Inventory of US Greenhouse Gas Emissions and Sinks: 1990-2015
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Chemical Characterization and Thermal Stressing Studies of Perfluorohexane Fluids for Space-Based Applications
Chemical Characterization and Thermal Stressing Studies of Perfluorohexane Fluids for Space-Based Applications William A. Arnold, Ph.D.1 ZIN Technologies, Inc., Brook Park, Ohio, 44142, USA Thomas G. Hartman, Ph.D.2 CAFT, Cook College, Rutgers the Sate University of New Jersey, New Brunswick, NJ, 08901 USA John McQuillen,3 NASA Glenn Research Center, Cleveland, Ohio, 44135, USA Perfluorohexane (PFH), C6F14, is a perfluorocarbon fluid. Several PFH fluids with different isomer concentrations were evaluated for use in an upcoming NASA space experiment. Samples tested included two commercially obtained high-purity n-perfluorohexane (n-PFH) fluids and a technical grade mixture of C6F14 branched and linear isomers (FC-72). These fluids were evaluated for exact chemical composition, impurity purity and high temperature degradation behavior (pyrolysis). Our investigation involved simulated thermal stressing studies of PFH fluids under conditions likely to occur in the event of an atmospheric breach within the International Space Station (ISS) and subsequent exposure of the vapors to the high temperature and catalyst present in its Trace Contaminant Control Subsystem (TCCS). Exposure to temperatures in the temperature range of 200-450°C in an inert or oxidizing atmosphere, with and without the presence of catalyst was investigated. The most aggressive conditions studied were exposure of PFH vapors to 450°C in air and in the presence of TCCS (palladium) catalyst. Gas chromatography-mass spectrometry (GC-MS) and gas chromatography (GC) analyses were conducted on the perfluorohexane samples before and after pyrolysis. The FC-72 and n-PFH samples showed no significant degradation following pyrolysis even under the most aggressive study conditions. -
1,1,1,2-Tetrafluoroethane
This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the United Nations Environment Programme, the International Labour Organisation, or the World Health Organization. Concise International Chemical Assessment Document 11 1,1,1,2-Tetrafluoroethane First draft prepared by Mrs P. Barker and Mr R. Cary, Health and Safety Executive, Liverpool, United Kingdom, and Dr S. Dobson, Institute of Terrestrial Ecology, Huntingdon, United Kingdom Please not that the layout and pagination of this pdf file are not identical to the printed CICAD Published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organisation, and the World Health Organization, and produced within the framework of the Inter-Organization Programme for the Sound Management of Chemicals. World Health Organization Geneva, 1998 The International Programme on Chemical Safety (IPCS), established in 1980, is a joint venture of the United Nations Environment Programme (UNEP), the International Labour Organisation (ILO), and the World Health Organization (WHO). The overall objectives of the IPCS are to establish the scientific basis for assessment of the risk to human health and the environment from exposure to chemicals, through international peer review processes, as a prerequisite for the promotion of chemical safety, and to provide technical assistance in strengthening national capacities for the sound management of chemicals. The Inter-Organization -
SAFETY DATA SHEET Halocarbon R-503
SAFETY DATA SHEET Halocarbon R-503 Section 1. Identification GHS product identifier : Halocarbon R-503 Other means of : Not available. identification Product type : Liquefied gas Product use : Synthetic/Analytical chemistry. SDS # : 007306 Supplier's details : Airgas USA, LLC and its affiliates 259 North Radnor-Chester Road Suite 100 Radnor, PA 19087-5283 1-610-687-5253 24-hour telephone : 1-866-734-3438 Section 2. Hazards identification OSHA/HCS status : This material is considered hazardous by the OSHA Hazard Communication Standard (29 CFR 1910.1200). Classification of the : GASES UNDER PRESSURE - Liquefied gas substance or mixture HAZARDOUS TO THE OZONE LAYER - Category 1 GHS label elements Hazard pictograms : Signal word : Warning Hazard statements : Contains gas under pressure; may explode if heated. May cause frostbite. May displace oxygen and cause rapid