EP0519485A1 - Treibmittel für Gasgeneratoren - Google Patents
Treibmittel für Gasgeneratoren Download PDFInfo
- Publication number
- EP0519485A1 EP0519485A1 EP92110353A EP92110353A EP0519485A1 EP 0519485 A1 EP0519485 A1 EP 0519485A1 EP 92110353 A EP92110353 A EP 92110353A EP 92110353 A EP92110353 A EP 92110353A EP 0519485 A1 EP0519485 A1 EP 0519485A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- derivatives
- propellant
- nitrate
- salts
- radical
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000003380 propellant Substances 0.000 title claims abstract description 30
- 239000000203 mixture Substances 0.000 claims abstract description 35
- 150000002978 peroxides Chemical class 0.000 claims abstract description 16
- 239000007800 oxidant agent Substances 0.000 claims abstract description 13
- 150000001875 compounds Chemical class 0.000 claims abstract description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 11
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000011575 calcium Substances 0.000 claims abstract description 9
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 9
- 239000011777 magnesium Substances 0.000 claims abstract description 9
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims abstract description 7
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000011591 potassium Substances 0.000 claims abstract description 7
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 7
- 239000011734 sodium Substances 0.000 claims abstract description 7
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 7
- 150000003536 tetrazoles Chemical class 0.000 claims abstract description 7
- 150000002823 nitrates Chemical class 0.000 claims abstract description 6
- 239000003054 catalyst Substances 0.000 claims abstract description 5
- 229910052742 iron Inorganic materials 0.000 claims abstract description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 4
- 239000004202 carbamide Substances 0.000 claims abstract description 4
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 4
- XLJMAIOERFSOGZ-UHFFFAOYSA-N cyanic acid Chemical class OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 claims abstract description 4
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims abstract description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000002826 coolant Substances 0.000 claims abstract description 3
- 229910052712 strontium Inorganic materials 0.000 claims abstract description 3
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 claims abstract description 3
- 150000003918 triazines Chemical class 0.000 claims abstract description 3
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 3
- 239000011701 zinc Substances 0.000 claims abstract description 3
- -1 amino, carboxyl Chemical group 0.000 claims description 29
- 239000007789 gas Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 13
- ULRPISSMEBPJLN-UHFFFAOYSA-N 2h-tetrazol-5-amine Chemical compound NC1=NN=NN1 ULRPISSMEBPJLN-UHFFFAOYSA-N 0.000 claims description 12
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- DLINORNFHVEIFE-UHFFFAOYSA-N hydrogen peroxide;zinc Chemical compound [Zn].OO DLINORNFHVEIFE-UHFFFAOYSA-N 0.000 claims description 8
- 229940105296 zinc peroxide Drugs 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical class NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 6
- 229910002651 NO3 Inorganic materials 0.000 claims description 6
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 6
- HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical compound NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 235000010344 sodium nitrate Nutrition 0.000 claims description 6
- 239000004317 sodium nitrate Substances 0.000 claims description 6
- JGZAFSFVZSXXCJ-ONEGZZNKSA-N (E)-bis(2H-tetrazol-5-yl)diazene Chemical compound N(=N\C1=NN=NN1)/C1=NN=NN1 JGZAFSFVZSXXCJ-ONEGZZNKSA-N 0.000 claims description 4
- 150000005840 aryl radicals Chemical class 0.000 claims description 4
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 4
- 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 4
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 238000003825 pressing Methods 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- OTXHZHQQWQTQMW-UHFFFAOYSA-N (diaminomethylideneamino)azanium;hydrogen carbonate Chemical compound OC([O-])=O.N[NH2+]C(N)=N OTXHZHQQWQTQMW-UHFFFAOYSA-N 0.000 claims description 3
