A Field Explosion Test of Hydrogen-Air Mixtures
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A Simple Approach to the Supernova Progenitor-Explosion Connection
A Simple Approach to the Supernova Progenitor-Explosion Connection Bernhard Müller Queen's University Belfast Monash Alexander Heger, David Liptai, Joshua Cameron (Monash University) Many potential/indirect observables from core-collapse supernovae, but some of the most direct ones (explosion energies, remnant masses) are heavy elements challenging for SN theory! massive star core-collapse supernovae neutron stars & gravitational waves neutrinos supernova remnants The neutrino-driven mechanism in its modern flavour shock ● Stalled accretion shock still oscillations (“SASI”) pushed outward to ~150km as matter piles up on the PNS, then recedes again convection ● Heating or gain region g develops some tens of ms n i t g a n after bounce e li h o o c ● Convective overturn & shock oscillations “SASI” enhance the efficiency of -heating, shock which finally revives the shock ● Big challenge: Show that this works! Status of 3D Neutrino Hydrodynamics Models with Multi-Group Transport First-principle 3D models: ● Mixed record, some failures ● Some explosions, delayed compared to 2D ● Models close to the threshold So what is missing? 27 M Hanke et al. (2013) 2 3/5 2 −3/5 ⊙ ● Lcrit ∝M˙ M 14 Ma /3 ● → Increase neutrino heating or Reynolds stresses ● Unknown/undetermined microphysics (e.g. Melson et al. 2015)? ● 20 M Melson et al. (2015) Lower explosion threshold in ⊙ SASI-dominated regime (Fernandez 2015)? 15 M⊙ Lentz et al. (2015) ● Better 1D/multi-D progenitor Or with simpler schemes: e.g. IDSA+leakage Takiwaki et al. (2014) models? Challenge: Connecting to Observables Several 50 diagnostic 10 erg with explosion sustained energy accretion . l a ) t 2 e 1 a 0 k 2 ( n Pejcha & Prieto (2015): Explosion energies a J vs. -
Thermodynamics of Ion Exchange
Chapter 1 Thermodynamics of Ion Exchange Ayben Kilislioğlu Additional information is available at the end of the chapter http://dx.doi.org/10.5772/53558 1. Introduction 1.1. Ion exchange equilibria During an ion exchange process, ions are essentially stepped from the solvent phase to the solid surface. As the binding of an ion takes place at the solid surface, the rotational and translational freedom of the solute are reduced. Therefore, the entropy change (ΔS) during ion exchange is negative. For ion exchange to be convenient, Gibbs free energy change (ΔG) must be negative, which in turn requires the enthalpy change to be negative because ΔG = ΔH - TΔS. Both enthalpic (ΔHo) and entropic (ΔSo) changes help decide the overall selectivity of the ion-exchange process [Marcus Y., SenGupta A. K. 2004]. Thermodynamics have great efficiency on the impulsion of ion exchange. It also sets the equilibrium distribution of ions between the solution and the solid. A discussion about the role of thermodynamics relevant to both of these phenomena was done by researchers [Araujo R., 2004]. As the basic rule of ion exchange, one type of a free mobile ion of a solution become fixed on the solid surface by releasing a different kind of an ion from the solid surface. It is a reversible process which means that there is no permanent change on the solid surface by the process. Ion exchange has many applications in different fields like enviromental, medical, technological,.. etc. To evaluate the properties and efficiency of the ion exchange one must determine the equilibrium conditions. -
Could a Nearby Supernova Explosion Have Caused a Mass Extinction? JOHN ELLIS* and DAVID N