suffocation. Harms public health and the environment by destroying ozone in the upper atmosphere. Precautionary statements General : Read and follow all Safety Data Sheets (SDS’S) before use. Read label before use. Keep out of reach of children. If medical advice is needed, have product container or label at hand. Close valve after each use and when empty. Use equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use a back flow preventative device in the piping. Use only equipment of compatible materials of construction. Always keep container in upright position. Prevention : Not applicable. Response : Not applicable. Storage : Protect from sunlight. Store in a well-ventilated place. Disposal : Refer to manufacturer or supplier for information on recovery or recycling. Hazards not otherwise : Liquid can cause burns similar to frostbite. -
Chlorofluorocarbons Chem 300A Tyler Jensen, Mackenzie Latimer, Jessie Luther, Jake Mcghee, Adeeb Noorani, Tyla Penner, & Maddy Springle
Chlorofluorocarbons Chem 300a Tyler Jensen, Mackenzie Latimer, Jessie Luther, Jake McGhee, Adeeb Noorani, Tyla Penner, & Maddy Springle 1.1: A Brief History of Chlorofluorocarbons Chlorofluorocarbons (CFCs), also known as Freons, were first synthesized in 1928 by Thomas Midgley Jr, who was working for General Motors trying to find a safe refrigerant to use in commercial applications. (Rosenbaum, n.d.). They are an anthropogenic compound containing fluorine, carbon, and chlorine atoms, and are classified as halocarbons. CFCs are a family of chemicals based upon hydrocarbon skeletons, where most hydrogens have been replaced with chlorine and/or fluorine atoms. They are chemically stable freons that are non-flammable, tasteless and odourless. CFCs are very volatile, which makes for ideal refrigerant gases, having a boiling point close to zero degrees (Rosenbaum, n.d) They were originally created to replace the toxic gases used in the late 1800’s and early 1900’s. Examples of the toxic gases replaced by CFCs as refrigerants are ammonia (NH3), methyl chloride (CH3Cl), and sulfur dioxide (SO2) (Wilkins, 1999). When first created dichlorodifloromethane was found to be less toxic than carbon dioxide, and as non-flammable as carbon tetrachloride (Midgley & Henne, 1930). The non-toxic, non-flammable, and non-reactive properties of CFCs made them ideal for use as refrigerants. CFCs were used in many developed countries for consumption and production as they were inflammable and non-toxic towards humanity. Chlorofluorocarbons can be used as refrigerants, cleaning agents, foaming agents, and propellants for aerosol sprays (Welch, n.d.). In 1974, Two University of California chemists, Professor F. Sherwood Rowland and Dr. -
CHAPTER12 Atmospheric Degradation of Halocarbon Substitutes
CHAPTER12 AtmosphericDegradation of Halocarbon Substitutes Lead Author: R.A. Cox Co-authors: R. Atkinson G.K. Moortgat A.R. Ravishankara H.W. Sidebottom Contributors: G.D. Hayman C. Howard M. Kanakidou S .A. Penkett J. Rodriguez S. Solomon 0. Wild CHAPTER 12 ATMOSPHERIC DEGRADATION OF HALOCARBON SUBSTITUTES Contents SCIENTIFIC SUMMARY ......................................................................................................................................... 12.1 12.1 BACKGROUND ............................................................................................................................................... 12.3 12.2 ATMOSPHERIC LIFETIMES OF HFCS AND HCFCS ................................................................................. 12.3 12.2. 1 Tropospheric Loss Processes .............................................................................................................. 12.3 12.2.2 Stratospheric Loss Processes .............................................................................................................. 12.4 12.3 ATMOSPHERIC LIFETIMES OF OTHER CFC AND HALON SUBSTITUTES ......................................... 12.4 12.4 ATMOSPHERIC DEGRADATION OF SUBSTITUTES ................................................................................ 12.5 12.5 GAS PHASE DEGRADATION CHEMISTRY OF SUBSTITUTES .............................................................. 12.6 12.5.1 Reaction with NO .............................................................................................................................. -
