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  • 1
    Description / Table of Contents: PREFACE Sulfate is an abundant and ubiquitous component of Earth’s lithosphere and hydrosphere. Sulfate minerals represent an important component of our mineral economy, the pollution problems in our air and water, the technology for alleviating pollution, and the natural processes that affect the land we utilize. Vast quantities of gypsum are consumed in the manufacture of wallboard, and calcium sulfates are also used in sculpture in the forms of alabaster (gypsum) and papier-mâché (bassanite). For centuries, Al-sulfate minerals, or “alums,” have been used in the tanning and dyeing industries, and these sulfate minerals have also been a minor source of aluminum metal. Barite is used extensively in the petroleum industry as a weighting agent during drilling, and celestine (also known as “celestite”) is a primary source of strontium for the ceramics, metallurgical, glass, and television face-plate industries. Jarosite is a major waste product of the hydrometallurgical processing of zinc ores and is used in agriculture to reduce alkalinity in soils. At many mining sites, the extraction and processing of coal or metal-sulfide ores (largely for gold, silver, copper, lead, and zinc) produce waste materials that generate acid-sulfate waters rich in heavy metals, commonly leading to contamination of water and sediment. Concentrated waters associated with mine wastes may precipitate a variety of metal-sulfate minerals upon evaporation, oxidation, or neutralization. Some of these sulfate minerals are soluble and store metals and acidity only temporarily, whereas others are insoluble and improve water quality by removing metals from the water column. There is considerable scientific interest in the mineralogy and geochemistry of sulfate minerals in both high-temperature (igneous and hydrothermal) and low-temperature (weathering and evaporite) environments. The physical scale of processes affected by aqueous sulfate and associated minerals spans from submicroscopic reactions at mineral-water interfaces to global issues of oceanic cycling and mass balance, and even to extraterrestrial applications in the exploration of other planets and their satellites. In mineral exploration, minerals of the alunite-jarosite supergroup are recognized as key components of the advanced argillic (acid-sulfate) hydrothermal alteration assemblage, and supergene sulfate minerals can be useful guides to primary sulfide deposits. The role of soluble sulfate minerals formed from acid mine drainage (and its natural equivalent, acid rock drainage) in the storage and release of potentially toxic metals associated with wet-dry climatic cycles (on annual or other time scales) is increasingly appreciated in environmental studies of mineral deposits and of waste materials from mining and mineral processing. This volume compiles and synthesizes current information on sulfate minerals from a variety of perspectives, including crystallography, geochemical properties, geological environments of formation, thermodynamic stability relations, kinetics of formation and dissolution, and environmental aspects. The first two chapters cover crystallography (Chapter 1) and spectroscopy (Chapter 2). Environments with alkali and alkaline earth sulfates are described in the next three chapters, on evaporites (Chapter 3). barite-celestine deposits (Chapter 4), and the kinetics of precipitation and dissolution of gypsum, barite, and celestine (Chapter 5). Acidic environments are the theme for the next four chapters, which cover soluble metal salts from sulfide oxidation (Chapter 6), iron and aluminum hydroxysulfates (Chapter 7), jarosites in hydrometallugy (Chapter 8), and alunite-jarosite crystallography, thermodynamics, and geochronology (Chapter 9). The next two chapters discuss thermodynamic modeling of sulfate systems from the perspectives of predicting sulfate-mineral solubilities in waters covering a wide range in composition and concentration (Chapter 10) and predicting interactions between sulfate solid solutions and aqueous solutions (Chapter 11). The concluding chapter on stable-isotope systematics (Chapter 12) discusses the utility of sulfate minerals in understanding the geological and geochemical processes in both high-and low-temperature environments, and in unraveling the past evolution of natural systems through paleoclimate studies. We thank the authors for their comprehensive and timely efforts, and for their cooperation with our various requests regarding consistency of format and nomenclature. Special thanks are due to the numerous scientists who provided peer reviews, which substantially improved the content of the chapters. This volume would not have been possible without the usual magic touch and extreme patience of Paul H. Ribbe, Series Editor for Reviews in Mineralogy and Geochemistry. Finally, we thank our families for their support and understanding during the past several months.
