Chapter 2 Minerals
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Download PDF About Minerals Sorted by Mineral Name
MINERALS SORTED BY NAME Here is an alphabetical list of minerals discussed on this site. More information on and photographs of these minerals in Kentucky is available in the book “Rocks and Minerals of Kentucky” (Anderson, 1994). APATITE Crystal system: hexagonal. Fracture: conchoidal. Color: red, brown, white. Hardness: 5.0. Luster: opaque or semitransparent. Specific gravity: 3.1. Apatite, also called cellophane, occurs in peridotites in eastern and western Kentucky. A microcrystalline variety of collophane found in northern Woodford County is dark reddish brown, porous, and occurs in phosphatic beds, lenses, and nodules in the Tanglewood Member of the Lexington Limestone. Some fossils in the Tanglewood Member are coated with phosphate. Beds are generally very thin, but occasionally several feet thick. The Woodford County phosphate beds were mined during the early 1900s near Wallace, Ky. BARITE Crystal system: orthorhombic. Cleavage: often in groups of platy or tabular crystals. Color: usually white, but may be light shades of blue, brown, yellow, or red. Hardness: 3.0 to 3.5. Streak: white. Luster: vitreous to pearly. Specific gravity: 4.5. Tenacity: brittle. Uses: in heavy muds in oil-well drilling, to increase brilliance in the glass-making industry, as filler for paper, cosmetics, textiles, linoleum, rubber goods, paints. Barite generally occurs in a white massive variety (often appearing earthy when weathered), although some clear to bluish, bladed barite crystals have been observed in several vein deposits in central Kentucky, and commonly occurs as a solid solution series with celestite where barium and strontium can substitute for each other. Various nodular zones have been observed in Silurian–Devonian rocks in east-central Kentucky. -
A Vibrational Spectroscopic Study of the Silicate Mineral Harmotome Â
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 137 (2015) 70–74 Contents lists available at ScienceDirect Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy journal homepage: www.elsevier.com/locate/saa A vibrational spectroscopic study of the silicate mineral harmotome – (Ba,Na,K)1-2(Si,Al)8O16Á6H2O – A natural zeolite ⇑ Ray L. Frost a, , Andrés López a, Lina Wang a,b, Antônio Wilson Romano c, Ricardo Scholz d a School of Chemistry, Physics and Mechanical Engineering, Science and Engineering Faculty, Queensland University of Technology, GPO Box 2434, Brisbane, Queensland 4001, Australia b School of Chemistry and Chemical Engineering, Tianjin University of Technology, No. 391, Bin Shui West Road, Xi Qing District, Tianjin, PR China c Geology Department, Federal University of Minas Gerais, Belo Horizonte, MG 31270-901, Brazil d Geology Department, School of Mines, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG 35400-00, Brazil highlights graphical abstract We have studied the mineral harmotome (Ba,Na,K)1- 2(Si,Al)8O16Á6H2O. It is a natural zeolite. Raman and infrared bands are attributed to siloxane stretching and bending vibrations. A sharp infrared band at 3731 cmÀ1 is assigned to the OH stretching vibration of SiOH units. article info abstract Article history: The mineral harmotome (Ba,Na,K)1-2(Si,Al)8O16Á6H2O is a crystalline sodium calcium silicate which has Received 31 March 2014 the potential to be used in plaster boards and other industrial applications. It is a natural zeolite with cat- Received in revised form 7 July 2014 alytic potential. Raman bands at 1020 and 1102 cmÀ1 are assigned to the SiO stretching vibrations of Accepted 28 July 2014 three dimensional siloxane units. -
Large-Scale Hydrothermal Zoning Reflectedin The
