US1906394A - Explosive - Google Patents
Explosive Download PDFInfo
- Publication number
- US1906394A US1906394A US635049A US63504932A US1906394A US 1906394 A US1906394 A US 1906394A US 635049 A US635049 A US 635049A US 63504932 A US63504932 A US 63504932A US 1906394 A US1906394 A US 1906394A
- Authority
- US
- United States
- Prior art keywords
- lead
- dinitrophenylazide
- mixture
- priming
- percent
- 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
Links
- 239000002360 explosive Substances 0.000 title description 5
- 239000000203 mixture Substances 0.000 description 21
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 20
- MTNOSUYWLTXJGO-UHFFFAOYSA-N 1-azido-2,3-dinitrobenzene Chemical class [O-][N+](=O)C1=CC=CC(N=[N+]=[N-])=C1[N+]([O-])=O MTNOSUYWLTXJGO-UHFFFAOYSA-N 0.000 description 16
- 230000037452 priming Effects 0.000 description 15
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 6
- MHWLNQBTOIYJJP-UHFFFAOYSA-N mercury difulminate Chemical compound [O-][N+]#C[Hg]C#[N+][O-] MHWLNQBTOIYJJP-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- IXHMHWIBCIYOAZ-UHFFFAOYSA-N styphnic acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1[N+]([O-])=O IXHMHWIBCIYOAZ-UHFFFAOYSA-N 0.000 description 5
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- RLJMLMKIBZAXJO-UHFFFAOYSA-N lead nitrate Chemical compound [O-][N+](=O)O[Pb]O[N+]([O-])=O RLJMLMKIBZAXJO-UHFFFAOYSA-N 0.000 description 4
- IUKSYUOJRHDWRR-UHFFFAOYSA-N 2-diazonio-4,6-dinitrophenolate Chemical compound [O-]C1=C([N+]#N)C=C([N+]([O-])=O)C=C1[N+]([O-])=O IUKSYUOJRHDWRR-UHFFFAOYSA-N 0.000 description 3
- 229910021346 calcium silicide Inorganic materials 0.000 description 3
- 239000005337 ground glass Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical compound [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 description 3
- QJGDGUBLGKFNDB-UHFFFAOYSA-N 1-azido-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1N=[N+]=[N-] QJGDGUBLGKFNDB-UHFFFAOYSA-N 0.000 description 2
- 244000215068 Acacia senegal Species 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920000084 Gum arabic Polymers 0.000 description 2
- 235000010489 acacia gum Nutrition 0.000 description 2
- 239000000205 acacia gum Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- KYYIDSXMWOZKMP-UHFFFAOYSA-N O-desmethylvenlafaxine Chemical compound C1CCCCC1(O)C(CN(C)C)C1=CC=C(O)C=C1 KYYIDSXMWOZKMP-UHFFFAOYSA-N 0.000 description 1
- 241000287181 Sturnus vulgaris Species 0.000 description 1
- OMBQIOZTGRITMM-UHFFFAOYSA-N [N+](=O)([O-])C=1C(=C(C=CC1)N=[N+]=[N-])[N+](=O)[O-].[Na] Chemical compound [N+](=O)([O-])C=1C(=C(C=CC1)N=[N+]=[N-])[N+](=O)[O-].[Na] OMBQIOZTGRITMM-UHFFFAOYSA-N 0.000 description 1
- 238000005267 amalgamation Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- -1 diazodin'itrophenol Chemical compound 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B41/00—Compositions containing a nitrated metallo-organic compound
- C06B41/02—Compositions containing a nitrated metallo-organic compound the compound containing lead
Definitions
- This invention relates to explosives and more particularly to the use of salts of dinitrophenylazide in the manufacture of priming mixtures "for small arms ammunition,
- This-material may be manufactured in various waysbut I prefer to prepare it by reaction between diazodinitrophenol, sodium azide and lead nitrate.
- the diazodinitrophenol is first dissolved in a'suitable solvent, such as acetone and an aqueous solution of sodium azide added thereto to form sodium dinitrophenylazide.
- aqueous solution of lead nitrate is then added and lead dinitrophenylazide precipitated from the solution.
- The'metal salts of dinitrophenylazide possess desirable properties for use as the initiator of priming compositions.
- mercury fulminate may be eliminated and a non-mercuric priming mixture provided.
- the sensitivity of lead dinitrophenylazide topercussion and friction is approximately the same as that of mer cury fulminate.
