Glaucochroite(Olivine, Camnsioo) from Franklin, New Jersey: Its Composition,Occurrence, and Formation Prrnn B
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
Metamorphism of Sedimentary Manganese Deposits
Acta Mineralogica-Petrographica, Szeged, XX/2, 325—336, 1972. METAMORPHISM OF SEDIMENTARY MANGANESE DEPOSITS SUPRIYA ROY ABSTRACT: Metamorphosed sedimentary deposits of manganese occur extensively in India, Brazil, U. S. A., Australia, New Zealand, U. S. S. R., West and South West Africa, Madagascar and Japan. Different mineral-assemblages have been recorded from these deposits which may be classi- fied into oxide, carbonate, silicate and silicate-carbonate formations. The oxide formations are represented by lower oxides (braunite, bixbyite, hollandite, hausmannite, jacobsite, vredenburgite •etc.), the carbonate formations by rhodochrosite, kutnahorite, manganoan calcite etc., the silicate formations by spessartite, rhodonite, manganiferous amphiboles and pyroxenes, manganophyllite, piedmontite etc. and the silicate-carbonate formations by rhodochrosite, rhodonite, tephroite, spessartite etc. Pétrographie and phase-equilibia data indicate that the original bulk composition in the sediments, the reactions during metamorphism (contact and regional and the variations and effect of 02, C02, etc. with rise of temperature, control the mineralogy of the metamorphosed manga- nese formations. The general trend of formation and transformation of mineral phases in oxide, carbonate, silicate and silicate-carbonate formations during regional and contact metamorphism has, thus, been established. Sedimentary manganese formations, later modified by regional or contact metamorphism, have been reported from different parts of the world. The most important among such deposits occur in India, Brazil, U.S.A., U.S.S.R., Ghana, South and South West Africa, Madagascar, Australia, New Zealand, Great Britain, Japan etc. An attempt will be made to summarize the pertinent data on these metamorphosed sedimentary formations so as to establish the role of original bulk composition of the sediments, transformation and reaction of phases at ele- vated temperature and varying oxygen and carbon dioxide fugacities in determin- ing the mineral assemblages in these deposits. -
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 -
Mineral Processing
Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19 -
Charlesite, a New Mineral of the Ettringite Group, from Franklin, New Jersey
American Mineralogist, Volume 68, pages 1033-1037,1983 Charlesite, a new mineral of the ettringite group, from Franklin, New Jersey PBre J. DuxN Department of Mineral Sciences SmithsonianInstitution, Washington,D. C. 20560 DoNero R. Peecon Department of GeologicalSciences University of Michigan, Ann Arbor, Michigan 48109 PBrnn B. LBavBNs Departmentof Geology Universityof Delaware, Newark, Delaware l97ll eNo JonN L. Beuu Franklin Mineral Museum Franklin. New Jersey 07416 Abstract Charlesite,ideally C4(AI,Si)z(SO4)2(B(OH)4)(OH,O)r2.26H2Ois a member of the ettrin- gite group from Franklin, New Jersey, and is the Al analogueof sturmanite. Chemical analysisyielded CaO27.3, Al2O3 5.1, SiO2 3.1, SO3 12.8,B2o33.2, H2O 48.6, sum : 100.1 percent.-Charlesiteis hexagonal,probable spacegroup P3lc, with a = ll.16(l), c = 21.21(2)4. The strongest lines in the X-ray powder difraction pattern (d, IlIo, hkl) are: 9.70,100, 100;5.58, 80, 110;3.855,80, ll4;2.749,70,304;2.538,70,126;2.193,70,2261 404. Charlesite occurs as simple hexagonal crystals tabular on {0001} and has a perfect {10T0}cleavage. The densityis 1.77glcm3 (obs.) and 1.79glcms (calc.). Optically, charlesite is uniaxial( -) with a : | .492(3)and e : 1.475(3).It occurswith clinohedrite,ganophyllite, xonotlite, prehnite, roeblingite and other minerals in severalparageneses at Franklin, New Jersey. Charlesite is named in honor of the late Professor Charles Palache. Introduction were approved, prior to publication, by the Commission Minerals and Mineral Names. I. M. A. The An ettringite-like mineral was first described from on New specimenwas divided into three portions. -
