US2970900A - Priming composition - Google Patents
Priming composition Download PDFInfo
- Publication number
- US2970900A US2970900A US101274A US10127449A US2970900A US 2970900 A US2970900 A US 2970900A US 101274 A US101274 A US 101274A US 10127449 A US10127449 A US 10127449A US 2970900 A US2970900 A US 2970900A
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- US
- United States
- Prior art keywords
- priming
- corrosive
- explosive
- red
- sensitivity
- 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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- 239000000203 mixture Substances 0.000 title claims description 46
- 230000037452 priming Effects 0.000 title claims description 35
- 239000002360 explosive Substances 0.000 claims description 33
- 230000009972 noncorrosive effect Effects 0.000 claims description 21
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 13
- 239000007800 oxidant agent Substances 0.000 claims description 11
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 9
- TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 claims description 9
- 239000000026 Pentaerythritol tetranitrate Substances 0.000 claims description 9
- 229960004321 pentaerithrityl tetranitrate Drugs 0.000 claims description 9
- 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 claims description 7
- 239000000015 trinitrotoluene Substances 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 6
- 230000035945 sensitivity Effects 0.000 description 14
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 13
- 239000004615 ingredient Substances 0.000 description 7
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 230000002411 adverse Effects 0.000 description 3
- WETZJIOEDGMBMA-UHFFFAOYSA-L lead styphnate Chemical compound [Pb+2].[O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C([O-])=C1[N+]([O-])=O WETZJIOEDGMBMA-UHFFFAOYSA-L 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- RLJMLMKIBZAXJO-UHFFFAOYSA-N lead nitrate Chemical compound [O-][N+](=O)O[Pb]O[N+]([O-])=O RLJMLMKIBZAXJO-UHFFFAOYSA-N 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- AGUIVNYEYSCPNI-UHFFFAOYSA-N N-methyl-N-picrylnitramine Chemical compound [O-][N+](=O)N(C)C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O AGUIVNYEYSCPNI-UHFFFAOYSA-N 0.000 description 1
- -1 Pentaerythritol tetranitrate Barium nitrate Chemical compound 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- YNJJRHZFIYPEEI-UHFFFAOYSA-N [N+](=O)([O-])[O-].[K+].[N+](=O)([O-])[O-].[Ba+2] Chemical compound [N+](=O)([O-])[O-].[K+].[N+](=O)([O-])[O-].[Ba+2] YNJJRHZFIYPEEI-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- MHWLNQBTOIYJJP-UHFFFAOYSA-N mercury difulminate Chemical compound [O-][N+]#C[Hg]C#[N+][O-] MHWLNQBTOIYJJP-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- C06B39/00—Compositions containing free phosphorus or a binary compound of phosphorus, except with oxygen
Definitions
- This invention relates generally to priming compositions and particularly to non-corrosive priming compositions foruse in small arms ammunition.
- non-corrosive primers heretofore disclosed it has been necessary to provide a highly sensitive primary explosive for initiating the priming mixture, as otherwise the sensitivity of the priming mixture was insufficient to be dependable.
- Red phosphorous has been suggested by numerous workers in the art as a material utilizable with non-corrosive ingredients and without the primary explosive initiator, but the priming compositions resulting from these suggestions have proven unsatisfactory either from the standpoint of sensitivity or from the standpoint of stability, to an extent such that they have not superceded non-corrosive priming mixtures containing the primary explosive ingredient despite the greater hazard involved in handling the latter.
- the object of the present invention is to provide a priming composition of the non-corrosive type, which is highly sensitive and satisfactorily stable, and which does not require the presence of a primary explosive.
- Another object of the invention is to improve the sensitivity of non-corrosive priming mixtures which do contain primary explosive ingredients, but whose sensitivity is lower than that of mercury fulminate, lead azide, and the like.
- a more specific object of the invention is to improve the stability and sensitivity of priming compositions containing red phosphorous.
- a non-corrosive priming composition having sensitivity, stability, and freedom-from-handling hazard on a parity with or better than potassium chlorate priming mixtures may be provided by the concurrent utilization of red phosphorus with a secondary explosive, such as pentaerythritol tetranitrate, trimethylenetrinitramine, and trinitrotoluene.
