Travelogue Series Discovered This Element in a Cobalt Mine in Los, East of the Mine in the Center of Falun
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Hjalmar Fors, the Limits of Matter—Chemistry, Mining & Enlightenment
Miner Econ (2015) 28:131–132 DOI 10.1007/s13563-015-0071-2 BOOK REVIEW Hjalmar Fors, The Limits of Matter—Chemistry, mining & enlightenment The University of Chicago Press Chicago USA 2015 Magnus Ericsson1 Published online: 15 September 2015 # Springer-Verlag Berlin Heidelberg 2015 Swedish chemists have discovered more elements than scien- though at that time not united into one yet), France and tists from any other nation. Over more than 100 years, from England? Part of the answer is surprisingly bureaucratisation the early 18th century to the end of the 19th century, 20 ele- or the creation of an administrative institution called ments of which 18 metals or non-metals and 2 gases, nitrogen Bergskollegium in Swedish or English Bureau of Mines as and chlorine were independently isolated and described. Some Hjalmar Fors calls it in his new and path-breaking study of these are as follows: The Limits of Matter—Chemistry, mining & enlightenment. Another part is the need of improved processes and better Element Name Year of discovery yields in Swedish mines, which played such a vital role in Cobalt Brandt 1735 the Swedish economy during this period. The Swedish ruling Nickel Cronstedt 1751 groups saw these demands and founded the Bureau of Mines, Manganese Gahn 1774 which acted in several ways to solve problems, that had arisen in the mining industry. R&D in those days was highly Molybdenum Hjelm 1781 applied but nevertheless led to important purely scientific Yttrium Gadolin 1794 results. Tantalum Ekeberg 1802 The Bureau was set up in 1634 based on a predecessor, Cerium Berzelius 1803 which was started already in 1630. -
RBRC-32 BNL-6835.4 PARITY ODD BUBBLES in HOT QCD D. KHARZEEV in This ~A~Er We Give a Pedawwicalintroduction~0 Recent Work Of
RBRC-32 BNL-6835.4 PARITY ODD BUBBLES IN HOT QCD D. KHARZEEV RIKEN BNL Research Center, Br$ookhauenNational Laboratory, . Upton, New York 11973-5000, USA R.D. PISARSKI Department of Physics, Brookhaven National Laboratoy, Upton, New York 11973-5000, USA M.H.G. TYTGAT Seruice de Physique Th&orique, (7P 225, Uniuersitc4Libre de Bruzelles, B[ud. du !t%iomphe, 1050 Bruxelles, Belgium We consider the topological susceptibility for an SU(N) gauge theory in the limit of a large number of colors, N + m. At nonzero temperature, the behavior of the topological susceptibility depends upon the order of the reconfining phrrse transition. The meet interesting possibility is if the reconfining transition, at T = Td, is of second order. Then we argue that Witten’s relation implies that the topological suscepti~lfity vanishes in a calculable fdion at Td. Ae noted by Witten, this implies that for sufficiently light quark messes, metaetable etates which act like regions of nonzero O — parity odd bubbles — can arise at temperatures just below Td. Experimentally, parity odd bubbles have dramatic signature% the rI’ meson, and especially the q meson, become light, and are copiously produced. Further, in parity odd bubbles, processes which are normally forbidden, such as q + rr”ro, are allowed. The most direct way to detect parity violation is by measuring a parity odd global seymmetry for charged pions, which we define. 1 Introduction In this .-~a~er we give a Pedawwicalintroduction~0 recent work of ours? We I consider an SU(IV) gau”ge t~e~ry in the limit of a large number of colors, N + co, This is, of course, a familiar limit? We use the large N expansion I to investigate the behavior of the theory at nonzero temperature, especially for the topological susceptibility. -
Hexagon Fall
