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WO 2017/106925 Al 29 June 2017 (29.06.2017) P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2017/106925 Al 29 June 2017 (29.06.2017) P O P C T (51) International Patent Classification: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, C22B 26/12 (2006.01) C22B 3/06 (2006.01) DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KH, KN, (21) International Application Number: KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, PCT/AU20 16/05 1278 MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, (22) International Filing Date: NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, 22 December 2016 (22. 12.2016) RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, (25) Filing Language: English ZA, ZM, ZW. (26) Publication Language: English (84) Designated States (unless otherwise indicated, for every (30) Priority Data: kind of regional protection available): ARIPO (BW, GH, 20159053 17 22 December 201 5 (22. 12.2015) AU GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, 2016900774 2 March 2016 (02.03.2016) AU TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, (72) Inventor; and DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, (71) Applicant : HUNWICK, Richard [AU/AU]; 59 Abing LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, don Road, Roseville, New South Wales 2069 (AU). -
Novel Triadius-Like N4 Specie of Iron Nitride Compounds Under High
www.nature.com/scientificreports OPEN Novel triadius-like N4 specie of iron nitride compounds under high pressure Received: 11 May 2018 Yuanzheng Chen1, Xinyong Cai1, Hongyan Wang1, Hongbo Wang2 & Hui Wang2 Accepted: 2 July 2018 Various nitrogen species in nitrides are fascinating since they often appear with these nitride as Published: xx xx xxxx superconductors, hard materials, and high-energy density. As a typical complex, though iron nitride has been intensively studied, nitrogen species in the iron–nitrogen (Fe-N) compounds only have been confned to single atom (N) or molecule nitrogen (N2). Using a structure search method based on the CALYPSO methodology, unexpectedly, we here revealed two new stable high pressure (HP) states at 1:2 and 1:4 compositions with striking nitrogen species. The results show that the proposed FeN2 stabilizes by a break up of molecule N2 into a novel planar N4 unit (P63/mcm, >228 GPa) while FeN4 stabilizes by a infnite 1D linear nitrogen chains N∞ (P-1, >50 GPa; Cmmm, >250 GPa). In the intriguing N4 specie of P63/mcm-FeN2, we fnd that it possesses three equal N = N covalent bonds and forms a perfect triadius-like confguration being never reported before. This uniqueness gives rise to a set of remarkable properties for the crystal phase: it is identifed to have a good mechanical property and a potential for phonon-mediated superconductivity with a Tc of 4–8 K. This discovery puts the Fe-N system into a new class of desirable materials combining advanced mechanical properties and superconductivity. Nitrogen (N) is the most abundant element in the earth’s atmosphere and is one of the least studied elements regarding the composition of the Earth1. -
Explosion of Lithium-Thionyl-Chloride Battery Due to Presence of Lithium Nitride
Downloaded from orbit.dtu.dk on: Sep 25, 2021 Explosion of lithium-thionyl-chloride battery due to presence of lithium nitride Hennesø, E.; Hedlund, Frank Huess Published in: Journal of Failure Analysis and Prevention Link to article, DOI: 10.1007/s11668-015-0004-y Publication date: 2015 Document Version Early version, also known as pre-print Link back to DTU Orbit Citation (APA): Hennesø, E., & Hedlund, F. H. (2015). Explosion of lithium-thionyl-chloride battery due to presence of lithium nitride. Journal of Failure Analysis and Prevention, 15(5), 600-603. https://doi.org/10.1007/s11668-015-0004-y General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. Users may download and print one copy of any publication from the public portal for the purpose of private study or research. You may not further distribute the material or use it for any profit-making activity or commercial gain You may freely distribute the URL identifying the publication in the public portal If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. This article appeared in Journal of Failure Analysis and Prevention, ISSN 1547-7029 http://dx.doi.org/10.1007/s11668-015-0004-y Explosion of lithium-thionyl- chloride battery due to presence of lithium nitride Document no. -
