GB2437076A - Primer composition - Google Patents
Primer composition Download PDFInfo
- Publication number
- GB2437076A GB2437076A GB0607472A GB0607472A GB2437076A GB 2437076 A GB2437076 A GB 2437076A GB 0607472 A GB0607472 A GB 0607472A GB 0607472 A GB0607472 A GB 0607472A GB 2437076 A GB2437076 A GB 2437076A
- Authority
- GB
- United Kingdom
- Prior art keywords
- primer
- composition
- dry weight
- phosphorus
- filler
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 181
- 239000000945 filler Substances 0.000 claims abstract description 38
- 229920002472 Starch Polymers 0.000 claims abstract description 26
- 239000008107 starch Substances 0.000 claims abstract description 26
- 235000019698 starch Nutrition 0.000 claims abstract description 26
- 239000007800 oxidant agent Substances 0.000 claims abstract description 25
- 239000002245 particle Substances 0.000 claims abstract description 23
- 239000011230 binding agent Substances 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 14
- 238000009527 percussion Methods 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000004816 latex Substances 0.000 claims abstract description 6
- 229920000126 latex Polymers 0.000 claims abstract description 6
- 239000004575 stone Substances 0.000 claims abstract description 6
- YALMXYPQBUJUME-UHFFFAOYSA-L calcium chlorate Chemical class [Ca+2].[O-]Cl(=O)=O.[O-]Cl(=O)=O YALMXYPQBUJUME-UHFFFAOYSA-L 0.000 claims abstract description 3
- 239000010433 feldspar Substances 0.000 claims abstract description 3
- 239000000454 talc Substances 0.000 claims abstract description 3
- 229910052623 talc Inorganic materials 0.000 claims abstract description 3
- 239000005337 ground glass Substances 0.000 claims abstract 2
- 229910052604 silicate mineral Inorganic materials 0.000 claims abstract 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 48
- 239000003380 propellant Substances 0.000 claims description 38
- 239000011574 phosphorus Substances 0.000 claims description 31
- 229910052698 phosphorus Inorganic materials 0.000 claims description 31
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 claims description 18
- 230000001590 oxidative effect Effects 0.000 claims description 13
- 229910001220 stainless steel Inorganic materials 0.000 claims description 6
- 239000010935 stainless steel Substances 0.000 claims description 6
- 240000008042 Zea mays Species 0.000 claims description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 4
- 229920002678 cellulose Polymers 0.000 claims description 3
- 235000010980 cellulose Nutrition 0.000 claims description 3
- WHQOKFZWSDOTQP-UHFFFAOYSA-N 2,3-dihydroxypropyl 4-aminobenzoate Chemical compound NC1=CC=C(C(=O)OCC(O)CO)C=C1 WHQOKFZWSDOTQP-UHFFFAOYSA-N 0.000 claims description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 2
- 240000005979 Hordeum vulgare Species 0.000 claims description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- 239000005909 Kieselgur Substances 0.000 claims description 2
- 240000007594 Oryza sativa Species 0.000 claims description 2
- 235000007164 Oryza sativa Nutrition 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 2
- 244000061456 Solanum tuberosum Species 0.000 claims description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 claims description 2
- 235000021307 Triticum Nutrition 0.000 claims description 2
- 241000209140 Triticum Species 0.000 claims description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 2
- KHPLPBHMTCTCHA-UHFFFAOYSA-N ammonium chlorate Chemical compound N.OCl(=O)=O KHPLPBHMTCTCHA-UHFFFAOYSA-N 0.000 claims description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 235000005822 corn Nutrition 0.000 claims description 2
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 claims description 2
- 235000009973 maize Nutrition 0.000 claims description 2
- 229910001487 potassium perchlorate Inorganic materials 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 claims 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 claims 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract description 2
- 239000011591 potassium Substances 0.000 abstract description 2
- 229910052700 potassium Inorganic materials 0.000 abstract description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 abstract 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 abstract 1
- 238000012549 training Methods 0.000 description 39
- 230000037452 priming Effects 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 10
- 238000001035 drying Methods 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 6
- 230000006378 damage Effects 0.000 description 5
- 238000010304 firing Methods 0.000 description 5
- 208000027418 Wounds and injury Diseases 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910001385 heavy metal Inorganic materials 0.000 description 4
- 208000014674 injury Diseases 0.000 description 4
- 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 4
- 238000002156 mixing Methods 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000007580 dry-mixing Methods 0.000 description 3
- 238000004880 explosion Methods 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 231100000489 sensitizer Toxicity 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 230000002269 spontaneous effect Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 150000004655 tetrazenes Chemical class 0.000 description 2
- 229920000856 Amylose Polymers 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
- 208000034656 Contusions Diseases 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical compound [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-N iodic acid Chemical class OI(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- -1 perchiorateS Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical compound [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B29/00—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B29/00—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate
- C06B29/02—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate of an alkali metal
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B31/00—Compositions containing an inorganic nitrogen-oxygen salt
- C06B31/02—Compositions containing an inorganic nitrogen-oxygen salt the salt being an alkali metal or an alkaline earth metal nitrate
- C06B31/08—Compositions containing an inorganic nitrogen-oxygen salt the salt being an alkali metal or an alkaline earth metal nitrate with a metal oxygen-halogen salt, e.g. inorganic chlorate, inorganic perchlorate
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C7/00—Non-electric detonators; Blasting caps; Primers
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C7/00—Non-electric detonators; Blasting caps; Primers
- C06C7/02—Manufacture; Packing
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C9/00—Chemical contact igniters; Chemical lighters
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F42—AMMUNITION; BLASTING
- F42C—AMMUNITION FUZES; ARMING OR SAFETY MEANS THEREFOR
- F42C19/00—Details of fuzes
- F42C19/08—Primers; Detonators
- F42C19/0803—Primers; Detonators characterised by the combination of per se known chemical composition in the priming substance
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F42—AMMUNITION; BLASTING
- F42C—AMMUNITION FUZES; ARMING OR SAFETY MEANS THEREFOR
- F42C19/00—Details of fuzes
- F42C19/08—Primers; Detonators
- F42C19/10—Percussion caps
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Paints Or Removers (AREA)
Abstract
A primer composition, possibly associated with a percussion cap or ammunition cartridge, comprises red phosphorous, an oxidising agent such as one or more of potassium, ammonium or calcium chlorates or perchlorates, and one or more components of a latex binding agent, gritty filler and/or starch. The inert gritty filler may be in the form of ground stone, ground glass, feldspar, talc or silicate minerals with particle sizes of 5-150m. The dry composition of the primer consists of 10-50% filler, 20-99% oxidising agent, 0.025-10% starch and approximately 6% red phosphorous. A method of preparing such a primer is also disclosed and includes adding 36% water to a dry composition of phosphorous, filler and starch, adding the oxidising agent before adding a suitable binding agent.
