Meyer R., Koehler J., Homburg A. Explosives. Wiley-VCH, 2002 / Explosives 5th ed by Koehler, Meyer, and Homburg (2002)
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Ethyl Picrate |
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128 |
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refractive index nD20: |
1.504 –1.507 |
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boiling analysis at 760 Torr: |
252 |
– 255 °C = |
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485 |
– 491°F |
acidity, as HCl: not more than |
0.004 % |
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reaction: |
neutral |
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Ethyl Picrate
2,4,6-trinitrophenetol; Ethylpikrat; picrate d’ethyle
pale yellow needles empirical formula: C8H7N3O7 molecular weight: 257.2
energy of formation: –167.1 kcal/kg = – 699 kJ/kg enthalpy of formation: –186.7 kcal/kg = – 781 kJ/kg oxygen balance: – 77.8 %
nitrogen content: 16.34 %
volume of explosion gases: 859 l/kg heat of explosion
(H2O liq.): 840 kcal/kg = 3515 kJ/kg (H2O gas): 805 kcal/kg = 3369 kJ/kg
specific energy: 86 mt/kg = 847 kJ/kg melting point: 78 °C = 172°F detonation velocity, confined:
6500 m/s =21 300 ft/s at r = 1.55 g/cm3
The preparation of this compound resembles that of W Trinitroanisol.
Ethyltetryl
2,4,6-trinitrophenylethylnitramine; trinitroph´enyl´ethylnitramine
green yellow crystals empirical formula: C8H7N5O8 molecular weight: 301.2
energy of formation: +5.4 kcal/kg = +22.5 kJ/kg enthalpy of formation: –14.3 kcal/kg = – 59.8 kJ/kg
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Exothermal |
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oxygen balance: – 61.1 % nitrogen content: 23.25 %
volume of explosion gases: 874 l/kg heat of explosion
(H2O liq.): 970 kcal/kg = 4058 kJ/kg (H2O gas): 939 kcal/kg = 3930 kJ/kg specific energy: 109 mt/kg = 1069 kJ/kg
density: 1.63 g/cm3
melting point: 95.8 °C = 204.4°F
heat of fusion: 18.7 kcal/kg = 78 kJ/kg lead block test: 325 cm3/10 g
impact sensitivity: 0.5 kp m = 5 N m friction sensitivity:
up to 36 kp = 353 N pistil load no reaction
The properties of this compound resemble those of Tetryl; it can be prepared from monoor diethylaniline.
Since the melting point of ethyltetryl is lower than that of Tetryl, the former can be more readily employed in energy-rich pourable mixtures.
EURODYN 2000®
EURODYN 2000® is the trade name of a gelatinous rock explosive made by the DYNAMIT NOBEL GmbH Company. In contrast to the classical W Ammongelites, this explosive does not contain any nitroaromatics harmful to health, such as W Dinitrotoluene and Trinitrotoluene.
EWALID W
EWALID W is the trade name of a new rock explosive made by the WASAG CHEMIE Sythen GmbH Company. Its good water resistance enables it to be used even in wet shotholes.
Exothermal*)
Process characterized by the evolution of heat (opposite of endothermal).
* Text quoted from glossary.
Explode |
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Explode*)
Explodieren; exploser
To be changed in chemical or physical state, usually from a solid or liquid to a gas (as by chemical decomposition or sudden vaporization) so as to suddenly transform considerable energy into the kinetic form (W Explosion).
Exploding Bridgewire*)
Detonator or initiator that is initiated by capacitor discharge that explodes (rather than merely heats) the bridgewire. Cannot be initiated by any normal shock or electrical energy.
Exploding BridgeWire Detonator (EBW)
An initiating device which utilizes the shock energy from the explosion of a fine metallic wire to directly initiate a secondary explosive train. Invented by Luis Alvarez for the Manhatten project in the early 1940’s, the basic EBW consists of a fine wire (typically gold, 0.038 mm in diameter, 1 mm long), next to a secondary explosive such asW PETN or W RDX. A large, fast current pulse (>200 amps in approximately 1 microsecond) through the wire causes it to rapidly vaporize generating a shock wave of about 15 kilobars. This intense shock wave is sufficient to directly initiate the low density explosive next to the exploding wire. The low density explosive is than used to initiate a higher density explosive output pellet which in turn can initiate main charge explosives.
Exploding Foil Initiator (EFI, Slapper)
Similar in some respects to an Exploding BridgeWire Detonator, the Exploding Foil Initiator uses a high electrical current to vaporize a foil and accelerate a dielectric flyer down a short barrel (typically about 0.2 mm long). The kinetic energy of the flyer is sufficient to initiate high density secondary explosives such as HNS directly. Invented in 1965 by John Stroud of the Lawrence Livermore National Laboratory.
* Text quoted from glossary.
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Explosive Forming and Cladding |
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Explosion*)
Chemical reaction or change of state effected in an exceedingly short period of time with the generation of a high temperature and generally a large quantity of gas. An explosion produces a shock wave in the surrounding medium. A detonation is a confined explosion, occuring e.g. in a closed chamber where volume is constant. An unconfined explosion is an explosion occuring in the open air where the (atmospheric) pressure is constant.
