Search results for "Anhydrite"

showing 7 items of 7 documents

Genesis of chlorine and sulphur in fumarolic emissions at Vulcano Island (Italy): assessment of pH and redox conditions in the hydrothermal system

2002

Chlorine- and sulphur-bearing compounds in fumarole discharges of the La Fossa crater at Vulcano Island (Italy) can be modelled by a mixing process between magmatic gases and vapour from a boiling hydrothermal system. This allows estimating the compounds in both endmembers. Magma degassing cannot explain the time variation of sulphur and HCl concentrations in the deep endmember, which are more probably linked to reactions of solid phases at depth, before mixing with the hydrothermal vapours. Based on the P–T conditions and speciation of the boiling hydrothermal system below La Fossa, the HCl and Stot contents in the hydrothermal vapours were used to compute the redox conditions and pH of th…

AnhydriteAqueous solutionMineralogyengineering.materialFumaroleHydrothermal circulationchemistry.chemical_compoundGeophysicschemistryGeochemistry and PetrologyEnvironmental chemistryBoilingengineeringSeawaterPyriteParagenesisGeologyJournal of Volcanology and Geothermal Research
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Carbonate deposition and diagenesis in evaporitic environments: The evaporative and sulphur-bearing limestones during the settlement of the Messinian…

2015

The depositional and diagenetic processes involved in the formation of carbonates in the evaporitic environment of the Messinian Salinity Crisis are investigated in Southern Italy (Sicily and Calabria). Strong differences are observed between the studied sections that reflect specific depositional and diagenetic evolution in the interconnected sub-basins resulting from the syn-sedimentary tectonic fragmentation of the Central Sicilian and Calabrian domains. These carbonates formed diachronously in restricted perched sub-basins between the Tripoli Formation and the hypersaline settings of the MSC. The Calcare di Base (CdB) that can be interbedded with gypsum layers occurs rhythmically at the…

Calcare di BaseGypsumBacterial sulphate reductionSettore GEO/02 - Geologia Stratigrafica E Sedimentologica010504 meteorology & atmospheric sciencesEvaporiteGeochemistryDiagenetic carbonateSulphur LimestoneMineralogy[PHYS.PHYS.PHYS-GEO-PH]Physics [physics]/Physics [physics]/Geophysics [physics.geo-ph]engineering.material010502 geochemistry & geophysicsOceanography01 natural scienceschemistry.chemical_compoundCelestineMessinian Salinity Crisis Carbonate SulphurEcology Evolution Behavior and SystematicsComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesEarth-Surface ProcessesCalciteAnhydriteSettore GEO/07 - Petrologia E PetrografiaMessinian Salinity CrisiPaleontologySettore GEO/01 - Paleontologia E PaleoecologiaSettore GEO/08 - Geochimica E VulcanologiaDiagenesisEvaporitechemistryengineeringHaliteCarbonateGeology
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Influence of temperature on the hydration products of low pH cements

2012

International audience; The chemical evolution of two hydrated "low pH" binders prepared from binary (60% Portland cement + 40% silica fume) or ternary (37.5% Portland cement +32.5% silica fume + 30% fly-ash) mixtures was characterized over one year at 20 degrees C. 50 degrees C, and 80 degrees C. The main hydrates were Al-substituted C-S-H. Raising the temperature from 20 to 80 degrees C caused a lengthening and cross-linking of their silicate chains. Ettringite that formed in pastes stored at 20 degrees C was destabilized. Only traces of calcium sulfate (gypsum and/or anhydrite) reprecipitated after one year in some materials cured at 50 degrees C and 80 degrees C. The sulfates released w…

EttringiteGypsumSilica fume[SDV]Life Sciences [q-bio]Inorganic chemistry0211 other engineering and technologiesMAS NMR-SPECTROSCOPYTRICALCIUM SILICATE02 engineering and technologyengineering.materialchemistry.chemical_compoundAdsorptionSI-29021105 building & construction[CHIM]Chemical SciencesGeneral Materials ScienceCALCIUM-SULFATEPART IIAL-27 NMRELEVATED-TEMPERATURESAnhydriteBuilding and ConstructionALUMINUM021001 nanoscience & nanotechnologyAlkali metalSilicateC-S-HchemistryChemical engineeringengineering0210 nano-technologyTernary operationPORTLAND-CEMENT
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Formation of secondary carbonates and native sulphur in sulphate-rich Messinian strata, Sicily

