NO310300B1 - Faste pyrotekniske blandinger - Google Patents
Faste pyrotekniske blandinger Download PDFInfo
- Publication number
- NO310300B1 NO310300B1 NO19945046A NO945046A NO310300B1 NO 310300 B1 NO310300 B1 NO 310300B1 NO 19945046 A NO19945046 A NO 19945046A NO 945046 A NO945046 A NO 945046A NO 310300 B1 NO310300 B1 NO 310300B1
- Authority
- NO
- Norway
- Prior art keywords
- weight
- mixture
- binder
- plasticizer
- solid pyrotechnic
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 89
- 239000007787 solid Substances 0.000 title claims description 20
- 239000011230 binding agent Substances 0.000 claims description 57
- 229920002857 polybutadiene Polymers 0.000 claims description 35
- 239000004014 plasticizer Substances 0.000 claims description 32
- 239000005062 Polybutadiene Substances 0.000 claims description 30
- 229920001169 thermoplastic Polymers 0.000 claims description 21
- 239000004416 thermosoftening plastic Substances 0.000 claims description 21
- FCBQZFWYMGKDNR-UHFFFAOYSA-N [Fe++].c1cc[cH-]c1.[SiH3][c-]1cccc1 Chemical group [Fe++].c1cc[cH-]c1.[SiH3][c-]1cccc1 FCBQZFWYMGKDNR-UHFFFAOYSA-N 0.000 claims description 20
- -1 alkali metal chlorates Chemical class 0.000 claims description 18
- 230000001590 oxidative effect Effects 0.000 claims description 18
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 claims description 16
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- 239000005977 Ethylene Substances 0.000 claims description 8
- 229910001963 alkali metal nitrate Inorganic materials 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims description 5
- 239000000028 HMX Substances 0.000 claims description 5
- UZGLIIJVICEWHF-UHFFFAOYSA-N octogen Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 UZGLIIJVICEWHF-UHFFFAOYSA-N 0.000 claims description 5
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- UAGLZAPCOXRKPH-UHFFFAOYSA-N nitric acid;1,2,3-triaminoguanidine Chemical compound O[N+]([O-])=O.NNC(NN)=NN UAGLZAPCOXRKPH-UHFFFAOYSA-N 0.000 claims description 3
- 229910001964 alkaline earth metal nitrate Inorganic materials 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 2
- 229920001971 elastomer Polymers 0.000 claims 1
- 239000000806 elastomer Substances 0.000 claims 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 33
- 238000002485 combustion reaction Methods 0.000 description 30
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical class [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 17
- 239000003380 propellant Substances 0.000 description 16
- 229910052742 iron Inorganic materials 0.000 description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 14
- 238000000034 method Methods 0.000 description 12
- 239000002904 solvent Substances 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 9
- 239000004449 solid propellant Substances 0.000 description 9
- 229920001187 thermosetting polymer Polymers 0.000 description 9
- 239000007789 gas Substances 0.000 description 8
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 230000005012 migration Effects 0.000 description 7
- 238000013508 migration Methods 0.000 description 7
- 229920000570 polyether Polymers 0.000 description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 7
- 229920002554 vinyl polymer Polymers 0.000 description 7
- 239000004952 Polyamide Substances 0.000 description 6
- 239000004721 Polyphenylene oxide Substances 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 229920001400 block copolymer Polymers 0.000 description 6
- 231100000252 nontoxic Toxicity 0.000 description 6
- 230000003000 nontoxic effect Effects 0.000 description 6
- 229920002647 polyamide Polymers 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 229920002725 thermoplastic elastomer Polymers 0.000 description 5
- 239000002341 toxic gas Substances 0.000 description 5
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 230000035945 sensitivity Effects 0.000 description 4
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 229920002614 Polyether block amide Polymers 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000000567 combustion gas Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- XIZNSFKZKZTGNG-UHFFFAOYSA-N 2-butylbenzenesulfonamide Chemical compound CCCCC1=CC=CC=C1S(N)(=O)=O XIZNSFKZKZTGNG-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 2
