore blending and so to reduce negative effects during ore treatment process. (author)

  13. Development of refractory ceramic using waste of petrochemical catalysts

    International Nuclear Information System (INIS)

    Pedroso, M.A.; Mymrine, V.

    2011-01-01

    The manufacturing of catalytic catalysts by the company FCC SA. for the Brazilian petrochemical industry is 25,000 tons per annum, which after going through the cracking process cannot undergo regeneration any longer, being wasted with humidity near 70%. To increase the economical and environmental efficiency of the use of this rejected catalyst, without preliminary drying, a method of using it as main raw material in composition like kaolin was developed, as well as in ash and glass for the manufacturing of common (regular) and refractory ceramic. The mixture of these components were burnt at temperatures of 1100 deg C, 1200°C, 1250°C and 1300°C. The ceramics with 30% and 40% in weight of wasted catalyst, sintered in 1250 deg C or 1300 deg C have flexion of 10,8 - 12,9 MPa. After burning the mixtures, the chemical interaction of the initial components was determined by the methods of RXD, MEV and EDS, synthesizing new minerals like Diopside Ca(Mg,Al)(Si,Al) 2 O 6 , Nepheline (K,Na)AlSiO 4 , Lazurite Na 8 [Al 2 SiO 4 ] 6 [SO 4 ,S] 2 , Magnetite Fe 3 O 4 , Albite Na Al Si 3 O 8 and high content of vitreous amorphous phase. (author)

  14. Study on the enhancement of hydrocarbon recovery by characterization of the reservoir

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, Tae-Jin; Kwak, Young-Hoon; Huh, Dae-Gee [Korea Institute of Geology Mining and Materials, Taejon (KR)] (and others)

    1999-12-01

    The reservoir geochemistry is to understand the origin of these heterogeneities and distributions of the bitumens within the reservoir and to use them not only for exploration but for the development of the petroleums. Methods and principles of the reservoir geochemistry, which are applicable to the petroleum exploration and development, are reviewed in the study. In addition, a case study was carried out on the gas, condensate, water and bitumen samples in the reservoir, taken from the Haenam, Pohang areas and the Ulleung Basin offshore Korea. Mineral geothermometers were studied to estimate the thermal history in sedimentary basins and successfully applied to the Korean onshore and offshore basins. The opal silica-to-quartz transformation was investigated in the Pohang basin as a geothermometer. In Korean basins, the smectite-to-illite changes indicate that smectite and illite can act as the geothermometer to estimate the thermal history of the basins. The albitization reaction was also considered as a temperature indicator. Naturally fractured reservoir is an important source of oil and gas throughout the world. The properties of matrix and fracture are the key parameters in predicting the performances of naturally fractured reservoirs. A new laboratory equipment has been designed and constructed by pressure pulse method to determine the properties, which are (1) the porosity of matrix, (2) the permeability of matrix, (3) the effective width of the fractures, and the permeability of the fractures. (author). 97 refs.

  15. Salinity variations and chemical compositions of waters in the Frio Formation, Texas Gulf Coast. Annual report

    Energy Technology Data Exchange (ETDEWEB)

    Morton, R.A.; Garrett, C.M. Jr.; Posey, J.S.; Han, J.H.; Jirik, L.A.

    1981-11-01

    Waters produced from sandstone reservoirs of the deep Frio Formation exhibit spatial variations in chemical composition that roughly coincide with the major tectonic elements (Houston and Rio Grande Embayments, San Marcos Arch) and corresponding depositional systems (Houston and Norias deltas, Greta-Carancahua barrier/strandplain system) that were respectively active along the upper, lower, and middle Texas Coast during Frio deposition. Within an area, salinities are usually depth dependent, and primary trends closely correspond to pore pressure gradients and thermal gradients. Where data are available (mainly in Brazoria County) the increases in TDS and calcium with depth coincide with the zone of albitization, smectite-illite transition, and calcite decrease in shales. Waters have fairly uniform salinities when produced from the same sandstone reservoir within a fault block or adjacent fault blocks with minor displacement. In contrast, stratigraphically equivalent sandstones separated by faults with large displacement usually yield waters with substantially different salinities owing to the markedly different thermal and pressure gradients across the faults that act as barriers to fluid movement.

  16. Uranium occurrences of the Thunder Bay-Nipigon-Marathon area

    International Nuclear Information System (INIS)

    Scott, J.F.

    1987-01-01

    During the 1981, 1982 and 1983 field seasons an inventory of all known uranium occurrences in the North Central Region of Ontario was undertaken. Three major categories of uranium occurrences were identified: uranium associated with the rocks of the Quetico Subprovince; uranium associated with the Proterozoic/Archean unconformity; and uranium associated with alkalic and carbonatite rocks of Late Precambrian age. Occurrences associated with the Quetico Belt are in white, albite-quartz-muscovite pegmatites. Occurrences associated with the Proterozoic/Archean unconformity are usually of high gradee (up to 12% U 3 O 8 ), nearly always hematized and are related to fault or shear zones proximal to the unconformity. Although of high grade, many of the unconformity related occurrences are very narrow (<1 m). Alkalic and carbonatite rocks of Late Precambrian age are an important source of uranium but possible metallurgical problems might downgrade their potential. The Quetico Subprovince is anomalously high in background uranium, and therefore contains important source rocks for uranium. Areas that have the highest potential for uranium deposits in the North Central Region are the Nipigon Basin area, and the areas underlain by the Gunflint and Rove Formations. All the high grade vein-type uranium deposits related to the unconformity are found within the Nipigon Basin. 126 refs

  17. Formation and damping of a shock wave induced by laser in a metallic target

    International Nuclear Information System (INIS)

    Cottet, F.

    1981-01-01

    In the first part of this work, a numerical simulation of the formation and of the damping of the shock wave induced in a solid target by a laser impulse is developed. It allows to interpret the experimental obtained in the second part of the study. Two series of experiments have been realized. An iron target metallographic study is intended to verify if laser shocks produce effects comparable with conventional shocks, particularly a deformation by albite twinning the existence of which is related to the shock amplitude and its evolution during the propagation in the target. Macles observation become a possible mean to estimate the value of the induced pressures. Another experiment series has been realized to determine more directly the shock parameters. Piezoelectric cermets have been used to detect a shock-wave passage and to measure the time taken to go through targets of variable thickness. The numerical solution allows, afterwards, to deduce the maximum pressure of the induced shock. The most part of the tests have been done on copper targets, the behaviour of which is well known in a large pressure domain. Some tests have been realized on aluminium and iron targets [fr

  18. Hydrogeochemical tracing of mineral water in Jingyu County, Northeast China.

    Science.gov (United States)

    Yan, Baizhong; Xiao, Changlai; Liang, Xiujuan; Wu, Shili

    2016-02-01

    The east Jilin Province in China, Jingyu County has been explored as a potential for enriching mineral water. In order to assess the water quality and quantity, it is of crucial importance to investigate the origin of the mineral water and its flow paths. In this study, eighteen mineral springs were sampled in May and September of 2012, May and September of 2013, and May 2014 and the environment, evolvement, and reaction mechanism of mineral water formation were analysed by hydrochemical data analysis, geochemical modelling and multivariate statistical analysis. The results showed that the investigated mineral water was rich in calcium, magnesium, potassium, sodium, bicarbonate, chloride, sulphate, fluoride, nitrate, total iron, silicate, and strontium, and mineral water ages ranged from 11.0 to more than 61.0 years. The U-shape contours of the mineral ages indicate a local and discrete recharge. The mineral compositions of the rocks were olivine, potassium feldspar, pyroxene, albite, and anorthite and were under-saturated in the mineral water. The origin of mineral water was from the hydrolysis of basalt minerals under a neutral to slightly alkaline and CO2-rich environment.

  19. Characterization of the Lime Mortars of the Rui Barbosa House Museum in Rio De Janeiro, Brazil

    Directory of Open Access Journals (Sweden)

    Daniele Pereira da Silva Dalto

    2018-02-01

    Full Text Available The aim of this research is to characterize the mortars of the Rui Barbosa House Museum, built in 1850, in the city of Rio de Janeiro, Brazil, using X-ray diffraction (XRD, gel-CSH determination, Fourier Transform Infrared spectrometry (FTIR, Wavelength-Dispersive X-ray Fluorescence spectrometry (WDXRF, Thermo gravimetric analysis (TG-DTG, and granulometric analysis. Also, petrographic and physical characteristics such as porosity, water absorption, and apparent density of the mortars were used to identify the raw materials employed in their preparation. Mineralogical associations found are similar (quartz, calcite, kaolinite, microcline, muscovite, and albite for the majority of samples and only vary in their proportions; the most prominent phases are quartz and calcite. The collected data, indicating that the binder is hydrated lime, lead us to conclude that the analyzed samples are lime mortars, discarding the possibility of cement as the binder material. Two samples, located on the corner of the building, which underwent repairs, present a differentiated behavior, with high levels of dolomite and the presence of pozzolanic material, with greater water absorption and higher density, indicating the use of a different mortar type. In addition, it was verified that the WDXRF and XRD methods are able to determine the trace element composition with comparable precision with respect to the methodological approach proposed by Teutonico (1988. In addition, it has been verified that the major pollutant causing degradation of building are sulfur emitted by the vehicles and saline spray.

  20. Alteration, age, and emplacement of the Tangihua Complex ophiolite, New Zealand

    International Nuclear Information System (INIS)

    Nicholson, K.N.; Black, P.M.; Picard, C.; Cooper, P.; Hall, C.M.; Itaya, T.

    2007-01-01

    The Tangihua Complex, New Zealand, represents an upper sequence of Late Cretaceous oceanic crustal material: massive basalt flows, pillow lavas, and dolerites. Three phases of alteration are preserved within the complex, each characterised by zeolite precipitation, which correlate to stratigraphic position. The mylonitised sole contains greenschist assemblages (c. 325 degrees C) grading upwards into the initial phase of alteration (250-300 degrees C), and is characterised by actinolite, epidote, albite, and Na-rich zeolites. This phase is cut by lower temperature veins of chlorite-smectite and Ca-rich zeolites. The final alteration phase ( + and Ca 2+ rich minerals, including apophyllite and calcite. Disruption of Ar/Ar spectra around 50 Ma correlate with rifting in the Loyalty Basin and initiation of obduction along the Loyalty-Three Kings Ridge system. We suggest that these events resulted in initial dismemberment, alteration, and movement of the ophiolite, whereas Ar/Ar plateaux at 25-35 Ma correspond to ophiolite emplacement and the last phases of alteration. (author). 49 refs., 5 figs., 3 tabs

  1. Experimental Study of Cement - Sandstone/Shale - Brine - CO2 Interactions.

    Science.gov (United States)

    Carroll, Susan A; McNab, Walt W; Torres, Sharon C

    2011-11-11

    Reactive-transport simulation is a tool that is being used to estimate long-term trapping of CO2, and wellbore and cap rock integrity for geologic CO2 storage. We reacted end member components of a heterolithic sandstone and shale unit that forms the upper section of the In Salah Gas Project carbon storage reservoir in Krechba, Algeria with supercritical CO2, brine, and with/without cement at reservoir conditions to develop experimentally constrained geochemical models for use in reactive transport simulations. We observe marked changes in solution composition when CO2 reacted with cement, sandstone, and shale components at reservoir conditions. The geochemical model for the reaction of sandstone and shale with CO2 and brine is a simple one in which albite, chlorite, illite and carbonate minerals partially dissolve and boehmite, smectite, and amorphous silica precipitate. The geochemical model for the wellbore environment is also fairly simple, in which alkaline cements and rock react with CO2-rich brines to form an Fe containing calcite, amorphous silica, smectite and boehmite or amorphous Al(OH)3. Our research shows that relatively simple geochemical models can describe the dominant reactions that are likely to occur when CO2 is stored in deep saline aquifers sealed with overlying shale cap rocks, as well as the dominant reactions for cement carbonation at the wellbore interface.

  2. The New Peruvian Meteorite Carancas: Mössbauer Spectroscopy and X-Ray Diffraction Studies

    Science.gov (United States)

    Munayco, P.; Munayco, J.; Varela, M. E.; Scorzelli, R. B.

    2013-02-01

    The Carancas meteorite fell on 15 September 2007 approximately 10 km south of Desaguadero, near Lake Titicaca, Peru, producing bright lights, clouds of dust in the sky and intense detonations. The Carancas meteorite is classified as a H4-5 ordinary chondrite with shock stage S3 and a degree of weathering W0. The Carancas meteorite is characterized by well defined chondrules composed either of olivine or pyroxene. The Mössbauer spectra show an overlapping of paramagnetic and magnetic phases. The spectra show two quadrupole doublets associated to olivine and pyroxene; and two magnetic sextets, associated with the primary phases kamacite/taenite and Troilite (Fe2+). Metal particles were extracted from the bulk powdered samples exhibit only kamacite and small amounts of the intergrowth tetrataenite/antitaenite. X-Ray diffractogram shows the primary phases olivine, pyroxene, troilite, kamacite, diopside and albite. Iron oxides has not been detected by Mössbauer spectroscopy or XRD as can be expected for a meteorite immediately recovered after its fall.

  3. Rare-earth element geochemistry in the Luanga Mafic-Ultramafic Complex, Para

    International Nuclear Information System (INIS)

    Suita, M.T.F.; Nilson, A.A.

    1989-01-01

    Six whole-rock samples (harzburgite, orthopyroxenic and norite) of the Luanga Mafic-Ultramafic Complex (Para) were analysed for rare-earth elements (REE) through plasma spectrometry. The Luanga Complex is a deformed and metamorphosed layered mafic-ultramafic body of Archaean age. The Complex underwent medium-grade metamorphism in three stages. The first stage (medium grade) involved local formation of tremolite and reduction of Ca content in plagioclase. The second stage (low grade) consisted of serpentinization of amphibole or ortopyroxene forming bastile and generation of albite + epidote + white mica + actinolite from plagioclase. The third stage involved renewed serpentinization and/or talcification of pre-existing minerals (including serpentine) along fracture and fault surfaces. The analysed rocks display light rare-earth element (LREE) enrichment up to sixty times the composition of the Leedly chondrite and La/Yb ratios from 6.2 to 20.0 they are low in medium rare-earth elements (MREE), displaying discrete to strong negative Eu anomaly even in plagioclase cumulates and are slightly enriched in heavy rare-earth elements (HREE), usually higher than chondrite values. The low MREE area related to the occurrence of orthopyroxene (bronzite) in a way similar to the pattern of alpine periodotites, while HREE enrichment is compatible with the presence of bronzite and Mg-olivine, probably an inherited igneous feature. (author) [pt

  4. Chemical treatment of kaolin. Case study of kaolin from the Tamazert– Jijel mine

    Directory of Open Access Journals (Sweden)

    Mohamed Chouafa

    2016-01-01

    Full Text Available The Tamazert-Jijel kaolin deposit is located in eastern Algeria, It was formed during a process of hydro-thermal alteration of feldspars rich in potassium. Kaolin, obtained at the mine, mainly contains varying amounts of impurities such as iron oxide (Fe2O3 and anatase (TiO2. These components negatively affect the quality of the commercial product. This research was performed to improve the quality of kaolin to be used in the paper industry with the goal of reducing the impurities of iron and titanium oxides. Different sized fractions of the original sample were analyzed by XRD. The results obtained showed that the mineralogical composition is: quartz, muscovite, kaolinite, dolomite, albite and orthoclase. Kaolin, like all clays, has a thin dissemination of minerals throughout it. After processing kaolin, the particle size fraction of less than 45μm, corresponding to the liberation mesh size, was retained for purification by chemical treatment with different acids of different concentrations (hydrochloric acid, sulfuric acid, acetic acid, heated to boiling point temperatures. The kaolin samples treated with the various acids above were analyzed by X-ray fluorescence and by XRD. The results obtained from the sample treated with hydrochloric acid show that the iron oxide content of acid is reduced by 1.65% to 0.88%. Meanwhile, the brightness of the sample reached 90% under the effect of the treatment with hydrochloric acid at concentration of 2 mole/dm3.

  5. Paleoproterozoic volcanic centers of the São Félix do Xingu region, Amazonian craton, Brazil: Hydrothermal alteration and metallogenetic potential

    Science.gov (United States)

    da Cruz, Raquel Souza; Fernandes, Carlos Marcello Dias; Villas, Raimundo Netuno Nobre; Juliani, Caetano; Monteiro, Lena Virgínia Soares; Lagler, Bruno; Misas, Carlos Mario Echeverri

    2016-06-01

    Geological, petrographic, scanning electron microscopy, and X-ray diffraction studies revealed hydrothermalized lithotypes evidenced by overprinted zones of potassic, propylitic, sericitic, and intermediate argillic alterations types, with pervasive and fracture-controlled styles, in Paleoproterozoic volcano-plutonic units of the São Félix do Xingu region, Amazonian craton, northern Brazil. The Sobreiro Formation presents propylitic (epidote + chlorite + carbonate + clinozoisite + sericite + quartz ± albite ± hematite ± pyrite), sericitic (sericite + quartz + carbonate), and potassic (potassic feldspar + hematite) alterations. The prehnite-pumpellyite pair that is common in geothermal fields also occurs in this unit. The Santa Rosa Formation shows mainly potassic (biotite + microcline ± magnetite), sericitic (sericite + quartz + carbonate ± chlorite ± gold), and intermediate argillic (montmorillonite + kaolinite/halloysite + illite) alterations. These findings strongly suggest the involvement of magma-sourced and meteoric fluids and draw attention to the metallogenetic potential of these volcanic units for Paleoproterozoic epithermal and rare and base metal porphyry-type mineralizations, similar to those already identified in other portions of the Amazonian craton.

  6. Hydrothermal alteration in the Matok Igneous Complex, Southern Marginal Zone of the Limpopo Belt, South Africa

    International Nuclear Information System (INIS)

    Sieber, T.; Van Reenen, D.D.; Barton, J.M.

    1991-01-01

    Ductile shear zones associated with the 2700 to 2650 Ma Limpopo Orogeny locally contained gold mineralization. Some of these shear zones were reactivated under brittle conditions and contain zones of hydrothermal alteration that are of potential economic significance. Within the approximately 2670 Ma Matok Complex, two examples of this shear zone controlled alteration are exposed, the Dwars River and Sand River alteration zones. The granitic rocks of this Complex experienced early selective sericitization of plagioclase and the subsequent development of perthitic porphyroblasts. This early regional alteration was overprinted along brittle shear zones by pervasive propylitization and vein controlled quartz-albite alteration. The setting, composition, and the age of the Matok Complex make it a possible source for Archaean gold mineralization. The Dwars River and Sand River alteration zones are characterized by the absence of significant gold mineralization. The pattern of wall-rock alteration indicates that the hydrothermal processes were different from typical Archaean lode gold deposits. P-T conditions during the shear-zone controlled alteration were less than 400 degrees C and 1,9 - 2,8 kb. The shear zone hosted alteration could have taken place anytime between emplacement of the Matok Complex and about 1315 Ma ago. 35 refs., 10 figs., 4 tabs

  7. The heterogeneous nature of mineral matter, fly-ash and deposits

    Energy Technology Data Exchange (ETDEWEB)

    Creelman, R.A.; Pohl, J.H.; Devir, G.P.; Su, S. [R.A. Creelman and Associates, Epping, NSW (Australia)

    2000-07-01

    This paper reports on a series of slagging studies investigating the heterogeneous nature of mineral matter, fly ash and deposits, and how this heterogeneity affects deposition. The data come from low temperature ashing (LTA) of pulverised coal, fly ash from boilers, and deposits from pilot-scale furnaces and boilers. The paper presents optical and scanning electron (SEM) micrographs, electron microprobe analysis (EMPA) and energy dispersive x-ray analysis (EDXRA) of mineral matter, individual fly ash particles, and localised regions of deposits. During combustion, the included mineral matter is transformed into fly ash, melts and partially adheres to the char surface, and may form agglomerated masses. Excluded mineral matter has little chance of encountering another ash particle and agglomerating in the gas phase, but can react with other particles in the wall deposits. Certain fly ash particles adhere to the wall where they can combine with other fly ash particles. Analyses of molten regions of deposits have shown, so far, four mineral phase fields to be responsible for forming difficult deposits with melting points below deposit surface temperatures of 1200 to 1350{sup o}C. These mineral fields include iron cordierite, albite and its silica undersaturated equivalent nepheline, anorthite, and compounds with ratios of Ca to P of 2.3-2.5.

  8. Geochemistry Petrography, thermobarometry and investigation of magmatic series in Mirabad- Chehel Khane granitoid body (east of Bouin– Miandasht, Isfahan province

    Directory of Open Access Journals (Sweden)

    Seyed Mohsen Tabatabaei Manesh

    2017-11-01

    Full Text Available On the base of petrology, the Mirabad- Chehel Khane granitoid, east of Bouin-Miandasht, dominantly consists of syenogranite, monzogranite, alkali granite and granodiorites. The main minerals of these rocks are quartz, alkali feldspar (Orthoclase, plagioclase (Albite - Oligoclase, biotite, ± amphibole with minor amount of allanite, zircon, titanite, apatite, ± tourmaline.  The biotite from the granites are Fe-rich type (annite and primary magmatic in origin. The composition of the biotites studied principally falls in the calc-alkaline subduction related I-type granite on the tectonomagmatic discrimination diagrams, which stand on their major element oxides. Which is consistent with the nature of their host rocks. The studied amphiboles are classified as calcic (ferro-hornblende which points to the I-type nature of the granitoid.  The tourmaline composition plots on the schorl - foitite field. The temperature for the alteration, on the base of chlorite composition from the syenogranite, is estimated around 350°C and from the monzogranite rocks about 341°C.  Based on the application of Al-in amphibole, a 3 Kbar pressure was determined for the syenogranite unit corresponding to the depth of 8-11 Km for the emplacement of the pluton. Hornblende- plagioclase thermometer shows 694 to 700°C for the equilibrium of these two minerals.

  9. Effect of addition of arc furnace dust in the microstructural properties of fly ash alkali-activated

    International Nuclear Information System (INIS)

    Vargas, Alexandre Silva de; Pavao, Bruno Barreto; Masuero, Angela Boreges; Dal Molin, Denise Carpena Coitinho; Vilela, Antonio Cezar Faria

    2010-01-01

    The search for alternative materials for construction, with less environmental impact, has been the subject of several studies. The alkali-activated cements have shown potential for the reuse of waste, and can be used in the technology of solidification/stabilization. Thus, this study aims to evaluate the main effect of adding arc furnace dust (AFD) in the microstructural properties of matrices based on fly ash alkali-activated. Three levels of AFD were studied: 0, 5, 15 and 25%. The curing was set at 70°C/24 h, and after, kept at room temperature until the age of analysis - 1, 28 and 180 days, with XRD and FTIR analysis. In the XRD spectres it was found that compounds of albite and natron decrease the intensity of their peaks in that there is an increase in the levels of AFD. Concerning to the FTIR, we observed that the band characteristic of the fly ash (FA) 1084 cm"-"1 was shifted to bands near 1000 cm"-"1, which shows that the residue does not interfere in the polymerization and aluminosilicate gel formation. Therefore, under the microstructural aspect, there were no major changes that would impair the use of this residue in alkali-activated matrices. (author)

  10. Isotopic and geochemical evidence of recharge sources and water quality in the Quaternary aquifer beneath Jinchang city, NW China

    International Nuclear Information System (INIS)

    Ma Jinzhu; Pan Feng; Chen Lihua; Edmunds, W. Mike; Ding Zhenyu; He Jianhua; Zhou Kunpeng; Huang Tianming

    2010-01-01

    Multiple isotopic and hydrogeochemical tracers were utilized to understand the recharge sources and geochemical evolution of groundwater in the Quaternary aquifer beneath Jinchang city and the adjacent Gobi desert area. The groundwater shows markedly depleted stable isotopic composition compared to modern rainfall. The signature of groundwaters from Jinchang and the northern Gobi desert area differ clearly from that of the alluvial fan in the south Yongchang basin and modern rainfall, and has lower or non-detectable 3 H activity, implying that the aquifer is likely maintained by palaeowater. This groundwater in the Gobi desert has a 14 C age older than 12 ka, indicating that the groundwater resources are non-renewable. The build-up of dissolved solids through evaporation is a major control on groundwater composition, and the dominant anion species change systematically from HCO 3 - , SO 4 2- to Cl - , but cations from weathering of albite, calcite, dolomite and gypsum also make a significant contribution. The scientific results have important implications for groundwater management in Jinchang city and as well as in the Shiyang River basin under China's West Development Strategy. It is recommended that the water allocation program of diverting water from the Dongda river to the Minqin basin be reconsidered.

  11. Characterization of rock samples localized in some sites of the Mexican Pacific coast

    International Nuclear Information System (INIS)

    Pena, P.; Torre, J. de la; Falcon, T.; Segovia, N.; Azorin, J.

    1999-01-01

    Geophysical studies in zones of high seismicity have showed differences in the content of radioactive material that is used in the study of the geochemical behavior of the subsoil. In an emanometric mapping of radon in soil realized in the Mexican Pacific coast were finding distinct levels in zones with different lithology. With the finality to know the mineralization types in two zones of study which are localized in the Guerrero coast and they belonging to terrains named Guerrero and Xolapa it was determined the mineralogic characteristics in two types of rocks. The identification of the rocks was realized by X-ray diffraction and was determined the elemental chemical composition using a scanning electron microscope. It was indicated in the results obtained that in the two types of rocks were found minerals such as: quartz, albite, microcline anortite, ferroactinolite and biotite. However, it was found differences between them by the presence of their mineralogic compounds because in the rock belonging to Xolapa terrain were presented whereas in the rock localized in the Guerrero terrain were presented sodic and potassic feldspars. The analysis by the Elemental Chemical Composition technique (Energy Dispersive Spectroscopy) corroborated the results obtained by the X-ray diffraction technique. (Author)

  12. Diagenesis and sedimentology of the Clearwater Formation at Tucker Lake

    Energy Technology Data Exchange (ETDEWEB)

    Hutcheon, I; Abercrombie, H J; Putnam, P; Gardner, R; Krouse, H R

    1989-03-01

    The Clearwater Formation at Tucker Lake Alberta, contains heavy oil and is the site of a steam simulation pilot. The best developed reservoir intervals are north-south oriented distributary channel fill and rivermouth bar sand-stones. Oil bearing sands are underlain by a water zone and calcite cements are more abundant in the transition zone. Mineralogy and petrography were studied by x-ray diffraction analysis and scanning electron microscopy, and carbon and oxygen isotope ratios were measured for calcite in the samples studied. The diagenetic history is complex. Early diagenetic minerals include pyrite, quarts, K-feldspar and albite overgrowths, isopachous calcite, iron-rich chlorite, siderite and smectite. Further burial and modification of fluid composition resulted in dissolution of framework mineral grains and precipitation of clinoptilolite and opal. The emplacement of oil retarded mineral diageneses, and was accompanied by a change in aqeous fluid composition. Kaolinite was deposited during and after oil deposition as relativley fresh water entered the Clearwater Formation. The degradation and fermentation of oil and introduction of meteoric water resulted in the production of a late, isotopically distinct, post-bitumen calite cement. 29 refs., 12 figs.

  13. A survey of lunar rock types and comparison of the crusts of earth and moon

    Science.gov (United States)

    Wood, J. A.

    1977-01-01

    The principal known types of lunar rocks are briefly reviewed, and their chemical relationships discussed. In the suite of low-KREEP highland rocks, Fe/(Fe + Mg) in the normative mafic minerals increases and the albite content of normative plagio-clase decreases as the total amount of normative plagioclase increases, the opposite of the trend predicted by the Bowen reaction principle. The distribution of compositions of rocks from terrestrial layered mafic intrusives is substantially different: here the analyses fall in several discrete clusters (anorthositic rocks, norites, granophyres and ferrogabbros, ultramafics), and the chemical trends noted above are not reproduced. It is suggested that the observed trends in lunar highland rocks could be produced by crystal fractionation in a deep global surface magma system if (1) plagiociase tended to float, upon crystallization, and (2) the magma was kept agitated and well mixed (probably by thermal convection) until crystallization was far advanced and relatively little residual liquid was left. After the crustal system solidified, but before extensive cooling had developed a thick, strong lithosphere, mantle convection was able to draw portions of the lunar anorthositic crust down into the mantle.

  14. Origin of Holocene trachyte lavas of the Quetrupillán volcanic complex, Chile: Examples of residual melts in a rejuvenated crystalline mush reservoir

    Science.gov (United States)

    Brahm, Raimundo; Parada, Miguel Angel; Morgado, Eduardo; Contreras, Claudio; McGee, Lucy Emma

    2018-05-01

    The Quetrupillán Volcanic Complex (QVC) is a stratovolcano placed in the center of a NW-SE volcanic chain, between Villarrica volcano and Lanín volcano, in the Central Southern Volcanic Zone of the Andes. Its youngest effusive products are dominated by crystal-poor (most samples with differentiation at shallow depth (<1 kbar) and NNO-QFM oxidation conditions were obtained from initial melt compositions equivalent to the Huililco basalts, a small eruptive centre located ca. 12 km NE of the QVC main vent. Pyroxene-bearing crystal clots, locally abundant in the trachytes, were formed at 900-960 °C (±55 °C) and represent a dismembered crystal mush from which interstitial trachytic melts were extracted and transported upward before eruption. Heating of the crystal mush by a hotter magma recharge is inferred from complex zoned plagioclases formed at higher crystallization temperatures (50-90 °C) than those obtained from pyroxene. Ca-rich plagioclase overgrowths around more albitic cores, followed by an external rim of similar composition to the core are interpreted as restoration to the initial conditions of plagioclase crystallization after the mentioned heating event. Additionally, a late heating of up to 150 °C just prior to eruption is recorded by Fe-Ti oxide thermometry.

  15. U-Pb ages related to uranium mineralization of Lagoa Real, Bahia - Brazil: tectonic implications

    Energy Technology Data Exchange (ETDEWEB)

    Chaves, Alexandre O.; Rios, Francisco J.; Oliveira, Lucilia A.R.; Alves, James V.; Fuzikawa, Kazuo; Neves, Jose M.C.; Chaves, Adriana M.D.V.; Prates, Sonia P. [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)]. E-mail: aoc@cdtn.br; Tubrett, Michael [Memorial University of Newfoundland, NL (Canada). Inco Innovation Centre. MicroAnalysis Facility; Matos, Evando C. [Industrias Nucleares do Brasil S.A. (INB), Rio de Janeiro, RJ (Brazil)

    2007-07-01

    The uranium from Lagoa Real (Bahia/Brazil) is associated with syenitic magmatism (1904 {+-}44 Ma minimum age from upper intercept of zircon U-Pb discordia by LA-ICP-MS) belonging to a mafic/ felsic lithologic association linked to the final stages of 2.05-1.80 Ga Orosirian Orogeny, which acted in the Paramirim Block. These syenitic rocks are rich not only in albite, but also in U-rich titanite (source of uranium). In association with the development of the Orosirian ductile shear zones, the syenites were crystallized and deformed. The metamorphic reactions, which include intense recrystallization of magmatic minerals, led uraninite to precipitate (1868 {+-} 69 Ma; U-Pb by LA-ICP MS) under Redox control. A second population of uraninites was also generated by shear zones reactivation during 0.6-0.5 Ga Brasiliano Orogeny (605 {+-} 170 Ma; U-Pb by LA-ICP-MS). The geotectonic implications are: a) the importance of the Orosirian event in the Paramirim Block during paleoproterozoic Sao Francisco/Congo Craton edification and b) the influence of the Brasiliano event in the Paramirim Block during the West-Gondwana assembly processes, indicated by the 605 {+-} 170 Ma uraninite (second population) age and by the 483 {+-} 100 Ma lower intercept of the metamorphosed syenite U-Pb discordia. (author)

  16. Adsorption of Radioactive Cesium to Illite-Sericite Mixed Clays

    Science.gov (United States)

    Hwang, J. H.; Choung, S.; Park, C. S.; Jeon, S.; Han, J. H.; Han, W. S.

    2016-12-01

    Once radioactive cesium is released into aquatic environments through nuclear accidents such as Chernobyl and Fukushima, it is harmful to human and ecological system for a long time (t1/2 = 30.2 years) because of its chemical toxicity and γ-radiation. Sorption mechanism is mainly applied to remove the cesium from aquatic environments. Illite is one of effective sorbent, considering economical cost for remediation. Although natural illite is typically produced as a mixture with sericite formed by phyllic alteration in hydrothermal ore deposits, the effects of illite-sericite mixed clays on cesium sorption was rarely studied. This study evaluated the sorption properties of cesium to natural illite collected at Yeongdong in Korea as the world-largest illite producing areas (termed "Yeongdong illite"). The illite samples were analyzed by XRF, XRD, FT-IR and SEM-EDX to determine mineralogy, chemical composition, and morphological characteristics, and used for batch sorption experiments. Most of "Yeongdong illite" samples predominantly consist of sericite, quartz, albite, plagioclase feldspar and with minor illite. Cesium sorption distribution coefficients (Kd,Cs) of various "Yeongdong illite" samples ranged from 500 to 4000 L/kg at low aqueous concentration (Cw 10-7 M). Considering Kd,Cs values were 400 and 6000 using reference sericite and illite materials, respectively, in this study, these results suggested that high contents of sericite significantly affect the decrease of sorption capabilities for radiocesium by natural illite (i.e., illite-sericite mixed clay).

  17. Isotopic studies of marbles in the Sanbagawa metamorphic terrain, central Shikoku, Japan

    International Nuclear Information System (INIS)

    Wada, Hideki; Enami, Masaki; Yanagi, Takeru.

    1984-01-01

    Carbon, oxygen and strontium isotopic studies were carried out on marbles occurring in crystalline schists and epidote amphibolites of the Sanbagawa metamorphic terrain, central Shikoku, Japan, in order to estimate metamorphic temperatures and to elucidate their origin. Carbon isotopic fractionation between calcite and graphite shows the metamorphic temperature of 460 deg C at the transitional part between the garnet and albite-biotite zones. Marbles are isotopically classified into two groups. (1) some marbles in epidote amphibolite masses show characteristically negative delta 13 C values and low 87 Sr/ 86 Sr ratios. These marbles are interpreted as have been derived from magmatic or deep-seated carbonates. (2) marbles collected from the crystalline schists and from the marginal part of epidote amphibolite masses, have high 87 Sr/ 86 Sr ratios and delta 13 C values similar to those of typical sedimentary carbonates. They were probably derived from sedimentary carbonates and/or carbonates re-equilibrated with metamorphic fluid segregated from crystalline schists during the Sanbagawa metamorphism. (author)

  18. The geomicrobiology of bauxite deposits

    Directory of Open Access Journals (Sweden)

    Xiluo Hao

    2010-10-01

    Full Text Available Bauxite deposits are studied because of their economic value and because they play an important role in the study of paleoclimate and paleogeography of continents. They provide a rare record of the weathering and evolution of continental surfaces. Geomicrobiological analysis makes it possible to verify that microorganisms have played a critical role during the formation of bauxite with the possibility already intimated in previous studies. Ambient temperature, abundance of water, organic carbon and bioavailable iron and other metal substrates provide a suitable environment for microbes to inhabit. Thiobacillus, Leptospirilum, Thermophilic bacteria and Heterotrophs have been shown to be able to oxidize ferrous iron and to reduce sulfate-generating sulfuric acid, which can accelerate the weathering of aluminosilicates and precipitation of iron oxyhydroxides. Microorganisms referred to the genus Bacillus can mediate the release of alkaline metals. Although the dissimilatory iron-reducing and sulfate-reducing bacteria in bauxites have not yet been identified, some recorded authigenic carbonates and “bacteriopyrites” that appear to be unique in morphology and grain size might record microbial activity. Typical bauxite minerals such as gibbsite, kaolinite, covellite, galena, pyrite, zircon, calcium plagioclase, orthoclase, and albite have been investigated as part of an analysis of microbial mediation. The paleoecology of such bauxitic microorganisms inhabiting continental (sub surfaces, revealed through geomicrobiological analysis, will add a further dimension to paleoclimatic and paleoenvironmental studies.

  19. Solubility of apatite in H2O-NaCl and silicate-bearing solutions at 0.7-3.0 GPa, 800° C

    Science.gov (United States)

    Antignano, A.; Manning, C. E.

    2004-12-01

    Apatite is a major reservoir for the rare-earth elements (REE) in the earth's crust. However, little is known about its solubility in metamorphic fluids. We measured the solubility of apatite in H2O-NaCl and silicate bearing fluids at 800° C and 1.0-2.0 GPa using a piston-cylinder apparatus with NaCl-graphite furnaces. A single Durango fluor-apatite crystal was loaded into a 1.6 mm OD Pt inner capsule, which was crimped and then placed in a 3.5 OD Pt outer capsule with ultra pure H2O and NaCl or powdered albite. Solubility was determined by the weight loss of the apatite grain after 24 hrs. In the H2O-NaCl experiments, total dissolved solids (TDS) were initially below detection (0.4 millimolal) between XNaCl= 0 and XNaCl= 0.025. At XNaCl= 0.035, solubility was 3.3(0.2) millimolal (errors are 1s), and it increased to 57.5(0.4) millimolal at XNaCl= 0.526. Our results show that there is an enhancement in apatite solubility with increasing pressure in pure H2O. Solubility is initially below detection at bearing solutions. This probably explains textures in which monazite mantles apatite, which are common in granulite metamorphic terranes, such as the Kiirunavaara magnetite-apatite ore.

  20. The Morro do Resende orthogneiss: mineralogy, petrography, geochemistry and geochronology

    International Nuclear Information System (INIS)

    Vasconcelos, Fabiana Franco de; Avila, Ciro Alexandre; Bongiolo, Everton Marques; Camara, Beatriz de Oliveira; Menezes, Victor Hugo Riboura; Cunha, Fernanda Caetano de Mattos; Neumann, Reiner; Teixeira, Wilson; Barbosa, Natali

    2017-01-01

    The Morro do Resende orthogneiss is a hololeucocratic to leucocratic, fine-grained body with monzogranitic to granodioritic composition, cropping out near the Volta Grande mine in Nazareno County, State of Minas Gerais, Brazil. It bears xenoliths of metamafic rocks of the Rio das Mortes metavolcano-sedimentary sequence and yields a U-Pb SHRIMP crystallization age of 2174 ± 4 Ma, relating it to one of the magmatic pulses of the Mineiro Belt. The primary mineralogy includes quartz, albite, microcline, biotite, allanite, zircon, magnetite, titanite and apatite, while sericite, epidote, zoisite, clinozoisite, carbonate and chlorite are metamorphic minerals. Maghemite, barite, fluorite, monazite, xenotime, garnet and REE fluorides (possibly gagarinite) are hydrothermal, as they fill the fractures, intergrow or replace the primary and metamorphic minerals. Fluid interaction was not homogeneous throughout the body. Metamorphic paragenesis points to greenschist facies conditions, which could be related to the Paleoproterozoic II event of the Mineiro Belt, which lasted from 2131 to 2101 Ma. The Morro do Resende orthogneiss is distinguished by significant REE enrichment, as well as a negative Eu anomaly linked to the magmatic crystallization and a negative Ce anomaly related to oxidizing hydrothermal fluids circulation. (author)

  1. Effect of addition of arc furnace dust in the microstructural properties of fly ash alkali-activated; Estudo do efeito da adicao do po de aciaria nas propriedades microestruturais de matrizes a base de cinzas volantes alcali-ativadas

    Energy Technology Data Exchange (ETDEWEB)

    Vargas, Alexandre Silva de [Centro de Estudos Superiores Feevale, Novo Hamburgo, RS (Brazil); Pavao, Bruno Barreto; Masuero, Angela Boreges; Dal Molin, Denise Carpena Coitinho; Vilela, Antonio Cezar Faria [Universidade Federal do Rio Grande do Sul (UFRS), RS (Brazil)

    2010-07-01

    The search for alternative materials for construction, with less environmental impact, has been the subject of several studies. The alkali-activated cements have shown potential for the reuse of waste, and can be used in the technology of solidification/stabilization. Thus, this study aims to evaluate the main effect of adding arc furnace dust (AFD) in the microstructural properties of matrices based on fly ash alkali-activated. Three levels of AFD were studied: 0, 5, 15 and 25%. The curing was set at 70°C/24 h, and after, kept at room temperature until the age of analysis - 1, 28 and 180 days, with XRD and FTIR analysis. In the XRD spectres it was found that compounds of albite and natron decrease the intensity of their peaks in that there is an increase in the levels of AFD. Concerning to the FTIR, we observed that the band characteristic of the fly ash (FA) 1084 cm{sup -1} was shifted to bands near 1000 cm{sup -1}, which shows that the residue does not interfere in the polymerization and aluminosilicate gel formation. Therefore, under the microstructural aspect, there were no major changes that would impair the use of this residue in alkali-activated matrices. (author)

  2. Optimization of NaOH Molarity, LUSI Mud/Alkaline Activator, and Na2SiO3/NaOH Ratio to Produce Lightweight Aggregate-Based Geopolymer

    Directory of Open Access Journals (Sweden)

    Rafiza Abdul Razak

    2015-05-01

    Full Text Available This paper presents the mechanical function and characterization of an artificial lightweight geopolymer aggregate (ALGA using LUSI (Sidoarjo mud and alkaline activator as source materials. LUSI stands for LU-Lumpur and SI-Sidoarjo, meaning mud from Sidoarjo which erupted near the Banjarpanji-1 exploration well in Sidoarjo, East Java, Indonesia on 27 May 2006. The effect of NaOH molarity, LUSI mud/Alkaline activator (LM/AA ratio, and Na2SiO3/NaOH ratio to the ALGA are investigated at a sintering temperature of 950 °C. The results show that the optimum NaOH molarity found in this study is 12 M due to the highest strength (lowest AIV value of 15.79% with lower water absorption and specific gravity. The optimum LUSI mud/Alkaline activator (LM/AA ratio of 1.7 and the Na2SiO3/NaOH ratio of 0.4 gives the highest strength with AIV value of 15.42% with specific gravity of 1.10 g/cm3 and water absorption of 4.7%. The major synthesized crystalline phases were identified as sodalite, quartz and albite. Scanning Electron Microscope (SEM image showed more complete geopolymer matrix which contributes to highest strength of ALGA produced.

  3. Optimization of NaOH Molarity, LUSI Mud/Alkaline Activator, and Na2SiO3/NaOH Ratio to Produce Lightweight Aggregate-Based Geopolymer

    Science.gov (United States)

    Abdul Razak, Rafiza; Abdullah, Mohd Mustafa Al Bakri; Hussin, Kamarudin; Ismail, Khairul Nizar; Hardjito, Djwantoro; Yahya, Zarina

    2015-01-01

    This paper presents the mechanical function and characterization of an artificial lightweight geopolymer aggregate (ALGA) using LUSI (Sidoarjo mud) and alkaline activator as source materials. LUSI stands for LU-Lumpur and SI-Sidoarjo, meaning mud from Sidoarjo which erupted near the Banjarpanji-1 exploration well in Sidoarjo, East Java, Indonesia on 27 May 2006. The effect of NaOH molarity, LUSI mud/Alkaline activator (LM/AA) ratio, and Na2SiO3/NaOH ratio to the ALGA are investigated at a sintering temperature of 950 °C. The results show that the optimum NaOH molarity found in this study is 12 M due to the highest strength (lowest AIV value) of 15.79% with lower water absorption and specific gravity. The optimum LUSI mud/Alkaline activator (LM/AA) ratio of 1.7 and the Na2SiO3/NaOH ratio of 0.4 gives the highest strength with AIV value of 15.42% with specific gravity of 1.10 g/cm3 and water absorption of 4.7%. The major synthesized crystalline phases were identified as sodalite, quartz and albite. Scanning Electron Microscope (SEM) image showed more complete geopolymer matrix which contributes to highest strength of ALGA produced. PMID:26006238

  4. In-situ high-temperature Raman spectroscopic studies of aluminosilicate liquids

    Science.gov (United States)

    Daniel, Isabelle; Gillet, Philippe; Poe, Brent T.; McMillan, Paul F.

    1995-03-01

    We have measured in-situ Raman spectra of aluminosilicate glasses and liquids with albite (NaAlSi3 O8) and anorthite (CaAl2Si2O8) compositions at high temperatures, through their glass transition range up to 1700 and 2000 K, respectively. For these experiments, we have used a wire-loop heating device coupled with micro-Raman spectroscopy, in order to achieve effective spatial filtering of the extraneous thermal radiation. A major concern in this work is the development of methodology for reliably extracting the first and second order contributions to the Raman scattering spectra of aluminosilicate glasses and liquids from the high temperature experimental data, and analyzing these in terms of vibrational (anharmonic) and configurational changes. The changes in the first order Raman spectra with temperature are subtle. The principal low frequency band remains nearly constant with increasing temperature, indicating little change in the T-O-T angle, and that the angle bending vibration is quite harmonic. This is in contrast to vitreous SiO2, studied previously. Above Tg, intensity changes in the 560 590 cm-1 regions of both sets of spectra indicate configurational changes in the supercooled liquids, associated with formation of additional Al-O-Al linkages, or 3-membered (Al, Si)-containing rings. Additional intensity at 800 cm-1 reflects also some rearrangement of the Si-O-Al network.

  5. Colloidal behavior of Np(V) in aqueous systems

    International Nuclear Information System (INIS)

    Zhao Xin; Zhang Yingjie; Wei Liansheng; Lin Zhangji

    2004-01-01

    The speciation of Np(V) in solutions is measured by means of FT-Raman spectrometer. The formation of colloid of Np(V) in aqueous solutions is studied with the variation of pH(2-12), ionic strength (0.01 mol/L, 0.1 mol/L, 1.0 mol/L), storage time (6h, 30h, 1 week, 6 weeks) and neptunium concentration. The adsorption behavior of Np(V) on granite and its rock-forming minerals (quartz, microcline, albite, biotite and hornblende) is also studied in an aqueous phase of artificial ground water. The experiments are performed at ambient temperature. Experimental results show that a small fraction of Np removed from the solution is adsorbed on the walls of container at the pH above 6 due to the formation of colloid of Np. The formation of colloid of Np depends on its hydrolytic extent, ionic strength, and storage time. The adsorption of Np on granite and the individual mineral depends strongly on the formation of the colloids with the variation of pH in solutions. (author)

  6. Using presence of calcite cap rock in shales to predict occurrence of reservoirs composed of leached secondary porosity in the geopressured zone. Annual report, June 1, 1980-October 31, 1980

    Energy Technology Data Exchange (ETDEWEB)

    Kaiser, W.R.; Magara, K.; Milliken, K.L.; Richmann, D.L.

    1981-01-01

    The distribution of high-resistivity shale in the Frio Formation between hydropressured and geopressured strata has been mapped along the Texas Gulf Coast. Two high-resistivity intervals more than 1000 ft thick have been mapped, one in Brazoria and Galveston Counties and the other in Kenedy County. They coincide with Frio delta systems and may be related to extraordinary quantities of CO/sub 2/ produced by deltaic sediments rich in woody and herbaceous matter. Beyond being calcareous, the nature of the high-resistivity interval is enigmatic and its relationship to deep secondary porosity problematic. Most of the contained carbonate is microscopically and isotopically skeletal in origin, revealing no evidence of diagenetic modification. Minor rhombs of iron-bearing carbonate tens of microns in size were identified. Detrital feldspar compositions are being established to test subsequent changes in feldspar composition resulting from progressive burial and albitization. Hydrolysis reactions for authigenic minerals and reactions between key pairs of minerals have been written. Thermodynamic functions for complex phyllosilicates at temperatures up to 200/sup 0/C have been calculated. From thermodynamic calculations it was predicted that ferroan calcite would be the favored authigenic carbonate in shales.

  7. Clays for brick manufacturing in Actopan, Hidalgo: physical, chemical and mineralogical characterization

    Energy Technology Data Exchange (ETDEWEB)

    Moreno-Tovar, Raul; Yañez-Hernández, Osiris Annel; Pérez-Moreno, Fidel; Rodríguez-Lugo, Ventura [Área de Ciencias de la Tierra y Materiales, Universidad Autónoma del Estado de Hidalgo (Mexico); Rivera, José de Jesús Cruz [Universidad Autónoma de San Luis Potosí (Mexico); Rivera, Ana Leonor, E-mail: analeonor.ventura.2016@gmail.com [Universidad Nacional Autónoma de México, DF (Mexico)

    2017-10-15

    Samples of clays from Actopan, Hidalgo employed in brick manufacturing are physical, chemical and mineralogical characterized. Transmitted polarized light microscopy showed a uniform particle size with grain morphology characteristic of euhedral crystals with quartz, feldspars, nontronite, and iron oxides particles. Scanning Electron Microscopy revealed 75 μm to 90 μm wide subhedral structures formed by particles from 2.0 μm to 5.0 μm; and rombohedrales forms 40 μm wide, 70 µm long, constituted of silicon, aluminum, iron, titanium, calcium, minor amounts of potassium, magnesium, and sodium. Minerals such as quartz, albite, cristobalite, calcium and Hematite phases were recognized by X-Ray Diffraction technique. Chemical analysis by atomic emission spectrometry with Inductively Coupled Plasma confirmed this mineralogy composition while laser granulometry method found the same particle size. Grain size analysis determined submicrometric dimensions, and multimodal type curves, that can be interpreted as the mixing of two or more different mineral phases in each sample. (author)

  8. Structure-dependent interactions between alkali feldspars and organic compounds: implications for reactions in geologic carbon sequestration.

    Science.gov (United States)

    Yang, Yi; Min, Yujia; Jun, Young-Shin

    2013-01-02

    Organic compounds in deep saline aquifers may change supercritical CO(2) (scCO(2))-induced geochemical processes by attacking specific components in a mineral's crystal structure. Here we investigate effects of acetate and oxalate on alkali feldspar-brine interactions in a simulated geologic carbon sequestration (GCS) environment at 100 atm of CO(2) and 90 °C. We show that both organics enhance the net extent of feldspar's dissolution, with oxalate showing a more prominent effect than acetate. Further, we demonstrate that the increased reactivity of Al-O-Si linkages due to the presence of oxalate results in the promotion of both Al and Si release from feldspars. As a consequence, the degree of Al-Si order may affect the effect of oxalate on feldspar dissolution: a promotion of ~500% in terms of cumulative Si concentration was observed after 75 h of dissolution for sanidine (a highly disordered feldspar) owing to oxalate, while the corresponding increase for albite (a highly ordered feldspar) was ~90%. These results provide new insights into the dependence of feldspar dissolution kinetics on the crystallographic properties of the mineral under GCS conditions.

  9. A test of the 40Ar/39Ar age spectrum technique on some terrestrial materials

    Science.gov (United States)

    Lanphere, M.A.; Brent, Dalrymple G.

    1971-01-01

    40Ar/39Ar age spectra were determined for 10 terrestrial rock and mineral samples whose geologic history is known from independent evidence. The spectra for six mineral and whole rock samples, including biotite, feldspar, hornblende, muscovite, and granodiorite, that have experienced post-crystallization heating did not reveal the age of crystallization in any obvious way. Minima in the spectra, however, give reasonable maximum ages for reheating and high-temperature maxima can be interpreted as minimum crystallization ages. High-temperature ages of microcline and albite that have not been reheated are approximately 10% younger than the known crystallization age. Apparently there are no domains in these feldspars that have retained radiogenic 40Ar quantitatively. Spectra from two diabase samples that contain significant quantities of excess argon might mistakenly be interpreted as spectra from reheated samples and do not give the age of emplacement. The 40Ar/39Ar age spectrum technique may be a potentially valuable tool for the study of geologic areas with complex histories, but the interpretation of age spectra from terrestrial samples seems to be more difficult than suggested by some previous studies. ?? 1971.

  10. Characterization of some archaeological ceramics and clay samples from Zamala - Far-northern part of Cameroon (West Central Africa)

    Energy Technology Data Exchange (ETDEWEB)

    Ntah, Z.L. Epossi; Sobott, R.; Bente, K., E-mail: zoilaepossi@yahoo.fr [Institute of Mineralogy, Crystallography and Materials Science, University of Leipzig (Germany); Fabbri, B. [Institute of Science and Technology for Ceramics, National Research Council (CNR) of Italy, Faenza (Italy)

    2017-07-15

    Seventeen ceramics samples (515±95 BP, about 580 years old) and two clay raw materials from Zamala (Far-northern, Cameroon) were characterized by X-ray diffraction (XRD), thermal analysis (DTA/TG) and X-ray fluorescence spectroscopy. The aim of the work was the deduction of the production technology and provenance of these ceramics. With the exception of one sample the analysed ceramics formed a homogeneous chemical and mineralogical group. The observed mineralogical phases were quartz, mica (biotite), potassium feldspar (microcline) and plagioclase (albite and oligoclase). The XRD study of two local clays yielded the presence of quartz, kaolinite, mica, feldspar and plagioclase. The presence of the broad endothermic peak in the DTA/TG curves of the clays and its absence in the curves of the ceramics indicated that the firing temperature of the ceramics was above 550-600 °C, which is the temperature of the kaolinite-metakaolinite transformation. The firing experiments of the clay between 400-1200 °C in oxidizing atmosphere showed that mica disappeared above 900 °C. Therefore, the firing temperature of the sherds should have been between 600-900 °C. The chemical correlation between ceramics and local clay materials pointed out to a local production of these ceramics. (author)

  11. Analysis of 19th century ceramic fragments excavated from Pirenópolis (Goiás, Brazil) using FT-IR, Raman, XRF and SEM

    Science.gov (United States)

    Freitas, Renato P.; Coelho, Filipe A.; Felix, Valter S.; Pereira, Marcelo O.; de Souza, Marcos André Torres; Anjos, Marcelino J.

    2018-03-01

    This study used Raman, FT-IR and XRF spectroscopy and SEM to analyze ceramic fragments dating from the 19th century, excavated from an old farm in the municipality of Pirenópolis, Goiás, Brazil. The results show that the samples were produced in an open oven at a firing temperature below 500 °C, using raw materials including kaolinite, hematite, magnetite, quartz, microcline, albite, anhydrite, calcite, illite, orthoclase and MnO2. Although the analyses showed similarities in the manufacturing process and the presence of many minerals was common in all samples, multivariate statistical methods (PCA) allowed a more detailed assessment of similarities and differences in the mineral composition of the samples. The results of the PCA showed that the samples excavated in one of the slave quarters (senzalas) group with those excavated at the farmhouse, where the landowner lived, which indicates a paternalistic attitude towards captives, including the sharing of ceramic materials of everyday use.

  12. Luminescence characterization of a sodium rich feldspar

    International Nuclear Information System (INIS)

    Correcher, V.; Sanchez M, L.; Garcia G, J.; Rivera, T.

    2006-01-01

    This paper reports on the radioluminescence (RL) and thermoluminescence (TL) properties of a sodium rich feldspar ((Na,K)[AlSi 3 O 8 ]) with a mean molecular composition of orthoclase (Or) and albite (Ab) of Or 1 Ab 99 . Despite the complexity of the luminescence signals of the sample, it is possible to determine six different emission bands at about 300, 380, 420, 460, 550 and 680 nm. The 300 nm emission can be associated to structural defects related to the recombination process in which the Na + ion diffusion-limited is involved. The UV-blue emission band at (i) 380 nm is characteristic of mineral phases containing SiO 4 tetrahedral and could be related to intrinsic defects in the lattice, (ii) the 420 nm band could be associated to the presence of Cu (II) ions placed next to the hole traps or the recombination on a centre formed from a hole-oxygen atom adjacent to two Al atoms (Al-O-Al) and (iii) the 460 nm waveband could be due to the presence of Ti 4+ . The green and red emissions are respectively associated to the presence of Mn 2+ and Fe 3+ ions. The ratio between the relative intensities, peaked at 290 (the more intense waveband) and 550 nm is about 10:1 in both TL and RL; this fact indicates that the efficiency of recombination centres does no changes regardless on the type of the process. (Author)

  13. Thermoluminescent characteristics of oregano and paprika

    Energy Technology Data Exchange (ETDEWEB)

    Cruz Z, E.; Furetta, C.; Teuffer Z, C. [ICN-UNAM, A.P. 70-543, 04510 Mexico D.F. (Mexico); Melendrez, R.; Barboza F, M. [Universidad de Sonora, A.P. 5-88, Hermosillo, Sonora (Mexico); Kitis, G. [Nuclear Physics Laboratory, Aristotle University of Thessaloniki, 54006 Thessaloniki (Greece)

    2005-07-01

    The poly minerals from oregano and paprika were selected according to different sizes, i.e 10, 53, 74, 149 {mu}m, and they were exposed to ionizing gamma radiation in the range of doses 0.5-45 kGy. The glow curves from these spices show an abroad TL band, centered around 150 C and by XRD analysis shows a mono mineral composition mainly quartz and feldspar, including albite, ortose and clay. The fading behavior was related to the quartz, feldspar and calcite TL properties and shown the stability of the traps associated to the defects generated by irradiation in the samples. The tendency of the TL integrated was increased with the grain size for oregano and can be related to the different energy values associated to the activation energy of the traps in the monominerals. The glow curve TL from poly minerals was analyzed and it is possible to use the dosimetric property of the poly minerals from spices for detect irradiated foodstuffs. (Author)

  14. The Lagoa Real uranium province, Bahia state, Brazil: some petrographic aspects and fluid inclusion studies

    International Nuclear Information System (INIS)

    Fuzikawa, K.; Alves, J.V.; Cuney, M.; Kostolanyl, C.; Poti, B.

    1988-01-01

    The Lagoa Real Uranium Province in the central-southern Bahia State, consisting of six deposits and several prospects, has a reserve of near one hundred tons of U 3 O 8 . The main lithological unit in the area is the Lagoa Real Complex which is formed by granites and gneisses derived from them. The unit overthrusts the Espinhaco metasediments the west. The Complex is the host of albities which may contain uraninite. The mineralization is manly associated with pyroxene and garnet. Petrographic and field relations indicate the overthrusting as the latest event, having left implants in the orebodies and their hosts. Fluid inclusion studies indicated fluids of different characteristics in the Espinhaco and the Lagoa Real Complex although they were similar in composition (carbonic and aqueous). The types inclusions detected are in agreement with the geologic processes suggested for the area: emplacement of the Sao Timoteo granite at 1.72 Ga; albitization and uranium mineralization at ∼ 1.4 Ga; and metamorphism at ∼ 0.49 Ga. The study is an example of fluid inclusion behaviour in a metamorphic process with very limited amount of fluids. (author) [pt

  15. Studies of mineralogy and geochemistry of Rare Earth Elements in permo-Triassic Bauxite deposit, Northeast of Bukan, North West of Iran

    International Nuclear Information System (INIS)

    Abedini, A.; Calagari, A. A.; Hadjalilu, B.; Jahangiri, A.

    2008-01-01

    Bauxite deposit of Permo-Triassic age in northeast of Bukan was developed stratiformly along the boundary between Ruteh and Elika formations, and includes four distinct rock units. This deposit was affected by tectonic and morphological processes. Mineralogical and geochemical investigations showed that during weathering processes, two mechanisms of ferrugenization and deferrugenization played crucial role in formation of minerals such as Diaspora, boehmite, hematite, goethite, kaolinite, pyrophyllite, clinochlore, illite, montmorillonite, anatase, rutile, albite, sanidine, quartz, and calcite in this deposit. By taking notice of field evidence and of mineralogical and geochemical data, the basalts (whose remnants are still present along the contact of this deposit with carbonate bedrock) are the potential parent rock of this deposit. The distribution pattern of rare earth elements (normalized to chondrite and basaltic parent rock) along with anomaly variations of Eu, Ce, and (La/Yb) N indicates differentiation of LREEs from HREEs during bauxitization processes. Further geochemical considerations indicate that the concentrations of LREEs were occurred by hematite, goethite, manganese oxides, cerianite, and secondary phosphates (rhabdophane, vitusite, gorceixite, monazite) and of HREEs by clay minerals; rutile, anatase, zircon, euxenite, and fergusonite. Incorporation of the results obtained from mineralogical and geochemical investigations suggests that in addition to factors such as p H of weathering solutions, ionic potential, composition of the parent rock, and fixation by residual minerals, adsorption processes also played crucial role in enrichment of rare earth elements during moderate to intense lateritization in the study area

  16. Geothermal System as the Cause of the 1979 Landslide Tsunami in Lembata Island, Indonesia

    Directory of Open Access Journals (Sweden)

    Yudhicara Yudhicara

    2015-05-01

    Full Text Available DOI:10.17014/ijog.2.2.91-99A tsunami landslide which caused hundreds casualties and lots of damage took place on Lembata Island in 1979. In order to understand the characteristics of the landslide mechanism, a field survey was conducted in 2013 which sampled both the origin soil and landslide material, and the water from hotspring around the landslide site. The physical properties of the soil obtained show that the original soil has dominantly coarser grain than the landslide material (80.5% coarser grain compared to 11.8% coarse grain respectively which indicates that the soil has become finer and softer. Hot spring analysis indicated that the mineral content of the water was 99.48% SO4. This shows that magmatism processes are involved which caused the soil to become acidic and may have fragilised the system. Results of X-ray Diffraction Mineralogy Analysis (XRD show that the original soil is composed of minerals of cristobalite, quartz, and albite, while the landslide material consists of clay minerals such as quartz, saponite, chabazite, silicon oxide, and coesite which are typical minerals in a hydrothermal environment. Based on these results, it can be concluded that the area was influenced by an active geothermal system that could be the main source mechanism behind this disastrous event. 