Reactions of Lithium Nitride with Some Unsaturated Organic Compounds. Perry S
Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1963 Reactions of Lithium Nitride With Some Unsaturated Organic Compounds. Perry S. Mason Jr Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Mason, Perry S. Jr, "Reactions of Lithium Nitride With Some Unsaturated Organic Compounds." (1963). LSU Historical Dissertations and Theses. 898. https://digitalcommons.lsu.edu/gradschool_disstheses/898 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has been 64—5058 microfilmed exactly as received MASON, Jr., Perry S., 1938- REACTIONS OF LITHIUM NITRIDE WITH SOME UNSATURATED ORGANIC COMPOUNDS. Louisiana State University, Ph.D., 1963 Chemistry, organic University Microfilms, Inc., Ann Arbor, Michigan Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. REACTIONS OF LITHIUM NITRIDE WITH SOME UNSATURATED ORGANIC COMPOUNDS A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requireiaents for the degree of Doctor of Philosophy in The Department of Chemistry by Perry S. Mason, Jr. B. S., Harding College, 1959 August, 1963 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. -
1 Understanding Continuous Lithium-Mediated Electrochemical Nitrogen Reduction Nikifar Lazouski,1 Zachary J Schiffer,1 Kindle Wi
© 2019 This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ doi: 10.1016/j.joule.2019.02.003 Understanding Continuous Lithium-Mediated Electrochemical Nitrogen Reduction Nikifar Lazouski,1 Zachary J Schiffer,1 Kindle Williams,1 and Karthish Manthiram1* 1Department of Chemical Engineering; Massachusetts Institute of Technology; Cambridge, MA 02139, USA *Corresponding Author: [email protected] 1 © 2019 This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ doi: 10.1016/j.joule.2019.02.003 Summary Ammonia is a large-scale commodity chemical that is crucial for producing nitrogen- containing fertilizers. Electrochemical methods have been proposed as renewable and distributed alternatives to the incumbent Haber-Bosch process, which utilizes fossils for ammonia production. Herein, we report a mechanistic study of lithium-mediated electrochemical nitrogen reduction to ammonia in a non-aqueous system. The rate laws of the main reactions in the system were determined. At high current densities, nitrogen transport limitations begin to affect the nitrogen reduction process. Based on these observations, we developed a coupled kinetic-transport model of the process, which we used to optimize operating conditions for ammonia production. The highest Faradaic efficiency observed was 18.5 ± 2.9%, while the highest production rate obtained was (7.9 ± 1.6) × 10-9 mol cm-2 s-1. Our understanding of the reaction network and the influence of transport provides foundational knowledge for future improvements in continuous lithium- mediated ammonia synthesis. -
Table of Contents
