US20130305952A1 - Ignition powder composition for igniter - Google Patents
Ignition powder composition for igniter Download PDFInfo
- Publication number
- US20130305952A1 US20130305952A1 US13/810,120 US201113810120A US2013305952A1 US 20130305952 A1 US20130305952 A1 US 20130305952A1 US 201113810120 A US201113810120 A US 201113810120A US 2013305952 A1 US2013305952 A1 US 2013305952A1
- Authority
- US
- United States
- Prior art keywords
- igniter
- powder
- ignition
- mass
- metal
- 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.)
- Abandoned
Links
- 239000000843 powder Substances 0.000 title claims abstract description 184
- 239000000203 mixture Substances 0.000 title claims abstract description 120
- 229910052751 metal Inorganic materials 0.000 claims abstract description 49
- 239000002184 metal Substances 0.000 claims abstract description 49
- 229910052987 metal hydride Inorganic materials 0.000 claims abstract description 26
- 150000004681 metal hydrides Chemical class 0.000 claims abstract description 26
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims abstract description 23
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims abstract description 21
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims abstract description 20
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims abstract description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 6
- -1 titanium hydride Chemical compound 0.000 claims description 15
- 229910000048 titanium hydride Inorganic materials 0.000 claims description 11
- QSGNKXDSTRDWKA-UHFFFAOYSA-N zirconium dihydride Chemical compound [ZrH2] QSGNKXDSTRDWKA-UHFFFAOYSA-N 0.000 claims description 10
- 229910000568 zirconium hydride Inorganic materials 0.000 claims description 10
- 230000035945 sensitivity Effects 0.000 abstract description 57
- 238000010304 firing Methods 0.000 abstract description 38
- 238000000034 method Methods 0.000 description 25
- 239000011230 binding agent Substances 0.000 description 23
- MLFHJEHSLIIPHL-UHFFFAOYSA-N isoamyl acetate Chemical compound CC(C)CCOC(C)=O MLFHJEHSLIIPHL-UHFFFAOYSA-N 0.000 description 22
- 239000002245 particle Substances 0.000 description 20
- 238000012360 testing method Methods 0.000 description 19
- 238000004519 manufacturing process Methods 0.000 description 18
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 description 14
- 229910001487 potassium perchlorate Inorganic materials 0.000 description 14
- 238000004880 explosion Methods 0.000 description 11
- 229940117955 isoamyl acetate Drugs 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 229910052721 tungsten Inorganic materials 0.000 description 11
- 239000010937 tungsten Substances 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 9
- 239000003623 enhancer Substances 0.000 description 9
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 7
- 239000008187 granular material Substances 0.000 description 7
- 239000007800 oxidant agent Substances 0.000 description 7
- 229910052726 zirconium Inorganic materials 0.000 description 7
- 239000000395 magnesium oxide Substances 0.000 description 6
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 6
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 6
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 6
- 238000002485 combustion reaction Methods 0.000 description 5
- 238000005469 granulation Methods 0.000 description 5
- 230000003179 granulation Effects 0.000 description 5
- 239000000020 Nitrocellulose Substances 0.000 description 4
- 238000007605 air drying Methods 0.000 description 4
- 229920001220 nitrocellulos Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000002923 metal particle Substances 0.000 description 3
- 235000010333 potassium nitrate Nutrition 0.000 description 3
- 239000004323 potassium nitrate Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 229910001485 alkali metal perchlorate Inorganic materials 0.000 description 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- KOPBYBDAPCDYFK-UHFFFAOYSA-N caesium oxide Chemical compound [O-2].[Cs+].[Cs+] KOPBYBDAPCDYFK-UHFFFAOYSA-N 0.000 description 2
- 229910001942 caesium oxide Inorganic materials 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- XXQBEVHPUKOQEO-UHFFFAOYSA-N potassium superoxide Chemical compound [K+].[K+].[O-][O-] XXQBEVHPUKOQEO-UHFFFAOYSA-N 0.000 description 2
- CPRMKOQKXYSDML-UHFFFAOYSA-M rubidium hydroxide Chemical compound [OH-].[Rb+] CPRMKOQKXYSDML-UHFFFAOYSA-M 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 description 2
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Chemical compound [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- MFGOFGRYDNHJTA-UHFFFAOYSA-N 2-amino-1-(2-fluorophenyl)ethanol Chemical compound NCC(O)C1=CC=CC=C1F MFGOFGRYDNHJTA-UHFFFAOYSA-N 0.000 description 1
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 1
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 description 1
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 description 1
- 239000004343 Calcium peroxide Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229910001051 Magnalium Inorganic materials 0.000 description 1
- SPAGIJMPHSUYSE-UHFFFAOYSA-N Magnesium peroxide Chemical compound [Mg+2].[O-][O-] SPAGIJMPHSUYSE-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- KHPLPBHMTCTCHA-UHFFFAOYSA-N ammonium chlorate Chemical compound N.OCl(=O)=O KHPLPBHMTCTCHA-UHFFFAOYSA-N 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- ZJRXSAYFZMGQFP-UHFFFAOYSA-N barium peroxide Chemical compound [Ba+2].[O-][O-] ZJRXSAYFZMGQFP-UHFFFAOYSA-N 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 1
- 229910000024 caesium carbonate Inorganic materials 0.000 description 1
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- YALMXYPQBUJUME-UHFFFAOYSA-L calcium chlorate Chemical compound [Ca+2].[O-]Cl(=O)=O.[O-]Cl(=O)=O YALMXYPQBUJUME-UHFFFAOYSA-L 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 description 1
- 235000019402 calcium peroxide Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- HPGPEWYJWRWDTP-UHFFFAOYSA-N lithium peroxide Chemical compound [Li+].[Li+].[O-][O-] HPGPEWYJWRWDTP-UHFFFAOYSA-N 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 229910012375 magnesium hydride Inorganic materials 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 229960004995 magnesium peroxide Drugs 0.000 description 1
- NNNSKJSUQWKSAM-UHFFFAOYSA-L magnesium;dichlorate Chemical compound [Mg+2].[O-]Cl(=O)=O.[O-]Cl(=O)=O NNNSKJSUQWKSAM-UHFFFAOYSA-L 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 150000004972 metal peroxides Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- WKMKTIVRRLOHAJ-UHFFFAOYSA-N oxygen(2-);thallium(1+) Chemical compound [O-2].[Tl+].[Tl+] WKMKTIVRRLOHAJ-UHFFFAOYSA-N 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- WPFGFHJALYCVMO-UHFFFAOYSA-L rubidium carbonate Chemical compound [Rb+].[Rb+].[O-]C([O-])=O WPFGFHJALYCVMO-UHFFFAOYSA-L 0.000 description 1
- 229910000026 rubidium carbonate Inorganic materials 0.000 description 1
- 229910001952 rubidium oxide Inorganic materials 0.000 description 1
- CWBWCLMMHLCMAM-UHFFFAOYSA-M rubidium(1+);hydroxide Chemical compound [OH-].[Rb+].[Rb+] CWBWCLMMHLCMAM-UHFFFAOYSA-M 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 1
- 229910001488 sodium perchlorate Inorganic materials 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229910000018 strontium carbonate Inorganic materials 0.000 description 1
- FRTABACCYANHFP-UHFFFAOYSA-L strontium chlorate Chemical compound [Sr+2].[O-]Cl(=O)=O.[O-]Cl(=O)=O FRTABACCYANHFP-UHFFFAOYSA-L 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- UHCGLDSRFKGERO-UHFFFAOYSA-N strontium peroxide Chemical compound [Sr+2].[O-][O-] UHCGLDSRFKGERO-UHFFFAOYSA-N 0.000 description 1
- 229910003438 thallium oxide Inorganic materials 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D5/00—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
- C06D5/06—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets by reaction of two or more solids
-
- 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
- C06C9/00—Chemical contact igniters; Chemical lighters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R21/00—Arrangements or fittings on vehicles for protecting or preventing injuries to occupants or pedestrians in case of accidents or other traffic risks
- B60R21/02—Occupant safety arrangements or fittings, e.g. crash pads
- B60R21/16—Inflatable occupant restraints or confinements designed to inflate upon impact or impending impact, e.g. air bags
- B60R21/26—Inflatable occupant restraints or confinements designed to inflate upon impact or impending impact, e.g. air bags characterised by the inflation fluid source or means to control inflation fluid flow
- B60R2021/26029—Ignitors
Definitions
- the present invention relates to an ignition powder composition for igniter and an igniter using the ignition powder composition.
- the present invention relates to an ignition powder composition for igniter used in electric initiators or airbags built in automobiles, and to an igniter (so-called squib) using the ignition powder composition.
- the present invention relates to an ignition powder composition for igniter meeting the required firing current sensitivity with lowered friction sensitivity and an igniter using the ignition powder composition.
- igniters have been developed as igniters provided for gas generators used in safety equipment of automobiles such as airbags or seat belt pretensioners. Such an igniter is generally charged with ignition powder which is ignited with little electrical energy, and the ignition powder works to activate the gas generator by ignition in immediate response to the thermal energy converted from the electrical energy.
