Lithium Market Outlook
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Standardal /Z<-Z
Hamilton Ui StandardAl HANL1r0N STNTVI) Bi;.TVGircr1h VP0FT SVHCA, 5712 1 0 L 'K-KY-o LaIUI P~FrcX.-19F TEST2 ?i0&at CONrxyhCT NO. TIAS 9-8159 NASA Aid!,zj.. SACECAFT CF.CErR ,_eb-r 1970 Prepared Byi/kA / 70 L.A. Wilis, axrer.mwtal Enineer Pae Aproved ByA1"" /Z<-Z -;' W. A. Blezhcr0 Chiet Pa tc Advanced -nginee.rin ONUMBE) AHRU) U NASA CR OR ?MX OR AD NUMBER) (CATEGORY) Hamilton L Standard cnisni _ This report contairs test results defining the operating chsractcristics of lithin peroxide to the extcnt required to quantify system level ponalties. The effects of chemical caulysts, bed cooling, che.,ical Panufacturing tech uiques, opera ing conditions, and cheaica) handling jroc Curea are evaluated. ii! StandardHamilton i5U TAlBLE OF CO_&E!PS Section me No. 1.0 SUMM4ARY 1 2 .0 INTRODUCTION 3 3.0 PROGRAM DEFINITION 3.1 Program Objectives 4 3.2 Test Objectives 4 3.3 Program Description 5 3.4 Test Conitions T 3.5 Test Facility 7 3.6 - Test Hardware 12 3.7 Planned Test Sequence 18 3.8 Test.Results 21 ho TEST DATA PRESENTATION 22 4.1 Performance Data 22 4.2 Chemical Analysis Data 1o6 5.0 PERFOrd4ICE ANALYSIS 109 5.1 Catalyst Evaluation 109 5.2 Bed Cooling Evaluation 134 5.3 Procedural Test Evaluation 0h5 5.4 Off Design Test Evaluation 153 5.5 End Item Canister Evaluation 157 5.6 Li 2O2 System Penalty Evaluation 163 6.0 RECOM ENDED FUTURE EFFORT 165 7.0 APPENDIX 167 7.1 Specification for Lithium Peroxide 167 Manufacturing 7.2 Specification for Lithium Peroxide Storage a68 7.3 Specification for Lithium Peroxide 170 Cartridge Loading iv Standard 5712 LIST OP TABLFS Table No. -
Transport of Dangerous Goods
ST/SG/AC.10/1/Rev.16 (Vol.I) Recommendations on the TRANSPORT OF DANGEROUS GOODS Model Regulations Volume I Sixteenth revised edition UNITED NATIONS New York and Geneva, 2009 NOTE The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. ST/SG/AC.10/1/Rev.16 (Vol.I) Copyright © United Nations, 2009 All rights reserved. No part of this publication may, for sales purposes, be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, electrostatic, magnetic tape, mechanical, photocopying or otherwise, without prior permission in writing from the United Nations. UNITED NATIONS Sales No. E.09.VIII.2 ISBN 978-92-1-139136-7 (complete set of two volumes) ISSN 1014-5753 Volumes I and II not to be sold separately FOREWORD The Recommendations on the Transport of Dangerous Goods are addressed to governments and to the international organizations concerned with safety in the transport of dangerous goods. The first version, prepared by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods, was published in 1956 (ST/ECA/43-E/CN.2/170). In response to developments in technology and the changing needs of users, they have been regularly amended and updated at succeeding sessions of the Committee of Experts pursuant to Resolution 645 G (XXIII) of 26 April 1957 of the Economic and Social Council and subsequent resolutions. -
CCXL1.- the Electrochemistry of Solutions in Acetone. Part I
View Article Online / Journal Homepage / Table of Contents for this issue 2 I38 ROSHDESTWENSKY AND LEWlS THE CCXL1.- The Electrochemistry of Solutions in Acetone. Part I. By ALEXANDERROSHDESTWENSEY and WILLIAM CUDMORE MCCULLAGHLEWIS. WHILSTa considerable amount of attention has been directed to the electrochemical behaviour of methyl and ethyl alcohols, rela- tively few measurements are recorded in the caw of solutions in acetone. The present paper contains the resulk of an investigation undertaken to supply to a certain extent this deficiency. The solutes employed were lithium nitrate and silver nitrate, the latter being examined in greater detail. Before giving our own meamrements, it is necessary to indicate briefly some of the results obtained by other observers which bear directly on the results obtained by us.* As regards the electrolysis of saturated silver nitrate solutions in acetone, Kahlenberg (J. physicd C‘Aem., 1900,4, 349) found that the metal was precipitated in a coherent form, but “the solution conducts so poorly ” that it was impossible to verify Faxaday’s law. In the same paper Kahlenberg gives some results of electromotive force measurements of Ag i AgNO, concentration cells in pyridine and acetonitrile respectively, with regard to which he concludes that the Nernst expressions are inapplicable. Kahlenberg asumes that the liquid/liquid potential difference is negligible, which, in the case of acetone at least, we shall show later is not the case. The specific conductivity of acetone itself has been meamred by Dutoit and Levier (J. Chim. phys., 1905, 3,435), the value obtained Published on 01 January 1911. Downloaded by Freie Universitaet Berlin 09/04/2018 17:53:03. -