- IDCPFAYURAQKDZ-UHFFFAOYSA-N 1-nitroguanidine Chemical compound NC(=N)N[N+]([O-])=O IDCPFAYURAQKDZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000004604 Blowing Agent Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 3
- 125000006501 nitrophenyl group Chemical group 0.000 claims description 3
- DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 claims description 3
- IATXFPUBPMZBPH-UHFFFAOYSA-N (n'-carbamoylcarbamimidoyl)azanium;sulfate Chemical compound OS(O)(=O)=O.NC(N)=NC(N)=O.NC(N)=NC(N)=O IATXFPUBPMZBPH-UHFFFAOYSA-N 0.000 claims description 2
- FYADHXFMURLYQI-UHFFFAOYSA-N 1,2,4-triazine Chemical class C1=CN=NC=N1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 claims description 2
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052582 BN Inorganic materials 0.000 claims description 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 2
- 239000004343 Calcium peroxide Substances 0.000 claims description 2
- SQSPRWMERUQXNE-UHFFFAOYSA-N Guanylurea Chemical compound NC(=N)NC(N)=O SQSPRWMERUQXNE-UHFFFAOYSA-N 0.000 claims description 2
- 229920000877 Melamine resin Polymers 0.000 claims description 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 2
- 239000004809 Teflon Substances 0.000 claims description 2
- 229920006362 Teflon® Polymers 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 claims description 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 2
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 claims description 2
- 235000019402 calcium peroxide Nutrition 0.000 claims description 2
- FFNKZSVHHUBFHT-UHFFFAOYSA-N cyanamide;sodium Chemical compound [Na].[Na].NC#N FFNKZSVHHUBFHT-UHFFFAOYSA-N 0.000 claims description 2
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 2
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 claims description 2
- 239000010439 graphite Substances 0.000 claims description 2
- 229910002804 graphite Inorganic materials 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 2
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- JCLYRAQECYMILR-UHFFFAOYSA-M potassium;5-aminotetrazole-5-carboxylate Chemical compound [K+].[O-]C(=O)C1(N)N=NN=N1 JCLYRAQECYMILR-UHFFFAOYSA-M 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- 150000004655 tetrazenes Chemical class 0.000 claims description 2
- 150000003672 ureas Chemical class 0.000 claims description 2
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 2
- BAKYASSDAXQKKY-UHFFFAOYSA-N 4-Hydroxy-3-methylbenzaldehyde Chemical compound CC1=CC(C=O)=CC=C1O BAKYASSDAXQKKY-UHFFFAOYSA-N 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000000306 component Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 6
- 238000000465 moulding Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000007792 addition Methods 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000036541 health Effects 0.000 description 4
- 230000035945 sensitivity Effects 0.000 description 4
- 239000003981 vehicle Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 231100001261 hazardous Toxicity 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 2
- 239000000006 Nitroglycerin Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000004200 deflagration Methods 0.000 description 2
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 description 2
- 229960003711 glyceryl trinitrate Drugs 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- LQICKCWPFRQEFI-UHFFFAOYSA-N n-methyl-2h-tetrazol-5-amine Chemical compound CNC=1N=NNN=1 LQICKCWPFRQEFI-UHFFFAOYSA-N 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000002341 toxic gas Substances 0.000 description 2
- VKGQPUZNCZPZKI-UHFFFAOYSA-N (diaminomethylideneamino)azanium;sulfate Chemical compound NN=C(N)N.NN=C(N)N.OS(O)(=O)=O VKGQPUZNCZPZKI-UHFFFAOYSA-N 0.000 description 1
- IBMCQJYLPXUOKM-UHFFFAOYSA-N 1,2,2,6,6-pentamethyl-3h-pyridine Chemical compound CN1C(C)(C)CC=CC1(C)C IBMCQJYLPXUOKM-UHFFFAOYSA-N 0.000 description 1
- NHYHTYJIILODSA-UHFFFAOYSA-N 1-(4-nitrophenyl)tetrazole Chemical compound C1=CC([N+](=O)[O-])=CC=C1N1N=NN=C1 NHYHTYJIILODSA-UHFFFAOYSA-N 0.000 description 1
- OMAFFHIGWTVZOH-UHFFFAOYSA-N 1-methyltetrazole Chemical compound CN1C=NN=N1 OMAFFHIGWTVZOH-UHFFFAOYSA-N 0.000 description 1
