The Rutile Deposits of the Eastern United States
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CRYSTAL SRUKTUR of CALCIUM TITANATE (Catio3) PHOSPHOR DOPED with PRASEODYMIUM and ALUMINIUM IONS
CRYSTAL SRUKTUR OF CALCIUM TITANATE (CaTiO3) PHOSPHOR DOPED WITH PRASEODYMIUM AND ALUMINIUM IONS STRUKTUR KRISTAL FOSFOR KALSIUM TITANIA DIDOPKAN DENGAN ION PRASEODYMIUM DAN ALUMINIUM IONS Siti Aishah Ahmad Fuzi1* and Rosli Hussin2 1 Material Technology Group, Industrial Technology Division, Malaysian Nuclear Agency, Bangi, 43000 Kajang, Selangor Darul Ehsan, Malaysia. 2 Department of Physics, Faculty of Science, Universiti Teknologi Malaysia, 81310 Skudai, Johor 1*[email protected], [email protected] Abstract The past three decades have witnessed rapid growth in research and development of luminescence phenomenon because of their diversity in applications. In this paper, Calcium Titanate (CaTiO3) was studied to find a new host material with desirable structural properties for luminescence-based applications. Solid state reactions o 3+ methods were used to synthesis CaTiO3 at 1000 C for 6 hours. Crystal structure of CaTiO3 co-doped with Pr 3+ and Al were investigated using X-Ray Diffraction (XRD) method. Optimum percentage to synthesis CaTiO3 was 3+ obtained at 40 mol%CaO-60 mol%TiO2 with a single doping of 1 mol%Pr . However, a crystal structure of 4 mol% of Al3+ co-doped with Pr3+ was determined as an optimum parameter which suitable for display imaging. Keywords: calcium titanate, anatase, rutile Abstrak Semenjak tiga dekad yang lalu telah menunjukkan peningkatan yang ketara bagi kajian dan pembangunan dalam bidang fotolumiscen. Peningkatan ini berkembang dengan meluas disebabkan oleh kebolehannya untuk diaplikasikan dalam pelbagai kegunaan harian. Dalam manuskrip ini, kalsium titania (CaTiO3) telah dikaji untuk mencari bahan perumah dengan sifat struktur yang bersesuaian bagi aplikasi luminescen. Tindak balas keadaan o pepejal telah digunakan bagi mensintesis CaTiO3 pada suhu 1000 C selama 6 jam. -
New Minerals Approved in 1998 by The
247 The Canadian Mineralogist Vol. 37, pp. 247-252 (1999) NEW MINERALSAPPROVED IN 1998 BY THE COMMISSIONON NEW MINERALS AND MINERALNAMES. INTERNATIONAL MINERALOGICAL ASSOCIATION JOEL D. GRICE* CanadianMuseum of Nttture,P.O. Box 3443A,Station "D", Ottawa,Ontario KIP 6P4 GIOVANNI FERRARISX* Dipanimentodi ScienzeMineralogiche e Petrologiche,Universitd di Torino,Via ValpergaCaluso 35, I-10125Torino, Italy The information given here is provided by the Commission on New Minerals and Mineral Names (CNMMN), Intemational Mineralogical Association (IMA), for comparative purposesand as a service to mineralogists work- ing on new species.Each mineral is described in the following format: IMA Number Chemical Formula (any relationship to other minerals; structure analysis) Crystal system, spacegroup unit-cell parameters Color; luster; diaphaneity Optical properties Strongestlines in the X-ray powder-diffraction pattern td in A(I)l The namesof these approved speciesare consideredconfidential information until the authors have published their descriptions or releasedinformation themselves.No other information will be releasedby the Commission. 1998Pnoposers IMA No. 98-002 Ca:Ge(OH)6(SO+XCO:).12HzO A memberof IMA No. 98-001 the ettringitegroup; Cu3(AsOa)2.4H2O New structure-type structure OrthorhombiciPnma Hexagonal:P63/m a 5.6906.b t7.06I.c 9.82 A, a 11.056,c 10.629A Bottle green;vitreous; transparent White; vitreous;transparent Biaxial(-), u 1.745,B 1.755,1 1.760,2V(meas)11", Uniaxial(-), to 1.509,e 1.479 2V (calc)70" 8.52(100),3.721(60), 3.221(90), 9.57 (vs), 5. 5 3 (s), 3. 8 3 (s), 3. 56(ms), 3.44(m), 2.7 4(ms), 3.ro2(40), 2.8 r7 (3 5), 2.79 s (3 s), 2.3s0(25) 2.53(m) \ * Chairman, CNMMN. -
