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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. -
Ion Sources for High-Power Hadron Accelerators
Ion sources for high-power hadron accelerators Daniel C. Faircloth Rutherford Appleton Laboratory, Chilton, Oxfordshire, UK Abstract Ion sources are a critical component of all particle accelerators. They create the initial beam that is accelerated by the rest of the machine. This paper will introduce the many methods of creating a beam for high-power hadron accelerators. A brief introduction to some of the relevant concepts of plasma physics and beam formation is given. The different types of ion source used in accelerators today are examined. Positive ion sources for producing H+ ions and multiply charged heavy ions are covered. The physical principles involved with negative ion production are outlined and different types of negative ion sources are described. Cutting edge ion source technology and the techniques used to develop sources for the next generation of accelerators are discussed. 1 Introduction 1.1 Ion source basics An ion is an atom or molecule in which the total number of electrons is not equal to the total number of protons, thus giving it a net positive or negative electrical charge. The name ion (from the Greek ιον, meaning "going") was first suggested by William Whewell in 1834. Michael Faraday used the term to refer to the charged particles that carry current in his electrolysis experiments. Ion sources consist of two parts: a plasma generator and an extraction system. The plasma generator must be able to provide enough of the correct ions to the extraction system. There are numerous ways of making plasma: electrical discharges in all of their forms; heating by many different means; using lasers; or even being hit by beams of other particles. -
Used at Rocky Flats
. TASK 1 REPORT (Rl) IDENTIFICATION OF CHEMICALS AND RADIONUCLIDES USED AT ROCKY FLATS I PROJECT BACKGROUND ChemRisk is conducting a Rocky Flats Toxicologic Review and Dose Reconstruction study for The Colorado Department of Health. The two year study will be completed by the fall of 1992. The ChemRisk study is composed of twelve tasks that represent the first phase of an independent investigation of off-site health risks associated with the operation of the Rocky Flats nuclear weapons plant northwest of Denver. The first eight tasks address the collection of historic information on operations and releases and a detailed dose reconstruction analysis. Tasks 9 through 12 address the compilation of information and communication of the results of the study. Task 1 will involve the creation of an inventory of chemicals and radionuclides that have been present at Rocky Flats. Using this inventory, chemicals and radionuclides of concern will be selected under Task 2, based on such factors as the relative toxicity of the materials, quantities used, how the materials might have been released into the environment, and the likelihood for transport of the materials off-site. An historical activities profile of the plant will be constructed under Task 3. Tasks 4, 5, and 6 will address the identification of where in the facility activities took place, how much of the materials of concern were released to the environment, and where these materials went after the releases. Task 7 addresses historic land-use in the vicinity of the plant and the location of off-site populations potentially affected by releases from Rocky Flats. -
US2278550.Pdf
April 7, 1942. D. J. OER E. A. 2,278,550 PREPARATION OF ALKALI METAL ALKOXIDES Filed June 21, 1939 REACTION ------ REGENERATION OFMX FROM M-represents an alkali metal N-represents a number from 2 to 3 R-represents an alkyl group X-represents the anion of a weak acid Donald D. Lee Donald J. Loder NVENTOR BY 232 az - ATTORNEY Patented Apr. 7, 1942 2,278,550 UNITED STATES PATENT OFFICE 2,278,550 PREPARATION OF ALKALI METAL ALKOXDES Donald J. Loder and Donald D. Lee, Wilmington, Del, assignors to E. I. du Pont de Nemours & Company, Wilmington, Del., a corporation of Delaware Application June 21, 1939, Serial No. 280,308 16 Claims. (CI. 260-632) The invention relates to improvements in the and R is an alkyl, or aralkyl radical which may be manufacture of metal alkoxides and more particu Saturated, unsaturated, substituted or unsub larly to the preparation of alkali metal alkoxides stituted. by the interaction of alcohols with alkali metal In Reactions 1 and 2, an alkali metal salt of a salts of weak acids. weak acid is digested with an alcohol at an ap Alkali metal alkoxides have been prepared by propriate temperature, the digestion being Con. direct reaction of the alkali metal as such with tinued until equilibrium has been substantially an alcohol. or by action of an alkali metal hy reached. The equilibrium mixture is filtered for. droxide. upon an alcohol. The higher cost of the the separation of any undissolved (MX or M3X) first of these methods has limited somewhat the O salt and the resulting solution (or filtrate) is industrial use of the alkoxide thus prepared and found to contain an alkali metal alkoxide, or much effort has been expended in endeavors to aralkoxide, (MOR) hereinafter called 'al make the second more commercially practicable. -
