US20080271825A1 - Gas generant - Google Patents

Gas generant Download PDF

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US20080271825A1
US20080271825A1 US12/217,577 US21757708A US2008271825A1 US 20080271825 A1 US20080271825 A1 US 20080271825A1 US 21757708 A US21757708 A US 21757708A US 2008271825 A1 US2008271825 A1 US 2008271825A1
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gas generant
generant composition
weight
metal
nitrate
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US12/217,577
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Jeffrey W. Halpin
Sean P. Burns
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Priority claimed from US11/540,841 external-priority patent/US20070084531A1/en
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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B23/00Compositions characterised by non-explosive or non-thermic constituents
    • C06B23/006Stabilisers (e.g. thermal stabilisers)
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06DMEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
    • C06D5/00Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
    • C06D5/06Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets by reaction of two or more solids

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  • the present invention relates generally to gas generating systems, and to gas generant compositions employed in gas generator devices for automotive restraint systems, for example.
  • the present invention relates to gas generant compositions that upon combustion produce a relatively small amount of solids and a relatively abundant amount of gas. It is an ongoing challenge to reduce the amount of solids and increase the amount of gas thereby decreasing the filtration requirements for an inflator. As a result, the filter may be either reduced in size or eliminated altogether thereby reducing the weight and/or size of the inflator.
  • gas generant compositions that produce relatively small amounts of solids, sometimes known as “smokeless” compositions, is that not all non-metallic constituents contribute to stable ballistic performance when subjected to environmental conditioning.
  • one fuel that is favored because of its propensity to produce all or mostly gas is the mono-ammonium salt of bis-1(2)H-tetrazol-5-yl)-amine (BTA-1NH3).
  • BTA-1NH3 bis-1(2)H-tetrazol-5-yl)-amine
  • compositions that contain BTA-1NH3 that contribute to a “smokeless” gas generant composition, or one that when combusted produces 90% or more of gas as a product, while yet passing thermal shock evaluations.
  • compositions including BTA-1NH3, an oxidizer such as phase stabilized ammonium nitrate, and a fumed oxide such as fumed silica or fumed alumina. It has been found that the addition of fumed silica or fumed oxides to compositions containing BTA-1NH3 has resulted in compositions that are now able to withstand thermal cycling/thermal shock evaluations.
  • a gas generator and a vehicle occupant protection system incorporating the gas generant composition are also included.
  • 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.
  • FIGS. 3 and 4 are graphical representations of a composition containing 0.25% by weight fumed silica.
  • FIGS. 5 and 6 are graphical representations of a composition containing 0.50% by weight fumed silica.
  • FIGS. 7 and 8 are graphical representations of a composition containing 0.75% by weight fumed silica.
  • the present invention includes gas generant compositions that in accordance with the present invention, incorporate an additive into compositions containing BTA-1NH3 that, when added at relatively low levels, stabilizes the propellant grains when subjected to thermal cycling or thermal shock conditioning, as required for use in the automotive industry.
  • These formulations generally contain the following:
  • a first oxidizer selected from the group including nonmetal and metal nitrate salts such as ammonium nitrate, phase-stabilized ammonium nitrate, potassium nitrate, strontium nitrate; nitrite salts such as potassium nitrite; chlorate salts such as potassium chlorate; metal and nonmetal perchlorate salts such as potassium or ammonium perchlorate; oxides such as iron oxide and copper oxide; basic nitrate salts such as basic copper nitrate and basic iron nitrate; and mixtures thereof.
  • the first oxidizer is generally provided at about 0.1-80 wt % of the gas generant composition, and more preferably at about 10-70 wt %.
  • An optional secondary oxidizer may also be provided and selected from the oxidizers described above, and when included is generally provided at about 0.1-50 wt %, and more preferably at about 0.1-30 wt %.
  • the total oxidizer component that is the combined weight percent of all oxidizers, will nevertheless only range from 0.1 to 80 wt %.
  • a first or primary fuel consists of mono-ammonium salt of bis-(1(2)H-tetrazol-5-yl)-amine (BTA-1NH3) and is generally provided at about 0.1-50 weight percent or wt %, and more preferably at about 10-30 wt %.
  • An optional secondary fuel is selected from the group containing derivatives of bis-(1(2)H-tetrazol-5-yl)-amine, including its anhydrous acid and its acid monohydrate, from metal salts thereof including the potassium, sodium, strontium, copper, boron, zinc salts of BTA-1NH3, and complexes thereof; azoles such as 5-aminotetrazole; metal salts of azoles such as potassium 5-aminotetrazole; nonmetal salts of azoles such as mono-or di-ammonium salt of 5,5′-bis-1H-tetrazole; nitrate salts of azoles such as 5-aminotetrazole nitrate; nitramine derivatives of azoles such as 5-nitraminotetrazole; metal salts of nitramine derivatives of azoles such as di-potassium 5-nitraminotetrazole; nonmetal salts of nitramine derivatives of azoles such as mono- or di-ammonium 5-nitram
  • a first or primary additive is selected from the group of fumed metal oxides including fumed silica and fumed alumina, and mixtures thereof, and is generally provided at about 0.05-10 wt %, and more preferably at about 0.05-5 wt %.
  • An optional second additive is selected from the group including silicon compounds including elemental silicon, silicon dioxide, and fused silica; silicones such as polydimethylsiloxane; silicates such as potassium silicates; natural minerals such as talc, mica, and clay; lubricants such as graphite powder or fibers, magnesium stearate, boron nitride, molybdenum sulfide; and mixtures thereof, and when included is generally provided at about 0.1-10%, and more preferably at about 0.1-5%.
  • silicones such as polydimethylsiloxane
  • silicates such as potassium silicates
  • natural minerals such as talc, mica, and clay
  • lubricants such as graphite powder or fibers, magnesium stearate, boron nitride, molybdenum sulfide; and mixtures thereof, and when included is generally provided at about 0.1-10%, and more preferably at about 0.1-5%.