  17. Clays for brick manufacturing in Actopan, Hidalgo: physical, chemical and mineralogical characterization

    International Nuclear Information System (INIS)

    Moreno-Tovar, Raul; Yañez-Hernández, Osiris Annel; Pérez-Moreno, Fidel; Rodríguez-Lugo, Ventura; Rivera, José de Jesús Cruz; Rivera, Ana Leonor

    2017-01-01

    Samples of clays from Actopan, Hidalgo employed in brick manufacturing are physical, chemical and mineralogical characterized. Transmitted polarized light microscopy showed a uniform particle size with grain morphology characteristic of euhedral crystals with quartz, feldspars, nontronite, and iron oxides particles. Scanning Electron Microscopy revealed 75 μm to 90 μm wide subhedral structures formed by particles from 2.0 μm to 5.0 μm; and rombohedrales forms 40 μm wide, 70 µm long, constituted of silicon, aluminum, iron, titanium, calcium, minor amounts of potassium, magnesium, and sodium. Minerals such as quartz, albite, cristobalite, calcium and Hematite phases were recognized by X-Ray Diffraction technique. Chemical analysis by atomic emission spectrometry with Inductively Coupled Plasma confirmed this mineralogy composition while laser granulometry method found the same particle size. Grain size analysis determined submicrometric dimensions, and multimodal type curves, that can be interpreted as the mixing of two or more different mineral phases in each sample. (author)

  18. Rare earth element geochemistry of feldspars: examples from Fe-oxide Cu-Au systems in the Olympic Cu-Au Province, South Australia

    Science.gov (United States)

    Kontonikas-Charos, Alkis; Ciobanu, Cristiana L.; Cook, Nigel J.; Ehrig, Kathy; Krneta, Sasha; Kamenetsky, Vadim S.

    2018-04-01

    Rare earth element (REE) fractionation trends in feldspars are reported from Olympic Dam (including Wirrda Well and Phillip's Ridge) and Cape Donington (Port Lincoln), for comparison with two other igneous-hydrothermal terranes within the eastern Gawler Craton: Moonta-Wallaroo and Hillside. The case studies were selected as they represent 1590 Ma Hiltaba Suite and/or 1845 - 1810 Ma Donington Suite granites, and, aside from Cape Donington, are associated with Mesoproterozoic iron-oxide copper gold (IOCG)-type mineralization. Both plagioclase and alkali feldspar were analyzed within selected samples with the purpose of constraining and linking changes in REE concentrations and fractionation trends in feldspars to local and whole-rock textures and geochemistry. Two unique, reproducible fractionation trends were obtained for igneous plagioclase and alkali feldspars, distinguished from one another by light rare earth element enrichment, Eu-anomalies and degrees of fractionation (e.g. La/Lu slopes). Results for hydrothermal albite and K-feldspar indicate that REE concentrations and fractionation trends are generally inherited from igneous predecessors, however in some instances, significant amounts of REE appear to have been lost to the fluid. These results may have critical implications for the formation of world-class IOCG systems, in which widespread alkali metasomatism plays a key role by altering the physical and chemical properties of the host rocks during early stages of IOCG formation, as well as trapping trace elements (including REE).

  19. Ferroan Dolomitization by Seawater Interaction with Mafic Igneous Dikes and Carbonate Host Rock at the Latemar Platform, Dolomites, Italy: Numerical Modeling of Spatial, Temporal, and Temperature Data

    Directory of Open Access Journals (Sweden)

    K. Blomme

    2017-01-01

    Full Text Available Numerous publications address the petrogenesis of the partially dolomitized Latemar carbonate platform, Italy. A common factor is interpretation of geochemical data in terms of heating via regional igneous activity that provided kinetically favorable conditions for replacement dolomitization. New field, petrographic, XRD, and geochemical data demonstrate a spatial, temporal, and geochemical link between replacement dolomite and local mafic igneous dikes that pervasively intrude the platform. Dikes are dominated by strongly altered plagioclase and clinopyroxene. Significantly, where ferroan dolomite is present, it borders dikes. We hypothesize that seawater interacted with mafic minerals, causing Fe enrichment in the fluid that subsequently participated in dolomitization. This hypothesis was tested numerically through thermodynamic (MELTS, Arxim-GEM and reactive flow (Arxim-LMA simulations. Results confirm that seawater becomes Fe-enriched during interaction with clinopyroxene (diopside-hedenbergite and plagioclase (anorthite-albite-orthoclase solid solutions. Reaction of modified seawater with limestone causes ferroan and nonferroan replacement dolomitization. Dolomite quantities are strongly influenced by temperature. At 40 to 80°C, ferroan dolomite proportions decrease with increasing temperature, indicating that Latemar dolomitization likely occurred at lower temperatures. This relationship between igneous dikes and dolomitization may have general significance due to the widespread association of carbonates with rifting-related igneous environments.

  20. A new type of Nb (Ta)-Zr(Hf)-REE-Ga polymetallic deposit in the late Permian coal-bearing strata, eastern Yunnan, southwestern China: Possible economic significance and genetic implications

    Energy Technology Data Exchange (ETDEWEB)

    Dai, Shifeng; Wang, Xibo; Luo, Yangbing; Song, Zhentao; Ren, Deyi [State Key Laboratory of Coal Resources and Safe Mining, China University of Mining and Technology, Beijing 100083 (China); Zhou, Yiping; Zhang, Mingquan; Wang, Jumin; Song, Xiaolin; Yang, Zong [Yunnan Institute of Coal Geology Prospection, Kunming 650218 (China); Jiang, Yaofa [Xuzhou Institute of Architectural Technology, Xuzhou 221116 (China)

    2010-07-01

    This paper describes a new type of Nb(Ta)-Zr(Hf)-REE-Ga polymetallic deposit of volcanic origin in the late Permian coal-bearing strata of eastern Yunnan, southwestern China. Well logging data (especially natural gamma-ray), geochemical data (high concentrations of Nb, Ta, Zr, Hf, REE, and Ga) and mineralogical compositions (Nb(Ta)-, Zr(Hf)-, or REE-bearing minerals rarely observed), together with the volcanic lithological characteristics indicate that there are thick (1-10 m, mostly 2-5 m) ore beds in the lower Xuanwei Formation (late Permian) in eastern Yunann of southwestern China. The ore beds are highly enriched in (Nb,Ta){sub 2}O{sub 5} (302-627 ppm), (Zr,Hf)O{sub 2} (3805-8468 ppm), REE (oxides of La-Lu + Y) (1216-1358 ppm), and Ga (52.4-81.3 ppm). The ore beds are mainly composed of quartz, mixed-layer illite-smectite, kaolinite, berthierine, and albite. Four types of ore beds in the study area were identified, namely, clay altered volcanic ash, tuffaceous clay, tuff, and volcanic breccia. Preliminary studies suggest that the high concentrations of otherwise rare metals were mainly derived from the alkalic pyroclastic rocks. The modes of occurrence, spatial distribution, and enrichment mechanism of the rare metals, however, require further study. (author)

  1. Propagation of hydroclimatic variability through the critical zone

    Science.gov (United States)

    Porporato, A. M.; Calabrese, S.; Parolari, A.

    2016-12-01

    The interaction between soil moisture dynamics and mineral-weathering reactions (e.g., ion exchange, precipitation-dissolution) affects the availability of nutrients to plants, composition of soils, soil acidification, as well as CO2 sequestration. Across the critical zone (CZ), this interaction is responsible for propagating hydroclimatic fluctuations to deeper soil layers, controlling weathering rates via leaching events which intermittently alter the alkalinity levels. In this contribution, we analyze these dynamics using a stochastic modeling approach based on spatially lumped description of soil hydrology and chemical weathering reactions forced by multi-scale temporal hydrologic variability. We quantify the role of soil moisture dynamics in filtering the rainfall fluctuations through its impacts on soil water chemistry, described by a system of ordinary differential equations (and algebraic equations, for the equilibrium reactions), driving the evolution of alkalinity, pH, the chemical species of the soil solution, and the mineral-weathering rate. A probabilistic description of the evolution of the critical zone is thus obtained, allowing us to describe the CZ response to long-term climate fluctuations, ecosystem and land-use conditions, in terms of key variables groups. The model is applied to the weathering rate of albite in the Calhoun CZ observatory and then extended to explore similarities and differences across other CZs. Typical time scales of response and degrees of sensitivities of CZ to hydroclimatic fluctuations and human forcing are also explored.

  2. Preliminary results on the petrology and fluid inclusions of the Rossing uraniferous alaskites

    International Nuclear Information System (INIS)

    Cuney, M.

    1980-01-01

    Petrography, radioactivity distribution and fluid inclusions have been studied in three samples of the Rossing alaskites from the S.H. anomaly outside of the Rossing deposit. After the crystallization of the alaskitic magma which involved oligoclase, biotite, orthoclase and quartz, a deuteric alteration produced a quartz, microcline, albite, muscovite, calcite plus minus chlorite mineral association similar to those observed in several French uraniferous granites. Uranium redistribution occurred during this alteration. From fluid inclusions data, the pressure at the time of the intrusion is estimated to have been at least 6kbar for a temperature of 625 degrees Celsius. Reaction of the magma with the marbles of the Rossing formation led to the boiling of the magma by an increase in the CO 2 partial pressure as well as to its crystallization. Immiscibility between a dense saline (more than 30 per cent NaCl) and CO 2 -rich fluid is proposed to have occurred simultaneously or after the fluid oversaturation of the magma. Part of uraninite is formed at the magmatic stage, another part crystallized from the magmatic fluids in the biotite-rich selvages of the alaskites or in the uraninite-fluorite veins. Uraninite crystallization appears to be mainly controlled by the oxygen fugacity prevailing in the magma and in the surrounding rocks

  3. Thermoluminescent characteristics of oregano and paprika

    International Nuclear Information System (INIS)

    Cruz Z, E.; Furetta, C.; Teuffer Z, C.; Melendrez, R.; Barboza F, M.; Kitis, G.

    2005-01-01

    The poly minerals from oregano and paprika were selected according to different sizes, i.e 10, 53, 74, 149 μm, and they were exposed to ionizing gamma radiation in the range of doses 0.5-45 kGy. The glow curves from these spices show an abroad TL band, centered around 150 C and by XRD analysis shows a mono mineral composition mainly quartz and feldspar, including albite, ortose and clay. The fading behavior was related to the quartz, feldspar and calcite TL properties and shown the stability of the traps associated to the defects generated by irradiation in the samples. The tendency of the TL integrated was increased with the grain size for oregano and can be related to the different energy values associated to the activation energy of the traps in the monominerals. The glow curve TL from poly minerals was analyzed and it is possible to use the dosimetric property of the poly minerals from spices for detect irradiated foodstuffs. (Author)

  4. Compositional controls on spinel clouding and garnet formation in plagioclase of olivine metagabbros, Adirondack Mountains, New York

    Science.gov (United States)

    McLelland, J.M.; Whitney, P.R.

    1980-01-01

    Olivine metagabbros from the Adirondacks usually contain both clear and spinel-clouded plagioclase, as well as garnet. The latter occurs primarily as the outer rim of coronas surrounding olivine and pyroxene, and less commonly as lamellae or isolated grains within plagioclase. The formation of garnet and metamorphic spinel is dependent upon the anorthite content of the plagioclase. Plagioclase more sodic than An38??2 does not exhibit spinel clouding, and garnet rarely occurs in contact with plagioclase more albitic than An36??4. As a result of these compositional controls, the distribution of spinel and garnet mimics and visually enhances original igneous zoning in plagioclase. Most features of the arrangement of clear (unclouded) plagioclase, including the shells or moats of clear plagioclase which frequently occur inside the garnet rims of coronas, can be explained on the basis of igneous zoning. The form and distribution of the clear zones may also be affected by the metamorphic reactions which have produced the coronas, and by redistribution of plagioclase in response to local volume changes during metamorphism. ?? 1980 Springer-Verlag.

  5. Effect of Al-B2O3-TiO2 Exothermic System on Performances of Fly Ash Glass/Ceramic Composite Coating

    Directory of Open Access Journals (Sweden)

    Yajun An

    2018-01-01

    Full Text Available Glass/ceramic composite coatings were prepared on 40Cr steel matrix by thermo-chemical reaction with fly ash and a small amount of SiO2, Al2O3, MgO, and albite as main raw materials. On this basis, adding 10% Al-TiO2-B2O3 exothermic system, the morphology, phase, thermal shock resistance, and corrosion resistance of the coating were tested, and the influence of exothermic system on the structure and properties of the composite coating was studied. The experimental results show that the addition of exothermic system can promote the formation of NaB15, TiB2, Na2B4O7, Ca2Al2SiO7, and other new phases by thermo-chemical reaction; when compared to the composite coating without addition of exothermic system, combined with a good interface, higher compactness, and lower porosity. The highest micro hardness can be reached 725HV0.1. The number of thermal shock from 700 °C to room temperature can reach more than 50 times; acid, salt, oil immersion corrosion test, composite coating with exothermic system relative to the matrix increased by 27.40 times, 3.97 times, and 1.88 times, respectively. The overall performance is better than that of the composite coating without exothermic system.

  6. 208-240 M.Y. old jadeite-glaucophane schists in the Kurosegawa tectonic zone near Kochi city, Shikoku

    International Nuclear Information System (INIS)

    Maruyama, Shigenori; Ueda, Yoshio; Banno, Shohei.

    1978-01-01

    A new member of the Kurosegawa tectonic zone was found in the serpentinite near Kochi city. They are high P and low T schists derived from basalt and chert. Three metamorphic events can be deciphered in the high-pressure schists, based upon the texture and mineral paragenesis: first, low P metamorphism at intermediate- to high-grade, second, high P and low T metamorphism of the jadeite-glaucophane facies and the third, retrograde crystallization of the second stage high P schists within the stability field of lawsonit + pumpellyite + glaucophane. Further, the formation of analcime replacing jadeite took place. The second and third metamorphism can be distinguished on pyroxene mineralogy that jadeite + quartz was stable in the second, but albite + quartz + aegirinejadeite in the third stage of metamorphism. Not all of the high P and low T schists had suffered low P metamorphism before they were metamorphosed by the high P one. Some basaltic rocks directly changed to high P and low T schists. Two muscovites in the schists give K-Ar ages of 208 - 240 m.y., and a relic igneous biotite, being partly replaced by chlorite, gives 225 m.y. of K-Ar age. These values are different not only from those of the Sanbagawa schists, but also from the other members of the Kurosegawa zone. (author)

  7. Moessbauer spectroscopy and X-ray diffraction analyses of clayey samples used as ceramic sourcing materials, in Peru

    Energy Technology Data Exchange (ETDEWEB)

    Quille, Ruben, E-mail: quilleruben@gmail.com; Bustamante, Angel [San Marcos National University, Laboratory of Ceramics and Nanomaterials, Faculty of Physical Sciences (Peru); Palomino, Ybar [National University of San Cristobal de Huamanga, Experimental Center of Ceramics (Peru)

    2011-11-15

    The ceramic industry is an important area of economic activity in the Ayacucho Region, in particular in the District of Quinua. As a consequence, there is a huge demand for clay to produce ceramic pastes in that region. This paper reports on results concerning the mineralogical characterization of four clayey samples, which were collected MAA and SPQA from the area Pampa de La Quinua with geographic coordinates 13 Degree-Sign 02 Prime 49 Double-Prime S 74 Degree-Sign 08 Prime 03 Double-Prime W, CE1M and CE2M from the Quinua locality 13 Degree-Sign 03 Prime 07 Double-Prime S 74 Degree-Sign 08 Prime 31 Double-Prime W, both in the District of Quinua, Province of Huamanga, Ayacucho, Peru. The chemical and mineralogical characterization of these samples was carried out with powder X-ray diffraction detecting quartz, albite, montmorillonite, kaolinite and glauconite mineral phases, Moessbauer spectroscopy detected iron in kaolinite, glauconite and montmorillonite minerals. Chemical analysis was performed through scanning electron microscopy and energy dispersive X-ray spectroscopy. Data obtained from the combination of these techniques provided relevant information about the morphology, chemical composition, and the mineralogy of samples.

  8. Mössbauer spectroscopy and X-ray diffraction analyses of clayey samples used as ceramic sourcing materials, in Peru

    Science.gov (United States)

    Quille, Rubén; Bustamante, Ángel; Palomino, Ybar

    2011-11-01

    The ceramic industry is an important area of economic activity in the Ayacucho Region, in particular in the District of Quinua. As a consequence, there is a huge demand for clay to produce ceramic pastes in that region. This paper reports on results concerning the mineralogical characterization of four clayey samples, which were collected MAA and SPQA from the area Pampa de La Quinua with geographic coordinates 13° 02' 49″ S 74° 08' 03″ W, CE1M and CE2M from the Quinua locality 13° 03' 07″ S 74° 08' 31″ W, both in the District of Quinua, Province of Huamanga, Ayacucho, Peru. The chemical and mineralogical characterization of these samples was carried out with powder X-ray diffraction detecting quartz, albite, montmorillonite, kaolinite and glauconite mineral phases, Mössbauer spectroscopy detected iron in kaolinite, glauconite and montmorillonite minerals. Chemical analysis was performed through scanning electron microscopy and energy dispersive X-ray spectroscopy. Data obtained from the combination of these techniques provided relevant information about the morphology, chemical composition, and the mineralogy of samples.

  9. Mössbauer spectroscopy and X-ray diffraction analyses of clayey samples used as ceramic sourcing materials, in Peru

    International Nuclear Information System (INIS)

    Quille, Rubén; Bustamante, Ángel; Palomino, Ybar

    2011-01-01

    The ceramic industry is an important area of economic activity in the Ayacucho Region, in particular in the District of Quinua. As a consequence, there is a huge demand for clay to produce ceramic pastes in that region. This paper reports on results concerning the mineralogical characterization of four clayey samples, which were collected MAA and SPQA from the area Pampa de La Quinua with geographic coordinates 13° 02′ 49″ S 74° 08′ 03″ W, CE1M and CE2M from the Quinua locality 13° 03′ 07″ S 74° 08′ 31″ W, both in the District of Quinua, Province of Huamanga, Ayacucho, Peru. The chemical and mineralogical characterization of these samples was carried out with powder X-ray diffraction detecting quartz, albite, montmorillonite, kaolinite and glauconite mineral phases, Mössbauer spectroscopy detected iron in kaolinite, glauconite and montmorillonite minerals. Chemical analysis was performed through scanning electron microscopy and energy dispersive X-ray spectroscopy. Data obtained from the combination of these techniques provided relevant information about the morphology, chemical composition, and the mineralogy of samples.

  10. On the geology of the uranium mineralization in the Swiss Alps

    International Nuclear Information System (INIS)

    Gillieron, F.

    1988-01-01

    Numerous radiometric anomalies and several uranium occurrences were found in the Swiss Alps by systematic prospecting of selected areas carried out between 1957 and 1984. Most of the uranium indications lie in a rather narrow belt that follows roughly the valleys of the Rhone und of the Rhine Anterior, from Martigny onto Ilanz and extending northwards towards the Lake of Walenstadt. The uranium occurrences were found in the following geological environments: - permocarboniferous continental, variably metamorphosed series, belonging either to the formation of the 'Verrucano' or to the Penninic St. Bernhard nappe; - muscovite-chlorite-albite gneisses belonging to the pre-Westphalian basement of the St. Bernhard nappe; - muscovite-chlorite gneisses and phyllites of the Hercynian Tavetsch massiv; - muscovite-biotite gneisses within the southern border of the Aar massif; - Vallorcine granite of the Auguilles-Rouges massiv and polymetamorphic biotite gneisses along its northwestern contact zone. The possible geological (or 'in situ') resources are estimated to be 50-250 tonnes uranium in each one of the investigated mineralization zones of some importance; the respective estimated grades are 50-250 ppm U. Therefore the occurrences are actually of no economic value. (author) 25 figs., 1 tab., refs

  11. Use of a cranium-vessel determined by means of compound analysis; Uso de una vasija-craneo determinada por medio de analisis de compuesto

    Energy Technology Data Exchange (ETDEWEB)

    Leboreiro, I.; Pijoan, C.M.; Mansilla, J. [Direccion de Antropologia Fisica, INAH, Gandhi s/n, Polanco, 11560 Mexico D. F. (Mexico); Bosch, P. [Instituto de Investigaciones en Materiales, UNAM, Circuito Exterior, Ciudad Universitaria, 04510 Mexico D. F. (Mexico)

    2004-07-01

    Many human remains as bones, skin, teeth and others, were used in pre-hispanic cultures as tools or ritual objects. A human cranial vault filed in the Direccion de Antropologia Fisica presented particular and interesting cultural modifications. There are twelve drills used to restore by sewing the crane, in this way the piece resembles a pot. It has been established that it comes from North Mexico where such restoration work has been reported (Aveleyra, 1956) for containers made of vegetables (guaje). As the utilization of this kind of archaeological remain is unknown, the study of dust samples from the inside and the outside of the crane should provide hints on the products stored into it. In this study we present the X-ray diffraction results which show that the outer dusts are mainly constituted by albite, andesite and quartz, whereas in the inside the substances were mainly aluminosilicates and magnesium compounds. Hence, most probably, this crane was not used as a conventional container and it is linked to the concoction of magnesium and aluminosilicates containing products. This conclusion has to be correlated to that even nowadays, in both alternative and conventional medicine. (Author) 7 refs., 7 figs.

  12. Propagation of a hyperalkaline plume into the geological barrier surrounding a radioactive waste repository

    International Nuclear Information System (INIS)

    Lichtner, P.C.; Eikenberg, J.

    1995-01-01

    A coupled geochemical transport model (MPATH) which includes chemical reaction kinetics is used to evaluate the alteration of Swiss argillaceous sediments in a high-pH environment and to predict the spatial propagation of the hyperalkaline plume with time. The calculations predict dissolution of quartz, clay minerals and chlorite, and precipitation of zeolite minerals such as analcime and natrolite as well as he feldspars K-feldspar and albite. In addition, Portland cement-hydrates such as calcium silicate and aluminate hydrates, ettringite and friedel-salt are also predicted to form, depending on the composition of the inlet fluid and the host rock. The dissolution of clay minerals reduces the pH of the hyperalkaline plume to levels between approximately 8 and 10, depending on the composition of the inlet fluid and the host rock. For pure advective transport through porous medium, neglecting changes in porosity and permeability, the migration velocity of the high-pH front is calculated to be approximately one to two orders of magnitude less than that of the infiltrating groundwater. However, due to precipitation of secondary phases, in the present model concept a rapid decrease in porosity of the marl occurs several meters from the repository. At the interface between the marl host rock and cement the porosity increases as a consequence of the low silica concentration of the cement pore fluid. (author) 10 figs., 7 tabs., refs

  13. Mineral shock signatures in rocks from Dhala (Mohar) impact structure, Shivpuri district, Madhya Pradesh, India

    Science.gov (United States)

    Roy, Madhuparna; Pandey, Pradeep; Kumar, Shailendra; Parihar, P. S.

    2017-12-01

    A concrete study combining optical microscopy, Raman spectroscopy and X-ray diffractometry, was carried out on subsurface samples of basement granite and melt breccia from Mohar (Dhala) impact structure, Shivpuri district, Madhya Pradesh, India. Optical microscopy reveals aberrations in the optical properties of quartz and feldspar in the form of planar deformation feature-like structures, lowered birefringence and mosaics in quartz, toasting, planar fractures and ladder texture in alkali feldspar and near-isotropism in bytownite. It also brings to light incidence of parisite, a radioactive rare mineral in shocked granite. Raman spectral pattern, peak positions, peak widths and multiplicity of peak groups of all minerals, suggest subtle structural/crystallographic deviations. XRD data further reveals minute deviations of unit cell parameters of quartz, alkali feldspar and plagioclase, with respect to standard α-quartz, high- and low albite and microcline. Reduced cell volumes in these minerals indicate compression due to pressure. The c0/a0 values indicate an inter-tetrahedral angle roughly between 120o and 144o, further pointing to a possible pressure maxima of around 12 GPa. The observed unit cell aberration of minerals may indicate an intermediate stage between crystalline and amorphous stages, thereby, signifying possible overprinting of decompression signatures over shock compression effects, from a shock recovery process.

  14. Use of a cranium-vessel determined by means of compound analysis

    International Nuclear Information System (INIS)

    Leboreiro, I.; Pijoan, C.M.; Mansilla, J.; Bosch, P.

    2004-01-01

    Many human remains as bones, skin, teeth and others, were used in pre-hispanic cultures as tools or ritual objects. A human cranial vault filed in the Direccion de Antropologia Fisica presented particular and interesting cultural modifications. There are twelve drills used to restore by sewing the crane, in this way the piece resembles a pot. It has been established that it comes from North Mexico where such restoration work has been reported (Aveleyra, 1956) for containers made of vegetables (guaje). As the utilization of this kind of archaeological remain is unknown, the study of dust samples from the inside and the outside of the crane should provide hints on the products stored into it. In this study we present the X-ray diffraction results which show that the outer dusts are mainly constituted by albite, andesite and quartz, whereas in the inside the substances were mainly aluminosilicates and magnesium compounds. Hence, most probably, this crane was not used as a conventional container and it is linked to the concoction of magnesium and aluminosilicates containing products. This conclusion has to be correlated to that even nowadays, in both alternative and conventional medicine. (Author) 7 refs., 7 figs

  15. Geochemistry and tectonic setting of basic dykes in the Boroujerd area (Sanandaj- Sirjan Zone

    Directory of Open Access Journals (Sweden)

    Zahra Tahmasbi

    2017-03-01

    Full Text Available Basic dykes, trending NE-SW and cross cutting the middle Jurassic granodioritic rocksexposed in the Boroujerd area. They are dark green and fine to medium–grained rocksand are characterized by ophitic to subophitic texture. These rocks are dominated bymajor minerals including amphibole and plagioclase as well as minor biotite, apatite,sphene and prehnite. Amphibole is calcic, with magnesia-hornblende to actinolitehornblendecomposition. T = 600-700ºC and P = 3.5-5.2 kbar were calculated forcrystallization of these minerals. The composition of plagioclases ranges from albite tooligoclase. The basic dykes studied are undeformed and the youngest magmatic activityin the area.. The collision of Arabian and Central Iranian plates, gave rise to the pressurein the Central Iranian plate, which expanded the extension fractures in the direction ofthe plate movement. As a result, the dykes in discussion formed in direction of platemovement. Thus, development of basic dykes in the Northeast-Southwest direction withrespect to the convergence zone is justified. The basic dykes, on the discriminationtectonic diagrams, are classified as alkaline series and plotted on within plateenvironment field, which originated from partial melting of an enriched mantle source.

  16. Geochemical significance of neoproterozoic rasimalai alkali syenite emplaced along Dharmapuri shear zone in the Northern part of Tamil Nadu

    International Nuclear Information System (INIS)

    Thangavel, S.; Balasubramani, S.; Nagaraju, M.; Bhattacharya, D.; Zakaulla, Syed; Rai, A.K.

    2015-01-01

    The Rasimalai alkali syenite complex is emplaced within Peninsular Gneissic complex and spatially associated with NE-SW trending major Dharmapuri shear zone (DSZ) in the northern part of Tamil Nadu. It is surrounded by epidote hornblend egneiss, which is the fenetised product of Charnockite and occurs about 20 km NE of Alangayam in Vellore district. It is mainly comprised of medium to coarse grained grey syenite (albite and orthoclase) and medium to micro grained pink syenite (orthoclase, microcline and perthite) at places porphyritic in nature with hornblende, riebeckitc, aegirine and acmite as accessory minerals. Grey syenite is non radioactive and uranium mineralisation is associated with pink syenite (syngenetic and disseminated type) and quartz-barite veins (hydrothermal type). Hydrothermal activity is manifested in the form of pyrite, chalcopyrite, galena, barite, calcite and calcian-strontianite which occur in the form of disseminations, stringers, lumps, aggregates, veinlets and veins. Presence of high silica (63.14-75.43%) with high field strength elements (U, Th, Nb and Pb) and large ion lithophile elements (Rb, Sr, K, Ba) possibly indicates that Rasimalai alkali syenite is the product of crustal communication and partial melting of protracted emplacement of parental alkali basaltic magma

  17. A kinetics database and scripts for PHREEQC

    Science.gov (United States)

    Hu, B.; Zhang, Y.; Teng, Y.; Zhu, C.

    2017-12-01

    Kinetics of geochemical reactions has been increasingly used in numerical models to simulate coupled flow, mass transport, and chemical reactions. However, the kinetic data are scattered in the literature. To assemble a kinetic dataset for a modeling project is an intimidating task for most. In order to facilitate the application of kinetics in geochemical modeling, we assembled kinetics parameters into a database for the geochemical simulation program, PHREEQC (version 3.0). Kinetics data were collected from the literature. Our database includes kinetic data for over 70 minerals. The rate equations are also programmed into scripts with the Basic language. Using the new kinetic database, we simulated reaction path during the albite dissolution process using various rate equations in the literature. The simulation results with three different rate equations gave difference reaction paths at different time scale. Another application involves a coupled reactive transport model simulating the advancement of an acid plume in an acid mine drainage site associated with Bear Creek Uranium tailings pond. Geochemical reactions including calcite, gypsum, and illite were simulated with PHREEQC using the new kinetic database. The simulation results successfully demonstrated the utility of new kinetic database.

  18. Analysis of the potential geochemical reactions in the Enceladus' hydrothermal environment

    Science.gov (United States)

    Ramirez-Cabañas, A. K.; Flandes, A.

    2017-12-01

    Enceladus is the sixth largest moon of Saturn and differs from its other moons, because of its cryovolcanic geysers that emanate from its south pole. The instruments of the Cassini spacecraft reveal different compounds in the gases and the dust of the geysers, such as salts (sodium chloride, sodium bicarbonate and/or sodium carbonate), as well as silica traces (Postberg et al., 2008, 2009) that could be the result of a hydrothermal environment (Hsu et al., 2014, Sekine et al., 2014). By means of a thermodynamic analysis, we propose and evaluate potential geochemical reactions that could happen from the interaction between the nucleus surface and the inner ocean of Enceladus. These reactions may well lead to the origin of the compounds found in the geysers. From this analysis, we propose that, at least, two minerals must be present in the condritic nucleus of Enceladus: olivines (fayalite and fosterite) and feldspar (orthoclase and albite). Subsequently, taking as reference the hydrothermal processes that take place on Earth, we propose the different stages of a potential hydrothermal scenario for Enceladus.

  19. A mineralogical investigation of a uranium-bearing phosphatic siltstone from Tsongnapan, Northwestern Cape Province

    International Nuclear Information System (INIS)

    Brynard, H.J.

    1980-02-01

    A sample of uranium-bearing phosphatic siltstone from Tsongnapan in the Northwestern Cape Province was investigated mineralogically. The siltstone consists of cyclically alternating apatite- and calcite spherulite-rich layers. The calcite content of the rock is 11,4% and the apatite content is 42,1%. The groundmass shows the presence of the following elements: Si, Ca, P, Fe, Mg, K, Al, Cu and Zn. Detrital quartz, albite and magnetite are mainly confined to calcite spherulitic layers. The uranium content of the siltstone is 1 120 ppm U 3 O 8 and the thorium content 638 ppm ThO 2 . Both uranium and thorium occur mainly in the apatite-rich groundmass and to a minor extent in subsidiary monazite and zircon. Laboratory-scale metallurgical tests showed that the uranium is almost wholly leachable by hydrochloric acid while sulphuric and acetic acid dissolve only a small percentage of the uranium with concomitant formation of calcium sulphate. The rock probably formed in a low-energy regime in a marine environment where apatite and calcite spherulites crystallised from a possibly colloidal state [af

  20. Characterization of rock samples localized in some sites of the Mexican Pacific coast; Caracterizacion de muestras de rocas localizadas en algunos sitios de la costa del Pacifico Mexicano

    Energy Technology Data Exchange (ETDEWEB)

    Pena, P.; Torre, J. de la; Falcon, T.; Segovia, N. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico); Azorin, J. [Universidad Autonoma Metropolitana-Iztapalapa C.P. 09340 Mexico D.F. (Mexico)

    1999-07-01

    Geophysical studies in zones of high seismicity have showed differences in the content of radioactive material that is used in the study of the geochemical behavior of the subsoil. In an emanometric mapping of radon in soil realized in the Mexican Pacific coast were finding distinct levels in zones with different lithology. With the finality to know the mineralization types in two zones of study which are localized in the Guerrero coast and they belonging to terrains named Guerrero and Xolapa it was determined the mineralogic characteristics in two types of rocks. The identification of the rocks was realized by X-ray diffraction and was determined the elemental chemical composition using a scanning electron microscope. It was indicated in the results obtained that in the two types of rocks were found minerals such as: quartz, albite, microcline anortite, ferroactinolite and biotite. However, it was found differences between them by the presence of their mineralogic compounds because in the rock belonging to Xolapa terrain were presented whereas in the rock localized in the Guerrero terrain were presented sodic and potassic feldspars. The analysis by the Elemental Chemical Composition technique (Energy Dispersive Spectroscopy) corroborated the results obtained by the X-ray diffraction technique. (Author)

  1. Use of basaltic waste as red ceramic raw material

    Directory of Open Access Journals (Sweden)

    T. M. Mendes

    Full Text Available Abstract Nowadays, environmental codes restrict the emission of particulate matters, which result in these residues being collected by plant filters. This basaltic waste came from construction aggregate plants located in the Metropolitan Region of Londrina (State of Paraná, Brazil. Initially, the basaltic waste was submitted to sieving (< 75 μm and the powder obtained was characterized in terms of density and particle size distribution. The plasticity of ceramic mass containing 0%, 10%, 20%, 30%, 40% and 50% of basaltic waste was measured by Atterberg method. The chemical composition of ceramic formulations containing 0% and 20% of basaltic waste was determined by X-ray fluorescence. The prismatic samples were molded by extrusion and fired at 850 °C. The specimens were also tested to determine density, water absorption, drying and firing shrinkages, flexural strength, and Young's modulus. Microstructure evaluation was conducted by scanning electron microscopy, X-ray diffraction, and mercury intrusion porosimetry. Basaltic powder has similar physical and chemical characteristics when compared to other raw materials, and contributes to ceramic processing by reducing drying and firing shrinkage. Mechanical performance of mixtures containing basaltic powder is equivalent to mixtures without waste. Microstructural aspects such as pore size distribution were modified by basaltic powder; albite phase related to basaltic powder was identified by X-ray diffraction.

  2. Geology and mineralization of the Jabalat alkali-feldspar granite, northern Asir region, Kingdom of Saudi Arabia

    Science.gov (United States)

    Al Tayyar, Jaffar; Jackson, Norman J.; Al-Yazidi, Saeed

    The Jabalat post-tectonic granite pluton is composed of albite- and oligoclase-bearing, low-calcium, F-, Sn- and Rb-rich subsolvus granites. These granites display evidence of late-magmatic, granitophile- and metallic-element specialization, resulting ultimately in the development of post-magmatic, metalliferous hydrothermal systems characterized by a Mo sbnd Sn sbnd Cu sbnd Pb sbnd Zn sbnd Bi sbnd Ag sbnd F signature. Two main types of mineralization are present within the pluton and its environs: (1) weakly mineralized felsic and aplitic dikes and veins enhanced in Mo, Bi, Ag, Pb and Cu; and (2) pyrite—molybdenite—chalcopyrite-bearing quartz and quartz—feldspar veins rich in Mo, Sn, Bi, Cu, Zn and Ag. A satellite stock, 3 km north of the main intrusion, is composed of fine-grained, miarolitic, muscovite—albite—microcline (microperthite) granite. The flanks of this intrusion and adjacent dioritic rocks are greisenized and highly enriched in Sn, Bi and Ag. Quartz veins which transect the satellite stock contain molybdenite and stannite.

  3. Mineralogical characterization of a meteorite impact in Carancas, Puno

    International Nuclear Information System (INIS)

    Ceron Loayza, Maria L.; Bravo Cabrejos, Jorge A.

    2009-01-01

    We report the results of the study of a meteorite that impacted an inhabited zone in the neighborhood of the town of Carancas, Puno Region, about 1,300 km south of Lima. The analysis carried out by X ray diffractometry, transmission Moessbauer spectroscopy (at room temperature and at 4,2 K), and by energy dispersive X ray fluorescence reveal the presence in the meteorite simple of magnetic sites assigned to the Fe-Ni and troilite (Fe,S) phases, and of 3 paramagnetic doublets, two of them assigned to Fe 2+ , one associated to olivine and the other to pyroxene, and the third one due to a site occupied by Fe 3+ , which can be associated to oxides in a superparamagnetic state and/or by an Fe hydroxide. The soil samples from the crater reveal a composition that consists mainly of quartz, albite and impactites such as coesite and stishovite (SiO 2 ). The occurrence of these phases with a high content of SiO 2 in the crater soils strengthens the hypothesis of their origin induced by impact; we observe also the presence of the Fe oxide hematite, of aluminum silicates such as illite and montmorillonite, and an unassigned phase of Fe 3+ . In general, the results obtained by these techniques complement each other rather well and allow the verification of the origin of the studied simples. (author).

  4. Geochemistry and paleotectonomagmatic setting of metabasites protolith from Asalem metamorphic complex (northwest Rasht

    Directory of Open Access Journals (Sweden)

    Mohsen Nasrabady

    2016-12-01

    Full Text Available Asalem metamorphic complex consists mostly of metabasite, metapelite and serpentinite. Metabasites display metamorphic features of greenschist and blueschist facies. Greenschist facies rocks that found as both foliated and massive types contain mineralogical assemblage of actinolite, chlorite, albite and epidote. Blueschists contain mineralogical assemblage of sodic amphibole, epidote and phengite. Whole rock analyses of the metabasites indicate basaltic to andesitic composition with mainly calcalkaline nature of their protolith. According to the discrimination diagrams of tectonomagmatic setting, the protolith of investigated metabasites has been islands arc and somewhat mid ocean ridge. The patterns of rare earth elements and spider diagrams of the Asalem metabasites resemble to the basic and intermediate magmatism of islands arc or suprasubduction setting as well. Greenschists and blueschists facies rocks of the Asalem metamorphic complex have been probably equivalent to islands arc or young and hot oceanic crust of suprasubduction zone setting. This portion of oceanic basin unlike the subducted even and thick oceanic lithosphere of Paleotethys during accretion in the shallower levels of accretionary prisms, have underwent metamorphic conditions of blueschist and greenschist facies and finally gave rise to the formation of the metabasites of the Asalem metamorphic complex.

  5. An exsolution silica-pump model for the origin of myrmekite

    Science.gov (United States)

    Castle, R.O.; Lindsley, D.H.

    1993-01-01

    Myrmekite, as defined here, is the microscopic intergrowth between vermicular quartz and modestly anorthitic plagioclase (calcic albite-oligoclase), intimately associated with potassium feldspar in plutonic rocks of granitic composition. Hypotheses previously invoked in explanation of myrmekite include: (1) direct crystallization; (2) replacement; (3) exsolution. The occurrence of myrmekite in paragneisses and its absence in rocks devold of discrete grains of potassium feldspar challenge those hypotheses based on direct crystallization or replacement. However, several lines of evidence indicate that myrmekite may in fact originate in response to kinetic effects associated with the exsolution of calcic alkali feldspar into discrete potassium feldspar and plagioclase phases. Exsolution of potassium feldspar system projected from [AlSi2O8] involves the exchange CaAlK-1Si-1, in which the AlSi-1 tetrahedral couple is resistant to intracrystalline diffusion. By contrast, diffusion of octahedral K proceeds relatively easily where it remains uncoupled to the tetrahedral exchange. We suggest here that where the ternary feldspar system is open to excess silica, the exchange reaction that produces potassium feldspar in the ternary plane is aided by the net-transfer reaction K+Si=Orthoclase, leaving behind indigenous Si that reports as modal quartz in the evolving plagioclase as the CaAl component is concomitantly incorporated in this same phase. Thus silica is "pumped" into the reaction volume from a "silica reservoir", a process that enhances redistribution of both Si and Al through the exsolving ternary feldspar. ?? 1993 Springer-Verlag.

  6. Metallogenetic modeling for uranium exploration in rocks of the Abaira-Jussiape Anticlinal nucleus, Chapada Diamantina, Bahia

    International Nuclear Information System (INIS)

    Santana, Jocilene dos Santos; Cruz, Simone Cerqueira Pereira; Barbosa, Johildo Salomao Figueiredo; Abram, Maisa Bastos; Martins, Adriano Alberto Marques

    2011-01-01

    The NNW-SSE-trending Abaira-Jussiape Anticlinal is an antiformal culmination of folding and shearing in the Paramirim Corridor of the Western Chapada Diamantina. In its core paleoproterozoic, mylonitized Caraguatai Suite, tonalites-granodiorites, alkali-feldspar granites, syenites to quartz-syenites and Jussiape Suite granites crop out. Compressional and distensional stresses mark the structural geology of the area. The compressional structures are related to two distinct deformation phases, named D1a and D1b. The main compressional phase is ductile D1a, which is related to the nucleation of dextral to dextral-reverse shearing zones. Deformation and syn-D1a recrystallization involving plagioclase and the K-feldspar suggest deformation temperature conditions above 550 deg C. The following phase D2 is of ductilebrittle nature and culminates in reverse shearing zones. The distensional structures correspond to the D3 phase and are represented by frontal shear zones with normal movement. The petrographic study helped identify a pre-D1a hydrothermal alteration process related to albitization and potassification, syn-D1 oxidation process, and hydration and saussuritization related to phases D2 and D3. The integration of lithological, petrographic, structural and geophysical data by means of the logic Fuzzy, plus the existing information regarding structural and lithologic controls of the known uranium mineralization in the Paramirim Corridor, led us to identify two promising areas for radioactive element exploration in the nucleus of Abaira-Jussiape Anticlinal. (author)

  7. Mecanismos de construcción-destrucción de patrones macroestructurales en microclimas como sistemas complejos

    Directory of Open Access Journals (Sweden)

    Sánchez-Muñoz, L.

    2006-10-01

    Full Text Available The structures of microcline perthites collected from granitic pegmatites have been studied at different observation scales using optical microscopy (OM, X-ray diffraction (XRD, 27Al MASS-NMR spectroscopy, and electron microprobe (EMPA with Na mappings. Pegmatite perthites are identified as complex systems. During the cooling process, K-rich feldspars display two separated genetic periods of recrystallization, each one with variable intensity along different samples. During the first period, in the mineral structure a progressive construction of macrostructural pseudo-periodic patterns is produced. These regular patterns emerge due to a combined mechanism of non-ergodic Si/Al local ordering and a global cooperative effect of the crystal structure. From the incoherent Na/K interfaces arise transformation fronts (avalanches which can coalesce longitudinally and juxtapose transversally to self-assemble into irregular domains. Finally, they can evolve up to create regular twin-domains (Albite and Pericline laws as the crystal unit of the macrostructural building. This selforganization process is activated when the system is open to water circulation acting as a catalyst of Al/Si ordering in the feldspar lattice linked with an external stimulation by shear tectonic stress. During the second period the structural patterns, previously created, are destroyed by (i relaxation and deformation twinning mechanisms, (ii coarsening of twin-domains produced by dissolution-precipitation due to aqueous fluids interactions at low temperature, (iii reorientation of Periclinelaw twin-domains to the Albite-law orientation.

    Se han estudiado estructuras de feldespatos potásicos triclínicos (microclinas intercrecidos con feldespatos sódicos en texturas pertíticas procedentes de pegmatitas graníticas a diferentes escalas de observación, mediante microscopía de luz transmitida (MLT, difracción de rayos-X (DRX, resonancia magnética nuclear de alta resoluci

  8. Magnetite-apatite mineralization in Khanlogh iron deposit, northwest of Neyshaboor, NE Iran

    Science.gov (United States)

    Najafzadeh Tehrani, Parvin; Asghar Calagari, Ali; Velasco Roldan, Francisco; Simmonds, Vartan; Siahcheshm, Kamal

    2016-04-01

    fluids. The high fluorine content of the apatite at Khanlogh may testify to the presence of Ti-fluoride complex in the fluids. Formation of apatite crystals was concurrent with development of titanium lamellae in magnetite. The apatite possesses high REE content which is possibly associated with monazite inclusions. The SEM studies better show these inclusions are occasionally present at the margin of apatite crystals and veins. Based upon field relations, microscopic examinations, and the results of XRD analyses, sodic (albite), propylitic (epidote, chlorite, calcite), and argillic (montmorillonite) alterations are developed in the study area. The principal minerals in these alteration zones are albite, epidote, sericite, chlorite, quartz, calcite, and montmorllonite. Mineralogy, alteration, geochemistry, structure, and texture of the ores at Khanlogh indicate that the magnetite and apatite were chiefly formed by hydrothermal solutions which were enriched in iron mainly transported by F- and Cl- rich fluids. Reference Hou,,T., Zhaochong, Z., Timothy, K., (2011). Gushan magnetite-apatite deposit in the Ningwu basin, Lower Yangtze River Valley, SE China: Hydrothermal or Kiruna-type? Ore geology review, 43, 333-346. Purtov, V.K., Kotelnikova, A.L. (1993). Solubility of titanium in chloride and fluoride hydrothermal solution. International Geology Review 35, 274 -287.

  9. Mineral chemistry and geochemistry of the Late Neoproterozoic Gabal Abu Diab granitoids, Central Eastern Dessert, Egypt: Implications for the origin of rare metal post-orogenic A-type granites

    Science.gov (United States)

    Sami, Mabrouk; Ntaflos, Theodoros; Farahat, Esam S.; Ahmed, Awaad F.; Mohamed, Haroun A.

    2015-04-01

    The Neoproterozoic Gabal Abu Diab pluton is a part of the Arabian Nubian shield (ANS) continental crust and located in the Central Eastern Desert (CED) of Egypt. It constitutes multiphase granitic pluton intruded into granodiorite and metagabbro-diorite rocks with sharp and nonreactive contacts. Based on field observations, colors, structural variations and petrographic investigations, this granitic outcrop consists of an inner core of two-mica granite (TMG) followed outward by garnet bearing muscovite granite (GBMG) and albite granite (AG). Petrographical study indicated that medium to coarse-grained TMG is dominated by K-feldspar (Or88-98), quartz, plagioclase (albite, An0-7), muscovite and biotite with hypidiomorphic texture. With exception the appearance of garnet and the disappearance of biotite the GBMG resembles the TGM, while AG is leucocratic without any mafic mineral. The main accessories are zircon, Nb and Ta-bearing rutile, columbite, ilmenorutile, ilmenite, magnetite and apatite. This mineralogical similarity and the existence of columbite group minerals (CGM) in all granitoids, indicates a cogenetic relationship. Microprobe analyses reveal that, besides the CGM, rutile and ilmenite are the main repository phases for Nb-Ta-Ti. Columbite-(Mn) exists as individual subhedral crystals (up to 100μm in size) or intimate intergrowth with Nb-bearing rutile and/or ilmenite. The CGM are represented mostly by columbite-(Mn) with Ta/(Ta+Nb) and Mn/(Mn+Fe) ratio ranging from 0.02-0.08 and 0.4-0.9, respectively suggesting extreme degree of magmatic fractionation. Rutile contains significant amounts of Ta (up to 4 wt.% Ta2O5) and Nb (up to 22 wt.% Nb2O5). Biotites are phlogopite-annite in composition (Ann47-60Phlog40-53,on average) and are enriched with AlIV that characterize peraluminous granites. Garnets contain 60-69 mol.% spessartine and 28-36 mol.% almandine where, the ratio of spessartine and almandine together exceeds 95 mole percent, similar to garnet occur

  10. ⁵³Mn-⁵³Cr and ²⁶Al-²⁶Mg ages of a feldspathic lithology in polymict ureilites

    Energy Technology Data Exchange (ETDEWEB)

    Goodrich, Cyrena Anne [Planetary Science Institute. Tucson, AZ (United States); Hutcheon, Ian D. [Glenn T. Seaborg Institute. Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kita, Noriko T. [Dept. of Geoscience. Univ. of Wisconsin, Madison, WI (United States); Huss, Gary R. [NASA Marshall Space Flight Center (MSFC), Huntsville, AL (United States); Cohen, Barbara Anne [Hawaii Institute of Geophysics and Planetology. Univ. of Hawaii, Honolulu, HI (United States); Keil, Klaus

    2010-07-01

    We report 53Mn–53Cr and 26Al–26Mg isotopic data, obtained by in-situ SIMS analysis, for feldspathic clasts in polymict ureilites DaG 319 and DaG 165. The analyzed clasts belong to the “albitic lithology,” the most abundant population of indigenous feldspathic materials in polymict ureilites, and are highly fractionated igneous assemblages of albitic plagioclase, Fe-rich pyroxenes, phosphates, ilmenite, silica, and Fe(Mn, K, P, Ti)-enriched glass. Glass in DaG 165 clast 19 has extremely high and variable 55Mn/52Cr ratios (500–58,000) and shows correlated 53Cr excesses up to ~ 1500‰, clearly indicating the presence of live 53Mn at the time of formation. The slope of the well-correlated isochron defined by glass and pyroxenes from this clast corresponds to (53Mn/55Mn) = (2.84 ± 0.10) × 10-6 (2σ). Data for less 55Mn/52Cr-enriched glasses from DaG 319 clast B1, as well as phosphates from several other clasts, are consistent with this isochron. The 53Mn/55Mn ratio obtained from the isochron implies that these clasts are 0.70 ± 0.18 Ma younger than the D'Orbigny angrite, corresponding to the absolute age of 4563.72 ± 0.22 Ma. Plagioclase in DaG 319 clast B1 has a fairly constant 27Al/24Mg ratio of ~ 900 and shows resolvable 26Mg excesses of ~ 2‰. The slope of the isochron defined by pyroxene and plagioclase in this clast is (3.0 ± 1.1) × 10-7 (2σ), corresponding to a time difference of 5.4 (-0.3/+0.5) Ma after CAI (assuming the canonical initial 26Al/27Al ratio of 5 × 10-5) and an age 0.5 (-0.3/+0.5) Ma younger than D'Orbigny. Its absolute age (relative to D'Orbigny) is 4563.9 (+ 0.4/-0.5) Ma, in agreement with the 53Mn–53Cr age from clast 19. These data provide the first

  11. Rb-Sr, K-Ar, and stable isotope evidence for the ages and sources of fluid components of gold-bearing quartz veins in the northern Sierra Nevada foothills metamorphic belt, California

    Science.gov (United States)

    Böhlke, John Karl; Kistler, R. W.

    1986-01-01

    Gold-bearing quartz veins occur in and near major fault zones in deformed oceanic and island-arc rocks west of the main outcrop of the Sierra Nevada composite batholith. Veins typically occupy minor reverse faults that crosscut blueschist to amphibolite-grade metamorphic rocks whose metamorphic ages range from early Paleozoic to Jurassic. Vein micas and carbonate-quartz-mica assemblages that formed by hydrothermal metasomatism of ultramafic wall rocks in the Alleghany, Grass Valley, Washington, and Mother Lode districts yield concordant K-Ar and Rb-Sr ages. The dated veins are significantly younger than prograde metamorphism, penetrative deformation, and accretion of their host rocks to the continental margin. New and previously published mineralization ages from 13 localities in the Sierra foothills range from about 140 to 110 m.y. ago, with mean and median between 120 and 115 m.y. The age relations suggest that mineralizing fluids were set in motion by deep magmatic activity related to the resumption of east-dipping subduction along the western margin of North America following the Late Jurassic Nevadan collision event.CO 2 -bearing fluids responsible for metasomatism and much of the vein mica, carbonate, albite, and quartz deposition in several northern mines were isotopically heavy (delta 18 O [asymp] 8-14ppm; delta D between about -10 and -50ppm) and do not resemble seawater, magmatic, or meteoric waters. Metasomatic and vein-filling mica, dolomite, magnesite, and quartz in altered ultramafic rocks generally formed from fluids with similar Sr and O isotope ratios at a given locality. Consistent quartz-mica delta 18 O fractionations (delta 18 O (sub Q-M) = 4.5-4.9ppm) from various localities imply uniform equilibration temperatures, probably between 300 degrees and 350 degrees C. On a local (mine) scale, fluids responsible for both carbonate alteration of mafic and ultramafic wall rocks and albitic alteration of felsic and pelitic rocks had similar Sr isotope

  12. Metal-rich fluid inclusions provide new insights into unconformity-related U deposits (Athabasca Basin and Basement, Canada)

    Science.gov (United States)

    Richard, Antonin; Cathelineau, Michel; Boiron, Marie-Christine; Mercadier, Julien; Banks, David A.; Cuney, Michel

    2016-02-01

    The Paleoproterozoic Athabasca Basin (Canada) hosts numerous giant unconformity-related uranium deposits. The scope of this study is to establish the pressure, temperature, and composition (P-T-X conditions) of the brines that circulated at the base of the Athabasca Basin and in its crystalline basement before, during and after UO2 deposition. These brines are commonly sampled as fluid inclusions in quartz- and dolomite-cementing veins and breccias associated with alteration and U mineralization. Microthermometry and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) data from five deposits (Rabbit Lake, P-Patch, Eagle Point, Millennium, and Shea Creek) complement previously published data for the McArthur River deposit. In all of the deposits investigated, fluid inclusion salinity is between 25 and 40 wt.% NaCl equiv., with compositions displaying a continuum between a "NaCl-rich brine" end-member (Cl > Na > Ca > Mg > K) and a "CaCl2-rich brine" end-member (Cl > Ca ≈ Mg > Na > K). The CaCl2-rich brine has the highest salinity and shows evidence for halite saturation at the time of trapping. The continuum of compositions between the NaCl-rich brine and the CaCl2-rich brine end-members combined with P-T reconstructions suggest anisothermal mixing of the two brines (NaCl-rich brine, 180 ± 30 °C and 800 ± 400 bars; CaCl2-rich brine, 120 ± 30 °C and 600 ± 300 bars) that occurred under fluctuating pressure conditions (hydrostatic to supra-hydrostatic). However, because the two brines were U bearing and therefore oxidized, brine mixing was probably not the driving force for UO2 deposition. Several scenarios are put forward to account for the Cl-Na-Ca-Mg-K composition of the brines, involving combinations of seawater evaporation, halite dissolution, mixing with a halite-dissolution brine, Mg/Ca exchange by dolomitization, Na/Ca exchange by albitization of plagioclase, Na/K exchange by albitization of K-feldspar, and Mg loss by Mg

  13. Greenschist-Facies Pseudotachylytes and Gouge: a Microstructural Study of the Deformation Propagation at the Boundary Between Hp-Metabasite and Calcite Bearing Metasediments

    Science.gov (United States)

    Crispini, L.; Scambelluri, M.; Capponi, G.

    2013-12-01

    Recent friction experiments on calcite-bearing systems reproduce pseudotachylyte structures, that are diagnostic of dinamic calcite recrystallization related to seismic slip in the shallow crust. Here we provide the study of a pseudotachylyte (PT) bearing low angle oblique-slip fault. The fault is linked to the exhumation of Alpine HP-ophiolites and it is syn- to post-metamorphic with respect to retrograde greenschist facies metamorphism. The observed microstructures developed at the brittle-ductile transition and suggest that seismic and interseismic slip was enhanced by interaction with fluids. The fault zone is in-between high-pressure eclogite-facies metabasites (hangingwall) and calcite bearing metasediments (footwall). The mafic rocks largely consist of upper greenschist facies hornblende, albite, chlorite, epidote with relict eclogitic garnet, Na-pyroxene and rutile; metasediments correspond to calcschist and micaschist with quartz, phengite, zoisite, chlorite, calcite and relics of garnet. Key features of the oucrop are: the thickness and geometry of the PT and gouge; the multiple production of PT characterized by overprinting plastic and brittle deformation; the occurrence in footwall metasediments of mm-thick bands of finely recrystallized calcite coeval with PT development in the hangingwall. The damage zone is ca. 2 m-thick and is characterized by two black, ultra-finegrained straight and sharp Principal Slip Zones (PSZ) marked by PT. The damage zone shows a variety of fault rocks (cataclasite and ultracataclasite, gouge and PT) with multiple crosscutting relationships. Within the two main PSZ, PT occurs in 10-20 cm thick layer, in small scale injection veins and in microfractures. In the mafic hanging wall, the PT is recrystallized and does not preserve glass: it shows flow structures with subrounded, embayed and rebsorbed quartz in a fine grained matrix composed of isotropic albite + chlorite + quartz + epidote + titanite, suggesting recrystallization

  14. Calculation of the 13C NMR shieldings of the C0 2 complexes of aluminosilicates

    Science.gov (United States)

    Tossell, J. A.

    1995-04-01

    complexation are much smaller. Complexation with CO 2 greatly increases the electric field gradient at the bridging oxygen of H 3AlOAlH 3-2, raising it to a value similar to that found for SiOSi linkages. Comparison of these results with the experimental 13C NMR spectra support the formation of CO 2-like complexes at SiOSi bridges in albite glasses and CO 3-like complexes at SiOAl and AlOAl bridges in albite and nepheline glasses. Changes in the calculated shieldings as Na + ions are added to the complexes suggest that some of the observed complexes may be similar in their CO 2-aluminosilicate interactions, but different with respect to the positions of the charge-compensating Na + ions.

  15. Inverse Geochemical Reaction Path Modelling and the Impact of Climate Change on Hydrologic Structure in Snowmelt-Dominated Catchments in the Southwestern USA

    Science.gov (United States)

    Driscoll, J. M.; Meixner, T.; Molotch, N. P.; Sickman, J. O.; Williams, M. W.; McIntosh, J. C.; Brooks, P. D.

    2011-12-01

    Snowmelt from alpine catchments provides 70-80% of the American Southwest's water resources. Climate change threatens to alter the timing and duration of snowmelt in high elevation catchments, which may also impact the quantity and the quality of these water resources. Modelling of these systems provides a robust theoretical framework to process the information extracted from the sparse physical measurement available in these sites due to their remote locations. Mass-balance inverse geochemical models (via PHREEQC, developed by the USGS) were applied to two snowmelt-dominated catchments; Green Lake 4 (GL4) in the Rockies and Emerald Lake (EMD) in the Sierra Nevada. Both catchments primarily consist of granite and granodiorite with a similar bulk geochemistry. The inputs for the models were the initial (snowpack) and final (catchment output) hydrochemistry and a catchment-specific suite of mineral weathering reactions. Models were run for wet and dry snow years, for early and late time periods (defined hydrologically as 1/2 of the total volume for the year). Multiple model solutions were reduced to a representative suite of reactions by choosing the model solution with the fewest phases and least overall phase change. The dominant weathering reactions (those which contributed the most solutes) were plagioclase for GL4 and albite for EMD. Results for GL4 show overall more plagioclase weathering during the dry year (214.2g) than wet year (89.9g). Both wet and dry years show more weathering in the early time periods (63% and 56%, respectively). These results show that the snowpack and outlet are chemically more similar during wet years than dry years. A possible hypothesis to explain this difference is a change in contribution from subsurface storage; during the wet year the saturated catchment reduces contact with surface materials that would result in mineral weathering reactions by some combination of reduced infiltration and decreased subsurface transit time. By

  16. Cachoeira Uranium Deposit, Lagoa Real, Bahia, Brazil – Kinematic, compositional and fluid evolution

    International Nuclear Information System (INIS)

    Pires, F.; Miano, S.

    2014-01-01

    The Cachoeira uranium albitite-type deposit occurs in a steep dip shear zone aligned with several other similar uranium deposits in the Lagoa Real Province. Uranium resources are estimated as about 90,000 t U_3O_8 [~76,000 t U] grading 2500 ppm U_3O_8 [~2100 ppm U]. Uraniferous albitite occupies a 15 m-thick strongly mylonitized shear zone structurally enclosed within “zebra” biotite gneiss. Uranium albitite mineralization forms cigar-shaped (prolate) and secondarily pancake-shaped (oblate) bodies composed of albite-hornblende-garnet-uraninite-magnetite ore grading to quartz-free skarntype rock with fluorite-kyanite-calcite-quartz concordant veins and pockets formed by late hydrothermal process. Brown chalcedony was the latest mineral to form. Fine-grained, disseminated uraninite is distributed and concentrated in the mafic portions of the gneiss consisting of hornblende andradite- sphene-apatite-epidote forming 30% and albite portions consisting of 70% of the albitite, which allows its gravitational treatment, thus decreasing acid leaching. While the host rock was severely affected by K-metasomatism the uraninite zone was deposited together with hornblende by Na- and Ca-metasomatism. Another reaction involves garnet crystallization exclusively together with uraninite, which liberates sílica and oxygen, differently from previous reaction which consumes silica and oxygen. Both reactions involve magnetite. The destabilization of biotite at the ore zone implies in the formation of GSPO-biotite overgrowing the LPO-biotite previously formed at host rock, due to the excess of K in the system. Magnetite is absent. The reaction represents the K-metasomatism at the host zebra gneiss: biotite + plagioclase + pyroxene + UO_2Cl"+ + Ca_2"+ = hornblende + uraninite + kyanite + quartz. The excess of Ca is allocated in the sphene, apatite and epidote structures. Consumption of Ca results in rutile deposition. As fluid composition was complex F and CO_2 were enriched in the

  17. Caracterización hidroquímica y análisis de los estados de equilibrio termodinámico en aguas termominerales de Alhama de Murcia (Murcia, Espana

    Directory of Open Access Journals (Sweden)

    Padilla Benítez, A.