- ignition powder compositions for igniter specifically, ignition powder such as a mixture of zirconium and potassium perchlorate (ZPP); a mixture of zirconium, tungsten, and potassium perchlorate (ZWPP); and the like.
- ZPP zirconium and potassium perchlorate
- ZWPP zirconium, tungsten, and potassium perchlorate
- various ignition powders have been practically developed in order to provide for the need for improved performance of safety equipment and improved safety in the production process of igniters for gas generators.
- JP 2007-518655T discloses a technique characterized by adding a combustion enhancer such as titanium hydride to a pyrotechnic composition which is a blend of zirconium and oxidizer.
- PTL 1 involves obtaining an ignition powder composition which is a single increment initiator charge containing zirconium as an essential ingredient, and ensures sufficient heat for ignition, and it is not aimed at lowering friction sensitivity of ignition powders.
- JP 2009-120424A discloses that an ignition powder composition for igniter in which metal powder contains potassium perchlorate and potassium nitrate can be used as ignition powder with lower friction sensitivity.
- the invention disclosed in PTL 2 lowers friction sensitivity of a conventional ignition powder by adding potassium nitrate thereto.
- JP 2001-348291A discloses a technique of controlling safety risk in handling metal powder while maintaining the firing current sensitivity with the use of metal powder formed of flat metal particles.
- this technique has the disadvantages that the metal powder is required to have specially shaped particles, production control of the metal powder is difficult, and the production cost is high.
- the purpose of the present invention is to solve the problems of existing techniques described above and to provide an ignition powder composition for igniter of which friction sensitivity is lowered with the required firing current sensitivity being achieved.
- the present inventor found that the friction sensitivity of an ignition powder composition for igniter can be lowered while achieving the firing current sensitivity required of ignition powder compositions for igniter, by preparing the ignition powder composition for igniter, containing metal hydride (A); metal powder (B) that is one or more selected from the group consisting of tungsten powder, molybdenum powder, aluminum powder, titanium powder, and magnesium powder; and perchlorate (C).
- A metal hydride
- B metal powder
- C perchlorate
- the present invention is as follows (1) to (8).
- the ignition powder composition for igniter according to the present invention can provide ignition powder for igniter, meeting the required firing current sensitivity with lowered friction sensitivity. Lowering friction sensitivity of ignition powder prevents accidents resulted from accidental ignition of ignition powder due to friction, which has been a problem in producing ignition powder and igniters. Safety in igniter production process can be improved, and quick response igniters can be produced. Moreover, a gas generator for seat belt pretensioner and a gas generator for airbag can be provided, which use igniters charged with such ignition powder compositions for igniter.
- FIG. 1 is a cross section view showing an example of an igniter of the present invention.
- FIG. 2 is a cross section view showing an example of a gas generator for seat belt pretensioner according to the present invention.
- FIG. 3 is a cross section view showing an example of a gas generator for airbag according to the present invention.
- An ignition powder composition for igniter according to the present invention is characterized by containing metal hydride (A); metal powder(s) (B) that is one or more selected from the group consisting of tungsten powder, molybdenum powder, aluminum powder, titanium powder, and magnesium powder; and perchlorate (C).
- A metal hydride
- B metal powder(s)
- C perchlorate
- the ignition powder composition for igniter according to the present invention will be described in detail below.
- Metal hydride (A) used in the present invention functions as a combustion component. Specifically, the metal hydride (A) works to generate heat by the oxidation in an ignition process and to provide heated metal particles and heated gas.
- Examples of the metal hydride (A) used in the present invention includes zirconium hydride, titanium hydride, aluminum hydride, magnesium hydride, calcium hydride, and the like. These metal hydrides (A) may be used alone or as a mixture of two or more of the metal hydrides. In terms of the stability and handleability of the ignition powder composition, zirconium hydride and/or titanium hydride are preferable; in particular, zirconium hydride is preferable.
- the particle size of the metal hydride (A) influences firing current sensitivity relating to the quick ignition response, and is determined as appropriate depending on the required performance of the igniter.
- the particle size used is preferably 1 ⁇ m to 10 ⁇ m.
- the content of the metal hydride (A) in the ignition powder composition for igniter according to the present invention is preferably 10 mass % to 50 mass %. More preferably, the content is in the range of 10 mass % to 40 mass %. When the content of metal hydride (A) is less than 10 mass %, sufficient output may not be achieved. When the content is more than 50 mass %, the firing current sensitivity required of the ignition powder composition for igniter may not be achieved.
- Metal powder (B) used in the present invention functions as a combustion component.
- the metal powder (B) used in the present invention is metal powder(s) (B) selected from the group consisting of tungsten powder, aluminum powder, magnesium powder, titanium powder, and molybdenum powder. These metal powders (B) may be used alone or as a mixture of two or more of the metal powders.
- the metal powder (B) content partly or entirely serves to generate heat in response to the oxidation in ignition and combustion processes, and to provide heated metal particles.
- tungsten powder or molybdenum powder is preferably used as the metal powder (B). In particular, it is more preferable to use tungsten powder.
- Metal powder (B) in a spherical shape, formed by a known method is preferably used.
- the particle size of the metal powder (B) influences firing current sensitivity relating to the quick ignition response, and is determined as appropriate depending on the required performance of the igniter.
- the metal powder (B) used preferably has a particle size of 0.01 ⁇ m to 5 ⁇ m.
- the content of the metal powder (B) used in the ignition powder composition for igniter according to the present invention is preferably in the range of 10 mass % to 50 mass % with respect to the ignition powder composition for igniter, more preferably in the range of 15 mass % to 45 mass %.
- the content of the metal powder (B) is less than 10 mass %, the firing current sensitivity required of the ignition powder composition for igniter may not be achieved. In contrast, a content of more than 50 mass % may results in lower output.
- Perchlorate (C) is used in the ignition powder composition for igniter according to the present invention, and the perchlorate (C) also serves as an oxidizer for oxidizing the metal hydride (A) and the metal powder (B).
- the perchlorate (C) include alkali metal perchlorate, alkaline earth metal perchlorate, ammonium perchlorate, and the like. Alkali metal perchlorate is preferable, and potassium perchlorate or sodium perchlorate is particularly preferable.
- the content of the perchlorate (C) in the ignition powder composition for igniter is preferably 20 mass % to 70 mass %, and more preferably in the range of 25 mass % to 60 mass %. When the content of the perchlorate (C) is less than 20 mass %, sufficient output may not be achieved. If the content is more than 70 mass %, the firing current sensitivity required of the ignition powder composition for igniter may not be achieved.
- the ignition powder composition for igniter of the present invention preferably has 10 mass % to 50 mass % of metal hydride (A), 10 mass % to 50 mass % of metal powder (B), and 20 mass % to 70 mass % of perchlorate (C). More preferably, the content of metal hydride (A) is in the range of 10 mass % to 40 mass %; metal powder (B): 15 mass % to 45 mass %; and perchlorate (C): 25 mass % to 60 mass %.
- the ignition powder composition for igniter of present invention more preferably contains zirconium hydride and/or titanium hydride as metal hydride (A), tungsten powder or molybdenum powder as metal powder (B), and potassium perchlorate as perchlorate (C).
- a preferred ignition powder composition include a composition containing zirconium hydride, tungsten, and potassium perchlorate.
- the composition preferably contains 10 mass % to 50 mass % of zirconium hydride, 10 mass % to 50 mass % of tungsten, and 20 mass % to 70 mass % of potassium perchlorate.
- Another preferable example may be a composition containing titanium hydride, tungsten, and potassium perchlorate.
- the composition preferably contains 10 mass % to 50 mass % of titanium hydride, 10 mass % to 50 mass % of tungsten, and 20 mass % to 70 mass % of potassium perchlorate.
- other metal powder As optional components, other metal powder, another oxidizer, a basic material, a binder, a compounding ingredient, and the like may be added as appropriate to the ignition powder composition for igniter of the present invention.
- metal powder may optionally be added to the metal powder (B) to be used together as a metal powder mixture.
- additional metal powders zirconium powder, magnalium powder, copper powder, beryllium powder, and the like can be used. It should be noted that the content of the additional metal powder to be added is preferably 10 mass % or less in the ignition powder composition for igniter.
- the ignition powder composition for igniter of the present invention can contain other oxidizer(s) as appropriate in addition to perchlorate (C).
- additional oxidizers include nitrates such as potassium nitrate, sodium nitrate, strontium nitrate, basic copper nitrate, magnesium nitrate, and ammonium nitrate; and chlorates such as sodium chlorate, potassium chlorate, magnesium chlorate, calcium chlorate, strontium chlorate, and ammonium chlorate.
- nitrates such as potassium nitrate, sodium nitrate, strontium nitrate, basic copper nitrate, magnesium nitrate, and ammonium nitrate
- chlorates such as sodium chlorate, potassium chlorate, magnesium chlorate, calcium chlorate, strontium chlorate, and ammonium chlorate.
