"Drill-Hole" Franklinite by F.W
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Znucalite Cazn11(UO2)(CO3)3(OH)20 • 4H2O C 2001-2005 Mineral Data Publishing, Version 1
Znucalite CaZn11(UO2)(CO3)3(OH)20 • 4H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: n.d. Crystals are thin lamellar, to 100 µm, in spherical boxworklike aggregates; forms coatings. Physical Properties: Cleavage: Perfect on {010}. Hardness = n.d. D(meas.) = 3.01–3.1 D(calc.) = 3.15 Radioactive; may fluoresce intense yellow-green under SW and LW UV. Optical Properties: Translucent. Color: White, pale grayish yellow, yellow. Luster: Silky. Optical Class: Biaxial (–). Orientation: X = c; Y = b; Z = a. α = 1.556–1.563 β = 1.600 γ = 1.620–1.621 2V(meas.) = 50◦–60◦ 2V(calc.) = 66.4◦ Cell Data: Space Group: n.d. a = 10.72(1) b = 25.16(1) c = 6.325(4) Z = 2 X-ray Powder Pattern: Pˇr´ıbram, Czech Republic. 2.708 (100), 2.728 (90), 6.141 (78), 3.165 (70), 25.1 (62), 2.682 (56), 5.650 (54) Chemistry: (1) (2) (3) CO2 8.25 n.d. 8.14 UO3 17.42 18.51 17.64 ZnO 56.75 53.52 55.21 CaO 4.06 3.55 3.46 H2O 15.37 n.d. 15.55 Total 101.85 100.00 (1) Pˇr´ıbram,Czech Republic; by electron microprobe, average of 15 analyses, CO2 and H2O • by thermal analysis; corresponds to Ca1.15Zn11.01(UO2)0.96(CO3)2.97(OH)20.30 3.34H2O. (2) Mas-d’Alary deposit, France; by electron microprobe, average of 17 partial analyses; utilizing • CO2 and H2O from (1), corresponds to Ca1.02Zn10.70(UO2)1.06(CO3)3.06(OH)19.44 4.16H2O. -
TRAVERTINE-MARL DEPOSITS of the VALLEY and RIDGE PROVINCE of VIRGINIA - a PRELIMINARY REPORT David A
- Vol. 31 February 1985 No. 1 TRAVERTINE-MARL DEPOSITS OF THE VALLEY AND RIDGE PROVINCE OF VIRGINIA - A PRELIMINARY REPORT David A. Hubbard, Jr.1, William F. Gianninil and Michelle M. Lorah2 The travertine and marl deposits of Virginia's Valley and Ridge province are the result of precipitation of calcium carbonate from fresh water streams and springs. Travertine is white to light yellowish brown and has a massive or concretionary structure. Buildups of this material tend to form cascades or waterfalls along streams (Figure 1). Marl refers to white to dark yellowish brown, loose, earthy deposits of calcium carbonate (Figure 2). Deposits of these carbonate materials are related and have formed during the Quaternary period. This preliminary report is a compilation of some litei-ature and observations of these materials. A depositional model is proposed. These deposits have long been visited by man. Projectile points, pottery fragments, and firepits record the visitation of American Indians to Frederick and Augusta county sites. Thomas Jefferson (1825) wrote an account of the Falling Spring Falls from a visit prior to 1781. Aesthetic and economic considerations eontinue to attract interest in these deposits. 'Virginia Division of Mineral Resources, Charlot- Figure 1. Travertine waterfall and cascade series tesville, VA on Falling Springs Creek, Alleghany County, 2Department of Environmental Sciences, Univer- Virginia. Note man standing in center of left sity of Virginia, Charlottesville, VA margin. 2 VIRGINIA DIVISION OF MINERAL RESOURCES Vol. 31 Figure 2. An extensive marl deposit located in Figure 3. Rimstone dam form resulting from Frederick County, Virginia. Stream, in fore- precipitation of calcium carbonate in Mill Creek, ground, has incised and drained the deposit. -
