Chemical Resistance Guide
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Precursors and Chemicals Frequently Used in the Illicit Manufacture of Narcotic Drugs and Psychotropic Substances 2017
INTERNATIONAL NARCOTICS CONTROL BOARD Precursors and chemicals frequently used in the illicit manufacture of narcotic drugs and psychotropic substances 2017 EMBARGO Observe release date: Not to be published or broadcast before Thursday, 1 March 2018, at 1100 hours (CET) UNITED NATIONS CAUTION Reports published by the International Narcotics Control Board in 2017 The Report of the International Narcotics Control Board for 2017 (E/INCB/2017/1) is supplemented by the following reports: Narcotic Drugs: Estimated World Requirements for 2018—Statistics for 2016 (E/INCB/2017/2) Psychotropic Substances: Statistics for 2016—Assessments of Annual Medical and Scientific Requirements for Substances in Schedules II, III and IV of the Convention on Psychotropic Substances of 1971 (E/INCB/2017/3) Precursors and Chemicals Frequently Used in the Illicit Manufacture of Narcotic Drugs and Psychotropic Substances: Report of the International Narcotics Control Board for 2017 on the Implementation of Article 12 of the United Nations Convention against Illicit Traffic in Narcotic Drugs and Psychotropic Substances of 1988 (E/INCB/2017/4) The updated lists of substances under international control, comprising narcotic drugs, psychotropic substances and substances frequently used in the illicit manufacture of narcotic drugs and psychotropic substances, are contained in the latest editions of the annexes to the statistical forms (“Yellow List”, “Green List” and “Red List”), which are also issued by the Board. Contacting the International Narcotics Control Board The secretariat of the Board may be reached at the following address: Vienna International Centre Room E-1339 P.O. Box 500 1400 Vienna Austria In addition, the following may be used to contact the secretariat: Telephone: (+43-1) 26060 Fax: (+43-1) 26060-5867 or 26060-5868 Email: [email protected] The text of the present report is also available on the website of the Board (www.incb.org). -
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. -
End-Of-Line Hyphenation of Chemical Names (IUPAC Provisional
Pure Appl. Chem. 2020; aop IUPAC Recommendations Albert J. Dijkstra*, Karl-Heinz Hellwich, Richard M. Hartshorn, Jan Reedijk and Erik Szabó End-of-line hyphenation of chemical names (IUPAC Provisional Recommendations) https://doi.org/10.1515/pac-2019-1005 Received October 16, 2019; accepted January 21, 2020 Abstract: Chemical names and in particular systematic chemical names can be so long that, when a manu- script is printed, they have to be hyphenated/divided at the end of a line. Many systematic names already contain hyphens, but sometimes not in a suitable division position. In some cases, using these hyphens as end-of-line divisions can lead to illogical divisions in print, as can also happen when hyphens are added arbi- trarily without considering the ‘chemical’ context. The present document provides recommendations and guidelines for authors of chemical manuscripts, their publishers and editors, on where to divide chemical names at the end of a line and instructions on how to avoid these names being divided at illogical places as often suggested by desk dictionaries. Instead, readability and chemical sense should prevail when authors insert optional hyphens. Accordingly, the software used to convert electronic manuscripts to print can now be programmed to avoid illogical end-of-line hyphenation and thereby save the author much time and annoy- ance when proofreading. The recommendations also allow readers of the printed article to determine which end-of-line hyphens are an integral part of the name and should not be deleted when ‘undividing’ the name. These recommendations may also prove useful in languages other than English. -
