JPWO2010103811A1 - GAS GENERATOR COMPOSITION, MOLDED BODY THEREOF, AND GAS GENERATOR USING THE SAME - Google Patents
GAS GENERATOR COMPOSITION, MOLDED BODY THEREOF, AND GAS GENERATOR USING THE SAME Download PDFInfo
- Publication number
- JPWO2010103811A1 JPWO2010103811A1 JP2011503708A JP2011503708A JPWO2010103811A1 JP WO2010103811 A1 JPWO2010103811 A1 JP WO2010103811A1 JP 2011503708 A JP2011503708 A JP 2011503708A JP 2011503708 A JP2011503708 A JP 2011503708A JP WO2010103811 A1 JPWO2010103811 A1 JP WO2010103811A1
- Authority
- JP
- Japan
- Prior art keywords
- mass
- gas
- perchlorate
- nitrate
- generant composition
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 141
- 239000007789 gas Substances 0.000 claims abstract description 300
- 239000002245 particle Substances 0.000 claims abstract description 46
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims abstract description 38
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims abstract description 37
- -1 nitrogen organic compound Chemical class 0.000 claims abstract description 34
- 239000007800 oxidant agent Substances 0.000 claims abstract description 33
- 230000001590 oxidative effect Effects 0.000 claims abstract description 30
- 229910002010 basic metal nitrate Inorganic materials 0.000 claims abstract description 21
- 229910001960 metal nitrate Inorganic materials 0.000 claims abstract description 19
- 239000000446 fuel Substances 0.000 claims abstract description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 87
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 claims description 25
- 229910001487 potassium perchlorate Inorganic materials 0.000 claims description 25
- NDEMNVPZDAFUKN-UHFFFAOYSA-N guanidine;nitric acid Chemical compound NC(N)=N.O[N+]([O-])=O.O[N+]([O-])=O NDEMNVPZDAFUKN-UHFFFAOYSA-N 0.000 claims description 19
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 claims description 18
- 239000011230 binding agent Substances 0.000 claims description 15
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 8
- 239000002893 slag Substances 0.000 claims description 7
- YTNLBRCAVHCUPD-UHFFFAOYSA-N 5-(1$l^{2},2,3,4-tetrazol-5-yl)-1$l^{2},2,3,4-tetrazole Chemical compound [N]1N=NN=C1C1=NN=N[N]1 YTNLBRCAVHCUPD-UHFFFAOYSA-N 0.000 claims description 6
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 claims description 6
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims description 6
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 claims description 6
- 150000003536 tetrazoles Chemical class 0.000 claims description 5
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 4
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 4
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 claims description 3
- 235000010333 potassium nitrate Nutrition 0.000 claims description 3
- 239000004323 potassium nitrate Substances 0.000 claims description 3
- 235000010344 sodium nitrate Nutrition 0.000 claims description 3
- 239000004317 sodium nitrate Substances 0.000 claims description 3
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 claims description 3
- 229910001488 sodium perchlorate Inorganic materials 0.000 claims description 3
- 150000003852 triazoles Chemical class 0.000 claims description 3
- 229910052728 basic metal Inorganic materials 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 238000002485 combustion reaction Methods 0.000 abstract description 35
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 238000012360 testing method Methods 0.000 description 47
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 41
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 28
- 230000000052 comparative effect Effects 0.000 description 24
- 239000000377 silicon dioxide Substances 0.000 description 20
- 239000008187 granular material Substances 0.000 description 18
- 235000019359 magnesium stearate Nutrition 0.000 description 14
- 239000004372 Polyvinyl alcohol Substances 0.000 description 13
- 239000000654 additive Substances 0.000 description 13
- 229920002451 polyvinyl alcohol Polymers 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 12
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 11
- 238000011049 filling Methods 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 230000000996 additive effect Effects 0.000 description 9
- 230000004043 responsiveness Effects 0.000 description 9
- 239000003623 enhancer Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000000465 moulding Methods 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 239000004927 clay Substances 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 230000007613 environmental effect Effects 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- 210000003141 lower extremity Anatomy 0.000 description 4
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 229910001485 alkali metal perchlorate Inorganic materials 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 230000001747 exhibiting effect Effects 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 3
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- IDCPFAYURAQKDZ-UHFFFAOYSA-N 1-nitroguanidine Chemical compound NC(=N)N[N+]([O-])=O IDCPFAYURAQKDZ-UHFFFAOYSA-N 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 2
- ULRPISSMEBPJLN-UHFFFAOYSA-N 2h-tetrazol-5-amine Chemical compound NC1=NN=NN1 ULRPISSMEBPJLN-UHFFFAOYSA-N 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 2
- 235000019399 azodicarbonamide Nutrition 0.000 description 2
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 229940075894 denatured ethanol Drugs 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 235000012438 extruded product Nutrition 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 2
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 2
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 2
- 238000007561 laser diffraction method Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
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- 239000013585 weight reducing agent Substances 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- MDTUWBLTRPRXBX-UHFFFAOYSA-N 1,2,4-triazol-3-one Chemical compound O=C1N=CN=N1 MDTUWBLTRPRXBX-UHFFFAOYSA-N 0.000 description 1
- WHQOKFZWSDOTQP-UHFFFAOYSA-N 2,3-dihydroxypropyl 4-aminobenzoate Chemical compound NC1=CC=C(C(=O)OCC(O)CO)C=C1 WHQOKFZWSDOTQP-UHFFFAOYSA-N 0.000 description 1
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 description 1
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- MTAYYBKXNAEQOK-UHFFFAOYSA-N 5-(2h-tetrazol-5-yl)-2h-tetrazole Chemical compound N1N=NC(C2=NNN=N2)=N1 MTAYYBKXNAEQOK-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
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- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 229910021503 Cobalt(II) hydroxide Inorganic materials 0.000 description 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 1
- 239000005750 Copper hydroxide Substances 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
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- MPCRDALPQLDDFX-UHFFFAOYSA-L Magnesium perchlorate Chemical compound [Mg+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O MPCRDALPQLDDFX-UHFFFAOYSA-L 0.000 description 1
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- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical compound [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- HURPOIVZCDCEEE-UHFFFAOYSA-N n-(2h-tetrazol-5-yl)nitramide Chemical compound [O-][N+](=O)NC=1N=NNN=1 HURPOIVZCDCEEE-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- UAGLZAPCOXRKPH-UHFFFAOYSA-N nitric acid;1,2,3-triaminoguanidine Chemical compound O[N+]([O-])=O.NNC(NN)=NN UAGLZAPCOXRKPH-UHFFFAOYSA-N 0.000 description 1
- TVIRJXQLFRFUCD-UHFFFAOYSA-N nitric acid;2h-tetrazol-5-amine Chemical compound O[N+]([O-])=O.NC1=NN=NN1 TVIRJXQLFRFUCD-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229940079938 nitrocellulose Drugs 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-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
- 229940068984 polyvinyl alcohol Drugs 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical group [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000452 restraining effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Images
Classifications
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- 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
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Organic Chemistry (AREA)
- Air Bags (AREA)
- Feeding, Discharge, Calcimining, Fusing, And Gas-Generation Devices (AREA)
Abstract
本発明は、優れた着火性及び燃焼性を有し、燃焼起動のための電気信号に迅速に呼応することが可能なガス発生剤組成物に関し、より詳細には、燃料成分（Ａ）として含窒素有機化合物と、酸化剤成分（Ｂ）として金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）並びに５０％粒径が１〜５０μｍの過塩素酸塩（Ｂ−２）とを含有し、酸化剤成分（Ｂ）の全質量中に占める前記過塩素酸塩（Ｂ−２）の含有量が５質量％以上で且つ３５質量％未満であることを特徴とするガス発生剤組成物に関するものである。The present invention relates to a gas generant composition having excellent ignitability and flammability and capable of quickly responding to an electrical signal for starting combustion, and more specifically, as a fuel component (A). Containing a nitrogen organic compound, metal nitrate and / or basic metal nitrate (B-1) as an oxidant component (B), and perchlorate (B-2) having a 50% particle size of 1 to 50 μm, The content of the perchlorate (B-2) in the total mass of the oxidant component (B) is 5% by mass or more and less than 35% by mass. It is.
Description
本発明は、ガス発生剤組成物及び該ガス発生剤組成物の成形体、並びに該ガス発生剤組成物の成形体を用いたガス発生器に関し、特には、燃焼起動のための電気信号に迅速に呼応し（即ち、燃焼起動のための電気信号に対する応答性に優れる）、車両搭乗者安全装置用ガス発生器への使用に好適なガス発生剤組成物に関するものである。 The present invention relates to a gas generant composition, a molded article of the gas generant composition, and a gas generator using the molded article of the gas generant composition, and more particularly to an electric signal for starting combustion. The gas generating composition is suitable for use in a gas generator for a vehicle occupant safety device.
自動車の安全性向上の方策において、近年、火薬を利用した車両搭乗者安全装置としてエアバッグ、シートベルトプリテンショナーが広く採用されている。エアバッグ装置の原理は、車両の衝突を検出したセンサーからの電気信号により、ガス発生器内に充填されているガス発生剤を燃焼させて大容量のガスを生成し、そのガス圧力によりエアバッグを乗員と車体内壁との間に展開させるものである。また、シートベルトプリテンショナーにおいても同様であり、車両の衝突をセンサーにより検知し、該センサーからの電気信号によりガス発生器に充填したガス発生剤を燃焼させてガスを生成し、そのガス圧力によりシートベルト巻取り機構を作動させ、そのシートベルトの拘束力を高めることにより乗員を保護するというものである。車両の衝突において、車両搭乗者安全装置用ガス発生器は、衝突感知センサーからの電気信号に対して極めて迅速な応答が要求される。即ち、該ガス発生器には、衝突感知センサーからの電気的な信号を受けてガス発生剤を燃焼させ、ガスを生成させると共に、その生成ガスの最大圧力に数十ミリ秒で到達する性能が要求される。 In the measures for improving the safety of automobiles, in recent years, airbags and seat belt pretensioners are widely used as vehicle occupant safety devices using explosives. The principle of the airbag device is that an electric signal from a sensor that detects a vehicle collision generates a large volume of gas by burning a gas generating agent filled in the gas generator. Is deployed between the occupant and the inner wall of the vehicle body. The same applies to a seat belt pretensioner, in which a vehicle collision is detected by a sensor, a gas generating agent filled in the gas generator is burned by an electric signal from the sensor, and a gas is generated. The occupant is protected by operating the seat belt winding mechanism and increasing the restraining force of the seat belt. In a vehicle collision, a gas generator for a vehicle occupant safety device is required to respond very quickly to an electrical signal from a collision detection sensor. That is, the gas generator has the ability to receive the electrical signal from the collision detection sensor, burn the gas generating agent to generate gas, and reach the maximum pressure of the generated gas in tens of milliseconds. Required.
車両搭乗者安全装置用ガス発生器としての極めて迅速な応答性能要求に応えるため、応答性に優れたガス発生剤が求められており、具体的には、ガス発生器内点火器の点火炎を受けて速やかに着火すると共に、短時間で完全に燃焼してガスを生成できるガス発生剤が求められている。そして、このような応答性に優れたガス発生剤により、車両搭乗者安全装置として好適で、衝突による起動信号を発してから生成ガスの最大圧力に到達するまでの時間が極めて短い、優れた応答性を示すガス発生器を提供することができる。 In order to meet the extremely quick response performance requirements of gas generators for vehicle occupant safety devices, there is a need for gas generators with excellent responsiveness. Specifically, the ignition flame of the igniter in the gas generator is required. There is a need for a gas generating agent that can be ignited and ignited promptly and that can completely burn in a short time to generate gas. With such a gas generating agent with excellent responsiveness, it is suitable as a vehicle occupant safety device, and has an extremely short response time from the start signal due to a collision until reaching the maximum pressure of the generated gas. A gas generator exhibiting properties can be provided.
また、車両安全機能に関する意識の高まりから、近年では、従来装備されてきた運転者及び助手席搭乗者のための前方衝突用エアバッグ以外にも、車両内側壁面及びガラス面並びに車両内天井面における衝突用エアバックの装備や下肢部保護用の衝突用エアバッグの装備が進められている。このような側面、頭部面、下肢部相対面は、搭乗者との距離が近いため、前方衝突用エアバッグより迅速に展開させる優れた応答性が要求され、このような位置への装備に適用可能な車両搭乗者安全装置用ガス発生器の開発が進められている。 In addition to the increasing awareness of vehicle safety functions, in recent years, in addition to the front collision airbags for drivers and passengers on the front passenger seat, the vehicle inner wall surface, glass surface, and vehicle interior ceiling surface Equipped with crash airbags and crash airbags for lower limb protection. Because these side, head, and lower limb relative surfaces are close to the occupant, excellent responsiveness is required to be deployed more quickly than the front collision airbag. Development of applicable gas generators for vehicle occupant safety devices is underway.