Canadian Mineralogist Vol. 27, pp. 383-400 (1989) LARGE-SCALE HYDROTHERMAL ZONING REFLECTED IN THE TETRAHEDRITE-FREIBERGITE SOLID SOLUTION, KENO HILL Ag-Pb-Zn DISTRICT, YUKON J.V. GREGORY LYNCH* Department of Geology, The University of Alberta, Edmonton, Alberta T6G 2E3 ABSTRACT en argent se distinguent aussi par une augmentation dans Ie nombre de cations dans leur formule chimique. Le rap- The zoned Keno Hill vein system of central Yukon port Sb/ As demeure uniformement eleve. extends laterally from a Cretaceous plutonic-metamorphic center and surrounding quartz-feldspar veins, to (Traduit par la Redaction) carbonate-Ag-Pb-Zn deposits, and further to peripheral veins having epithermal characteristics. Seven distinct Mots-cles: zonation hydrothermale, nappe aquifere, tetra- mineralogical zones are recognized, and the entire sequence edrite, solution solide, plutonique, epithermal, altera- is continuous from east to west in a 4O-km belt. The fault- tion, district de Keno Hill, Yukon. and fracture-controlled veins are stratabound to the brit- tle moderately dipping Keno Hill Quartzite unit, of Mis- INTRODUCTION sissippian age. The unit is graphitic and appears to have acted as a large-scale hydrothermal aquifer, restricting fluid This paper concerns the large-scale nature of the flow during minera1ization and" development of zoning predominantly to the lateral direction. Tetrahedrite is dis- Keno Hill hydrothermal system. A broad and con- tributed along a 25-km-Iong portion of the system, and is tinuous sequence of mineral zoning can be the principal ore mineral of Ag. Both Ag/Cu and Fe/Zn documented within veins distributed along an exten- values in tetrahedrite are highest at the outer extremity of sive portion of the Keno Hill Quartzite, which is the the system, where freibergite dominates over tetrahedrite; main host rock to the ore in the area. -
The Surface Reactions of Silicate Minerals
RESEARCH BULLETIN 614 SEPTEMBER, 1956 UNIVERSITY OF MISSOURI COLLEGE OF AGRICULTURE AGRICULTURAL EXPERIMENT STATION J. H. Longwell, Director The Surface Reactions Of Silicate Minerals PART II. REACTIONS OF FELDSPAR SURFACES WITH SALT SOLUTIONS. V. E. NASH AND C. E. MARSHALL (Publication authorized September 5, 1956) COLUMBIA, MISSOURI TABLE OF CONTENTS Introduction .......... .. 3 The Interaction of Albite with Salt Solutions . .. 4 The Interaction of Anorthite with Salt Solutions ........ .. 7 Relative Effectiveness of Ammonium Chloride and Magnesium Chloride on the Release of Sodium from Albite . .. 9 Surface Interaction of Albite with Salt Solutions in Methanol . .. 13 Experiments on Cationic Fixation ............................... 16 Detailed Exchange and Activity Studies with Individual Feldspars .......... .. 19 Procedure .. .. 20 Microcline . .. 21 Albite .................................................... 22 Oligoclase . .. 23 Andesine . .. 24 Labradori te . .. 25 Bytownite ................................................. 25 Anorthite . .. 27 Discussion ........ .. 28 Summary ..................................................... 35 References .. .. 36 Most of the experimental material of this and the preceding Research Bulletin is taken from the Ph.D. Thesis of Victor Nash, University of Missouri, June 1955. The experiments on cation fixation were carried our with the aid of a research grant from the Potash Rock Company of America, Lithonia, Georgia, for which the authors wish to record their appreciation. The work was part of Department of Soils Research Project No.6, entitled, "Heavy Clays." The Surface Reactions of Silicate Minerals PART II. REACTIONS OF FELDSPAR SURFACES WITH SALT SOLUTIONS. v. E. NASH AND C. E. MARSHALL INTRODUCTION The review of literature cited in Part I of this series indicates that little is known of the interaction of feldspar surfaces with salt solutions. The work of Breazeale and Magistad (1) clearly demonstrated that ex change reactions between potassium and calcium occur in the case of or thoclase surfaces. -
Analytical Methods to Differentiate Romanian Amber and Baltic Amber for Archaeological Applications
Cent. Eur. J. Chem. • 7(3) • 2009 • 560-568 DOI: 10.2478/s11532-009-0053-8 Central European Journal of Chemistry Analytical methods to differentiate Romanian amber and Baltic amber for archaeological applications Research Article Eugenia D. Teodor1*, Simona C. Liţescu1, Antonela Neacşu2, Georgiana Truică1 Camelia Albu1 1 National Institute for Biological Sciences, Centre of Bioanalysis, Bucharest, 060031, Romania 2 University of Bucharest, Faculty of Geology and Geophysics, Bucharest, 010041, Romania Received 27 August 2008; Accepted 02 March 2009 Abstract: The study aims to establish several definite criteria which will differentiate Romanian amber and Baltic amber to certify the local or Baltic origin of the materials found in archaeological sites on the Romanian territory, by using light microscopy and performing analytical methods, such as Fourier transform infrared spectroscopy-variable angle reflectance and liquid chromatography with mass spectrometry detection. Experiments especially by Fourier transformed infrared spectroscopy, were applied to a wide range of samples with controlled origin. The methods were optimised and resulted in premises to apply the techniques to analysis of the archaeological material. Keywords: Romanian amber • FTIR-VAR • LC-MS • Light microscopy © Versita Warsaw and Springer-Verlag Berlin Heidelberg. 