Explosion Heat
W Heat of Explosion
Explosion Temperature
Explosionstemperatur; temp´erature d’explosion
Explosion temperature is the calculated temperature of the fumes of an explosive material which is supposed to have been detonated while confined in a shell assumed to be indestructible and impermeable to heat; the calculation is based on the W Heat of Explosion and on the decomposition reaction, with allowance for the dissociation equilibria and the relevant gas reaction (W Thermodynamic Calculation of Decomposition Reactions). The real detonation temperature in the front of the shock wave of a detonating explosive can be estimated on the strength of the hydrodynamic shock wave theory, and is higher than the calculated explosion temperature.
Explosive Forming and Cladding
Metallbearbeitung durch Sprengstoffe; traitement des m´etaux par explosion
The applicability of explosive matrials for metal forming have been studied with three different objectives in view: sheet forming and matrix forming of flat items by pressure impact; metal plating; surface hardening of manganese hard steel.
The application of the pressure shock of an explosive to form very large workpieces is primarily intended, to achieve the shaping of a workpiece without using presses, which are very expensive. The transmission of the pressure impact takes place under water. Preliminary
* Text quoted from glossary.
Explosive Bolt |
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experiments gave encouraging results, but a large-scale industrial application has not yet been developed.
The development of explosive cladding is very much more advanced: the metal sheet to be cladded is exploded onto the base material, parallel to it or at a certain angle. In this way it is possible to effect cladding tasks which would be impossible to fulfil by manual welding, owing to the formation of brittle intermediate alloys between the plating material and the base material – as, for instance, in plating titanium onto a steel surface.
On the surface of manganese steel, the impact of the explosive layer onto the steel surface results in hardening; the only objective of this process is that it enables repair work to be carried out on railway tracks in remote regions, and there is no need to convey the defective parts over long distances. In densely populated areas, forming explosions are difficult to perform.
Explosive Bolt*)
Sprengriegel; verrou destructif
A bolt that is intended to be fractured by a contained or inserted explosive charge.
Explosive Loading Factor*)
Spezifischer Sprengstoffverbrauch; consommation specitique d’explosits
The amount of explosive used per unit of rock, usually expressed as pounds of explosives per cubic yard of rock or tons of rock per pound of explosives, or their reciprocals.
Explosive Materials*)
Sprengmittel; materiaux explosif (W Table 11)
These include explosives, blasting agents and detonators. The term includes, but is not limited to, dynamite and other high explosives, slurries and water gels, blasting agents, black powder pellet powder, initiating explosives, detonators, safety fuses, squibs, detonating cord, igniter cord and igniters. A list of explosive materials determined to be within the coverage of “18 U.S.C. Chapter 40, Importation, Manufacture, Distribution and Storage of Explosive Materials” is issued at
* Text quoted from glossary.
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Explosives |
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least annually by the Director of the Bureau of Alcohol, Tobacco and Firearms of the Department of the Treasury.
The United States Department of Transportation classifications of explosive materials used in commercial blasting operations are not identical with the statutory definitions of the Organized Crime Control Act of 1970, Title 18 U.S.C., Section 841. To achieve uniformity in transportation, the definitions of the United States Department of Transportation in Title 49 Transportation CFR, Parts I-999 subdivides these materials into:
W Class A Explosives |
– Detonating, or otherwise maximum haz- |
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ard. |
W Class S Explosives |
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Flammable hazard. |
W Class C Explosives |
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Minimum hazard. |
Oxidizing Material |
– A substance that yields oxygen readily to |
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stimulate the combustion of organic mat- |
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ter (W Oxidizer) |
Explosive Train*)
A train of combustible and explosive elements arranged in order of decreasing sensitivity. The explosive train accomplishes the controlled augmentation of a small impulse into one of suitable energy to actuate main charge. A fuze explosive train may consist of a primer, a detonator, a delay, a relay, a lead and booster charge, one or more of which may be either omitted or combined. If the bursting charge is added to the foregoing train it becomes a bursting charge explosive train. A propelling charge explosive train might consist of a primer, igniter or igniting charge, usually black powder, and finally, any of the various types of propellants (W Igniter Train).
Explosives
Explosivstoffe; explosifs
1. Definition
Explosives are solid or liquid**) substances, alone or mixed with one another, which are in a metastable state and are capable, for this
* Text quoted from glossary.
**Of course, gases and gaseous mixtures can also be explosive. Explosive mixtures are often generated spontaneously (leaks in gas pipes, solvent tanks; firedamp in coal mining).
Explosives |
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reason, of undergoing a rapid chemical reaction without the participation of external reactants such as atmospheric oxygen. The reaction can be initiated by mechanical means (impact, W Impact Sensitivity; friction, W Friction Sensitivity), by the action of heat (sparks, open flame, red-hot or white-hot objects), or by detonating shock (W Blasting Cap with or without a W Booster charge). The resistance of the metastable state to heat is known as W Stability. The ease with which the chemical reaction can be initiated is known as W Sensitivity.
