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WaTEn RESOURCESINVESTIGATIONS O'Brien and W J. Stone, 1984:Ground Water, Newpublications v.22, no. 6, pp.717-727. 83-4l18-B-Maps showing ground-water levels, Volcanogenic-exhalativetungsten mineralization springs, and depth to ground water, Basin and T{MBMMR of Proterozoic age near Santa Fe, New Mexico, Range Province, New Mexico, by B. T. Brady, *Circular L90--The skull of Sphenacodon and implicationsfor exploration,by M. S. Fulp ferocior, D. A. Mulvihill, D. L Hart, and W. H. Lan- and comoarisons with other sphenacodontines Jr., andJ.L. Renshaw,1985: Geology, v.73,pp.66- ger, 7984,6 pp., 2 sheets,scale 1:500,000 (ReptiliaiPelycosauria), by D.-A. Eberth, 1985, 69. 83-411.8-C-Maps showing distribution of dis- 39 pp., 2 tables, 39 figs $4.00 in Virtually complete, disarticulated cranial re- solved solids and dominant chemical type New 0pen-filereports ma\nsof Sohenacodonferociorfrom the Cutler and ground water, Basin and Range Province, and NMBMMR Abo Formations (Lower Permian) of north-cen- Mexico,by T. H. Thompson, R. Chappell, scale *215--Evaluation tral New Mexico are described in detail for the D. L. Hart, Jr., 7984, 5 pp., 2 sheets, of laboratory procedures for de- first time. These descriptions provide the basis 1:500,000. termining soil-water chloride, by B. E. McGurk for the most detailedcomparisons to datewithin 83-41.18-D-Map showing outcrops of granitic and W. f. Stone,1985, 36 pp., 12 tables,2 figs. and the subfamily Sphen- rocks and silicic shallow-intrusive rocks, Basin $7.20 the genus Sphenacodon *21.9-Geology acodontinae. -
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 -
Zektzerite, Nalizrsiuo,U: a Silicate with Six-Tetrahedral-Repeat Double
American Mineralogist, Volume 63, pages 304-310' 1978 Zektzerite, NaLiZrSiuO,u: a silicate with six-tetrahedral-repeatdouble chains SusnA.rnGHosn nNo Cus'Nc Wa'N Department of GeologicalSciences, Uniuersity of Washington Sealt le. Washinston98 I 95 Abstract : zektzerite, Nal-iZrSiuo,u, is orthorhombic, space group Cmca, with cell dimensions: a 14.330(2),b : 17.354(2),and c : 10.164(2)4;Z : 8.The crystal structurehas been determinedby the symbolic addition method and refinedby the method of leastsquares to an R factor of 0.040for 2389reflections, measured on an automaticsingle-crystal diffractometer. The crystal structureof zektzeriteis a three-dimensionalframework consistingof (a) edge- sharing Na-polyhedral chains, (b) octahedral-tetrahedralchains, formed by alternating Li tetrahedra andZr octahedrasharing edges, and (c) corrugateddouble-silicate chains with six- tetrahedraf repeat (Seclrser-Doppelkette)and three different four-membered rings. The Li tetrahedron,with an averageLi-O distanceof 1.959A,shows strong angular distortion. The Zr octahedronis nearly regular,with an averageZr-O distanceof 2.0'/4A.The sodium atom occurs in an irregular cavity formed by the corrugation of the silicatedouble chains; it is coordinatedto six oxygen atoms at distancesof 2.37-2.6'7A,and four more oxygenatoms at distancesof 3.12-3.23A.The averageSi-O bond lengthswithin the Si(l)' Si(2)' and Si(3) tetrahedraarel.6l4,l.6l6,andl.6l0A.TheSi-O-Si bondanglesinvolvingoxygenslyingon mirror planesaverage 155.7", whereas those within the singlesilicate chain averagel4'7.6". The larger Si-O-Si anglesare associatedwith shorter Si-O bonds. Zektzeriteis isostructural with tuhualite, (Na,K)Fer+Fe3+Si"O,u,and synthetic Na2MgrSiuo,r. -
Crystal Structure of Bage [Ge3 O9] and Its Relation to Benitoite