    1993-04-01

    Full Text Available The principal physico-chemical characteristics of sorne thermomineral waters of Alhama de Murcia detrital aquifer are studied. The waters show a temperature between 26-41 °C and they are calcium-magnesium chloride-sulphate type. The origin of ions has a direct relationship with the dissolution of evaporitic sulphate-chloride salts, carbonatic and silica rocks, agricultural contamination processes and possibly ore-deposits. Mixing processes with cold waters possibly also occur. By SOLMINEQ.88 program the thermodinamic equilibrium conditions in surface are studied; the samples are saturated in quartz, chalcedony and albite. A great part of the waters are also saturated in calcite, aragonite, dolomite, gypsum, barite and magnesite. Finally, the waters are undersaturated in cristobalite, anhydrite and fluorite. Conventional chemical geothermometers yield a broad range of temperatures. Both, calcite-dolomite and anhydrite-fluorite geothermometers was applied to two samples with anomalous results. The saturation index modeling, at a series of growing temperatures, shows an approach equilibrium with quartz, chalcedony, albite, sanidine, gipsum, anhydrite, gibbsite and halloisite between 80-110 °C. A spread in the apparent equilibration temperatures deduced from two metodology, should be a consequence of dilution by surface waters, effects of re-equilibration of minerals with waters and CO2 loss. Temperature and chemical composition of the waters shows a thermal anomaly directly related with the tectonic activity in the area.Se estudian las principales características físico-químicas de algunas aguas termominerales del acuífero detrítico de Alhama de Murcia cuya temperatura está comprendida entre 26 y 41 °C y son de facies clorurada-sulfatada cálcico-magnésica. El origen de los iones encontrados está relacionado con la disolución de materiales evaporíticos, sales sulfatadas y cloruradas, carbonatados y silicatados, procesos de

  18. Geochemistry of biotite granites from the Lamas de Olo Pluton, northern Portugal

    Science.gov (United States)

    Fernandes, Susana; Gomes, Maria; Teixeira, Rui; Corfu, Fernando

    2013-04-01

    In the Central Iberian Zone (CIZ) extensive crustal recycling occurred during the post-thickening extension stage of the Variscan orogeny (~330-290 Ma). After the ductile deformation phase D3 (~320-300 Ma), characterized by the intrusion of large volumes of highly peraluminous granitic magmas, rapid and drastic tectonic changes at about 300 Ma gave rise to the brittle phase of deformation D4 that controlled the emplacement of Fe-K subalkaline granites (296-290 Ma; Dias et al. 1998). The Lamas de Olo Pluton (LOP) is controlled by NE-SW and NW-SE fracture systems, probably related to the Régua-Verin fault zone (Pereira, 1989). The LOP is a medium to coarse-grained, porphyritic biotite granite, accompanied by medium- to fine grained, porphyritic biotite granite (Alto dos Cabeços- AC) and a more leucocratic, fine-grained, slightly porphyritic biotite-muscovite granite (Barragens- BA). The contacts between LO and AC are generally diffuse, whereas those to BA are sharp. In fact, the BA granite can occur in dykes and sills cutting LO and AC. Microgranular enclaves and xenoliths are very rare. The LOP intrudes the Douro Group, presumably of Precambrian to Cambrian age, and two-mica granites from the Vila Real composite massif. The LOP granites consist of quartz, microcline, plagioclase, biotite, zircon, titanite, tourmaline apatite, fluorite, ilmenite, magnetite, and rutile, with muscovite in BA granite and rare allanite in the LO and AC granites. The plagioclase composition is of oligoclase (An12) - andesine (An35) for LO granite, albite (An9) - andesine (An30) for CA granite and albite (An5) - oligoclase (An20) for BA granite. There are decreases in: a) anorthite content from phenocryst to matrix plagioclase; b) Ba content from phenocryst to matrix microcline in all granites. The Fe2+ biotite has a composition similar to that of biotite from calc-alkaline to sub-alkaline rock series. The LO and AC granites are meta- to peraluminous with ASI variable between 1.05 and 1

  19. Emplacement model of obsidian-rhyolite magma deduced from complete internal section of the Akaishiyama lava, Shirataki, northern Hokkaido, Japan

    Science.gov (United States)

    Wada, K.; Sano, K.

    2016-12-01

    Simultaneously explosive and effusive eruptions of silicic magmas has shed light on the vesiculation and outgassing history of ascending magmas in the conduit and emplacement model of obsidian-rhyolite lavas (Castro et al., 2014; Shipper et al, 2013). As well as the knowledge of newly erupted products such as 2008-2009 Chaitén and 2011-2012 Cordón Caule eruptions, field and micro-textural evidences of well-exposed internal structure of obsidian-rhyolite lava leads to reveal eruption processes of silicic magmas. The Shirataki monogenetic volcano field, 2.2 million year age, northern Hokkaido, Japan, contains many outcrops of obsidian and vesiculated rhyolite zones (SiO2=76.7-77.4 wt.%). Among their outcrops, Akaishiyama lava shows good exposures of internal sections from the top to the bottom along the Kyukasawa valley with thickness of about 190 meters, showing the symmetrical structure comprising a upper clastic zone (UCZ; 5m thick), an upper dense obsidian zone (UDO; 15m), an upper banded obsidian zone (UBO; 70-80m), a central rhyolite zone (CR; 65m), a lower banded obsidian zone (LBO; 15m), a lower dense obsidian zone (LDO; 20m), and a lower clastic zone (LCZ; 3m). The upper banded obsidian zone is characterized by existence of spherulite concentration layers with tuffisite veins and rhyolite enclaves. Spherulites consisting of albite, cristobalaite and obsidian glass, are clustered in the dense obsidian. Tuffisite veins show brecciated obsidians in tuffaceous matrix, showing an outgassing path during the emplacement of obsidian lava. Perpendicular dip of spherulite parallel rows indicates the banded zone itself was the domain of vent area. From the observation of these occurrences in the internal section and rock texture, we show the qualitative formation model of Shirataki obsidian-rhyolite lava.

  20. On the interaction of pure and impure supercritical CO2 with rock forming minerals in saline aquifers: An experimental geochemical approach

    International Nuclear Information System (INIS)

    Wilke, Franziska D.H.; Vásquez, Mónica; Wiersberg, Thomas; Naumann, Rudolf; Erzinger, Jörg

    2012-01-01

    The aim of this experimental study was to evaluate and compare the geochemical impact of pure and impure CO 2 on rock forming minerals of possible CO 2 storage reservoirs. This geochemical approach takes into account the incomplete purification of industrial captured CO 2 and the related effects during injection, and provides relevant data for long-term storage simulations of this specific greenhouse gas. Batch experiments were conducted to investigate the interactions of supercritical CO 2 , brine and rock-forming mineral concentrates (albite, microcline, kaolinite, biotite, muscovite, calcite, dolomite and anhydrite) using a newly developed experimental setup. After up to 42 day (1000 h) experiments using pure and impure supercritical CO 2 the dissolution and solution characteristics were examined by XRD, XRF, SEM and EDS for the solid, and ICP–MS and IC for the fluid reactants, respectively. Experiments with mixtures of supercritical CO 2 (99.5 vol.%) and SO 2 or NO 2 impurities (0.5 vol.%) suggest the formation of H 2 SO 4 and HNO 3 , reflected in pH values between 1 and 4 for experiments with silicates and anhydrite and between 5 and 6 for experiments with carbonates. These acids should be responsible for the general larger amount of cations dissolved from the mineral phases compared to experiments using pure CO 2 . For pure CO 2 a pH of around 4 was obtained using silicates and anhydrite, and 7–8 for carbonates. Dissolution of carbonates was observed after both pure and impure CO 2 experiments. Anhydrite was corroded by approximately 50 wt.% and gypsum precipitated during experiments with supercritical CO 2 + NO 2 . Silicates do not exhibit visible alterations during all experiments but released an increasing amount of cations in the reaction fluid during experiments with impure CO 2 . Nonetheless, precipitated secondary carbonates could not be identified.

  1. Geochemical effects of CO2 sequestration in sandstones under simulated in situ conditions of deep saline aquifers

    International Nuclear Information System (INIS)

    Wigand, M.; Carey, J.W.; Schuett, H.; Spangenberg, E.; Erzinger, J.

    2008-01-01

    The geochemical effects of brine and supercritical CO 2 (SCCO 2 ) on reservoir rocks from deep (1500-2000 m) saline aquifers were examined via experimental simulation at in situ conditions. Dry sandstone samples were mounted in a triaxial cell and autoclave system, evacuated, and saturated with 1 M NaCl solution. The brine-rock system was allowed to react at 30 MPa confining pressure, 15 MPa pore fluid pressure, and 60 deg. C while SCCO 2 was injected at a pressure gradient of 1-2 MPa. The experiment was conducted for a period of 1496 h, during which fluids were periodically sampled and analyzed. The pH measured in partially degassed fluid samples at 25 deg. C decreased from a starting value of 7.0-4.3 (9 days) and finally 5.1 after saturation with SCCO 2 . Fluid analyses indicate that most of the major (e.g. Ca, Mg, Fe, Mn) and trace elements (e.g. Sr, Ba, Pb) of the sandstone increase in concentration during the reaction with brine and SCCO 2 . These results are supported by scanning electron microscopy which indicates dissolution of dolomite cement, K-feldspar, and albite. In addition to dissolution reactions the formation of montmorillonite was observed. By adjusting surface area and reaction rates of dissolution and precipitation, geochemical modeling of the experiments could reproduce long-term trends in solution chemistry and indicated limited rates of dissolution as the system remained strongly undersaturated with most minerals, including carbonates. The geochemical models could not account for decreases in concentration of some elements, changes in solution composition resulting from changes in imposed pressure gradient, and the observed Ca/Mg and Si/Al ratios in solution

  2. Hydrochemical Characteristics and Evolution Laws of Drinking Groundwater in Pengyang County, Ningxia, Northwest China

    Directory of Open Access Journals (Sweden)

    Li Peiyue

    2011-01-01

    Full Text Available The purpose of the paper is to identify the chemical characteristics of drinking groundwater and its distribution patterns in Pengyang County and to discover the hydrochemical evolution laws of groundwater. The temporal and spatial variation of groundwater hydrochemical characteristics and evolution laws were comprehensively and systematically studied based on the understanding of the geological, hydrogeological, meteorological and hydrological conditions. Many analytical methods such as descriptive statistics, geostatistical analysis, ionic ratio coefficient method and correlation analysis were adopted based on the underground water quality analysis data. Study results showed that variation coefficients of chemical parameters of pore water in unconsolidated rocks were relatively high which indicated that water chemical compositions are vulnerable to topography, meteorology, hydrology and human activities. TDS variation was in accordance with the changes in Ca2+, Mg2+ and SO42- concentration. Hydrochemical type varied from HCO3•SO4-Na•Ca•Mg type and HCO3•SO4-Ca•Mg type at the upper reaches towards gradually to HCO3-Na type at the lower reaches. Ionic ratio coefficient analysis showed that the hydrodynamic conditions of the pore water in loose rocks were better than that of pore-fissure water in clastic rocks and groundwater was non-marine deposited water. Its formation effects include the weathering leaching effects of the formation containing rock salt, water-rock interaction and cation exchange reaction. Hydrochemical characteristics were mainly controlled by geological and hydrogeological conditions. Correlation analysis showed that the dissolution of rock salt and sodium sulfate salt as well as calcite precipitation occurred in pore water and in pore-crack water in clastic rocks the dissolution of albite, K-feldspar and the precipitation of dolomite were also important effects.

  3. Integrating petrography, mineralogy and hydrochemistry to constrain the influence and distribution of groundwater contributions to baseflow in poorly productive aquifers: insights from Gortinlieve catchment, Co. Donegal, NW Ireland.

    Science.gov (United States)

    Caulfield, John; Chelliah, Merlyn; Comte, Jean-Christophe; Cassidy, Rachel; Flynn, Raymond

    2014-12-01

    Identifying groundwater contributions to baseflow forms an essential part of surface water body characterisation. The Gortinlieve catchment (5 km(2)) comprises a headwater stream network of the Carrigans River, itself a tributary of the River Foyle, NW Ireland. The bedrock comprises poorly productive metasediments that are characterised by fracture porosity. We present the findings of a multi-disciplinary study that integrates new hydrochemical and mineralogical investigations with existing hydraulic, geophysical and structural data to identify the scales of groundwater flow and the nature of groundwater/bedrock interaction (chemical denudation). At the catchment scale, the development of deep weathering profiles is controlled by NE-SW regional scale fracture zones associated with mountain building during the Grampian orogeny. In-situ chemical denudation of mineral phases is controlled by micro- to meso-scale fractures related to Alpine compression during Palaeocene to Oligocene times. The alteration of primary muscovite, chlorite (clinochlore) and albite along the surfaces of these small-scale fractures has resulted in the precipitation of illite, montmorillonite and illite-montmorillonite clay admixtures. The interconnected but discontinuous nature of these small-scale structures highlights the role of larger scale faults and fissures in the supply and transportation of weathering solutions to/from the sites of mineral weathering. The dissolution of primarily mineral phases releases the major ions Mg, Ca and HCO3 that are shown to subsequently form the chemical makeup of groundwaters. Borehole groundwater and stream baseflow hydrochemical data are used to constrain the depths of groundwater flow pathways influencing the chemistry of surface waters throughout the stream profile. The results show that it is predominantly the lower part of the catchment, which receives inputs from catchment/regional scale groundwater flow, that is found to contribute to the

  4. Hydrochemical investigation and status of geochemical modeling of groundwater evolution at the Kamaishi in-situ tests site, Japan

    International Nuclear Information System (INIS)

    Sasamoto, Hiroshi; Yui, Mikazu; Arthur, Randolph C.

    1999-07-01

    The results of hydrochemical investigations of groundwaters in the Kurihashi granodiorite at JNC's Kamaishi in-situ tests site indicate that these solutions are: meteoric in origin, chemically reducing (at depths greater than a few hundreds meters), relatively young [residence times in the Kurihashi granodiorite generally less than about 40 years, but groundwaters older than several thousand years BP (before present) are also indicated by preliminary carbon-14 dating of samples obtained from the KH-1 borehole], Ca-HCO 3 type solutions near the surface, changing to Na-HCO 3 type groundwaters with increasing depth. The evolution of groundwater compositions in the Kurihashi granodiorite is modeled assuming local equilibrium for selected mineral-fluid reactions, taking into account the rainwater origin of these solutions. Results suggest it is possible to interpret approximately the 'real' groundwater chemistry (i.e., pH, Eh, total dissolved concentrations of Si, Na, Ca, K, Al, carbonate and sulfate) in the Kurihashi granodiorite if the following assumptions are adopted: CO 2 concentration in the gas phase contacting pore solutions in the overlying soil zone=10 -2 bar, minerals in the rock zone that control the solubility of respective elements in the groundwater include; chalcedony (Si), albite (Na), kaolinite (Al), calcite (Ca and carbonate), microcline (K) and pyrite (Eh and sulfate). Discussions with international experts suggest a systematic approach utilizing reaction-path models of irreversible water-rock interactions in open systems may be needed to more realistically model groundwater evolution at the Kamaishi test site. Detailed information characterizing certain site properties (e.g., fracture mineralogy) may be required to adequately constrain such models, however. (author)

  5. Metamorphic Evolution of Garnet-bearing Epidote-Barroisite Schist from the Meratus Complex in South Kalimantan, Indonesia

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    Nugroho Imam Setiawan

    2015-09-01

    Full Text Available DOI:10.17014/ijog.2.3.139-156This paper presents metamorphic evolution of metamorphic rocks from the Meratus Complex in South Kalimantan, Indonesia. Eight varieties of metamorphic rocks samples from this location, which are garnet-bearing epidote-barroisite schist, epidote-barroisite schist, glaucophane-quartz schist, garnet-muscovite schist, actinolite-talc schist, epidote schist, muscovite schist, and serpentinite, were investigated in detail its petrological and mineralogical characteristics by using polarization microscope and electron probe micro analyzer (EPMA. Furthermore, the pressure-temperature path of garnet-bearing epidote-barroisite schist was estimated by using mineral parageneses, reaction textures, and mineral chemistries to assess the metamorphic history. The primary stage of this rock might be represented by the assemblage of glaucophane + epidote + titanite ± paragonite. The assemblage yields 1.7 - 1.0 GPa in assumed temperature of 300 - 550 °C, which is interpreted as maximum pressure limit of prograde stage. The peak P-T condition estimated on the basis of the equilibrium of garnet rim, barroisite, phengite, epidote, and quartz, yields 547 - 690 °C and 1.1 - 1.5 GPa on the albite epidote amphibolite-facies that correspond to the depth of 38 - 50 km. The retrograde stage was presented by changing mineral compositions of amphiboles from the Si-rich barroisite to the actinolite, which lies near 0.5 GPa at 350 °C. It could be concluded that metamorphic rocks from the Meratus Complex experienced low-temperature and high-pressure conditions (blueschist-facies prior to the peak metamorphism of the epidote amphibolite-facies. The subduction environments in Meratus Complex during Cretaceous should be responsible for this metamorphic condition.

  6. Status of geochemical modeling of groundwater evolution at the Tono in-situ tests site, Japan

    International Nuclear Information System (INIS)

    Sasamoto, Hiroshi; Yui, Mikazu; Arthur, R.C.

    1999-12-01

    Hydrochemical investigation of Tertiary sedimentary rocks at JNC's Tono in-situ tests site indicate the groundwaters are: meteoric in origin, chemically reducing at depths greater than a few tens of meters in the sedimentary rock, relatively old [carbon-14 ages of groundwaters collected from the lower part of the sedimentary sequence range from 13,000 to 15,000 years BP (before present)]. Ca-Na-HCO 3 type solutions near the surface, changing to Na-HCO 3 type groundwaters with increasing depth. The chemical evolution of the groundwaters is modeled assuming local equilibrium for selected mineral-fluid reactions, taking into account the rainwater origin of these solutions. Results suggest it is possible to interpret approximately the 'real' groundwater chemistry (i.e., pH, Eh, total dissolved concentrations of Si, Na, Ca, K, Al, carbonate and sulfate) if the following assumptions are adopted: CO 2 concentration in the gas phase contacting pore solutions in the overlying soil zone=10 -1 bar, minerals in the rock zone that control the solubility of respective elements in the groundwater include; chalcedony (Si), albite (Na), kaolinite (Al), calcite (Ca and carbonate), muscovite (K) and pyrite (Eh and sulfate). It is noted, however, that the available field data may not be sufficient to adequately constrain parameters in the groundwater evolution model. In particular, more detailed information characterizing certain site properties (e.g., the actual mineralogy of 'plagioclase', 'clay' and 'zeolite') are needed to improve the model. Alternative conceptual models of key reactions may also be necessary. For this reason, a model that accounts for ion-exchange reactions among clay minerals, and which is based on the results of laboratory experiments, has also been evaluated in the present study. Further improvements of model considering ion-exchange reactions are needed in future, however. (author)

  7. Low temperature geothermal systems in carbonate-evaporitic rocks: Mineral equilibria assumptions and geothermometrical calculations. Insights from the Arnedillo thermal waters (Spain).

    Science.gov (United States)

    Blasco, Mónica; Gimeno, María J; Auqué, Luis F

    2018-02-15

    Geothermometrical calculations in low-medium temperature geothermal systems hosted in carbonate-evaporitic rocks are complicated because 1) some of the classical chemical geothermometers are, usually, inadequate (since they were developed for higher temperature systems with different mineral-water equilibria at depth) and 2) the chemical geothermometers calibrated for these systems (based on the Ca and Mg or SO 4 and F contents) are not free of problems either. The case study of the Arnedillo thermal system, a carbonate-evaporitic system of low temperature, will be used to deal with these problems through the combination of several geothermometrical techniques (chemical and isotopic geothermometers and geochemical modelling). The reservoir temperature of the Arnedillo geothermal system has been established to be in the range of 87±13°C being the waters in equilibrium with respect to calcite, dolomite, anhydrite, quartz, albite, K-feldspar and other aluminosilicates. Anhydrite and quartz equilibria are highly reliable to stablish the reservoir temperature. Additionally, the anhydrite equilibrium explains the coherent results obtained with the δ 18 O anhydrite - water geothermometer. The equilibrium with respect to feldspars and other aluminosilicates is unusual in carbonate-evaporitic systems and it is probably related to the presence of detrital material in the aquifer. The identification of the expected equilibria with calcite and dolomite presents an interesting problem associated to dolomite. Variable order degrees of dolomite can be found in natural systems and this fact affects the associated equilibrium temperature in the geothermometrical modelling and also the results from the Ca-Mg geothermometer. To avoid this uncertainty, the order degree of the dolomite present in the Arnedillo reservoir has been determined and the results indicate 18.4% of ordered dolomite and 81.6% of disordered dolomite. Overall, the results suggest that this multi

  8. Petrography, geochemistry and geochronology of the host porphyries and associated alteration at the Tuwu Cu deposit, NW China: a case for increased depositional efficiency by reaction with mafic hostrock?

    Science.gov (United States)

    Shen, Ping; Pan, Hongdi; Zhou, Taofa; Wang, Jingbin

    2014-08-01

    Tuwu is the largest porphyry copper deposit discovered in the Eastern Tianshan Mountains, Xinjiang, China. A newly recognized volcanic complex in the Early Carboniferous Qi'eshan Group at Tuwu consists of basalt, andesite, and diorite porphyry. The plagiogranite porphyry was emplaced into this complex at 332.8±2.5 Ma (U-Pb zircon SIMS determination). Whole-rock element geochemistry shows that the volcanic complex and plagiogranite porphyry formed in the same island arc, although the complex was derived by partial melting of the mantle wedge and the plagiogranite porphyry by partial melting of a subducting slab. The diorite and the plagiogranite porphyries have both been subjected to intense hydrothermal alteration and associated mineralization, but the productive porphyry is the plagiogranite porphyry. Three alteration and mineralization stages, including pre-, syn- and post-ore stages, have been recognized. The pre-ore stage formed a barren propylitic alteration which is widespread in the volcanic complex. The syn-ore stage is divided into three sub-stages: Stage 1 is characterized by potassic alteration with chalcopyrite + bornite + chalcocite; Stage 2 is marked by chlorite-sericite-albite alteration with chalcopyrite ± pyrite ± bornite; Stage 3 is represented by phyllic alteration with chalcopyrite + pyrite ± molybdenite. The post-ore stage produced a barren argillic alteration limited to the diorite porphyry. A specific feature of the Tuwu deposit is that the productive porphyry was emplaced into a very mafic package, and reaction of the resulting fluids with the ferrous iron-rich hostrocks was a likely reason that Tuwu is the largest porphyry in the district.

  9. Ore deposits and epithermal evidences associated with intra-magmatic faults at Aïn El Araâr-Oued Belif ring structure (NW of Tunisia)

    Science.gov (United States)

    Aissa, Wiem Ben; Aissa, Lassaâd Ben; Amara, Abdesslem Ben Haj; Tlig, Said; Alouani, Rabah

    2017-03-01

    Hydrothermal ore deposits at Aïn El Araâr-Oued Belif location are classified as epithermal deposits type. The ore bodies are hosted by upper Turonian (8-9 M.y) volcanic rhyodacitic complex. Polymetallic sulfide orebodies are mainly concentrated within intra-magmatic faults. Petrographic, XRD, and TEM-STEM investigations revealed that ore minerals are essentially, arsenopyrite, pyrite, chalcopyrite, pyrrhotite, hematite, goethite and magnetite with Au, Ag and Pt trace metals. Gangue minerals are mainly adularia, quartz, sericite, alunite, tridymite, chlorite, phlogopite and smectite. Epithermal alteration is well zoned with four successive characteristic zones: (1) zone of quartz-adularia-sericite and rare alunite; (2) zone of kaolinite and plagioclase albitization; (3) intermediate zone of illite-sericite; (4) sapropelic alteration type zone of chlorite-smectite and rare illite. This can be interpreted as a telescoping of two different acidity epithermal phases; low sulfidation (adularia-sericite) and high sulfidation (quartz-alunite), separated in time or due to a gradual increase of fluids acidity and oxicity within the same mineralization phase. Brecciated macroscopic facies with fragments hosting quartz-adularia-sericite minerals (low-sulfidation phase) without alunite, support the last hypothesis. Geodynamic context and mineral alteration patterns are closely similar to those of Maria Josefa gold mine at SE of Spain which exhibit a volcanic-hosted epithermal ore deposit in a similar vein system, within rhyolitic ignimbrites, altered to an argillic assemblage (illite-sericite abundant and subordinate kaolinite) that grades outwards into propylitic alteration (Sanger-von Oepen et al. (1990)). Mineralogical and lithologic study undertaken in the volcanic host rock at Aïn El Araâr-Oued Belif reveals a typical epithermal low-sulfidation and high-sulfidation ore deposits with dominance of low-sulfidation. Host rocks in these systems range from silicic to

  10. Geochemical behavior of rare earth elements of the hydrothermal alterations within the Tepeoba porphyry Cu-Mo-Au deposits at Balikesir, NW Turkey

    Science.gov (United States)

    Doner, Zeynep; Abdelnasser, Amr; Kiran Yildirim, Demet; Kumral, Mustafa

    2016-04-01

    This work reports the geochemical characteristics and behavior of the rare earth elements (REE) of the hydrothermal alteration of the Tepeoba porphyry Cu-Mo-Au deposit located in the Anatolian tectonic belt at Biga peninsula (Locally Balikesir province), NW Turkey. The Cu-Mo-Au mineralization at this deposit hosted in the hornfels rocks and related to the silicic to intermediate intrusion of Eybek pluton. It locally formed with brecciated zones and quartz vein stockworks, as well as the brittle fracture zones associated with intense hydrothermal alteration. Three main alteration zones with gradual boundaries formed in the mine area in the hornfels rock that represents the host rock, along that contact the Eybek pluton; potassic, propylitic and phyllic alteration zones. The potassic alteration zone that formed at the center having high amount of Cu-sulfide minerals contains biotite, muscovite, and sericite with less amount of K-feldspar and associated with tourmalinization alteration. The propylitic alteration surrounds the potassic alteration having high amount of Mo and Au and contains chlorite, albite, epidote, calcite and pyrite. The phyllic alteration zone also surrounds the potassic alteration containing quartz, sericite and pyrite minerals. Based on the REE characteristics and content and when we correlate the Alteration index (AI) with the light REEs and heavy REEs of each alteration zone, it concluded that the light REEs decrease and heavy REEs increase during the alteration processes. The relationships between K2O index with Eu/Eu* and Sr/Sr* reveals a positive correlation in the potassic and phyllic alteration zones and a negative correlation in the propylitic alteration zone. This refers to the hydrothermal solution which is responsible for the studied porphyry deposits and associated potassic and phyllic alterations has a positive Eu and Sr anomaly as well as these elements were added to the altered rock from the hydrothermal solution. Keywords: Rare

  11. A mineral quantification method for wall rocks at open pit mines, and application to the Martha Au-Ag mine, Waihi, New Zealand

    International Nuclear Information System (INIS)

    Castendyk, Devin N.; Mauk, Jeffrey L.; Webster, Jenny G.

    2005-01-01

    Pit lakes that result from open pit mining are potential water resources or potential environmental problems, depending on lake water quality. Wall rock mineralogy can affect lake chemistry if surface water inputs and/or groundwater inputs and/or lake water in contact with submerged wall rocks react with the wall rock minerals. This study presents a mineral quantification method to measure the distribution and concentration of wall rock minerals in open pit mines, and applies the method to the Martha epithermal Au-Ag mine, Waihi, New Zealand. Heterogeneous ore deposits, like Martha, require a large number of wall rock samples to accurately define mineral distributions. X-ray diffraction analyses of 125 wall rock samples identified the most abundant minerals in the wall rocks as quartz, adularia, albite, illite, chlorite, kaolinite, pyrite and calcite. Distribution maps of these minerals defined 8 relatively homogenous areas of wall rock referred to as 'mineral associations': weakly-altered, propylitic, fresh-argillic, weathered-argillic, oxidized, potassic, quartz veins, and post-mineralization deposits. X-ray fluorescence, Leco furnace, and neutron activation analyses of 46 representative samples produced the geochemical dataset used to assign quantities of elements to observed minerals, and to calculate average mineral concentrations in each association. Thin-section petrography and calcite concentrations from Sobek acid-digestions confirm the calculated mineralogy, providing validation for the method. Calcite and pyrite concentrations allowed advanced acid-base accounting for each mineral association, identifying 3 potential acid-producing associations and one potential acid-neutralizing association. The results target areas, where detailed hydrologic and kinetic tests would be valuable in the next stage of pit lake evaluation. Detailed understanding of wall rock mineralogy will help strengthen predictions of pit lake water quality

  12. A mineral quantification method for wall rocks at open pit mines, and application to the Martha Au-Ag mine, Waihi, New Zealand

    Energy Technology Data Exchange (ETDEWEB)

    Castendyk, Devin N. [Environmental Science, SGES, University of Auckland, Tamaki Campus, Private Bag 92019, Auckland (New Zealand)]. E-mail: d.castendyk@auckland.ac.nz; Mauk, Jeffrey L. [Geology Department, University of Auckland, Private Bag 92019, Auckland (New Zealand); Webster, Jenny G. [Environmental Science, SGES, University of Auckland, Tamaki Campus, Private Bag 92019, Auckland (New Zealand)

    2005-01-01

    Pit lakes that result from open pit mining are potential water resources or potential environmental problems, depending on lake water quality. Wall rock mineralogy can affect lake chemistry if surface water inputs and/or groundwater inputs and/or lake water in contact with submerged wall rocks react with the wall rock minerals. This study presents a mineral quantification method to measure the distribution and concentration of wall rock minerals in open pit mines, and applies the method to the Martha epithermal Au-Ag mine, Waihi, New Zealand. Heterogeneous ore deposits, like Martha, require a large number of wall rock samples to accurately define mineral distributions. X-ray diffraction analyses of 125 wall rock samples identified the most abundant minerals in the wall rocks as quartz, adularia, albite, illite, chlorite, kaolinite, pyrite and calcite. Distribution maps of these minerals defined 8 relatively homogenous areas of wall rock referred to as 'mineral associations': weakly-altered, propylitic, fresh-argillic, weathered-argillic, oxidized, potassic, quartz veins, and post-mineralization deposits. X-ray fluorescence, Leco furnace, and neutron activation analyses of 46 representative samples produced the geochemical dataset used to assign quantities of elements to observed minerals, and to calculate average mineral concentrations in each association. Thin-section petrography and calcite concentrations from Sobek acid-digestions confirm the calculated mineralogy, providing validation for the method. Calcite and pyrite concentrations allowed advanced acid-base accounting for each mineral association, identifying 3 potential acid-producing associations and one potential acid-neutralizing association. The results target areas, where detailed hydrologic and kinetic tests would be valuable in the next stage of pit lake evaluation. Detailed understanding of wall rock mineralogy will help strengthen predictions of pit lake water quality.

  13. Alteration and petrology of Intrusive Rocks associated with Gold Mineralization at Kuh-E-Zar Gold Deposit, Torbat-e-Heydaryeh

    Directory of Open Access Journals (Sweden)

    Alireza Mazloumi Bajestani

    2009-09-01

    Full Text Available Kuh- e -Zar gold deposit located 35 km west of Torbat-e-Heydaryeh, (Khorassan e- Razavi province, East of Iran. This deposit is a specularite-rich Iron oxide type (IOCG. This mine is situated within Khaf-Bardascan volcanic plutonic belt. Based on recent exploration along this belt, several IOCG type system plus Kuh-e-Zar deposit are discovered. In the study area, several type of tuff and lava having acid to intermediate composition are identified (upper Eocene. Oligo-Miocene granite, granodiorite, synogranite and monzonite intruded upper Eocene andesite-dacite-rhyolite. Intrusive rocks are meta-aluminous, medium to high-K series I-type. Based on spider diagram, intrusive rocks show enrichment in LILE = K, Th, Rb and depletion in HFSE = Nb, Sr, Ti. Based geochemistry of igneous rock, they formed in continental margin subduction zone. Propylitic (chlorite alteration is dominated and covers large area. Silicification is restricted only to mineralized zones. Argillic and albitization is found in certain location and cover small areas. The style of mineralization was controlled by the type and geometry of fault zones. Mineralization is found as vein, stockwork and breccias. Hypogene mineral Paragenesis include: specularite-quartz-gold-chlorite ± chalcopyrite ± pyrite ± galena ± barite. Secondary minerals formed due to oxidation are: goethite, limonite, lepidocrucite, Malachite, Azurite, Covelite, Cerucite, hydrocerucite, Pyrolusite and Smitsonite. In a few localities, chalcopyrite and minor pyrite and galena are found. Based on SEM analysis gold is present as electrum. Mineralization appeared in different type such as vein, stockwork and Hydrothermal breccia in strike sleep fault zone which are hidden inside volcano plutonic rocks. The average gold grade is between 3.02 ppm and ore reserve is estimated more than 3 million tons (cut off grade = 0.7 ppm.

  14. Investigation of Enhanced Leaching of Lithium from α-Spodumene Using Hydrofluoric and Sulfuric Acid

    Directory of Open Access Journals (Sweden)

    Hui Guo

    2017-10-01

    Full Text Available An effective method using hydrofluoric and sulfuric acid was proposed to enhance the leaching of lithium from α-spodumene, without calcination that is subjected to 1000 °C for phase transformation. The thermodynamic feasibility of the reactions was firstly verified. Dissolution conditions were tested to maximize the leaching efficiency of lithium and with efficient utilization of hydrofluoric acid (HF served as evaluation criteria. The results showed that 96% of lithium could be transferred into lixivium with an ore/HF/H2SO4 ratio of 1:3:2 (g/mL/mL, at 100 °C for 3 h. Due to the fact that HF molecules were the main reaction form, the dissolution behaviors were theoretically represented and investigated by dissolution in HF/H2SO4. When combined with chemical elements analyses and characterizations, the results of the dissolution behaviors revealed that α-spodumene and albite were preferentially dissolved over quartz. Insoluble fluoroaluminates, such as AlF3, cryolite (Na3AlF6 and cryolithionite (Na3Li3Al2F12, were generated and might be further partially dissolved by H2SO4. Fluorosilicates, such as K2SiF6, Na2SiF6, or KNaSiF6, were also generated as a part of the insoluble residues. This work provides fundamental insight into the role of HF/H2SO4 played in the dissolution of α-spodumene, and sheds light on a novel and promising process to efficiently extract lithium.

  15. Geochemical modelling of water-rock interactions at the Osamu Utsumi mine and Morro do Ferro analogue study sites, Pocos de Caldas, Brazil

    International Nuclear Information System (INIS)

    Nordstrom, D.K.; Puigdomenech, I.; McNutt, R.H.

    1990-01-01

    Geochemical processes involving water-rock interactions have been modelled using groundwater composition, mineralogical data, ion plots and computations of speciation, non-thermodynamic mass balance and thermodynamic mass transfer for two natural analogue sites near Pocos de Caldas, Brazil: the Osamu Utsumi mine and Morro do Ferro. The main rock type is an alkaline igneous complex composed of volcanic and sub-volcanic phonolites that have been hydrothermally altered and highly weathered. This altered rock mass grades from a laterite at the surface to a saprolite and finally to unweathered, hydrothermally altered bedrock at depth. The mine site contains high concentrations of uranium and Morro do Ferro contains high concentrations of thorium and rare-earths. The reaction models can reproduce the water chemistry and mineral occurences and they were validated by predicting the masses of minerals precipitated and the pH of the final water. The model computations can also reproduce the pH and iron concentrations of the water samples during CO 2 degassing and iron(II) oxidation from exposure to air. The results from the geochemical reaction models reveal that the dominant processes are production of CO 2 in the soil zone through aerobic decay of organic matter, dissolution of fluorite, calcite, K-feldspar, albite and manganese oxides, oxidation of pyrite and sphalerite and precipitation of ferric oxides, silica and kaolinite. Recharge waters are undersaturated with respect to barite and discharging waters and deeper groundwaters are saturated to supersaturated with respect to barite, demonstrating a strong equilibrium solubility control. Strontium isotope data demonstrate that sources other than calcium-bearing minerals are required to account for the dissolved strontium in the ground. These may include K-feldspar, smectite-chlorite mixed-layer clays and goyazite. (author) 24 figs., 4 tabs., 18 refs

  16. Geochemistry, mineralization and age of tin-bearing ganites from Pitinga, nortwestern Brazil

    International Nuclear Information System (INIS)

    Macambira, M.J.B.; Teixeira, J.T.; Daoud, W.E.K.; Costi, H.T.

    1987-01-01

    One of the important geological units of the Central Amazonian Provinceis formed by anarogenic granit plutons, some of them associated with important ore deposits. The larget ore deposits of SN,Zr,Nb,Ta, and REE in this Province are associeted with the madeira (MD) and Agua Boa (AB) plutons, Pitinga region, NW Brazil. These plutons crosscut the volcanic rocks from Iricoume Group and sediments from Urupi formation, and follow the regional trend, suggesting magma ascension along deep faults. These plutons are composed by three granitic units, which are, in order of emplacement: granite with rapakivi tendency; fine-grained porphyritic granite; and biotite granite. There are metasomatic variations to greisen (in AB pluton) and apogranite (in MD pluton) associated genetically with ore deposits. Major and trace elements contents shown sub-alkalic to peraluminous characteristics, with an increasing of SiO 2 , F,Sn,Rb, and Y, and a decreasing of Al 2 O 3 , FeO,Fe 2 O 3 ,CaO,MgO,TiO 2 ,Sr,Zr and Nb toward the biotite granite. As a whole, AB pluton has the lowest Nb contents, while the MD pluton has the lowest Y and REE contents. The REE patterns of AB and MD are similar, showing high absolute contents, pronounced negative Eu anomalies, and a little fractionated patterns. The apogranite is depleted in LREE by albitization process. Rb-Sr whole-rock isochron constructed with nine samples from AB and MD plutons indicates an age of 1,691 +- 34 Ma with initial ratio of 0.7062 +- 0.0067. The geological and geochemical features of AB and MD plutons are similar with cratogenic bodies originated in tensional regions, as A-type granites. However, the classifications of these plutons in separated regional suites is not well established due to absence of more strong criteria to do so, up to now. (author) [pt

  17. Petrology of Terra Nova pluton, Brazil, and associated ultrapotassic dykes

    International Nuclear Information System (INIS)

    Silva Filho, A.F. da; Thompson, R.N.; Leat, P.T.

    1987-01-01

    The Upper Precambrian Terra Nova Pluton, situated 550 Km inland from Recife, Brazil, is 220 Km 2 in area and intrudes deformed metasedimentary rocks of the Pianco-Alto Brigida Mobile Belt. The Pluton shows complex petrological relationships. It consists of subalkaline quartz-monzonites and quartz-syenites, and the major minerals are K-feldspars, albite, hornblende, and quartz. The pluton is intermediate in composition (SiO 2 = 58.9-65.6 wt%, MgO=0.9-3.7 wt%) and is dominantly potassic (K 2 O=3.3-5.6 wt %; K 2 O/Na 2 O=0.9-1.8). Ba (up to 2.300 ppm) and Sr (up to 1,100 ppm) are abundant in the rocks, and LREE are enriched relative to HREE (La N /Lu N = 25.6-43.2). There is no significant Eu Anomaly. Rounded autoliths within the pluton are similar, but more mafic in composition (SiO 2 =54.6-57.5 wt %; MgO=4.9-6.4 wt %). A suite of dykes cut pluton and the surrounding country rocks. These dykes are varied in composition, encompassing most of the chemical range shown by the pluton and associated autoliths. The dykes are holocrystalline, peralkaline, and strongly enriched in both K 2 O(K 2 O=5.3-11.4 wt %) and Ba (Ba=2,400 ppm-10,500 ppm), which are considered to be magmatic abundances. The dykes have similar REE and other trace elements and ratios to the autoliths and plutonic rocks, and the dykes and the pluton are thought to be chemically related. The Terra Nova Pluton records the fractionation of mantle-derived ultrapotassic magma from mafic to intermediate compositions. (author) [pt

  18. Paleotransport of lanthanides and strontium recorded in calcite compositions from tuffs at Yucca Mountain, Nevada, USA

    International Nuclear Information System (INIS)

    Vaniman, D.T.; Chipera, S.J.

    1996-01-01

    Secondary calcite occurs in both saturated and unsaturated hydrologic zones (SZ and UZ, respectively) in the tuffs at Yucca Mountain, Nevada, USA. In the upper UZ, the major constituents of the calcite crystal structure (C, O) have surface origins. At greater depth there is a open-quotes barren zone,close quotes straddling the water table, where calcite is rare and mixing of surface and subsurface sources may occur. Deep in the SZ, distinctive Mn calcites reflect deep sources, including Ca released as analcime or albite formed and carbonates derived from underlying Paleozoic rocks. In the UZ and in the barren zone, above the deep Mn calcites, variations in calcite lanthanide chemistry can be used to distinguish rhyolitic from quartz-latitic sources. Lanthanide ratios and Sr contents of calcites record the chemical evolution of waters flowing through the UZ and upper SZ. Variations in calcite chemistry in the UZ and in the barren zone show that (1) Sr, which is readily exchanged with clays or zeolites, is essentially removed from some flowpaths that are in contact with these minerals and (2) traces of Mn oxides found in the tuffs have a significant effect of groundwater chemistry in the UZ and in the barren zone by removing almost all Ce from solution (evidenced by characteristic Ce depletions in calcite throughout this zone). Extreme Ce removal may be a result of Ce oxidation (Ce 3+ → Ce 4+ ) at the surfaces of some Mn oxides, particularly rancieite. Higher Sr contents and lack of Ce depletions in the deeper Mn calcites reflect different ages, origins, and transport systems. The calcite record of lanthanide and Sr transport in the UZ shows that minor minerals (clays and zeolites) and even trace minerals (Mn oxides) will affect the compositions of groundwaters that flow over distances greater than a few tens of meters. 43 refs., 8 figs., 4 tabs

  19. Site investigation SFR. Fracture mineralogy and geochemistry of borehole sections sampled for groundwater chemistry and Eh. Results from boreholes KFR01, KFR08, KFR10, KFR19, KFR7A and KFR105

    Energy Technology Data Exchange (ETDEWEB)

    Sandstroem, Bjoern (WSP Sverige AB (Sweden)); Tullborg, Eva-Lena (Terralogica AB, Grabo (Sweden))

    2011-01-15

    This report is part of the complementary site investigations for the future expansion of SFR. The report presents the results obtained during a detailed mineralogical and geochemical study of fracture minerals in drill cores from borehole section sampled for groundwater chemistry and where downhole Eh measurements have been performed. The groundwater redox system comprises not only the water, but also the bedrock/fracture mineral system in contact with this water. It is thus important to gain knowledge of the solid phases in contact with the groundwater, i.e. the fracture minerals. The samples studied for mineralogy and geochemistry, here reported, were selected to represent the fracture surfaces in contact with the groundwater in the sampled borehole sections and will give input to the hydrogeochemical model (SFR SDM). The mineralogy was determined using SEM-EDS and XRD and the geochemistry of fracture filling material was analysed by ICP-AES and ICP-QMS. The most common fracture minerals in the samples are mixed layer clay (smectite-illite), illite, chlorite, calcite, quartz, adularia and albite. Other minerals identified in the borehole sections include laumontite, pyrite, barite, chalcopyrite, hematite, Fe-oxyhydroxide, muscovite, REE-carbonate, allanite, biotite, asphaltite, galena, sphalerite, arsenopyrite, uranium phosphate, uranium silicate, Y-Ca silicate, monazite, xenotime, harmotome and fluorite. There are no major differences between the fracture mineralogy of the investigated borehole sections from SFR and the fracture mineralogy of the Forsmark site investigation area. The four fracture mineral generations distinguished within the Forsmark site investigation are also found at SFR. However, some differences have been observed: 1) Barite and uranium minerals are more common in the SFR fractures, 2) clay minerals like mixed layer illite-smectite and illite dominates in contrast to Forsmark where corrensite is by far the most common clay mineral and, 3

  20. Rocha com espodumênio como fundente para massas cerâmicas tradicionais Spodumene rock as a flux for traditional ceramic bodies

    Directory of Open Access Journals (Sweden)

    S. R. Bragança

    2010-07-01

    Full Text Available Investigou-se a atuação de uma rocha com espodumênio como fundente em massas cerâmicas, analisando-se sua reatividade com outras matérias-primas, como quartzo e caulim. Primeiramente, caracterizou-se petrograficamente o pegmatito de onde se extrai esse fundente. Posteriormente avaliou-se o comportamento de moabilidade, fundência e deformação piroplástica da rocha com espodumênio. Analisou-se então sua influência nas propriedades tecnológicas finais das peças, principalmente em relação à temperatura de queima, às fases e à microestrutura. Comparou-se a gresificação com outros fundentes comerciais como a albita e o feldspato. O espodumênio mostrou maior capacidade de reduzir a temperatura de gresificação das peças que os fundentes tradicionais, promovendo a densificação por fluxo viscoso.A spodumene rock was used as a flux in ceramic bodies, analyzing its reactivity to other raw materials such as quartz and kaolin. The petrology properties of the pegmatite (parent rock from which the flux is extracted was characterized. The grindability, fluxing strength and pyroplastic deformation of the spodumene rock were investigated. The influence on technological properties of the final pieces, mainly in relation to the firing temperature, phases formation and microstructure were also further analyzed. The firing behavior to other commercial flux such as albite and feldspar were then compared. The spodumene rock was considered an effective flux, capable of reducing the firing temperatures of the tested bodies by viscous flow.

  1. Preliminary stratigraphic and petrologic characterization of core samples from USW-G1, Yucca Mountain, Nevada

    International Nuclear Information System (INIS)

    Waters, A.C.; Carroll, P.R.

    1981-11-01

    Tuffs of the Nevada Test Site are currently under investigation to determine their potential for long-term storage of radioactive waste. As part of this program, hole USW-G1 was drilled to a depth of 6000 ft below the surface, in the central part of the Yucca Mountain area, Nevada Test Site, Nevada. Petrographic study of the USW-G1 core is presented in this report and shows the tuffs (which generally were variably welded ash flows) are partly recrystallized to a variety of secondary minerals. The important alteration products are zeolites (heulandite, clinoptilolite, mordenite and analcime), smectite clays with minor interstratified illite, albite, micas, potassium feldspar, and various forms of silica. Iijima's zeolite zones I through IV of burial metamorphism can be recognized in the core. Zeolites are first observed at about the 1300-ft depth, and the high-temperature boundary of zeolite stability in this core occurs at about 4350 ft. Analcime persists, either metastably or as a retrograde mineral, deeper in the core. The oxidation state of Fe-Ti oxide minerals, through most of the core, increases as the degree of welding decreases, but towards the bottom of the hole, reducing conditions generally prevail. Four stratigraphic units transected by the core may be potentially favorable sites for a waste repository. These four units, in order of increasing depth in the core, are (1) the lower cooling unit of the Topopah Spring Member, (2) cooling unit II of the Bullfrog Member, (3) the upper part of the Tram tuff, and (4) the Lithic-rich tuff

  2. Atmospheric weathering and silica-coated feldspar: analogy with zeolite molecular sieves, granite weathering, soil formation, ornamental slabs, and ceramics.

    Science.gov (United States)

    Smith, J V

    1998-03-31

    Feldspar surfaces respond to chemical, biological, and mechanical weathering. The simplest termination is hydroxyl (OH), which interacts with any adsorption layer. Acid leaching of alkalis and aluminum generated a silica-rich, nanometers-thick skin on certain feldspars. Natural K, Na-feldspars develop fragile surfaces as etch pits expand into micrometer honeycombs, possibly colonized by lichens. Most crystals have various irregular coats. Based on surface-catalytic processes in molecular sieve zeolites, I proposed that some natural feldspars lose weakly bonded Al-OH (aluminol) to yield surfaces terminated by strongly bonded Si-OH (silanol). This might explain why some old feldspar-bearing rocks weather slower than predicted from brief laboratory dissolution. Lack of an Al-OH infrared frequency from a feldspar surface is consistent with such a silanol-dominated surface. Raman spectra of altered patches on acid-leached albite correspond with amorphous silica rather than hydroxylated silica-feldspar, but natural feldspar may respond differently. The crystal structure of H-exchanged feldspar provides atomic positions for computer modeling of complex ideas for silica-terminated feldspar surfaces. Natural weathering also depends on swings of temperature and hydration, plus transport of particles, molecules, and ionic complexes by rain and wind. Soil formation might be enhanced by crushing granitic outcrops to generate new Al-rich surfaces favorable for chemical and biological weathering. Ornamental slabs used by architects and monumental masons might last longer by minimizing mechanical abrasion during sawing and polishing and by silicifying the surface. Silica-terminated feldspar might be a promising ceramic surface.

  3. Why is Dawsonite Absent in CO2 Charged Reservoirs?

    International Nuclear Information System (INIS)

    Hellevang, H.; Declercq, J.; Aagaard, P.

    2011-01-01

    Growth of the sodium-aluminium-hydroxy carbonate dawsonite (NaAl(OH) 2 CO 3 ) after charging saline aquifers with CO 2 has been assumed in a plethora of numerical simulations at different mineralogies, aqueous solutions, pressures and temperatures. It appears however that dawsonite is less abundant than expected in natural CO 2 storage analogues if we take into account the thermodynamic stability alone. We have mapped the thermodynamic stability of dawsonite relative to mineral phases like albite, kaolinite and analcime from 37 to 200 C and performed closed-system batch kinetic simulations using a new kinetic expression including a nucleation term based on classical nucleation theory, and a growth term that was based on BCF growth theory. Using this rate equation, we have performed a sensitivity study on dawsonite growth on mineralogy, temperature, CO 2 pressure, nucleation rate and its dependencies on temperature and affinity, and on the dawsonite precipitation rate coefficient. Simulations with dawsonite growth disabled showed that the maximum over-saturation reached for dawsonite for seawater-like solutions never exceeded 3-4 times over-saturation. The positive effect on dawsonite growth of increasing the CO 2 pressure was mostly neutralized by higher acidity. Decreasing the precipitation rate coefficient by 5 orders of magnitude had a limited effect on the onset of significant growth, but the amount of dawsonite formed at the end of the 1 000 years simulated time was only 37% below the high-rate case. Reducing the nucleation rates had similar effects leading to postponed dawsonite growth. Finally, based on thermodynamic considerations and numerical simulations, we suggest that the potential of dawsonite growth is limited to a medium-temperature window framed by a high thermodynamic stability relative to competing mineral phases at low temperatures, but with rapidly diminishing nucleation and growth rates at lower temperatures constrained by energy barriers

  4. New geological model of the Lagoa Real uraniferous albitites from Bahia (Brazil)

    Science.gov (United States)

    de Oliveira Chaves, Alexandre

    2013-09-01

    New evidence supported by petrography (including mineral chemistry), lithogeochemistry, U-Pb geochronology by Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS), and physicochemical study of fluid and melt inclusions by LA-ICP-MS and microthermometry, point to an orogenic setting of Lagoa Real (Bahia-Brazil) involving uraniferous mineralization. Unlike the previous models in which uraniferous albitites represent Na-metasomatised 1.75 Ga anorogenic granitic rocks, it is understood here that they correspond to metamorphosed sodium-rich and quartz-free 1.9 Ga late-orogenic syenitic rocks (Na-metasyenites). These syenitic rocks are rich not only in albite, but also in U-rich titanite (source of uranium). The interpretation of geochemical data points to a petrogenetic connection between alkali-diorite (local amphibolite protolith) and sodic syenite by fractional crystallization through a transalkaline series. This magmatic differentiation occurred either before or during shear processes, which in turn led to albitite and amphibolite formation. The metamorphic reactions, which include intense recrystallization of magmatic minerals, led uraninite to precipitate at 1.87 Ga under Oxidation/Reduction control. A second population of uraninites was also generated by the reactivation of shear zones during the 0.6 Ga Brasiliano Orogeny. The geotectonic implications include the importance of the Orosirian event in the Paramirim Block during paleoproterozoic Săo Francisco Craton edification and the influence of the Brasiliano event in the Paramirim Block during the West-Gondwana assembly processes. The regional microcline-gneiss, whose protolith is a 2.0 Ga syn-collisional potassic granite, represents the albitite host rock. The microcilne-gneiss has no petrogenetic association to the syenite (albitite protolith) in magmatic evolutionary terms.

  5. Gold mineralisation near the Main Divide, upper Wilberforce valley, Southern Alps, New Zealand

    International Nuclear Information System (INIS)

    Becker, J.A.; Craw, D.; Horton, T.; Chamberlain, C.P.

    2000-01-01

    Veins up to 8 m wide fill extensional fractures in Torlesse Terrane metasediments near the Main Divide in the upper Wilberforce valley, Canterbury, New Zealand. The upper Wilberforce veins are part of a prominent 40 km long, NNE-trending swarm of gold-bearing veins formed across the Main Divide during the Late Cenozoic rise of the Southern Alps. The veins occur within, and near, a prominent set of faults which constitute the Main Divide Fault Zone. The veins are irregular in shape due to contrasting host rock properties, and have been only weakly sheared and deformed. Veins cut across greywacke beds and follow irregularly along argillite beds, on the 1-10 m scale. Quartz dominates vein mineralogy, but albite forms up to 45% of some veins, and minor chlorite, pyrite, arsenopyrite, chalcopyrite, and gold occur sporadically, especially in breccias near vein margins. Fluid inclusions in vein quartz homogenise at 180-253 degrees C, and arsenopyrite composition (28.3-30.8 at.% As) suggest formation temperatures of 250-350 degrees C. Elevated arsenic levels (up to 200 ppm above a background of 10 ppm) in some host greywackes and argellites suggest that hydrothermal activity pervaded host rocks as well as forming veins, but there is no textural evidence for this fluid flow. Late-stage carbonates in faults adjacent to the quartz veins, but which postdate the quartz veins, have δ 18 O ranging from 11.1 to 25.6 per thousand, and δ 13 C ranging from -12.5 to -1.1 per thousand. These carbonates were deposited by a mixture of meteoric and crustally isotopically exchanged fluid as a shallow-level manifestation of the same hydrothermal system which deposited the quartz veins. The upper Wilberforce veins structurally and mineralogically resemble some Late Cenozoic gold-bearing vein systems in the Mt Cook area, 100 km to the southwest along the Southern Alps. (author). 52 refs., 9 figs., 3 tabs

  6. Distribution of magnetic particulates in a roadside snowpack based on magnetic, microstructural and mineralogical analyses

    Science.gov (United States)

    Bućko, Michał S.; Mattila, Olli-Pekka; Chrobak, Artur; Ziółkowski, Grzegorz; Johanson, Bo; Čuda, Jan; Filip, Jan; Zbořil, Radek; Pesonen, Lauri J.; Leppäranta, Matti

    2013-10-01

    Vehicle traffic is at present one of the major sources of environmental pollution in urban areas. Magnetic parameters are successfully applied in environmental studies to obtain detailed information about concentrations and quality of iron-bearing minerals. A general aim of this research was to investigate the magnetic, microstructural and mineralogical properties of dust extracted from the roadside snowpack accumulated on the side of an urban highway, northern Helsinki. Vertical snow profiles were taken at different distances (5, 10 and 15 m) from the road edge, during winter season 2010-2011. The temporal distribution of mass magnetic susceptibility (χ) of the road dust shows that the concentration of magnetic particles increases in the snowpack during winter. Roadside snowpack preserves a large fraction of the magnetic particulate until the late stages of melting and this could be considered as one of the main factors responsible for the resuspension phenomenon observed in Nordic countries. The vertical distribution of χ and SIRM (saturation isothermal remanent magnetization)/χ ratio may indicate the migration of magnetic particles down in the snowpack during melting conditions. Ultrafine to coarse-grained (superparamagnetic to multidomain) magnetite was identified as the primary magnetic mineral in all the studied road dust samples. The examined road dust contains significant amount of dia/paramagnetic minerals (e.g. quartz, albite, biotite) and the content of magnetite is relatively low (below 1 weight percent, wt%). The roadside snowpack is enriched in anthropogenic particles such as angular and spherical iron-oxides, tungsten-rich particles and sodium chloride. This study demonstrates the suitability of snow as an efficient collecting medium of magnetic particulates generated by anthropogenic activities.

  7. Evaluation of the potential of indigenous calcareous shale for neutralization and removal of arsenic and heavy metals from acid mine drainage in the Taxco mining area, Mexico.

    Science.gov (United States)

    Romero, F M; Núñez, L; Gutiérrez, M E; Armienta, M A; Ceniceros-Gómez, A E

    2011-02-01

    In the Taxco mining area, sulfide mineral oxidation from inactive tailings impoundments and abandoned underground mines has produced acid mine drainage (AMD; pH 2.2-2.9) enriched in dissolved concentrations (mg l⁻¹) sulfate, heavy metals, and arsenic (As): SO₄²⁻ (pH 1470-5454), zinc (Zn; 3.0-859), iron (Fe; pH 5.5-504), copper (Cu; pH 0.7-16.3), cadmium (Cd; pH 0.3-6.7), lead (Pb; pH acid-neutralizing potential of limestone decreases when surfaces of the calcite particles become less reactive as they are progressively coated by metal precipitates. This study constitutes first-stage development of passive-treatment systems for treating AMD in the Taxco mine area using indigenous calcareous shale. This geologic material consists of a mixture of calcite, quartz, muscovite, albite, and montmorillonite. Results of batch leaching test indicate that calcareous shale significantly increased the pH (to values of 6.6-7.4) and decreased heavy metal and As concentrations in treated mine leachates. Calcareous shale had maximum removal efficiency (100%) for As, Pb, Cu, and Fe. The most mobile metals ions were Cd and Zn, and their average percentage removal was 87% and 89%, respectively. In this natural system (calcareous shale), calcite provides a source of alkalinity, whereas the surfaces of quartz and aluminosilicate minerals possibly serve as a preferred locus of deposition for metals, resulting in the neutralizing agent (calcite) beings less rapidly coated with the precipitating metals and therefore able to continue its neutralizing function for a longer time.

  8. Diagenesis of amorphous organic matter as an essential aspect of genesis and alteration of tabular-type uranium-vanadium deposits, Colorado Plateau

    International Nuclear Information System (INIS)

    Spirakis, C.S.; Hansley, P.L.

    1987-01-01

    Organic matter was the key to the initial concentration of uranium and vanadium (during the sulfate reduction stage of early diagenesis) in all sandstone-hosted, tabular deposits in the Morrison Formation, Colorado Plateau. In deposits rich in amorphous organic matter, as are many in the Grants uranium region (GUR), diagenesis did not proceed beyond sulfate reduction. In contrast, in organic-poor, chlorite deposits of the Henry Mountains district, 13 C- and 18 O-enriched dolomites preserve evidence of a subsequent methanogenic stage. In these and similar organic-poor deposits in the Slick Rock district and in parts of the GUR, aluminosilicate dissolution (including a distinctive, organic-acid-induced etching of garnets) and growth of coarse-grained coffinite, albite, ankerite, and chlorite suggest diagenesis reached the organic acid stage. Temperature and thermal maturation indicators (vitrinite reflectance, type IIb chlorite, ordered illite/smectite, and fluid inclusion data) are consistent with temperatures of organic-acid stage diagenesis (∼ 100 0 C). The localization of these alterations in and around organic-poor, clay-rich ore; the similarities in type and sequence of these alterations to the normal alteration of organic-bearing sediments; the alteration of iron-titanium oxides (attributed to the action of soluble organic complexes) around both organic-rich and organic-poor deposits; and the gradation from organic-rich to organic-poor, chlorite-rich deposits (in GUR) suggest that (1) amorphous organic matter was involved in the genesis of all of these deposits and (2) differences among deposits may reflect varying degrees of diagenesis of the organic matter

  9. Jerusalem artichoke decreased salt content and increased diversity of bacterial communities in the rhizosphere soil in the coastal saline zone

    Science.gov (United States)

    Shao, Tianyun; Li, Niu; Cheng, Yongwen; Long, Xiaohua; Shao, Hongbo; Zed, Rengel

    2017-04-01

    Soil salinity is one of the main environmental constraints that restrict plant growth and agricultural productivity; however, utilization of salt-affected land can bring substantial benefits. This study used an in-situ remediation method by planting Jerusalem artichoke in naturally occurring saline alkali soils with different salinity (high salinity (H, >4.0 g•salt kg-1 soil), moderate salinity (M, 2.0-4.0 g•salt kg-1 soil) and low salinity (L, 1.0-2.0 g•salt kg-1 soil) in the coastal saline zone in southeast China in comparison with the respective controls without Jerusalem artichoke planting (undisturbed soil). Soil pH and salinity increased sequentially from the rhizosphere to the bulk soil and the unplanted controls. The activity of neutral phosphatase and invertase decreased in the order L > M > H, whereas that of catalase was reverse. The minimum content of calcite, muscovite and quartz, and maximum content of chlorite and albite, were found in the control soils. Planting of Jerusalem artichoke enhanced bacterial microflora in saline alkali soil. Proteobacteria, Acidobacteria, Actinobacteria and Bacteroidetes were the dominant phyla in all samples, accounting for more than 80% of the reads. The number of Operational Taxonomic Units (OTU) in the rhizosphere soil was, respectively, 1.27, 1.02 and 1.25 times higher compared with the bulk soil, suggesting that Jerusalem artichoke played a significant role in increasing abundance and diversity of soil microbial populations. The study showed that Jerusalem artichoke could be used to improve saline alkali soil by enriching bacterial communities, enhancing the activity of phosphatase and invertase, and decreasing soil salinity.

