CODE of COLORADO REGULATIONS 6 CCR 1007-3 Part 8 Hazardous Materials and Waste Management Division
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Industry Compliance Programme
Global Chemical Industry Compliance Programme GC-ICP Chemical Weapons Convention December 2006 Version 1.0 GLOBAL CHEMICAL INDUSTRY COMPLIANCE PROGRAMME FOR IMPLEMENTING THE CHEMICAL WEAPONS CONVENTION The purpose of the handbook is to provide guidance to chemical facilities, traders and trading companies in developing a Global Chemical Industry Compliance Programme (GC-ICP) to comply with the Chemical Weapons Convention (CWC). The GC-ICP focuses first on determining if there is a reporting requirement to your National Authority and second on collecting the relevant support data used to complete the required reports. The GC-ICP is designed to provide a methodology to comply with the CWC and establish systems that facilitate and demonstrate such compliance. Each facility/company should also ensure that it follows its country’s CWC specific laws, regulations and reporting requirements. • Sections 2, 3, and 4 guide you through the process of determining if chemicals at your facility/ company should be reported to your National Authority for compliance with the CWC. • Section 5 provides recommended guidance on information that you may use to determine your reporting requirements under the CWC and administrative tools that your facility/company may use to ensure compliance with the CWC. • Section 6 provides a glossary of terms and associated acronyms. • Section 7 provides a listing of all National Authorities by country. CWC Global Chemical Industry Compliance Programme 1 TABLE OF CONTENTS Section 1 Overview What is the Chemical Weapons Convention? -
Responding to a Chemical Warfare Agent Incident: from Sampling and Analysis to Decontamination and Waste Management Stuart Willi
Responding to a Chemical Warfare Agent Incident: from sampling and analysis to decontamination and waste management Stuart Willison & Lukas Oudejans U. S. EPA National Homeland Security Research Center 1 Outline • Homeland Security Relevance to Chemical (Warfare Agent) Incidents and Incident Response Cycle • Identification of Gaps/Needs: PARTNER Process and Stakeholder Priorities • Current High Stakeholder Priorities • Research Efforts to meet these Needs/Gaps Selected Analytical Methods (SAM) Document CWA Method Development and Wipe Efficiency Studies on Surfaces Fate and Transport of CWAs Natural Attenuation of VX Decontamination of Vesicant/Blister CWAs HD, L, HL Analytical Method Development: Lewisite; EA 2192 Best Practices Document for Waste Media from Remediation Activities • Summary 2 Response to Contamination Events Since 9/11, multiple chemical/biotoxin contamination events have occurred in the United States and worldwide: • Several ricin incidents (2002-2014) • Deepwater Horizon oil spill (April 2010) • Kalamazoo River oil spill (July 2010) • CWA sulfur mustard clam shells (2010) • CWA chemical attacks (Syria, Middle East) (March-August 2013 and April 2014-current) • Elk River chemical spill in West Virginia (January 2014) • Toxic algae blooms in Toledo, OH (August 2014) • Arsenic-contaminated soil in Kentucky potentially containing CWA Lewisite (March 2015) • (Organophosphate-) Pesticide over- or misuse across USA in relation to bed bug epidemic (current) 3 Response Cycle Contaminant Release Reduce Vulnerabilities Lessons -
Supplement to All Hazards Receipt Facility (AHRF) Screening Protocol
EPA/600/R-10/155 December 2010 Supplement to All Hazards Receipt Facility (AHRF) Screening Protocol SCIENCE Office of Research and Development National Homeland Security Research Center Supplement to All Hazards Receipt Facility (AHRF) Screening Protocol December 2010 Office of Research and Development National Homeland Security Research Center Acknowledgments This document is intended to be supplementary to the U.S. Environmental Protection Agency (EPA) and U.S. Department of Homeland Security (DHS) September 2008 All Hazards Receipt Facility Protocol (AHRF Protocol), and attempts to address considerations raised by stakeholders since publication of the protocol. Development of this document was funded by the U.S. Environmental Protection Agency (EPA) National Homeland Security Research Center (NHSRC), and includes information provided by EPA Regions 1, 6, and 10; EPA Office of Radiation and Indoor Air (ORIA), the Association of Public Health Laboratories (APHL): State Public Health Laboratories of Connecticut, Delaware, Massachusetts, Minnesota, New Jersey, New York, and Virginia; and New York City; and the Canadian Defence Research and Development Laboratory. This document was prepared by CSC under Contract EP-W-06- 046. Disclaimer This document is intended to be supplementary to the guidance provided in the U.S. Environmental Protection Agency (EPA) and U.S. Department of Homeland Security (DHS) September 2008 All Hazards Receipt Facility Protocol (AHRF Protocol), and attempts to address considerations raised by stakeholders since publication of the protocol. This supplement assumes that: • The September 2008 AHRF Protocol was developed and provided as a guide; implementation of the protocol and the screening equipment included in the protocol may vary among locations, depending on the goals and capabilities of the laboratory to which the facility is attached. -