1. Introduction (Oligocene). The resin-bearing strata are intercalated within the lower and medium part of the lower Kliwa Amber is a fossil resin originating from different types sandstone (0.20-1.40 m). They consist of siliceous clay of Conifers and certain flowering trees, especially in hot (0.20-1.40 m) always containing thin intercalations of climates. From the mineralogical point of view amber bituminous shales (2-5 cm) and of preanthracite coal could be considered a mineraloid. -
Noritic Anorthosite Bodies in the Sierra Nevada Batholith
MINERALOGICAL SOCIETY OF AMERICA, SPECIAL PAPER 1, 1963 INTERNATIONALMINERALOGICAL ASSOCIATION,PAPERS, THIRD GENERAL MEETING NORITIC ANORTHOSITE BODIES IN THE SIERRA NEVADA BATHOLITH ALDEN A. LOOMISl Department of Geology, Stanford University, Stanford, California ABSTRACT A group of small noritic plutons were intruded prior to the immediately surrounding granitic rocks in a part of the composite Sierra Nevada batholith near Lake Tahoe. Iron was more strongly concentrated in the late fluids of individual bodies than during the intrusive sequence as a whole. Pyroxenes are more ferrous in rocks late in the sequence, although most of the iron is in late magnetite which replaces pyroxenes. Both Willow Lake type and normal cumulative layering are present. Cumulative layering is rare; Willi ow Lake layering is common and was formed early in individual bodies. Willow Lake layers require a compositional uniqueness providing high ionic mobility to explain observed relations. The Sierran norites differ from those in large stratiform plutons in that (1) the average bulk composition is neritic anorthosite in which typical rocks contain over 20% AbO" and (2) differentiation of both orthopyroxene and plagioclase produced a smooth progressive sequence of mineral compositions. A plot of modal An vs. En for all the rocks in the sequence from early Willow Lake-type layers to late no rite dikes defines a smooth non-linear trend from Anss-En76 to An,,-En54. TLe ratio An/ Ab decreased faster than En/Of until the assemblage Anso-En65 was reached and En/Of began to decrease more rapidly. Similar plots for large stratiform bodies show too much scatter to define single curves. -
Christie's Presents Jewels: the Hong Kong Sale
FOR IMMEDIATE RELEASE October 28, 2008 Contact: Kate Swan Malin +852 2978 9966 [email protected] CHRISTIE’S PRESENTS JEWELS: THE HONG KONG SALE Jewels: The Hong Kong Sale Tuesday, December 2 Christie’s Hong Kong Hong Kong – Christie’s announces the fall sale of magnificent jewellery, Jewels: The Hong Kong Sale, which will take place on December 2 at the Hong Kong Convention and Exhibition Centre. This sale features an exquisite selection of over 300 extraordinary jewels across a spectrum of taste and style, from masterpieces of the Belle Époque to contemporary creations, and from the rarest of white and coloured diamonds to important coloured stones. COLOURLESS DIAMONDS Leading the auction is a rare pair of D colour, Flawless diamonds weighing 16.11 and 16.08 carats (illustrated right, estimate: HK$40,000,000-60,000,000 / US$5,000,000-8,000,000). These marvellous stones are also graded ‘Excellent’ for polish, symmetry and cut grade, making them exceedingly rare for their superb quality. Classified as Type IIa, these diamonds are the most the chemically pure type of diamonds known, with no traces of the colorant nitrogen. The absence of this element, seen in 98% of diamonds, gives these stones a purity of colour and degree of transparency that is observed only in the finest white diamonds. The modern round brilliant cut is the diamond’s most basic and popular shape, as it allows the potential for the highest degree of light return. But more importantly, the round diamond sustains the highest value as its production requires riddance of the greatest amount of diamond rough. -
The Red Diamond
