Acenaphthene Environmental Summary
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Estimation of Enthalpy of Bio-Oil Vapor and Heat Required For
Edinburgh Research Explorer Estimation of Enthalpy of Bio-Oil Vapor and Heat Required for Pyrolysis of Biomass Citation for published version: Yang, H, Kudo, S, Kuo, H-P, Norinaga, K, Mori, A, Masek, O & Hayashi, J 2013, 'Estimation of Enthalpy of Bio-Oil Vapor and Heat Required for Pyrolysis of Biomass', Energy & Fuels, vol. 27, no. 5, pp. 2675-2686. https://doi.org/10.1021/ef400199z Digital Object Identifier (DOI): 10.1021/ef400199z Link: Link to publication record in Edinburgh Research Explorer Document Version: Early version, also known as pre-print Published In: Energy & Fuels 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: 04. Oct. 2021 Estimation of Enthalpy of Bio-oil Vapor and Heat Required for Pyrolysis of Biomass Hua Yang,† Shinji Kudo,§ Hsiu-Po Kuo,‡ Koyo Norinaga, ξ Aska Mori, ξ Ondřej Mašek,|| and Jun-ichiro Hayashi †, ξ, §, * †Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, -
Summary of Information for ABC for Polycyclic Aromatic Hydrocarbons
Air Toxics Science Advisory Committee Summary of Information for ABC for Polycyclic Aromatic Hydrocarbons September 16, 2015 ATSAC Meeting #10 Presenter: Sue MacMillan, DEQ ATSAC lead Sue MacMillan | Oregon Department of Environmental Quality 26 Individual PAHs to Serve as Basis of ABC for Total PAHs Acenaphthene Cyclopenta(c,d)pyrene Acenaphthylene Dibenzo(a,h)anthracene Anthracene Dibenzo(a,e)pyrene Anthanthrene Dibenzo(a,h)pyrene Benzo(a)pyrene Dibenzo(a,i)pyrene Naphthalene Benz(a)anthracene Dibenzo(a,l)pyrene has separate Benzo(b)fluoranthene Fluoranthene ABC. Benzo(k)fluoranthene Fluorene Benzo( c)pyrene Indeno(1,2,3-c,d)pyrene Benzo(e)pyrene Phenanthrene Benzo(g,h,i)perylene Pyrene Benzo(j)fluoranthene 5-Methylchrysene Chrysene 6-Nitrochrysene Use of Toxic Equivalency Factors for PAHs • Benzo(a)pyrene serves as the index PAH, and has a documented toxicity value to which other PAHs are adjusted • Other PAHs adjusted using Toxic Equivalency Factors (TEFs), aka Potency Equivalency Factors (PEFs). These values are multipliers and are PAH-specific. • Once all PAH concentrations are adjusted to account for their relative toxicity as compared to BaP, the concentrations are summed • This summed concentration is then compared to the toxicity value for BaP, which is used as the ABC for total PAHs. Source of PEFs for PAHs • EPA provides a range of values of PEFs for each PAH • Original proposal suggested using upper-bound value of each PEF range as the PEF to use for adjustment of our PAHs • Average PEF value for each PAH is a better approximation of central tendency, and is consistent with the use of PEFs by other agencies • Result of using average, rather than upper-bound PEFs: slightly lower summed concentrations for adjusted PAHs, thus less apt to exceed ABC for total PAHs Documents can be provided upon request in an alternate format for individuals with disabilities or in a language other than English for people with limited English skills. -
Polycyclic Aromatic Hydrocarbons (Pahs)
Polycyclic Aromatic Hydrocarbons (PAHs) Factsheet 4th edition Donata Lerda JRC 66955 - 2011 The mission of the JRC-IRMM is to promote a common and reliable European measurement system in support of EU policies. European Commission Joint Research Centre Institute for Reference Materials and Measurements Contact information Address: Retiewseweg 111, 2440 Geel, Belgium E-mail: [email protected] Tel.: +32 (0)14 571 826 Fax: +32 (0)14 571 783 http://irmm.jrc.ec.europa.eu/ http://www.jrc.ec.europa.eu/ Legal Notice Neither the European Commission nor any person acting on behalf of the Commission is responsible for the use which might be made of this publication. Europe Direct is a service to help you find answers to your questions about the European Union Freephone number (*): 00 800 6 7 8 9 10 11 (*) Certain mobile telephone operators