  • An optional binder is selected from the group of cellulose derivatives such as cellulose acetate, cellulose acetate butyrate, carboxymethycellulose, salts of carboxymethylcellulose, carboxymethylcellulose acetate butyrate; silicone; polyalkene carbonates such as polypropylene carbonate and polyethylene carbonate; and mixtures thereof, and when included is generally provided at about 0.1-10%, and more preferably at about 0.1-5%.
  • BTA-1NH3 When combined with PSAN, exhibits many favorable qualities for use in automotive passenger restraints, and therefore forms preferred gas generating compositions.
  • BTA-1NH3 is a high energy, high-nitrogen fuel which exhibits excellent stability and very favorable levels of hygroscopicity and sensitivity.
  • the properties of ammonium nitrate and potassium nitrate, for example, are well known throughout the propellant industry.
  • PSAN more specifically, exhibits no sensitivity when subjected to impact, friction, or electrostatic discharge stimuli.
  • gas generant compositions made in accordance with the present invention exhibit many favorable characteristics for use in the auto industry, while avoiding many of the drawbacks of gas generants listed in the prior art.
  • a smokeless gas generant was produced by mixing Phase-Stabilized Ammonium Nitrate (PSAN) containing 10% by weight Potassium Nitrate, with bis-(1(2)H-tetrazol-5-yl)-amine, mono-ammonium salt (BTA-1NH3). The mixture was substantially in stoichiometric balance. The components were ground dry for about 15 minutes within a Sweco Vibratory Jar Mill.
  • PSAN Phase-Stabilized Ammonium Nitrate
  • BTA-1NH3 mono-ammonium salt
  • the resultant mixture was pressed into tablets, as is standard in the industry.
  • the tablets were then loaded into a single-stage driver-side inflator for ballistic evaluation.
  • Several inflators were deployed to provide baseline data while other inflators were subjected to thermal shock conditioning by varying the temperature from ⁇ 40 C to 90 C in accordance with typical thermal shock cycling.
  • Upon completion of 100 thermal shock cycles several inflators were deployed to compare with baseline ballistics.
  • Relative to thermal shock evaluations inflators were deployed at temperatures of ⁇ 40 C, +23 C, and +85 C. The ⁇ 40 C and +23 C deployments match the baseline data fairly well, while the +85 C ballistic data indicated less than desirable ballistic behavior.
  • fumed silica was commercially available as M-5 Grade provided by Cabot Corporation. Initially, the fumed silica was added at levels between about 3-6% by mass. The stoichiometric balance of the fuel and oxidizer and processing were kept the same. The resultant gas generants were then ballistically evaluated via the same method described above. After thermal shock conditioning, no change had occurred in the ballistic performance. However, the addition of such a large amount of “inert” material detracted from or inhibited the energy of the system. Although these compositions were acceptable, the lessened energy made the formulations not as desirable.
  • FIGS. 3 and 4 The ballistic data for the mixture containing 0.25% silica is illustrated in FIGS. 3 and 4 .
  • the pressure was measured inside the inflator and inside a 60-L tank during deployment prior to thermal shock tests and is represented in FIG. 3 .
  • FIG. 4 illustrates the results of combusting this mixture after thermal shock testing where the ballistic performance is less than desirable.
  • a few tablets were weighed and measured to determine density both before and after thermal shock conditioning. The crush strength was also measured for comparison. This data is shown in Table 1.
  • the ballistic data for the mixture containing 0.5% silica can be seen in FIGS. 5 and 6 .
  • the pressure was measured inside the inflator and inside a 60-L tank during deployment prior to thermal shock tests and is represented in FIG. 5 .
  • FIG. 6 illustrates the results of combusting this mixture after thermal shock testing wherein the pressure curves indicate less than desirable ballistic performance.
  • the pressure was measured inside the inflator and inside a 60-L tank during deployment.
  • the data from the thermal shock inflators showed an improvement over the mixture containing 0.25% silica.
  • a few tablets were weighed and measured to determine density both before and after thermal shock conditioning. The crush strength was also measured for comparison. This data is shown in Table 1.
  • FIGS. 7 and 8 The ballistic data for the mixture containing 0.75% silica can be seen in FIGS. 7 and 8 .
  • the pressure was measured inside the inflator and inside a 60-L tank during deployment prior to thermal shock tests and is represented in FIG. 7 .
  • FIG. 8 illustrates the results of combusting this mixture after thermal shock testing wherein the pressure indicates consistent ballistic performance before and after thermal shock.
  • the pressure was measured inside the inflator and inside the 60-L tank during deployment.
  • the data from the thermal shock inflators again showed an improvement over the mixture containing 0.5% silica.
  • the ballistic performance after thermal shock indicates a minimal change.
  • a few tablets were weighed and measured to determine density both before and after thermal shock conditioning.
  • the crush strength was also measured for comparison. This data can be seen in Table 1.
  • an exemplary inflator incorporates a dual chamber design to tailor the force of deployment an associated airbag.
  • an inflator containing a primary gas generant 12 formed as described herein may be manufactured as known in the art.
  • U.S. Pat. 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, 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. Pat. 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. Further, the compositions described above do not limit the present invention.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Air Bags (AREA)

Abstract

Gas generant compositions contain the mono-ammonium salt of bis (1(2)H-tetrazol-5-yl)-amine, an oxidizer such as phase stabilized ammonium nitrate, and a first additive selected from fumed oxides such as fumed silica. Gas generators 10 and gas generating systems 200 incorporating the compositions are also contemplated.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation-in-part of co-pending application U.S. application Ser. No. 11/540,841 filed on Sep. 29, 2006, and claims the benefit thereof.