Selected Analytical Methods for Environmental Remediation and Recovery (SAM) 2017
EPA/600/R-17/356 | September 2017 www.epa.gov/homeland-security-research Selected Analytical Methods for Environmental Remediation and Recovery (SAM) 2017 Office of Research and Development Homeland Security Research Program This page left intentionally blank EPA/600/R-17/356 | September 2017 Selected Analytical Methods for Environmental Remediation and Recovery (SAM) 2017 UNITED STATES ENVIRONMENTAL PROTECTION AGENCY Cincinnati, OH 45268 Office of Research and Development Homeland Security Research Program Disclaimer Disclaimer The U.S. Environmental Protection Agency (EPA) through its Office of Research and Development funded and managed the research described here under Contract EP-C-15-012 to CSRA Inc. This document is undergoing review and has not been approved for publication. The contents reflect the views of the contributors and technical work groups and do not necessarily reflect the views of the Agency. Mention of trade names or commercial products in this document or in the methods referenced in this document does not constitute endorsement or recommendation for use. Questions concerning this document or its application should be addressed to: Romy Campisano National Homeland Security Research Center Office of Research and Development (NG16) U.S. Environmental Protection Agency 26 West Martin Luther King Drive Cincinnati, OH 45268 (513) 569-7016 [email protected] Kathy Hall National Homeland Security Research Center Office of Research and Development (NG16) U.S. Environmental Protection Agency 26 West Martin Luther King -
UAH Chemical Hygiene Plan
UAH CHEMICAL HYGIENE Effective Date: Feb. 2014 PLAN The Campus Chemical Hygiene Plan (Campus CHP) was developed to ensure the safety of laboratory employees and maintain compliance with the OSHA Laboratory Standard. In addition to OSHA regulations, this document also presents key information on the practices and procedures that must be implemented to maintain compliance with other state, federal, and local regulations required for the use and storage of hazardous chemicals. Prepared by: The Office of Environmental Health & Safety Contents 1. Introduction .............................................................................................................................. 1 1.1 Purpose .................................................................................................................................................. 1 1.2 Background on Regulatory Compliance .................................................................................... 1 1.3 Chemical Hygiene Plan Overview ................................................................................................. 2 1.4 Scope and Applicability .................................................................................................................... 3 1.5 Implementation of the Plan ............................................................................................................ 4 1.6 Availability of the Plan ..................................................................................................................... 4 1.7 Annual -
Things to Be Done
DRAFT MAY 2003 ANNEX 1: CHEMICAL AGENTS 1. Introduction The large-scale use of toxic chemicals as weapons first became possible during the First World War (1914–1918) thanks to the growth of the chemical industry. More than 110 000 tonnes were disseminated over the battlefields, the greater part on the western front. Initially, the chemicals were used, not to cause casualties in the sense of putting enemy combatants out of action, but rather to harass. Though the sensory irritants used were powerful enough to disable those who were exposed to them, they served mainly to drive enemy combatants out of the trenches or other cover that protected them from conventional fire, or to disrupt enemy artillery or supplies. About 10% of the total tonnage of chemical warfare agents used during the war were chemicals of this type, namely lacrimators (tear gases), sternutators and vomiting agents. However, use of more lethal chemicals soon followed the introduction of disabling chemicals. In all, chemical agents caused some 1.3 million casualties, including 90 000 deaths. During the First World War, almost every known noxious chemical was screened for its potential as a weapon, and this process was repeated during the Second World War (1939–1945), when substantial stocks of chemical weapons were accumulated, although rarely used in military operations. Between the two world wars, a high proportion of all the new compounds that had been synthesized, or isolated from natural materials, were examined to determine their utility as lethal or disabling chemical weapons. After 1945, these systematic surveys continued, together with a search for novel agents based on advances in biochemistry, toxicology and pharmacology. -