ガス発生器に用いるガス発生剤は、一般に、燃料成分と酸化剤成分との混合組成物を主成分として調製される。燃料成分としては、かつて用いられてきたアジ化金属化合物に代えて含窒素有機化合物が使用されており、該含窒素有機化合物と無機酸化剤を組み合わせてなる非アジド系ガス発生剤組成物が提案されている。酸化剤成分の役割としては、燃料成分に酸素を供給し燃焼性を向上させると共に、一酸化炭素、アンモニア、一酸化窒素、二酸化窒素、塩化水素等の好ましくないガス成分の生成を抑制する機能が要求される。ここで、ガス発生剤組成物の酸化剤成分としては、各種硝酸塩が広く使用されており、具体的には、金属硝酸塩、塩基性金属硝酸塩、硝酸アンモニウム、相安定化硝酸アンモニウム等が知られている。更に、酸化剤成分としてかかる硝酸塩と過塩素酸塩とを併用したガス発生剤組成物の例が知られている。特許文献１には、含窒素化合物、塩基性金属硝酸塩及び塩素酸化合物を含有するガス発生剤組成物が開示されている。また、特許文献２には、窒素含有燃料、銅含有化合物及び平均粒径が１００ミクロンを超えるアルカリ金属過塩素酸塩を含有するガス発生剤組成物が開示されている。これらの特許文献は、いずれも生成ガス成分中に含まれる窒素酸化物やアンモニア等の有毒なガス成分の生成を抑制できるガス発生剤組成物に関するものである。しかしながら、これらの特許文献に記載のガス発生剤組成物は、十分な燃焼速度を有するものではない。
The gas generating agent used for the gas generator is generally prepared with a mixed composition of a fuel component and an oxidant component as a main component. As the fuel component, a nitrogen-containing organic compound is used instead of the metal azide compound that has been used before, and a non-azide gas generant composition comprising a combination of the nitrogen-containing organic compound and an inorganic oxidizing agent is proposed. Has been. The role of the oxidant component is to supply oxygen to the fuel component to improve combustibility and to suppress the generation of undesirable gas components such as carbon monoxide, ammonia, nitric oxide, nitrogen dioxide, hydrogen chloride and the like. Required. Here, various nitrates are widely used as the oxidant component of the gas generant composition, and specifically, metal nitrate, basic metal nitrate, ammonium nitrate, phase-stabilized ammonium nitrate, and the like are known. Furthermore, examples of gas generant compositions using such nitrate and perchlorate in combination as oxidant components are known. Patent Document 1 discloses a gas generating composition containing a nitrogen-containing compound, a basic metal nitrate, and a chloric acid compound.
そこで、本発明の目的は、上記従来技術の問題を解決し、着火性及び燃焼性が向上したガス発生剤組成物及び該ガス発生剤組成物の成形体を提供することにある。また、本発明の他の目的は、該ガス発生剤組成物の成形体を備えることで、燃焼起動のための電気信号の発信から生成ガスの最大圧力に到達するまでの時間が極めて短い、即ち優れた応答性を示すガス発生器を提供することにある。 Accordingly, an object of the present invention is to solve the above-described problems of the prior art and provide a gas generant composition with improved ignitability and combustibility and a molded body of the gas generant composition. Another object of the present invention is to provide a molded product of the gas generant composition, so that the time from the transmission of an electric signal for starting combustion to the maximum pressure of the generated gas is extremely short, that is, An object of the present invention is to provide a gas generator exhibiting excellent responsiveness.
本発明者らは、上記目的を達成するために鋭意検討した結果、燃料成分として含窒素有機化合物と、酸化剤成分として金属硝酸塩及び／又は塩基性金属硝酸塩並びに過塩素酸塩とを含有するガス発生剤組成物において、該過塩素酸塩の５０％粒径を１〜５０μｍの範囲に限定し、酸化剤成分の全質量中に占める該過塩素酸塩の含有量を５質量％以上で且つ３５質量％未満の範囲に限定することで、ガス発生剤組成物の着火性及び燃焼性が顕著に向上できることを見出し、本発明を完成させるに至った。 As a result of intensive studies to achieve the above object, the present inventors have found that a gas containing a nitrogen-containing organic compound as a fuel component and a metal nitrate and / or a basic metal nitrate and a perchlorate as an oxidant component. In the generator composition, the 50% particle size of the perchlorate is limited to a range of 1 to 50 μm, and the content of the perchlorate in the total mass of the oxidant component is 5% by mass or more and By limiting to the range of less than 35% by mass, it was found that the ignitability and combustibility of the gas generant composition can be remarkably improved, and the present invention has been completed.
即ち、本発明のガス発生剤組成物は、燃料成分（Ａ）として含窒素有機化合物と、酸化剤成分（Ｂ）として金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）並びに５０％粒径が１〜５０μｍの過塩素酸塩（Ｂ−２）とを含有し、酸化剤成分（Ｂ）の全質量中に占める前記過塩素酸塩（Ｂ−２）の含有量が５質量％以上で且つ３５質量％未満であることを特徴とする。 That is, the gas generant composition of the present invention comprises a nitrogen-containing organic compound as the fuel component (A), a metal nitrate and / or basic metal nitrate (B-1) as the oxidant component (B), and a 50% particle size. 1 to 50 μm perchlorate (B-2), and the content of the perchlorate (B-2) in the total mass of the oxidant component (B) is 5% by mass or more. And less than 35% by mass.
本発明のガス発生剤組成物の好適例においては、前記含窒素有機化合物が、グアニジン、トリアゾール、テトラゾール、ビトリアゾール、ビテトラゾール及びそれらの誘導体からなる群から選択される少なくとも１種である。 In a preferred example of the gas generant composition of the present invention, the nitrogen-containing organic compound is at least one selected from the group consisting of guanidine, triazole, tetrazole, vitriazole, bitetrazole and derivatives thereof.
本発明のガス発生剤組成物の他の好適例においては、金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）が、硝酸カリウム、硝酸ナトリウム、硝酸ストロンチウム及び塩基性硝酸銅からなる群から選択される少なくとも１種である。 In another preferred embodiment of the gas generant composition of the present invention, the metal nitrate and / or the basic metal nitrate (B-1) is selected from the group consisting of potassium nitrate, sodium nitrate, strontium nitrate and basic copper nitrate. At least one kind.
本発明のガス発生剤組成物の他の好適例においては、前記過塩素酸塩（Ｂ−２）が、過塩素酸カリウム、過塩素酸ナトリウム及び過塩素酸アンモニウムからなる群から選択される少なくとも１種である。 In another preferred embodiment of the gas generant composition of the present invention, the perchlorate (B-2) is at least selected from the group consisting of potassium perchlorate, sodium perchlorate and ammonium perchlorate. One type.
本発明のガス発生剤組成物においては、前記含窒素有機化合物の含有量が３５〜６０質量％で、前記金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）の含有量が２０〜５０質量％で、前記過塩素酸塩（Ｂ−２）の含有量が１〜２０質量％であることが好ましい。ここで、前記含窒素有機化合物が硝酸グアニジンであり、前記金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）が塩基性金属硝酸銅であり、前記過塩素酸塩（Ｂ−２）が過塩素酸カリウムであることが更に好ましい。 In the gas generant composition of the present invention, the content of the nitrogen-containing organic compound is 35 to 60% by mass, and the content of the metal nitrate and / or the basic metal nitrate (B-1) is 20 to 50% by mass. %, And the content of the perchlorate (B-2) is preferably 1 to 20% by mass. Here, the nitrogen-containing organic compound is guanidine nitrate, the metal nitrate and / or basic metal nitrate (B-1) is basic metal copper nitrate, and the perchlorate (B-2) is excessive. More preferably, it is potassium chlorate.
本発明のガス発生剤組成物において、前記過塩素酸塩（Ｂ−２）は、５０％粒径が１〜３０μｍであることが好ましい。 In the gas generant composition of the present invention, the perchlorate (B-2) preferably has a 50% particle size of 1 to 30 μm.
本発明のガス発生剤組成物の他の好適例においては、更にバインダー剤（Ｃ）を含む。 In another preferred embodiment of the gas generant composition of the present invention, a binder agent (C) is further contained.
本発明のガス発生剤組成物の他の好適例においては、更にスラグ形成剤（Ｄ）を含む。 In another preferred embodiment of the gas generant composition of the present invention, a slag forming agent (D) is further contained.
また、本発明のガス発生剤組成物の成形体は、上述のガス発生剤組成物の成形体である。 Moreover, the molded object of the gas generant composition of this invention is a molded object of the above-mentioned gas generant composition.
本発明のガス発生剤組成物の成形体の好適例においては、成形体の形状が円柱状であり、その直径が４ｍｍ以下である。 In the suitable example of the molded object of the gas generant composition of this invention, the shape of a molded object is a column shape and the diameter is 4 mm or less.
更に、本発明のガス発生器は、上述のガス発生剤組成物の成形体を備えることを特徴とし、長尺筒状のハウジングを備えることが好ましい。 Furthermore, the gas generator of the present invention is characterized by including a molded body of the above gas generant composition, and preferably includes a long cylindrical housing.
本発明によれば、燃料成分として含窒素有機化合物と、酸化剤成分として金属硝酸塩及び／又は塩基性金属硝酸塩並びに過塩素酸塩とを含有するガス発生剤組成物において、該過塩素酸塩の５０％粒径を１〜５０μｍの範囲に限定し、酸化剤成分の全質量中に占める該過塩素酸塩の含有量を５質量％以上で且つ３５質量％未満の範囲に限定することで、着火性及び燃焼性に優れるガス発生剤組成物及び該ガス発生剤組成物の成形体を提供することができ、該ガス発生剤組成物及びその成形体は、車両搭乗者安全装置用ガス発生器への使用に好適である。なお、本発明のガス発生剤組成物及びその成形体は、熱安定性にも優れる。また、かかるガス発生剤組成物の成形体を備えることで、燃焼起動のための電気信号の発信から生成ガスの最大圧力に到達するまでの時間が極めて短い、即ち優れた応答性を示すガス発生器を提供することができる。なお、本発明のガス発生器は、ガス発生剤組成物が着火性に優れることから、従来のエアバック用インフレータ等に使用されるエンハンサー剤の使用が不要であり、ガス発生器の小型化を達成でき、特に迅速な応答が要求される側面衝突（側突）用エアバック用ガス発生器として好適である。また、本発明のガス発生器は、ガス発生剤組成物が燃焼性に優れることから、一酸化炭素、アンモニア及び窒素酸化物成分が比較的少なく、更には塩素や塩化水素をほとんど含んでいない清浄な排気ガスを生成することが可能である。 According to the present invention, in a gas generant composition containing a nitrogen-containing organic compound as a fuel component and a metal nitrate and / or a basic metal nitrate and a perchlorate as an oxidant component, By limiting the 50% particle size to a range of 1 to 50 μm, and limiting the content of the perchlorate in the total mass of the oxidizer component to a range of 5% by mass or more and less than 35% by mass, A gas generant composition excellent in ignitability and combustibility and a molded product of the gas generant composition can be provided, and the gas generant composition and the molded product are used as a gas generator for a vehicle occupant safety device. Suitable for use in. In addition, the gas generant composition of the present invention and the molded body thereof are excellent in thermal stability. Further, by providing a molded body of such a gas generant composition, the time from the transmission of an electrical signal for starting combustion to the maximum pressure of the generated gas being extremely short, that is, gas generation exhibiting excellent responsiveness Can be provided. Since the gas generator composition of the present invention has excellent ignitability, it is not necessary to use an enhancer agent used in conventional air bag inflators, etc., and the gas generator can be downsized. It can be achieved, and is particularly suitable as a gas generator for a side impact (side impact) airbag that requires a quick response. In addition, the gas generator of the present invention has a gas generator composition that is excellent in flammability, and therefore has a relatively small amount of carbon monoxide, ammonia, and nitrogen oxide components, and further contains no chlorine or hydrogen chloride. It is possible to generate exhaust gas.
以下に、本発明を詳細に説明する。本発明のガス発生剤組成物は、燃料成分（Ａ）として含窒素有機化合物と、酸化剤成分（Ｂ）として金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）並びに５０％粒径が１〜５０μｍの過塩素酸塩（Ｂ−２）とを含有し、酸化剤成分（Ｂ）の全質量中に占める前記過塩素酸塩（Ｂ−２）の含有量が５質量％以上で且つ３５質量％未満であることを特徴とし、着火性及び燃焼性に優れ、車両搭乗者安全装置用ガス発生器への使用に好適である。 The present invention is described in detail below. The gas generant composition of the present invention has a nitrogen-containing organic compound as the fuel component (A), a metal nitrate and / or basic metal nitrate (B-1) as the oxidant component (B), and a 50% particle size of 1 To 50 μm perchlorate (B-2), and the content of the perchlorate (B-2) in the total mass of the oxidant component (B) is 5% by mass or more and 35 It is characterized by being less than mass%, has excellent ignitability and combustibility, and is suitable for use in a gas generator for a vehicle occupant safety device.