Mineral Collecting Sites in North Carolina by W
.'.' .., Mineral Collecting Sites in North Carolina By W. F. Wilson and B. J. McKenzie RUTILE GUMMITE IN GARNET RUBY CORUNDUM GOLD TORBERNITE GARNET IN MICA ANATASE RUTILE AJTUNITE AND TORBERNITE THULITE AND PYRITE MONAZITE EMERALD CUPRITE SMOKY QUARTZ ZIRCON TORBERNITE ~/ UBRAR'l USE ONLV ,~O NOT REMOVE. fROM LIBRARY N. C. GEOLOGICAL SUHVEY Information Circular 24 Mineral Collecting Sites in North Carolina By W. F. Wilson and B. J. McKenzie Raleigh 1978 Second Printing 1980. Additional copies of this publication may be obtained from: North CarOlina Department of Natural Resources and Community Development Geological Survey Section P. O. Box 27687 ~ Raleigh. N. C. 27611 1823 --~- GEOLOGICAL SURVEY SECTION The Geological Survey Section shall, by law"...make such exami nation, survey, and mapping of the geology, mineralogy, and topo graphy of the state, including their industrial and economic utilization as it may consider necessary." In carrying out its duties under this law, the section promotes the wise conservation and use of mineral resources by industry, commerce, agriculture, and other governmental agencies for the general welfare of the citizens of North Carolina. The Section conducts a number of basic and applied research projects in environmental resource planning, mineral resource explora tion, mineral statistics, and systematic geologic mapping. Services constitute a major portion ofthe Sections's activities and include identi fying rock and mineral samples submitted by the citizens of the state and providing consulting services and specially prepared reports to other agencies that require geological information. The Geological Survey Section publishes results of research in a series of Bulletins, Economic Papers, Information Circulars, Educa tional Series, Geologic Maps, and Special Publications. -
Development of Highly Transparent Zirconia Ceramics
11 Development of highly transparent zirconia ceramics Isao Yamashita *1 Masayuki Kudo *1 Koji Tsukuma *1 Highly transparent zirconia ceramics were developed and their optical and mechanical properties were comprehensively studied. A low optical haze value (H<1.0 %), defined as the diffuse transmission divided by the total forward transmission, was achieved by using high-purity powder and a novel sintering process. Theoretical in-line transmission (74 %) was observed from the ultraviolet–visible region up to the infra-red region; an absorption edge was found at 350 nm and 8 µm for the ultraviolet and infrared region, respectively. A colorless sintered body having a high refractive index (n d = 2.23) and a high Abbe’s number (νd = 27.8) was obtained. A remarkably large dielectric constant (ε = 32.7) with low dielectric loss (tanδ = 0.006) was found. Transparent zirconia ceramics are candidates for high-refractive index lenses, optoelectric devices and infrared windows. Transparent zirconia ceramics also possess excellent mechanical properties. Various colored transparent zirconia can be used as exterior components and for complex-shaped gemstones. fabricating transparent cubic zirconia ceramics.9,13-19 1.Introduction Transparent zirconia ceramics using titanium oxide as Transparent and translucent ceramics have been a sintering additive were firstly reported by Tsukuma.15 studied extensively ever since the seminal work on However, the sintered body had poor transparency translucent alumina polycrystal by Coble in the 1960s.1 and low mechanical strength. In this study, highly Subsequently, researchers have conducted many transparent zirconia ceramics of high strength were studies to develop transparent ceramics such as MgO,2 developed. -