Provisional Peer-Reviewed Toxicity Values for Lewisite (Casrn 541-25-3)
EPA/690/R-15/009F l Final 9-30-2015 Provisional Peer-Reviewed Toxicity Values for Lewisite (CASRN 541-25-3) Superfund Health Risk Technical Support Center National Center for Environmental Assessment Office of Research and Development U.S. Environmental Protection Agency Cincinnati, OH 45268 AUTHORS, CONTRIBUTORS, AND REVIEWERS CHEMICAL MANAGER Dan D. Petersen, PhD, DABT National Center for Environmental Assessment, Cincinnati, OH DRAFT DOCUMENT PREPARED BY SRC, Inc. 7502 Round Pond Road North Syracuse, NY 13212 PRIMARY INTERNAL REVIEWERS Jeffery Swartout, PhD, DABT National Center for Environmental Assessment, Cincinnati, OH This document was externally peer reviewed under contract to: Eastern Research Group, Inc. 110 Hartwell Avenue Lexington, MA 02421 3136 Questions regarding the contents of this document may be directed to the U.S. EPA Office of Research and Development’s National Center for Environmental Assessment, Superfund Health Risk Technical Support Center (513-569-7300). ii Lewisite TABLE OF CONTENTS COMMONLY USED ABBREVIATIONS AND ACRONYMS .................................................. iv BACKGROUND .............................................................................................................................1 DISCLAIMERS ...............................................................................................................................1 QUESTIONS REGARDING PPRTVs ............................................................................................1 INTRODUCTION ...........................................................................................................................2 -
Lewisite (L) Team (NRT) Quick Reference Guides (Qrgs) for Chemical Warfare Agents
NRT Quick Reference Guide: For references, please see Key References Cited/Used in National Response Lewisite (L) Team (NRT) Quick Reference Guides (QRGs) for Chemical Warfare Agents. [July 2015 Update] QRGs are intended for Federal OSC/RPMs. Agent Classification: Schedule 1 Chemical Warfare Blister (Vesicant) Agent; CAS: 541-25-3; Formula: C2H2AsCl3; Molecular Weight: 207.35 g/mol. Description: Lewisite is referred to as L-1 and is oily, colorless and odorless. When impure, it is a yellow brown through violet black liquid with a strong penetrating geranium odor. The manufacturing process affects physical properties, appearance, persistence, and analytical detection limits. Common impurities include two related compounds, lewisite 2 (L-2) and lewisite 3 (L-3). This QRG is based on L-1 but includes aspects of L-2 and L-3, and will use “L” as the collective abbreviation. L is a blister (vesicant) agent that produces immediate burning pain with blistering starting within a few hours. L is less volatile than Sarin (GB); it is much more volatile than persistent agents VX or HD. Environmental breakdown products of L are easily formed and include highly toxic arsenic (III) compounds, such as arsenites, lewisite oxide, and 2-chlorovinyl arsenous acid (CVAA); some cause similar blistering as L. Decontamination by-products of L include arsenic (V) compounds, which are generally less toxic than arsenic (III) compounds, but may be considered hazardous. Persistence: L is considered a “low to moderate persistent” chemical warfare agent. Vapor: minutes to hours; liquid: hours to days. Persistence will depend upon amount and purity of the agent, method of release, environmental conditions, and the types of surfaces and materials impacted. -
University Micrdrilms International 300 N
A COMPARISON OF THE EFFECTIVENESS OF SEVERAL THIOLIC CHELATING AGENTS ON THE MOBILIZATION OF ARSENIC IN THE RABBIT. Item Type text; Thesis-Reproduction (electronic) Authors Hoover, Todd David. Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 24/09/2021 12:49:10 Link to Item http://hdl.handle.net/10150/274892 INFORMATION TO USERS This reproduction was made from a copy of a document sent to us for microfilming. While the most advanced technology has been used to photograph and reproduce this document, the quality of the reproduction is heavily dependent upon the quality of the material submitted. The following explanation of techniques is provided to help clarify markings or notations which may appear on this reproduction. 1.The sign or "target" for pages apparently lacking from the document photographed is "Missing Page(s)". If it was possible to obtain the missing page(s) or section, they are spliced into the film along with adjacent pages. This may have necessitated cutting through an image and duplicating adjacent pages to assure complete continuity. 2. When an image on the film is obliterated with a round black mark, it is an indication of either blurred copy because of movement during exposure, duplicate copy, or copyrighted materials that should not have been filmed. For blurred pages, a good image of the page can be found in the adjacent frame. -