- an oxidizer mixture of perchlorate(s) (C) and nitrates is anticipated to balance the firing current sensitivity and lower friction sensitivity, so that it is preferably expected to improve the effect of the ignition powder composition according to the present invention.
- the content of the additional oxidizer is preferably 30 mass % or less in the ignition powder composition for igniter.
- the ignition powder composition for igniter of the present invention preferably contains a further additional basic material as appropriate.
- the blending of the basic material can suppress corrosion of metal parts of the igniter.
- Specific examples of the basic material include metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide, rubidium hydroxide, cesium hydroxide, magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide, and aluminum hydroxide; metal oxides such as lithium oxide, sodium oxide, potassium oxide, rubidium oxide, cesium oxide, magnesium oxide, calcium oxide, strontium oxide, barium oxide, zinc oxide, thallium oxide, and cesium oxide; metal peroxides such as lithium peroxide, sodium peroxide, potassium peroxide, rubidium peroxide, cesium peroxide, magnesium peroxide, calcium peroxide, strontium peroxide, and barium peroxide; and metal carbonates such as lithium carbonate, sodium carbonate, potassium carbonate, rubidium carbonate, cesium carbonate
- the content of the basic material is preferably 10 mass % or less in the ignition powder composition for igniter. Considering the relative proportions of each component in the ignition powder composition, in particular, the content is preferably 5 mass % or less.
- the ignition powder composition for igniter of the present invention preferably contains a binder in addition.
- the blending of the binder makes it possible to improve breaking strength and various mechanical properties of the ignition powder composition for igniter to be consolidated.
- organic binders such as a metal salt of carboxymethyl cellulose; polysaccharide derivatives such as hydroxyethyl cellulose, cellulose acetate, cellulose propionate, cellulose acetate butyrate, nitrocellulose, guar gum, polyvinyl alcohol, polyacrylamide, and starch; salt of stearic acid; fluoro-rubber; SBS rubber; and the like can be used.
- These binders may be used alone or as a mixture of two or more of the binders.
- the content of the binder is preferably 5 mass % or less in the ignition powder composition for igniter.
- the binder may be mixed to the ignition powder composition as it is, or may be mixed to the ignition powder composition with a suitable solvent added to the binder.
- a suitable solvent can be used without any particular problem as long as it is inert against the binder and excellent in dispersibility or in solubility.
- the solvent preferably has a property of being vaporizable in a drying process in view of the production process, and vaporizable organic solvents such as hydrocarbons, esters, or ketones are preferably used.
- the ignition powder composition for igniter of the present invention can be obtained by blending various combinations of any components suitably selected depending on the necessity into the metal hydride (A), the metal powder (B), and the perchlorate (C) and mixing them, thus producing powdered ignition powder for igniter.
- the mixture of the composition components may be granulated to produce the ignition powder for igniter as granules.
- the mixing may be performed by a mixing method, for example, the metal hydride (A), the metal powder (B), the perchlorate (C), and the optional components are mixed in a mixer to obtain a mixture thereof.
- a binder dissolved in a solvent is added to a mixture in which a given component such as other metal powder is added to the mixture of the metal hydride (A) and the metal powder (B), and they are mixed in a mixer.
- perchlorate (C) a given other oxidizer, a basic material, and the like are added to the above mixture, and they are further mixed to obtain a mixture of them.
- Examples of the granulation method include a method of adding a binder component to obtain a mixture through a mixing process, air-drying the mixture on a pallet, and then passing it through a screen to obtain granules.
- the particle size of the granules to be obtained is determined depending on the mesh size of the screen.
- the particle size is preferably in the range of 1.0 mm or less, more preferably in the range of 0.8 mm or less.
- the particle size is preferably regular. However, when the mesh is excessively coarse, regular particle size is not achieved, whereas the mixture hardly passes through a screen having excessively fine mesh. The mesh size should be determined carefully.
- ignition powder is prepared through operation processes, in which the ignition powder composition is vulnerable to mechanical contact or it is physically moved, such as measurement or transfer of each material component, in addition to the mixing process and the granulation process. Therefore, the production of ignition powder with high friction sensitivity requires careful handling.
- the ignition powder composition for igniter of the present invention has lower friction sensitivity, has such properties that greatly improve handling safety in the production process, and thus has significantly beneficial effects.
- the ignition powder composition for igniter of the present invention can achieve lower friction sensitivity while maintaining the firing current sensitivity.
- the ignition powder composition has an effect of improving safety in the ignition powder preparation process. Applying the ignition powder to an igniter can ensure safety in the igniter production process while ensuring quick response of the igniter.
- the present invention involves an igniter using the above ignition powder composition for igniter.
- the igniter of the present invention is not limited in particular except that the above ignition powder composition for igniter is used.
- the igniter can be produced by a known method.
- the igniter of the present invention will be described in detail below with reference to FIG. 1 .
- FIG. 1 is a cross section view of an example of an igniter of the present invention.
- An igniter 1 shown in FIG. 1 is equipped with a cup 6 for containing ignition powder 2 , a cover 9 for holding a cup 6 , a plug 7 in which connector pins 8 for electrical connection to the outside are fixed by insulator 4 , and a bridge wire 3 connected between the connector pins 8 , in contact with the ignition powder 2 .
- the joint area between the plug 7 and the cup 6 and the joint areas between the plug 7 and the connector pins 8 are covered with an insulating resin 5 to be protected.
- the igniter 1 of the present invention may be further equipped with known components ordinarily used for igniters.
- the igniter 1 of the present invention is required to use ignition powder which is the above ignition powder composition for igniter of the present invention or consolidated powder, as the ignition powder 2 .
- the operation of the igniter 1 in FIG. 1 will be described. Detecting a collision of a vehicle, a sensor (not shown) sends a signal to a control unit (an energy source)(not shown), and the control unit having detected this signal supplies energy to the connector pins 8 .
- the bridge wire 3 generates Joule heat due to electric current supplied by the energy source; the ignition powder 2 in contact with the bridge wire 3 is ignited by the heat; the cup 6 is broken by the heat energy and the generated pressure; and the flame propagates out of the igniter 1 ; thus, the function of an igniter is achieved.
- the ignition powder 2 is required to have sufficient ignition sensitivity performance to ignite in quick response to the heat generated by the bridge wire 3 .
- a plug assembly in which the plug 7 is equipped with the connector pins 8 , the bridge wire 3 , and the like, is installed into the cup 6 charged with the ignition powder 2 and fixed. After that, the periphery of the cup 6 is covered with the cover 9 , and they are fixed with insulating resin 5 by over molding. Thus, the igniter 1 can be produced.
- the ignition powder 2 undergoes physical movement and mechanical contact friction through a measuring process, a loading process of loading the cup 6 , a plug assembly installing process, and a plug fixing process. Thus, the igniter 1 is produced.
- the ignition powder composition for igniter of the present invention has quick igniting properties while maintaining the same firing current sensitivity as existing generally used ignition powders. Further, the ignition powder composition has lowered friction sensitivity, and has such properties that significantly improve handling safety in production of the igniter.
- the ignition powder composition of the present invention is applied to the igniter, so that the production safety is improved and the igniter meeting the specified sensitivity performance can be provided.
- the present invention includes a gas generator using the above igniter.
- the gas generator is preferably used as a micro gas generator used for the activation of a seat belt pretensioner. Alternatively, it is preferably used as a gas generator for deploying an airbag.
- FIG. 2 is a cross section view of an example of a gas generator for seat belt pretensioner using an igniter of the present invention.
- a gas generator 11 shown in FIG. 2 is equipped with a cup 13 for containing gas generants 12 which generates gas by combustion; an igniter 14 placed inside the cup 13 , for igniting the gas generants 12 by supplied energy, which is provided with connector pins 16 for electrical connection to the outside; and a holder 15 for fixing the cup 13 and the igniter 14 .
- the gas generator 11 may be further equipped with known components ordinarily used for gas generators.
- a sensor sends a signal to a control unit (an energy source)(not shown), and the control unit having detected this signal supplies energy to the connector pins 16 .
- a bridge wire inside the igniter 14 generates heat, and the ignition powder, with which the igniter 14 is loaded, is ignited by the generated heat, so that the flame propagates in the cup 13 of the igniter 14 .
- the flame combusts the gas generants 12 to generate a large amount of gas.
- the large amount of gas generated is introduced into the seat belt pretensioner (not shown) to increase the pressure in the seat belt pretensioner; thus, the seat belt pretensioner is operated and the seat belt is fastened.
- a gas generator for airbag of the present invention will be described in detail with reference to FIG. 3 .
- FIG. 3 is a cross section view of an example of a gas generator for airbag using an igniter of the present invention.
- a gas generator 21 shown in FIG. 3 has an outer envelope including a upper housing 22 which is made of a metal container provided with some gas outlets 26 , and an igniter 23 of the present invention and a filter 25 are installed inside the gas generator 21 .
