Interagency Committee on Chemical Management
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Calcium Stearate Processing
National Organic Standards Board Technical Advisory Panel (TAP) Review Compiled by University of California Sustainable Agriculture Research and Education Program (UC SAREP) for the USDA National Organic Program Calcium Stearate Processing Executive Summary1 A petition is under consideration with respect to NOP regulations subpart G §205.605, governing the use of substances in processed products: Petitioned: Inclusion of calcium stearate on National List of nonagricultural substances allowed in or on processed products labeled as “organic” or “made with organic (specified ingredients or food group(s)).” Calcium stearate is a compound of calcium with a mixture of solid organic acids obtained from edible sources. It is generally used as a solid-phase lubricant that reduces friction between particles of the substance to which it is added. The Petitioner’s intended use is “as a flow agent (anti-dusting agent)” to be used in dry flour based ingredients sold to bakeries (NOSB Petition). The NOP has no prior listing or ruling on the substance. All three reviewers agreed that the substance should be considered synthetic. The reviewers were divided over the use of calcium stearate in food labeled as “organic.” Two of the reviewers felt it should not be allowed in these foods, while one reviewer felt it should be accepted. One reviewer who voted to restrict its use indicated that more information was needed on the nature of the substance and its potential applications, and the other reviewer felt that inclusion of a “synthetic” substance in organics runs contrary to consumer’s expectations regarding organic products. All three reviewers agreed that the substance should be allowed in products labeled as “made with organic…” ingredients. -
New Synthesis Routes for Production of Ε-Caprolactam by Beckmann
New synthesis routes for production of ε-caprolactam by Beckmann rearrangement of cyclohexanone oxime and ammoximation of cyclohexanone over different metal incorporated molecular sieves and oxide catalysts Von der Fakultät für Mathematik, Informatik und Naturwissenschaften der RWTH Aachen University zur Erlangung des akademischen Grades eines Doktors der Naturwissenschaften genehmigte Dissertation vorgelegt von Anilkumar Mettu aus Guntur/Indien Berichter: Universitätprofessor Dr. Wolfgang F. Hölderich Universitätprofessor Dr. Carsten Bolm Tag der mündlichen Prüfung: 29.01.2009 Diese Dissertation ist auf den Internetseiten der Hochschulbibliothek online verfügbar. Dedicated to my Parents This work reported here has been carried out at the Institute for Chemical Technolgy and Heterogeneous Catalysis der Fakultät für Mathematik, Informatik und Naturwissenschaften in the University of Technology, RWTH Aachen under supervision of Prof. Dr. Wolfgang F. Hölderich between June 2005 and August 2008. ACKNOWLEDGEMENTS I would like to express my deepest sence of gratitude to my supervisor Prof. Dr. rer. nat. W. F. Hölderich for giving me the opportunity to do my doctoral study in his group. His guidance and teaching classes have allowed me to grow and learn my subject during my Ph.d. He has provided many opportunities for me to increase my abilities as a researcher and responsibilities as a team member. I am grateful for the financial support of this work from Sumitomo Chemicals Co., Ltd, Niihama, Japan (Part One) and Uhde Inventa-Fischer GmBH, Berlin (Part Two). Our collaborators at Sumitomo Chemicals Co., Ltd (Dr. C. Stoecker) and Uhde Inventa- Fischer GmBH (Dr. R. Schaller and Dr. A. Pawelski) provided thoughtful guidance and suggestions for each project. -
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. -
Selective Hydrogenation of Phenol to Cyclohexanol Over Ni/CNT in the Absence of External Hydrogen
energies Article Selective Hydrogenation of Phenol to Cyclohexanol over Ni/CNT in the Absence of External Hydrogen Changzhou Chen 1,2, Peng Liu 1,2, Minghao Zhou 1,2,3,*, Brajendra K. Sharma 3,* and Jianchun Jiang 1,2,* 1 Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Key Laboratory of Biomass Energy and Material, Jiangsu Province, National Engineering Laboratory for Biomass Chemical Utilization, Key and Open Laboratory on Forest Chemical Engineering, SFA, Nanjing 210042, China; [email protected] (C.C.); [email protected] (P.L.) 2 Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, Nanjing 210037, China 3 Illinois Sustainable Technology Center, Prairie Research Institute, one Hazelwood Dr., Champaign, University of Illinois at Urbana-Champaign, Champaign, IL 61820, USA * Correspondence: [email protected] (M.Z.); [email protected] (B.K.S.); [email protected] (J.J.) Received: 7 January 2020; Accepted: 11 February 2020; Published: 14 February 2020 Abstract: Transfer hydrogenation is a novel and efficient method to realize the hydrogenation in different chemical reactions and exploring a simple heterogeneous catalyst with high activity is crucial. Ni/CNT was synthesized through a traditional impregnation method, and the detailed physicochemical properties were performed by means of XRD, TEM, XPS, BET, and ICP analysis. Through the screening of loading amounts, solvents, reaction temperature, and reaction time, 20% Ni/CNT achieves an almost complete conversion of phenol after 60 min at 220 ◦C in the absence of external hydrogen. Furthermore, the catalytic system is carried out on a variety of phenol derivatives for the generation of corresponding cyclohexanols with good to excellent results. -
