WO2007016594A2 - Composition d'autocompression/de surpression - Google Patents
Composition d'autocompression/de surpression Download PDFInfo
- Publication number
- WO2007016594A2 WO2007016594A2 PCT/US2006/030002 US2006030002W WO2007016594A2 WO 2007016594 A2 WO2007016594 A2 WO 2007016594A2 US 2006030002 W US2006030002 W US 2006030002W WO 2007016594 A2 WO2007016594 A2 WO 2007016594A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- acid
- oxidizer
- autoignition
- gas
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 91
- 239000000446 fuel Substances 0.000 claims abstract description 19
- 239000007800 oxidant agent Substances 0.000 claims abstract description 18
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 claims abstract description 16
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 claims abstract description 15
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims abstract description 8
- FEWJPZIEWOKRBE-XIXRPRMCSA-N Mesotartaric acid Chemical compound OC(=O)[C@@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-XIXRPRMCSA-N 0.000 claims abstract description 7
- 229940048879 dl tartaric acid Drugs 0.000 claims abstract description 7
- ULRPISSMEBPJLN-UHFFFAOYSA-N 2h-tetrazol-5-amine Chemical compound NC1=NN=NN1 ULRPISSMEBPJLN-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000001735 carboxylic acids Chemical class 0.000 claims abstract description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 7
- -1 furazans Chemical class 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 6
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 4
- KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Substances C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- DSLZVSRJTYRBFB-UHFFFAOYSA-N Galactaric acid Natural products OC(=O)C(O)C(O)C(O)C(O)C(O)=O DSLZVSRJTYRBFB-UHFFFAOYSA-N 0.000 claims description 4
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
- DSLZVSRJTYRBFB-DUHBMQHGSA-N galactaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O DSLZVSRJTYRBFB-DUHBMQHGSA-N 0.000 claims description 4
- 150000002823 nitrates Chemical class 0.000 claims description 4
- 229910052755 nonmetal Inorganic materials 0.000 claims description 4
- 150000003536 tetrazoles Chemical class 0.000 claims description 4
- 150000003852 triazoles Chemical class 0.000 claims description 4
- 150000002826 nitrites Chemical class 0.000 claims description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 2
- 239000001361 adipic acid Substances 0.000 claims description 2
- 235000011037 adipic acid Nutrition 0.000 claims description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- 239000004220 glutamic acid Substances 0.000 claims description 2
- 235000013922 glutamic acid Nutrition 0.000 claims description 2
- 229940116298 l- malic acid Drugs 0.000 claims description 2
- 235000011090 malic acid Nutrition 0.000 claims description 2
- 235000006408 oxalic acid Nutrition 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052728 basic metal Inorganic materials 0.000 claims 1
- 150000003818 basic metals Chemical class 0.000 claims 1
- 229960001367 tartaric acid Drugs 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- 235000002906 tartaric acid Nutrition 0.000 claims 1
- 239000007789 gas Substances 0.000 description 49
- 239000000470 constituent Substances 0.000 description 16
- 238000009472 formulation Methods 0.000 description 10
- 230000035945 sensitivity Effects 0.000 description 7
- 238000000113 differential scanning calorimetry Methods 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 238000004891 communication Methods 0.000 description 5
- 230000007246 mechanism Effects 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 239000003380 propellant Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 229910021485 fumed silica Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 239000002360 explosive Substances 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
- 238000004806 packaging method and process Methods 0.000 description 2
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229960000250 adipic acid Drugs 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 150000003851 azoles Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910002010 basic metal nitrate Inorganic materials 0.000 description 1
- BGECDVWSWDRFSP-UHFFFAOYSA-N borazine Chemical compound B1NBNBN1 BGECDVWSWDRFSP-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229960001270 d- tartaric acid Drugs 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229960002989 glutamic acid Drugs 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- FEWJPZIEWOKRBE-LWMBPPNESA-N levotartaric acid Chemical compound OC(=O)[C@@H](O)[C@H](O)C(O)=O FEWJPZIEWOKRBE-LWMBPPNESA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc 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
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C9/00—Chemical contact igniters; Chemical lighters
Definitions
- the present invention relates generally to gas generating systems, and to autoignition compositions employed in gas generator devices for automotive restraint systems, for example.
- the present invention relates to autoignition compositions that upon ignition provide the flame front and pressure front necessary to safely ignite gas generant compositions in combustible communication therewith.