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. -
Sussexite Mn2+BO2(OH)
2+ Sussexite Mn BO2(OH) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. As bladed acicular crystals, to 7 mm; cross-vein or radial fibrous, in felted or matted aggregates, nodular. Twinning: Submicroscopic twinning on {100} which cannot be resolved optically. Physical Properties: Tenacity: Inflexible. Hardness = 3–3.5 D(meas.) = 3.30 D(calc.) = 3.335 Optical Properties: Semitransparent. Color: White to buff, straw-yellow, pale pink; colorless in transmitted light. Streak: White. Luster: Silky, dull, earthy. Optical Class: Biaxial (–). Orientation: Parallel extinction; X = elongation; Z ⊥ flattening. Dispersion: r> v. α= 1.670 β = 1.728 γ = 1.732 2V(meas.) = ∼25◦ Cell Data: Space Group: P 21/a. a = 12.866(3) b = 10.718(2) c = 3.287(1) β =94.75(3)◦ Z=8 X-ray Powder Pattern: N’chwaning II mine, South Africa. 6.43 (10), 2.773 (7), 3.34 (6), 2.632 (6), 2.494 (6), 2.741 (5), 2.694 (5) Chemistry: (1) (3) B2O3 30.52 30.33 FeO 0.16 MnO 49.40 61.82 MgO 9.56 CaO 2.03 H2O 8.33 7.85 Total [100.00] 100.00 (1) Franklin, New Jersey, USA; recalculated to 100% after deduction of willemite 4.5%. (2) N’chwaning II mine, South Africa; by electron microprobe, analysis not given; stated to correspond to (Mn0.95Mg0.05)Σ=1.00BO2(OH). (3) MnBO2(OH). Polymorphism & Series: Forms a series with szaib´elyite. Occurrence: A rare hydrothermal mineral typically in veinlets in boron-bearing metamorphosed Mn–Fe–Zn deposits. -
Download the Scanned
JOURNAL MINERALOGICAL SOCIETY OF AMERICA 193 Boyle, Blank, Biernbaum, Clay, Frankenfield, Gordon, Oldach, Knabe, and Trudell. At Branchville, albite crystals, beryl, margarodite, spodumene, and cyrnatolite were obtained; at East Hampton, golden beryl; at White Rocks, masses of pink and greenish tourmaline; at Strickland's quarry' green tourmaline, albite, beryl, and spoctumene. Ihe report was illustrated with lantern slides of photographs taken on the trip, and exhibits of specimens. Mr. George Vaux, Jr. described a trip to Franklin, N. J. with Mr. Gordon, where some exceptionally 6ne specimens were obtained, including the following minerals: apatite, copper, rhodonite, datolite, willemite, glaucochroite, Ieuco- phoenicite, hancockite, wernerite, franklinite, and arsenopyrite. Seuurr, G. Goroon, SecretarY, BOOK REVIEW A LIST OF NEW CRYSTAL FORMS OF MINERALS. Hnnstnr P Wurrrocr. Bur,retrn ol Tnr: Auenlcau Museunr ol NATURAT-Ifrsronv, Vor. xrvr, Ant. II, pp.89-278,1[ewYorh,1922. In July 1910, the author published. in The Sthool of Mines Quarterl,L (Vol. 31, No. 4 and VoI. 32, No. 1) a list of new crystal forms which had been recorded in the literature since the appearance of Goldschmidt's Index der Krystallformen der Mineralien (1336_91). The present bulletin includes the former data and extends the compilation to 1920, thus furnishing crystallographers with a most useful reference work covering a period of thirty years (1890-1920). References prior to 1890 being available in Goldschmidt's "Index." Where a new orientation of a species has been proposed and accepted, forms previously cited have been transposed to correspond with the new axial elements In such cases the elements used are given at the head of the species. -
Clinohedrite Caznsio4 ² H2O C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Monoclinic