- 229920000834 poly(ferrocenylene) polymer Polymers 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 235000010344 sodium nitrate Nutrition 0.000 description 2
- 239000004317 sodium nitrate Substances 0.000 description 2
- 230000035882 stress Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- ZQXWPHXDXHONFS-UHFFFAOYSA-N 1-(2,2-dinitropropoxymethoxy)-2,2-dinitropropane Chemical compound [O-][N+](=O)C([N+]([O-])=O)(C)COCOCC(C)([N+]([O-])=O)[N+]([O-])=O ZQXWPHXDXHONFS-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 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
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical class OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/04—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
- C06B45/06—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component
- C06B45/10—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component the organic component containing a resin
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B23/00—Compositions characterised by non-explosive or non-thermic constituents
- C06B23/007—Ballistic modifiers, burning rate catalysts, burning rate depressing agents, e.g. for gas generating
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Air Bags (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Feeding, Discharge, Calcimining, Fusing, And Gas-Generation Devices (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9315790A FR2714374B1 (fr) | 1993-12-29 | 1993-12-29 | Compositions pyrotechniques solides à liant thermoplastique et plastifiant polybutadiène silylferrocénique. |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO945046D0 NO945046D0 (no) | 1994-12-27 |
| NO945046L NO945046L (no) | 1995-06-30 |
| NO310300B1 true NO310300B1 (no) | 2001-06-18 |
Family
ID=9454515
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19945046A NO310300B1 (no) | 1993-12-29 | 1994-12-27 | Faste pyrotekniske blandinger |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5458706A (it) |
| JP (1) | JP3802094B2 (it) |
| DE (1) | DE4446976B4 (it) |
| FR (1) | FR2714374B1 (it) |
| GB (1) | GB2285256B (it) |
| IT (1) | IT1267339B1 (it) |
| NO (1) | NO310300B1 (it) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5542688A (en) * | 1992-10-27 | 1996-08-06 | Atlantic Research Corporation | Two-part igniter for gas generating compositions |
| DE19531288A1 (de) * | 1995-08-25 | 1997-02-27 | Temic Bayern Chem Airbag Gmbh | Pyrotechnische Gasgeneratoren mit verbessertem Anbrennverhalten |
| US5847311A (en) * | 1996-10-22 | 1998-12-08 | Trw Vehicle Safety Systems Inc. | Hybrid inflator with crystalline and amorphous block copolymer |
| US5847315A (en) * | 1996-11-29 | 1998-12-08 | Ecotech | Solid solution vehicle airbag clean gas generator propellant |
| JP3608902B2 (ja) * | 1997-03-24 | 2005-01-12 | ダイセル化学工業株式会社 | ガス発生剤組成物及びその成型体 |
| US6740180B1 (en) | 1997-07-15 | 2004-05-25 | Anthony Joseph Cesaroni | Thermoplastic polymer propellant compositions |
| US6852182B1 (en) * | 2000-02-04 | 2005-02-08 | The United States Of America As Represented By The Secretary Of The Navy | Hydrolyzable prepolymers for explosive and propellant binders |
| FR2818636B1 (fr) * | 2000-12-22 | 2003-02-28 | Poudres & Explosifs Ste Nale | Compositions pyrotechniques generatrices de gaz a liant hydrocarbone et procede de fabrication en continu |
| JP3972628B2 (ja) * | 2001-10-23 | 2007-09-05 | 日本油脂株式会社 | ガス発生剤組成物及びガス発生器 |
| US6884307B1 (en) * | 2002-04-12 | 2005-04-26 | Diehl Munitionssysteme Gmbh & Co. Kg | Insensitive explosive molding powder, paste process |
| DE102007004316B4 (de) | 2007-01-29 | 2015-06-11 | Trw Airbag Systems Gmbh | Gaserzeugende Masse und deren Verwendung |
| FR3007659B1 (fr) | 2013-06-28 | 2017-03-24 | Herakles | Procede de delivrance d'un liquide pressurise par les gaz de combustion d'au moins un chargement pyrotechnique |
| FR3037812B1 (fr) | 2015-06-29 | 2017-08-04 | Herakles | Extincteur d'incendie |
| FR3077989B1 (fr) | 2018-02-20 | 2021-11-19 | Arianegroup Sas | Extincteur d'incendie |