Redis co very of the Elements The Rare Earth s–The Beginnings I I I James L. Marshall, Beta Eta 1971 , and Virginia R. Marshall, Beta Eta 2003 , Department of Chemistry, University of North Texas, Denton, TX 76203-5070, [email protected] 1 Rare earths —introduction. The rare earths Figure 1. The “rare earths” are defined by IUPAC as the 15 lanthanides (green) and the upper two elements include the 17 chemically similar elements of the Group III family (yellow). These elements have similar chemical properties and all can exhibit the +3 occupying the f-block of the Periodic Table as oxidation state by the loss of the highest three electrons (two s electrons and either a d or an f electron, well as the Group III chemical family (Figure 1). depending upon the particular element). A few rare earths can exhibit other oxidation states as well; for These elements include the 15 lanthanides example, cerium can lose four electrons —4f15d 16s 2—to attain the Ce +4 oxidation state. (atomic numbers 57 through 71, lanthanum through lutetium), as well as scandium (atomic number 21) and yttrium (atomic number 39). The chemical similarity of the rare earths arises from a common ionic configuration of their valence electrons, as the filling f-orbitals are buried in an inner core and generally do not engage in bonding. The term “rare earths” is a misnome r—these elements are not rare (except for radioactive promethium). They were named as such because they were found in unusual minerals, and because they were difficult to separate from one another by ordinary chemical manipula - tions. -
Peaceful Berkelium
in your element Peaceful berkelium The first new element produced after the Second World War has led a rather peaceful life since entering the period table — until it became the target of those producing superheavy elements, as Andreas Trabesinger describes. f nomenclature were transitive, element 97 with the finding that in Bk(iii) compounds would be named after an Irish bishop spin–orbit coupling leads to a mixing of the Iwhose philosophical belief was that first excited state and the ground state. This material things do not exist. But between gives rise to unexpected electronic properties the immaterialist George Berkeley and the not present in analogous lanthanide element berkelium stands, of course, the structures containing terbium. Even more fine Californian city of Berkeley (pictured), recently5, a combined experimental and where the element was first produced in computational study revealed that berkelium December 1949. The city became the eponym can have stabilized +iii and +iV oxidation of element 97 “in a manner similar to that states also under mild aqueous conditions, used in naming its chemical homologue indicating a path to separating it from other terbium […] whose name was derived from lanthanides and actinides. the town of Ytterby, Sweden, where the rare The main use of berkelium, however — earth minerals were first found”1. arguably one that wouldn’t have met with A great honour for the city? The mayor Bishop Berkeley’s approval — remains a of Berkeley at the time reportedly displayed PHOTO STOCK / ALAMY AF ARCHIVE distinctly material one: as the target for “a complete lack of interest when he was the synthesis of other transuranium and called with the glad tidings”2. -
Ytterby: Where It All Began (For Tantalum, at Least, See Page 4)
TANTALUM-NIOBIUM INTERNATIONAL STUDY CENTER Bulletin No 175: October 2018 Ytterby: where it all began (for tantalum, at least, see page 4) Contents To join the Bulletin mailing list email [email protected] President’s Letter 2 Tantalum-niobium intellectual property update 21 Director’s Letter 3 Diary of forthcoming events 22 In the footsteps of Anders Gustaf Ekeberg 4 Member company and T.I.C. updates 23 Temperature stability assessment of GaN power 10 Members of the Executive Committee 23 amplifiers with matching tantalum capacitors Ekeberg Prize: Winner 2018 24 Ultra-low profile tantalum capacitors 12 ISSN 1019-2026 Bulletin_175 MDA.pdf 1 24/09/2018 15:18 President’s Letter Dear Fellow Members and Friends, It is my great privilege to welcome all of you to central Africa this October, a region where I spend much of my time, and from which our members source a large percentage of our industries’ supply. I think you will find the conference will be in a very convenient African location, with a first class hotel, in a modern, safe, beautiful and clean country. Rwanda is known for its regional pro-business environment, capable of attracting foreign investments and business entrepreneurs. In Rwanda, it only takes a few days to incorporate a company, and you will find the government will provide needed assistance along the way. Rwanda is the easiest place in central Africa to set up and manage a business. Businesses do not exist in a vacuum – they need a supportive political infrastructure to grow and thrive. Rwanda’s political system is one that enacts laws, decides priorities and sets regulations using a rational, pro-business approach. -