Mineral Processing
Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19 -
(12) Patent Application Publication (10) Pub. No.: US 2005/0124724 A1 Burton Et Al
US 2005O124724A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2005/0124724 A1 Burton et al. (43) Pub. Date: Jun. 9, 2005 (54) POLYMER COMPOSITIONS WITH (21) Appl. No.: 10/728,439 BIOACTIVE AGENT, MEDICAL ARTICLES, AND METHODS (22) Filed: Dec. 5, 2003 (75) Inventors: Scott A. Burton, Woodbury, MN (US); Publication Classification Patrick D. Hyde, Burnsville, MN (US); Prabhakara S. Rao, Maplewood, MN (51) Int. Cl." ....................................................... C08K 3/00 (US); Caroline M. Ylitalo, Stillwater, (52) U.S. Cl. .............................................................. 523/122 MN (US) (57) ABSTRACT Correspondence Address: A polymer composition that includes a hydrophilic polymer, 3M INNOVATIVE PROPERTIES COMPANY an optional Secondary organic polymer, and a bioactive PO BOX 33427 agent distributed therein, wherein the bioactive agent is ST. PAUL, MN 55133-3427 (US) Selected from the group consisting of a Silver compound, a copper compound, a Zinc compound, and combinations (73) Assignee: 3M Innovative Properties Company thereof. US 2005/O124724 A1 Jun. 9, 2005 POLYMER COMPOSITIONS WITH BOACTIVE comprising absorbent hydrophilic microparticles, a metal AGENT, MEDICAL ARTICLES, AND METHODS compound Selected from the group consisting of a Silver compound, a copper compound, a Zinc compound, and BACKGROUND combinations thereof, wherein the Silver compound has a 0001 Polymer compositions that include bioactive Solubility of at least 0.1 gram per liter in water; and a agents (e.g., antimicrobial agents) are used for a variety of hydroxide Source that converts the metal compound to the applications, particularly medical applications Such as corresponding metal oxide. The components are combined wound dressings and wound packing materials. Conven in a manner to incorporate the metal oxide within the tional antimicrobial agents include ionizable Silver com microparticles. -
Aniline and Aniline Hydrochloride
SOME AROMATIC AMINES AND RELATED COMPOUNDS VOLUME 127 This publication represents the views and expert opinions of an IARC Working Group on the Identification of Carcinogenic Hazards to Humans, which met remotely, 25 May–12 June 2020 LYON, FRANCE - 2021 IARC MONOGRAPHS ON THE IDENTIFICATION OF CARCINOGENIC HAZARDS TO HUMANS ANILINE AND ANILINE HYDROCHLORIDE 1. Exposure Characterization 1.1.2 Structural and molecular formulae, and relative molecular mass 1.1 Identification of the agent (a) Aniline 1.1.1 Nomenclature NH2 (a) Aniline Chem. Abstr. Serv. Reg. No.: 62-53-3 EC No.: 200-539-3 Molecular formula: C H N IUPAC systematic name: aniline 6 7 Relative molecular mass: 93.13 (NCBI, 2020a). Synonyms and abbreviations: benzenamine; phenylamine; aminobenzene; aminophen; (b) Aniline hydrochloride aniline oil. NH2 (b) Aniline hydrochloride Chem. Abstr. Serv. Reg. No.: 142-04-1 EC No.: 205-519-8 HCl IUPAC systematic name: aniline hydro - Molecular formula: C6H8ClN chloride Relative molecular mass: 129.59 (NCBI, Synonyms: aniline chloride; anilinium chlo- 2020b). ride; benzenamine hydrochloride; aniline. HCl; phenylamine hydrochloride; phenylam- monium chloride. 1.1.3 Chemical and physical properties of the pure substance Aniline is a basic compound and will undergo acid–base reactions. Aniline and its hydrochlo- ride salt will achieve a pH-dependent acid–base equilibrium in the body. 109 IARC MONOGRAPHS – 127 (a) Aniline Octanol/water partition coefficient (P): log Kow, 0.936, predicted median (US EPA, 2020b) Description: aniline appears as a yellowish Conversion factor: 1 ppm = 5.3 mg/m3 [calcu- to brownish oily liquid with a musty fishy lated from: mg/m3 = (relative molecular odour (NCBI, 2020a), detectable at 1 ppm 3 mass/24.45) × ppm, assuming temperature [3.81 mg/m ] (European Commission, 2016; (25 °C) and pressure (101 kPa)]. -
