Studies of the Manganese Oxides. Iv. Todorokite* J. A
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Characterization of Sulfide Minerals from Gabbroic and Ultramafic Rocks by Electron Microscopy1 D.J
Blackman, D.K., Ildefonse, B., John, B.E., Ohara, Y., Miller, D.J., MacLeod, C.J., and the Expedition 304/305 Scientists Proceedings of the Integrated Ocean Drilling Program, Volume 304/305 Data report: characterization of sulfide minerals from gabbroic and ultramafic rocks by electron microscopy1 D.J. Miller,2 T. Eisenbach,2 and Z.P. Luo3 Chapter contents Abstract Abstract . 1 This objective of this research was to investigate the potential of using transmission electron microscopy (TEM) to determine sul- Introduction . 1 fide mineral speciation in gabbroic rocks from Atlantis Massif, the Geologic background . 2 site of Integrated Ocean Drilling Program Expedition 304/305. Method development . 2 The method takes advantage of TEM analysis techniques and Results . 2 proved successful in sulfide mineral identification. TEM can pro- Discussion . 3 vide imaging of the sample morphology, crystal structure through Acknowledgments. 4 the electron diffraction, and chemical compositional information References . 4 through X-ray energy dispersive spectroscopy. Electron probe mi- Figures . 5 croanalysis was also used to determine the chemical composition. Table . 11 Introduction Integrated Ocean Drilling Program (IODP) Expedition 304/305 at Atlantis Massif, 30°N on the Mid-Atlantic Ridge (MAR) (Fig. F1) comprised a coordinated, dual-expedition drilling program aimed at investigating oceanic core complex (OCC) formation and the exposure of ultramafic rocks in young oceanic lithosphere. One of the scientific objectives of this drilling program is to investigate the role of magmatism in the development of OCCs. Whereas precruise submersible and geophysical surveys suggested the po- tential of recovering substantial amounts of serpentinized perido- tite and possibly fresh residual mantle, coring on the central dome of the massif returned a 1.4 km thick section of plutonic mafic rock with only a thin (<150 m) interval of ultramafic or near-ultramafic composition rocks of indeterminate origin. -
Washington State Minerals Checklist
Division of Geology and Earth Resources MS 47007; Olympia, WA 98504-7007 Washington State 360-902-1450; 360-902-1785 fax E-mail: [email protected] Website: http://www.dnr.wa.gov/geology Minerals Checklist Note: Mineral names in parentheses are the preferred species names. Compiled by Raymond Lasmanis o Acanthite o Arsenopalladinite o Bustamite o Clinohumite o Enstatite o Harmotome o Actinolite o Arsenopyrite o Bytownite o Clinoptilolite o Epidesmine (Stilbite) o Hastingsite o Adularia o Arsenosulvanite (Plagioclase) o Clinozoisite o Epidote o Hausmannite (Orthoclase) o Arsenpolybasite o Cairngorm (Quartz) o Cobaltite o Epistilbite o Hedenbergite o Aegirine o Astrophyllite o Calamine o Cochromite o Epsomite o Hedleyite o Aenigmatite o Atacamite (Hemimorphite) o Coffinite o Erionite o Hematite o Aeschynite o Atokite o Calaverite o Columbite o Erythrite o Hemimorphite o Agardite-Y o Augite o Calciohilairite (Ferrocolumbite) o Euchroite o Hercynite o Agate (Quartz) o Aurostibite o Calcite, see also o Conichalcite o Euxenite o Hessite o Aguilarite o Austinite Manganocalcite o Connellite o Euxenite-Y o Heulandite o Aktashite o Onyx o Copiapite o o Autunite o Fairchildite Hexahydrite o Alabandite o Caledonite o Copper o o Awaruite o Famatinite Hibschite o Albite o Cancrinite o Copper-zinc o o Axinite group o Fayalite Hillebrandite o Algodonite o Carnelian (Quartz) o Coquandite o o Azurite o Feldspar group Hisingerite o Allanite o Cassiterite o Cordierite o o Barite o Ferberite Hongshiite o Allanite-Ce o Catapleiite o Corrensite o o Bastnäsite -
16 /75 / 7 ~ -% in +~ In