- FYYACQQSYSDVJB-UHFFFAOYSA-N 1-phenyl-2h-tetrazol-5-one Chemical compound OC1=NN=NN1C1=CC=CC=C1 FYYACQQSYSDVJB-UHFFFAOYSA-N 0.000 description 1
- ULIDRMKBVYYVIQ-UHFFFAOYSA-N 1-phenyltetrazol-5-amine Chemical compound NC1=NN=NN1C1=CC=CC=C1 ULIDRMKBVYYVIQ-UHFFFAOYSA-N 0.000 description 1
- IYPXPGSELZFFMI-UHFFFAOYSA-N 1-phenyltetrazole Chemical compound C1=NN=NN1C1=CC=CC=C1 IYPXPGSELZFFMI-UHFFFAOYSA-N 0.000 description 1
- JXBKZAYVMSNKHA-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-olate Chemical compound OC=1N=NNN=1 JXBKZAYVMSNKHA-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- SUEIINDYWPMJEW-UHFFFAOYSA-N 2-ethyltetrazol-5-amine Chemical compound CCN1N=NC(N)=N1 SUEIINDYWPMJEW-UHFFFAOYSA-N 0.000 description 1
- AZUKLCJYWVMPML-UHFFFAOYSA-N 2-methyltetrazol-5-amine Chemical compound CN1N=NC(N)=N1 AZUKLCJYWVMPML-UHFFFAOYSA-N 0.000 description 1
- VRESBNUEIKZECD-UHFFFAOYSA-N 2-methyltetrazole Chemical compound CN1N=CN=N1 VRESBNUEIKZECD-UHFFFAOYSA-N 0.000 description 1
- VQHZPBXUOJDGTE-UHFFFAOYSA-N 2-methyltetrazole-5-carboxylic acid Chemical compound CN1N=NC(C(O)=O)=N1 VQHZPBXUOJDGTE-UHFFFAOYSA-N 0.000 description 1
- QLDFMNWSPWEFIM-UHFFFAOYSA-N 2-phenyltetrazole Chemical compound N1=CN=NN1C1=CC=CC=C1 QLDFMNWSPWEFIM-UHFFFAOYSA-N 0.000 description 1
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 description 1
- JRRAUWWVBVECPY-UHFFFAOYSA-N 4-(tetrazol-1-yl)aniline Chemical compound C1=CC(N)=CC=C1N1N=NN=C1 JRRAUWWVBVECPY-UHFFFAOYSA-N 0.000 description 1
- BCCJIAZPYBJASR-UHFFFAOYSA-N 5-(4-methylphenyl)-2H-tetrazole Chemical compound C1=CC(C)=CC=C1C1=NNN=N1 BCCJIAZPYBJASR-UHFFFAOYSA-N 0.000 description 1
- XZGLNCKSNVGDNX-UHFFFAOYSA-N 5-methyl-2h-tetrazole Chemical compound CC=1N=NNN=1 XZGLNCKSNVGDNX-UHFFFAOYSA-N 0.000 description 1
- MARUHZGHZWCEQU-UHFFFAOYSA-N 5-phenyl-2h-tetrazole Chemical compound C1=CC=CC=C1C1=NNN=N1 MARUHZGHZWCEQU-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical compound NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- VBIXEXWLHSRNKB-UHFFFAOYSA-N ammonium oxalate Chemical compound [NH4+].[NH4+].[O-]C(=O)C([O-])=O VBIXEXWLHSRNKB-UHFFFAOYSA-N 0.000 description 1
- IMHBYKMAHXWHRP-UHFFFAOYSA-N anilazine Chemical compound ClC1=CC=CC=C1NC1=NC(Cl)=NC(Cl)=N1 IMHBYKMAHXWHRP-UHFFFAOYSA-N 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000013590 bulk material Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940087373 calcium oxide Drugs 0.000 description 1
- DWPDSISGRAWLLV-JHZYRPMRSA-L calcium;(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Ca+2].C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C([O-])=O.C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C([O-])=O DWPDSISGRAWLLV-JHZYRPMRSA-L 0.000 description 1
- GJTDGCRKKXOTQZ-UHFFFAOYSA-L calcium;5-aminotetrazole-5-carboxylate Chemical compound [Ca+2].[O-]C(=O)C1(N)N=NN=N1.[O-]C(=O)C1(N)N=NN=N1 GJTDGCRKKXOTQZ-UHFFFAOYSA-L 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- HYAJTKXLVUMUKG-UHFFFAOYSA-N cerium(3+) lead(2+) oxygen(2-) Chemical compound [Pb+2].[O-2].[O-2].[Ce+3] HYAJTKXLVUMUKG-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- XOYUVEPYBYHIFZ-UHFFFAOYSA-L diperchloryloxylead Chemical compound [Pb+2].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O XOYUVEPYBYHIFZ-UHFFFAOYSA-L 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052806 inorganic carbonate Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910001484 inorganic perchlorate Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 1
- FBRRQXJRKCVETE-UHFFFAOYSA-N n,1-dimethyltetrazol-5-amine Chemical compound CNC1=NN=NN1C FBRRQXJRKCVETE-UHFFFAOYSA-N 0.000 description 1
- QKCLDBIRKLLWHT-UHFFFAOYSA-N n,2-dimethyltetrazol-5-amine Chemical compound CNC=1N=NN(C)N=1 QKCLDBIRKLLWHT-UHFFFAOYSA-N 0.000 description 1
- ROAFQARTWKYLPD-UHFFFAOYSA-N n,n,1-trimethyltetrazol-5-amine Chemical compound CN(C)C1=NN=NN1C ROAFQARTWKYLPD-UHFFFAOYSA-N 0.000 description 1
- XUYRDKGAGMTGRC-UHFFFAOYSA-N n,n-dimethyl-2h-tetrazol-5-amine Chemical compound CN(C)C=1N=NNN=1 XUYRDKGAGMTGRC-UHFFFAOYSA-N 0.000 description 1
- KTNSUVMJIFVCRV-UHFFFAOYSA-N n-decyl-2h-tetrazol-5-amine Chemical compound CCCCCCCCCCNC=1N=NNN=1 KTNSUVMJIFVCRV-UHFFFAOYSA-N 0.000 description 1