Synthesis of Bromochloromethane Using Phase Transfer Catalysis
1 SYNTHESIS OF BROMOCHLOROMETHANE USING PHASE TRANSFER CATALYSIS By LANCELOT LUCRETIUS BROOKS Baccalaureus Scientiae Honores-Chemistry, Nelson Mandela Metropolitan University A dissertation submitted in fulfillment of the requirements for the Masters Degree in Chemistry In the Faculty of Science at the NELSON MANDELA METROPOLITAN UNIVERSITY Nov. 2011 Promoter : Dr G. Dugmore Co-Promoter : Prof B. Zeelie 2 DECLARATION I, Lancelot Brooks, hereby declare that the above-mentioned treatise is my own work and that it has not previously been submitted for assessment to another University, or for another qualification. ……………………………….. ……………………….. Mr. L.L. Brooks Date 3 ACKNOWLEDGEMENTS To my promoters Dr. Gary Dugmore, and Prof. Ben Zeelie for their invaluable input, help and guidance. To NRF and NMMU for financial assistance To my parents and brothers for their love and support To Peter, Batsho, Unati, and friends in NMMU chemistry research laboratory, thank you guys. To my dearest fiancée, Natasha, a very special thank you for always being there and supporting me. Love you angel. “And we know that all things work together for good to those who love God, to those who are called according to His purpose” -Romans 8:28. 4 TABLE OF CONTENTS DECLARATION……………………………………………………………………. 2 ACKNOWLEDGEMENTS……………………………………………………………. 3 TABLE OF CONTENTS………………………………………………………………. 4 LIST OF FIGURES…………………………………………………………………….. 8 LIST OF TABLES……………………………………………………………………… 9 LIST OF EQUATIONS………………………………………………………………… 11 SUMMARY……………………………………………………………………………… 12 CHAPTER 1…………………………………………………………………………….. 14 INTRODUCTION………………………………………………………………………. 14 1.1. Technology of leather production……………………………………………….. 14 1.2. Synthesis of TCMTB……………………………………………………………… 17 1.3. Bromine……………………………………………………………………………. 20 1.3.1. Overview……………………………………………………………. 20 1.3.2. Applications of bromine compounds…………..…………………. 22 1.3.2.1. Photography……………………………………………… 22 1.3.2.2. -
Development of Monitoring Technology for Environmental Radioactivity
KAERI/RR-2037/99 KR0000197 Development of Environmental Radiation Protection Technology Development of Monitoring Technology for Environmental Radioactivity 31/40 Please be aware that all of the Missing Pages in this document were originally blank pages KAERI/RR-2037/99 2=1 # a Development of Environmental Radiation Protection Technology Development of Monitoring Technology for Environmental Radioactivity 2000^ : 0| o| I. II- EML ^-A>^ B \f $14. III. o) 4^0. 9Sr Tc-99 )14^H Tc-991- Tc-95m ^^^>* if?!: 7l^^ TBP TBP ^-^^i TEVA ?l^-^ 7] (Quantulus 1220)-!: 44^ *1^^ Pu-241 ^1-Jl £^7l^ 6}-g-«l-^ ^^^ PSA ^^1 Pu-241 a^^l^^: ^1-g-^^ FOM (figure of-merit)7> Pu-241 31# ^fl^l- S^^>^4. FOM° (Ultima gold-AB) ^4^ ^^^^4. S^ ^ 2]^^-€ Pu-241 ^^£ Pu-241 5H ^^^ PERALS® -g-nfl PERALS® PSA 7]^^; 7>*1 ^^]^^-7)]^7l(Quantulus 1220™, Wallac Rn-222 ^ Ra Rn-222 2. on-line «H3-3|i£ £^7l#-ir 7fl#§|-7] $«H ion chromatography£f <SH^% U-A>^^#7|1- ^l-g-^ «j-A}^ ^1#7]1- 7fl^Sl-^4. ion chromatographyS £|M 4^ 14^4^ ^^ #4^ 3. : 7fl#§V7| ^§1] Pu-242 ^«fi^ pH U-232, Th-229 ^ Am-243 Talvitie IV. (Sr-Spec)i 92 % oR1"^ fe^ ^t^: ^.$1^ £lfe Ba, Ca, Y 4. 111 7} %$\ £#*l|3. DC18C6 0.1 Mi tflsfl DNNS 25 mM ^£7} JL 6I *H 90 %°]$£\ ^S^-f- 4i^ > 1 : 5 - 1 ^^4J^A], ^ aflui*l<g<3 (20 - 500 keV) ^A^ ^S 90 % °1&JL 90Y^ 34.2 %, ne)jL 89Sr^r 50.6 % ^1-1^1^^(500 - 1400 keV)iAi^ 7fl#^^^: ^Sr0] 1.7 %, 90Y7} 49.7 %, nelJL 89Sr^l 44.9 % 3£t- .^-^4. -
