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Transport of Dangerous Goods
ST/SG/AC.10/1/Rev.16 (Vol.I) Recommendations on the TRANSPORT OF DANGEROUS GOODS Model Regulations Volume I Sixteenth revised edition UNITED NATIONS New York and Geneva, 2009 NOTE The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. ST/SG/AC.10/1/Rev.16 (Vol.I) Copyright © United Nations, 2009 All rights reserved. No part of this publication may, for sales purposes, be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, electrostatic, magnetic tape, mechanical, photocopying or otherwise, without prior permission in writing from the United Nations. UNITED NATIONS Sales No. E.09.VIII.2 ISBN 978-92-1-139136-7 (complete set of two volumes) ISSN 1014-5753 Volumes I and II not to be sold separately FOREWORD The Recommendations on the Transport of Dangerous Goods are addressed to governments and to the international organizations concerned with safety in the transport of dangerous goods. The first version, prepared by the United Nations Economic and Social Council's Committee of Experts on the Transport of Dangerous Goods, was published in 1956 (ST/ECA/43-E/CN.2/170). In response to developments in technology and the changing needs of users, they have been regularly amended and updated at succeeding sessions of the Committee of Experts pursuant to Resolution 645 G (XXIII) of 26 April 1957 of the Economic and Social Council and subsequent resolutions. -
CL-20-Based Cocrystal Energetic Materials: Simulation, Preparation and Performance
molecules Review CL-20-Based Cocrystal Energetic Materials: Simulation, Preparation and Performance Wei-qiang Pang 1,2,* , Ke Wang 1, Wei Zhang 3 , Luigi T. De Luca 4 , Xue-zhong Fan 1 and Jun-qiang Li 1 1 Xi’an Modern Chemistry Research Institute, Xi’an 710065, China; [email protected] (K.W.); [email protected] (X.-z.F.); [email protected] (J.-q.L.) 2 Science and Technology on Combustion and Explosion Laboratory, Xi’an 710065, China 3 School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China; [email protected] 4 Department of Aerospace Science and Technology, Politecnico di Milano, 20156 Milan, Italy; [email protected] * Correspondence: [email protected]; Tel.: +86-029-8829-1765 Academic Editor: Svatopluk Zeman Received: 3 September 2020; Accepted: 17 September 2020; Published: 20 September 2020 Abstract: The cocrystallization of high-energy explosives has attracted great interests since it can alleviate to a certain extent the power-safety contradiction. 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12- hexaaza-isowurtzitane (CL-20), one of the most powerful explosives, has attracted much attention for researchers worldwide. However, the disadvantage of CL-20 has increased sensitivity to mechanical stimuli and cocrystallization of CL-20 with other compounds may provide a way to decrease its sensitivity. The intermolecular interaction of five types of CL-20-based cocrystal (CL-20/TNT, CL-20/HMX, CL-20/FOX-7, CL-20/TKX-50 and CL-20/DNB) by using molecular dynamic simulation was reviewed. The preparation methods and thermal decomposition properties of CL-20-based cocrystal are emphatically analyzed. -
May 25, 1965 M. A. COOK ETAL 3,185,017 METHOD of MAKING an EXPLOSIVE BOOSTER Original Filed July 13, 1959
May 25, 1965 M. A. COOK ETAL 3,185,017 METHOD OF MAKING AN EXPLOSIVE BOOSTER Original Filed July 13, 1959 FLS-1 INVENTORS AE1M at OOC AOWGLMS Al ACA 3,185,017 United States Patent Office Patented May 25, 1965 2 3,185,017 pressed pentolite (PETN-TNT), TNT, tetryl, tetrytol METHOD OF MAKING AN EXPLGSWE GOSTER (tetryl-TNT), cyclotol (RDX-TNT), composition B Melvin A. Cook and Dotigias E. Pack, 3: it lake City, (RDX-TNT-wax) and Ednatol (EDNA-TNT). The Utah, assig Rors to Intertanozzataia Researcia and Engi more inexpensive of these explosives are not detonatable eering Company, Inc., Saitake City, Utah, a cospera by Prinnacord, however. tion of Utah 5 Original application July 13, 1959, Ser. No. 826,539, how It has been found that PETN, PETN-TNT mixtures, Patent No. 3,637,453, dated June 5, 1932, Cisie at: RDX and cyclotol are detonated by Primacord, but their this application Oct. 24, 1960, Ser. No. 70,334 high cost and the relatively large quantities required make 2 Clairls. (C. 86-) it uneconomical to use them as boosters. O The improved boost cr of the invention generally com This invention relates to detonating means for ex prises a core of Primacord-sensitive explosive material plosives and more particularly to boosters for relatively sit trol inted by a compacted sheath of Primacord-insensi insensitive explosive compositions. This application is tive explosive imaterial of high brisance, said booster a division of our copending application Serial No. 826,539, having at cast one perforation extending through said filed July 13, 1959, now U.S. -