本発明のガス発生剤組成物の燃料成分（Ａ）は、含窒素有機化合物であり、ここで、該含窒素有機化合物としては、特に限定されず、車両搭乗者安全装置用ガス発生器用ガス発生剤組成物に通常使用される含窒素有機化合物を好適に使用できるが、グアニジン又はその誘導体、トリアゾール又はその誘導体、テトラゾール又はその誘導体、ビトリアゾール又はその誘導体、ビテトラゾール又はその誘導体、アゾジカルボンアミド又はその誘導体、ヒドラジン又はその誘導体、及びヒドラジド誘導体が好ましく、より具体的には、５−オキソ−１，２，４−トリアゾール、テトラゾール、５−アミノテトラゾール、硝酸アミノテトラゾール、ニトロアミノテトラゾール、ビテトラゾール（５，５'−ビ−１Ｈ−テトラゾール）、５，５'−ビ−１Ｈ−テトラゾールジアンモニウム塩、アゾビステトラゾール、５，５'−アゾビステトラゾールジグアニジウム塩、グアニジン、ニトログアニジン、シアノグアニジン、トリアミノグアニジン硝酸塩、硝酸グアニジン、硝酸アミノグアニジン、ビウレット、アゾジカルボンアミド、カルボヒドラジド、カルボヒドラジド硝酸塩錯体、シュウ酸ヒドラジド、ヒドラジン硝酸塩錯体、アンミン錯体等が好適に挙げられる。これらの含窒素有機化合物の中でも、安価で反応性が良く比較的取り扱いが容易であることから、テトラゾール誘導体、ビテトラゾール誘導体及びグアニジン誘導体が好ましく、ニトログアニジン、硝酸グアニジン、ビテトラゾール、アゾビステトラゾール及び５−アミノテトラゾールが更に好ましい。これらの中でも、硝酸グアニジンは、分子中に酸素を含有するため酸化剤成分の配合量を低減でき、また良好な熱安定性を有し、更には低コスト、燃焼時の高いガス収率が期待できる等のメリットがあり、特に好ましい。なお、これら含窒素有機化合物は、一種単独で用いてもよく、二種以上を組み合わせて用いてもよい。 The fuel component (A) of the gas generant composition of the present invention is a nitrogen-containing organic compound, and the nitrogen-containing organic compound is not particularly limited, and is a gas generator for a gas generator for a vehicle occupant safety device. Nitrogen-containing organic compounds usually used in the agent composition can be preferably used, but guanidine or a derivative thereof, triazole or a derivative thereof, tetrazole or a derivative thereof, vitriazole or a derivative thereof, bitetrazole or a derivative thereof, azodicarbonamide or Derivatives thereof, hydrazine or derivatives thereof, and hydrazide derivatives are preferred, and more specifically, 5-oxo-1,2,4-triazole, tetrazole, 5-aminotetrazole, aminotetrazole nitrate, nitroaminotetrazole, bitetrazole ( 5,5′-bi-1H-tetrazole), 5,5′-bi-1 -Tetrazole diammonium salt, azobistetrazole, 5,5'-azobistetrazole diguanidinium salt, guanidine, nitroguanidine, cyanoguanidine, triaminoguanidine nitrate, guanidine nitrate, aminoguanidine nitrate, biuret, azodicarbonamide, carbo Preferred examples include hydrazide, carbohydrazide nitrate complex, oxalic hydrazide, hydrazine nitrate complex, and ammine complex. Among these nitrogen-containing organic compounds, tetrazole derivatives, bitetrazole derivatives and guanidine derivatives are preferred because they are inexpensive, reactive and relatively easy to handle, and nitroguanidine, guanidine nitrate, bitetrazole, azobistetrazole and More preferred is 5-aminotetrazole. Among these, guanidine nitrate contains oxygen in the molecule, so the amount of the oxidant component can be reduced, it has good thermal stability, and further, low cost and high gas yield during combustion are expected. There is a merit that it can be performed, and it is particularly preferable. In addition, these nitrogen-containing organic compounds may be used individually by 1 type, and may be used in combination of 2 or more type.
また、上記含窒素有機化合物は、取り扱いが容易であることから粉末若しくは顆粒状であることが好ましく、その５０％粒径は、５〜８０μｍが好ましく、１０〜５０μｍが更に好ましい。なお、含窒素有機化合物の５０％粒径は、大き過ぎるとガス発生剤組成物成形体の強度が低下する一方で、小さ過ぎると粉砕に多大なコストを必要とする。また、本発明において、５０％粒径とは、測定粒子数基準の５０％粒径を意味し、例えばレーザー回折・散乱法等で測定できる。 The nitrogen-containing organic compound is preferably in the form of powder or granule because it is easy to handle, and the 50% particle size is preferably 5 to 80 μm, more preferably 10 to 50 μm. When the 50% particle size of the nitrogen-containing organic compound is too large, the strength of the molded product of the gas generant composition is lowered. On the other hand, when the particle size is too small, a large cost is required for pulverization. In the present invention, the 50% particle size means a 50% particle size based on the number of measured particles, and can be measured by, for example, a laser diffraction / scattering method.
本発明のガス発生剤組成物中に占める含窒素有機化合物の含有率（配合割合）は、３５〜６０質量％が好ましく、４０〜５８質量％が更に好ましい。該含窒素有機化合物の含有率（配合割合）が３５質量％未満では、ガス発生剤組成物１００ｇ当たりの発生ガスモル数が減少し、酸素過剰で窒素酸化物の発生が増加する傾向にある。一方、含窒素有機化合物の含有率（配合割合）が６０質量％を超えると、有機物が多くなるため、ガス発生剤組成物の真比重が減少し、体積当たりの充填量が減少し、また、酸化剤成分が不足するために有毒な一酸化炭素が多く発生する傾向にある。 The content (mixing ratio) of the nitrogen-containing organic compound in the gas generating composition of the present invention is preferably 35 to 60% by mass, and more preferably 40 to 58% by mass. When the content (mixing ratio) of the nitrogen-containing organic compound is less than 35% by mass, the number of generated gas moles per 100 g of the gas generant composition tends to decrease, and the generation of nitrogen oxides tends to increase due to excess oxygen. On the other hand, when the content (mixing ratio) of the nitrogen-containing organic compound exceeds 60% by mass, the organic matter increases, so the true specific gravity of the gas generant composition decreases, the filling amount per volume decreases, There is a tendency to generate a lot of toxic carbon monoxide due to a shortage of oxidant components.
本発明のガス発生剤組成物の酸化剤成分（Ｂ）は、金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）と５０％粒径が１〜５０μｍの過塩素酸塩（Ｂ−２）を併用する。 The oxidizing agent component (B) of the gas generant composition of the present invention is composed of metal nitrate and / or basic metal nitrate (B-1) and perchlorate (B-2) having a 50% particle size of 1 to 50 μm. Use together.
上記金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）としては、例えば、アルカリ金属、アルカリ土類金属、鉄、銅、マグネシウム、コバルト、ニッケル、亜鉛等から選択される金属塩が挙げられる。具体的には、アルカリ金属の硝酸塩として硝酸ナトリウム、硝酸カリウム等、アルカリ土類金属の硝酸塩として硝酸マグネシウム、硝酸カルシウム、硝酸ストロンチウム、硝酸バリウム等が挙げられる。なお、これら金属硝酸塩は、一種単独で用いてもよく、二種以上を組み合わせて用いてもよい。また、塩基性金属硝酸塩としては、塩基性硝酸銅、塩基性硝酸コバルト、塩基性硝酸亜鉛、塩基性硝酸マグネシウム、塩基性硝酸鉄等が挙げられる。これらの中でも、塩基性硝酸銅が特に好ましい。なお、これら塩基性金属硝酸塩は、一種単独で用いてもよく、二種以上を組み合わせて用いてもよい。 Examples of the metal nitrate and / or basic metal nitrate (B-1) include metal salts selected from alkali metals, alkaline earth metals, iron, copper, magnesium, cobalt, nickel, zinc, and the like. Specific examples of the alkali metal nitrate include sodium nitrate and potassium nitrate, and examples of the alkaline earth metal nitrate include magnesium nitrate, calcium nitrate, strontium nitrate, and barium nitrate. In addition, these metal nitrates may be used individually by 1 type, and may be used in combination of 2 or more type. Examples of basic metal nitrates include basic copper nitrate, basic cobalt nitrate, basic zinc nitrate, basic magnesium nitrate, and basic iron nitrate. Among these, basic copper nitrate is particularly preferable. In addition, these basic metal nitrates may be used individually by 1 type, and may be used in combination of 2 or more type.
また、上記金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）は、取り扱いが容易であることから粉末若しくは顆粒状であることが好ましく、その５０％粒径は、１〜８０μｍが好ましく、１〜５０μｍが更に好ましい。なお、金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）の５０％粒径は、大き過ぎるとガス発生剤組成物成形体の強度が低下する一方で、小さ過ぎると粉砕に多大なコストを必要とする。 The metal nitrate and / or basic metal nitrate (B-1) is preferably in the form of powder or granules because it is easy to handle, and the 50% particle size is preferably 1 to 80 μm. More preferably, it is ˜50 μm. In addition, while the 50% particle diameter of the metal nitrate and / or basic metal nitrate (B-1) is too large, the strength of the molded product of the gas generant composition is lowered. I need.
上記過塩素酸塩（Ｂ−２）としては、例えば、アルカリ金属の過塩素酸塩、アルカリ土類金属の過塩素酸塩、過塩素酸アンモニウム等が挙げられる。具体的には、アルカリ金属の過塩素酸塩として過塩素酸ナトリウム、過塩素酸カリウム等、アルカリ土類金属の過塩素酸として過塩素酸マグネシウム、過塩素酸カルシウム、過塩素酸バリウム、過塩素酸ストロンチウム等が挙げられる。なお、これら過塩素酸塩は、一種単独で用いてもよく、二種以上を組み合わせて用いてもよい。 Examples of the perchlorate (B-2) include alkali metal perchlorate, alkaline earth metal perchlorate, and ammonium perchlorate. Specifically, sodium perchlorate, potassium perchlorate, etc. as alkali metal perchlorate, magnesium perchlorate, calcium perchlorate, barium perchlorate, perchlorate as perchloric acid of alkaline earth metals Examples include strontium acid. In addition, these perchlorate may be used individually by 1 type, and may be used in combination of 2 or more type.
また、上記過塩素酸塩（Ｂ−２）は、その粒径が小さい程、燃料成分（Ａ）との接触面積が増大し、該燃料成分（Ａ）に対して優れた反応性を示すため、ガス発生剤組成物の着火性及び燃焼性を大幅に向上できることから、その５０％粒径を１〜５０μｍの範囲にすることが必要であり、１〜３０μｍの範囲が好ましく、５〜３０μｍの範囲が更に好ましく、８〜２５μｍの範囲が一層好ましい。なお、上記過塩素酸塩（Ｂ−２）の５０％粒径が１μｍ未満では、粉砕に多大なコストを必要とする一方、５０μｍを超えると、ガス発生剤組成物成形体の強度が低下することに加えて、着火性、燃焼性等のガス発生特性の向上効果が十分に得られない。 Further, the perchlorate (B-2) has a smaller contact size with the fuel component (A) as its particle size is smaller, and exhibits excellent reactivity with the fuel component (A). Since the ignitability and combustibility of the gas generant composition can be greatly improved, it is necessary to make the 50% particle size in the range of 1 to 50 μm, preferably in the range of 1 to 30 μm, and in the range of 5 to 30 μm. The range is more preferable, and the range of 8 to 25 μm is more preferable. In addition, when the 50% particle size of the perchlorate (B-2) is less than 1 μm, a large cost is required for pulverization, while when it exceeds 50 μm, the strength of the gas generant composition molded product is reduced. In addition, the effect of improving gas generation characteristics such as ignitability and combustibility cannot be sufficiently obtained.