Clinohedrite CaZnSiO4 ² H2O c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Monoclinic. Point Group: m: Crystals typically prismatic or tabular, to 4 mm; may be wedge-shaped re°ecting the domatic class in which the species crystallizes. Physical Properties: Cleavage: Perfect on 010 . Hardness = 5.5 D(meas.) = 3.28{3.335 D(calc.) = [3.32] Strongly pyroelectric. f g Optical Properties: Transparent to translucent. Color: Amethystine, colorless to white. Luster: Brilliant, glassy; pearly on 010 . f g Optical Class: Biaxial ({). Orientation: Z = b; Y c = 28±. ® = 1.662 ¯ = 1.667 ° = 1.669 2V(meas.) = Large. ^ Cell Data: Space Group: Cc: a = 5.090{5.131 b = 15.829{15.928 c = 5.386{5.422 ¯ = 103:39± 103:43± Z = 4 ¡ X-ray Powder Pattern: Franklin, New Jersey, USA. (ICDD 17-214). 2.76 (100), 3.23 (70), 2.50 (60), 7.81 (50), 3.97 (50), 2.36 (50), 2.47 (40) Chemistry: (1) (2) (3) SiO2 27.22 26.73 27.87 (Fe; Al)2O3 0.28 0.37 MnO 0.50 1.11 ZnO 37.44 37.13 37.76 MgO 0.07 CaO 26.25 26.25 26.01 + H2O 8.56 8.09 8.36 Total 100.32 99.68 100.00 (1) Franklin, New Jersey, USA; average of two analyses. (2) Do. (3) CaZnSiO4 ² H2O: Occurrence: In a metamorphosed stratiform zinc orebody (Franklin, New Jersey, USA). Association: Hancockite, nasonite, glaucochroite, roeblingite, calcite, willemite, axinite, larsenite, hodgkinsonite, franklinite (Franklin, New Jersey, USA); stringhamite, kinoite, apophyllite (Christmas mine, Arizona, USA). Distribution: From Franklin, Sussex Co., New Jersey; in the Christmas mine, Gila Co., Arizona, USA. -
The Picking Table Volume 27, No. 1 – Spring 1986
TABLE JOURNAL of the FRANKLIN-OGDENSBURG MINERALOGICAL SOCIETY, INC. SPRING. 1986 VOLUME 27, NO.l The contents of The Picking Table are licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. F.QM.S. Notes prise a spectacular fluorescent display. For PRESIDENT'S MESSAGE years the Gerstmann Mineral Museum has displayed the collection for the delight and With the melting of the snow, the rocks of education of amateur and professional mineralo- the Buckwheat Dump emerge from their white gists alike. The Franklin Mineral Museum mantle, and the seismic tremors rumble through is most grateful to Arthur and Harriet Mitteldorf the souls of the collector community. Whatever for this most generous donation and to Ewald Spring may mean to the average mortal, to Gerstmann for its accumulation and for his FOMS members it brings a special appeal to sponsorship of the Franklin Mineral Museum dig in the dirt, not to plant, but to explore as the recipient. Transfer of the collection again the crystalline mysteries of Nature. will be effected as soon as suitable space is available to house it. Let us not lose sight of the fact that we are a community, however widespread, dedicated JLB to a great common interest and purpose: the expansion and preservation of knowledge about the world's most remarkable mineral location. ABOUT THE COVER SKETCH Like all great enterprises, this demands the efforts and participation of many. To the Located Sphalerite Occurrences—Franklin Mine extent that we share our knowledge, our time, and our interest with each other and the world, It is suggested that you refer to this hand Franklin lives. -
Canadian Mineralogist, 51
785 The Canadian Mineralogist Vol. 51, pp. 785-800 (2013) DOI : 10.3749/canmin.51.5.785 A COMBINED GEOCHEMICAL AND GEOCHRONOLOGICAL INVESTIGATION OF NIOCALITE FROM THE OKA CARBONATITE COMPLEX, CANADA WEI CHEN§, ANTONIO SIMONETTI, AND PETER C. BURNS* Department of Civil & Environmental Engineering & Earth Sciences, 156 Fitzpatrick Hall, University of Notre Dame, Notre Dame IN, 46556 USA ABSTRACT This study is the first to report a detailed geochemical investigation and in situ U-Pb ages for niocalite, which occurs within carbonatite from the Bond Zone area of the Oka Carbonatite Complex (Canada). Niocalite is a Nb-disilicate member of the låvenite−cuspidine group. The major element composition of the niocalite studied here is relatively homogeneous with the average formula of: (Na0.34Fe0.06Mn0.19Mg0.09Ca13.40REE0.15Ti0.02)Σ14.25Nb2.12Ta0.06(Si2O7)4O7.65F2.44. Niocalite is enriched in minor and trace elements [i.e., Ta, Ti, and rare earth elements (REEs) up to 4.35 wt.