The Role of the Clinical Laboratory in Managing Chemical Or Biological Terrorism
Clinical Chemistry 46:12 1883–1893 (2000) Review The Role of the Clinical Laboratory in Managing Chemical or Biological Terrorism Saeed A. Jortani,1 James W. Snyder,1 and Roland Valdes, Jr.1,2* Background: Domestic and international acts of terror- to respond to such attacks. Accurate assessment of ism using chemicals and pathogens as weapons have resources in clinical laboratories is important because it recently attracted much attention because of several will provide local authorities with an alternative re- hoaxes and real incidents. Clinical laboratories, espe- source for immediate diagnostic analysis. It is, therefore, cially those affiliated with major trauma centers, should recommended that clinical laboratories identify their be prepared to respond rapidly by providing diagnostic current resources and the extent of support they can tests for the detection and identification of specific provide, and inform the authorities of their state of agents, so that specific therapy and victim management readiness. can be initiated in a timely manner. As first-line re- © 2000 American Association for Clinical Chemistry sponders, clinical laboratory personnel should become familiar with the various chemical or biological agents Release of chemical and biological warfare agents threat- and be active participants in their local defense pro- ens civilian populations throughout the world. Potential grams. sources of exposure include accidental release from mili- Approach: We review the selected agents previously tary factories and stockpiles, -
The Three Schedules
Scheduled Chemicals under the Chemical Weapons Convention (CWC) Schedule 1 Schedule 2 Schedule 3 Guidelines for Schedule 1 Guidelines for Schedule 2 Guidelines for Schedule 3 The following criteria shall be taken into account in considering whether a toxic The following criteria shall be taken into account in considering whether a toxic The following criteria shall be taken into account in considering whether a toxic chemical or precursor should be included in Schedule 1: chemical not listed in Schedule 1 or a precursor to a Schedule 1 chemical or to a chemical or precursor, not listed in other Schedules, should be included in (a) It has been developed, produced, stockpiled or used as a chemical weapon as chemical listed in Schedule 2, part A, should be included in Schedule 2: Schedule 3: defined in Article II; (a) It poses a significant risk to the object and purpose of this Convention because (a) It has been produced, stockpiled or used as a chemical weapon; (b) It poses otherwise a high risk to the object and purpose of this Convention by it possesses such lethal or incapacitating toxicity as well as other properties (b) It poses otherwise a risk to the object and purpose of this Convention because it virtue of its high potential for use in activities prohibited under this that could enable it to be used as a chemical weapon; possesses such lethal or incapacitating toxicity as well as other properties that Convention because one or more of the following conditions are met: (b) It may be used as a precursor in one of the chemical reactions -
Federal Register/Vol. 64, No. 95/Tuesday, May 18, 1999/Rules
27138 Federal Register / Vol. 64, No. 95 / Tuesday, May 18, 1999 / Rules and Regulations DEPARTMENT OF COMMERCE ADDRESSES: Written comments should families of chemicals. The United States be sent to Nancy Crowe, Regulatory is a participant in the Australia Group Bureau of Export Administration Policy Division, Bureau of Export (AG), a 30-nation multilateral chemical Administration, Room 2705, 14th Street and biological weapons non- 15 CFR Parts 734, 736, 738, 740, 742, and Pennsylvania Ave., NW, proliferation regime. All AG 745, 748, 758, 772 and 774 Washington, DC 20230. participants have national export [Docket No. 990416098±9098±01] FOR FURTHER INFORMATION CONTACT: controls on 54 precursor chemicals, Nancy Crowe, Regulatory Policy some of which are listed on the CWC RIN 0694±AB67 Division, Bureau of Export Schedules, and on chemical-related Implementation of the Chemical Administration, at (202) 482±2440. production equipment. Two Schedule 1 Weapons Convention; Revisions to the SUPPLEMENTARY INFORMATION: toxins, ricin and saxitoxin, are subject to Export Administration Regulations the EAR, are listed in Export Control Background Classification Number (ECCN) 1C351 on AGENCY: Bureau of Export As a party to the Convention on the the Commerce Control List (CCL), and Administration, Commerce. Prohibition of the Development, currently require a license for chemical ACTION: Interim rule. Production, Stockpiling, and Use of and biological (CB) non-proliferation Chemical Weapons and on Their reasons for export to all destinations SUMMARY: On