Supplement to the Role of Internal Standards and Their Interaction With
Supplement to: Hiatt, M., “The Role of Internal Standards and their Interaction with Soils Impact Accuracy of Volatile Organics Determinations,” Int. J. of Environ. Anal. Chem., 2010 90:8 591-604. Please note that this is a non-copyrighted web version of supplemental information belonging to the above-cited journal article. There are formatting and page-numbering differences between this web version and the actual published version. There are also minor content differences. This version can be accessed at: http://www.epa.gov/nerlesd1/chemistry/vacuum/reference/pubs.htm This publication is also available from Informaworld: http://www.informaworld.com/smpp/content~db=all~content=a921288588 Web version, 27 April 2010 1 Supplement to: The Role of Internal Standards and their Interaction with Soils Impact Accuracy of Volatile Organics Determinations Michael H. Hiatt U.S. Environmental Protection Agency, National Exposure Research Laboratory Environmental Sciences Division. P.O. Box 93478, Las Vegas, Nevada 89193-3478 Phone: 702 798 2381. Fax: 702 798 2142. E-mail: [email protected]. Supplementary Information Data that was too detailed for “The Role of Internal Standards and their Interaction with Soils Impact Accuracy of Volatile Organics Determinations” is presented as supplemental information. This information includes each analyte by matrix and includes the accuracy evaluation, analyte results impacted by criteria, and results from varying spike equilibration times. The list of internal standards and their chemical properties are presented in Table S1 while the surrogates are listed in Table S2. Tables of results by analyte are included as Tables S3-8. These tables include the data by matrix and combined. -
Hydrothermal Synthesis of Molybdenum Based Oxides for The
Hydrothermal synthesis of molybdenum based oxides for the application in catalysis Zur Erlangung des akademischen Grades eines DOKTORS DER NATURWISSENSCHAFTEN (Dr. rer. nat.) Fakultät für Chemie und Biowissenschaften Karlsruher Institut für Technologie (KIT) - Universitätsbereich genehmigte DISSERTATION von Dipl.-Ing. (FH) Kirsten Schuh aus Mainz Dekan: Prof. Dr. Peter Roesky Referent: Prof. Dr. Jan-Dierk Grunwaldt Korreferent: Prof. Dr. Anker Degn Jensen Tag der mündlichen Prüfung: 17. April 2014 Acknowledgements Acknowledgements I owe many thanks to a lot of people who have helped, supported and encouraged me during my doctoral studies, not just scientifically but also personally. First I would like to thank my supervisor Prof. Dr. Jan-Dierk Grunwaldt for the opportunity to complete my doctoral studies in his group and for providing me with a very interesting and diversified topic. I am grateful for the scientific freedom he gave me, the possibility to spend several months at the Technical University of Denmark as well as University of Zurich and for the opportunity to attend international conferences. I am grateful to Dr. Wolfgang Kleist for his scientific help especially with presentations and publications making the manuscripts reader friendly. I would also like to thank Prof. Dr. Anker Degn Jensen for agreeing to be my co- supervisor, for very helpful corrections and suggestions of abstracts, manuscripts and presentations and for giving me the opportunity to spend four months in his group at the Technical University of Denmark (DTU), where I felt very welcome. I am especially grateful for the help of Dr. Martin Høj, who put the selective oxidation set- up at DTU into operation, tested several of my samples for selective oxidation of propylene and performed TEM measurements of my FSP samples. -
Cheminformatics Tools for Enabling Metabolomics by Yannick Djoumbou Feunang
