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Primary explosives explosive power

For primary explosives the power or the energy in a nanosecond laser pulse is sufficient to initiate these explosives. For example, lead azide or silver azide require only a few mJ s in a nanosecond laser pulse, while most nanosecond pulse lasers deliver at least several tens... [Pg.663]

It explodes without melting when heated [1]. The title compound and its barium, lead(II), and mercury(II) salts were studied by DTA and DSC techniques. The lead salt is the least stable and most powerful primary explosive of the 4 compounds [2],... [Pg.310]

Primary explosives differ from secondary explosives in that they undergo a rapid transition from burning to detonation and have the ability to transmit the detonation to less sensitive (but more powerful) secondary explosives. Primary explosives have high degrees of sensitivity to initiation through shock, friction, electric spark, or high temperature, and explode whether confined or unconfined. Some widely used primary explosives include lead azide, silver azide, tetrazene, lead styphnate, mercury fulminate, and diazodinitrophenol. Nuclear weapon applications normally limit the use of primary explosives to lead azide and lead styphnate. [Pg.51]

Secondary explosives (also known as high explosives) are different from primary explosives in that they cannot be detonated readily by heat or shock and are generally more powerful. Secondary explosives can be initiated to detonation only by a shock produced by the explosion of a primary explosive. Widely used secondary explosives include trinitrotoluene (TNT), tetryl, picric acid, nitrocellulose, nitroglycerine, nitroguanidine, cyclotrimethylenetrinitramine (RDX), cyclotetramethylenetetranit-... [Pg.52]

Pentaerythritol tetranitrate (PETN) is a colorless crystalline solid that is very sensitive to initiation by a primary explosive. It is a powerful secondary explosive that has a great shattering effect. It is used in commercial blasting caps, detonation cords, and boosters. PETN is not used in its pure form because it is too sensitive to friction and impact. It is usually mixed with plasticized nitrocellulose or with synthetic rubbers to form PBXs. The most common form of explosive composition containing PETN is Pentolite, a mixture of 20 to 50% PETN and TNT. PETN can be incorporated into gelatinous industrial explosives. The military has in most cases replaced PETN with RDX because RDX is more thermally stable and has a longer shelf life. PETN is insoluble in water, sparingly soluble in alcohol, ether, and benzene, and soluble in acetone and methyl acetate. [Pg.55]

The five primary threats from a nuclear explosion are the destructive power of the nuclear explosion, the intense initial heat, the initial radiation, the air blast, and fallout. Almost nothing can be done to avoid the explosive power of a nuclear blast, but an individual can take some steps to avoid exposure to the remaining factors. [Pg.142]

Explosives are classed as primary or secondary. Typically, a small quantity of a primary explosive would be used in a detonator (known colloquially as a cap ), whereas larger quantities of secondary explosives are used in the booster and the main charge of a device. This collection of explosives is known as an explosive train in which a signal (mechanical, thermal, or electrical) from the control system is converted first into a small explosive shock from the detonator, which in turn initiates a more powerful explosion in the booster, which amplifies the shock into the main charge. [Pg.12]

Primary explosives are sensitive to modest stimuli such as heat, spark, or friction application of the correct stimulus will lead to a detonation. The primary explosives used in detonators are typically extremely sensitive but not particularly powerful common examples are mercury fulminate, lead azide, and lead styphnate. In principle, the heavy metals present in most primary explosives should be a good cue for detection however, there are primary explosives that do not contain such elements. [Pg.13]

Interest has focused on derivatives of mannitol hexanitrate (14) as potential explosives because although this nitrate ester is a powerful explosive it has some property characteristics of a primary explosive. Treatment of mannitol hexanitrate (14) with pyridine or ammonium carbonate " in aqueous acetone leads to a very selective denitration with the formation of mannitol-1,2,3,5,6-pentanitrate (77). Marans and co-workers synthesized the acetate (78), the propionate (79), and the phenylacetate (80) derivatives of mannitol-1,2,3,5,6-pentanitrate and all have significantly lower melting points than mannitol hexanitrate. The incorporation of such groups can also help to increase the solubility of an explosive in the melt of another explosive. [Pg.110]

The chemical properties of primary and secondary nitramines are important in relation to their use as explosives. Primary nitramines contain acidic hydrogen in the form of —N//NO2 and, consequently, in the presence of moisture, primary nitramines corrode metals and form metal salts, some of which are primary explosives. This is one reason why powerful explosives like methyinitramine (1) have not found practical use. Ethylenedinitramine (EDNA) (2) suffers from similar problems but its high brisance (VOD 8240 m/s, d = 1.66 g/cm ) and low sensitivity to impact have seen it used for some applications. [Pg.192]