Ionic Compound Ratios Time: 1 -2 Class Periods
Collisions Lesson Plan Ionic Compound Ratios Time: 1 -2 class periods Lesson Description In this lesson, students will use Collisions to explore the formation of ionic compounds and compound ratios. Key Essential Questions 1. What makes up an ionic compound? 2. Are ionic compounds found in common ratios? Learning Outcomes Students will be able to determine the ionic compound ratio of an ionic compound. Prior Student Knowledge Expected Cations are postiviely charged ions and anions are negatively charged ions. Lesson Materials • Individual student access to Collisions on tablet, Chromebook, or computer. • Projector / display of teacher screen • Accompanying student resources (attached) Standards Alignment NGSS Alignment Science & Enginnering Practices Disciplinary Core Ideas Crosscutting Concepts • Developing and using • HS-PS-12. Construct and • Structure and Function models revise an explanation for the • Construcing explanations outcome of a simple chemical and designing solutions rection based on the outermost electron states of atoms, trends int he periodic table, and knowl- edge of the partterns of chemi- cal properties. www.playmadagames.com ©2018 PlayMada Games LLC. All rights reserved. 1 PART 1: Explore (15 minutes) Summary This is an inquiry-driven activity where students will complete the first few levels of the Collisions Ionic Bonding game to become introduced to the concept of ionic bonding and compound ratios. Activity 1. Direct students to log into Collisions with their individual username and password. 2. Students should enter the Ionic Bonding game and play Levels 1-6 levels. 3. Have your students answer the following questions during gameplay: 1. What combination of ions did you use to successfully match a target? 2. -
United States Patent Office Patented May 26, 964 1
3,134,646 United States Patent Office Patented May 26, 964 1. 2 3,134,646 anhydrous lithium peroxide. The rapid drying step PREPARATION 6Fiff UM PEROXIDE. serves not only to effect the removal of water added Ricardo O. Bach, Gastonia, N.C., assignor to Lithium through the water solutions of the reactants and, addi Corporation of America, inc., New York, N.Y., a cor tionally, formed in the course of the reaction, but serves, poration of Minnesota also, and quite surprisingly, to bring about the important No Drawing, Filed Jan. 5, 1962, Set. No. 166,395 function of effecting rapid transfer of the active oxygen 10 Claims. (CI. 23-184) of the hydrogen peroxide to the lithium hydroxide to consummate formation of the desired lithium peroxide. This invention relates to an improved method of pro The lithium hydroxide (which term also includes ducing substantially anhydrous lithium peroxide, and to O lithium hydroxide hydrates such as lithium hydroxide the product produced thereby. monohydrate) is most advantageously used in the form Methods for the production of substantially anhydrous of a strong to substantially saturated aqueous solution, lithium peroxide have long been known in the art. More for instance, from about 8 or 10 to 12% concentration. recently, improvements in such methods have been pro In those instances where the resulting lithium hydroxide posed as disclosed, for instance, in U.S. Patents Nos. 5 solutions contain insoluble impurities as, for instance, 2,448,485 and 2,962,358. However, each of the methods lithium carbonate, it is desirable to filter the solutions disclosed in these patents has certain significant disad to remove said impurities so as to bring about greater vantages, particularly from an economic standpoint, purity of the final substantially anhydrous lithium which make their utilization in commercial operations peroxide. -
