A (Sixth) List of New Mineral Names
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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 -
Mercury--Quicksilver
scueu« No. 12 Mineral Technology Series No 6 University of Arizona Bulletin Mercury---Quicksilver By P. E. JOSEPH SECOND ISSUE NOVEMBER, 1916. Entered as second class matter November 2:1, 191~, at the postoftice at Tucson, Arizona. under the Act ot August 24, 1912. Issued weekb". September to Ya)·. PUBLISHED BY THE University of Arizona Bureau of Mines CHARLES F. WILLIS, Director TUCSON, ARIZONA 1916-17 BIBLIOGRAPHY Bancroft, Howland. Notes on the occurrence of cinnabar in central western Arizona. U. S. G. S. Bull. 430, pp. 151-153, 1910. Becker, G. F. Geology of- the quicksilver deposits of the Pacific slope, with atlas. Mon. 13, p. 486, 1888. Only the atlas in stock. Quicksilver Ore Deposits; Mineral Resources U. S. for 1892, pp. 139-168, 1893. Christy, S. B. Quicksilver reduction at New Almaden, Cal. Min- eral Resources U. S. for 1883-1884, pp. 603-636, 1885. Hillebrand, W. F., and Schaller, W. T. Mercury miner-als from Terlingua, Tex. U. S. G. S. Bull. 405, pp. 174, 1909. McCaskey, H. D. Quicksilver in 1912; Mineral Resources U. S. for 1912, Pt. 1, pp. 931-948, 1913. Quicksilver in 1913-Production and Resources; Mineral Resources U. S. for 1913, Pt. 1, pp. 197-212, 1914. Melville, W. H., and Lindgren, Waldemar. Contributions to the mineralogy of the Pacific coast. U. S. G. S. Bull. 61, 30 pp., 1890. Parker, E. W. Quicksilver; Twenty-first Ann. Rept. U. S. G. S., Pt. 6, pp. 273-283, 1901. University of Arizona Bulletin BULLETIN No. 12 SECOND ISSUE, NOVEMBER, 1916 MERCURY-QUICKSILVER By P. -
Minerals of the System Stichtite–Pyroaurite–Iowaite–Woodallite from Serpentinites of the Terekta Ridge (Gorny Altai, Russia)
Russian Geology and Geophysics © 2020, V.S. Sobolev IGM, Siberian Branch of the RAS Vol. 61, No. 1, pp. 36–46, 2020 DOI:10.15372/RGG2019076 Geologiya i Geofizika Minerals of the System Stichtite–Pyroaurite–Iowaite–Woodallite from Serpentinites of the Terekta Ridge (Gorny Altai, Russia) E.S. Zhitovaa, , I.V. Pekovb, N.V. Chukanovb,c, V.O. Yapaskurtb, V.N. Bocharova aSt. Petersburg University, Universitetskaya nab. 7/9, St. Petersburg, 199034 Russia bLomonosov Moscow State University, Leninskie Gory GSP-1, Moscow, 119991, Russia cInstitute of Problems of Chemical Physics of RAS, pr. Akademika Semenova 1, Chernogolovka, 142432, Russia Received 26 April 2018; accepted 17 September 2018 Abstract—Hydrotalcite supergroup minerals stichtite, pyroaurite, iowaite, and woodallite form a complex solid-solution system at the Kyzyl-Uyuk locality (Terekta Ridge, Gorny Altai, Russia). The diversity of these minerals is due to: (1) subdivision by anionic interlayer composition into carbonate (stichtite and pyroaurite) and chloride (iowaite and woodallite) species and (2) isomorphism of M 3+ cations, mainly between Cr- (stichtite and woodallite) and Fe3+-dominant species (pyroaurite and iowaite), with a quantitative predominance of stichtite and iowaite. Most of the studied samples correspond to stichtite and woodallite with high Fe3+ contents or pyroaurite and iowaite with high Cr3+ contents. According to vibrational (IR and Raman) spectroscopy data, the interlayer Cl– is partially substituted by OH– rather 2– –1 than CO3 groups. We suppose that the presence/absence of a band in the region 1400–1350 cm in the Raman spectra of stichtite can be explained by the local distortion of triangular CO3 groups. -