| CN115650811B (zh) * | 2022-11-09 | 2023-08-25 | 湖南恒达烟花有限公司 | 一种烟花微烟引线药剂 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4023994A (en) * | 1963-09-09 | 1977-05-17 | Thiokol Corporation | Solid propellant containing ferrocene plasticizer |
| US3954527A (en) * | 1970-03-24 | 1976-05-04 | The United States Of America As Represented By The Secretary Of The Army | Solid propellant with iron-carbonyl containing polymer binder |
| US3723205A (en) * | 1971-05-07 | 1973-03-27 | Susquehanna Corp | Gas generating composition with polyvinyl chloride binder |
| US3932240A (en) * | 1973-06-04 | 1976-01-13 | The United States Of America As Represented By The Secretary Of The Navy | Burning rate modifying binder for propellant and method |
| US4097662A (en) * | 1976-10-29 | 1978-06-27 | The United States Of America As Represented By The Secretary Of The Army | Co-polymers of butadiene and carboranyl methacrylate |
| US4092188A (en) * | 1977-05-16 | 1978-05-30 | Lovelace Alan M Acting Adminis | Nitramine propellants |
| FR2567895B1 (fr) * | 1984-07-20 | 1986-11-21 | Poudres & Explosifs Ste Nale | Polymere a insaturations ethyleniques comportant des groupements silylmetallocenes, procede de fabrication de ce polymere, et composition propulsive ayant comme liant ce polymere |
| DE3872380D1 (de) * | 1988-03-21 | 1992-07-30 | Thiokol Corp | Hochenergetische zusammmensetzungen mit einem giessbaren thermoplastischen binder. |
| US4919737A (en) * | 1988-08-05 | 1990-04-24 | Morton Thiokol Inc. | Thermoplastic elastomer-based low vulnerability ammunition gun propellants |
-
1993
- 1993-12-29 FR FR9315790A patent/FR2714374B1/fr not_active Expired - Fee Related
-
1994
- 1994-11-29 GB GB9424093A patent/GB2285256B/en not_active Expired - Fee Related
- 1994-12-13 JP JP30888094A patent/JP3802094B2/ja not_active Expired - Fee Related
- 1994-12-16 IT IT94TO001031A patent/IT1267339B1/it active IP Right Grant
- 1994-12-27 NO NO19945046A patent/NO310300B1/no unknown
- 1994-12-28 DE DE4446976A patent/DE4446976B4/de not_active Expired - Fee Related
- 1994-12-29 US US08/366,603 patent/US5458706A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH07257985A (ja) | 1995-10-09 |
| DE4446976A1 (de) | 1995-07-06 |
| GB9424093D0 (en) | 1995-01-18 |
| ITTO941031A1 (it) | 1996-06-16 |
| GB2285256A (en) | 1995-07-05 |
| IT1267339B1 (it) | 1997-01-28 |
| NO945046D0 (no) | 1994-12-27 |
| ITTO941031A0 (it) | 1994-12-16 |
| NO945046L (no) | 1995-06-30 |
| GB2285256B (en) | 1998-02-11 |
| FR2714374B1 (fr) | 1996-01-26 |
| JP3802094B2 (ja) | 2006-07-26 |
| DE4446976B4 (de) | 2005-07-14 |
| US5458706A (en) | 1995-10-17 |
| FR2714374A1 (fr) | 1995-06-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO310300B1 (no) | Faste pyrotekniske blandinger | |
| USRE36296E (en) | Propellant composition for automotive safety applications | |
| US6682616B1 (en) | Gas generating composition for use in a pretensioner | |
| US5525171A (en) | Pyrotechnic compositions generating clean and nontoxic gases, containing a thermoplastic elastomer binder | |
| US4244758A (en) | Ignition enhancer coating compositions for azide propellant | |
| KR20010033307A (ko) | 높은 산소 발란스의 연료를 포함하는 피로테크닉 가스발생제 조성물 | |
| US20110041969A1 (en) | Gas-generating pyrotechnic compound and production process | |
| JPH0692770A (ja) | 非毒性ホットガスを生成する組成物及び自動車の乗客を保護するための装置へのその使用 | |
| JP2007523823A (ja) | 特に自動車の安全装置用の発火性ガス発生用組成物及び発火性化合物 | |
| US6673172B2 (en) | Gas generant compositions exhibiting low autoignition temperatures and methods of generating gases therefrom | |
| JP2002511829A (ja) | モレキュラーシーブを含む硝酸アンモニウム噴射剤 | |
| US5566543A (en) | PVC-based gas generant for hybrid gas generators | |
| KR100656304B1 (ko) | 높은 산소 발란스의 연료를 포함하는 피로테크닉 가스발생제 조성물 | |
| JP4805833B2 (ja) | ガス発生剤のためのバインダーマトリックス並びに関連する組成物及び方法 | |
| CA1341397C (en) | Propellant compositions | |
| WO1997012847A1 (en) | Extrudable gas-generating compositions | |
| JPH07133180A (ja) | ガス発生剤組成物 | |
| EP0853603B1 (en) | Molded gas generating compositions containing a quick cure hydroxyl-terminated binder system and process for producing the same | |
| Singh et al. | Studies on low vulnerability gun propellants based on conventional binders and energetic plasticizers | |
| JP3370669B2 (ja) | 非晶質ポリエーテル／発熱性可塑剤バインダーを含有する固体推進薬 | |
| NO313324B1 (no) | Ammoniumnitrat-drivladningssammensetning |