  10. Fabrication and characterization of fine ceramic based on alumina, bentonite, and glass bead

    Science.gov (United States)

    Sebayang, P.; Nurdina; Simbolon, S.; Kurniawan, C.; Yunus, M.; Setiadi, E. A.; Sitorus, Z.

    2018-03-01

    Fabrication of fine ceramics based on alumina, bentonite and glass bead has been carried out by powder metallurgy. The preparation of powder has been performed using High Energy Milling (HEM) with wet milling process and using toluene as medium for 2 hours. The powder milling result was dried in oven at 100 °C for 24 hours. After that, the powder was compacted into pellet by using hydraulic press with 80 kgf/cm2 pressure at room temperature. Then, the pellet was sintered at 900 °C for 4 hours. Materials characterization such as physical properties (true density, bulk density, porosity, and water absorption), average particle diameter, hardness, microstructure and phase were measured by Archimedes method, Particle Size Analyzer (PSA), Hardness Vickers (HV), Scanning Electron Microscope (SEM-EDX) and X-Ray Diffraction (XRD). From the result, the optimum condition is sample D (with addition of 30 wt.% γ-Al2O3) with sintering temperature of 900 °C for 4 hours. At this condition, these properties were measured: average particle diameter of 4.27 μm, true density of 2.32 g/cm3, porosity of 5.57%, water absorption of 2.46%, bulk density of 2.39 g/cm3, and hardness of 632 HV. The fine ceramic has four phases with albite (Al2NaO8Si3) and quartz (SiO2) as dominant phases and corundum (Al2O3) and nepheline (AlNaO4Si) as minor phases.

  11. Microstructures in landslides in northwest China - Implications for creeping displacements?

    Science.gov (United States)

    Schäbitz, M.; Janssen, C.; Wenk, H.-R.; Wirth, R.; Schuck, B.; Wetzel, H.-U.; Meng, X.; Dresen, G.

    2018-01-01

    Microstructures, mineralogical composition and texture of selected landslide samples from three landslides in the southern part of the Gansu Province (China) were examined with optical microscopy, transmission electron microscopy (TEM), x-ray diffraction (XRD) and synchrotron x-ray diffraction measurements. Common sheet silicates are chlorite, illite, muscovite, kaolinite, pyrophyllite and dickite. Other minerals are quartz, calcite, dolomite and albite. In one sample, graphite and amorphous carbon were detected by TEM-EDX analyses and TEM high-angle annular dark-field images. The occurrence of graphite and pyrophyllite with very low friction coefficients in the gouge material of the Suoertou and Xieliupo landslides is particularly significant for reducing the frictional strength of the landslides. It is proposed that the landslides underwent comparable deformation processes as fault zones. The low friction coefficients provide strong evidence that slow-moving landsliding is controlled by the presence of weak minerals. In addition, TEM observations document that grain size reduction in clayey slip zone material was produced mainly by mechanical abrasion. For calcite and quartz, grain size reduction was attributed to both pressure solution and cataclasis. Therefore, besides landslide composition, the occurrence of ultrafine-grained slip zone material may also contribute to weakening processes of landslides. TEM images of slip-zone samples show both locally aligned clay particles, as well as kinked and folded sheet silicates, which are widely disseminated in the whole matrix. Small, newly formed clay particles have random orientations. Based on synchrotron x-ray diffraction measurements, the degree of preferred orientation of constituent sheet silicates in local shear zones of the Suoertou and Duang-He-Ba landslide is strong. This work is the first reported observation of well-oriented clay fabrics in landslides.

  12. Water management of the uranium production facility in Brazil (Caetite, BA): potential impacts over groundwater quality

    International Nuclear Information System (INIS)

    Lamego, Fernando; Santos, Robson Rodger; Silva, L. Ferreira da; Fernandes, Horst Monken

    2008-01-01

    The uranium unit of Caetite - in charge of all the 'yellow cake' produced in Brazil - is located in the semi-arid Northeast region at Bahia State. The geological uranium content of the ore is 3000 ppm, which is mainly associated with albite (NaAlSi 8 O 8 ), and its extraction is achieved by means of a Heap-Leach process. This process has a low water demand, which is supplied by a network of wells, but can contribute to change the groundwater quality and in some cases the extinguishing of wells was observed. The managing of liquid mining wastes formed by drainage waters from mine pit and solid waste piles is not enough to avoid unwarranted releases in the environment, which turn necessary the waste treatment through passing them into the industrial plant in order to reduce radionuclide concentrations. The groundwater is Na-HCO 3 type water and relative high concentration of Cl are observed in some groundwater. It seems that levels of uranium in groundwaters are mainly a consequence of the complexation of the metal by carbonates (or other anions) and not by any sort of the contamination of these waters by the drainage accumulated in the open pit. The speciation modelling allows identifying some areas where the replenishment of the aquifer is more active, but in general the recharge is a fast process run by direct infiltration. The stable isotope data (δ 2 H and δ 18 O) showed that evaporation plays a role during the infiltration, causing the groundwater salinization. These data discard the possibility that groundwater salinization was caused by discharge of deeper saline groundwater through faults associated to a regional groundwater flow system. The presence of an active shallow groundwater flow system offers better possibility for sustainable use of the groundwater resources in this semi-arid region of Brazil. (author)

  13. Geochemical features of the geothermal fluids from the Mapamyum non-volcanic geothermal system (Western Tibet, China)

    Science.gov (United States)

    Wang, Peng; Chen, Xiaohong; Shen, Licheng; Wu, Kunyu; Huang, Mingzhi; Xiao, Qiong

    2016-06-01

    Mapamyum geothermal field (MGF) in western Tibet is one of largest geothermal areas characterized by the occurrence of hydrothermal explosions on the Tibetan Plateau. The geochemical properties of hydrothermal water in the MGF system were investigated to trace the origin of the solutes and to determine the equilibrium temperatures of the feeding reservoir. The study results show that the geochemistry of hydrothermal waters in the MGF system is mainly of the Na-HCO3 type. The chemical components of hydrothermal waters are mainly derived from the minerals in the host rocks (e.g., K-feldspar, albite, Ca-montmorillonite, and Mg-montmorillonite). The hydrothermal waters are slightly supersaturated or undersaturated with respect to aragonite, calcite, dolomite, chalcedony and quartz (saturation indices close to 0), but are highly undersaturated with respect to gypsum and anhydrite (saturation indices < 0). Mixing models and Na-K-Mg ternary diagrams show that strong mixing between cold meteoric water and deeply-seated thermal fluids occurred during the upward flowing process. δD and δ18O data confirm that the meteoric water acts as the water source of the geothermal waters. An 220 °C equilibrated reservoir temperature of hydrothermal spring waters was calculated via both the Na-K-Mg ternary diagrams and the cationic chemical geothermometers. The logpCO2 of hydrothermal waters in the MGF system ranges from - 2.59 to - 0.57 and δ13C of the total dissolved inorganic carbon ranges from - 5.53‰ to - 0.94‰, suggesting that the carrier CO2 in hydrothermal water are mainly of a magmatic or metamorphic CO2 origin.

  14. Fundamental study of CO2-H2O-mineral interactions for carbon sequestration, with emphasis on the nature of the supercritical fluid-mineral interface.

    Energy Technology Data Exchange (ETDEWEB)

    Bryan, Charles R.; Dewers, Thomas A.; Heath, Jason E.; Wang, Yifeng; Matteo, Edward N.; Meserole, Stephen P.; Tallant, David Robert

    2013-09-01

    In the supercritical CO2-water-mineral systems relevant to subsurface CO2 sequestration, interfacial processes at the supercritical fluid-mineral interface will strongly affect core- and reservoir-scale hydrologic properties. Experimental and theoretical studies have shown that water films will form on mineral surfaces in supercritical CO2, but will be thinner than those that form in vadose zone environments at any given matric potential. The theoretical model presented here allows assessment of water saturation as a function of matric potential, a critical step for evaluating relative permeabilities the CO2 sequestration environment. The experimental water adsorption studies, using Quartz Crystal Microbalance and Fourier Transform Infrared Spectroscopy methods, confirm the major conclusions of the adsorption/condensation model. Additional data provided by the FTIR study is that CO2 intercalation into clays, if it occurs, does not involve carbonate or bicarbonate formation, or significant restriction of CO2 mobility. We have shown that the water film that forms in supercritical CO2 is reactive with common rock-forming minerals, including albite, orthoclase, labradorite, and muscovite. The experimental data indicate that reactivity is a function of water film thickness; at an activity of water of 0.9, the greatest extent of reaction in scCO2 occurred in areas (step edges, surface pits) where capillary condensation thickened the water films. This suggests that dissolution/precipitation reactions may occur preferentially in small pores and pore throats, where it may have a disproportionately large effect on rock hydrologic properties. Finally, a theoretical model is presented here that describes the formation and movement of CO2 ganglia in porous media, allowing assessment of the effect of pore size and structural heterogeneity on capillary trapping efficiency. The model results also suggest possible engineering approaches for optimizing trapping capacity and for

  15. Preliminary stratigraphic and petrologic characterization of core samples from USW-G1, Yucca Mountain, Nevada

    Energy Technology Data Exchange (ETDEWEB)

    Waters, A.C.; Carroll, P.R. (eds.)

    1981-11-01

    Tuffs of the Nevada Test Site are currently under investigation to determine their potential for long-term storage of radioactive waste. As part of this program, hole USW-G1 was drilled to a depth of 6000 ft below the surface, in the central part of the Yucca Mountain area, Nevada Test Site, Nevada. Petrographic study of the USW-G1 core is presented in this report and shows the tuffs (which generally were variably welded ash flows) are partly recrystallized to a variety of secondary minerals. The important alteration products are zeolites (heulandite, clinoptilolite, mordenite and analcime), smectite clays with minor interstratified illite, albite, micas, potassium feldspar, and various forms of silica. Iijima`s zeolite zones I through IV of burial metamorphism can be recognized in the core. Zeolites are first observed at about the 1300-ft depth, and the high-temperature boundary of zeolite stability in this core occurs at about 4350 ft. Analcime persists, either metastably or as a retrograde mineral, deeper in the core. The oxidation state of Fe-Ti oxide minerals, through most of the core, increases as the degree of welding decreases, but towards the bottom of the hole, reducing conditions generally prevail. Four stratigraphic units transected by the core may be potentially favorable sites for a waste repository. These four units, in order of increasing depth in the core, are (1) the lower cooling unit of the Topopah Spring Member, (2) cooling unit II of the Bullfrog Member, (3) the upper part of the Tram tuff, and (4) the Lithic-rich tuff.

  16. Preferential Treatment: Interaction Between Amino Acids and Minerals

    Science.gov (United States)

    Crapster-Pregont, E. J.; Cleaves, H. J.; Hazen, R. M.

    2008-12-01

    Amino acids are the building blocks of proteins and are important for some models of the origin of life. Polymerization of amino acids from dilute solution is unlikely without a scaffold or catalyst. The surfaces of early Earth minerals are the most likely candidates for this role. The surface adsorption behavior of 12 amino acids (L-alanine, L-serine, L-aspartic acid, L-proline, L- phenylalanine, L-valine, L-arginine, d-amino valeric acid, glycine, L-lysine, L-isoleucine, and B-alanine) on 21 minerals (quartz, calcite, enstatite, illite, olivine, pyrrhotite, pyrite, alkali basalt, albite, analcime, chlorite, barite, hydroxyl apatite, hematite, magnetite, aluminum hydroxide, kaolin, silica gel, corundum, rutile, and montmorillonite) was determined via batch adsorption experiments. Absorption was determined for concentrations between 10-4M and 10-6M in the presence of 0.1M NaCl, and between pH values of 3 and 9 at 25 degrees C. The equilibrated solutions were centrifuged, filtered, derivatized using a fluorescent amino group tag (dansyl-chloride) and analyzed by HPLC. Adsorption was standardized using BET surface area measurements for each mineral to give the number of mols of each amino acid adsorbed per square meter for each mineral. The results indicate an enormous difference in the adsorption of amino acids between minerals, along with major differences in the adsorption of individual amino acids on the same mineral surface. There is also a change in the absorbance of amino acids as the pH changes. Many previous studies of amino acid concentration and catalysis by minerals have used clay minerals because of their high surface areas, however, this data suggests that the surfaces of minerals such as calcite, quartz and pyrite have even higher affinities for amino acids. The results suggest mineral surfaces that could be optimal locations for the polymerization of molecules linked to the origin of life.

  17. Hydrothermal alteration of plagioclase and growth of secondary feldspar in the Hengill Volcanic Centre, SW Iceland

    Science.gov (United States)

    Larsson, D.; Grönvold, K.; Oskarsson, N.; Gunnlaugsson, E.

    2002-05-01

    Dissolution of igneous feldspar and the formation and occurrence of secondary feldspar in tholeiitic basalts from the Hengill volcanic centre, in SW Iceland was studied by microprobe analysis of cuttings from two ca. 2000 m deep geothermal wells. Well NG-7 in Nesjavellir represents a geothermal system in a rift zone where the intensity of young, insignificantly altered intrusions increases with depth. Well KhG-1 in Kolviðarhóll represents the margin of a rift zone where the intensity of intrusives is lower and the intensity of alteration higher. This marginal well represents altered basaltic crust in an early retrograde state. The secondary plagioclase in both wells is mainly oligoclase, occurring in association with K-feldspar and chlorite±actinolite. The texture of this assemblage depends on the lithology and intensity of alteration. In Nesjavellir (NG-7) the composition of secondary albite-oligoclase is correlated with the host-rock composition. This connection is not apparent in more intensely altered samples from Kolviðarhóll (KhG-1). The influence of temperature on composition of secondary Na-feldspar is unclear in both wells although Ca is expected to increase with temperature. Any temperature dependence may be suppressed by the influence of rock composition in Nesjavellir and by retrograde conditions at Kolviðarhóll. The absence of clear compositional gradients between igneous plagioclase and secondary feldspar and between Na-feldspar and K-feldspar suggests that secondary feldspars formed by dissolution precipitation reactions.

  18. Diagenesis of the Mucuri Member sandstones, lower cretaceous in the Espirito Santo and Mucuri Basins; Diagenese dos arenitos do Membro Mucuri, cretaceo inferior das Bacias do Espirito Santo e de Mucuri

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Carlos Manuel de Assis; Anjos, Sylvia Maria Couto dos [PETROBRAS, Rio de Janeiro, RJ (Brazil). Centro de Pesquisas. Dib. de Geologia e Engenharia de Reservatorios

    1996-01-01

    The diagenetic evolution of the sandy conglomerate sediments belonging to the Mucuri Member was regionally defined in the basins of Espirito Santo and Mucuri from samples collected in 24 wells at depths varying from 500 m to 3,000 m. Nine hundred meters of core samples were described, and 600 thin sections were prepared to be studied at the petrographic microscope and later at the scanning electron microscope (SEM). Samples were also analyze using X-ray diffraction in order to determine the clay minerals content as well as carbon and oxygen isotopic determination of the carbonate cements. The Mucuri Member consists of Alagoas and pre-Alagoas age sediments from alluvial-fluvial-deltaic environments, of arid climate, deposited during the rift phase of the Espirito Santo and Mucuri basins. The Aptian portion (Alagoas age) presents intercalations of typically marine shales. Thus, the Alagoas age sediments present formation water with a distinctive composition from the pre-Alagoas age sediments (continental) responsible for different diagenetic changes in both packages. Moreover, the pre-Alagoas sediments had a burial history characterized by a longer residence time at greater depths than the Alagoas package, and thereby being more susceptible to mesodiagnetic processes. Most reservoirs of the Mucuri Member are of the Alagoas age, and because of better sampling a more detailed description is given. These reservoirs were also deeply affected by eodiagenesis, with particular emphasis in calcite precipitation in zones of sulfate reduction and methagenesis and authigenesis of smectites, which is the main agent responsible for the large amounts of clay minerals present in these reservoirs. several other diagenetic processes were identified in the Mucuri Member being however less efficient in reducing the pore space. The progressive utilization of the clay minerals, the albitization of the feldspar and the precipitation of quartz overgrowth were the mesodiagenetic features

  19. Characteristics of the Late Devonian Tsagaan Suvarga Cu-Mo deposit, Southern Mongolia

    Science.gov (United States)

    Tungalag, Naidansuren; Jargalan, Sereenen; Khashgerel, Bat-Erdene; Mijiddorj, Chuluunbaatar; Kavalieris, Imants

    2018-05-01

    The Late Devonian Tsagaan Suvarga deposit (255 Mt at 0.55% Cu, 0.02% Mo) is located on the NW margin of the Tsagaan Suvarga Complex (TSC), which extends ENE over 15 × 10 km and comprises mainly medium-grained equigranular hornblende-biotite quartz monzonite and monzodiorite. Distinct mineralized intrusions are inferred from distribution of Cu-Mo mineralization but are not clearly discernible. The Tsagaan Suvarga Complex is a window within Carboniferous volcanic and sedimentary rocks, and wall rocks to the TSC are not known or exposed in the nearby district. Whole-rock analyses and Sr-Nd isotopes, 87Sr/86Sr0 = 0.7027 to 0.7038 (n = 12) and ɛNd0 = + 4.26 to + 2.77 (n = 12), show that the granitoids are subduction-related I-type, high K-calc-alkaline to shoshonitic series and derived from a mantle source. They exhibit fractionated light rare earth elements, without depleted Eu and depleted middle heavy rare earth elements and Y, typical of oxidized, fertile porphyry magmatic suites. Early porphyry-style quartz veins include A- and B-type. Molybdenite occurs in monomineralic veins (1-5 mm) or A veins. Copper mineralization occurs mainly as chalcopyrite and subordinate bornite, disseminated and associated with quartz-muscovite veins. Pyrite (vol%) content is less than chalcopyrite and bornite combined. Deep oxidation to about 50 m depth has formed zones of malachite and covellite in late fractures. The most important alteration is actinolite-biotite-chlorite-magnetite replacing hornblende and primary biotite. Quartz-K-feldspar alteration is minor. Late albite replaces primary K-feldspar and enhances sodic rims on plagioclase crystals. Quartz-muscovite (or sericitic alteration) overprints actinolite-biotite and porphyry-type quartz veins. Field observations and petrographic studies suggest that the bulk of the chalcopyrite-bornite mineralization at the Tsagaan Suvarga formed together with coarse muscovite alteration.

  20. Sericitization of illite decreases sorption capabilities for cesium

    Science.gov (United States)

    Choung, S.; Hwang, J.; Han, W.; Shin, W.

    2017-12-01

    Release of radioactive cesium (137Cs) to environment occurs through nuclear accidents such as Chernobyl and Fukushima. The concern is that 137Cs has long half-life (t1/2 = 30.2 years) with chemical toxicity and γ-radiation. Sorption techniques are mainly applied to remove 137Cs from aquatic environment. In particular, it has been known well that clay minerals (e.g, illite) are effective and economical sorbents for 137Cs. Illite that was formed by hydrothermal alteration exist with sericite through "sericitization" processes. Although sericite has analogous composition and lattice structure with illite, the sorptive characteristics of illite and sericite for radiocesium could be different. This study evaluated the effects of hydrothermal alteration and weathering process on illite cesium sorption properties. Natural illite samples were collected at Yeongdong area in Korea as the world-largest hydrothermal deposits for illite. The samples were analyzed by XRF, XRD and SEM-EDX to determine mineralogy, chemical compositions and morphological characteristics, and used for batch sorption experiments. The Yeongdong illites predominantly consist of illite, sericite, quartz, and albite. The measured cesium sorption distribution coefficients (Kd,Cs) of reference illite and sericite were approximately 6000 and 400 L kg-1 at low aqueous concentration (Cw 10-7 M), respectively. In contrast, Kd,Cs values for the Yeongdong illite samples ranged from 500 to 4000 L kg-1 at identical concentration. The observed narrow and sharp XRD peak of sericite indicated that the sericite has better crystallinity compared to illite. These experimental results suggested that sericitization processes of illite can decline the sorption capabilities of illite for cesium under various hydrothermal conditions. In particular, weathering experiments raised the cesium sorption to illite, which seems to be related to the increase of preferential sorption sites for cesium through crystallinity destruction

  1. Evidence of Metasomatism in the Lowest Petrographic Types Inferred from A Na(-), K, Rich Rim Around A LEW 86018 (L3.1) Chondrule

    Science.gov (United States)

    Mishra, Ritesh Kumar; Marhas, Kuljeet Kaur; Simon, Justin I.; Ross, Daniel Kent

    2015-01-01

    Ordinary chondrites (OCs) represent the most abundant extraterrestrial materials and also record the widest range of alteration of primary, pristine minerals of early Solar system material available for study. Relatively few investigations, however, address: (1) the role of fluid alteration, and (2) the relationship between thermal metamorphism and metasomatism in OCs, issues that have been extensively studied in many other meteorite groups e.g., CV, CO, CR, and enstatite chondrites. Detailed elemental abundances profiles across individual chondrules, and mineralogical studies of Lewis Hills (LEW) 86018 (L3.1), an unequilibrated ordinary chondrite (UOC) of low petrographic type of 3.1 returned from Antarctica, provide evidence of extensive alteration of primary minerals. Some chondrules have Na(-), K(-), rich rims surrounded by nepheline, albite, and sodalite-like Na(-), Cl(-), Al-rich secondary minerals in the near vicinity within the matrices. Although, limited evidences of low temperature (approximately 250 C) fluid-assisted alteration of primary minerals to phyllosilicates, ferroanolivine, magnetite, and scapolite have been reported in the lowest grades (less than 3.2) Semarkona (LL3.00) and Bishunpur (LL3.10), alkali-rich secondary mineralization has previously only been seen in higher grade greater than 3.4 UOCs. This preliminary result suggests highly localized metamorphism in UOCs and widens the range of alteration in UOCs and complicates classification of petrographic type and extent of thermal metamorphism or metasomatism. The work in progress will document the micro-textures, geochemistry (Ba, Ca, REE), and isotopic composition (oxygen, Al(-)- 26 Mg-26) of mineral phases in chondrules and adjoining objects to help us understand the formation scenario and delineate possible modes of metamorphism in UOCs.

  2. Deposition and diagenesis of the Brushy Basin Member and upper part of the Westwater Canyon member of the Morrison Formation, San Juan Basin, New Mexico

    International Nuclear Information System (INIS)

    Bell, T.E.

    1986-01-01

    The Brushy Basin Member and the upper part of the Westwater Canyon Member of the Morrison Formation in northwest New Mexico are nonmarine sedimentary rocks of Late Jurassic age. This stratigraphic interval consists of as many as four lithofacies deposited in fluvial and playa-lake environments. Lithofacies A is composed of crossbed feldspathic sandstone and was deposited by braided streams on an alluvial plain. Lithofacies B is composed of crossbedded feldspathic sandstone and tuffaceous mudstone, and was deposited by braided and anastomosing streams at the distal end of the alluvial plain. Lithofacies C is composed of calcareous, tuffaceous mudstone and was deposited on a mudflat between the alluvial plain and a playa lake. Lithofacies D is composed of zeolitic, tuffaceous mudstone and was deposited in a playa lake. The distribution of diagenetic facies in mudstones and tuffs in the Brushy Basin Member and upper part of the Westwater Canyon Member reflects the pH and salinity gradients common to fluvial/playa-lake systems. The abundant vitric ash in the sediments reacted to form montmorillonite in the fluvial facies. Calcite and montmorillonite were the reaction products where the fluvial and outermost playa facies met. Vitric ash reacted to form clinoptilolite and heulandite along the playa margins. In the center of the playa facies, analcime replaced clinoptilolite, an early zeolite. These early diagenetic minerals were replaced by albite, quartz, and mixed-layer illitemontmorillonite where the Brushy Basin Member and upper part of the Westwater Canyon Member have been deeply buried in the San Juan basin

  3. Site investigation SFR. Fracture mineralogy and geochemistry of borehole sections sampled for groundwater chemistry and Eh. Results from boreholes KFR01, KFR08, KFR10, KFR19, KFR7A and KFR105

    International Nuclear Information System (INIS)

    Sandstroem, Bjoern; Tullborg, Eva-Lena

    2011-01-01

    This report is part of the complementary site investigations for the future expansion of SFR. The report presents the results obtained during a detailed mineralogical and geochemical study of fracture minerals in drill cores from borehole section sampled for groundwater chemistry and where downhole Eh measurements have been performed. The groundwater redox system comprises not only the water, but also the bedrock/fracture mineral system in contact with this water. It is thus important to gain knowledge of the solid phases in contact with the groundwater, i.e. the fracture minerals. The samples studied for mineralogy and geochemistry, here reported, were selected to represent the fracture surfaces in contact with the groundwater in the sampled borehole sections and will give input to the hydrogeochemical model (SFR SDM). The mineralogy was determined using SEM-EDS and XRD and the geochemistry of fracture filling material was analysed by ICP-AES and ICP-QMS. The most common fracture minerals in the samples are mixed layer clay (smectite-illite), illite, chlorite, calcite, quartz, adularia and albite. Other minerals identified in the borehole sections include laumontite, pyrite, barite, chalcopyrite, hematite, Fe-oxyhydroxide, muscovite, REE-carbonate, allanite, biotite, asphaltite, galena, sphalerite, arsenopyrite, uranium phosphate, uranium silicate, Y-Ca silicate, monazite, xenotime, harmotome and fluorite. There are no major differences between the fracture mineralogy of the investigated borehole sections from SFR and the fracture mineralogy of the Forsmark site investigation area. The four fracture mineral generations distinguished within the Forsmark site investigation are also found at SFR. However, some differences have been observed: 1) Barite and uranium minerals are more common in the SFR fractures, 2) clay minerals like mixed layer illite-smectite and illite dominates in contrast to Forsmark where corrensite is by far the most common clay mineral and, 3

  4. Reaction softening by dissolution–precipitation creep in a retrograde greenschist facies ductile shear zone, New Hampshire, USA

    Science.gov (United States)

    McAleer, Ryan J.; Bish, David L.; Kunk, Michael J.; Sicard, Karri R.; Valley, Peter M.; Walsh, Gregory J.; Wathen, Bryan A.; Wintsch, R.P.

    2016-01-01

    We describe strain localization by a mixed process of reaction and microstructural softening in a lower greenschist facies ductile fault zone that transposes and replaces middle to upper amphibolite facies fabrics and mineral assemblages in the host schist of the Littleton Formation near Claremont, New Hampshire. Here, Na-poor muscovite and chlorite progressively replace first staurolite, then garnet, and finally biotite porphyroblasts as the core of the fault zone is approached. Across the transect, higher grade fabric-forming Na-rich muscovite is also progressively replaced by fabric-forming Na-poor muscovite. The mineralogy of the new phyllonitic fault-rock produced is dominated by Na-poor muscovite and chlorite together with late albite porphyroblasts. The replacement of the amphibolite facies porphyroblasts by muscovite and chlorite is pseudomorphic in some samples and shows that the chemical metastability of the porphyroblasts is sufficient to drive replacement. In contrast, element mapping shows that fabric-forming Na-rich muscovite is selectively replaced at high-strain microstructural sites, indicating that strain energy played an important role in activating the dissolution of the compositionally metastable muscovite. The replacement of strong, high-grade porphyroblasts by weaker Na-poor muscovite and chlorite constitutes reaction softening. The crystallization of parallel and contiguous mica in the retrograde foliation at the expense of the earlier and locally crenulated Na-rich muscovite-defined foliation destroys not only the metastable high-grade mineralogy, but also its stronger geometry. This process constitutes both reaction and microstructural softening. The deformation mechanism here was thus one of dissolution–precipitation creep, activated at considerably lower stresses than might be predicted in quartzofeldspathic rocks at the same lower greenschist facies conditions.

  5. Mineralogy, geochemistry and low grade metamorphism of green tuffs of Karaj formation in Hesarbon area (south west Firoozkooh

    Directory of Open Access Journals (Sweden)

    Shiva Bahrami

    2017-03-01

    Full Text Available Green tuffs of middle Eocene age in Hesarbon area, south west of Firoozkuh (East of Central Alborz consist of a thick sequence of lithic-, crystal-,vitric-and calcareous-tuffs. Microscopic and x-ray diffraction studies show plagioclase (albite and oligoclase, alkali feldspar (sanidine, quartz, cristobalite, biotite and hornblende are the major minerals in the rocks studied. Secondary minerals such as analcime, chlorite, prehnite and clay minerals are mainly present in the groundmass of the rocks. Extensive tectonic activities have created a variety of structural features including numerous folds and faults and therefore, have caused the green tuffs to be crushed and converted to breccia tuffs in many parts. Veins and cavities are filled by considerable amounts of zeolitic minerals including heulandite group, clinoptilolite and natrolite along with calcite and secondary quartz. Based on geochemical data, they lie on the dacite and rhyodacite field showing a calc-alkaline nature in the corresponding diagrams. According to the chondrite and primitive mantle normalized diagrams of trace elements, negative anomalies of Eu, Nb, Ti, P and depletion of HFSE together with their position in the petrogenesis discrimination diagrams, it is most likely that these rocks are formed in the active continental margin of a subduction zone. The existence of analcime and prehnite in the groundmass demonstrate that these rocks have undergone some degrees of low-grade metamorphism due to the overburden of the layers in the temperature range 200-300 °C. The present study shows that zeolite minerals filling the fractures and cavities of tuffs are precipitated by hydrothermal fluids with a neutral pH to acidic

  6. Rock–water interactions and pollution processes in the volcanic aquifer system of Guadalajara, Mexico, using inverse geochemical modeling

    International Nuclear Information System (INIS)

    Morán-Ramírez, J.; Ledesma-Ruiz, R.; Mahlknecht, J.; Ramos-Leal, J.A.

    2016-01-01

    In order to understand and mitigate the deterioration of water quality in the aquifer system underlying Guadalajara metropolitan area, an investigation was performed developing geochemical evolution models for assessment of groundwater chemical processes. The models helped not only to conceptualize the groundwater geochemistry, but also to evaluate the relative influence of anthropogenic inputs and natural sources of salinity to the groundwater. Mixing processes, ion exchange, water–rock–water interactions and nitrate pollution and denitrification were identified and confirmed using mass-balance models constraint by information on hydrogeology, groundwater chemistry, lithology and stability of geochemical phases. The water–rock interactions in the volcanic setting produced a dominant Na−HCO_3 water type, followed by Na−Mg−Ca−HCO_3 and Na−Ca−HCO_3. For geochemical evolution modeling, flow sections were selected representing recharge and non-recharge processes and a variety of mixing conditions. Recharge processes are dominated by dissolution of soil CO_2 gas, calcite, gypsum, albite and biotite, and Ca/Na exchange. Non-recharge processes show that the production of carbonic acid and Ca/Na exchange are decreasing, while other minerals such as halite and amorphous SiO_2 are precipitated. The origin of nitrate pollution in groundwater are fertilizers in rural plots and wastewater and waste disposal in the urban area. This investigation may help water authorities to adequately address and manage groundwater contamination. - Highlights: • The Inverse geochemical modeling was used to study to processes occurring in a volcanic aquifer. • Three flow sections were selected to apply inverse hydrogeochemical modeling. • Three main groundwater flows were identified: a local, intermediate and regional flow. • The models show that in the study area that groundwater is mixed with local recharge. • In the south, the aquifer has thermal influence.

  7. Isotope geochemistry of drainage from an acid mine impaired watershed, Oakland, California

    International Nuclear Information System (INIS)

    Butler, Thomas W.

    2007-01-01

    Oxidation of sulfides at the Leona Heights Sulfur Mine has resulted in the liberation of acid, SO 4 and metals to Leona Creek. Previous research at the site has indicated Fe(II) oxidation at rates faster than would be predicted by abiotic oxidation alone, particularly in the segment of stream between the Adit and Leona Street sample stations. In order to assess the mechanisms responsible for sulfide oxidation, samples were collected for isotopic analysis of water and SO 4 , the results of which were used to develop a stoichiometric isotope-balance model. This exercise indicated that the percentage of water-derived oxygen in SO 4 increased spatially from between 56% and 64% at the Adit to between 71% and 72% at Leona Street, illustrating that increased sulfide oxidation via Fe(III) was occurring within, or as water flows over, the waste rock, relative to water emanating directly from the former mine. The incorporation of water-derived oxygen in SO 4 during pyrite oxidation is a process controlled by Fe oxidizing bacteria such as A. ferrooxidans at low pH. The role of bacteria was further supported by estimates of the rate constant for Fe oxidation between sampling stations, yielding values that were approximately 10 6 faster than abiotic Fe oxidation alone. Stable isotopic analysis of water further indicates a close correlation of adit spring water to the local meteoric water line, while 3 H data indicate a groundwater apparent age, or time of travel from its primary zone of recharge, of 34 S data, in conjunction with reported albitized feldspars within the Leona Rhyolite host rock, indicate a magmatic origin of ore sulfur, contrary to previous interpretations at the site

  8. Timing of multiple hydrothermal events in the iron oxide-copper-gold deposits of the Southern Copper Belt, Carajás Province, Brazil

    Science.gov (United States)

    Moreto, Carolina P. N.; Monteiro, Lena V. S.; Xavier, Roberto P.; Creaser, Robert A.; DuFrane, S. Andrew; Melo, Gustavo H. C.; Delinardo da Silva, Marco A.; Tassinari, Colombo C. G.; Sato, Kei

    2015-06-01

    The Southern Copper Belt, Carajás Province, Brazil, hosts several iron oxide-copper-gold (IOCG) deposits, including Sossego, Cristalino, Alvo 118, Bacuri, Bacaba, Castanha, and Visconde. Mapping and U-Pb sensitive high-resolution ion microprobe (SHRIMP) IIe zircon geochronology allowed the characterization of the host rocks, situated within regional WNW-ESE shear zones. They encompass Mesoarchean (3.08-2.85 Ga) TTG orthogneiss, granites, and remains of greenstone belts, Neoarchean (ca. 2.74 Ga) granite, shallow-emplaced porphyries, and granophyric granite coeval with gabbro, and Paleoproterozoic (1.88 Ga) porphyry dykes. Extensive hydrothermal zones include albite-scapolite, biotite-scapolite-tourmaline-magnetite alteration, and proximal potassium feldspar, chlorite-epidote and chalcopyrite formation. U-Pb laser ablation multicollector inductively coupled mass spectrometry (LA-MC-ICP-MS) analysis of ore-related monazite and Re-Os NTIMS analysis of molybdenite suggest multiple Neoarchean (2.76 and 2.72-2.68 Ga) and Paleoproterozoic (2.06 Ga) hydrothermal events at the Bacaba and Bacuri deposits. These results, combined with available geochronological data from the literature, indicate recurrence of hydrothermal systems in the Southern Copper Belt, including 1.90-1.88-Ga ore formation in the Sossego-Curral ore bodies and the Alvo 118 deposit. Although early hydrothermal evolution at 2.76 Ga points to fluid migration coeval with the Carajás Basin formation, the main episode of IOCG genesis (2.72-2.68 Ga) is related to basin inversion coupled with Neoarchean (ca. 2.7 Ga) felsic magmatism. The data suggest that the IOCG deposits in the Southern Copper Belt and those in the Northern Copper Belt (2.57-Ga Salobo and Igarapé Bahia-Alemão deposits) do not share a common metallogenic evolution. Therefore, the association of all IOCG deposits of the Carajás Province with a single extensive hydrothermal system is precluded.

  9. Use of high-resolution satellite images for detection of geological structures related to Central Andes geothermal field, Chile.

    Science.gov (United States)

    Benavides-Rivas, C. L.; Soto-Pinto, C. A.; Arellano-Baeza, A. A.

    2014-12-01

    Central valley and the border with Argentina in the center, and in the fault system Liquiñe-Ofqui in the South of the country. High resolution images from the LANDSAT 8 satellite have been used to delineate the geological structures related to the potential geothermal reservoirs located at the northern end of the Southern Volcanic Zone of Chile. It was done by applying the lineament extraction technique, using the ADALGEO software, developed by [Soto et al., 2013]. These structures have been compared with the distribution of main geological structures obtained in the field. It was found that the lineament density increases in the areas of the major heat flux indicating that the lineament analysis could be a power tool for the detection of faults and joint zones associated to the geothermal fields. A lineament is generally defined as a straight or slightly curved feature in the landscape visible satellite image as an aligned sequence of pixel intensity contrast compared to the background. The system features extracted from satellite images is not identical to the geological lineaments that are generally determined by ground surveys, however, generally reflects the structure of faults and fractures in the crust. A temporal sequence of eight Landsat multispectral images of Central Andes geothermal field, located in VI region de Chile, was used to study changes in the configuration of the lineaments during 2011. The presence of minerals with silicification, epidotization, and albitization, which are typical for geothrmal reservoirs, was also identified, using their spectral characteristics, and subsequently corroborated in the field. Both lineament analysis and spectral analysis gave similar location of the reservoir, which increases reliability of the results.

  10. Hydrochemistry and geothermometrical modeling of low-temperature Panticosa geothermal system (Spain)

    Science.gov (United States)

    Asta, Maria P.; Gimeno, Maria J.; Auqué, Luis F.; Gómez, Javier; Acero, Patricia; Lapuente, Pilar

    2012-08-01

    The chemical characteristics of the low-temperature geothermal system of Panticosa (Spain) were investigated in order to determine the water temperature at the reservoir and to identify the main geochemical processes that affect the water composition during the ascent of the thermal waters. In general, the studied waters are similar to other geothermal systems in the Pyrenees, belonging to the group of granite-related alkaline thermal waters (high pH, low total dissolved solids, very low magnesium concentration, and sodium as the dominant cation). According to the alkaline pH of these waters, they have a very low CO2 partial pressure, bicarbonate is the dominant anion and silica is partially ionized as H3SiO4-. The unusually active acid-base pairs (HCO3-/CO32 - and, mainly, H4SiO4/H3SiO4-) act as homogeneous pH buffers and contribute to the total alkalinity in these alkaline waters. On the basis of the study of the conservative elements, a mixing process between a hot and a cold end-member has been identified. Additionally, in order to determinate the water temperature at the reservoir, several geothermometric techniques have been applied, including both geothermometrical modeling and classical geothermometrical calculations. The geothermometrical modeling seems to indicate that thermal waters re-equilibrate with respect to calcite and kaolinite during their ascent to the surface. Modeling results suggest that these thermal waters would be in equilibrium with respect to albite, K-feldspar, quartz, calcite, kaolinite and zoisite at a similar temperature of 90 ± 20 °C in the reservoir, which is in good agreement with the results obtained by applying the classical geothermometers.

  11. Intensive low-temperature tectono-hydrothermal overprint of peraluminous rare-metal granite: a case study from the Dlhá dolina valley (Gemericum, Slovakia

    Directory of Open Access Journals (Sweden)

    Breiter Karel

    2015-02-01

    Full Text Available A unique case of low-temperature metamorphic (hydrothermal overprint of peraluminous, highly evolved rare-metal S-type granite is described. The hidden Dlhá dolina granite pluton of Permian age (Western Carpathians, eastern Slovakia is composed of barren biotite granite, mineralized Li-mica granite and albitite. Based on whole-rock chemical data and evaluation of compositional variations of rock-forming and accessory minerals (Rb-P-enriched K-feldspar and albite; biotite, zinnwaldite and di-octahedral micas; Hf-(Sc-rich zircon, fluorapatite, topaz, schorlitic tourmaline, the following evolutionary scenario is proposed: (1 Intrusion of evolved peraluminous melt enriched in Li, B, P, F, Sn, Nb, Ta, and W took place followed by intrusion of a large body of biotite granites into Paleozoic metapelites and metarhyolite tuffs; (2 The highly evolved melt differentiated in situ forming tourmaline-bearing Li-biotite granite at the bottom, topaz-zinnwaldite granite in the middle, and quartz albitite to albitite at the top of the cupola. The main part of the Sn, Nb, and Ta crystallized from the melt as disseminated cassiterite and Nb-Ta oxide minerals within the albitite, while disseminated wolframite appears mainly within the topaz-zinnwaldite granite. The fluid separated from the last portion of crystallized magma caused small scale greisenization of the albitite; (3 Alpine (Cretaceous thrusting strongly tectonized and mylonitized the upper part of the pluton. Hydrothermal low-temperature fluids enriched in Ca, Mg, and CO2 unfiltered mechanically damaged granite. This fluid-driven overprint caused formation of carbonate veinlets, alteration and release of phosphorus from crystal lattice of feldspars and Li from micas, precipitating secondary Sr-enriched apatite and Mg-rich micas. Consequently, all bulk-rock and mineral markers were reset and now represent the P-T conditions of the Alpine overprint.

  12. Early Jurassic Carbon and Sodium Sequestration in a CAMP basalt flow

    Science.gov (United States)

    Block, K. A.; Puffer, J. H.

    2017-12-01

    The initial HTQ-type CAMP Orange Mountain Basalt flow, as well as related pillowed flows and the overlying Preakness flows, locally underwent substantial and well documented albitization, chloritization, and sulphate, carbonate, and zeolite mineralization. Layers representing at least 25 vol % of the Orange Mountain Basalt have undergone a major net increase in sodium and carbon content and a major redistribution of magnesium and calcium. Most alteration occurred during the development of a widespread early Jurassic geothermal system similar to the active system of Iceland. In both cases alteration was controlled by active circulation of basin brines through vesicular layers during rapid burial at temperatures that were kept elevated by recurring magmatism. Whole rock Na2O levels typically increased from 2.2 wt. % in unaltered layers to 3.2 wt. % in vesicular layers, and commonly reached levels exceeding 5 wt. %. The environmental implications of the removal of such massive amounts of sodium from the geothermal system on the chlorine budget and the salt content of Early Jurassic lakes are currently being evaluated. Massive amounts of carbon sequestration from the geothermal system may have mitigated an increased burden on the early Jurassic atmosphere where geothermal CO2 may have otherwise been vented at hot springs or solfataras. Calcite amygdules typically account for 5 to 10 vol. % of the vesiculated layers amounting to 66 to 132 kg of CO2 per m3 of basalt. If 25 vol. % of the 160 thick Orange Mountain Basalt is vesiculated that would equate to about 2640 to 5280 kg of CO2 per m2 of basalt. The full extent of calcite enrichment across the entire CAMP province, however, has not yet been determined.

  13. Intensive low-temperature tectono-hydrothermal overprint of peraluminous rare-metal granite: a case study from the Dlhá dolina valley (Gemericum, Slovakia)

    Science.gov (United States)

    Breiter, Karel; Broska, Igor; Uher, Pavel

    2015-02-01

    A unique case of low-temperature metamorphic (hydrothermal) overprint of peraluminous, highly evolved rare-metal S-type granite is described. The hidden Dlhá dolina granite pluton of Permian age (Western Carpathians, eastern Slovakia) is composed of barren biotite granite, mineralized Li-mica granite and albitite. Based on whole-rock chemical data and evaluation of compositional variations of rock-forming and accessory minerals (Rb-P-enriched K-feldspar and albite; biotite, zinnwaldite and di-octahedral micas; Hf-(Sc)-rich zircon, fluorapatite, topaz, schorlitic tourmaline), the following evolutionary scenario is proposed: (1) Intrusion of evolved peraluminous melt enriched in Li, B, P, F, Sn, Nb, Ta, and W took place followed by intrusion of a large body of biotite granites into Paleozoic metapelites and metarhyolite tuffs; (2) The highly evolved melt differentiated in situ forming tourmaline-bearing Li-biotite granite at the bottom, topaz-zinnwaldite granite in the middle, and quartz albitite to albitite at the top of the cupola. The main part of the Sn, Nb, and Ta crystallized from the melt as disseminated cassiterite and Nb-Ta oxide minerals within the albitite, while disseminated wolframite appears mainly within the topaz-zinnwaldite granite. The fluid separated from the last portion of crystallized magma caused small scale greisenization of the albitite; (3) Alpine (Cretaceous) thrusting strongly tectonized and mylonitized the upper part of the pluton. Hydrothermal low-temperature fluids enriched in Ca, Mg, and CO2 unfiltered mechanically damaged granite. This fluid-driven overprint caused formation of carbonate veinlets, alteration and release of phosphorus from crystal lattice of feldspars and Li from micas, precipitating secondary Sr-enriched apatite and Mg-rich micas. Consequently, all bulk-rock and mineral markers were reset and now represent the P-T conditions of the Alpine overprint.

  14. Oxygen isotope partitioning between rhyolitic glass/melt and CO2: An experimental study at 550-950 degrees C and 1 bar

    International Nuclear Information System (INIS)

    Palin, J.M.; Epstein, S.; Stolper, E.M.

    1996-01-01

    Oxygen isotope partitioning between gaseous CO 2 and a natural rhyolitic glass and melt (77.7 wt% SiO 2 , 0.16 wt% H 2 O total ) has been measured at 550-950 degrees C and approximately 1 bar. Equilibrium oxygen isotope fractionation factors (α CO2-rhyolite = ( 18 O/ 16 O) rhyolite ) determined in exchange experiments of 100-255 day duration. These values agree well with predictions based on experimentally determined oxygen isotope fractionation factors for CO 2 -silica glass and CO 2 -albitic glass/melt, if the rhyolitic glass is taken to be a simple mixture of normative silica and alkali feldspar components. The results indicate that oxygen isotope partitioning in felsic glasses and melts can be modeled by linear combinations of endmember silicate constituents. Rates of oxygen isotope exchange observed in the partitioning experiments are consistent with control by diffusion of molecular H 2 O dissolved in the glass/melt and are three orders of magnitude faster than predicted for rate control solely by diffusion of dissolved molecular CO 2 under the experimental conditions. Additional experiments using untreated and dehydrated (0.09 wt% H 2 O total ) rhyolitic glass quantatively support these interpretations. We conclude that diffusive oxygen isotope exchange in rhyolitic glass/melt, and probably other polymerized silicate materials, it controlled by the concentrations and diffusivities of dissolved oxygen-bearing volatile species rather than diffusion of network oxygen under all but the most volatile-poor conditions. 25 refs., 6 figs., 1 tab

  15. Structural and metamorphic evolution of the Orocopia Schist and related rocks, southern California: Evidence for late movement on the Orocopia fault

    Science.gov (United States)

    Jacobson, Carl E.; Dawson, M. Robert

    1995-08-01

    The Pelona, Orocopia, and Rand Schists (POR schists) of southern California and southwesternmost Arizona are late Mesozoic or early Tertiary subduction complexes that underlie Precambrian to Mesozoic continental basement along the low-angle Vincent-Chocolate Mountains (VCM) fault system. The VCM faults are often considered to be remnants of the original subduction zone, but recent work indicates that many have undergone substantial postsubduction reactivation. In the Orocopia Mountains, for example, the Orocopia Schist exhibits an exceptionally complex structural and metamorphic history due to multiple periods of movement along the Orocopia fault. Structures in the schist include isoclinal folds with axial-planar schistosity, open-to-tight folds that fold schistosity, penetrative stretching lineations, and crenulation lineations, all of which show a nearly 360° range in trend. Folds and lineations that trend approximately NE-SW occur throughout the schist and are thought to be part of an early phase of deformation related to subduction. Folds of this orientation show no consistent vergence. Folds and lineations that trend approximately NW-SE are concentrated near the Orocopia fault and are interpreted to have formed during exhumation of the schist. The NW-SE trending folds, and shear indicators in late-stage mylonite at the top of the schist, consistently verge NE. The exhumation event culminated in emplacement of the schist against brittlely deformed upper plate. Exhumation of the Orocopia Schist was accompanied by retrograde replacement of garnet, biotite, epidote, and calcic amphibole by chlorite, calcite, and sericite. Matrix amphibole has a lower Na/Al ratio than amphibole inclusions in albite, consistent with a late-stage decrease in pressure. As NE vergence in the Orocopia Mountains is associated with exhumation of the schist, the NE movement along other segments of the VCM fault may also be late and therefore have no bearing on the facing direction of the

  16. Mineral chemistry and petrogenesis of the Gurgur Mount volcanic rocks (Northeast Takab

    Directory of Open Access Journals (Sweden)

    Dariush Esmaeily

    2016-12-01

    Full Text Available Andesitic and andesitic-basaltic lavas are widespread over most of the ground surface of the Gurgur area altered mostly by the hydrothermal solutions. The main rock forming minerals in these rocks are plagioclase, pyroxene and olivine affected by the hydrothermal solutions. The altered rocks do contain minerals including calcite, sericite and chlorite. Given the results obtained and the mineral chemistry studies, the clinopyroxenes formed in the area are, chemically, calkalkaline and of diopside-augite type formed in subvolcanic to near surface levels contemporaneous with magma ascending. Plagioclase minerals show zoning textures and lie within the two andesine and albite-oligoclase fields. These units, in terms of total rock chemistry, are classified as the calk-alkaline volcanic rocks formed in the continental arcs. On the other hand, on the trace elements chondrite-normalized diagrams and enriched mantle-normalized multi- element diagrams, the LREE enrichment relative to the HREE is observed. The LILE (i.e. Rb, K and Th and the LREE (e.g. La, Ce and Nd show an enrichment in comparison to the HFSE (Zr, Hf, Nb, Yb, Y and Sm. Given the Nd/Th (1.42-1.15, Zr/Nb (12.27-21.22, Ba/La (18.64-29.77 as well as LILE enrichment associated with depletion in Nb, Ta and Ti, an environment related to the subduction zones can be proposed for the area under study. Moreover, the similarity between the REE distribution pattern and the incompatible elements point to the genetic relationship between these rocks. Finally, on the base of the obtained data, it can be concluded that the volcanic rocks in the Gurgur Mountain were likely formed during the extended magmatism of the Urumieh-Dokhtar in the Cenozoic.

  17. What classic greywacke (litharenite) can reveal about feldspar diagenesis: An example from Permian Rotliegend sandstone in Hessen, Germany

    Science.gov (United States)

    Molenaar, Nicolaas; Felder, Marita; Bär, Kristian; Götz, Annette E.

    2015-08-01

    Rotliegend siliciclastic sediments in southern Hessen (Germany) are a good example of dissolution of detrital feldspars, which is a common feature in many sandstones. Dissolution occurred after mechanical compaction of the lithic-rich sandstone, which experienced framework collapse with pores and pore connections filled and obstructed by deformed ductile lithic grains (pseudomatrix) thereby reducing pore space to microporosity., The advanced degree of compaction and reduced porosity caused low permeability and low hydraulic conductivity of the rock mass. This is further reduced by the presence of wackes and shales that occur intercalated with the sandstones. Feldspar dissolution thus took place in low permeable sediments when large-scale flow of meteoric or acidic fluids is ruled out as a cause of feldspar dissolution. Mineral precipitation (illite, kaolinite, and albite) took place within pseudomatrix and detrital matrix as well as in secondary pores created by feldspar dissolution. Feldspar was the source for the authigenesis. The system was thus closed during burial after framework collapse, and diagenetic reactants in the form of detrital components were already present within the system. The original mass was preserved, but redistributed and diagenetic minerals were the local sinks for the dissolved reactants, precipitating within the system. This also suggests that burial diagenesis in general might be more mass conservative than usually assumed. Rotliegend sandstones thus form a case where, despite of the lack of external exchange of mass by fluid flow, major diagenetic processes did take place and significantly modified the original mineralogy and texture. Feldspar diagenesis can take place from other processes than mere large-scale flushing of open systems as often supposed. It implies that the volumes of rock affected by feldspar diagenesis may be much larger than anticipated based upon the common hold believe that feldspar diagenesis is linked to

  18. U(VI) sorption on granite: prediction and experiments

    International Nuclear Information System (INIS)

    Nebelung, C.; Brendler, V.

    2010-01-01

    One widely accepted approach - component additivity (CA) - to describe the sorption of contaminants onto complex materials such as rocks or soils is based on the assumption that the surface of a complex mineral assemblage is composed of a mixture of mineral constituents whose surface properties are known from independent studies. An internally consistent SCM (surface complexation model) database can be developed that describes the adsorption reactions of solutes to each phase. Here, the capability of such a methodology was tested, using the code MINTEQA2 including thermodynamic data of the NEA-TDB, and literature data for SCM, namely the DDL model. The sorption characteristics of U(VI) on granite (from Eibenstock, Saxony, Germany, with the main components quartz, albite, orthoclase, and muscovite) was predicted and then compared to batch experiments. Granite plays an important role in the remediation of former uranium ore mining and milling sites, but is also one of the host rocks considered for final disposal of nuclear materials. Safety assessment requires a detailed understanding of this system and its retention potential with regard to hazardous components. Namely the sorption of uranium in this complex rock is not fully understood yet. The experiments thus also provided a better understanding of the far-field behaviour in granitic geological nuclear repositories. The robustness of the prediction was tested by variation of the granite composition and the variation of the specific surface area (SSA) - first all components were predicted with a uniform granite SSA, second with a distinct SSA for each granite component (determined on pure minerals for the same grain size fractions). Changes in compositions yielded only marginal differences in the prediction. Different approaches to SSA showed somewhat larger deviations. In conclusion, the CA methodology is a valid and robust approach to U(VI) sorption onto complex substrates such as granite, provided sufficient

  19. Scintilometry in pegmatitcs of the region of Cristais

    International Nuclear Information System (INIS)

    Marinho, J.M.L.

    1981-01-01

    The objective of this paper is to show the use of cintilometry in the delimitation of pegmatites of the region of Cristais, northeast of Ceara State. It is a part of the Project Litium-Ce and it receives a financial aid from FINEP. Four on-the-spot surveys have been made with a rectangules 5 x 15 m mesh on heterogeneous and little or not exploited pegmatite revealed on the surface by a residual mantle of milky quartz and slabs of muscovite. A cintilometer Saphyro Srat, model SPP-2 was used for readings in counts per second (c/s). Three of the surveys were performed on medium-sized pegmatites ( 5 - 15 m of width) and show that their measurement are in the 15-60 c/s range while those on the host rock (biotite-gneiss) vary from 70 to 130 c/s. One of the surveys was made over a pegmatitic dyke, with 1,5 meter width, in a sand-covered area of 1 meter, and it shows that the portion of the pegmatite may hardly by suggested, pointing out only at the southwest corner of the area the presence of biotite-gneiss through the increase in the readings. The cintilometry may be used on a more detailed scale in areas with superficial signs of the presence of pegmatites, in order to determine their position and to guide a superficial prospection. The low value reading (15 - 60 c/s) on the pegmatites are bound to be related to the absence of U and Th minerals and to the presence of a nucleus of quartz and albite, replacing largely the potassium feldspars. The reading in the 70 - 130 c/s range on the biotite-gneiss should be linked with the presence in their mineralogic composition of biotite muscovite, potassium feldspars and zircon. A sandy corer disguises the anomalies. (author) [pt

  20. Modelización del proceso de episienitización (decuarcificación-albitización: formulación cinética y transporte advectivo en medio continuo

    Directory of Open Access Journals (Sweden)

    Caballero, J. M.

    1999-04-01

    Full Text Available The development of episyenites from Sierra de Guadarrama has been modelized. The process mainly consists in a coupled process of dequartztification-albitization. The model is based on pure advective mass transport in a continuum medium, where the reactive process is formulated from a kinetic point of view. It is demonstrated the possibility of its formation through the action of low-salinity fluids (2,32 wt % NaCl equiv., partially equilibrated with a biotite monzogranite, linked to isobaric reaction paths across negative geothermal gradients, intersecting the quartz retrograde solubility field, and associated to a quick fluid-resident mobilisation due to the environment tectonic opening. The model explains the albitic nature of the alteration against former models. These predict microcline formation from the gradient relations ∂logKmic/∂T > ∂logKab/∂T (0.05739 and 0.05735 and ∂logKKCl/∂T NaCl/∂T (-0.038 and -0.036. Albite formation arises from the anortite component presence, because ∂logKan/∂T =0,1293 ≻ ∂logKmic/∂T. Non-equilibrium relations are very small, which implies that alteration intensity arises from the circulation of huge fluid volumes. This process feature together the kinetic rate constants result in a small change, spatial and temporal, of the fluid composition, being practically null for its main components (Na, K and, subordinately to these, the pH. The model also shows the necessity of handling geochemical systems as complex as possible. In this way, the proposed aqueous speciation proves that pH evolution along decreasing temperature is not necessarily acid, but inlet fluid pH dependent due to the calculated concentrations show that its behaviour mainly depends as much from Hel as from the NaOH base dissociation.Se modeliza teóricamente la formación de las episienitas de la Sierra de Guadarrama, consistente básicamente en un proceso acoplado de decuarcificaci

  1. Petrology of blueschist and meta-greywacke along the Turkmeni-Ordib fault (Turkmeni area, SE of Anarak

    Directory of Open Access Journals (Sweden)

    Fereshteh Bayat

    2015-10-01

    Full Text Available Introduction The occurrence of blueschist metamorphic facies is believed to mark the existence of former subduction zones. This facies is represented in the main constituents of subduction-accretion complexes, where it occurs in separate tectonic sheets, imbricated slices, lenses, or exotic blocks within a serpentinite mélange (Volkova et al., 2011. The evidence of the presence and maturity of Paleo- Tethys oceanic crust in the CEIM (define this in Paleo-Tethys branches, subduction and collision has been studied by various authors (Bagheri, 2007; Zanchi et al., 2009; Bayat and Torabi, 2011; Torabi 2011. Late Paleozoic blueschists have recognized in the western part of the CEIM (e. g. Anarak, Chupanan and Turkmeni in linear trends. Metamorphic rocks of the Turkmeni area (SE of Anarak are composed of blueschist and meta-greywacke and are situated along the Turkmeni-Ordib fault associated with Paleozoic rock units and serpentinized peridotite bodies. Turkmeni blueschist and meta-greywackes have not been studied by previous workers. The Turkmeni blueschists consist of albite, winchite, actinolite and epidote. Granoblastic, nematoblastic and lepidoblastic are main textures in these rocks. Winchite is found in the matrix and around epidote grains. This sodic-calcic amphibole serves as an index mineral in blueschist facies. Actinolite and epidote formed during retrograde metamorphism of blueschists in the greenschist facies. The mineral assemblage of albite, epidote, chlorite and phengite ± garnet is present in meta-greywackes in the Turkmeni blueschists. Veins of garnet, muscovite, quartz and opaque minerals are extensive in these rocks. Epidote and chlorite formed in meta-greywackes by retrograde metamorphism in the greenschist facies. The aim of the present study is to determine the petrological and geochemical characteristics, P-T condition of blueschists and meta-greywackes, as well as the geotectonic setting of primary basaltic rocks of the

  2. Metamorphic assemblages and the direction of flow of metamorphic fluids in four instances of serpentinization

    Science.gov (United States)

    Barnes, I.; Rapp, J.B.; O'Neil, J.R.; Sheppard, R.A.; Gude, A.J.

    1972-01-01

    Fluids related to Serpentinization are of at least three types. The first reported (Barnes and O'Neil, 1969) is a fluid of local meteoric origin, the chemical and thermodynamic properties of which are entirely controlled by olivine, orthopyroxene, brucite, and serpentine reactions. It is a Ca+2-OH-1 type and is shown experimentally to be capable of reacting with albite to yield calcium hydroxy silicates. Rodingites may form where the Ca+2-OH-1 type waters flow across the ultramafic contact and react with siliceous country rock. The second type of fluid has its chemical composition largely controlled before it enters the ultramafic rocks, but reactions within the ultramafic rocks fix the thermodynamic properties by reactions of orthopyroxene, olivine, calcite, brucite, and serpentine. The precipitation of brucite from this fluid clearly shows that fluid flow allows reaction products to be deposited at a distance from the point of solution. Thus, textural evidence for volume relations during Serpentinization may not be valid. The third type of fluid has its chemical properties fixed in part before the reactions with ultramafic rocks, in part by the reactions of orthopyroxene, olivine, and serpentine and in part by reactions with siliceous country rock at the contact. The reactions of the ultramafic rock and country rock with the fluid must be contemporaneous and require flow to be along the contact. This third type of fluid is grossly supersaturated with talc and tremolite, both found along the contact. The occurrence of magadiite, kenyaite, mountainite, and rhodesite along the contact is probably due to a late stage low-temperature reaction of fluids of the same thermodynamic properties as those that formed the talc and tremolite at higher temperatures. Oxygen isotope analyses of some of these minerals supports this conclusion. Rodingites form from Ca+2-rich fluids flowing across the contact; talc and tremolite form from silica-rich fluids flowing along the contact

  3. Micro-Raman and micro-XRF analysis of glass beads from the Chungde site, Taiwan

    Science.gov (United States)

    Liou, Y. S.; Wang, S. C.; Liu, Y. C.

    2014-12-01

    A large number of ancient glass beads dating back from Late Neolithic Age to early Historical Period (ca. 2300-400 BP) of Taiwan have been uncovered from archaeological sites. These glass beads with variant colors, shapes, and stylistics have long been considered to possess socio-cultural significance. Due to the color and chemical composition of glass bead might be determined by raw materials, fluxing agents, colorants, opacifiers and stabilizers. In addition, ancient glass beads are rare and precious, non-destructive analysis has been employed to decipher about the provenances, manufacturing techniques, and exchange/trade routes. In this work, micro-Raman spectroscopy and micro X-ray fluorescent spectrometer (μ-XRF) were used to examine ten ancient glass beads excavated from the Chungde site, Hualien, Taiwan, dating back to 1500-800 BP, to unravel the mineralogical and chemical compositions. Micro Raman experimental results show that glass and anorthite glass are the main constituents accompanying with trace level of quartz, albite, siderite, ankerite, and amazonite. The Raman Index of Polymerization (Ip) indicate that the sintering temperature of the glass beads is in the range of 1000~1400°C. Furthermore, the chemical compositions are corresponding to the maximum stretching vibration peak wave number (νmax Si-O Stretching) and the maximum bending vibration peak wave number (δmax Si-O Bending), which are essentially consistent with that of the India-Pacific beads. The μ-XRF results indicate the presence of oxides including SiO2, Al2O3, Fe2O3, Na2O, K2O, CaO, MgO, SnO2, TiO2, CuO, etc., and could be classified to high aluminum of soda-lime glass system. According to ternary phase diagram analysis of CaO-K2O-Na2O and K2O-Al2O3-CaO, the ancient glass beads analyzed could be attributed to the India-Pacific beads, and is in accordance with that of Raman spectra. The combination of these facts leads to the conclusion that glass beads obtained from the Chungde

  4. Estimations of durability of fracture mineral buffers in the Olkiluoto bedrock

    International Nuclear Information System (INIS)

    Luukkonen, A.