Mount Lyell Abt Railway Tasmania
Mount Lyell Abt Railway Tasmania Nomination for Engineers Australia Engineering Heritage Recognition Volume 2 Prepared by Ian Cooper FIEAust CPEng (Retired) For Abt Railway Ministerial Corporation & Engineering Heritage Tasmania July 2015 Mount Lyell Abt Railway Engineering Heritage nomination Vol2 TABLE OF CONTENTS BIBLIOGRAPHIES CLARKE, William Branwhite (1798-1878) 3 GOULD, Charles (1834-1893) 6 BELL, Charles Napier, (1835 - 1906) 6 KELLY, Anthony Edwin (1852–1930) 7 STICHT, Robert Carl (1856–1922) 11 DRIFFIELD, Edward Carus (1865-1945) 13 PHOTO GALLERY Cover Figure – Abt locomotive train passing through restored Iron Bridge Figure A1 – Routes surveyed for the Mt Lyell Railway 14 Figure A2 – Mount Lyell Survey Team at one of their camps, early 1893 14 Figure A3 – Teamsters and friends on the early track formation 15 Figure A4 - Laying the rack rail on the climb up from Dubbil Barril 15 Figure A5 – Cutting at Rinadeena Saddle 15 Figure A6 – Abt No. 1 prior to dismantling, packaging and shipping to Tasmania 16 Figure A7 – Abt No. 1 as changed by the Mt Lyell workshop 16 Figure A8 – Schematic diagram showing Abt mechanical motion arrangement 16 Figure A9 – Twin timber trusses of ‘Quarter Mile’ Bridge spanning the King River 17 Figure A10 – ‘Quarter Mile’ trestle section 17 Figure A11 – New ‘Quarter Mile’ with steel girder section and 3 Bailey sections 17 Figure A12 – Repainting of Iron Bridge following removal of lead paint 18 Figure A13 - Iron Bridge restoration cross bracing & strengthening additions 18 Figure A14 – Iron Bridge new -
Optical Properties of Common Rock-Forming Minerals
AppendixA __________ Optical Properties of Common Rock-Forming Minerals 325 Optical Properties of Common Rock-Forming Minerals J. B. Lyons, S. A. Morse, and R. E. Stoiber Distinguishing Characteristics Chemical XI. System and Indices Birefringence "Characteristically parallel, but Mineral Composition Best Cleavage Sign,2V and Relief and Color see Fig. 13-3. A. High Positive Relief Zircon ZrSiO. Tet. (+) 111=1.940 High biref. Small euhedral grains show (.055) parallel" extinction; may cause pleochroic haloes if enclosed in other minerals Sphene CaTiSiOs Mon. (110) (+) 30-50 13=1.895 High biref. Wedge-shaped grains; may (Titanite) to 1.935 (0.108-.135) show (110) cleavage or (100) Often or (221) parting; ZI\c=51 0; brownish in very high relief; r>v extreme. color CtJI\) 0) Gamet AsB2(SiO.la where Iso. High Grandite often Very pale pink commonest A = R2+ and B = RS + 1.7-1.9 weakly color; inclusions common. birefracting. Indices vary widely with composition. Crystals often euhedraL Uvarovite green, very rare. Staurolite H2FeAI.Si2O'2 Orth. (010) (+) 2V = 87 13=1.750 Low biref. Pleochroic colorless to golden (approximately) (.012) yellow; one good cleavage; twins cruciform or oblique; metamorphic. Olivine Series Mg2SiO. Orth. (+) 2V=85 13=1.651 High biref. Colorless (Fo) to yellow or pale to to (.035) brown (Fa); high relief. Fe2SiO. Orth. (-) 2V=47 13=1.865 High biref. Shagreen (mottled) surface; (.051) often cracked and altered to %II - serpentine. Poor (010) and (100) cleavages. Extinction par- ~ ~ alleL" l~4~ Tourmaline Na(Mg,Fe,Mn,Li,Alk Hex. (-) 111=1.636 Mod. biref. -
Mercury Isotope Fractionation During Ore Retorting in the Almadén Mining District, Spain