7-'<16_ /75_ / 7 ~ R.6l3. Wolframite concentration, Scamander Mining Corporation N.L. A chip sample for the determination of the maximum recoverable amount of wolframite was supplied by the Scamander Mining Corporation and stated to be from their Scamander Tier lease. Special consideration was to be given to the production of a high grade wolframite concentrate and the rejection of the coarsest possible tailing. The chip sample was given the registered number 700174. • The chip sample was initially c rushed to -\ in and found to contain 0.82\ W03' The sample consisted mainly of quartz plus some dolerite with minor amounts of an iron oxide mineral. Large slivers of wolframite up to • 5/16 in were present. SAMPLE PREPARATION The -\ in ore was stage crushed to %" in in a laboratory Chipmunk jaw crusher, mixed, then riffled into four identical parts. One part was further riffled to supply samples for a siie analysis and a further head assay. The second part was wet, then dry screened to provide the following fractions for concentration: Size Range Concentrating Operation -% in +~ in 1 -\ in +10. 2 -10* +22. 3 • -22. +52# 4 -52. +100. 5 -100. +200# 6 • - 200. 7 The remaining two identical parts were retained for possible further work. PROCEDURE The sized fractions of the ore were gravity and magnetically concen t trated (Table 1). II Jig Concentration Jig conditions are shown in Table 2. As the jig concentration operat ions were not continuous , each fraction was fed through its respective jig ~ three times. Table Concentration Minimum amounts of water and l ow feed rates were used to obtain quartz free concentrates from each fraction. -
Moon Minerals a Visual Guide
Moon Minerals a visual guide A.G. Tindle and M. Anand Preliminaries Section 1 Preface Virtual microscope work at the Open University began in 1993 meteorites, Martian meteorites and most recently over 500 virtual and has culminated in the on-line collection of over 1000 microscopes of Apollo samples. samples available via the virtual microscope website (here). Early days were spent using LEGO robots to automate a rotating microscope stage thanks to the efforts of our colleague Peter Whalley (now deceased). This automation speeded up image capture and allowed us to take the thousands of photographs needed to make sizeable (Earth-based) virtual microscope collections. Virtual microscope methods are ideal for bringing rare and often unique samples to a wide audience so we were not surprised when 10 years ago we were approached by the UK Science and Technology Facilities Council who asked us to prepare a virtual collection of the 12 Moon rocks they loaned out to schools and universities. This would turn out to be one of many collections built using extra-terrestrial material. The major part of our extra-terrestrial work is web-based and we The authors - Mahesh Anand (left) and Andy Tindle (middle) with colleague have build collections of Europlanet meteorites, UK and Irish Peter Whalley (right). Thank you Peter for your pioneering contribution to the Virtual Microscope project. We could not have produced this book without your earlier efforts. 2 Moon Minerals is our latest output. We see it as a companion volume to Moon Rocks. Members of staff -
Technologic Tests of Turkey-Gordes Zeolite Minerals
Journal of Minerals and Materials Characterization and Engineering, 2017, 5, 252-265 http://www.scirp.org/journal/jmmce ISSN Online: 2327-4085 ISSN Print: 2327-4077 Technologic Tests of Turkey-Gordes Zeolite Minerals Oyku Bilgin Department of Mining Engineering, Sirnak University, Sirnak, Turkey How to cite this paper: Bilgin, O. (2017) Abstract Technologic Tests of Turkey-Gordes Zeo- lite Minerals. Journal of Minerals and Ma- Natural zeolites are found at many points of the world in the form of miner- terials Characterization and Engineering, 5, als. As for Turkey, quite large volumes of zeolites reserves are available in the 252-265. following regions: Ankara (Nallihan, Beypazari, Polatli etc.), Kütahya-Sa- https://doi.org/10.4236/jmmce.2017.55021 phane, Manisa-Gördes, Manisa-Demirci, Izmir-Urla, Balıkesir-Bigadiç and Received: February 23, 2017 Cappadocia. By means of the works carried out only at the field in Balikesir- Accepted: August 11, 2017 Bigadiç region, one of the detected reserves in Turkey, it was understood that Published: August 14, 2017 an easily workable potential around 500 million ton is available. According to Copyright © 2017 by author and the very limited observations made until today, it is stated that the total re- Scientific Research Publishing Inc. serve in our country may be around 500 billion ton. In these regions, the types This work is licensed under the Creative of clinoptilolite, hoylandit, chabazite, analcime and erionite from the zeolite Commons Attribution International minerals exist. Zeolites are widely used in many sectors such as energy, envi- License (CC BY 4.0). http://creativecommons.org/licenses/by/4.0/ ronment, construction, detergent, chemistry, medicine, mining, agriculture Open Access and livestock. -
