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(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization llllllllllllllllllllllllllllllll^ International Bureau (10) International Publication Number (43) International Publication Date WO 2018/097733 A3 31 May 2018 (31.05.2018) WIPO I PCT (51) International Patent Classification: (88) Date of publication of the international search report: A61K31/194 (2006.01) A61P 9/00 (2006.01) 02 August 2018 (02.08.2018) A61K31/195 (2006.01) A61P 3/00 (2006.01) A61P 21/00 (2006.01) GOIN 33/48 (2006.01) (21) International Application Number: PCT/NO2017/000032 (22) International Filing Date: 23 November 2017 (23.11.2017) (25) Filing Language: English (26) Publication Language: English (30) Priority Data: 20161866 23 November2016 (23.11.2016) NO (71) Applicant: BOHNE ASK0Y AS [NO/NO]; Romledalen 51, 5310 Hauglandshella (NO). (72) Inventors: BOHNE, Oyvind; Romledalen 51, 5310 Haug- landshella (NO). BOHNE, Victoria; Romledalen 51, 5310 Hauglandshella (NO). (74) Agent: ACAPO AS; P.O. Box 1880 Nordnes, 5817 Bergen (NO). (81) Designated States (unless otherwise indicated, for every kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, HN, HR, HU, ID, IL, IN, IR, IS, JO, JP, KE, KG, KH, KN, KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, 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, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. -
Aldrich FT-IR Collection Edition I Library
Aldrich FT-IR Collection Edition I Library Library Listing – 10,505 spectra This library is the original FT-IR spectral collection from Aldrich. It includes a wide variety of pure chemical compounds found in the Aldrich Handbook of Fine Chemicals. The Aldrich Collection of FT-IR Spectra Edition I library contains spectra of 10,505 pure compounds and is a subset of the Aldrich Collection of FT-IR Spectra Edition II library. All spectra were acquired by Sigma-Aldrich Co. and were processed by Thermo Fisher Scientific. Eight smaller Aldrich Material Specific Sub-Libraries are also available. Aldrich FT-IR Collection Edition I Index Compound Name Index Compound Name 3515 ((1R)-(ENDO,ANTI))-(+)-3- 928 (+)-LIMONENE OXIDE, 97%, BROMOCAMPHOR-8- SULFONIC MIXTURE OF CIS AND TRANS ACID, AMMONIUM SALT 209 (+)-LONGIFOLENE, 98+% 1708 ((1R)-ENDO)-(+)-3- 2283 (+)-MURAMIC ACID HYDRATE, BROMOCAMPHOR, 98% 98% 3516 ((1S)-(ENDO,ANTI))-(-)-3- 2966 (+)-N,N'- BROMOCAMPHOR-8- SULFONIC DIALLYLTARTARDIAMIDE, 99+% ACID, AMMONIUM SALT 2976 (+)-N-ACETYLMURAMIC ACID, 644 ((1S)-ENDO)-(-)-BORNEOL, 99% 97% 9587 (+)-11ALPHA-HYDROXY-17ALPHA- 965 (+)-NOE-LACTOL DIMER, 99+% METHYLTESTOSTERONE 5127 (+)-P-BROMOTETRAMISOLE 9590 (+)-11ALPHA- OXALATE, 99% HYDROXYPROGESTERONE, 95% 661 (+)-P-MENTH-1-EN-9-OL, 97%, 9588 (+)-17-METHYLTESTOSTERONE, MIXTURE OF ISOMERS 99% 730 (+)-PERSEITOL 8681 (+)-2'-DEOXYURIDINE, 99+% 7913 (+)-PILOCARPINE 7591 (+)-2,3-O-ISOPROPYLIDENE-2,3- HYDROCHLORIDE, 99% DIHYDROXY- 1,4- 5844 (+)-RUTIN HYDRATE, 95% BIS(DIPHENYLPHOSPHINO)BUT 9571 (+)-STIGMASTANOL -
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. -
Phosphate-Based Treatments for Conservation of Stone
RILEM Technical Letters (2017) 2: 14‐19 DOI: http://dx.doi.org/10.21809/rilemtechlett.2017.34 Phosphate‐based treatments for conservation of stone Enrico Sassoni a* a Department of Civil, Chemical, Environmental and Materials Engineering, University of Bologna, Via Terracini 28, 40131, Bologna, Italy Received: 30 May 2017 / Accepted: 09 August 2017 / Published online: 9 October 2017 © The Author(s) 2017. This article is published with open access and licensed under a Creative Commons Attribution 4.0 International License. Abstract To overcome the limitations of currently available protectives and consolidants for carbonate stones (such as marble and limestone), in 2011 the use of calcium phosphate was proposed. The idea is forming calcium phosphates (ideally hydroxyapatite) as the reaction product between the substrate and an aqueous solution of a phosphate salt that the stone is treated with. In this paper, the studies aimed at identifying