2010

Abstract Microbially formed authigenic carbonates accompanied by native sulphur are present in the ‘Calcare Solfifero’ below a thick succession of gypsum deposited during the Messinian salinity crisis in Sicily. We sampled these carbonates and associated sulphur in five former sulphur mines to subject them to a detailed petrographic and geochemical study in order to explore their different modes of formation. Native sulphur formed in conjunction with microbial sulphate reduction, which is reflected in its depletion in 34S (δ34S values as low as − 2‰ vs. V-CDT) and an enrichment of 34S in the residual sulphate (δ34S values as high as + 61‰). The oxidation of organic matter by sulphate reduct…

GypsumSettore GEO/02 - Geologia Stratigrafica E Sedimentologica010504 meteorology & atmospheric sciences[SDU.STU.GP]Sciences of the Universe [physics]/Earth Sciences/Geophysics [physics.geo-ph]StratigraphyAlkalinityGeochemistryCarbonate minerals[PHYS.PHYS.PHYS-GEO-PH]Physics [physics]/Physics [physics]/Geophysics [physics.geo-ph]engineering.material010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundδ34SMessinian salinity crisiSicilyComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesSettore GEO/06 - MineralogiaAnhydriteGeologyAuthigenicSettore GEO/01 - Paleontologia E PaleoecologiaNative sulphurSettore GEO/08 - Geochimica E VulcanologiaDiagenesischemistry13. Climate actionengineeringCarbonateMicrobial sulphate reductionAuthigenic carbonateGeology
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CaSO4 and its pressure-induced phase transitions. A density functional theory study

2012

Theoretical investigations concerning possible calcium sulfate, CaSO(4), high-pressure polymorphs have been carried out. Total-energy calculations and geometry optimizations have been performed by using density functional theory at the B3LYP level for all crystal structures considered. The following sequence of pressure-driven structural transitions has been found: anhydrite, Cmcm (in parentheses the transition pressure) → monazite-type, P2(1)/n (5 GPa) → barite-type, Pnma (8 GPa), and scheelite-type, I4(1)/a (8 GPa). The equation of state of the different polymorphs is determined, while their corresponding vibrational properties have been calculated and compared with previous theoretical r…

Phase transitionAnhydriteCrystallographyLiquid crystalschemistry.chemical_elementThermodynamicsAnhydriteCalciumInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryLiquid crystalDensity functional theoryPhysical and Theoretical ChemistryPolymorphs
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Sulfur isotope ratio measurements of individual sulfate particles by NanoSIMS

2008

Abstract The sulfur isotopic compositions of barite (BaSO4), anhydrite (CaSO4), gypsum (CaSO4·2H2O), mascagnite ((NH4)2SO4), thenardite (Na2SO4), boetite (K2SO4), epsomite (MgSO4·7H2O), magnesium sulfate (MgSO4·xH2O) and cysteine (an amino acid) were determined with a Cameca NanoSIMS 50 ion microprobe employing a Cs+ primary ion beam and measuring negative secondary ions. This ion microprobe permits the analysis of sulfur isotope ratios in sulfates on 0.001–0.5 ng of sample material, enabling the analysis of individual S-bearing particles with diameters as small as 500 nm. The grain-to-grain reproducibility of measurements is typically 5‰ (1σ) for micron-sized grains,

ThenarditeMicroprobeAnhydriteIon beamMagnesiumEpsomiteAnalytical chemistrychemistry.chemical_elementCondensed Matter PhysicsSulfurchemistry.chemical_compoundchemistryPhysical and Theoretical ChemistrySulfateInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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Irreversible modifications of the porous microstructure of soluble anhydrite β-CaSO4 induced by hydration-dehydration cycles

2006

26 pages; The internal surface area of hexagonal (soluble) primary anhydrite CaSO4 produced by dehydration of gypsum decreases by about 70 % when the anhydrite is successively subjected to rehydration and dehydration at room temperature in humid air and in vacuum respectively. In the rehydration step, the hemihydrate is formed; its dehydration yields secondary anhydrite. Additional hydration-dehydration cycles in the same conditions have a much smaller effect. The first cycle also brings about a modification of the t-plot, which reveals that the micropores of primary anhydrite are irreversibly healed. Mercury intrusion porosimetry shows that the primary dehydration of gypsum also generates …

[CHIM.INOR] Chemical Sciences/Inorganic chemistryhemihydrateporosity[ SPI.MAT ] Engineering Sciences [physics]/Materialsdehydration[ CHIM.INOR ] Chemical Sciences/Inorganic chemistrysurface area[CHIM.INOR]Chemical Sciences/Inorganic chemistry[SPI.MAT] Engineering Sciences [physics]/Materialsgypsumanhydrite[SPI.MAT]Engineering Sciences [physics]/Materials
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