    Pages: Online-Ressource (VIII, 608 Seiten)
    ISBN: 0939950529
    Language: English
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. 629-630 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The monoclinic modification of dipotassium dichromate, β-K2Cr2O7, has been synthesized in the K2Cr2O7–H2O system. The structure consists of K+ cations and Cr2O72− dimers. In contrast with triclinic α-K2Cr2O7 [Kuz'min, Ilyukhin, Kharitonov & Belov (1969). Krist. Tech. 4, 441–461], the Cr2O72− groups in β-K2Cr2O7 have twofold crystallographic symmetry and are parallel to each other.
    Type of Medium: Electronic Resource
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  • 3
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    MDPI - Multidisciplinary Digital Publishing Institute
    Publication Date: 2023-12-20
    Description: The Arctic zone of the Earth is a major source of mineral and other natural resources for the future development of science and technology. It contains a large supply of strategic mineral deposits, including rare earths, copper, phosphorus, niobium, platinum-group elements, and other critical metals. The continued melting of the sea ice due to climate change makes these resources more accessible than ever before. However, the mineral exploration in the Arctic has always been a challenge due to the climatic restrictions, remote location, and vulnerability of Arctic ecosystems. This book covers a broad range of topics related to the problem of Arctic mineral resources, including geological, geochemical, and mineralogical aspects of their occurrence and formation; chemical technologies; and environmental and economic problems related to mineral exploration. The contributions can be tentatively classified into four major types: geodynamics and metallogeny, mineralogy and petrology, mineralogy and crystallography, and mining and chemical technologies associated with the exploration of mineral deposits and the use of raw materials for manufacturing new products. The book can be of interest for all those interested in Arctic issues and especially in Arctic mineral resources and associated problems of mineralogy, geology, geochemistry, and technology.
    Keywords: Q1-390 ; U mineralization ; n/a ; ivanyukite ; Kovdor phoscorite–carbonatite complex ; Precambrian ; Kovdor phoscorite-carbonatite complex ; hydrothermal deposits ; chalcopyrite ; cathodoluminescence ; PGE ; low-grade copper-nickel ore ; Northern Karelia ; diamond processing plants ; transformation mineral species ; batievaite-(Y) ; rock alteration ; Khibiny ; bacterial leaching ; cryomineralogenesis ; beryllium minerals ; Siberian craton ; apatite-nepheline deposit ; apatite ; gold ; hainite-(Y) ; Keivy alkaline province ; zircon ; niobium ; zeolite group minerals ; shkatulkalite ; zircon dating ; electrochemical separation ; hydrothermal synthesis ; pyrrhotite ; Breivikbotn ; crystal fractionation ; Sakharjok massif ; Palaeoproterozoic ; titanosilicate ; Pechenga structure ; LIP ; antigorite ; nepheline ; forsterite ; Arctic ; saponite-containing waters ; chemical composition ; Khibiny promising structures ; melteigite ; sulfuric-acidic decomposition ; petroleum potential ; mineralogy ; mafic intrusion ; Paleoproterozoic ; vuonnemite ; calcite ; garnet ; raw materials ; search of trend differences ; metallogeny ; Lovozero alkaline massif ; isotopes ; kimberlite ; phase diagram apatite-nepheline-diopside ; mineral data ; ore dressing tailings ; geochronology ; geodynamic evolution ; pyrochlore supergroup minerals ; pentlandite ; saponite product applications ; basic rocks ; Plume ; West-Pana intrusion ; Rb-Sr ; U-Pb ; heap leaching ; rinkite group minerals ; Arctic zone ; Ti-in-zircon geothermometry ; apatite-nepheline-titanite ore ; cobaltpentlandite ; silicocarbonatite ; Fennoscandian Shield ; titanium ; MHD-source “Khibiny” ; Fedorova-Pana Complex ; Northern Norway ; evolution of the composition ; trace elements ; oil ; vanadium mineralization ; geodynamics ; gas ; greenstone belt ; South Reef ; typochemistry ; mechanical activation ; alkali-activated binder ; Kola region ; hydrothermal veins ; Kola Peninsula ; macrocrysts ; titanyl sulfate ; alkaline rocks ; cryogenic treatment ; granite ; Yenisei-Khatanga basin ; crystal structure ; pegmatites ; conductive layers ; bic Book Industry Communication::G Reference, information & interdisciplinary subjects::GP Research & information: general