上述のように、上記過塩素酸塩（Ｂ−２）は、該燃料成分（Ａ）に対して反応性が非常に高いので、例えば、ガス発生剤組成物に必要とされる酸化剤成分の全てを該過塩素酸塩（Ｂ−２）としてしまうと、反応性が鋭敏すぎ、その取り扱いが非常に困難になる。このため、本発明のガス発生剤組成物においては、酸化剤成分中に占める過塩素酸塩（Ｂ−２）の含有量の制御が非常に重要であり、本発明者らが最適化を試みたところ、酸化剤成分（Ｂ）の全質量中に占める過塩素酸塩（Ｂ−２）の含有量を５質量％以上で且つ３５質量％未満の範囲に限定する必要があることを見出した。本発明のガス発生剤組成物において、酸化剤成分（Ｂ）の全質量中に占める過塩素酸塩（Ｂ−２）の含有量が３５質量％以上では、上記した通り、反応性が高くなり過ぎ、その取り扱いが困難になる他、作動時に塩素由来のガス成分の発生量が増加し、該ガス成分を回収するための添加剤が必要となり、ガス発生剤組成物の有効成分（燃焼成分及び酸化剤成分）の含有量を低減するため回避すべきである。また、自立燃焼性を喪失し、場合によっては燃焼が中断してしまうおそれがある。なお、ここでいう自立燃焼性とは、着火後に燃焼が中断せずに完全に燃え尽きる性質を意味する。一方、酸化剤成分（Ｂ）の全質量中に占める過塩素酸塩（Ｂ−２）の含有量が５質量％未満では、着火性、燃焼性等のガス発生特性の向上効果が十分に得られない。なお、本発明のガス発生剤組成物において、酸化剤成分（Ｂ）の全質量中に占める過塩素酸塩（Ｂ−２）の含有量は、着火性、燃焼性等のガス発生特性を更に向上させる観点から、８質量％以上で且つ３５質量％未満の範囲が好ましく、１０質量％以上で且つ３５質量％未満の範囲が更に好ましい。 As described above, since the perchlorate (B-2) is very reactive with the fuel component (A), for example, an oxidant component required for the gas generant composition is used. If all the perchlorate (B-2) is used, the reactivity is too sensitive and the handling becomes very difficult. For this reason, in the gas generant composition of the present invention, it is very important to control the content of perchlorate (B-2) in the oxidant component, and the present inventors have attempted optimization. As a result, it has been found that it is necessary to limit the content of perchlorate (B-2) in the total mass of the oxidant component (B) to a range of 5% by mass or more and less than 35% by mass. . In the gas generant composition of the present invention, when the content of perchlorate (B-2) in the total mass of the oxidant component (B) is 35% by mass or more, the reactivity becomes high as described above. In addition to being difficult to handle, the generation amount of chlorine-derived gas components increases during operation, and an additive for recovering the gas components is required. The effective components of the gas generant composition (combustion components and It should be avoided to reduce the content of the oxidant component). In addition, the self-sustainability may be lost, and in some cases, combustion may be interrupted. Here, the self-sustained combustibility means a property that the combustion is completely burned out without being interrupted after ignition. On the other hand, when the content of the perchlorate (B-2) in the total mass of the oxidant component (B) is less than 5% by mass, the effect of improving the gas generation characteristics such as ignitability and combustibility is sufficiently obtained. I can't. In the gas generant composition of the present invention, the content of perchlorate (B-2) in the total mass of the oxidant component (B) further increases gas generation characteristics such as ignitability and combustibility. From the viewpoint of improvement, a range of 8% by mass or more and less than 35% by mass is preferable, and a range of 10% by mass or more and less than 35% by mass is more preferable.
本発明のガス発生剤組成物中に占める酸化剤成分（Ｂ）の含有率（配合割合）は、上記燃料成分（Ａ）の種類、添加剤の種類、酸素バランス等によって異なるが、３０〜６５質量％が好ましく、３５〜６０質量％が更に好ましい。ここで、本発明のガス発生剤組成物中に占める上記金属硝酸塩及び／又は塩基性金属硝酸塩（Ｂ−１）の含有量（配合割合）は、２０〜５０質量％が好ましく、２５〜５０質量％が更に好ましい。また、本発明のガス発生剤組成物中に占める上記過塩素酸塩（Ｂ−２）の含有量（配合割合）は、１〜２０質量％が好ましく、３〜１８質量％が更に好ましい。 The content (mixing ratio) of the oxidant component (B) in the gas generant composition of the present invention varies depending on the type of the fuel component (A), the type of additive, the oxygen balance, etc., but is 30 to 65. % By mass is preferable, and 35 to 60% by mass is more preferable. Here, the content (mixing ratio) of the metal nitrate and / or basic metal nitrate (B-1) in the gas generant composition of the present invention is preferably 20 to 50% by mass, and preferably 25 to 50% by mass. % Is more preferable. Moreover, 1-20 mass% is preferable and, as for content (mixing ratio) of the said perchlorate (B-2) which occupies in the gas generating composition of this invention, 3-18 mass% is still more preferable.
本発明のガス発生剤組成物は、更に添加剤を含有していてもよい。該添加剤としては、一般的に車両搭乗者安全装置用ガス発生器用のガス発生剤組成物に使用可能な添加剤を用いることができる。例えば、好適な燃焼特性を維持するために成形性や形状保持性を付与するためのバインダー剤（Ｃ）、燃焼残渣を容易にろ過することを可能にするためのスラグ形成剤（Ｄ）、燃焼調整剤、滑剤等の添加剤を用いることができる。これら添加剤の含有量は、その用途により異なるが、いずれの用途においても、添加剤の含有量が多くなり過ぎると、燃焼性等の性能が低下するため、ガス発生剤組成物中に占める添加剤の含有量は、０．１〜１５質量％が好ましく、０．１〜１０質量％が更に好ましい。 The gas generant composition of the present invention may further contain an additive. As this additive, the additive which can generally be used for the gas generant composition for gas generators for vehicle occupant safety devices can be used. For example, a binder agent (C) for imparting moldability and shape retention to maintain suitable combustion characteristics, a slag forming agent (D) for enabling easy filtration of combustion residues, combustion Additives such as regulators and lubricants can be used. The content of these additives varies depending on the application, but in any application, if the content of the additive is excessive, the performance such as flammability deteriorates, so the addition in the gas generant composition 0.1-15 mass% is preferable and, as for content of an agent, 0.1-10 mass% is still more preferable.
上記バインダー剤（Ｃ）は、好適な燃焼特性を維持させるために成形性、形状保持性を付与する添加剤であり、例えば、ガス発生剤組成物がバインダー剤（Ｃ）を含有する場合、インフレータが使用される過酷な環境下であっても、燃焼性能を保持することができる。該バインダー剤（Ｃ）としては、ガス発生剤組成物の燃焼挙動に大幅な悪影響を与えなければ特に制限なく使用でき、例えば、カルボキシメチルセルロースの金属塩、ヒドロキシエチルセルロース、ヒドロキシプロピルメチルセルロース、酢酸セルロース、プロピオン酸セルロース、酢酸酪酸セルロース、ニトロセルロース、微結晶性セルロース、グアガム、ポリビニルアルコール、ポリビニルピロリドン、ポリアクリルアミド、デンプン等の多糖誘導体、ステアリン酸塩等の有機バインダー、二硫化モリブデン、合成ヒドロタルサイト、酸性白土、タルク、ベントナイト、ケイソウ土、カオリン、シリカ、アルミナ等の無機バインダーが好適に挙げられる。これらの中でも、セルロース系バインダー、酸性白土等が特に好ましい。本発明のガス発生剤組成物中におけるバインダー剤（Ｃ）の含有量は、１．０〜１０質量％が好ましく、１．０〜５質量％が更に好ましい。バインダー剤（Ｃ）の含有量が高いと、成形体の破壊強度を高めることができるが、組成物中の炭素元素及び水素元素の数が増大し、炭素元素の不完全燃焼生成物である一酸化炭素ガスの濃度が増大し、発生ガスの品質を低下させ、また燃焼を阻害してしまうおそれもあることから、ガス発生剤組成物の形状を維持できる最低量での使用が好ましい。特に、バインダー剤（Ｃ）の含有量が１０質量％を超えると、酸化剤成分の相対的存在割合の増大が必要となり、ガス発生剤組成物中における燃料成分（含窒素有機化合物）の相対的存在割合が低下し、ガス発生器の実用化が困難になるおそれがある。 The binder agent (C) is an additive that imparts moldability and shape retention in order to maintain suitable combustion characteristics. For example, when the gas generant composition contains the binder agent (C), an inflator The combustion performance can be maintained even under the harsh environment in which is used. The binder agent (C) can be used without any particular limitation as long as it does not have a significant adverse effect on the combustion behavior of the gas generant composition. Cellulose acid, cellulose acetate butyrate, nitrocellulose, microcrystalline cellulose, guar gum, polyvinyl alcohol, polyvinylpyrrolidone, polyacrylamide, starch and other polysaccharide derivatives, stearates and other organic binders, molybdenum disulfide, synthetic hydrotalcite, acidic Preferable examples include inorganic binders such as white clay, talc, bentonite, diatomaceous earth, kaolin, silica, and alumina. Among these, cellulosic binders, acid clay and the like are particularly preferable. 1.0-10 mass% is preferable and, as for content of the binder agent (C) in the gas generating composition of this invention, 1.0-5 mass% is still more preferable. When the content of the binder agent (C) is high, the fracture strength of the molded product can be increased, but the number of carbon elements and hydrogen elements in the composition increases, and this is an incomplete combustion product of carbon elements. Since the concentration of the carbon oxide gas is increased, the quality of the generated gas is lowered, and combustion may be hindered, it is preferable to use it in the minimum amount capable of maintaining the shape of the gas generant composition. In particular, if the content of the binder agent (C) exceeds 10% by mass, it is necessary to increase the relative proportion of the oxidant component, and the relative proportion of the fuel component (nitrogen-containing organic compound) in the gas generant composition. There is a risk that the existing ratio is lowered and it is difficult to put the gas generator into practical use.
上記スラグ形成剤（Ｄ）は、ガス発生剤組成物の燃焼後に生成する燃焼残渣を容易にろ過することを可能にする添加剤であり、インフレータの外に放出することを防ぐことを目的に添加される。該スラグ形成剤（Ｄ）の具体例としては、例えば、窒化珪素、炭化珪素、二酸化珪素、珪酸塩、酸化アルミニウム、酸化チタン、酸性白土、クレー等の天然鉱物等が挙げられる。本発明のガス発生剤組成物中におけるスラグ形成剤（Ｄ）の含有量は、０．５〜１０質量％が好ましく、１．０〜５．０質量％が更に好ましい。スラグ形成剤（Ｄ）の含有量が高いと、燃焼性を低下させ、更には発生ガスのモル数を低下させることから、乗員保護性能が十分に発揮されないおそれがある。 The slag forming agent (D) is an additive that enables easy filtration of the combustion residue generated after combustion of the gas generant composition, and is added for the purpose of preventing it from being released out of the inflator. Is done. Specific examples of the slag forming agent (D) include natural minerals such as silicon nitride, silicon carbide, silicon dioxide, silicate, aluminum oxide, titanium oxide, acidic clay, and clay. 0.5-10 mass% is preferable and, as for content of the slag formation agent (D) in the gas generating composition of this invention, 1.0-5.0 mass% is still more preferable. If the content of the slag forming agent (D) is high, the combustibility is lowered, and further the number of moles of the generated gas is lowered, so that the passenger protection performance may not be sufficiently exhibited.
上記滑剤は、ガス発生剤組成物の調製時において原料成分の混合性向上、流動性改善を目的として添加される。該滑剤の具体例としては、例えば、グラファイト、ステアリン酸マグネシウム、ステアリン酸亜鉛、ステアリン酸カルシウム、ステアリン酸ナトリウム、窒化ホウ素、高分散シリカ（二酸化珪素）、タルク等が挙げられる。これらの中でも、高分散シリカ（二酸化珪素）は、原料混合時の固着や凝集を抑制して均一に分散混合する機能を有しており、各成分の粒度特性・作用を維持する効果があり、特に有用である。本発明のガス発生剤組成物中における滑剤の含有量は、０．１〜５．０質量％が好ましく、０．１〜２．０質量％が更に好ましい。滑剤の含有量が高いと、燃焼性の低下、発生ガスのモル数の低下、更には発生ガス中の一酸化炭素の濃度の増大等が起きるおそれがある。 The above-mentioned lubricant is added for the purpose of improving the mixing property and fluidity of the raw material components during the preparation of the gas generant composition. Specific examples of the lubricant include graphite, magnesium stearate, zinc stearate, calcium stearate, sodium stearate, boron nitride, highly dispersed silica (silicon dioxide), talc and the like. Among these, highly dispersed silica (silicon dioxide) has a function of uniformly dispersing and mixing while suppressing sticking and agglomeration during raw material mixing, and has the effect of maintaining the particle size characteristics and action of each component. It is particularly useful. The content of the lubricant in the gas generant composition of the present invention is preferably 0.1 to 5.0% by mass, and more preferably 0.1 to 2.0% by mass. When the content of the lubricant is high, there is a risk that the combustibility decreases, the number of moles of the generated gas decreases, and further the concentration of carbon monoxide in the generated gas increases.
上記燃焼調整剤は、ガス発生剤組成物の燃焼を調整するための添加剤であり、具体例としては、酸化鉄、酸化ニッケル、酸化銅、酸化亜鉛、酸化マンガン、酸化クロム、酸化コバルト、酸化モリブデン、酸化バナジウム、酸化タングステン等の金属酸化物、水酸化銅、水酸化コバルト、水酸化亜鉛、水酸化アルミニウム等の金属水酸化物、活性炭粉末、グラファイト、カーボンブラック等の炭素類等が挙げられる。本発明のガス発生剤組成物中における燃焼調整剤の含有量は、１０質量％以下が好ましく、５質量％以下が更に好ましい。 The combustion modifier is an additive for adjusting the combustion of the gas generant composition. Specific examples thereof include iron oxide, nickel oxide, copper oxide, zinc oxide, manganese oxide, chromium oxide, cobalt oxide, and oxidation. Metal oxides such as molybdenum, vanadium oxide, and tungsten oxide, metal hydroxides such as copper hydroxide, cobalt hydroxide, zinc hydroxide, and aluminum hydroxide, carbons such as activated carbon powder, graphite, and carbon black . The content of the combustion regulator in the gas generant composition of the present invention is preferably 10% by mass or less, and more preferably 5% by mass or less.
