US1054411A - Detonating cap. - Google Patents

Detonating cap. Download PDF

Info

Publication number
US1054411A
US1054411A US71956212A US1912719562A US1054411A US 1054411 A US1054411 A US 1054411A US 71956212 A US71956212 A US 71956212A US 1912719562 A US1912719562 A US 1912719562A US 1054411 A US1054411 A US 1054411A
Authority
US
United States
Prior art keywords
acid
explosives
detonating
detonating cap
shell
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US71956212A
Inventor
Edmund Herz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US71956212A priority Critical patent/US1054411A/en
Application granted granted Critical
Publication of US1054411A publication Critical patent/US1054411A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F42AMMUNITION; BLASTING
    • F42BEXPLOSIVE CHARGES, e.g. FOR BLASTING, FIREWORKS, AMMUNITION
    • F42B3/00Blasting cartridges, i.e. case and explosive
    • F42B3/10Initiators therefor

Definitions

  • This invention relate. to a novel detonating cap containingan explosive which is designed to replaoe'tho t'ulniinatiiu;v .mercury hitherto generally employed t'or this purpose.
  • lfuhninating mercury has the disadvantage that it is extremely poisonous and that its manufacture is oangerous and complicated, thus ehtailingf a couiparatively high cost of production.
  • the detonati. -pld sives, such as aromatic dia'lo conipminds which, have been suggested for replacing' the ulniinating mercury are not reliable and Jfail frequently to oli other explosives, due to a relatively sinall amount. of oxygen.
  • diazo comH pounds of perchloriu acid are used as det.- onating explosives more particularly for the reason thatl tney contain a large per4 centage of oxygen.
  • diazoporcl'iloratcs of the simple, as well as of the aromatio l1ydrocarbons constitute extremely powerful and rcliable (tetonating-l explosives, which' inezizponsiie may be nianutzu'tured without danger, and are fire damp prooi".
  • the diazoperchlorates surpass other diano salts not only in explosive power and briskness, but thoy are of superior stability and sensitiveness to mechanical influences. ln
  • diazoperchlorates are scantily soluble 1n pure water
  • the diezo compound thus formed is precipitated as i tine powder, thus simplifying the manutan-iure thereof.
  • the diazoperohlorates are not hygroscopic, so that they possess a superior staoi'lity a. iinst humidity and-'may be exposed to air saturated with aqueous vapors without becoming decomposed and without an impairment of their explosive qualities.
  • the indifference ot these salts afiaiiisty water ⁇ etc., is still increased by the presence ot' halogens, negative groups such as Clit), lUOl-li, or thi.l nitro group NO2.
  • This latter group is more particularly adapted t'or thisl purpose, on account ot its high percentage oi oxygen. so thatthe eX- plosive power of the Haal-product is correspondingly increased.
  • - is to the uunibe of nitro groups which may be added to tht; salt ⁇ r it may be stated that no more than two j; 'oups should be introduced, while the inavinnun ell'oct attained by adding butl a sii Asgroup.
  • the following salts may be produced in analogous manner: diazotoluolperchlorato. diazoxylolperchloyrate, diazonaphthaleneperohloratc, diazoanthraceneperchlorate. nitrodiazotoluolper# consequently best vacid solution. Ylhus for instance Jr'roni nitropnrepheng-'lenet inniin, there' may be obtained nitrobisdiezobenzolperchlorate under the condition, that nitrous acid is innintained in excess, as otherwise-triominoozoor aziinido compounds would be formed.
  • a charge of picric acid contained in a cartridge may be fully eriplodedA by 0.015 to 0.02 frrani of nitrodinZobenzolperchlorute.
  • nitrodinZobenzolperchlorute For exploding kel-dynamite, gelatin dynamite, clieddite, picric acid and trinitro toluol, 0.02 to 0.05 grain of nitrodiazobenzolperchlorate is .sulicient and eren the leest.
  • sensitive annnoniuin nitrate explosives may be set olin by O l to 9.3 grano of said perchlorate.
  • the diazoperchlorates are used either alone ond erefiled into a. shell No. 2 or 3, or they are combined with some other brisk explosive. So' for instance, l gram picric acid is filled into shell No 8 and then say about 0.02 groin of nitrodiezobenzolperchlorete is pressed into said shell. Care should however be teken to avoid a direct; contact between these tiro explosives,
  • the separation of the explosives tray be effected by4 interposingtherebetweena. sheet of tin foil, copper, etc. It is further advisable thatfthe entire charge of the shell be closed by tin foil or by a perforated sheet of copper, which besides confining' the charge, prevents any dangerous friction during the insertion of the fuse. lf desired, the shells may finally be var nislied in order to render them perfectly tight.
  • the numerell indicates the shell into which is pressed n chargeA 2 of say picric acid, and u superposed charge Bof say nitrodinzobenzolperchlorate. These charges are separated from each other by a sheet of tin toil 4, while a copper cap 5 connes them within shell l, said cup being perforated as et 6 for the introduction-oi" the fuse.
  • detonating cap for explosives composed of n shell containing :i diazoperchlorate of -eneromatic hydrocarbon.
  • Q. A detonating cap for explosives, coinposed of a shell containing a diazoperchl'orate of n nitreted aromatic hydrocarbon.