- Space inside the gas generator 21 is filled with a gas generants 24 , and an enhancer chamber is provided in the proximity of the igniter 23 .
- the enhancer chamber is charged with enhancer (booster charge) 27 which propagates the ignition flame generated by the igniter 23 to the gas generants 24 .
- the gas generator 21 may be further equipped with known components ordinarily used for gas generators. Generally used known materials can be used for the enhancer 27 .
- FIG. 3 illustrates a so-called disk-shaped gas generator having a short cylindrical shape.
- the gas generator for deploying an airbag according to the present invention is not limited, and the igniter of the present invention can be suitably applied to a cylinder gas generator having a long cylindrical shape or a hybrid gas generator including a small amount of pyrotechnic ignition composition and a high pressure gas cylinder as well.
- a sensor (not shown) sends a signal to a control unit (an energy source)(not shown), and the control unit having detected this signal sends energy to the igniter 23 .
- a bridge wire provided inside the igniter 23 generates heat, and the ignition powder, with which the igniter 23 is loaded, is ignited by the generated heat, so that the flame propagates in the enhancer chamber of the igniter 23 .
- the enhancer with which the enhancer chamber is loaded, is ignited by the flame; more intense flame and high temperature and pressure gas are passed to the gas generants 24 ; and the gas generants 24 are combusted and generate a large amount of gas.
- the large amount of generated gas passes through the filter 25 , flows out through gas outlets 26 to be introduced into the airbag, and thus deploys the airbag.
- Nitrocellulose was dissolved as a binder in isoamyl acetate to prepare an isoamyl acetate solution having a binder concentration of 2 mass %.
- 1.5 g of the isoamyl acetate solution of the above binder (binder concentration: 2 mass %) was added to a mixture of 8.55 g of zirconium hydride (particle size: 2.5 ⁇ m), 9.6 g of tungsten (particle size: 0.6 ⁇ m to 0.8 ⁇ m), 11.85 g of potassium perchlorate (particle size: 12 ⁇ m to 18 ⁇ m), and 0.15 g of magnesium oxide.
- 11 g of isoamyl acetate was further added and mixed together in a mixer.
- Example 1 After the mixing, the obtained mixture was spread on a palette and air-dried. After the air-drying, the mixture was passed through a 24 mesh (about 0.8 to 0.6 mm aperture) screen for granulation, and the obtained granules were introduced into a dryer to be dried at 60° C. Thus, ignition powder for igniter (approximately 30 g) of Example 1 was obtained.
- ignition powders for igniter of Examples 2 to 4 were prepared by the same preparation method as Example 1 with the component ratios of the components being altered as shown in Table 1.
- Nitrocellulose was dissolved as a binder in isoamyl acetate to prepare an isoamyl acetate solution having a binder concentration of 1.3 mass %.
- 45 g of the above isoamyl acetate solution (binder concentration: 1.3 mass %) was added to a mixture of 150 g of zirconium (particle size: 2 ⁇ m) and 175 g of tungsten (particle size: 0.6 ⁇ m to 0.8 ⁇ m), and after that, 50 g of isoamyl acetate was further added and mixed together in a mixer. Then, 175 g of potassium perchlorate, 2.5 g of magnesium oxide, and 60 g of isoamyl acetate were added and mixed in the mixer.
- ignition powder for igniter (approximately 500 g) was obtained.
- compositions of the ignition powders for igniter of Examples 1 to 4 and Comparative Example are shown in Table 1. The contents are each expressed in mass ratio in reference to the whole composition.
- Friction Sensitivity Test (Test Method Based on JIS K 4810)
- the ignition powder of Examples or Comparative Example was held between a ceramic friction peg and a ceramic friction plate attached to the BAM friction tester, and the friction plate was moved horizontally with a load being applied thereto. Thus, a friction sensitivity test was performed. The friction sensitivity level was examined from the relationship between the applied load and whether explosion occurred or not. The level was evaluated by determining the load of the 1 ⁇ 6 explosion point with which explosion occurs once or was assumed to occur once in six times of continuous tests with the same load being applied.
- the firing current sensitivity was evaluated by the Bruceton test process used as a statistical method for calculating the minimum firing current and the maximum non-firing current.
- the igniter shown in FIG. 1 was loaded with 215 mg of the ignition powders of Examples 1 to 4 and Comparative Example to manufacture test igniters.
- the firing current was supplied depending on whether the test device was fired by the firing current or not.
- This test procedure was repeated 40 times, and the results were finally processed statically to find the mean value and estimate the standard deviation of the minimum firing current and maximum non-firing current.
- the confidence level was 95%, and the reliability was 99.9999%, with respect to the minimum firing current and the maximum non-firing current.
- the load of the 1 ⁇ 6 explosion point for each ignition powder of Examples 1 to 4 was found to be 5600 gf to 10800 gf.
- the load corresponding to the 1 ⁇ 6 explosion point was determined to be a load between 50 gf and 75 gf.
- the results of the friction sensitivity test showed that the load of 1 ⁇ 6 explosion points with the ignition powder compositions for igniter of Examples 1 to 4 was heavier than the ignition powder composition for igniter of Comparative Example. It was found that the friction sensitivities of the ignition powder compositions for igniter of Examples 1 to 4 were significantly lowered and accordingly they became less sensitive.
- Ignition powder for igniter of Example 5 was prepared by the same preparation method as Example 1 (1.5 g of an isoamyl acetate solution (binder concentration: 2 mass %) containing nitrocellulose as a binder was added to 0.15 g of magnesium oxide), except for using the composition containing 6.3 g of titanium hydride (particle size: 8.0 ⁇ m), 9.6 g of tungsten (particle size: 0.6 ⁇ m to 0.8 ⁇ m), and 14.1 g of potassium perchlorate (particle size: 12 ⁇ m to 18 ⁇ m).
- compositions of the ignition powders for igniter of Examples 5 and 6 are shown in Table 3. The contents are each expressed in mass ratio in reference to the whole composition.
- Example 5 Titanium hydride 21 13.9 Tungsten 32 32.9 Potassium perchlorate 47 53.2 Magnesium oxide 0.5 — Binder 0.1 —
- the igniters shown in FIG. 1 were loaded with 215 mg of the ignition powders for igniter of Examples 5 and 6 as the ignition powder 2 and test igniters were manufactured. A current of 1.2 A was supplied to the connector pins 8 for 2 ms to determine whether ignition occurred or not.
- the ignition powders of Examples 5 and 6 were found to be significantly less sensitive for friction from the load of 1 ⁇ 6 explosion point found in the friction sensitivity test.
- the ignition powders of Examples 5 and 6 were found to ignite by the method for checking activation of igniters under the conditions of supplying a current 1.2 A for 2 ms. Accordingly, it was determined that the ignition powders of Examples 5 and 6 can be used as the ignition powder compositions for igniter without any problem.
- the ignition powder compositions for igniter of the present invention were demonstrated to achieve the performance of lower friction sensitivity, meeting the required firing current sensitivity.
- the ignition powder having sensitivity that ensures ignition with very low current is obtained, and the ignition powder becomes less sensitive with lower friction sensitivity, which is significantly beneficial in improving safety in the production process.
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Abstract
An ignition powder composition for igniter of which friction sensitivity can be lowered with the required firing current sensitivity being achieved is provided as ignition powder for an igniter that is activated by an electrical signal. The ignition powder composition for igniter contains metal hydride (A); metal powder (B) that is one or more selected from the group consisting of tungsten powder, molybdenum powder, aluminum powder, titanium powder, and magnesium powder; and perchlorate (C).
Description
- The present invention relates to an ignition powder composition for igniter and an igniter using the ignition powder composition. In particular, the present invention relates to an ignition powder composition for igniter used in electric initiators or airbags built in automobiles, and to an igniter (so-called squib) using the ignition powder composition. In more particular, the present invention relates to an ignition powder composition for igniter meeting the required firing current sensitivity with lowered friction sensitivity and an igniter using the ignition powder composition.
- Various igniters have been developed as igniters provided for gas generators used in safety equipment of automobiles such as airbags or seat belt pretensioners. Such an igniter is generally charged with ignition powder which is ignited with little electrical energy, and the ignition powder works to activate the gas generator by ignition in immediate response to the thermal energy converted from the electrical energy. There are techniques using ignition powder compositions for igniter, specifically, ignition powder such as a mixture of zirconium and potassium perchlorate (ZPP); a mixture of zirconium, tungsten, and potassium perchlorate (ZWPP); and the like. Further, various ignition powders have been practically developed in order to provide for the need for improved performance of safety equipment and improved safety in the production process of igniters for gas generators.
- For example, JP 2007-518655T (PTL 1) discloses a technique characterized by adding a combustion enhancer such as titanium hydride to a pyrotechnic composition which is a blend of zirconium and oxidizer. However, PTL 1 involves obtaining an ignition powder composition which is a single increment initiator charge containing zirconium as an essential ingredient, and ensures sufficient heat for ignition, and it is not aimed at lowering friction sensitivity of ignition powders.