WO 2016/074683 Al 19 May 2016 (19.05.2016) W 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 2016/074683 Al 19 May 2016 (19.05.2016) W P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C12N 15/10 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/DK20 15/050343 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 11 November 2015 ( 11. 1 1.2015) KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, (25) Filing Language: English PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, (26) Publication Language: English SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: PA 2014 00655 11 November 2014 ( 11. 1 1.2014) DK (84) Designated States (unless otherwise indicated, for every 62/077,933 11 November 2014 ( 11. 11.2014) US kind of regional protection available): ARIPO (BW, GH, 62/202,3 18 7 August 2015 (07.08.2015) US GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, (71) Applicant: LUNDORF PEDERSEN MATERIALS APS TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, [DK/DK]; Nordvej 16 B, Himmelev, DK-4000 Roskilde DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, (DK). -
Anti-Aging Effects of Deuterium Depletion on Mn-Induced Toxicity in a C
Toxicology Letters 211 (2012) 319–324 Contents lists available at SciVerse ScienceDirect Toxicology Letters jou rnal homepage: www.elsevier.com/locate/toxlet Anti-aging effects of deuterium depletion on Mn-induced toxicity in a C. elegans model a,c b b c,d,e,∗ Daiana Silva Ávila , Gábor Somlyai , Ildikó Somlyai , Michael Aschner a Universidade Federal do Pampa, BR 472 Km 585, CEP 97500-970, Uruguaiana, RS, Brazil b HYD LLC for Cancer Research and Drug Development, Furj u.2., Budapest H-1124, Hungary c Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA d Department of Pharmacology, Vanderbilt University Medical Center, Nashville, TN, USA e Kennedy Center for Research on Human Development, Vanderbilt University Medical Center, Nashville, TN, USA a r t i c l e i n f o a b s t r a c t Article history: Work with sub-natural levels of deuterium (D) in animals has demonstrated an anti-cancer effect of low Received 17 February 2012 D-concentration in water. Our objective was to investigate whether deuterium-depleted water (DDW) Received in revised form 19 April 2012 can overturn reverse manganese (Mn)-induced reduction in life span, using the Caenorhabditis elegans (C. Accepted 20 April 2012 elegans) as a model system. DDW per se had no effect on worm’s life span 48 h after treatment; however, it Available online 26 April 2012 reversed the Mn-induced decrease in C. elegans life span. Mn reduced DAF-16 levels, a transcription factor strongly associated with life-span regulation. Low D-concentration (90 ppm) restored the Mn-induced Keywords: changes in DAF-16 to levels indistinguishable from controls, suggesting DDW can regulate the DAF-16 Deuterium depletion DDW pathway. -
Light-Assisted Delithiation of Lithium Iron Phosphate Nanocrystals Towards Photo-Rechargeable Lithium Ion Batteries
ARTICLE Received 7 Nov 2016 | Accepted 17 Jan 2017 | Published 10 Apr 2017 DOI: 10.1038/ncomms14643 OPEN Light-assisted delithiation of lithium iron phosphate nanocrystals towards photo-rechargeable lithium ion batteries Andrea Paolella1,2, Cyril Faure1, Giovanni Bertoni3, Sergio Marras4, Abdelbast Guerfi1, Ali Darwiche1, Pierre Hovington1, Basile Commarieu1, Zhuoran Wang2, Mirko Prato4, Massimo Colombo4, Simone Monaco4, Wen Zhu1, Zimin Feng1, Ashok Vijh1, Chandramohan George5, George P. Demopoulos2, Michel Armand6 & Karim Zaghib1 Recently, intensive efforts are dedicated to convert and store the solar energy in a single device. Herein, dye-synthesized solar cell technology is combined with lithium-ion materials to investigate light-assisted battery charging. In particular we report the direct photo- oxidation of lithium iron phosphate nanocrystals in the presence of a dye as a hybrid photo-cathode in a two-electrode system, with lithium metal as anode and lithium hexafluorophosphate in carbonate-based electrolyte; a configuration corresponding to lithium ion battery charging. Dye-sensitization generates electron–hole pairs with the holes aiding the delithiation of lithium iron phosphate at the cathode and electrons utilized in the formation of a solid electrolyte interface at the anode via oxygen reduction. Lithium iron phosphate acts effectively as a reversible redox agent for the regeneration of the dye. Our findings provide possibilities in advancing the design principles for photo-rechargeable lithium ion batteries. 