Landscapes

  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Air Bags (AREA)

Description

E. HERZ.
DETONATING GAP.
APLwATIoN FILED SEPT. 1o, 1912.
atmted Feb. 25, 97.3
vplosifon.'
EBMUND HERZ, OF VIENNA, AUS'RIA-BSUNGRY.
DETONATING CAP.
.Specification of Letters Patent.
Application filed September l0, 1912. Serial No. 719,562.
To aU whom 1i 'muy concern Be, 1t. lfnoivn that l, EDML'ND Hmz, a citi# zen of Austria. resi/dino at Vienna. Austriany Hungary, have invented a new and lin proved Detonatiug tap7 ot' which the fol lowing is a specification.
This invention relate. to a novel detonating cap containingan explosive which is designed to replaoe'tho t'ulniinatiiu;v .mercury hitherto generally employed t'or this purpose.
lfuhninating mercury has the disadvantage that it is extremely poisonous and that its manufacture is oangerous and complicated, thus ehtailingf a couiparatively high cost of production. The detonati. -pld sives, such as aromatic dia'lo conipminds which, have been suggested for replacing' the ulniinating mercury are not reliable and Jfail frequently to oli other explosives, due to a relatively sinall amount. of oxygen. so that the carbon present in 'those conipounds was insulieiently oxidized thus resulting-iii a rather lon' tcnnlieinture ot exil reliable and e lectivo detonatoi' must not only cause a violent detonating` shock, but should develop sutiicient heat to bring the explosive to beset oil lo the necessary highv temperati'u'c at its point of Contact.
`ocordinfr to niy invention. diazo comH pounds of perchloriu acid are used as det.- onating explosives more particularly for the reason thatl tney contain a large per4 centage of oxygen. 'The diazoporcl'iloratcs of the simple, as well as of the aromatio l1ydrocarbons constitute extremely powerful and rcliable (tetonating-l explosives, which' inezizponsiie may be nianutzu'tured without danger, and are lire damp prooi".
The diazoperchlorates surpass other diano salts not only in explosive power and briskness, but thoy are of superior stability and sensitiveness to mechanical influences. ln
oontradistinotion tothe diazochlorids,'diazosulfates and diazonitrates the, diazoperchlorates are scantily soluble 1n pure water, and
lare almost insoluble in water containingr erclilorio acid, thus showing a close resemM glance to the slight-ly soluble potassium perchloratcs. -This t'actl is ot considerable importance for the manu'tzu'ture ot' the iazoperohloratcs, for the reason that it a solution of an aromatic amin in perchlorio acid'in excess is mixed with sodium nitrite,
the diezo compound thus formed is precipitated as i tine powder, thus simplifying the manutan-iure thereof. -ln connection with their scant solubility, the diazoperohlorates are not hygroscopic, so that they possess a superior staoi'lity a. iinst humidity and-'may be exposed to air saturated with aqueous vapors without becoming decomposed and without an impairment of their explosive qualities. The indifference ot these salts afiaiiisty water` etc., is still increased by the presence ot' halogens, negative groups such as Clit), lUOl-li, or thi.l nitro group NO2. This latter group is more particularly adapted t'or thisl purpose, on account ot its high percentage oi oxygen. so thatthe eX- plosive power of the Haal-product is correspondingly increased. -is to the uunibe of nitro groups which may be added to tht; salt`r it may be stated that no more than two j; 'oups should be introduced, while the inavinnun ell'oct attained by adding butl a sii Asgroup. s furthermore the br ,JlinesxI of coinposiion of the diamiperehlorates is uit a high order, while thc formation ot llames i'niniuuun, percussion caps lilled with these salts arc notI liable to ignite tire damp or any whirling coal dust'.
lhe most. stable and brisk salt of perchloric acid which is adapted for filling perci..ion Caps, is the inononitratcdbcnxolcompound. lnnianufacturingl this salt.y puro crystallized nitraniliu (the motaooinpound beingy preferable) is dissolved in diluted peroliloric acid of the specific gravity of 1.19, the acid being' hon'- evcr employed to such an excess that attcr the completion ol" the reaction`v troc acid is still present'. 'lo the solution thus obtained. there isi-added sodium nitrite in such a quantity as is necessary for diaf/,otizinxe` the sodium nitrite being used either in solid forni or in highly concentrated solution. Although the. heat yfreed during' this roaction is but small. it is advisable to provide somel cooling means, inore Imrticularly ,when Working" in large quantities. The nitrodiazobenrcolperchlorate thus formed is `inimediately precipitated as a fino crystallized powder, which after settling, may be readily separated from the liquid to be then 'repeatedly Washed with highly diluted perchloric acid, alcohol and ether. The following salts may be produced in analogous manner: diazotoluolperchlorato. diazoxylolperchloyrate, diazonaphthaleneperohloratc, diazoanthraceneperchlorate. nitrodiazotoluolper# consequently best vacid solution. Ylhus for instance Jr'roni nitropnrepheng-'lenet inniin, there' may be obtained nitrobisdiezobenzolperchlorate under the condition, that nitrous acid is innintained in excess, as otherwise-triominoozoor aziinido compounds would be formed.
The igniting capacity of the above de-` scribed compounds is considerable find superior to that o" fulininuting mercury sind other detonating explosives. Thus, for instance, a charge of picric acid contained in a cartridge may be fully eriplodedA by 0.015 to 0.02 frrani of nitrodinZobenzolperchlorute. For exploding fuhr-dynamite, gelatin dynamite, clieddite, picric acid and trinitro toluol, 0.02 to 0.05 grain of nitrodiazobenzolperchlorate is .sulicient and eren the leest.
sensitive annnoniuin nitrate explosives may be set olin by O l to 9.3 grano of said perchlorate.
lfn practice, the diazoperchlorates are used either alone ond erefiled into a. shell No. 2 or 3, or they are combined with some other brisk explosive. So' for instance, l gram picric acid is filled into shell No 8 and then say about 0.02 groin of nitrodiezobenzolperchlorete is pressed into said shell. Care should however be teken to avoid a direct; contact between these tiro explosives,
so' that they will not actupon each other upon decompositionA The separation of the explosives tray be effected by4 interposingtherebetweena. sheet of tin foil, copper, etc. It is further advisable thatfthe entire charge of the shell be closed by tin foil or by a perforated sheet of copper, which besides confining' the charge, prevents any dangerous friction during the insertion of the fuse. lf desired, the shells may finally be var nislied in order to render them perfectly tight.
l detonating cap of the character' above f 'lescrihed4 is illustrated in longitudinal section in the accompanying drawing.
The numerell indicates the shell into which is pressed n chargeA 2 of say picric acid, and u superposed charge Bof say nitrodinzobenzolperchlorate. These charges are separated from each other by a sheet of tin toil 4, while a copper cap 5 connes them within shell l, said cup being perforated as et 6 for the introduction-oi" the fuse.
For the purpose of this invention.- the homologues or substitute products of the diazoperclilorates of the aromatic hydrocarbons are equivalents of the latter.
claim:
l. e, detonating cap for explosives, composed of n shell containing :i diazoperchlorate of -eneromatic hydrocarbon. Q. A detonating cap for explosives, coinposed of a shell containing a diazoperchl'orate of n nitreted aromatic hydrocarbon.
. EDMUND HERZ.
vVJitnesses t AUGUST Focene, ADA MARIA BERGER.
US71956212A 1912-09-10 1912-09-10 Detonating cap. Expired - Lifetime US1054411A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US71956212A US1054411A (en) 1912-09-10 1912-09-10 Detonating cap.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US71956212A US1054411A (en) 1912-09-10 1912-09-10 Detonating cap.