Human Health Toxicity Values for Perfluorobutane Sulfonic Acid (CASRN 375-73-5) and Related Compound Potassium Perfluorobutane Sulfonate (CASRN 29420 49 3)
EPA-823-R-18-307 Public Comment Draft Human Health Toxicity Values for Perfluorobutane Sulfonic Acid (CASRN 375-73-5) and Related Compound Potassium Perfluorobutane Sulfonate (CASRN 29420-49-3) This document is a Public Comment draft. It has not been formally released by the U.S. Environmental Protection Agency and should not at this stage be construed to represent Agency policy. This information is distributed solely for the purpose of public review. This document is a draft for review purposes only and does not constitute Agency policy. DRAFT FOR PUBLIC COMMENT – DO NOT CITE OR QUOTE NOVEMBER 2018 Human Health Toxicity Values for Perfluorobutane Sulfonic Acid (CASRN 375-73-5) and Related Compound Potassium Perfluorobutane Sulfonate (CASRN 29420 49 3) Prepared by: U.S. Environmental Protection Agency Office of Research and Development (8101R) National Center for Environmental Assessment Washington, DC 20460 EPA Document Number: 823-R-18-307 NOVEMBER 2018 This document is a draft for review purposes only and does not constitute Agency policy. DRAFT FOR PUBLIC COMMENT – DO NOT CITE OR QUOTE NOVEMBER 2018 Disclaimer This document is a public comment draft for review purposes only. This information is distributed solely for the purpose of public comment. It has not been formally disseminated by EPA. It does not represent and should not be construed to represent any Agency determination or policy. Mention of trade names or commercial products does not constitute endorsement or recommendation for use. i This document is a draft for review purposes only and does not constitute Agency policy. DRAFT FOR PUBLIC COMMENT – DO NOT CITE OR QUOTE NOVEMBER 2018 Authors, Contributors, and Reviewers CHEMICAL MANAGERS Jason C. -
"Fluorine Compounds, Organic," In: Ullmann's Encyclopedia Of
Article No : a11_349 Fluorine Compounds, Organic GU¨ NTER SIEGEMUND, Hoechst Aktiengesellschaft, Frankfurt, Federal Republic of Germany WERNER SCHWERTFEGER, Hoechst Aktiengesellschaft, Frankfurt, Federal Republic of Germany ANDREW FEIRING, E. I. DuPont de Nemours & Co., Wilmington, Delaware, United States BRUCE SMART, E. I. DuPont de Nemours & Co., Wilmington, Delaware, United States FRED BEHR, Minnesota Mining and Manufacturing Company, St. Paul, Minnesota, United States HERWARD VOGEL, Minnesota Mining and Manufacturing Company, St. Paul, Minnesota, United States BLAINE MCKUSICK, E. I. DuPont de Nemours & Co., Wilmington, Delaware, United States 1. Introduction....................... 444 8. Fluorinated Carboxylic Acids and 2. Production Processes ................ 445 Fluorinated Alkanesulfonic Acids ...... 470 2.1. Substitution of Hydrogen............. 445 8.1. Fluorinated Carboxylic Acids ......... 470 2.2. Halogen – Fluorine Exchange ......... 446 8.1.1. Fluorinated Acetic Acids .............. 470 2.3. Synthesis from Fluorinated Synthons ... 447 8.1.2. Long-Chain Perfluorocarboxylic Acids .... 470 2.4. Addition of Hydrogen Fluoride to 8.1.3. Fluorinated Dicarboxylic Acids ......... 472 Unsaturated Bonds ................. 447 8.1.4. Tetrafluoroethylene – Perfluorovinyl Ether 2.5. Miscellaneous Methods .............. 447 Copolymers with Carboxylic Acid Groups . 472 2.6. Purification and Analysis ............. 447 8.2. Fluorinated Alkanesulfonic Acids ...... 472 3. Fluorinated Alkanes................. 448 8.2.1. Perfluoroalkanesulfonic Acids -
United Nations Sc
UNITED NATIONS SC UNEP/POPS/POPRC.12/INF/16 Distr.: General 2 August 2016 English only Stockholm Convention on Persistent Organic Pollutants Persistent Organic Pollutants Review Committee Twelfth meeting Rome, 19–23 September 2015 Item 4 (d) of the provisional agenda Technical work: consolidated guidance on alternatives to perfluorooctane sulfonic acid and its related chemicals Comments and responses relating to the draft consolidated guidance on alternatives to perfluorooctane sulfonic acid and its related chemicals Note by the Secretariat As referred to in the note by the Secretariat on guidance on alternatives to perfluorooctane sulfonic acid and its related chemicals (UNEP/POPS/POPRC.12/7), the annex to the present note contains a table listing the comments and responses relating to the draft guidance. The present note, including its annex, has not been formally edited. UNEP/POPS/POPRC.12/1. 