- gas generators are typically provided with an autoignition composition that in the event of a fire ignites responsive to a desired threshold temperature. As a result, the gas generant is ignited prior to melting for example, thereby safely igniting the main gas generant composition to inhibit or prevent theJikelihood of an explosive event once the gas generant begins to combust.
- compositions are provided to serve correspondingly discrete functions. These compositions often include a primary gas generating composition that when combusted is employed to provide sufficient quantities of gaseous products to operate the associated restraint device, such as an airbag or seatbelt pretensioner.
- a booster composition is utilized to elevate the pressure and heat within the gas generator prior to combustion of the primary gas generant, thereby creating favorable conditions within the inflator for acceptable combustion of the primary gas generant.
- the auto-ignition composition employed to provide safe combustion of the other compositions in the event of a fire.
- the auto-ignition composition is designed to ignite at temperatures below the melting point of the primary gas generant for example, thereby ensuring the controlled combustion of the primary gas generant, as opposed to an explosive reaction perhaps.
- gas generating systems including an autoignition composition containing a first oxidizer selected from metal chlorates, such as potassium chlorate, a carboxylic acid or dicarboxylic acid as a primary fuel, a secondary oxidizer selected from metal and nonmetal nitrates, nitrites, oxides, basic metal nitrates, and other known oxidizers, and a secondary fuel selected from azoles including tetrazoles, triazoles, and furazans, and salts thereof.
- a first oxidizer selected from metal chlorates, such as potassium chlorate, a carboxylic acid or dicarboxylic acid as a primary fuel
- a secondary oxidizer selected from metal and nonmetal nitrates, nitrites, oxides, basic metal nitrates, and other known oxidizers
- a secondary fuel selected from azoles including tetrazoles, triazoles, and furazans, and salts thereof.
- FIG. 1 is a cross-sectional side view showing the general structure of an inflator in accordance with the present invention
- FIG. 2 is a schematic representation of an exemplary vehicle occupant restraint system containing a gas generant composition in accordance with the present invention.
- the present compositions contain a first oxidizer selected from alkali, alkaline earth, and transitional metal chlorates, and mixtures thereof, such as potassium chlorate, at about 10-60 weight%; a primary fuel selected from carboxylic acids and dicarboxylic acids, such as DL-tartaric acid, at about 15-45 weight%; a secondary oxidizer selected from metal and nonmetal nitrates, nitrites, oxides, and other known oxidizers at about 30-50%; and a secondary fuel selected from tetrazoles, triazoles, furazans, and salts thereof at about 0-30 weight %, said weight percent calculated with regard to the weight of the total composition.
- Extrusion aids or processing additives such as graphite or fumed silica may be added in relatively smaller amounts, such as 0.1-2% by weight of the total composition for example.
- compositions contain a metal chlorate such as potassium chlorate; a primary fuel selected from carboxylic acids and dicarboxylic including DL-tartaric acid, L- tartaric acid, D-tartaric acid, succinic acid, glutamic acid, adipic acid, mucic acid, fumaric acid, oxalic acid, galactaric acid, citric acid, glycolic acid, L-malic acid, and compounds having at least one -COOH- group, and mixtures thereof; a second fuel selected from an azole including tetrazoles, triazoles, furazans, salts thereof, and mixtures thereof; a secondary oxidizer selected from metal and nonmetal nitrates or other known oxidizers not containing a perchlorate.
- a metal chlorate such as potassium chlorate
- a primary fuel selected from carboxylic acids and dicarboxylic including DL-tartaric acid, L- tartaric acid, D-tartaric acid, succinic acid, glut
- the carboxylic acid or dicarboxylic acid will preferably have a primary hydrogen or PKA less than or equal to 3. Nevertheless, it has been found that with certain fuels/salts, the pKa of the base acid may range up to 5.0 or less.
- the total fuel constituent including he carboxylic fuel and the second fuel is provided at about 20-45% by weight of the total composition; the oxidizer constituent is provided at about 20-50% by weight of the total composition; and the potassium chlorate or metal chlorate is provided at about 10-60% by weight of the total composition wherein the weight percent of the chlorate is separately calculated from that of the oxidizer.
- the composition may be formed by wet or dry mixing the constituents in a granulated form in a known manner, and then pelletizing or otherwise forming the composition for further use.
- the constituents may be provided by Fisher Chemical, Aldrich Chemical, GFS, and other known suppliers.