Proc. Natl. Acad. Sci. USA Vol. 92, pp. 235-238, January 1995 Astronomy Could a nearby supernova explosion have caused a mass extinction? JOHN ELLIS* AND DAVID N. SCHRAMMtt *Theoretical Physics Division, European Organization for Nuclear Research, CH-1211, Geneva 23, Switzerland; tDepartment of Astronomy and Astrophysics, University of Chicago, 5640 South Ellis Avenue, Chicago, IL 60637; and *National Aeronautics and Space Administration/Fermilab Astrophysics Center, Fermi National Accelerator Laboratory, Batavia, IL 60510 Contributed by David N. Schramm, September 6, 1994 ABSTRACT We examine the possibility that a nearby the solar constant, supernova explosions, and meteorite or supernova explosion could have caused one or more of the comet impacts that could be due to perturbations of the Oort mass extinctions identified by paleontologists. We discuss the cloud. The first of these has little experimental support. possible rate of such events in the light of the recent suggested Nemesis (4), a conjectured binary companion of the Sun, identification of Geminga as a supernova remnant less than seems to have been excluded as a mechanism for the third,§ 100 parsec (pc) away and the discovery ofa millisecond pulsar although other possibilities such as passage of the solar system about 150 pc away and observations of SN 1987A. The fluxes through the galactic plane may still be tenable. The supernova of y-radiation and charged cosmic rays on the Earth are mechanism (6, 7) has attracted less research interest than some estimated, and their effects on the Earth's ozone layer are of the others, perhaps because there has not been a recent discussed. -
NUCLEAR WEAPONS EFFECTS Introduction: the Energy Characteristics and Output from Nuclear Weapons Differ Significantly from Conve
NUCLEAR WEAPONS EFFECTS Introduction: The energy characteristics and output from nuclear weapons differ significantly from conventional weapons. Nuclear detonations exhibit much higher temperature within the fireball and produce peak temperatures of several hundred million degrees and intense x-ray heating that results in air pressure pulses of several million atmospheres. Conventional chemical explosions result in much lower temperatures and release the bulk of their energy as air blast and shock waves. In an atmospheric detonation, such as was deployed in Japan, it is the blast and thermal component of the nuclear explosion that is the major factor in destruction and death, not nuclear radiation, as the public believes. The effective range of immediate harm to humans from nuclear radiation from the atmospheric explosion is much less than the effective range from blast and thermal heating. In order to limit the discussion of weapons effects to elementary terms, this discussion is based upon a single worst-case scenario. Probably the largest weapon that might be employed against a population would have a yield of less than one-megaton (or 1 million tons of TNT equivalent energy or simply 1 MT). However, a crude terrorist nuclear device would probably be in the range of a few thousand tons of TNT equivalent energy or a few KT). The discussion here is based upon a nuclear detonation of 1 MT. Yield: The destructive power of a nuclear weapon, when compared to the same amount of energy produced by TNT is defined as the ‘yield’ of the nuclear weapon. A 20-kiloton (KT) weapon, such as was detonated over Japan in World War II was equivalent in energy yield to 20,000 tons of TNT. -
Sample Chapter Template for AFFA
The Training Material on “Dangerous Goods Handling (All modes)” has been produced under Project Sustainable Human Resource Development in Logistic Services for ASEAN Member States with the support from Japan-ASEAN Integration Fund (JAIF). Copyright Association of Southeast Asian Nations (ASEAN) 2014. All rights reserved. Dangerous Goods Handling Chapter 2: International Classification of Dangerous Goods Objectives This chapter will explain UN Transport regulations, its history and basis as model regulations for international classification system for other modes of transport. The linkage into the ASEAN Protocol 9 framework on the international carriage of dangerous goods in ASEAN will also be explained. 9 classes of dangerous goods classification shall be key content in this chapter. Other relevant basic terms such as Class, Division, Packaging Group (PG), UN Number (UNNO) and Proper Shipping Names (PSN) will also be covered. As supplement knowledge in classification of substances or mixtures that have more than one hazard, the explanation on precedence of hazard characteristics will be given. Basic hazard communication such as Labelling requirements, Dangerous Goods Declaration (DGD) or Multi-modal Dangerous Goods Form shall be explained. 1. Introduction 1.1 United Nations Recommendations on the Transport of Dangerous Goods (UNTDG/UNRTDG) These Recommendations have been developed by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods in the light of technical progress, the advent of new substances and materials, the exigencies of modern transport systems and, above all, the requirement to ensure the safety of people, property and the environment. They are addressed to governments and international organizations concerned with the regulation of the transport of dangerous goods. -