本発明のガス発生剤組成物は、適当な形状を有する成形体として使用することが好ましい。以下、ガス発生剤組成物の成形体をガス発生剤とも称する。なお、ガス発生剤組成物は、ガス発生剤組成物の燃焼性能、ガス発生器の燃焼特性に合わせて様々な形状に成形することができる。その成形方法としては、加圧成形方法、押出成形方法が挙げられる。本発明のガス発生剤組成物の成形体の形状は、特に限定されず、ペレット状、ディスク状、球状、棒状、円柱状、円筒状、金平糖状、テトラポット状等が挙げられる。また、該成形体は、無孔のものでもよいし、単孔又は多孔といった有孔のもの（例えば、単孔円筒状又は多孔円筒状）でもよい。更に、ペレット状、ディスク状の成形体は、片面又は両面に１〜数個程度の突起を設けてもよい。突起の形状は特に制限されず、例えば、円柱状、円筒状、円錐状、多角錘状等が挙げられる。 The gas generant composition of the present invention is preferably used as a molded product having an appropriate shape. Hereinafter, the molded body of the gas generating agent composition is also referred to as a gas generating agent. The gas generant composition can be formed into various shapes according to the combustion performance of the gas generant composition and the combustion characteristics of the gas generator. Examples of the molding method include a pressure molding method and an extrusion molding method. The shape of the molded article of the gas generant composition of the present invention is not particularly limited, and examples thereof include pellets, discs, spheres, rods, columns, cylinders, confetti, tetrapots, and the like. The molded body may be non-porous, or may be single-hole or porous (for example, single-hole cylindrical shape or porous cylindrical shape). Furthermore, the pellet-shaped or disk-shaped molded body may be provided with one to several protrusions on one side or both sides. The shape of the protrusion is not particularly limited, and examples thereof include a columnar shape, a cylindrical shape, a conical shape, and a polygonal pyramid shape.
本発明のガス発生剤組成物の加圧成形体において、その形状が円柱状である場合、該成形体の円柱直径が小さいと、ガス発生剤の燃焼性を顕著に向上できることを見出した。加えて、円柱状成形体の直径が小さいと、ガス発生剤の嵩密度が高くなることを見出した。ガス発生器に該ガス発生剤を充填した場合、円柱直径が大きいものと同程度の充填量において、ガス発生特性の向上が期待される。また、嵩密度が高いと、単位体積当たりのガス発生剤充填量の増量が可能となり、ガス発生器の高出力を図るこが可能となるため望ましい。また、別の観点では、嵩密度が高いと、ガス発生剤を充填する空間の小容量化が可能となり、ガス発生器の小型化が達成できるため望ましい。特に、ガス発生剤を充填する空間の形状が制限される長尺円筒状のハウジングを備えるガス発生器においては、該ガス発生器に適用されるガス発生剤の充填性の向上が重要な課題となる。従って、本発明のガス発生剤組成物の成形体を長尺円筒状のハウジングを備えるガス発生器に充填する場合、該ガス発生器への充填性を向上させる観点から、成形体の形状を円柱状とし、その円柱直径を小さくすることが好ましい。具体的には、円柱状成形体の直径は、好ましくは４．０ｍｍ以下、より好ましくは３．２ｍｍ以下、更に好ましくは２．５ｍｍ以下である。また、特に限定されるものではないが、円柱状成形体の直径は、２．０ｍｍ以上が好ましい。更に、円柱状成形体の厚み（高さ）は、薄く（低く）すると、燃焼性能は向上するものの充填性が低下し、一方、厚く（高く）すると、充填性は向上するものの燃焼性能が低下するため、厚み／直径の比率は、３０〜８０％が好ましく、３０〜６０％が更に好ましい。加えて、燃焼性、充填性、成形体の強度等を考慮した場合、円柱状成形体の厚みは３．０ｍｍ以下が好ましく、２．０ｍｍ以下が更に好ましく、１．５ｍｍ以下が一層好ましい。また、特に限定されるものではないが、円柱状成形体の厚みは、１．０ｍｍ以上が好ましい。なお、円柱状成形体としては、厚みが２．０ｍｍ以下で、直径が４．０ｍｍ以下の加圧成形体が、最も好適である。また、円柱状成形体とは、該円柱状成形体の表面に曲面を形成した形状も含まれるものであり、その曲面高さは０．５ｍｍ以下が好ましく、０．３ｍｍ以下が更に好ましく、０．１ｍｍ以下が一層好ましい。また、成形体角面の面取りをした形状も含まれる。 It has been found that when the shape of the pressure-formed product of the gas generant composition of the present invention is a columnar shape, the combustibility of the gas generant can be significantly improved if the columnar diameter of the molded product is small. In addition, it has been found that when the diameter of the cylindrical molded body is small, the bulk density of the gas generating agent increases. When the gas generator is filled with the gas generator, an improvement in gas generation characteristics is expected at a filling amount similar to that of a cylinder having a large diameter. Moreover, it is desirable that the bulk density is high, because it is possible to increase the amount of the gas generating agent charged per unit volume and to achieve high output of the gas generator. From another viewpoint, it is desirable that the bulk density is high because the space for filling the gas generating agent can be reduced, and the gas generator can be reduced in size. In particular, in a gas generator having a long cylindrical housing in which the shape of the space filled with the gas generating agent is limited, it is important to improve the filling property of the gas generating agent applied to the gas generator. Become. Therefore, when the gas generator composition molded body of the present invention is filled in a gas generator having a long cylindrical housing, the shape of the molded body is circular from the viewpoint of improving the filling property of the gas generator. It is preferable to use a columnar shape and reduce the diameter of the column. Specifically, the diameter of the cylindrical molded body is preferably 4.0 mm or less, more preferably 3.2 mm or less, and still more preferably 2.5 mm or less. Moreover, although it does not specifically limit, the diameter of a cylindrical molded object has preferable 2.0 mm or more. Further, when the thickness (height) of the cylindrical molded body is thin (lower), the combustion performance is improved, but the fillability is lowered. On the other hand, when the thickness (high) is increased, the fillability is improved, but the combustion performance is lowered. Therefore, the thickness / diameter ratio is preferably 30 to 80%, and more preferably 30 to 60%. In addition, when considering combustibility, filling properties, strength of the molded body, etc., the thickness of the cylindrical molded body is preferably 3.0 mm or less, more preferably 2.0 mm or less, and even more preferably 1.5 mm or less. Moreover, although not particularly limited, the thickness of the cylindrical molded body is preferably 1.0 mm or more. As the cylindrical molded body, a pressure molded body having a thickness of 2.0 mm or less and a diameter of 4.0 mm or less is most preferable. Further, the columnar molded body includes a shape in which a curved surface is formed on the surface of the columnar molded body, and the height of the curved surface is preferably 0.5 mm or less, more preferably 0.3 mm or less, and 0 More preferably, it is 1 mm or less. Moreover, the shape which chamfered the molded object square surface is also contained.
次に、本発明のガス発生剤組成物の成形体の加圧成形方法による製造方法を例示する。加圧成形により、錠剤状、ペレット状又はディスク状にガス発生剤組成物を成形する場合、燃料成分、酸化剤成分、任意の各種添加剤をＶ型混合機又はロッキングミキサー等の乾式混合機にて混合する。混合の際には、該成分の混合物中に球体を分散し介在させることで、該成分の粉末が球体による力を細部にわたって受けるため、組成物中に各成分が均一に分散する。ロッキングミキサーのような回転と揺動運動を行う混合機を用いることで、各成分がより均一に分散したガス発生剤組成物を得ることができるため望ましい。得られたガス発生剤組成物（粉末）に、バインダー剤（Ｃ）を含有する溶液（バインダー溶液）を添加し、撹拌造粒機等の湿式造粒機を用いて該ガス発生剤組成物を造粒する。バインダー溶液の添加量は、一概には言えないが、混合粉末に対して５〜２０質量％添加することができる。その後、８０〜１００℃にて熱処理して顆粒を得る。熱処理後の顆粒の水分量は、１％を超えると流動性の低下が起こり、安定して次工程の加圧成形を行うことができないおそれがあるため、顆粒中の水分量は１質量％以下、好ましくは０．５質量％以下が望ましい。次に、該顆粒をロータリー打錠機によって所望の形状に加圧成形する。加圧成形の際、通常使用されるステアリン酸マグネシウム等の滑剤を０．１〜５質量％の範囲で添加することも可能である。加圧成形された成形体は、１００〜１１０℃で５〜２０時間熱処理した後、ガス発生剤として使用できる。熱処理後のガス発生剤中の水分量は１質量％以下、好ましくは０．５質量％以下、更に好ましくは０．３質量％以下が望ましい。 Next, the manufacturing method by the press molding method of the molded object of the gas generant composition of this invention is illustrated. When molding a gas generant composition into tablets, pellets, or disks by pressure molding, the fuel component, oxidant component, and various additives are added to a dry mixer such as a V-type mixer or rocking mixer. And mix. At the time of mixing, the spheres are dispersed and interposed in the mixture of the components, so that the powder of the components is subjected to force by the spheres in detail, so that each component is uniformly dispersed in the composition. Use of a mixer that rotates and swings like a rocking mixer is desirable because a gas generating composition in which each component is more uniformly dispersed can be obtained. A solution (binder solution) containing the binder agent (C) is added to the obtained gas generant composition (powder), and the gas generant composition is added using a wet granulator such as a stirring granulator. Granulate. The amount of the binder solution added cannot be generally specified, but 5 to 20% by mass can be added to the mixed powder. Then, it heat-processes at 80-100 degreeC, and obtains a granule. If the moisture content of the granule after heat treatment exceeds 1%, the fluidity is lowered, and there is a risk that the subsequent pressure molding cannot be performed stably. Preferably, it is 0.5% by mass or less. Next, the granules are pressed into a desired shape by a rotary tableting machine. During the pressure molding, a commonly used lubricant such as magnesium stearate can be added in the range of 0.1 to 5% by mass. The pressure-molded molded body can be used as a gas generating agent after heat treatment at 100 to 110 ° C. for 5 to 20 hours. The water content in the gas generating agent after the heat treatment is 1% by mass or less, preferably 0.5% by mass or less, more preferably 0.3% by mass or less.
一方、押出成形方法により本発明のガス発生剤組成物の成形体を製造する場合には、燃料成分、酸化剤成分、各種添加剤を混合機にて混合し、得られた混合粉末に外割で１０〜２０質量％の水又は有機溶媒を加えて十分に混練し、粘性を有する湿薬にする。その後、所望の形状に押出成形可能なダイスに該湿薬を通し、押出成形体を適宜切断していく。押出成形体は柱状体であり、より好ましい形体としては長尺円柱状成形体である。その形状は、直径が３．０ｍｍ以下、より好ましくは２．５ｍｍ以下、更に好ましくは２．０ｍｍ以下である。また、特に限定されるものではないが、該直径は、１．０ｍｍ以上が好ましい。長さ／直径の比率は、１３０〜３５０％が好ましく、１３０〜２５０％が更に好ましく、１３０〜２００％が一層好ましい。加えて、燃焼性、充填性等を考慮した場合、長尺円柱状成形体の長さは、６．５ｍｍ以下、好ましくは４．５ｍｍ以下、更に好ましくは２．５ｍｍ以下が望ましい。また、特に限定されるものではないが、長さは、２．０ｍｍ以上が好ましい。押出成形体としては、長さが２．５ｍｍ以下で、直径が２．０ｍｍ以下の長尺円柱状成形体が、最も好適である。このようにして得られた押し出し成形体を熱処理し、ガス発生剤として使用できる。 On the other hand, when the molded product of the gas generant composition of the present invention is produced by an extrusion molding method, a fuel component, an oxidant component, and various additives are mixed in a mixer, and the obtained mixed powder is externally divided. Add 10-20% by mass of water or an organic solvent and knead thoroughly to obtain a viscous moistening agent. Thereafter, the wet agent is passed through a die that can be extruded into a desired shape, and the extruded product is appropriately cut. The extruded molded body is a columnar body, and a more preferable form is a long cylindrical shaped body. The shape has a diameter of 3.0 mm or less, more preferably 2.5 mm or less, and still more preferably 2.0 mm or less. Further, although not particularly limited, the diameter is preferably 1.0 mm or more. The length / diameter ratio is preferably 130 to 350%, more preferably 130 to 250%, and still more preferably 130 to 200%. In addition, when considering combustibility, filling properties, etc., the length of the long cylindrical shaped body is 6.5 mm or less, preferably 4.5 mm or less, more preferably 2.5 mm or less. Although not particularly limited, the length is preferably 2.0 mm or more. As the extruded molded body, a long cylindrical molded body having a length of 2.5 mm or less and a diameter of 2.0 mm or less is most preferable. The extruded product thus obtained can be heat-treated and used as a gas generating agent.