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. -
Research School of Physical Sciences, Australian National University
604 SHORT COMMUNICATIONS (Na light) a 1"741, fl 1"746, y 1"755 (all • Ferrous iron was determined by fusion of the mineral in sodium metafluoroborate, following the procedure given by Groves (1951); water by a modified Penfield method, the minera] sample being heated in a silica tube for half an hour by an oxy-coal gas burner, the temperature reached being about 1300 ~ C. The number of metal atoms have been calculated on the basis of 48(0,0H) to the unit cell: Si 7.807, A1 17.163, Fe" 0-706, Ti 0-178, Mg 0.874, Fe" 2-515, Mn 0.015, Ca 0-064, OH 3-510; AI+Fe" 17.869 ; Fe"+Ti &c., 3.646. If Ti and Ca are grouped with Fe", Mg, and Mn, the resultant formula agrees best with that proposed by Juurinen (1956), namely Fe4AllsSisO4,(OH)4. Research School of Physical Sciences, 5[. J. SNELLING. Australian National University, Canberra, Australia. BAEROW (G.) et al., 1912a. Explanation of Sheet 65. Mem. Geol. Surv. Scotland. BARROW(G.), 1912b. Prec. Geol. Assoc., voh 23, p. 274. GROVES (A. W.), 1951. Silicate Analysis. 2nd edn., London. JIIVRI~N (A.), 1956. Ann. Acad. Scient. Fenn., ser. A, vol. 3, no. 47. Serpierite .from the Lake District. SEaP~ERITE, a basic sulphate of copper, zinc, and calcium, was first described in 1881 from the Camareza section of the Laurium mines in Greece; in 1927 Sir Arthur RusselP described a second occurrence at Ross Island, Killarney, Co. Kerry, in Ireland, this being the first and hitherto only known locality in the British Isles. -
Jarosewichite and a Related Phase: Basic Manganese Arsenates of the Chlorophoenicite Group from Franklin, New Jersey
American Mineralogist, Volume 67, pages 1043-1047,1962 Jarosewichite and a related phase: basic manganese arsenates of the chlorophoenicite group from Franklin, New Jersey Pe,re J. DUNN Department of Mineral Sciences Smit hsonian I nstit utio n Washington, D.C.20560 DoNelo R. Pr,econ Department of Geological Sciences University of Michigan Ann Arbor, Michigan 48109 PBrBn B. LBeveNs Department of Geology University of Delaware Newark, Delaware l97II eNo Wrllreu B. SIuuoNs Department of Earth Sciences University of New Orleans New Orleans. Louisiana 70148 Abstract Jarosewichite,Mn3+Mn3+(AsOn)(OH)0, is a new mineral, closely related to chloro- phoenicite,from the Franklin mine, Franklin, SussexCounty, New Jersey,where it occurs associatedwith andradite,franklinite, flinkite, cahniteand hausmannite.Jarosewichite is orthorhombic,space grotp C2lmLlm2lm,C222 or Cmm2,with a : 6.56(3),b : 25.20(10),c : 10.00(5)4,and Z : 8. The strongestlines in the X-ray powder difraction patternare (d, I, hkD2.669 100 222,082;3.91 60 042,061;1.788 50 (notindexed);2.503 30 242,261,004,0 l0 0. Jarosewichiteis dark red, occursin prismaticbarrel-shaped aggregates, has a density of 3.66(obs),3.70glcm3(calc).Itisbiaxial(-)withrefractiveindicesd= 1.780(5),p= 1.795(5)and y= 1.805(5);theorientationisX:a,Y: b,Z = c;pleochroismisweak,Z) X. Microprobeanalysis with Mn3+calculated, yields: FeO 0.4, MgO 2.l,CaO0.2,ZnO 1.2, MnO 42.3, Mn2O317.7 (IMn = 45.1 wt.%), AszOs24.0, with H2O 12.1 percent by difference,sum : 100.0percent. A secondmanganese arsenate from Franklin, New Jersey,is alsorelated to chlorophoen- icite, but may be heterogeneous.Although optical, chemicaland crystallographicproper- ties are characterized,there is sufficient ambiguity to deny it speciesstatus at this time. -