Background Document on Cadmium ______
Hazardous Substances Series -------------------------------------------------------------------------------------------------------------------------------------------- Cadmium OSPAR Commission 2002 (2004 Update) OSPAR Commission, 2002: OSPAR Background Document on Cadmium _______________________________________________________________________________________________________ The Convention for the Protection of the Marine Environment of the North-East Atlantic (the “OSPAR Convention”) was opened for signature at the Ministerial Meeting of the former Oslo and Paris Commissions in Paris on 22 September 1992. The Convention entered into force on 25 March 1998. It has been ratified by Belgium, Denmark, Finland, France, Germany, Iceland, Ireland, Luxembourg, Netherlands, Norway, Portugal, Sweden, Switzerland and the United Kingdom and approved by the European Community and Spain. La Convention pour la protection du milieu marin de l'Atlantique du Nord-Est, dite Convention OSPAR, a été ouverte à la signature à la réunion ministérielle des anciennes Commissions d'Oslo et de Paris, à Paris le 22 septembre 1992. La Convention est entrée en vigueur le 25 mars 1998. La Convention a été ratifiée par l'Allemagne, la Belgique, le Danemark, la Finlande, la France, l’Irlande, l’Islande, le Luxembourg, la Norvège, les Pays-Bas, le Portugal, le Royaume-Uni de Grande Bretagne et d’Irlande du Nord, la Suède et la Suisse et approuvée par la Communauté européenne et l’Espagne. © OSPAR Commission, 2002. Permission may be granted by the publishers for the report to be wholly or partly reproduced in publications provided that the source of the extract is clearly indicated. © Commission OSPAR, 2002. La reproduction de tout ou partie de ce rapport dans une publication peut être autorisée par l’Editeur, sous réserve que l’origine de l’extrait soit clairement mentionnée. -
Disinfection Byproducts in Chlorinated Drinking Water
International Journal of Water and Wastewater Treatment SciO p Forschene n HUB for Sc i e n t i f i c R e s e a r c h ISSN 2381-5299 | Open Access RESEARCH ARTICLE Volume 4 - Issue 2 | DOI: http://dx.doi.org/10.16966/2381-5299.156 Disinfection Byproducts in Chlorinated Drinking Water Malia Vester1, Hany F Sobhi2 and Mintesinot Jiru1* 1Department of Natural Sciences, Coppin State University, Maryland, USA 2Center for Organic Synthesis, Department of Natural Sciences, Coppin State University, Maryland, USA *Corresponding author: Mintesinot Jiru, Department of Natural Sciences, Coppin State University, Maryland, USA, Tel: 410-951-4139; E-mail: [email protected] Received: 07 Jul, 2018 | Accepted: 14 Nov, 2018 | Published: 20 Nov, 2018 Citation: Vester M, Sobhi HF, Jiru M (2018) Disinfection Byproducts in Chlorinated Drinking Water. Int J Water Wastewater Treat 4(2): dx.doi. org/10.16966/2381-5299.156 Copyright: © Vester M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Abstract Trihalomethanes (THMs) are disinfection byproducts formed through the reaction of chlorine and organic matter. There are four forms of Trihalomethanes: chloroform, bromoform, dibromochloromethane and bromodichloromethane. Studies have shown that chloroform, a principal disinfection byproduct, is carcinogenic in rodents. Although the presence of these hazardous materials are constantly being monitored by Water Treatment Plant and the Environmental Protection Agency (EPA), they continue to be present at an unpredictable levels and the full effects of these byproducts are not fully understood. -
Hydrofluoric Acid Reduction Project – TURI Grant 2017