The Elements.Pdf
A Periodic Table of the Elements at Los Alamos National Laboratory Los Alamos National Laboratory's Chemistry Division Presents Periodic Table of the Elements A Resource for Elementary, Middle School, and High School Students Click an element for more information: Group** Period 1 18 IA VIIIA 1A 8A 1 2 13 14 15 16 17 2 1 H IIA IIIA IVA VA VIAVIIA He 1.008 2A 3A 4A 5A 6A 7A 4.003 3 4 5 6 7 8 9 10 2 Li Be B C N O F Ne 6.941 9.012 10.81 12.01 14.01 16.00 19.00 20.18 11 12 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 3 Na Mg IIIB IVB VB VIB VIIB ------- VIII IB IIB Al Si P S Cl Ar 22.99 24.31 3B 4B 5B 6B 7B ------- 1B 2B 26.98 28.09 30.97 32.07 35.45 39.95 ------- 8 ------- 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 4 K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr 39.10 40.08 44.96 47.88 50.94 52.00 54.94 55.85 58.47 58.69 63.55 65.39 69.72 72.59 74.92 78.96 79.90 83.80 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 5 Rb Sr Y Zr NbMo Tc Ru Rh PdAgCd In Sn Sb Te I Xe 85.47 87.62 88.91 91.22 92.91 95.94 (98) 101.1 102.9 106.4 107.9 112.4 114.8 118.7 121.8 127.6 126.9 131.3 55 56 57 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 6 Cs Ba La* Hf Ta W Re Os Ir Pt AuHg Tl Pb Bi Po At Rn 132.9 137.3 138.9 178.5 180.9 183.9 186.2 190.2 190.2 195.1 197.0 200.5 204.4 207.2 209.0 (210) (210) (222) 87 88 89 104 105 106 107 108 109 110 111 112 114 116 118 7 Fr Ra Ac~RfDb Sg Bh Hs Mt --- --- --- --- --- --- (223) (226) (227) (257) (260) (263) (262) (265) (266) () () () () () () http://pearl1.lanl.gov/periodic/ (1 of 3) [5/17/2001 4:06:20 PM] A Periodic Table of the Elements at Los Alamos National Laboratory 58 59 60 61 62 63 64 65 66 67 68 69 70 71 Lanthanide Series* Ce Pr NdPmSm Eu Gd TbDyHo Er TmYbLu 140.1 140.9 144.2 (147) 150.4 152.0 157.3 158.9 162.5 164.9 167.3 168.9 173.0 175.0 90 91 92 93 94 95 96 97 98 99 100 101 102 103 Actinide Series~ Th Pa U Np Pu AmCmBk Cf Es FmMdNo Lr 232.0 (231) (238) (237) (242) (243) (247) (247) (249) (254) (253) (256) (254) (257) ** Groups are noted by 3 notation conventions. -
From Bedrock to Porcelain a Study Regarding The
Bachelor Thesis Degree Project in Geology 15 hp From Bedrock to Porcelain A study regarding the history of porcelain, Ytterby mine and the discovery of yttrium in Sweden Timmy Kärrström Stockholm 2017 Department of Geological Sciences Stockholm University SE-106 91 Stockholm Sweden Abstract Porcelain is a translucent vitreous material that consists of clay (kaolin), feldspar and quartz which has been mixed and heated together to cause a metamorphic reaction. In Sweden, the Porcelain industry was established in 1726 at Rörstrands castle in Stockholm and is today one of the oldest industries in Europe to produce porcelain. Around the 1790’s Rörstrand got its feldspars and quartz from the Ytterby mine that was located at Resarö in Stockholm’s archipelago making the raw material somewhat easy to access. Rörstrand owned the mine in the 1850’s to 1926. During the time Ytterby mine was active, an amateur geologist by the name of Carl Axel Arrhenius, discovered an unusual black mineral in the quarry ore in 1787 which later led to the discovery of 8 new rare earth elements (REE) with the help of several Swedish chemists throughout time. These elements are Yttrium, Ytterbium, Gadolinium, Terbium, Thulium, Erbium, Holmium and scandium. This study will focus on the Swedish porcelain industry and how it has evolved throughout history and Rörstrand’s role in the discovery of yttrium. PAGE 1 Contents Abstract ........................................................................................................................................... 1 -
Experimental Investigation of Recycling Rare Earth Elements from Waste Fluorescent Lamp Phosphors