Description
<p>Primer Compositions</p>
<p>FIELD OF THE INVENTION</p>
<p>This invention relates to a novel primer composition, and particularly but not exclusively to a priming composition for percussion caps for small arms ammunition (SAA) capable of meeting military standards, its method of manufacture and to percussion caps and cartridges containing the composition. The primer composition of the present invention is particularly useful in the manufacture of training ammunition.</p>
<p>BACKGROUND ART</p>
<p>* It is well known that the main propellant charge contained within the cartridge case of a round of ammunition is relatively insensitive and **** requires a significant amount of energy to ensure that rapid and complete : *. ignition successfully occurs. This energy is conventionally provided by a I...</p>
<p>* primer composition located at the rear end of the cartridge case. Such *..</p>
<p>primer compositions typically comprise an energetic material which is sensitive to the input of energy generated through heat, friction or * percussion and provides in response thereto a flame and/or hot S..</p>
<p>particulates for activating the propellant charge present in the cartridge.</p>
<p>A percussion primer typically comprises a cap formed of a cup having a priming composition therein. The cup is typically covered with waxed or varnished paper or the like to exclude moisture. The cap is then placed in a pocket in the cartridge case. In a Boxer primer, there is also an anvil pressed into the open end of the cup. For Berdan primers, the casing of the cartridge includes an anvil integrally formed therewith. In each case, ignition of the priming composition is initiated by the impact of the firing pin of a weapon against the central portion of the cup thereby compressing the priming composition between the anvil and the cup. The heat generated by the compressive and/or frictional forces generated within the cup causes the composition to ignite almost instantaneously, and to burn very rapidly. The hot gases and/or parliculates generated are forced into contact with the propellant through flash holes in the casing pocket. The energy generated by the burning of the primer/propellant combination typically causes the projectile to be expelled from the barrel of the gun at velocities in excess of 700ft/sec [ 2l3mtr/sec].</p>
<p>Common priming compositions typically comprise a main energetic ingredient, an oxidant and a sensitiser which increases the susceptibility of the main ingredient to the effect of the impact from the firing pin of the weapon. One or more secondary energetic ingredients and fuels, which modify the output of the primer, by for example providing more heat or producing more gas, hot particles may also be present.</p>
<p>With certain ammunition rounds, depending upon the design of the propellant, the production of a flame or hot gas only can be insufficient to a *..</p>
<p>S..'.' promote efficient ignition of the propellant because the gas only tends to * .. impact and activate the surface region of thereof. Activation of the remaining propellant therefore depends upon the propagation of the *5s primer initiated reaction from the surface region of the propellant : . . throughout the remaining volume. Efficient propagation of the primer *..* initiated reaction can be achieved through the incorporation into the n primer of particulate matter, which generates hot particles upon ignition of the primer. The production of hot particles can be beneficial to the subsequent ignition of the propellant, because they can be directed in such a way that they are able to efficiently penetrate the propellant and simultaneously cause activation thereof over a larger volume than would otherwise be the case.</p>
<p>Many priming compositions contain heavy metal elements as their principle components. For example, lead styphnate is typically used as a main energetic component; barium nitrate is a common oxidant and antimony sulphide is a common fuel. The presence of heavy metal elements in priming compositions is undesirable due to environmental concerns and priming mixtures containing strontium nitrate as an oxidant have been proposed (US 4 693 2010) in order to avoid the use of heavy metals.</p>
<p>Although the use of both potassium dinitrobenzofuroXafl (KDNBF) and diazodinitropheflOl (DDNP) as energetic ingredients (US 4 693 201), is known, the use of KDNBF as the sole energetic ingredient results in primers that are inconsistent or insensitive in their performance. Although this problem can be partially overcome through the addition of tetrazene as a sensitiser to the KDNBF or DDNP mixture, the long term stability of the resulting mixtures is poor, leading to an explosives hazard.</p>
<p>Primer mixtures containing KDNBF, tetrazene and strontium nitrate are known. Such mixtures can be formed through either a wet or a dry mixing * process. However, a disadvantage with this type of primer is that, in general they are frequently too energetic and cartridges containing these a.., primer compositions often burn too rapidly upon ignition, which is undesirable. * . .</p>
<p>Cartridges used for training munitions are preferably designed to mimic * real-life situations as much as possible without the need for extensive safety measures. Such cartridges differ from those used in live ammunition principally in the energy at which the bullets are expelled from the muzzle of the gun. Live ammunition is typically expelled from the barrel of a gun at energies of over 60 ft lbs (81.35 joules) whereas the cartridges of training munitions are typically expelled at 4 ft lbs (5.43 joules). Thus, although it is known to use training cartridges containing both a primer and a propellant, the use of such cartridges is associated with relatively high energy and necessitates the use of bulky and expensive protective clothing, which means that training does not take place under realistic circumstances.</p>