The Seven Crystal Systems
Learning Series: Basic Rockhound Knowledge The Seven Crystal Systems The seven crystal systems are a method of classifying crystals according to their atomic lattice or structure. The atomic lattice is a three dimensional network of atoms that are arranged in a symmetrical pattern. The shape of the lattice determines not only which crystal system the stone belongs to, but all of its physical properties and appearance. In some crystal healing practices the axial symmetry of a crystal is believed to directly influence its metaphysical properties. For example crystals in the Cubic System are believed to be grounding, because the cube is a symbol of the element Earth. There are seven crystal systems or groups, each of which has a distinct atomic lattice. Here we have outlined the basic atomic structure of the seven systems, along with some common examples of each system. Cubic System Also known as the isometric system. All three axes are of equal length and intersect at right angles. Based on a square inner structure. Crystal shapes include: Cube (diamond, fluorite, pyrite) Octahedron (diamond, fluorite, magnetite) Rhombic dodecahedron (garnet, lapis lazuli rarely crystallises) Icosi-tetrahedron (pyrite, sphalerite) Hexacisochedron (pyrite) Common Cubic Crystals: Diamond Fluorite Garnet Spinel Gold Pyrite Silver Tetragonal System Two axes are of equal length and are in the same plane, the main axis is either longer or shorter, and all three intersect at right angles. Based on a rectangular inner structure. Crystal shapes include: Four-sided prisms and pyramids Trapezohedrons Eight-sided and double pyramids Icosi-tetrahedron (pyrite, sphalerite) Hexacisochedron (pyrite) Common Tetragonal Crystals: Anatase Apophyllite Chalcopyrite Rutile Scapolite Scheelite Wulfenite Zircon Hexagonal System Three out of the four axes are in one plane, of the same length, and intersect each other at angles of 60 degrees. -
Rutile Mineral Chemistry and Zr-In-Rutile Thermometry In
minerals Article Rutile Mineral Chemistry and Zr-in-Rutile Thermometry in Provenance Study of Albian (Uppermost Lower Cretaceous) Terrigenous Quartz Sands and Sandstones in Southern Extra-Carpathian Poland Jakub Kotowski * , Krzysztof Nejbert and Danuta Olszewska-Nejbert Faculty of Geology, University of Warsaw, Zwirki˙ i Wigury 93, 02-089 Warszawa, Poland; [email protected] (K.N.); [email protected] (D.O.-N.) * Correspondence: [email protected] Abstract: The geochemistry of detrital rutile grains, which are extremely resistant to weathering, was used in a provenance study of the transgressive Albian quartz sands in the southern part of extra-Carpathian Poland. Rutile grains were sampled from eight outcrops and four boreholes located on the Miechów, Szydłowiec, and Puławy Segments. The crystallization temperatures of the rutile grains, calculated using a Zr-in-rutile geothermometer, allowed for the division of the study area into three parts: western, central, and eastern. The western group of samples, located in the Citation: Kotowski, J.; Nejbert, K.; Miechów Segment, is characterized by a polymodal distribution of rutile crystallization temperatures ◦ ◦ ◦ Olszewska-Nejbert, D. Rutile Mineral (700–800 C; 550–600 C, and c. 900 C) with a significant predominance of high-temperature forms, Chemistry and Zr-in-Rutile and with a clear prevalence of metapelitic over metamafic