- COMPARATIVE EXAMPLE 1 A known autoignition composition was prepared by homogeneously mixing dried and granulated D-glucose at about 26.875 wt% and potassium chlorate at about 73.125 wt%, the percents stated by weight of the total composition. The composition autoignited at about 144 C as measured by DSC analysis. The propellant formed from the constituents resulted in an approximate 55.5% gas yield. The impact sensitivity of this formulation had an HD50 of 2.0 inches as conducted in conformance with the Bruceton Test.
- An exemplary formulation was provided that functions as a booster, an autoignition, and a gas generant composition.
- the formulation contains 5-aminotetrazole at about 19.0 wt%, DL-tartaric acid at about 20.0 wt%, strontium nitrate at about 35.0 wt%, and potassium chlorate at about 26.0 wt%.
- the constituents were previously and separately ground to a relatively small size in a known manner. They were then dry-mixed to form a substantially homogeneous composition.
- the composition autoignited at about 140 C as measured by DSC analysis.
- the propellant formed from the constituents resulted in an approximate 67% gas yield.
- the impact sensitivity of this formulation had an HD50 of 1 1 .5 inches as conducted in conformance with the Bruceton Test.
- the composition was aged for about 480 hours at 107C and still autoignited at about 145.1 C as determined by DSC analysis.
- EXAMPLE 3 An exemplary formulation was provided that functions as a booster, an autoignition, and a gas generant composition.
- the formulation contains 5-aminotetrazole at about 19.0 wt%, DL-tartaric acid at about 19.0 wt%, strontium nitrate at about 50.0 wt%, and potassium chlorate at about 12.0 wt%.
- the constituents were granulated and dry-mixed to form a substantially homogeneous composition.
- the composition autoignited at about 141 C as measured by DSC analysis.
- the propellant formed from the constituents resulted in an approximate 68.2% gas yield.
- the impact sensitivity of this formulation had an HD50 of 8.8 inches as conducted in conformance with the Bruceton Test. As shown in FIG.
- the composition reflected a relatively strong burn rate across several pressure regimes, and in particular indicated burn rates of over 0.8 inches per second (ips).
- ips inches per second
- FIG. 3 it can be seen that the composition exhibited a burn rate of about 0.2 ips at about 200 psig, about 0.35 ips at about 550 psig, about 0.5 ips at about 1000 psig, about 0.55 ips at about 1500 psig, about 0.85 ips at about 2000 psig, about 0.9 ips at about 2500 psig, about 0.85 ips at about 3000 psig; and about 1.2 ips at about 3900 psig.
- a composition in accordance with the present invention exhibits a satisfactory burn rate (typically 0.4 ips or more at about 2500-3000 psig) thereby ensuring satisfactory functionality as a primary gas generant.
- the composition was aged for about 480 hours at 107C and still autoignited at about 174.7C as determined by DSC analysis.
- An exemplary formulation was provided that functions as a booster, an autoignition, and a gas generant composition.
- the formulation contains DL-tartaric acid at about 28.0 wt%, strontium nitrate at about 32.0 wt%, and potassium chlorate at about 30.0 wt%.
- the constituents were previously and separately ground to a relatively small size in a known manner. They were then dry-mixed to form a substantially homogeneous composition.
- the composition autoignited at about 1 53 C as measured by DSC analysis.
- the propellant formed from the constituents resulted in an approximate 66.1 % gas yield.
- the impact sensitivity of this formulation had an HD50 of 8.1 inches as conducted in conformance with the Bruceton Test.
- compositions formed in accordance with the present invention preferably autoignite at or below about 18OC and provide a booster function as well.
- the compositions of the present invention may also produce substantial quantities of gas, and exhibit sufficient burn rates thereby producing sufficient amounts of gas when activated.
- Compositions employing a secondary oxidizer, such as strontium nitrate provide relative increased quantities of gas and an improved sensitivity.
- compositions formed in this manner may be provided to singularly replace the three discrete booster, autoignition, and primary gas generant compositions normally found in a gas generator.
- gas generators made as known in the art and also vehicle occupant protection systems manufactured as known in the art are also contemplated.
- autoignition compositions of the present invention are employed in gas generators, seat belt assemblies, and/or vehicle occupant protection systems, all manufactured as known in the art.
- the present compositions may be employed within a gas generating system.
- a vehicle occupant protection system made in a known way contains crash sensors in electrical communication with an airbag inflator in the steering wheel, and also with a seatbelt assembly.