  • TECHNICAL FIELD
  • The present invention relates generally to gas generating systems, and to gas generant compositions employed in gas generator devices for automotive restraint systems, for example.
  • BACKGROUND OF THE INVENTION
  • The present invention relates to gas generant compositions that upon combustion produce a relatively small amount of solids and a relatively abundant amount of gas. It is an ongoing challenge to reduce the amount of solids and increase the amount of gas thereby decreasing the filtration requirements for an inflator. As a result, the filter may be either reduced in size or eliminated altogether thereby reducing the weight and/or size of the inflator.
  • An equally important challenge is to manufacture gas generants that exhibit relatively low sensitivity with regard to impact, friction, or electrostatic discharge stimuli.
  • Yet another challenge with gas generant compositions that produce relatively small amounts of solids, sometimes known as “smokeless” compositions, is that not all non-metallic constituents contribute to stable ballistic performance when subjected to environmental conditioning. In fact, one fuel that is favored because of its propensity to produce all or mostly gas is the mono-ammonium salt of bis-1(2)H-tetrazol-5-yl)-amine (BTA-1NH3). When combined with other gas generant constituents such as an oxidizer, and formed into a gas generant composition, this fuel contributes to greater amounts of gas upon combustion of the composition.
  • Accordingly, it would be an improvement in the art to provide compositions that contain BTA-1NH3 that contribute to a “smokeless” gas generant composition, or one that when combusted produces 90% or more of gas as a product, while yet passing thermal shock evaluations.
  • SUMMARY OF THE INVENTION
  • The above-referenced concerns are resolved by gas generating compositions including BTA-1NH3, an oxidizer such as phase stabilized ammonium nitrate, and a fumed oxide such as fumed silica or fumed alumina. It has been found that the addition of fumed silica or fumed oxides to compositions containing BTA-1NH3 has resulted in compositions that are now able to withstand thermal cycling/thermal shock evaluations. Other constituents including processing aids such as graphite, may be included in relatively small amounts.
  • In further accordance with the present invention, a gas generator and a vehicle occupant protection system incorporating the gas generant composition are also included.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • 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.
  • FIGS. 3 and 4 are graphical representations of a composition containing 0.25% by weight fumed silica.
  • FIGS. 5 and 6 are graphical representations of a composition containing 0.50% by weight fumed silica.
  • FIGS. 7 and 8 are graphical representations of a composition containing 0.75% by weight fumed silica.
  • DETAILED DESCRIPTION
  • The present invention includes gas generant compositions that in accordance with the present invention, incorporate an additive into compositions containing BTA-1NH3 that, when added at relatively low levels, stabilizes the propellant grains when subjected to thermal cycling or thermal shock conditioning, as required for use in the automotive industry. These formulations generally contain the following:
  • A first oxidizer selected from the group including nonmetal and metal nitrate salts such as ammonium nitrate, phase-stabilized ammonium nitrate, potassium nitrate, strontium nitrate; nitrite salts such as potassium nitrite; chlorate salts such as potassium chlorate; metal and nonmetal perchlorate salts such as potassium or ammonium perchlorate; oxides such as iron oxide and copper oxide; basic nitrate salts such as basic copper nitrate and basic iron nitrate; and mixtures thereof. The first oxidizer is generally provided at about 0.1-80 wt % of the gas generant composition, and more preferably at about 10-70 wt %.
  • An optional secondary oxidizer may also be provided and selected from the oxidizers described above, and when included is generally provided at about 0.1-50 wt %, and more preferably at about 0.1-30 wt %. The total oxidizer component, that is the combined weight percent of all oxidizers, will nevertheless only range from 0.1 to 80 wt %.
  • A first or primary fuel consists of mono-ammonium salt of bis-(1(2)H-tetrazol-5-yl)-amine (BTA-1NH3) and is generally provided at about 0.1-50 weight percent or wt %, and more preferably at about 10-30 wt %.
  • An optional secondary fuel is selected from the group containing derivatives of bis-(1(2)H-tetrazol-5-yl)-amine, including its anhydrous acid and its acid monohydrate, from metal salts thereof including the potassium, sodium, strontium, copper, boron, zinc salts of BTA-1NH3, and complexes thereof; azoles such as 5-aminotetrazole; metal salts of azoles such as potassium 5-aminotetrazole; nonmetal salts of azoles such as mono-or di-ammonium salt of 5,5′-bis-1H-tetrazole; nitrate salts of azoles such as 5-aminotetrazole nitrate; nitramine derivatives of azoles such as 5-nitraminotetrazole; metal salts of nitramine derivatives of azoles such as di-potassium 5-nitraminotetrazole; nonmetal salts of nitramine derivatives of azoles such as mono- or di-ammonium 5-nitraminotetrazole and; guanidines such as dicyandiamide; salts of guanidines such as guanidine nitrate; nitro derivatives guanidines such as nitroguanidine; azoamides such as azodicarbonamide; nitrate salts of azoamides such as azodicarbonamidine dinitrate; and mixtures thereof, and when included is generally provided at about 0.149.9 wt %, more preferably 0.1-30 wt %. The total fuel component, that is the combined amount of all of the fuels of the composition, will nevertheless only range from 0.1-50 wt %, and more preferably about 0.1-30 wt %.
  • In accordance with the present invention, a first or primary additive is selected from the group of fumed metal oxides including fumed silica and fumed alumina, and mixtures thereof, and is generally provided at about 0.05-10 wt %, and more preferably at about 0.05-5 wt %.
  • All percentages for the constituents described herein are presented as weight percents of a total gas generant weight.
  • An optional second additive is selected from the group including silicon compounds including elemental silicon, silicon dioxide, and fused silica; silicones such as polydimethylsiloxane; silicates such as potassium silicates; natural minerals such as talc, mica, and clay; lubricants such as graphite powder or fibers, magnesium stearate, boron nitride, molybdenum sulfide; and mixtures thereof, and when included is generally provided at about 0.1-10%, and more preferably at about 0.1-5%.