------------- ., JOURNAL OF RESEARCH of the National Bureau of Standards - A. Physics and Chemistry Vol. 70A, No.5, September-October 1966 Crystal Structure of BaGe [ Ge3 0 9 Jand Its Relation to Benitoite I I C. Robbins, A. Perloff, and S. Block ~ ( Institute for Materials Research, National Bureau of Standards, Washington, D.C. 20234 I (May 23, 1966) BaGe[Ge30gl is trigonal, space group P3, with lattice constants a= 11.61, c=4.74 A, and Z =3. The structure was established by three·dimensional Patterson and electron density syntheses. Three·dimensional least·squares refinement resulted in a final R value of 6.8 percent (observed data only). The previously proposed structural relationship of this compound with benitoite, BaTiSbOg, has been confirmed. The structure can be considered as composed of Ge30g rings, in which the Ge is tetrahedrally coordinated, linked through octahedrally coordinated Ge atoms to form a three·dimen· sional Ge·O network. All Ge polyhedra are linked by corner sharing. The Ba ions occupy positions in channels of the network. Key Words: Barium tetragermanate, structure, benitoite, crystal, x·ray. 1. Introduction Robbins and Levin [lJ. Their data plus the space group information are: The synthesis of three germanates of formula type MeGe4 0g (Me = Sr, Pb, Ba) was reported by Robbins a=lL61 A w= L797±0.003 and Levin [lJ .1 A comparison of indexed powder c=4.74A E= 1.783 ± 0.003 patterns suggested that the compounds were isostruc S.G.=P3 p (obs) = 5.1 gcm - 3 turaL This was later confirmed by Eulenberger, Z =3 p (calc) = 5.12 gcm- 3 Wittman, and Nowotny [2]. -
List of New Mineral Names: with an Index of Authors
415 A (fifth) list of new mineral names: with an index of authors. 1 By L. J. S~v.scs~, M.A., F.G.S. Assistant in the ~Iineral Department of the,Brltish Museum. [Communicated June 7, 1910.] Aglaurito. R. Handmann, 1907. Zeita. Min. Geol. Stuttgart, col. i, p. 78. Orthoc]ase-felspar with a fine blue reflection forming a constituent of quartz-porphyry (Aglauritporphyr) from Teplitz, Bohemia. Named from ~,Xavpo~ ---- ~Xa&, bright. Alaito. K. A. ~Yenadkevi~, 1909. BuU. Acad. Sci. Saint-P6tersbourg, ser. 6, col. iii, p. 185 (A~am~s). Hydrate~l vanadic oxide, V205. H~O, forming blood=red, mossy growths with silky lustre. Founi] with turanite (q. v.) in thct neighbourhood of the Alai Mountains, Russian Central Asia. Alamosite. C. Palaehe and H. E. Merwin, 1909. Amer. Journ. Sci., ser. 4, col. xxvii, p. 899; Zeits. Kryst. Min., col. xlvi, p. 518. Lead recta-silicate, PbSiOs, occurring as snow-white, radially fibrous masses. Crystals are monoclinic, though apparently not isom0rphous with wol]astonite. From Alamos, Sonora, Mexico. Prepared artificially by S. Hilpert and P. Weiller, Ber. Deutsch. Chem. Ges., 1909, col. xlii, p. 2969. Aloisiite. L. Colomba, 1908. Rend. B. Accad. Lincei, Roma, set. 5, col. xvii, sere. 2, p. 233. A hydrated sub-silicate of calcium, ferrous iron, magnesium, sodium, and hydrogen, (R pp, R',), SiO,, occurring in an amorphous condition, intimately mixed with oalcinm carbonate, in a palagonite-tuff at Fort Portal, Uganda. Named in honour of H.R.H. Prince Luigi Amedeo of Savoy, Duke of Abruzzi. Aloisius or Aloysius is a Latin form of Luigi or I~ewis. -
(12) United States Patent (10) Patent No.: US 7.449,161 B2 Boryta Et Al
USOO74491.61B2 (12) United States Patent (10) Patent No.: US 7.449,161 B2 Boryta et al. (45) Date of Patent: Nov. 11, 2008 (54) PRODUCTION OF LITHIUM COMPOUNDS 4,207,297 A * 6/1980 Brown et al. ............. 423,179.5 DIRECTLY FROM LITHIUM CONTAINING 4,243,641 A * 1/1981 Ishimori et al. .......... 423/179.5 BRINES 4.261,960 A * 4/1981 Boryta ............. ... 423,179.5 4,271,131. A * 6/1981 Brown et al. ...... ... 423,179.5 4,274,834. A 6/1981 Brown et al. .............. 23,302 R (75) Inventors: Daniel Alfred Boryta, Cherryville, NC 4,463,209 A * 7/1984 Kursewicz et al. .......... 