United States Patent (19) 11 Patent Number: 5,693,794 Nielsen 45 Date of Patent: Dec
USOO5693794A United States Patent (19) 11 Patent Number: 5,693,794 Nielsen 45 Date of Patent: Dec. 2, 1997 54). CAGED POLYNTRAMINE COMPOUND R.D. Gilardi. “The Crystal Structure of CHNO, a Heterocyclic Cage Compound." Acta Chystallographica, 75 Inventor: Arnold T. Nielsen, Santa Barbara, vol. B28, Part 3 (Mar. 1972), pp. 742-746. Calif. A.T. Nielsen and R.A. Nissan, "Polynitropolyaza Caged 73) Assignee: The United States of America as Explosives-Part 5." Naval Weapons Center Technical Pub represented by the Secretary of the lication 6692 (Publication Unclassified), China Lake, Ca. , Navy, Washington, D.C. Mar. 1986, pp. 10-23. (21) Appl. No.: 253,106 Primary Examiner-Richard D. Lovering 22 Filed: Sep. 30, 1988 Attorney, Agent, or Firm--Melvin J. Sliwka; Stephen J. Church 51 .................. CO7D 259/00 52 . 540/554; 14992; 540/556 (57) ABSTRACT 58 Field of Search ...................................... 54.0/554, 556 A new compound, 2.4.6.8, 10.12-hexanitro-2,4,6,8,10,12 56 References Cited8. hexaazaisowurtzitane12-hexaazatetracyclo[5.5.0.0'dodecane) (2,4,6,8,10.12-hexanitro-2,4,6,8,10, is disclosed PUBLICATIONS and a method of preparation thereof. The new compound is useful as a high energy, high density explosive. J.M. Kliegman and R.K. Barnes. "Glyoxal Derivatives-I 3. rgy, high Conjugated Aliphatic Dimines From Glyoxal and Aliphatic Primary Amines." Tetrahedron, vol. 26 (1970), pp. ONN NNO 2555-2560. ONN NNO J.M. Kliegman and R.K. Barnes. "Glyoxal Derivatives-II. Reaction of Glyoxal With Aromatic Primary Amines,” Jour nal Organic Chemistry, vol. -
Recovery of Ammonium Nitrate and Reusable Acetic Acid from Effluent Generated During HMX Production
CORE Metadata, citation and similar papers at core.ac.uk Provided by Defence Science Journal RAUT, era/.: RECOVERY OFACE~CACU)~OMEFF~UENTGENERATEDDUR~G HMXPRODUCTION ,/ Defence Science Journal, Vol. 54, No. 2, April 2004, pp. 161-167 O 2004. DESIDOC Recovery of Ammonium Nitrate and Reusable Acetic Acid from Effluent Generated during HMX Production V.D. Raut, R.S. Khopade, M.V. Rajopadhye, and V.L. Narasimhan High Energy Materials Research Laboratory, Pune-411 021 ABSTRACT Production of HMX on commercial scale is mainly carried out by modified Bachmann process, and acetic acid constitutes major portion of effluenttspent liquor produced during this process. The recovery of glacial acetic acid from this spent liquor is essential to make the process commercially viable besides making it eco-friendly by minimising the quantity of disposable effluent. The recovery of glacial acetic acid from spent liquor is not advisable by simple distillation since it contains, in addition to acetic acid, a small fraction of nitric acid, traces of RDX, HMX, and undesired nitro compounds. The process normally involves neutralising the spent mother liquor with liquor ammonia and then distillating the ueutralised mother liquor under vacuum to recover dilute acetic acid (strength approx. 30 %). The dilute acetic acid, in turn, is concentrated to glacial acetic acid by counter current solvent extraction, followed by distillation. The process is very lengthy and the energy requirement is also very high, rendering the process economically unviable. Hence, a novel method has been developed on bench-scale to obtain glacial acetic acid directly from the mother liquor after the second ageing process. -
Detonation Cord, Detacord, Det