%], with double- and triple-valenced elements (i.e., Sr, Y, REEs) substituting at different Ca-occupied lattice sites. The chondrite-normalized REE patterns for niocalite are LREE-enriched (~104 times chondrite) and negatively sloped. In addition, niocalite has higher HREE contents compared to those for co-existing apatite from the identical carbonatite sample. This result is expected based on bond valence data because of differing cation sizes. In situ U-Pb ages for niocalite from three carbonatite samples obtained by LA-ICP-MS define a wide range of ages, between ~111 and ~133 Ma. Niocalite from one carbonatite sample yields a bimodal distribution with weighted mean 206Pb/238U ages of 110.1 ± 5.0 Ma and 133.2 ± 6.1 Ma, and overlap those of co-existing apatite for the same sample. -
Zincite (Zn, Mn2+)O
Zincite (Zn, Mn2+)O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 6mm. Crystals rare, typically pyramidal, hemimorphic, with large {0001}, to 2.5 cm, rarely curved; in broad cleavages, foliated, granular, compact, massive. Twinning: On {0001}, with composition plane {0001}. Physical Properties: Cleavage: {1010}, perfect; parting on {0001}, commonly distinct. Fracture: Conchoidal. Tenacity: Brittle. Hardness = 4 VHN = 205–221 (100 g load). D(meas.) = 5.66(2) D(calc.) = 5.6730 Rare pale yellow fluorescence under LW UV. Optical Properties: Translucent, transparent in thin fragments. Color: Yellow-orange to deep red, rarely yellow, green, colorless; deep red to yellow in transmitted light; light rose-brown in reflected light, with strong red to yellow internal reflections. Streak: Yellow-orange. Luster: Subadamantine to resinous. Optical Class: Uniaxial (+). ω = 2.013 = 2.029 R1–R2: (400) 13.0–13.6, (420) 12.8–13.2, (440) 12.6–12.8, (460) 12.3–12.6, (480) 12.1–12.4, (500) 12.0–12.2, (520) 11.8–12.1, (540) 11.8–12.0, (560) 11.7–11.9, (580) 11.6–11.8, (600) 11.4–11.7, (620) 11.3–11.6, (640) 11.2–11.5, (660) 11.1–11.4, (680) 11.0–11.2, (700) 11.0–11.2 Cell Data: Space Group: P 63mc (synthetic). a = 3.24992(5) c = 5.20658(8) Z = 2 X-ray Powder Pattern: Synthetic. 2.476 (100), 2.816 (71), 2.602 (56), 1.626 (40), 1.477 (35), 1.911 (29), 1.379 (28) Chemistry: (1) (2) SiO2 0.08 FeO 0.01 0.23 MnO 0.27 0.29 ZnO 99.63 98.88 Total 99.99 [99.40] (1) Sterling Hill, New Jersey, USA. -
51St Annual Franklin-Sterling Gem and Mineral Show
ANNUAL Franklin - Sterling GEM & MINERAL SHOW SATURDAY & SUNDAY SEPTEMBER 29th & 30th, 2007 Sponsored By ;FRANKLIN. MI M I ; I' N 1 S F E R i U A i ■ N I I, '.--...., - Franklin, New Jersey The Fluorescent Mineral Capital Of The World STERLING HILL MINING MUSEUM 30 PLANT STREET OGDENSBURG, NJ 07439-1126 Welcome to The Sterling Hill Mine in Ogdensburg, NJ UNDERGROUND MINE TOURS • • • PASSAIC & NOBLE PIT • • COLLECTING OPEN TO THE PUBLIC • • • • During the Franklin-Sterling Hill Mineral Show, Sept. 30, 2007 • • Open Sunday, 9 AM to 3 PM • Admission: $5.00 per person, $1.50 per pound for anything taken • • • • • • STERLING HILL GARAGE SALE • • • • September 29th and 30th • Saturday and Sunday, from 11 AM to 3 PM • FRANKLIN MINE TOUR ADMISSION Citi N a. ADULT 10.00 CHILDREN (UNDER 12) 7.50 SENIOR CITIZEN (65+) 9.00 HOURS STERLING HILL OPEN 7 DAYS A WEEK MINING MUSEUM NEW YORK HOURS 10 AM TO 3 PM TOURS AT 1:00 PM DAILY OGDENSBURG & OTHER TIMES BY CHANCE I OR APPOINTMENT (:) GREEN THUMB FROM APRIL 1 TO NOV. 30 NURSERY MARCH AND DEC., WEEKENDS ONLY OTHER TIMES BY APPOINTMENT SPARTA JAN AND FEB., WEEKENDS ONLY FRANKLIN OTHER TIMES BY APPOINTMENT EXIT Nite Collecting Sat. Sept. 29th from 6-11 PM GROUP RATES AVAILABLE EXIT 34B For information call DOVER (973)209-7212 COLLECTING AVAILABLE FAX 973-209-8505 7 Days A Week, April to Nov. 10 AM to 3 PM www.sterlinghill.org MINERAL SPECIES FOUND AT FRANKLIN-STERLING HILL, NJ (Revised by FOMS Mineral List Committee September 2007) Acanthite Birnessite Cuprite Actinolite Bornite Cuprostibite Adamite Bostwickite