585/467 (US); Teresita Frianeza Kullberg, 4,465,659 A * 8/1984 Cambridge et al. ......... 423,495 Gastonia, NC (US); Anthony Michael 4,588,565 A * 5/1986 Schultze et al. .......... 423,179.5 Thurston, Edmond, OK (US) 4,747.917 A * 5/1988 Reynolds et al. ............ 205,512 4,859,343 A * 8/1989 Frianeza-Kullberg (73) Assignee: Chemetall Foote Corporation, Kings et al. .......................... 210,679 Mountain, NC (US) 4,980,136 A * 12/1990 Brown et al. ... 423,179.5 5,049,233 A 9, 1991 Davis .......................... 216.93 (*) Notice: Subject to any disclaimer, the term of this 5,219,550 A * 6/1993 Brown et al. ............. 423 (419.1 patent is extended or adjusted under 35 5,599,516 A * 2/1997 Bauman et al. .......... 423/179.5 U.S.C. 154(b) by 0 days. 5,939,038 A * 8/1999 Wilkomirsky ............... 423,276 5.993,759 A * 1 1/1999 Wilkomirsky ........... -
The Secondary Phosphate Minerals from Conselheiro Pena Pegmatite District (Minas Gerais, Brazil): Substitutions of Triphylite and Montebrasite Scholz, R.; Chaves, M
The secondary phosphate minerals from Conselheiro Pena Pegmatite District (Minas Gerais, Brazil): substitutions of triphylite and montebrasite Scholz, R.; Chaves, M. L. S. C.; Belotti, F. M.; Filho, M. Cândido; Filho, L. Autor(es): A. D. Menezes; Silveira, C. Publicado por: Imprensa da Universidade de Coimbra URL persistente: URI:http://hdl.handle.net/10316.2/31441 DOI: DOI:http://dx.doi.org/10.14195/978-989-26-0534-0_27 Accessed : 2-Oct-2021 20:21:49 A navegação consulta e descarregamento dos títulos inseridos nas Bibliotecas Digitais UC Digitalis, UC Pombalina e UC Impactum, pressupõem a aceitação plena e sem reservas dos Termos e Condições de Uso destas Bibliotecas Digitais, disponíveis em https://digitalis.uc.pt/pt-pt/termos. Conforme exposto nos referidos Termos e Condições de Uso, o descarregamento de títulos de acesso restrito requer uma licença válida de autorização devendo o utilizador aceder ao(s) documento(s) a partir de um endereço de IP da instituição detentora da supramencionada licença. Ao utilizador é apenas permitido o descarregamento para uso pessoal, pelo que o emprego do(s) título(s) descarregado(s) para outro fim, designadamente comercial, carece de autorização do respetivo autor ou editor da obra. Na medida em que todas as obras da UC Digitalis se encontram protegidas pelo Código do Direito de Autor e Direitos Conexos e demais legislação aplicável, toda a cópia, parcial ou total, deste documento, nos casos em que é legalmente admitida, deverá conter ou fazer-se acompanhar por este aviso. pombalina.uc.pt digitalis.uc.pt 9 789892 605111 Série Documentos A presente obra reúne um conjunto de contribuições apresentadas no I Congresso Imprensa da Universidade de Coimbra Internacional de Geociências na CPLP, que decorreu de 14 a 16 de maio de 2012 no Coimbra University Press Auditório da Reitoria da Universidade de Coimbra. -
Rare Earth Element Potential of the Felsite Dykes of Phulan Area, Siwana Ring Complex, Rajasthan, India
SCIENTIFIC CORRESPONDENCE Rare earth element potential of the felsite dykes of Phulan area, Siwana Ring Complex, Rajasthan, India The global demand of rare earth elements (REE) is increasing at present due to their unique magnetic, high electrical and thermal conductance, fluorescent, chemi- cal properties and their uses in high- technology applications and in the quest for green energy. China, the largest pro- ducer of REE, has largely reduced its export since 2010. As a consequence, all the other countries in the world have in- tensified their search for REE to meet their demands. The present study may lead to enhancing the REE resources of India. The Neo-proterozoic Malani Igneous Suite occurring in western Rajasthan, west of the Aravalli