US3028229A - Pyrotechnic compositions - Google Patents
Pyrotechnic compositions Download PDFInfo
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- US3028229A US3028229A US758173A US75817358A US3028229A US 3028229 A US3028229 A US 3028229A US 758173 A US758173 A US 758173A US 75817358 A US75817358 A US 75817358A US 3028229 A US3028229 A US 3028229A
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- Prior art keywords
- finely divided
- pyrotechnic
- burning
- mixtures
- delay
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 50
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 description 19
- 229940083898 barium chromate Drugs 0.000 description 19
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 description 19
- 229910001487 potassium perchlorate Inorganic materials 0.000 description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 14
- 239000002184 metal Substances 0.000 description 14
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 11
- 229910052721 tungsten Inorganic materials 0.000 description 10
- 239000010937 tungsten Substances 0.000 description 10
- 239000005909 Kieselgur Substances 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 5
- 229910052750 molybdenum Inorganic materials 0.000 description 5
- 239000011733 molybdenum Substances 0.000 description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- 238000001994 activation Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-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
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 235000015842 Hesperis Nutrition 0.000 description 1
- 235000012633 Iberis amara Nutrition 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- ZJRXSAYFZMGQFP-UHFFFAOYSA-N barium peroxide Chemical compound [Ba+2].[O-][O-] ZJRXSAYFZMGQFP-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- BCFSVSISUGYRMF-UHFFFAOYSA-N calcium;dioxido(dioxo)chromium;dihydrate Chemical compound O.O.[Ca+2].[O-][Cr]([O-])(=O)=O BCFSVSISUGYRMF-UHFFFAOYSA-N 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-YPZZEJLDSA-N chromium-50 Chemical compound [50Cr] VYZAMTAEIAYCRO-YPZZEJLDSA-N 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229960004643 cupric oxide Drugs 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 229910003439 heavy metal oxide Inorganic materials 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- ZOKXTWBITQBERF-VENIDDJXSA-N molybdenum-90 Chemical compound [90Mo] ZOKXTWBITQBERF-VENIDDJXSA-N 0.000 description 1
- ZSJFLDUTBDIFLJ-UHFFFAOYSA-N nickel zirconium Chemical compound [Ni].[Zr] ZSJFLDUTBDIFLJ-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- PWZUUYSISTUNDW-VAFBSOEGSA-N quinestrol Chemical compound C([C@@H]1[C@@H](C2=CC=3)CC[C@]4([C@H]1CC[C@@]4(O)C#C)C)CC2=CC=3OC1CCCC1 PWZUUYSISTUNDW-VAFBSOEGSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B33/00—Compositions containing particulate metal, alloy, boron, silicon, selenium or tellurium with at least one oxygen supplying material which is either a metal oxide or a salt, organic or inorganic, capable of yielding a metal oxide
- C06B33/06—Compositions containing particulate metal, alloy, boron, silicon, selenium or tellurium with at least one oxygen supplying material which is either a metal oxide or a salt, organic or inorganic, capable of yielding a metal oxide the material being an inorganic oxygen-halogen salt
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C5/00—Fuses, e.g. fuse cords
- C06C5/06—Fuse igniting means; Fuse connectors
Definitions
- This invention relates in general to certain new and useful improvements in pyrotechnic compositions and, more particularly, to pyrotechnic compositions having predetermined burning rates by reason of which such compositions can'be utilized as so-called delay mixturesi
- Compressed columns of solid powder mixtures have long been used for initiating some desired pyrotechnic result under time delay at the end of a predettermined time-delay period.
- the earliest form of such pyrotechnic device consisted of a confined column of black powder which could be ignited at one end so that the flame and glow front could advance along the column to the other end at a substantially uniform and predetermined rate.
- so called delay mixtures consisting of powdered manganese, silicon, boron, and zirconium nickel alloys in combination with soiid oxidizers, such as barium chromate, lead chromate, and potassium perchlorate.
- delay mixtures are subject to a number of serious limitations. Where the mixture must perform reliably extremes of low temperature within the range of 65 F. to 90 F. in a reasonsably narrow column not exceeding 0.250 inch in diameter, the range of burning time per lineal inch is restricted to a maximum of about 10-13 seconds. Many of the conventional delay mixtures not only fail to perform reliably extremes of temperature, but are also subject to undesirable variations in burning rate responsive to changes in temperature. Furthermore, such delay mixtunes are extremely sensitive to pressure changes. Consequently, if substantial quantities of gas are evolved during burning, the internal pressure buildup will cause the delay mixture to burn erratically.