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. -
MINERALS and MINERAL VARIETIES from METAMORPHOSED Mn DEPOSITS of BISTRITA MOUNTAINS, ROMANIA
Acta Mineralogica-Petrographica, Abstract Series 1, Szeged, 2003 MINERALS AND MINERAL VARIETIES FROM METAMORPHOSED Mn DEPOSITS OF BISTRITA MOUNTAINS, ROMANIA HÎRTOPANU, P.1 & SCOTT, P.2 1 Geological Institute of Romania, Caransebeş 1, RO-78344 Bucharest, Romania. E-mail: [email protected] 2 Camborne School of Mines, Redruth, Cornwall, United Kingdom. The Bistrita Mountains belong to the Crystalline Meso- mation of some amphiboles and some pyroxenes into other zoic Zone of the East Carpathians, which consists of super- phases, there are drastical transformations of pyroxenes into posed Variscan and Alpine Nappes, overthrusted eastwards pyroxenoids (johannsenite into rhodonite), pyroxenoids into over the Flysch Zone. The manganese ore is contained by pyroxenoids (pyroxmangite into rhodonite), pyroxmangite Tulghes Group (Tg2 level) of the Variscan Putna Nappe, into manganogrunerite, garnets into garnets (spessartine- situated over the Pietrosu Bistritei Nappe and supporting the calderite into spessartine, spessartine into anisotropic spes- thrusting of the Rebra Nappe. All these Variscan nappes sartine-andradite-grossular), calderite into pyroxmangite- constitute the Alpine Sub-Bucovinian Nappe localised be- magnetite, etc. are the best evidences of continuous variation tween Alpine Infrabucovinian Nappe in the East and the of formation conditions. Alpine Bucovinian Nappe in the West. The Mn ore have a predominant carbonate rather than The mineralogy of Mn metamorphosed deposits from silicate mineralogical composition, which means a great CO2 Bistrita Mts. includes 328 minerals and mineral varieties. fluid control in the carbonation and dehydration processes They may count among the mineralogically the most com- along the many stages of the whole history of the ore and the plex deposits of the world. -
THE CRYSTAL STRUCTURE of CAHNITE, Cabaso4 (OH)4
THE CRYSTAL STRUCTURE OF CAHNITE, CaBAsO4 (OH)4 by Charles T. Prewitt S.B., M.I.T.AAT.rc (1955) SUBMITTED IN PARTIAL YULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE at the MASSACHUSETTS INSTITUTE OF TECHNOLOGY (1960) Signature of Author .,. ..... .. ... .... Department of>Geolgy nd Geophysics, May 20, 1960 Certified by . t -.. 4-w.Vi 4 ... .. ... , . Thesis Supervisor Accepted by . .* . .... ... Chairman, Departmental Committee on Graduate Students THE CRYSTAL STRUCTURE OF CAHNITE, Ca2 BAs04 (OH)4 Charles T. Prewitt Submitted to the Department of Geology on May 20, 1960 in partial fulfillment of the requirements for the degree of Master of Science. Cahnite is one of the few crystals which had been assigned to crystal class 4. A precession study showed that its diffraction sphol is 4/m I-/-, which contains space groups I4, I4E, and14/. Because of the known 4 morphology, it must be assigned to space group I4. The unit cell, whose dimensions are a = 7.11A, o = 6.201, contains two formula weights of Ca BAsO (OH)L. The structure was studied with the aid of in ensity medsurements made with a single-crystal diffractometer. Patterson s ntheses were first made for projections along the c, a, and 110 directions. The atomic numbers of the atoms are in the ratio As:Ca.0:B = 33:20:8:5, so that the Patterson peaks are dominated by the atom pairs containing arsenic as one member of the pair. Since there are only two arsenic atoms in a body-centered cell, one As can be arbitrarily assigned to the origin. -