- AYZFMCOIISJDHU-UHFFFAOYSA-N n-ethyl-2h-tetrazol-5-amine Chemical compound CCNC=1N=NNN=1 AYZFMCOIISJDHU-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- VHXONGYTQILYGR-UHFFFAOYSA-N n-heptyl-2h-tetrazol-5-amine Chemical compound CCCCCCCNC=1N=NNN=1 VHXONGYTQILYGR-UHFFFAOYSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- RDLLWXSEEYESKC-UHFFFAOYSA-N n-octyl-2h-tetrazol-5-amine Chemical compound CCCCCCCCNC=1N=NNN=1 RDLLWXSEEYESKC-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JJGVUQXLNNGWPZ-UHFFFAOYSA-N n-phenyl-2h-tetrazol-5-amine Chemical compound C=1C=CC=CC=1NC1=NN=NN1 JJGVUQXLNNGWPZ-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 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
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- ZVCDLGYNFYZZOK-UHFFFAOYSA-M sodium cyanate Chemical compound [Na]OC#N ZVCDLGYNFYZZOK-UHFFFAOYSA-M 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- UHCGLDSRFKGERO-UHFFFAOYSA-N strontium peroxide Chemical compound [Sr+2].[O-][O-] UHCGLDSRFKGERO-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
- 235000009529 zinc sulphate Nutrition 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D5/00—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
- C06D5/06—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets by reaction of two or more solids
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B43/00—Compositions characterised by explosive or thermic constituents not provided for in groups C06B25/00 - C06B41/00
Definitions
- Gas generators are finding increasing interest in saving lives, for example in vehicles.
- the most widely used gas generation mixture in the world contains sodium azide.
- sodium azide is toxic, which requires special measures in the manufacture of the raw material, the gas mixture, its processing, quality control and disposal. This applies in particular to the scrapping of vehicles.
- DE-A-21 42 578 describes a compressed propellant charge for rapidly inflating a hollow body by reacting tetrazylazen with oxygen carriers.
- DE-A-18 06 550 proposes a propellant gas-generating, cool gas-producing propellant based on ammonium nitrate, activated carbon and an endothermic decomposing or sublimating compound.
- this system supplies a large proportion of water vapor, which is disadvantageous because water leads to a sharp increase in temperature due to its high heat of condensation.
- DE-A-12 22 418 describes mixtures which develop pressurized gas on the basis of inorganic perchlorate oxidizers, polymeric fuel binders and a coolant.
- preparations with high levels of chlorate or perchlorate lead to chlorine levels in the reaction gases.
- EP-A-372 733 describes an unsatisfactory mixture since the propellant charge of the proposed airbag contains about 40% ammonium perchlorate.
- Even nitrocellulose and nitroglycerin masses can be found in the literature. Such proposals cannot be used for use in life-saving systems. Nitrocellulose and nitroglycerin mixtures or other carbon-rich, energetic compounds are eliminated due to the formation of carbon monoxide.
- the propellants of DE-A-12 50 318 which contain aminotetrazole, potassium dichromate, calcium resinate and metallic silicon, do not meet today's safety requirements. The same applies to DE-C-20 04 620, whose charge gas-generating charge contains azotetrazole and / or ditetrazole and chlorates or perchlorates.
- the propellants of US Pat. No. 3,734,789 which contain 5-aminotetrazole nitrate and polyisoprene binder, burn off quickly, but also generate carbon monoxide in concentrations which are hazardous to health due to the carbon-rich binder fraction.
- the invention is therefore based on the object of providing gas sets whose production and processing or handling are harmless and whose reaction products are not toxic.
- the nitrogen-containing compounds to be used according to the invention are those which, when mixed with oxidizing agents, form mainly CO2, N2 and H2O in their thermal / chemical reaction, but do not develop gases such as CO or NO x in concentrations which are hazardous to health. It is particularly important that the addition of binders is not absolutely necessary.
- R1 is preferably hydrogen, amino, hydroxy, carboxyl, a methyl, ethyl, propyl or isopropyl, butyl, isobutyl or tert-butyl, n-pentyl, n-hexyl or n-heptyl radical, one Methylamino, ethylamino, dimethylamino, n-heptylamino, n-octylamino or n-decylamino, a phenylamino, a phenyl, nitrophenyl or aminophenyl group.