Chemical Geology 357 (2013) 150–157 Contents lists available at ScienceDirect Chemical Geology journal homepage: www.elsevier.com/locate/chemgeo Mercury isotope fractionation during ore retorting in the Almadén mining district, Spain John E. Gray a,⁎, Michael J. Pribil a, Pablo L. Higueras b a U.S. Geological Survey, P.O. Box 25046, MS 973, Denver, CO 80225, USA b Universidad de Castilla-La Mancha, Plaza M. Meca 1, 13400 Almadén, Spain article info abstract Article history: Almadén, Spain, is the world's largest mercury (Hg) mining district, which has produced over 250,000 metric Received 28 May 2013 tons of Hg representing about 30% of the historical Hg produced worldwide. The objective of this study was to Received in revised form 20 August 2013 0 measure Hg isotopic compositions of cinnabar ore, mine waste calcine (retorted ore), elemental Hg (Hg (L)), Accepted 22 August 2013 and elemental Hg gas (Hg0 ), to evaluate potential Hg isotopic fractionation. Almadén cinnabar ore δ202Hg Available online 30 August 2013 (g) varied from −0.92 to 0.15‰ (mean of −0.56‰, σ = 0.35‰, n = 7), whereas calcine was isotopically heavier δ202 − ‰ ‰ ‰ σ ‰ δ202 Editor: J. Fein and Hg ranged from 0.03 to 1.01 (mean of 0.43 , =0.44 ,n = 8).Theaverage Hg enrichment of 0.99‰ between cinnabar ore and calcines generated during ore retorting indicated Hg isotopic mass depen- Keywords: dent fractionation (MDF). Mass independent fractionation (MIF) was not observed in any of the samples in Mercury isotopes this study. Laboratory retorting experiments of cinnabar also were carried out to evaluate Hg isotopic fractionation 0 0 0 Retorting of products generated during retorting such as calcine, Hg (L),andHg(g). -
C:\Documents and Settings\Alan Smithee\My Documents\MOTM
Itkx1//7Lhmdq`knesgdLnmsg9Rshbgshsd Our ongoing search for new minerals to feature finds us scouring the more than forty separate shows that comprise the Tucson Gem & Mineral show every year, looking for large lots of interesting and attractive minerals. The search is rewarded when we make a new contact and find something especially vibrant like this month’s combination of lavender stichtite in green serpentinite! OGXRHB@K OQNODQSHDR Chemistry: Mg6Cr2(CO3)(OH)16A4H2O Basic Hydrous Magnesium Chromium Carbonate (Hydrous Magnesium Chromium Carbonate Hydroxide) Class: Carbonates Subclass: Carbonates with hydroxyl or halogen radicals Group: Hydrotalcite Crystal System: Trigonal Crystal Habits: Crystals rarely macroscopic; usually as crust-like aggregates in matrix; sometimes radiating, micaceous with flexible plates, and nodular with tuberous, irregular surface projections; also massive and fibrous. Color: Lavender, lilac, light violet, pink, or purplish. Luster: Waxy, greasy, sometimes pearly. Transparency: Transparent to translucent Streak: White to pale lilac Refractive Index: 1.516-1.542 Cleavage: Perfect in one direction Fracture: Uneven, brittle. Hardness: 1.5-2.0 Specific Gravity: 2.2 Luminescence: None Distinctive Features and Tests: Softness, color, crystal habits, occurrence in chromium-rich metamorphic environments, and frequent association with serpentinite (a greenish metamorphic rock). Stichtite can be confused with similarly colored sugilite [potassium sodium iron manganese aluminum lithium silicate, KNa2(Fe,Mn,Al)2Li2Si12O30]. -
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 -
Stichtite Mg6cr2co3(OH)16∙4H2O - Crystal Data: Hexagonal