Hydrofluoric Acid Reduction Project – TURI Grant 2017 Sponsored by: Toxics Use Reduction Institute 126 John St Lowell, MA 01854 TURI Report 2018-001 Authors: Tyler DeFosse David Demarey Supervisor: Paul Watson Special Thanks to: Joy Onasch – Toxics Use Reduction Institute John Raschko – Massachusetts Office of Technical Assistance and Technology 1 Table of Contents 1.0 Executive Summary .......................................................................................................................... 3 2.0 Background ....................................................................................................................................... 5 2.1 Introduction ......................................................................................................................................... 5 2.2 Literature Searches .......................................................................................................................... 6 2.2.1 Diffusion Dialysis ...................................................................................................................... 6 2.2.2 Reverse Osmosis ....................................................................................................................... 7 2.2.3 Hydrofluoric Acid Wastewater Recycling Method ............................................................... 7 2.2.4 Issues Regarding the Etching of Silicon Dioxide ................................................................. 8 2.3 Alternative Strategies ..................................................................................................................... -
Barium Nitrate Solution 0.1M
Safety Data Sheet Barium Nitrate Solution 0.1M 1. PRODUCT AND COMPANY IDENTIFICATION Product Name: Barium Nitrate Solution 0.1M Synonyms/Generic Names: None SDS Number: 85.20 Product Use: For Educational Use Only Manufacturer: Columbus Chemical Industries, Inc. N4335 Temkin Rd. Columbus, WI. 53925 For More Information Contact: Ward's Science 5100 West Henrietta Rd. PO Box 92912-9012 Rochester, NY 14692 (800) 962-2660 (Monday-Friday 7:30-7:00 Eastern Time) In Case of Emergency Call: CHEMTREC - 800-424-9300 or 703-527-3887 (24 Hours/Day, 7 Days/Week) 2. HAZARDS IDENTIFICATION OSHA Hazards: Oxidizer, Toxic by ingestion, Toxic by inhalation, Irritant Target Organs: Kidney, Liver, Blood, Heart, Gastrointestinal system, Bone marrow, Spleen, Nerves Signal Words: Warning Pictograms: GHS Classification: Oxidizing liquid Category 3 Acute toxicity, Oral Category 4 Acute toxicity, Inhalation Category 4 Skin irritation Category 3 Eye irritation Category 2A GHS Label Elements, including precautionary statements: Hazard Statements: H272 May intensify fire; oxidizer. H302+H332 Harmful if swallowed or in contact with skin. H316 Causes mild skin irritation. H319 Causes serious eye irritation. Revised on 01/08/2013 Page 1 of 6 Precautionary Statements: P220 Keep/store away from clothing/combustible materials. P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do so. Continue rinsing. Potential Health Effects Eyes Causes eye irritation. Inhalation Toxic if inhaled. Causes respiratory tract irritation. Skin May be harmful if absorbed through skin. Causes skin irritation. Ingestion Toxic if swallowed. NFPA Ratings HMIS Ratings Health 2 Health 2 Flammability 0 Fire 0 Reactivity 0 Reactivity 0 Specific hazard N/A Personal E 3. -
CA004600 SDS.Pdf
Safety Data Sheet SECTION 1: Identification 1.1. Product Identifier Trade Name or Designation: Ammonium Bifluoride, 15.5 g/L, Aqueous Product Number: A-0046 Other Identifying Product Numbers: A-0046-4L 1.2. Recommended Use and Restrictions on Use General Laboratory Reagent 1.3. Details of the Supplier of the Safety Data Sheet Company: Reagents Inc. Address: 4746 Sweden Road Charlotte, NC 28224 USA Telephone: 800-732-8484 1.4. Emergency Telephone Number (24 hr) CHEMTREC (USA) 800-424-9300 CHEMTREC (International) 1+ 703-527-3887 SECTION 2: Hazard(s) Identification 2.1. Classification of the Substance or Mixture (in accordance with OSHA HCS 29 CFR 1910.1200) For the full text of the Hazard and Precautionary Statements listed below, see Section 16. Hazard Hazard Class Category Statement Precautionary Statements Skin Corrosion / Irritation Category 1 H314 P260, P264, P280, P301+P330+P331, P303+P361+P353, P363, P304+P340, P310, P321, P305+P351+P338, P405, P501 Eye Damage / Irritation Category 1 H318 P280, P305+P351+P338, P310 Specific Target Organs/Systemic Toxicity Following Single Category 1 H370 P260, P264, P270, P307+P311, P321, P405, Exposure P501 Specific Target Organs/Systemic Toxicity Following Repeated Category 2 H373 P260, P314, P501 Exposure Corrosive to Metals Category 1 H290 P234, P390, P406 Product Number: A-0046 Page 1 of 10 Safety Data Sheet 2.2. GHS Label Elements Pictograms: Signal Word: Danger Hazard Statements: Hazard Number Hazard Statement H290 May be corrosive to metals. H314 Causes severe skin burns and eye damage. H318 Causes serious eye damage. H370 Causes damage to organs. H373 May cause damage to organs through prolonged or repeated exposure. -
Polyvinyl Chloride - Wikipedia Polyvinyl Chloride