- the present invention resides in the discovery that finely divided or powdered metals of the class consisting of chromium, molybdenum and Wolfram can be intimately intermixed with potassium perchlorate and a secondary oxidizer, the quantity of potassium perchlorate being less than the stoichiometric equivalent of the metal powder present in the mixture.
- Such mixtures form a pyrotechnic composition which, when compressed into a column of selected cross-sectional area, will have a precisely predetermined lineal burning rate.
- compositions formulated in accordance with the present invention have extremely low gas evolution and, therefore the burning rate is not rendered erratic due to pressure changes.
- the primary oxidizer is finely powdered potassium perchlorate.
- the secondary oxidizer which acts as a reaction modifier to slow the burning rate, is, preferably, barium chromate, but numerous other oxidizers which contain no potentially volatile components except oxygen have proven to be satisfactory, such as, for example, all metal chromates and all heavy metal oxides. More particularly, the following are substances which have been found to function effectively as secondary oxidizers: Barium chromate, strontium chromate, calcium chromate, silver oxide, barium peroxide, manganese dioxide, cupric oxide, and lead dioxide.
- the pyrotechnic composition contain substantially less potassium perchlorate than stoichiometrically combines with the metal regardless of other ingredients which may be present.
- the other ingredients may consist of varying amounts of barium chromate and excess metal or excess metal alone without addition of barium chromate. These mixtures evolve only as much gas as is liberated due to incidental presence of gas formers such as adsorbed gases or unremovable traces of moisture.
- chromium or molybdenum containing mixtures are best suitable for extremely reliable combinations in the conventional burning rate ranges, namely, from I to 10 second per inch. Molybdenum also forms excellent mixtures below one second per inch of burning time. Tungsten containing mixtures form reliably burning mixtures of as high as 40 seconds per inch. For all tungsten containing mixtures which range from about 1 to 40 sec./in., it has been found that the addition of siliceous matter, such as finely ground calcined infusorial earth has a beneficial effect on the control of compaction and upon the reproducibility of the burning rate.
- Example V Powdered metallic molybdenum 33.25 Finely divided potassium perchlorate 9.5 Finely divided barium chromate 52.25
- Example VIII Powdered metallic tungsten 49.5 Finely divided potassium perchlorate 4.5 Finely divided barium chromate 36.0 Finely ground calcined infusorial earth (diatomaceous earth) 10 Burning rate10 sec/in.
- Example IX Powdered metallic tungsten 38.00 Finely divided potassium perchlorate 4.75 Finely divided barium chromate 52.25 Finely ground calcined infusorial earth (diatomaceous earth) Burning rate20 see/in.
- Example X Powdered metallic tungsten 30.8 Finely divided potassium perchlorate 8.8 Finely divided barium chromate 48.4 Finely ground calcined infusorial earth (diatomaceous earth) 12.0 Burning rate30 sec./ in.
- compositions are rich in metal fuel and contain a considerable amount of unreacted metal after burning, they are mostly good conductors for electricity before and after reaction. Such conductivity can be further enhanced by replacing some of the excess metal by an inert but electrically highly conductive metal, such as silverpowder.
- an inert but electrically highly conductive metal such as silverpowder.
- compositions of the present invention form extremely compact, sintered and highly cohesive residues which are fully retained within the delay column during and after burning.
- This property makes the delay mixtures suitable for activation during exertion of high spin rates, set-back forces, acceleration and deceleration, shock and vibration.
- a further advantage of the invention is that the metal powders employed are more or less passive to oxidation by aid and hardly affected by water, so that it is not necessary to treat them with protective coatings as has formerly been practiced with certain metal powders and which is a tedious and costly burden for the manufacturer.
- the metals of the present invention are not easily ignited by sparks or other accidental means.
- the mixing of the ingredients can be done safely in small quantities by dry mixing, such as repeated screening, but because of the potential hazard innate in all pyrotechnic loose powder mixtures, it is preferable to mix larger quantities by vigorous mechanical stirring in slurry form in an easily removable liquid, such as methanol.