Stichtite Mg6Cr2CO3(OH)16∙4H2O - Crystal Data: Hexagonal. Point Group: 3 2/m or 6/m 2/m 2/m. As aggregates of fibers or plates, commonly matted, contorted; as cross-fiber veinlets and micaceous scales. Physical Properties: Cleavage: Perfect on {0001}. Tenacity: Laminae flexible, not elastic; greasy feel. Hardness = 1.5-2 D(meas.) = 2.16 D(calc.) = 2.11 Optical Properties: Transparent. Color: Lilac to rose-pink; lilac to rose-pink in transmitted light. Streak: Very pale lilac to white. Luster: Waxy to resinous, somewhat pearly. Optical Class: Uniaxial (–); may be anomalously biaxial. ω = 1.545(3) ε = 1.518(3) 2V(meas.) = Small. Pleochroism: Weak; O = dark rose-pink to lilac; E = light rose-pink to lilac. - Cell Data: Space Group: R3 m. a = 3.09575(3) c = 23.5069(6) Z = 3/8 (stichtite-3R) Space Group: P63/mmc. a = 3.09689(6) c = 15.6193(8) Z = 1/4 (stichtite-2H) X-ray Powder Pattern: Dundas, Tasmania, Australia. (ICDD 14-330) 7.8 (100), 3.91 (90), 2.60 (40), 2.32 (30), 1.97 (30), 1.54 (20), 1.51 (20) Chemistry: (1) (2) Al2O3 2.30 Fe2O3 4.18 Cr2O3 14.15 23.24 MgO 37.72 36.98 H2O 34.14 33.05 CO2 7.15 6.73 Total [100.00] 100.00 (1) Dundas, Tasmania, Australia; probably intermixed with stichtite-2H, original total of 99.27% recalculated to 100% after deduction of SiO2 2.09%, FeO 0.28% as chromite. (2) Mg6Cr2(CO3)(OH)16•4H2O. Polymorphism & Series: Polytypes 3R and 2H (formerly barbertonite). -
Clintonite-Bearing Assemblages in Chondrodite Marbles from the Contact Aureole of the Tøebíè Pluton, Moldanubian Zone, Bohemian Massif
Journal of the Czech Geological Society 51/34(2006) 249 Clintonite-bearing assemblages in chondrodite marbles from the contact aureole of the Tøebíè Pluton, Moldanubian Zone, Bohemian Massif Asociace obsahující clintonit v chondroditových mramorech moldanubika z kontaktní aureoly tøebíèského plutonu, Èeský masiv (6 figs, 4 tabs) STANISLAV HOUZAR1 MILAN NOVÁK2 1 Department of Mineralogy and Petrography, Moravian Museum, Zelný trh 6, CZ-659 37 Brno, Czech Republic; [email protected] 2 Institute of Geological Sciences, Masaryk University, Kotláøská 2, CZ-611 37 Brno, Czech Republic; [email protected] Clintonite is a minor to accessory mineral in chondrodite marbles. They represent a rare type of metacarbonate rocks in the Varied Unit of the Moldanubian Zone, forming thin bodies enclosed in migmatites. Clintonite occurs exclusively in marbles from contact aureole of melanocratic ultrapotassic granites (durbachites) of the Tøebíè Pluton. Chondrodite marbles consist of dominant calcite, less abundant dolomite; amounts of silicates vary from ~ 5 to 30 vol. %. The early mineral assemblage Dol+Cal+Prg ±Phl is replaced by the assemblage Chn+Cli+Cal ±Chl I ±Spl. Accessory minerals include fluorapatite, diopside, tremolite, pyrrhotite, and rare zircon and baddeleyite. Violet fluorite occurs on late fissures. Clintonite forms colourless to pale green flakes and sheaf-like aggregates, up to 2 mm in size. It has extraordinary high Si (2.7392.986 apfu) and Si/Al ratio (0.520.60). The contents of Fe (0.0410.128 apfu), Na (0.0350.134 apfu), tot Ti (0.0040.024 apfu) and K (≤ 0.005 apfu) are low. High concentrations of F (0.4371.022 apfu) corresponding up to 26 % of the F-component are the highest ever-recorded in clintonite. -
A Specific Gravity Index for Minerats