- red phosphorous pentaerythritol tetranitrate and trimethylenetrinitramine, in particular, and trinitrotoluene, to a lesser degree, do exhibit the property of radically increasing the sensitivity of the composition without adversely affecting its stability.
- the sensitivity of the red phosphorous-secondary-explosive-containing priming composition is not adversely affected as the size of the pellet increases. Consequently, the weight of the pellet of priming for any 2,970,900 Patented Feb. 7, 1961 2 given round of ammunition can be increased to insure ignition of the propellant and eliminate the possibility of dangerous squibs in small arms ammunition.
- the invention is characterized by the concurrent use of red phosphorous and one of the three secondary explosives, to-wit2 pentaerythritol tetranitrate, trimethylenetrinitramine, and trinitrotoluene, or mixtures thereof. While some other compounds having the characteristics of a secondary explosive may be utilized with red phosphorous to achieve an increased sensitivity, the three aforesaid are the only ones revealed by our investigation which exhibit the synergetic eifect of increased sensitivity without adversely alfecting stability. For example, trinitrophenylmethylnitramine, when incorporated with red; phosphorous in a non-corrosive priming composition, results in a composition which is relatively unstable.
- red phosphorous incorporated in the priming mixtures in accordance with the present invention, must itself be as stable as possible, within practical limits. Consequently, it is contemplated that, prior to incorporation with the other components, the ordinary red phosphorous of commerce may be purified and have its stability improved by any known method, such for example as that published in Industrial and Engineering Chemistry 40, 301 (1948), in which the phosphorous is first subjected to an acid treatment, an elutriation, and a coating with aluminum hydroxide.
- any of the Well known non-corrosive oxidizing agents such as barium nitrate, potassium nitrate, lead nitrate, lead dioxide, basic lead nitrate, and barium nitrate-potassium nitrate double salt, may be utilized.
- Priming compositions of the present invention may be compounded with or without primary explosive ingredients. Since one of the objectives of all endeavors in this branch of the explosives art is to reduce the hazards of manufacture, it is desirable to makeuse of the less sensitive members of the primary explosive family, for example, lead trinitro resorcinate. In priming co-mpositions which contain lead trinitro resorcinate as a primary explosive initiator, the sensitivity can be decidedly improved by the incorporation of the red phosphoroussecondary explosive sub-composition aforesaid.
- the several ingredients may be mixed and charged in the usual manner.
- Such coating may be accomplished by dissolving the secondary explosive in any suitable solvent, mixing the phosphorous with the solution to form a homogeneous paste, then precipitating the secondary explosive from the solvent, then separating the solvent liquor and drying the solid residue. If acetone is used as the solvent for the secondary explosive, precipitation of the latter may be accomplished by the addition of water.
- proportions of the several ingredients of the composition are preferably within the ranges indicated in the following table:
- the secondary explosive indicated in the foregoing table is one selected from the group consisting of pentaerythritol tetranitrate trimethylenetrinitramine, and trinitrotoluene.
- the oxidizer is preferably a non-corrosive one.
- composition containing primary explosive initiator whose sensitivity is improved in accordance with the present invention, the following formula is representative:
- compositions of this invention are preferably loaded in caps having a surface of a compatible metal such as aluminum, lead, or zinc, which will not promote decomposition of the mixtures particularly under hot and moist storage conditions. Such modifications or adjustments may be made in accordance with the custom in the art, and without departing from the spirit of the present invention or the scope of the appended claims.
- a priming mixture comprising substantial quantities of red phosphorus, a non-corrosive solid oxidizing agent therefor, and a secondary explosive selected from the group consisting of pentaerythritol tetranitrate, trimethylenetrinitramine, and trinitrotoluene, and mixtures thereof.
- the priming mixture of claim 1 which includes a primary explosive initiator.
- a non-corrosive priming mixture containing substantial quantities of red phosphorus, a solid oxidizing agent therefor, and pentaerythritol tetranitrate.
- a non-corrosive priming mixture containing substantial quantities of red phosphorus, a solid oxidizing agent therefor, and trimethylenetrinitramine.
- a non-corrosive priming mixture consisting essentially of:
- a non-corrosive priming mixture consisting essentially of:
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Fireproofing Substances (AREA)
Description
United States Patent PRIMING COMPOSITION William B. Woodring, Hamden, Conn., and Hiramie T. McAdams, ,Bethalto, Ill., assignors to Olin Mathieson Chemical Corporation, a corporation of Virginia N0 Drawing. Filed June 24, 1949, Ser. No. 101,274
8 Claims. (Cl. 52-4) This invention relates generally to priming compositions and particularly to non-corrosive priming compositions foruse in small arms ammunition.