- As a method of ensuring safety in igniter production process by lowering friction sensitivity of an ignition powder composition for igniter, JP 2009-120424A (PTL 2) discloses that an ignition powder composition for igniter in which metal powder contains potassium perchlorate and potassium nitrate can be used as ignition powder with lower friction sensitivity. The invention disclosed in
PTL 2 lowers friction sensitivity of a conventional ignition powder by adding potassium nitrate thereto. - For metal powder which can be used in an ignition powder composition for igniter, it is known that the firing current sensitivity is generally improved as the metal powder is refined. On the other hand, the risk of accidental ignition in handling of the metal powder during production is increased, so that safety has been an issue. It is particularly known that zirconium generally used as metal powder contained in ignition powder is excellent in ignition performance, but is at high risk of accidental ignition when being handled during production.
- For such problems, JP 2001-348291A (PTL 3) discloses a technique of controlling safety risk in handling metal powder while maintaining the firing current sensitivity with the use of metal powder formed of flat metal particles. However, this technique has the disadvantages that the metal powder is required to have specially shaped particles, production control of the metal powder is difficult, and the production cost is high.
- PTL 1: JP 2007-518655T
- PTL 2: JP 2009-120424A PTL 3: JP 2001-348291A
- In order to improve safety in handling in production of an ignition powder composition for igniter, it is desired that the friction sensitivity of an ignition powder composition be lowered. However, in cases where the friction sensitivity of an ignition powder composition for igniter is lowered, the firing current sensitivity is simultaneously lowered, which has been a problem.
- The purpose of the present invention is to solve the problems of existing techniques described above and to provide an ignition powder composition for igniter of which friction sensitivity is lowered with the required firing current sensitivity being achieved.
- As a result of various studies made to achieve the above object, the present inventor found that the friction sensitivity of an ignition powder composition for igniter can be lowered while achieving the firing current sensitivity required of ignition powder compositions for igniter, by preparing the ignition powder composition for igniter, containing metal hydride (A); metal powder (B) that is one or more selected from the group consisting of tungsten powder, molybdenum powder, aluminum powder, titanium powder, and magnesium powder; and perchlorate (C). Thus, the present invention has been completed.
- The present invention is as follows (1) to (8).
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- (1) An ignition powder composition for igniter which contains metal hydride (A); metal powder (B) that is one or more selected from the group consisting of tungsten powder, molybdenum powder, aluminum powder, titanium powder, and magnesium powder; and perchlorate (C).
- (2) The ignition powder composition for igniter according to (1), in which the metal hydride (A) contains zirconium hydride and/or titanium hydride.
- (3) The ignition powder composition for igniter according to (1) or (2), in which the metal powder (B) contains tungsten powder.
- (4) The ignition powder composition for igniter according to any one of (1) to (3), in which the content of the metal hydride (A) is 10 mass % to 50 mass %.
- (5) The ignition powder composition for igniter according to any one of (1) to (4), in which the content of the metal hydride (A) is 10 mass % to 50 mass %, the content of the metal powder (B) is 10 mass % to 50 mass %, and the content of the perchlorate (C) is 20 mass % to 70 mass %.
- (6) An igniter using the ignition powder composition for igniter according to any one of (1) to (5).
- (7) A gas generator for seat belt pretensioner, using the igniter according to (6).
- (8) A gas generator for airbag, using the igniter according to (6).
- The ignition powder composition for igniter according to the present invention can provide ignition powder for igniter, meeting the required firing current sensitivity with lowered friction sensitivity. Lowering friction sensitivity of ignition powder prevents accidents resulted from accidental ignition of ignition powder due to friction, which has been a problem in producing ignition powder and igniters. Safety in igniter production process can be improved, and quick response igniters can be produced. Moreover, a gas generator for seat belt pretensioner and a gas generator for airbag can be provided, which use igniters charged with such ignition powder compositions for igniter.
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FIG. 1 is a cross section view showing an example of an igniter of the present invention. -
FIG. 2 is a cross section view showing an example of a gas generator for seat belt pretensioner according to the present invention. -
FIG. 3 is a cross section view showing an example of a gas generator for airbag according to the present invention. - An ignition powder composition for igniter according to the present invention is characterized by containing metal hydride (A); metal powder(s) (B) that is one or more selected from the group consisting of tungsten powder, molybdenum powder, aluminum powder, titanium powder, and magnesium powder; and perchlorate (C).
- The ignition powder composition for igniter according to the present invention will be described in detail below.
- Metal hydride (A) used in the present invention functions as a combustion component. Specifically, the metal hydride (A) works to generate heat by the oxidation in an ignition process and to provide heated metal particles and heated gas.
- Examples of the metal hydride (A) used in the present invention includes zirconium hydride, titanium hydride, aluminum hydride, magnesium hydride, calcium hydride, and the like. These metal hydrides (A) may be used alone or as a mixture of two or more of the metal hydrides. In terms of the stability and handleability of the ignition powder composition, zirconium hydride and/or titanium hydride are preferable; in particular, zirconium hydride is preferable.
- The particle size of the metal hydride (A) influences firing current sensitivity relating to the quick ignition response, and is determined as appropriate depending on the required performance of the igniter. The particle size used is preferably 1 μm to 10 μm.
- The content of the metal hydride (A) in the ignition powder composition for igniter according to the present invention is preferably 10 mass % to 50 mass %. More preferably, the content is in the range of 10 mass % to 40 mass %. When the content of metal hydride (A) is less than 10 mass %, sufficient output may not be achieved. When the content is more than 50 mass %, the firing current sensitivity required of the ignition powder composition for igniter may not be achieved.
- Metal powder (B) used in the present invention functions as a combustion component. The metal powder (B) used in the present invention is metal powder(s) (B) selected from the group consisting of tungsten powder, aluminum powder, magnesium powder, titanium powder, and molybdenum powder. These metal powders (B) may be used alone or as a mixture of two or more of the metal powders. The metal powder (B) content partly or entirely serves to generate heat in response to the oxidation in ignition and combustion processes, and to provide heated metal particles. In terms of reducing friction sensitivity of the ignition powder composition for igniter and facilitating handling in production, tungsten powder or molybdenum powder is preferably used as the metal powder (B). In particular, it is more preferable to use tungsten powder. Metal powder (B) in a spherical shape, formed by a known method is preferably used. The particle size of the metal powder (B) influences firing current sensitivity relating to the quick ignition response, and is determined as appropriate depending on the required performance of the igniter. The metal powder (B) used preferably has a particle size of 0.01 μm to 5 μm.
- The content of the metal powder (B) used in the ignition powder composition for igniter according to the present invention is preferably in the range of 10 mass % to 50 mass % with respect to the ignition powder composition for igniter, more preferably in the range of 15 mass % to 45 mass %. When the content of the metal powder (B) is less than 10 mass %, the firing current sensitivity required of the ignition powder composition for igniter may not be achieved. In contrast, a content of more than 50 mass % may results in lower output.
- Perchlorate (C) is used in the ignition powder composition for igniter according to the present invention, and the perchlorate (C) also serves as an oxidizer for oxidizing the metal hydride (A) and the metal powder (B). Examples of the perchlorate (C) include alkali metal perchlorate, alkaline earth metal perchlorate, ammonium perchlorate, and the like. Alkali metal perchlorate is preferable, and potassium perchlorate or sodium perchlorate is particularly preferable.
- The content of the perchlorate (C) in the ignition powder composition for igniter is preferably 20 mass % to 70 mass %, and more preferably in the range of 25 mass % to 60 mass %. When the content of the perchlorate (C) is less than 20 mass %, sufficient output may not be achieved. If the content is more than 70 mass %, the firing current sensitivity required of the ignition powder composition for igniter may not be achieved.
- The ignition powder composition for igniter of the present invention preferably has 10 mass % to 50 mass % of metal hydride (A), 10 mass % to 50 mass % of metal powder (B), and 20 mass % to 70 mass % of perchlorate (C). More preferably, the content of metal hydride (A) is in the range of 10 mass % to 40 mass %; metal powder (B): 15 mass % to 45 mass %; and perchlorate (C): 25 mass % to 60 mass %.
- The ignition powder composition for igniter of present invention more preferably contains zirconium hydride and/or titanium hydride as metal hydride (A), tungsten powder or molybdenum powder as metal powder (B), and potassium perchlorate as perchlorate (C).
- Specific examples of a preferred ignition powder composition include a composition containing zirconium hydride, tungsten, and potassium perchlorate. In this case, the composition preferably contains 10 mass % to 50 mass % of zirconium hydride, 10 mass % to 50 mass % of tungsten, and 20 mass % to 70 mass % of potassium perchlorate. Another preferable example may be a composition containing titanium hydride, tungsten, and potassium perchlorate. In this case, the composition preferably contains 10 mass % to 50 mass % of titanium hydride, 10 mass % to 50 mass % of tungsten, and 20 mass % to 70 mass % of potassium perchlorate.