DDEPATMENT OF MINING ENGINEERING INTRODUCTION:- What are explosives? An explosive (or explosive material) is a reactive substance that contains a great amount of potential energy that can produce an explosion if released suddenly, usually accompanied by the production of light, heat, sound, and pressure. An explosive charge is a measured quantity of explosive material, which may either be composed solely of one ingredient or be a mixture containing at least two substances. The potential energy stored in an explosive material may, for example, be chemical energy, such as nitro glycerine or grain dust DDEPATMENT OF MINING ENGINEERING pressurized gas, such as a gas cylinder or aerosol can nuclear energy, such as in the fissile isotopes uranium-235 and plutonium-239 Explosive materials may be categorized by the speed at which they expand. Materials that detonate (the front of the chemical reaction moves faster through the material than the speed of sound) are said to be "high explosives" and materials that deflagrate are said to be "low explosives". Explosives may also be categorized by their sensitivity. Sensitive materials that can be initiated by a relatively small amount of heat or pressure are primary explosives and materials that are relatively insensitive are secondary or tertiary explosives. A wide variety of chemicals can explode; a smaller number are manufactured specifically for the purpose of being used as explosives. The remainder are too dangerous, sensitive, toxic, expensive, DDEPATMENT OF MINING ENGINEERING unstable, or prone to decomposition or degradation over short time spans. DDEPATMENT OF MINING ENGINEERING HISTORY:- The use of explosives in mining goes back to the year 1627, when gunpowder was first used in place of mechanical tools in the Hungarian (now Slovak) town of Banská Štiavnica. -
Guide for the Selection of Commercial Explosives Detection Systems For
2.5.3.8 EXPRAY Field Test Kit EXPRAY is a unique, aerosol-based field test kit for the detection of what the manufacturer refers to as Group A explosives (TNT, DNT, picric acid, etc.), Group B explosives (Semtex H, RDX, PETN, NG, smokeless powder, etc.), and compounds that contain nitrates that are used in improvised explosives. Detection of explosive residue is made by observing a color change of the test paper. EXPRAY can be used in a variety of applications, and although in some aspects it does not perform as well as many of the other trace detectors discussed in this section, it costs only $250. This very low cost, coupled with simplicity and ease of use, may make it of interest to many law enforcement agencies (see the EXPRAY kit in fig. 13). The EXPRAY field kit2 is comprised of the following items: - one can of EXPRAY-1 for Group A explosives, - one can of EXPRAY-2 for Group B explosives, - one can of EXPRAY-3 for nitrate-based explosives (ANFO, black powder, and commercial and improvised explosives based on inorganic nitrates), - special test papers which prevent cross contamination. Figure 13. Photo of the EXPRAY Field Test Kit for explosives Initially, a suspected surface (of a package, a person’s clothing, etc.) is wiped with the special test paper. The paper is then sprayed with EXPRAY-1. The appearance of a dark violet-brown color indicates the presence of TNT, a blue-green color indicates the presence of DNT, and an orange color indicates the presence of other Group A explosives. -
Explosive Characteristics and Performance Larry Mirabelli Design Factors for Chemical Crushing
Explosive Characteristics and Performance Larry Mirabelli Design Factors for Chemical Crushing Controllable EXPLOSIVEEXPLOSIVE Uncontrollable GEOLOGYROCK CONFINEMENT DISTRIBUTION Course Agenda What is an Explosive Explosive Types What are best to fuel “chemical crusher” Explosive Properties Explosive types Characteristics General Application Explosive selection to meet blasting objectives What is an Explosive Intimate mixture of fuel and oxidizer. Can be a molecular solid, liquid or gas and/or mixtures of them. When initiated reacts very quickly to form heat, solids and gas. Violent exothermic oxidation-reduction reaction. Detonates instead of burning. Rate of reaction is its detonation velocity. Explosive Types Main Explosive Charge Explosive for use in primer make up. Initiation System Explosive Types – Main Explosive Charge Bulk Explosive Blasting Agent, 1.5 D (not detonator sensitive) • Repumpable – Emulsion (available with field density adjustment and/or homogenization) • Repumpable ANFO Blend – Emulsion (available with field density adjustment) • Heavy ANFO Blend – Emulsion • ANFO For fueling chemical crusher, application flexibility for changing design is best decision. Explosive Types – Main Explosive Charge Packaged Explosive Explosive, 1.1D (detonator sensitive) • Emulsion • Dynamite Blasting Agent, 1.5 D (not detonator sensitive) • Emulsion • Water Gel • WR ANFO • ANFO For fueling chemical crusher, it is best to optimize explosive distribution. Explosive Types Explosive for use in primer make up. Explosive, 1.1D (detonator sensitive) • Cast Booster • Dynamite • Emulsion For fueling chemical crusher, cast booster is recommended explosive for primer make up. Explosive Types Initiation System Electronic Non Electric Electric For fueling chemical crusher, Electronic Detonator is recommended. Explosive Properties Safety properties Characterize transportation, storage, handling and use Physical properties Characterize useable applications and loading equipment requirements. -
European Patent Office
Europäisches Patentamt (19) European Patent Office Office européen des brevets (11) EP 0 968 983 A1 (12) EUROPEAN PATENT APPLICATION published in accordance with Art. 158(3) EPC (43) Date of publication: (51) Int. Cl.7: C06B 25/34 05.01.2000 Bulletin 2000/01 (86) International application number: (21) Application number: 98912736.0 PCT/JP98/01634 (22) Date of filing: 09.04.1998 (87) International publication number: WO 99/26900 (03.06.1999 Gazette 1999/22) (84) Designated Contracting States: (72) Inventor: BAZAKI, Hakobu CH DE FR GB LI SE Oita 870-1109 (JP) (30) Priority: 26.11.1997 JP 33948497 (74) Representative: Blake, John Henry Francis (71) Applicant: Brookes & Martin Asahi Kasei Kogyo Kabushiki Kaisha High Holborn House Osaka-shi, Osaka 530-8205 (JP) 52/54 High Holborn London WC1V 6SE (GB) (54) HEXANITROHEXAAZAISOWURTZITANE COMPOSITION AND EXPLOSIVE COMPOSITION CONTAINING SAID COMPOSITION (57) Hexanitrohexaazaisowurtzitane-containing compositions which comprise hexanitrohexaazaisowurtzitane, polynitropolyacetylhexaazaisowurtzitanes and one or more of oxaisowurtzitane compounds represented by the speci- fied formulae. The explosive compositions which contain the hexanitrohexaazaisowurtzitane-containing compositions have improved handling safety by lowering their sensitivity without degrading combustibility and detonability. EP 0 968 983 A1 Printed by Xerox (UK) Business Services 2.16.7/3.6 (Cont. next page) EP 0 968 983 A1 2 EP 0 968 983 A1 Description Technical Field 5 [0001] The present invention relates to compositions which contain hexanitrohexaazaisowurtzitane as a major com- ponent and explosive compositions which contain the hexanitrohexaazaisowurtzitane-containing compositions. The compositions of the present invention are excellent in not only performance in terms of ignitability, combustibility, deton- ability and the like, but also insensitivity to provide improved handling safety. -
Enhanced Performance from Insensitive Explosives
Calhoun: The NPS Institutional Archive Faculty and Researcher Publications Faculty and Researcher Publications Collection 2013 Enhanced performance from insensitive explosives Brown, Ronald Monterey, California. Naval Postgraduate School 2013 Insensitive Munitions and Energetic Materials Technology SymposiumPaper 16169 http://hdl.handle.net/10945/47519 Approved for Public Release ENHANCED PERFORMANCE FROM INSENSITIVE EXPLOSIVES Ronald Brown, John Gamble, Dave Amondson, Ronald Williams, Paul Murch, and Joshua Lusk Physics Department Naval Postgraduate School, Monterey, CA 93943 Contact: [email protected] 2013 Insensitive Munitions and Energetic Materials Technology Symposium Paper 16169 Approved for Public Release Acknowledgement Dr. Kevin Vandersall Lawrence Livermore National Laboratory Technical Staff ANSYS-AUTODYN Berkeley, CA 2013 Insensitive Munitions and Energetic Materials Technology Symposium Paper 16169 Approved for Public Release Projected 14 Demonstrated Levels of Increase 12 “ONC” = Octanitrocubane “N8” = Octaazacubane > - e Overview of s c a e 10 e s r / c > - Achievements n m I e k s , a y e t i Relative to 8 r c