- smaller percentages of lead dinitrophenylazide maybe employed with substantially the same results ⁇ that are obtained from the use of mercury fulminate, due to its lower density and eater ability for'flame propagation. Its
- cartridges maybe formed by mixing the fol lowing ingredients in substantially the following PlOPOItlQDS;
- Per cent Lead dinitrophenylazide 15 Barium nitrate 30 Lead peroxide 25 Antimony sulphide 18 Calcium silicide 6 Trinitroresorcinol 6 cc Proportions of these ingredients may; of course, be varied depending upon the commercial strength of the ingredients and to I Per cent Lead dinitrophenylazide 15 Barium nitrate 25 Lead peroxide 12 Diazodin'itrophenol l7 rinitroresorcinol .8 Ground -glass u 2 Gum arabic 1 As in the case of center fire mixtures, the proportions of the ingredients may be varied depending upon the properties desired in the individual case and the commercial strength of the ingredients.
- the rim fire mixture is prepared in the usual way, poured into individual pellets of the proper size for the individual charges by means of a charge plate in the usual manner and then transferred to empty rim fire cartridge shells.
- the prim- 1 ing mixture is then forced to distribute itself into the hollow rim of the cartridge shell by spinning the'shell in the customary machine.
- the shells are then loaded with powder and bullets in the customary way.
- the material may also be used in the manufacture of detonators and in high explosive shells. When so used it is used in place of the known and heretofore employed materials having similar properties.
- oxygen supplying elements and fuels mentioned above are referred to by Way of example. Known equivalents may be substituted for any or all of them without departing'from the spirit of the invention.
- lead nitrate may be employed in place of barium nitrate, the quantity of lead nitrate to be employed varying slightly from the quantity of barium nitrate given above to obtain substantially the same qualities in the resulting mixture.
- a priming mixture comprising lead dinitrophenylazide.
- a priming mixture comprising lead (li nitrophenylazide and an oxidizer.
- a priming mixture comprising lead dinitrophenylazide, an oxidizer and a fuel.
- a priming mixture comprising lead dinitrophenylazide and trinitroresorclnol.
- a priming mixture comprising lead dinitrophenylazide, barium nitrate and a fuel.
- a priming mixture comprising lead dinitrophenylazide, barium nitrate, lead peroxide and a fuel.
- a priming mixture comprising lead dinitrophenylazide, barium nitrate, lead peroxide, antimony sulphide, calcium silicide and trinitroresorcinol.
- a priming mixture comprising lead nitrophenylazide, barium nitrate, lead peroxide, diazodin'itrophenol, trinitroresorcinol and ground glass.
- a priming mixture comprising substantially 15 percent lead 'dinitrophenylazide, substantially 30 percent barium nitrate, substantially 25 percent lead peroxide, substantially 18 percent antimony sulphide, substantially 6 percent calcium silicide, and substantially 6 percent trinitroresorcinol;
- a priming mixture comprising sub stantially 15 percent lead dinitrophenylazide, substantially 25 percent barium nitrate, substantially 12 percent lead peroxide,-substantlally 17 percent diazodinitrophenol, substan-
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Description
Patented May 2, llfi stares Parana? onion JO$EPE D MCNUTT, OF NEW VEN, CONNECTICUT, ASSIONOR TO WINCHESTER RE- PEA'IDIGr MEWS COHPANY, OF NEW HAVEN, CONNECTICUT, A CORPORATION OF W ZLQA "m EXPLOSIVE lilo Brawing.
This invention relates to explosives and more particularly to the use of salts of dinitrophenylazide in the manufacture of priming mixtures "for small arms ammunition,
5 in commercial detonators, in high explosive shells and the like.
The material which I have found'particu; larly useful for thesepurposes is the normal lead salt of dinitrophenylazide having the m empirical formula Pb C 0 N and whose structural formula may be illustrated by the -following:
o Pb
N .N i 1 o N om N a a t INC: N0:
* This-material may be manufactured in various waysbut I prefer to prepare it by reaction between diazodinitrophenol, sodium azide and lead nitrate.
The diazodinitrophenol is first dissolved in a'suitable solvent, such as acetone and an aqueous solution of sodium azide added thereto to form sodium dinitrophenylazide. An
aqueous solution of lead nitrate is then added and lead dinitrophenylazide precipitated from the solution.
The'metal salts of dinitrophenylazide possess desirable properties for use as the initiator of priming compositions. By employing this material, mercury fulminate may be eliminated and a non-mercuric priming mixture provided. The sensitivity of lead dinitrophenylazide topercussion and friction is approximately the same as that of mer cury fulminate. However, smaller percentages of lead dinitrophenylazide maybe employed with substantially the same results \that are obtained from the use of mercury fulminate, due to its lower density and eater ability for'flame propagation. Its
risance when explodedis between that of mercury fulminate and lead azide. It possesses' great chemical stability and is compatible with most of the common ingred ents 0 'ofgrimingmixtures. 5
suitable pr mixture for c enterjfire meet the requirements of various uses of the mixture.