Explosives and Terminal Ballistics
AND TERMINAL BALLISTICS A REPORT PREPARED FOR THE AAF SCIEN'rIFIC ADVISORY GROUP By D. P. MAC DOUGALL Naval Ordnance Laboratory, Washington, D. C. N. M. NEWMARK Department oj Civil Engineering, University oj Illinois • PMblished May, 1946 by HEADQUARTERS AIR MATERIEL COMMAND PUBLICATIONS BRANCH, INTEJtJYiE~9) '1001 WRIGHT FIELD, DAYTON, OHIO V-46579 The AAF Scientific Advisory Group was activated late in 1944 by General of the Army H. H. Arnold. He se cured the services of Dr. Theodore von Karman, re nowned scientist and consultant in aeronautics, who agreed to organize and direct the group. Dr. von Karman gathered about him a group of Ameri can scientists from every field of research having a bearing on air power. These men then analyzed im portant developments in the basic sciences, both here and abroad, and attempted to evaluate the effects of their application to air power. This volume is one of a group of reports made to the Army Air Forces by the Scientific Advisory Group. Thil document contolnl Information affecting the notional defenle of the United Statel within the meaning of the Espionage Ad, SO U. S. C., 31 and 32, 01 amended. Its tronsmiulon or the revelation of Its contents In any manner to on unauthorized person II prohibited by low. AAF SCIENTIFIC ADVISORY GROUP Dr. Th. von Karman Director Colonel F. E. Glantzberg Dr. H. L. Dryden Deputy Director, Military Deputy Director, Scientific Lt Col G. T. McHugh, Executive Capt C. H. Jackson, Jr., Secretary CONSULTANTS Dr. C. W. Bray Dr. A. J. Stosick Dr. L. A. -
Energy and the Hydrogen Economy
Energy and the Hydrogen Economy Ulf Bossel Fuel Cell Consultant Morgenacherstrasse 2F CH-5452 Oberrohrdorf / Switzerland +41-56-496-7292 and Baldur Eliasson ABB Switzerland Ltd. Corporate Research CH-5405 Baden-Dättwil / Switzerland Abstract Between production and use any commercial product is subject to the following processes: packaging, transportation, storage and transfer. The same is true for hydrogen in a “Hydrogen Economy”. Hydrogen has to be packaged by compression or liquefaction, it has to be transported by surface vehicles or pipelines, it has to be stored and transferred. Generated by electrolysis or chemistry, the fuel gas has to go through theses market procedures before it can be used by the customer, even if it is produced locally at filling stations. As there are no environmental or energetic advantages in producing hydrogen from natural gas or other hydrocarbons, we do not consider this option, although hydrogen can be chemically synthesized at relative low cost. In the past, hydrogen production and hydrogen use have been addressed by many, assuming that hydrogen gas is just another gaseous energy carrier and that it can be handled much like natural gas in today’s energy economy. With this study we present an analysis of the energy required to operate a pure hydrogen economy. High-grade electricity from renewable or nuclear sources is needed not only to generate hydrogen, but also for all other essential steps of a hydrogen economy. But because of the molecular structure of hydrogen, a hydrogen infrastructure is much more energy-intensive than a natural gas economy. In this study, the energy consumed by each stage is related to the energy content (higher heating value HHV) of the delivered hydrogen itself. -
Recent Developments in Composition C-4: Towards an Alternate Binder and Reduced Sensitivity