TABLE OF CONTENTS ACKNOWLEDGEMENTS iii TABLE OF CONTENTS iv LIST OF TABLES vi LIST OF FIGURES viii ABSTRACT xii CHAPTER 1 INTRODUCTION 1 1.1 Overview 1 1.2 Research Objectives and Organization of the Dissertation 2 CHAPTER 2 ALKLI SILICA REACTION AND RECYCLED CONCRETE 4 AGGREGATE 2.1 Alkali Silica Reaction (ASR) 4 2.1.1 ASR essentials 4 2.1.2 ASR mechanisms 5 2.1.3 ASR test methods review 7 2.1.4 Potential mitigation methods 9 2.2 Recycled Concrete Aggregate (RCA) 11 2.2.1 Recycled aggregate preview 11 2.2.2 RCA with ASR distress 13 2.2.3 RCA alkali contribution and alkali leaching 17 CHAPTER 3 PORE SOLUTION 19 3.1 Pore solution extraction 19 3.1.1 Instrumental introduction and description 19 3.1.2 Sample preparation 24 3.1.3 Extraction method and load scheme 25 3.2 Pore Solution Chemical Analysis 27 3.2.1 Alkali evolution process in pore solution 27 3.2.2 Pore solution test schemes and methods 29 3.2.3 Test results and analysis 32 iv CHAPTER 4 RCA ASR MITIGATION USING MINERAL ADMIXTURES 35 4.1 Fly Ash Mitigation 35 4.1.1 Fly ash as a concrete admixture 35 4.1.2 Mortar bar expansion test 38 4.1.3 Expansion results and comparison 42 4.1.4 Pore solution analysis 45 4.1.5 Mitigation mechanism analysis 49 4.2 Ground Granulated Blast Furnace Slag (GGBFS) Mitigation 54 4.2.1 Slag production and use in concrete 54 4.2.2 Expansion test results and comparison 55 4.2.3 Pore solution analysis and TGA 57 4.3 Silica Fume Mitigation 59 4.3.1 Expansion results and comparison 60 4.3.2 Pore solution analysis and TGA 65 4.3.3 Particle size issue 66 4.4 -
Stable Lithium Diisopropylamide and Method of Preparation
Europaisches Patentamt J European Patent Office Publication number: 0 205 583 Office europeen des brevets B1 EUROPEAN PATENT SPECIFICATION (45) Date of publication of patent specification: 30.01.91 Intel.5: C 07 C 211/65 (3) Application number: 86900522.3 @ Date of filing: 17.12.85 (8) International application number: PCT/US85/02509 ® International publication number: WO 86/03744 03.07.86 Gazette 86/14 STABLE LITHIUM DIISOPROPYLAMIDE AND METHOD OF PREPARATION. (M) Priority: 24.12.84 US 685318 Proprietor: LITHIUM CORPORATION OF AMERICA, INC. Post Office Box 795 Date of publication of application: Bessemer City, NC 28016 (US) 30.12.86 Bulletin 86/52 Inventor: MORRISON, Robert, Charles Publication of the grant of the patent: 1946 Elmwood Drive 30.01.91 Bulletin 91/05 Gastonia, NC 28054 (US) Inventor: HALL, Randy, Winf red Route 4 Box 697 (M) Designated Contracting States: Kings Mountain, NC 28086 (US) AT BE CH DE FR GB IT LI LU NL SE Inventor: RATHMAN, Terry, Lee 3843 Gardner Park Drive Gastonia, NC 28054 (US) References cited: US-A-3197 516 US-A-3 694516 US-A-3388178 US-A-4 006187 Representative: Gore, Peter Manson et al US-A-3446 860 US-A-4399 078 W.P. THOMPSON & CO. Coopers Building Church Street JOURNAL OF ORGANOMETALLIC CHEMISTRY, Liverpool L1 3AB (GB) vol. 4, 1965; GILMAN et al.: "Stabilities of some n-alkyllithium compounds in mixed solvent CO I References cited: 00 systems", pp. 483-487 JOURNAL OF ORGANOMETTALIC CHEMISTRY, m JOURNAL OF AMERICAN CHEMICAL SOCIETY, vol. 29, 1971; HONEYCUTT: "Kinetics of the in vol. -
Lithium Nitride
TECHNICAL DATA SHEET Date of Issue: 2016/12/12 Lithium Nitride CAS-No. 26134-62-3 EC-No. 247-475-2 Molecular Formula Li3N Product Number 401121 SPECIFICATION Lithium Nitride: min. 94% METHOD OF ANALYSIS Assay by determination of nitrogen by the method of Kjeldahl. A detailed laboratory instruction is available on request. PHYSICAL PROPERTIES Appearance fine powder Color red brown Melting point/ range ca. 840 - 845 °C Density ca. 1.38 g/cm3 at 20 °C Water solubility (Not applicable) Molecular weight 34.82 g/mol Additional Physical Theoretical lithium weight: 59.8 % Properties The information presented herein is believed to be accurate and reliable, but is presented without guarantee or responsibility on the part of Albemarle Corporation and its subsidiaries and affiliates. It is the responsibility of the user to comply with all applicable laws and regulations and to provide for a safe workplace. The user should consider any health or safety hazards or information contained herein only as a guide, and should take those precautions which are necessary or prudent to instruct employees and to develop work practice procedures in order to promote a safe work environment. Further, nothing contained herein shall be taken as an inducement or recommendation to manufacture or use any of the herein materials or processes in violation of existing or future patent. Technical data sheets may change frequently. You can download the latest version from our website www.albemarle-lithium.com. Please contact us at www.albemarle-lithium.com/contact with questions. Lithium Nitride Page 2 / 3 Product Number: 401121 Date of Issue: 2016/12/12 HANDLING & STORAGE Handling Lithium Nitride should be handled under inert gas atmosphere. -