rutile. The eastern group of samples, Thermometry in Provenance Study of corresponding to the Lublin Area, is monomodal and their crystallization temperatures peak at Albian (Uppermost Lower 550–600 ◦C. The contents of metapelitic to metamafic rutile in the study area are comparable. The Cretaceous) Terrigenous Quartz central group of rutile samples with bimodal distribution (550–600 ◦C and 850–950 ◦C) most likely Sands and Sandstones in Southern represents a mixing zone, with a visible influence from the western and, to a lesser extent, the eastern Extra-Carpathian Poland. -
Scandium Mineralization Associated with Hydrothermal Lazulite-Quartz Veins in the Lower Austroalpine Grobgneis Complex, Eastern Alps, Austria
Bernhard, F. (2001): Scandium mineralization associated with hydrothermal lazulite-quartz veins in the Lower Austroalpine Grobgneis complex, Eastern Alps, Austria. In: Piestrzynski A. et al. (eds.): Mineral Deposits at the Beginning of the 21st Century. Proceedings of the joint sixth biennial SGA-SEG meeting. Kraków, Poland. A.A.Balkema Publishers, 935-938. Scandium mineralization associated with hydrothermal lazulite-quartz veins in the Lower Austroalpine Grobgneis complex, Eastern Alps, Austria F. Bernhard Institut für Technische Geologie und Angewandte Mineralogie, Technische Universität Graz, Rechbauerstraße 12, A-8010 Graz, Austria ABSTRACT: Lazulite (MgAl2(PO4)2(OH)2)-quartz veins within the Lower Austroalpine Grobgneis complex, Austria, have Sc-contents up to 200 ppm. The predominant Sc-carrier is pretulite, ScPO4, and this phase oc- curs as a wide-spread accessory mineral. Vein formation took place at temperatures of 300-500° C and low pressure during Permo-Triassic extensional tectonics and fluid flow. Mg-enriched alteration zones suggest that vein material was not derived from the immediate host rocks. Eo-Alpine metamorphism and deformation overprinted the veins to varying degrees. Despite the low tonnage of the Sc-rich veins, this new type of Sc- mineralization may point to larger Sc-accumulations in similar phosphate-rich hydrothermal environments. 1 INTRODUCTION The long-known lazulite (MgAl2(PO4)2(OH)2)- quartz veins in northeastern Styria and southern Scandium is a moderately abundant transition ele- Lower Austria contain significant Sc-enrichments in ment with an average content ca. 7 ppm in the upper the form of pretulite, ScPO4 (Bernhard et al. 1998b). and ca. 25 ppm in the lower continental crust (We- This contribution gives data on the geology, miner- depohl 1995). -
Compositional Asymmetry in Replacement Tourmaline – an Example from the Tauern Window, Eastern Alps
Geological Volume 4 Number 2 Mater ials August 12, 2002 Researc h Compositional asymmetry in replacement tourmaline – An example from the Tauern Window, Eastern Alps Darrell J. Henry1, Barbara L. Dutrow2 and Jane Selverstone3 1, 2Department of Geology and Geophysics, Louisiana State University, Baton Rouge, Louisiana 70808, USA 1<[email protected]>, 2<[email protected]>, 3Department of Earth and Planetary Sciences, University of New Mexico, Albuquerque, New Mexico 87131, USA 3<[email protected] > Abstract Tourmaline, partially replacing pre-existing tourmaline from a tectonically-dismembered tourmalinite vein, has developed distinctive compositional asymmetry that reflects influx of reac- tive fluids. The tourmalinite clast, enclosed in a quartzite from the Tauern Window, Eastern Alps, experienced a clockwise P-T-t path with maximal burial depths of 35-40 km (10-11 kbar), peak temperatures of ~550°C and major deformation preceding peak thermal conditions. The primary tourmaline of the tourmalinite clast, generation-1, is texturally and compositionally heterogeneous, ranging from schorl to dravite [Mg / (Mg + Fe) = 0.27 - 0.61] with highly-variable Al consistent X X with combinations of the Al(NaR)-1 and AlO(R(OH))-1 exchange vectors, where represents X-site vacancy and R is Fe2+ + Mn + Mg. Generation-2 tourmaline is manifest as distinctive compo- sitionally-asymmetric bands of colorless foitite (zone 1) and blue schorl (zone 2) replacing genera- tion-1 tourmaline. Replacement takes place along a scalloped margin and advances preferentially towards the analogous pole (-c) of generation-1 tourmaline. The two zones of generation-2 range from foitite to schorl with a restricted ratio of Mg / (Mg + Fe) of 0.32 - 0.41, but with variable X, X Al, Na and R predominantly reflecting Al(NaR)-1. -
Khmaralite, a New Beryllium-Bearing Mineral Related to Sapphirine: a Superstructure Resulting from Partial Ordering of Be, Al, and Si on Tetrahedral Sites
American Mineralogist, Volume 84, pages 1650–1660, 1999 Khmaralite, a new beryllium-bearing mineral related to sapphirine: A superstructure resulting from partial ordering of Be, Al, and Si on tetrahedral sites JACQUES BARBIER,1,* EDWARD S. GREW,2 PAULUS B. MOORE,3 AND SHU-CHUN SU4 1Department of Chemistry, McMaster University, Hamilton, Ontario, L8S 4M1 Canada 2Department of Geological Sciences, University of Maine 5790 Bryand Center Orono, Maine 04469, U.S.A. 3P.O. Box 703, Warwick, New York,10990, U.S.A. 4Hercules Research Center, 500 Hercules Road, Wilmington, Delaware 19808, U.S.A. ABSTRACT 3+ 2+ Khmaralite, Ca0.04Mg5.46Fe 0.12Fe 1.87Al14.26Be1.43B0.02Si4.80O40, is a new mineral closely related to sapphirine from Khmara Bay, Enderby Land, Antarctica. It occurs in a pegmatite metamorphosed at T ≥ 820 °C, P ≥ 10 kbar. The minerals surinamite, musgravite, and sillimanite associated with khmaralite at Casey Bay saturate it in BeO, and thus its BeO content could be close to the maximum possible. Optically, khmaralite is biaxial (–); at λ = 589 nm, α = 1.725(2), β = 1.740(2), γ = 1.741(2), 2Vmeas = 34.4 (1.8)°, v > r strong, and β b. The weak superstructure reported using electron diffraction has been confirmed by single-crystal X-ray diffraction. The superstructure corresponds to a doubling of the a axis in monoclinic sapphirine-2M (P21/c setting) with the following unit-cell parameters: a = 3 19.800(1), b = 14.371(1), c = 11.254(1) Å, β = 125.53(1)°, Z = 4, Dcalc = 3.61 g/cm . -
List of Abbreviations
List of Abbreviations Ab albite Cbz chabazite Fa fayalite Acm acmite Cc chalcocite Fac ferroactinolite Act actinolite Ccl chrysocolla Fcp ferrocarpholite Adr andradite Ccn cancrinite Fed ferroedenite Agt aegirine-augite Ccp chalcopyrite Flt fluorite Ak akermanite Cel celadonite Fo forsterite Alm almandine Cen clinoenstatite Fpa ferropargasite Aln allanite Cfs clinoferrosilite Fs ferrosilite ( ortho) Als aluminosilicate Chl chlorite Fst fassite Am amphibole Chn chondrodite Fts ferrotscher- An anorthite Chr chromite makite And andalusite Chu clinohumite Gbs gibbsite Anh anhydrite Cld chloritoid Ged gedrite Ank ankerite Cls celestite Gh gehlenite Anl analcite Cp carpholite Gln glaucophane Ann annite Cpx Ca clinopyroxene Glt glauconite Ant anatase Crd cordierite Gn galena Ap apatite ern carnegieite Gp gypsum Apo apophyllite Crn corundum Gr graphite Apy arsenopyrite Crs cristroballite Grs grossular Arf arfvedsonite Cs coesite Grt garnet Arg aragonite Cst cassiterite Gru grunerite Atg antigorite Ctl chrysotile Gt goethite Ath anthophyllite Cum cummingtonite Hbl hornblende Aug augite Cv covellite He hercynite Ax axinite Czo clinozoisite Hd hedenbergite Bhm boehmite Dg diginite Hem hematite Bn bornite Di diopside Hl halite Brc brucite Dia diamond Hs hastingsite Brk brookite Dol dolomite Hu humite Brl beryl Drv dravite Hul heulandite Brt barite Dsp diaspore Hyn haiiyne Bst bustamite Eck eckermannite Ill illite Bt biotite Ed edenite Ilm ilmenite Cal calcite Elb elbaite Jd jadeite Cam Ca clinoamphi- En enstatite ( ortho) Jh johannsenite bole Ep epidote -
The Crystal Structure of Aenigmatite E
THE AMERICAN MINERALOGIST, VOL. 56, MARCH-APRIL, 1971 THE CRYSTAL STRUCTURE OF AENIGMATITE E. CANNILLO AND F. MAZZI, Centro di studio del C.N.R. per la cristal- lografia struturale, Istituto di Mineralogia dell' Universita di Pavia, Italy. AND J. H. FANG, PAUL D. ROBINSON, AND Y. OHYA, Department of Geology, Southern Illinois University, Carbondale, Illinois, U.S.A. ABSTRACT Aenigmatite, Na2Fe.TiSi602Q, is triclinic PI, with a= 10.406(13), b = 10.813(14), c=8.926(6) A, <>= 104° 56'(9), ~=96°52'(11), 1'= 125°19'(6), and Z = 2. The structure was solved, independently and simultaneously, by Patterson syntheses and by the symbolic addition procedure. Three-dimensional refinement with 921 "observed" reflections (photo- graphic data) from a Naujakasik, Greenland, crystal gave RhkZ=0.075 and with 1501 "observed" reflections (counter data) from a Kola, Greenland crystal gave Rhkl=O.072. A distinct pseudo-monoclinic symmetry, based on a cell with parameters: 11m= 12.120, b1O=2X14.815, c1O=1O.406 A, <>10=90°4', ~1O=127°9', 1'10=89°44' (matrix of transforma- tion [011jI22/100j), Z = 8, emphasizes the similarity of its crystal structure with that of sapphirine [(Mg, Alh02(Si, Al)6018, a=11.266, b=14.401, c=9.929 A, ~=125 °46', Z=4, space group P2i!a]. The crystal structure consists of two sets of polyhedral layers parallel to the pseudo- monoclinic (100) plane which alternate along the x*-direction. The first layer is formed by Fe-octahedra, Ti-octahedra and distorted Na-square antiprisms and the second by [Si601s]" chains connected by Fe-octahedra. -
'Uravesmountain Artd-·
/' ;~~ . - . :-.--... -~~;~-'. ' ) ;;. :,~~., . -'uravesMountain artd-· . ',MagrudetMine·, " . WiIkes_ Lmeolll~Gee"'.- .··~-SOUth~(JeolegicalSoc~~ OOidebOOk;NWIlber~3B- - April- 23-25, 1999 -. GRAVES MOUNTAIN AND MAGRUDER MINE Compiled and Edited by: Marc V. Hurst and Cornelis Winkler III - GUIDEBOOK NtTMBER 38 Prepared for the Annual Field Trip of the Southeastern Geological Society April 23-25, 1999 Published by the Southeastern Geological Society P.O. Box 1634 Tallahassee, Florida 32302 TABLE OF CONTENTS LOCATIONS OF GRAVES MOUNTAIN AND MAGRUDERMINE...................................... 1 INTRODUCTION TO GRAVES MOUNTAIN by John S. Whatley, JM. Huber Corporation.................................................................3 PHOSPHATE MINERALS OF GRAVES MOUNTAIN, GEORGIA by Henry BatWood............. .............................................................................................5 GRAVES MOUNTAIN, SLATE BELT, GEORGIA GEOLOGY by Gilles O. Allard, University of Georgia.................................................................... 11 GEOLOGY AND ECONOMIC POTENTIAL OF THE MAGRUDER MINE AND VICINITY by Norman L. Bryan ..................................................................................................... 17 \ \ \ \ \ \ \ \ \ \ Magruder Mme ~\ \ ,\(". ~\1- "'..,.. \9 \'> <'\'ci0;: \ I I I I l-s £-''d C!.'s., "I~ ~ \«\ (>\~ o I' I \ i-20 \ \ I \ \ I \ \ \ \ ~ \ '\ '\ '\ LOCATIONS OF GRAVES MOUNTAIN AND MAGRUDER MINE 2 J 5 ! ! I Scole in Hites Ap,.it 15. 1'J'J'J INTRODUCTION TO GRAVES MOUNTAIN by John S.