Because of the corrosive effect of potassium chlorate, numerous efforts have been addressed toward the problem of finding a priming composition as sensitive and as stable, yet as free of manufacturing hazards, as was the potassium chlorate priming of old.
In the non-corrosive primers heretofore disclosed, it has been necessary to provide a highly sensitive primary explosive for initiating the priming mixture, as otherwise the sensitivity of the priming mixture was insufficient to be dependable. In some instances, it has been proposed to utilize non-corrosive oxidizing agents and fuels without the highly sensitive primary explosive, in order to reduce the hazard of manufacture, but in those cases where adequate sensitivity has been achieved, instability of the mixture has been encountered. Red phosphorous has been suggested by numerous workers in the art as a material utilizable with non-corrosive ingredients and without the primary explosive initiator, but the priming compositions resulting from these suggestions have proven unsatisfactory either from the standpoint of sensitivity or from the standpoint of stability, to an extent such that they have not superceded non-corrosive priming mixtures containing the primary explosive ingredient despite the greater hazard involved in handling the latter.
The object of the present invention, generally stated, is to provide a priming composition of the non-corrosive type, which is highly sensitive and satisfactorily stable, and which does not require the presence of a primary explosive.
Another object of the invention is to improve the sensitivity of non-corrosive priming mixtures which do contain primary explosive ingredients, but whose sensitivity is lower than that of mercury fulminate, lead azide, and the like. l
A more specific object of the invention is to improve the stability and sensitivity of priming compositions containing red phosphorous.
The present invention is predicated upon the discovery that a non-corrosive priming composition having sensitivity, stability, and freedom-from-handling hazard on a parity with or better than potassium chlorate priming mixtures may be provided by the concurrent utilization of red phosphorus with a secondary explosive, such as pentaerythritol tetranitrate, trimethylenetrinitramine, and trinitrotoluene. When incorporated in a non-corrosive priming mixture With red phosphorous, pentaerythritol tetranitrate and trimethylenetrinitramine, in particular, and trinitrotoluene, to a lesser degree, do exhibit the property of radically increasing the sensitivity of the composition without adversely affecting its stability. Unlike other priming compositions, the sensitivity of the red phosphorous-secondary-explosive-containing priming composition is not adversely affected as the size of the pellet increases. Consequently, the weight of the pellet of priming for any 2,970,900 Patented Feb. 7, 1961 2 given round of ammunition can be increased to insure ignition of the propellant and eliminate the possibility of dangerous squibs in small arms ammunition.
The invention is characterized by the concurrent use of red phosphorous and one of the three secondary explosives, to-wit2 pentaerythritol tetranitrate, trimethylenetrinitramine, and trinitrotoluene, or mixtures thereof. While some other compounds having the characteristics of a secondary explosive may be utilized with red phosphorous to achieve an increased sensitivity, the three aforesaid are the only ones revealed by our investigation which exhibit the synergetic eifect of increased sensitivity without adversely alfecting stability. For example, trinitrophenylmethylnitramine, when incorporated with red; phosphorous in a non-corrosive priming composition, results in a composition which is relatively unstable.
It is to be understood, of course, thatthe red phosphorous incorporated in the priming mixtures, in accordance with the present invention, must itself be as stable as possible, within practical limits. Consequently, it is contemplated that, prior to incorporation with the other components, the ordinary red phosphorous of commerce may be purified and have its stability improved by any known method, such for example as that published in Industrial and Engineering Chemistry 40, 301 (1948), in which the phosphorous is first subjected to an acid treatment, an elutriation, and a coating with aluminum hydroxide.
In the manufacture of non-corrosive primers in accordance with the present invention, any of the Well known non-corrosive oxidizing agents, such as barium nitrate, potassium nitrate, lead nitrate, lead dioxide, basic lead nitrate, and barium nitrate-potassium nitrate double salt, may be utilized. Priming compositions of the present invention may be compounded with or without primary explosive ingredients. Since one of the objectives of all endeavors in this branch of the explosives art is to reduce the hazards of manufacture, it is desirable to makeuse of the less sensitive members of the primary explosive family, for example, lead trinitro resorcinate. In priming co-mpositions which contain lead trinitro resorcinate as a primary explosive initiator, the sensitivity can be decidedly improved by the incorporation of the red phosphoroussecondary explosive sub-composition aforesaid.