Safe Handling of Organolithium Compounds in the Laboratory
FEATURE Safe handling of organolithium compounds in the laboratory Organolithium compounds are extremely useful reagents in organic synthesis and as initiators in anionic polymerizations. These reagents are corrosive, flammable, and in certain cases, pyrophoric. Careful planning prior to execution of the experiment will minimize hazards to personnel and the physical plant. The proper personal protective equipment (PPE) for handling organolithium compounds will be identified. Procedures to minimize contact with air and moisture will be presented. Solutions of organolithium compounds can be safely transferred from the storage bottles to the reaction flask with either a syringe or a cannula. With the utilization of these basic techniques, organolithium compounds can be safely handled in the laboratory. By James A. Schwindeman, oxides (typi®ed by lithium t-butoxide). various classes of organolithium com- Chris J. Woltermann, and These organolithium compounds have pounds, with pKa from 15.2 (lithium Robert J. Letchford found wide utility as reagents for methoxide) to 53 (t-butyllithium).5 organic synthesis in a variety of appli- Fourth, organolithium reagents demon- cations. For example, they can be strate enhanced nucleophilicity com- INTRODUCTION employed as strong bases (alkyl- pared to the corresponding organo- When properly handled, organo- lithiums, aryllithiums, lithium amides magnesium compound. Finally, they lithiums provide unique properties and lithium alkoxides), nucleophiles are convenient, as a variety of organo- that allow for -
Lithium Diisopropylamide: Nonequilibrium Kinetics and Lessons Learned About Rate Limitation Russell F
Perspective pubs.acs.org/joc Lithium Diisopropylamide: Nonequilibrium Kinetics and Lessons Learned about Rate Limitation Russell F. Algera, Lekha Gupta, Alexander C. Hoepker, Jun Liang, Yun Ma, Kanwal J. Singh, and David B. Collum* Department of Chemistry and Chemical Biology Baker Laboratory, Cornell University, Ithaca, New York 14853-1301, United States *S Supporting Information ABSTRACT: The kinetics of lithium diisopropylamide (LDA) in tetrahydrofuran under nonequilibrium conditions are reviewed. These conditions correspond to a class of substrates in which the rates of LDA aggregation and solvation events are comparable to the rates at which various fleeting intermediates react with substrate. Substrates displaying these reactivities, by coincidence, happen to be those that react at tractable rates on laboratory time scales at −78 °C. In this strange region of nonlimiting behavior, rate-limiting steps are often poorly defined, sometimes involve deaggregation, and at other times include reaction with substrate. Changes in conditions routinely cause shifts in the rate-limiting steps, and autocatalysis is prevalent and can be acute. The studies are described in three distinct portions: (1) methods and strategies used to deconvolute complex reaction pathways, (2) the resulting conclusions about organolithium reaction mechanisms, and (3) perspectives on the concept of rate limitation reinforced by studies of LDA in tetrahydrofuran at −78 °C under nonequilibrium conditions. ithium diisopropylamide (LDA), a highly reactive and at −78 °Cconditions that are of singular importance in L selective Brønsted base, stands among the most prominent organic synthesisoccur at nearly the rates at which the reagents in organic synthesis.1 A survey of 500 total syntheses aggregates in Scheme 1 exchange. -