- R2 or R3 is preferably hydrogen, a methyl or ethyl radical, a phenyl, nitrophenyl or aminophenyl radical.
- the tetrazole derivatives are particularly preferred: 5-aminotetrazole, sodium, potassium or calcium 5-aminotetrazolate, 1- (4-aminophenyl) tetrazole, 1- (4-nitrophenyl) tetrazole, 1-methyl-5-dimethylamino-tetrazole, 1-methyl 5-methylaminotetrazole, 1-methyl-tetrazole, 1-phenyl-5-aminotetrazole, 1-phenyl-5-hydroxy-tetrazole, 1-phenyl-tetrazole, 2-ethyl-5-aminotetrazole, 2-methyl- 5-amino-tetrazole, 2-methyl-5-carboxyl-tetrazole, 2-methyl-5-methylamino-tetrazole, 2-methyl-tetrazole, 2-phenyl-tetrazole, 5- (p-tolyl) -tetrazole, 5- Diallyl-aminotetrazole, 5-dimethylamino-tetrazole
- cyanic acid derivatives 1,3,5-triazine, cyanuric acid ester and / or cyanuric acid amide (melamine) as triazine derivatives and biuret, guanidine, nitroguanidine, guanidine nitrate, aminoguanidine, guanidine nitrate, aminoguanidine as urea derivatives.
- Triaminoguanidine nitrate aminoguanidine hydrogen carbonate, azodicarboxylic acid diamide, dicyandiamidine nitrate, dicyandiamidine sulfate, tetrazene and / or semicarbazide nitrate are used.
- the mixtures according to the invention have high thermal and climatic stability, which is a prerequisite for a perfect effect even after long storage.
- Nitrates of ammonium, sodium, potassium, magnesium, calcium or iron, preferably sodium nitrate or peroxides of zinc, calcium, strontium or magnesium can be used as the oxidizing agent.
- the peroxides are used with an oxygen value that can be obtained from stable compounds. For zinc peroxide, this is about 11 to 14% by weight.
- the corresponding molar ratio of nitrogen-containing compound to peroxide is in the range from 1: 2 to 5.5.
- Calcium peroxide can have an active oxygen value of, for example, 18.62% by weight and grain sizes of 15.5 ⁇ m and is advantageously used in a molar ratio of nitrogenous compound / peroxide of 1: 3.
- the above-mentioned peroxides can be used in a molar ratio of 1: 1 to 20.
- Calcium and / or zinc peroxide is preferably used. Mixtures of the peroxides with one another or with other oxidizing agents can also be used.
- Other oxidizing agents are, for example, the above-mentioned nitrates of ammonium, sodium, potassium, magnesium, calcium or iron, preferably sodium nitrate.
- the alkaline hydrolysis products can cause reactions with the other components of the mixture.
- coating the peroxides with inorganic or organic materials by methods known per se is expedient. Such a coating also offers the advantage of better handling, since the blowing agent treated in this way no longer produces dust.
- the mixtures of the tetrazole or its derivatives to be used according to the invention with the compounds from groups A), B) and / or C) enable the propellants to be graded with respect to their reaction rate and the vapors and gases that develop.
- a gradation that is necessary in order to be able to use the propellants according to the invention as widely as possible.
- the propellant charges according to the invention must be mixed in a targeted manner. This is the only way to find the optimal one To achieve effect.
- the efficiency of the propellants according to the invention is influenced not only by the composition, but also by the ignition, and also by the insulation caused by the construction and by the outflow behavior of the developing swaths and gases.
- the efficiency can be assessed, for example, by determining the gas pressure increase gradient of the respective mixture in the design-related, predetermined external environment and the type of ignition selected.
- the developing gas concentrations, especially those of the gases hazardous to health, must not exceed certain maximum values. These values result from the MAK values (or from the TLV values in the USA). From these values together with the permitted exposure times, technical requirements are created which the respective propellant charges have to meet. When defining these requirements, for example, the different passenger cells are also taken into account. In order to meet these requirements, it is necessary to mix the respective propellant in a targeted manner.
- the gas temperature can be kept low by adding diammonium oxalate, oxalic acid diamide, dicyandiamide or carbonates or bicarbonates. If thermal stability is not important and smoke formation is to be avoided when inorganic carbonates or bicarbonates are added, aminoguanidine bicarbonate can be used as the organic bicarbonate. Additional additives can be oxalic acid or urea, which are generally added in an amount of up to 5% by weight, based on the mixture.