Recent Developments in Composition C-4: Towards an Alternate Binder and Reduced Sensitivity NDIA Insensitive Munitions & Energetic Materials Technology Symposium 2009 Jim Owens* BAE SYSTEMS OSI, Holston Army Ammunition Plant Paul Vinh RDECOM-ARDEC, Picatinny Arsenal IMEMTS 2009 – Tucson, AZ Cleared for Public Release by BAE Systems 1 Presentation Outline • Research Extrudable Moldable Insensitive eXplosive (OSX-REMIX) • Background • Program Objectives • Technical Approach • Formulation and Evaluation • Summary • Alternate Plastic-binder Extrudable eXplosive (OSX-APEX) • Background • Program Objectives • Technical Approach • Formulation • Modified Accelerated Aging Trial • Summary IMEMTS 2009 – Tucson, AZ Cleared for Public Release by BAE Systems 2 Acknowledgement • PM-CCS • Mr. Felix Costa • RDECOM-ARDEC • Mr. Paul Vinh • Mr. Sanjeev Singh • Mr. Gregory Tremarco • BAE SYSTEMS OSI • Mr. Jim Haynes • Ms. Kelly Guntrum • Mr. Alberto Carrillo • Mr. Matt Hathaway • Mr. Brian Alexander IMEMTS 2009 – Tucson, AZ Cleared for Public Release by BAE Systems 3 OSX-REMIX – Program Objectives • Composition C-4 already fares well in the arena of insensitivity, due to relatively large amount of binder. • Passes Bullet Impact and Fragment Impact (Army) sensitivity tests at ambient temperature. • Fails shock stimulus – Sympathetic Detonation and Shaped Charge Jet. • BAE’s task – to develop an alternate extrudable formulation with similar physical and energy output characteristics, while enhancing its insensitivity. • Maintain current binder configuration for comparison to standard C-4. • Identify modifications to process or alternate input energetics. • Formulate and evaluate physical and energetic properties. IMEMTS 2009 – Tucson, AZ Cleared for Public Release by BAE Systems 4 OSX-REMIX – Technical Approach • Modification to manufacturing process. • Maintain aqueous slurry-coating process. • Premixing RDX with fluid portion of binder (DOA/Oil). -
Dangerous Goods Classifications
Dangerous Goods Classifications Dangerous Goods Classifications Click on a class to read more details: 1. Explosives 2. Gases 3. Flammable Liquids 4. Flammable Solids 5. Oxidizing Substances 6. Toxic & Infectious Substances 7. Radioactive Material 8. Corrosives 9. Miscellaneous Dangerous Goods CLASS 1: EXPLOSIVES Explosives are materials or items which have the ability to rapidly conflagrate or detonate as a consequence of chemical reaction. Subclass Subclass 1.1: Explosives with a mass explosion hazard Consists of explosives that have a mass explosion hazard. A mass explosion is one which affects almost the entire load instantaneously. Subclass 1.2: Explosives with a severe projection hazard Consists of explosives that have a projection hazard but not a mass explosion hazard. Subclass 1.3: Explosives with a fire Consists of explosives that have a fire hazard and either a minor blast hazard or a minor projection hazard or both but not a mass explosion hazard. Subclass 1.4: Minor fire or projection hazard Consists of explosives that present a minor explosion hazard. The explosive effects are largely confined to the package and no projection of fragments of appreciable size or range is to be expected. An external fire must not cause virtually instantaneous explosion of almost the entire contents of the package. Subclass 1.5: An insensitive substance with a mass explosion hazard Consists of very insensitive explosives with a mass explosion hazard (explosion similar to 1.1). This division is comprised of substances which have a mass explosion hazard but are so insensitive that there is very little probability of initiation or of transition from burning to detonation under normal conditions of transport. -
Tnt Equivalence of C-4 and Pe4: a Review of Traditional Sources and Recent Data
TNT EQUIVALENCE OF C-4 AND PE4: A REVIEW OF TRADITIONAL SOURCES AND RECENT DATA D. Bogosian1, M. Yokota1, S. Rigby2 1Baker Engineering and Risk Consultants, 360 N. Sepulveda Blvd., Ste 1090, El Segundo, CA 90245, USA; 2University of Sheffield, Department of Civil & Structural Engineering, Sir Frederick Mappin Building, Mappin Street, Sheffield, S1 3JD, United Kingdom ABSTRACT Since standard engineering-level blast models are typically developed to predict airblast parameters (pressure and impulse) from TNT bursts, prediction of airblast from other materials uses an equivalence factor by which an equivalent TNT weight is computed and used in the source term of the model. This approach is widespread in the industry and has been codified in numerous manuals, books, and