<p>There are several types of training ammunition available. These include Live training ammunition, Live low energy training ammunition and Low energy man on man training ammunition.</p>
<p>Live training ammunition is designed to allow shooting in areas and ranges in which the danger zone is below that of live combat ammunition. These products can still kill but their range is reduced.</p>
<p>Live low energy training ammunition is designed to further reduce the danger zone and risk of fatal injury. It also reduces the damage caused to training areas. These products are still dangerous and cannot be used man on man. .</p>
<p>Low energy man on man training ammunition is designed to eliminate the risk of : fatal and minor injury during firearms training. The training of man on man is the nearest and most realistic training for real life combat situations. The guns muzzle energy must be kept below 3 ft/lbs and the projectile velocity kept below 400 ft/sec if even minor injury [broken skin is to be eliminated. Protective clothing is still worn to cover eyes, ears, face, throat and bare skin to further reduce the risk of minor injury such as bruising.</p>
<p>In order to obviate the need for extensive protective clothing in training exercises and to enhance the realism thereof, a double primer propellant free cartridge has been proposed. Such cartridges can be used in live ammunition but find particular application with training ammunition.</p>
<p>Cartridges of this type are described in United Kingdom patent application number US 6 422 149. Such cartridges typically comprise a front primer positioned adjacent the bullet to be expelled from the cartridge and a rear primer positioned adjacent the rear end of the cartridge against which the firing pin impacts when the gun is fired. Impact of the firing pin on the rear primer results in ignition of the primer composition present therein and causes a ball (typically plastic or steel) to be driven at high energy against the front primer. Upon impact of the rear primer driven ball against the front primer, ignition of the front primer composition occurs and causes the bullet to be expelled from the barrel of the gun.</p>
<p>The choice of primer compositions used in both the front and rear primers will depend upon the application in which the cartridge is to be used. The primer compositions of the rear primers tend to be relatively energetic to ensure that despite the relatively low energy at which the firing pin impacts the rear primer, efficient ignition of the primer composition occurs and results in the ball being driven at relatively high energy against the front primer. Typically the rear primer provides energies of 10 to 30 ft lbs (13.56 to 40.67 Joules) upon ignition. If the cartridge is to be used for live low energy training ammunition, the priming composition of the front a..</p>
<p>primer is also itself relatively energetic to ensure that the energy at which the bullet is expelled from the barrel of the gun is relatively high. Typically if a double primer propellant free cartridge is to be use for live low energy training ammunition, the front primer suitably provides energies of 5 to 10 ft lbs (6.8 to 13.6 Joules) upon ignition. If the cartridge is to be used for Is..</p>
<p>low energy man on man training ammunition, the priming composition of the front primer is less energetic to ensure that the muzzle energy of the bullet expelled does not exceed 3 ft lbs (4.08 Joules).</p>
<p>The use of the double primer propellant free cartridges described above has made it possible to better control muzzle velocities. Using known primer compositions (such as lead styphnate) muzzle velocities not exceeding 2ft/lbs (2.72 Joules) have been observed for Man Marker Rounds (MMR) and for Live Low Energy Reduced Range (LERR) ammunition the muzzle velocities not exceeding 8ft/lbs (10.87 Joules) have been achieved.</p>
<p>However, the use of primer mixtures containing lead styphnate as an energetic component, for example, in double primer propellant free cartridges frequently results in inconsistent and unpredictable results. It is not unusual for a double primer propellant free cartridge either to fail to fire the bullet out of the muzzle or to be expelled at a rate which greatly exceeds the desired muzzle velocities for training munitions due to the rapid and unpredictable burning of the lead styphnate.</p>
<p>There is, therefore, a need for a priming composition that is free of toxic heavy metals, provides consistent and controlled burning on ignition and is suitable for use in both live and training munitions, particularly in double primer propellant free cartridges.</p>
<p>The present invention addresses that need.</p>
<p>: SUMMARY OF THE INVENTION sc S...</p>
<p>A first aspect of the present invention provides a primer composition : *. comprising phosphorus and an oxidising agent. Depending upon the * required energenicity of the primer further optional components may also be present. These additional components include one or more of a gritty ::. filler, a starch and a binding agent. S...</p>
<p>The phosphorus is preferably red phosphorus rather than white or black phosphorus due to its greater stability and reduced toxicity compared to white phosphorus, for example. The phosphorus acts as an energetic agent and the amount of phosphorus present will depend upon a number of factors, which include the particle size of the phosphorus, the method used to initiate ignition of the primer compositions, including the force of impact, whether the primer composition is to be used in live or training ammunition and if it is to be used in a double primer propellant free cartridge, whether it is to be placed in the front or rear primer. The presence or absence of one or more additional components such as a gritty filler, a starch and a binding agent will also influence the amount of phosphorus present.</p>