Range, covering an area of 20,000 sq. km, is a favourable geological province for the search of REE and rare metals (RM)1,2 (S. Majum- dar; S. K. Rastogi and T. Mukherjee un- published). The well-studied Siwana Ring Complex (SRC), Rajasthan, India comprises bimodal volcanic sequence of basaltic and rhyolitic flows intruded by different phases of plutonic rocks like peralkaline granite, microgranite, felsite and aplite dykes, which are characterized by significant abundances of REE and RM (Figure 1). Earlier studies of SRC indicated 250 ppm Nb, 500 ppm La, Figure 1. Location map of the study area in Siwana Ring Complex, Barmer district, 700 ppm Y and greater than 1000 ppm Zr Rajasthan, India. on an average (S. Majumdar, unpub- lished). Anomalous concentrations of Rb, Ba, Sr, K, Zr, Nb, REE in granites and microgranites of SRC indicate the potentiality for RM and rare earth miner- alization1. -
New Minerals Approved Bythe Ima Commission on New
NEW MINERALS APPROVED BY THE IMA COMMISSION ON NEW MINERALS AND MINERAL NAMES ALLABOGDANITE, (Fe,Ni)l Allabogdanite, a mineral dimorphous with barringerite, was discovered in the Onello iron meteorite (Ni-rich ataxite) found in 1997 in the alluvium of the Bol'shoy Dolguchan River, a tributary of the Onello River, Aldan River basin, South Yakutia (Republic of Sakha- Yakutia), Russia. The mineral occurs as light straw-yellow, with strong metallic luster, lamellar crystals up to 0.0 I x 0.1 x 0.4 rnrn, typically twinned, in plessite. Associated minerals are nickel phosphide, schreibersite, awaruite and graphite (Britvin e.a., 2002b). Name: in honour of Alia Nikolaevna BOG DAN OVA (1947-2004), Russian crys- tallographer, for her contribution to the study of new minerals; Geological Institute of Kola Science Center of Russian Academy of Sciences, Apatity. fMA No.: 2000-038. TS: PU 1/18632. ALLOCHALCOSELITE, Cu+Cu~+PbOZ(Se03)P5 Allochalcoselite was found in the fumarole products of the Second cinder cone, Northern Breakthrought of the Tolbachik Main Fracture Eruption (1975-1976), Tolbachik Volcano, Kamchatka, Russia. It occurs as transparent dark brown pris- matic crystals up to 0.1 mm long. Associated minerals are cotunnite, sofiite, ilin- skite, georgbokiite and burn site (Vergasova e.a., 2005). Name: for the chemical composition: presence of selenium and different oxidation states of copper, from the Greek aA.Ao~(different) and xaAxo~ (copper). fMA No.: 2004-025. TS: no reliable information. ALSAKHAROVITE-Zn, NaSrKZn(Ti,Nb)JSi401ZJz(0,OH)4·7HzO photo 1 Labuntsovite group Alsakharovite-Zn was discovered in the Pegmatite #45, Lepkhe-Nel'm MI. -
Mineralogicai, Radiographic and Uranium Leaching Studies on the Uranium Ore from Kvanefjeld, Ilimaussaq Complex, South Greenland
T><2too/t6' Risø-R-416 Mineralogicai, Radiographic and Uranium Leaching Studies on the Uranium Ore from Kvanefjeld, Ilimaussaq Complex, South Greenland Milota Makovicky, Emil Makovicky, Bjarne Leth Nielsen, Svend Karup-Møller, and Emil Sørensen Risø National Laboratory, DK-4000 Roskilde, Denmark June 1980 RISØ-R-416 MINERALOGICAL, RADIOGRAPHIC AND URANIUM LEACHING STUDIES ON THE URANIUM ORE FROM KVANEFJELD, ILIMAUSSAQ. COMPLEX, 'SOUTH GREENLAND Milota Makovickyl , Emil Makovicky2, Bjarne Leth Nielsen-! , Sven Karuo-Møller^ and Emil Sørensen^ Abstract. 102 samples of low-grade uranium ore from 70 drill holes at Kvanefjeld, Ilimaussaq alkaline intrusion, South Green land were studied by means of autoradiography, fission-track investigations, microscopy, microprobe analyses and uranium- leaching experiments. The principal U-Th bearing mineral, steen- strupine, and several less common uranium minerals are dis seminated in lujavrite 'nepheline syenite) and altered volcanic rocks. Stenstrupine has a/erage composition Na6.7HxCai.n e Al (REE+Y)5.8(Th,l')o.5 ( ""1 . 