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Developments in Uranium Resources, Production, Demand and the Environment
IAEA-TECDOC-1425 Developments in uranium resources, production, demand and the environment Proceedings of a technical committee meeting held in Vienna, 15–18 June 1999 January 2005 IAEA-TECDOC-1425 Developments in uranium resources, production, demand and the environment Proceedings of a technical committee meeting held in Vienna, 15–18 June 1999 January 2005 The originating Section of this publication in the IAEA was: Nuclear Fuel Cycle and Materials Section International Atomic Energy Agency Wagramer Strasse 5 P.O. Box 100 A-1400 Vienna, Austria DEVELOPMENTS IN URANIUM RESOURCES, PRODUCTION, DEMAND AND THE ENVIRONMENT IAEA, VIENNA, 2004 IAEA-TECDOC-1425 ISBN 92–0–112904–1 ISSN 1011–4289 © IAEA, 2005 Printed by the IAEA in Austria January 2005 FOREWORD Globalization has led to the growing importance of the uranium production industries of the world’s developing countries. Though trade restrictions continue to impede completely free access to the worldwide uranium market, the uranium resources and production capabilities of the developing countries are becoming increasingly important in assuring the adequacy of uranium supplies to meet projected worldwide demand. Therefore, papers presented at this meeting provide an important overview of uranium production operations in developing countries as well as offering insight into future production plans and potential. Along with their increasing contribution to worldwide uranium supply, the environmental impact of uranium production in developing countries has come under increasing scrutiny -
Uranium and Thorium Resources in India: UNFC System
Uranium and thorium resources in India: UNFC system P.S.Parihar Atomic Minerals Directorate for Exploration and Research Department of Atomic Energy Government of India 1 21/08/2013 Government of India’s Policy on Atomic Minerals The federal status of the DAE and the powers invested in it under the Indian Atomic Energy Act (1948 and 1962) as amended from time to time, bestow upon it several rights to facilitate atomic mineral exploration. The more significant ones are- . Exclusive rights to conduct exploration for uranium, thorium and other prescribed minerals such as beryllium, lithium, niobium, tantalum and rare-earth elements all over the country . Exclusive rights to buy prescribed minerals from private mine owners produced incidental to mining of other economic minerals. 30/10/2013 - . Rights to access to surface and sub-surface data on areas under exploration or mining/recovery for oil, coal, minerals and ground water by Government or Public Sector Organisations. The facility includes carrying out of gamma-ray logging of boreholes and checking of mine workings and collection of samples etc. 2 UNFC workshop, New Delhi workshop, UNFC Government of India’s Policy on Atomic Minerals Uranium exploration, production and utilisation are under the control of Central Government. Only public sector companies under Government of India are allowed to explore and mine atomic minerals viz. U, Th, etc. Present system of reporting of uranium reserves in India is as per the IAEA system of uranium resource classification . Indicated – [Reasonable -
Info Sheet This Is Followed by Heliborne Gamma-Ray Studies of Ore, As a Prelude to Commercial Mining
Research and Development: In order to multidisciplinary geoscientific skills. AMD will understand the genesis and controls of uranium continue its exploration efforts to fullfil the atomic ATOMIC MINERALS DIRECTORATE FOR mineralisation, basic research in the fields of minerals requirement of country’s nuclear power geology, geophysics, geochemistry and also programme. EXPLORATION AND RESEARCH (AMD) in allied topics such as physics, chemistry and electronics is being carried out. Atomic Minerals Directorate for Exploration spectrometric and geophysical surveys1 to identify Other Activities: and Research (AMD) is one of the oldest units potential targets with abnormal radioelemental *AMD is also entrusted to carry out geological / of Department of Atomic Energy (DAE) and plays concentration. geotechnical