<p>If the composition is to be used in live ammunition or in the rear primer of a double primer propellant free cartridge, for a maximum particle size of pm, the amount of phosphorus suitably comprises 1.1 to 10.0 % of the dry weight of the primer composition. Preferably the phosphorus comprises 4 to 8% of the dry weight of the composition, especially 6% of the dry weight of the composition. Under these conditions energies in the range 10 to 30 ft lbs (13.56 to 40.67 Joules) can be achieved upon ignition. If the particle size of the phosphorus is larger, a smaller amount of phosphorus may be required, depending upon the energies required from the primer and the method of impact. Given these requirements, it will be within the skill of a skilled person to determine the optimum amount of phosphorus required for any particular application. However, for a phosphorus particle size of 75 to 500pm, the amount of phosphorus suitably comprises 0.5 to 7.0 % of the dry weight of the composition, preferably 1.0 to 6.0% by weight of the composition and especially 2.5% by weight of the composition.</p>
<p>If the composition is to be used in low energy man on man training ammunition, for example in the front primer of a double primer propellant I.e.</p>
<p>free cartridge, the amount of phosphorus suitably comprises 0.25 to 5 % of the dry weight of the composition. Preferably the phosphorus comprises 0.5 to 3% of the dry weight of the composition, especially 0.5 to 1.0 % of the dry weight of the composition. Under these conditions energies in the range 1.5 to 3.5 ft lbs (2.03 to 4.74 Joules) can be achieved. Energy levels of 1.5 ft lbs (2.03 Joules) have been obtained with double primer propellant free cartridges using either 1.5% by weight of phosphorus having a particle size of 5Opm and a steel ball or 2.0% by weight of phosphorus having a particle size of 5Opm and a plastic ball. If the particle size of the phosphorus is larger, a smaller amount of phosphorus may be required, depending upon the energies required from the primer and the method of impact. Given these requirements, it will be within the skill of a skilled person to determine the optimum amount of phosphorus required for any particular application.</p>
<p>The amount of phosphorus used in the primer compositions will also depend, in part, on the type and presence of any additional components.</p>
<p>If a gritty filler is present, the amount of phosphorus required will be less.</p>
<p>The amount of phosphorus will also depend upon the particle size of the gritty filler; as the particle size of the gritty filler increases less phosphorus, in general, is needed.</p>
<p>Since some of the further components such as starch or binding agent do in themselves increase the rate of burn and or the amount of gas provided by the primer composition, the amount of phosphorus used will also depend upon the presence and nature of these additional components. If a binding agent or a starch is present, less phosphorus will be required if : *. these components do in themselves increase the rate of burn and or the S...</p>
<p>es amount of gas provided by the primer composition. The effect of the *S..</p>
<p>additional ingredients on the rate of burn of the primer compositions can ::::. be readily determined by comparing the burning properties of the * compositions with and without the presence of the additional components : * and changing the amount of phosphorus present if necessary.</p>
<p>In general phosphorus having a particle size in the range 10 to 500 pm *.*.</p>
<p>can be used in the preparation of the primer compositions of the present invention. It will be appreciated from the foregoing discussion that if the primer composition is to be used in training ammunition or in the front primer of a double primer propellant free cartridge (for use in live or training ammunition), particle sizes in the range 10 to 200 pm can be used, with particle sizes in the range 10 to 50 pm being preferred. If the primer composition is to be use in live ammunition or in the rear primer of a double primer propellant free cartridge (for use in live or training ammunition), particle sizes in the range 40 to 500 pm can be used, with particle sizes in the range 100 to 500 pm being preferred.</p>
<p>A stabiliser may also be present in the event that the components of the primer composition are found to degrade over a period of time. Potassium carbonate may suitably be used as a stabilising agent. A skilled person will be aware of other stabilising agents that may also be used.</p>
<p>The oxidising agent may be any oxidant that reacts with the other components of the primer composition upon ignition only. The oxidant must be sufficiently stable so that spontaneous ignition of percussion caps containing the primer mixture does not occur in storage. Suitable oxidants include nitrates, bromateS, iodates, chlorates, perchiorateS, peroxides and oxides. Typical oxidants include potassium chlorate, potassium perchlorate, ammoniUm chlorate, ammonium perchiorate, calcium chlorate and calcium perchlorate. The use of potassium chlorate is particularly preferred, since it has been found that its presence means ::::. that the activation energy required for ignition of a primer composition containing this oxidant is negligible.</p>
<p>::::. The amount of oxidant present will depend upon whether the composition is to be used in live or training ammunition or in a front or a rear primer * of a double primer propellant free cartridge. In addition, the amount of oxidant present will depend upon whether any additional components such S...</p>