030816 UNEP/POPS/POPRC.12/INF/16 Annex Comments and responses relating to the draft consolidated guidance on alternatives to perfluorooctane sulfonic acid and its related chemicals Minor grammatical or spelling changes have been made without acknowledgment. Only substantial comments are listed. Yellow highlight indicates addition of text while green highlight indicates deletion. Source of Page Para Comments on the second draft Response Comment Austria 7 2 This statement is better placed in Chapter VII Rejected. accompanied with a justification for those “critical applications”. For clarification “where it is not currently possible without the use of PFOS” is added Austria 15 47 According to May be commercialized is revised to http://poppub.bcrc.cn/col/1413428117937/index.html “are commercialized” F-53 and F-53B have a long history of usage and have been commercialized before PFOS related Reference substances were used (cf. -
Alkane Coiling in Perfluoroalkane Solutions
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Repositório Científico da Universidade de Évora Article Cite This: Langmuir 2017, 33, 11429-11435 pubs.acs.org/Langmuir Alkane Coiling in Perfluoroalkane Solutions: A New Primitive Solvophobic Effect † ‡ § † ∥ ‡ Pedro Morgado, Ana Rosa Garcia, , Luís F. G. Martins, , Laura M. Ilharco,*, † and Eduardo J. M. Filipe*, † ‡ Centro de Química Estrutural, Instituto Superior Tecnicó and Centro de Química-Física Molecular and Institute of Nanoscience and Nanotechnology, Instituto Superior Tecnico,́ Universidade de Lisboa, 1049-001 Lisboa, Portugal § Departamento de Química e Farmacia,́ FCT, Universidade do Algarve, 8000 Faro, Portugal ∥ Centro de Química de Évora, Escola de Cienciaŝ e Tecnologia, Universidade de Évora, 7000-671 Évora, Portugal *S Supporting Information ABSTRACT: In this work, we demonstrate that n-alkanes coil when mixed with perfluoroalkanes, changing their conformational equilibria to more globular states, with a higher number of gauche conformations. The new coiling effect is here observed in fluids governed exclusively by dispersion interactions, contrary to other examples in which hydrogen bonding and polarity play important roles. FTIR spectra of liquid mixtures of n-hexane and perfluorohexane unambiguously reveal that the population of n-hexane molecules in all-trans conformation reduces from 32% in the pure n-alkane to practically zero. The spectra of perfluorohexane remain unchanged, suggesting nanosegregation of the hydrogenated and fluorinated chains. Molecular dynamics simulations support this analysis. The new solvophobic effect is prone to have a major impact on the structure, organization, and therefore thermodynamic properties and phase equilibria of fluids involving mixed hydrogenated and fluorinated chains. -
Methane Emissions from Forests Ecosystems Enhance Global Warming? : Keppler Et.Al.(2006)
Methane emissions from forests ecosystems enhance global warming? : Keppler et.al.(2006). Methane emissions from terrestrial plants under aerobic conditions. Nature 439: 187-191 Quantifications of possible effects and comments Summary The results of this study could affect attractiveness and returns of CDM carbon offset projects and future negotiations about carbon sinks in the second commitment period. If confirmed independently, they represent a paradigm shift regarding methane formation in plant physiology. When extrapolated, net greenhouse gas removals by growing forests, e.g. existing forests or forests created by afforestation projects under the Clean Development Mechanism, could be reduced by maximally 4-8% though aerobic emissions of methane by trees. Net actual effects are likely to be lower. However, transposing and up-scaling results obtained in containers on small samples, seedlings, and on only one tree species to global forests and other biomes is not a valid “first estimate”, but at best a hypothesis which should be tested. Results do not invalidate the role of forests as carbon sinks; they also do not support the view that deforestation mitigates global warming via reduced emissions of methane. Background The paper postulates a sizeable, previously unknown methane source of 60-240 Mt from forests and other biomes, and an additional source of 1-7 Mt CH4 from litter. Plant physiology has up to now not recognized the possibility of aerobic methane formation by intact plants or litter. Methane, a powerful greenhouse gas with a global warming potential of 23 times that of CO2, has been thought to originate in rice patties, natural wetlands, landfills, natural gas reservoirs, biomass burning and in the digestive tracts of cattle.If these methane emissions can be corroborated, the discovery amounts to a paradigm shift in plant physiology. -