1 Institute de Recherche d-Hydro-Que´bec (IREQ), 1800 Boulevard Lionel Boulet, Varennes, Quebec, Canada J3X 1S1. 2 Department of Mining and Materials Engineering, McGill University, Wong Building, 3610 University Street, Montreal, Quebec, Canada H3A OC5. 3 IMEM-CNR, Parco Area delle Scienze 37/A, 43124 Parma, Italy. -
Deuterated Molecules in Star-Forming Regions
Jagiellonian University Faculty of Physics, Astronomy and Applied Computer Science Deuterated Molecules in Star-Forming Regions Magdalena Jastrzębska Dissertation for the degree Doctor of Philosophy Promotor: prof. dr hab. Ryszard Szczerba co-promotor: dr Agata Karska "Not all who wander are lost." J.R.R. Tolkien–Lord of the Rings Rodzicom Danucie i Antoniemu i Chciałabym serdecznie podziękować Panu profesorowi Darkowi Lisowi, bez którego moja rozprawa doktorska by nie powstała. Pani profesor Maryvonne Gerin, która wprowadzała mnie w tajniki redukcji danych spektroskopowych i której wyjątkowe zaangażowanie przyczyniło się do powstania moich artykułów. Panu profesorowi dr hab. Ryszardowi Szczerbie za cierpliwość i merytoryczną pomoc podczas pisania pracy. Paniom dr Agacie Karskiej i dr Nataszy Siódmiak za wnikliwą analizę tekstu. Rodzinie za wsparcie, Kindze i Stasiowi za twórczą obecność, a sobie za kosmiczną determinację. ii Oświadczenie Ja niżej podpisana Magdalena Jastrzębska (nr indeksu: WFAI-D-150) doktorantka Wydziału Fizyki, Astronomii i Informatyki Stosowanej Uniwersytetu Jagiellońskiego oświadczam, że przedłożona przeze mnie rozprawa doktorska pt. „Deuterated Molecules in Star-Forming Regions” jest oryginalna i przedstawia wyniki badań wykonanych przeze mnie osobiście, pod kierunkiem prof. dr hab. Ryszarda Szczerby. Pracę napisałam samodzielnie. Oświadczam, że moja rozprawa doktorska została opracowana zgodnie z Ustawą o prawie autorskim i prawach pokrewnych z dnia 4 lutego 1994 r (Dziennik Ustaw 1994 nr 24 poz. 83 z późniejszymi zmianami). Jestem świadoma, że niezgodność niniejszego oświadczenia z prawdą ujawniona w dowolnym czasie, niezależnie od skutków prawnych wynikających z ww. ustawy, może spowodować unieważnienie stopnia na podstawie tej rozprawy. ................................. ................................. Data Podpis autora pracy iii Contents Contents 1 Abstract 2 2 Summary in Polish 4 3 Synopsis 6 3.1 A brief history ............................... -
Treaty Series
Treaty Series Treaties and internationalagreements registered or filed and recorded with the Secretariat of the United Nations VOLUME 446 Recueil des Traites Traites et accords internationaux enregistres ou classes et inscrits au repertoire au Secrtariat de l'Organisationdes Nations Unies United Nations * Nations Unies New York, 1963 Treaties and international agreements registered or filed and recorded with the Secretariat of the United Nations VOLUME 446 1962 I. Nos. 6397-6409 TABLE OF CONTENTS Treaties and internationalagreements registered /rom 29 November 1962,to 4 December 1962 Page No. 6397. Denmark and People's Republic of China: Exchange of notes constituting an agreement relating to mutual exemption from taxation of residents of either State who are temporarily staying in the other State for educational purposes. Copenhagen, 7 and 23 Septem- ber 1961 .............. .............. ........ 3 No. 6398. United States of America and Denmark: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). Signed at Geneva, on 5 March 1962 ............ 9 No. 6399. United States of America and Finland: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). Signed at Geneva, on 5 March 1962 ......... ... 19 No. 6400. United States of America and Israel: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). Signed at Geneva, on 5 March 1962 ......... ... 29 No. 6401. United States of America and New Zealand: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). Signed at Geneva, on 5 March 1962 ......... ... 39 No. 6402. United States of America and Norway: Interim Agreement relating to the General Agreement on Tariffs and Trade (with schedules). -