    2006-12-01

    This study attempts to make scenarios for the geochemical effects that the underground excavations in the Olkiluoto bedrock have on naturally occurring fracture mineral buffers. The excavations of underground research facilities and final repository galleries probably cause steep hydraulic gradients in some bedrock fractures. These gradients likely draw surficial waters within the fracture network and activate weathering processes deeper in rock fractures than in the natural undisturbed conditions. The present studies concentrate on the meteoric infiltration in a single rock fracture, and on the selected set of minerals believed to be significant buffers against pH/redox variations in groundwater. The modelling considers the possibility that the infiltrating meteoric water is soil water rich in dissolved inorganic carbon. Calcite, pyrite, quartz, amorphous silica, cordierite, hornblende, albite, K-feldspar, kaolinite, and illite are taken into account as reacting minerals. Simulations are done by varying the flow rate of water from 1 L/h to 100 L/h. The effects of mineral reactions onto porosity and permeability values are monitored as well. In the present study, however, the changes in physical properties of the fracture channel do not affect the flow rate of water. Furthermore, calculations also describe how cation exchange affects the studied fracture channel system. The simulations coupling the hydraulic flow and water-rock interaction were done with TOUGHREACT V1.0 code and with the EQ3/6-database implemented in the code. In part, the simulations were evaluation of the code capabilities, and verification of results to earlier PHREEQC-2 simulation results. The calculation results confirm the assumption that principal buffer against pH changes is calcite. All silicate reactions, with considered reactive surface areas, are by comparison of marginal importance. The only redox buffer in the calculations is pyrite, and consequently significant amounts of oxygen runs

  5. A Case for Nebula Scale Mixing Between Non-Carbonaceous and Carbonaceous Chondrite Reservoirs: Testing the Grand Tack Model with Chromium Isotopic Composition of Almahata Sitta Stone 91A

    Science.gov (United States)

    Sanborn, M. E.; Yin, Q.-Z.; Goodrich, C. A.; Zolensky, M.; Fioretti, A. M.

    2017-01-01

    There is an increasing number of Cr-O-Ti isotope studies that show solar system materials are divided into two main populations, one carbonaceous chondrite (CC)-like and the other is non-carbonaceous (NC)-like, with minimal mixing attributed to a gap opened in the protoplanetary disk due to Jupiter's formation. The Grand Tack model suggests there should be large-scale mixing between S- and C-type asteroids, an idea supported by our recent work on chondrule (Delta)17O-e54Cr isotope systematics. The Almahata Sitta (AhS) meteorite provides a unique opportunity to test the Grand Tack model. The meteorite fell to Earth in October 2008 and has been linked to the asteroid 2008 TC3 which was discovered just prior to the fall of the AhS stones. The AhS meteorite is composed of up to 700 individual pieces with approx.140 of those pieces having some geochemical and/or petrologic studies. Almahata Sitta is an anomalous polymict ureilite with other meteorite components, including enstatite, ordinary, and carbonaceous chondrites with an approximate abundance of 70% ureilites and 30% chondrites. This observation has lead to the suggestion that TC3 2008 was a loosely aggregated rubble pile-like asteroid with the non-ureilite sample clasts within the rubble-pile. Due to the loosely-aggregated nature of AhS, the object disintegrated during atmospheric entry resulting in the weakly held clasts falling predominantly as individual stones in the AhS collection area. However, recent work has identified one sample of AhS, sample 91A, which may represent two different lithologies coexisting within a single stone. The predominate lithology type in 91A appears to be that of a C2 chondrite based on mineralogy but also contains olivine, pyroxene, and albite that have ureilite-like compositions. Previous Cr isotope investigations into AhS stones are sparse and what data is available show nearly uniform isotopic composition similar to that of typical ureilites with negative e54Cr values.

  6. Crystallization conditions and petrogenesis of the lava dome from the ˜900 years BP eruption of Cerro Machín Volcano, Colombia

    Science.gov (United States)

    Laeger, Kathrin; Halama, Ralf; Hansteen, Thor; Savov, Ivan P.; Murcia, Hugo F.; Cortés, Gloria P.; Garbe-Schönberg, Dieter

    2013-12-01

    The last known eruption at Cerro Machín Volcano (CMV) in the Central Cordillera of Colombia occurred ˜900 years BP and ended with the formation of a dacitic lava dome. The dome rocks contain both normally and reversely zoned plagioclase (An24-54), unzoned and reversely zoned amphiboles of dominantly tschermakite and pargasite/magnesio-hastingsite composition and olivine xenocrysts (Fo = 85-88) with amphibole/clinopyroxene overgrowth, all suggesting interaction with mafic magma at depth. Plagioclase additionally exhibits complex oscillatory zoning patterns reflecting repeated replenishment, fractionation and changes in intrinsic conditions in the magma reservoir. Unzoned amphiboles and cores of the reversely zoned amphiboles give identical crystallization conditions of 910 ± 30 °C and 360 ± 70 MPa, corresponding to a depth of about 13 ± 2 km, at moderately oxidized conditions (f = +0.5 ± 0.2 ΔNNO). The water content in the melt, calculated based on amphibole chemistry, is 7.1 ± 0.4 wt.%. Rims of the reversely zoned amphiboles are relatively enriched in MgO and yield higher crystallization temperatures (T = 970 ± 25 °C), slightly lower melt H2O contents (6.1 ± 0.7 wt.%) and overlapping pressures (410 ± 100 MPa). We suggest that these rims crystallized following an influx of mafic melt into a resident magma reservoir at mid-crustal depths, further supported by the occurrence of xenocrystic olivine. Crystallization of biotite, albite-rich plagioclase and quartz occurred at comparatively low temperatures (probably during early stages of ascent or storage at shallower levels. Based on amphibole mineral chemistry, the felsic resident melt had a rhyolitic composition (71 ± 2 wt.% SiO2), whereas the hybrid magma, from which the amphibole rims crystallized, was dacitic (64 ± 3 wt.% SiO2). The bulk rock chemistry of the CMV lava dome dacites is homogenous. They have elevated (La/Nb)N ratios of 3.8-4.5, typical for convergent margin magmas, and display several

  7. Early Jurassic mafic dykes from the Aigao uranium ore deposit in South China: Geochronology, petrogenesis and relationship with uranium mineralization

    Science.gov (United States)

    Zhang, Di; Zhao, Kui-Dong; Chen, Wei; Jiang, Shao-Yong

    2018-05-01

    Mafic dykes are abundant and widely distributed in many granite-hosted uranium ore deposits in South China. However, their geochronology, petrogenesis and relationship with uranium mineralization were poorly constrained. In this study, apatite U-Pb dating, whole-rock major and trace element and Sr-Nd-Pb isotope analysis were conducted for the dolerite dykes from the Aigao uranium ore deposit. Apatite U-Pb isotopic data indicate that the mafic dykes were emplaced at Early Jurassic (189 ± 4 Ma), which provides new evidence for the rarely identified Early Jurassic magmatism in South China. Pyroxene from the dykes is mainly augite, and plagioclase belongs to albite. The dolerite samples have relatively low SiO2 contents (45.33-46.79 wt%), relatively high total alkali contents (K2O + Na2O = 4.11-4.58 wt%) and Al2O3 contents (13.39-13.80 wt%), and medium MgO contents (4.29-5.16 wt%). They are enriched in Nb, Ta, Ti, rare earth elements and depleted in Rb, K, Sr, Th, showing the typical OIB-like geochemical affinity. All the dolerite samples show homogeneous Sr-Nd-Pb isotopic compositions, with (87Sr/86Sr)i varying from 0.706049 to 0.707137, εNd(t) from +4.6 to +5.2, 206Pb/204Pb from 19.032 to 19.126 and 207Pb/204Pb from 15.641 to 15.653. The mafic dykes in the Aigao deposit should be derived from the partial melting of the asthenospheric mantle and formed in a within-plate extensional environment. The emplacement age of the mafic dykes is older than the uranium mineralization age. Therefore, CO2 in ore-forming fluids couldn't originate from the basaltic magma as suggested by previous studies. The dolerite dykes might only provide a favorable reducing environment to promote the precipitation of uraninite from oxidize hydrothermal fluids.

  8. An exotic terrane in the Sulu UHP region, China

    Science.gov (United States)

    Chu, W.; Zhang, R.; Tsujimori, T.; Liou, J. G.

    2004-12-01

    The Haiyangsuo region of about 15 km2 along the coast in the NE part of the Triassic Sulu UHP terrane occurs three major rock types: amphibolitized metagabbro, gneiss and granitic dikes. Three different gneisses were observed in the field: A) Light color felsic gneiss is the dominant country rock and contains Qtz, Pl, Ms and Bi. B) Dark color plagioclase-amphibole gneiss occurs as thin layers within country rock; C) Granulite facies rock occurs as discontinuous lens. The amphibolitized metagabbros intrude into the gneisses as massive bodies (several m to hundreds of m in size) and thin dikes. Both metamorphic intrusives and gneisses are cross-cut by granitic dikes. The amphibolitized metagabbro was divided into three types: coronal metagabbro, transitional rock and garnet amphibolite: 1) Coronal metagabbro preserves gabbroic texture and primary assemblage of Opx+Cpx+Pl+Amp+Ilm. Most pyroxene grains are partially rimmed by thin corona of Amp+Ab+Qtz. Garnet occurs as fine-grained coronas at interface between plagioclase, pyroxene or ilmenite. 2) Transitional rocks contain similar assemblage and texture but most orthopyroxenes were partially or totally replaced by Amp+Qtz; garnet increases in content and size. Some gabbroic textures are preserved, but calcic plagioclase was replaced by zoisite, albite and muscovite. 3) Garnet amphibolite occurs at the margins of intrusive bodies and boudins where only minor relict clinopyroxenes preserve. Garnet coronal chains are not clear any more. Granitic dikes show pronounced deformation with mylonitic texture and contain 40-50% quartz porphyroclasts. Zircon separates from 2 metagabbros, 4 gneisses and 1 granitic rock were dated by using Stanford SHRIMP-RG. Metagabbroic zircons are angular and fractured shapes. The upper-intercept ages of gneisses rang from 1730 to about 2400 Ma, indicating variable protoith age. The 2 garnet amphibolites have upper-intercept ages 1734±5Ma and 1735±21Ma respectively. They are much older than

  9. The Saint Martin de Belleville syncline and its uraniferous permian sandstone

    International Nuclear Information System (INIS)

    Schade, Johannes

    1983-01-01

    This dissertation (these de specialite) is a study of the geology of the St.Martin d.B. syncline and the uranium prospect 'le Cochet' in the Carboniferous Brianconnais Zone of Savoy. Stratigraphy and sedimentology: This syncline presents continental detrital sediments ranging from U.Carboniferous to L.Triassic. In the U.Carboniferous, magmatic activity begins with the Moriaz Layers acid volcanics that are considered as a lateral equivalent of the Stephanian Courchevel Conglomerates. In Permian times, parts of an alluvial fan seem to occupy the north of the study area (gray and green conglomeratic sandstone). Southwards these inter-finger with flood plain sediments (red slate) including a locally oolitic limestone. Volcanic detritus is important in the Permian. Tourmalinite pebbles are frequent and seem to be related to the regional Permian magmatism. Albitization of feldspars is general in the Carboniferous and the Permian. The Permo-triassic typically shows microcline bearing dolomitic sandstones. In the Scythian quartzites orthoclase is the dominant feldspar. The quartzites are overlain by L.Triassic evaporites identified by the sulfur isotope ratio of their gypsum. The morphology of the zircons in the sandstones has been investigated using the typological method of J.P. Pupin. Regional Permian magmatism apparently produces volcanics of the calc-alkalic and tholeiitic series as well as a high level granitic intrusion of anatectic origin. The uranium occurrences are strata-bound on a kilometric and hecto-metric scale. They are developed almost exclusively in the gray variety of the Permian sandstones whose gray and red varieties are always barren. Within this unit, the mineralization impregnates irregularly distributed lenses and pods of coal material. Uranium is accompanied by vanadium occurring as roscoelite. The association U-V, of bio-philic character, reflects the concentration in the sedimentary environment and argues for a quite indirect relation with the

  10. Gamma-spectrometric surveys in differentiated granites. II: the Joaquim Murtinho Granite in the Cunhaporanga Granitic Complex, Parana, SE Brazil; Levantamentos gamaespectrometricos em granitos diferenciados. II: O exemplo do Granito Joaquim Murtinho, Complexo Granitico Cunhaporanga, Parana

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Francisco Jose Fonseca [Universidade Federal do Parana (UFPR), Curitiba, PR (Brazil). Dept. de Geologia. Lab. de Pesquisas em Geofisica Aplicada; Fruchting, Allan [Votorantim Metais, Sao Paulo, SP (Brazil)], e-mail: allan.fruchting@vmetais.com.br; Guimaraes, Gilson Burigo [Universidade Estadual de Ponta Grossa (UEPG), PR (Brazil). Dept. de Geociencias], e-mail: gburigo@ig.com.br; Alves, Luizemara Soares [PETROBRAS S.A., Rio de Janeiro, RJ (Brazil)], e-mail: luizemara@petrobras.com.br; Martin, Victor Miguel Oliveira; Ulbrich, Horstpeter Herberto Gustavo Jose [Universidade de Sao Paulo (USP), SP (Brazil). Inst. de Geociencias. Dept. de Mineralogia e Geotectonica], e-mail: vicmartin6@ig.com.br, e-mail: hulbrich@usp.br

    2009-07-01

    Detailed mapping at the NW corner of the large Neo proterozoic Cunhaporanga Granitic Complex (CGC), Parana state, SE Brazil, redefined the Joaquim Murtinho Granite (JMG), a late intrusion in CGC with an exposed area of about 10 km{sup 2}, made up mainly by evolved 'alaskites' (alkali-feldspar leuco granites). This unit is in tectonic contact with the Neoproterozoic-Eocambrian volcano-sedimentary Castro Group, to the W, and is intrusive into other less evolved granitic units of the CGC to the E. Petrographically, JMG shows mainly mesoperthite and quartz, with subordinate amounts of altered micas and some accessory phases, mainly zircon. The equi to inequigranular granites are usually deformed with cataclastic textures, are often brecciated, and may have miarolitic structures. Formation of late albite, sericite, carbonate and hematite was caused by deuteric and hydrothermal alteration. A gamma-ray spectrometric survey at 231 stations which measured total counts (TC), Ueq K%, eU ppm and eTh ppm was used to construct several direct and derived maps. Compared to neighboring units the JMG has significant anomalies, especially in the TC, %K, eTh and eU maps, although the differences are less obvious in some derived maps. These evolved granites are enriched in these three elements. Geochemical behavior of K, Th and U is used to analyse the results observed in maps. Enhanced weathering under a subtropical climate with moderate to high average temperatures and heavy rainfall affects mainly feldspars and biotite, and may also destabilize most U and Th-bearing accessory phases. Th is most likely retained in restite minerals in soils, being relatively immobile, while part of U may migrate as uranyl ion in oxidizing media. K is especially affected by feldspar alteration to K-free clays (mainly kaolinite), and may be completely leached. Gamma-ray spectrometric methods are valid tools to study facies in granitic rocks, especially in those that are enriched in K, Th and U

  11. CARACTERÍSTICAS QUÍMICO-MINERALÓGICAS DE FONTES DE PIGMENTOS MINERAIS EM DEPÓSITOS NATURAIS DO ENTORNO DO SÍTIO ARQUEOLÓGICO PEDRA DO CANTAGALO I, EM PIRIPIRI, PIAUÍ, BRASIL (Chemical-Mineralogical Features of Mineral Pigments Sources in Natural Deposits Surrounding the Pedra do Cantagalo I Archaeological Site, in Piripiri, Piauí, Brazil

    Directory of Open Access Journals (Sweden)

    Heralda Kelis Sousa Bezerra da Silva

    2017-12-01

    , which are assignable to superparamagnetic species, more likely including goethite, of small particle sizes, or the paramagnetic iron in the crystalline structure of aluminosilicates. The XRD patterns show characteristic reflections of quartz, muscovite, kaolinite, illite, albite, hematite, rutile and anatase.

  12. Cl-rich hydrous mafic mineral assemblages in the Highiș massif, Apuseni Mountains, Romania

    Science.gov (United States)

    Bonin, Bernard; Tatu, Mihai

    2016-08-01

    The Guadalupian (Mid-Permian) Highiș massif (Apuseni Mountains, Romania) displays a bimodal igneous suite of mafic (gabbro, diorite) and A-type felsic (alkali feldspar granite, albite granite, and hybrid granodiorite) rocks. Amphibole is widespread throughout the suite, and yields markedly high chlorine contents. Three groups are identified: Cl-rich potassic hastingsite (2.60-3.40 wt% Cl) within A-type felsic rocks and diorite, mildly Cl-rich pargasite to hornblende (0.80-1.90 wt% Cl) within gabbro, and low F-Cl hornblende within gabbro and hybrid granodiorite. Coexisting biotite is either Cl-rich within diorite, or F-Cl-poor to F-rich within A-type felsic rocks. Chlorine and fluorine are distributed in both mafic phases, according to the F-Fe and Cl-Mg avoidance rules. The low-Ti contents suggest subsolidus compositions. Cl-rich amphibole within diorite and A-type felsic rocks yields a restricted temperature range - from 575 °C down to 400 °C, whereas mildly Cl-rich amphibole within gabbro displays the highest range - from 675 to 360 °C. Temperatures recorded by Cl-rich biotite within diorite range from 590 to 410 °C. Biotite within A-type felsic rocks yields higher temperatures than amphibole: the highest values- from 640 to 540 °C - are recorded in low-F-Cl varieties, whereas the lowest values- from 535 to 500 °C - are displayed by F-rich varieties. All data point to halogen-rich hydrothermal fluids at upper greenschist facies conditions percolating through fractures and shear zones and pervasively permeating the whole Highiș massif, with F precipitating as interstitial fluorite and Cl incorporating into amphibole, during one, or possibly several, hydrothermal episodes that would have occurred during a ~ 150 My-long period of time extending from the Guadalupian (Mid-Permian) to the Albian (Mid-Cretaceous).

  13. Internal structure of the Supragetic Unit basement in the Serbian Carpathians and its significance for the late Early Cretaceous nappe-stacking

    Directory of Open Access Journals (Sweden)

    Krstekanić Nemanja

    2017-01-01

    Full Text Available Fault-related folds and hanging-wall structures reflect the geometry of the main thrusts in foldthrust belts. The results of the structural analysis of the Supragetic Unit metamorphic basement in eastern Serbia at map-, outcrop- and thin-section scale, and its importance for the late Early Cretaceous nappe-stacking are presented in this paper. The Supragetic Unit metamorphic basement includes various volcano-sedimentary rocks of Ordovician-Silurian protolith age. They were metamorphosed to the low greenschist facies with temperatures reaching 300-350°C and pressure reaching 0.3-0.5 GPa. The microscale studies show that quartz and albite demonstrate dominantly bulging and locally subgrain rotation recrystallisation, while chlorite, sericite and muscovite define spaced to continuous foliation recognised both at the outcrop- and the thin-section-scale. The statistical analysis based on the available map data shows low- to high-angle west-dipping foliation which is interpreted as an indicator of flat-ramp geometry of the Supragetic thrust, rather than east-vergent tight to isoclinal folding. At the thin-section scale ductile to semi-ductile C’-S structures indicate top to ESE thrusting. Subsequent kinking, recognised both at the outcrop- and the thin-section-scale, deform the older foliation. Those kink bands are the result of WNW-ESE to NW-SE compression and could represent the later stage of a continuous deformation event during which C’-S structures were formed. The youngest, brittle deformation is represented by subvertical joints with no offset recognised in thin-sections. The structural characteristics of the Supragetic Unit low-grade metamorphic basement in the studied areas, combined with tectonothermal events recognised elsewhere in Dacia mega-unit, could imply a possible initiation of the late Early Cretaceous nappe-stacking in the ductile to semi-ductile/semi-brittle domain. [Project of the Serbian Ministry of Education, Science and

  14. Hydrothermal titanite from the Chengchao iron skarn deposit: temporal constraints on iron mineralization, and its potential as a reference material for titanite U-Pb dating

    Science.gov (United States)

    Hu, Hao; Li, Jian-Wei; McFarlane, Christopher R. M.

    2017-09-01

    Uranium-lead isotopes and trace elements of titanite from the Chengchao iron skarn deposit (Daye district, Eastern China), located along the contact zones between Triassic marine carbonates and an early Cretaceous intrusive complex consisting of granite and quartz diorite, were analyzed using laser ablation inductively coupled plasma mass spectrometry to provide temporal constraints on iron mineralization and to evaluate its potential as a reference material for titanite U-Pb geochronology. Titanite grains from mineralized endoskarn have simple growth zoning patterns, exhibit intergrowth with magnetite, diopside, K-feldspar, albite and actinolite, and typically contain abundant primary two-phase fluid inclusions. These paragenetic and textural features suggest that these titanite grains are of hydrothermal origin. Hydrothermal titanite is distinct from the magmatic variety from the ore-related granitic intrusion in that it contains unusually high concentrations of U (up to 2995 ppm), low levels of Th (12.5-453 ppm), and virtually no common Pb. The REE concentrations are much lower, as are the Th/U and Lu/Hf ratios. The hydrothermal titanite grains yield reproducible uncorrected U-Pb ages ranging from 129.7 ± 0.7 to 132.1 ± 2.7 Ma (2σ), with a weighted mean of 131.2 ± 0.2 Ma [mean standard weighted deviation (MSWD) = 1.7] that is interpreted as the timing of iron skarn mineralization. This age closely corresponds to the zircon U-Pb age of 130.9 ± 0.7 Ma (MSWD = 0.7) determined for the quartz diorite, and the U-Pb ages for zircon and titanite (130.1 ± 1.0 Ma and 131.3 ± 0.3 Ma) in the granite, confirming a close temporal and likely genetic relationship between granitic magmatism and iron mineralization. Different hydrothermal titanite grains have virtually identical uncorrected U-Pb ratios suggestive of negligible common Pb in the mineral. The homogeneous textures and U-Pb characteristics of Chengchao hydrothermal titanite suggest that the mineral might be a

  15. Prediction of Nanoparticle and Colloid Attachment on Unfavorable Mineral Surfaces Using Representative Discrete Heterogeneity.

    Science.gov (United States)

    Trauscht, Jacob; Pazmino, Eddy; Johnson, William P

    2015-09-01

    Despite several decades of research there currently exists no mechanistic theory to predict colloid attachment in porous media under environmental conditions where colloid-collector repulsion exists (unfavorable conditions for attachment). It has long been inferred that nano- to microscale surface heterogeneity (herein called discrete heterogeneity) drives colloid attachment under unfavorable conditions. Incorporating discrete heterogeneity into colloid-collector interaction calculations in particle trajectory simulations predicts colloid attachment under unfavorable conditions. As yet, discrete heterogeneity cannot be independently measured by spectroscopic or other approaches in ways directly relevant to colloid-surface interaction. This, combined with the fact that a given discrete heterogeneity representation will interact differently with differently sized colloids as well as different ionic strengths for a given sized colloid, suggests a strategy to back out representative discrete heterogeneity by a comparison of simulations to experiments performed across a range of colloid size, solution IS, and fluid velocity. This has recently been performed for interaction of carboxylate-modified polystyrene latex (CML) microsphere attachment to soda lime glass at pH 6.7 with NaCl electrolyte. However, extension to other surfaces, pH values, and electrolytes is needed. For this reason, the attachment of CML (0.25, 1.1, and 2.0 μm diameters) from aqueous suspension onto a variety of unfavorable mineral surfaces (soda lime glass, muscovite, and albite) was examined for pH values of 6.7 and 8.0), fluid velocities (1.71 × 10(-3) and 5.94 × 10(-3) m s(-1)), IS (6.0 and 20 mM), and electrolytes (NaCl, CaSO4, and multivalent mixtures). The resulting representative heterogeneities (heterodomain size and surface coverage, where heterodomain refers to nano- to microscale attractive domains) yielded colloid attachment predictions that were compared to predictions from existing

  16. Mineralogy of the Chaparra IOCG deposit, southern Peru

    Science.gov (United States)

    Yáñez, Juan; Alfonso, Pura

    2014-05-01

    The Chaparra IOCG, located in southern Peru, near Chala, is mined and exploited by small-scale miners for gold, however, it has not been studied until now. Here we present a preliminary geological and mineralogic study of this deposit. Powder X ray diffraction, electron microscopy and electron microprobe were used to characterize the mineralization. This deposit is hosted in magmatic rocks from the Coastal Batholith. Host rocks belong to the Linga Super-unit, of Upper Cretaceous age and are mainly constituted by monzonites, monzogabbros and diorites. Major alterations are the propylitic (chlorite - albite - quartz), advanced argillic (jarosite - natrojarosite) and sericitic (muscovite-sericite-quartz). Gypsum and other alteration minerals such as potassium feldspar and phlogopite, vermiculite and natrolite are widespread. Mineralization occurs mainly in quartz veins up to 1 m thick, emplaced filling fractures. Ore mineralogy is mainly composed of hematite, goethite, and sulphides (mainly pyrite, chalcopyrite and covellite). Gold and REE-rich minerals also occur. Native gold can reach up to 1 mm in size, but usually is few μm in size. Its composition is 82-92 wt% Au, up to 12 wt% of Ag and Fe can reach up to 4 wt%. The paragenetic sequence in the Chaparra deposit was divided into three stages: (I) primary mineralization, (II) Fracture filling, and (III) supergene alteration. The sequence begins with the crystallization of magnetite, quartz, pyrrhotite and pyrite. Subsequently, native gold, native Bismuth and uraninite crystallices together with the former minerals, in which are enclosed. Later, monacite is formed, being enclosed in quartz. Pyrite also presents small grains of chalcopyrite inside. Galena, sphalerite and arsenopyrite also are formed, whether included in pyrite or outside. Scarce grains of sakuraiite also occur in this stage. Structural formula of sakuraiie from this deposit is Cu 01.78-1.90 Zn 0.07-12Fe 1.16-124In 0.22-0.26Sn 0.79-082S4). Indium

  17. Effects of chemical alteration on fracture mechanical properties in hydrothermal systems

    Science.gov (United States)

    Callahan, O. A.; Eichhubl, P.; Olson, J. E.

    2015-12-01

    Fault and fracture networks often control the distribution of fluids and heat in hydrothermal and epithermal systems, and in related geothermal and mineral resources. Additional chemical influences on conduit evolution are well documented, with dissolution and precipitation of mineral species potentially changing the permeability of fault-facture networks. Less well understood are the impacts of chemical alteration on the mechanical properties governing fracture growth and fracture network geometry. We use double-torsion (DT) load relaxation tests under ambient air conditions to measure the mode-I fracture toughness (KIC) and subcritical fracture growth index (SCI) of variably altered rock samples obtained from outcrop in Dixie Valley, NV. Samples from southern Dixie Valley include 1) weakly altered granite, characterized by minor sericite in plagioclase, albitization and vacuolization of feldspars, and incomplete replacement of biotite with chlorite, and 2) granite from an area of locally intense propylitic alteration with chlorite-calcite-hematite-epidote assemblages. We also evaluated samples of completely silicified gabbro obtained from the Dixie Comstock epithermal gold deposit. In the weakly altered granite KIC and SCI are 1.3 ±0.2 MPam1/2 (n=8) and 59 ±25 (n=29), respectively. In the propylitic assemblage KIC is reduced to 0.6 ±0.1 MPam1/2 (n=11), and the SCI increased to 75 ±36 (n = 33). In both cases, the altered materials have lower fracture toughness and higher SCI than is reported for common geomechanical standards such as Westerly Granite (KIC ~1.7 MPam1/2; SCI ~48). Preliminary analysis of the silicified gabbro shows a significant increase in fracture toughness, 3.6 ±0.4 MPam1/2 (n=2), and SCI, 102 ±45 (n=19), compared to published values for gabbro (2.9 MPam1/2 and SCI = 32). These results suggest that mineralogical and textural changes associated with different alteration assemblages may result in spatially variable rates of fracture

  18. Water-rock interaction in the magmatic-hydrothermal system of Nisyros Island (Greece)

    Science.gov (United States)

    Ambrosio, Michele; Doveri, Marco; Fagioli, Maria Teresa; Marini, Luigi; Principe, Claudia; Raco, Brunella

    2010-04-01

    In this work, we investigated the water-rock interaction processes taking place in the hydrothermal reservoir of Nisyros through both: (1) a review of the hydrothermal mineralogy encountered in the deep geothermal borehole Nisyros-2; and (2) a comparison of the analytically-derived redox potentials and acidities of fumarolic-related liquids, with those controlled by redox buffers and pH buffers, involving hydrothermal mineral phases. The propylitic zone met in the deep geothermal borehole Nisyros-2, from 950 to 1547 m (total depth), is characterised by abundant, well crystallised epidote, adularia, albite, quartz, pyrite, chlorite, and sericite-muscovite, accompanied by less abundant anhydrite, stilpnomelane, wairakite, garnet, tremolite and pyroxene. These hydrothermal minerals were produced in a comparatively wide temperature range, from 230 to 300 °C, approximately. Hydrothermal assemblages are well developed from 950 to 1360 m, whereas they are less developed below this depth, probably due to low permeability. Based on the RH values calculated for fumarolic gases and for the deep geothermal fluids of Nisyros-1 and Nisyros-2 wells, redox equilibrium with the (FeO)/(FeO 1.5) rock buffer appears to be closely attained throughout the hydrothermal reservoir of Nisyros. This conclusion may be easily reconciled with the nearly ubiquitous occurrence of anhydrite and pyrite, since RH values controlled by coexistence of anhydrite and pyrite can be achieved by gas separation. The pH of the liquids feeding the fumarolic vents of Stephanos and Polybote Micros craters was computed, by means of the EQ3 code, based on the Cl- δD relationship which is constrained by the seawater-magmatic water mixing occurring at depth in the hydrothermal-magmatic system of Nisyros. The temperature dependence of analytically-derived pH values for the reservoir liquids feeding the fumarolic vents of Stephanos and Polybote Micros craters suggests that some unspecified pH buffer fixes the

  19. U-Pb zircon and biostratigraphic data of high-pressure/low-temperature metamorphic rocks of the Talea Ori: tracking the Paleotethys suture in central Crete, Greece

    Science.gov (United States)

    Zulauf, G.; Dörr, W.; Krahl, J.; Lahaye, Y.; Chatzaras, V.; Xypolias, P.

    2016-10-01

    Inherited deformation microfabrics of detrital quartz grains and U-Pb (Laser ablation (LA)-ICPMS and ID TIMS) ages of detrital zircons separated from the Phyllite-Quartzite Unit s.l. of the Talea Ori, central Crete, suggest strikingly different source rocks. Albite gneiss of the lower Rogdia Beds includes Cambrian and Neoproterozoic rounded zircons with main U-Pb age peaks at 628 and 988 Ma. These and minor Paleoproterozoic and Archean peaks, together with the lack of Variscan-aged and Mesoproterozoic zircons, are similar to the age spectra obtained from the Phyllite-Quartzite Unit s.str. of the Peloponnesus and eastern Crete and from the Taurides. All of these zircons should be derived from the northeastern passive margin of Gondwana (Cimmeria). Metatuffites of the uppermost Rogdia Beds and metasandstone of Bali beach, on the other hand, include euhedral detrital zircons displaying a Variscan U-Pb age spectra at ca. 300 Ma with concordia ages at 291 ± 3, 300 ± 1 Ma (Rogdia) and 286 ± 3, 300 ± 3, 313 ± 2 Ma (Bali). Both types of metasediments and their zircons are similar to those of the pre-Alpine basement and overlying Tyros Beds of eastern Crete, revealing a provenance at the southern active margin of Laurasia. Thus, in central Crete the Paleotethys suture should be situated inside the Rogdia Beds. Magmatic zircons separated from a rhyolite boulder of the lower Achlada Beds yielded a concordant U-Pb zircon age at 242 ± 2 Ma placing a maximum age for the deposition of the (meta)conglomerate from which the boulder was collected. This age is compatible with an Olenekian-early Anisian age of the underlying Vasilikon marble suggested by new findings of the foraminifera Meandrospira aff. pusilla. Both the Achlada Beds and the Vasilikon marble can be attributed to the lower Tyros Beds of eastern Crete. The Alpine deformation led to a pervasive mylonitic foliation, which is affecting most of the studied rocks. This foliation results from D2 top

  20. Solid oxide electrolyser cell

    Energy Technology Data Exchange (ETDEWEB)

    Hoejgaard Jensen, S.

    2006-12-15

    Solid oxide fuel cells (SOFCs) produced at Riso National Laboratory was tested as steam electrolysers under various current densities, operating temperatures and steam partial pressures. At 950 deg. C and a cell voltage of 1.48V the current density was -3.6 A/cm{sup 2} with app. 30% H{sub 2} + 70% H{sub 2}O in the inlet gas and a H{sub 2}O utilization of app. 40%. The tested SOECs were also used for CO{sub 2} electrolysis. Economy studies of CO and H2 production show that especially H{sub 2} production can be competitive in areas with cheap electricity. Assuming the above described initial performance and a lifetime of 10 years it is possible to achieve a production price of 0.7 US dollar/kg H{sub 2} with an electricity price of 1.3 US cent/kWh. The cell voltage was measured as function of time. In test of about two month of duration a long-term degradation was observed. At 850 deg. C, -0.5 A/cm{sup 2} with 50 vol% H{sub 2} the degradation rate was app. 20 mV/1000h. It was shown that the degradation happens at Ni/YSZ-electrode. The long term degradation is probably caused by coarsening of the Ni-particles. After onset of electrolysis operation a transient passivation/reactivation phenomena with duration of several days was observed. It was shown that the phenomenon is attributed to the SiO{sub 2} contamination at the Ni/YSZ electrode-electrolyte interface. The SiO{sub 2} arises from the albite glass sealing (NaAlSi{sub 3}O{sub 8}) that surrounds the electrode. Si may enter the Ni/YSZ electrode via the reaction Si(OH){sub 4}(g) {r_reversible} SiO{sub 2}(l)+H{sub 2}O(g). At the active sites of the Ni/YSZ electrode steam is reduced via the reaction H{sub 2}O - 2e {yields} H{sub 2}+O{sup 2-} . This shifts the equilibrium of the first reaction to form SiO{sub 2}(l) at the active sites. After a certain time the sealing crystallizes and the SiO{sub 2}(l) evaporates from the active sites and the cell reactivates. The passivation is shown to relate to a build up of a

  1. Processing of Vietnamese lithium ores to produce LiCl

    Energy Technology Data Exchange (ETDEWEB)

    Dinh, Thi Thu Hien

    2015-11-16

    A potential lithium deposit has been discovered in the La Vi mining district, located in Quang Ngai Province, Central Vietnam. The Li-rich rocks (average contents: 1.3±0.9 wt.% Li{sub 2}O) are highly fractionated, peraluminous granites, which are further characterized by high contents of Al{sub 2}O{sub 3}, Na{sub 2}O, K{sub 2}O, F, and P{sub 2}O{sub 5}, but very low concentrations of all other main components (MgO, CaO, Fe{sub 2}O{sub 3}tot, TiO{sub 2}). The granites exhibit a light pink color and contain mainly albite, quartz, muscovite, lithian muscovite, and lepidolite, with minor amounts of amblygonite-montebrasite, herderite, fluorapatite, topaz, and cassiterite, and accessory beryl and goyazite. Lepidolite from La Vi deposit was extracted to produce lithium chloride by using iron II sulphide (FeS)-CaO roasting and water leaching. The HSC program was applied for the simulation of the behavior of lepidolite and the additives during roasting, confirming the important role of SO{sub 2}/SO{sub 3} gas for extracting lithium from lepidolite. At optimum conditions roasting at 750 C using FeS/Li and Ca/F molar ratios of 5:1 and 1:1, respectively, followed by leaching at 50 C using water/calcine mass ratios of >5:1 could yield a maximum of ∝85% Li recovery (at <1 g/L Li concentration). Addition of CaO led to a decrease in the liberation of HF gas and insoluble LiF formation. NaOH and BaCl{sub 2} were used for removing the metal and sulphate impurities from the leach liquor by precipitation at ambient temperature. The efficiency of lithium extraction reached ∝100 % with washing of the precipitates after filtering. Alkali salts were separated from the LiCl solution via solar evaporation and isopropanol leaching. 96.3 wt.% LiCl could be produced using an isopropanol/salt mass ratio of 5:1 at ambient temperature in 3 h.

  2. Magmatic evolution and controls on rare metal-enrichment of the Strange Lake A-type peralkaline granitic pluton, Québec-Labrador

    Science.gov (United States)

    Siegel, Karin; Vasyukova, Olga V.; Williams-Jones, Anthony E.

    2018-05-01

    Although it is well known that A-type granites are enriched in the rare earth elements (REE) and other high field strength elements (HFSE), the magmatic processes that concentrate these elements are still poorly understood. The 1.24 Ga Strange Lake pluton in northern Québec-Labrador provides an extraordinary example of hyper-enrichment in the REE, Zr, and Nb in a peralkaline A-type granite. The pluton consists of two hypersolvus granite units (southern and northern) and a transsolvus granite, all of which contain perthitic alkali feldspar as the earliest major mineral; the transsolvus granite also contains separate albite and microcline crystals. Arfvedsonite, a sodic amphibole, occurs exclusively as phenocrysts in the transsolvus granite, whereas in the hypersolvus granite it is present as a late, interstitial phase. The primary HFSE minerals are zircon, monazite-(Ce), gagarinite-(Ce) and the pyrochlore group minerals. Magma evolution was monitored by the alumina content in the bulk rock, which decreases from the southern to the northern hypersolvus granite and is lowest in the transsolvus granite. Alkalinity indices and bulk Si, Fe, Rb, REE, Zr, Nb concentrations show the opposite trend. Alkali feldspar compositions mirror the trend shown by the bulk rock, i.e., decreasing Al contents are accompanied by increasing Si, Fe3+, REE, Zr and Nb contents. The major driving forces for the evolution of the hypersolvus magma prior to emplacement were the early separation of a fluoride melt from the silicate melt and the crystallization of alkali feldspar and HFSE-rich phases (zircon, monazite-(Ce), pyrochlore group). An alkali feldspar-rich crystal-mush containing LREE-fluoride melt droplets was emplaced as the least evolved southern hypersolvus granite. Massive fractionation of alkali feldspar led to a sharp increase in ƒH2O and F- activity in the magma chamber that triggered the crystallization of arfvedsonite and was followed by emplacement of the northern hypersolvus

  3. A middle Permian ophiolite fragment in Late Triassic greenschist- to blueschist-facies rocks in NW Turkey: An earlier pulse of suprasubduction-zone ophiolite formation in the Tethyan belt

    Science.gov (United States)

    Topuz, Gültekin; Okay, Aral I.; Schwarz, Winfried H.; Sunal, Gürsel; Altherr, Rainer; Kylander-Clark, Andrew R. C.

    2018-02-01

    The Eastern Mediterranean region within the Tethyan belt is characterised by two main pulses of suprasubduction-zone ophiolite formation during the Early-Middle Jurassic and Late Cretaceous. Despite vast exposures of the Permo-Triassic accretionary complexes, related suprasubduction-zone ophiolites and the timing of subduction initiation leading to the formation of Permo-Triassic accretionary complexes are unknown so far. Here we report on a 40 km long and 0.3 to 1.8 km wide metaophiolite fragment within transitional greenschist- to blueschist-facies oceanic rocks from NW Turkey. The metaophiolite fragment is made up mainly of serpentinite and minor dykes or stocks of strongly sheared metagabbro with mineral assemblages involving actinolite/winchite, chlorite, epidote, albite, titanite and phengite. The metagabbro displays (i) variable CaO and MgO contents, (ii) anomalously high Mg# (= 100 ∗ molar MgO/(MgO + FeOtot)) of 75-88, and (iii) positive Eu anomalies, together with low contents of incompatible elements such as Ti, P and Zr, suggesting derivation from former plagioclase cumulates. The serpentinites comprise serpentine, ± chlorite, ± talc, ± calcite and relict Cr-Al spinel surrounded by ferrichromite to magnetite. Relict Cr-Al spinels are characterised by (i) Cr/(Cr + Al) ratios of 0.45-0.56 and Mg/(Mg + Fe2 +) ratio of 0.76-0.22, (ii) variable contents of ZnO and MnO, and (iii) extremely low TiO2 contents. Zn and Mn contents are probably introduced into Cr-Al spinels during greenschist- to blueschist metamorphism. Compositional features of the serpentinite such as (i) Ca- and Al-depleted bulk compositions, (ii) concave U-shaped, chondrite-normalised rare earth element patterns (REE) with enrichment of light and heavy REEs, imply that serpentinites were probably derived from depleted peridotites which were refertilised by light rare earth element enriched melts in a suprasubduction-zone mantle wedge. U-Pb dating on igneous zircons from three metagabbro

  4. The LaPaz Icefield 04840 meteorite: Mineralogy, metamorphism, and origin of an amphibole- and biotite-bearing R chondrite

    Science.gov (United States)

    McCanta, M. C.; Treiman, A. H.; Dyar, M. D.; Alexander, C. M. O.'D.; Rumble, D., III; Essene, E. J.

    2008-12-01

    The R chondrite meteorite LaPaz Icefield (LAP) 04840 is unique among metamorphosed, non-carbonaceous chondrites in containing abundant OH-bearing silicate minerals: ˜13% ferri-magnesiohornblende and ˜0.4% phlogopite by volume. Other minerals include olivine (Fo 62), orthopyroxene (En 69Fs 30Wo 1), albite (An 8Ab 90Or 2), magnetite, pyrrhotite, pentlandite, and apatite. Ferromagnesian minerals are rich in Fe 3+, as determined by Mössbauer spectrometry and electron microprobe chemical analyses. Fe 3+/Fe tot values are olivine ⩽5%, amphibole 80%, phlogopite 65%, and magnetite 42%. Mineral compositions are nearly constant across grains and the section, except for a small variability in amphibole compositions reflecting the edenite exchange couple ( ANa + IVAl ↔ A□ + Si). These mineral compositions, the absence of Fe-Ni metal, and the oxygen isotope data support its classification as an R (Rumuruti) chondrite. LAP 04840 is classified as petrologic grade 5, based on the chemical homogeneity of its minerals, and the presence of distinctly marked chondrules and chondrule fragments in a fine-grained crystalline matrix. The mineral assemblage of LAP 04840 allows calculation of physical and chemical conditions at the peak of its metamorphism: T = 670 ± 60 °C from a amphibole-plagioclase thermometer; PO between 250 and 500 bars as constrained by the assemblage phlogopite + orthopyroxene + olivine + feldspar and the absence of diopside; P unconstrained; f at QFM + 0.5 log units; log(f/fO)≈-5.8;log(f/fO)≈-3.3;andlog(f/f)≈-2.6. The hydrogen in LAP 04840 is very heavy, an average δD value of +3660 ± 75‰ in the magnesiohornblende. Only a few known sources of hydrogen have such high δD and are suitable sources for LAP 04840: ordinary chondrite phyllosilicates (as in the Semarkona chondrite), and insoluble organic matter (IOM) in ordinary chondrites and CR chondrites. Hydrogen from the IOM could have been released by oxidation, and then reacted with an anhydrous

  5. Site investigation SFR. Boremap mapping of core drilled borehole KFR106

    Energy Technology Data Exchange (ETDEWEB)

    Winell, Sofia (Geosigma AB (Sweden))

    2010-06-15

    This report presents the result from the Boremap mapping of the core drilled borehole KFR106, drilled from an islet ca 220 m southeast of the pier above SFR. The borehole has a length of 300.13 m, and a bearing and inclination of 195.1 deg and -69.9 deg, respectively. The purpose of the location and orientation of the borehole is to investigate the possible occurrence of gently dipping, water-bearing structures in the area. The geological mapping is based on simultaneous study of drill core and borehole image (BIPS). The two lowermost meters of the drill core was mapped in Boremap without access to complementary BIPS-image. The dominating rock type, which occupies 72% of KFR106, is fine- to medium-grained, metagranite granodiorite (rock code 101057), which is foliated with a medium to strong intensity. Pegmatite to pegmatitic granite (rock code 101061) is the second most common rock type and it occupies 16% of the mapped interval. It is also frequent as smaller rock occurrences (< 1 m) in other rock types throughout the borehole. Subordinate rock types are fine- to medium-grained granite (rock code 111058), felsic to intermediate meta volcanic rock (rock code 103076), fine- to medium-grained metagranitoid (rock code 101051) and amphibolite (rock code 102017). Totally 49% of the rock in KFR106 has been mapped as altered, where muscovitization and oxidation is the two most common. Additional shorter intervals of alterations are in decreasing order of abundance quartz dissolution, epidotization, argillization, albitization, chloritization, laumontization and carbonatization. A total number of 2801 fractures are registered in KFR106. Of these are 1059 open, 1742 sealed and 84 partly open. This result in the following fracture frequencies: 6.0 sealed fractures/m, 3.7 open fractures/m and 0.3 partly open fractures/m. In addition there are 5 narrow brecciated zones, and 20 sealed networks with a total length of 18 m. The most frequent fracture fillings in KFR106 are

  6. From Compression to Extension: Cretaceous A-type Granite as Indicator of Geodynamic Changes in the Adria Part of the European Neotethys Suture Zone

    Science.gov (United States)

    Balen, D.; Schneider, P.; Massonne, H. J.; Opitz, J.; Petrinec, Z.

    2017-12-01

    The Cretaceous suture zone between the colliding plates of European and Adria (Gondwana) marks the closure of the W Neotethys branch. This zone, partly located in the northern Croatia, comprises reddish alkali granite which is mainly composed of alkali feldspar and quartz, with small amounts of albite, white mica and hematite with ilmenite exsolutions. Accessory minerals include zircon, apatite and Fe-(Ti)-oxides. This granite shows a geochemical signature typical for A2-type granite characterized by a highly siliceous composition and an enrichment in alkalies (high-K calc-alkaline series) and Al (strongly peraluminous, ASI>1.1). The rock belongs to the group of oxidized and ferroan granites with low CaO, MgO, MnO and FeO* contents. Characteristic trace element ratios, primitive mantle and OIB normalized spider-diagrams show significant positive anomalies of Rb, Th, U, K, Zr and Pb accompanied with clear negative anomalies of Ba, Nb, Sr, P, Eu and Ti. The negative anomalies suggest fractionation of plagioclase, apatite and Fe-Ti oxide. Based on the geochemical characteristics the magma originated mainly from melting of lower continental crust (granulite facies metasediments) although a mantle contribution cannot be excluded. The melting process could have been triggered by a heat from the upwelling upper mantle as inferred from zircon typology (D and J5 types prevail), as well from the zircon and whole-rock chemistry accompanied with high zircon saturation temperatures (T=860-950°C). Subsequent ascent of granitic magma was localized along the Europe-Adria suture i.e. the Sava Zone segment of the Late Cretaceous collisional zone where granite was emplaced at ca. 20 km depth. The emplacement followed a long period of Mesozoic orogenic compressional activity. Typical for A-type granites, although in our case related to the subduction of the Adria plate underneath the European plate, is their formation in an extensional tectonic regime. Thus, the studied A

  7. Metabasalts from the Mid-Atlantic Ridge: new insights into hydrothermal systems in slow-spreading crust

    Science.gov (United States)

    Gillis, Kathryn M.; Thompson, Geoffrey

    1993-12-01

    An extensive suite of hydrothermally altered rocks were recovered by Alvin and dredging along the MARK [Mid-Atlantic Ridge, south of the Kane Fracture Zone (23 24°N)] where detachment faulting has provided a window into the crustal component of hydrothermal systems. Rocks of basaltic composition are altered to two assemblages with these characteristics: (i) type I: albitic plagioclase (An02 10)+mixed-layer smectite/chlorite or chlorite±actinolite±quartz±sphene, 20% of the clinopyroxene is altered, and Cu and Zn are leached. The geochemical signature of these alteration types reflects the relative proportion and composition of secondary minerals, and the degree of alteration of primary phases, and does not show simple predictive relationships. Element mobilities indicate that both alteration types formed at low water/rock ratios. The MARK assemblages are typical of the greenschist and transition to the amphibolite facies, and represent two distinct, albeit overlapping, temperature regimes: type I-180 to 300°C and type II-250 to 450°C. By analogy with DSDP/ODP Hole 504B and many ophiolites, the MARK metabasalts were altered within the downwelling limb of a hydrothermal cell and type I and II samples formed in the upper and lower portions of the sheeted like complex, respectively. Episodic magmatic and hydrothermal events at slow-spreading ridges suggest that these observed mineral assemblages represent the cumulative effects of more than one hydrothermal event. Groundmass and vein assemblages in the MARK metabasalts indicate either that alteration conditions did not change during successive hydrothermal events or that these assemblages record only the highest temperature event. Lack of retrograde reactions or overprinting of lower temperature assemblages (e.g., zeolites) suggests that there is a continuum in alteration conditions while crustal segments remain in the ridge axis environment. The type II samples may be representative of the reaction zone where

  8. Hydrothermal alteration of a rhyolitic hyaloclastite from Ponza Island, Italy

    Science.gov (United States)

    Ylagan, Robert F.; Altaner, Stephen P.; Pozzuoli, Antonio

    1996-12-01

    A rhyolitic hyaloclastite from Ponza island, Italy, has been hydrothermally altered producing four distinct alteration zones based on XRD and field textures: (1) non-pervasive argillic zone; (2) propylitic zone; (3) silicic zone; and (4) sericitic zone. The unaltered hyaloclastite is a volcanic breccia with clasts of vesiculated obsidian in a matrix of predominantly pumice lapilli. Incomplete alteration of the hyaloclastite resulted in the non pervasive argillic zone, characterized by smectite and disordered opal-CT. Obsidian clasts, some pumice lapilli, and pyrogenic plagioclase and biotite are unaltered. Smectite has an irregular flakey morphology, although euhedral particles are occasionally observed. The propylitic zone is characterized by mixed-layer illite/smectite (I/S) with 10 to 85% illite (I), mordenite, opal-C and authigenic K-feldspar (akspar). The matrix of the hyaloclastite is completely altered and obsidian clasts are silicified; however, plagioclase and biotite phenocrysts remain unaltered. Flakey I/S replaces pumice, and mordenite, akspar and silica line and fill pores. I/S particles are composed predominantly of subequant plates and euhedral laths. The silicic zone is characterized by highly illitic I/S with ≥ 90% I, quartz, akspar and occasional albite. In this zone the matrix and clasts are completely altered, and pyrogenic plagioclase shows significant alteration. Illitic I/S has a euhedral lath-like morphology. In the sericitic zone the hyaloclastite altered primarily to illitic I/S with ≥ 66% I, quartz, and minor akspar and pyrite. Clay minerals completely replace pyrogenic feldspars and little evidence remains of the original hyaloclastite texture. Unlike other zones, illitic I/S is fibrous and pure illite samples are composed of euhedral laths and hexagonal plates. The temperatures of hydrothermal alteration likely ranged from 30 to 90 °C for the argillic zone, from 110 to 160 °C for the propylitic zone, from 160 to 270 °C for the

  9. Caracterización geoquímica y estudio comparativo de plagiogranitos de las Zonas Surportuguesa y Ossa-Morena (SO del Macizo Ibérico, España

    Directory of Open Access Journals (Sweden)

    Bellido, F.

    2010-06-01

    Full Text Available Plagiogranites and albitic rocks belonging to contrasted magmatic associations of different ages and geodynamic environments outcrop in Ossa-Morena (OMZ and Surportuguese (SPZ Zones. OMZ plagiogranites are related with Cambrian-Ordovician rifting and represent a part of the felsic members of a bimodal magmatic suite and show oceanic plagiogranites affinities. SPZ plagiogranites are related with a Carboniferous volcano-plutonic calc-alkaline suite related with Variscan Orogeny. Both plagiogranites show many similar petrological and geochemical characteristics but display some different immobile elements ratios as La/Nb, Th/Nb, Th/La that are unaltered by metamorphism, magmatic differentiation and alteration processes and prove differences in their sources. SPZ plagiogranites show a more compositional homogeneity than OMZ ones. This is interpreted as a proof of cogenetic origin for SPZ plagiogranites and heterogeneous origin for OMZ plagiogranites, derived from the mix of different sources (astenospheric, lithospheric and crustal.

    En la Zona de Ossa-Morena (ZOM y en la Zona Surportuguesa (ZSP se encuentran plagiogranitos pertenecientes a asociaciones magmáticas y ambientes geodinámicos muy contrastados. Los primeros pertenecen a una asociación bimodal máfica-félsica relacionada con el rifting cámbrico-ordovícico y presentan bastantes afinidades con plagiogranitos oceánicos. Los segundos forman parte de una asociación volcánico-plutónica calcoalcalina carbonífera relacionada con la Orogenia Varisca. Ambos plagio-granitos son semejantes en diversos aspectos petrológicos y geoquímicos pero muestran diferencias en algunas relaciones de elementos inmóviles tales como La/Nb, Th/Nb, Th/La poco sensibles a los procesos de evolución magmática, metamorfismo y alteración y que son reflejo de la composición de las fuentes. Los plagiogranitos de la ZSP presentan una mayor homogeneidad composicional que los de la ZOM. Esto se

  10. Ionoluminiscencia de silicatos de utilización en cerámica a temperaturas criogenicas

    Directory of Open Access Journals (Sweden)

    García-Guinea, J.

    2004-10-01

    Full Text Available Requirements on accurate physical properties need new characterization techniques for structural defects. The use of light ions such as H+ and He+ with MeV energies allows penetration to a depth of several microns in most materials producing strong luminescence to gain information on the defect structures present. Examples of ionoluminescence spectra of silicates for ceramic uses are included such as Mn2+-Fe3+ coupled pairs in quartz, Dy3+ in zircon, hatch-twinning in microcline and spontaneous strain and sodium in albite. In cryogenic thermal conditions tectosilicates display both, reorganization of Mn2+ and Fe3+ centres plus a large enlargement of the UV-blue emissions by stress mechanisms. Nesosilicates, i.e., zircon, shows differences such as existence of REE and (Dy3+ and a selective reduction of some UV-blue peaks, e.g., at 340 and 400 nm.

    El requerimiento de propiedades físicas muy controladas en los nuevos materiales cerámicos precisa de nuevas técnicas de caracterización de defectos estructurales. Al incidir sobre un material un flujo de iones ligeros, como 1 1H+, 2 1H+, 3 2He+ y 4 2He+, acelerados a energías de MeV, estos iones pueden penetrar varias micras en muchos materiales emitiendo un fuerte espectro luminiscente con mucha información sobre defectos estructurales. Se presentan algunos ejemplos de espectros de ionoluminiscencia de silicatos de uso cerámico con diferentes tipos de defectos como Mn2+, Fe3+, Ti4+ en cuarzo, Dy3+ en circón, maclados tartán en microclina y estrés espontáneo y potasio en albita. En tectosilicatos a temperaturas criogénicas se aprecia una reorganización del par Mn2+ y Fe3+ mas un crecimiento de las emisiones espectrales ultravioleta-azules atribuibles a mecanismos de estrés en redes silicatadas. En nesosilicatos (circón se observan diferencias como presencia de tierras raras (Dy3+ y reducción selectiva de algunos picos ultravioleta-azules (340 y 400 nm.

  11. Volcanic ash in feed coal and its influence on coal combustion products

    Energy Technology Data Exchange (ETDEWEB)

    Brownfield, M.E.; Affolter, R.H.; Cathcart, J.D.; Brownfield, I.K.; Hower, J.C.; Stricker, G.D.; O' Connor, J.T.

    2000-07-01

    The US Geological Survey and the University of Kentucky Center for Applied Energy Research are collaborating with an Indiana Utility to determine the physical and chemical properties of feed coal and coal combustion products (CCPs) from a coal-fired power plant. The plant utilizes a low-sulfur (.23--.47 weight percent S) coal from the Powder River Basin, Wyoming. Scanning Electron Microscope (SEM) and X-ray diffraction (XRD) analysis of feed coal samples identified two mineral suites. A primary suite (not authigenic) consisting of quartz (detrital and volcanic beta-form grains), biotite, and minor zircon and a secondary authigenic mineral suite containing calcite, alumino-phosphates (crandallite and gorceixite), kaolinite, quartz, anatase, barite, and pyrite. The authigenic minerals are attributed to air-fall and reworked volcanic ash that was deposited in peat-forming mires. The Powder River Basin feed coals contain higher amounts of Ba, Ca, Mg, Na, Sr, and P compared to other analyzed eastern coals. These elements are associated with alumino-phosphate, biotite, calcite, and clay minerals. The element associations are indicative of coal that incorporated volcanic ash during deposition. XRD analysis of CCPs revealed a predominance of glass, perovskite, lime, gehlenite, quartz, and phosphates with minor amounts of periclase, anhydrite, hematite, and spinel group minerals in the fly ash; and quartz, plagioclase (albite and anorthite), pyroxene (augite and fassaite), rhodonite, and akermanite in the bottom ash. Microprobe and SEM analysis of fly ash samples revealed quartz, zircon, monazite, euhedral laths of corundum with merrillite, hematite, dendritic spinels/ferrites, and rounded grains of wollastonite with periclase. The abundant Ca and Mg mineral phases in the fly ashes are related to the presence of carbonate, clay, and phosphate minerals in the feed coal. The Ca- and Mg-rich mineral phases in the CCPs can be attributed to volcanic minerals deposited in the

  12. Geology of the Mid-Miocene Rooster Comb Caldera and Lake Owyhee Volcanic Field, eastern Oregon: Silicic volcanism associated with Grande Ronde flood basalt

    Science.gov (United States)

    Benson, Thomas R.; Mahood, Gail A.

    2016-01-01

    The Lake Owyhee Volcanic Field (LOVF) of eastern Oregon consists of rhyolitic caldera centers and lava fields contemporaneous with and spatially related to Mid-Miocene Columbia River flood basalt volcanism. Previous studies delineated two calderas in the southeastern part of LOVF near Owyhee Reservoir, the result of eruptions of two ignimbrites, the Tuff of Leslie Gulch and the Tuff of Spring Creek. Our new interpretation is that these two map units are differentially altered parts of a single ignimbrite produced in a major phreatomagmatic eruption at 15.8 Ma. Areas previously mapped as Tuff of Spring Creek are locations where the ignimbrite contains abundant clinoptilolite ± mordenite, which made it susceptible to erosion. The resistant intracaldera Tuff of Leslie Gulch has an alteration assemblage of albite ± quartz, indicative of low-temperature hydrothermal alteration. Our new mapping of caldera lake sediments and pre- and post-caldera rhyolitic lavas and intrusions that are chemically similar to intracaldera Tuff of Leslie Gulch point to a single 20 × 25 km caldera, which we name the Rooster Comb Caldera. Erosion of the resurgently uplifted southern half of the caldera created dramatic exposures of intracaldera Tuff of Leslie Gulch cut by post-caldera rhyolite dikes and intrusions that are the deeper-level equivalents of lava domes and flows that erupted into the caldera lake preserved in exposures to the northeast. The Rooster Comb Caldera has features in common with more southerly Mid-Miocene calderas of the McDermitt Volcanic Field and High Rock Caldera Complex, including formation in a basinal setting shortly after flood basalt eruptions ceased in the region, and forming on eruption of peralkaline ignimbrite. The volcanism at Rooster Comb Caldera postdates the main activity at McDermitt and High Rock, but, like it, begins 300 ky after flood basalt volcanism begins in the area, and while flood basalts don't erupt through the silicic focus, are

  13. Brittle deformation in Southern Granulite Terrane (SGT): A study of pseudotachylyte bearing fractures along Gangavalli Shear Zone (GSZ), Tamil Nadu, India.