A Study of Lithium Precursors on Nanoparticle Quality
Electronic Supplementary Material (ESI) for Nanoscale. This journal is © The Royal Society of Chemistry 2021 Electronic Supplementary Information Elucidating the role of precursors in synthesizing single crystalline lithium niobate nanomaterials: A study of lithium precursors on nanoparticle quality Rana Faryad Ali, Byron D. Gates* Department of Chemistry and 4D LABS, Simon Fraser University, 8888 University Drive Burnaby, BC, V5A 1S6, Canada * E-mail: [email protected] This work was supported in part by the Natural Sciences and Engineering Research Council of Canada (NSERC; Grant No. RGPIN-2020-06522), and through the Collaborative Health Research Projects (CHRP) Partnership Program supported in part by the Canadian Institutes of Health Research (Grant No. 134742) and the Natural Science Engineering Research Council of Canada (Grant No. CHRP 462260), the Canada Research Chairs Program (B.D. Gates, Grant No. 950-215846), CMC Microsystems (MNT Grant No. 6345), and a Graduate Fellowship (Rana Faryad Ali) from Simon Fraser University. This work made use of 4D LABS (www.4dlabs.com) and the Center for Soft Materials shared facilities supported by the Canada Foundation for Innovation (CFI), British Columbia Knowledge Development Fund (BCKDF), Western Economic Diversification Canada, and Simon Fraser University. S1 Experimental Materials and supplies All chemicals were of analytical grade and were used as received without further purification. Niobium ethoxide [Nb(OC2H5)5, >90%] was obtained from Gelest Inc., and benzyl alcohol (C7H7OH, 99%) and triethylamine [N(C2H5)3, 99.0%] were purchased from Acros Organics and Anachemia, respectively. Lithium chloride (LiCl, ~99.0%) was obtained from BDH Chemicals, and lithium bromide (LiBr, ≥99.0%), lithium fluoride (LiF, ~99.9%), and lithium iodide (LiI, 99.0%) were purchased from Sigma Aldrich. -
The Structure of Alkali Silicate Glasses and Melts: a Multi-Spectroscopic Approach
The structure of alkali silicate glasses and melts: A multi-spectroscopic approach by Cedrick A. O'Shaughnessy A thesis submitted in conformity with the requirements for the degree of Doctor of Philosophy in Geology Graduate Department of Earth Sciences University of Toronto c Copyright 2019 by Cedrick A. O'Shaughnessy Abstract The structure of alkali silicate glasses and melts: A multi-spectroscopic approach Cedrick A. O'Shaughnessy Doctor of Philosophy in Geology Graduate Department of Earth Sciences University of Toronto 2019 The structure of alkali silicate glasses and melts is investigated using a multi-spectroscopic approach. Raman spectroscopy is used to characterize the local to intermediate range order within the glasses. We show that the distribution of rings varies as a function of composition, with 3-membered rings gaining importance with increasing alkali content. We apply a newly developed model for the fitting of the high n frequency envelope related to SiO4 symmetric stretch vibrations of Q species. These fits are interpreted using the idea of modifier bound bridging oxygen. The proportions of the different Qn species vary with alkali concentration with Q4 species breaking down to form lower order Qn species with increasing alkali 2 content. The Q peak appears at increasingly higher concentrations of M2O with increasing cation size. This leads us to believe that cations with a higher charge density cluster more readily than cations with a lower charge density. At the ∼20 mol. % composition we see a change in the silicate network, as shown by the absence of a Q4 peak and the proportion of 3-membered rings. -
Design Guidelines for Carbon Dioxide Scrubbers I
