US1054411A - Detonating cap. - Google Patents
Detonating cap. Download PDFInfo
- 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
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- 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
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- 239000002360 explosive Substances 0.000 description 14
- 239000002253 acid Substances 0.000 description 6
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 6
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 235000010288 sodium nitrite Nutrition 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LJCZNYWLQZZIOS-UHFFFAOYSA-N 2,2,2-trichlorethoxycarbonyl chloride Chemical compound ClC(=O)OCC(Cl)(Cl)Cl LJCZNYWLQZZIOS-UHFFFAOYSA-N 0.000 description 1
- SPSSULHKWOKEEL-UHFFFAOYSA-N 2,4,6-trinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O SPSSULHKWOKEEL-UHFFFAOYSA-N 0.000 description 1
- 101100460704 Aspergillus sp. (strain MF297-2) notI gene Proteins 0.000 description 1
- 241000570863 Brunfelsia uniflora Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241000905957 Channa melasoma Species 0.000 description 1
- 101100284008 Dictyostelium discoideum comH gene Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 241001245789 Goodea atripinnis Species 0.000 description 1
- 206010021703 Indifference Diseases 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- 241000986339 Percis Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000002817 coal dust Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 210000004013 groin Anatomy 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- 238000009527 percussion Methods 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F42—AMMUNITION; BLASTING
- F42B—EXPLOSIVE CHARGES, e.g. FOR BLASTING, FIREWORKS, AMMUNITION
- F42B3/00—Blasting cartridges, i.e. case and explosive
- F42B3/10—Initiators 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.
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- 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.
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) |
-
1912
- 1912-09-10 US US71956212A patent/US1054411A/en not_active Expired - Lifetime
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