なお、上記熱処理では、５０〜１５０℃の温度で１０〜２０時間程度熱処理を行うことにより、経時変化の少ないガス発生剤組成物の成形体を得ることができる。押出成形による製造方法では、水分を１０〜２０質量％含んだ成形体を熱処理するため、低温で長時間熱処理することが必要である。特に、１０７℃×４００時間の過酷な耐熱老化試験にパスするためには、この熱処理が極めて有効である。なお、熱処理時間が１０時間未満では、熱処理が不十分であり、一方、２０時間を超える熱処理時間も意味が無いため、１０〜２０時間の範囲で適宜選択するのが良い。また、熱処理温度は、５０℃未満では、成形体の品質を向上させる効果が小さく、８０℃を超えると、水分の蒸発速度が早すぎるため、成形体内に気泡が生じ、成形体の強度不足、燃焼中の異常燃焼の原因となる。そのため、５０〜７０℃にて一次熱処理を行い、ガス発生剤中の水分量を７％以下、好ましくは５％以下とし、その後、８０〜１５０℃にて二次熱処理を行い、ガス発生剤中の水分量を１質量％以下、好ましくは０．５質量％以下にすることが望ましい。 In addition, in the said heat processing, the molded object of a gas generant composition with little change with time can be obtained by performing heat processing for about 10 to 20 hours at the temperature of 50-150 degreeC. In the production method by extrusion molding, a molded body containing 10 to 20% by mass of water is heat-treated, and therefore it is necessary to heat-treat at a low temperature for a long time. In particular, this heat treatment is extremely effective in order to pass a severe heat aging test of 107 ° C. × 400 hours. Note that if the heat treatment time is less than 10 hours, the heat treatment is insufficient. On the other hand, the heat treatment time exceeding 20 hours is meaningless, so it is preferable to select the heat treatment time in the range of 10 to 20 hours. Also, if the heat treatment temperature is less than 50 ° C., the effect of improving the quality of the molded product is small, and if it exceeds 80 ° C., the moisture evaporation rate is too fast, resulting in bubbles in the molded product, insufficient strength of the molded product, Causes abnormal combustion during combustion. Therefore, the primary heat treatment is performed at 50 to 70 ° C., and the moisture content in the gas generating agent is set to 7% or less, preferably 5% or less, and then the secondary heat treatment is performed at 80 to 150 ° C. in the gas generating agent. It is desirable that the water content is 1 mass% or less, preferably 0.5 mass% or less.
本発明のガス発生剤組成物の成形体は、車両搭乗者安全装置用ガス発生器への使用に好適で、特にエアバッグ装置用ガス発生器への使用に好適である。 The molded article of the gas generant composition of the present invention is suitable for use in a gas generator for a vehicle occupant safety device, and particularly suitable for use in a gas generator for an airbag device.
以下に、図を参照しながら本発明のガス発生器を詳細に説明する。本発明のガス発生器は、上述のガス発生剤組成物の成形体を備えることを特徴とする。本発明のガス発生器は、かかるガス発生剤組成物の成形体を備えることで、燃焼起動のための電気信号の発信から生成ガスの最大圧力に到達するまでの時間が極めて短いため、車両搭乗者安全装置用ガス発生器として好適である。なお、車両搭乗者安全装置用ガス発生器としては、特に限定されるものではないが、例えば、図１及び図２に示されるような、エアバック装置用ガス発生器が挙げられる。 Hereinafter, the gas generator of the present invention will be described in detail with reference to the drawings. The gas generator of the present invention is characterized by comprising a molded body of the above gas generant composition. Since the gas generator of the present invention is provided with a molded body of such a gas generant composition, the time from the transmission of an electric signal for starting combustion to the maximum pressure of the generated gas is extremely short. It is suitable as a gas generator for personal safety devices. The gas generator for the vehicle occupant safety device is not particularly limited, and examples thereof include a gas generator for an airbag device as shown in FIGS. 1 and 2.
図１は、本発明のガス発生器の一例の断面図であり、該ガス発生器は、通常、前方衝突用エアバッグ装置に使用される。図１に示すガス発生器１は、ガス放出孔６が複数個設置された金属製容器からなるハウジング２を備え、該ハウジング２により外殻が形成されている。また、該ハウジング２の内部には、点火装置３、フィルター５が装備され、ガス発生剤４が充填されている。上記点火装置３の近接部には、点火室７が設置されおり、通常、点火装置３から発生する点火炎をガス発生剤４に伝達するエンハンサー剤（伝火薬）が充填されている。なお、本発明のガス発生剤組成物は、着火性に優れるため、エンハンサー剤が不要又は少量化することが可能となる。従って、点火室７が不要であったり、小容積化することが可能であるため、ガス発生器の小型化、軽量化及び低コスト化を達成することができる。
FIG. 1 is a cross-sectional view of an example of the gas generator of the present invention, and the gas generator is usually used in a front collision airbag apparatus. A gas generator 1 shown in FIG. 1 includes a
図２は、本発明のガス発生器の他の例の断面図であり、該ガス発生器は、長尺筒状のハウジングを備えており、側突用エアバック装置に好適に使用される。なお、ここでいう長尺とは、長さ（Ｌ）と断面の径（Ｄ）の比（Ｌ／Ｄ）が３以上であることを意味し、また、断面の形状が円以外の場合は、面積円相当径をＤとする。また、長尺筒状のハウジングの断面形状には、例えば、三角形、四角形、台形、円形、楕円形等がある。図２に示すガス発生器１１は、ガス放出孔１６が複数個設置された金属製容器からなる長尺筒状ハウジング１２を備え、該ハウジング１２により外殻が形成されている。また、該ハウジング１２の内部には、点火装置１３、フィルター１５が装備され、ガス発生剤１４が充填されている。上記点火装置１３の近接部には、点火室１７が設置されおり、通常、点火装置１３から発生する点火炎をガス発生剤１４に伝達するエンハンサー剤（伝火薬）が充填されている。なお、本発明のガス発生剤組成物は、着火性に優れるため、エンハンサー剤が不要又は少量化することが可能となる。従って、点火室１７が不要であったり、小容積化することが可能であるため、ガス発生器の小型化、軽量化及び低コスト化を達成することができる。また、図２に示すガス発生器１１は、図１に示すガス発生器１に比べて小型化が容易であり、車両内の設置スペースが小さい場所で使用されるエアバック用ガス発生器として好適である。その上、本発明のガス発生器は優れた応答性を示すため、図２に示すガス発生器１１は、側突用、下肢部保護用又はシート座面上昇用エアバッグ装置用ガス発生器として特に好適である。
FIG. 2 is a cross-sectional view of another example of the gas generator of the present invention. The gas generator includes a long cylindrical housing and is preferably used for a side-impact airbag device. In addition, the long term here means that the ratio (L / D) of the length (L) to the diameter (D) of the cross section is 3 or more, and when the shape of the cross section is other than a circle. The area equivalent circle diameter is D. The cross-sectional shape of the long cylindrical housing includes, for example, a triangle, a quadrangle, a trapezoid, a circle, and an ellipse. A
以下、実施例及び比較例を挙げて本発明をより詳細に説明するが、本発明はこれらに限定されるものではない。なお、各試験は以下の方法で行った。 EXAMPLES Hereinafter, although an Example and a comparative example are given and this invention is demonstrated in detail, this invention is not limited to these. Each test was conducted by the following method.
１．粒度測定法
レーザー回折・散乱法式粒度測定装置（日機装株式会社製 マイクロトラック ＭＴ３３００ＩＩ）を用いて、５０％粒径を測定した。なお、５０％粒径とは、上述の通り、測定粒子数基準の５０％粒径を指す。1. Particle
２．耐環境試験（高温安定性試験）
ガス発生剤組成物の成形体（ガス発生剤）をアルミ容器に入れて密封した後、１０７℃に調温された恒温槽に入れて放置した。その後、任意の時間でガス発生剤を取り出し、ガス発生剤の重量減少率を測定し、分解の有無について確認した。2. Environmental resistance test (high temperature stability test)
A molded article (gas generating agent) of the gas generating agent composition was put in an aluminum container and sealed, and then placed in a thermostatic chamber adjusted to 107 ° C. and left standing. Thereafter, the gas generating agent was taken out at an arbitrary time, the weight reduction rate of the gas generating agent was measured, and the presence or absence of decomposition was confirmed.
３．燃焼性試験（１８ｃｃタンク試験）
ガス発生剤組成物の成形体（ガス発生剤）２．０ｇを容積１８ｃｃの燃焼用密閉容器に充填してガス発生剤を燃焼させ、最大到達圧力及び最大圧力への到達時間を計測した。また、この計測値に基づき、圧力発生速度を求めた。3. Flammability test (18cc tank test)
2.0 g of a molded product (gas generating agent) of the gas generating agent composition was filled in a closed container for combustion having a volume of 18 cc to burn the gas generating agent, and the maximum pressure reached and the time to reach the maximum pressure were measured. Further, the pressure generation speed was obtained based on the measured value.
４．排ガス測定（１８ｃｃタンク試験）
１８ｃｃタンク試験後、タンク内のガスをテドラーバックに回収し、ガステック製検知管を用いて生成ガス成分の濃度分析を実施した。4). Exhaust gas measurement (18cc tank test)
After the 18 cc tank test, the gas in the tank was collected in a Tedlar bag, and the concentration analysis of the produced gas component was performed using a gas-tech detector tube.
５．燃焼性試験（２８．３Ｌタンク試験）
ガス発生剤組成物の成形体（ガス発生剤）９．９ｇを、長尺筒状のハウジングを備えたガス発生器に充填し、２８．３Ｌタンク試験を実施し、圧力−時間曲線を計測した。5. Flammability test (28.3L tank test)
A gas generator having a long cylindrical housing was charged with 9.9 g of a molded product (gas generant) of the gas generant composition, a 28.3 L tank test was performed, and a pressure-time curve was measured. .
６．着火性試験
ガス発生剤組成物の成形体（ガス発生剤）０．５ｇを大気中でバーナーにより着火し、ガス発生剤が着火し燃焼するかどうかについて確認した。6). Ignition test 0.5 g of a molded product (gas generant) of the gas generant composition was ignited by a burner in the atmosphere, and it was confirmed whether the gas generant was ignited and combusted.
（実施例１）
硝酸グアニジン５５質量部、塩基性硝酸銅４０質量部、５０％粒径が１９．８４μｍの過塩素酸カリウム５質量部、高分散シリカ０．４質量部を混合し、更に０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、次いで、９０℃で５時間熱処理して顆粒を作製した。その後、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。Example 1
Mixing 55 parts by mass of guanidine nitrate, 40 parts by mass of basic copper nitrate, 5 parts by mass of potassium perchlorate having a 50% particle size of 19.84 μm, 0.4 parts by mass of highly dispersed silica, and further 0.6% by
（実施例２）
硝酸グアニジン５６質量部、塩基性硝酸銅３４質量部、５０％粒径が１９．８４μｍの過塩素酸カリウム１０質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Example 2)
56 parts by mass of guanidine nitrate, 34 parts by mass of basic copper nitrate, 10 parts by mass of potassium perchlorate having a 50% particle size of 19.84 μm, and 0.4 parts by mass of highly dispersed silica were mixed, and then 0.6% by
（実施例３）
硝酸グアニジン４５質量部、塩基性硝酸銅３１．２質量部、５０％粒径が１９．８４μｍの過塩素酸カリウム１５質量部、ポリビニルピロリドン１．４質量部、ヒドロキシプロピルメチルセルロース２．２質量部、高分散シリカ０．４質量部、酸性白土４．８質量部を混合し、次いで、水１６質量部、変性エタノール３質量部を添加し、万能混合機で混練した。その後、押出機にて直径φ１．５ｍｍ、長さ２．５ｍｍの円柱物に成形した後、５５℃で８時間、１１０℃で８時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Example 3)
45 parts by mass of guanidine nitrate, 31.2 parts by mass of basic copper nitrate, 15 parts by mass of potassium perchlorate having a 50% particle size of 19.84 μm, 1.4 parts by mass of polyvinylpyrrolidone, 2.2 parts by mass of hydroxypropylmethylcellulose, 0.4 parts by mass of highly dispersed silica and 4.8 parts by mass of acid clay were mixed, then 16 parts by mass of water and 3 parts by mass of denatured ethanol were added and kneaded with a universal mixer. Thereafter, it was molded into a cylindrical product having a diameter of 1.5 mm and a length of 2.5 mm with an extruder, and then heat treated at 55 ° C. for 8 hours and at 110 ° C. for 8 hours, and the molded product of the gas generant composition of the present invention ( Gas generating agent) was obtained.