A SPECIFICGRAVITY INDEX FOR MINERATS c. A. MURSKyI ern R. M. THOMPSON, Un'fuersityof Bri.ti,sh Col,umb,in,Voncouver, Canad,a This work was undertaken in order to provide a practical, and as far as possible,a complete list of specific gravities of minerals. An accurate speciflc cravity determination can usually be made quickly and this information when combined with other physical properties commonly leads to rapid mineral identification. Early complete but now outdated specific gravity lists are those of Miers given in his mineralogy textbook (1902),and Spencer(M,i,n. Mag.,2!, pp. 382-865,I}ZZ). A more recent list by Hurlbut (Dana's Manuatr of M,i,neral,ogy,LgE2) is incomplete and others are limited to rock forming minerals,Trdger (Tabel,l,enntr-optischen Best'i,mmungd,er geste,i,nsb.ildend,en M,ineral,e, 1952) and Morey (Encycto- ped,iaof Cherni,cal,Technol,ogy, Vol. 12, 19b4). In his mineral identification tables, smith (rd,entifi,cati,onand. qual,itatioe cherai,cal,anal,ys'i,s of mineral,s,second edition, New york, 19bB) groups minerals on the basis of specificgravity but in each of the twelve groups the minerals are listed in order of decreasinghardness. The present work should not be regarded as an index of all known minerals as the specificgravities of many minerals are unknown or known only approximately and are omitted from the current list. The list, in order of increasing specific gravity, includes all minerals without regard to other physical properties or to chemical composition. The designation I or II after the name indicates that the mineral falls in the classesof minerals describedin Dana Systemof M'ineralogyEdition 7, volume I (Native elements, sulphides, oxides, etc.) or II (Halides, carbonates, etc.) (L944 and 1951). -
Titanian Clinohumite in the Carbonatites of the Jacupiranga
American Mineralogist, Volume 77, pages 168-178, 1992 Titanian clinohumite in the carbonatitesof the JacupirangaComplex, Brazil: Mineral chemistry and comparisonwith titanian clinohumite from other environments Josf C. Glspan Departamento de Mineralogia e Petrologia, Instituto de Geoci€ncias,Universidade de Brasilia, 70910 Brasilia DF, Brazil Ansrucr Titanian clinohumite (TiCl) occurs in the carbonatites of the Jacupiranga Complex, Brazil, either as the result of alteration of olivine (Mitchell, 1978) or in the reaction rock developed in the contact ofthe carbonatitesand the host magnetite pyroxenite, where it may not be related to olivine. Lamellae of titanian chondrodite (TiCh) are found, and the presenceof lamellae of polysomesrepresenting n > 4 is inferred. The TiCl samplescontain TiO, up to 3.78 wto/0,FeO up to 3.09 wto/0,and F up to 2.34 wto/o.Fe and Ti show a positive correlation. Complex zoning is always present. The only consistenttrend is that of increasingTiO, toward the margins, but even this trend is only observedin the crystals of the reaction rock. The partitioning of Fe and Mg between TiCl and olivine indicates enrichment of Mg in the TiCl and is different for samples from the three sovites. The characteristicsof the TiCl are thought to derive from a changing metasomatic environ- ment, and all TiCl so far reported from carbonatite complexesis possibly of metasomatic origin. The JacupirangaTiCl is similar in composition to TiCl from marbles, an obser- vation that cannot be extendedto TiCl from carbonatitesin general.Samples of TiCl from kimberlites have compositions similar to those from some Alpine peridotites. Fluorine TiCl is certainly stable in the upper mantle, but becauseof its rarity it is considered a mineral of no importance to mantle geology.