1/24/2020 Polyvinyl chloride - Wikipedia Polyvinyl chloride Polyvinyl chloride (/ˌpɒlivaɪnəl ˈklɔːraɪd/;[5] colloquial: Polyvinyl chloride polyvinyl, vinyl;[6] abbreviated: PVC) is the world's third-most widely produced synthetic plastic polymer, after polyethylene and polypropylene.[7] About 40 million tonnes are produced per year. PVC comes in two basic forms: rigid (sometimes abbreviated as RPVC) and flexible. The rigid form of PVC is used in construction for pipe and in profile applications such as doors and windows. It is also used in making bottles, non-food packaging, food-covering sheets,[8] and cards (such as bank or membership cards). It can be made softer and more flexible by the addition of plasticizers, the most widely used being phthalates. In this form, it is also used in plumbing, electrical cable insulation, imitation leather, flooring, signage, phonograph records,[9] inflatable products, and many applications where it replaces rubber.[10] With cotton or linen, it is used to make canvas. Pure polyvinyl chloride is a white, brittle solid. It is insoluble in alcohol but slightly soluble in tetrahydrofuran. Contents Discovery Production Microstructure Names Producers IUPAC name Additives poly(1-chloroethylene)[1] Phthalate plasticizers Di-2ethylhexylphthalate Other names Metal stabilizers Polychloroethylene Heat stabilizers Identifiers Properties CAS Number 9002-86-2 (http://ww Mechanical w.commonchemistry. Thermal and fire org/ChemicalDetail.a Electrical spx?ref=9002-86-2) Chemical Abbreviations PVC Applications ChEBI CHEBI:53243 -
Toxicological Profile for Bromodichloromethane
BROMODICHLOROMETHANE 89 CHAPTER 5. POTENTIAL FOR HUMAN EXPOSURE 5.1 OVERVIEW Bromodichloromethane has been identified in at least 238 of the 1,854 hazardous waste sites that have been proposed for inclusion on the EPA National Priorities List (NPL) (ATSDR 2017). However, the number of sites in which bromodichloromethane has been evaluated is not known. The number of sites in each state is shown in Figure 5-1. Of these sites, 233 are located within the United States, 2 are located in the Virgin Islands, and 3 are located in Puerto Rico (not shown). Figure 5-1. Number of NPL Sites with Bromodichloromethane Contamination • The most likely route of exposure for the general public to bromodichloromethane is through ingestion, inhalation, and dermal contact of chlorinated drinking water. • A median bromodichloromethane intake of 2.8–4.2 µg/day from drinking water has been estimated; inhalation and dermal exposure would add to this daily intake. BROMODICHLOROMETHANE 90 5. POTENTIAL FOR HUMAN EXPOSURE • Bromodichloromethane is formed as a byproduct of water disinfection methods using chlorination. This is the primary source of bromodichloromethane in the environment. • Its principal use is as a chemical intermediate for organic synthesis and as a chemical reagent. • Volatilization is an important fate process. Bromodichloromethane evaporates from sources and enters the environment as a gas, which is slowly broken down in air. Residual bromodichloromethane may be broken down slowly by bacteria. • In the atmosphere, bromodichloromethane is thought to undergo slow degradation through oxidative pathways, with a half-life of about 2–3 months. 5.2 PRODUCTION, IMPORT/EXPORT, USE, AND DISPOSAL 5.2.1 Production The principal anthropogenic source of bromodichloromethane is its unintentional formation as a byproduct during the chlorination of water containing organic materials and bromide. -
Ammonium Bifluoride CAS No
Product Safety Summary Ammonium Bifluoride CAS No. 1341-49-7 This Product Safety Summary is intended to provide a general overview of the chemical substance. The information on the summary is basic information and is not intended to provide emergency response information, medical information or treatment information. The summary should not be used to provide in-depth safety and health information. In-depth safety and health information can be found in the Safety Data Sheet (SDS) for the chemical substance. Names • Ammonium bifluoride (ABF) • Ammonium difluoride • Ammonium acid fluoride • Ammonium hydrogen difluoride • Ammonium fluoride compound with hydrogen fluoride (1:1) Product Overview Solvay Fluorides, LLC does not sell ammonium bifluoride directly to consumers. Ammonium bifluoride is used in industrial applications and in other processes where workplace exposures can occur. Ammonium bifluoride (ABF) is used for cleaning and etching of metals before they are further processed. It is used as an oil well acidifier and in the etching of glass or cleaning of brick and ceramics. It may also be used for pH adjustment in industrial textile processing or laundries. ABF is available as a solid or liquid solution (in water). Ammonium bifluoride is a corrosive chemical and contact can severely irritate and burn the skin and eyes causing possible permanent eye damage. Breathing ammonium bifluoride can severely irritate and burn the nose, throat, and lungs, causing nosebleeds, cough, wheezing and shortness of breath. On contact with water or moist skin, ABF can release hydrofluoric acid, a very dangerous acid. Inhalation or ingestion of large amounts of ammonium bifluoride can cause nausea, vomiting and loss of appetite.