- the gas generating compositions of the present invention may be employed in both subassemblies within the broader vehicle occupant protection system or gas generating system. More specifically, each gas generator employed in the automotive gas generating system may contain a gas generating composition as described herein.
- Extrusion aides may be selected from the group including talc, graphite, borazine [(BN) 3 ], boron nitride, fumed silica, and fumed alumina.
- the extrusion aid preferably constitutes 0-10% and more preferably constitutes 0-5% of the total composition.
- the compositions may be dry or wet mixed using methods known in the art.
- the various constituents are generally provided in particulate form and mixed to form a uniform mixture with the other gas generant constituents.
- an exemplary inflator incorporates a dual chamber design to tailor the force of deployment of an associated airbag.
- an inflator containing a primary gas generant 12 and an autoignition/booster composition 14 formed as described herein may be manufactured as known in the art.
- U.S. Patent Nos. 6,422,601 , 6,805,377, 6,659,500, 6,749,219, and 6,752,421 exemplify typical airbag inflator designs and are each incorporated herein by reference in their entirety.
- Airbag system 200 includes at least one airbag 202 and an inflator 10 containing a gas generant composition 12 in accordance with the present invention, coupled to airbag 202 so as to enable fluid communication with an interior of the airbag.
- Airbag system 200 may also include ⁇ or be in communication with) a crash event sensor 210.
- Crash event sensor 210 includes a known crash sensor algorithm that signals actuation of airbag system 200 via, for example, activation of airbag inflator 10 in the event of a collision.
- FIG. 2 shows a schematic diagram of one exemplary embodiment of such a restraint system.
- Safety belt assembly 150 includes a safety belt housing 152 and a safety belt 100 extending from housing 152.
- a safety belt retractor mechanism 154 (for example, a spring-loaded mechanism) may be coupled to an end portion of the belt.
- a safety belt pretensioner 156 containing propellant 12 and autoignition 14 may be coupled to belt retractor mechanism 154 to actuate the retractor mechanism in the event of a collision.
- Typical seat belt retractor mechanisms which may be used in conjunction with the safety belt embodiments of the present invention are described in U.S. Pat. Nos. 5,743,480, 5,553,803, 5,667,161 , 5,451 ,008, 4,558,832 and 4,597,546, each incorporated herein by reference.
- Illustrative examples of typical pretensioners with which the safety belt embodiments of the present invention may be combined are described in U.S. Pat. Nos. 6,505,790 and 6,419,177, incorporated herein by reference.
- Safety belt assembly 150 may also include (or be in communication with) a crash event sensor 158 (for example, an inertia sensor or an accelerometer) including a known crash sensor algorithm that signals actuation of belt pretensioner 156 via, for example, activation of a pyrotechnic igniter (not shown) incorporated into the pretensioner.
- a crash event sensor 158 for example, an inertia sensor or an accelerometer
- U.S. Patent Nos. 6,505,790 and 6,419,177 previously incorporated herein by reference, provide illustrative examples of pretensioners actuated in such a manner.
- safety belt assembly 150 airbag system 200, and more broadly, vehicle occupant protection system 180 exemplify but do not limit gas generating systems contemplated in accordance with the present invention.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- General Chemical & Material Sciences (AREA)
- Air Bags (AREA)
- Feeding, Discharge, Calcimining, Fusing, And Gas-Generation Devices (AREA)
Abstract
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008524284A JP5156627B2 (ja) | 2005-07-29 | 2006-07-31 | 自己発火/ブースター組成物 |
DE112006002030T DE112006002030T5 (de) | 2005-07-29 | 2006-07-31 | Selbstzündungs-/Booster-Zusammensetzung |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US70399805P | 2005-07-29 | 2005-07-29 | |