- As optional components, other metal powder, another oxidizer, a basic material, a binder, a compounding ingredient, and the like may be added as appropriate to the ignition powder composition for igniter of the present invention.
- In the present invention, other metal powder may optionally be added to the metal powder (B) to be used together as a metal powder mixture. As the additional metal powders, zirconium powder, magnalium powder, copper powder, beryllium powder, and the like can be used. It should be noted that the content of the additional metal powder to be added is preferably 10 mass % or less in the ignition powder composition for igniter.
- Further, the ignition powder composition for igniter of the present invention can contain other oxidizer(s) as appropriate in addition to perchlorate (C). Specific examples of the additional oxidizers include nitrates such as potassium nitrate, sodium nitrate, strontium nitrate, basic copper nitrate, magnesium nitrate, and ammonium nitrate; and chlorates such as sodium chlorate, potassium chlorate, magnesium chlorate, calcium chlorate, strontium chlorate, and ammonium chlorate. These additional oxidizers may be used alone or as a mixture of two or more of the oxidizers. In particular, an oxidizer mixture of perchlorate(s) (C) and nitrates is anticipated to balance the firing current sensitivity and lower friction sensitivity, so that it is preferably expected to improve the effect of the ignition powder composition according to the present invention. The content of the additional oxidizer is preferably 30 mass % or less in the ignition powder composition for igniter.
- The ignition powder composition for igniter of the present invention preferably contains a further additional basic material as appropriate. The blending of the basic material can suppress corrosion of metal parts of the igniter. Specific examples of the basic material include metal hydroxides such as lithium hydroxide, sodium hydroxide, potassium hydroxide, rubidium hydroxide, cesium hydroxide, magnesium hydroxide, calcium hydroxide, strontium hydroxide, barium hydroxide, and aluminum hydroxide; metal oxides such as lithium oxide, sodium oxide, potassium oxide, rubidium oxide, cesium oxide, magnesium oxide, calcium oxide, strontium oxide, barium oxide, zinc oxide, thallium oxide, and cesium oxide; metal peroxides such as lithium peroxide, sodium peroxide, potassium peroxide, rubidium peroxide, cesium peroxide, magnesium peroxide, calcium peroxide, strontium peroxide, and barium peroxide; and metal carbonates such as lithium carbonate, sodium carbonate, potassium carbonate, rubidium carbonate, cesium carbonate, magnesium carbonate, calcium carbonate, strontium carbonate, and barium carbonate. These basic materials may be used alone or as a mixture of two or more of the basic materials. Further, theses basic materials may be either water-soluble or water-insoluble. Among them, metal oxides are preferable, and magnesium oxide is particularly preferable.
- The content of the basic material is preferably 10 mass % or less in the ignition powder composition for igniter. Considering the relative proportions of each component in the ignition powder composition, in particular, the content is preferably 5 mass % or less.
- The ignition powder composition for igniter of the present invention preferably contains a binder in addition. The blending of the binder makes it possible to improve breaking strength and various mechanical properties of the ignition powder composition for igniter to be consolidated. Specifically, organic binders such as a metal salt of carboxymethyl cellulose; polysaccharide derivatives such as hydroxyethyl cellulose, cellulose acetate, cellulose propionate, cellulose acetate butyrate, nitrocellulose, guar gum, polyvinyl alcohol, polyacrylamide, and starch; salt of stearic acid; fluoro-rubber; SBS rubber; and the like can be used. These binders may be used alone or as a mixture of two or more of the binders.
- The content of the binder is preferably 5 mass % or less in the ignition powder composition for igniter.
- In a method used in the present invention, the binder may be mixed to the ignition powder composition as it is, or may be mixed to the ignition powder composition with a suitable solvent added to the binder. The above solvent can be used without any particular problem as long as it is inert against the binder and excellent in dispersibility or in solubility. In addition, the solvent preferably has a property of being vaporizable in a drying process in view of the production process, and vaporizable organic solvents such as hydrocarbons, esters, or ketones are preferably used.
- The ignition powder composition for igniter of the present invention can be obtained by blending various combinations of any components suitably selected depending on the necessity into the metal hydride (A), the metal powder (B), and the perchlorate (C) and mixing them, thus producing powdered ignition powder for igniter. Alternatively, the mixture of the composition components may be granulated to produce the ignition powder for igniter as granules.
- In the production of the ignition powder for igniter of the present invention, the mixing may be performed by a mixing method, for example, the metal hydride (A), the metal powder (B), the perchlorate (C), and the optional components are mixed in a mixer to obtain a mixture thereof. In another alternative method, a binder dissolved in a solvent is added to a mixture in which a given component such as other metal powder is added to the mixture of the metal hydride (A) and the metal powder (B), and they are mixed in a mixer. After that, perchlorate (C), a given other oxidizer, a basic material, and the like are added to the above mixture, and they are further mixed to obtain a mixture of them.
- Examples of the granulation method include a method of adding a binder component to obtain a mixture through a mixing process, air-drying the mixture on a pallet, and then passing it through a screen to obtain granules. The particle size of the granules to be obtained is determined depending on the mesh size of the screen. For the ignition powder composition for igniter of the present invention, the particle size is preferably in the range of 1.0 mm or less, more preferably in the range of 0.8 mm or less. In a case of measuring the granules in a certain volume, the particle size is preferably regular. However, when the mesh is excessively coarse, regular particle size is not achieved, whereas the mixture hardly passes through a screen having excessively fine mesh. The mesh size should be determined carefully.
- As described above, ignition powder is prepared through operation processes, in which the ignition powder composition is vulnerable to mechanical contact or it is physically moved, such as measurement or transfer of each material component, in addition to the mixing process and the granulation process. Therefore, the production of ignition powder with high friction sensitivity requires careful handling. The ignition powder composition for igniter of the present invention has lower friction sensitivity, has such properties that greatly improve handling safety in the production process, and thus has significantly beneficial effects.
- The ignition powder composition for igniter of the present invention can achieve lower friction sensitivity while maintaining the firing current sensitivity. The ignition powder composition has an effect of improving safety in the ignition powder preparation process. Applying the ignition powder to an igniter can ensure safety in the igniter production process while ensuring quick response of the igniter. The present invention involves an igniter using the above ignition powder composition for igniter. The igniter of the present invention is not limited in particular except that the above ignition powder composition for igniter is used. The igniter can be produced by a known method.
- The igniter of the present invention will be described in detail below with reference to
FIG. 1 . -
FIG. 1 is a cross section view of an example of an igniter of the present invention. An igniter 1 shown inFIG. 1 is equipped with acup 6 for containingignition powder 2, acover 9 for holding acup 6, aplug 7 in which connector pins 8 for electrical connection to the outside are fixed byinsulator 4, and abridge wire 3 connected between the connector pins 8, in contact with theignition powder 2. The joint area between theplug 7 and thecup 6 and the joint areas between theplug 7 and the connector pins 8 are covered with an insulatingresin 5 to be protected. The igniter 1 of the present invention may be further equipped with known components ordinarily used for igniters. The igniter 1 of the present invention is required to use ignition powder which is the above ignition powder composition for igniter of the present invention or consolidated powder, as theignition powder 2. - The operation of the igniter 1 in
FIG. 1 will be described. Detecting a collision of a vehicle, a sensor (not shown) sends a signal to a control unit (an energy source)(not shown), and the control unit having detected this signal supplies energy to the connector pins 8. Thebridge wire 3 generates Joule heat due to electric current supplied by the energy source; theignition powder 2 in contact with thebridge wire 3 is ignited by the heat; thecup 6 is broken by the heat energy and the generated pressure; and the flame propagates out of the igniter 1; thus, the function of an igniter is achieved. Theignition powder 2 is required to have sufficient ignition sensitivity performance to ignite in quick response to the heat generated by thebridge wire 3. - Next, a general method for producing the igniter 1 will be described.
- A plug assembly, in which the
plug 7 is equipped with the connector pins 8, thebridge wire 3, and the like, is installed into thecup 6 charged with theignition powder 2 and fixed. After that, the periphery of thecup 6 is covered with thecover 9, and they are fixed with insulatingresin 5 by over molding. Thus, the igniter 1 can be produced. Theignition powder 2 undergoes physical movement and mechanical contact friction through a measuring process, a loading process of loading thecup 6, a plug assembly installing process, and a plug fixing process. Thus, the igniter 1 is produced. - The ignition powder composition for igniter of the present invention has quick igniting properties while maintaining the same firing current sensitivity as existing generally used ignition powders. Further, the ignition powder composition has lowered friction sensitivity, and has such properties that significantly improve handling safety in production of the igniter. The ignition powder composition of the present invention is applied to the igniter, so that the production safety is improved and the igniter meeting the specified sensitivity performance can be provided.
- The present invention includes a gas generator using the above igniter. The gas generator is preferably used as a micro gas generator used for the activation of a seat belt pretensioner. Alternatively, it is preferably used as a gas generator for deploying an airbag.