Cheminformatics Tools for Enabling Metabolomics by Yannick Djoumbou Feunang A thesis submitted in partial fulfillment of requirements for the degree of Doctor of Philosophy in Microbiology and Biotechnology Department of Biological Sciences University of Alberta ©Yannick Djoumbou Feunang, 2017 ii Abstract Metabolites are small molecules (<1500 Da) that are used in or produced during chemical reactions in cells, tissues, or organs. Upon absorption or biosynthesis in humans (or other organisms), they can either be excreted back into the environment in their original form, or as a pool of degradation products. The outcome and effects of such interactions is function of many variables, including the structure of the starting metabolite, and the genetic disposition of the host organism. For this reasons, it is usually very difficult to identify the transformation products as well as their long-term effect in humans and the environment. This can be explained by many factors: (1) the relevant knowledge and data are for the most part unavailable in a publicly available electronic format; (2) when available, they are often represented using formats, vocabularies, or schemes that vary from one source (or repository) to another. Assuming these issues were solved, detecting patterns that link the metabolome to a specific phenotype (e.g. a disease state), would still require that the metabolites from a biological sample be identified and quantified, using metabolomic approaches. Unfortunately, the amount of compounds with publicly available experimental data (~20,000) is still very small, compared to the total number of expected compounds (up to a few million compounds). For all these reasons, the development of cheminformatics tools for data organization and mapping, as well as for the prediction of biotransformation and spectra, is more crucial than ever. -
Harmonized Tariff Schedule of the United States (2020) Revision 14 Annotated for Statistical Reporting Purposes
Harmonized Tariff Schedule of the United States (2020) Revision 14 Annotated for Statistical Reporting Purposes SECTION VI PRODUCTS OF THE CHEMICAL OR ALLIED INDUSTRIES VI-1 Notes 1. (a) Goods (other than radioactive ores) answering to a description in heading 2844 or 2845 are to be classified in those headings and in no other heading of the tariff schedule. (b) Subject to paragraph (a) above, goods answering to a description in heading 2843, 2846 or 2852 are to be classified in those headings and in no other heading of this section. 2. Subject to note 1 above, goods classifiable in heading 3004, 3005, 3006, 3212, 3303, 3304, 3305, 3306, 3307, 3506, 3707 or 3808 by reason of being put up in measured doses or for retail sale are to be classified in those headings and in no other heading of the tariff schedule. 3. Goods put up in sets consisting of two or more separate constituents, some or all of which fall in this section and are intended to be mixed together to obtain a product of section VI or VII, are to be classified in the heading appropriate to that product, provided that the constituents are: (a) Having regard to the manner in which they are put up, clearly identifiable as being intended to be used together without first being repacked; (b) Entered together; and (c) Identifiable, whether by their nature or by the relative proportions in which they are present, as being complementary one to another. Additional U.S. Notes 1. In determining the amount of duty applicable to a solution of a single compound in water subject to duty in this section at a specific rate, an allowance in weight or volume, as the case may be, shall be made for the water in excess of any water of crystallization which may be present in the undissolved compound.