- Metal powders of iron, magnesium, zirconium or titanium can be added as reducing agents, which in contrast to non-metal boron do not have a strong influence on the rate of combustion, but in the latter case they do have a strong influence on the heat of the reaction and the reaction products.
- the proportion of reducing agents can be up to 5% by weight.
- Catalysts are metal complexes, of which ferrocene is mentioned here by way of example, the addition of which increases the reaction rate significantly by up to about 3% by weight.
- the gas sets described in accordance with the invention are produced by mixing the components by methods known per se, if appropriate with the preparation of a harmless premix, to which further components are added.
- This mixture can already be used in powdered form. Demixing due to different density of the components can be countered by granulating the mixture.
- the mixture will be molded by pressing or similar measures.
- pressing aids can be added to the mixture.
- graphite, molybdenum disulfide, Teflon, talc, zinc stearate or boron nitride come into question. These agents work even in the smallest amounts and do not or only slightly influence the properties and the burning behavior.
- One such method is to add additives such as salts to the mixture before the actual molding process, which can be removed by extraction with water or solvents after the molding.
- Another method is to add substances which are not very thermally resistant and which decompose when the molding is heated.
- the surface of the mixture can also be increased by adding hollow microspheres made of glass or plastics to the mixture prior to pressing.
- the density of the compact to be achieved in this way can deviate by up to 20% from that of the untreated compact, this value being intended only as a rough guide and not a limitation. This treatment leads to an extreme acceleration of the burning process.
- a further treatment of the moldings can consist in a surface coating.
- protection against environmental influences is achieved in particular.
- Such a measure can also be used to increase the strength of the molded body.
- suitable fibers for stabilization would also have to be provided here.
- a side effect of the coating is the reduction of the abrasion during the transport stress of the parts.
- the moldings treated in this way can be introduced in bulk or directed into appropriate pressure-resistant containers. They are ignited using conventional methods with the aid of ignition kits or thermal charges, the resulting gases possibly filling the life-saving system in a split second after flowing through a suitable filter.
- the propellants according to the invention are particularly suitable for so-called airbags, impact bags, which are used in motor vehicles or aircraft to protect the occupants.
- the airbag In the event of a motor vehicle crash, the airbag must be filled with gas quantities of approximately 50 to 300 liters within a very short time, depending on the system and car size.
- the propellants according to the invention are also suitable for use in belt tensioners.
- Life saving systems containing the propellants according to the invention are also the subject of the present invention.
- 5-ATZ and ZnO2 as components for non-toxic gas sets, are homogenized together in a weight ratio of 1 to 7 (this corresponds to a molar ratio of approx. 1: 5) in plastic containers in a tumble mixer for 1-2 hours. 3.0 g of the sample are reacted as bulk in a 25 ml stainless steel pressure bomb by means of an electrically heatable Fe wire and the pressure-time profile is recorded by means of a piezoelectric measuring device. After about 30 ms, a maximum gas pressure of about 200 bar arises, which is mainly due to the formation of CO2, N2, O2 and H2O. The reaction has a strongly exothermic character of approx.
- the gas set mixtures described in Examples 1 to 24 can also be used in compressed form.
- Example 1 As described in Example 1, further mixtures of gas-generating components and oxygen suppliers such as zinc peroxide with an active oxygen content of 13.07% by weight and an average grain size of 11.8 ⁇ m or, in the case of sodium nitrate, with an average grain size of ⁇ 45 ⁇ m produced.
- gas-generating components and oxygen suppliers such as zinc peroxide with an active oxygen content of 13.07% by weight and an average grain size of 11.8 ⁇ m or, in the case of sodium nitrate, with an average grain size of ⁇ 45 ⁇ m produced.
- Table 4 below contains further information on the mixtures.
- Table 5 shows the values for the maximum pressure (bar) and the time in ms to the maximum pressure, which are in the range of those described in Example 1 for a gas set consisting of 5-aminotetrazole and zinc peroxide. In addition, the time between 40-60% of the maximum pressure was determined. Table 5 Example No. Maxim Pressure (bar) Time (ms) to maxim. print up to 40-60% of the max. print 26 359 30th 1.2 27th 217 123 13.1 28 352 29 1.5 29 473 39 1.3 30th 549 14 0.5 31 917 7 0.2 32 148 220 20.1
- the parameters required for the respective gas set can be set by coordinating the parameters and adding other components.
- the components are suitable for the production of gas sets due to their miscibility, processability, compressibility for shaping and compatibility with one another and with additional additives as well as their safety-related characteristics.