- The gas generator of the present invention will be described in detail with reference to
FIG. 2 .FIG. 2 is a cross section view of an example of a gas generator for seat belt pretensioner using an igniter of the present invention. Agas generator 11 shown inFIG. 2 is equipped with acup 13 for containinggas generants 12 which generates gas by combustion; anigniter 14 placed inside thecup 13, for igniting thegas generants 12 by supplied energy, which is provided withconnector pins 16 for electrical connection to the outside; and aholder 15 for fixing thecup 13 and theigniter 14. Thegas generator 11 may be further equipped with known components ordinarily used for gas generators. - The operations of the
gas generator 11 inFIG. 2 will be described. Detecting a collision, a sensor (not shown) sends a signal to a control unit (an energy source)(not shown), and the control unit having detected this signal supplies energy to the connector pins 16. In response, a bridge wire inside theigniter 14 generates heat, and the ignition powder, with which theigniter 14 is loaded, is ignited by the generated heat, so that the flame propagates in thecup 13 of theigniter 14. The flame combusts thegas generants 12 to generate a large amount of gas. The large amount of gas generated is introduced into the seat belt pretensioner (not shown) to increase the pressure in the seat belt pretensioner; thus, the seat belt pretensioner is operated and the seat belt is fastened. - A gas generator for airbag of the present invention will be described in detail with reference to
FIG. 3 . -
FIG. 3 is a cross section view of an example of a gas generator for airbag using an igniter of the present invention. Agas generator 21 shown inFIG. 3 has an outer envelope including aupper housing 22 which is made of a metal container provided with somegas outlets 26, and anigniter 23 of the present invention and afilter 25 are installed inside thegas generator 21. Space inside thegas generator 21 is filled with agas generants 24, and an enhancer chamber is provided in the proximity of theigniter 23. For a normal gas generator structure, the enhancer chamber is charged with enhancer (booster charge) 27 which propagates the ignition flame generated by theigniter 23 to thegas generants 24. Thegas generator 21 may be further equipped with known components ordinarily used for gas generators. Generally used known materials can be used for theenhancer 27. -
FIG. 3 illustrates a so-called disk-shaped gas generator having a short cylindrical shape. However, the gas generator for deploying an airbag according to the present invention is not limited, and the igniter of the present invention can be suitably applied to a cylinder gas generator having a long cylindrical shape or a hybrid gas generator including a small amount of pyrotechnic ignition composition and a high pressure gas cylinder as well. - The operations of the
gas generator 21 inFIG. 3 will be described. Detecting a collision of a vehicle, a sensor (not shown) sends a signal to a control unit (an energy source)(not shown), and the control unit having detected this signal sends energy to theigniter 23. In response, a bridge wire provided inside theigniter 23 generates heat, and the ignition powder, with which theigniter 23 is loaded, is ignited by the generated heat, so that the flame propagates in the enhancer chamber of theigniter 23. The enhancer, with which the enhancer chamber is loaded, is ignited by the flame; more intense flame and high temperature and pressure gas are passed to thegas generants 24; and thegas generants 24 are combusted and generate a large amount of gas. The large amount of generated gas passes through thefilter 25, flows out throughgas outlets 26 to be introduced into the airbag, and thus deploys the airbag. - The present invention will be described in more detail by means of the following examples. It should be noted that the present invention is not limited to the following examples.
- Nitrocellulose was dissolved as a binder in isoamyl acetate to prepare an isoamyl acetate solution having a binder concentration of 2 mass %. Next, 1.5 g of the isoamyl acetate solution of the above binder (binder concentration: 2 mass %) was added to a mixture of 8.55 g of zirconium hydride (particle size: 2.5 μm), 9.6 g of tungsten (particle size: 0.6 μm to 0.8 μm), 11.85 g of potassium perchlorate (particle size: 12 μm to 18 μm), and 0.15 g of magnesium oxide. Then, 11 g of isoamyl acetate was further added and mixed together in a mixer. After the mixing, the obtained mixture was spread on a palette and air-dried. After the air-drying, the mixture was passed through a 24 mesh (about 0.8 to 0.6 mm aperture) screen for granulation, and the obtained granules were introduced into a dryer to be dried at 60° C. Thus, ignition powder for igniter (approximately 30 g) of Example 1 was obtained.
- Further, ignition powders for igniter of Examples 2 to 4 were prepared by the same preparation method as Example 1 with the component ratios of the components being altered as shown in Table 1.
- Nitrocellulose was dissolved as a binder in isoamyl acetate to prepare an isoamyl acetate solution having a binder concentration of 1.3 mass %. Next, 45 g of the above isoamyl acetate solution (binder concentration: 1.3 mass %) was added to a mixture of 150 g of zirconium (particle size: 2 μm) and 175 g of tungsten (particle size: 0.6 μm to 0.8 μm), and after that, 50 g of isoamyl acetate was further added and mixed together in a mixer. Then, 175 g of potassium perchlorate, 2.5 g of magnesium oxide, and 60 g of isoamyl acetate were added and mixed in the mixer. After the mixing, the obtained mixture were spread on a palette and air-dried. After the air-drying, the mixture was passed through a 24 mesh screen for granulation, and the obtained granules were introduced into a dryer to be dried at 60° C. Thus, ignition powder for igniter (approximately 500 g) was obtained.
- The compositions of the ignition powders for igniter of Examples 1 to 4 and Comparative Example are shown in Table 1. The contents are each expressed in mass ratio in reference to the whole composition.
-
TABLE 1 Compara- Exam- Exam- Exam- Exam- tive (Unit: mass ratio) ple 1 ple 2ple 3ple 4Example Zirconium hydride 28.5 30 40 20 — Zirconium — — — — 30 Tungsten 32.0 35 20 40 35 Potassium 39.5 35 40 40 35 perchlorate Magnesium oxide 0.5 0.5 0.5 0.5 0.5 Binder 0.1 0.1 0.1 0.1 0.1 - The friction sensitivity test and the firing current sensitivity test were performed on each of the ignition powders for igniter obtained in accordance with Examples 1 to 4 and Comparative Example by the following method. Table 2 shows the results.
- (1) Friction Sensitivity Test (Test Method Based on JIS K 4810)
- The ignition powder of Examples or Comparative Example was held between a ceramic friction peg and a ceramic friction plate attached to the BAM friction tester, and the friction plate was moved horizontally with a load being applied thereto. Thus, a friction sensitivity test was performed. The friction sensitivity level was examined from the relationship between the applied load and whether explosion occurred or not. The level was evaluated by determining the load of the ⅙ explosion point with which explosion occurs once or was assumed to occur once in six times of continuous tests with the same load being applied.
- (2) Firing Current Sensitivity Test
- The firing current sensitivity was evaluated by the Bruceton test process used as a statistical method for calculating the minimum firing current and the maximum non-firing current. In brief, the igniter shown in
FIG. 1 was loaded with 215 mg of the ignition powders of Examples 1 to 4 and Comparative Example to manufacture test igniters. For the test igniter, some equally spaced levels were determined with respect to the firing current, and the firing current was supplied depending on whether the test device was fired by the firing current or not. This test procedure was repeated 40 times, and the results were finally processed statically to find the mean value and estimate the standard deviation of the minimum firing current and maximum non-firing current. Thus, the minimum firing current and maximum non-firing current meeting the desired reliability were determined. The confidence level was 95%, and the reliability was 99.9999%, with respect to the minimum firing current and the maximum non-firing current. -
TABLE 2 Firing current sensitivity Friction sensitivity Minimum Maximum Load of ⅙ firing non-firing explosion point current current [gf] [A] [A] Example 1 8000 1.20 0.53 Example 2 5600 0.93 0.47 Example 3 8000 1.02 0.52 Example 4 10800 0.92 0.40 Comparative 50 to 75 1.12 0.42 Example - In the friction sensitivity test, the load of the ⅙ explosion point for each ignition powder of Examples 1 to 4 was found to be 5600 gf to 10800 gf. On the other hand, for Comparative Example using conventional ignition powder, explosion occurred twice with a load of 75 gf, and no explosion occurred with a load of 50 gf. Therefore, the load corresponding to the ⅙ explosion point was determined to be a load between 50 gf and 75 gf. The results of the friction sensitivity test showed that the load of ⅙ explosion points with the ignition powder compositions for igniter of Examples 1 to 4 was heavier than the ignition powder composition for igniter of Comparative Example. It was found that the friction sensitivities of the ignition powder compositions for igniter of Examples 1 to 4 were significantly lowered and accordingly they became less sensitive.
- On the other hand, in terms of the firing current sensitivity, the minimum firing current and maximum non-firing current of ignition powders of Examples 1 to 4 were almost the same as those of the conventional ignition powder used in Comparative Example. Examples 1 to 4 had no trouble in using the ignition powders for igniter; they were found to meet the required firing current sensitivity.
- Ignition powder for igniter of Example 5 was prepared by the same preparation method as Example 1 (1.5 g of an isoamyl acetate solution (binder concentration: 2 mass %) containing nitrocellulose as a binder was added to 0.15 g of magnesium oxide), except for using the composition containing 6.3 g of titanium hydride (particle size: 8.0 μm), 9.6 g of tungsten (particle size: 0.6 μm to 0.8 μm), and 14.1 g of potassium perchlorate (particle size: 12 μm to 18 μm).