- the pyrotechnic compositions of'the present invention can be formulated by varying the proportions of the metal powders and oxidizers to achieve variations in burning times from a fraction of one second to forty seconds per lineal inch. It has also been found that the pyrotechnic compositions of the present invention perform reliably over wide variations in ambient temperature ranging from l65 F. to +165 F.
- the temperature coeflicients of the pyrotechnic mixtures over the aforesaid ambient temperature range does not exceed a maximum of 0.08% per degree F.
- the gas evolution of the pyrotechnic mixtures of the present invention does not w exceed 10 ml. of gas per gram of mixture at standard conditions of temperature and pressure, a factor which is far below previously experienced values and is of great advantage in fuse design.
- a pyrotechnic composition having substantially the following constituency:
- a pyrotechnic composition having substantially the following constituency:
- a pyrotechnic composition having substantially the following constituency:
- a pyrotechnic composition having substantially the following constituency:
- a pyrotechnic composition having substantially the following constituency:
- Powdered metallic tungsten 79.54r Finely divided potassium perchlorate 4.85 Finely divided barium chromate 12.61 Finely ground calcined infusorial earth (diatomaceous earth) 3.
- Powdered metallic tungsten 49.5 Finely divided potassium perchlorate 4.5 Finely divided barium chromate 36.0 Finely ground calcined infusorial earth (diatomaceous earth) 10.
- a pyrotechnic composition having substantially the following constituency:
- Finely round calcined infusorial earth (diatornaceous earth) 5.
- a pyrotechnic composition having substantially the following constituency:
- a pyrotechnic composition havin substantially the following constituency:
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Air Bags (AREA)
Description
atent @fiiee 3,028,229 Patented Apr. 3, 1962 3,028,229 PYRGTECHNIC COIVHOSITIONS Donald E. (llander, Florissant, Mo., assignor to Universal Match Corporation, Ferguson, Mo., a corporation of Delaware No Drawing. Filed Aug. 27, 1958, Ser. No. 758,173 Claims. (Cl. 149-40) This invention relates in general to certain new and useful improvements in pyrotechnic compositions and, more particularly, to pyrotechnic compositions having predetermined burning rates by reason of which such compositions can'be utilized as so-called delay mixturesi Compressed columns of solid powder mixtures have long been used for initiating some desired pyrotechnic result under time delay at the end of a predettermined time-delay period. The earliest form of such pyrotechnic device consisted of a confined column of black powder which could be ignited at one end so that the flame and glow front could advance along the column to the other end at a substantially uniform and predetermined rate. More recently, so called delay mixtures have been developed consisting of powdered manganese, silicon, boron, and zirconium nickel alloys in combination with soiid oxidizers, such as barium chromate, lead chromate, and potassium perchlorate.
All existing types of so-called delay mixtures, however, are subject to a number of serious limitations. Where the mixture must perform reliably extremes of low temperature within the range of 65 F. to 90 F. in a reasonsably narrow column not exceeding 0.250 inch in diameter, the range of burning time per lineal inch is restricted to a maximum of about 10-13 seconds. Many of the conventional delay mixtures not only fail to perform reliably extremes of temperature, but are also subject to undesirable variations in burning rate responsive to changes in temperature. Furthermore, such delay mixtunes are extremely sensitive to pressure changes. Consequently, if substantial quantities of gas are evolved during burning, the internal pressure buildup will cause the delay mixture to burn erratically.
Most existing types of delay mixtures are not ignitible in a rarefield atmosphere or, at least, do not burn consistently under such conditions. In addition, the formulation of conventional delay mixtures has been such that the electrical conductivity of the mixture is low both before and after the pyrotechnic reaction. This matter of electrical conductivity is not, of course, particularly significant for delay trains as such but constitutes a serious deficiency where the delay train is utilized in multi-stage rockets and similar modern applications.
It is, therefore, one of the primary objects of the present invention to provide pyrotechnic compositions, or socalled delay mixtures, which react exothermically without producing any appreciable quantity of gaseous reaction products and, therefore, are not adversely affected by either internal or ambient pressure conditions.
It is another object of the present invention to provide pyrotechnic delay mixtures which have a very broad range of burning times and which will perform reliably over a wide range of ambient temperatures.
