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Lead azide, detonation

Type 97 Land Bomb Gaine A and Type 99 Ordinary Bomb Gaine A length 4V4 inches, depth 1-3/8 inches. Explosive Train Primer compn in upper plug BkPdr delay (0.03 sec) over flash pdr relay in middle plug Lead Azide detonator over Tetryl in lower plug and PA Booster (p 192 Fig 140)... [Pg.476]

Lead azide is an explosive solid that can be detonated by shock (or by heating to 350 °C), while sodium azide exists as stable white crystals that decompose smoothly on heating (unless allowed to react with extraneous material). Why are heavy metal azides so explosive Why are lead azide detonators not sheathed in copper or brass ... [Pg.45]

Lead azide detonators for use in coal mining have copper capsules for all other blastings, aluminum caps are used. [Pg.255]

Lead azide detonators for coal mining have copper tubes. For all other blasting aluminium caps are used. [Pg.256]

In the case of lead azide, Andreev [42] and Bowden and Yoffe [43] suggest that lead azide detonates immediately after being ignited and that a burning regime is absent. The theory of fracture that was subsequently developed to explain the initiation of fast reaction [44,45], and the previous observations lead to the conclusion that the shock initiation mechanism of this primary explosive is not likely to exhibit the same characteristics as those exhibited by the secondary explosives. However, examination of the shock sensitivity of dextrinated and polyvinyl lead azide to pulse durations vaiying from 0.1 to 4.0 psec shows that the initiation characteristics are indeed similar to those observed for heterogeneous explosives. [Pg.276]

NO DEXTRINATED LEAD AZIDE DETONATIONS AT THIS LEVEL OR BELOW... [Pg.282]

A suitable replacement for lead azide in detonators still does not exist even though new candidates, mostly based on tetrazole complexes, have been proposed and to a certain limited extent even employed. There are also some alternative approaches which eliminate toxic metals from the detonator by eliminating the primary explosive but they have not yet succeeded in replacing lead azide detonators. [Pg.9]

Only relatively few compounds can act as primary explosives and still meet the restrictive military and industrial requirements for reflabiUty, ease of manufacture, low cost, compatibiUty, and long-term storage stabiUty under adverse environmental conditions. Most initiator explosives are dense, metaHoorganic compounds. In the United States, the most commonly used explosives for detonators include lead azide, PETN, and HMX. 2,4,6-Triamino-l,3,5-triuitrobenzene (TATB) is also used in electric detonators specially designed for use where stabiUty at elevated temperatures is essential. [Pg.10]

Lead Azide. The azides belong to a class of very few useflil explosive compounds that do not contain oxygen. Lead azide is the primary explosive used in military detonators in the United States, and has been intensively studied (see also Lead compounds). However, lead azide is being phased out as an ignition compound in commercial detonators by substances such as diazodinitrophenol (DDNP) or PETN-based mixtures because of health concerns over the lead content in the fumes and the explosion risks and environmental impact of the manufacturing process. [Pg.10]

Lead azide is not readily dead-pressed, ie, pressed to a point where it can no longer be initiated. However, this condition is somewhat dependent on the output of the mixture used to ignite the lead azide and the degree of confinement of the system. Because lead azide is a nonconductor, it may be mixed with flaked graphite to form a conductive mix for use in low energy electric detonators. A number of different types of lead azide have been prepared to improve its handling characteristics and performance and to decrease sensitivity. In addition to the dextrinated lead azide commonly used in the United States, service lead azide, which contains a minimum of 97% lead azide and no protective colloid, is used in the United Kingdom. Other varieties include colloidal lead azide (3—4 pm), poly(vinyl alcohol)-coated lead azide, and British RE) 1333 and RE) 1343 lead azide which is precipitated in the presence of carboxymethyl cellulose (88—92). [Pg.10]

D. E. Seeger, and R. H. Stresau, "Lead Azide Precipitated with Polyvlayl Alcohol," ia 2nd ONR Symposium on Detonation, Office of Naval Research, Washiagton, D.C., 1955, p. 92. [Pg.27]

Lead azide, Pb(N3)2, is used as a detonator in car airbags. The impact of a collision causes PMN to be converted into an enormous amount of gas that fills the airbag. A125°C, a saturated solution of lead azide is prepared by dissolving 25 mg in water to make 100.0 mL of solution. What is Kv for lead azide ... [Pg.446]

Not detonated by 0.35g of Lead Azide and 0.2g of Tetryl, or by 0.5g of Mercury Fulminate 6 minutes Good... [Pg.487]

In general terms, PETN can be characterized as a sensitive , brisant, and powerful high expl. Explosive sensitivity is a rather nebulous quantity, but there can be no doubt that PETN is a much more sensitive material than TNT, but rather less sensitive than Lead Azide. In particular, PETN requires very little priming i charge (less than 1 mg LA) to initiate its detonation. This is the characteristic that makes PETN so widely used in blasting cap base charges, in detonating cord and in boosters... [Pg.571]

Mechanical treatment alone may be sufficient to induce significant decomposition such processes are termed mechanochemical or tribo-chemical reactions and the topic has been reviewed [385,386]. In some brittle crystalline solids, for example sodium and lead azides [387], fracture can result in some chemical change of the substance. An extreme case of such behaviour is detonation by impact [232,388]. Fox [389] has provided evidence of a fracture initiation mechanism in the explosions of lead and thallium azide crystals, rather than the participation of a liquid or gas phase intermediate. The processes occurring in solids during the action of powerful shock waves have been reviewed by Dremin and Breusov [390]. [Pg.35]