studies related to site selection for an important role in the front and back end of nuclear power plants and repositories for the the nuclear fuel cycle. AMD was established as The potential areas delineated by heliborne disposal of radioactive wastes generated from Rare Minerals Survey Unit in 1949, subsequently surveys are taken up for ground reconnaissance these plants. renamed as Raw Materials Division (RMD) and radiometrics2 using portable gamma-ray *AMD provides professional and analytical brought under the Atomic Energy Commission measuring instruments such as Scintillometer, services. on October 3, 1950. RMD was later renamed as Gamma Ray Spectrometer etc., regional/detailed *AMD Studentship Programme has been initiated Atomic Minerals Division in 1958 and rechristened geological, geochemical (rock, soil, radon, water to impart basic field training and to encourage as Atomic Minerals Directorate for Exploration and and stream sediments) and ground-geophysical university students to take up their dissertation Research (AMD) in 1998. -
Iidentilica2tion and Occurrence of Uranium and Vanadium Identification and Occurrence of Uranium and Vanadium Minerals from the Colorado Plateaus
IIdentilica2tion and occurrence of uranium and Vanadium Identification and Occurrence of Uranium and Vanadium Minerals From the Colorado Plateaus c By A. D. WEEKS and M. E. THOMPSON A CONTRIBUTION TO THE GEOLOGY OF URANIUM GEOLOGICAL S U R V E Y BULL E TIN 1009-B For jeld geologists and others having few laboratory facilities.- This report concerns work done on behalf of the U. S. Atomic Energy Commission and is published with the permission of the Commission. UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1954 UNITED STATES DEPARTMENT OF THE- INTERIOR FRED A. SEATON, Secretary GEOLOGICAL SURVEY Thomas B. Nolan. Director Reprint, 1957 For sale by the Superintendent of Documents, U. S. Government Printing Ofice Washington 25, D. C. - Price 25 cents (paper cover) CONTENTS Page 13 13 13 14 14 14 15 15 15 15 16 16 17 17 17 18 18 19 20 21 21 22 23 24 25 25 26 27 28 29 29 30 30 31 32 33 33 34 35 36 37 38 39 , 40 41 42 42 1v CONTENTS Page 46 47 48 49 50 50 51 52 53 54 54 55 56 56 57 58 58 59 62 TABLES TABLE1. Optical properties of uranium minerals ______________________ 44 2. List of mine and mining district names showing county and State________________________________________---------- 60 IDENTIFICATION AND OCCURRENCE OF URANIUM AND VANADIUM MINERALS FROM THE COLORADO PLATEAUS By A. D. WEEKSand M. E. THOMPSON ABSTRACT This report, designed to make available to field geologists and others informa- tion obtained in recent investigations by the Geological Survey on identification and occurrence of uranium minerals of the Colorado Plateaus, contains descrip- tions of the physical properties, X-ray data, and in some instances results of chem- ical and spectrographic analysis of 48 uranium arid vanadium minerals. -
A New Method of the Qualitative Chemical Analysis of Common Cations
A New Method of the Qualitative Chemical Analysis of Common Cations by Keiichiro MATS UOKA* Introductory A qualitative analysis of inorganic substances is concerned with the methods of determining the species of base-forming and acid-forming constituents that are pre- sent in a substance. A qualitative analysis admits of twofold classification ; one is chemical and the other is physical method. Recent progress has introduced into the physical method many useful instruments and, for this reason, it is possible for the physical method to perform a very minute analysis in the accurate manner. Yet these instruments are regrettably too high to be within the reach of an average chemical laboratory. In any qualitative chemical analysis important procedures are separation, detec- tion and confirmatory test of the obtained result. With this method it is imperative that a very minute and accurate determination should be performed in less time. A chemical method is also divided into two kinds ; dry and wet methods. The former consists of heating test which contains blowpipe test as a sub-class and bead reaction including borax bead test, microscopic bead test, etc. Though the dry method is useful, its main value is derived from being used as a preliminary procedure. The latter method is further divided into four classes as follows. 1. Method by the use of H2S. 2. Method which uses substitutes for H2S. 3. Method which uses organic reagents instead of sulfide. 4. Method which detects each element on an individual basis. Methods in (1), (2) and (3) are systematic separating methods. And method in (1) and (2) are analyses based on the same principle. -