It is a further object of the present invention to provide pyrotechnic delay mixtures which are easily ignitible, consistently burning, chemically stable, precisely reproducible, and which produce very compactly sintered residues.
It is likewise an object of the present invention to provide pyrotechnic compositions of the type stated which are electrically conductive both before and after ignition.
Broadly speaking, the present invention resides in the discovery that finely divided or powdered metals of the class consisting of chromium, molybdenum and Wolfram can be intimately intermixed with potassium perchlorate and a secondary oxidizer, the quantity of potassium perchlorate being less than the stoichiometric equivalent of the metal powder present in the mixture. Such mixtures form a pyrotechnic composition which, when compressed into a column of selected cross-sectional area, will have a precisely predetermined lineal burning rate. Moreover, compositions formulated in accordance with the present invention have extremely low gas evolution and, therefore the burning rate is not rendered erratic due to pressure changes. -Within the scope of the present invention, the primary oxidizer is finely powdered potassium perchlorate. The secondary oxidizer, which acts as a reaction modifier to slow the burning rate, is, preferably, barium chromate, but numerous other oxidizers which contain no potentially volatile components except oxygen have proven to be satisfactory, such as, for example, all metal chromates and all heavy metal oxides. More particularly, the following are substances which have been found to function effectively as secondary oxidizers: Barium chromate, strontium chromate, calcium chromate, silver oxide, barium peroxide, manganese dioxide, cupric oxide, and lead dioxide.
As heretofore noted, it is an essential part of the present invention that the pyrotechnic composition contain substantially less potassium perchlorate than stoichiometrically combines with the metal regardless of other ingredients which may be present. The other ingredients may consist of varying amounts of barium chromate and excess metal or excess metal alone without addition of barium chromate. These mixtures evolve only as much gas as is liberated due to incidental presence of gas formers such as adsorbed gases or unremovable traces of moisture.
It has been found in connection with the present invention that chromium or molybdenum containing mixtures are best suitable for extremely reliable combinations in the conventional burning rate ranges, namely, from I to 10 second per inch. Molybdenum also forms excellent mixtures below one second per inch of burning time. Tungsten containing mixtures form reliably burning mixtures of as high as 40 seconds per inch. For all tungsten containing mixtures which range from about 1 to 40 sec./in., it has been found that the addition of siliceous matter, such as finely ground calcined infusorial earth has a beneficial effect on the control of compaction and upon the reproducibility of the burning rate.
Burning rate1.5 sec./ in.
Example IV Percent by wt.
Powdered metallic molybdenum 90 Finely divided potassium perchlorate 10' Finely divided potassium cerchlorate 10 Burning rate-01 sec./ in.
Example V Powdered metallic molybdenum 33.25 Finely divided potassium perchlorate 9.5 Finely divided barium chromate 52.25
Finely ground calcined infusorial earth (diatomaceous earth) Burning rate-6 sec/in.
Burning rate-1.4 see/in.
Example VIII Powdered metallic tungsten 49.5 Finely divided potassium perchlorate 4.5 Finely divided barium chromate 36.0 Finely ground calcined infusorial earth (diatomaceous earth) 10 Burning rate10 sec/in.
Example IX Powdered metallic tungsten 38.00 Finely divided potassium perchlorate 4.75 Finely divided barium chromate 52.25 Finely ground calcined infusorial earth (diatomaceous earth) Burning rate20 see/in.
Example X Powdered metallic tungsten 30.8 Finely divided potassium perchlorate 8.8 Finely divided barium chromate 48.4 Finely ground calcined infusorial earth (diatomaceous earth) 12.0 Burning rate30 sec./ in.
Example XI Powdered metallic tungsten 26.6 Finely divided potassium perchlorate 9.5 Finely divided barium chromate 58.9 Finely ground calcined infusorial earth (diatomaceous earth) Burning rate-40 see/in.
Because all these compositions are rich in metal fuel and contain a considerable amount of unreacted metal after burning, they are mostly good conductors for electricity before and after reaction. Such conductivity can be further enhanced by replacing some of the excess metal by an inert but electrically highly conductive metal, such as silverpowder. By embedding metal wires insu lated with a suitable thin organic coating into the delay column, it is possible to close electric currents triggered by the burning off of the insulation coating due to the advancing glow front and the establishing of electrical contact between the delay column and the wire and thus affect in an extremely simple manner an electric activation or a series of such activations at specified time intervals.