- the mixtures of Examples 33 to 44 were made of zinc peroxide (active oxygen content 12.8% by weight, average particle size 4.8 ⁇ m), aminotetrazole (average particle size ⁇ 125 ⁇ m), sodium nitrate (particle size ⁇ 45 ⁇ m) and the listed components with a grain size of ⁇ 125 ⁇ m.
- the additionally listed components are described in the literature.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Air Bags (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4120599 | 1991-06-21 | ||
DE4120599 | 1991-06-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0519485A1 true EP0519485A1 (de) | 1992-12-23 |
Family
ID=6434491
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP92110353A Withdrawn EP0519485A1 (de) | 1991-06-21 | 1992-06-19 | Treibmittel für Gasgeneratoren |
Country Status (4)
Country | Link |
---|---|
US (2) | US20030145923A1 (cs) |
EP (1) | EP0519485A1 (cs) |
CZ (1) | CZ291570B6 (cs) |
DE (1) | DE4220019A1 (cs) |
Cited By (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4411654A1 (de) * | 1993-10-20 | 1995-04-27 | Temic Bayern Chem Airbag Gmbh | Gaserzeugendes Gemisch |
WO1995018780A1 (en) * | 1994-01-10 | 1995-07-13 | Thiokol Corporation | Non-azide gas generant compositions containing dicyanamide salts |
EP0659711A3 (en) * | 1993-12-10 | 1995-08-09 | Morton Int Inc | Processing aids for gas generating compositions. |
EP0659714A3 (en) * | 1993-12-10 | 1995-09-13 | Morton Int Inc | Gas generating composition for use with aluminum building elements. |
EP0661253A3 (en) * | 1993-12-10 | 1995-09-13 | Morton Int Inc | Gas generating compositions using dicyanamide salts as fuel. |
US5451682A (en) * | 1994-01-10 | 1995-09-19 | Thiokol Corporation | Method for synthesizing 5-aminotetrazole |
US5467715A (en) * | 1993-12-10 | 1995-11-21 | Morton International, Inc. | Gas generant compositions |
US5468866A (en) * | 1994-01-04 | 1995-11-21 | Thiokol Corporation | Methods for synthesizing and processing bis-(1(2)H-tetrazol-5-yl)-amine |
US5516377A (en) * | 1994-01-10 | 1996-05-14 | Thiokol Corporation | Gas generating compositions based on salts of 5-nitraminotetrazole |
DE19505568A1 (de) * | 1995-02-18 | 1996-08-22 | Dynamit Nobel Ag | Gaserzeugende Mischungen |
EP0723530A4 (en) * | 1993-08-02 | 1996-09-25 | Thiokol Corp | METHOD FOR PRODUCING A WATER-FREE GAS-GENERATING TETRAZOLE COMPOSITION |
EP0712384A4 (en) * | 1993-08-02 | 1996-09-25 | Thiokol Corp | WATER-FREE GAS GENERATING TETRAZOLE COMPOSITION AND METHOD FOR THE PRODUCTION THEREOF |
EP0694511A4 (en) * | 1994-02-15 | 1997-02-26 | Nippon Koki Kk | Gas generator composition, process for producing tablet therefrom, and transportation method |
WO1997023434A1 (de) * | 1995-12-23 | 1997-07-03 | Dynamit Nobel Gmbh Explosivstoff- Und Systemtechnik | Initialsprengstoff-freie anzündmischung |
EP0795528A1 (en) * | 1996-03-15 | 1997-09-17 | Morton International, Inc. | Gas generant compositions containing amine nitrates plus basic copper (II) nitrate and/or cobalt(III) triammine trinitrate |
WO1997042142A1 (de) * | 1996-05-02 | 1997-11-13 | Trw Airbag Systems Gmbh & Co. Kg | Gaserzeugendes, azidfreies stoffgemisch |
EP0811589A1 (en) * | 1996-06-03 | 1997-12-10 | Daicel Chemical Industries, Ltd. | Composition of gas generating agent |
WO1998003450A1 (en) * | 1994-12-13 | 1998-01-29 | United Technologies Corporation | Breathable gas generators |
EP0844223A1 (en) * | 1996-11-26 | 1998-05-27 | Nederlandse Organisatie voor Toegepast Natuurwetenschappelijk Onderzoek TNO | Gas-generating preparation and use thereof in an air bag |
WO1998055428A1 (en) * | 1997-05-21 | 1998-12-10 | Försvarets Forskningsanstalt | New chemical compound, explosive containing the compound and use of the compound in gas generators |
EP0813512A4 (en) * | 1995-03-03 | 1999-03-17 | Primex Tech Inc | THERMOSTABLE GAS COMPOSITION |