  • An optional binder is selected from the group of cellulose derivatives such as cellulose acetate, cellulose acetate butyrate, carboxymethycellulose, salts of carboxymethylcellulose, carboxymethylcellulose acetate butyrate; silicone; polyalkene carbonates such as polypropylene carbonate and polyethylene carbonate; and mixtures thereof, and when included is generally provided at about 0.1-10%, and more preferably at about 0.1-5%.
  • All percentages for the constituents described herein are presented as weight percents of the total gas generant weight.
  • It has been determined that the addition of small amounts of fumed metal oxides, such as fumed silica (M-5 Grade provided by the Cabot Corporation), to these formulations provides a gas generant which exhibits all of the favorable properties listed above, and, more importantly, exhibits stable ballistic performance when subjected to thermal cycling or thermal shock conditioning.
  • The mono-ammonium salt of BTA-1NH3, when combined with PSAN, exhibits many favorable qualities for use in automotive passenger restraints, and therefore forms preferred gas generating compositions. BTA-1NH3 is a high energy, high-nitrogen fuel which exhibits excellent stability and very favorable levels of hygroscopicity and sensitivity. The properties of ammonium nitrate and potassium nitrate, for example, are well known throughout the propellant industry. PSAN, more specifically, exhibits no sensitivity when subjected to impact, friction, or electrostatic discharge stimuli.
  • Dry mixes of formulations containing these materials were made. The raw materials were ground together for 15 minutes in a Sweco vibratory mill. The dry material was then tableted, loaded into inflators, and subjected to desired thermal shock conditioning (100 Cycles, −40 C to 90 C). These formulations showed less than desirable ballistic performance when deployed at +85 C.
  • Next, the same process was used to make gas generants containing the above listed materials with 0.25%, 0.5%, and 0.75% M-5 Silica by weight. After the thermal shock conditioning indicated above, it was found that the ballistic stability of the gas generant increased with the amount of fumed silica, thereby providing the stability required for use in the automotive industry. Iterative analysis of various amounts of fumed silica in various compositions determined the amount of fumed silica or fumed oxide employed to assure acceptable ballistic performance. Accordingly, gas generant compositions made in accordance with the present invention exhibit many favorable characteristics for use in the auto industry, while avoiding many of the drawbacks of gas generants listed in the prior art.
  • Example 1 Silica-Free Mixtures
  • A smokeless gas generant was produced by mixing Phase-Stabilized Ammonium Nitrate (PSAN) containing 10% by weight Potassium Nitrate, with bis-(1(2)H-tetrazol-5-yl)-amine, mono-ammonium salt (BTA-1NH3). The mixture was substantially in stoichiometric balance. The components were ground dry for about 15 minutes within a Sweco Vibratory Jar Mill.
  • The resultant mixture was pressed into tablets, as is standard in the industry. The tablets were then loaded into a single-stage driver-side inflator for ballistic evaluation. Several inflators were deployed to provide baseline data while other inflators were subjected to thermal shock conditioning by varying the temperature from −40 C to 90 C in accordance with typical thermal shock cycling. Upon completion of 100 thermal shock cycles, several inflators were deployed to compare with baseline ballistics. Relative to thermal shock evaluations, inflators were deployed at temperatures of −40 C, +23 C, and +85 C. The −40 C and +23 C deployments match the baseline data fairly well, while the +85 C ballistic data indicated less than desirable ballistic behavior.
  • Example 2 High Silica Levels
  • To alleviate this problem, varying amounts of fumed silica were added to the mixture. The fumed silica was commercially available as M-5 Grade provided by Cabot Corporation. Initially, the fumed silica was added at levels between about 3-6% by mass. The stoichiometric balance of the fuel and oxidizer and processing were kept the same. The resultant gas generants were then ballistically evaluated via the same method described above. After thermal shock conditioning, no change had occurred in the ballistic performance. However, the addition of such a large amount of “inert” material detracted from or inhibited the energy of the system. Although these compositions were acceptable, the lessened energy made the formulations not as desirable.
  • Example 3 Lower Silica Levels
  • Next, the amount of fumed silica was reduced to test what level was required to pass thermal shock conditioning. Three new mixtures were made via the same processing using 0.25%, 0.5%, and 0.75% fumed silica by mass. The new mixtures were tableted and ballistically evaluated via the same method as described above.
  • 0.25% Silica (mixture 1)
  • The ballistic data for the mixture containing 0.25% silica is illustrated in FIGS. 3 and 4. The pressure was measured inside the inflator and inside a 60-L tank during deployment prior to thermal shock tests and is represented in FIG. 3. FIG. 4 illustrates the results of combusting this mixture after thermal shock testing where the ballistic performance is less than desirable. A few tablets were weighed and measured to determine density both before and after thermal shock conditioning. The crush strength was also measured for comparison. This data is shown in Table 1.
  • 0.5% silica (mixture 2)
  • The ballistic data for the mixture containing 0.5% silica can be seen in FIGS. 5 and 6. The pressure was measured inside the inflator and inside a 60-L tank during deployment prior to thermal shock tests and is represented in FIG. 5. FIG. 6 illustrates the results of combusting this mixture after thermal shock testing wherein the pressure curves indicate less than desirable ballistic performance. The pressure was measured inside the inflator and inside a 60-L tank during deployment. The data from the thermal shock inflators showed an improvement over the mixture containing 0.25% silica. A few tablets were weighed and measured to determine density both before and after thermal shock conditioning. The crush strength was also measured for comparison. This data is shown in Table 1.