The foregoing functions are greatly aided by the fact that all the compositions of the present invention form extremely compact, sintered and highly cohesive residues which are fully retained within the delay column during and after burning. This property makes the delay mixtures suitable for activation during exertion of high spin rates, set-back forces, acceleration and deceleration, shock and vibration. A further advantage of the invention is that the metal powders employed are more or less passive to oxidation by aid and hardly affected by water, so that it is not necessary to treat them with protective coatings as has formerly been practiced with certain metal powders and which is a tedious and costly burden for the manufacturer. In addition, the metals of the present invention are not easily ignited by sparks or other accidental means. The mixing of the ingredients can be done safely in small quantities by dry mixing, such as repeated screening, but because of the potential hazard innate in all pyrotechnic loose powder mixtures, it is preferable to mix larger quantities by vigorous mechanical stirring in slurry form in an easily removable liquid, such as methanol. Furthermore, the pyrotechnic compositions of'the present invention can be formulated by varying the proportions of the metal powders and oxidizers to achieve variations in burning times from a fraction of one second to forty seconds per lineal inch. It has also been found that the pyrotechnic compositions of the present invention perform reliably over wide variations in ambient temperature ranging from l65 F. to +165 F. The temperature coeflicients of the pyrotechnic mixtures over the aforesaid ambient temperature range does not exceed a maximum of 0.08% per degree F. The gas evolution of the pyrotechnic mixtures of the present invention does not w exceed 10 ml. of gas per gram of mixture at standard conditions of temperature and pressure, a factor which is far below previously experienced values and is of great advantage in fuse design.
It should be understood that changes in the methods, compositions, and combinations above set forth may be made without departing from the nature and principle of my invention.
Having thus described my invention, what I claim and desire to secure by Letters Patent is:
l. A pyrotechnic composition having substantially the following constituency:
Percent by weight Powered metallic chromium Finely divided potassium perchlorate l0 Finely divided barium chromate l0 2. A pyrotechnic composition having substantially the following constituency:
Percent by weight Powdered metallic chromium 50 Finely divided potassium perchlorate 25 Finely divided barium chromate 25 3. A pyrotechnic composition having substantially the following constituency:
Percent by weight Powdered metallic chromium 55 Finely divided potassium perchlorate l0 Finely divided barium chromate l0 Finely divided silver 25 4. A pyrotechnic composition having substantially the following constituency:
Percent by weight following constituency:
Percent by Weight Powdered metallic molybdenum 30 Finely divided potassium perchlorate 5 Finely divided barium chromate 65 aoaaaao U 5. A pyrotechnic composition having substantially the following constituency:
Percent by weight Powdered metallic tungsten 79.54r Finely divided potassium perchlorate 4.85 Finely divided barium chromate 12.61 Finely ground calcined infusorial earth (diatomaceous earth) 3.
7. A pyrotechnic composition having substantially the foilowing constituency:
Percent by Weight Powdered metallic tungsten 49.5 Finely divided potassium perchlorate 4.5 Finely divided barium chromate 36.0 Finely ground calcined infusorial earth (diatomaceous earth) 10.
8. A pyrotechnic composition having substantially the following constituency:
Percent by Weight Powdered metallic tungsten 38.00 Finely divided potassium perchlorate 4.75 Finely divided barium chromate 52.25
Finely round calcined infusorial earth (diatornaceous earth) 5.
9. A pyrotechnic composition having substantially the following constituency:
Percent by Weight Powdered metallic tungsten 30.8 Finely divided potassium perchlorate 8.8 Finely divided barium chromate 48.4 Finely ground calcined infusorial earth (diatornaceous earth) 12.0
10. A pyrotechnic composition havin substantially the following constituency:
Percent by weight References Cited in the file of this patent UNITED STATES PATENTS Pratt Feb. 2, 1943 Carr Aug. 16, 1949 -UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No, 3,028,229 April 3, 1962 Donald E. Olander It is hereby certified that ent requiring correction and that corrected below.
error appears in th the said Letters Column 1, line 16, for
predettermined" rea determined d prelines 29 and 35, after "reliably" Pence insert each occurat column 3, line 5, for "potassium Q fihlOrate" read barium chromate Signed and sealed this 19th day of February 1963.