    Science.gov (United States)

    mohan Behera, Bhuban; Thirukumaran, Venugopal; Biswal, Tapas kumar

    2016-04-01

    High grade metamorphism and intense deformation have given a well recognition to the Southern Granulite Terrane (SGT) in India. TTG-Charnockite and basic granulites constitute the dominant lithoassociation of the area. Dunite-peridotite-anorthosite-shonkinite and syenites are the intrusives. TTG-charnockite-basic granulite have undergone F1 (isoclinal recumbent), F2 (NE-SW) and F3 (NW-SE) folds producing several interference pattern. E-W trending Neoarchean and Palaeoproterozoic Salem-Attur Shear Zone exhibits a low angle ductile thrust as well as some foot print of late stage brittle deformation near Gangavalli area of Tamil Nadu. The thrust causes exhumation of basic granulites to upper crust. Thrusting along the decollement has retrograded the granulite into amphibolite rock. Subsequently, deformation pattern of Gangavalli area has distinctly marked by numerous vertical to sub-vertical fractures mostly dominating along 0-15 and 270-300 degree within charnockite hills that creates a maximum stress (σ1) along NNW and minimum stress (σ3) along ENE. However, emplacement of pseudotachylyte vein along N-S dominating fracture indicates a post deformational seismic event. Extensive fractures produce anastomose vein with varying thickness from few millimeters to 10 centimeters on the outcrop. ICP-AES study results an isochemical composition of pseudotachylyte vein that derived from the host charnockitic rock where it occurs. But still some noticeable variation in FeO-MgO and Na2O-CaO are obtained from different parts within the single vein showing heterogeneity melt. Electron probe micro analysis of thin sections reveals the existence of melt immiscibility during its solidification. Under dry melting condition, albitic rich melts are considered to be the most favorable composition for microlites (e.g. sheaf and acicular micro crystal) re-crystallization. Especially, acicular microlites preserved tachylite texture that suggest its formation before the final coagulation

  14. Study on Gold and base metal occurrence in Uluwai Prospect, Western Latimojong Mountain, South Sulawesi

    Science.gov (United States)

    Maulana, Adi; Jaya, Asri; Imai, Akira

    2018-02-01

    Uluwai Prospect is located in the northern part of South Arm of Sulawesi along the eastern part of the Kalosi Fold Belt and Latimojong Mountain. The area is generally characterized by moderate to rugged topography area with elevation in the range of 700 to 1400 m above sea level in the mountainous complex called Latimojong Mountain Complex. The mineralization is characterized by a relatively simple sulphide ore mineral assemblage consists of pyrite, sphalerite and chalcopyrite. Samples were collected in areas showing abundant sulphide minerals where younger faults cut the bedding and foliation of country rocks. A number of silicified zones have been observed, as well as float material containing disseminated pyrite, chalcopyrite, and sphalerite with hematite, goethite and limonite. Some alteration types have been observed including sericitization, albitization, carbonatization and silisification. The samples collected indicated that the mineralisation is contained within metasedimentary (sandstone to mudstone) and greenschist. Geochemical analyses from 16 samples including 5 stream sediment samples indicated that the most promising mineralization occur in the prospect area are copper (Cu) and zinc (Zn). This is also supported by the abundance of chalcopyrite and sphalerite in some highly altered samples. Assaying of the collected samples revealed most of samples contain relatively low gold (Au) concentration. However, two samples contain 0.007 and 0.01 ppm of Au. In the mineralized area, Zn concentrations are up to 134 ppm, Cu up to 120 ppm and Pb up to 18 ppm and As up to 70 ppm. There is no clear relationship that exists between Au and the base metals except that one of the samples with highest Au values tend to have high Zn and As. This unclear pattern also shown by Cu, Pb and Zn. Base metal concentration in stream sediment samples show a relatively stable pattern than in rock samples. Arsenic tends to be elevated in base metal rich samples. Sb and Mo are

  15. Characterization of the Fault Core and Damage Zone of the Borrego Fault, 2010 M7.2 Rupture

    Science.gov (United States)

    Dorsey, M. T.; Rockwell, T. K.; Girty, G.; Ostermeijer, G.; Mitchell, T. M.; Fletcher, J. M.

    2017-12-01

    We collected a continuous sample of the fault core and 23 samples of the damage zone out to 52 m across the rupture trace of the 2010 M7.2 El Mayor-Cucapa earthquake to characterize the physical damage and chemical transformations associated with this active seismic source. In addition to quantifying fracture intensity from macroscopic analysis, we cut a continuous thin section through the fault core and from various samples in the damage zone, and ran each sample for XRD analyses for clay mineralogy, XRF for bulk geochemical analyses, and bulk and grain density from which porosity and volumetric strain were derived. The parent rock is a hydrothermally-altered biotite tonalite, with biotite partially altered to chlorite. The presence of epidote with chlorite suggests that these rocks were subjected to relatively high temperatures of 300-400° C. Adjacent to the outermost damage zone is a chaotic breccia zone with distinct chemical and physical characteristics, indicating possible connection to an ancestral fault to the southwest. The damage zone consists of an outer zone of protocataclasite, which grades inward towards mesocataclasite with seams of ultracataclasite. The fault core is anomalous in that it is largely composed of a sliver of marble that has been translated along the fault, so direct comparison with the damage zone is impaired. From collected data, we observe that chloritization increases into the breccia and damage zones, as does the presence of illite. Porosity reaches maximum values in the damage zone adjacent to the core, and closely follows trends in fracture intensity. Statistically significant gains in Mg, Na, K, Mn, and total bulk mass occurred within the inner damage zone, with losses of Ca and P mass, which led to the formation of chlorite and albite. The outer damage zone displays gains in Mg and Na mass with losses in Ca and P mass. The breccia zone shows gains in mass of Mg and Mn and loss in total bulk mass. A gain in LOI in both the

  16. Archaeological jade mystery solved using a 119-year-old rock collection specimen

    Science.gov (United States)

    Harlow, G. E.; Davies, H. L.; Summerhayes, G. R.; Matisoo-Smith, E.

    2012-12-01

    In a recent publication (Harlow et al. 2012), a ~3200-year old small stone artefact from an archaeological excavation on Emirau Island, Bismarck Archipelago, Papua New Guinea was described and determined to be a piece of jadeite jade (jadeitite). True jadeitite from any part of New Guinea was not previously known, either in an archaeological or geological context, so this object was of considerable interest with respect to its geological source and what that would mean about trade between this source and Emirau Island. Fortuitously, the artefact, presumably a wood-carving gouge, is very unusual with respect to both pyroxene composition and minor mineral constituents. Pyroxene compositions lie essentially along the jadeite-aegirine join: Jd94Ae6 to Jd63Ae36, and without any coexisting omphacite. This contrasts with Jd-Di or Jd-Aug compositional trends commonly observed in jadeitites worldwide. Paragonite and albite occur in veins and cavities with minor titanite, epidote-allanite, and zircon, an assemblage seen in a few jadeitites. Surprisingly, some titanite contains up to 6 wt% Nb2O5 with only trace Ta and a single grain of a Y-Nb phase (interpreted as fergusonite) is present; these are unique for jadeitite. In a historical tribute to C.E.A. Wichmann, a German geologist who taught at Utrecht University, the Netherlands, a previously unpublished description of chlormelanite from the Torare River in extreme northeast Papua, Indonesia was given. The bulk composition essentially matches the pyroxene composition of the jade, so this sample was hypothesized as coming from the source. We were able to arrange a loan from the petrology collection at Utrecht University of the specimen acquired by Wichmann in 1893. In addition we borrowed stone axes from the Natural History Museum - Naturalis in Leiden obtained from natives near what is now Jayapura in eastern-most Papua. Petrography and microprobe analysis of sections of these samples clearly show that (1) Wichmann's 1893

  17. Mineralogy and geochemistry of triassic carbonatites in the Matcha alkaline intrusive complex (Turkestan-Alai Ridge, Kyrgyz Southern Tien Shan), SW Central Asian orogenic belt

    Science.gov (United States)

    Vrublevskii, V. V.; Morova, A. A.; Bukharova, O. V.; Konovalenko, S. I.

    2018-03-01

    Postorogenic intrusions of essexites and alkaline and nepheline syenites in the Turkestan-Alai segment of the Kyrgyz Southern Tien Shan coexist with dikes and veins of carbonatites dated at ∼220 Ma by the Ar-Ar and Rb-Sr age methods. They are mainly composed of calcite and dolomite (60-85%), as well as sodic amphibole, phlogopite, clinopyroxene, microcline, albite, apatite, and magnetite, with accessory niobate, ilmenite, Nb-rutile, titanite, zircon, baddeleyite, monazite-(Ce), barite, and sulfides. The rocks share mineralogical and geochemical similarity with carbonatites that originated by liquid immiscibility at high temperatures above 500 °C. Alkaline silicate and salt-carbonate melts are derived from sources with mainly negative bulk εNd(t) ∼ from -11 to 0 and high initial 87Sr/86Sr ratios (∼0.7061-0.7095) which may be due to mixing of PREMA and EM-type mantle material. Pb isotopic ratios in accessory pyrrhotite (206Pb/204Pb = 18.38; 207Pb/204Pb = 15.64; 208Pb/204Pb = 38.41) exhibit an EM2 trend. The intrusions bear signatures of significant crustal contamination as a result of magma genesis by syntexis and hybridism. Concordant isotope composition changes of δ13C (-6.5 to -1.9‰), δ18O (9.2-23‰), δD (-58 to -41‰), and δ34S (12.6-12.8‰) in minerals and rocks indicate inputs of crustal material at the stage of melting and effect of hot fluids released during dehydration of metamorphosed oceanic basalts or sediments. The observed HFSE patterns of the oldest alkaline gabbro may be due to interaction of the primary mafic magma with IAB-type material. The isotope similarity of alkaline rocks with spatially proximal basalts of the Tarim large igneous province does not contradict the evolution of the Turkestan-Alai Triassic magmatism as the "last echo" of the Tarim mantle plume.

  18. Hydrothermal reequilibration of igneous magnetite in altered granitic plutons and its implications for magnetite classification schemes: Insights from the Handan-Xingtai iron district, North China Craton

    Science.gov (United States)

    Wen, Guang; Li, Jian-Wei; Hofstra, Albert H.; Koenig, Alan E.; Lowers, Heather A.; Adams, David

    2017-09-01

    Magnetite is a common mineral in igneous rocks and has been used as an important petrogenetic indicator as its compositions and textures reflect changing physiochemical parameters such as temperature, oxygen fugacity and melt compositions. In upper crustal settings, igneous rocks are often altered by hydrothermal fluids such that the original textures and compositions of igneous magnetite may be partly or completely obliterated, posing interpretive problems in petrological and geochemical studies. In this paper, we present textural and compositional data of magnetite from variably albitized granitoid rocks in the Handan-Xingtai district, North China Craton to characterize the hydrothermal reequilibration of igneous magnetite. Four types of magnetite have been identified in the samples studied: pristine igneous magnetite (type 1), reequilibrated porous magnetite (type 2), reequilibrated nonporous magnetite (type 3), and hydrothermal magnetite (type 4). Pristine igneous magnetite contains abundant well-developed ilmenite exsolution lamellae that are largely replaced by titanite during subsequent hydrothermal alteration. The titanite has a larger molar volume than its precursor ilmenite and thus causes micro-fractures in the host magnetite grains, facilitating dissolution and reprecipitation of magnetite. During sodic alteration, the igneous magnetite is extensively replaced by type 2 and type 3 magnetite via fluid-induced dissolution and reprecipitation. Porous type 2 magnetite is the initial replacement product of igneous magnetite and is subsequently replaced by the nonoporous type 3 variety as its surface area is reduced and compositional equilibrium with the altering fluid is achieved. Hydrothermal type 4 magnetite is generally euhedral and lacks exsolution lamellae and porosity, and is interpreted to precipitate directly from the ore-forming fluids. Hydrothermal reequilibration of igneous magnetite has led to progressive chemical purification, during which trace

  19. Origin and evolution of formation water at the Jujo-Tecominoacan oil reservoir, Gulf of Mexico. Part 1: Chemical evolution and water-rock interaction

    Energy Technology Data Exchange (ETDEWEB)

    Birkle, Peter, E-mail: birkle@iie.org.mx [Instituto de Investigaciones Electricas (IIE), Gerencia de Geotermia, Av. Reforma 113, Cuernavaca, Morelos 62490 (Mexico); Garcia, Bernardo Martinez; Milland Padron, Carlos M. [PEMEX Exploracion y Produccion, Region Sur, Activo Integral Bellota-Jujo, Diseno de Explotacion, Cardenas, Tabasco (Mexico)

    2009-04-15

    The origin and evolution of formation water from Upper Jurassic to Upper Cretaceous mudstone-packstone-dolomite host rocks at the Jujo-Tecominoacan oil reservoir, located onshore in SE-Mexico at a depth from 5200 to 6200 m.b.s.l., have been investigated, using detailed water geochemistry from 12 producer wells and six closed wells, and related host rock mineralogy. Saline waters of Cl-Na type with total dissolved solids from 10 to 23 g/L are chemically distinct from hypersaline Cl-Ca-Na and Cl-Na-Ca type waters with TDS between 181 and 385 g/L. Bromine/Cl and Br/Na ratios suggest the subaerial evaporation of seawater beyond halite precipitation to explain the extreme hypersaline components, while less saline samples were formed by mixing of high salinity end members with surface-derived, low salinity water components. The dissolution of evaporites from adjacent salt domes has little impact on present formation water composition. Geochemical simulations with Harvie-M{phi}ller-Weare and PHRQPITZ thermodynamic data sets suggest secondary fluid enrichment in Ca, HCO{sub 3} and Sr by water-rock interaction. The volumetric mass balance between Ca enrichment and Mg depletion confirms dolomitization as the major alteration process. Potassium/Cl ratios below evaporation trajectory are attributed to minor precipitation of K feldspar and illitization without evidence for albitization at the Jujo-Tecominoacan reservoir. The abundance of secondary dolomite, illite and pyrite in drilling cores from reservoir host rock reconfirms the observed water-rock exchange processes. Sulfate concentrations are controlled by anhydrite solubility as indicated by positive SI-values, although anhydrite deposition is limited throughout the lithological reservoir column. The chemical variety of produced water at the Jujo-Tecominoacan oil field is related to a sequence of primary and secondary processes, including infiltration of evaporated seawater and original meteoric fluids, the subsequent

  20. Tectonic origin and deformation process of the Mayer Kangri medium-high pressure metamorphic dome in Central Qiangtang of Tibet

    Science.gov (United States)

    Wang, Y.; Liang, X.

    2016-12-01

    The metamorphic characteristics, deformation process, geochronology of the medium-high pressure metamorphic rocks in blueschist bearing Central Qiangtang Metamorphic belt (CQMB) of Tibet were less well constrained. It is, however, commonly assumed that these rock slices in the margin also contain important implications on the evolution of the entire metamorphic belt. The well-exposed Mayer Kangri medium-high pressure metamorphic dome in north flank of the CQMB provides an unique opportunity to investigate the outer part of the CQMB, which could facilitate the study on the subduction-exhumation-post orogenic scenarios of the Triassic accretionary orogeny in Central Qiangtang. Field structural analyses indicate the Mayer Kangri metamorphic dome are bounded by low-angle normal faults (LANF) within the hanging wall of low-green schist facies mélange. It majorly consists of epidote-amphibolites, quartz-phengite schist, epidote-albite schist. The outcrop and micro structural observations of footwall metamorphic rocks show an open anticline with multiple foliation replacement, which largely differentiate themselves from the dextral strike-slip shearing of the hanging wall. Well-zoned amphiboles were found within the epidote-amphibolite after micro-structural observations and electron probe microanalyses (EPMA), which indicate that the amphibole zonation demonstrates a Hastingsite core, a Ferro-actinolite mantle and a Ferro-winchite rim in most cases. The mean temperature and pressure estimates of the zoned amphibolites change from 544 °, 0.98Gpa in the core, to 426°, 0.34Gpa in the mantle, and to ca.364° and 0.70 GPa in the rim. The detailed analyses on the stepwise-heating Ar-Ar results of the zoned amphiboles provide good constrains on the episodic deformation process of the CQMB. For Hast-cores, we obtained near plateau ages of 242.4-241.2 Ma, indicating the onset of the oceanic subduction is earlier than the Anisian stage of Middle Triassic. The subsequent

  1. Diagenesis and reservoir quality evolution of palaeocene deep-water, marine sandstones, the Shetland-Faroes Basin, British continental shelf

    Energy Technology Data Exchange (ETDEWEB)

    Mansurbeg, H. [Department of Earth Sciences, Uppsala University, Villavaegen 16, SE 752 36 Uppsala (Sweden); Morad, S. [Department of Earth Sciences, Uppsala University, Villavaegen 16, SE 752 36 Uppsala (Sweden); Department of Petroleum Geosciences, The Petroleum Institute, P.O. Box 2533, Abu Dhabi (United Arab Emirates); Salem, A. [Faculty of Education at Kafr El-Sheikh, Tanta University, Kafr El-Sheikh (Egypt); Marfil, R.; Caja, M.A. [Departmento Petrologia y Geoquimica, Facultad de Geologia, UCM, 28040 Madrid (Spain); El-ghali, M.A.K. (Geology Department, Al-Fateh University, P.O. Box 13696, Libya); Nystuen, J.P. [Department of Geosciences, University of Oslo, P.O. Box 1047 Blindern, NO-0316 Oslo (Norway); Amorosi, A. [Department of Earth Sciences, University of Bologna, Via Zamboni 67, 40127 Bologna (Italy); Garcia, D. [Centre SPIN, Department GENERIC, Ecole Nationale Superieure des Mines de Saint Etienne 158, Cours Fauriel 42023, Saint-Etienne (France); La Iglesia, A. [Instituto de Geologia Economica (CSIC-UCM), Facultad de Geologia, UCM, 28040 Madrid (Spain)

    2008-06-15

    eogenetic kaolinite, smectite and mesogenetic illite and chlorite. Kaolinite has been subjected to mesogenetic replacement by dickite. The K-feldspar and plagioclase grains have been albitized. Dissolution of calcite cement and of framework grain (feldspar, volcanic fragments and mud intraclasts) has resulted in a considerable enhancement of reservoir quality. (author)

  2. Incorporation of cooling-induced crystallization into a 2-dimensional axisymmetric conduit heat flow model

    Science.gov (United States)

    Heptinstall, David; Bouvet de Maisonneuve, Caroline; Neuberg, Jurgen; Taisne, Benoit; Collinson, Amy

    2016-04-01

    Heat flow models can bring new insights into the thermal and rheological evolution of volcanic 3 systems. We shall investigate the thermal processes and timescales in a crystallizing, static 4 magma column, with a heat flow model of Soufriere Hills Volcano (SHV), Montserrat. The latent heat of crystallization is initially computed with MELTS, as a function of pressure and temperature for an andesitic melt (SHV groundmass starting composition). Three fractional crystallization simulations are performed; two with initial pressures of 34MPa (runs 1 & 2) and one of 25MPa (run 3). Decompression rate was varied between 0.1MPa/° C (runs 1 & 3) and 0.2MPa/° C (run 2). Natural and experimental matrix glass compositions are accurately reproduced by all MELTS runs. The cumulative latent heat released for runs 1, 2 and 3 differs by less than 9% (8.69E5 J/kg*K, 9.32E5 J/kg*K, and 9.49E5 J/kg*K respectively). The 2D axisymmetric conductive cooling simulations consider a 30m-diameter conduit that extends from the surface to a depth of 1500m (34MPa). The temporal evolution of temperature is closely tracked at depths of 10m, 750m and 1400m in the centre of the conduit, at the conduit walls, and 20m from the walls into the host rock. Following initial cooling by 7-15oC at 10m depth inside the conduit, the magma temperature rebounds through latent heat release by 32-35oC over 85-123 days to a maximum temperature of 1002-1005oC. At 10m depth, it takes 4.1-9.2 years for the magma column to cool by 108-131oC and crystallize to 75wt%, at which point it cannot be easily remobilized. It takes 11-31.5 years to reach the same crystallinity at 750-1400m depth. We find a wide range in cooling timescales, particularly at depths of 750m or greater, attributed to the initial run pressure and the dominant latent heat producing crystallizing phase, Albite-rich Plagioclase Feldspar. Run 1 is shown to cool fastest and run 3 cool the slowest, with surface emissivity having the strongest cooling

  3. Physical volcanology, geochemistry and basin evolution of the Ediacaran volcano-sedimentary succession in the Bas Draâ inlier (Ouarzazate Supergroup, Western Anti-Atlas, Morocco)

    Science.gov (United States)

    Karaoui, Brahim; Breitkreuz, Christoph; Mahmoudi, Abdelkader; Youbi, Nasrrddine

    2014-11-01

    New geologic mapping, lithofacies and granulometric analysis, and geochemistry from the volcano-sedimentary successions of the central part of the Bas Draâ inlier, Western Anti-Atlas, constrain the Ediacaran Ouarzazate Supergroup evolution during the post-collisional stage of the Pan-African orogeny. Volcanosedimentary facies analysis is the key aspect of the present contribution. We distinguished sixteen terrestrial volcanosedimentary lithofacies in the Bas Draâ succession (BDS), which reaches a total thickness of 2000 m. BDS evolution can be grouped into four units (Aouinet Aït Oussa I to IV, AO I-AO IV). The earliest volcanic activity produced rhyolitic ignimbrite sheets (AO I), which had been considered as lava flows by previous workers, and which were presumably related to caldera system(s). During AO II, a complex of high-silica andesitic and rhyolitic lavas formed, punctuated by the explosive eruption of a high-temperature silica-rich magma leading to the formation of parataxitic ignimbrite. AO III consists of basalt and andesite lava fields and small explosive, in parts phreatomagmatic volcanic vents. It is dissected by fluvial systems depositing external non-volcanic and local volcanic debris. BDS evolution terminated with the formation of a large SiO2-rich lava dome complex (AO IV), accompanied by small basalt effusive event. Volcanosedimentary facies analysis infers that the BDS evolved in a continental extensional setting developing in a low topography under humid paleoclimatic conditions. Alteration textures are dominated by a piemontite-calcite-albite-quartz (+ iron oxides) assemblage. Chemical analysis of BDS volcanic and subvolcanic rocks belongs to high-k calc-alkaline and alkali-calcic to alkaline magmatic trend typical for a post-collision setting. Trace elements spidergrams show a pattern typical for subduction-related suites of orogenic belts. REE patterns show moderate enrichment in LREE relative to flat HREE, with strong negative Eu

  4. Processing of Vietnamese lithium ores to produce LiCl

    International Nuclear Information System (INIS)

    Dinh, Thi Thu Hien

    2015-01-01

    A potential lithium deposit has been discovered in the La Vi mining district, located in Quang Ngai Province, Central Vietnam. The Li-rich rocks (average contents: 1.3±0.9 wt.% Li 2 O) are highly fractionated, peraluminous granites, which are further characterized by high contents of Al 2 O 3 , Na 2 O, K 2 O, F, and P 2 O 5 , but very low concentrations of all other main components (MgO, CaO, Fe 2 O 3 tot, TiO 2 ). The granites exhibit a light pink color and contain mainly albite, quartz, muscovite, lithian muscovite, and lepidolite, with minor amounts of amblygonite-montebrasite, herderite, fluorapatite, topaz, and cassiterite, and accessory beryl and goyazite. Lepidolite from La Vi deposit was extracted to produce lithium chloride by using iron II sulphide (FeS)-CaO roasting and water leaching. The HSC program was applied for the simulation of the behavior of lepidolite and the additives during roasting, confirming the important role of SO 2 /SO 3 gas for extracting lithium from lepidolite. At optimum conditions roasting at 750 C using FeS/Li and Ca/F molar ratios of 5:1 and 1:1, respectively, followed by leaching at 50 C using water/calcine mass ratios of >5:1 could yield a maximum of ∝85% Li recovery (at <1 g/L Li concentration). Addition of CaO led to a decrease in the liberation of HF gas and insoluble LiF formation. NaOH and BaCl 2 were used for removing the metal and sulphate impurities from the leach liquor by precipitation at ambient temperature. The efficiency of lithium extraction reached ∝100 % with washing of the precipitates after filtering. Alkali salts were separated from the LiCl solution via solar evaporation and isopropanol leaching. 96.3 wt.% LiCl could be produced using an isopropanol/salt mass ratio of 5:1 at ambient temperature in 3 h.

  5. Pressure-temperature evolution of eclogites from the Kechros complex in the Eastern Rhodope (NE Greece)

    Science.gov (United States)

    Mposkos, E.; Baziotis, I.; Proyer, A.

    2012-06-01

    The Rhodope Domain in NE Greece consists of different tectonometamorphic complexes involved in the Alpine collisional history between the Eurasian and African plates. In the Kechros Complex, which is the lowermost tectonic unit in the East Rhodope, a lense of kyanite eclogite occurs within orthogneiss and common eclogites are found between serpentinized peridotite and underlying pelitic gneisses. In kyanite eclogite, the high-pressure (HP) mineral assemblage is Grt + Omp (Jd35-55) + Ky + Ph + Qz + Rt + (indirectly inferred Tlc + Law); a Na-rich tremolite and zoisite formed at or near peak metamorphic conditions. In common eclogites, the HP mineral assemblage is Grt + Omp (Jd29-41) + Rt and, with less certainty, Amp (Gln-rich + Brs + Wnc + Hbl) ± Czo. The inclusions in garnet are glaucophane, actinolite, barroisite, hornblende, omphacite, clinozoisite, titanite, rutile and rarely paragonite and albite. In kyanite eclogite, peak P- T conditions are constrained at 2.2 GPa and 615°C using garnet-omphacite-phengite geothermobarometry and very similar values of 585 ± 32°C and 2.17 ± 0.11 GPa with the average P- T method, by which conditions of formation could also be narrowed down for the common eclogite (619 ± 53°C and 1.69 ± 0.17 GPa) and for a retrogressed eclogite (534 ± 36°C and 0.77 ± 0.11 GPa). Ages for the HP metamorphism in the Kechros Complex are not yet available. A Rb-Sr white mica age of 37 Ma from orthogneiss records a stage of the exhumation. The HP event may be coeval with the Eocene HP metamorphism (49-55 Ma) recorded in the Nestos Shear Zone in Central Rhodope and in the Attic-Cycladic crystalline belt, where it is interpreted as the result of subduction and final closure of the Axios/Vardar ocean and subsequent subduction of the Apulian continental crust (a promontory of the Africa continent) under the southern margin of the European continent in the late Cretaceous and early Tertiary.

  6. Zoning and exsolution in cumulate alkali feldspars from the eruption (12.9 Ka) of Laacher see volcano (Western Germany) as an indicator of time-scales and dynamics of carbonate-silicate unmixing

    Science.gov (United States)

    Sourav Rout, Smruti; Wörner, Gerhard

    2017-04-01

    Time-scales extracted from the detailed analysis of chemically zoned minerals provide insights into crystal ages, magma storage and compositional evolution, including mixing and unmixing events. This allows having a better understanding of pre-eruptive history of large and potentially dangerous magma chambers. We present a comprehensive study of chemical diffusion across zoning and exsolution patterns of alkali feldspars in carbonatite-bearing cognate syenites from the 6.3 km3 (D.R.E) phonolitic Laacher See Tephra (LST) eruption 12.9 ka ago. The Laacher See volcano is located in the Quaternary East Eifel volcanic field of the Paleozoic Rhenish Massif in Western Germany and has produced a compositionally variable sequence in a single eruption from a magma chamber that was zoned from mafic phonolite at the base to highly evolved, actively degassing phonolite magma at the top. Diffusion chronometry is applied to major and trace element compositions obtained on alkali feldspars from carbonate-bearing syenitic cumulates. Methods used were laser ablation inductively coupled plasma mass spectrometry (LA ICP-MS) in combination with energy-dispersive and wavelength-dispersive electron microprobe analyses (EDS & WDS-EMPA). The grey scale values extracted from multiple accumulations of back-scattered electron images represent the K/Na ratio owing to the extremely low concentrations of Ba and Sr (transition and phase separation). A distinctive uphill diffusive analysis is used specifically for the phase separation in the case of exsolution features (comprising of albite- and orthoclase-rich phases) in sanidines. The error values are aggregates of propagated error through calculations and the uncertainty in temperature values. Trace element compositional data of distinct feldspar compositions that are assumed to have grown before and after silicate-carbonate unmixing are used to estimate partition coefficients between carbonate and silicate melt. The resulting values correlate

  7. The natural radioactivity in the Serido Pegmatite Province - Rio Grande do Norte State (Brazil): assessment and monitoring of water's source

    International Nuclear Information System (INIS)

    Campos, Thomas F.C; Petta, Reinaldo A.; Malanca, Alberto; Guimaraes Guedes, Anderson; Pastura, Valeria F.S.; Sindern, Sven

    2008-01-01

    Full text: This abstract show the preliminary considerations of a study accomplished on the radioactive minerals, primary and secondary uranium minerals that occur in the pegmatites of the Serido Region, State of Rio Grande do Norte, Brazil and their influence on the several sources of water provision and on population nuclei of the area from the municipal district of Parelhas and Ecuador. In general, the pegmatite from the area of Ecuador-Parelhas present high environmental radioactivity so much due to the dispersed uranium in the crystalline structure of minerals (columbite-tantalite, albite, microcline, quartz, phosphate minerals, tourmaline, lepidolite and apatite), as primary and secondary uranium minerals (uraninite, pitchblende, gummite, autunite, torbernite, and uranium-bearing opal, etc.). These uranium minerals appear associates to the fracture and voids in the pegmatite and in the tourmaline-bearing granite. These minerals were identified by petrography, X-Rays diffraction, ultraviolet fluorescence analysis, infrared spectroscopy, radioactivity (HPGe gamma spectrometry), thermal behavior and chemical analysis (ICP-MS and AAS, Microprobe). Geochemistry and hydrochemistry preliminary environmental studies on the pegmatites bodies from Serido Region show gamma radiation level which between 150 to 30.000 cps; uranium (U 3 O 8 ) and thorium (ThO 2 ) content in Columbite-Tantalite (and/or polycrase) varying between 0,3% - 3,0% and 0,1% - 0,5% respectively, and the coating existent in these minerals show uranium contents varying between 20% to 60%. While the soil samples gathered in Ecuador/Parelhas districts show an average activity of 226 Ra, 232 Th, and 40 K of 27.1/39.1; 33.74/48.5; 260.1/234.8 (Bq.kg -1 , dry-weight), respectively, and the corresponding kerma rate (l) in air are 50 and 67 nGyh -1 ], suggesting that the acid underground waters and others oxidizers attack and dissolve the radioactive minerals from pegmatite, generating solutions rich in U 6

  8. Complex Diffusion Mechanisms for Li in Feldspar: Re-thinking Li-in-Plag Geospeedometry

    Science.gov (United States)

    Holycross, M.; Watson, E. B.

    2017-12-01

    In recent years, the lithium isotope system has been applied to model processes in a wide variety of terrestrial environments. In igneous settings, Li diffusion gradients have been frequently used to time heating episodes. Lithium partitioning behavior during decompression or cooling events drives Li transfer between phases, but the extent of Li exchange may be limited by its diffusion rate in geologic materials. Lithium is an exceptionally fast diffuser in silicate media, making it uniquely suited to record short-lived volcanic phenomena. The Li-in-plagioclase geospeedometer is often used to time explosive eruptions by applying laboratory-calibrated Li diffusion coefficients to model concentration profiles in magmatic feldspar samples. To quantify Li transport in natural scenarios, experimental measurements are needed that account for changing temperature and oxygen fugacity as well as different feldspar compositions and crystallographic orientation. Ambient pressure experiments were run at RPI to diffuse Li from a powdered spodumene source into polished sanidine, albite, oligoclase or anorthite crystals over the temperature range 500-950 ºC. The resulting 7Li concentration gradients developed in the mineral specimens were evaluated using laser ablation ICP-MS. The new data show that Li diffusion in all feldspar compositions simultaneously operates by both a "fast" and "slow" diffusion mechanism. Fast path diffusivities are similar to those found by Giletti and Shanahan [1997] for Li diffusion in plagioclase and are typically 10 to 20 times greater than slow path diffusivities. Lithium concentration gradients in the feldspar experiments plot in the shape of two superimposed error function curves with the slow diffusion regime in the near-surface of the crystal. Lithium diffusion is most sluggish in sanidine and is significantly faster in the plagioclase feldspars. It is still unclear what diffusion mechanism operates in nature, but the new measurements may impact

  9. Uranium mobility in mine areas: evaluation of the water-rock interaction

    Energy Technology Data Exchange (ETDEWEB)

    Zuddas, P. [UFR Sciences de la Terre. PEPS. Universite Claude Bernard. Lyon (France); Rocha Scislewski, A.; Faivre, D.; Lopez, O. [Institut de Physique du Globe de Paris (France)

    2005-07-01

    Full text of publication follows: Toxicity and natural radioactivity of uranium are among the main environmental concerns for exploitation and processing of uranium ore. Weathering processes and potential contamination paths of these areas have to be identified to preserve the water resources. In this work, leaching experiments were carried out in flow-through reactors. Approximately 750 g of crushed rock of selected grain size between 0.35 and 0.80 mm were introduced into a Pyrex column. Distilled and deionized water, saturated with 5% CO{sub 2}/95% air mixture, was introduced through a glass inlet fitted at the base of the column. Input solution pH was constantly equal to 4.2 while the low flow rate was obtained from a peristaltic pump. The output solution was sampled periodically for about 1 year. Three different rock samples were used: an untreated granite rock with high levels of uranium minerals, a rock with low uranium content and a rock rejected after the lixiviation process for uranium industrial extraction. For untreated rocks pH and silica decrease by 1-2 orders of magnitude while sodium decreases by 2-3 orders of magnitude. This indicates the strong albitite dissolution. Total dissolved uranium has a rather constant level indicating the constant dissolution rate of the uranium mineral assemblage. Thermodynamic modelling of the interacting output solutions indicates that 80% of the dissolved uranium content is under the form of two main carbonate complexes (i.e. UO{sub 2}(CO{sub 3}){sub 2}{sup 2-} and UO{sub 2}(CO{sub 3}){sub 3}{sup 4-}), while solutions are saturated on chalcedony, kaolinite and calcium clay minerals. Solutions are under saturated with respect to uraninite and low-temperature albite. In experiments where material was treated with sulphuric acid in the plant, pH is constantly equal to 4 indicating the lack of rock buffering properties. Na, Ca, and SO{sub 4} decrease by several orders of magnitude (from some initial mmol/kg) reaching

  10. High salinity volatile phases in magmatic Ni-Cu-platinum group element deposits

    Science.gov (United States)

    Hanley, J. J.; Mungall, J. E.

    2004-12-01

    The role of "deuteric" fluids (exsolved magmatic volatile phases) in the development of Ni-Cu-PGE (platinum group element) deposits in mafic-ultramafic igneous systems is poorly understood. Although considerable field evidence demonstrates unambiguously that fluids modified most large primary Ni-Cu-PGE concentrations, models which hypothesize that fluids alone were largely responsible for the economic concentration of the base and precious metals are not widely accepted. Determination of the trace element composition of magmatic volatile phases in such ore-forming systems can offer considerable insight into the origin of potentially mineralizing fluids in such igneous environments. Laser ablation ICP-MS microanalysis allows researchers to confirm the original metal budget of magmatic volatile phases and quantify the behavior of trace ore metals in the fluid phase in the absence of well-constrained theoretical or experimental predictions of ore metal solubility. In this study, we present new evidence from major deposits (Sudbury, Ontario, Canada; Stillwater Complex, Montana, U.S.A.) that compositionally distinct magmatic brines and halide melt phases were exsolved from crystallizing residual silicate melt and trapped within high-T fluid conduits now comprised of evolved rock compositions (albite-quartz graphic granite, orthoclase-quartz granophyre). Petrographic evidence demonstrates that brines and halide melts coexisted with immiscible carbonic phases at the time of entrapment (light aliphatic hydrocarbons, CO2). Brine and halide melt inclusions are rich in Na, Fe, Mn, K, Pb, Zn, Ba, Sr, Al and Cl, and homogenize by either halite dissolution at high T ( ˜450-700° C) or by melting of the salt phase (700-800° C). LA-ICPMS analyses of single inclusions demonstrate that high salinity volatile phases contained abundant base metals (Cu, Fe, Sn, Bi) and precious metals (Pt, Pd, Au, Ag) at the time of entrapment. Notably, precious metal concentrations in the inclusions

  11. Evidence for intense hydrothermal alteration associated with flood basalt volcanism during the birth of the Azores Plateau

    Science.gov (United States)

    Bach, W.; Busch, A.; Genske, F. S.; Beier, C.; Krumm, S.

    2017-12-01

    A stratigraphic section comprising >1000 m of upper crust in the Princess Alice Bank (PAB) of the western Azores Plateau was sampled during RV Meteor cruise M128 in July of 2016, using the ROV MARUM Quest 4000m. Twenty-two samples were recovered between 2484 and 1439 m water depth from the southfacing footwall of the Master fault bounding a prominent NW-SE striking rift zone within the PAB. Our geochemical and petrographic results show that virtually all samples are pervasively altered. The deeper part of the section (up to 1750 m water depth) was altered under greenschist-facies conditions to assemblages that include epidote, chlorite, albite, titanite, and actinolite. These rocks show 87Sr/86Sr values between 0.7036 and 0.7050. The topmost section was altered under lower metamorphic grades to chlorite/smectite-quartz-anatase. These rocks show severe losses of Ca and Sr, and gains in Mg, Li, and B, with 87Sr/86Sr ratios as high as 0.708. These geochemical signatures indicate an intensity of hydrothermal exchange between seawater and crust that is unmatched by any in situ section of upper ocean crust sampled by ocean drilling to date. Oxygen isotope data for epidote-calcite veins indicate temperatures of 250-300°C. Later quartz gives about 200°C. The implications of the intense hydrothermal alteration for crust-seawater exchange budgets can be evaluated in the light of the geological evolution of the PAB. Based on immobile element ratios of whole rocks and REE characteristics of relict clinopyroxene in the only incompletely altered sample, an E-type MORB primary composition of the basalts can be reconstructed. Our data suggest that the degrees of mantle melting were much higher than during extrusion of the <4 Ma old alkali-basalts recovered from the top of PAB (Beier et al., 2015, doi:10.1130/2015.2511(02)), and even higher than modern MORB at the adjacent mid-Atlantic Ridge. These results lead us to suggest that the deeper sections of the PAB formed during the

  12. Mineralogical, IR-spectral and geochemical monitoring of hydrothermal alteration in a deformed and metamorphosed Jurassic VMS deposit at Arroyo Rojo, Tierra del Fuego, Argentina

    Science.gov (United States)

    Biel, C.; Subías, I.; Acevedo, R. D.; Yusta, I.; Velasco, F.

    2012-04-01

    The Arroyo Rojo Zn-Pb-Cu volcanogenic massive sulfide deposit is the main deposit of the Fin del Mundo District in the Fuegian Andes, Argentina. This deposit is hosted by a Middle Jurassic volcanic and volcanoclastic sequence forming the Lemaire Formation. The latter consists, from the base up, of the following: rhyolitic and dacitic porphyritic rocks, ignimbrite, tuff, and flow. It is underlain by a pre-Jurassic basement and overlain by the hyaloclastic andesites of the Yahgán Formation. The Arroyo Rojo consists of stacked lenticular lenses that are associated with disseminated mineralization in both the footwall and the hanging wall. The internal structure of the ore lenses is marked by the occurrence of massive, semi-massive and banded facies, along with stringer and brecciated zones and minor ore disseminations. The mineral assemblage comprises mainly pyrite and sphalerite, with minor amounts of galena and chalcopyrite and rare pyrrhotite, arsenopyrite, tetrahedrite and bournonite. The ores and the volcanic host rocks have metamorphosed to greenschist facies and were overprinted by a penetrative tectonic foliation, which led to the development of mylonitic, and cataclastic textures, recrystallization and remobilization. Primary depositional characteristics and regional and hydrothermal alteration patterns were preserved despite deformation and metamorphism. Therefore, primary banding was preserved between facies boundaries. In addition, some remnants of magmatic origin are recognizable in preserved phenocrysts and volcaniclastic phenoclasts. Most of the volcanic and volcaniclastic rocks of the host sequence show a rhyolitic to rhyo-dacitic composition. Regional seafloor alteration, characterized by the presence of clinozoisite, Fe-chlorite and titanite, along with quartz and albite, is partially obliterated by hydrothermal alteration. The hydrothermal alteration is stratabound with the following assemblages, which developed from the base to top: (1) Quartz

  13. Geochemistry of komatiites and basalts from the Rio das Velhas and Pitangui greenstone belts, São Francisco Craton, Brazil: Implications for the origin, evolution, and tectonic setting

    Science.gov (United States)

    Verma, Sanjeet K.; Oliveira, Elson P.; Silva, Paola M.; Moreno, Juan A.; Amaral, Wagner S.

    2017-07-01

    The Neoarchean Rio das Velhas and Pitangui greenstone belts are situated in the southern São Francisco Craton, Minas Gerais, Brazil. These greenstone belts were formed between ca. 2.79-2.73 Ga, and consist mostly of mafic to ultramafic volcanics and clastic sediments, with minor chemical sediments and felsic volcanics that were metamorphosed under greenschist facies. Komatiites are found only in the Rio das Velhas greenstone belt, which is composed of high-MgO volcanic rocks that have been identified as komatiites and high-Mg basalts, based on their distinctive geochemical characteristics. The Rio das Velhas komatiites are composed of tremolite + actinolite + serpentine + albite with a relict spinifex-texture. The Rio das Velhas komatiites have a high magnesium content ((MgO)adj ≥ 28 wt.%), an Al-undepleted Munro-type [(Al2O3/TiO2)adj and (CaO/Al2O3)adj] ratio ranging from 27 to 47 and 0.48 to 0.89, relatively low abundances of incompatible elements, a depletion of light rare earth elements (LREE), a pattern of non-fractionated heavy rare- earth elements (HREE), and a low (Gd/Yb)PM ratio (≤ 1.0). Negative Ce anomalies suggest that alteration occurred during greenschist facies metamorphism for the komatiites and high-Mg basalts. The low [(Gd/Yb)PM 18] and high HREE, Y, and Zr content suggest that the Rio das Velhas komatiites were derived from the shallow upper mantle without garnet involvement in the residue. The chemical compositions [(Al2O3/TiO2)adj, (FeO)adj, (MgO)adj, (CaO/Al2O3)adj, Na, Th, Ta, Ni, Cr, Zr, Y, Hf, and REE] indicate that the formation of the komatiites, high-Mg basalts and basalts occurred at different depths and temperatures in a heterogeneous mantle. The komatiites and high-Mg basalts melted at liquidus temperatures of 1450-1550 °C. The Pitangui basalts are enriched in the highly incompatible LILE (large-ion lithophile elements) relative to the moderately incompatible HFS (high field strength) elements. The Zr/Th ratio ranging from 76 to

  14. Modern sedimentary facies, depositional environments, and major controlling processes on an arid siliciclastic coast, Al qahmah, SE Red Sea, Saudi Arabia

    Science.gov (United States)

    Nabhan, Abdullah I.; Yang, Wan

    2018-04-01

    The facies and environments along the arid siliciclastic coast of Red Sea in Al Qahmah, Saudi Arabia are studied to establish a depositional model for interpretation of ancient rocks deposited in rift settings. Field and petrographic studies of 151 sediment samples in an area of 20 km2 define seven main facies types: beach, washover fan, tidal channel, dune, sabkha, delta, and wadi (seasonal stream). The wadi and delta facies are composed of poorly to moderately well-sorted, gravelly, medium-to-fine sands. Delta-front sands are redistributed by southward longshore currents to form a beach. Beach facies is composed of well-to-moderately sorted fine sands with minor gravels, which contain high concentrations of magnetite, ilmenite, garnet, pyroxene, amphibole, epidote, titanite, and apatite grains, indicating strong winnowing. Crabs and other burrowers destroy primary sedimentary structures and mix sediments in foreshore and backshore of the beaches. Wind and storm surge rework foreshore and backshore sediments to form washover fans. Sabkha facies occurs extensively in supratidal depressions behind beach, are flooded by rainstorms and spring tide, and capped by a 5-cm-thick crust composed of interlaminated halite, quartz, albite, minor gypsum and biotite, and rarely calcium carbonate. Halite occurs as thin sheets and gypsum as nodules with a chicken-wire structure. Clastic fraction in sabkha sediments ranges from coarse silt to coarse sand with moderate sorting, and is transported by currents and wind. Tidal inlets and tidal creeks assume abandoned wadis and are filled by muddy sand. Sand dunes and sand sheets are 1-7 m high and widely distributed due to variable wind directions. Fine-grained dune sands are moderately well sorted, whereas sheet sands are coarser and poorly sorted due to vegetation baffling. Most eolian sands are sourced from beach deposits. This suite of complex riverine, wave, tidal, wind, chemical, and biological processes form the facies mosaic

  15. Quality Aspects of a Marine Aggregate Deposit off the SE Euboea Island, Greece, for its Exploitation - Preliminary Results

    Science.gov (United States)

    Anastasatou, Marianthi; Kapsimalis, Vasilios; Stamatakis, Michael; Tsoutsia, Antonia; Poulos, Serafeim; Rousakis, Grigoris; Karditsa, Aikaterini; Petrakis, Stelios; Aspiotis, Konstantinos; Papavlasopoulou, Nafsika; Stamatakis, Giorgos

    2015-04-01

    % according to a semi-quantitative estimation) with minor trace minerals, such as albite and clay minerals. On the basis of the qualitative characteristics, sediments on the inner continental shelf of SE Euboea can be classified as siliceous and being considered appropriate for potential exploitation, that is related also to its quantitatively characteristics. The relatively shallow depths (<40 m) and the absence of any beach nearby together with the ordinary population of benthic community support such an extraction. Definitive decisions for the commercial interest of the specific deposit will be concluded after the accomplished quality characterization and the estimation of the proven and inferred reserves of the deposit. Acknowledgemts: This work is supported by the research program THALES-MARE (MIS: 375655) that is funded by the Operational Programme ''Education and lifelong learning, 2007-2013'' of the Ministry of Education and Religious Affairs, Culture and Sports.

  16. Origin and evolution of formation water at the Jujo-Tecominoacan oil reservoir, Gulf of Mexico. Part 1: Chemical evolution and water-rock interaction

    International Nuclear Information System (INIS)

    Birkle, Peter; Garcia, Bernardo Martinez; Milland Padron, Carlos M.

    2009-01-01

    The origin and evolution of formation water from Upper Jurassic to Upper Cretaceous mudstone-packstone-dolomite host rocks at the Jujo-Tecominoacan oil reservoir, located onshore in SE-Mexico at a depth from 5200 to 6200 m.b.s.l., have been investigated, using detailed water geochemistry from 12 producer wells and six closed wells, and related host rock mineralogy. Saline waters of Cl-Na type with total dissolved solids from 10 to 23 g/L are chemically distinct from hypersaline Cl-Ca-Na and Cl-Na-Ca type waters with TDS between 181 and 385 g/L. Bromine/Cl and Br/Na ratios suggest the subaerial evaporation of seawater beyond halite precipitation to explain the extreme hypersaline components, while less saline samples were formed by mixing of high salinity end members with surface-derived, low salinity water components. The dissolution of evaporites from adjacent salt domes has little impact on present formation water composition. Geochemical simulations with Harvie-Mφller-Weare and PHRQPITZ thermodynamic data sets suggest secondary fluid enrichment in Ca, HCO 3 and Sr by water-rock interaction. The volumetric mass balance between Ca enrichment and Mg depletion confirms dolomitization as the major alteration process. Potassium/Cl ratios below evaporation trajectory are attributed to minor precipitation of K feldspar and illitization without evidence for albitization at the Jujo-Tecominoacan reservoir. The abundance of secondary dolomite, illite and pyrite in drilling cores from reservoir host rock reconfirms the observed water-rock exchange processes. Sulfate concentrations are controlled by anhydrite solubility as indicated by positive SI-values, although anhydrite deposition is limited throughout the lithological reservoir column. The chemical variety of produced water at the Jujo-Tecominoacan oil field is related to a sequence of primary and secondary processes, including infiltration of evaporated seawater and original meteoric fluids, the subsequent mixing of

  17. Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions

    Science.gov (United States)

    Watkins, James M.; DePaolo, Donald J.; Ryerson, Frederick J.; Peterson, Brook T.

    2011-06-01

    Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl 2Si 2O 8; denoted AN), albite (NaAlSi 3O 8; denoted AB), and diopside (CaMgSi 2O 6; denoted DI) were held at 1450 °C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB-AN experiment, D Ca/ D Si ≈ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D Ca/ D Si ≈ 1. In the AB-DI experiment, D Ca/ D Si ≈ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB-AN experiment. In the AB-DI experiment, D Mg/ D Si ≈ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity - the ratio of the diffusivity of the cation ( D Ca) to the diffusivity of silicon ( D Si). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D cation/ D Si. Cations diffusing in aqueous solutions display a similar relationship

  18. Thermodynamic modeling of phase relations and metasomatism in shear zones

    Science.gov (United States)

    Goncalves, P.; Oliot, E.; Marquer, D.

    2009-04-01

    granodiorite (Swiss Alps). Fourteen samples have been taken along a 80 meter-wide strain gradient from the undeformed granodiorite protolith to the ultramylonitic zone. The metastable magmatic assemblage consists of oligoclase (50 vol%), quartz ( 20 vol%), K-feldspar (17 vol%), and biotite (13 %). With increasing strain, K-feldspar and oligoclase rapidly disappear to produce albite and epidote porphyroblast (up to 45 and 5 vol% respectively) with phengite in shear planes (15 vol%). In the mylonite and ultramylonite, magmatic phases have been completely recrystallized and the metamorphic albite volume decreases down to 25 vol% whereas phengite constitutes up to 30 vol% of the rock. Epidote is absent in the ultramylonite. In localized shear bands, the metamorphic assemblage consists of phengite, chlorite, biotite and quartz. Mass balance calculations show that the ultramylonite is enriched in MgO (up to 130%) while CaO and Na2O are remove (80% and 45% respectively). However, mass transfer is even stronger in the chlorite-bearing shear bands, where CaO and Na2O have been completely leached out. Chemical potential pseudosections are constructed using the bulk composition of the unaltered granodiorite, with K2O, FeO, Al2O3 and SiO2 content remaining constant. Deformation occurred under water-saturated conditions at 6 kbar and 450°C. MgO, CaO and Na2O are considered as "perfectly mobile" components and therefore their chemical potentials, which is fixed by the externally-derived fluid, control the stability of the phases. μMgO vs μCaO and μMgO vs μNa2O diagrams, show that the breakdown of a Kf-ab-ep assemblage into phengite and the subsequent crystallization of chlorite require the introduction of a fluid with a μCaO and μNa2O significantly lower than in the unaltered metamorphic assemblage (Kf-ab-ep-Kf-Bio-q). Equalizing the chemical potential gradient of CaO and Na2O, established between the fluid and the metamorphic assemblage, is achieved by the complete removal of Ca

  19. Mineral-deposit model for lithium-cesium-tantalum pegmatites

    Science.gov (United States)

    Bradley, Dwight C.; McCauley, Andrew D.; Stillings, Lisa L.

    2017-06-20

    Lithium-cesium-tantalum (LCT) pegmatites comprise a compositionally defined subset of granitic pegmatites. The major minerals are quartz, potassium feldspar, albite, and muscovite; typical accessory minerals include biotite, garnet, tourmaline, and apatite. The principal lithium ore minerals are spodumene, petalite, and lepidolite; cesium mostly comes from pollucite; and tantalum mostly comes from columbite-tantalite. Tin ore as cassiterite and beryllium ore as beryl also occur in LCT pegmatites, as do a number of gemstones and high-value museum specimens of rare minerals. Individual crystals in LCT pegmatites can be enormous: the largest spodumene was 14 meters long, the largest beryl was 18 meters long, and the largest potassium feldspar was 49 meters long.Lithium-cesium-tantalum pegmatites account for about one-fourth of the world’s lithium production, most of the tantalum production, and all of the cesium production. Giant deposits include Tanco in Canada, Greenbushes in Australia, and Bikita in Zimbabwe. The largest lithium pegmatite in the United States, at King’s Mountain, North Carolina, is no longer being mined although large reserves of lithium remain. Depending on size and attitude of the pegmatite, a variety of mining techniques are used, including artisanal surface mining, open-pit surface mining, small underground workings, and large underground operations using room-and-pillar design. In favorable circumstances, what would otherwise be gangue minerals (quartz, potassium feldspar, albite, and muscovite) can be mined along with lithium and (or) tantalum as coproducts.Most LCT pegmatites are hosted in metamorphosed supracrustal rocks in the upper greenschist to lower amphibolite facies. Lithium-cesium-tantalum pegmatite intrusions generally are emplaced late during orogeny, with emplacement being controlled by pre-existing structures. Typically, they crop out near evolved, peraluminous granites and leucogranites from which they are inferred to be

  20. Long-Term CO2 Exposure Experiments - Geochemical Effects on Brine-Saturated Reservoir Sandstone

    Science.gov (United States)

    Fischer, Sebastian; Zemke, Kornelia; Liebscher, Axel; Wandrey, Maren

    2010-05-01

    The injection of CO2 into deep saline aquifers is the most promising strategy for the reduction of CO2 emissions to the atmosphere via long-term geological storage. The study is part of the CO2SINK project conducted at Ketzin, situated 40 km west of Berlin. There, food grade CO2 has been pumped into the Upper Triassic Stuttgart Formation since June 2008. The main objective of the experimental program is to investigate the effects of long-term CO2 exposure on the physico-chemical properties of the reservoir rock. To achieve this goal, core samples from observation well Ktzi 202 have been saturated with synthetic brine and exposed to CO2 in high quality steel autoclaves at simulated reservoir P-T-conditions of 5.5 MPa and 40 ° C. The synthetic brine had a composition representative of the formation fluid (Förster et al., 2006) of 172.8 g/l NaCl, 8.0 g/l MgCl2×2H2O, 4.8 g/l CaCl2×2H2O and 0.6 g/l KCl. After 15 months, the first set of CO2-exposed samples was removed from the pressure vessels. Thin sections, XRD, SEM as well as EMP data were used to determine the mineralogical features of the reservoir rocks before and after the experiments. Additionally, NMR relaxation and MP was performed to measure poroperm and pore size distribution values of the twin samples. The analyzed samples are fine- to medium grained, moderately well- to well sorted and weakly consolidated sandstones. Quartz and plagioclase are the major components, while K-feldspar, hematite, white & dark mica, chlorite and illite are present in minor and varying amounts. Cements are composed of analcime, dolomite and anhydrite. Some samples show mm- to cm-scale cross-beddings. The laminae comprise lighter, quartz- and feldspar-dominated layers and dark-brownish layers with notably less quartz and feldspars. The results are consistent with those of Blaschke et al. (2008). The plagioclase composition indicates preferred dissolution of the Ca-component and a trend toward albite-rich phases or even pure

  1. Influence of liquid structure on diffusive isotope separation in molten silicates and aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Watkins, J.M.; DePaolo, D.J.; Ryerson, F.J.; Peterson, B.

    2011-03-01

    Molecular diffusion in natural volcanic liquids discriminates between isotopes of major ions (e.g., Fe, Mg, Ca, and Li). Although isotope separation by diffusion is expected on theoretical grounds, the dependence on mass is highly variable for different elements and in different media. Silicate liquid diffusion experiments using simple liquid compositions were carried out to further probe the compositional dependence of diffusive isotopic discrimination and its relationship to liquid structure. Two diffusion couples consisting of the mineral constituents anorthite (CaAl{sub 2}Si{sub 2}O{sub 8}; denoted AN), albite (NaAlSi{sub 3}O{sub 8}; denoted AB), and diopside (CaMgSi{sub 2}O{sub 6}; denoted DI) were held at 1450°C for 2 h and then quenched to ambient pressure and temperature. Major-element as well as Ca and Mg isotope profiles were measured on the recovered quenched glasses. In both experiments, Ca diffuses rapidly with respect to Si. In the AB–AN experiment, D{sub Ca}/D{sub Si} ~ 20 and the efficiency of isotope separation for Ca is much greater than in natural liquid experiments where D{sub Ca}/D{sub Si} ~ 1. In the AB–DI experiment, D{sub Ca}/D{sub Si} ~ 6 and the efficiency of isotope separation is between that of the natural liquid experiments and the AB–AN experiment. In the AB–DI experiment, D{sub Mg}/D{sub Si} ~ 1 and the efficiency of isotope separation for Mg is smaller than it is for Ca yet similar to that observed for Mg in natural liquids. The results from the experiments reported here, in combination with results from natural volcanic liquids, show clearly that the efficiency of diffusive separation of Ca isotopes is systematically related to the solvent-normalized diffusivity—the ratio of the diffusivity of the cation (D{sub Ca}) to the diffusivity of silicon (D{sub Si}). The results on Ca isotopes are consistent with available data on Fe, Li, and Mg isotopes in silicate liquids, when considered in terms of the parameter D{sub cation

  2. Sedimentary carbonate-hosted giant Bayan Obo REE-Fe-Nb ore deposit of Inner Mongolia, China; a cornerstone example for giant polymetallic ore deposits of hydrothermal origin

    Science.gov (United States)

    Chao, E.C.T.; Back, J.M.; Minkin, J.A.; Tatsumoto, M.; Junwen, Wang; Conrad, J.E.; McKee, E.H.; Zonglin, Hou; Qingrun, Meng; Shengguang, Huang

    1997-01-01

    Detailed, integrative field and laboratory studies of the textures, structures, chemical characteristics, and isotopically determined ages and signatures of mineralization of the Bayan Obo deposit provided evidence for the origin and characteristics favorable for its formation and parameters necessary for defining giant polymetallic deposits of hydrothermal origin. Bayan Obo is an epigenetic, metasomatic, hydrothermal rare earth element (REE)-Fe-Nb ore deposit that is hosted in the metasedimentary H8 dolostone marble of the Middle Proterozoic Bayan Obo Group. The metasedimentary sequence was deposited on the northern continental slope of the North China craton. The mine area is about 100 km south of the suture marking Caledonian subduction of the Mongolian oceanic plate from the north beneath the North China craton. The mineralogy of the deposit is very complex, consisting of more than 120 different minerals, some of which are epigenetic minerals introduced by hydrothermal solutions, and some of which are primary and secondary metamorphic minerals. The major REE minerals are monazite and bastnaesite, whereas magnetite and hematite are the dominant Fe-ore minerals, and columbite is the most abundant Nb mineral. Dolomite, alkali amphibole, fluorite, barite, aegirine augite, apatite, phlogopite, albite, and microcline are the most widespread gangue minerals. Three general types of ores occur at Bayan Obo: disseminated, banded, and massive ores. Broad zoning of these ore types occurs in the Main and East Orebodies. Disseminated ores are in the outermost zone, banded ores are in the intermediate zone, and massive ores are in the cores of the orebodies. On the basis of field relations, host rocks, textures, structures, and mineral assemblages, many varieties of these three types of ores have been recognized and mapped. Isotopic dating of monazite, bastnaesite, aeschynite, and metamorphic and metasomatic alkali amphiboles associated with the deposit provides constraints

  3. Isotope age of the rare metal pegmatite formation in the Kolmozero-Voron'ya greenstone belt (Kola region of the Fennoscandian shield): U-Pb (TIMS) microlite and tourmaline dating

    Science.gov (United States)

    Kudryashov, Nikolay; Lyalina, Ludmila; Mokrushin, Artem; Zozulya, Dmitry; Groshev, Nikolay; Steshenko, Ekaterina; Kunakkuzin, Evgeniy

    2016-04-01

    The Kolmozero-Voron'ya greenstone belt is located in the central suture zone, which separates the Murmansk block from the Central-Kola and the Keivy blocks. The belt is represented by volcano-sedimentary rocks of Archaean age of 2.9-2.5 Ga. Rare metal pegmatites (Li, Cs with accessory Nb, Ta, and Be) occur among amphibolite and gabbroid intrusions in the northwestern and southeastern parts of the belt. According to the Rb-Sr data, the age of pegmatites was considered to be 2.7 Ga. Until recently there was no generally accepted point of view on the origin of pegmatites. Now we have isotopic data for a range of rock complexes that could pretend to be parental granites for the rare metal pegmatites. These are granodiorites with the zircon age of 2733±Ma, and microcline and tourmaline granites, which Pb-Pb isochronal age on tourmaline from the tourmaline granite located near the deposit is estimated to be 2520±70 Ma. The pegmatite field of the Vasin Myl'k deposit with the lepidolite--albite--microcline--spodumene--pollucite association is located among amphibolites in the northwestern part of the belt. The deposit is represented by subparallel low-angle zoned veins up to 220 m long and 5 m thick dipping in the southeastern direction at an angle of 10° too 30°. The minerals of the columbite--tonalite group from Vasin Myl'k deposit include microlite, simpsonite, and torolite, and are the oldest among different minerals represented by several generations in pegmatites under consideration. Zircons from the pegmatites are mostly represented by crystals with the structure affected by the action of fluids that put certain restrictions on its use as a geochronometer of the crystallization process. Microlite from the pegmatite taken from the dump of a prospecting drill hole was used for U--Pb (TIMS). The mineral is represented by 0.5--1.0 mm long euhedral octahedral crystals. It is brown in color, and transparent. The microlite crystals were preliminarily cleaned from

  4. Large-scale recumbent isoclinal folds in the footwall of the West Cycladic Detachment System (Greece)

    Science.gov (United States)

    Rice, A. Hugh N.; Grasemann, Bernhard

    2017-04-01

    The Pindos Zone in the Cyclades underwent Eocene high-pressure metamorphism and syn-orogenic exhumation, overprinted by Miocene low-angled extension. Although this represents a combination of likely high-strain-events, structural evidence of large-scale folding is rare. Here potential examples of such folding on Kea and Kythnos, in the Western Cyclades, are evaluated. These islands lie within the Cycladic Blueschist Nappe (lower nappe) of the Pindos Zone and in the footwall of the top-to-SSW West Cycladic Detachment System (WCDS). On Kea, no lithostratigraphy can be established in the 450 m thick greenschist facies mixed sedimentary-volcanoclastic-marble mylonite/phyllonite succession. On the east side of the island, lensoid marble layers frequently bifurcate, which might be reflecting early, sheared-out isoclinal folding, although no evidence of folded compositional layering has been found in potential fold-hinge zones and the bifurcation points are not arranged in a way suggestive of a fold axes parallel to the NNE-SSW oriented stretching lineation. However, at two localities, medium-scale recumbent isoclinal folding has been mapped, with NNE-SSW fold-axes exposed for up to 250 m and amplitudes of up to 170 m. On Kythnos, stretching lineations in greenschist facies rocks show a rotation from ENE-WSW in the north to NNE-SSW in the south, taken to represent a reorientation of the Eocene exhumation strain during block rotation coincident with top-to-SSW movement of the WCDS. The distribution of the three marble units that crop out in central/southern Kythnos suggest large-scale, likely isoclinal folding occurred. (1) Petroussa Lithodeme - a blue-grey calcite (BGC) marble with quartz-calcite-white-mica (QCWM) schists, forming a continuous outcrop around the island, thinning from >16m in the SE to <8m thick mylonites in the SW, overlain by grey sericite-albite-graphite-schists (Flabouria Lithodeme); (2) Rizou Lithodeme - massive grey to BGC marble, with abundant

  5. Siudaite, Na8(Mn2+ 2Na)Ca6Fe3+ 3Zr3NbSi25O74(OH)2Cl·5H2O: a new eudialyte-group mineral from the Khibiny alkaline massif, Kola Peninsula

    Science.gov (United States)

    Chukanov, Nikita V.; Rastsvetaeva, Ramiza K.; Kruszewski, Łukasz; Aksenov, Sergey M.; Rusakov, Vyacheslav S.; Britvin, Sergey N.; Vozchikova, Svetlana A.