c o n l I e V n o 6 i t Explosives a n o t Chronology e D 4 2 0 TNT RDX HMX CL-20 ONC N8 IMX HPX HPX+ 2013 Insensitive Munitions and Energetic Materials Technology Symposium Paper 16169 Approved for Public Release OUTLINE • Objective • Background • Modeling & Validations • Effect of Detonation Convergence on Energy Partitioning • Coaxial Initiation Limitations • Results of Novel Dynamic Compression • Conclusions 2013 Insensitive Munitions and Energetic Materials Technology Symposium Paper 16169 Approved for Public Release Develop means for enhancing directed energy from explosive weapon systems by exploiting the effects of overdriven detonation. Explore means for overcoming the limitations of coaxial charges. -
Local Minima Then Are Used As Starting Points for the Third Step of the Procedure
LA-I142-MSI CiC-14REPO”RTCollection -- c. 3 REPRODUCTION ‘“” COPY ~ -.;,. .1.! Los Alamos Nal,onal Laboratory IS operated by the Unwersity of Cal,fornla for the Umted States Department of Energy under conlracl W.7405.ENG.36. 1 -——.Procedqre for Estima ting the Crystal SN- ,-:~.-.....—.-:”.–:,--- ~~~=m --:.”-”..... ... Densities of Organzc ~xploswes ““”P. ~-. -. .. ...- .. ‘= - - -- .- — . Los Alamos National Laboratory ~O~~l~~~~LOSA,amOSN.WM~x,Co,,,,, 9 This work was supported by the U.S. Department of Energyand the Naval Surface Weapons Center, Silver Spring, Maryland. DISCLAIMER This repon waspreparedasanaeeount of worksponsoredbyan ageneyofthe UnitedStatesGovernment. Neithcrthe UnitedStatesGovernment noranyagcney thereof,noranyoftheiremployecs, makesany warmnty,expressor implied,or assumesany legalliabilityor responsibilityfor theaccuracy, completeness, or usefulnessof any information,apparatus.product, or prmessdiselosed,or representsthat its usewould not infringeprivatelyownedrighls.Referencehereinto any specificcommercial product, process,or service bytradersame, trademark,manufacturer,or otherwise,does not necessarilyconstituteor implyits endorsemermrecommendation,or favoringby~heUnitedStatesGovemmenl or any agencythereof.The viewsandopinionsof authorsexpressedhereindo not necessarilystateor reflect!hoseof the Uni~edStates Govemmermorany ageniy thereof. LA-11142-MS UC-45 Issued: November 1987 A Procedure for Estimatingthe Crystal Densities of Organic Explosives Don T. Cromer Herman L. Ammon’ James R. Holden** . -- , “. .—.-—. ,..—,.-- -
Design and Synthesis of Explosives: Polynitrocubanes and High Nitrogen Content Heterocycles Reported by Andrew L
Design and Synthesis of Explosives: Polynitrocubanes and High Nitrogen Content Heterocycles Reported by Andrew L. LaFrate March 17th, 2005 Introduction In the ninth century, Chinese alchemists discovered black powder, a mixture of sulfur, charcoal, 1 and saltpeter (KNO3), while trying to invent a formula for immortality. Since then humans have been fascinated by explosives and have strived to develop more powerful formulations. In 1846, the Italian chemist Ascanio Sobrero, prepared nitroglycerine (1) by adding glycerine to concentrated HNO3 and H2SO4. Nitroglycerine was not used as an explosive until 1863 when Alfred Nobel stabilized it by adding a nitrocellulose binder, a mixture he termed “dynamite” (from Greek: dynamis meaning power).2 Dynamite and 2,4,6-trinitrotoluene (2) were the explosives of choice until the advent of the nitramine explosives RDX (3) and HMX (4) prior to the second World War. More than 60 years later, HMX (and its formulations) is still O N CH3 2 ONO the workhorse for most 2 O N NO NO N NO 2 2 2 N 2 N military and heavy duty ONO2 N O2N N N N civilian applications. ONO2 NO2 O2N NO2 NO2 Nitroglycerine (1) TNT (2) RDX (3) HMX (4) Background The two most common methods used to quantitate the performance of explosives are the velocity of detonation (VOD) and the detonation pressure (PD). VOD is the rate at which the chemical reaction propagates through the solid explosive or the velocity of the shockwave produced by an explosion. PD is a measure of the increase in pressure followed by detonation of an explosive.3 Despite the development of high explosives such as HMX, active efforts have continued within the military and scientific communities to produce better explosives to complement emerging weapons and space technologies.