The reaction products are predominantly gaseous (W Fumes). The propagation rate from the initiation site outwards through the explosive material may be much slower than the velocity of sound (W Deflagration; W Gunpowder) or may be supersonic (W Detonation). Explosives are solid, liquid, or gelatinous substances or mixtures of individual substances, which have been manufactured for blasting or propulsion purposes. For their effectiveness: W Strength; W Burning Rate; W Brisance.
Materials which are not intended to be used for blasting or shooting may also be explosive. They include, for example, organic peroxide catalysts, gas-liberating agents employed in the modern manufacture of plastic materials and plastic foams, certain kinds of insecticides etc. Table 11 gives a an overview of explosive materials.
2. Important Explosives
Of the many explosive chemicals discussed in this book, the following are, at present, of industrial or military importance:
Nitro compounds:
W TNT in various degrees of purity, as defined by the solidification point of the material; pure 2,4- and 2,6-iso- mers of dinitrotoluene (as propellant components) and low-melting isomer mixtures (for commercial explosives);
Aromatic nitramines:
W Tetryl (trinitrophenylnitramine) for booster charges and secondary blasting cap charges;
Aliphatic nitramines:
WCyclonite (RDX) and W Octogen (HMX) as components for high-brisance compositions (W Compositions B;
WHollow Charges); W Nitroguanidine as the main component in powders with low explosion heat and in rocket propellants.
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Explosives |
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Nitrate esters:
WNitroglycerine, which is still of primary importance in commercial explosives, smokeless powders and rocket propellants;
WNitroglycol in commercial explosives only;*)
WPETN as a high-brisance component, which is phlegmatized and pressed for booster charges; it is also employed as a secondary charge of blasting caps and as a detonating cord charge;
WDiethyleneglycol Dinitrate for smokeless (cold) powders;
WNitrocellulose, which is the most important component of single-base and double-base powders and multibase rocket propellants. It is also used to gelatinize commercial explosives. Outside the explosives industry, it is also used in the manufacture of lacquers and varnishes;
WPolyvinyl Nitrate in rocket compositions.
Initiating explosives:
WMercury Fulminate, and other fulminates, which are now used to a much smaller extent;
WLead Azide, alone and in mixtures with Lead Trinitroresorcinate, as primary charges in blasting caps; also for firedamp-proof cooper caps in coal mining, and in military primers of all kinds;
WLead Styphnate (Lead Trinitroresorcinate) mixtures, which may or may not contain W Tetrazene, for percussion caps.
Many nitro derivatives of benzene and naphthalene were of importance in the past, since toluene – the starting compound in the manufacture of TNT – could only be prepared by distillation of coal. Owing to the advances in petrochemistry, toluene is now available in practically unlimited amounts; the bulk of the toluene now produced is employed as the starting material for the preparation of toluene diisocyanate (TDI) used in the production of plastics.
3. Quality Requirements for Industrial and Military Explosives
The quality requirements for industrial explosives are quite different from those valid for military explosives. It follows that their compositions and the mode of their preparation must be different as well. Table 4 gives an overview.
*Nitroglycol-based gelatinous explosives being replaced by W Emulsion Slurries.
Table 11. Explosive Materials and their Application
Explosives
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Table 12. Requirements on Industrial and Military Explosives
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Industrial Explosives |
Military Explosives |
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performance |
large gas volume and high heat of explosion = |
according to the purpose of the weapon: |
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high strength |
mines, bombs, mine projectiles, rocket war head |
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charges: |
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high detonation velocity not needed, except: |
high gas impact |
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special gelatins for seismic prospecting |
large gas volume |
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high heat of explosion |
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(high detonation velocity not needed) |
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grenades: |
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high speed splinter formation |
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high loading density |
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high detonation velocity |
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medium strength is sufficient |
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shaped (hollow charge effect): |
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extremely high values for density |
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and detonation velocity (HMX best |
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component) |
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high strength + high brisance |
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sensitivity |
safe in handling |
as unsensitive as possible |
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cap-sensitive (except: blasting agents and slur- |
firing safety |
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ries) |
impact safety |
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safe flash over capacity in long columns |
W projectile impact safety |
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stability and behavior on |
storage life about 6 months or longer neutral |
storage life 10 years or longer |
storage |
(e.g. no nitric acid as component) |
neutral |
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no reaction with metals such as picrate formation |
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water |
when cartridged, should withstand 2 h in stag- |
completely waterproof, at least when loaded in the |
resistance |
nant water (for seismic prospecting shots even |
weapon |
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longer) |
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consistency |
formable (gelatinous or powder form) to be able |
castable or pressible |
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to introduce the cap |
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thermal behavior |
must not freeze above – 25 °C (–13°F) |
fully functional between – 40 °C (– 40°F) |
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must withstand about +60 °C (140°F) for |
and 60 °C (140°F) or even higher for special purposes. |
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several hours (e.g. in deep mining) |
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Explosives