    2018-03-01

    The new eudialyte-group mineral siudaite, ideally Na8(Mn2+ 2Na)Ca6Fe3+ 3Zr3NbSi25O74(OH)2Cl·5H2O, was discovered in a peralkaline pegmatite situated at the Eveslogchorr Mt., Khibiny alkaline massif, Kola Peninsula, Russia. The associated minerals are aegirine, albite, microcline, nepheline, astrophyllite, and loparite-(Ce). Siudaite forms yellow to brownish-yellow equant anhedral grains up to 1.5 cm across. Its lustre is vitreous, and the streak is white. Cleavage is none observed. The Mohs' hardness is 4½. Density measured by hydrostatic weighing is 2.96(1) g/cm3. Density calculated using the empirical formula is equal to 2.973 g/cm3. Siudaite is nonpleochroic, optically uniaxial, negative, with ω = 1.635(1) and ɛ = 1.626(1) (λ = 589 nm). The IR spectrum is given. The chemical composition of siudaite is (wt%; electron microprobe, H2O determined by HCN analysis): Na2O 8.40, K2O 0.62, CaO 9.81, La2O3 1.03, Ce2O3 1.62, Pr2O3 0.21, Nd2O3 0.29, MnO 6.45, Fe2O3 4.51. TiO2 0.54, ZrO2 11.67, HfO2 0.29, Nb2O5 2.76, SiO2 47.20, Cl 0.54, H2O 3.5, -O = Cl - 0.12, total 99.32. According to Mössbauer spectroscopy data, all iron is trivalent. The empirical formula (based on 24.5 Si atoms pfu, in accordance with structural data) is [Na7.57(H2O)1.43]Σ9(Mn1.11Na0.88Ce0.31La0.20Nd0.05Pr0.04K0.41)Σ3(H2O)1.8(Ca5.46Mn0.54)Σ6(Fe3+ 1.76Mn2+ 1.19)Σ2.95Nb0.65(Ti0.20Si0.50)Σ0.71(Zr2.95Hf0.04Ti0.01)Σ3Si24.00Cl0.47O70(OH)2Cl0.47·1.82H2O. The crystal structure was determined using single-crystal X-ray diffraction data. The new mineral is trigonal, space group R3m, with a = 14.1885(26) Å, c = 29.831(7) Å, V = 5200.8(23) Å3 and Z = 3. Siudaite is chemically related to georgbarsanovite and is its analogue with Fe3+-dominant M2 site. The strongest lines of the powder X-ray diffraction pattern [d, Å (I, %) (hkl)] are: 6.38 (60) (-114), 4.29 (55) (-225), 3.389 (47) (131), 3.191 (63) (-228). 2.963 (100) (4-15), 2.843 (99) (-444), 2.577 (49) (3-39). Siudaite is named after the Polish

  6. The ophiolite of the Eohellenic nappe in the island of Skyros, Greece: Geotectonic environment of formation and metamorphic conditions inferred by mineralogical and geochemical data

    Science.gov (United States)

    Karkalis, Christos; Magganas, Andreas; Koutsovitis, Petros

    2014-05-01

    The island of Skyros is located in the Sporades-Aegean region. It includes an ophiolitic mélange sequence consisting of serpentinites, gabbroic and doleritic rocks, and also lavas which mostly appear in massive form, but in rare cases as deformed pillows. The ophiolitic mélange sequence also includes rodingites, ophicalcites, as well as radiolarites. This formation belongs to the Eohellenic tectonic nappe, which encompasses marbles, sandstones and schists and was emplaced onto the Pelagonian Zone during Early Cretaceous [1, 2]. Serpentinites were most likely formed after serpentinization of harzburgitic protoliths and consist of serpentine, bastite, spinel and magnetite. The chemistry of spinels (TiO2=0.14-0.25 wt.%, Al2O3=35.1-35.21 wt.%, Cr#=37.38-38.87), shows that the harzburgitic protoliths plausibly resemble back-arc basin peridotites [3]. Gabbros and dolerites present mostly subophitic textures, between the hornblende/clinopyroxene and plagioclase grains. Based upon their petrography and on their mineral chemistry hornblendes have been distinguished into magmatic and metamorphic hornblendes, with the first occurring mostly in gabbroic rocks. Magmatic hornblendes exhibit relatively high TiO2 (1.42-1.62 wt.%), Al2O3 (5.11-5.86 wt.%) and Na2O (1.01-1.09 wt.%) contents, with their presence implying that the magma was at least to some degree hydrous. Lavas are tholeiitic basalts with relatively high FeOt≡12 wt.% and low K2O and Th contents, consisting mostly albite, altered clinopyroxene and devitrified glass. Tectonomagmatic discrimination diagrams [4, 5] illustrate that the studied gabbros and lavas of Skyros are most likely associated with SSZ processes. Gabbroic rocks, subvolcanic dolerites and lavas have been subjected to greenschist/subgreenschist metamorphic processes, as confirmed by the presence of secondary amphiboles (metamorphic hornblende, actinolite/tremolite), epidote, pumpellyite and chlorite in all of the studied samples. On the other hand

  7. Epidotisation and fluid flow in sheeted dyke complex : new field and experimental constraints

    Science.gov (United States)

    Coelho, Gabriel; Sizaret, Stanislas; Arbaret, Laurent; Branquet, Yannick; Champallier, Rémi

    2013-04-01

    Hydrothermal system in oceanic crust is usually studied via dredge samples and drilled holes but their equivalent are also found in ophiolitic complexes (Oman, Cyprus). In the deepest zone, the fluids react with the sheeted diabase dikes at 400°C and 400 bars to form epidosites by enrichment in epidote and quartz [1]. Mineralogy and chemistry of epidosites have been widely studied on fields [1] and hydrology is generally studied using numerical models [2]. However, the relations and the timing of the emplacement of diabase dikes, their alteration in epidosite and the regional deformation remain unclear. We performed experiments on diabase sampled in the Troodos complex (Cyprus), 1) to stress the P-T-fO2-fluid composition conditions of the reaction of epidotisation and, 2) to quantify interrelations between the permeability and the epidotisation during deformation. In Troodos, we observed two major types of epidosite: 1) a pervasive epidosite in the core of dikes and a banding which is parallel to chilled margins and, 2) assemblages of epidote and quartz as alteration fronts in cooling joints or in the form of veins cross-cutting non-epidotised dikes. This last type of epidotisation clearly appears to be a hydrothermal veining process. We synthesized epidote in a static autoclave with external heating at 500°C and 2500 bars. Epidote was formed by the following reaction: 6 albite + 2 hematite + anorthite + 7 Ca2+ + 6 H2O → 4 epidote + 8 quartz + 6 Na+ + 8 H+. The calculated variation of the molar volume is about -3% (creation of porosity). Two parameters are essential to synthesize epidote from diabase: the oxygen fugacity and the composition of the fluid (enriched in Ca and Fe). However, there is an obvious problem of nucleation at 400°C and 400 bars. In order to understand how fluid flows throughout sheeted dikes, in situ measurements of permeability during coaxial deformation have been performed in a Paterson apparatus by infiltration of Argon and water. The

  8. Domain structure and texture in fine grained symplectite from garnet breakdown in peridotite xenoliths (Zinst, Bavaria, Bohemian Massif)

    Science.gov (United States)

    Habler, G.; Špaček, P.; Abart, R.

    2012-04-01

    changes continuously along subdomain boundaries and perpendicular to the grain elongation. Type B symplectite has the same phase content and topotactic relations as type A, but the aspect ratio of the grains is smaller, and straight phase boundary segments occur. Furthermore, changes in lattice orientations differ from symplectite A. The crystallographic orientation of Opx and Spl shows a discontinuous scatter around the elongation (=growth) direction. Besides there is a continuous lattice orientation change in growth direction. Changes in crystallographic orientations have significantly larger rotation angles than the SPO changes within a single domain. In type C symplectite the Pl content is increased at the expense of Opx. Plagioclase has a higher albite component indicating that these domains had interacted with fluid or melt. Spinel displays rounded grain shapes and occurs both within Opx and Pl. All phases recrystallized with isometric grain shapes. Whereas symplectite A and B reflect reaction microstructures of garnet breakdown, symplectite C is a retrogression product of precursor symplectites A and B. The changes in crystallographic orientation along and across the SPO are interpreted as due to plastic deformation during symplectite growth. The formation of Opx + Pl + Spl from garnet has a positive reaction volume of about 10%. As the area of the reaction front is supposed not to change during a reaction increment, this volume increase leads to a mechanically driven outward flow of symplectite material. It is hypothesized, that reaction induced strain may have led to plastic deformation and modulation of the crystallographic orientation during propagation of the reaction front.

  9. Solid oxide electrolysis cells - Performance and durability

    Energy Technology Data Exchange (ETDEWEB)

    Hauch, A.

    2007-10-15

    In this work H2 electrode supported solid oxide cells (SOC) produced at Risoe National Laboratory, DTU, have been used for steam electrolysis. Electrolysis tests have been performed at temperatures from 650AeC to 950AeC, p(H2O)/p(H2) from 0.99/0.01 to 0.30/0.70 and current densities from -0.25 A/cm2 to -2 A/cm2. The solid oxide electrolysis cells (SOEC) have been characterised by iV curves and electrochemical impedance spectroscopy (EIS) at start and end of tests and by EIS under current load during electrolysis testing. The tested SOCs have shown the best initial electrolysis performance reported in literature to date. Area specific resistances of 0.26 Oecm2 at 850AeC and 0.17 Oecm2 at 950AeC were obtained from electrolysis iV curves. The general trend for the SOEC tests was: 1) a short-term passivation in first few hundred hours, 2) then an activation and 3) a subsequent and underlying long-term degradation. The transient phenomenon (passivation/activation) was shown to be a set-up dependent artefact caused by the albite glass sealing with a p(Si(OH)4) of 1.10-7 atm, leading to silica contamination of the triple-phase boundaries (TPBs) of the electrode. The long-term degradation for the SOECs was more pronounced than for fuel cell testing of similar cells. Long-term degradation of 2%/1000 h was obtained at 850AeC, p(H2O)/p(H2) = 0.5/0.5 and -0.5 A/cm2, whereas the degradation rate increased to 6%/1000h at 950AeC, p(H2O)/p(H2) = 0.9/0.1 and -1.0 A/cm2. Both the short-term passivation and the long-term degradation appear mainly to be related to processes in the H2 electrode. Scanning electron microscopy micrographs show that only limited changes occur in the Ni particle size distribution and these are not the main degradation mechanism for the SOECs. Micro and nano analysis using energy dispersive spectroscopy in combination with transmission electron microscopy (TEM) and scanning TEM reveals that glassy phase impurities have accumulated at the TPBs as a result of

  10. Transmission Electron Microscopy of Itokawa Regolith Grains

    Science.gov (United States)

    Keller, Lindsay P.; Berger, E. L.

    2013-01-01

    Introduction: In a remarkable engineering achievement, the JAXA space agency successfully recovered the Hayabusa space-craft in June 2010, following a non-optimal encounter and sur-face sampling mission to asteroid 25143 Itokawa. These are the first direct samples ever obtained and returned from the surface of an asteroid. The Hayabusa samples thus present a special op-portunity to directly investigate the evolution of asteroidal sur-faces, from the development of the regolith to the study of the effects of space weathering. Here we report on our preliminary TEM measurements on two Itokawa samples. Methods: We were allocated particles RA-QD02-0125 and RA-QD02-0211. Both particles were embedded in low viscosity epoxy and thin sections were prepared using ultramicrotomy. High resolution images and electron diffraction data were ob-tained using a JEOL 2500SE 200 kV field-emission scanning-transmission electron microscope. Quantitative maps and anal-yses were obtained using a Thermo thin-window energy-dispersive x-ray (EDX) spectrometer. Results: Both particles are olivine-rich (Fo70) with µm-sized inclusions of FeS and have microstructurally complex rims. Par-ticle RA-QD02-0125 is rounded and has numerous sub-µm grains attached to its surface including FeS, albite, olivine, and rare melt droplets. Solar flare tracks have not been observed, but the particle is surrounded by a continuous 50 nm thick, stuctur-ally disordered rim that is compositionally similar to the core of the grain. One of the surface adhering grains is pyrrhotite show-ing a S-depleted rim (8-10 nm thick) with nanophase Fe metal grains (<5 nm) decorating the outermost surface. The pyrrhotite displays a complex superstructure in its core that is absent in the S-depleted rim. Particle RA-QD02-0211 contains solar flare particle tracks (2x109 cm-2) and shows a structurally disordered rim 100 nm thick. The track density corresponds to a surface exposure of 103-104 years based on the track production rate

  11. Compilation of kinetic data for geochemical calculations

    International Nuclear Information System (INIS)

    Arthur, R.C.; Savage, D.; Sasamoto, Hiroshi; Shibata, Masahiro; Yui, Mikazu

    2000-01-01

    physical properties of the fracture must be homogeneous over a characteristic length that is greater than or equal to the equilibration length. If these conditions are met, calculations suggest local equilibrium would be a valid assumption in groundwater evolution models applied to the Kamaishi site if: it applies to reactions involving calcite, stilbite (assuming its dissolution / precipitation behavior is similar to that of heulandite), laumontite, albite and prehnite, but not quartz; Darcy flow velocities are relatively low (e.g., less than about 0.1 m yr-1), and it is based on the assumption that equilibrium corresponds to an uncertainty in the saturation index of 0.0±0.4. If, however, actual reaction rates in the field are lower than expected, possibly because reactive surface areas are overestimated, the modeling approach may be inappropriate because it is probably unrealistic to assume that fracture mineralogy is homogeneous over fracture lengths exceeding a few meters or tens of meters. An analytical model of redox-front migration behavior based on the stationary-state approximation, and JNC's conceptual model of a natural events scenario involving the migration of oxidizing surface waters in fractures, suggests that oxidizing solutions could travel from the surface to the depth of a repository in crystalline rock within 400 to 50,000 years. These estimates are relatively short compared with time periods considered in safety assessments of repository performance, which suggests that time-dependent variations in the redox environment of both the near field and geosphere may need to be accounted for in these assessments. The flow velocities and concentrations of reducing minerals assumed in JNC's conceptual model may be overly conservative, however. (author)

  12. Effects of glacial/post-glacial weathering compared with hydrothermal alteration - implications for matrix diffusion. Results from drillcore studies in porphyritic quartz monzodiorite from Aespoe SE Sweden

    International Nuclear Information System (INIS)

    Landstroem, Ove; Tullborg, Eva-Lena

    2001-08-01

    The effects of hydrothermal + subsequent low temperature alteration and glacial/post-glacial weathering have been studied in two cores of quartz monzodiorite. One core (YA 1192) was drilled into the hydrothermally altered wall rock of a water-conducting fracture exposed at 170 m depth in the access tunnel to the Aespoe Hard Rock Laboratory. The other one (Bas 1) was drilled from an outcrop with a glacially polished surface, 1 km north of the YA 1192 site. Both drill cores were sectioned into mm-thick slices perpendicular to the core axis. The fracture filling of the YA 1192 core, the weathered surface of the BAS 1 core and the different slices were analysed for major and trace elements and isotopes of U and Th. The altered zone of the YA 1192 core extends to approx. 2.5 cm from the fracture surface. The alteration (mainly plagioclase → albite + sericite + epidote) has resulted in a higher porosity and formation of sorbing secondary minerals (e.g. sericite), favouring matrix diffusion. Increased Br concentrations in the altered zone are indicative of saline water in pores and micro fractures i.e. the presence of a diffusion medium. 234U/238U activity ratios > 1 and increased Cs in the altered zone are then interpreted as diffusion of U and Cs from fracture groundwater and subsequent sorption. The U migration is geologically recent (< 1 Ma). The 2.5 cm altered zone (corresponding to the zone of active matrix diffusion) significantly exceeds the visible red staining zone (0.5 cm) caused by hematite/FeOOH micrograins, emphasizing the need of microscopy to identify zones of alteration. The conspicuous weathering at the BAS 1 site is confined to a narrow rim of the bedrock surface (approx. 0.2-0.5 cm thick). Mass balance calculations for this rim (based on immobility of K) indicate that mechanical erosion has dominated over chemical dissolution processes (is roughly 10 times greater). The chemical weathering has affected mainly plagioclase and chlorite resulting in

  13. Gneiss wastes as secondary raw material for the ceramic industry: an example from the Verbano Cusio Ossola district (Piedmont, north-western Alps, Italy)

    Science.gov (United States)

    Cavallo, Alessandro

    2015-04-01

    -feldspathic rocks (i.e. Serizzo and Beola), are potential sources of secondary raw materials for the ceramic industry. To assess the feasibility of a reuse of these waste materials, an extensive sampling was performed on the main quarry dumps. The waste rocks were characterized by polarized light optical microscopy (OM) on thin sections, scanning electron microscopy (SEM), quantitative X-ray powder diffraction (XRD-QPA with the Rietveld method), electron microprobe (WDS and EDS) and whole-rock geochemistry (ICP-AES, ICP-MS and LECO®). The performed analyzes show a marked mineralogical and chemical heterogeneity (e.g. highly variable content of phyllosilicates, FeOtot content between 0.39 and 6.99 wt.%), as well as important textural and granulometric differences. On the other hand, the composition of feldspars is quite homogeneous, with the plagioclase ranging from almost pure albite to oligoclase (An 25 - 30%). Some varieties of Serizzo and Beola (Serizzo Sempione, Serizzo Formazza and Beola Bianca) are preferable because of their relatively low FeOtot content, but granulometric and textural factors should never be overlooked, as they have an important feedback in the efficiency and feasibility of the industrial treatments (e.g. magnetic separation). Specifically, some Beola varieties with particularly fine grain size and mylonitic texture, are poorly-suited to industrial ore treatments. On the contrary, the Serizzo varieties, although with a generally higher FeOtot content, have a coarser and homogeneous (and therefore preferable) grain size. Waste materials with different composition could be mixed properly until reaching the desired "ideal" compositions for the following industrial treatments. In any case, an accurate characterization of the waste materials from each of quarry dump is of fundamental importance.

  14. The crystal structure of galgenbergite-(Ce), CaCe2(CO3)4•H2O

    Science.gov (United States)

    Walter, Franz; Bojar, Hans-Peter; Hollerer, Christine E.; Mereiter, Kurt

    2013-04-01

    Galgenbergite-(Ce) from the type locality, the railroad tunnel Galgenberg between Leoben and St. Michael, Styria, Austria, was investigated. There it occurs in small fissures of an albite-chlorite schist as very thin tabular crystals building rosette-shaped aggregates associated with siderite, ancylite-(Ce), pyrite and calcite. Electron microprobe analyses gave CaO 9.49, Ce2O3 28.95, La2O3 11.70, Nd2O3 11.86, Pr2O3 3.48, CO2 30.00, H2O 3.07, total 98.55 wt.%. CO2 and H2O calculated by stoichiometry. The empirical formula (based on Ca + REE ∑3.0) is C{{a}_{1.00 }}{{( {C{{e}_{1.04 }}L{{a}_{0.42 }}N{{d}_{0.42 }}P{{r}_{0.12 }}} )}_{2.00 }}{{( {C{{O}_3}} )}_4}\\cdot {{H}_2}O , and the simplified formula is CaC{{e}_2}{{( {C{{O}_3}} )}_4}\\cdot {{H}_2}O . According to X-ray single crystal diffraction galgenbergite-(Ce) is triclinic, space group Poverline{1},a=6.3916(5) , b = 6.4005(4), c = 12.3898(9) Å, α = 100.884(4), β = 96.525(4), γ = 100.492(4)°, V = 483.64(6) Å3, Z = 2. The eight strongest lines in the powder X-ray diffraction pattern are [ d calc in Å/( I)/ hkl]: 5.052/(100)/011; 3.011/(70)/0-22; 3.006/(66)/004; 5.899/(59)/-101; 3.900/(51)/1-12; 3.125/(46)/-201; 2.526/(42)/022; 4.694/(38)/-102. The infrared absorption spectrum reveals H2O (OH-stretching mode at 3,489 cm-1, HOH bending mode at 1,607 cm-1) and indicates the presence of distinctly non-equivalent CO3-groups by double and quadruple peaks of their ν1, ν2, ν3 and ν4 modes. The crystal structure of galgenbergite-(Ce) was refined with X-ray single crystal data to R1 = 0.019 for 2,448 unique reflections ( I > 2 σ( I)) and 193 parameters. The three cation sites of the structure Ca(1), Ce(2) and Ce(3) have a modest mixed site occupation by Ca and small amount of REE (Ce, La, Pr, Nd) and vice versa. The structure is based on double layers parallel to (001), which are composed of Ca(1)Ce(2)(CO3)2 single layers with an ordered chessboard like arrangement of Ca and Ce, and with a roof tile

  15. Mineralogy of metasomatic rocks and geochronology of the Olhovka porphyry-copper deposit, Chukotka, Russia

    Science.gov (United States)

    Rogacheva, Lyuba; Baksheev, Ivan

    2010-05-01

    The Olkhovka porphyry-copper deposit located on the border of foreland of the Okhotsk-Chukotka volcanic belt (OCVB) and a ledge composed of the Late Jurassic-Early Cretaceous Uda-Murgal arc (J3-K1) rocks is hosted by monzonite stock attributed to the Upper Cretaceous Kavralyan complex - K2) We estimated age of the Olkhovka monzonite by Rb-Sr and U-Pb methods. Rb-Sr age was determine om the basis of isotopic analysis of 8 monomineralic samples (potassium feldspar, plagioclase, amphibole, and dark mica). Isochron constructed on the basis of Rb-Sr data corresponds to the age of 78 + 2.6 Ma (MSWD=0.23). The Rb-Sr age is supported by U-Pb data derived from zircon of the same rock. One hundred and three single crystals of zircon were analyzed. Uranium content ranges from 52.66 ppm to 579.64 ppm; U/Th isotopic ratio varies from 0.567 to 1.746; age is 78.02+0.65 Ma (MSWD = 2.8). Monzonite is propylitized in variable degree. Propylite is composed of actinolite, chlorite, albite, quartz, and calcite. Propylite are cut by quartz-tourmaline veins. In addition, quartz-tourmaline metasomatic rock was identified in rhyolite ignimbrite out of the stock. Microscopically, tourmaline crystals of both types are oscilatory zoned that is caused by variable Fe content. Tourmalines of both assemblages can be classified as intermediate member of the schorl ("oxy-schorl")-dravite ("oxy-dravite") series. The Fetot/ (Fetot+Mg) varies from 0.31 to 0.95 in propylitic tourmaline and from 0.11 to 0.49, in quartz-tourmaline altered rocks from ignimbrite. Despite similar composition of both tourmalines, the major isomorphic substitutions in them are different. In propylite tourmaline, it is Fe → Al, whereas in the second case, it is Fe → Mg with certain effect of the Fe → Al type. Fe → Al isomorphic substitution is typical of porphyry style deposits (Baksheev et al., 2009 [1]). Therefore, we can conclude that quartz-tourmaline alteration in ignimbrite does not related to the formation of

  16. Geology and porphyry copper-type alteration-mineralization of igneous rocks at the Christmas Mine, Gila County, Arizona

    Science.gov (United States)

    Koski, Randolph A.

    1979-01-01

    igneous rocks is progressively more alkaline and silicic from basalt to granodiorite. Early (Stage I) chalcopyrite-bornite (-molybdenite) mineralization and genetically related K-silicate alteration are centered on the Christmas stock. K-silicate alteration is manifested by pervasive hornblende-destructive biotitization in the stock, biotitization of basaltic volcanic wall rocks, and a continuous stockwork of K-feldspar veinlets and quartz-K-feldspar veins in the stock and quartz-sulfide veins in volcanic rocks. Younger (Stage II) pyrite-chalcopyrite mineralization and quartz-sericite-chlorite alteration occur in a zone overlapping with but largely peripheral to the zone of Stage I stockwork veins. Within the Christmas intrusive complex, K-silicate-altered rocks in the central stock are flanked east and west by zones of fracture-controlled quartz-sericite alteration and strong pyritization. In volcanic rocks quartz-chlorite-pyrite-chalcopyrite veins are superimposed on earlier biotitization and crosscut Stage I quartz-sulfide veins. Beyond the zones of quartz-sericite alteration, biotite rhyodacite porphyry dikes contain the propylitic alteration assemblage epidote-chlorite-albite-sphene. Chemical analyses indicate the following changes during pervasive alteration of igneous rocks: (1) addition of Si, K, H, S, and Cu, and loss of Fe 3+ and Ca during intense biotitization of basalt; (2) loss of Na and Ca, increase of Fe3+/Fe2+, and strong H-metasomatism during sericitization of quartz diorite; and (3) increase in Ca, Na, and Fe3+/Fe2+, and loss of K during intense propylitization of biotite rhyodacite porphyry dikes. Thorough biotitization of biotite granodiorite porphyry in the Christmas stock was largely an isochemical process. Fluid-inclusion petrography reveals that Stage I veins are characterized by low to moderate populations of moderate-salinity and gas-rich inclusions, and sparse but ubiquitous halite-bearing inclusions. Moderate-salinity an

  17. Geothermometry, geochronology, and mass transfer associated with hydrothermal alteration of a rhyolitic hyaloclastite from Ponza Island, Italy

    Science.gov (United States)

    Altaner, S.P.; Ylagan, R.F.; Savin, S.M.; Aronson, J.L.; Belkin, H.E.; Pozzuoli, A.

    2003-01-01

    A rhyolitic hyaloclastite from Ponza Island, Italy, was hydrothermally altered, producing four distinct alteration zones based on X-ray diffraction mineralogy and field textures: (1) nonpervasive argillic zone; (2) propylitic zone; (3) silicic zone; and (4) sericitic zone. The unaltered hyaloclastite is volcanic breccia with clasts of vesiculated obsidian in a matrix of predominantly pumice lapilli. Incomplete alteration of the hyaloclastite resulted in the nonpervasive argillic zone, characterized by smectite and disordered opal-CT. The other three zones exhibit more complete alteration of the hyaloclastite. The propylitic zone is characterized by mixed-layer illite-smectite (I-S) with 10 to 85% I, mordenite, opal-C, and authigenic K-feldspar (akspar). The silicic zone is characterized by I-S with ???90% I, pure illite, quartz, akspar, and occasional albite. The sericitic zone consists primarily of I-S with ???66% I, pure illite, quartz, and minor akspar and pyrite. K/Ar dates of I-S indicate hydrothermal alteration occurred at 3.38 ?? 0.08 Ma. Oxygen isotope compositions of I-S systematically decrease from zones 1 to 4. In the argillic zone, smectite has ??18 O values of 21.7 to 22.0??? and I-S from the propylitic, silicic, and sericitic zones ranges from 14.5 to 16.3???, 12.5 to 14.0???, and 8.6 to 11.9???, respectively. ??18 O values for quartz from the silicic and sericitic zones range from 12.6 to 15.9???. By use of isotope fractionation equations and data from authigenic quartz-hosted primary fluid inclusions, alteration temperatures ranged from 50 to 65 ??C for the argillic zone, 85 to 125 ??C for the propylitic zone, 110 to 210 ??C for the silicic zone, and 145 to 225 ??C for the sericitic zone. Fluid inclusion data and calculated ??18 O water values indicate that hydrothermal fluids were seawater dominated. Mass-transfer calculations indicate that hydrothermal alteration proceeded in a relatively open chemical system and alteration in the sericitic zone

  18. Structure, alteration, and geochemistry of the Charlotte quartz vein stockwork, Mt Charlotte gold mine, Kalgoorlie, Australia: time constraints, down-plunge zonation, and fluid source

    Science.gov (United States)

    Mueller, Andreas G.

    2015-02-01

    The Kalgoorlie district in the Archean Yilgarn Craton, Western Australia, comprises two world-class gold deposits: Mt Charlotte (144 t Au produced to 2013) in the northwest and the Golden Mile (1,670 t Au) in the southeast. Both occur in a folded greenschist-facies gabbro sill adjacent to the Golden Mile Fault (D2) in propylitic alteration associated with porphyry dikes. At Mt Charlotte, a shear array of fault-fill veins within the Golden Mile Fault indicates sinistral strike-slip during Golden Mile-type pyrite-telluride mineralization. The pipe-shaped Charlotte quartz vein stockwork, mined in bulk more than 1 km down plunge, is separated in time by barren D3 thrusts from Golden Mile mineralization and alteration, and occurs between two dextral strike-slip faults (D4). Movement on these faults generated an organized network of extension and shear fractures opened during the subsequent infiltration of high-pressure H2S-rich fluid at 2,655 ± 13 Ma (U-Pb xenotime). Gold was deposited during wall rock sulphidation in overlapping vein selvages zoned from deep albite-pyrrhotite (3 g/t Au) to upper muscovite-pyrite assemblages (5 g/t Au bulk grade). Chlorite and fluid inclusion thermometry indicate that this kilometre-scale zonation is due to fluid cooling from 410-440 °C at the base to 350-360 °C at the top of the orebody, while the greenstone terrane remained at 250 °C ambient temperature and at 300 MPa lithostatic pressure. The opened fractures filled with barren quartz and scheelite during the retrograde stage (300 °C) of the hydrothermal event. During fracture sealing, fluid flux was periodically restricted at the lower D3 thrust. Cycles of high and low up-flow, represented by juvenile H2O-CO2 and evolved H2O-CO2-CH4 fluid, respectively, are recorded by the REE and Sr isotope compositions of scheelite oscillatory zones. The temperature gradient measured in the vein stockwork points to a hot (>600 °C) fluid source 2-4 km below the mine workings, and several

  19. The Damage and Geochemical Signature of a Crustal Scale Strike-Slip Fault Zone

    Science.gov (United States)

    Gomila, R.; Mitchell, T. M.; Arancibia, G.; Jensen Siles, E.; Rempe, M.; Cembrano, J. M.; Faulkner, D. R.

    2013-12-01

    . Whole-rock XRF analyses show Al and Ca content decrease with increasing Si, whereas Na increases towards the core. This can be interpreted as compositional changes of plagioclase to albite-rich ones due to chloritic-propylitic alteration. In the damage zone, LOI increases towards the core but decreases inside of it. This is explained by H2O-rich clays and gypsum in the fault core boundary represented as fault gouge zones whereas in the cataclastic core zone, the decrease in LOI is explained by epidote. Our results show the JF had an evolving permeability structure where a cataclasite-rich core is formed at an early stage, and then a gouge-bounded core is developed which acted as a barrier to fluid from east to west of the fault.

  20. Petrogénesis del plutón monzogranítico peralumínico de Santa Eufemia (Batolito de los Pedroches, Córdoba

    Directory of Open Access Journals (Sweden)

    Fenoll Hach-Alí, P.

    1989-04-01

    Full Text Available The Santa Eufemia pluton is part of the composite magmatic assoclatlon of Los Pedroches batholith, located in the southern branch of the Central Iberian Zone of the Hercynian orogenic belt of Spain. This high-Ievel postkynematic batholith consists of three main types of plutonic rocks: boitite±amphibole granodiorites, biotite-cordierite porphiritic monzogranites and cordierite leucogranites. The Santa Eufemia pluton consists of biotite-cordierite monzogranites, and in a lesser extent of cordierite leucogranites. Scarce enclaves of different type are found in the monzogranites, biotiteplagioclase- eordierite and fine grained porphiritic monzogranite enclaves being the most common. The petrographic, structural and geochemical (major and trace elements data suggests a compiex evolutionary history of a metasedimentary-source monzogranitic magma with no genetical relationships with more basic magmas such as the one which is now represented by the granodiorite facies of the batholith. Non-minimum melt and reequilibrated source material (secondary restites mixing during the ortomagmatic evolution of the magma accounts for the compositional heterogenities of the monzogranites. The ultimate product of this evolution is the segregation of a fluid-saturated residual liquid in the final level of intrusion of the magma, leading to the emplacement of leucogranite masses and dikes and the exsolution of a supercritical fluid phase related with the late magmatic recrystallization of sorne mineral phases (muscovite, albite, quartz, tourmaline, topaz, the geochemical removilization of sorne incompatible trace elements (Rb, Cs, Li, Be, Sn, Nb due to fluid-rock interactions and the formation of periplutonic wolframite-arsenopyritequartz mineralizations.El plutón de Santa Eufemia forma parte del batolito de Los Pedroches, situado en el extremo sudoccidental de la Zona Centro-Ibérica del Macizo Hercínico español. Este batolito de carácter epizonal y postcinem

  1. Micro-structural and compositional variations of hydrothermal epidote-group minerals from a peralkaline granite, Corupá Pluton, Graciosa Province, South Brazil, and their petrological implications

    Directory of Open Access Journals (Sweden)

    Silvio R.F. Vlach

    2012-06-01

    Full Text Available Epidote-group minerals, together with albite, quartz, fluorite, Al-poor and Fe-rich phyllosilicates, zircon, and minor oxides and sulphides, are typical hydrothermal phases in peralkaline alkali-feldspar granites from the Corupá Pluton, Graciosa Province, South Brazil. The epidote-group minerals occur as single crystals and as aggregates filling in rock interstices and miarolitic cavities. They display complex recurrent zoning patterns with an internal zone of ferriallanite-(Ce, followed by allanite-(Ce, then epidote-ferriepidote, and an external zone with allanite-(Ce, with sharp limits, as shown in BSE and X-ray images. REE patterns show decreasing fractionation degrees of LREE over HREE from ferriallanite to epidote. The most external allanite is enriched in MREE. LA-ICP-MS data indicate that ferriallanite is enriched (>10-fold in Ti, Sr and Ga, and depleted in Mg, Rb, Th and Zr relative to the host granite. Allanite has lower Ga and Mn and higher Zr, Nb and U contents as compared to ferriallanite, while epidote is enriched in Sr, U and depleted in Pb, Zr, Hf, Ti and Ga. The formation of these minerals is related to the variable concentrations of HFSE, Ca, Al, Fe and F in fluids remaining from magmatic crystallization, in an oxidizing environment, close to the HM buffer. L-MREE were in part released by the alteration of chevkinite, their main primary repository in the host rocks.Minerais do grupo do epidoto, com albita, quartzo, fluorita, filossilicatos pobres em Al e ricos em Fe, zircão e quantidades menores de óxidos e sulfetos são fases hidrotermais típicas em álcali-feldpato granitos peralcalinos do Pluton Corupá, Província Graciosa, Sul do Brasil. Os minerais do grupo do epidoto ocorrem como cristais individuais ou agregados que preenchem interstícios e cavidades miarolíticas na rocha. Mostram zonamento complexo, recorrente, descrito por uma zona interna de ferriallanita-(Ce, seguida por allanita-(Ce, epidoto-ferriepidoto e uma

  2. Strongly foliated garnetiferous amphibolite clasts in ophiolitic melanges, Yarlung Zangbo Suture Zone, Tibet; Early Cretaceous disruption of a back-arc basin?

    Science.gov (United States)

    Guilmette, C.; Hebert, R.; Wang, C.; Indares, A. D.; Ullrich, T. D.; Dostal, J.; Bedard, E.

    2007-12-01

    Metre to decameter-size clasts of amphibolite are found embedded in ophiolitic melanges underlying the Yarlung Zangbo Suture Zone Ophiolites, South Tibet, China. These ophiolites and melanges occur at the limit between Indian and Tibetan-derived rocks and represent remnants of an Early Cretaceous intraoceanic supra-subduction zone domain, the Neo-Tethys. In the Saga-Dazuka segment (500 km along-strike), we discovered new occurrences of strongly foliated amphibolites found as clasts in the ophiolitic melange. In garnet-free samples, hornblende is green-blue magnesio-hornblende and cpx is low-Al diopside. In garnet- bearing samples, garnet is almandine with a strong pyrope component (up to 30 mol%) whereas coexisting hornblende is brown Ti-rich tschermakite and clinopyroxene is Al-diopside. Plagioclase composition was ubiquitously shifted to albite during a late metasomatic event. Geochemistry of these rocks indicates that their igneous protoliths crystallized from a slightly differentiated tholeiitic basaltic liquid that did not undergo major fractionation. Trace element patterns reveal geochemical characteristics identical to those of the overlying ophiolitic crust. These are 1) trace element abundances similar to that of N-MORBs or BABBs, 2) a slight depletion of LREE and 3) a moderate to strong Ta-Nb negative anomaly and a slight Ti anomaly. Such characteristics suggest genesis over a spreading center close to a subduction zone, possibly a back-arc basin. Step-heating Ar/Ar plateau ages were obtained from hornblende separates. All ages fall in the range of 123-128 Ma, overlapping the crystallization ages from the overlying ophiolite (126-131 Ma). Pseudosections were built with the THERMOCALC software in the system NCFMASH. Results indicate that the observed assemblage Hb+Pl+Gt+Cpx is stable over a wide range of P-T conditions, between 10-18 kbars and at more than 800°C. Measured mineral modes and solid solution compositions were successfully modeled, indicating

  3. Cataclastic rocks of the San Gabriel fault—an expression of deformation at deeper crustal levels in the San Andreas fault zone

    Science.gov (United States)

    Anderson, J. Lawford; Osborne, Robert H.; Palmer, Donald F.

    1983-10-01

    The San Gabriel fault, a deeply eroded late Oligocene to middle Pliocene precursor to the San Andreas, was chosen for petrologic study to provide information regarding intrafault material representative of deeper crustal levels. Cataclastic rocks exposed along the present trace of the San Andreas in this area are exclusively a variety of fault gouge that is essentially a rock flour with a quartz, feldspar, biotite, chlorite, amphibole, epidote, and Fe-Ti oxide mineralogy representing the milled-down equivalent of the original rock (Anderson and Osborne, 1979; Anderson et al., 1980). Likewise, fault gouge and associated breccia are common along the San Gabriel fault, but only where the zone of cataclasis is several tens of meters wide. At several localities, the zone is extremely narrow (several centimeters), and the cataclastic rock type is cataclasite, a dark, aphanitic, and highly comminuted and indurated rock. The cataclastic rocks along the San Gabriel fault exhibit more comminution than that observed for gouge along the San Andreas. The average grain diameter for the San Andreas gouge ranges from 0.01 to 0.06 mm. For the San Gabriel cataclastic rocks, it ranges from 0.0001 to 0.007 mm. Whereas the San Andreas gouge remains particulate to the smallest grain-size, the ultra-fine grain matrix of the San Gabriel cataclasite is composed of a mosaic of equidimensional, interlocking grains. The cataclastic rocks along the San Gabriel fault also show more mineralogiec changes compared to gouge from the San Andreas fault. At the expense of biotite, amphibole, and feldspar, there is some growth of new albite, chlorite, sericite, laumontite, analcime, mordenite (?), and calcite. The highest grade of metamorphism is laumontite-chlorite zone (zeolite facies). Mineral assemblages and constrained uplift rates allow temperature and depth estimates of 200 ± 30° C and 2-5 km, thus suggesting an approximate geothermal gradient of ~50°C/km. Such elevated temperatures imply a

  4. The role of reaction affinity and secondary minerals in regulating chemical weathering rates at the Santa Cruz Soil Chronosequence, California

    Science.gov (United States)

    Maher, K.; Steefel, Carl; White, A.F.; Stonestrom, David A.

    2009-01-01

    In order to explore the reasons for the apparent discrepancy between laboratory and field weathering rates and to determine the extent to which weathering rates are controlled by the approach to thermodynamic equilibrium, secondary mineral precipitation, and flow rates, a multicomponent reactive transport model (CrunchFlow) was used to interpret soil profile development and mineral precipitation and dissolution rates at the 226 ka Marine Terrace Chronosequence near Santa Cruz, CA. Aqueous compositions, fluid chemistry, transport, and mineral abundances are well characterized [White A. F., Schulz M. S., Vivit D. V., Blum A., Stonestrom D. A. and Anderson S. P. (2008) Chemical weathering of a Marine Terrace Chronosequence, Santa Cruz, California. I: interpreting the long-term controls on chemical weathering based on spatial and temporal element and mineral distributions. Geochim. Cosmochim. Acta 72 (1), 36-68] and were used to constrain the reaction rates for the weathering and precipitating minerals in the reactive transport modeling. When primary mineral weathering rates are calculated with either of two experimentally determined rate constants, the nonlinear, parallel rate law formulation of Hellmann and Tisserand [Hellmann R. and Tisserand D. (2006) Dissolution kinetics as a function of the Gibbs free energy of reaction: An experimental study based on albite feldspar. Geochim. Cosmochim. Acta 70 (2), 364-383] or the aluminum inhibition model proposed by Oelkers et al. [Oelkers E. H., Schott J. and Devidal J. L. (1994) The effect of aluminum, pH, and chemical affinity on the rates of aluminosilicate dissolution reactions. Geochim. Cosmochim. Acta 58 (9), 2011-2024], modeling results are consistent with field-scale observations when independently constrained clay precipitation rates are accounted for. Experimental and field rates, therefore, can be reconciled at the Santa Cruz site. Additionally, observed maximum clay abundances in the argillic horizons occur at

  5. The Friningen Garnet Peridotite (central Swedish Caledonides). A good example of the characteristic PTt path of a cold mantle wedge garnet peridotite

    Science.gov (United States)

    Gilio, Mattia; Clos, Frediano; van Roermund, Herman L. M.

    2015-08-01

    We present pseudosections of Cr-bearing garnet peridotite that together with new mineral-chemical data allow quantification of the early PT conditions of the original lithospheric mantle assemblage (M1) of the Friningen Garnet Peridotite (FGP) located in the central/middle belt of the Seve Nappe Complex in central Sweden. Results indicate that the early, coarse grained, olivine + orthopyroxene + clinopyroxene + "high Cr" garnet assemblage (M1a) was formed at 1100 ± 100 °C and 5.0 ± 0.5 GPa. These metamorphic conditions were followed by an inferred late Proterozoic exhumation event down to 850-900 °C and 1.5 GPa (M1b). The latter PT estimate is based on the breakdown of high-Cr M1a garnet (Cr# = 0.065) + olivine into an orthopyroxene + clinopyroxene + spinel (Cr# = 0.15-0.25) ± pargasite kelyphite (M1b) and the exsolution of garnet from Al-rich orthopyroxene and clinopyroxene. The M1b kelyphite is overprinted by an early-Caledonian UHPM mineral assemblage (M2; T = 800 °C and P = 3.0 GPa), equivalent to the earlier discovered UHP assemblage within an eclogitic dyke that cross-cuts FGP. In the garnet peridotite M2 is displayed by low-Cr garnet (Cr# = 0.030) growing together with spinel (Cr# = 0.35-0.45), both these minerals form part of the olivine + orthopyroxene + clinopyroxene + garnet + spinel + pargasite M2 assemblage. The formation of plagioclase + diopside symplectites after omphacite and breakdown of kyanite to sapphirine + albite in internal eclogite and the breakdown of M2 olivine + garnet to amphibole + orthopyroxene + spinel assemblages (M3) in garnet peridotite indicate post-UHP isothermal decompression down to 750-800 °C and 0.8-1.0 GPa (= M3). Multiphase solid-and fluid inclusion assemblages composed of Sr-bearing magnesite, dolomite or carbon decorate linear defect structures within M1a-b minerals and/or form subordinate local assemblages together with M2 minerals. The latter are interpreted as evidence for infiltration of early-Caledonian COH

  6. Mianningite, (□,Pb,Ce,Na) (U{sup 4+},Mn,U{sup 6+}) Fe{sup 3+}{sub 2}(Ti,Fe{sup 3+}){sub 18}O{sub 38}, a new member of the crichtonite group from Maoniuping REE deposit, Mianning county, southwest Sichuan, China

    Energy Technology Data Exchange (ETDEWEB)

    Ge, Xiangkun; Fan, Guang; Chen, Zhangru; Ai, Yujie [Beijing Research Institute of Uranium Geology, Beijing (China); Li, Guowu [China Univ. of Geosciences, Beijing (China). Lab. of Crystal Structure; Shen, Ganfu [Chengdu Institute of Geology and Mineral Resources, Chengdu (China)

    2017-05-15

    Mianningite (IMA 2014-072), ideally (□,Pb,Ce,Na)(U{sup 4+},Mn,U{sup 6+}) Fe{sup 3+}{sub 2}(Ti,Fe{sup 3+}){sub 18}O{sub 38}, is a new member of the crichtonite group from the Maoniuping REE deposit, Mianning county, Sichuan province, China. It was found in fractures of lamprophyre veins and in the contact between lamprophyre and a later quartz-alkali feldspar syenite dyke with REE mineralization, and is named after its type locality. Associated minerals are microcline, albite, quartz, iron-rich phlogopite, augite, muscovite, calcite, baryte, fluorite, epidote, pyrite, magnetite, hematite, galena, hydroxylapatite, titanite, ilmenite, rutile, garnet-group minerals, zircon, allanite-(Ce), monazite-(Ce), bastnaesite-(Ce), parisite-(Ce), maoniupingite-(Ce), thorite, pyrochlore-group minerals and chlorite. Mianningite occurs as opaque subhedral to euhedral tabular crystals, up to 1-2 mm in size, black in color and streak, and with a submetallic luster. Mianningite is brittle, with a conchoidal fracture. Its average micro-indentation hardness is 83.8 kg/mm{sup 2} (load 0.2 kg), which is equivalent to ∝6 on the Mohs hardness scale. Its measured and calculated densities are 4.62 (8) g/cm{sup 3} and 4.77 g/cm{sup 3}, respectively. Under reflected light, mianningite is grayish white, with no internal reflections. It appears isotropic and exhibits neither bireflectance nor pleochroism. The empirical formula, calculated on the basis of 38 O atoms per formula unit (apfu), is [□{sub 0.322}(Pb{sub 0.215}Ba{sub 0.037}Sr{sub 0.036}Ca{sub 0.010}){sub Σ0.298}(Ce{sub 0.128}La{sub 0.077}Nd{sub 0.012}){sub Σ0.217} (Na{sub 0.127}K{sub 0.036}){sub Σ0.163}]{sub Σ01.000}(U{sup 4+}{sub 0.447}Mn{sub 00.293}U{sup 6} {sup +}{sub 0.112}Y{sub 0.091}Zr{sub 0.023}Th{sub 0.011}){sub Σ0.977}(Fe{sup 3+}{sub 1.224}Fe{sup 2+}{sub 0.243}Mg{sub 0.023}P{sub 0.008}Si{sub 0.006} □{sub 0.496}){sub Σ2.000}(Ti{sub 12.464}Fe{sup 3+}{sub 5.292}V{sup 5+}{sub 0.118}Nb{sub 0.083}Al{sub 0.026}Cr{sup 3

  7. Organic petrology and geochemistry of mudrocks from the lacustrine Lucaogou Formation, Santanghu Basin, northwest China: Application to lake basin evolution

    Science.gov (United States)

    Hackley, Paul C.; Fishman, Neil; Wu, Tao; Baugher, Gregory

    2016-01-01

    inertinite is present in the upper section, indicating greater terrestrial influx and consistent with higher quartz and plagioclase content (dominantly authigenic chalcedony and albite). Laminated mudstones in the upper section indicate anoxia prevented bioturbation from benthic grazing, also indicating stratified water column conditions. A decrease upsection in authigenic dolomite with reciprocal increase of ankerite/siderite is consistent with decreasing salinity, as is an overall decrease in gammacerane index values. These observations suggest evolution from a shallow, stratified evaporative (saline) setting to a deeper, stratified freshwater basin with higher water input during Lucaogou deposition. The evolution from an under-filled to balance-filled lake in Santanghu Basin is similar to Lucaogou deposition in Junggar Basin, suggesting similar tectonic and climatic controls. Paleoclimate interpretations from other researchers in this area suggested an evolution from semi-arid to humid conditions during the Roadian; we interpret that the evolution from an under-filled to balanced-filled lake seen in our data is in response to climate change, and may represent increased groundwater delivery to the Santanghu Basin.

  8. Deformation of quartz and feldspar at mid-crustal depths in an extensional normal fault (Viveiro Fault, NW Spain)

    Science.gov (United States)

    López-Sánchez, M. A.; Llana-Fúnez, S.; Marcos, A.; Martínez, F. J.

    2012-04-01

    Metamorphic reactions, deformation mechanism and chemical changes during mylonitization and ultramylonitization of granite affected by a crustal-scale shear zone are investigated using microstructural observations and quantitative analysis. The Vivero Fault (VF) is a large extensional shear zone (>140Km) in NW of Iberia that follows the main Variscan trend dipping 60° toward the West. The movement accumulated during its tectonic history affects the major lithostratigraphic sequence of Palaeozoic and Neoproterozoic rocks and the metamorphic facies developed during Variscan orogenesis. Staurolite, and locally, andalucite plus biotite grew in the hangingwall during the development of VF, overprinted the previous regional Variscan greenschist facies metamorphism. Andalusite growth took place during the intrusion of syntectonic granitic bodies, such as the deformed granite studied here. The Penedo Gordo granite is coarse-grained two-mica biotite-rich granite intruding the VF and its hangingwall. This granite developed a localized deformation consisting of a set of narrow zones (mm to metric scales) heterogeneously distributed subsequently to its intrusion. Based on pseudosections for representative hangingwall pelites hosting the granite and the inferred metamorphic evolution, the shear zone that outcrops at present-day erosion surface was previously active at 14,7-17 km depth (390-450 MPa). Temperature estimates during deformation reach at least the range 500-600° C, implying a local gradient of 35±6°C/km. Microstructures in the mylonites are characterized by bulging (BLG) to subgrain rotation (SGR) recristallization in quartz with the increasing of deformation. Albitisation, flame-perthite and tartan twining are common in K-feldspar at the early stage of deformation. The inferred dominant deformation mechanisms are: i) intracrystalline plasticity in quartz, ii) cataclasis with syntectonic crystallisation of very fine albite-oligoclase and micas in K-feldspar, and

  9. The brittle-viscous-plastic evolution of shear bands in the South Armorican Shear Zone

    Science.gov (United States)

    Bukovská, Zita; Jeřábek, Petr; Morales, Luiz F. G.; Lexa, Ondrej; Milke, Ralf

    2014-05-01

    Shear bands are microscale shear zones that obliquely crosscut an existing anisotropy such as a foliation. The resulting S-C fabrics are characterized by angles lower than 45° and the C plane parallel to shear zone boundaries. The S-C fabrics typically occur in granitoids deformed at greenschist facies conditions in the vicinity of major shear zones. Despite their long recognition, mechanical reasons for localization of deformation into shear bands and their evolution is still poorly understood. In this work we focus on microscale characterization of the shear bands in the South Armorican Shear Zone, where the S-C fabrics were first recognized by Berthé et al. (1979). The initiation of shear bands in the right-lateral South Armorican Shear Zone is associated with the occurrence of microcracks crosscutting the recrystallized quartz aggregates that define the S fabric. In more advanced stages of shear band evolution, newly formed dominant K-feldspar, together with plagioclase, muscovite and chlorite occur in the microcracks, and the shear bands start to widen. K-feldspar replaces quartz by progressively bulging into the grain boundaries of recrystallized quartz grains, leading to disintegration of quartz aggregates and formation of fine-grained multiphase matrix mixture. The late stages of shear band development are marked by interconnection of fine-grained white mica into a band that crosscuts the original shear band matrix. In its extremity, the shear band widening may lead to the formation of ultramylonites. With the increasing proportion of shear band matrix from ~1% to ~12%, the angular relationship between S and C fabrics increases from ~30° to ~40°. The matrix phases within shear bands show differences in chemical composition related to distinct evolutionary stages of shear band formation. The chemical evolution is well documented in K-feldspar, where the albite component is highest in porphyroclasts within S fabric, lower in the newly formed grains within

  10. Steatite and schist as contenders for the Global Heritage Stone Resource due to their importance in Brazil's natural stone built heritage

    Science.gov (United States)

    Gilberto Costa, Antônio

    2013-04-01

    In Brazil, European natural stones, such as marble and limestone, were used as building material at historically important buildings and monuments, mainly in coastal cities, as well as in contemporary urban centers. However, in the country's central region, these Italian and Portuguese marbles and limestones were scarcely used. Instead, they were substituted for soapstone and several types of schist. As of 1755, the former was employed because of the ease with which it can be worked, essentially in the sculptural art and in the production of ornamental elements. Characterized by the presence of talc, steatite can feature other minerals such as serpentine, chlorite, carbonate, amphiboles, oxides like hematite and magnetite, and sulfites like pyrite, all in broadly variable amounts, which can result in modification of its technological properties (Volumetric Weight, Porosity, Water Absorption, Uniaxial Compression, Abrasion Resistance, Thermal Expansion etc.). In such rocks, talc content will be a decisive factor in their coloration. The higher its talc content is the clearer and softer the stone type will be, which ends up being known as talc stone. In such cases, the rock can display different hues of green, blue and gray. When compared to other rocks, texture patterns containing talc crystals, chlorite and carbonate contribute to low absorption and porosity for steatites. Schists were equally used at historical buildings in the Brazilian inland, especially in constructions in Minas Gerais towns, both in the production of structural elements such as bases, corners, pillars and foundations and in the creation of ornaments. Featuring different compositions, such rocks - which almost always occur interlayered with other ones such as quartzite - display coloration ranging from hues of gray to green to blue. They can be quartz-sericite-albite-chlorite schists featuring great or no amounts of carbonate, magnetite, epidote and tourmaline, sometimes with garnet, such as in

  11. Deep subduction of hot young oceanic slab required by the Syros eclogites

    Science.gov (United States)

    Flemetakis, Stamatis; Moulas, Evangelos; Kostopoulos, Dimitrios; Chatzitheodoridis, Elias

    2014-05-01

    The Cycladic islands of Syros and Siphnos, Aegean Sea, Greece, represent subducted IAT and BABB remnants of the Neotethyan Pindos Ocean. Garnet porphyroblasts (Ø=1mm) in a glaucophane-zoisite eclogite from Kini locality on Syros are compositionally zoned and display a unique prograde heating path from a high-pressure greenschist-facies core with high XSps and low Mg# via a blueschist-facies mantle with moderate XSps and Mg# to an eclogite-facies rim with low XSps and high Mg#. The outermost 35 μm of the garnet rims show flat XSps with rapidly increasing outwards Mg#. Na-Act-Chl-Ph rimmed by Gln mark the greenschist-blueschist facies transition, whereas Pg rimmed by Omp and the incoming of Rt at the expense of Ttn signify the blueschist-eclogite facies transition. Raman barometry of quartz inclusions in the eclogitic garnet rims coupled with elastic modelling of the garnet host [1], and Zr-in-Rt and Grt-Cpx-Ph thermobarometry revealed near-UHP P-T conditions of the order of 2.6 GPa/660°C (maximum residual pressure was 0.8-0.9GPa). By contrast, the greenschist-blueschist transition lies at ~0.75 GPa/355°C. This pressure is in excellent agreement with the position of the albite = jadeite + quartz boundary calculated at 350°C using the observed omphacite composition corrected for jadeite activity (Koons & Thompson, 1985) [2]. As a result, Cpx inclusions in garnet core signify the early entrance of garnet in the subduction zone history of the slab. Furthermore, the early growth of garnet (in lower pressures) observed in eclogites from Syros lies in great agreement with published slab-geotherms that indicate hot subduction and show a precocious garnet growth (Baxter and Caddick, 2013) [3]. The complete absence of lawsonite and the great abundance of zoisite crystals, based on the stability fields of both minerals (Poli et al., 2009) [4], further constrain the P-T trajectory of the slab. Our new P-T estimates match published T distributions on the slab surface

  12. The interplay of evolved seawater and magmatic-hydrothermal fluids in the 3.24 Ga panorama volcanic-hosted massive sulfide hydrothermal system, North Pilbara Craton, Western Australia

    Science.gov (United States)

    Drieberg, Susan L.; Hagemann, Steffen G.; Huston, David L.; Landis, Gary; Ryan, Chris G.; Van Achterbergh, Esmé; Vennemann, Torsten

    2013-01-01

    The ~3240 Ma Panorama volcanic-hosted massive sulfide (VHMS) district is unusual for its high degree of exposure and low degree of postdepositional modification. In addition to typical seafloor VHMS deposits, this district contains greisen- and vein-hosted Mo-Cu-Zn-Sn mineral occurrences that are contemporaneous with VHMS orebodies and are hosted by the Strelley granite complex, which also drove VHMS circulation. Hence the Panorama district is a natural laboratory to investigate the role of magmatic-hydrothermal fluids in VHMS hydrothermal systems. Regional and proximal high-temperature alteration zones in volcanic rocks underlying the VHMS deposits are dominated by chlorite-quartz ± albite assemblages, with lesser low-temperature sericite-quartz ± K-feldspar assemblages. These assemblages are typical of VHMS hydrothermal systems. In contrast, the alteration assemblages associated with granite-hosted greisens and veins include quartz-topaz-muscovite-fluorite and quartz-muscovite (sericite)-chlorite-ankerite. These vein systems generally do not extend into the overlying volcanic pile. Fluid inclusion and stable isotope studies suggest that the greisens were produced by high-temperature (~590°C), high-salinity (38–56 wt % NaCl equiv) fluids with high densities (>1.3 g/cm3) and high δ18O (9.3 ± 0.6‰). These fluids are compatible with the measured characteristics of magmatic fluids evolved from the Strelley granite complex. In contrast, fluids in the volcanic pile (including the VHMS ore-forming fluids) were of lower temperature (90°–270°C), lower salinity (5.0–11.2 wt % NaCl equiv), with lower densities (0.88–1.01 g/cm3) and lower δ18O (−0.8 ± 2.6‰). These fluids are compatible with evolved Paleoarchean seawater. Fluids that formed the quartz-chalcopyrite-sphalerite-cassiterite veins, which are present within the granite complex near the contact with the volcanic pile, were intermediate in temperature and isotopic composition between the greisen

  13. Rapid sedimentation of iron oxyhydroxides in an active hydrothermal shallow semi-enclosed bay at Satsuma Iwo-Jima Island, Kagoshima, Japan

    Science.gov (United States)

    Kiyokawa, Shoichi; Ueshiba, Takuya

    2015-04-01

    Hydrothermal activity is common in the fishing port of Nagahama Bay, a small semi-enclosed bay located on the southwest coast of Satsuma Iwo-Jima Island (38 km south of Kyushu Island, Japan). The bay contains red-brown iron oxyhydroxides and thick deposits of sediment. In this work, the high concentration and sedimentation rates of oxyhydroxide in this bay were studied and the sedimentary history was reconstructed. Since dredging work in 1998, a thickness of 1.0-1.5 m of iron oxyhydroxide-rich sediments has accumulated on the floor of the bay. To estimate the volume of iron oxyhydroxide sediments and the amount discharged from hydrothermal vents, sediment traps were operated for several years and 13 sedimentary core samples were collected to reconstruct the 10-year sedimentary history of Nagahama Bay. To confirm the timing of sedimentary events, the core data were compared with meteorological records obtained on the island, and the ages of characteristic key beds were thus identified. The sedimentation rate of iron oxyhydroxide mud was calculated, after correcting for sediment input from other sources. The sediments in the 13 cores from Nagahama Bay consist mainly of iron oxyhydroxide mud, three thick tephra beds, and a topmost thick sandy mud bed. Heavy rainfall events in 2000, 2001, 2002, and 2004-2005 coincide with tephra beds, which were reworked from Iwo-Dake ash deposits to form tephra-rich sediment. Strong typhoon events with gigantic waves transported outer-ocean-floor sediments and supplied quartz, cristobalite, tridymite, and albite sands to Nagahama Bay. These materials were redeposited together with bay sediments as the sandy mud bed. Based on the results from the sediment traps and cores, it is estimated that the iron oxyhydroxide mud accumulated in the bay at the relatively rapid rate of 33.3 cm/year (from traps) and 2.8-4.9 cm/year (from cores). The pore water contents within the sediment trap and core sediments are 73%-82% and 47%-67%, respectively

  14. Central Ukraine Uranium Province: The genetic model

    International Nuclear Information System (INIS)

    Emetz, A.; Cuney, M.