WO 2016/196440 Al 8 December 2016 (08.12.2016) 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 2016/196440 Al 8 December 2016 (08.12.2016) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every A61P 3/04 (2006.01) A61K 33/40 (2006.01) kind of national protection available): AE, AG, AL, AM, A61P 9/10 (2006.01) A61K 38/44 (2006.01) AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, A61K 35/74 (2015.01) A61K 31/17 (2006.01) BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (21) International Application Number: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, PCT/US20 16/034973 KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, (22) International Filing Date: MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, 3 1 May 2016 (3 1.05.2016) PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, (25) Filing Language: English TR, TT, TZ, UA, UG, US, UZ, VC, VN, 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, 62/169,480 1 June 2015 (01 .06.2015) US GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, 62/327,283 25 April 2016 (25.04.2016) US TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, (71) Applicant: XENO BIOSCIENCES INC. -
Hydrophobically Functionalized Poly (Acrylic Acid) Comprising the Ester
polymers Article Hydrophobically Functionalized Poly(Acrylic Acid) Comprising the Ester-Type Labile Spacer: Synthesis and Self-Organization in Water Łukasz Lamch 1,*, Sylwia Ronka 2, Izabela Moszy ´nska 1, Piotr Warszy ´nski 3 and Kazimiera A. Wilk 1,* 1 Department of Engineering and Technology of Chemical Processes, Faculty of Chemistry, Wrocław University of Science and Technology, Wybrze˙zeWyspia´nskiego27, 50-370 Wrocław, Poland; [email protected] 2 Department of Engineering and Technology of Polymers, Faculty of Chemistry, Wrocław University of Science and Technology, Wybrze˙zeWyspia´nskiego27, 50-370 Wrocław, Poland; [email protected] 3 Jerzy Haber Institute of Catalysis and Surface Chemistry, Polish Academy of Sciences, Niezapominajek 8, 30-239 Kraków, Poland; [email protected] * Correspondence: [email protected] (Ł.L.); [email protected] (K.A.W.) Received: 22 April 2020; Accepted: 18 May 2020; Published: 22 May 2020 Abstract: One of the most important properties of hydrophobically functionalized polyelectrolytes (HF-PEs) and their assemblies is their ability to encapsulate hydrophobic/amphiphilic agents and provide release on demand of the entrapped payload. The aim of the present work was to synthesize and study self-organization behavior in aqueous solution of hydrophobically functionalized poly(acrylic acid) (PAA) comprising the ester-type pH labile moiety with various degrees of hydrophobization and side-chain lengths in the absence and presence of appropriate mono- and polyvalent electrolytes (i.e., NaCl or CaCl2). The synthesis and purification of hydrophobically functionalized PAA were performed under mild conditions in order to avoid chemical degradation of the polymers. -
N FUEL CHEMISTRY DIVISION ANNUAL PROGRESS REPORT for 1988 S. Vaidyanathan
2-o3 BARC/1991/P/002 00 > n o o to FUEL CHEMISTRY DIVISION ANNUAL PROGRESS REPORT FOR 1988 S. Vaidyanathan 1991 GOVERNMENT OF INDIA ATOMIC ENERGY COMMISSION o o U a: < CD FUEL CHEMISTRY DIVISION ANNUAL PROGRESS REPORT FOR 1908 EdiLecl by S. VaidyanaLhan BHADHA ATOMIC RLSLAROI CLN7KI HOMHAY, INDIA 199 I BARC/1991/P/002 BIBLIOGRAPHIC DESCRIPTION SHEET FOR TECHNICAL REPORT (as per IS : 9400 - 1980) 01 Security classification : Uncl assi-f ied 02 Distribution : External 03 Report status : New 04 Series : BARC External 05 Report type : Progress Report 06 Report ND. : BARC/1991/P/002 07 Part No. or Volume No. : 08 Contract No. ; 10 Title and subtitle : Fuel Chemistry Division : annual progress report for 19BB 11 Collation : 158 p., 61 tabs., 13 figs. 13 Project No. : 20 Personal author(s) : S. Vaidyanathan <ed.) 21 Affiliation Df author(s) :Fuel Chemistry Division , Bhabha Atomic Research Centre, Bombay 22 Corporate author(s) : Bhabha Atomic Research Centre, Bombay - 400 0B5 23 Originating unit : Fuel Chemistry Division, BARC, BDHIIJU 24 Sponsor(s) Name ; Department of Atomic Energy Type : Government 30 Date of submission : July 1991 31 Publication/Issue date : August 1991 Contd... <i i) (ii) 40 Publisher/Distributor : Head, Library and Information Division, Bhabha Atomic Research Centre, Bombay 42 Form of distribution : Hard Copy 50 Language of text : Engli sh 51 Language of summary : English 52 No. of references : 53 Gives data on : 60 Abstract : The progress report gives the brief descriptions of various activities of the Fuel Chemistry Division of Bhabha Atomic Research Centre, Bombay for the year 1988.