（実施例４）
硝酸グアニジン５５質量部、塩基性硝酸銅４０質量部、５０％粒径が１４．８９μｍの過塩素酸カリウム５質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。Example 4
55 parts by mass of guanidine nitrate, 40 parts by mass of basic copper nitrate, 5 parts by mass of potassium perchlorate having a 50% particle size of 14.89 μm, and 0.4 parts by mass of highly dispersed silica are mixed, and then 0.6% by
（実施例５）
硝酸グアニジン５５質量部、塩基性硝酸銅４０質量部、５０％粒径が４４．４１μｍの過塩素酸カリウム５質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Example 5)
55 parts by mass of guanidine nitrate, 40 parts by mass of basic copper nitrate, 5 parts by mass of potassium perchlorate having a 50% particle size of 44.41 μm, and 0.4 parts by mass of highly dispersed silica are mixed, and then 0.6% by
（実施例６）
硝酸グアニジン５６質量部、塩基性硝酸銅３４質量部、５０％粒径が１９．８４μｍの過塩素酸カリウム１０質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径３．２ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Example 6)
56 parts by mass of guanidine nitrate, 34 parts by mass of basic copper nitrate, 10 parts by mass of potassium perchlorate having a 50% particle size of 19.84 μm, and 0.4 parts by mass of highly dispersed silica were mixed, and then 0.6% by
（実施例７）
硝酸グアニジン５６質量部、塩基性硝酸銅３４質量部、５０％粒径が１９．８４μｍの過塩素酸カリウム１０質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径２．５ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Example 7)
56 parts by mass of guanidine nitrate, 34 parts by mass of basic copper nitrate, 10 parts by mass of potassium perchlorate having a 50% particle size of 19.84 μm, and 0.4 parts by mass of highly dispersed silica were mixed, and then 0.6% by
（比較例１）
硝酸グアニジン５３質量部、塩基性硝酸銅４７質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１２質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で熱処理をして比較例用のガス発生剤組成物の成形体（ガス発生剤）を得た。(Comparative Example 1)
53 parts by mass of guanidine nitrate, 47 parts by mass of basic copper nitrate, and 0.4 parts by mass of highly dispersed silica were mixed, and then 12 parts by mass of a 0.6% by mass aqueous polyvinyl alcohol solution was added by spraying. Granules were prepared by heat treatment for 5 hours. Next, 0.4 parts by mass of magnesium stearate was added and formed into a cylinder having a diameter of 4.0 mm and a thickness of 1.50 mm, and then heat-treated at 110 ° C. to prepare a gas generating composition for a comparative example. A molded body (gas generating agent) was obtained.
（比較例２）
硝酸グアニジン５５質量部、塩基性硝酸銅４０質量部、５０％粒径が１９４．４μｍの過塩素酸カリウム５質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Comparative Example 2)
55 parts by mass of guanidine nitrate, 40 parts by mass of basic copper nitrate, 5 parts by mass of potassium perchlorate having a 50% particle size of 194.4 μm, and 0.4 parts by mass of highly dispersed silica were mixed, and then 0.6% by
（比較例３）
硝酸グアニジン４０．２質量部、塩基性硝酸銅５１質量部、ポリビニルピロリドン１．４質量部、ヒドロキシプロピルメチルセルロース２．２質量部、高分散シリカ０．４質量部、酸性白土４．８質量部を混合し、次いで、水１６質量部、変性エタノール３質量部を添加し、万能混合機で混練した。その後、押出機にて直径φ１．５ｍｍ、長さ２．５ｍｍの円柱物に成形した後、５５℃で８時間、１１０℃で８時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Comparative Example 3)
40.2 parts by mass of guanidine nitrate, 51 parts by mass of basic copper nitrate, 1.4 parts by mass of polyvinylpyrrolidone, 2.2 parts by mass of hydroxypropylmethylcellulose, 0.4 parts by mass of highly dispersed silica, 4.8 parts by mass of acid clay Next, 16 parts by mass of water and 3 parts by mass of denatured ethanol were added and kneaded with a universal mixer. Thereafter, it was molded into a cylindrical product having a diameter of 1.5 mm and a length of 2.5 mm with an extruder, and then heat treated at 55 ° C. for 8 hours and at 110 ° C. for 8 hours, and the molded product of the gas generant composition of the present invention ( Gas generating agent) was obtained.
（比較例４）
硝酸グアニジン５９質量部、塩基性硝酸銅２１質量部、５０％粒径が１９．８４μｍの過塩素酸カリウム２０質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Comparative Example 4)
59 parts by mass of guanidine nitrate, 21 parts by mass of basic copper nitrate, 20 parts by mass of potassium perchlorate having a 50% particle size of 19.84 μm, and 0.4 parts by mass of highly dispersed silica were mixed, and then 0.6% by
（比較例５）
硝酸グアニジン５５質量部、塩基性硝酸銅４０質量部、５０％粒径が９２．７３μｍの過塩素酸カリウム５質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Comparative Example 5)
55 parts by mass of guanidine nitrate, 40 parts by mass of basic copper nitrate, 5 parts by mass of potassium perchlorate having a 50% particle size of 92.73 μm, and 0.4 parts by mass of highly dispersed silica were mixed, and then 0.6% by
（比較例６）
硝酸グアニジン５５質量部、塩基性硝酸銅４０質量部、５０％粒径が１４４．８μｍの過塩素酸カリウム５質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Comparative Example 6)
55 parts by mass of guanidine nitrate, 40 parts by mass of basic copper nitrate, 5 parts by mass of potassium perchlorate having a 50% particle size of 144.8 μm, and 0.4 parts by mass of highly dispersed silica are mixed, and then 0.6% by
（比較例７）
硝酸グアニジン５５質量部、塩基性硝酸銅４０質量部、５０％粒径が２２２．９μｍの過塩素酸カリウム５質量部、高分散シリカ０．４質量部を混合し、次いで、０．６質量％のポリビニルアルコール水溶液１１質量部を噴霧添加し、その後、９０℃で５時間熱処理して顆粒を作製した。次に、ステアリン酸マグネシウム０．４質量部を添加し、直径４．０ｍｍ、厚さ１．５０ｍｍの円柱物に成形した後、１１０℃で１０時間熱処理して本発明のガス発生剤組成物の成形体（ガス発生剤）を得た。(Comparative Example 7)
55 parts by mass of guanidine nitrate, 40 parts by mass of basic copper nitrate, 5 parts by mass of potassium perchlorate having a 50% particle size of 222.9 μm, and 0.4 parts by mass of highly dispersed silica are mixed, and then 0.6% by
＜試験例１．耐環境試験（高温安定性試験）＞
実施例２のガス発生剤組成物の成形体を、１０７℃にて４００時間、８００時間、１２００時間の耐環境試験に投入した。初期重量及び試験後重量から算出した重量減少率を表１に示す。実施例２の重量減少率は１％以下であり、高温条件下における分解はほとんどなくガス発生剤として容認できる性能であることを確認できる。また、この耐環境試験に供した実施例２のガス発生剤について、上記燃焼性試験（１８ｃｃタンク試験）にて性能評価を行なった。その結果を表２に示す。耐環境試験を経た実施例２のガス発生剤は、最大到達圧力（ＰＭａｘ）及び最大圧力への到達時間（ｔＰｍａｘ）、並びに圧力発生速度（ｄＰ／ｄｔ）が、初期と比較して変化しておらず、高温安定性に優れていることが分かる。<Test Example 1. Environmental resistance test (high temperature stability test)>
The molded product of the gas generant composition of Example 2 was put into an environmental resistance test at 107 ° C. for 400 hours, 800 hours, and 1200 hours. Table 1 shows the weight loss rate calculated from the initial weight and the weight after the test. The weight reduction rate of Example 2 is 1% or less, and it can be confirmed that the performance is acceptable as a gas generating agent with almost no decomposition under high temperature conditions. Moreover, about the gas generating agent of Example 2 used for this environmental resistance test, performance evaluation was performed in the said flammability test (18cc tank test). The results are shown in Table 2. In the gas generating agent of Example 2 that passed the environmental resistance test, the maximum ultimate pressure (PMax), the time to reach the maximum pressure (tPmax), and the pressure generation rate (dP / dt) changed compared to the initial stage. It can be seen that the high temperature stability is excellent.
＜試験例２．燃焼性試験（１８ｃｃタンク試験）＞
実施例１、実施例２、比較例１及び比較例２のガス発生剤組成物成形体について、１８ｃｃタンク試験を実施した。その結果を表３に示す。実施例１及び実施例２は、比較例１より最大圧力到達時間（ｔＰｍａｘ）が短く、圧力上昇速度（ｄＰ／ｄｔ）も高い値を示しており、燃焼速度が速くなっていることが分かる。また、５０％粒径が異なる過塩素酸カリウムを使用した実施例１と比較例２の比較では、実施例１の方が、最大圧力到達時間（ｔＰｍａｘ）が短く、圧力上昇速度（ｄＰ／ｄｔ）も大きいことから、燃焼速度が速くなっていることを確認できる。また、最大到達圧力（Ｐｍａｘ）も、実施例１の方が比較例２より高くなることが確認できる。<Test Example 2. Flammability test (18cc tank test)>
For the gas generant composition molded bodies of Example 1, Example 2, Comparative Example 1 and Comparative Example 2, an 18 cc tank test was conducted. The results are shown in Table 3. In Examples 1 and 2, the maximum pressure arrival time (tPmax) is shorter than that in Comparative Example 1, and the pressure increase rate (dP / dt) is also high, indicating that the combustion rate is high. Further, in comparison between Example 1 and Comparative Example 2 using potassium perchlorate having different 50% particle size, Example 1 has a shorter maximum pressure arrival time (tPmax) and a pressure increase rate (dP / dt). ) Is also large, so it can be confirmed that the combustion speed is high. It can also be confirmed that the maximum ultimate pressure (Pmax) is higher in Example 1 than in Comparative Example 2.
＜試験例３．排ガス測定（１８ｃｃタンク試験）＞
実施例１、実施例２、比較例１及び比較例２のガス発生剤組成物成形体について、１８ｃｃタンク試験後の排ガスを回収し、燃焼後の発生ガス分析を実施した。その結果を表４に示す。実施例１は、発生ガス成分の全てにおいて比較例１及び比較例２より発生量が少ないことを確認できる。また、実施例２においても、実施例１と同程度の結果が得られることが分かる。なお、全てのガス発生剤において塩化水素の生成は認められない。<Test Example 3. Exhaust gas measurement (18cc tank test)>
For the gas generant composition molded bodies of Example 1, Example 2, Comparative Example 1 and Comparative Example 2, the exhaust gas after the 18 cc tank test was collected, and the generated gas after combustion was analyzed. The results are shown in Table 4. In Example 1, it can be confirmed that the amount of generated gas is less than that of Comparative Example 1 and Comparative Example 2 in all of the generated gas components. Also, it can be seen that the same result as in Example 1 is obtained in Example 2. In all gas generating agents, hydrogen chloride is not generated.
＜試験例４．燃焼性試験（２８．３Ｌタンク試験）＞
実施例３及び比較例３のガス発生剤組成物成形体について、２８．３Ｌタンク試験を実施した。通常、ガス発生器には点火具からの火炎を増幅させるエンハンサー剤が使用されているが、この実験では、エンハンサー剤を取り除いた仕様で行った。その結果を図３に示す。実施例３は、エンハンサー剤がなくても着火しタンク圧を上昇させているが、比較例３では、着火が起きていないことが分かる。このことから、実施例３のガス発生剤は、着火性に優れることが分かる。また、得られた圧力−時間曲線の結果から、実施例３のガス発生剤が、優れた応答性と十分なガス発生特性とを有することは明らかである。<Test Example 4. Flammability test (28.3L tank test)>
For the gas generant composition molded bodies of Example 3 and Comparative Example 3, a 28.3 L tank test was conducted. Normally, an enhancer that amplifies the flame from the igniter is used in the gas generator, but in this experiment, the specification was made with the enhancer removed. The result is shown in FIG. Although Example 3 ignites and raises the tank pressure without an enhancer, it can be seen that in Comparative Example 3, no ignition occurred. From this, it can be seen that the gas generating agent of Example 3 is excellent in ignitability. Moreover, it is clear from the result of the obtained pressure-time curve that the gas generating agent of Example 3 has excellent responsiveness and sufficient gas generation characteristics.
＜試験例５．着火性試験＞
実施例１、実施例２、実施例３及び比較例４のガス発生剤組成物成形体について、バーナーを用いた着火性試験を実施した。その結果を表５に示す。比較例４のガス発生剤は、酸化剤成分中に占める過塩素酸カリウムの含有量が高過ぎるため、自立燃焼が困難になることが分かる。<Test Example 5. Ignition test>
The gas generant composition molded bodies of Example 1, Example 2, Example 3 and Comparative Example 4 were subjected to an ignitability test using a burner. The results are shown in Table 5. It can be seen that the gas generating agent of Comparative Example 4 has difficulty in self-sustained combustion because the content of potassium perchlorate in the oxidant component is too high.