Salt Analysis(Qualitative Inorganic Chemistry)
AtoZ CHEMISTRY Salt Analysis Salt Analysis(Qualitative Inorganic Chemistry) 1. Solubility & Colour of Compounds 2. Properties of Gases & Compounds Q 1. Which one has the minimum solubility product? Q 1. Zn and Hg metals can be distinguished by using (A) AgCl (B) AlCl3 (A) NaOH (B) HCl (C) BaCl2 (D) NH4Cl (C) Both A & B (D) None of these Q 2. Which of the following sulphate is insoluble in Q 2. Which Metal dissolve in both NH3 & NaOH ? water? (A) Zn (B) Fe (A) CuSO4 (B) CdSO4 (C) Al (D) Pb (C) PbSO4 (D) Bi2(SO4)3 Q 3. Bromine is recognized by its Q 3. Mark the compound which is soluble in Hot (A) Pungent smelling dark red vapours water? (B) Ability to turn FeSO4 solution black (A) Lead Chloride (B) Mercurous chloride (C) Ability to turn starch iodide paper blue (C) Stronsium Sulphate (D) Silver chloride (D) Ability to dissolve in CS2 to give an orange Q 4. Which of the following basic radical is most colour to the organic layer difficult to precipitate? Q 4. Hydrochloric acid gas can be identified by its 3+ 2+ 2+ + (A) Characteristic pungent smell. (A) Fe (B) Cu (C) Ba (D) NH4 (B) Reaction with ammonia to give white fumes Q 5. Which of the following is most soluble in water? of NH4Cl. (A) AgCl (B) AgBr (C) Reaction AgNO3 to give white precipitate (C) AgI (D) AgF insoluble with in NH4OH. Q 6. PbCl2 dissolves in (D) Reaction with MnO2 to liberate Cl2 gas. (A) NH3 (B) H2O Q 5. -
Welding Inspection and Metallurgy
Welding Inspection and Metallurgy API RECOMMENDED PRACTICE 577 FIRST EDITION, OCTOBER 2004 --`,````,,,``,````,,,,,,``,,,,`-`-`,,`,,`,`,,`--- Copyright American Petroleum Institute Reproduced by IHS under license with API Licensee=YPF/5915794100 No reproduction or networking permitted without license from IHS Not for Resale, 12/07/2005 14:51:07 MST --`,````,,,``,````,,,,,,``,,,,`-`-`,,`,,`,`,,`--- Copyright American Petroleum Institute Reproduced by IHS under license with API Licensee=YPF/5915794100 No reproduction or networking permitted without license from IHS Not for Resale, 12/07/2005 14:51:07 MST Welding Inspection and Metallurgy Downstream Segment API RECOMMENDED PRACTICE 577 FIRST EDITION, OCTOBER 2004 --`,````,,,``,````,,,,,,``,,,,`-`-`,,`,,`,`,,`--- Copyright American Petroleum Institute Reproduced by IHS under license with API Licensee=YPF/5915794100 No reproduction or networking permitted without license from IHS Not for Resale, 12/07/2005 14:51:07 MST SPECIAL NOTES API publications necessarily address problems of a general nature. With respect to partic- ular circumstances, local, state, and federal laws and regulations should be reviewed. API is not undertaking to meet the duties of employers, manufacturers, or suppliers to warn and properly train and equip their employees, and others exposed, concerning health and safety risks and precautions, nor undertaking their obligations under local, state, or fed- eral laws. Information concerning safety and health risks and proper precautions with respect to par- ticular materials and conditions should be obtained from the employer, the manufacturer or supplier of that material, or the material safety data sheet. Nothing contained in any API publication is to be construed as granting any right, by implication or otherwise, for the manufacture, sale, or use of any method, apparatus, or prod- uct covered by letters patent. -
TDC Part I Paper I, Group B Inorganic Chemistry Department of Chemistry