<p>as a gritty filler, a starch component or a binding agent are present. The oxidant suitably comprises 20.0 to 99.0% by weight of the primer composition if no gritty filler is present, preferably 40.0% to 99.0% of the dry weight of the composition and especially 97.00% by dry weight of the composition. In a particularly preferred embodiment of the first aspect of the invention, the composition comprises 97.OO% of potassium chlorate of the dry weight of the composition and no gritty filler. Such compositions find particular application when used in a front primer for a double primer propellant free cartridge.</p>
<p>If the composition includes a gritty filler, the oxidant suitably comprises 20.0 to 60.0% by dry weight of the composition, preferably 40.0 to 60.0% by dry weight of the composition and especially 60.0% by weight of the dry weight of the composition. In a particularly preferred embodiment of the first aspect of the invention, the primer composition comprises 60.0% by weight of potassium chlorate and 29.5 to 33.0% by weight of a gritty filler. Such compositions find particular application use as a rear primer in a double primer propellant free cartridge.</p>
<p>The presence of a gritty filler prevents spontaneous explosion of the active ingredients of the primer and provides sufficient friction on ignition of the primer to ensure that controlled and efficient burning occurs. Examples of suitable fillers for use in the primers of the first aspect of the invention include ground stone, glass, talc, feldspar and silicates of diatomaceouS earth minerals. Preferably the inert filler is ground stone. Preferably the ground stone has particles in the range 5 to 150pm.</p>
<p>The presence or otherwise of a gritty filler depends upon the desired muzzle velocities required and whether the compositions are to be used in S...</p>
<p>live or training ammunition or in the front or rear primer of a double : primer propellant free cartridge (for use in either live or training I...</p>
<p>ammunition). If a composition is to be used in the manufacture of a primer for training purposes such as in the front primer of a double primer propellant free cartridge the composition will suitably either contain no filler at all or will typically contain a filler such that its amount and particle size result in a primer having an energy of 1.5 to 3. 5 ft lbs (2.03 to 4.75 Joules) upon ignition.</p>
<p>If the composition is to be used in the manufacture of a primer for live ammunition or in the rear primer of a double primer propellant free cartridge (either for training purposes or otherwise) the composition will suitably contain inert fillers having larger particle sizes. Typically the inert fillers for use in such applications have particle sizes in the range 60 to 120pm. Where an inert filler is present, it suitably comprises 10.00 to 50.00% of the dry weight of the composition, preferably 25.00 to 35.00% of the dry weight of the composition, especially 29.50 to 33.00% of the dry weight of the composition. In a particularly preferred embodiment of the first aspect of the invention, the inert filler comprises 29.5 to 33.00% of the dry weight of the composition of the primer composition.</p>
<p>A starch component may be included in the primer mixture to facilitate the controlled burning of the primer mixture on ignition and thus the controlled generation of gases associated with combustion. It will be appreciated that the rate of combustion of the primer mixture of the present invention depends to a large extent on the amount and the type of the starch component present. The starch component typically comprises between 0.025 and 10.00% by weight of the dry weight of the primer composition. Preferably the starch component comprises 0.75 to 5 Io by weight of the dry composition, especially 1.00 to 3.00% by weight of the dry composition. It will therefore be appreciated that the presence of a starch component is associated with a higher gas production compared to compositions in which none is present and that primer :.:::. compositions containing starch will most suitably be used in either in live S...</p>
<p>ammunition or in the rear primer of a double primer propellant free : * cartridge (either for training purposes or otherwise) where higher energies are required. Although compositions for use in training ammunition *0 * (including those used in the front primer of a double primer propellant ::. free cartridge) may contain starch, the amount and type of starch present will depend upon the other components present and desired energenicity.</p>
<p>Suitable starch components include powders derived from sources such as paper, cellulose, corn, rice, wheat, potato, maize and barley. In general it is preferred that when a starch component is present in a composition, the ratio of starch to oxidant is of the order of 1:6. Particularly good results have been achieved through the use of cornflour. In a particularly preferred embodiment of the first aspect of the invention, the primer composition contains 0.025 to 10.00% of cornflour by dry weight of the composition, particularly 0.75 to 5% by dry weight of the composition and especially 0.50 to 4.00 Io by weight of the dry composition. For preferred compositions including cornflour the ratio of cornflour to potassium chlorate is 1:6. Such compositions find particular application as the rear primer of a double primer propellant free cartridge (either for training purposes or otherwise).</p>