do not allow access to 00 800 numbers or these calls may be billed. A great deal of additional information on the European Union is available on the Internet. It can be accessed through the Europa server http://europa.eu/ JRC 66955 © European Union, 2011 Reproduction is authorised provided the source is acknowledged Printed in Belgium Table of contents Chemical structure of PAHs................................................................................................................................. 1 PAHs included in EU legislation.......................................................................................................................... 6 Toxicity of PAHs included in EPA and EU -
Polycyclic Aromatic Hydrocarbons in Water, Sediment, and Snow, from Lakes in Grand Teton National Park, Wyoming
POLYCYCLIC AROMATIC HYDROCARBONS IN WATER, SEDIMENT, AND SNOW, FROM LAKES IN GRAND TETON NATIONAL PARK, WYOMING Final Report, USGS-CERC-91344 February 2005 Darren T. Rhea1, Robert W. Gale2, Carl E. Orazio2, Paul H. Peterman2, David D. Harper1, and Aїda M. Farag1* 1U.S. Geological Survey, Columbia Environmental Research Center, Jackson Field Research Station, P.O. Box 1089, Jackson, WY 83001 2U.S. Geological Survey, Columbia Environmental Research Center, 4200 New Haven Rd., Columbia, MO 65201 *Corresponding author: [email protected] U.S. Department of the Interior U.S. Geological Survey Any use of trade, product, or firm names in this publication is for descriptive purposes only and does not imply endorsement by the U.S. Government. CONTENTS PAGE Abstract…………………………………………………………………………………... 3 Introduction……………………………………………………………………………… 4 Methods…………………………………………………………………………………... 5 Study areas…………………………………………………………………........... 5 Sample collection…………………………………………………………………. 6 Sample analysis……………………………………………………….................... 6 Results…………………………………………………………………………………..... 8 Quality assurance/quality control……………………………………………….....8 PAH concentrations…………………………………………………………......... 8 Organic carbon concentrations………………………………………………….... 9 Discussion………………………………………………………………………………..10 Literature Cited………………………………………………………………................14 Tables Table 1…………………………………………………………………................16 Table 2………………………………………………………………………........17 Figures Figure 1………………………………………………………………….............. 18 Appendices Appendix A……………………………………………………………………… -
Thermodynamics and Phase Behavior of Polycyclic Aromatic
Thermodynamics and Phase Behavior of Polycyclic Aromatic Hydrocarbon Mixtures By James William Rice B.S., Northeastern University, 2006 Sc.M., Brown University, 2008 A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the School of Engineering at Brown University PROVIDENCE, RHODE ISLAND MAY 2011 © Copyright 2011 by James W. Rice This dissertation by James W. Rice is accepted in its present form by the School of Engineering as satisfying the dissertation requirement for the degree of Doctor of Philosophy Date: _________________ ________________________________________________ Eric Suuberg, Advisor Recommended to the Graduate Council Date: _________________ ________________________________________________ Joseph Calo, Reader Date: _________________ ________________________________________________ Gerald Diebold, Reader Approved by the Graduate Council Date: _________________ ________________________________________________ Peter Weber, Dean of the Graduate School iii Curriculum Vitae for James W. Rice BORN on July 26, 1983 in Beverly, Massachusetts USA EDUCATION PhD Brown University, Providence, RI, Chemical Engineering (May 2011) ScM Brown University, Providence, RI, Engineering (May 2008) BS Northeastern University, Boston, MA, Chemical Engineering (May 2006) PUBLICATIONS J.W. Rice, J. Fu, E.M. Suuberg. “Anthracene + Pyrene Solid Mixtures: Eutectic and Azeotropic Character.” Journal of Chemical & Engineering Data (2010). J.W. Rice, E.M. Suuberg. “Thermodynamic Study of (Anthracene + Benzo[a]Pyrene) Solid Mixtures.” Journal of Chemical Thermodynamics (2010). J.W. Rice, J. Fu, E.M. Suuberg. “Thermodynamics of Multicomponent PAH Mixtures and Development of Tarlike Behavior.” Industrial and Engineering Chemistry Research (2011) J. Fu, J.W. Rice, E.M. Suuberg. “Phase Behavior and Vapor Pressures of the Pyrene + 9,10‐ Dibromoanthracene System.” Fluid Phase Equilibria (2010). CONFERENCE PRESENTATIONS J.W. -
Coal Tar Creosote
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 Organization, or the World Health Organization. Concise International Chemical Assessment Document 62 COAL TAR CREOSOTE Please note that the layout and pagination of this pdf file are not identical to the document being printed First draft prepared by Drs Christine Melber, Janet Kielhorn, and Inge Mangelsdorf, Fraunhofer Institute of Toxicology and Experimental Medicine, Hanover, Germany Published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organization, 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, 2004 The International Programme on Chemical Safety (IPCS), established in 1980, is a joint venture of the United Nations Environment Programme (UNEP), the International Labour Organization (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 Programme for the Sound Management of Chemicals (IOMC) was established in 1995 by UNEP, ILO, the Food and Agriculture Organization of the United Nations, WHO, the United Nations Industrial Development Organization, the United Nations Institute for Training and Research, and the Organisation for Economic Co-operation and Development (Participating Organizations), following recommendations made by the 1992 UN Conference on Environment and Development to strengthen cooperation and increase coordination in the field of chemical safety. -
Provisional Peer-Reviewed Toxicity Values For
EPA/690/R-11/001F l Final 4-6-2011 Provisional Peer-Reviewed Toxicity Values for Acenaphthene (CASRN 83-32-9) 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 J. Phillip Kaiser, PhD National Center for Environmental Assessment, Cincinnati, OH DRAFT DOCUMENT PREPARED BY ICF International 9300 Lee Highway Fairfax, VA 22031 PRIMARY INTERNAL REVIEWERS Paul G. Reinhart, PhD, DABT National Center for Environmental Assessment, Research Triangle Park, NC Q. Jay Zhao, PhD, MPH, 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). TABLE OF CONTENTS COMMONLY USED ABBREVIATIONS .................................................................................... ii BACKGROUND .............................................................................................................................1 HISTORY ....................................................................................................................................1 DISCLAIMERS ...........................................................................................................................1 -
Solubility of Acenaphthene in Pure Non-Aqueous Solvents Between 298.15 and 333.15 K
Indian Journal of Chemical Technology Vol. 14, March 2007, pp. 183-188 Solubility of acenaphthene in pure non-aqueous solvents between 298.15 and 333.15 K M Thenmozhi*, S Parvin Banu & T Karunanithi Department of Chemical Engineering, Annamalai University, Annamalai Nagar 608 002, India Email: [email protected] Received 2 September 2005; revised received 7 November 2006; accepted 3 January 2007 Binary solid-liquid equilibria (SLE) for the systems acenaphthene +benzene, +methanol, +2-propanol, +2-methyl- propan-1-ol, +ethyl acetate, +methyl ethyl ketone, +acetone, +chloroform are reported in the temperature range of 298.15 K to 333.15 K. The predictive ability of UNIFAC model as applied to SLE data of these systems is evaluated by comparing with the experimental values using percent relative deviation (%RD). Scope for improvements in UNIFAC model is analyzed based on the application of this model to SLE involving polycyclic aromatic compounds. Keywords: SLE, Acenaphthene, UNIFAC, Polycyclic aromatic hydrocarbons (PAHs) IPC Code: C10H35/00 Acenaphthene, also known as 1,2-dihydroacenaph- by Acree et al9-12. Of the nine solvent + solute systems thylene or 1,8-ethylenenaphthalene, is a tricyclic studied in the present work, excepting benzene and aromatic hydrocarbon. Acenaphthene belongs to a chloroform, SLE data are available only at the larger group of compounds called polycylic aromatic reference temperature of 298.15 K. In the case of hydrocarbons (PAH’s). It is used as a dye acenaphthene in benzene or chloroform, SLE data are intermediate, in the manufacture of some plastics, and available. Both Choi et al.13 and McLaughlin and as an insecticide and fungicide. -
Guidance for Evaluating the Cancer Potency of PAH Mixtures
Environmental Health Division, Environmental Surveillance and Assessment Section PO Box 64975 St. Paul, MN 55164-0975 651-201-5000 www.health.state.mn.us Guidance for Evaluating the Cancer Potency of Polycyclic Aromatic Hydrocarbon (PAH) Mixtures in Environmental Samples Minnesota Department of Health February 8, 2016 Guidance for Evaluating the Cancer Potency of Polycyclic Aromatic Hydrocarbon (PAH) Mixtures in Environmental Samples February 8, 2016 For more information, contact: Environmental Health Division, Environmental Surveillance and Assessment Section PO Box 64975 St. Paul, MN 55164-0975 Phone: 651-201-5000 Fax: 651-201-4606 This report describes guidance for conducting risk assessments. This work was conducted by the Site Assessment and Consultation Unit, Carl Herbrandson, PhD, senior toxicologist, under the supervision of Rita Messing, PhD, with the collaboration of the Health Risk Assessment Unit, Helen Goeden, PhD, senior toxicologist, and Kate Sande, MS, Research Scientist, under the supervision of Pamela Shubat, PhD. Questions on the content of this report should be directed to the Health Risk Assessment Unit, 651-201- 4899 or by email to [email protected]. Information about this work is also posted on the MDH website at Guidance for PAHs (http://www.health.state.mn.us/divs/eh/risk/guidance/pahmemo.html) Upon request, this material will be made available in an alternative format such as large print, Braille or audio recording. Printed on recycled paper. Guidance for Evaluating the Cancer Potency of Polycyclic Aromatic Hydrocarbon (PAH) Mixtures in Environmental Samples Executive Summary The Minnesota Department of Health (MDH) offers guidance for a wide range of risk assessment needs. -
SAFETY DATA SHEETS According to the UN GHS Revision 8
www.targetmol.com Target Molecule Corp. SAFETY DATA SHEETS According to the UN GHS revision 8 Version: 1.0 Creation Date: July 15, 2019 Revision Date: July 15, 2019 1. Identification 1.1 GHS Product identifier Product name Acenaphthylene 1.2 Other means of identification Other names 1.3 Recommended use of the chemical and restrictions on use Identified uses Industrial and scientific research uses. Uses advised against no data available 1.4 Supplier's details Company Target Molecule Corp. Address Suite 260, 36 Washington Street, Wellesley Hills, Massachusetts, USA Tel/Fax +1 (857) 239-0968 1.5 Emergency phone number Emergency phone number 400-821-2233 Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours). 2. Hazard identification 2.1 Classification of the substance or mixture Acute toxicity - Dermal, Category 1 Acute toxicity - Inhalation, Category 1 2.2 GHS label elements, including precautionary statements Pictogram(s) Signal word Danger Hazard statement(s) H310 Fatal in contact with skin H330 Fatal if inhaled Precautionary statement(s) Prevention P262 Do not get in eyes, on skin, or on clothing. P264 Wash ... thoroughly after handling. P270 Do not eat, drink or smoke when using this product. P280 Wear protective gloves/protective clothing/eye protection/face protection. P260 Do not breathe dust/fume/gas/mist/vapours/spray. P271 Use only outdoors or in a well-ventilated area. P284 [In case of inadequate ventilation] wear respiratory protection. Response P302+P352 IF ON SKIN: Wash with plenty of water/... P310 Immediately call a POISON CENTER/doctor/… P321 Specific treatment (see .. -
Screening and Determination of Polycyclic Aromatic Hydrocarbons
METHOD NUMBER: C-002.01 POSTING DATE: November 1, 2017 POSTING EXPIRATION DATE: November 1, 2023 PROGRAM AREA: Seafood METHOD TITLE: Screening and Determination of Polycyclic Aromatic Hydrocarbons in Seafoods Using QuEChERS-Based Extraction and High-Performance Liquid Chromatography with Fluorescence Detection VALIDATION STATUS: Equivalent to Level 3 Multi-laboratory validation (MLV) AUTHOR(S): Samuel Gratz, Angela Mohrhaus Bryan Gamble, Jill Gracie, David Jackson, John Roetting, Laura Ciolino, Heather McCauley, Gerry Schneider, David Crockett, Douglas Heitkemper, and Fred Fricke (FDA Forensic Chemistry Center) METHOD SUMMARY/SCOPE: Analyte(s): Polycyclic aromatic hydrocarbons (PAH): acenaphthene, anthracene, benzo[a]anthracene, benzo[a]pyrene, benzo[b]fluoranthene, benzo[g,h,i]perylene, benzo[k]fluoranthene, chrysene, dibenzo[a,h]anthracene, fluoranthene, fluorene, indeno[1,2,3-cd]pyrene, naphthalene, phenanthrene, pyrene Matrices: Oysters, shrimp, crabs, and finfish The method provides a procedure to screen for fifteen targeted parent polycyclic aromatic hydrocarbons (PAHs) and provides an estimate of total PAH concentration including alkylated homologs in oysters, shrimp, crabs, and finfish. PAHs are extracted from seafood matrices using a modified QuEChERS sample preparation procedure. The method utilizes High-Performance Liquid Chromatography with Fluorescence Detection (HPLC-FLD) for the determination step. This procedure is applicable to screen a variety of seafood matrices including oysters, shrimp, finfish and crab for the presence of parent PAHs and the common alkylated homologs due to oil contamination. This method was originally developed and validated in response to the 2010 Gulf of Mexico oil spill. REVISION HISTORY: OTHER NOTES: Method was originally posted on November 1, 2017. It was approved for re-posting by the Chemistry Research Coordination Group for 3 years in December 2020. -
Supplementary Information
Supplementary Information Investigating PAH Relative Reactivity using Congener Profiles, Quinone Measurements and Back Trajectories Mohammed S. Alam, Juana Maria Delgado-Saborit, Christopher Stark and Roy M. Harrison*† * To whom correspondence should be addressed (Tel: +44 121 414 3494; Fax: +44 121 414 3709; Email: [email protected]) † Also at: Department of Environmental Sciences / Center of Excellence in Environmental Studies, King Abdulaziz University, Jeddah, 21589, Saudi Arabia 1 Sampling Analysis List of chemicals HPLC grade dichloromethane (DCM) was purchased from Fischer Scientific (Loughborough, UK) and nonane 99% purum, zinc powder 99% purum, pentane 99% GC grade and acetic anhydride 99% puriss were supplied by Sigma-Aldrich (Dorset, UK). Certified standard 16 EPA Priority PAH pollutant mixture CERTAN 100 µg/mL of each analyte in toluene was purchased from LGC Promochem (Teddington, UK). Coronene standard solution 100 µg/mL in toluene, acenaphthylene-d8 200 µg/mL in isooctane, pyrene-d10 500 µg/mL in acetone, chrysene-d12 2000 µg/mL in dichloromethane, benzo[a]pyrene-d12 200 µg/mL in isooctane, indeno[1,2,3-cd]pyrene-d12 200 µg/mL in isooctane, benzo[ghi]perylene-d12 200 µg/mL in toluene were supplied by Greyhound ChemService (Birkenhead, UK), benz[a]anthracene-d12 and phenanthrene-d10 1000 µg/mL in DCM were purchased from UltraScientific (North Kingstown, RI, USA) whilst anthracene-d10 and p-terphenyl-d14 2000 µg/mL in dichloromethane were purchased from Greyhound ChemService and UltraScientific. Quinone standards and internal standards were purchased as powders (>97% purity) from Sigma-Aldrich (Dorset, UK) with the exception of benzo[a]pyrene-1,6-dione and benzo[a]pyrene-6,12-dione, which were purchased from NCI Chemical Reference Standard Repository.