"NCSCTECH MAN 4110-1-83 I (REVISION A) S00 TECHNICAL MANUAL tow DESIGN GUIDELINES FOR CARBON DIOXIDE SCRUBBERS I MAY 1983 REVISED JULY 1985 Prepared by M. L. NUCKOLS, A. PURER, G. A. DEASON I OF * Approved for public release; , J 1"73 distribution unlimited NAVAL COASTAL SYSTEMS CENTER PANAMA CITY, FLORIDA 32407 85. .U 15 (O SECURITY CLASSIFICATION OF TNIS PAGE (When Data Entered) R O DOCULMENTATIONkB PAGE READ INSTRUCTIONS REPORT DOCUMENTATION~ PAGE BEFORE COMPLETING FORM 1. REPORT NUMBER 2a. GOVT AQCMCSION N (.SAECIP F.NTTSChALOG NUMBER "NCSC TECHMAN 4110-1-83 (Rev A) A, -NI ' 4. TITLE (and Subtitle) S. TYPE OF REPORT & PERIOD COVERED "Design Guidelines for Carbon Dioxide Scrubbers '" 6. PERFORMING ORG. REPORT N UMBER A' 7. AUTHOR(&) 8. CONTRACT OR GRANT NUMBER(S) M. L. Nuckols, A. Purer, and G. A. Deason 9. PERFORMING ORGANIZATION NAME AND ADDRESS 10. PROGRAM ELEMENT, PROJECT. TASK AREA 6t WORK UNIT NUMBERS Naval Coastal PanaaLSystems 3407Project CenterCty, S0394, Task Area Panama City, FL 32407210,WrUnt2 22102, Work Unit 02 II. CONTROLLING OFFICE NAME AND ADDRE1S t2. REPORT 3ATE May 1983 Rev. July 1985 13, NUMBER OF PAGES 69 14- MONI TORING AGENCY NAME & ADDRESS(if different from Controtling Office) 15. SECURITY CLASS. (of this report) UNCLASSIFIED ISa. OECL ASSI FICATION/DOWNGRADING _ __N•AEOULE 16. DISTRIBUTION STATEMENT (of thia Repott) Approved for public release; distribution unlimited. 17. DISTRIBUTION STATEMENT (of the abstract entered In Block 20, If different from Report) IS. SUPPLEMENTARY NOTES II. KEY WORDS (Continue on reverse side If noceassry and Identify by block number) Carbon Dioxide; Scrubbers; Absorption; Design; Life Support; Pressure; "Swimmer Diver; Environmental Effects; Diving., 20. -
S41467-020-19206-W.Pdf
ARTICLE https://doi.org/10.1038/s41467-020-19206-w OPEN Unravelling the room-temperature atomic structure and growth kinetics of lithium metal Chao Liang 1, Xun Zhang1, Shuixin Xia1, Zeyu Wang1, Jiayi Wu1, Biao Yuan 1, Xin Luo1, Weiyan Liu1, ✉ Wei Liu 1 &YiYu 1 Alkali metals are widely studied in various fields such as medicine and battery. However, limited by the chemical reactivity and electron/ion beam sensitivity, the intrinsic atomic 1234567890():,; structure of alkali metals and its fundamental properties are difficult to be revealed. Here, a simple and versatile method is proposed to form the alkali metals in situ inside the transmission electron microscope. Taking alkali salts as the starting materials and electron beam as the trigger, alkali metals can be obtained directly. With this method, atomic resolution imaging of lithium and sodium metal is achieved at room temperature, and the growth of alkali metals is visualized at atomic-scale with millisecond temporal resolution. Furthermore, our observations unravel the ambiguities in lithium metal growth on garnet-type solid electrolytes for lithium-metal batteries. Finally, our method enables a direct study of physical contact property of lithium metal as well as its surface passivation oxide layer, which may contribute to better understanding of lithium dendrite and solid electrolyte interphase issues in lithium ion batteries. ✉ 1 School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China. email: [email protected] NATURE COMMUNICATIONS | (2020) 11:5367 | https://doi.org/10.1038/s41467-020-19206-w | www.nature.com/naturecommunications 1 ARTICLE NATURE COMMUNICATIONS | https://doi.org/10.1038/s41467-020-19206-w t has been a long history for the research on alkali metals1, the to control the dose-rate of the electron beam. -
LISTA PUBLIKACJI 2009 LIST of PUBLICATIONS
Instytut Niskich Temperatur i Badań Strukturalnych PAN Wrocław, 2011.12 31 LISTA PUBLIKACJI 2009 LIST of PUBLICATIONS KSIĄŻKI, MONOGRAFIE i ARTYKUŁY PRZEGLĄDOWE Books, Monographs & Reviews 1. R. Troć, 6.β Actinide monochalcogenides. In: Landolt–Börnstein Numerical Data and Functional Relationship in Science and Technology, New Series, ed. by W.Martienssen, Group III: Condensed Matter, Vol. 27: Magnetic Properties of Non-Metallic Inorganic Compounds Based on Transition Elements, ed. by H.P.J. Wijn, Subvol. B Pnictides and Chalcogenides III (Berlin: Springer-Vg 2009) Pt 6β, X + 574 pp. ARTYKUŁY W CZASOPISMACH NAUKOWYCH Articles in Scientific Journals 2. L.C.Alves, M.M.M.Rubinger, R.H.Lindemann, G.J.Perpétuo, J. Janczak, L.D.L.Miranda, L.Zambolim, M.R.L.Oliveira, Syntheses, Crystal Structure, Spectroscopic Characterization and Antifungal Activity of New N -R-Sulfonyldithiocarbimate Metal Complexes. J. Inorg. Biochem. 103 7 (2009) 1045–53. [DOI] 3. R.Acevedo, A.Soto-Bubert, M.E.G.Valerio, W. Stręk, On the Theory of Interaction Potentials in Ionic Crystals: An Application to the Thermodynamics of Lanthanide Type Crystals. Asian J. Spectrosc. 13 1 (2009) 43–65. 4. L.G.Akselrud, I.A.Ivashchenko, O.F.Zmiy, I.D.Olekseyuk, J. Stępień-Damm, Description of Concentration Polytypism in Cd1−xCuxIn2Se4 by Commensurately Modulated Structures. Chem. Met. Alloys 2 1/2 (2009) 108–14. 5. Tran Kim Anh, Dinh Xuan Loc, Lam thi Kieu Giang, W. Stręk, Le Quoc Minh, Preparation, Optical Properties of ZnO, ZnO : Al Nanorods and Y(OH)3 : Eu Nanotube. J. Phys. Conf. Ser. 146 (2009) 012001 (5). [DOI] II Kraj.Konf. -