<p>The primer composition of the first aspect of the invention preferably contains one or more binding agents, the presence of which facilitates the formation of the primer composition into a paste and its loading into percussion caps for subsequent insertion into a cartridge. Preferably the binder doesn't burn or requires a very high activation energy in order for burning to occur. Any suitable binding composition that facilitates the formation of a paste can be used, providing the storage stability of the composition is not compromised. Examples of suitable binding compositions include latex emulsions such as BAL, shellac, resins, glues, lacquers or any of the polysaccharides (such as gels or gums) used for setting or thickening purposes within the food industry or used as adhesives. Synthetic vinyl based polymers can also be used as can wall paper paste. Gelatines, alginates, celluloses, amyloses and other S. polysaccharides having the desired properties to facilitate the formation of : a paste are known to a person skilled in the art. However, preferably the binding agent is a wall paper paste comprising carboxymethylcellulose and I..</p>
<p>* sodium hydroxymethylcellulose that has optionally been formaldehyde : * . treated. Preferably the wall paper paste comprises 0. 25 to 0.90% of the dry weight of the composition, especially 0.50% of the dry weight of the S...</p>
<p>composition.</p>
<p>In a most preferred embodiment of the first aspect of the invention, the primer composition comprises 6.00% red phosphorus, 60.00% potassium chlorate; 29.5 to 33% inert filler, 0.50 to 4.00% cornflour and 0.5% of wallpaper paste by dry weight of the composition. This composition is suitably used in live ammunition or in the rear primer of a double primer propellant free cartridge (for either live or training purposes).</p>
<p>In a further preferred embodiment of the first aspect of the invention, the primer composition comprises 2.00% by weight red phosphorus, 97.00% by weight potassium chlorate, 0.50% by weight of a wallpaper paste and 0.50% by weight of BAL latex binder. All weights are quoted with reference to the dry weight of the composition. This composition is suitably used in training ammunition, particularly in the front primer of a double primer propellant free cartridge.</p>
<p>It is known that primer compositions can be prepared through the use of either wet mixing or dry mixing techniques. Wet mixing techniques have been found to produce the most homogeneous products but require the use of a drying step. It will be appreciated, however, that the drying of a bulk volume of a primer composition is inherently associated with the risk of explosion. Although dry mixing techniques can be used in the production of primer compositions, the technique is less suited for the production of bulk quantities of the primer composition and the homogeneity of the resulting compositions, generally, is not as good as that achieved through the use of wet mixing techniques. S...</p>
<p>The compositions of the present invention are, therefore, preferably prepared through the use of a wet mixing technique and a second aspect S...</p>
<p>of the invention provides a method for the preparation of the primer compositions according to the first aspect of the invention. Typically the wet mix comprises 25g of water per lOOg of dry ingredients. To prevent the risk of explosion, the red phosphorus and oxidant are only mixed together in the presence of water.</p>
<p>For the preparation of a composition suitable for use in a front primer of a double primer propellant free cartridge, phosphorus is firstly added to water and thoroughly mixed. Potassium chlorate is then thoroughly incorporated into the mixture and finally the binder (BAL and/or wallpaper paste) is added. The resulting paste is then loaded into primer caps and dried in a drying oven. Potassium carbonate may be added to the mixture to improve its long term stability in the event that the stability of the dry composition is less than optimal.</p>
<p>For the preparation of a composition suitable for use in live ammunition or in a rear primer of a double primer propellant free cartridge water is added to a dry mixture of red phosphorus, inert filler and the starch component. The oxidising agent is then added to the wet mixture and thoroughly combined therewith. Finally the binding agent is added to the mixture which results in the formation of a workable paste. The resultant paste is then metered into suitable containers for each application and then dried.</p>
<p>In a preferred embodiment of the second aspect of the invention, water is added to a dry mixture of red phosphorus, inert filler and cornftour to give a liquid slurry. Potassium chlorate is then added to the liquid slurry and mixed thoroughly. Wall paper paste is then added to the resulting mixture to give a paste, which can be readily loaded into the percussion caps used in cartridges. * S.</p>
<p>: The compositions are preferably dried at a temperature of between 60 C and 100 C. If it is desired to dry at 100 C, it is preferably toinclude a BAL : *". latex binder in the composition to prevent shrinkage of the dry S...</p>
<p>composition away from the wall of the cup. Drying at 60 C results in less shrinkage. * S a S * *5SS</p>
<p>It has been found that the primer composition of the present invention S...</p>
<p>reacts with the brass cups typically used in the manufacture of percussion caps and that stainless steel caps should be used instead. A third aspect of the invention provides a percussion cap for use in ammunition comprising a stainless steel cap containing the primer composition according to the first aspect of the invention.</p>
<p>DETAILED DESCRIPTION OF THE EMBODIMENTS</p>
<p>The invention will now be described with reference to the following non-limiting examples. Variations on these examples falling within the scope of the present invention will be apparent to a person skilled in the art.</p>
<p>ExamDle 1 A primer composition was prepared by adding 36 g of water to a dry mixture containing 6g of red phosphorus, 33g of inert filler and 0.5g of cornflour. 60g of potassium chlorate was added to the wet mixture and thoroughly combined. 0.5g of wallpaper paste was added to the resulting mixture and stirred until a paste-like consistency was achieved (15 -30 seconds). The resultant paste-like mixture was metered into a stainless steel cups and placed in a drying oven.</p>