    Language: English
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  • 4
    Publication Date: 2020-07-08
    Description: We report the crystal structures of four synthetic members of the variscite group (space group type Pbca) and of bonacinaite, the first naturally occurring scandium arsenate member of the metavariscite group. All structures were determined using single-crystal X-ray intensity data. The following members were all synthesised under either mild hydrothermal conditions or by wet-chemical methods (
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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  • 5
    Publication Date: 2018
    Description: 〈div data-abstract-type="normal"〉〈p〉Hydroxynatropyrochlore, (Na,Сa,Ce)〈span〉2〈/span〉Nb〈span〉2〈/span〉O〈span〉6〈/span〉(OH), is a new Na–Nb–OH-dominant member of the pyrochlore supergroup from the Kovdor phoscorite–carbonatite pipe, Kola Peninsula, Russia. It is cubic, 〈span〉Fd〈/span〉〈span〉〈span〉〈img data-mimesubtype="gif" data-type="simple" src="http://static.cambridge.org/resource/id/urn:cambridge.org:id:binary:20190313104343836-0311:S0026461X18001056:S0026461X18001056_inline1.gif"〉 〈span data-mathjax-type="texmath"〉 〈/span〉 〈/span〉〈/span〉〈span〉m〈/span〉, 〈span〉a〈/span〉 = 10.3211(3) Å, 〈span〉V〈/span〉 = 1099.46(8) Å〈span〉3〈/span〉 and 〈span〉Z〈/span〉 = 8 (from powder diffraction data) or 〈span〉a〈/span〉 = 10.3276(5) Å, 〈span〉V〈/span〉 = 1101.5(2) Å〈span〉3〈/span〉 and 〈span〉Z〈/span〉 = 8 (from single-crystal diffraction data). Hydroxynatropyrochlore is a characteristic accessory mineral of the low-carbonate phoscorite in the contact zone of the phoscorite–carbonatite pipe with host foidolite as well as in the carbonate-rich phoscorite and carbonatite of the pipe axial zone. It usually forms zonal cubic or cubooctahedral crystals (up to 0.5 mm in diameter) with irregularly shaped relics of amorphous U–Ta-rich hydroxykenopyrochlore inside. Characteristic associated minerals include rock-forming calcite, dolomite, forsterite, hydroxylapatite, magnetite and phlogopite, accessory baddeleyite, baryte, barytocalcite, chalcopyrite, chamosite–clinochlore, galena, gladiusite, juonniite, ilmenite, magnesite, pyrite, pyrrhotite, quintinite, spinel, strontianite, valleriite and zirconolite. Hydroxynatropyrochlore is pale brown, with an adamantine to greasy lustre and a white streak. The cleavage is average on {111} and the fracture is conchoidal. Mohs hardness is ~5. In transmitted light, the mineral is light brown, isotropic and 〈span〉n〈/span〉 = 2.10(5) (λ = 589 nm). The calculated and measured densities are 4.77 and 4.60(5) g cm〈span〉−3〈/span〉, respectively. The mean chemical composition determined by electron microprobe is: F 0.05, Na〈span〉2〈/span〉O 7.97, CaO 10.38, TiO〈span〉2〈/span〉 4.71, FeO 0.42, Nb〈span〉2〈/span〉O〈span〉5〈/span〉 56.44, Ce〈span〉2〈/span〉O〈span〉3〈/span〉 3.56, Ta〈span〉2〈/span〉O〈span〉5〈/span〉 4.73, ThO〈span〉2〈/span〉 5.73, UO〈span〉2〈/span〉 3.66, total 97.65 wt.%. The empirical formula calculated on the basis of Nb + Ta + Ti = 2 apfu is (Na〈span〉1.02〈/span〉Ca〈span〉0.73〈/span〉Ce〈span〉0.09〈/span〉Th〈span〉0.09〈/span〉 U〈span〉0.05〈/span〉〈span〉〈span〉〈img data-mimesubtype="gif" data-type="simple" src="http://static.cambridge.org/resource/id/urn:cambridge.org:id:binary:20190313104343836-0311:S0026461X18001056:S0026461X18001056_inline2.gif"〉 〈span data-mathjax-type="texmath"〉 〈/span〉 〈/span〉〈/span〉)〈span〉Σ2.00〈/span〉(Nb〈span〉1.68〈/span〉Ti〈span〉0.23〈/span〉Ta〈span〉0.09〈/span〉)〈span〉Σ2.00〈/span〉O〈span〉6.03〈/span〉(OH〈span〉1.04〈/span〉F〈span〉0.01〈/span〉)〈span〉Σ1.05〈/span〉. The simplified formula is (Na,Ca,Ce)〈span〉2〈/span〉Nb〈span〉2〈/span〉O〈span〉6〈/span〉(OH). The mineral dissolves slowly in hot HCl. The strongest X-ray powder-diffraction lines [listed as (〈span〉d〈/span〉 in Å)(〈span〉I〈/span〉)(〈span〉hkl〈/span〉)] are as follows: 5.96(47)(111), 