US60/703,998 | 2005-07-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007016594A2 true WO2007016594A2 (fr) | 2007-02-08 |
WO2007016594A3 WO2007016594A3 (fr) | 2007-10-04 |
Family
ID=37709331
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/030002 WO2007016594A2 (fr) | 2005-07-29 | 2006-07-31 | Composition d'autocompression/de surpression |
Country Status (4)
Country | Link |
---|---|
US (1) | US20070034307A1 (fr) |
JP (1) | JP5156627B2 (fr) |
DE (1) | DE112006002030T5 (fr) |
WO (1) | WO2007016594A2 (fr) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2870234B1 (fr) * | 2004-05-13 | 2007-02-09 | Snpe Materiaux Energetiques Sa | Compostion pyrotechnique dosable utilisee comme fusible thermique dans un generateur de gaz et generateur de gaz incluant un compose ayant ladite composition |
US20080078486A1 (en) * | 2006-09-30 | 2008-04-03 | Khandhadia Paresh S | Gas generating system and composition |
US20070169863A1 (en) * | 2006-01-19 | 2007-07-26 | Hordos Deborah L | Autoignition main gas generant |
US20100326575A1 (en) * | 2006-01-27 | 2010-12-30 | Miller Cory G | Synthesis of 2-nitroimino-5-nitrohexahydro-1,3,5-triazine |
US7959749B2 (en) * | 2006-01-31 | 2011-06-14 | Tk Holdings, Inc. | Gas generating composition |
US20080271825A1 (en) * | 2006-09-29 | 2008-11-06 | Halpin Jeffrey W | Gas generant |
US9556078B1 (en) | 2008-04-07 | 2017-01-31 | Tk Holdings Inc. | Gas generator |
US8657974B1 (en) * | 2009-08-31 | 2014-02-25 | Tk Holdings, Inc. | Gas generator |
US10919818B1 (en) * | 2010-08-23 | 2021-02-16 | Joyson Safety Systems Acquisition Llc | Auto-ignition composition |
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US3880595A (en) * | 1972-06-08 | 1975-04-29 | Hubert G Timmerman | Gas generating compositions and apparatus |
JPS5128616B2 (fr) * | 1973-04-17 | 1976-08-20 | ||
DE3215925C2 (de) | 1982-04-29 | 1985-11-28 | Bayern-Chemie Gesellschaft für flugchemische Antriebe mbH, 8261 Aschau | Aufwickelvorrichtung mit Rückstrammer für Sicherheitsgurte |
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US5553803A (en) | 1994-09-13 | 1996-09-10 | Takata Vehicle Safety Technology Gmbh | Belt tensioner for safety belts for motor vehicles |
DE19503150A1 (de) | 1995-02-01 | 1996-08-08 | Takata Europ Gmbh | Einen Gurtstraffer aufweisende Sicherheitsgurtanordnung in Kraftfahrzeugen |
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EP1061057B1 (fr) * | 1998-02-25 | 2010-10-27 | Nippon Kayaku Kabushiki Kaisha | Composition generatrice de gaz |
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JP4500399B2 (ja) * | 2000-02-04 | 2010-07-14 | ダイセル化学工業株式会社 | トリアジン誘導体を含むガス発生剤組成物 |
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US6659500B2 (en) | 2000-05-11 | 2003-12-09 | Automotive Systems Laboratory, Inc. | Multi-chamber inflator |
US6505790B2 (en) | 2000-06-05 | 2003-01-14 | Automotive Systems Laboratory, Inc. | Pretensioner device |
DE10064285C1 (de) * | 2000-12-22 | 2002-10-17 | Nigu Chemie Gmbh | Gasgeneratortreibstoff-Zusammensetzung und deren Verwendung |
WO2003022645A1 (fr) * | 2001-08-09 | 2003-03-20 | Nippon Kayaku Kabushiki-Kaisha | Generateur de gaz |
US6749219B2 (en) | 2001-09-12 | 2004-06-15 | Automotive Systems Laboratory | Inflator |
EP1470028A1 (fr) | 2002-01-03 | 2004-10-27 | Automotive Systems Laboratory Inc. | Dispositif de gonflage d'airbag |
JP2010513186A (ja) * | 2006-12-15 | 2010-04-30 | ティー ケー ホールディングス インク | 自己発火/ブースター組成物 |
-
2006
- 2006-07-31 WO PCT/US2006/030002 patent/WO2007016594A2/fr active Application Filing
- 2006-07-31 JP JP2008524284A patent/JP5156627B2/ja not_active Expired - Fee Related
- 2006-07-31 US US11/497,149 patent/US20070034307A1/en not_active Abandoned
- 2006-07-31 DE DE112006002030T patent/DE112006002030T5/de not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
DE112006002030T5 (de) | 2008-07-10 |
WO2007016594A3 (fr) | 2007-10-04 |
US20070034307A1 (en) | 2007-02-15 |
JP5156627B2 (ja) | 2013-03-06 |
JP2009502718A (ja) | 2009-01-29 |
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