EXPERIMENTAL INVESTIGATION OF RECYCLING RARE EARTH ELEMENTS FROM WASTE FLUORESCENT LAMP PHOSPHORS by Patrick Max Eduafo A thesis submitted to the Faculty and the Board of Trustees of the Colorado School of Mines in partial fulfillment of the requirements for the degree of Master of Science (Metallurgical and Material Engineering). Golden, Colorado Date: Signed: Patrick Max Eduafo Signed: Dr. Brajendra Mishra Thesis Advisor Golden, Colorado Date: Signed: Dr. Michael Kaufman Professor and Head Department of Metallurgical & Material Engineering ii ABSTRACT Characterization techniques and experimental measurements were used to evaluate a process for recycling rare earth elements (REEs) from spent fluorescent lamp phosphors. QEMSCAN analysis revealed that 70% of the rare earth bearing minerals was less than 10 µm in size. Feeds of varying characteristic were received throughout the course of the experimental analysis. A representative sample of the as-received feed contained 5.8% total rare earth elements (TREE) and upon sieving to below 44 µm, the grade increased to 16.5% TREE. By sieving further to below 10 µm, the grade increased to 19.8% TREE. Hydrochloric acid was used as lixiviant in batch leach experiments on the phosphor powder. The maximum extraction obtained was 90% for europium and yttrium at the following conditions: 1.5 M HCl, 70˚C, 1 hr, 30 g/L and 200 rpm. However, the solubility of cerium, lanthanum and terbium remained low under these conditions. Multistage leaching and calcination followed by leaching processes also resulted in poor extraction of cerium, lanthanum and terbium. Based on experimental results a new process for extracting the chief REEs from end of life fluorescent lamps has been developed. -
CW Scheele, from Pharmacist's Apprentice to Man of Science
ambix, vol. 55, No. 1, March 2008, 29–49 Stepping through Science’s Door: C. W. Scheele, from Pharmacist’s Apprentice to Man of Science1 HJALMAR FORS Division of History of Science and Technology, Royal Institute of Technology, Stockholm This reinterpretation of Carl Wilhelm Scheele’s (1742–86) early life and career analyses the social interplay between Scheele and other chemists who were active in eighteenth-century Sweden. It is argued that Scheele, a rather lowly journeyman working in peripheral pharmacies, had to work hard and traverse several geographical and social boundaries to gain a foothold in the scientifi c community. Eventually, Scheele’s skilful analysis of the mineral magnesia nigra would establish him as one of the pivotal Swedish chemists. However, this happened only after Scheele had managed to prove himself as a knowledgeable chemist who did not threaten the authority of certain socially superior colleagues. When Scheele had gained a place in the scien- tifi c community, the exchange logic of the eighteenth-century republic of letters permitted him to trade experimental results for other kinds of resources. Hence, he gained in both social status, economic prosperity and scientifi c prominence in a relatively short time. Carl Wilhelm Scheele has been, and still is, the object of much admiration. In biographical texts he is often portrayed as the perfect scientifi c hero: humble begin- nings, miraculous discovery, worldwide fame, and an early death caused by long hours spent working over poisonous substances in a drafty chemical laboratory. The legacy of his short life is said to be the discovery of a great number of chemical 1 This paper is based on chapter 6 in the author’s doctoral thesis Mutual Favours: The Social and Scientifi c Practice of Eighteenth-century Swedish chemistry, Institutionen för idé- och lärdomshistoria: skrifter 30 (Uppsala: Uppsala University, 2003). -
THE MAJOR RARE-EARTH-ELEMENT DEPOSITS of AUSTRALIA: GEOLOGICAL SETTING, EXPLORATION, and RESOURCES Figure 1.1
CHAPTER ONE WHAT ARE RARE- EARTH ELEMENTS? 1.1. INTRODUCTION latter two elements are classified as REE because of their similar physical and chemical properties to the The rare-earth elements (REE) are a group of seventeen lanthanides, and they are commonly associated with speciality metals that form the largest chemically these elements in many ore deposits. Chemically, coherent group in the Periodic Table of the Elements1 yttrium resembles the lanthanide metals more closely (Haxel et al., 2005). The lanthanide series of inner- than its neighbor in the periodic table, scandium, and transition metals with atomic numbers ranging from if its physical properties were plotted against atomic 57 to 71 is located on the second bottom row of the number then it would have an apparent number periodic table (Fig. 1.1). The lanthanide series of of 64.5 to 67.5, placing it between the lanthanides elements are often displayed in an expanded