3.110(30)(311), 2.580(100)(222), 2.368(19)(400), 1.9875(6)(333), 1.8257(25)(440) and 1.5561(14)(622). The crystal structure of hydroxynatropyrochlore was refined to 〈span〉R〈/span〉〈span〉1〈/span〉 = 0.026 on the basis of 80 unique observed reflections. The mineral belongs to the pyrochlore structure type 〈span〉A〈/span〉〈span〉2〈/span〉〈span〉B〈/span〉〈span〉2〈/span〉O〈span〉6〈/span〉〈span〉Y〈/span〉〈span〉1〈/span〉 with octahedral framework of corner-sharing 〈span〉B〈/span〉O〈span〉6〈/span〉 octahedra with 〈span〉A〈/span〉 cations and OH groups in the interstices. The Raman spectrum of hydroxynatropyrochlore contains characteristic bands of the lattice, 〈span〉B〈/span〉O〈span〉6〈/span〉, 〈span〉B〈/span〉–O and O–H vibrations and no characteristic bands of the H〈span〉2〈/span〉O vibrations. Within the Kovdor phoscorite–carbonatite pipe, hydroxynatropyrochlore is the latest hydrothermal mineral of the pyrochlore supergroup, which forms external rims around grains of earlier U-rich hydroxykenopyrochlore and separated crystals in voids of dolomite carbonatite veins. The mineral is named in accordance with the pyrochlore supergroup nomenclature.〈/p〉〈/div〉
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
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  • 6
    Publication Date: 2005-02-01
    Print ISSN: 0002-7863
    Electronic ISSN: 1520-5126
    Topics: Chemistry and Pharmacology
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  • 7
    Publication Date: 2002-08-01
    Print ISSN: 0020-1669
    Electronic ISSN: 1520-510X
    Topics: Chemistry and Pharmacology
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  • 8
    Publication Date: 2012-07-01
    Description: Leucostaurite is a new nanoporous lead borate discovered in samples from the Mina Asunción, Sierra Gorda, Atacama Desert, Chile, preserved since 1912 in the collections of the Natural History Museum of Bern, Switzerland. Leucostaurite formed via the oxidation of base-metal ores in the presence of B-rich brines. The mineral name is derived from the Greek “leukos” (white) and “stauros” (cross), and alludes to the white or transparent, colorless cruciform twinned crystals. Leucostaurite forms thin-tabular {010}, striated //[100], interpenetrated twinned crystals, and sheaf-like aggregates up to 0.8 mm on a paralaurionite and boleite matrix. The streak is white and the luster adamantine. Leucostaurite shows a weak, light-yellow fluorescence under short-wavelength UV but no fluorescence under long-wavelength UV light. The mineral is brittle, Mohs hardness ~4, with perfect cleavage parallel to {010} and good cleavage parallel to {100}; calculated density is 5.071 g/cm3. Leucostaurite is biaxial, 2V (meas) ~30°, dispersion: r 〉 v, strong. Optic sign and refractive indices could not be measured, but the average index calculated from the Gladstone-Dale relationship is 1.849. The empirical formula based on Pb + Sr + Ca = 2 atoms per formula unit (apfu), 1 H apfu and B + Si = 5 apfu, is (Pb1.967Sr0.026Ca0.007)∑2.000 (B4.983Si0.017)∑5.000(Cl1.073I0.004)∑1.077O8.971·0.5H2O, which simplifies to Pb2[B5O9]Cl·0.5H2O. The boron content was measured on two crystal fragments using proton-induced γ-ray emission spectroscopy; the analytical value [26.7(3) wt% B2O3] is within error of the stoichiometric value of 26.5 wt% B2O3. Leucostaurite is orthorhombic, space group Pnn2, a = 11.376(2), b = 11.505(2), c = 6.5558(7) Å, V = 858.1(2) Å3, Z = 4. The seven strongest lines measured in the X-ray powder diffraction pattern are [d in Å/Irel in %]: 4.04/100; 2.84/100; 5.71/80; 2.019/70; 3.29/40; 2.55/40; 1.877/40. The crystal structure of leucostaurite (R1 = 6.2%) contains a hilgardite-type three-dimensional [B5O9]3− framework. Leucostaurite is the first mineral of the hilgardite group with orthorhombic (Pnn2) symmetry. However, several borates synthesized for their non-linear optical properties are structurally and chemically closely related to leucostaurite. For example in Na0.5Pb2(B5O9)Cl(OH)0.5, one type of channels contains Cl− ions, the other contains OH−, Cl−, and Na+ ions; in leucostaurite these channels are occupied by Cl− ions, and Cl− ions + H2O groups, respectively.