  • 0.75% silica (mixture 3)
  • The ballistic data for the mixture containing 0.75% silica can be seen in FIGS. 7 and 8. The pressure was measured inside the inflator and inside a 60-L tank during deployment prior to thermal shock tests and is represented in FIG. 7. FIG. 8 illustrates the results of combusting this mixture after thermal shock testing wherein the pressure indicates consistent ballistic performance before and after thermal shock. The pressure was measured inside the inflator and inside the 60-L tank during deployment. The data from the thermal shock inflators again showed an improvement over the mixture containing 0.5% silica. Stated another way, the ballistic performance after thermal shock indicates a minimal change. A few tablets were weighed and measured to determine density both before and after thermal shock conditioning. The crush strength was also measured for comparison. This data can be seen in Table 1.
  • TABLE 1
    Physical Properties of 0.25″ OD × 0.125″ Tablets
    Propellant Density (g/cm{circumflex over ( )}3) Crush Strength (kp)
    Mixture 1
    0.25% Baseline 1.65 21.0
    0.25% Thermal Shock 1.60 18.3
    Mixture 2
    0.5% Baseline 1.65 23.2
    0.5% Thermal Shock 1.60 21.0
    Mixture 3
    0.75% Baseline 1.66 24.6
    0.75% Thermal Shock 1.61 22.9
  • The results of this experiment are counterintuitive according to the density and crush strength of the individual tablets. All three mixtures appear to be nearly identical in density and crush strength, both before and after thermal shock. Accordingly, it is not apparent that the use of fumed silica in the varying amounts would improve the ballistic properties as described. Mixture 3, however, performs significantly better than Mixture 2, which performs significantly better than Mixture 1.
  • As shown in FIG. 1, an exemplary inflator incorporates a dual chamber design to tailor the force of deployment an associated airbag. In general, an inflator containing a primary gas generant 12 formed as described herein, may be manufactured as known in the art. U.S. Pat. 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.
  • Referring now to FIG. 2, the exemplary inflator 10 described above may also be incorporated into a gas generating system or airbag system 200. 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.
  • Referring again to FIG. 2, airbag system 200 may also be incorporated into a broader, more comprehensive vehicle occupant restraint system 180 including additional elements such as a safety belt assembly 150. 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. In addition, 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, 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. U.S. Pat. Nos. 6,505,790 and 6,419,177, previously incorporated herein by reference, provide illustrative examples of pretensioners actuated in such a manner.
  • It should be appreciated that 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. Further, the compositions described above do not limit the present invention.
  • It should be understood that the preceding is merely a detailed description of various embodiments of this invention and that numerous changes to the disclosed embodiments can be made in accordance with the disclosure herein without departing from the scope of the invention. The preceding description, therefore, is not meant to limit the scope of the invention. Rather, the scope of the invention is to be determined only by the appended claims and their equivalents.

Claims (20)

1. A gas generant composition comprising:
a first oxidizer selected from metal and nonmetal nitrates; metal nitrites, metal and nonmetal perchlorates, metal oxides, basic metal nitrates, said first oxidizer provided at about 0.1 to 80% by weight of the gas generant composition;
a first fuel consisting of mono-ammonium salt of bis-(1(2) H-tetrazol-5-yl)amine, said first fuel provided at about 0.1 to 50% by weight of the gas generant composition; and
a first additive selected from fumed metal oxides and mixtures thereof, said first additive provided in amounts no greater than 10% by weight of the gas generant composition.
2. The gas generant composition of claim 1 further comprising:
a second fuel selected from derivatives of bis-(1(2) H-tetrazol-5-yl)-amine including its anhydrous acid, its acid monohydrate, metal salts, and complexes thereof; azoles, metal salts of azoles, nonmetal and metal salts of nitramine derivatives of azoles; guanidines; salts of guanidines; nitro derivatives of guanidines; azoamides; nitrate salts of azoamides, and mixtures thereof; said second fuel provided at about 0.1-49.9% by weight of the gas generant composition.
3. The gas generant composition of claim 1 further comprising:
a second additive selected from silicon, silicon dioxide, fused silicon, silicones; silicates; natural minerals including clay, mica, and talc; lubricants including graphite, magnesium stearate, boron nitride, molybdenum sulfide; and mixtures thereof, said second additive provided at about 0.1 to 10% by weight of the gas generant composition.
4. The gas generant composition of claim 1 further comprising a secondary oxidizer.
5. The gas generant composition of claim 1 further comprising a binder selected from cellulose derivatives, polyalkenes carbonates, and mixtures thereof, said binder provides at about 0.1 to 10% by weight of the gas generant composition.
6. A gas generator containing the composition of claim 1.
7. A vehicle occupant protection system containing the composition of claim 1.
8. The gas generant composition of claim 1 comprising the mono-ammonium salt of bis (1(2) H-tetrazol-5-yl)-amine at about 0.1 to 50% by weight of the gas generant composition, phase stabilized ammonium nitrate at about 0.1 to 80% by weight of the gas generant composition, and fumed silica at about 0.1 to 10% by weight of the gas generant composition.
9. The gas generant composition of claim 1 wherein said first oxidizer is selected from ammonium nitrate, phase stabilized ammonium nitrate, potassium nitrate, strontium nitrate, potassium nitrite, potassium chlorate, potassium perchlorate, ammonium perchlorate, iron oxide, copper oxide, basic copper nitrate, basic iron nitrate, and mixtures thereof.
10. The gas generant composition of claim 2 wherein said second fuel is selected from a potassium, sodium, strontium, copper, boron and zinc salt of bis-(1(2)H-tetrazol-5-yl)-amine; 5-aminotetrazole; potassium 5-aminotetrazole; mono-ammonium salt of 5,5-bis-1H-tetrazole and di-ammonium salt of 5,5-bis-1H-tetrazole; 5-aminotetrazole nitrate; nitraminotetrazole; di-potassium 5-nitraminotetrazole; mono-ammonium nitraminotetrazole and di-ammonium nitraminotetrazole; dicyandiamide; guanidine nitrate; nitroguanidine; azodicarbonamide, azodicarbonamidine di-nitrate; and mixtures thereof.