<p>The use of the percussion caps of example 1 in training ammunition resulted in an impact energy of the cartridge projectile of 3 ft/lbs or less.</p>
<p>ExamDle 2 A primer composition was prepared by adding 36g of water to a dry mixture containing 6g of red phosphorus, 32.5g of inert filler and 1.Og of ::. cornflour. 60g of potassium chlorate was added to the wet mixture and thoroughly combined. 0.5g of wallpaper paste was added to the resulting * S..</p>
<p>mixture and stirred until a paste-like consistency was achieved (15 -30 seconds). The resultant paste-like mixture was metered into a stainless steel cup and placed in a drying oven.</p>
<p>ExamDle3 S... * . 0I**</p>
<p>A primer composition was prepared by adding 36g of water to a dry mixture containing 6g of red phosphorus, 32.75g of inert filler and 0.75g of cornflour. 60g of potassium chlorate was added to the wet mixture and thoroughly combined. 0.5g of wallpaper paste was added to the resulting mixture and stirred until a paste-like consistency was achieved (15 -30 seconds). The resultant paste-like mixture was metered into a stainless steel cup and placed in a drying oven.</p>
<p>Example 4</p>
<p>A primer composition was prepared by adding 36g of water to a dry mixture containing 6g of red phosphorus, 30.5g of inert filler and 3.Og of cornflour. 60g of potassium chlorate was added to the wet mixture and thoroughly combined. 0.5g of wallpaper paste was added to the resulting mixture and stirred until a paste-like consistency was achieved (how long does this take -approximately?). The resultant paste-like mixture was pressed into rimfire primer cases using a small press at 30 psi with an angled punch and placed in a drying oven.</p>
<p>This product was able to cycle the M16 and the G36 OK over repeated rounds of ammunition.</p>
<p>ExamDle 5 A primer composition was prepared by adding 36g of water to a dry mixture containing 6g of red phosphorus, 29.5g of inert filler and 4.Og of cornflour. 60g of potassium chlorate was added to the wet mixture and thoroughly combined. 0.5g of wallpaper paste was added to the resulting mixture and stirred until a paste-like consistency was achieved (15 -30 *S..</p>
<p>seconds). The resultant paste-like mixture was pressed into a stainless : ** steel cup and the cup and primer dried. *.I.</p>
<p>S</p>
<p>I * .</p>
<p>I S *... S... * I.</p>
Claims (2)
- <p>CLAIMS</p><p>1. A primer composition comprising red phosphorus and an oxidising agent.</p><p>2. A primer composition according to claim 1, which also comprises one or more components selected from a gritty filler, a starch and a binding agent.</p><p>3. A primer composition according to claim 1 or claim 2, wherein the phosphorus comprises 0.25 to l0.00 Io, particularly 0.50 to 8.00% and especially 1.50 to 6.00% of the dry weight of the composition.</p><p>4. A primer composition according to any one of the preceding claims, I...</p><p>wherein the oxidising agent is selected from one or more of * S..</p><p>potassium chlorate, potassium perchlorate, ammonium chlorate, :.:::. ammonium perchlorate, calcium chlorate and calcium perchlorate.</p><p>5. A primer composition according to claim 4, wherein the oxidising :::*. agent comprises 20.00 to 99.00%, especially 60.00 to 97.00% of the dry weight of the composition.</p><p>6. A composition according to claim 4 or claim 5, wherein the oxidising agent is potassium chlorate.</p><p>7. A primer composition according to any one of the preceding claims wherein the inert filler is selected from ground stone, ground glass, talc, feldspar, and silicate minerals of diatomaceous earth elements having a particle size in the range 5 to 150pm.</p><p>8. A primer according to claim 7, wherein the inert filler comprises 10.00 to 50.00%, preferably 25.00 to 35.00 Io and especially 29.5 to 33.00% of the dry weight of the composition.</p><p>9. A primer according to claim 8, wherein the inert filler is ground stone.</p><p>10. A primer according to any one of the preceding claims, wherein the starch component is selected from one or more of powders derived from paper, cellulose, corn, wheat, potato, rice, maize and barley.</p><p>11. A primer according to claim 10, wherein the starch component is cornflour.</p><p>12. A primer according to claim 10 or claim 11, wherein the starch component comprises 0.025 to 10.00%, preferably 0.75 to 5% and especially 1.00 to 4.00% by weight of the dry weight of the composition.</p><p>13. A primer composition according to any one of claims 10 to 12, wherein the ratio of the starch component to the oxidant is 1:6. I...</p><p>I *1*.</p><p>14. A primer composition according to any one of the preceding claims, a binding agent selected from BAL latex binder or a wallpaper paste comprising carboxymethylcellUlose and sodium hydroxyethylcellu lose.</p><p>15. A primer according to any one of the preceding claims comprising 6.00% of red phosphorus, 60.00% of potassium chlorate, 29.50 to 33.00% of an inert filler, 0.50 to 4.00% of cornflour and 0.50% of wallpaper paste by dry weight of the composition.</p><p>16. A primer according to any one of claims 1 to 14 comprising
- 2.00% of red phosphorus, 97.00% of potassium chlorate, 0.50% of wallpaper paste and 0.50% of a BAL latex binder by dry weight of the composition.</p><p>17. A method of preparing a primer according to any one of the preceding claims comprising the steps of a. combining water in an amount of 36% of the final weight of the dry composition to a mixture of phosphorus, inert filler and starch component; -g-b. adding the oxidising agent to the wet mixture and thoroughlY combining the resulting mixture of components; and c. adding the binding agent to the mixture obtained from (b) thereby to give a paste suitab'e for placement in a cup of a perCUSSiOfl cap.</p><p>18. A percuSSIOfl cap comprising a stainless steel cup and a primer composition according to any one of claims 1 to 16.</p><p>19. An ammunition cartridge comprising one or more percussion caps according to claim 18.</p><p>20. An ammunition cartridge according to claim 19 which is a double rSS primer propellant free cartridge.</p><p>21. An ammunition cartridge according to claim 19, which further comprises a propellant. * . I *11 4 I</p><p>* * *,</p>