    2014-01-01

    Ukraine produces ~1,100 t U per year from the Michurinske, Centralne, Novokostantynivske and Vatutinske U deposits in the Kirovograd U district of the Central Ukraine Uranium Province (CUUP) consisting of about 20 deposits and numerous showings related to ~1.8 Ga sodium metasomatites developed in the Lower Paleoproterozoic granite-gneiss and iron formations of the Ingul Megablock of the Ukrainian Shield. Two deposits (the Zhovta Richka and Pervomayske) were mined out tens kilometers eastward in iron formations of the Kryvy Rig – Kremenchug mining district. Nametasomatite fields with scarce sub-economical U-mineralization were revealed by geophysical (magnetometry and gravimetry) and drilling programs northward in granitised gneisses around the younger Korsun-Novomyrgorod rapakivi pluton consisting of A2-type within plate granitoids which were emplaced during decompression melting at ~1.75 Ga. The present work aims to demonstrate structural and geochemical factors related to Na-metasomatism, and to mark out geochemical and tectonical parameters which were favorable for U-accumulation using data on deep seismic survey, geological structure analysis, and mineralogical and geochemical investigations of metasomatites. In the Ingul Megablock, Na-metasomatites occur along shear fault zones mostly oriented N-S. Metasomatites form complicate systems of plate- and lens-like bodies of aegirine-riebeckite albitites surrounded by dequartzified host rocks. Elemental alteration during Na-metasomatism demonstrates simple exchange of Si, K, Rb, Ba and Cs by Na, Ca, and locally V and U. δ 18 O H 2 O (300-400ºC) for albitizing hydrothermal solutions is near “zero”, typically for surficial water. These data suggest host rock interaction with hot marine waters. Persistent Na-metasomatic alterations extend along major tectonic faults for several kilometres with variable thicknesses reaching some hundreds meters in the zones of intense brecciation developed in the places of fault

  15. Los sistemas geotermales del Pirineo central. I. Caracteres geoquímicos y fisicoquímicos de los manantiales termales

    Directory of Open Access Journals (Sweden)

    Gómez, J.

    1996-08-01

    Full Text Available The compositional characters of selected hot springs from the Panticosa, Benasque, Arties, Caldas de Bohí, Luchon and Cauterets geothermal systems in the Central Pyrenees have been studied. All the springs have the same global geochemical features (high pH, low total dissolved solids, very low Mg concentrations, Na as the dominant cation, and absence of a dominant anion and belong to the same granite-related alkaline thermal waters group. Chemical composition of the springs is similar to each other, and to that found in other Pyrenean geothermal systems. A more detailed comparison shows, however, that Panticosa and Benasque systems have the lowest sodium and potassium concentrations found in any water belonging to the group of alkaline waters. Differences in pH values among the springs are related to emergence temperature as it occurs in the Pyrenean geothermal systems. According to the high pH of these waters, speciation calculations at emergence temperature show a very low CO2 partial pressure, dissolved silica partially ionized as H3Si04-, and Al(OH4- as the dominant aluminium species. Saturation indexes show that almost al1 the waters are highly oversaturated with quartz (close to equilibrium with chalcedony, potassium feldspar, and albite, which are the minerals equilibrated at depth with the solutions. Furthermore, all waters are in equilibrium with kaolinite and ca1cite at emergence conditions, showing the existence of a reequilibrium process during their ascent to the surface. This process happens to be one of the most important in the geochemical evo1ution of these alkaline systems.Las aguas de los sistemas geotermales de Panticosa, Benasque, Arties, Caldas de Bohí, Luchon y Cauterets en el Pirineo Central presentan rasgos geoquímicos similares (valores de pH elevados, bajo contenido de sólidos disueltos, muy bajas concentraciones de Mg, sodio como catión dominante y sin un anión en proporciones preponderantes sobre los dem

  16. The Thermal Expansion Of Feldspars

    Science.gov (United States)

    Hovis, G. L.; Medford, A.; Conlon, M.

    2009-12-01

    Hovis and others (1) investigated the thermal expansion of natural and synthetic AlSi3 feldspars and demonstrated that the coefficient of thermal expansion (α) decreases significantly, and linearly, with increasing room-temperature volume (VRT). In all such feldspars, therefore, chemical expansion limits thermal expansion. The scope of this work now has been broadened to include plagioclase and Ba-K feldspar crystalline solutions. X-ray powder diffraction data have been collected between room temperature and 925 °C on six plagioclase specimens ranging in composition from anorthite to oligoclase. When combined with thermal expansion data for albite (2,3,4) a steep linear trend of α as a function of VRT emerges, reflecting how small changes in composition dramatically affect expansion behavior. The thermal expansion data for five synthetic Ba-K feldspars ranging in composition from 20 to 100 mole percent celsian, combined with data for pure K-feldspar (3,4), show α-VRT relationships similar in nature to the plagioclase series, but with a slope and intercept different from the latter. Taken as a group all Al2Si2 feldspars, including anorthite and celsian from the present study along with Sr- (5) and Pb-feldspar (6) from other workers, show very limited thermal expansion that, unlike AlSi3 feldspars, has little dependence on the divalent-ion (or M-) site occupant. This apparently is due to the necessitated alternation of Al and Si in the tetrahedral sites of these minerals (7), which in turn locks the tetrahedral framework and makes the M-site occupant nearly irrelevant to expansion behavior. Indeed, in feldspar series with coupled chemical substitution it is the change away from a 1:1 Al:Si ratio that gives feldspars greater freedom to expand. Overall, the relationships among α, chemical composition, and room-temperature volume provide useful predictive tools for estimating feldspar thermal expansion and give insight into the controls of expansion behavior in

  17. The Itataia phosphate-uranium deposit (Ceará, Brazil) new petrographic, geochemistry and isotope studies

    Science.gov (United States)

    Veríssimo, César Ulisses Vieira; Santos, Roberto Ventura; Parente, Clóvis Vaz; Oliveira, Claudinei Gouveia de; Cavalcanti, José Adilson Dias; Nogueira Neto, José de Araújo

    2016-10-01

    The Itataia phosphate-uranium deposit is located in Santa Quitéria, in central Ceará State, northeastern Brazil. Mineralization has occurred in different stages and involves quartz leaching (episyenitization), brecciation and microcrystalline phase formation of concretionary apatite. The last constitutes the main mineral of Itatiaia uranium ore, namely collophane. Collophanite ore occurs in massive bodies, lenses, breccia zones, veins or episyenite in marble layers, calc-silicate rocks and gneisses of the Itataia Group. There are two accepted theories on the origin of the earliest mineralization phase of Itataia ore: syngenetic (primary) - where the ore is derived from a continental source and then deposited in marine and coastal environments; and epigenetic (secondary) - whereby the fluids are of magmatic, metamorphic and meteoric origin. The characterization of pre- or post-deformational mineralization is controversial, since the features of the ore are interpreted as deformation. This investigation conducted isotopic studies and chemical analyses of minerals in marbles and calc-silicate rocks of the Alcantil and Barrigas Formations (Itataia Group), as well as petrographic and structural studies. Analysis of the thin sections shows at least three phosphate mineral phases associated with uranium mineralizaton: (1) A prismatic fluorapatite phase associated with chess-board albite, arfvedsonite and ferro-eckermannite; (2) a second fluorapatite phase with fibrous radial or colloform habits that replaces calcium carbonate in marble, especially along fractures, with minerals such as quartz, chlorite and zeolite also identified in calc-silicate rocks; and (3) an younger phosphate phase of botryoidal apatite (fluorapatite and hydroxyapatite) related with clay minerals and probably others calcium and aluminum phosphates. Detailed isotopic analysis carried out perpendicularly to the mineralized levels and veins in the marble revealed significant variation in isotopic

  18. Mixing of fluids in hydrothermal ore-forming (Sn,W) systems: stable isotope and rare earth elements data

    Science.gov (United States)

    Sushchevskaya, T. M.; Popova, J. A.; Velivetskaya, T. A.; Ignatiev, A. V.; Matveeva, S. S.; Limantseva, O. A.

    2012-04-01

    Experimental and physico-chemical modeling data witness to important role of mixing of different type of fluids during tin and tungsten ore formation in hydrothermal systems. Mixing of magmatogeneous fluids, exsolved from granite melts, with exogenic, initially meteoric waters in hydrothermal ore-forming systems may change chemical composition of ore-forming fluid, causing cassiterite and/or wolframite precipitation (Heinrich, 1990; Sushchevskaya, Ryzhenko, 2002). We studied the process of genetically different fluids mixing for two economic Sn-W deposits, situated in the Iultin ore region (North-East of Russia, Chukotka Penninsula). The Iultin and Svetloe deposits are located in the apical parts of close situated leucogranite stocks, formed at the final stage of the Iultin complex emplacement. Both deposits are composed of a series of quartz veins among the flyschoid rocks (T 1-2), cut by the dikes (K1) of lamprophyre, granodiorite porphyre and alpite. The veins of the deposits are dominated by the productive quartz-wolframite-cassiterite-arsenopyrite-muscovite mineral assemblage. Topaz, beryl, fluorite, and albite occur sporadically. The later sulfide (loellingite-stannite-chalcopyrite) and quartz-fluorite-calcite assemblages show insignificant development. The preore quartz veinlets in host hornfels contain disseminated iron sulfides, chalcopyrite, muscovite. Isotopic (H, O, Ar) study of minerals, supplemented by oxygen isotope data of host granites and metamorphic rocks gave us possibility to conclude, that at the Iultin and the Svetloye deposits fluid mixing was fixed on the early stages of deposit formation and could be regarded as probable cause of metal (W, Sn) precipitation. During postore time the intensive involvement of isotopically light exogenic waters have changed: a) the initial character of oxygen isotope zonality; b) the initial hydrogen isotope composition of muscovites, up to meteoric calculated values for productive fluid (while the δ18O

  19. A geochemical and petrological study of the Late Cretaceous banatites from the Apuseni Mountains, Romania

    Science.gov (United States)

    Vander Auwera, Jacqueline; Berza, Tudor; Dupont, Alain; Gesels, Julie; Pin, Christian

    2014-05-01

    Banatites from western Romania belong to the more than 1000 km long and 30 to 70 km wide Late Cretaceous magmatic belt that spreads across southeastern Europe (Apuseni-Banat-Timok-Srednogorie). These banatites (Apuseni Mts. in the north and Banat in the south) occupy a particularly important area as they were emplaced across a major boundary between the Tisza and Dacia mega-units. Given their calc-alkaline signature and depletion in HFSE, they are interpreted as subduction related. Mineralogical, geochemical and isotopic (Sr, Nd) data were acquired on a series of samples from a selection of intrusions of the Apuseni Mountains in order to model their possible differentiation processes and to compare them with published results on banatites from Banat and Serbia (Timok and Ridanj-Krepolijn). Samples from the Apuseni Mts. display high-K calc-alkaline differentiation trends of decreasing FeOt, MgO, CaO, P2O5, TiO2, Sr, Zn, Co, V and increasing Rb and Th with increasing SiO2 (54.4 wt. % to 72 wt. %). Mixing is a plausible differentiation process as mingling relationships have been observed between microdiorites and granodiorites in Pietroasa but is not supported by geochemical data. These are better predicted by fractional crystallization but phenocrysts unmixing cannot be precluded. The fractional crystallization process has been modelled in three steps using the least square regression method : a gabbronoritic cumulate is subtracted in the first step whereas apatite-bearing dioritic cumulates are subtracted in the two later steps with a more albitic plagioclase in the third cumulate. The trace elements composition of the samples support the proposed model. The composition of the least differentiated samples collected in the Apuseni Mts. preclude them as being primary magmas in equilibrium with a mantle source. We however suggest that these least differentiated compositions were derived by limited differentiation of a mantle-derived magma that either was trapped in the

  20. Experimental determination of liquidus H2O contents of haplogranite at deep-crustal conditions

    Science.gov (United States)

    Makhluf, A. R.; Newton, R. C.; Manning, C. E.

    2017-09-01

    The liquidus water content of a haplogranite melt at high pressure ( P) and temperature ( T) is important, because it is a key parameter for constraining the volume of granite that could be produced by melting of the deep crust. Previous estimates based on melting experiments at low P (≤0.5 GPa) show substantial scatter when extrapolated to deep crustal P and T (700-1000 °C, 0.6-1.5 GPa). To improve the high-P constraints on H2O concentration at the granite liquidus, we performed experiments in a piston-cylinder apparatus at 1.0 GPa using a range of haplogranite compositions in the albite (Ab: NaAlSi3O8)—orthoclase (Or: KAlSi3O8)—quartz (Qz: SiO2)—H2O system. We used equal weight fractions of the feldspar components and varied the Qz between 20 and 30 wt%. In each experiment, synthetic granitic composition glass + H2O was homogenized well above the liquidus T, and T was lowered by increments until quartz and alkali feldspar crystalized from the liquid. To establish reversed equilibrium, we crystallized the homogenized melt at the lower T and then raised T until we found that the crystalline phases were completely resorbed into the liquid. The reversed liquidus minimum temperatures at 3.0, 4.1, 5.8, 8.0, and 12.0 wt% H2O are 935-985, 875-900, 775-800, 725-775, and 650-675 °C, respectively. Quenched charges were analyzed by petrographic microscope, scanning electron microscope (SEM), X-ray diffraction (XRD), and electron microprobe analysis (EMPA). The equation for the reversed haplogranite liquidus minimum curve for Ab36.25Or36.25Qz27.5 (wt% basis) at 1.0 GPa is T = - 0.0995 w_{{{H}_{ 2} {O}}}^{ 3} + 5.0242w_{{{H}_{ 2} {O}}}^{ 2} - 88.183 w_{{{H}_{ 2} {O}}} + 1171.0 for 0 ≤ w_{{{H}_{ 2} {O}}} ≤ 17 wt% and T is in °C. We present a revised P - T diagram of liquidus minimum H2O isopleths which integrates data from previous determinations of vapor-saturated melting and the lower pressure vapor-undersaturated melting studies conducted by other workers on

  1. Mineralogical controls on surface colonization by sulfur-metabolizing microbial communities

    Science.gov (United States)

    Jones, A. A.; Bennett, P.

    2012-12-01

    When characterizing microbial diversity and the microbial ecosystem of the shallow subsurface the mineral matrix is generally assumed to be homogenous and unreactive. We report here experimental evidence that microorganisms colonize rock surfaces according to the rock's chemistry and the organism's metabolic requirements and tolerances. We investigated this phenomenon using laboratory biofilm reactors with both a pure culture of sulfur-oxidizing Thiothrix unzii and a mixed environmental sulfur-metabolizing community from Lower Kane, Cave, WY, USA. Reactors contained rock and mineral chips (calcite, albite, microcline, quartz, chert, Madison Limestone (ML), Madison Dolostone (MD), and basalt) amended with one of the two inoculants. Biomass of attached microorganisms on each mineral surface was quantified. The 16S rRNA of attached microbial communities were compared using Roche FLX and Titanium 454 next generation pyrosequencing. A primary controlling factor on taxonomy of attached microorganisms in both pure and mixed culture experiments was mineral buffering capacity. In mixed culture experiments acid-buffering carbonates were preferentially colonized by neutrophilic sulfur-oxidizing microorganisms (~18% to ~27% of microorganisms), while acidophilic sulfur-oxidizing microorganisms colonized non-buffering quartz exclusively (~46% of microorganisms). The nutrient content of the rock was a controlling factor on biomass accumulation, with neutrophilic organisms selecting between carbonate surfaces of equivalent buffer capacities according to the availability of phosphate. Dry biomass on ML was 17.8 ± 2.3 mg/cm2 and MD was 20.6 ± 6.8 mg/cm2; while nutrient poor calcite accumulated 2.4 ± 0.3 mg/cm2. Biomass accumulation was minimal on non-buffering nutrient-limited surfaces. These factors are countered by the competitive exclusion of some populations. A pure culture of T. unzii preferentially colonizes carbonates while a very closely related Thiothrix spp is excluded

  2. Ar and K partitioning between clinopyroxene and silicate melt to 8 GPa

    Science.gov (United States)

    Chamorro, E. M.; Brooker, R. A.; Wartho, J.-A.; Wood, B. J.; Kelley, S. P.; Blundy, J. D.

    2002-02-01

    The relative incompatibility of Ar and K are fundamental parameters in understanding the degassing history of the mantle. Clinopyroxene is the main host for K in most of the upper mantle, playing an important role in controlling the K/Ar ratio of residual mantle and the subsequent time-integrated evolution of 40Ar/36Ar ratios. Clinopyroxene also contributes to the bulk Ar partition coefficient that controls the Ar degassing rate during mantle melting. The partitioning of Ar and K between clinopyroxene and quenched silicate melt has been experimentally determined from 1 to 8 GPa for the bulk compositions Ab80Di20 (80 mol% albite-20 mol% diopside) and Ab20Di80 with an ultraviolet laser ablation microprobe (UVLAMP) technique for Ar analysis and the ion microprobe for K. Data for Kr (UVLAMP) and Rb (ion probe) have also been determined to evaluate the role of crystal lattice sites in controlling partitioning. By excluding crystal analyses that show evidence of glass contamination, we find relatively constant Ar partition coefficients (DAr) of 2.6 × 10-4 to 3.9 × 10-4 for the Ab80Di20 system at pressures from 2 to 8 GPa. In the Ab20Di80 system, DAr shows similar low values of 7.0 × 10-5 and 3.0 × 10-4 at 1 to 3 GPa. All these values are several orders of magnitude lower than previous measurements on separated crystal-glass pairs. DK is 10 to 50 times greater than DRb for all experiments, and both elements follow parallel trends with increasing pressure, although these trends are significantly different in each system studied. The DK values for clinopyroxene are at least an order of magnitude greater than DAr under all conditions investigated here, but DAr appears to show more consistent behavior between the two systems than K or Rb. The partitioning behavior of K and Rb can be explained in terms of combined pressure, temperature, and crystal chemistry effects that result in changes for the size of the clinopyroxene M2 site. In the Ab20Di80 system, where

  3. Hydrothermal modification of host rock geochemistry within Mo-Cu porphyry deposits in the Galway Granite, western Ireland

    Science.gov (United States)

    Tolometti, Gavin; McCarthy, Will

    2016-04-01

    Hydrothermal alteration of host rock is a process inherent to the formation of porphyry deposits and the required geochemical modification of these rocks is regularly used to indicate proximity to an economic target. The study involves examining the changes in major, minor and trace elements to understand how the quartz vein structures have influenced the chemistry within the Murvey Granite that forms part of the 380-425Ma Galway Granite Complex in western Ireland. Molybdenite mineralisation within the Galway Granite Complex occurred in close association with protracted magmatism at 423Ma, 410Ma, 407Ma, 397Ma and 383Ma and this continues to be of interest to active exploration. The aim of the project is to characterize hydrothermal alteration associated with Mo-Cu mineralisation and identify geochemical indicators that can guide future exploration work. The Murvey Granite intrudes metagabbros and gneiss that form part of the Connemara Metamorphic complex. The intrusion is composed of albite-rich pink granite, garnetiferous granite and phenocrytic orthoclase granite. Minor doleritic dykes post-date the Murvey Granite, found commonly along its margins. Field mapping shows that the granite is truncated to the east by a regional NW-SE fault and that several small subparallel structures host Mo-Cu bearing quartz veins. Petrographic observations show heavily sericitized feldspars and plagioclase and biotite which have undergone kaolinization and chloritisation. Chalcopyrite minerals are fine grained, heavily fractured found crystallized along the margins of the feldspars and 2mm pyrite crystals. Molybdenite are also seen along the margins of the feldspars, crystallized whilst the Murvey Granite cooled. Field and petrographic observations indicate that mineralisation is structurally controlled by NW-SE faults from the selected mineralization zones and conjugate NE-SW cross cutting the Murvey Granite. Both fault orientations exhibit quartz and disseminated molybdenite

  4. Ilyukhinite (H3O,Na)14Ca6Mn2Zr3Si26O72(OH)2 • 3H2O, a New Mineral of the Eudialyte Group

    Science.gov (United States)

    Chukanov, N. V.; Rastsvetaeva, R. K.; Rozenberg, K. A.; Aksenov, S. M.; Pekov, I. V.; Belakovsky, D. I.; Kristiansen, R.; Van, K. V.

    2017-12-01

    A new eudialyte-group mineral, ilyukhinite, ideally (H3O,Na)14Ca6Mn2Zr3Si26O72(OH)2 · 3H2O, has been found in peralkaline pegmatite at Mt. Kukisvumchorr, Khibiny alkaline pluton, Kola Peninsula, Russia. It occurs as brownish orange, with vitreous luster anhedral grains up to 1 mm across in hydrothermally altered peralkaline rock, in association with aegirine, murmanite, albite, microcline, rhabdophane-(Ce), fluorite, sphalerite and molybdenite. The Mohs hardness is 5; cleavage is not observed. D meas 2.67(2), D calc 2.703 g/cm3. Ilyukhinite is optically uniaxial (-): ω = 1.585(2), ɛ = 1.584(2). The IR spectrum is given. The average chemical composition of ilyukhinite (wt %; electron microprobe, ranges given in parentheses; H2O determined by gas chromatography) is as follows: 3.07 (3.63-4.43) Na2O, 0.32 (0.28-0.52) K2O, 10.63 (10.26-10.90) CaO, 3.06 (2.74-3.22) MnO, 1.15 (0.93-1.37) FeO, 0.79 (0.51-0.89) La2O3, 1.21 (0.97-1.44) Ce2O3, 0.41 (0.30-0.56) Nd2O3, 0.90 (0.77-1.12) TiO2, 10.94 (10.15-11.21) ZrO2, 1.40 (0.76-1.68) Nb2O5, 51.24 (49.98-52.28) SiO2, 1.14 (0.89-1.37) SO3, 0.27 (0.19—0.38) Cl, 10.9(5 )H2O,-0.06-O = C1, total is 98.27. The empirical formula is H36.04(Na3.82K0.20)(Ca5.65Ce0.22La0.14Nd0.07)(Mn1.285Fe0.48)(Zr2.645Ti0.34)Nb0.31Si25.41S0.42Cl0.23O86.82. The crystal structure has been solved ( R = 0.046). Ilyukhinite is trigonal, R3 m; a = 14.1695(6) Å, b = 31.026(1) Å, V = 5394.7(7) Å3, Z = 3. The strongest XRD reflections [ d, Å (I, %) ( hkl)] are 11.44 (82) (101), 7.09 (70) (110), 6.02 (44) (021), 4.371 (89) 205), 3.805 (47) (303, 033), 3.376 (41) (131), 2.985 (100) (315, 128), 2.852 (92) (404). Ilyukhinite was named in memory of Vladimir V. Ilyukhin (1934-1982), an outstanding Soviet crystallographer. The type specimen of ilyukhinite has been deposited in the collection of the Natural History Museum, University of Oslo, Norway.

  5. Los sistemas geotermales del Pirineo Central. II. Resultados de la aplicación de técnicas geotermométricas

    Directory of Open Access Journals (Sweden)

    Gimeno, M. J.

    1997-04-01

    Full Text Available Reservoir temperatures are calculated for six geothermal systems in the Central Pyrenees (Arties, Caldas de Bohí, Benasque, Panticosa, Luchon and Cauterets using different geothermometrical methods. In general, the selected hot springs have similar geochemical features belonging to the group of alkaline thermal systems installed in granitic environments. More in detail, however, it is important to note that Na and K concentrations of Panticosa and Benasque thermal springs are the lowest found in this water group to date. Both classical geothermometers and modeling calculations agree within a few degrees for the Arties, Caldas and Luchon geothermal systems: thermal waters are in equilibrium in their reservoirs with a common mineral association (quartz, albite, K-feldspar, caolinite and some calc-aluminum silicate at 103, 107 and 127° C, respectively. Cauterets, Panticosa and Benasque thermal waters appear to be equilibrated with the same mineral association at 98, 107 and 94° C, respectively as deduced from silica and Na-K geothermometers. Na-K-Ca and Ca-K geothermometers provide lower temperatures for these systems, probably because of some exchange of calcium between rock and water during the ascent of solutions. Nevertheless, the modeling calculations fail to represent the composition of Panticosa and Benasque thermal springs: these waters are out of equilibrium with the selected mineral association at the temperatures given by Na-K and SiO2-quartz geothermometers Therefore, the agreement between these geothermometers appear to be fortuitous, specially for Benasque thermal waters.Mediante la utilización de distintas técnicas geotermométricas se han estimado las temperaturas en el reservorio de seis sistemas geotermales (Arties, Caldas de Bohí, Benasque, Panticosa, Luchon y Cauterets instalados en los materiales graníticos del Pirineo Central. Los manantiales seleccionados para realizar los cálculos muestran similares caracteres

  6. Spatial and temporal zoning of hydrothermal alteration and mineralization in the Sossego iron oxide-copper-gold deposit, Carajás Mineral Province, Brazil: Paragenesis and stable isotope constraints

    Science.gov (United States)

    Monteiro, Lena V.S.; Xavier, R.P.; Carvalho, E.R.; Hitzman, M.W.; Johnson, C.A.; Souza, Filho C.R.; Torresi, I.

    2008-01-01

    The Sossego iron oxide–copper–gold deposit (245 Mt @ 1.1% Cu, 0.28 g/t Au) in the Carajás Mineral Province of Brazil consists of two major groups of orebodies (Pista–Sequeirinho–Baiano and Sossego–Curral) with distinct alteration assemblages that are separated from each other by a major high angle fault. The deposit is located along a regional WNW–ESE-striking shear zone that defines the contact between metavolcano–sedimentary units of the ∼2.76 Ga Itacaiúnas Supergroup and tonalitic to trondhjemitic gneisses and migmatites of the ∼2.8 Ga Xingu Complex. The deposit is hosted by granite, granophyric granite, gabbro, and felsic metavolcanic rocks. The Pista–Sequeirinho–Baiano orebodies have undergone regional sodic (albite–hematite) alteration and later sodic–calcic (actinolite-rich) alteration associated with the formation of massive magnetite–(apatite) bodies. Both these alteration assemblages display ductile to ductile–brittle fabrics. They are cut by spatially restricted zones of potassic (biotite and potassium feldspar) alteration that grades outward to chlorite-rich assemblages. The Sossego–Curral orebodies contain weakly developed early albitic alteration and very poorly developed subsequent calcic–sodic alteration. These orebodies contain well-developed potassic alteration assemblages that were formed during brittle deformation that resulted in the formation of breccia bodies. Breccia matrix commonly displays coarse mineral infill suggestive of growth into open space. Sulfides in both groups of deposits were precipitated first with potassic alteration and more importantly with a later assemblage of calcite–quartz–epidote–chlorite. In the Sequeirinho orebodies, sulfides range from undeformed to deformed; sulfides in the Sossego–Curral orebodies are undeformed. Very late, weakly mineralized hydrolytic alteration is present in the Sossego/Currral orebodies. The sulfide assemblage is dominated by chalcopyrite with

  7. Petrogenetic and geodynamic origin of the Neoarchean Doré Lake Complex, Abitibi subprovince, Superior Province, Canada

    Science.gov (United States)

    Polat, Ali; Frei, Robert; Longstaffe, Fred J.; Woods, Ryan

    2018-04-01

    The Neoarchean (ca. 2728 Ma) anorthosite-bearing Doré Lake Complex in the northeastern Abitibi subprovince, Quebec, was emplaced into an association of intra-oceanic tholeiitic basalts and gabbros known as the Obatogamau Formation. The Obatogamau Formation constitutes the lower part of the Roy Group, which is composed of two cycles of tholeiitic-to-calc-alkaline volcanic and volcaniclastic rocks, siliciclastic and chemical sedimentary rocks, and layered mafic-to-ultramafic sills. In this study, we report major and trace element results, and Nd, Sr, Pb and O isotope data for anorthosites, leucogabbros, gabbros and mafic dykes from the Doré Lake Complex and spatially associated basalts and gabbros of the Obatogamau Formation to assess their petrogenetic origin and geodynamic setting. Field and petrographic observations indicate that the Doré Lake Complex and associated volcanic rocks underwent extensive metamorphic alteration under greenschist facies conditions, resulting in widespread epidotization (20-40%) and chloritization (10-40%) of many rock types. Plagioclase recrystallized mainly to anorthite and albite endmembers, erasing intermediate compositions. Metamorphic alteration also led to the mobilization of many elements (e.g., LILE and transition metals) and to significant disturbance of the Rb-Sr and U-Pb isotope systems, resulting in 1935 ± 150 and 3326 ± 270 Ma errorchron ages, respectively. The Sm-Nd isotope system was less disturbed, yielding an errorchron age of 2624 ± 160 Ma. On many binary major and trace element diagrams, the least altered anorthosites and leucogabbros, and the gabbros and mafic dykes of the Doré Lake Complex plot in separate fields, signifying the presence of two distinct magma types in the complex. The gabbros and mafic dykes in the Doré Lake Complex share the geochemical characteristics of tholeiitic basalts and gabbros in the Obatogamau Formation, suggesting a possible genetic link between the two rock associations. Initial

  8. Is there a geochemical link between volcanic and plutonic rocks in the Organ Mountains caldera?

    Science.gov (United States)

    Memeti, V.; Davidson, J.

    2013-12-01

    determine within-crystal geochemical variations. Our current conclusions and working hypotheses are: 1) All igneous rocks from the Organ Mountains are crustal-mantle melt mixtures indicating two component mixing; 2) the caldera-forming ignimbrites are likely derived from a fractionating Organ Needle pluton; 3) pre- and post-caldera lavas are isotopically similar to the post-caldera Sugarloaf Peak quartz-monzonite; 4) K-feldspar cumulate textures in the structurally top 0.5-1 km of the Organ Needle pluton indicate that interstitial melt was lost from the magma mush, which likely fed the ignimbrite eruptions. 5) Plutonic feldspar textures are complex compared to rather simple zoned volcanic feldspars including K-feldspar rimmed plagioclase, plagioclase rimmed K-feldspar and unrimmed feldspars occurring over a range of grain sizes at thin section scale. Some volcanic feldspar phenocrysts have any previous zonation erased due to late stage albitization. Although the single mineral studies are still work in progress and details need resolving, our data so far suggest a geochemical link between volcanic and plutonic rocks of the Organ Mountains caldera, albeit a complex one; and greater complexity in plutonic versus volcanic minerals. [1] Seager (1980), NM Bureau of Mines and Min. Res. Memoir 36, 97 p. [2] Zimmerer & McIntosh (2013) Journal of Geophysical Research, v. 93, p. 4421-4433

  9. Red-staining of the wall rock and its influence on the reducing capacity around water conducting fractures

    International Nuclear Information System (INIS)

    Drake, Henrik; Tullborg, Eva-Lena; Annersten, Hans

    2008-01-01

    Red-staining and alteration of wall rock is common around water conducting fractures in the Laxemar-Simpevarp area (SE Sweden), which is currently being investigated by the Swedish Nuclear Fuel and Waste Management Co. (SKB) in common with many other places. Red-staining is often interpreted as a clear sign of oxidation but relevant analyses are seldom performed. The area is dominated by Palaeoproterozoic crystalline rocks ranging in composition from quartz monzodiorite to granite. In this study wall rock samples have been compared with reference samples from within 0.1 to 1 m of the red-stained rock, in order to describe mineralogical and geochemical changes but also changes in redox conditions. A methodology for tracing changes in mineralogy, mineral and whole rock chemistry and Fe 3+ /Fe tot ratio in silicates and oxides in the red-stained wall rock and the reference rock is reported. The results show that the red-stained rock adjacent to the fractures displays major changes in mineralogy; biotite, plagioclase and magnetite have been altered and chlorite, K-feldspar, albite, sericite, prehnite, epidote and hematite have been formed. The changes in chemistry are however moderate; K-enrichment, Ca-depletion and constant Fe tot are documented. The Fe 3+ /Fe tot ratio in the oxide phase is higher in the red-stained samples whereas the Fe 3+ /Fe tot ratio in the silicate phase is largely similar in the wall rock and the reference samples. Because most of the Fe is hosted in the silicate phase the decrease in reducing capacity (Fe 2+ ), if any, in the red-stained wall rock is very small and not as high as macroscopic observations might suggest. Instead, the mineralogical changes in combination with the modest oxidation and formation of minute hematite grains in porous secondary minerals in pseudomorphs after plagioclase have produced the red-staining. Increased porosity is also characteristic for the red-stained rock. Moderate alteration in the macroscopically fresh

  10. Predictive modeling of CO2 sequestration in deep saline sandstone reservoirs: Impacts of geochemical kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Balashov, Victor N.; Guthrie, George D.; Hakala, J. Alexandra; Lopano, Christina L.; Rimstidt, J. Donald; Brantley, Susan L.

    2013-03-01

    maximum CO{sub 2} sequestration, 34.5 kg CO{sub 2} per m{sup 3} of sandstone, is attained by 4000 years even though the system does not achieve chemical equilibrium until ~25,000 years. This maximum represents about 20% CO{sub 2} dissolved as CO{sub 2},aq, 50% dissolved as HCO{sub 3}{sup -}{sub ,aq}, and 30% precipitated as calcite. The extent of sequestration as HCO{sub 3}{sup -} at equilibrium can be calculated from equilibrium thermodynamics and is roughly equivalent to the amount of Na+ in the initial sandstone in a soluble mineral (here, oligoclase). Similarly, the extent of trapping in calcite is determined by the amount of Ca2+ in the initial oligoclase and smectite. Sensitivity analyses show that the rate of CO{sub 2} sequestration is sensitive to the mineral-water reaction kinetic constants between approximately 10 and 4000 years. The sensitivity of CO{sub 2} sequestration to the rate constants decreases in magnitude respectively from oligoclase to albite to smectite.

  11. Mianningite, (□,Pb,Ce,Na) (U"4"+,Mn,U"6"+) Fe"3"+_2(Ti,Fe"3"+)_1_8O_3_8, a new member of the crichtonite group from Maoniuping REE deposit, Mianning county, southwest Sichuan, China

    International Nuclear Information System (INIS)

    Ge, Xiangkun; Fan, Guang; Chen, Zhangru; Ai, Yujie; Li, Guowu

    2017-01-01

    Mianningite (IMA 2014-072), ideally (□,Pb,Ce,Na)(U"4"+,Mn,U"6"+) Fe"3"+_2(Ti,Fe"3"+)_1_8O_3_8, is a new member of the crichtonite group from the Maoniuping REE deposit, Mianning county, Sichuan province, China. It was found in fractures of lamprophyre veins and in the contact between lamprophyre and a later quartz-alkali feldspar syenite dyke with REE mineralization, and is named after its type locality. Associated minerals are microcline, albite, quartz, iron-rich phlogopite, augite, muscovite, calcite, baryte, fluorite, epidote, pyrite, magnetite, hematite, galena, hydroxylapatite, titanite, ilmenite, rutile, garnet-group minerals, zircon, allanite-(Ce), monazite-(Ce), bastnaesite-(Ce), parisite-(Ce), maoniupingite-(Ce), thorite, pyrochlore-group minerals and chlorite. Mianningite occurs as opaque subhedral to euhedral tabular crystals, up to 1-2 mm in size, black in color and streak, and with a submetallic luster. Mianningite is brittle, with a conchoidal fracture. Its average micro-indentation hardness is 83.8 kg/mm"2 (load 0.2 kg), which is equivalent to ∝6 on the Mohs hardness scale. Its measured and calculated densities are 4.62 (8) g/cm"3 and 4.77 g/cm"3, respectively. Under reflected light, mianningite is grayish white, with no internal reflections. It appears isotropic and exhibits neither bireflectance nor pleochroism. The empirical formula, calculated on the basis of 38 O atoms per formula unit (apfu), is [□_0_._3_2_2(Pb_0_._2_1_5Ba_0_._0_3_7Sr_0_._0_3_6Ca_0_._0_1_0)_Σ_0_._2_9_8(Ce_0_._1_2_8La_0_._0_7_7Nd_0_._0_1_2)_Σ_0_._2_1_7 (Na_0_._1_2_7K_0_._0_3_6)_Σ_0_._1_6_3]_Σ_0_1_._0_0_0(U"4"+_0_._4_4_7Mn_0_0_._2_9_3U"6 "+_0_._1_1_2Y_0_._0_9_1Zr_0_._0_2_3Th_0_._0_1_1)_Σ_0_._9_7_7(Fe"3"+_1_._2_2_4Fe"2"+_0_._2_4_3Mg_0_._0_2_3P_0_._0_0_8Si_0_._0_0_6 □_0_._4_9_6)_Σ_2_._0_0_0(Ti_1_2_._4_6_4Fe"3"+_5_._2_9_2V"5"+_0_._1_1_8Nb_0_._0_8_3Al_0_._0_2_6Cr"3"+_0_._0_1_7)_Σ_1_8_._0_0_0O_3_8. Mianningite is trigonal, belongs to the space group R anti 3, and has

  12. Geology of the Stroudsburg quadrangle and Adjacent areas, Pennsylvania--New Jersey

    Science.gov (United States)

    Epstein, Jack Burton

    1971-01-01

    structures, including the prominent regional cleavage, were produced during the late Paleozoic Appalachian orogeny and are superimposed upon larger Taconic folds and faults. Field relations and microscopic study suggest that the regional cleavage in the Stroudsburg area is due to laminar flow of pelitic material along cleavage folia accompanied by mechanical reorientation of platy and elongate minerals and neocrystallization of mica, quartz, chlorite, and probably albite. Numerous lines of evidence point to the conclusion that cleavage developed after the rock was indurated and formed at, and Just below, conditions of low-grade metamorphism. Intensity of cleavage development increases to the southeast across the area. Second-generation slip cleavage, also believed to be Appalachian in age, formed by mechanical reorientation of minerals as well as by limited new mineral growth. The topography had a profound effect on the direction of movement of the Wisconsin glacier, as well as the manner of its retreat and the deposits that were formed. Till and stratified drift of Wisconsin age and till of Illinoian(?) age are common in the area. Wisconsin deglaciation occurred by northeastward retreat and by stagnation. A conspicuous terminal moraine marks the limit of Wisconsin ice movement. Lake Sciota was dammed between the retreating ice, the moraine, and the surrounding ridges north of Godfrey Ridge. Several deltas mark ice stand positions during the retreat of the ice. Lake-bottom and kame deposits are locally common in Cherry Valley. South of Kittatinny Mountain, on the other hand, melt water was freely discharged to the south. The wind and water gaps in the Stroudsburg area (including Delaware Water Gap and Wind Gap) are structurally controlled; specifically they are located where folds die out in short distances, where folding is locally more intense, or where resistant rocks dip steeply and have a narrow width of outcrop. This conclusion is contrary to

  13. Regional paleohydrologic and paleoclimatic settings of wetland/lacustrine depositional systems in the Morrison Formation (Upper Jurassic), Western Interior, USA

    Science.gov (United States)

    Dunagan, S.P.; Turner, C.E.

    2004-01-01

    and shoreline deposits. Marginal lacustrine deposits include ooid and skeletal packstone-grainstone, siltstone, and sandstone. Distal lacustrine units are skeletal mudstone-wackestone, microbialites, and laminated (siliciclastic) mudstone. Differentiation between wetlands and distal lacustrine units is not always possible. Palustrine features, Magadi-type chert (MTC), and evaporites record episodes of increased aridity and exposure. Farther upstream, during deposition of the upper part of the Brushy Basin Member, the ancestral Uncompahgre Uplift imposed a barrier to shallow, eastward-flowing groundwater that discharged into the San Juan/Paradox Basin on the upstream side of the uplift. This created the closed hydrologic setting necessary for development of an alkaline-saline wetland/lacustrine complex ("Lake" T'oo'dichi'). Silicic volcanic ash, delivered by prevailing winds from calderas west and southwest of the basin, contributed to the pore-water evolution in the sediments. A distinctive lateral hydrogeochemical gradient, reflecting increasing salinity and alkalinity in the pore waters, altered the ash to a variety of authigenic minerals that define concentric zones within the basin. The basinward progression of diagenetic mineral zones is smectite???clinoptilolite???analcime ??potassium feldspar???albite. The groundwater-fed wetlands were shallow and frequently evaporated to dryness. Scarce laminated gray mudstone beds record distinct episodes of freshwater lacustrine deposition that resulted from intermittent streams that carried detritus well out into the basin. ?? 2004 Elsevier B.V. All rights reserved.

  14. Microtectonic-assisted P-T determination on low-grade Alpine metamorphic rocks from the "Tisia Mega-Unit" of the Slavonian Mountains in Croatia

    Science.gov (United States)

    Balen, Dražen; Lihter, Iva; Massonne, Hans-Joachim

    2016-04-01

    The internal structure of the Tisia (Tisza) Mega-Unit in the Alpine-Carpathian-Dinaridic orogenic system encompasses large Alpine nappe systems brought to its present-day position by complex regional-scale movements. The Slavonian Mountains are part of the Bihor nappe system which is below the Codru and above the Mecsek nappe systems. The low-grade metamorphic schist unit of the Slavonian Mountains includes numerous rocks which were previously related to Precambrian and/or Lower Paleozoic orogeneses. However, recent studies (e.g. Balen, 2014, European Geosciences Union General Assembly, EGU 2014-6122) show that the metapelites of this unit should be attributed to the Alpine orogeny and the poorly known P-T conditions, which they experienced, should be refined. Although metapelites can be sensitive to changes of metamorphic conditions and, therefore, be suitable for the P-T estimation of metamorphic event(s), the extraction of mineral assemblages, being in equilibrium, and associated microtectonic data for particular low-grade metamorphic rocks is not straightforward. On the contrary, due to lack of suitable minerals and complex mictotectonic features, one can be faced with a severe problem concerning (dis)equilibrium. To avoid this, the observation scale in the research was set to the sub-mm level taking into account microtectonic positions of minerals. The investigated samples from the Slavonian Mountains are fine-grained schists consisting of chlorite (15-30 vol. %), white mica (15-25 vol. %), quartz (10-25 vol. %), feldspars (albite 10-15 vol. %; some K-feldspar), biotite (<5 vol. %), opaques (<5 vol. %), and accessory minerals (zircon, monazite, xenotime, apatite, chalcopyrite, pyrite, barite, parisite-(Ce), rutile). The schists show complex microtectonic fabric including well-developed foliations, pervasive folding, crenulation and cleavage. Foliations are defined by the preferred orientation of phyllosilicates and thin quartz and feldspar ribbons. Chlorite

  15. Phase relations in the hydrous CMAS pyrolite in presence of KCl at 2 GPa

    Science.gov (United States)

    Safonov, O.

    2012-04-01

    In the upper mantle, chlorides are constituents of concentrated aqueous solutions (brines), as well as chloride-carbonate and carbonatite melts. Mineral assemblages coming from diverse depth levels show that mobile (K, Na)Cl-bearing fluids are able to provoke intensive metasomatism of the peridotitic mantle accompanied by melting. Scarce experimental studies on influence of brines on mineral equilibria in the peridotitic mantle (Stalder et al., 2008; Chu et al., 2011) indicate that influence of chlorides on water activity in a fluid equilibrated with forsterite enstatite at pressures above 2 GPa is very similar to their effect at lower "crustal" pressures (e.g. Aranovich, Newton, 1997): decrease of the H2O activity with an increase of the salt content results in an increase of the melting temperature of silicates. Nevertheless, these experiments were performed in the Al-free systems. Presence of Al would provoke an active interaction of alkali chlorides, namely KCl, with silicates with formation of new K-Al-bearing phases, such as phlogopite (in presence of H2O), which would influence on the melting of complex assemblages. In order to investigate an effect of KCl on phase relations in the Al2O3, CaO, Na2O-rich hydrous peridotite and on stability of garnet, pyroxenes, and amphiboles, in particular, experiments on interaction of the model CMAS pyrolite Fo57En17Prp14Di12 (+0.3 wt. % of Na2O) with the H2O-KCl fluid were performed at 2 GPa in the temperature interval 900-1200. Mixtures of synthetic forsterite, diopside, enstatite and pyrope in the above weight ratio were mixed with 14 wt. % of Mg(OH)2 corresponding to 4.4 wt. % of H2O in the system. 2.4, 3.7, 5 and 10 wt. % of KCl were added to silicate-H2O mixture. Experiments were performed using a piston-cylinder apparatus with ½-inch talc high-pressure cells calibrated via brucite = periclase + H2O and albite = jadeite + quartz equilibria curves. Temperature was controlled with accuracy ?1 with the W95Re5/W80Re20

  16. Au-bearing magnetite mineralizaion in Kashmar (alteration, mineralization, geochemistry, geochemistry and fluid inclusions;

    Directory of Open Access Journals (Sweden)

    Alireza Almasi

    2017-02-01

    amounts of sulfide minerals in Kashmar, all represent the oxidized conditions of hydrothermal fluid and the impact of CO2-bearing chloride complex in transport, non-interference of meteoric waters and precipitation of metallic elements with reducing of temperature. Discussion Most important IOCG deposits of south America (Candelaria, Mantoverde and Raul Condstable have Au-bearing massive magnetite bodies accompanied with Potassium (actinolite, biotite and K-feldspar alterations with high temperatures (500-700 O C and salinities (>40%wt NaCl at deepest parts (Sillitoe, 2003. At the upper levels, there are magnetite changes to hematite (Specular and the possibility of coarse calcite (± silver mineralisation. Hematite zone may display hydrothermal/tectonic brecciation. The hematite-rich veins tend to contain sericite and/or chlorite, with or without K-feldspar or albite, and to possess alteration haloes characterized by these same minerals. Both the magnetite- and specular hematite-rich IOCG veins contain chalcopyrite and generally subordinate Pyrite (Fuller et al., 1965. References Almasi, A., Karimpour, M.H., Ebrahimi Nasrabadi, Kh., Rahimi, B. and KlÖtzli, U, 2016. Geology and geochemistry of sub-volcanic and plutonic bodies of Kashmar (North of Lut Block. Iranian Journal of Crystallography and Mineralogy, 24 (3: 539-556. (in Persian Fuller, R.C., Corvala´n, J., Klohn, C., Klohn, E. and Levi, B., 1965. Geologı´a y yacimientos metalı´feros de Chile. Instituto de Investigaciones Geolo´ gicas, Santiago, 305 pp. Sillitoe, R.H., 2003. Iron oxide-copper-gold deposits: An Andean view. Mineralium Deposita, 38(7: 787–812.

  17. Gulf of Mexico miocene CO₂ site characterization mega transect

    Energy Technology Data Exchange (ETDEWEB)

    Meckel, Timothy [Univ. of Austin, Austin, TX (United Staes); Trevino, Ramon [Univ. of Austin, Austin, TX (United Staes)

    2014-12-01

    m) of data allowed for the identification and mapping of unconformable surfaces including what is probably a surface associated with the last Pleistocene glacial lowstand. The identification of a previously unrecognized (in commercial seismic data) gas chimney that was clearly defined in the 2013 HR3D survey, indicates that HR3D surveys may be useful as both a characterization tool for the overburden of a potential carbon sequestration site and as an additional monitoring tool for future engineered injection sites. Geochemical modeling indicated that injection of CO₂ would result in minor dissolution of calcite, K-feldspar and albite. In addition, modeling of typical brines in Miocene age rocks indicate that approximately 5% of injection capacity would result from CO₂ dissolution into the brine. After extensive searches, no rock samples of the Marginulina A and Amphistegina B seals (“caprocks”) were obtained, but analyses of available core samples of other Miocene age mudrocks (seals or caprocks) indicate that they have sealing ability sufficient for potential CO2 storage in underlying sandstone units.

  18. Thermal expansion behavior of fluor-chlorapatite crystalline solutions

    Science.gov (United States)

    Hovis, G.; Harlov, D.; Gottschalk, M.; Hudacek, W.; Wildermuth, S.

    2009-04-01

    diagnostics. Mineralogical Magazine 61, 65-77. Hovis, G.L., Brennan, S., Keohane, M., Crelling, J. (1999) High-temperature X-ray investigation of sanidine - analbite crystalline solutions: Thermal expansion, phase transitions, and volumes of mixing. The Canadian Mineralogist 37, 701-709. Hovis, G.L., Crelling, J., Wattles, D., Dreibelbis, B., Dennison, A., Keohane, M., and Brennan, S. (2003) Thermal expansion of nepheline - kalsilite crystalline solutions. Mineralogical Magazine 67, 535-546. Hovis, G.L. and Graeme-Barber, A. (1997) Volumes of K-Na mixing for low albite - microcline crystalline solutions at elevated temperature: A test of regular solution thermodynamic models. American Mineralogist 82, 158-164. Hovis, G.L., Harlov, D.E., Hahn, A., and Steigert, H. (2007) Enthalpies and volumes of F-Cl mixing in fluorapatite - chlorapatite crystalline solutions. Geophysical Research Abstracts 9, abstract 01748. Hovis, G.L., Morabito, J.R. Spooner, R., Mott, A. Person, E.L., Henderson, C. Michael B., Roux, J., and Harlov, D. (2008) A simple predictive model for the thermal expansion of AlSi3 feldspars. American Mineralogist 98, 1568-1573. Hovis, G.L., Person, E., Spooner, A., and Roux, J. (2006) Thermal expansion of highly silicic nepheline - kalsilite crystalline solutions. Mineralogical Magazine 70, 383-396. O'Reilly, S.Y. and Griffin, W.L. (2000) Apatite in the mantle: implications for metasomatic processes and high heat production in Phanerozoic mantle. Lithos 53, 217-232. Parrish, W. (1953) X-Ray reflection angle tables for several standards. Technical Report No. 68, Philips Laboratories Incorporated, Irvington on Hudson, New York.

  19. TIME-TEMPERATURE-TRANSFORMATION DIAGRAMS FOR THE SLUDGE BATCH 3 - FRIT 418 GLASS SYSTEM

    International Nuclear Information System (INIS)

    Billings, A.; Edwards, Tommy

    2009-01-01

    transition temperature measurement and TTT diagram development. The glass transition temperature (Tg) was measured using differential scanning calorimetry (DSC) and was recorded to be 443 ± 3 C. Using the previous TTT diagrams as guidance, subsamples of the glass were isothermally heat treated for 0.5 to 768 hours at temperatures between 400 C to 1100 C. Each of the 56 heat treated samples, along with quenched and centerline canister cooled (CCC) treated samples, were analyzed using Xray diffraction (XRD) and the PCT. Crystallization was detected only in samples treated at 600 C for more than 192 hours, and 700, 800, and 900 C for more than 48 hours. Phases crystallized were similar in composition if not the same as those found in the previous TTT studies. Six different crystalline phases were detected, including nepheline, acmite, lithium silicate, trevorite, krinovite, and albite. Overall, phases were spinel (iron) based, lithium metasilicate, sodium aluminosilicate or sodium transition metal silicate in composition. No new crystalline families were detected. Durability, as measured by the PCT, decreased when lithium silicate or nepheline crystals were present. Only one heat treated sample had a measured PCT response exceeding the benchmark EA glass, which was a sample treated at 600 C for 768 hours. During normal processing at the DWPF these conditions would be highly unlikely to occur, even in an extreme accident scenario. In order to continue to meet the requirements of the WCP, a simplified strategy is suggested for the generation of future TTT diagrams. A strategy has been developed that would require completing two more TTT diagrams for two averaged, future, predicted waste types. By creating diagrams for the resulting glass compositions of encompassing waste types, it will give insight to the crystallization regions possible for those averages. As discussed in the report, 'Initial MAR Assessments to Access the Impact of Al-Dissolution on DWPF Operating Windows

  20. Changes on the mineralogical and physico-chemical properties of a compacted bentonite in contact with hyperalkaline pore fluids

    International Nuclear Information System (INIS)

    Fernandez, A.M.; Melon, A.; Sanchez, D.M.

    2010-01-01

    in the Na-smectite and K-smectite type particles (increasing the percentage of illite/smectite mixed-layers up to 40%); and a tri-octahedral smectite (saponite) was observed. Accessory minerals, such as feldspars (anorthite and albite) and quartz, do not present any dissolution signs; and the precipitation of CSH minerals, CASH-phases were not detected. However, zeolites were identified by XRD. It seems that at these experimental conditions, the montmorillonite has undergone an alteration that seems to affect the total length of the sample (2.5 cm). (authors)

  1. Metallogenetic systems associated with granitoid magmatism in the Amazonian Craton: An overview of the present level of understanding and exploration significance

    Science.gov (United States)

    Bettencourt, Jorge Silva; Juliani, Caetano; Xavier, Roberto P.; Monteiro, Lena V. S.; Bastos Neto, Artur C.; Klein, Evandro L.; Assis, Rafael R.; Leite, Washington Barbosa, Jr.; Moreto, Carolina P. N.; Fernandes, Carlos Marcello Dias; Pereira, Vitor Paulo

    2016-07-01

    íder and Teles Pires suites). The Transamazonas Province corresponds to a N-S-trending orogenic belt, consolidated during the Transamazonian cycle (2.26-1.95 Ga), comprising the Lourenço, Amapá, Carecuru, Bacajá, and Santana do Araguaia tectonic domains. They show a protracted tectonic evolution, and are host to the pre-, syn-, and post-orogenic to anorogenic granitic magmatism. Gold mineralization associated with magmatic events is still unclear. Greisen and pegmatite Sn-Nb-Ta deposits are related to 1.84 to 1.75 Ga late-orogenic to anorogenic A-type granites. The Pitinga Tin Province includes the Madeira Sn-Nb-Ta-F deposit, Sn-greisens and Sn-episyenites. These are associated with A-type granites of the Madeira Suite (1.84-1.82 Ga), which occur within a cauldron complex (Iricoumé Group). The A-type magmatism evolved from a post-collisional extension, towards a within-plate setting. The hydrothermal processes (400 °C-100 °C) resulted in albitization and formation of disseminated cryolite, pyrochlore columbitization, and formation of a massive cryolite deposit in the core of the Madeira deposit. The Rondônia Tin Province hosts rare-metal (Ta, Nb, Be) and Sn-W mineralization, which is associated with the São Lourenço-Caripunas (1.31-1.30 Ga), related to the post-collisional stage of the Rondônia San Ignácio Province (1.56-1.30 Ga), and to the Santa Clara (1.08-1.07 Ga) and Younger Granites of Rondônia (0.99-0.97 Ga) A-type granites. The latter are linked to the evolution of the Sunsás-Aguapeí Province (1.20-0.95 Ga). Rare-metal polymetallic deposits are associated with late stage peraluminous granites, mainly as greisen, quartz vein, and pegmatite types.

  2. Black and red granites in the Egyptian Antiquity Museum of Turin. A minero-petrographic and provenance study.

    Science.gov (United States)

    Serra, M.; Borghi, A.; Vaggelli, G.; D'Amicone, E.; Vigna, L.

    2009-04-01

    materials used for two of the best known masterpieces of Egyptian art. As regards to red granites, it has been observed that most of the exposed sculptures were made of rocks closely akin to Aswan granite. Just in one case, the Ram headed sphinx (cat. 836), macroscopic differences in colour index, grain size and isoorientation of feldspar phenocrysts, suggested a different provenance of the source material and determined the choice of picking up a small fragment for minero-petrographic analysis. The sample collected from the sarcophagus of Nefertari (suppl. 5153) during the recent restoration of the sculpture, was analysed in order to test the accuracy of the results, as the provenance of the material used for its realization was already certain. Petrographic observations and chemical analysis were undertaken by a scanning electron microscope equipped with an energy-dispersive spectrometer. Minero-petrographic data primarily showed that all samples vary in composition from granite (red granites) to granodiorite and tonalite (black granites). The main sialic phases are represented by plagioclase (albite to oligoclase), alkali-feldspar (microcline) and quartz, while femic phases are amphibole (green horneblende) and biotite (Fe- to Mg-biotite), always coexisting in variable relative percentages. Minor amount of apatite (≈ 1 wt.%), magnetite, ilmenite, often associated to sphene, zircon, pyrite and allanite also occur. The identification of some compositional markers in all samples suggested a common provenance for all the rocks used for the sculptures. Thus, it was supposed that they could all have been quarried in the famous district of Aswan, well known at least since Dynastic period. This provenance hypothesis was confirmed by geological literature and archeological evidences, considering the relative proximity of Aswan quarries to Nile river and to the key centres of power in the New Kingdom. Therefore, several geological samples were collected in Aswan area, in order

  3. Ore genesis constraints on the Idaho Cobalt Belt from fluid inclusion gas, noble gas isotope, and ion ratio analyses

    Science.gov (United States)

    Hofstra, Albert H.; Landis, Gary P.

    2012-01-01

    38Ar produced by nucleogenic production from 41K. In contrast, some ore and gangue minerals yield significant SO2 and have low RH and RS values of a more oxidized fluid. Three extracts from gangue quartz have high helium R/RA values indicative of a mantle source and neon isotope compositions that require nucleogenic production of 22Ne in fluorite from U ± Th decay. Two extracts from gangue quartz have estimated 40K/40Ar that permit a Precambrian age. Extracts from gangue quartz in three different ore zones are biased toward the hypersaline population of inclusions and have a tight range of ion ratios (Na, K, NH4, Cl, Br, F) suggestive of a single fluid. Their Na, Cl, Br ratios suggest this fluid was a mixture of magmatic and basinal brine. Na-K-Ca temperatures (279°-347°C) are similar to homogenization temperatures of hypersaline inclusions. The high K/Na of the brine may be due to albitization of K silicate minerals in country rocks. Influx of K-rich brines is consistent with the K metasomatism necessary to form gangue biotite with high Cl. An extract from a post-ore quartz vein is distinct and has Na, Cl, Br ratios that resemble metamorphic fluids in Cretaceous silver veins of the Coeur d'Alene district in the Belt Basin. The results show that in some samples, for certain components, it is possible to "see through" the Cretaceous metamorphic overprint. Of great import for genetic models, the volatiles trapped in gangue quartz have 3He derived from a mantle source and 22Ne derived from fluorite, both of which may be attributed to nearby ~1377 Ma basalt-rhyolite magmatism. The brine trapped in gangue quartz is a mixture of magmatic fluid and evaporated seawater. The former requires a granitic intrusion that is present in the bimodal intrusive complex, and the latter equatorial paleolatitudes that existed in the Mesoproterozoic. The results permit genetic models involving heat and fluids from the neighboring bimodal plutonic complex and convection of basinal brine

  4. Response to the contribution: On Neolithic authenticity of finds from Belica by Dragana Antonović and Slaviša Perić

    Directory of Open Access Journals (Sweden)

    Stojić Milorad

    2013-01-01

    types of stone which are not found in the region, such as serpentine and albite, and to make several dozen objects from them; to find animal bones (Bos/Cervus, from the protostarčevo period and make a large number of figurines exclusively of this material; then using baked clay (as A-P state, also from the protostarčevo period, make anthropomorphic figurines. He would then have to put all these objects into a pit which he dug out in the centre of the Neolithic site, surrounded by a trench 75 m in diameter and then cover it with a great quantity of ochre. To fill up the pit clay of specific content would have to be transport from somewhere else. He would also need to have excellent knowledge of the religious symbols of Neolith, (particularly the connection of the symbolism of woman and moon, as well as the symbolism of moon, woman, snake etc., to shape such objects which stylistically, typologically, chronologically and symbolically completely correspond with the cultural tradition of the Stone Age of Europe, Asia Minor, Near and Middle East, including the ambivalent figures (which represent at the same time man and woman, i.e. male and female symbols, otherwise a recent term in archaeology and to know how the vulva looks immediately before birth which was depicted on all figurines of woman in childbirth in Belica. The statement by A-P that 'there are no analogies' is not correct because numerous analogies are known in Serbia and other parts of the Balkan Peninsula as well as in Asia Minor, the Near and Middle East. As geomagnetic investigations confirm, the protostarčevo settlement in Belica, contrary to the opinion of A-P that it is 'a small Neolithic settlement', is one of the largest settlements from the Early Neolith in Serbia, covering an area of more than 7 ha. Also the statement, that parallel traces, such as those which exist on the surface and in grooves on the stone objects, are the remains of work with 'contemporary grind tools with a large number of

  5. Estudo colorimétrico de fritas feldspáticas Colorimetric study of feldsphatic frits

    Directory of Open Access Journals (Sweden)

    S. F Santos

    2010-03-01

    minerals at high temperatures (about 1500 ºC. Glazes prepared exclusively from frits are used to manufacture ceramic pieces where the aesthetic component is more important than structural features, such as in the case of tiles, decorative ceramics and dental restorations. To improve the decorative effect the ceramic tile has to be colorimetrically stable in order to preserve the color provided by the pigment. In this context, the present work presents the results obtained in a color study carried out by application of ceramic pigments in transparent frits, produced with feldspar from Borborema-Seridó (PB/RN region, Brazil. The chemical analysis of feldspar evidenced that this mineral present the requested characteristics for the application as glaze, once its impurities content (iron and other colorant oxides are low grade. The mineral was characterized by X-ray diffraction (albite and orthoclase and size distribution was determined by screening (Tyler sieves, as being less than 100 µm. The colorimetric evaluation by using CIELab standards and reflectance measurements allowed characterizing the color of the ceramic tiles obtained under different light sources and illuminants. The results indicated that the feldspar from Seridó presents potential for application as colored ceramic tile and hereafter it could be applied in the area of dental restorations, since that mineral is one of the main components of the dental porcelains, however, until the present, all dental restorative material used in Brazil is of foreign origin.

  6. Hydrogeochemical evaluation. Preliminary site description Forsmark area - version 1.2

    International Nuclear Information System (INIS)

    Laaksoharju, Marcus