the best treatment conditions (in terms of nature and concentration of the phosphate precursor, solution pH, reaction time, ionic and organic additions) are first briefly summarized. Then, the efficacy of the phosphate treatment in protecting marble from dissolution in rain and restoring cohesion of weathered marble and limestone is discussed. Some recent studies on the use of the phosphate treatment on alternative substrates and some future steps for research on the topic are finally outlined. Keywords: Cultural heritage; Marble; Hydroxyapatite; Protection; Consolidation 1 Introduction improve mechanical properties, by providing a binding action between the stone grains. Organic products are A great part of cultural heritage objects (e.g. monuments, effective in improving mechanical properties, but again architectural decorations and statues) is made of carbonate they lack compatibility and durability. -
Durham E-Theses
Durham E-Theses Halogenated diazines and triazines Wood, D. E. How to cite: Wood, D. E. (1978) Halogenated diazines and triazines, Durham theses, Durham University. Available at Durham E-Theses Online: http://etheses.dur.ac.uk/8324/ Use policy The full-text may be used and/or reproduced, and given to third parties in any format or medium, without prior permission or charge, for personal research or study, educational, or not-for-prot purposes provided that: • a full bibliographic reference is made to the original source • a link is made to the metadata record in Durham E-Theses • the full-text is not changed in any way The full-text must not be sold in any format or medium without the formal permission of the copyright holders. Please consult the full Durham E-Theses policy for further details. Academic Support Oce, Durham University, University Oce, Old Elvet, Durham DH1 3HP e-mail: [email protected] Tel: +44 0191 334 6107 http://etheses.dur.ac.uk UNIVERSITY OF Du'RKAM A THESIS entitled HALOGENATED DIAZINES AND TRIAZINES Submitted by D E. WOOD (Grey), B Sc (London) The copyright of this thesis rests with the author No quotation from it should be published without his prior written consent and information derived from it should be acknowledged A candidate for the degree of Doctor of Philosophy 19 78 sr i i > j J To my MoLhcr and FaLhcr WLLII Lh.inks for .ill LhaL Lhey have done ACKNOWLEDGEMLNTS I would like LO express my thanks Lo Professor R D Chambers i under whose guidance this research was undertaken, for considerable encouragement, advice and discussion Thanks are due to Dr R S Matthews for his expert advice with n in r. -
1,45%,562 UNITED SATES P All.‘ Bl If" Til?
Patented May 1, 1923. 1,45%,562 UNITED SATES P All.‘ bl if" til? . ROBERT E. WILSON, LEON ‘JV. PARSONS, AND STANLEY 1E. OHXSHOLIYI, OF WASHINGTON, DISTRICT OF COLUMBIA. PROCESS THE PRODUCTION OE‘ All‘HALLEAETELMLETAL PERTJIANGANATES. N0 Drawing". Application ?led September 27, 1918. Serial No. 255,975. To (all to]: am it may concern. .' manganate by oxidation or acidification, Be it known that we, Romain‘ E. lllinsou, metatheses into calcium pern'iangamite by LEON “7. Parsons, and STANLEY L. Unis treatment With calcium sulphate or milk at HoLM, citizens of the United States. and sta lime. tioned at ViTashington, District of Columbia, O'li' these four possible methods, (1.) is not 60 in the o?icc of the Director the Chemical a possible large scale method. on account l/Varfare Service, Research Division, have in of its use ot silver; (2) and are elec vented a Process for the ll’roduction oif Al trolytic methods Without a. great deal out kali-Earth-l\letal Permanpjanates, of which promise, and are to be considered elsewhere; ll) the ‘following is a speci?cation. (ll) the principal subject of this applica G3 in The present invention relates to the pro tion. duction oi? alkah» earth metal permangam Three distinct methods for preparing: ba~ nates and especially the permanganates of rium (or strontium) manganate have been calcium and magnesium as these have beenv here investigated. The ?rst of? these meth found to be very ellicient oxidizing agents ods involves heating together barium perox 70 for certain purposes, more e?icient even. than ide, hydroxide, or a salt, such as the nitrate the permanganates of the allmliearth metals. -