Publications (1)

Publication Number Publication Date
US1054411A true US1054411A (en) 1913-02-25

Family

ID=3122671

Family Applications (1)

Application Number Title Priority Date Filing Date
US71956212A Expired - Lifetime US1054411A (en) 1912-09-10 1912-09-10 Detonating cap.

Country Status (1)

Country Link
US (1) US1054411A (en)

Similar Documents

Publication Publication Date Title
US2195965A (en) Gas producing cartridge
US2194480A (en) Noncorrosive priming composition
US2877709A (en) Cartridge
US1935495A (en) Slow match composition
US2420201A (en) Blasting cap
US3048103A (en) Blasting assembly
US2011578A (en) Explosive
US3184286A (en) Cs2b12h12*csno3 product and process for making same
US2525397A (en) Blasting initiator
US1797509A (en) Electric blasting cap and ignition material for the same
US4676164A (en) Sporting ammunition
US3132585A (en) Detonator having a priming sponge
US2475281A (en) Delay electric initiator
Bebie Manual of explosives military pyrotechnics and chemical warfare agents
RU2026276C1 (en) Gun-powder composition
US2422043A (en) Compound detonator
US1185830A (en) Detonator.
US2268372A (en) Ignition composition comprising pyro-lead salt-chlorate
US1350465A (en) Primer for small-arms ammunition
US2125221A (en) Blasting cap
Taylor et al. HMTD—A new detonating explosive
US2159229A (en) Manufacture of fuse heads for electrical firing
US2104513A (en) Blasting cap composition
US2908559A (en) Ignition mixtures and electric initiators
US904289A (en) Charge for detonator-casings.