11. The gas generant composition of claim 1 wherein said fumed metal oxide is selected from at least one of fumed silica, fumed alumina, and mixtures thereof.
12. The gas generant composition of claim 1 wherein said fumed metal oxide is fumed silica provided at about 0.75% by weight of the gas generant composition.
13. A gas generant composition comprising:
a first oxidizer selected from metal and nonmetal nitrates; metal nitrites, metal and nonmetal perchlorates, metal oxides, basic metal nitrates, said first oxidizer provided at about 0.1 to 80% by weight of the gas generant composition;
a first fuel consisting of mono-ammonium salt of bis-(1(2)H-tetrazol-5-yl)amine, said first fuel provided at about 0.1 to 50% by weight of the gas generant composition; and
a first additive selected from the group consisting of fumed silica, fumed alumina, and mixtures thereof, said first additive provided at about 0.05 to 10% by weight of the gas generant composition.
14. The gas generant composition of claim 13 wherein said first additive is provided at about 0.05 to 5% by weight of the gas generant composition.
15. The gas generant composition of claim 13 wherein said first additive is provided at about 0.05 to 0.75% by weight of the gas generant composition.
16. A gas generant composition comprising:
a first oxidizer selected from metal and nonmetal nitrates; metal nitrites, metal and nonmetal perchlorates, metal oxides, basic metal nitrates, said first oxidizer provided at about 0.1 to 80% by weight of the gas generant composition;
a first fuel consisting of mono-ammonium salt of bis-(1(2)H-tetrazol-5-yl)amine, said first fuel provided at about 0.1 to 50% by weight of the gas generant composition; and
fumed silica provided in amounts no greater than 10% by weight of the gas generant composition.
17. The gas generant composition of claim 16 wherein said fumed silica is provided at about 0.05 to 0.75% by weight of the gas generant composition.
18. The gas generant composition of claim 16 wherein said fumed silica is provided at about 0.25 to 0.75% by weight of the gas generant composition.
19. The gas generant composition of claim 16 wherein said fumed silica is provided at about 0.75% by weight of the gas generant composition.
20. A vehicle occupant protection system containing the composition of claim 16.
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070169863A1 (en) * 2006-01-19 2007-07-26 Hordos Deborah L Autoignition main gas generant
US20070175553A1 (en) * 2006-01-31 2007-08-02 Burns Sean P Gas Generating composition
US20100024931A1 (en) * 2007-04-16 2010-02-04 Zevenbergen John Franciscus Pyrotechnic colour composition
US20100326575A1 (en) * 2006-01-27 2010-12-30 Miller Cory G Synthesis of 2-nitroimino-5-nitrohexahydro-1,3,5-triazine
CN102876415A (en) * 2012-10-09 2013-01-16 浙江大学 Boron-based solid fuel and preparation method thereof
CN102898262A (en) * 2011-07-27 2013-01-30 奥托里夫Asp股份有限公司 Gas generation via elemental carbon-based compositions
USRE44721E1 (en) * 2007-03-31 2014-01-21 Tk Holdings Inc. Method of making monoammonium salt of bis-(1(2)H-tetrazol-5-yl)-amine
US9556078B1 (en) 2008-04-07 2017-01-31 Tk Holdings Inc. Gas generator
CN108456126A (en) * 2017-02-20 2018-08-28 比亚迪股份有限公司 A kind of starting mix of gas generator and preparation method thereof and a kind of gas generator for automobile safety gas bag

Citations (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3785149A (en) * 1972-06-08 1974-01-15 Specialty Prod Dev Corp Method for filling a bag with water vapor and carbon dioxide gas
US3880595A (en) * 1972-06-08 1975-04-29 Hubert G Timmerman Gas generating compositions and apparatus
US3923884A (en) * 1973-04-17 1975-12-02 Mitsubishi Gas Chemical Co Process for producing DL-tartaric acid
US5035757A (en) * 1990-10-25 1991-07-30 Automotive Systems Laboratory, Inc. Azide-free gas generant composition with easily filterable combustion products
US5084118A (en) * 1990-10-23 1992-01-28 Automotive Systems Laboratory, Inc. Ignition composition for inflator gas generators
US5139588A (en) * 1990-10-23 1992-08-18 Automotive Systems Laboratory, Inc. Composition for controlling oxides of nitrogen
US5380380A (en) * 1994-02-09 1995-01-10 Automotive Systems Laboratory, Inc. Ignition compositions for inflator gas generators
US5386775A (en) * 1993-06-22 1995-02-07 Automotive Systems Laboratory, Inc. Azide-free gas generant compositions and processes
US5387296A (en) * 1991-08-23 1995-02-07 Morton International, Inc. Additive approach to ballistic and slag melting point control of azide-based gas generant compositions
US5460668A (en) * 1994-07-11 1995-10-24 Automotive Systems Laboratory, Inc. Nonazide gas generating compositions with reduced toxicity upon combustion
US5460671A (en) * 1994-04-04 1995-10-24 Automotive Systems Laboratory, Inc. Ignition compositions for inflator gas generators
US5514230A (en) * 1995-04-14 1996-05-07 Automotive Systems Laboratory, Inc. Nonazide gas generating compositions with a built-in catalyst
US5531941A (en) * 1993-08-04 1996-07-02 Automotive Systems Laboratory, Inc Process for preparing azide-free gas generant composition