field at gadolinium and erbium. Some investigators who want the base of the table directly above the actinide series to emphasise the lanthanide connection of the REE of elements. In order of increasing atomic number the group, use the prefix ‘lanthanide’ (e.g., lanthanide REE: REE are: lanthanum (La), cerium (Ce), praseodymium see Chapter 2). In some classifications, the second element of the actinide series, thorium (Th: Mernagh (Pr), neodymium (Nd), promethium (Pm), samarium 1 (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), and Miezitis, 2008), is also included in the REE dysprosium (Dy), holmium (Ho), erbium (Er), thulium group, while promethium (Pm), which is a radioactive (Tm), ytterbium (Yb), and lutetium (Lu). -
The Rare Earths I
The Mountain Pass rare earth ore body in Southern California, 86 km (54 mi) south-southwest of LasLas Vegas,Vegas, Nevada,Nevada, isis oneone ofof thethe largest,largest, richest,richest, andand mostmost readilyreadily mineablemineable rarerare earthearth depositsdeposits inin thethe worldworld (N35°(N35° 28.7428.74 W115°W115° 31.98).31.98). ItsIts provenproven andand probableprobable reservesreserves exceedexceed 1.31.3 millionmillion metricmetric tonstons ofof rarerare earthearth oxideoxide (REO)(REO) equivalentequivalent containedcontained inin 18.418.4 millionmillion metricmetric tonstons ofof oreore withwith ~8%~8% ore grade and a 5% cut-off grade. ItIt containscontains allall ofof thethe naturallynaturally occurringoccurring rarerare earthearth elements.elements. Photo,Photo, courtesycourtesy ofof Molycorp,Molycorp, Inc.Inc. Rediscovery ...pg 40 2016 Solicitation...pg 52 2015 Awards . ..pg 54 Collegiate News ...pg 57 FALL 2015 THE Rediscovering The Rare Earths A new series starts on page 40. Redis co very of the Elements The Rare Earth s–The Beginnings I I I James L. Marshall, Beta Eta 1971 , and Virginia R. Marshall, Beta Eta 2003 , Department of Chemistry, University of North Texas, Denton, TX 76203-5070, [email protected] 1 Rare earths —introduction. The rare earths Figure 1. The “rare earths” are defined by IUPAC as the 15 lanthanides (green) and the upper two elements include the 17 chemically similar elements of the Group III family (yellow). These elements have similar chemical properties and all can exhibit the +3 occupying the f-block of the Periodic Table as oxidation state by the loss of the highest three electrons (two s electrons and either a d or an f electron, well as the Group III chemical family (Figure 1). -
The Coordination Chemistry of Solvated Metal Ions in DMPU
The Coordination Chemistry of Solvated Metal Ions in DMPU A Study of a Space-Demanding Solvent Daniel Lundberg Faculty of Natural Resources and Agricultural Sciences Department of Chemistry Uppsala Doctoral thesis Swedish University of Agricultural Sciences Uppsala 2006 Acta Universitatis Agriculturae Sueciae 2006: 23 ISSN 1652-6880 ISBN 91-576-7072-2 © 2006 Daniel Lundberg, Uppsala Tryck: SLU Service/Repro, Uppsala 2006 Abstract Lundberg, D., 2006, The Coordination Chemistry of Solvated Metal Ions in DMPU – A Study of a Space-Demanding Solvent. Doctor’s dissertation. ISSN 1652-6880, ISBN 91-576-7072-2 This thesis summarizes and discusses the results of several individual studies on the solvation of metal ions in the solvent N,N’-dimethylpropyleneurea, DMPU, including the iron(II), iron(III), zinc(II), cadmium(II), and lanthanoid(III) ions. These studies have shown that the solvation process in DMPU is sometimes very different to those in corresponding aqueous systems. This is due to the the space-demanding properties the DMPU molecule has when coordinating to metal ions, with its two methyl groups close to the coordinating oxygen atom. The methyl groups effectively hinder/hamper the metal ion from reaching the coordination numbers present in hydrate and solvate complexes with solvent molecules with much lower spatial demands. The investigations were performed with different X-ray techniques, including extended X-ray absorption fine structure (EXAFS), large angle X-ray scattering (LAXS), and single crystal X-ray diffraction (XRD) and included both studies in solution (EXAFS and LAXS) and solid state (EXAFS and XRD). A coordination number reduction, compared to the corresponding hydrates, was found in all of the studied systems, except cadmium(II).