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. -
Kinoshitalite (Ba,K)(Mg,Mn,Al)3Si2al2o10(OH)2
Kinoshitalite (Ba; K)(Mg; Mn; Al)3Si2Al2O10(OH)2 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Monoclinic. Point Group: 2=m: Forms small scales, < 1 mm. Physical Properties: Cleavage: 001 , perfect. Tenacity: Brittle. Hardness = 2.5{3 D(meas.) = 3.30 D(calc.) = 3.33 f g Optical Properties: Semitransparent. Color: Yellow-brown to colorless; light yellow to colorless in thin section. Luster: Vitreous. Optical Class: Biaxial ({). Pleochroism: X = very light yellow to light yellow; Y = Z = light yellow with brownish tinge. Absorption: Y Z > X. ® = 1.619 ¯ = 1.628{1.633 ° = 1.635 ' 2V(meas.) = 23± Cell Data: Space Group: C2=m: a = 5.345(3) b = 9.250(4) c = 10.256(8) ¯ = 99:99(6)± Z = 2 X-ray Powder Pattern: Noda-Tamagawa mine, Japan. 3.37 (100), 2.52 (55), 2.020 (55), 5.05 (50), 10.1 (45), 1.684 (15), 3.16 (5) Chemistry: (1) (2) (1) (2) SiO2 24.58 23.43 BaO 17.85 27.60 TiO2 0.16 Na2O 0.68 0.11 Al2O3 22.06 19.25 K2O 3.30 0.24 Fe2O3 0.71 1.87 F 0.21 + Mn2O3 3.24 H2O 2.90 FeO 0.04 H2O¡ 0.20 MnO 7.38 2.62 H2O 3.50 MgO 16.60 21.95 O = F 0.09 ¡ 2 CaO 0.05 0.05 Total 99.87 100.62 2+ (1) Noda-Tamagawa mine, Japan; corresponds to (Ba0:58K0:35Na0:11Ca0:01)§=1:05(Mg2:06Mn0:52 3+ 3+ Al0:22Mn0:21Fe0:04Ti0:01)§=3:06Si2:05Al1:94O10[(OH)1:62O0:33F0:06]§=2:01: (2) Netra, India; by electron microprobe, total Fe as Fe2O3; corresponding to (Ba0:93K0:03Na0:02Ca0:01)§=0:99 (Mg2:80Mn0:19Fe0:08)§=3:07Si2:01(Al1:94Fe0:05)§=1:99O10(OH)2: Polymorphism & Series: 1M, 2M1 polytypes. -
General Index
CAL – CAL GENERAL INDEX CACOXENITE United States Prospect quarry (rhombs to 3 cm) 25:189– Not verified from pegmatites; most id as strunzite Arizona 190p 4:119, 4:121 Campbell shaft, Bisbee 24:428n Unanderra quarry 19:393c Australia California Willy Wally Gully (spherulitic) 19:401 Queensland Golden Rule mine, Tuolumne County 18:63 Queensland Mt. Isa mine 19:479 Stanislaus mine, Calaveras County 13:396h Mt. Isa mine (some scepter) 19:479 South Australia Colorado South Australia Moonta mines 19:(412) Cresson mine, Teller County (1 cm crystals; Beltana mine: smithsonite after 22:454p; Brazil some poss. melonite after) 16:234–236d,c white rhombs to 1 cm 22:452 Minas Gerais Cripple Creek, Teller County 13:395–396p,d, Wallaroo mines 19:413 Conselheiro Pena (id as acicular beraunite) 13:399 Tasmania 24:385n San Juan Mountains 10:358n Renison mine 19:384 Ireland Oregon Victoria Ft. Lismeenagh, Shenagolden, County Limer- Last Chance mine, Baker County 13:398n Flinders area 19:456 ick 20:396 Wisconsin Hunter River valley, north of Sydney (“glen- Spain Rib Mountain, Marathon County (5 mm laths donite,” poss. after ikaite) 19:368p,h Horcajo mines, Ciudad Real (rosettes; crystals in quartz) 12:95 Jindevick quarry, Warregul (oriented on cal- to 1 cm) 25:22p, 25:25 CALCIO-ANCYLITE-(Ce), -(Nd) cite) 19:199, 19:200p Kennon Head, Phillip Island 19:456 Sweden Canada Phelans Bluff, Phillip Island 19:456 Leveäniemi iron mine, Norrbotten 20:345p, Québec 20:346, 22:(48) Phillip Island 19:456 Mt. St-Hilaire (calcio-ancylite-(Ce)) 21:295– Austria United States