In compounding the priming composition in accordance with the present invention, the several ingredients may be mixed and charged in the usual manner. In order to assure the maintenance of intimate contact between the red phosphorous and the secondary explosive, it is preferable to coat the red phosphorous with the secondary explosive. Such coating may be accomplished by dissolving the secondary explosive in any suitable solvent, mixing the phosphorous with the solution to form a homogeneous paste, then precipitating the secondary explosive from the solvent, then separating the solvent liquor and drying the solid residue. If acetone is used as the solvent for the secondary explosive, precipitation of the latter may be accomplished by the addition of water.
The proportions of the several ingredients of the composition are preferably within the ranges indicated in the following table:
Percent Primary explosive 0-30 Secondary explosive 5-10 Red phosphorous 15-25 Oxidizer 50-70 The secondary explosive indicated in the foregoing table is one selected from the group consisting of pentaerythritol tetranitrate trimethylenetrinitramine, and trinitrotoluene. The oxidizer is preferably a non-corrosive one.
As an example of a composition containing primary explosive initiator, whose sensitivity is improved in accordance with the present invention, the following formula is representative:
Percent Normal lead trinitro resorcinate 25 Red phosphorus 17 Pentaerythritol tetranitrate Barium nitrate 53 Trimethylenetrinitramine may be substituted for pentaerythritol tetranitrate in each of the foregoing examples without substantial variation in proportions or results.
In sensitivity tests conducted to compare the priming compositions of the present invention with others, it has been ascertained that, of a test lot charged with noncorrosive priming composition containing both red phosphorus and a secondary explosive of the class aforesaid, 100% fired when a four-ounce ball was dropped a distance of 2 /2 inches thereon, while primers otherwise comparable in composition, but omitting either the red phosphorus or the secondary explosive, did not all fire even when the four-ounce ball was dropped thereon for a distance of 3% inches. When impacted by the fourounce ball dropping 2% inches, 79% of the primers, constituted according to the first specific example above given, fired, but only 18% of the test lot, charged with 25% red phosphorus and 75% barium nitrate, fired at this distance.
From the foregoing disclosure, those skilled in the art will find that the invention accomplishes its objects and provides a priming composition having all the virtues of a potassium chlorate primer, but being non-corrosive and without requiring the use of hazardous materials. While two specific examples have been given and various alternatives suggested, it is to be distinctly understood that the invention is not limited to the particular ingredients, or the proportions thereof, indicated in the examples, but that various adjustments in the compositions may be made in order to fit the primer to the requirements of any given round or any given propellent. It will also be understood that the compositions of this invention are preferably loaded in caps having a surface of a compatible metal such as aluminum, lead, or zinc, which will not promote decomposition of the mixtures particularly under hot and moist storage conditions. Such modifications or adjustments may be made in accordance with the custom in the art, and without departing from the spirit of the present invention or the scope of the appended claims.
Having thus described the invention, what is claimed and desired to be secured by Letters Patent is:
1. A priming mixture comprising substantial quantities of red phosphorus, a non-corrosive solid oxidizing agent therefor, and a secondary explosive selected from the group consisting of pentaerythritol tetranitrate, trimethylenetrinitramine, and trinitrotoluene, and mixtures thereof.
2. The priming mixture of claim 1 which includes a primary explosive initiator.
3. A non-corrosive priming mixture containing substantial quantities of red phosphorus, a solid oxidizing agent therefor, and pentaerythritol tetranitrate.
4. A non-corrosive priming mixture containing substantial quantities of red phosphorus, a solid oxidizing agent therefor, and trimethylenetrinitramine.
5. A non-corrosive priming mixture consisting essentially of:
Percent Solid oxidizer 50-70 Red phosphorus 15-25 Secondary explosive 5-10 in which the secondary explosive is selected from a group consisting of pentaerythritol tetranitrate, trimethylenetrinitramine, and trinitrotoluene, and mixtures thereof, and in which the oxidizer is capable of oxidizing red phosphorus.