The Red Diamond John Fitzgerald Rob Floyd The Red Diamond Text and image copyright © John Fitzgerald and Rob Floyd 2012 Thalassa by Louis MacNeice is reproduced by kind permission of David Higham literary, film and TV agents. The authors would also like to thank Penguin Books for permission to quote from King Arthur and His Knights of the Round Table by Roger Lancelyn Green, and Colin Wilson for the phrase, ‘Imagination is the Herald of Change’. Contents Welcome The Sulphurous Heart Seekers in the Sunrise Britain is Our Playground Daughters of the Revolution The Arch of Constantine The Lantern Bearer Temenos The Mind and the World The Room of the Golden Dance Glittering Prize Rebel Angels Useful Idiots Panache, Power and Pride Visions and Ruins The God Abandons Antony The Red Diamond The Far Wall Welcome Man is in love with what abandons him. That’s the starting point of every quest. Meister Eckhart ******* Hello, thank you and welcome to The Red Diamond. We hope it stirs your imaginations and that you enjoy it in every way. The Red Diamond is essentially an Art Book, with Rob’s illustrations playing as central a role in the story’s unfolding as does my text. Our intent has not been so much to say, ‘this happened here, that happened there and here’s the picture to prove it’, but rather to allow words and pictures to come together in the hope of creating new contemplative spaces – evocative spaces – spaces of growth, possibility and playful creative change. The text tends therefore to concentrate more on atmosphere and mood than the adoption of a purely realistic approach to the story’s development. -
Carbonation and Decarbonation Reactions: Implications for Planetary Habitability K
American Mineralogist, Volume 104, pages 1369–1380, 2019 Carbonation and decarbonation reactions: Implications for planetary habitability k E.M. STEWART1,*,†, JAY J. AGUE1, JOHN M. FERRY2, CRAIG M. SCHIFFRIES3, REN-BIAO TAO4, TERRY T. ISSON1,5, AND NOAH J. PLANAVSKY1 1Department of Geology & Geophysics, Yale University, P.O. Box 208109, New Haven, Connecticut 06520-8109, U.S.A. 2Department of Earth and Planetary Sciences, Johns Hopkins University, 3400 N. Charles Street, Baltimore, Maryland 21218, U.S.A. 3Geophysical Laboratory, Carnegie Institution for Science, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 4School of Earth and Space Sciences, MOE Key Laboratory of Orogenic Belt and Crustal Evolution, Peking University, Beijing 100871, China 5School of Science, University of Waikato, 101-121 Durham Street, Tauranga 3110, New Zealand ABSTRACT The geologic carbon cycle plays a fundamental role in controlling Earth’s climate and habitability. For billions of years, stabilizing feedbacks inherent in the cycle have maintained a surface environ- ment that could sustain life. Carbonation/decarbonation reactions are the primary mechanisms for transferring carbon between the solid Earth and the ocean–atmosphere system. These processes can be broadly represented by the reaction: CaSiO3 (wollastonite) + CO2 (gas) ↔ CaCO3 (calcite) + SiO2 (quartz). This class of reactions is therefore critical to Earth’s past and future habitability. Here, we summarize their significance as part of the Deep Carbon Obsevatory’s “Earth in Five Reactions” project. In the forward direction, carbonation reactions like the one above describe silicate weathering and carbonate formation on Earth’s surface. Recent work aims to resolve the balance between silicate weathering in terrestrial and marine settings both in the modern Earth system and through Earth’s history. -
Chemical Oxides Analysis from Azara Baryte
African Journal of Pure and Applied Chemistry Vol. 1 (2), pp. 015-017, November 2007 Available online at http://www.academicjournals.org/AJCAB ISSN 1996 - 0840 © 2007 Academic Journals Short Communication Chemical oxides analysis from Azara Baryte Hauwa Isa Department of Science Laboratory Technology School of Applied Sciences, Nuhu Bamalli Polytechnic, Zaria Nigeria. E- mail: [email protected] Accepted 26 September, 2007 Physical and chemical analysis of the two samples A and B of Azara baryte were conducted, such as moisture content, loss on ignition and elemental composition by the use of atomic absorption spectrophotometer(ASS) and flame photometer. The oxides values in 1.000 g sample of each element were obtained. Sample A (lower layer): moisture content = 0.020, loss on ignition = 0.060, Na2O = 0.250, K2O = 