Study on Extraction of Lanthanum Oxide from Monazite Concentrate
World Academy of Science, Engineering and Technology International Journal of Materials and Metallurgical Engineering Vol:2, No:10, 2008 Study on Extraction of Lanthanum Oxide from Monazite Concentrate Nwe Nwe Soe, Lwin Thuzar Shwe, and Kay Thi Lwin La2O3 has more extensive applications. It is a white Abstract—Lanthanum oxide is to be recovered from monazite, amorphous powder; insoluble in water improves the alkali which contains about 13.44% lanthanum oxide. The principal resistance of glass. The Kodak's camera objectives contain objective of this study is to be able to extract lanthanum oxide from from 20 to 40% La2O3. Lanthanum oxide can also be used in monazite of Moemeik Myitsone Area. The treatment of monazite in optical glasses where it imparts improved alkali resistance, this study involves three main steps; extraction of lanthanum La-Ce-Tb phosphors for fluorescent lamps, dielectric and hydroxide from monazite by using caustic soda, digestion with nitric conductive ceramics, Barium titanate capacitors, X-Ray acid and precipitation with ammonium hydroxide and calcination of lanthanum oxalate to lanthanum oxide. intensifying screens and lanthanum metal production [1]. Keywords—Calcination, Digestion, Precipitation. II. EXPERIMENTAL PROCEDURE Monazite from Moemeik Myitsone Area was used as raw I. INTRODUCTION material for the experiments. Monazite was ground to obtain - ANTHANUM was discovered in 1839 by Swedish 325 mesh. It has beach color. The flow diagram of the L Chemist Carl Gustav Mosandar when he partially extraction of lanthanum oxide is shown in Fig. 1. decomposed a sample of cerium nitrate by heating and treating Monazite the resulting salt with nitric acid. -
United States Patent [151 3,642,527 Purdes Et Al
United States Patent [151 3,642,527 Purdes et al. v [45] Feb. 15, 1972 [54] METHOD OF MODIFYING va dielectric substrate, such as barium titanate, may be ELECTRICAL RESISTIVITY modi?ed by ?rst forming a relatively porous substrate which CHARACTERISTICS OF DIELECTRIC may be handled without breaking, as by pre?ring the sub SUBSTRATES strate, masking selected portions of the substrate with a material such as a photoresist material which will vaporize [72] Inventors: Andrew J. Purdes, Pawtucket, R.I.; Ernest during ?nal ?ring of the substrate, contacting the substrate ' M. Just, Plainville, Mass. with a solution of a ?rst reactant, immersing at least a portion [ 73] Assignee: Texas Instruments Incorporated, Dallas, of the substrate in a solution of a second reactant which will Tex. react with the ?rst reactant to precipitate in situ in a portion of the substrate a compound which is insoluble in the solutions [22] Filed: Dec. 30, 1968 and which is adapted to modify the electrical resistivity characteristics of the substrate, and thereafter ?ring the sub [21] Appl. No.: 787,989 strate at a temperature on the order of l,400°-l,450° C. to reduce the porosity of the substrate and to incorporate the in {52] us. c1 ....................................... ..117/212, 117/223 soluble compound into the lattice of selected portions of the [511 1m. (:1 ...................................... ..B44d l/l8 substrate. Where it is desired to dope selected portions of an [58] Field 6: Search .................. ..106/39; 117/212, 213, 123, undoped substrate to the desired thickness and form thick ?lm positive temperature coef?cient (PTC) thermistors, the ‘ 117/223 starting material may be an undoped barium titanate, for ex~ [56] References Cited ample, the solution of the ?rst reactant may be an aqueous solution of a compound such as ammonium hydroxide, and UNITED STATES PATENTS the ‘solution of the second reactant may be an aqueous solu tion of a compound such as lanthanum acetate which reacts 3,296,359 1/1967 Ramsey, Jr.