6. The priming mixture of claim 1 wherein the secondary explosive is coated on the red phosphorus.
7. A non-corrosive priming mixture consisting essentially of:
Percent Oxidizer 50-70 Red phosphorus 15-25 Secondary explosive 5-10 References Cited in the file of this patent UNITED STATES PATENTS 1,185,830 Runge June 6, 1916 2,194,480 Pritham Mar. 26, 1940 2,350,172 Lawrence May 30, 1944 FOREIGN PATENTS 2,377 Great Britain of 1856
Claims (1)
1. A PRIMING MIXTURE COMPRISING SUBSTANTIAL QUANTITIES OF RED PHOSPHORUS, A NON-CORROSIVE SOLID OXIDIZING AGENT THEREFOR, AND A SECONDARY EXPLOSIVE SELECTED FROM THE GROUP CONSISTING OF PENTAERYTHRITOL TETRANITRATE, TRIMETHYLENETRINITRAMINE, AND TRINITROTOLUENE, AND MIXTURES THEREOF.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US101274A US2970900A (en) | 1949-06-24 | 1949-06-24 | Priming composition |
| BE601305A BE601305A (en) | 1949-06-24 | 1961-03-14 | Priming compound. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US101274A US2970900A (en) | 1949-06-24 | 1949-06-24 | Priming composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2970900A true US2970900A (en) | 1961-02-07 |
Family
ID=22283795
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US101274A Expired - Lifetime US2970900A (en) | 1949-06-24 | 1949-06-24 | Priming composition |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2970900A (en) |
| BE (1) | BE601305A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3120459A (en) * | 1959-11-20 | 1964-02-04 | Arthur D Coates | Composite incendiary powder containing metal coated oxidizing salts |
| US3401633A (en) * | 1967-07-06 | 1968-09-17 | Ralph H. Allen | Fire cartridge |
| EP1829849A1 (en) * | 2006-03-02 | 2007-09-05 | Alliant Techsystems Inc. | Nontoxic, noncorrosive phosphorus based primer composition, a percussion cap primer comprising the same and ordnance including the same |
| EP1876160A1 (en) * | 2006-07-04 | 2008-01-09 | Diehl BGT Defence GmbH & Co.KG | Active blasting charge |
| US20080245252A1 (en) * | 2007-02-09 | 2008-10-09 | Alliant Techsystems Inc. | Non-toxic percussion primers and methods of preparing the same |
| US20100116385A1 (en) * | 2005-03-30 | 2010-05-13 | Alliant Techsystems Inc. | Methods of forming a sensitized explosive and a percussion primer |
| US20110000390A1 (en) * | 2007-02-09 | 2011-01-06 | Alliant Techsystems Inc. | Non-toxic percussion primers and methods of preparing the same |
| US20120132099A1 (en) * | 2008-08-19 | 2012-05-31 | Busky Randall T | Nontoxic, noncorrosive phosphorus-based primer compositions and an ordnance element including the same |
| US8206522B2 (en) | 2010-03-31 | 2012-06-26 | Alliant Techsystems Inc. | Non-toxic, heavy-metal free sensitized explosive percussion primers and methods of preparing the same |
| US8641842B2 (en) | 2011-08-31 | 2014-02-04 | Alliant Techsystems Inc. | Propellant compositions including stabilized red phosphorus, a method of forming same, and an ordnance element including the same |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1185830A (en) * | 1913-06-30 | 1916-06-06 | Du Pont Powder Co | Detonator. |
| US2194480A (en) * | 1938-03-07 | 1940-03-26 | Charles H Pritham | Noncorrosive priming composition |
| US2350172A (en) * | 1940-05-17 | 1944-05-30 | Hercules Powder Co Ltd | Electric blasting cap |
-
1949
- 1949-06-24 US US101274A patent/US2970900A/en not_active Expired - Lifetime
-
1961
- 1961-03-14 BE BE601305A patent/BE601305A/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1185830A (en) * | 1913-06-30 | 1916-06-06 | Du Pont Powder Co | Detonator. |
| US2194480A (en) * | 1938-03-07 | 1940-03-26 | Charles H Pritham | Noncorrosive priming composition |