0.015, CaO = 0.014, MgO = 0.018, Fe2O3 = 0.029, SiO2 = 9.310, BaO = 89.630, Al2O3 = 6.200 Sample B (upper layer): moisture content = 0.030, loss on ignition = 0.040, Na2O = 0.030, K2O = 0.001, CaO = 0.006, MgO = 0.030, Fe2O3 = 0.028, SiO2 =18.12, BaO = 65.020, Al2O3 = 16.120. The result of the analysis revealed that the Azara baryte could use as source of inorganic chemical oxides and for the production of some laboratory chemicals such as barium sulphate and aluminum oxides Key words: Azara Baryte,Chemical oxides,analysis INTRODUCTION Baryte (BaSO4) – Barium sulphate is found naturally in mineral collector's market (RMRDC, 2005) Natural bary- the form of witherite (Othmer, 1964). It has various tes are chemically stable and highly temperature-resis- colours but mostly yellow, isomorphous orthorhombic tant. -
Compilation of Reported Sapphire Occurrences in Montana
Report of Investigation 23 Compilation of Reported Sapphire Occurrences in Montana Richard B. Berg 2015 Cover photo by Richard Berg. Sapphires (very pale green and colorless) concentrated by panning. The small red grains are garnets, commonly found with sapphires in western Montana, and the black sand is mainly magnetite. Compilation of Reported Sapphire Occurrences, RI 23 Compilation of Reported Sapphire Occurrences in Montana Richard B. Berg Montana Bureau of Mines and Geology MBMG Report of Investigation 23 2015 i Compilation of Reported Sapphire Occurrences, RI 23 TABLE OF CONTENTS Introduction ............................................................................................................................1 Descriptions of Occurrences ..................................................................................................7 Selected Bibliography of Articles on Montana Sapphires ................................................... 75 General Montana ............................................................................................................75 Yogo ................................................................................................................................ 75 Southwestern Montana Alluvial Deposits........................................................................ 76 Specifi cally Rock Creek sapphire district ........................................................................ 76 Specifi cally Dry Cottonwood Creek deposit and the Butte area .................................... -
Carbonation and Decarbonation Reactions: Implications for Planetary Habitability K
American Mineralogist, Volume 104, pages 1369–1380, 2019 Carbonation and decarbonation reactions: Implications for planetary habitability k E.M. STEWART1,*,†, JAY J. AGUE1, JOHN M. FERRY2, CRAIG M. SCHIFFRIES3, REN-BIAO TAO4, TERRY T. ISSON1,5, AND NOAH J. PLANAVSKY1 1Department of Geology & Geophysics, Yale University, P.O. Box 208109, New Haven, Connecticut 06520-8109, U.S.A. 2Department of Earth and Planetary Sciences, Johns Hopkins University, 3400 N. Charles Street, Baltimore, Maryland 21218, U.S.A. 3Geophysical Laboratory, Carnegie Institution for Science, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 4School of Earth and Space Sciences, MOE Key Laboratory of Orogenic Belt and Crustal Evolution, Peking University, Beijing 100871, China 5School of Science, University of Waikato, 101-121 Durham Street, Tauranga 3110, New Zealand ABSTRACT The geologic carbon cycle plays a fundamental role in controlling Earth’s climate and habitability. For billions of years, stabilizing feedbacks inherent in the cycle have maintained a surface environ- ment that could sustain life. Carbonation/decarbonation reactions are the primary mechanisms for transferring carbon between the solid Earth and the ocean–atmosphere system. These processes can be broadly represented by the reaction: CaSiO3 (wollastonite) + CO2 (gas) ↔ CaCO3 (calcite) + SiO2 (quartz). This class of reactions is therefore critical to Earth’s past and future habitability. Here, we summarize their signifcance as part of the Deep Carbon Obsevatory’s “Earth in Five Reactions” project. In the forward direction, carbonation reactions like the one above describe silicate weathering and carbonate formation on Earth’s surface. Recent work aims to resolve the balance between silicate weathering in terrestrial and marine settings both in the modern Earth system and through Earth’s history.