TDC Part I Paper I, Group B Inorganic Chemistry Department of Chemistry L.S COLLEGE MUZAFFARPUR B. R. A. BIHAR UNIVERSITY Dr. Priyanka TOPIC: - p-block group 13 Oxides, oxoacids and hydroxides Oxides, oxoacids and hydroxides Trioxides of all elements (M2O3) are known Thallium forms the monoxide. On moving down the group, the basicity of the oxide increases along with increase in metallic character of the element. Thus B2O3 is acidic, Al2O3 and Ga2O3 amphoteric while In2O3 and Tl2O3 are basic. Tl2O is strongly basic; it dissolves in water forming TlOH, which is as strong a base as KOH. B2O3 is obtained by direct combination or by dehydration of boric acid. 2B + 3O2 B2O3 1000C red heat 2H3BO3 2HBO2 B2O3 Orthoboric acid -2H2O metaboric acid -H2O Being the oxide of a non-metal it is acidic in nature. It is the anhydride of boric acid. When fused with metal oxides or salts it forms metaborates. The metaborates of transition metals have characteristic colours and form the basis of borax-bead test of identification of metals. CoO + B2O3 Co(BO2)2 deep blue CuSO4 + B2O3 Cu(BO2)2 +SO3 Blue Cr2O3 + 3B2O3 2Cr(BO2)3 Green However when B2O3 is treated with strongly acidic compounds like phosphorus pentoxide, it is forced to behave as a base. B2O3 + P2O5 2BPO4 Aluminium oxide occurs in nature as bauxite and corundum and also as gemstones – ruby, emerald, sapphire etc. the colour is due to transition metal ions like iron, chromium, titanium etc. Anhydrous aluminium oxide exists in two forms- α-Al2O3 and r- Al2O3. -
Application No. AU 2008221580 Al (19) AUSTRALIAN PATENT OFFICE
(12) STANDARD PATENT APPLICATION (11) Application No. AU 2008221580 Al (19) AUSTRALIAN PATENT OFFICE (54) Title The technology of producing ferrotitanium (51) International Patent Classification(s) C22B 5/04 (2006.01) C22B 5/10 (2006.01) (21) Application No: 2008221580 (22) Date of Filing: 2008.09.25 Priority Data (31) Number (32) Date (33) Country 2007905269 2007.09.26 AU (43) Publication Date: 2009.04.09 (43) Publication Journal Date: 2009.04.09 (71) Applicant(s) Alexey Nosenkov;Nosenkova Margarita (72) Inventor(s) Nosenkov, Alexey;Nosenkova, Margarita (74) Agent Attorney Alexey Nosenkov, 50 Mundy Street, Mentone, VIC, 3194 THE TECHNOLOGY OF PRODUCING FERROTITANIUM 00 O Abstract. (N Method of alumothermal and carbothermal production of ferrotitanium has been offered. Charge consisting of oxides of titanium, iron, calcium and metallic aluminum is being heated to V) the temperature of 800-1000OC and set on fire with ignition mixture. Carbon can be used instead of aluminum. As the second option the following process is offered: titanium oxide is being mixed with any source of carbon (soot, coal etc.), heated and soaked at temperatures up to 1000 0C-25000 C. Then in the process of melting oxides of titanium, iron and/or metallic iron are being added. 00 00 (N, THE TECHNOLOGY OF PRODUCING FERROTITANIUM 00 0 Ferrotitanium is a metallic alloy of titanium and iron and it is widely used as an active alloying Cq addition in the production of stainless and interstitial free steels. Traditionally ferrotitanium is produced by using metallic scrap. However production of ferrotitanium by reduction of titanium V oxides did not find wide application due to the absence of robust technology that would allow to produce ferrotitanium with 70% titanium contents. -
Assessment of the Risk to Consumers from Borates and the Impact of Potential Restrictions on Their Marketing and Use
Ref. Ares(2014)76743 - 15/01/2014 Assessment of the Risk to Consumers from Borates and the Impact of Potential Restrictions on their Marketing and Use Final Report prepared for European Commission DG Enterprise and Industry RPA November 2008 Assessment of the Risk to Consumers from Borates and the Impact of Potential Restrictions on their Marketing and Use Final Report – November 2008 prepared for European Commission Directorate-General Enterprise and Industry by Risk & Policy Analysts Limited, Farthing Green House, 1 Beccles Road, Loddon, Norfolk, NR14 6LT, UK Tel: +44 1508 528465 Fax: +44 1508 520758 Email: [email protected] Web: www.rpaltd.co.uk RPA REPORT – ASSURED QUALITY Project: Ref/Title J612/Borates In accordance with the Project Specifications and Approach: associated discussions with the Commission Report Status: Final Report Prepared by: Pete Floyd, Director Tobe Nwaogu, Senior Consultant Nigel Tuffnell, Consultant Approved for issue by: Pete Floyd, Director