- In a mixer, 2.782 g of titanium hydride (particle size: 8.0 μm), 6.572 g of tungsten (particle size: 0.6 μm to 0.8 μm), 10.646 g of potassium perchlorate (particle size: 12 μm to 18 μm), and 7 g of isoamyl acetate were mixed together. After the mixing, the obtained mixture was spread on a palette and air-dried. After the air-drying, the mixture was passed through a 24 mesh (about 0.8 mm to 0.6 mm aperture) screen for granulation, and the obtained granules were introduced into a dryer to be dried at 60° C. Thus, ignition powder for igniter (approximately 20 g) of Example 6 was obtained.
- The compositions of the ignition powders for igniter of Examples 5 and 6 are shown in Table 3. The contents are each expressed in mass ratio in reference to the whole composition.
-
TABLE 3 Example 5 Example 6 Titanium hydride 21 13.9 Tungsten 32 32.9 Potassium perchlorate 47 53.2 Magnesium oxide 0.5 — Binder 0.1 — - The friction sensitivity test based on JIS K 4810 was performed on the ignition powders for igniter of Examples 5 and 6. Further, in order to confirm whether the ignition powders had an ignition function or not, the function test was carried out under the following test conditions. Table 4 shows the results.
- (3) Function Test
- The igniters shown in
FIG. 1 were loaded with 215 mg of the ignition powders for igniter of Examples 5 and 6 as theignition powder 2 and test igniters were manufactured. A current of 1.2 A was supplied to the connector pins 8 for 2 ms to determine whether ignition occurred or not. -
TABLE 4 Friction sensitivity; load Function of ⅙ explosion point (gf) test Example 5 10800 Ignition Example 6 19200 Ignition - The ignition powders of Examples 5 and 6 were found to be significantly less sensitive for friction from the load of ⅙ explosion point found in the friction sensitivity test. The ignition powders of Examples 5 and 6 were found to ignite by the method for checking activation of igniters under the conditions of supplying a current 1.2 A for 2 ms. Accordingly, it was determined that the ignition powders of Examples 5 and 6 can be used as the ignition powder compositions for igniter without any problem.
- The ignition powder compositions for igniter of the present invention were demonstrated to achieve the performance of lower friction sensitivity, meeting the required firing current sensitivity. The ignition powder having sensitivity that ensures ignition with very low current is obtained, and the ignition powder becomes less sensitive with lower friction sensitivity, which is significantly beneficial in improving safety in the production process.
- 1, 14, 23: Igniter
- 2: Ignition powder
- 3: Bridge wire
- 4: Insulator
- 5: Insulating resin
- 6, 13: Cup
- 7: Plug
- 8, 16: Connector pins
- 9: Cover
- 11, 21: Gas generator
- 12, 24: Gas generants
- 15: Holder
- 22: Upper housing
- 25: Filter
- 26: Gas outlets
- 27: Enhancer
Claims (9)
1. An ignition powder composition for igniter, comprising:
metal hydride (A);
metal powder (B) that is one or more selected from the group consisting of tungsten powder, molybdenum powder, aluminum powder, titanium powder, and magnesium powder; and
perchlorate (C).
2. The ignition powder composition for igniter according to claim 1 , wherein the metal hydride (A) contains zirconium hydride and/or titanium hydride.
3. The ignition powder composition for igniter according to claim 1 , wherein the metal powder (B) contains tungsten powder.
4. The ignition powder composition for igniter according to claim 1 , wherein the content of the metal hydride (A) is 10 mass % to 50 mass %.
5. The ignition powder composition for igniter according to claim 1 , wherein:
the content of the metal hydride (A) is 10 mass % to 50 mass %,
the content of the metal powder (B) is 10 mass % to 50 mass %, and
the content of the perchlorate (C) is 20 mass % to 70 mass %.
6. An igniter using the ignition powder composition for igniter according to claim 1 .
7. A gas generator for seat belt pretensioner, using the igniter according to claim 6 .
8. A gas generator for airbag, using the igniter according to claim 6 .
9. The ignition powder composition for igniter according to claim 2 , wherein the metal powder (B) contains tungsten powder.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
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| JP2010-160464 | 2010-07-15 | ||
| JP2010160464 | 2010-07-15 | ||
| PCT/JP2011/004023 WO2012008161A1 (en) | 2010-07-15 | 2011-07-14 | Igniting powder composition for igniters |
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| Publication Number | Publication Date |
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| US20130305952A1 true US20130305952A1 (en) | 2013-11-21 |
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ID=45469175
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/810,120 Abandoned US20130305952A1 (en) | 2010-07-15 | 2011-07-14 | Ignition powder composition for igniter |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20130305952A1 (en) |
| EP (1) | EP2594545B1 (en) |
| JP (1) | JP5819829B2 (en) |
| CN (1) | CN103052609B (en) |
| MX (1) | MX2013000536A (en) |
| SG (1) | SG186824A1 (en) |
| WO (1) | WO2012008161A1 (en) |
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| JP2023096436A (en) | 2021-12-27 | 2023-07-07 | 日本化薬株式会社 | igniters, and igniters containing them |
| CN115583862B (en) * | 2022-11-02 | 2023-06-16 | 中国科学技术大学 | Multi-acid-base low-power laser ignition method |
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| DE19823999C2 (en) * | 1998-05-28 | 2002-07-18 | Nico Pyrotechnik | Process for the manufacture of pyrotechnic igniters |
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| US6165296A (en) * | 1999-02-02 | 2000-12-26 | Autoliv Development As | Gas generant igniter composition and method |
| JP3819216B2 (en) | 2000-06-05 | 2006-09-06 | 住友チタニウム株式会社 | Metal powder for ignition |
| CZ305185B6 (en) * | 2001-05-10 | 2015-06-03 | Nippon Kayaku Kabushiki Kaisha | Igniting agent composition and fuse using such composition |
| US6941868B2 (en) * | 2003-06-26 | 2005-09-13 | Autoliv Asp, Inc. | Single increment initiator charge |
| US6905562B2 (en) * | 2003-09-04 | 2005-06-14 | Autoliv Asp, Inc. | Low density slurry bridge mix |
| FR2861389B1 (en) * | 2003-10-22 | 2006-03-10 | Davey Bickford | LOW SENSITIVE PYROTECHNIC COMPOSITION WITH STATIC ELECTRICITY AND ULTRASOUND. |
| JP2009120424A (en) * | 2007-11-13 | 2009-06-04 | Nippon Kayaku Co Ltd | Granular firing powder composition for igniter and igniter using the same |
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- 2011-07-14 EP EP11806494.8A patent/EP2594545B1/en not_active Not-in-force
- 2011-07-14 CN CN201180034704.5A patent/CN103052609B/en not_active Expired - Fee Related
- 2011-07-14 WO PCT/JP2011/004023 patent/WO2012008161A1/en active Application Filing
- 2011-07-14 MX MX2013000536A patent/MX2013000536A/en not_active Application Discontinuation
- 2011-07-14 US US13/810,120 patent/US20130305952A1/en not_active Abandoned
- 2011-07-14 JP JP2012524456A patent/JP5819829B2/en active Active
- 2011-07-14 SG SG2012095451A patent/SG186824A1/en unknown
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| US4757764A (en) * | 1985-12-20 | 1988-07-19 | The Ensign-Bickford Company | Nonelectric blasting initiation signal control system, method and transmission device therefor |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9051225B1 (en) * | 2009-06-12 | 2015-06-09 | Tk Holdings Inc. | Gas generator |
| US20160052481A1 (en) * | 2013-03-18 | 2016-02-25 | Hitachi Systems, Ltd. | Igniter, igniter assembly, and detection system and detection method therefor |
| US9688235B2 (en) * | 2013-03-18 | 2017-06-27 | Hitachi Systems, Ltd. | Igniter, igniter assembly, and detection system and detection method therefor |
| CN104311374A (en) * | 2014-10-20 | 2015-01-28 | 宜兴市阳生化工有限公司 | Novel sensitization bubble carrier colloidal emulsion explosive and preparation method thereof |
| US10107601B2 (en) * | 2015-10-06 | 2018-10-23 | Raytheon Company | Electrically operated pulse initiators and ignition |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5819829B2 (en) | 2015-11-24 |
| CN103052609B (en) | 2015-10-07 |
| SG186824A1 (en) | 2013-02-28 |
| EP2594545B1 (en) | 2015-09-09 |
| EP2594545A4 (en) | 2014-01-22 |
| MX2013000536A (en) | 2013-07-29 |
| EP2594545A1 (en) | 2013-05-22 |
| JPWO2012008161A1 (en) | 2013-09-05 |
| WO2012008161A1 (en) | 2012-01-19 |
| CN103052609A (en) | 2013-04-17 |
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| AS | Assignment |
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