A Vibrational Spectroscopic Study of the Silicate Mineral Inesite Ca2
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 128 (2014) 207–211 Contents lists available at ScienceDirect Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy journal homepage: www.elsevier.com/locate/saa A vibrational spectroscopic study of the silicate mineral inesite Ca2(Mn,Fe)7Si10O28(OH)Á5H2O ⇑ Ray L. Frost a, , Andrés López a, Yunfei Xi a, Ricardo Scholz b a School of Chemistry, Physics and Mechanical Engineering, Science and Engineering Faculty, Queensland University of Technology, GPO Box 2434, Brisbane, Queensland 4001, Australia b Geology Department, School of Mines, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG 35,400-00, Brazil highlights graphical abstract We have studied the hydrated hydroxyl silicate mineral inesite. Of formula Ca2(Mn,Fe)7Si10O28(OH)Á5H2O. Using a combination of scanning electron microscopy with EDX and Raman and infrared spectroscopy. OH stretching vibrations are readily studied. The application of vibrational spectroscopy has enabled an assessment of the molecular structure of inesite. article info abstract Article history: We have studied the hydrated hydroxyl silicate mineral inesite of formula Ca2(Mn,Fe)7Si10O28(OH)Á5H2O Received 14 October 2013 using a combination of scanning electron microscopy with EDX and Raman and infrared spectroscopy. Received in revised form 2 February 2014 SEM analysis shows the mineral to be a pure monomineral with no impurities. Semiquantitative analysis Accepted 19 February 2014 shows a homogeneous phase, composed by Ca, Mn2+, Si and P, with minor amounts of Mg and Fe. Available online 12 March 2014 Raman spectrum shows well resolved component bands at 997, 1031, 1051, and 1067 cmÀ1 attributed to a range of SiO symmetric stretching vibrations of [Si10O28] units. -
1 a Vibrational Spectroscopic Study of the Silicate Mineral Inesite 1
1 A vibrational spectroscopic study of the silicate mineral inesite 2 Ca2(Mn,Fe)7Si10O28(OH)∙5H2O 3 4 Ray L. Frost,a Andrés López,a Yunfei Xia and Ricardo Scholzb 5 6 a School of Chemistry, Physics and Mechanical Engineering, Science and Engineering 7 Faculty, Queensland University of Technology, GPO Box 2434, Brisbane Queensland 8 4001, Australia. 9 10 b Department of Geology, Faculty of Science, University of Zagreb, Horvatovac 95, 10000 11 Zagreb, Croatia 12 13 c Geology Department, School of Mines, Federal University of Ouro Preto, Campus Morro do 14 Cruzeiro, Ouro Preto, MG, 35,400-00, Brazil 15 16 ABSTRACT 17 18 We have studied the hydrated hydroxyl silicate mineral inesite of formula 19 Ca2(Mn,Fe)7Si10O28(OH)∙5H2O using a combination of scanning electron microscopy with 20 EDX and Raman and infrared spectroscopy. SEM analysis shows the mineral to be a pure 21 monomineral with no impurities. Semiquantitative analysis shows a homogeneous phase, 22 composed by Ca, Mn2+, Si and P, with minor amounts of Mg and Fe. 23 Raman spectrum shows well resolved component bands at 997, 1031, 1051, and 1067 cm-1 24 attributed to a range of SiO symmetric stretching vibrations of [Si10O28] units. Infrared bands 25 found at 896, 928, 959 and 985 cm-1 are attributed to the OSiO antisymmetric stretching 26 vibrations. An intense broad band at 653 cm-1 with shoulder bands at 608, 631 and 684 cm-1 27 are associated with the bending modes of the OSiO units of the 6- and 8-membered rings of -1 - -1 28 the [Si10O28] units. -
Distribution and Chemistry of Fracture-Lining Minerals at Yucca Mountain, Nevada
LA-12977-MS UC-814 Issued: December 1995 Distribution and Chemistry of Fracture-Lining Minerals at Yucca Mountain, Nevada Barbara A. Carlos Steve f. Chipera David L. Bish Los Alamos NATIONAL LABORATORY Los Alamos, New Mexico 87545 DISCLAIMER Portions of this document may be illegible in electronic image products. Images are produced from the best available original document. DISTRIBUTION AND CHEMISTRY OF FRACTURE-LINING MINERALS AT YUCCA MOUNTAIN, NEVADA by Barbara A. Carlos, Steve J. Chipera, and David L. Bish ABSTRACT Yucca Mountain, a >1.5-km-thick sequence of tuffs and subordinate lavas in southwest Nevada, is being investigated as a potential high-level nuclear waste repository site. Fracture- lining minerals have been studied because they may provide information on past fluid transport and because they may act as natural barriers to radionuclide migration within the fractures. Cores from seven drill holes have been studied to determine the distribution and chemistry of minerals lining fractures at Yucca Mountain. Fracture-lining minerals in tuffs of the Paintbrush Group, which is above the static water level at Yucca Mountain, are highly variable in distribution, both vertically and laterally across the mountain, with the zeolites mordenite, heulandite, and stellerite widespread in fractures even though the tuff matrix is generally devitrified and nonzeolitic. Where heulandite occurs as both tabular and prismatic crystals in the same fracture, the two morphologies have different compositions, suggesting multiple episodes of zeolite formation within the fractures. Manganese-oxide minerals within the Paintbrush Group are rancieite and lithiophorite. The silica polymorphs (quartz, tridymite, and cristobalite) generally exist in fractures where they exist in the matrix, suggesting that they formed in the fractures at the same time they formed in the matrix. -
Newmineraloccurr17farr.Pdf
'SSO • E5 ~ * • 1 v' •* C3 5 Field Columbian Museum Publication 44. Geological Series. Vol. I, No. 7. NEW MINERAL OCCURRENCES. 11. CRYSTAL FORMS OF CALCITE FROM JOPLIN, MISSOURI. BY Oliver Cummings Farrington, Ph.D., Curator, Department of Geology. Chicago, U. S. A. February, 1900. TABLE OF CONTENTS. New Mineral Occurrences, ----- 221 Inesite, ----..'.. 221 Caledonite, ------- 224 Gay-lussite, . 226 - - Kpsomite, - ..... 22g Golden Calcite, ---.... 22Q Dolomite Used as Indian Money, ..... 2 \o Crystal Forms of - - - Calcite from Joplin, Mo., 232 Localities of - - . Large Crystals, . 232 Forms of Large Crystals, ...... 233 Forms of Smaller ' * * • - Crystals, • 237 Forms of Twinned Crystals, ...... 238 NEW MINERAL OCCURRENCES. 1NESITE. SAN CAYETANO MINE NEAR VILLA CORONA, STATE OF DURANGO. MEXICO. MUSEUM No. M 5> A specimen of inesite from the above locality was first secured by the writer in the spring of 1896 while at Villa Corona. Having later determined the mineral by its blowpipe characters as inesite, a request was sent to Mr. John D. Almy, one of the proprietors of the mine, to procure more specimens if possible. Through his kindness, and that of Mr. W. H. Schlemm, a few more specimens were obtained, and were generously placed at the writer's disposal for study. The rarity of the mineral makes the find of interest, as it is known at only three other localities in the world, viz. : The manganese mines at Nanzenbach, northeast of Dillenburg, Ger- many; the Harstig mine, Pajsberg, Wermland, Sweden,* and Jakobsberg, Nordmark, Sweden. t In the specimens from the San Cayetano mine the mineral occurs partly in cavities and partly in- tergrown with calcite and a flesh-colored manganesian calcite. -
An Unusual Titanium-Rich Oxide Mineral from Oslo, Norway Tovr Vrcron
American Mineralogist, Volume 69, pages 36E-390,I9U An unusual titanium-rich oxide mineral from Oslo, Norway Tovr Vrcron Secersrno Mineralo gic al-Ge olo gic al M us e um, Universityof Oslo Sars gate l, Oslo 5, Norway Abstract An unusual Ti-rich oxide mineral of composition Sre.21REEs.26Sis.a3Ti1a.0oFe3.5sV1.2s Cr1.5sO3shas been found in an anatase-albititedike at Oslo, Norway. The mineral is metamict becauseof a small Th content, and contains abundant water (12.14 wt.Vo\.It is black with a metallic to adamantine luster and gives a black-brown streak. The Mohs hardnessis 6. The reflectivity is 17.0-17.4%(546 nm) in air, weakly anisotropic. Heating in air or nitrogen gives X-ray powder lines of rutile (7fi), 8fi), and 900"C)or brannerite (10fi) and 12fi)'C). The chemistry of the mineral resemblesthat of crichtonite. 0ccurrence endothermicpeak. This is believed to representmetamict Three samples containing small, black, shiny crystals water loss. The microprobe analysis, including 12.14 surrounded by reaction halos and occurring in a 20-cm wt.Vowater,totals 10il..78%,assuming all iron to be Fe3*. wide dike were sampled by the author during 1965in a Traces of Y, Pr, Eu, Tb, and Ho were also found. All other elements were below their limits of detection as quarry for road-material (Huken Quarry) near the aban- doned Aanerud copper mine near Grorud in Oslo. The seen by spectrometer scanning. material has subsequently been removed by quarrying Table I shows the unit cell contents normalized to 6 operations and spread over the streets of Oslo. -
Interfacial Precipitation of Phosphate on Hematite and Goethite
minerals Article Interfacial Precipitation of Phosphate on Hematite and Goethite Lijun Wang 1,* ID , Christine V. Putnis 2,3,*, Jörn Hövelmann 4 and Andrew Putnis 2,5 1 College of Resources and Environment, Huazhong Agricultural University, Wuhan 430070, China 2 Institut für Mineralogie, University of Münster, 48149 Münster, Germany 3 Department of Chemistry, Curtin University, Perth, WA 6845, Australia 4 GFZ German Research Centre for Geosciences, 14473 Potsdam, Germany; [email protected] 5 The Institute for Geoscience Research (TIGeR), Curtin University, Perth, WA 6102, Australia; [email protected] * Correspondence: [email protected] (L.W.); [email protected] (C.V.P.); Tel.: +86-27-87288382 (L.W.); +49-251-8333454 (C.V.P.) Received: 19 March 2018; Accepted: 9 May 2018; Published: 10 May 2018 Abstract: Adsorption and subsequent precipitation of dissolved phosphates on iron oxides, such as hematite and goethite, is of considerable importance in predicting the bioavailability of phosphates. We used in situ atomic force microscopy (AFM) to image the kinetic processes of phosphate-bearing solutions interacting with hematite or goethite surfaces. The nucleation of nanoparticles (1.0–4.0 nm in height) of iron phosphate (Fe(III)-P) phases, possibly an amorphous phase at the initial stages, was observed during the dissolution of both hematite and goethite at the earliest crystallization stages. This was followed by a subsequent aggregation stage where larger particles and layered precipitates are formed under different pH values, ionic strengths, and organic additives. Kinetic analysis of the surface nucleation of Fe-P phases in 50 mM NH4H2PO4 at pH 4.5 showed the nucleation rate was greater on goethite than hematite. -
Mineralogy of Mafic and Fe.Ti Oxide-Rich Differentiates of The
American Mineralogist, Volume 67, pages 14J7, 1982 Mineralogy of mafic and Fe.Ti oxide-rich differentiatesof the Marcy anorthositemassif, Adirondacks, New york LBwrs D. Asuwnl Lunar and Plnnetary Institute 3303 NASA Road l, Houston, Texas 77058 Abstract Rocks enriched in mafic silicates, Fe-Ti oxides and apatite form a minor but ubiquitous facies of nearly all Proterozoic massif-typeanorthosite complexes.In the Marcy massif of the Adirondack highlands,New York, the mafic rocks have two modesof occurrence: l) as conformable segregationsinterpreted as cumulate layers in the border zones, and 2) as dikes throughout the massif, interpreted as having crystallized from residual liquids extracted at varying stagesduring differentiation. Primary mineral compositions in these rocks are commonly preserved,despite the effectsof subsolidusrecrystallization in the high pressure granulite facies. In the mafic rock suite, primary compositions of mafic silicates reveal an iron enrichment trend which is broadly similar to that of basic layered intrusions, but suggestive of somewhat higher crystallization temperatures. Textural relationships suggest the following crystallization sequence: plagioclase, pigeonite + augite, hemo-ilmenite * magnetite,apatite. Fe-rich olivine replacedpigeonite in the latest- stage residual liquids. The mineralogy and field relationships of these mafic rocks are consistent with their origin as diferentiates from the same melts which produced the anorthosites. This conclusion agrees with recent geochemical data that suggest an