(SEAL) Attest:
ESTON G. JOHNSON DAVID L, LADD Attesting Officer Commissioner of Patents
Claims (1)
1. A PYROTECHNIC COMPOSITION HAVING SUBSTANTIALLY THE FOLLOWING CONSTITUENCY:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US758173A US3028229A (en) | 1958-08-27 | 1958-08-27 | Pyrotechnic compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US758173A US3028229A (en) | 1958-08-27 | 1958-08-27 | Pyrotechnic compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3028229A true US3028229A (en) | 1962-04-03 |
Family
ID=25050798
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US758173A Expired - Lifetime US3028229A (en) | 1958-08-27 | 1958-08-27 | Pyrotechnic compositions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3028229A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3142253A (en) * | 1962-05-16 | 1964-07-28 | Olin Mathieson | Ignition composition and electric squib containing it |
| US3972673A (en) * | 1974-09-23 | 1976-08-03 | General Electric Company | Photoflash lamp |
| FR2603576A1 (en) * | 1986-09-09 | 1988-03-11 | Bickford Davey | PYROTECHNIC COMPOSITION FOR "ANTIGRISOU" SHORT-DELAY DETONATORS |
| US4963204A (en) * | 1988-03-12 | 1990-10-16 | Dynamit Nobel Aktiengesellschaft | Pyrotechnic delay compositions |
| FR2706449A1 (en) * | 1993-06-18 | 1994-12-23 | Giat Ind Sa | Pyrotechnic composition for delay cords. |
| EP0902773A4 (en) * | 1996-05-14 | 2000-05-24 | Talley Defence Systems Inc | Autoignition composition |
| RU2421438C1 (en) * | 2009-10-14 | 2011-06-20 | Виктория Геннадьевна Никулова | Igniter composition |
| WO2016075091A1 (en) * | 2014-11-10 | 2016-05-19 | Dynitec Gmbh | Pyrotechnical retarding element |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2309978A (en) * | 1940-06-21 | 1943-02-02 | Atlas Powder Co | Propellent fuel assembly |
| US2479470A (en) * | 1944-03-13 | 1949-08-16 | Union Oil Co | Asphaltic jet propulsion fuel |
-
1958
- 1958-08-27 US US758173A patent/US3028229A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2309978A (en) * | 1940-06-21 | 1943-02-02 | Atlas Powder Co | Propellent fuel assembly |
| US2479470A (en) * | 1944-03-13 | 1949-08-16 | Union Oil Co | Asphaltic jet propulsion fuel |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3142253A (en) * | 1962-05-16 | 1964-07-28 | Olin Mathieson | Ignition composition and electric squib containing it |
| US3972673A (en) * | 1974-09-23 | 1976-08-03 | General Electric Company | Photoflash lamp |
| FR2603576A1 (en) * | 1986-09-09 | 1988-03-11 | Bickford Davey | PYROTECHNIC COMPOSITION FOR "ANTIGRISOU" SHORT-DELAY DETONATORS |
| EP0267058A1 (en) * | 1986-09-09 | 1988-05-11 | Davey Bickford | "Anti-firedamp" pyrotechnical composition for short-delay detonators |
| US4963204A (en) * | 1988-03-12 | 1990-10-16 | Dynamit Nobel Aktiengesellschaft | Pyrotechnic delay compositions |
| FR2706449A1 (en) * | 1993-06-18 | 1994-12-23 | Giat Ind Sa | Pyrotechnic composition for delay cords. |
| EP0630876A1 (en) * | 1993-06-18 | 1994-12-28 | GIAT Industries | Pyrotechnic composition for delay fuses |
| EP0902773A4 (en) * | 1996-05-14 | 2000-05-24 | Talley Defence Systems Inc | Autoignition composition |
| US6749702B1 (en) * | 1996-05-14 | 2004-06-15 | Talley Defense Systems, Inc. | Low temperature autoignition composition |
| RU2421438C1 (en) * | 2009-10-14 | 2011-06-20 | Виктория Геннадьевна Никулова | Igniter composition |
| WO2016075091A1 (en) * | 2014-11-10 | 2016-05-19 | Dynitec Gmbh | Pyrotechnical retarding element |
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