FR2772370A1 (fr) * | 1997-12-12 | 1999-06-18 | Poudres & Explosifs Ste Nale | Compositions pyrotechniques generatrices de gaz non toxiques a base de perchlorate d'ammonium |
EP0951923A1 (en) | 1998-01-29 | 1999-10-27 | Primex Aerospace Company | Chemically active fire suppression composition |
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US6241281B1 (en) | 1996-07-25 | 2001-06-05 | Cordant Technologies Inc. | Metal complexes for use as gas generants |
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US6550808B1 (en) | 2000-11-17 | 2003-04-22 | Autoliv Asp. Inc. | Guanylurea nitrate in gas generation |
US6602365B1 (en) | 2000-11-17 | 2003-08-05 | Autoliv Asp, Inc. | Gas generation via metal complexes of guanylurea nitrate |
US6969435B1 (en) | 1994-01-19 | 2005-11-29 | Alliant Techsystems Inc. | Metal complexes for use as gas generants |
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DE4423088A1 (de) * | 1994-07-01 | 1996-01-04 | Temic Bayern Chem Airbag Gmbh | Gaserzeugendes, azidfreies Stoffgemisch |
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WO2007130676A2 (en) * | 2006-05-05 | 2007-11-15 | Tk Holdings, Inc. | Gas generant compositions |
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FR2950624B1 (fr) * | 2009-09-25 | 2013-05-10 | Snpe Materiaux Energetiques | Compose pyrotechnique generateur de gaz |
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JP5639137B2 (ja) * | 2012-10-15 | 2014-12-10 | 積水化学工業株式会社 | ガス発生材及びマイクロポンプ |
CN104350030B (zh) | 2012-10-15 | 2017-09-15 | 积水化学工业株式会社 | 气体发生材料及微型泵 |
JP6970190B2 (ja) | 2016-05-23 | 2021-11-24 | ジョイソン セーフティー システムズ アクウィジション エルエルシー | ガス発生組成物ならびにそれらの製造方法及び使用方法 |
KR20210141456A (ko) * | 2019-03-15 | 2021-11-23 | 에이와 가세이 고교 가부시키가이샤 | 가스발생제, 발포용 조성물, 발포체, 및 발포체의 제조방법 |
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US5468866A (en) * | 1994-01-04 | 1995-11-21 | Thiokol Corporation | Methods for synthesizing and processing bis-(1(2)H-tetrazol-5-yl)-amine |
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DE19505568A1 (de) * | 1995-02-18 | 1996-08-22 | Dynamit Nobel Ag | Gaserzeugende Mischungen |
WO1996026169A1 (de) * | 1995-02-18 | 1996-08-29 | Dynamit Nobel Gmbh | Gaserzeugende mischungen |
CZ298208B6 (cs) * | 1995-02-18 | 2007-07-25 | Delphi Technologies, Inc. | Látka produkující plyn z dusíkatých sloucenin, zpusob výroby této látky, systém záchrany zivota tvorený plynovým generátorem s látkou produkující plyn a pouzití látky produkující plyn |
RU2250207C2 (ru) * | 1995-02-18 | 2005-04-20 | Динамит Нобель Гмбх Эксплозивштофф-Унд Зистемтехник | Газообразующий состав для газогенератора (его варианты) и система безопасности газогенераторная |
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WO1997023434A1 (de) * | 1995-12-23 | 1997-07-03 | Dynamit Nobel Gmbh Explosivstoff- Und Systemtechnik | Initialsprengstoff-freie anzündmischung |
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WO1997042142A1 (de) * | 1996-05-02 | 1997-11-13 | Trw Airbag Systems Gmbh & Co. Kg | Gaserzeugendes, azidfreies stoffgemisch |
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US6291711B2 (en) | 1997-05-21 | 2001-09-18 | Totalforsvarets Forskningsinstitut (Foi) | Guanylurea dinitramide, an explosive, propellant, rocket motor charge and gas generator |
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US6602365B1 (en) | 2000-11-17 | 2003-08-05 | Autoliv Asp, Inc. | Gas generation via metal complexes of guanylurea nitrate |
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EP2038146A4 (en) * | 2006-05-05 | 2009-09-30 | Tk Holdings Inc | GAS PRODUCTION COMPOSITIONS |
Also Published As
Publication number | Publication date |
---|---|
US20040226639A1 (en) | 2004-11-18 |
DE4220019A1 (de) | 1992-12-24 |
CZ189792A3 (en) | 1993-01-13 |
CZ291570B6 (cs) | 2003-04-16 |
US20030145923A1 (en) | 2003-08-07 |
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