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0607472A GB2437076A (en) | 2006-04-13 | 2006-04-13 | Primer composition |
PCT/GB2007/000555 WO2007119037A1 (en) | 2006-04-13 | 2007-02-16 | Primer compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0607472A GB2437076A (en) | 2006-04-13 | 2006-04-13 | Primer composition |
Publications (2)
Publication Number | Publication Date |
---|---|
GB0607472D0 GB0607472D0 (en) | 2006-05-24 |
GB2437076A true GB2437076A (en) | 2007-10-17 |
Family
ID=36571799
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB0607472A Withdrawn GB2437076A (en) | 2006-04-13 | 2006-04-13 | Primer composition |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB2437076A (en) |
WO (1) | WO2007119037A1 (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3437534A (en) * | 1963-11-18 | 1969-04-08 | Us Navy | Explosive composition containing aluminum,potassium perchlorate,and sulfur or red phosphorus |
GB1286612A (en) * | 1969-02-19 | 1972-08-23 | Catalyst Research Corp | Pyrotechnic primers |
GB1445564A (en) * | 1973-07-31 | 1976-08-11 | Pains Wessex Ltd | Pyrotechnic or other combustible devices |
GB2273702A (en) * | 1991-01-08 | 1994-06-29 | Bryant & May Ltd | Match Head Formulations |
WO1999036745A1 (en) * | 1998-01-13 | 1999-07-22 | Senco Products. Inc. | Propellant strip assembly and propellant charge structure |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US157856A (en) * | 1874-12-15 | Improvement in explosive compounds | ||
US1831760A (en) * | 1928-07-11 | 1931-11-10 | Wieben Anella | Igniting composition |
US2194480A (en) * | 1938-03-07 | 1940-03-26 | Charles H Pritham | Noncorrosive priming composition |
US2649047A (en) * | 1945-03-13 | 1953-08-18 | Martin S Silverstein | Primer |
US3118798A (en) * | 1961-10-26 | 1964-01-21 | Olin Mathieson | Composition and method of forming |
US3187671A (en) * | 1962-08-01 | 1965-06-08 | Quinlan Joseph | Primer for consumable round |
US3420137A (en) * | 1967-08-18 | 1969-01-07 | Olin Mathieson | Contained compacted ammunition primer composition and method of preparation |
US5945627A (en) * | 1996-09-19 | 1999-08-31 | Ici Canada | Detonators comprising a high energy pyrotechnic |
GB9920205D0 (en) * | 1999-08-27 | 1999-10-27 | Lambeth Pty Ltd | Training cartridge of a self loading gun |
GB0002767D0 (en) * | 2000-02-08 | 2000-03-29 | Lambeth Pty Ltd | Improvements in and relating to training ammunition |
DE102004001980A1 (en) * | 2003-01-14 | 2004-07-22 | Ruag Ammotec Gmbh | Propellant charge useful in weapons training systems comprises a soft friction material |
GB0327492D0 (en) * | 2003-11-26 | 2003-12-31 | Utm Ip Ltd | Low energy training cartridge |
-
2006
- 2006-04-13 GB GB0607472A patent/GB2437076A/en not_active Withdrawn
-
2007
- 2007-02-16 WO PCT/GB2007/000555 patent/WO2007119037A1/en active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3437534A (en) * | 1963-11-18 | 1969-04-08 | Us Navy | Explosive composition containing aluminum,potassium perchlorate,and sulfur or red phosphorus |
GB1286612A (en) * | 1969-02-19 | 1972-08-23 | Catalyst Research Corp | Pyrotechnic primers |
GB1445564A (en) * | 1973-07-31 | 1976-08-11 | Pains Wessex Ltd | Pyrotechnic or other combustible devices |
GB2273702A (en) * | 1991-01-08 | 1994-06-29 | Bryant & May Ltd | Match Head Formulations |
WO1999036745A1 (en) * | 1998-01-13 | 1999-07-22 | Senco Products. Inc. | Propellant strip assembly and propellant charge structure |
Also Published As
Publication number | Publication date |
---|---|
WO2007119037A1 (en) | 2007-10-25 |
GB0607472D0 (en) | 2006-05-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU2714187C1 (en) | Non-rusting impact ignition composition | |
US8784583B2 (en) | Priming mixtures for small arms | |
CA2794793C (en) | Non-toxic, heavy-metal free sensitized explosive percussion primers and methods of preparing the same | |
AU2008258443B2 (en) | Cartridged ammunition, particularly blank ammunition | |
JPH09506326A (en) | Lead-free detonation mixture for percussion tubes | |
JPH11512697A (en) | Non-toxic rimfire primer | |
RU2415831C1 (en) | Explosive composition with multifunctional action | |
US4570540A (en) | LOVA Type black powder propellant surrogate | |
RU2110505C1 (en) | Pyrotechnic impact composition for central impact detonators in shooting arm cartridges | |
GB2437076A (en) | Primer composition | |
US4534810A (en) | Red phosphorous smoke producing composition | |
JP4057779B2 (en) | Illumination bullet with igniter prepared from an extrudable igniter composition | |
GB2437077A (en) | Primer cup and composition | |
GB2446600A (en) | Training cartridge utilising a primer composition that eliminates the need for a primer cup | |
CA2972106C (en) | Tungsten oxide primer compositions | |
RU2484076C2 (en) | Pyrotechnical ignition-blow-out and ignition-rupture composition | |
AU759857B2 (en) | Priming composition | |
US3556009A (en) | Delay initiators | |
US5189249A (en) | Gel propellant ammunition | |
US1312156A (en) | Pbjming charge | |
RU2144523C1 (en) | Pyrotechnic percussion inflammable composition for circular inflammation cartridges | |
RU2253084C1 (en) | High-explosive ammunition | |
US20190023629A1 (en) | Pyrotechnic compositions | |
Dahlberg | New low-sensitivity modular charge propellant based on GUDN | |
US1106343A (en) | Priming charge. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |