Combustion of a Renewable and Fossil Fuel: Teacher Manual
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Module III – Fire Analysis Fire Fundamentals: Definitions
Module III – Fire Analysis Fire Fundamentals: Definitions Joint EPRI/NRC-RES Fire PRA Workshop August 21-25, 2017 A Collaboration of the Electric Power Research Institute (EPRI) & U.S. NRC Office of Nuclear Regulatory Research (RES) What is a Fire? .Fire: – destructive burning as manifested by any or all of the following: light, flame, heat, smoke (ASTM E176) – the rapid oxidation of a material in the chemical process of combustion, releasing heat, light, and various reaction products. (National Wildfire Coordinating Group) – the phenomenon of combustion manifested in light, flame, and heat (Merriam-Webster) – Combustion is an exothermic, self-sustaining reaction involving a solid, liquid, and/or gas-phase fuel (NFPA FP Handbook) 2 What is a Fire? . Fire Triangle – hasn’t change much… . Fire requires presence of: – Material that can burn (fuel) – Oxygen (generally from air) – Energy (initial ignition source and sustaining thermal feedback) . Ignition source can be a spark, short in an electrical device, welder’s torch, cutting slag, hot pipe, hot manifold, cigarette, … 3 Materials that May Burn .Materials that can burn are generally categorized by: – Ease of ignition (ignition temperature or flash point) . Flammable materials are relatively easy to ignite, lower flash point (e.g., gasoline) . Combustible materials burn but are more difficult to ignite, higher flash point, more energy needed(e.g., wood, diesel fuel) . Non-Combustible materials will not burn under normal conditions (e.g., granite, silica…) – State of the fuel . Solid (wood, electrical cable insulation) . Liquid (diesel fuel) . Gaseous (hydrogen) 4 Combustion Process .Combustion process involves . – An ignition source comes into contact and heats up the material – Material vaporizes and mixes up with the oxygen in the air and ignites – Exothermic reaction generates additional energy that heats the material, that vaporizes more, that reacts with the air, etc. -
Safety Data Sheet
Coghlan’s Magnesium Fire Starter #7870 SAFETY DATA SHEET This Safety Data Sheet complies with the Canadian Hazardous Product Regulations, the United States Occupational Safety and Health Administration (OSHA) Hazard Communication Standard, 29 CFR 1910 (OSHA HCS), and the European Union Directives. 1. Product and Supplier Identification 1.1 Product: Magnesium Fire Starter 1.2 Other Means of Identification: Coghlan’s #7870 1.3 Product Use: Fire starter 1.4 Restrictions on Use: None known 1.5 Producer: Coghlan’s Ltd., 121 Irene Street, Winnipeg, Manitoba Canada, R3T 4C7 Telephone: +1(204) 284-9550 Facsimile: +1(204) 475-4127 Email: [email protected] Supplier: As above 1.6 Emergencies: +1(877) 264-4526 2. Hazards Identification 2.1 Classification of product or mixture This product is an untested preparation. GHS classification for this preparation is based upon its use as a fire starter by making shavings and small particulate from the metal block. As shipped in mass form, this preparation is not considered to be a hazardous product and is not classifiable under the requirements of GHS. GHS Classification: Flammable Solids, Category 1 2.2 GHS Label Elements, including precautionary statements Pictogram: Signal Word: Danger Page 1 of 11 October 18, 2016 Coghlan’s Magnesium Fire Starter #7870 GHS Hazard Statements: H228: Flammable Solid GHS Precautionary Statements: Prevention: P210: Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P280: Wear protective gloves, eye and face protection Response: P370+P378: In case of fire use water as first choice. Sand, earth, dry chemical, foam or CO2 may be used to extinguish. -
Operating and Maintaining a Wood Heater
OPERATING AND MAINTAINING A WOODHEATER FIREWOOD ASSOCIATION THE FIREWOODOF AUSTRALIA ASSOCIATION INC. OF AUSTRALIA INC. Building a wood fire Maintaining a wood heater For any fire to start and keep going three things are needed, Even in correctly operated wood heaters and fireplaces, some fuel, oxygen and heat. In wood fires the fuel is provided by the of the combustion gases will condense on the inside of the wood, the oxygen comes from the air, and the initial heat comes flue or chimney as a black tar-like substance called creosote. from burning paper or a fire lighter. In a going fire the heat is If this substance is allowed to build up it will restrict the air flow provided by the already burning wood. Without fuel, heat and in the heater or fireplace, reducing its efficiency. Eventually oxygen the fire will go out. When the important role of oxygen a build up of creosote can completely block the flue, making is understood, it is easy to see why you need plenty of air space around each piece of kindling when setting up the fire. the fire impossible to operate. One sign of a blocked flue is smoke coming into the room when you open the heater door. Kindling catches fire easily because it has a large surface Creosote appearing on the glass door is another indication area and small mass, which allows it to reach combustion that your heater is not working properly. Because creosote temperature quickly. The surface of a large piece of wood is flammable, if the chimney or flue gets hot enough the will not catch fire until it has been brought up to combustion creosote can catch alight, causing a dangerous chimney fire. -
Learn the Facts: Fuel Consumption and CO2
Auto$mart Learn the facts: Fuel consumption and CO2 What is the issue? For an internal combustion engine to move a vehicle down the road, it must convert the energy stored in the fuel into mechanical energy to drive the wheels. This process produces carbon dioxide (CO2). What do I need to know? Burning 1 L of gasoline produces approximately 2.3 kg of CO2. This means that the average Canadian vehicle, which burns 2 000 L of gasoline every year, releases about 4 600 kg of CO2 into the atmosphere. But how can 1 L of gasoline, which weighs only 0.75 kg, produce 2.3 kg of CO2? The answer lies in the chemistry! Î The short answer: Gasoline contains carbon and hydrogen atoms. During combustion, the carbon (C) from the fuel combines with oxygen (O2) from the air to produce carbon dioxide (CO2). The additional weight comes from the oxygen. The longer answer: Î So it’s the oxygen from the air that makes the exhaust Gasoline is composed of hydrocarbons, which are hydrogen products heavier. (H) and carbon (C) atoms that are bonded to form hydrocarbon molecules (C H ). Air is primarily composed of X Y Now let’s look specifically at the CO2 reaction. This reaction nitrogen (N) and oxygen (O2). may be expressed as follows: A simplified equation for the combustion of a hydrocarbon C + O2 g CO2 fuel may be expressed as follows: Carbon has an atomic weight of 12, oxygen has an atomic Fuel (C H ) + oxygen (O ) + spark g water (H O) + X Y 2 2 weight of 16 and CO2 has a molecular weight of 44 carbon dioxide (CO2) + heat (1 carbon atom [12] + 2 oxygen atoms [2 x 16 = 32]). -
Combustion Chemistry William H
Combustion Chemistry William H. Green MIT Dept. of Chemical Engineering 2014 Princeton-CEFRC Summer School on Combustion Course Length: 15 hrs June 2014 Copyright ©2014 by William H. Green This material is not to be sold, reproduced or distributed without prior written permission of the owner, William H. Green. 1 Combustion Chemistry William H. Green Combustion Summer School June 2014 2 Acknowledgements • Thanks to the following people for allowing me to show some of their figures or slides: • Mike Pilling, Leeds University • Hai Wang, Stanford University • Tim Wallington, Ford Motor Company • Charlie Westbrook (formerly of LLNL) • Stephen J. Klippenstein (Argonne) …and many of my hard-working students and postdocs from MIT 3 Overview Part 1: Big picture & Motivation Part 2: Intro to Kinetics, Combustion Chem Part 3: Thermochemistry Part 4: Kinetics & Mechanism Part 5: Computational Kinetics Be Prepared: There will be some Quizzes and Homework 4 Part 1: The Big Picture on Fuels and Combustion Chemistry 5 What is a Fuel? • Fuel is a material that carries energy in chemical form. • When the fuel is reacted (e.g. through combustion), most of the energy is released as heat • Though sometimes e.g. in fuel cells or flow batteries it can be released as electric power • Fuels have much higher energy densities than other ways of carrying energy. Very convenient for transportation. • The energy is released via chemical reactions. Each fuel undergoes different reactions, with different rates. Chemical details matter. 6 Transportation Fuel: Big Issues •People want, economy depends on transportation • Cars (growing rapidly in Asia) • Trucks (critical for economy everywhere) • Airplanes (growing rapidly everywhere) • Demand for Fuel is “Inelastic”: once they have invested in a vehicle, people will pay to fuel it even if price is high •Liquid Fuels are Best • Liquids Flow (solids are hard to handle!) • High volumetric and mass energy density • Easy to store, distribute. -
Fundamentals of Applied Smouldering Combustion
Western University Scholarship@Western Electronic Thesis and Dissertation Repository 6-20-2018 10:00 AM Fundamentals of Applied Smouldering Combustion Marco Zanoni The University of Western Ontario Supervisor Gerhard, Jason I. The University of Western Ontario Co-Supervisor Torero, Jose L. The University of Western Ontario Graduate Program in Civil and Environmental Engineering A thesis submitted in partial fulfillment of the equirr ements for the degree in Doctor of Philosophy © Marco Zanoni 2018 Follow this and additional works at: https://ir.lib.uwo.ca/etd Part of the Environmental Engineering Commons, and the Heat Transfer, Combustion Commons Recommended Citation Zanoni, Marco, "Fundamentals of Applied Smouldering Combustion" (2018). Electronic Thesis and Dissertation Repository. 5410. https://ir.lib.uwo.ca/etd/5410 This Dissertation/Thesis is brought to you for free and open access by Scholarship@Western. It has been accepted for inclusion in Electronic Thesis and Dissertation Repository by an authorized administrator of Scholarship@Western. For more information, please contact [email protected]. Abstract Smouldering combustion is defined as a flameless oxidation reaction occurring on the surface of the condensed phase (i.e., solid or liquid). Traditional research on smouldering was related to economic damages, fire risk, and death, due to the release of toxic gases and slow propagation rates. Recently, smouldering has been applied as an intentional, engineering technology (e.g., waste and contaminant destruction). Smouldering involves the transport of heat, mass, and momentum in the solid and fluid phases along with different chemical reactions. Therefore, numerical models are essential for the fundamental understanding of the process. Smouldering models either neglected heat transfer between phases (i.e., assumed local thermal equilibrium) or employed heat transfer correlations (i.e., under local thermal non- equilibrium conditions) not appropriate for smouldering. -
EMPLOYEE FIRE and LIFE SAFETY: Developing a Preparedness Plan and Conducting Emergency Evacuation Drills
EMPLOYEE FIRE AND LIFE SAFETY: Developing a Preparedness Plan and Conducting Emergency Evacuation Drills The following excerpts are taken from the book Introduction to Employee Fire and Life Safety, edited by Guy Colonna, © 2001 National Fire Protection Association. EXCERPTS FROM CHAPTER 3: Quick Tip Developing a Preparedness Plan To protect employees from fire and other emergencies and to prevent Jerry L. Ball property loss, whether large or small, companies use preparedness plans Fire is only one type of emergency that happens at work. Large and (also called pre-fire plans or pre- small workplaces alike experience fires, explosions, medical emergen- incident plans). cies, chemical spills, toxic releases, and a variety of other incidents. To protect employees from fire and other emergencies and to prevent property loss, whether large or small, companies use preparedness plans (also called pre-fire plans or pre-incident plans). The two essential components of a fire preparedness plan are the following: 1. An emergency action plan, which details what to do when a fire occurs 2. A fire prevention plan, which describes what to do to prevent a fire from occurring Of course, these two components of an overall preparedness plan are inseparable and overlap each other. For the purposes of this discus- sion, however, this chapter subdivides these two components into even smaller, more manageable subtopics. OSHA REGULATIONS uick ip Emergency planning and training directly influence the outcome of an Q T emergency situation. Facilities with well-prepared employees and Emergency planning and training directly influence the outcome of an well-developed preparedness plans are likely to incur less structural emergency situation. -
Ammonia, Anhydrous Ama
AMMONIA, ANHYDROUS AMA CAUTIONARY RESPONSE INFORMATION 4. FIRE HAZARDS 7. SHIPPING INFORMATION 4.1 Flash Point: 7.1 Grades of Purity: Commercial, industrial, Common Synonyms Liquefied compressed Colorless Ammonia odor Not flammable under conditions likely to refrigeration, electronic, and metaflurgical Liquid ammonia gas be encountered grades all have purity greater than 99.5% 4.2 Flammable Limits in Air: 15.50%- 7.2 Storage Temperature: Ambient for pressurized 27.00% ammonia; low temperature for ammonia at Floats and boils on water. Poisonous, visible vapor cloud is produced. 4.3 Fire Extinguishing Agents: Stop flow of atmospheric pressure Avoid contact with liquid and vapor. Keep people away. gas or liquid. Let fire burn. 7.3 Inert Atmosphere: No requirement Wear goggles, self-contained breathing apparatus, and rubber overclothing (including gloves). 4.4 Fire Extinguishing Agents Not to Be 7.4 Venting: Safety relief 250 psi for ammonia Stop discharge if possible. Used: None under pressure. Pressure-vacuum for Stay upwind and use water spray to ``knock down'' vapor. 4.5 Special Hazards of Combustion ammonia at atmospheric pressure. Call fire department. Products: Not pertinent Isolate and remove discharged material. 7.5 IMO Pollution Category: Currently not available 4.6 Behavior in Fire: Not pertinent Notify local health and pollution control agencies. 7.6 Ship Type: 2 4.7 Auto Ignition Temperature: 1204°F Protect water intakes. 7.7 Barge Hull Type: 2 4.8 Electrical Hazards: Class I, Group D Combustible. 4.9 Burning Rate: 1 mm/min. Fire 8. HAZARD CLASSIFICATIONS Wear goggles, self-contained breathing apparatus, and rubber over- 4.10 Adiabatic Flame Temperature: Currently clothing (including gloves). -
HEATS of COMBUSTION of DIAMOND and of GRAPHITE by Ralph S
r---------------___........,._ . _____~ ~_ U. S. DEPARTMENT OF COMMERCE NATIONAL BUREAU OF STANDARDS RESEARCH PAPER RP1140 Part of Journal of Research of the }.{ational Bureau of Standards, Volume 21, October 1938 HEATS OF COMBUSTION OF DIAMOND AND OF GRAPHITE By Ralph S. Jessup ABSTRACT Measurements were made of the heats of combustion of one artificial graphite, two natural graphites, and two samples of diamond. The bomb calorimeter used was calibrated electrically and by means of benzoic acid. The amount of reaction in each combustion experiment was determined from the mass of carbon dioxide formed. This method of determining the amount of reaction automatically eliminates the effect of unburned carbon and of some impurities. It was found, however, that results for different samples did not agree unless the samples were purified. Two methods of purification were used: (a) heating in vacuo to 1,800° C and (b) treatment with hydrochloric and hydrofluoric acids and subsequent heating in vacuo to 200° C to remove traces of the acids. Both methods yielded graphite containing only small amounts of impurities. The mean value obtained for the heat of combustion (-/lH) of the purified graphites in oxygen at 25° C and a constant pressure of 1 atmosphere to form gaseous carbon dioxide at the same temperature and pressure was 393.396 international kilojoules per mole (44.010 g of CO2). The maximum deviation of the mean value for anyone of the purified samples from this value was 0.021 percent. The two samples of diamond, purified by treatment with aqueous hydrochloric and hydrofluoric acids and subsequently heated in vacuo to about 570° C, had average particle sizes of 2.5 I'- and 39.5 1'-, respectively, and yielded the following respective mean values for the heat of combustion (-/lH) at 25° C and 1 atmos phere, in oxygen to form gaseous carbon dioxide: 395.771 and 395.287 interna tional kilojoules per mole. -
Thermochemistry of Heteroatomic Compounds:Calculation of the Heat
Open Journal of Physical Chemistry, 2011, 1, 1-5 doi:10.4236/ojpc.2011.11001 Published Online May 2011 (http://www.SciRP.org/journal/ojpc) Thermochemistry of Heteroatomic Compounds: Calculation of the heat of Combustion and the heat of Formation of some Bioorganic Molecules with Different Hydrophenanthrene Rows Vitaly V. Ovchinnikov Tupolev Kazan State Technical University, St- K. Marks 10, 420111 Kazan, Russian Federation E-mail: [email protected] Received March 23rd, 2011; revised April 10th, 2011; accepted May 10th, 2011. Abstract On the basis of the known experimental heats of combustions of the seventeen alkanes in condensed state, the general equation comb HifNg has been deduced, in which i and f are correlation coefficients, N and g are a numbers of valence electrons and lone electron pairs of heteroatoms in molecule. The pre- sented dependence has been used for the calculation of the heats of combustion of thirteen organic molecules with biochemical properties: holestan, cholesterol, methyl-cholesterol, ergosterol, vitamin-D2, estradiol, an- drostenone, testosterone, androstanedione, morphine, morphinanone, codeine and pentasozine. It is noted that good convergence was obtained within the limits of errors of thermochemical experiments known in the literature and calculations of the heats of combustion for some of them were conducted. With the application of Hess law and the heats of vaporization vap H , which has been calculated with the use of a topological 1 s solvation index of the first order x , the heats of formation f H for condensed and gaseous phases were calculated for the listed bioorganic molecules. Keywords: Alkanes, Biochemical Molecules, the Heat of Combustion, Heat of Formation, Heat of Vaporiza- tion, Topological Solvation Index 1. -
&EPA Ambient Water Quality Criteria for Toluene
United States Cffice of Water EPA 440/5-80-075 Environmental Protection Regula.ions and Standards O,:tober 1980 Agency Criteria and Standards Division Washington DC 20480 c.). & EPA Ambient Water Quality Criteria for Toluene tz r AMBIENT WATER QUALITY CRITERIA FOR TOLUENE Prepared By U.S. ENVIRONMENTAL PROTECTION AGENCY Office of Water Regulations and Standards Criteria and Standards Division Washington, D.C. Office of Research and Development Environmental Criteria and Assessment Office Cincinnati, Ohio Carcinogen Assessment Group Washington, D.C. Environmental Research Laboratories Corvalis, Oregon Duluth, Minnesota Gulf Breeze, Florida Narragansett, Rhode Island DISCLAIMER This report has been reviewed by the Environmental Criteria and Assessment Office, U.S. Environmental Protection Agency, and approved for publication. Mention of trade names or commercial products does not constitute endorsement or recommendation for use. AVAILABILITY NOTICE This document is available to the public through the National Technical Information Service, (NTIS), Springfield, Virginia 22161. El~TAL l'R~e1'!tjf A~ ii FOREWORD Section 304 (a)(1) of the Clear Water Act of 1977 (P.L. 95-217), requires the Administrator of the Environmental Protection Agency to publish criteria for water quality accurately reflecting the latest scientific knowledge on the kind and extent of all identifiable effects on health and welfare which may be expected from the presence of pollutants in any body of water, including ground water. Proposed water quality criteria for the 65 toxic pollutants listed under section 307 (a) (1) of the Cl ean Water Act were deve loped and a notice of thei r availability was published for public comment on March 15, 1979 (44 FR 15926), July 25, 1979 (44 FR 43660), and October 1, 1979 (44 FR 56628). -
Introduction to Alkenes and Alkynes in an Alkane, All Covalent Bonds
Introduction to Alkenes and Alkynes In an alkane, all covalent bonds between carbon were σ (σ bonds are defined as bonds where the electron density is symmetric about the internuclear axis) In an alkene, however, only three σ bonds are formed from the alkene carbon -the carbon thus adopts an sp2 hybridization Ethene (common name ethylene) has a molecular formula of CH2CH2 Each carbon is sp2 hybridized with a σ bond to two hydrogens and the other carbon Hybridized orbital allows stronger bonds due to more overlap H H C C H H Structure of Ethylene In addition to the σ framework of ethylene, each carbon has an atomic p orbital not used in hybridization The two p orbitals (each with one electron) overlap to form a π bond (p bonds are not symmetric about the internuclear axis) π bonds are not as strong as σ bonds (in ethylene, the σ bond is ~90 Kcal/mol and the π bond is ~66 Kcal/mol) Thus while σ bonds are stable and very few reactions occur with C-C bonds, π bonds are much more reactive and many reactions occur with C=C π bonds Nomenclature of Alkenes August Wilhelm Hofmann’s attempt for systematic hydrocarbon nomenclature (1866) Attempted to use a systematic name by naming all possible structures with 4 carbons Quartane a alkane C4H10 Quartyl C4H9 Quartene e alkene C4H8 Quartenyl C4H7 Quartine i alkine → alkyne C4H6 Quartinyl C4H5 Quartone o C4H4 Quartonyl C4H3 Quartune u C4H2 Quartunyl C4H1 Wanted to use Quart from the Latin for 4 – this method was not embraced and BUT has remained Used English order of vowels, however, to name the groups