US5538567A (en) * 1994-03-18 1996-07-23 Olin Corporation Gas generating propellant
US5545272A (en) * 1995-03-03 1996-08-13 Olin Corporation Thermally stable gas generating composition
US5567905A (en) * 1996-01-30 1996-10-22 Morton International, Inc. Gas generant compositions containing D 1-tartaric acid
US5756929A (en) * 1996-02-14 1998-05-26 Automotive Systems Laboratory Inc. Nonazide gas generating compositions
US5783773A (en) * 1992-04-13 1998-07-21 Automotive Systems Laboratory Inc. Low-residue azide-free gas generant composition
US5872329A (en) * 1996-11-08 1999-02-16 Automotive Systems Laboratory, Inc. Nonazide gas generant compositions
US5962808A (en) * 1997-03-05 1999-10-05 Automotive Systems Laboratory, Inc. Gas generant complex oxidizers
US6007647A (en) * 1996-08-16 1999-12-28 Automotive Systems Laboratory, Inc. Autoignition compositions for inflator gas generators
US6074502A (en) * 1996-11-08 2000-06-13 Automotive Systems Laboratory, Inc. Smokeless gas generant compositions
US6077371A (en) * 1997-02-10 2000-06-20 Automotive Systems Laboratory, Inc. Gas generants comprising transition metal nitrite complexes
US6287400B1 (en) * 1999-03-01 2001-09-11 Automotive Systems Laboratory, Inc. Gas generant composition
US6306232B1 (en) * 1996-07-29 2001-10-23 Automotive Systems Laboratory, Inc. Thermally stable nonazide automotive airbag propellants
US6475312B1 (en) * 1999-04-07 2002-11-05 Automotive Systems Laboratory, Inc. Method of formulating a gas generant composition
US6620266B1 (en) * 1999-07-02 2003-09-16 Automotive Systems Laboratory, Inc. Gas generant compositions containing a silicone coating
US20040016480A1 (en) * 2002-04-04 2004-01-29 Williams Graylon K. Nonazide gas generant compositions
US6789326B1 (en) * 2003-04-14 2004-09-14 Yin-Hai Huang Structure of handle for mini-handsaw
US20050011135A1 (en) * 2003-07-18 2005-01-20 Stageright Corporation Variable height fold and roll staging and method of assembling same
US6860951B2 (en) * 1995-03-10 2005-03-01 Talley Defense Systems, Inc. Gas generating compositions
US20050067074A1 (en) * 1994-01-19 2005-03-31 Hinshaw Jerald C. Metal complexes for use as gas generants
US20050230017A1 (en) * 2003-10-09 2005-10-20 Williams Graylon K Gas generant compositions
US20050235863A1 (en) * 2004-01-28 2005-10-27 Stevens Bruce A Auto igniting pyrotechnic booster
US20050257866A1 (en) * 2004-03-29 2005-11-24 Williams Graylon K Gas generant and manufacturing method thereof
US20050263223A1 (en) * 2004-03-30 2005-12-01 Halpin Jeffrey W Gas generating system
US20050272873A1 (en) * 2004-06-02 2005-12-08 Miller Cory G Gas generant and synthesis
US20060021340A1 (en) * 2003-04-15 2006-02-02 Volvo Construction Equipment Holding Sweden Ab System and method for controlling viscosity of a fluid and a working vehicle containing such a system
US20060022443A1 (en) * 2004-07-27 2006-02-02 Stevens Bruce A Gas generator containing a flash suppressant
US20060043716A1 (en) * 2004-08-31 2006-03-02 Quioc Eduardo L Gas generating system
US7094296B1 (en) * 1999-09-16 2006-08-22 Automotive Systems Laboratory, Inc. Gas generants containing silicone fuels
US20070034307A1 (en) * 2005-07-29 2007-02-15 Hordos Deborah L Autoignition/booster composition
US20070040167A1 (en) * 2005-06-01 2007-02-22 Miller Cory G Water-based synthesis of poly(tetrazoles) and articles formed therefrom
US20070044675A1 (en) * 2005-08-31 2007-03-01 Burns Sean P Autoignition compositions
US20070084532A1 (en) * 2005-09-30 2007-04-19 Burns Sean P Gas generant
US20070084531A1 (en) * 2005-09-29 2007-04-19 Halpin Jeffrey W Gas generant

Patent Citations (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3880595A (en) * 1972-06-08 1975-04-29 Hubert G Timmerman Gas generating compositions and apparatus
US3785149A (en) * 1972-06-08 1974-01-15 Specialty Prod Dev Corp Method for filling a bag with water vapor and carbon dioxide gas
US3923884A (en) * 1973-04-17 1975-12-02 Mitsubishi Gas Chemical Co Process for producing DL-tartaric acid
US5084118A (en) * 1990-10-23 1992-01-28 Automotive Systems Laboratory, Inc. Ignition composition for inflator gas generators
US5139588A (en) * 1990-10-23 1992-08-18 Automotive Systems Laboratory, Inc. Composition for controlling oxides of nitrogen
US5035757A (en) * 1990-10-25 1991-07-30 Automotive Systems Laboratory, Inc. Azide-free gas generant composition with easily filterable combustion products
US5387296A (en) * 1991-08-23 1995-02-07 Morton International, Inc. Additive approach to ballistic and slag melting point control of azide-based gas generant compositions
US5783773A (en) * 1992-04-13 1998-07-21 Automotive Systems Laboratory Inc. Low-residue azide-free gas generant composition
US5386775A (en) * 1993-06-22 1995-02-07 Automotive Systems Laboratory, Inc. Azide-free gas generant compositions and processes
US5531941A (en) * 1993-08-04 1996-07-02 Automotive Systems Laboratory, Inc Process for preparing azide-free gas generant composition
US20050067074A1 (en) * 1994-01-19 2005-03-31 Hinshaw Jerald C. Metal complexes for use as gas generants