papers. A recent effort co-sponsored by TSWG (U.S.) and FSTD (Singapore) collected and compiled equivalence data for a wide variety of explosive materials (both military grade as well as home-made) into a single software tool named STREET. The database thus assembled provides a comprehensive and expandable repository for equivalence data. Two of the main achievements in STREET are the consideration of equivalence as a function of scaled standoff (rather than a scalar), and the documentation of uncertainty in the estimated value. In this paper, we consider specifically the manual- and test-derived data related to Composition C-4, and as a first step, we draw some judgments regarding the equivalence implicit in blast curves provided by UFC 3-340-02, for both pressure and impulse. Next, we consider PE4, which is similar in composition to C-4 and is used widely in the UK. -
2,4,6-Trinitrotoluene (Tnt)
2,4,6-TRINITROTOLUENE (TNT) What is 2,4,6-TRINITROTOLUENE? 2,4,6-trinitrotoluene, also called TNT, is a man-made compound. The odorless, yellow solid is used in explosives. In the United States, TNT is primarily made at military sites. Where can TNT be found and how is it used? TNT is an explosive used by the military in artillery shells, grenades and airborne bombs. TNT may be found in old artillery shells that wash up or are dredged up on beaches. Industries use TNT to make dye and photography chemicals. How can people be exposed to TNT? You could be exposed to TNT through: Breathing vapor or dust containing TNT. This might happen if your work involves TNT. Drinking water polluted with TNT. This could happen if you drink water polluted by a waste site containing TNT. Eating fruits and vegetables grown in soil containing TNT. Touching soil that contacted TNT. You can also touch it if you work with TNT. Eye Contact by touching the eyes with hands contaminated with TNT, or getting TNT-contaminated dust in them. How does TNT work? When you breathe in air or drink water with TNT in it, the chemical enters your body quickly and completely. If TNT touches the skin, the body absorbs it more slowly. Regardless of the type of exposure, TNT is absorbed by the bloodstream and travels to the organs. When it reaches the liver, it breaks down and changes into several different substances. Not all of these substances have been identified, so it is not known if they are harmful. -
Explosive Chemical Hazards & Risk
Safe Operating Procedure (1/13) EXPLOSIVE CHEMICAL HAZARDS & RISK MINIMIZATION _____________________________________________________________________ (For assistance, please contact EHS at (402) 472-4925, or visit our web site at http://ehs.unl.edu/) Background The Globally Harmonized System (GHS) of classification and labeling of chemicals defines an explosive materials as follows: a solid or liquid substance (or mixture of substances) which is in itself capable by chemical reaction of producing gas at such temperature and pressure and at such speed as to cause damage to the surroundings. Under the GHS system, there are seven divisions for explosives. • Unstable explosives • Division 1.1 – mass explosion hazards (i.e., nearly instant detonation of the entire quantity of explosive present) • Division 1.2 – projection hazards but not mass explosion hazards • Division 1.3 – minor mass explosion or projection hazards • Divisions 1.4 through 1.6 – very insensitive substances; negligible probability of accidental initiation or propagation Explosive chemicals will be identified with the pictogram shown below. In addition, Section 2 of the Safety Data Sheet (SDS) will include one or more of the hazard statements indicated below. • H200 Unstable; explosive • H201 Explosive; mass explosion hazard • H202 Explosive; severe projection hazard • H203 Explosive; fire, blast or projection hazard • H204 Fire or projection hazard • H205 May explode in fire Scope This SOP is limited in scope to those chemicals that meet the GHS definition of an explosive. However, it is important to understand that explosions can occur with chemicals that are not considered GHS explosives. For example, an explosion can occur with large-scale polymerization of a monomer. The reaction of monomers forming polymers is exothermic.