    Print ISSN: 0003-004X
    Electronic ISSN: 1945-3027
    Topics: Geosciences
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  • 9
    Publication Date: 2018
    Description: 〈div data-abstract-type="normal"〉〈p〉Hydrotalcite, ideally [Mg〈span〉6〈/span〉Al〈span〉2〈/span〉(OH)〈span〉16〈/span〉](CO〈span〉3〈/span〉)(H〈span〉2〈/span〉O)〈span〉4〈/span〉, was studied in samples from Dypingdal, Snarum, Norway (3〈span〉R〈/span〉 and 2〈span〉H〈/span〉), Zelentsovskaya pit (2〈span〉H〈/span〉) and Praskovie–Evgenievskaya pit (2〈span〉H〈/span〉) (both Southern Urals, Russia), Talnakh, Siberia, Russia (3〈span〉R〈/span〉), Khibiny, Kola, Russia (3〈span〉R〈/span〉), and St. Lawrence, New York, USA (3〈span〉R〈/span〉 and 2〈span〉H〈/span〉). Two polytypes, 3〈span〉R〈/span〉 and 2〈span〉H〈/span〉 (both ‘classical’), were confirmed on the basis of single-crystal and powder X-ray diffraction data. Their chemical composition was studied by electron-microprobe analysis, infrared spectroscopy, differential scanning calorimetry, and thermogravimetric analysis. The crystal structure of hydrotalcite-3〈span〉R〈/span〉 was solved by direct methods in the space group 〈span〉R〈/span〉〈span〉〈span〉〈img data-mimesubtype="gif" data-type="simple" src="http://static.cambridge.org/resource/id/urn:cambridge.org:id:binary:20190522072108342-0385:S0026461X18001457:S0026461X18001457_inline1.gif"〉 〈span data-mathjax-type="texmath"〉 〈/span〉 〈/span〉〈/span〉〈span〉m〈/span〉 on three crystals (two data collections at 290 K and one at 120 K). The unit-cell parameters are as follows (290/290/120 K): 〈span〉a〈/span〉 = 3.0728(9)/3.0626(3)/3.0617(4), 〈span〉c〈/span〉 = 23.326(9)/23.313(3)/23.203(3) Å and 〈span〉V〈/span〉 = 190.7(1)/189.37(4)/188.36(4) Å〈span〉3〈/span〉. The crystal structures were refined on the basis of 304/150/101 reflections to 〈span〉R〈/span〉〈span〉1〈/span〉 = 0.075/0.041/0.038. Hydrotalcite-2〈span〉H〈/span〉 crystallises in the 〈span〉P〈/span〉6〈span〉3〈/span〉/〈span〉mmc〈/span〉 space group; unit-cell parameters for two crystals are (data collection at 290 K and 93 K): 〈span〉a〈/span〉 = 3.046(1)/3.0521(9), 〈span〉c〈/span〉 = 15.447(6)/15.439(4) Å, 〈span〉V〈/span〉 = 124.39(8)/124.55(8) Å〈span〉3〈/span〉. The crystal structures were refined on the basis of 160/142 reflections to 〈span〉R〈/span〉〈span〉1〈/span〉 = 0.077/0.059. This paper reports the first single-crystal structure data on hydrotalcite. Hydrotalcite distribution in Nature, diagnostic features, polytypism, interlayer topology and localisation of 〈span〉M〈/span〉〈span〉2+〈/span〉–〈span〉M〈/span〉〈span〉3+〈/span〉 cations within metal hydroxide layers are discussed.〈/p〉〈/div〉
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  • 10
    Publication Date: 2003-02-01
    Print ISSN: 1293-2558
    Electronic ISSN: 1873-3085
    Topics: Chemistry and Pharmacology , Physics
    Published by Elsevier
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