2013
DOI: 10.1007/978-3-642-28436-6
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Primary Explosives

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Cited by 164 publications
(90 citation statements)
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“…For example, the sensitivity of MF is mostly reported as being from 0.4 J to 1.2 J [3]; we obtained 0.62 J. PETN is mostly reported as being between 3 J and 4.1 J [3]; 50% probability of initiation determined in the present study was 3.93 J. …”
Section: Sensitivity Of Tnadazt and Agtnadazt To Impactsupporting
confidence: 54%
See 1 more Smart Citation
“…For example, the sensitivity of MF is mostly reported as being from 0.4 J to 1.2 J [3]; we obtained 0.62 J. PETN is mostly reported as being between 3 J and 4.1 J [3]; 50% probability of initiation determined in the present study was 3.93 J. …”
Section: Sensitivity Of Tnadazt and Agtnadazt To Impactsupporting
confidence: 54%
“…The results of the electric spark sensitivity tests are presented in Table 4. TNADAzT is significantly less sensitive to electric discharge than PETN and RDX; the sensitivity of its silver salt is lower than that of MF and comparable with that of lead azide [3]. …”
Section: Sensitivity To Electric Dischargementioning
confidence: 87%
“…It is commonly agreed that the highly toxic mercury fulminate (1), adopted for use in some of the first percussion primer formulations in the early 1800s [6] and later by Alfred Nobel for some of the first blasting caps in 1867 [7], is the first primary explosive to see practical application. The high costs associated with mercury, the high sensitivity of mercury fulminate, and its ability to lose performance under high loading pressures paved the way for lead azide (2) to replace the compound starting in the early 1900s [8]. Today, lead azide (including its less sensitive dextrin-coated form) finds wide-ranging application in energetic materials as the main primary explosive ingredient in blasting caps and detonators.…”
Section: Legacy Primary Explosivesmentioning
confidence: 99%
“…Treatment of picric acid (7) with a controlled simultaneous addition of aqueous sodium sulfide yields sodium picramate (8), which is then converted to DDNP via the Griess diazotization. DDNP has found explosive use since the early 20th century [1].…”
Section: -Diazo-46-dinitrophenol (Ddnp)mentioning
confidence: 99%
“…N-heterocycles with sulfhydryl ligands are capable of -N(H)-C(=S) $ -N=C(-SH) tautomerization. Heterocyclic nitrogen can participate in coordination, while the sulfhydryl moiety can be used as a bridging group [8][9][10][11][12][13][14]. The soft sulfhydryl group has good coordination ability, because it has empty 3d orbital that can accept electrons from the metal [8,[14][15][16].…”
Section: Introductionmentioning
confidence: 99%