Zllniit?Dstates Patent' ”
, 2,962,358 zllniit?dstates Patent‘ ” ICC. Patented Nov. 29,1969 7 l . , r 2 . percent recovery of the theoretical amount of lithium peroxide available-can be obtained. 2,96%“ The drying may bedone underatmosphen'c pressure at 1 METHOD on MAKING LITHIUM PERoxmE suitable temperatures to keep decomposition of the lithium IN METHANOL peroxide at a ' ‘Ethyl alcohol can be used, as well as methanol, and Henry H. Strater, May?eld Heights, Ohio, assignor to commercial strength alcohols are satisfactory. The re 8: Chemicals, Willoughby, Ohio, a corporation action of the invention will occur at room tempera 0 o ture. No Drawing. Filed June 2, 1958, Ser. No. 738,959 10 Should it be desired to recover the lithium present in the end ?ltrate material, the ?ltrate can be heated to 4 Claims. (Cl. 23-184) distill the alcohol therein which can be recovered for further use. The water present also is evaporated o? and the residue material will have been partially con The present invention relates to a method of preparing 15 verted from lithium peroxide over to lithium hydroxide. lithium' peroxide, and particularly relates to the prepara Such end product can be puri?ed in any conventional tion of such material in an alcohol reacting medium. manner and be again used in the practice of the process, Heretofore there have been some methods proposed or it can be used for other purposes, as desired. for the production of lithium peroxide, vbut none of such The reaction conditions are readily controllable by methods have been completely satisfactory for low cost 20 the process described, as the hydrogen peroxide is slowly eifective production of lithium peroxide, so far as I am added to the reacting materials and no excessive tem aware. -
Ionic Conductivity of Solid Mixtures
NASA TECHNICAL NOTE NASA-- TN D-4606 d./ *o 0 *o nP LOAN COPY: RRURN TO AFWL (WLIL-2) KIRTLAND AFB, N MEX IONIC CONDUCTIVITY OF SOLID MIXTURES by William L. Fielder Lewis Research Celzter 3 ._i _... Cleveland, Ohio r I t , 1 NATIONAL AERONAUTICS AND SPACE ADMINISTRATION WASHINGTON, D. C. MAY 1968 ,/ I I TECH LIBRARY KAFB, NM ,lllllllllll__ .llllllllll I1111 lllllllllllllllll I 023L03b NASA TN D-4606 IONIC CONDUCTIVITY OF SOLID MIXTURES By William L. Fielder Lewis Research Center Cleveland, Ohio NATIONAL AERONAUTICS AND SPACE ADMINISTRATION For sale by the Clearinghouse for Federal Scientific and Technicol Information Springfield, Virginia 22151 - CFSTI price $3.00 IONIC CONDUCTIVITY OF SOLID MIXTURES by William L. Fielder Lewis Research Center SUMMARY The conductivities of four solid mixtures were determined as a function of tempera ture: (1) the lithium fluoride - lithium chloride eutectic, (2) the lithium chloride - potassium chloride eutectic, (3) the lithium fluoride - sodium chloride eutectic, and (4) a 50-mole-percent mixture of sodium chloride and potassium chloride. Two conductivity regions were obtained for each of the four mixtures. The activation energies for the conductivity for the lower-temperature regions ranged from 14 to 27 kilocalories per mole (59 to 114 kJ/mole). These energies were similar to the cation migration energies for the single crystals of the alkali halides. The conductivity of the mixtures in the lower-temperature regions is best explained by the following mechanism: (1) formation of cation vacancies primarily by multivalent impurities, and (2) migration of the cations through these vacancies. The activation energies for the conductivity of the solid mixtures in the upper- temperature regions ranged from 5 to 9 kilocalories per mole (20 to 39 kJ/mole).