| US2350172A (en) * | 1940-05-17 | 1944-05-30 | Hercules Powder Co Ltd | Electric blasting cap |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3120459A (en) * | 1959-11-20 | 1964-02-04 | Arthur D Coates | Composite incendiary powder containing metal coated oxidizing salts |
| US3401633A (en) * | 1967-07-06 | 1968-09-17 | Ralph H. Allen | Fire cartridge |
| US8460486B1 (en) | 2005-03-30 | 2013-06-11 | Alliant Techsystems Inc. | Percussion primer composition and systems incorporating same |
| US20100116385A1 (en) * | 2005-03-30 | 2010-05-13 | Alliant Techsystems Inc. | Methods of forming a sensitized explosive and a percussion primer |
| US8282751B2 (en) | 2005-03-30 | 2012-10-09 | Alliant Techsystems Inc. | Methods of forming a sensitized explosive and a percussion primer |
| EP1829849A1 (en) * | 2006-03-02 | 2007-09-05 | Alliant Techsystems Inc. | Nontoxic, noncorrosive phosphorus based primer composition, a percussion cap primer comprising the same and ordnance including the same |
| US20100288403A1 (en) * | 2006-03-02 | 2010-11-18 | Busky Randall T | Nontoxic, noncorrosive phosphorus-based primer compositions |
| US7857921B2 (en) * | 2006-03-02 | 2010-12-28 | Alliant Techsystems Inc. | Nontoxic, noncorrosive phosphorus-based primer compositions |
| US9199887B2 (en) | 2006-03-02 | 2015-12-01 | Orbital Atk, Inc. | Propellant compositions including stabilized red phosphorus and methods of forming same |
| US20110100246A1 (en) * | 2006-03-02 | 2011-05-05 | Alliant Techsystems Inc. | Percussion primers comprising a primer composition and ordnance including the same |
| US8524018B2 (en) | 2006-03-02 | 2013-09-03 | Alliant Techsystems Inc. | Percussion primers comprising a primer composition and ordnance including the same |
| US20080006167A1 (en) * | 2006-07-04 | 2008-01-10 | Diehl Bgt Defence Gmbh & Co., Kg | Blast effect charge |
| EP1876160A1 (en) * | 2006-07-04 | 2008-01-09 | Diehl BGT Defence GmbH & Co.KG | Active blasting charge |
| US8192568B2 (en) | 2007-02-09 | 2012-06-05 | Alliant Techsystems Inc. | Non-toxic percussion primers and methods of preparing the same |
| US8202377B2 (en) | 2007-02-09 | 2012-06-19 | Alliant Techsystems Inc. | Non-toxic percussion primers and methods of preparing the same |
| US8454769B2 (en) | 2007-02-09 | 2013-06-04 | Alliant Techsystems Inc. | Non-toxic percussion primers and methods of preparing the same |
| US8454770B1 (en) | 2007-02-09 | 2013-06-04 | Alliant Techsystems Inc. | Non-toxic percussion primers and methods of preparing the same |
| US20080245252A1 (en) * | 2007-02-09 | 2008-10-09 | Alliant Techsystems Inc. | Non-toxic percussion primers and methods of preparing the same |
| US20110000390A1 (en) * | 2007-02-09 | 2011-01-06 | Alliant Techsystems Inc. | Non-toxic percussion primers and methods of preparing the same |
| US20120132099A1 (en) * | 2008-08-19 | 2012-05-31 | Busky Randall T | Nontoxic, noncorrosive phosphorus-based primer compositions and an ordnance element including the same |
| US8540828B2 (en) * | 2008-08-19 | 2013-09-24 | Alliant Techsystems Inc. | Nontoxic, noncorrosive phosphorus-based primer compositions and an ordnance element including the same |
| US8470107B2 (en) | 2010-03-31 | 2013-06-25 | Alliant Techsystems Inc. | Non-toxic, heavy-metal free explosive percussion primers and methods of preparing the same |
| US8206522B2 (en) | 2010-03-31 | 2012-06-26 | Alliant Techsystems Inc. | Non-toxic, heavy-metal free sensitized explosive percussion primers and methods of preparing the same |
| US8641842B2 (en) | 2011-08-31 | 2014-02-04 | Alliant Techsystems Inc. | Propellant compositions including stabilized red phosphorus, a method of forming same, and an ordnance element including the same |
Also Published As
| Publication number | Publication date |
|---|---|
| BE601305A (en) | 1961-09-14 |
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