- The ingredients are first thoroughly and J homogeneously mixed and then poured into U Application filed September 27, 1932. Serial No. 635,049.
cartridges maybe formed by mixing the fol lowing ingredients in substantially the following PlOPOItlQDS;
Per cent Lead dinitrophenylazide 15 Barium nitrate 30 Lead peroxide 25 Antimony sulphide 18 Calcium silicide 6 Trinitroresorcinol 6 cc Proportions of these ingredients may; of course, be varied depending upon the commercial strength of the ingredients and to I Per cent Lead dinitrophenylazide 15 Barium nitrate 25 Lead peroxide 12 Diazodin'itrophenol l7 rinitroresorcinol .8 Ground -glass u 2 Gum arabic 1 As in the case of center fire mixtures, the proportions of the ingredients may be varied depending upon the properties desired in the individual case and the commercial strength of the ingredients. The rim fire mixture is prepared in the usual way, poured into individual pellets of the proper size for the individual charges by means of a charge plate in the usual manner and then transferred to empty rim fire cartridge shells. The prim- 1 ing mixture is then forced to distribute itself into the hollow rim of the cartridge shell by spinning the'shell in the customary machine. The shells are then loaded with powder and bullets in the customary way.
As stated above, the material may also be used in the manufacture of detonators and in high explosive shells. When so used it is used in place of the known and heretofore employed materials having similar properties.
The advantages of the non-mercuric priming mixtures set forth above over priming mixtures containing mercury fulminate, will be apparent to those skilled in the art. The elimination, of mercury fulminate and the resulting amalgamation of the cartridge shell permits reloading and reuse of center fire cartridge cases.
The oxygen supplying elements and fuels mentioned above are referred to by Way of example. Known equivalents may be substituted for any or all of them without departing'from the spirit of the invention. As an example, lead nitrate may be employed in place of barium nitrate, the quantity of lead nitrate to be employed varying slightly from the quantity of barium nitrate given above to obtain substantially the same qualities in the resulting mixture.
I claim: 1. A priming mixture comprising lead dinitrophenylazide.
eoaeea V tially 8 per cent trinitroresorcinol, substantially 22 per cent ground glass and substantially 1 per cent gum arabic.
In testimony whereof aflixmy signature.
JOSEPH 1D. MCNUTT.
2. A priming mixture comprising lead (li nitrophenylazide and an oxidizer.
3. A priming mixture comprising lead dinitrophenylazide, an oxidizer and a fuel.
4. A priming mixture comprising lead dinitrophenylazide and trinitroresorclnol.
5. A priming mixture comprising lead dinitrophenylazide, barium nitrate and a fuel.
. 6. A priming mixture comprising lead dinitrophenylazide, barium nitrate, lead peroxide and a fuel.
7. A priming mixture comprising lead dinitrophenylazide, barium nitrate, lead peroxide, antimony sulphide, calcium silicide and trinitroresorcinol.
8. A priming mixture comprising lead nitrophenylazide, barium nitrate, lead peroxide, diazodin'itrophenol, trinitroresorcinol and ground glass.
9. A priming mixture comprising substantially 15 percent lead 'dinitrophenylazide, substantially 30 percent barium nitrate, substantially 25 percent lead peroxide, substantially 18 percent antimony sulphide, substantially 6 percent calcium silicide, and substantially 6 percent trinitroresorcinol;
10. A priming mixture comprising sub stantially 15 percent lead dinitrophenylazide, substantially 25 percent barium nitrate, substantially 12 percent lead peroxide,-substantlally 17 percent diazodinitrophenol, substan-
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US635049A US1906394A (en) | 1932-09-27 | 1932-09-27 | Explosive |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US635049A US1906394A (en) | 1932-09-27 | 1932-09-27 | Explosive |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1906394A true US1906394A (en) | 1933-05-02 |
Family
ID=24546225
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US635049A Expired - Lifetime US1906394A (en) | 1932-09-27 | 1932-09-27 | Explosive |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1906394A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0704415A1 (en) * | 1994-08-27 | 1996-04-03 | Eley Limited | Primer composition |
-
1932
- 1932-09-27 US US635049A patent/US1906394A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0704415A1 (en) * | 1994-08-27 | 1996-04-03 | Eley Limited | Primer composition |
| US5538569A (en) * | 1994-08-27 | 1996-07-23 | Eley Limited | Primer compositions containing dinitrobenzofuroxan compounds |
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