The Need for Fast Near-Term Climate Mitigation to Slow Feedbacks and Tipping Points
The Need for Fast Near-Term Climate Mitigation to Slow Feedbacks and Tipping Points Critical Role of Short-lived Super Climate Pollutants in the Climate Emergency Background Note DRAFT: 27 September 2021 Institute for Governance Center for Human Rights and & Sustainable Development (IGSD) Environment (CHRE/CEDHA) Lead authors Durwood Zaelke, Romina Picolotti, Kristin Campbell, & Gabrielle Dreyfus Contributing authors Trina Thorbjornsen, Laura Bloomer, Blake Hite, Kiran Ghosh, & Daniel Taillant Acknowledgements We thank readers for comments that have allowed us to continue to update and improve this note. About the Institute for Governance & About the Center for Human Rights and Sustainable Development (IGSD) Environment (CHRE/CEDHA) IGSD’s mission is to promote just and Originally founded in 1999 in Argentina, the sustainable societies and to protect the Center for Human Rights and Environment environment by advancing the understanding, (CHRE or CEDHA by its Spanish acronym) development, and implementation of effective aims to build a more harmonious relationship and accountable systems of governance for between the environment and people. Its work sustainable development. centers on promoting greater access to justice and to guarantee human rights for victims of As part of its work, IGSD is pursuing “fast- environmental degradation, or due to the non- action” climate mitigation strategies that will sustainable management of natural resources, result in significant reductions of climate and to prevent future violations. To this end, emissions to limit temperature increase and other CHRE fosters the creation of public policy that climate impacts in the near-term. The focus is on promotes inclusive socially and environmentally strategies to reduce non-CO2 climate pollutants, sustainable development, through community protect sinks, and enhance urban albedo with participation, public interest litigation, smart surfaces, as a complement to cuts in CO2. -
Synthetic Greenhouse Gases
Synthetic Greenhouse Gases How are they different to What are ‘synthetic greenhouse gases’? ‘greenhouse gases’? Synthetic greenhouse gases are man made Greenhouse gases are naturally occurring. chemicals. They are commonly used in They include carbon dioxide (CO2), methane refrigeration and air conditioning, fire (CH4) and nitrous oxide (N2O). Synthetic extinguishing, foam production and in greenhouse gases are man made chemicals medical aerosols. When they are released, and generally have a much higher global synthetic greenhouse gases trap heat in warming potential than naturally occurring the atmosphere. greenhouse gases. What is global warming potential? Global warming potential (GWP) is a measure of how much heat a greenhouse gas traps in the atmosphere over a specific time compared to a similar mass of carbon dioxide (CO2). CO2, with a global warming potential of 1, is used as the base figure for measuring global warming potential. The higher the global warming potential number, the more heat a gas traps. The most common synthetic greenhouse gas in Australia is HFC-134a, which is mostly used in refrigerators and air conditioners. It has a global warming potential of 1430; this means the release of one tonne of HFC-134a is equivalent to releasing 1430 tonnes of CO2 into the atmosphere. Which synthetic greenhouse gases does 22,800 Australia regulate? SF6 the global warming potential of sulfur hexafluoride (SF6) • hydrofluorocarbons (HFCs) • perfluorocarbons (PFCs) • sulfur hexafluoride (SF6) Synthetic • nitrogen trifluoride (NF3) greenhouse gases account for around 2% of all greenhouse gas emissions in Australia How do we use synthetic greenhouse gases? They are man made chemicals with a wide variety of uses.