Aminotetrazole (91) reacts with potassium permanganate in excess aqueous sodium hydroxide to yield the disodium salt of 5-azotetrazole (92). 5-Azotetrazole is unstable and attempts to isolate it by acidification yields 5-hydrazinotetrazole (93). Diazotization of 5-aminotetrazole (91) in the presence of excess sodium nitrite yields 5-nitrotetrazole (94), a powerful explosive whose mercury and silver salts are primary explosives. ... [Pg.344]

TABLE 3.2 Comparisons of Initiating Powers of Primary Explosives... [Pg.48]

Values of power index for some primary and secondary explosives are given in the Table 1.7 which shows that the values for power index of secondary explosives are more than the values for primary explosives. [Pg.33]

The erstwhile Explosives Research and Development Laboratory (ERDL), now High Energy Materials Research Laboratory (HEMRL), Pune, had undertaken a study on primary explosives with a view to synthesizing a series of new explosives, which are safer, powerful and free from the drawbacks of lead azide and MF. As a result of these sustained efforts, HEMRL has successfully synthesized and developed a new and safer initiatory explosive called basic lead azide (BLA). [Pg.132]

A plant used for drying, grinding, sieving, weighing and stirring primary explosives must be designed to minimize friction, and power units should be located in a separate building. [Pg.130]

Nitromannite is about as sensitive as nitroglycerin to shock and to friction. It detonates under a 4-cm. drop of a 2-kilogram weight, and may be exploded readily on a concrete surface by a blow of a carpenter s hammer. It is not fired by the spit of a fuse, but is made to detonate by the flame of a match which causes local overheating. It is almost, but not quite, a primary explosive. It is used as the high-explosive charge in compound detonators which contain the relatively safe diazodinitrophenol as the primary explosive. A mixture of nitromannite and tetra-cene is a powerful and brisant primary explosive which detonates from moderate heat. [Pg.238]

Typical primary explosives are lead azide and lead styphnate (see Fig. 1.17). The latter one is less powerful than LA but easier to initiate. Tetrazene (Fig. 2.2) is often added to the latter in order to enhance the response (sensitizer). (N.B. mercury fulminate used to be used as a sensitizer). Tetrazene is an effective primer which decomposes without leaving any residue behind. It has been introduced as an additive to erosion-free primers based on lead trinitroresorcinate. Unfortunately, tetrazene is hydrolytically not entirely stable and in long term studies decomposes at temperatures above 90 °C. Diazodinitrophenol (Fig. 2.2) is also a primary explosive and is primarily used in the USA. However, the compound quickly darkens in sun-... [Pg.45]

While Region II can be compared with the hot-wire initiation of primary explosives or pyrotechnic compositions, the laser power densities in region IV also make it possible to directly shock initiate secondary explosives by laser irradiation. The laser power densities of Region IV are achieved by solid-state lasers with laser powers of at least 100 W. In contrast, laser diodes ( 1-10 W) only provide power densities which fall into the regions II and III. However, more powerful laser diodes have been gradually developed and therefore, laser diode initiators (LDI) have be-... [Pg.145]

Properties More sensitive and powerful than those high explosives which are used as main bursting charge, but less sensitive than primary explosives. [Pg.37]

CDNTA form a white to bluish white powder, crystals, or granules. The crystals are sensitive to shock, friction, and percussion. CDNTA is a powerful primary explosive that demonstrates outstanding potential as a future replacement for mercury fulminate, lead styphnate, lead azide, and diazodinitrophenol for use in blasting caps and detonators. It should not be stored dry, and should be desensitized with dextrose, sulfur, starch, wood pulp, dextrin, or gum Arabic after preparation... [Pg.269]


See other pages where Primary explosives explosive power is mentioned: [Pg.61]    [Pg.50]    [Pg.53]    [Pg.103]    [Pg.413]    [Pg.84]    [Pg.219]    [Pg.219]    [Pg.494]    [Pg.369]    [Pg.149]    [Pg.45]    [Pg.3]    [Pg.419]    [Pg.421]    [Pg.45]    [Pg.2289]    [Pg.27]    [Pg.146]    [Pg.86]    [Pg.24]    [Pg.27]    [Pg.231]    [Pg.261]   
See also in sourсe #XX -- [ Pg.90 , Pg.91 ]




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