Crown Chemical Resistance Chart
Crown Polymers, Corp. 11111 Kiley Drive Huntley, IL. 60142 USA www.crownpolymers.com 847-659-0300 phone 847-659-0310 facisimile 888-732-1270 toll free Chemical Resistance Chart Crown Polymers Floor and Secondary Containment Systems Products: CrownShield covers the following five (4) formulas: CrownShield 50, Product No. 320 CrownCote, Product No. 401 CrownShield 40-2, Product No. 323 CrownShield 28, Product No. 322 CrownPro AcidShield, Product No. 350 CrownCote AcidShield, Product No. 430 CrownPro SolventShield, Product No. 351 CrownCote SolventShield, Product No. 440 This chart shows chemical resistance of Crown Polymers foundational floor and secondary containment product line that would be exposed to chemical spill or immersion conditions. The chart was designed to provide general product information. For specific applications, contact your local Crown Polymers Floor and Secondary Containment Representative or call direct to the factory. ; Resistant to chemical immersion up to 7 days followed by wash down with water 6 Spillage environments that will be cleaned up within 72 hours after initial exposure. 9 Not Recommended Chemical CrownShield SolventShield AcidShield Chemical CrownShield SolventShield AcidShield 1, 4-Dichloro-2-butene 9 6 6 Aluminum Bromate ; ; ; 1, 4-Dioxane 9 6 6 Aluminum Bromide ; ; ; 1-1-1 Trichloroethane 9 ; ; Aluminum Chloride ; ; ; 2, 4-Pentanedione 6 ; 6 Aluminum Fluoride (25%) ; ; ; 3, 4-Dichloro-1-butene 6 6 6 Aluminum Hydroxide ; ; ; 4-Picoline (0-50%) 9 6 6 Aluminum Iodine ; ; ; Acetic Acid (0-15%) 9 6 6 -
Safety Practices in Chemistry Laboratories
4/24/2012 Safety Practices in Chemistry Laboratory Sam Tung, HSE Specialist, CIH, RSO Health Safety and Environment Office, Hong Kong University of Science and Technology Contents 1. Introduction to Legislations related to Chemistry Laboratories 2. Introduction to Chemical Hazards 3. Criteria of Design for Laboratory Ventilation 4. Operations and Maintenance of Laboratory Fume hood 5. Case Studies of Laboratory Accidents 6. Handling of Chemical Spills 7. Emergency Response Equipment 1 4/24/2012 Importance of Health and Safety To protect your health and safety (and environment) To protect your colleagues’ and students’ health and safety Case Study: Laboratory Fire Kills UCLA Researcher A 23-year-old research assistant working at UCLA who was seriously burned in a lab fire in December 2008 recently died from her injuries. She was trying to transfer up to 2 ounces (~50ml) of t-butyl lithium (pyrophoric chemical), which was dissolved in pentane from one sealed container to another by a 50 ml syringe. The barrel of the syringe was either ejected or pulled out of the syringe, causing liquid to be released. A flash fire set her clothing ablaze and spread second- and third-degree burns over 43% of her body. 2 4/24/2012 Root Causes of the Accident Poor technique and improper method Use a 50ml syringe to transfer~50 ml pyrophoric chemical Should use a 100ml syringe Should use Cannula Method for transfer of pyrophoric chemical > 50 ml Lack of proper training No safety training record Lack of supervision No follow up actions had been -
1 Abietic Acid R Abrasive Silica for Polishing DR Acenaphthene M (LC
1 abietic acid R abrasive silica for polishing DR acenaphthene M (LC) acenaphthene quinone R acenaphthylene R acetal (see 1,1-diethoxyethane) acetaldehyde M (FC) acetaldehyde-d (CH3CDO) R acetaldehyde dimethyl acetal CH acetaldoxime R acetamide M (LC) acetamidinium chloride R acetamidoacrylic acid 2- NB acetamidobenzaldehyde p- R acetamidobenzenesulfonyl chloride 4- R acetamidodeoxythioglucopyranose triacetate 2- -2- -1- -β-D- 3,4,6- AB acetamidomethylthiazole 2- -4- PB acetanilide M (LC) acetazolamide R acetdimethylamide see dimethylacetamide, N,N- acethydrazide R acetic acid M (solv) acetic anhydride M (FC) acetmethylamide see methylacetamide, N- acetoacetamide R acetoacetanilide R acetoacetic acid, lithium salt R acetobromoglucose -α-D- NB acetohydroxamic acid R acetoin R acetol (hydroxyacetone) R acetonaphthalide (α)R acetone M (solv) acetone ,A.R. M (solv) acetone-d6 RM acetone cyanohydrin R acetonedicarboxylic acid ,dimethyl ester R acetonedicarboxylic acid -1,3- R acetone dimethyl acetal see dimethoxypropane 2,2- acetonitrile M (solv) acetonitrile-d3 RM acetonylacetone see hexanedione 2,5- acetonylbenzylhydroxycoumarin (3-(α- -4- R acetophenone M (LC) acetophenone oxime R acetophenone trimethylsilyl enol ether see phenyltrimethylsilyl... acetoxyacetone (oxopropyl acetate 2-) R acetoxybenzoic acid 4- DS acetoxynaphthoic acid 6- -2- R 2 acetylacetaldehyde dimethylacetal R acetylacetone (pentanedione -2,4-) M (C) acetylbenzonitrile p- R acetylbiphenyl 4- see phenylacetophenone, p- acetyl bromide M (FC) acetylbromothiophene 2- -5- -
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. -
Chemistry Inventory; Fall
CHEMISTRY FALL 2005 MSDS Mfg.'s Name Chemical Name Quantity Stored Storage Conditions (on file = 9) Aluminum 9 1.5 kg Aluminum chloride, anhydrous, 98.5% 9 0.2 kg Aluminum chloride · 6H2O 9 0.5 kg Aluminum hydroxide 9 0.5 kg Aluminum nitrate 9 0.5 kg Aluminum sulfate 9 0.5 kg Ammonia, concentrated 9 4.0 L Ammonium acetate 9 0.2 kg Ammonium chloride 9 Ammonium dihydrogen phosphate (monobasic) 9 0.4 kg J.T. Baker Ammonium hydrogen phosphate (dibasic) No 0.5 kg Ammonium nitrate 9 2.5 kg Ammonium oxalate 9 0.7 kg Ammonium peroxydisulfate 9 0.5 kg Ammonium sulfate 9 0.2 kg Antimony 9 0.4 kg Barium chloride, anhydrous 9 2.5 kg Barium chloride · 2H2O 9 2.5 kg Barium nitrate 9 0.8 kg Bismuth 9 2.0 kg Boric Acid 9 0.4 kg Brass 9 Bromine 9 2.5 kg Cadmium 9 0.1 kg Cadmium nitrate 9 0.3 kg Calcium acetate · xH2O 9 0.5 kg Calcium carbide 9 1.0 kg Calcium carbonate 9 2.2 kg Calcium chloride 9 1.0 kg Calcium hydroxide 9 0.3 kg Calcium nitrate · 4H2O 9 1.0 kg Calcium oxide 9 0.3 kg Calcium sulfate · 2H2O 9 1.0 kg Carbon 9 0.1 kg Ceric ammonium nitrate 9 0.5 kg Cesium chloride 9 0.01 kg Chromium 9 0.01 kg Chromium chloride 9 0.5 kg Chromium nitrate 9 0.5 kg Cobalt 9 0.025 kg Cobalt chloride 9 0.7 kg Cobalt nitrate 9 0.6 kg Copper (assorted) 9 4.0 kg Copper acetate 9 0.05 kg Copper chloride 9 0.1 kg Copper nitrate 9 3.5 kg Copper oxide 9 0.4 kg Cupric sulfate, anhydrous 9 0.5 kg Cupric sulfate · 5H2O 9 2.75 kg EDTA 9 0.6 kg Iodine 9 2.0 kg Iron (assorted) 9 5.0 kg MSDS Mfg.'s Name Chemical Name Quantity Stored Storage Conditions (on file = 9) Ferric ammonium -
Crystallization and Preliminary X-Ray Analysis of Ocr, the Product of Gene 0.3 of Bacteriophage T7
Edinburgh Research Explorer Crystallization and preliminary X-ray analysis of ocr, the product of gene 0.3 of bacteriophage T7 Citation for published version: Sturrock, SS, Dryden, DTF, Atanasiu, C, Dornan, J, Bruce, S, Cronshaw, A, Taylor, P & Walkinshaw, MD 2001, 'Crystallization and preliminary X-ray analysis of ocr, the product of gene 0.3 of bacteriophage T7', Acta Crystallographica Section D: Biological Crystallography, vol. 57, no. Part 11, pp. 1652-1654. https://doi.org/10.1107/S0907444901011623 Digital Object Identifier (DOI): 10.1107/S0907444901011623 Link: Link to publication record in Edinburgh Research Explorer Document Version: Publisher's PDF, also known as Version of record Published In: Acta Crystallographica Section D: Biological Crystallography Publisher Rights Statement: RoMEO green General rights Copyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorer content complies with UK legislation. If you believe that the public display of this file breaches copyright please contact [email protected] providing details, and we will remove access to the work immediately and investigate your claim. Download date: 27. Sep. 2021 crystallization papers Acta Crystallographica Section D Crystallization and preliminary X-ray analysis of Biological Crystallography ocr, the product of gene 0.3 of bacteriophage T7 ISSN 0907-4449 Shane S. Sturrock,a David T. F.