Date: 25 November 2008 If printed by RPA, this report is published on chlorine free, 100% recycled paper. While RPA considers that the information and opinions given in this report are sound, the report is based on assumptions and information that are subject to uncertainties. Due to such uncertainties and because events may not occur as expected, there is a possibility that the results presented in this report will be different from situations which occur in the future. This report has been prepared for the client in accordance with the associated contract and RPA will accept no liability for any loss or damage arising out of the provision of the report to third parties. -
Dry Tests Physical Examination in Physical
www.thechemistryguru.com 1 Dry Tests Physical Examination In physical examination of compound colour, smell, density etc, are observed. Physical Examination Observation Inference (A) colour of Compound 2+ 2 (i) Blue, Whose aqueous Hydrated salts of Cu (except CO3 solution is also blue. and Cl-) (ii) Blue, Whose aqueous Anhydrous salts of cobalt solution is pink (iii) Colourless substance Transition metals absent (except some salts of Mn2+) (iv) Green, Whose aqueous Slats of Ni2+, Cr3+ solution is also green and on dilution colour is not changed too much (v) yellow-green, aqueous Salts if Fe2+ solution is light green or almost colourless (vi) Yellow-brown, aqueous Salts of Fe3+ solution is yellow (vii) Violet-pink, aqueous Salts of cobalt solution is pink www.thechemistryguru.com 2 (viii) Black, Substance. CuO, Nio, SnO, FeS, CuS, HgS, PbS, NiS, CoS, CuBr2, Ag2S, Cu2S, MnO2, Fe3O4, FeO, Co3O4, Ni2O3 etc. (ix) Brown Substance CdO, PbO2, SnS, Bi2S3 MnCO3 (pale brown), CuCrO4, SnS. (x) Yellow substance Bi2O3, CdS, SnS2, As2S3, PbI2, Chromates, As2S5, AgI etc. (xi) Red substance Cu2O, HgO, Pb3O4, HgI2 etc. 2 (xii) Orange substance Cr2 O 7 salts, Sb2S3 etc. (xiii) Green substance K2MnO4, Carbonate or Chloride ofCu2+ (xiv) Light pink Hydrated Mn2+ salts (xv) Purple. KMnO4 & other permanganates, some Cr3+ salts. (B) Odour of Compound (i) Ammonical smell NH4 salts (ii) Vinegar like smell Acetates (iii) Like smell from rotten S2- salts. eggs. (C) Density (i) Mixture or salt is heavy Hg and Pb salts (ii) Mixture or salt is light. Salts of Zn, Al, Bi, Ca, Ba, Sr, Mg etc. -
Light Due to Multiple Surface-Plasmon-Polariton Waves
Pennsylvania State University Engineering Science and Mechanics 2012 ESM TODAY Abstract Book PRESENTATIONS (Presentation) SHAPE-CONTROLLABLE SYNTHESIS OF HYBRID STRUCTURES BY 3D HYDRODYNAMIC FOCUSING METHOD Mengqian Lu , Qingzhen Hao, Ahmad Ahsan Nawaz, Tony Jun Huang Department of Engineering Science and Mechanics, The Pennsylvania State University Biofunctionalized NEMS Laboratory, the Huang Research Group, PA-16802, USA Micro-/nano- structures (MNS) have shown reaction region contacts the top and bottom walls of potential applications in electronics, materials the microfluidic channels. The aggregation of the science and chemical, physical and biomedical product on the channel wall results in clogging of fields.[1] In micro/nano scale, the size or shape the channels, which substantially reduces the change can affect the materials properties, such as robustness and stability during synthesis process, optical, chemical, electrical properties.[2] and finally causes the failure of the device.[5] Therefore, it is very important to fabricate MNS with uniform size and shape. Three-dimensional (3D) HF method can provide uniform environment both horizontally and Conventional method, which simply mix reagents vertically and confined the reagent streams at the by vortex mixing, is difficult to control the size and center of the channel. Multi-step photolithography shape distribution of the product. During reaction, and assembly protocols have been developed for the addition of reagents, rate of stirring, local fabricating the 3D HF devices. However, these temperature and concentration fluctuations can methods require either tedious assembly of affect the forming process of the product. individual components or multiple alignments and Conventional method cannot make good control of exposures during mold fabrication.