US5380380A (en) * 1994-02-09 1995-01-10 Automotive Systems Laboratory, Inc. Ignition compositions for inflator gas generators
US5538567A (en) * 1994-03-18 1996-07-23 Olin Corporation Gas generating propellant
US5460671A (en) * 1994-04-04 1995-10-24 Automotive Systems Laboratory, Inc. Ignition compositions for inflator gas generators
US5460668A (en) * 1994-07-11 1995-10-24 Automotive Systems Laboratory, Inc. Nonazide gas generating compositions with reduced toxicity upon combustion
US5545272A (en) * 1995-03-03 1996-08-13 Olin Corporation Thermally stable gas generating composition
US6860951B2 (en) * 1995-03-10 2005-03-01 Talley Defense Systems, Inc. Gas generating compositions
US5514230A (en) * 1995-04-14 1996-05-07 Automotive Systems Laboratory, Inc. Nonazide gas generating compositions with a built-in catalyst
US5567905A (en) * 1996-01-30 1996-10-22 Morton International, Inc. Gas generant compositions containing D 1-tartaric acid
US5756929A (en) * 1996-02-14 1998-05-26 Automotive Systems Laboratory Inc. Nonazide gas generating compositions
US6306232B1 (en) * 1996-07-29 2001-10-23 Automotive Systems Laboratory, Inc. Thermally stable nonazide automotive airbag propellants
US6007647A (en) * 1996-08-16 1999-12-28 Automotive Systems Laboratory, Inc. Autoignition compositions for inflator gas generators
US5872329A (en) * 1996-11-08 1999-02-16 Automotive Systems Laboratory, Inc. Nonazide gas generant compositions
US6210505B1 (en) * 1996-11-08 2001-04-03 Automotive Systems Laboratory Inc High gas yield non-azide gas generants
US6074502A (en) * 1996-11-08 2000-06-13 Automotive Systems Laboratory, Inc. Smokeless gas generant compositions
US6077371A (en) * 1997-02-10 2000-06-20 Automotive Systems Laboratory, Inc. Gas generants comprising transition metal nitrite complexes
US5962808A (en) * 1997-03-05 1999-10-05 Automotive Systems Laboratory, Inc. Gas generant complex oxidizers
US6287400B1 (en) * 1999-03-01 2001-09-11 Automotive Systems Laboratory, Inc. Gas generant composition
US6475312B1 (en) * 1999-04-07 2002-11-05 Automotive Systems Laboratory, Inc. Method of formulating a gas generant composition
US6620266B1 (en) * 1999-07-02 2003-09-16 Automotive Systems Laboratory, Inc. Gas generant compositions containing a silicone coating
US7094296B1 (en) * 1999-09-16 2006-08-22 Automotive Systems Laboratory, Inc. Gas generants containing silicone fuels
US20040016480A1 (en) * 2002-04-04 2004-01-29 Williams Graylon K. Nonazide gas generant compositions
US6789326B1 (en) * 2003-04-14 2004-09-14 Yin-Hai Huang Structure of handle for mini-handsaw
US20060021340A1 (en) * 2003-04-15 2006-02-02 Volvo Construction Equipment Holding Sweden Ab System and method for controlling viscosity of a fluid and a working vehicle containing such a system
US20050011135A1 (en) * 2003-07-18 2005-01-20 Stageright Corporation Variable height fold and roll staging and method of assembling same
US20050230017A1 (en) * 2003-10-09 2005-10-20 Williams Graylon K Gas generant compositions
US20050235863A1 (en) * 2004-01-28 2005-10-27 Stevens Bruce A Auto igniting pyrotechnic booster
US20050257866A1 (en) * 2004-03-29 2005-11-24 Williams Graylon K Gas generant and manufacturing method thereof
US20050263223A1 (en) * 2004-03-30 2005-12-01 Halpin Jeffrey W Gas generating system
US20050272873A1 (en) * 2004-06-02 2005-12-08 Miller Cory G Gas generant and synthesis
US20060022443A1 (en) * 2004-07-27 2006-02-02 Stevens Bruce A Gas generator containing a flash suppressant
US20060043716A1 (en) * 2004-08-31 2006-03-02 Quioc Eduardo L Gas generating system
US20070040167A1 (en) * 2005-06-01 2007-02-22 Miller Cory G Water-based synthesis of poly(tetrazoles) and articles formed therefrom
US20070034307A1 (en) * 2005-07-29 2007-02-15 Hordos Deborah L Autoignition/booster composition
US20070044675A1 (en) * 2005-08-31 2007-03-01 Burns Sean P Autoignition compositions
US20070084531A1 (en) * 2005-09-29 2007-04-19 Halpin Jeffrey W Gas generant
US20070084532A1 (en) * 2005-09-30 2007-04-19 Burns Sean P Gas generant

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US20070175553A1 (en) * 2006-01-31 2007-08-02 Burns Sean P Gas Generating composition
US7959749B2 (en) 2006-01-31 2011-06-14 Tk Holdings, Inc. Gas generating composition
USRE44721E1 (en) * 2007-03-31 2014-01-21 Tk Holdings Inc. Method of making monoammonium salt of bis-(1(2)H-tetrazol-5-yl)-amine
US20100024931A1 (en) * 2007-04-16 2010-02-04 Zevenbergen John Franciscus Pyrotechnic colour composition
US8142581B2 (en) * 2007-04-16 2012-03-27 Clearspark, Llc Pyrotechnic colour composition
US9556078B1 (en) 2008-04-07 2017-01-31 Tk Holdings Inc. Gas generator
CN102898262A (en) * 2011-07-27 2013-01-30 奥托里夫Asp股份有限公司 Gas generation via elemental carbon-based compositions
CN102876415A (en) * 2012-10-09 2013-01-16 浙江大学 Boron-based solid fuel and preparation method thereof
CN108456126A (en) * 2017-02-20 2018-08-28 比亚迪股份有限公司 A kind of starting mix of gas generator and preparation method thereof and a kind of gas generator for automobile safety gas bag

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