The increase in volume as gaseous products are formed in a chemical reaction is even larger if several gas molecules are produced from each reactant molecule, such as the formation of CO and CO, from a solid fuel (Fig. 4.17). Lead azide, Pb(N3)2, which is used as a detonator for explosives, suddenly releases a large volume of nitrogen gas when it is struck ... [Pg.276]

Lead azide, Pb(N,)2, is used as a detonator, i i) What volume of nitrogen at STP (1 atm, 0°Ci does 1.5, of It id azide produce when it decomposes into lead metal and nitrogen gas (b) Would 1.5 g of mercury(ll) azide, Hg(N which is also used as a detonator, produce a larger or smallei volume, given that its decomposition products i c elemental mercury and nitrogen gas (c) Metal azides in general are potent explosives. Why ... [Pg.771]

Mass effects due to some ions in salts. It is generally observed that there is a greater instability amongst compounds containing heavy atoms compared with elements in the first periods of the periodic tabie.This can be observed by analysing enthalpies of formation of ammonia, phosphine, arsine and stibine (see previous table for the last three). In the same way, it is easier to handle sodium azide than lead azide, which is a primary explosive for detonators. It is exactly the same with the relatively highly stable zinc and cadmium thiocyanates and the much less stable mercury thiocyanate. [Pg.99]

Lead azide is manufactured by reaction of sodium azide with either lead nitrate or lead acetate. It is a white crystalline solid, insoluble in cold water and stable on storage. It is very sensitive to friction and impact and has a velocity of detonation, when pressed to a density of 3-8, of4500 ms 1. [Pg.96]

Two crystallographic forms of lead azide are important, the ordinary alpha form which is orthorhombic and the beta form which is monoclinic. The densities of these forms are 4-71 and 4-93 respectively. It was for many years believed that the beta form is the more sensitive to friction and impact and accounted for detonations which have occurred in the manufacture and handling of the substance. It is now known that the beta form is in fact no more sensitive than the alpha. Even the alpha form, when present as large crystals, is very sensitive and conditions can arise (particularly when the formation of the lead azide is controlled by diffusion effects) where spontaneous detonation occurs. Although with modern knowledge these hazards can be avoided, pure lead azide is nevertheless a dangerous compound and is now made only for military purposes. [Pg.96]

Many other methods of making lead azide in a safe form have been described, but the only one to have found commercial importance consists of replacing the dextrine by a small proportion of gelatine. When properly made this form of lead azide is as safe to handle as the dextrinated form and has improved sensitiveness to flame. It can therefore be used by itself in electric and delay detonators, but not in plain detonators as it is not ignited with certainty by safety fuse. [Pg.97]

Lead styphnate is a poor initiating explosive which when dry is very sensitive to friction and impact, to electrostatic discharge, and to flame. Its main use is as an additive to lead azide to improve flame sensitiveness (see p. 101). When pressed to a density of 2-6 g ml-1 it has a velocity of detonation of4900 m s l. [Pg.97]

The original initiating explosive used by Nobel and all manufacturers for many years was mercury fulminate. This had the disadvantage of decomposing slowly in hot climates, particularly under moist conditions. For this reason mercury fulminate is no longer widely used. In most countries it has been replaced by a mixture of dextrinated lead azide and lead styphnate. In the U.S.A. some detonators are made containing diazodinitrophenol. [Pg.101]

The introduction of lead azide led to a difficulty in the choice of metal for the detonator tube. Under moist conditions, lead azide and copper can react to form cuprous azide on the inner wall of the tube and thus in a particularly dangerous position. Therefore with plain detonators, which cannot be sealed, copper cannot be used when lead azide is employed. Such detonators are usually made from aluminium tubes, or occasionally zinc. [Pg.101]

The initiating explosive used must ignite with certainty from the spit of a safety fuse. It must be remembered that the intensity of the spit can be reduced if the safety fuse is not cut squarely and also that the fuse may in practice not always be fully inserted into the detonator. Lead azide by itself is not sufficiently easily ignited to give a satisfactory plain detonator and it is therefore used in admixture with lead styphnate, which is very readily ignited by flame. The proportions of such mixtures vary from 25 to 50% of lead styphnate. Mercury fulminate and diazodinitrophenol are sufficiently sensitive to flame not to require such additives. [Pg.101]

Although the requirement for flame sensitiveness is the main consideration for initiating explosives for plain detonators, others are important in manufacture. The explosive must be capable of compression into a coherent mass and at the same time leave the equipment free from adhesions. Lead azide can be somewhat deficient in cohesion, and to improve this a small proportion of tetryl is sometimes added to the... [Pg.101]

The normal initiating charge in a British detonator is lead azide modified with gelatine. In the case of plain detonators a small proportion of lead styphnate is added to the azide to ensure satisfactory ignition from safety fuse. [Pg.104]


See other pages where Lead azide, detonation is mentioned: [Pg.41]    [Pg.172]    [Pg.421]    [Pg.41]    [Pg.430]    [Pg.72]    [Pg.41]    [Pg.172]    [Pg.421]    [Pg.41]    [Pg.430]    [Pg.72]    [Pg.10]    [Pg.10]    [Pg.70]    [Pg.266]    [Pg.556]    [Pg.144]    [Pg.146]    [Pg.417]    [Pg.597]    [Pg.1002]    [Pg.232]    [Pg.97]   
See also in sourсe #XX -- [ Pg.336 ]




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