＜試験例６．燃焼性試験（１８ｃｃタンク試験）；過塩素酸カリウム粒径の影響＞
過塩素酸カリウム（ＰＰ）の５０％粒径が異なる実施例１、実施例４、実施例５及び比較例５〜７のガス発生剤組成物成形体について、１８ｃｃタンク試験を実施した。その結果を表６に示す。使用した過塩素酸カリウムの５０％粒径が小さい程、最大圧力到達時間（ｔＰｍａｘ）が速く、圧力上昇速度（ｄＰ／ｄｔ）が大きくなる傾向を示しており、燃焼速度が速くなることが分かる。その上、５０％粒径が小さい程、最大到達圧力（ＰＭａｘ）も大きくなる傾向を示す。これらの例では、酸化剤成分中に占める過塩素酸カリウムの含有量が同一であるため、過塩素酸カリウムの５０％粒径を小さくすることで、ガス発生剤の性能向上が達成できることが明らかとなる。また、５０％粒径が５０μｍ以下の過塩素酸カリウムを用いることにより、ガス発生剤の燃焼性を向上できることが分かる。<Test Example 6. Flammability test (18cc tank test); Effect of particle size of potassium perchlorate>
The 18 cc tank test was implemented about the gas generating agent molded object of Example 1, Example 4, Example 5, and Comparative Examples 5-7 from which the 50% particle size of potassium perchlorate (PP) differs. The results are shown in Table 6. It can be seen that the smaller the 50% particle size of the potassium perchlorate used, the faster the maximum pressure arrival time (tPmax) and the higher the pressure increase rate (dP / dt), and the faster the combustion rate. . In addition, the smaller the 50% particle size, the greater the maximum ultimate pressure (PMax). In these examples, since the content of potassium perchlorate in the oxidant component is the same, it is clear that the performance improvement of the gas generating agent can be achieved by reducing the 50% particle size of potassium perchlorate. It becomes. Moreover, it turns out that the combustibility of a gas generating agent can be improved by using potassium perchlorate whose 50% particle size is 50 micrometers or less.
＜試験例７．燃焼性試験（１８ｃｃタンク試験）；ガス発生剤組成物の成形体形状の影響＞
本発明のガス発生剤組成物の成形体において、成形体の形状が燃焼性に与える影響を検証するため、打錠成形体の直径が異なる実施例２、実施例６及び実施例７のガス発生剤組成物の成形体について、１８ｃｃタンク試験を実施した。結果を表７に示す。実施例２、実施例６及び実施例７は、同一の組成であるにもかかわらず、直径が小さい程、最大圧力到達時間（ｔＰｍａｘ）が短くなるため、最大到達圧力（ＰＭａｘ）の差異は認められないが、結果として、圧力上昇速度（ｄＰ／ｄｔ）が速くなることが分かる。<Test Example 7. Flammability test (18 cc tank test); Influence of molded product shape of gas generant composition>
In the molded article of the gas generant composition of the present invention, in order to verify the influence of the shape of the molded article on the flammability, the gas generation of Examples 2, 6 and 7 with different diameters of the tableting molded article The molded product of the agent composition was subjected to an 18 cc tank test. The results are shown in Table 7. Although Example 2, Example 6 and Example 7 have the same composition, the smaller the diameter, the shorter the maximum pressure attainment time (tPmax). Therefore, a difference in the maximum attainment pressure (PMax) is recognized. However, as a result, it can be seen that the pressure increase rate (dP / dt) is increased.
＜試験例８．嵩密度測定；ガス発生剤組成物の成形体形状の影響＞
実施例２、実施例６及び実施例７のガス発生剤組成物の成形体について、容積１００ｃｃの円筒容器を用いて、成形体の嵩密度の測定を行った。測定結果を表７に示す。ガス発生剤の直径が小さい程、嵩密度が高くなることが分かる。<Test Example 8. Measurement of bulk density; influence of the shape of the gas generant composition>
About the molded object of the gas generant composition of Example 2, Example 6, and Example 7, the bulk density of the molded object was measured using a cylindrical container with a capacity of 100 cc. Table 7 shows the measurement results. It can be seen that the smaller the diameter of the gas generating agent, the higher the bulk density.
ガス発生剤組成物の成形体形状に関する試験例７及び試験例８の結果から、本発明に係るガス発生剤組成物の成形体は、円柱直径が小さい程、圧力上昇速度が速く、燃焼性を向上できることが分かる。この理由は解明されていないが、成形体の直径が小さい程、ガス発生剤単位質量当たりのガス発生剤表面積が大きいため、燃焼性の向上に寄与するものと予想される。 From the results of Test Example 7 and Test Example 8 relating to the shape of the molded article of the gas generant composition, the molded article of the gas generant composition according to the present invention has a higher pressure rise rate and lower flammability as the cylinder diameter is smaller. It can be seen that it can be improved. Although the reason for this has not been elucidated, it is expected that the smaller the diameter of the molded body, the larger the surface area of the gas generant per unit mass of the gas generant, which contributes to the improvement of combustibility.
更に、本発明のガス発生剤組成物の円柱状成形体においては、直径が小さい程、嵩密度が大きくなるという結果が得られた。これは、該ガス発生剤のガス発生器への充填性が向上することを示すものであるため、単位容積当たりのガス発生剤の充填量を増加でき、ガス発生器の高出力化を達成できるという効果を奏する。また、本発明のガス発生剤組成物の円柱状成形体の直径を小さくすれば、充填性が向上する上、応答性に優れるため、ガス発生器へガス発生剤を充填する容積を小さくすることが可能であり、ガス発生器の小型化を達成できるという効果を奏する。 Furthermore, in the cylindrical molded body of the gas generant composition of the present invention, the result was obtained that the smaller the diameter, the larger the bulk density. This indicates that the filling property of the gas generating agent into the gas generator is improved, so that the filling amount of the gas generating agent per unit volume can be increased, and high output of the gas generator can be achieved. There is an effect. Moreover, if the diameter of the cylindrical molded body of the gas generant composition of the present invention is reduced, the filling property is improved and the responsiveness is excellent. Therefore, the volume for filling the gas generator with the gas generant is reduced. It is possible to achieve a reduction in the size of the gas generator.
本発明のガス発生剤組成物は、着火性及び燃焼性に優れるため、燃焼起動のための電気信号に迅速に呼応し、速やかに着火して大量の燃焼ガスは発生させるものであり、該電気起信号の発信から生成ガスの最大圧力に到達するまでの時間を極めて短くすることができる。このため、優れた応答性が望まれる車両搭乗者安全装置用ガス発生器への使用に好適で、特には、側突用、下肢部保護用又はシート座面上昇用エアバッグ装置用ガス発生器への使用に好適である。 Since the gas generant composition of the present invention is excellent in ignitability and combustibility, it quickly responds to an electrical signal for starting combustion and quickly ignites to generate a large amount of combustion gas. The time from the generation of the starting signal until the maximum pressure of the product gas is reached can be extremely shortened. For this reason, it is suitable for use in a gas generator for a vehicle occupant safety device for which excellent responsiveness is desired, and in particular, a gas generator for an airbag device for side impact, for lower limb protection, or for raising a seat seat surface. Suitable for use in.
１，１１ ガス発生器
２，１２ ハウジング
３，１３ 点火装置
４，１４ ガス発生剤
５，１５ フィルター
６，１６ ガス放出孔
７，１７ 点火室DESCRIPTION OF
Claims (13)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
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| JP2011503708A JP5719763B2 (en) | 2009-03-13 | 2010-03-09 | GAS GENERATOR COMPOSITION, MOLDED BODY THEREOF, AND GAS GENERATOR USING THE SAME |
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| JP2009061450 | 2009-03-13 | ||
| JP2009061450 | 2009-03-13 | ||
| PCT/JP2010/001665 WO2010103811A1 (en) | 2009-03-13 | 2010-03-09 | Gas generant composition, molded object thereof, and gas generator using same |
| JP2011503708A JP5719763B2 (en) | 2009-03-13 | 2010-03-09 | GAS GENERATOR COMPOSITION, MOLDED BODY THEREOF, AND GAS GENERATOR USING THE SAME |
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| JPWO2010103811A1 true JPWO2010103811A1 (en) | 2012-09-13 |
| JP5719763B2 JP5719763B2 (en) | 2015-05-20 |
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| US (1) | US20120000583A1 (en) |
| EP (1) | EP2407443A4 (en) |
| JP (1) | JP5719763B2 (en) |
| CN (1) | CN102414147A (en) |
| WO (1) | WO2010103811A1 (en) |
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| FR2949778B1 (en) * | 2009-09-10 | 2013-05-10 | Snpe Materiaux Energetiques | PYROTECHNIC COMPOUNDS GENERATORS OF GAS |
| FR2975097B1 (en) * | 2011-05-09 | 2015-11-20 | Sme | PYROTECHNIC COMPOUNDS GENERATORS OF GAS |
| WO2014173504A1 (en) * | 2013-04-25 | 2014-10-30 | Fischerwerke Gmbh & Co. Kg | Electrically-ignitable caseless propellant, and the production and use of same |
| JP6310735B2 (en) * | 2014-03-12 | 2018-04-11 | 日本化薬株式会社 | Gas generator |
| CN105157493B (en) * | 2015-09-30 | 2016-08-24 | 马卫国 | A kind of explosion expansion tube and blasting method thereof |
| WO2017205257A1 (en) | 2016-05-23 | 2017-11-30 | Tk Holdings Inc. | Gas generating compositions and methods of making and using thereof |
| CN110317120B (en) * | 2019-05-30 | 2020-10-20 | 湖北航鹏化学动力科技有限责任公司 | Ignition powder, preparation method and application thereof and safety airbag gas generator |
| AU2020210211B2 (en) | 2019-09-18 | 2022-09-08 | Innovatus Design Pty Ltd | A modular partition and fabrication thereof |
| US20230312431A1 (en) * | 2020-01-22 | 2023-10-05 | Xi'an Crysten Materials Technology Corporation Limited | Compounds and preparation method therefor and use thereof as energetic materials |
| CN116789506A (en) * | 2023-06-30 | 2023-09-22 | 陕西庆华汽车安全***有限公司 | Gas generating composition for automobile safety belt pretensioner and preparation method thereof |
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| JPH10297419A (en) * | 1997-05-01 | 1998-11-10 | Nippon Kayaku Co Ltd | Gas generator |
| JP2926040B2 (en) * | 1997-05-09 | 1999-07-28 | ダイセル化学工業株式会社 | Gas generator and airbag device for airbag |
| JP2000103692A (en) * | 1998-09-30 | 2000-04-11 | Daicel Chem Ind Ltd | Gas generator composition molding product for air bag |
| JP2000319086A (en) * | 1999-05-10 | 2000-11-21 | Nippon Kayaku Co Ltd | Gas generating agent molding |
| WO2001023304A1 (en) * | 1999-09-27 | 2001-04-05 | Daicel Chemical Industries, Ltd. | Basic metal nitrate, method for producing the same and gas-generating agent composition |
| JP4641130B2 (en) * | 2000-10-10 | 2011-03-02 | 日本化薬株式会社 | Gas generating composition and gas generator using the same |
| CZ20033057A3 (en) * | 2001-04-10 | 2004-03-17 | Nippon Kayaku Kabushiki-Kaisha | Gas generator |
| WO2002092539A1 (en) * | 2001-05-10 | 2002-11-21 | Nippon Kayaku Kabushiki Kaisha | Igniting agent composition, and igniter using the igniting agent composition |
| US6875295B2 (en) * | 2001-12-27 | 2005-04-05 | Trw Inc. | Cool burning gas generating material for a vehicle occupant protection apparatus |
| AU2003207250A1 (en) * | 2002-02-06 | 2003-09-02 | Nippon Kayaku Kabushiki-Kaisha | Gas generator |
| JP4302442B2 (en) * | 2002-09-12 | 2009-07-29 | ダイセル化学工業株式会社 | Gas generant composition |
| JP4767487B2 (en) * | 2003-10-20 | 2011-09-07 | ダイセル化学工業株式会社 | Gas generant composition |
| US20050127324A1 (en) * | 2003-10-22 | 2005-06-16 | Jianzhou Wu | Gas generating composition |
| US7665764B2 (en) * | 2004-01-15 | 2010-02-23 | Daicel Chemical Industries, Ltd. | Gas generator for air bag |
| US20050161135A1 (en) * | 2004-01-28 | 2005-07-28 | Williams Graylon K. | Auto-igniting pyrotechnic booster composition |
| JP2006076849A (en) * | 2004-09-10 | 2006-03-23 | Nippon Kayaku Co Ltd | Gas producing agent composition and gas producer having the same |
| EP1990088B1 (en) * | 2006-01-18 | 2019-09-25 | Nippon Kayaku Kabushiki Kaisha | Small gas-generating device for gas actuator and pretensioner system |
| FR2949778B1 (en) * | 2009-09-10 | 2013-05-10 | Snpe Materiaux Energetiques | PYROTECHNIC COMPOUNDS GENERATORS OF GAS |
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| US20120000583A1 (en) | 2012-01-05 |
| EP2407443A4 (en) | 2013-11-27 |
| JP5719763B2 (en) | 2015-05-20 |
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