6*" 1 . S^Q. 3^0. l 0. 2 ) Sii2036 (P4.3Si-) ,7 )024 (F,OH). nH20; n and x are variable. It either is of magmatic origin (type A) or connected with metasomatic processes (type B), or occurs in late veins (Type C). Preponder ance of grains are metamict (usually 2000-5000 ppm U3O8) or al tered (usually above 5000 ppm U3O8), sometimes zoned with both (continue on next page) June 1980 Pisø National Laboratory, DK-4000 Roskilde, Denmark components present. Occasionally they are extremely altered with U content falling to 500-5000 ppm U3O8 and local accumulations of high-U minerals formed. -
Reflective Index Reference Chart
REFLECTIVE INDEX REFERENCE CHART FOR PRESIDIUM DUO TESTER (PDT) Reflective Index Refractive Reflective Index Refractive Reflective Index Refractive Gemstone on PDT/PRM Index Gemstone on PDT/PRM Index Gemstone on PDT/PRM Index Fluorite 16 - 18 1.434 - 1.434 Emerald 26 - 29 1.580 - 1.580 Corundum 34 - 43 1.762 - 1.770 Opal 17 - 19 1.450 - 1.450 Verdite 26 - 29 1.580 - 1.580 Idocrase 35 - 39 1.713 - 1.718 ? Glass 17 - 54 1.440 - 1.900 Brazilianite 27 - 32 1.602 - 1.621 Spinel 36 - 39 1.718 - 1.718 How does your Presidium tester Plastic 18 - 38 1.460 - 1.700 Rhodochrosite 27 - 48 1.597 - 1.817 TL Grossularite Garnet 36 - 40 1.720 - 1.720 Sodalite 19 - 21 1.483 - 1.483 Actinolite 28 - 33 1.614 - 1.642 Kyanite 36 - 41 1.716 - 1.731 work to get R.I. values? Lapis-lazuli 20 - 23 1.500 - 1.500 Nephrite 28 - 33 1.606 - 1.632 Rhodonite 37 - 41 1.730 - 1.740 Reflective indices developed by Presidium can Moldavite 20 - 23 1.500 - 1.500 Turquoise 28 - 34 1.610 - 1.650 TP Grossularite Garnet (Hessonite) 37 - 41 1.740 - 1.740 be matched in this table to the corresponding Obsidian 20 - 23 1.500 - 1.500 Topaz (Blue, White) 29 - 32 1.619 - 1.627 Chrysoberyl (Alexandrite) 38 - 42 1.746 - 1.755 common Refractive Index values to get the Calcite 20 - 35 1.486 - 1.658 Danburite 29 - 33 1.630 - 1.636 Pyrope Garnet 38 - 42 1.746 - 1.746 R.I value of the gemstone. -
PABSTITE from the DARA-I-PIOZ MORAINE (TADJIKISTAN)
New data on minerals. M.: 2003. Volume 38 UDC 549.6 PABSTITE FROM THE DARA-i-PIOZ MORAINE (TADJIKISTAN) Leonid A. Pautov Fersman Mineralogical Museum of the Russian Academy of Science. Moscow, [email protected] Pabstite was discovered in the moraine of the Dara-i-Pioz glacier (Garmsky district, Tadjikistan) in a leuco- cratic rock mainly composed of microcline, quartz, and albite. Subordinated minerals are aegirine, titanite, astrophyllite, bafertisite, galena, sphalerite, ilmenite, pyrochlore, fluorite, zircon, fluorapatite, and calcite. Pabstite forms grains and well-faced crystals (0.1-0.5 mm), growing on quartz crystals in small cavities abun- dant in the rock. Its composition is close to the final member BaSnSi:P9 in the series pabstite-benitoite. Microprobe analysis has shown: SiO, - 37.43; Ti02 - 0.19; Zr02 - 0.16; Sn02 - 30.05; BaO - 32.41; total 100.24. The empirical formula is Balo2(Sno96Tio.01Zroo,)o98Si3o,09'Refraction parameters of pabstite are no = 1.668(2); 1.657(2), which is much lower than cited figures for pabstite from the type locality. Strong n" = dependence of pabstite optical properties on titanium contents is shown. The find of pabstite at Dara-i-Pioze is the first find of pabstite in alkaline rocks and, apparently, the second find of this mineral in the world. 2 tables, 3 figures and 13 references. Pabstite BaSnSi30g, the tin analogue of beni- aegirine syenites and foyaites. The first data on toite, was described as a new mineral from the massif were received at works of Tadjik- Santa Cruz (California, USA), where it was met Pamirs expedition of 1932 - 1936.